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Sample records for biomimetic nanoparticles preparation

  1. Biomimetic nanoparticles: preparation, characterization and biomedical applications

    Directory of Open Access Journals (Sweden)

    Ana Maria Carmona-Ribeiro

    2010-04-01

    Full Text Available Ana Maria Carmona-RibeiroBiocolloids Lab, Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo, BrazilAbstract: Mimicking nature is a powerful approach for developing novel lipid-based devices for drug and vaccine delivery. In this review, biomimetic assemblies based on natural or synthetic lipids by themselves or associated to silica, latex or drug particles will be discussed. In water, self-assembly of lipid molecules into supramolecular structures is fairly well understood. However, their self-assembly on a solid surface or at an interface remains poorly understood. In certain cases, hydrophobic drug granules can be dispersed in aqueous solution via lipid adsorption surrounding the drug particles as nanocapsules. In other instances, hydrophobic drug molecules attach as monomers to borders of lipid bilayer fragments providing drug formulations that are effective in vivo at low drug-to-lipid-molar ratio. Cationic biomimetic particles offer suitable interfacial environment for adsorption, presentation and targeting of biomolecules in vivo. Thereby antigens can effectively be presented by tailored biomimetic particles for development of vaccines over a range of defined and controllable particle sizes. Biomolecular recognition between receptor and ligand can be reconstituted by means of receptor immobilization into supported lipidic bilayers allowing isolation and characterization of signal transduction steps.Keywords: cationic lipid, phospholipids, bilayer fragments, vesicles, silica, polymeric particles, antigens, novel cationic immunoadjuvants, drugs

  2. Biomimetic Preparation and Dual-Color Bioimaging of Fluorescent Silicon Nanoparticles.

    Science.gov (United States)

    Wu, Sicong; Zhong, Yiling; Zhou, Yanfeng; Song, Bin; Chu, Binbin; Ji, Xiaoyuan; Wu, Yanyan; Su, Yuanyuan; He, Yao

    2015-11-25

    Fluorescent silicon nanoparticles (SiNPs), as the most important zero-dimensional silicon nanostructures, hold high promise for long-awaited silicon-based optic applications. There currently remain major challenges for the green, inexpensive, and mass production of fluorescent SiNPs, resulting in difficulties in sufficiently exploiting the properties of these remarkable materials. Here, we show that fluorescent small-sized (∼3.8 nm) SiNPs can be produced through biomimetic synthesis in rapid (10 min), low-cost, and environmentally benign manners. The as-prepared SiNPs simultaneously feature bright fluorescence (quantum yield (QY), ∼15-20%), narrow emission spectral width (full width at half-maximum (fwhm), ∼30 nm), and nontoxicity, making them as high-quality fluorescent probes for biological imaging in vitro and in vivo.

  3. Biomimetic magnetic nanoparticles

    Directory of Open Access Journals (Sweden)

    Michael T. Klem

    2005-09-01

    Full Text Available Magnetic nanoparticles are of considerable interest because of their potential use in high-density memory devices, spintronics, and applications in diagnostic medicine. The conditions for synthesis of these materials are often complicated by their high reaction temperatures, costly reagents, and post-processing requirements. Practical applications of magnetic nanoparticles will require the development of alternate synthetic strategies that can overcome these impediments. Biomimetic approaches to materials chemistry have provided a new avenue for the synthesis and assembly of magnetic nanomaterials that has great potential for overcoming these obstacles.

  4. Plasmonic nanoparticles tuned thermal sensitive photonic polymer for biomimetic chameleon

    Science.gov (United States)

    Yan, Yang; Liu, Lin; Cai, Zihe; Xu, Jiwen; Xu, Zhou; Zhang, Di; Hu, Xiaobin

    2016-08-01

    Among many thermo-photochromic materials, the color-changing behavior caused by temperature and light is usually lack of a full color response. And the study on visible light-stimuli chromic response is rarely reported. Here, we proposed a strategy to design a thermo-photochromic chameleon biomimetic material consisting of photonic poly(N-isopropylacrylamide-co-methacrylic acid) copolymer and plasmonic nanoparticles which has a vivid color change triggered by temperature and light like chameleons. We make use of the plasmonic nanoparticles like gold nanoparticles and silver nanoparticles to increase the sensitivity of the responsive behavior and control the lower critical solution temperature of the thermosensitive films by tuning the polymer chain conformation transition. Finally, it is possible that this film would have colorimetric responses to the entire VIS spectrum by the addition of different plasmonic nanoparticles to tune the plasmonic excitation wavelength. As a result, this method provides a potential use in new biosensors, military and many other aspects.

  5. Gambogic acid-loaded biomimetic nanoparticles in colorectal cancer treatment

    Science.gov (United States)

    Zhang, Zhen; Qian, Hanqing; Yang, Mi; Li, Rutian; Hu, Jing; Li, Li; Yu, Lixia; Liu, Baorui; Qian, Xiaoping

    2017-01-01

    Gambogic acid (GA) is expected to be a potential new antitumor drug, but its poor aqueous solubility and inevitable side effects limit its clinical application. Despite these inhe rent defects, various nanocarriers can be used to promote the solubility and tumor targeting of GA, improving antitumor efficiency. In addition, a cell membrane-coated nanoparticle platform that was reported recently, unites the customizability and flexibility of a synthetic copolymer, as well as the functionality and complexity of natural membrane, and is a new synthetic biomimetic nanocarrier with improved stability and biocompatibility. Here, we combined poly(lactic-co-glycolic acid) (PLGA) with red blood-cell membrane (RBCm), and evaluated whether GA-loaded RBCm nanoparticles can retain and improve the antitumor efficacy of GA with relatively lower toxicity in colorectal cancer treatment compared with free GA. We also confirmed the stability, biocompatibility, passive targeting, and few side effects of RBCm-GA/PLGA nanoparticles. We expect to provide a new drug carrier in the treatment of colorectal cancer, which has strong clinical application prospects. In addition, the potential antitumor drug GA and other similar drugs could achieve broader clinical applications via this biomimetic nanocarrier.

  6. Preparation of biomimetic photoresponsive polymer springs.

    Science.gov (United States)

    Iamsaard, Supitchaya; Villemin, Elise; Lancia, Federico; Aβhoff, Sarah-Jane; Fletcher, Stephen P; Katsonis, Nathalie

    2016-10-01

    Polymer springs that twist under irradiation with light, in a manner that mimics how plant tendrils twist and turn under the effect of differential expansion in different sections of the plant, show potential for soft robotics and the development of artificial muscles. The soft springs prepared using this protocol are typically 1 mm wide, 50 μm thick and up to 10 cm long. They are made from liquid crystal polymer networks in which an azobenzene derivative is introduced covalently as a molecular photo-switch. The polymer network is prepared by irradiation of a twist cell filled with a mixture of shape-persistent liquid crystals, liquid crystals having reactive end groups, molecular photo-switches, some chiral dopant and a small amount of photoinitiator. After postcuring, the soft polymer film is removed and cut into springs, the geometry of which is determined by the angle of cut. The material composing the springs is characterized by optical microscopy, scanning electron microscopy and tensile strength measurements. The springs operate at ambient temperature, by mimicking the orthogonal contraction mechanism that is at the origin of plant coiling. They shape-shift under irradiation with UV light and can be pre-programmed to either wind or unwind, as encoded in their geometry. Once illumination is stopped, the springs return to their initial shape. Irradiation with visible light accelerates the shape reversion.

  7. Biomimetic synthesis of highly biocompatible gold nanoparticles with amino acid-dithiocarbamate as a precursor for SERS imaging

    Science.gov (United States)

    Li, Li; Liu, Jianbo; Yang, Xiaohai; Huang, Jin; He, Dinggeng; Guo, Xi; Wan, Lan; He, Xiaoxiao; Wang, Kemin

    2016-03-01

    Amino acid-dithiocarbamate (amino acid-DTC) was developed as both the reductant and ligand stabilizer for biomimetic synthesis of gold nanoparticles (AuNPs), which served as an excellent surface-enhanced Raman scattering (SERS) contrast nanoprobe for cell imaging. Glycine (Gly), glutamic acid (Glu), and histidine (His) with different isoelectric points were chosen as representative amino acid candidates to synthesize corresponding amino acid-DTC compounds through mixing with carbon disulfide (CS2), respectively. The pyrogenic decomposition of amino acid-DTC initiated the reduction synthesis of AuNPs, and the strong coordinating dithiocarbamate group of amino acid-DTC served as a stabilizer that grafted onto the surface of the AuNPs, which rendered the as-prepared nanoparticles a negative surface charge and high colloidal stability. MTT cell viability assay demonstrated that the biomimetic AuNPs possessed neglectful toxicity to the human hepatoma cell, which guaranteed them good biocompatibility for biomedical application. Meanwhile, the biomimetic AuNPs showed a strong SERS effect with an enhancement factor of 9.8 × 105 for the sensing of Rhodamine 6G, and two distinct Raman peaks located at 1363 and 1509 cm-1 could be clearly observed in the cell-imaging experiments. Therefore, biomimetic AuNPs can be explored as an excellent SERS contrast nanoprobe for biomedical imaging, and the amino acid-DTC mediated synthesis of the AuNPs has a great potential in bio-engineering and biomedical imaging applications.

  8. Biomimetics

    Indian Academy of Sciences (India)

    P Ramachandra Rao

    2003-06-01

    The well-organised multifunctional structures, systems and biogenic materials found in nature have attracted the interest of scientists working in many disciplines. The efforts have resulted in the development of a new and rapidly growing field of scientific effort called biomimetics. In this article we present a few natural materials and systems and explore how ideas from nature are being interpreted and modified to suit efforts aimed at designing better machines and synthesising newer materials.

  9. Preparation, anti-biofouling and drag-reduction properties of a biomimetic shark skin surface

    Directory of Open Access Journals (Sweden)

    Xia Pu

    2016-04-01

    Full Text Available Shark skin surfaces show non-smoothness characteristics due to the presence of a riblet structure. In this study, biomimetic shark skin was prepared by using the polydimethylsiloxane (PDMS-embedded elastomeric stamping (PEES method. Scanning electron microscopy (SEM was used to examine the surface microstructure and fine structure of shark skin and biomimetic shark skin. To analyse the hydrophobic mechanism of the shark skin surface microstructure, the effect of biomimetic shark skin surface microstructure on surface wettability was evaluated by recording water contact angle. Additionally, protein adhesion experiments and anti-algae adhesion performance testing experiments were used to investigate and evaluate the anti-biofouling properties of the surface microstructure of biomimetic shark skin. The recorded values of the water contact angle of differently microstructured surfaces revealed that specific microstructures have certain effects on surface wettability. The anti-biofouling properties of the biomimetic shark skin surface with microstructures were superior to a smooth surface using the same polymers as substrates. Moreover, the air layer fixed on the surface of the biomimetic shark skin was found to play a key role in their antibiont adhesion property. An experiment into drag reduction was also conducted. Based on the experimental results, the microstructured surface of the prepared biomimetic shark skin played a significant role in reducing drag. The maximum of drag reduction rate is 12.5%, which is higher than the corresponding maximum drag reduction rate of membrane material with a smooth surface.

  10. Biomimetic Mussel Adhesive Inspired Clickable Anchors Applied to the Functionalization of Fe3O4 Nanoparticles

    NARCIS (Netherlands)

    Goldmann, Anja S.; Schoedel, Christine; Walther, Andreas; Yuan, Jiayin; Loos, Katja; Mueller, Axel H. E.; Müller, Axel H.E.

    2010-01-01

    The functionalization of magnetite (Fe3O4) nanoparticles with dopamine-derived clickable biomimetic anchors is reported. Herein, an alkyne-modified catechol-derivative is employed as the anchor, as i) the catechol-functional anchor groups possess irreversible covalent binding affinity to Fe3O4 nanop

  11. Characterization of antiseptic apatite powders prepared at biomimetics temperature and pH

    Directory of Open Access Journals (Sweden)

    Soumia Belouafa

    2008-03-01

    Full Text Available Antiseptic apatite-based calcium phosphates were prepared as the single-phase powders. Phosphocalcic oxygenated apatites were synthesized from calcium salts and orthophosphate dissolved in oxygenated water solution at 30%, under the biomimetic conditions of 37 °C and pH 7.4. The characterization and chemical analysis of the synthesized biomimetic apatite powders were performed by scanning electron microscopy (SEM, powder X ray diffraction (XRD, Fourier-transformed infrared spectroscopy (FT-IR and chemical analysis. The obtained materials are a calcium deficient apatites with different morphologies.

  12. Preparation of microcellular composites with biomimetic structure via supercritical fluid technology

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    A new microcellular composite material with a biomimetic structure has been prepared via the supercritical fluid (SCF) technology. The resultant material has a clear biomimetic structure like bamboo and wood. The skin region is enriched with oriented high-strength thermotropic liquid crystal polymer fibrils, while the core region with polystyrene (PS) micro-cells. The diameter and density of micro- cells can be controlled by the processing parameters such as temperature and pressure. And the skin thickness can be controlled conveniently by varying the composition of polystyrene and liquid crystal polymer.

  13. Preparation of biomimetic hydrophobic coatings on AZ91D magnesium alloy surface

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The hydrophobic coating has been a promising technology for improving surface performance. The surface performance of magnesium alloy has been limited in application. Furthermore, the hydrophobic of magnesium alloy is rarely investigated because magnesium alloy is an active metal alloy. In this paper, inspired by microstructure character of typical plant leaf surface such as lotus, the biomimetic hydrophobic coatings on AZ91D magnesium alloy surface were prepared by means of wet-chemical combining electroless. The samples were immersed into AgNO3 solution in wet-chemical method firstly. Then, biomimetic hydrophobic coatings were prepared by electroless after wet-method pretreatment. The microstructure was observed by SEM and the contact angles were measured by contact angle tester. The results indicated that the biomimetic hydrophobic coatings with uniform crystalline and dense structure could be obtained on AZ91D magnesium alloy surface. The results of contact angle revealed that the biomimetic nano-composite coatings were hydrophobic. The wet-chemical method treatment on the AZ91D magnesium alloy substrate provided a rough microstructure, thus improving adhesion of the coating and the substrate.

  14. Biomimetic Hierarchical Assembly of Helical Supraparticles from Chiral Nanoparticles.

    Science.gov (United States)

    Zhou, Yunlong; Marson, Ryan L; van Anders, Greg; Zhu, Jian; Ma, Guanxiang; Ercius, Peter; Sun, Kai; Yeom, Bongjun; Glotzer, Sharon C; Kotov, Nicholas A

    2016-03-22

    Chiroptical materials found in butterflies, beetles, stomatopod crustaceans, and other creatures are attributed to biocomposites with helical motifs and multiscale hierarchical organization. These structurally sophisticated materials self-assemble from primitive nanoscale building blocks, a process that is simpler and more energy efficient than many top-down methods currently used to produce similarly sized three-dimensional materials. Here, we report that molecular-scale chirality of a CdTe nanoparticle surface can be translated to nanoscale helical assemblies, leading to chiroptical activity in the visible electromagnetic range. Chiral CdTe nanoparticles coated with cysteine self-organize around Te cores to produce helical supraparticles. D-/L-Form of the amino acid determines the dominant left/right helicity of the supraparticles. Coarse-grained molecular dynamics simulations with a helical pair-potential confirm the assembly mechanism and the origin of its enantioselectivity, providing a framework for engineering three-dimensional chiral materials by self-assembly. The helical supraparticles further self-organize into lamellar crystals with liquid crystalline order, demonstrating the possibility of hierarchical organization and with multiple structural motifs and length scales determined by molecular-scale asymmetry of nanoparticle interactions.

  15. Preparation methods of alginate nanoparticles

    NARCIS (Netherlands)

    Paques, J.P.; Linden, van der E.; Rijn, van C.J.M.; Sagis, L.M.C.

    2014-01-01

    This article reviews available methods for the formation of alginate nano-aggregates, nanocapsules and nanospheres. Primarily, alginate nanoparticles are being prepared by two methods. In the “complexation method”, complex formation on the interface of an oil droplet is used to form alginate nanocap

  16. Tuning mechanical properties of polymer-grafted nanoparticle networks by using biomimetic catch bonds

    Science.gov (United States)

    Mbanga, Badel L.; Iyer, Balaji V. S.; Yashin, Victor V.; Balazs, Anna C.

    Cross-linked networks of polymer-grafted nanoparticles (PGNs) constitute a class of composites with tunable mechanical properties that exhibit a self-healing behavior. A PGN network consists of nanoparticles that are decorated with end-grafted polymer chains. Reactive groups on the free ends of these grafted chains can form bonds with the chain ends on the nearby particles. We study these materials using a 3D computational model that encompasses the particle-particle interactions, the kinetics of bond formation and rupture, and the external forces applied to the network. In our model, a fraction of cross-links is formed through biomimetic ``catch'' bonds. In contrast to conventional ``slip'' bonds, catch bonds can effectively become stronger under a deformation. We show that by varying the fraction of these catch bonds in the network, the toughness, ductility, and tensile strength of the material could be tuned to desired levels.

  17. Preparation of biomimetic nano-structured films with multi-scale roughness

    Science.gov (United States)

    Shelemin, A.; Nikitin, D.; Choukourov, A.; Kylián, O.; Kousal, J.; Khalakhan, I.; Melnichuk, I.; Slavínská, D.; Biederman, H.

    2016-06-01

    Biomimetic nano-structured films are valuable materials in various applications. In this study we introduce a fully vacuum-based approach for fabrication of such films. The method combines deposition of nanoparticles (NPs) by gas aggregation source and deposition of overcoat thin film that fixes the nanoparticles on a surface. This leads to the formation of nanorough surfaces which, depending on the chemical nature of the overcoat, may range from superhydrophilic to superhydrophobic. In addition, it is shown that by proper adjustment of the amount of NPs it is possible to tailor adhesive force on superhydrophobic surfaces. Finally, the possibility to produce NPs in a wide range of their size (45-240 nm in this study) makes it possible to produce surfaces not only with single scale roughness, but also with bi-modal or even multi-modal character. Such surfaces were found to be superhydrophobic with negligible water contact angle hysteresis and hence truly slippery.

  18. Process variables in biomimetic synthesis of silver nanoparticles by aqueous extract of Azadirachta indica (Neem) leaves

    Energy Technology Data Exchange (ETDEWEB)

    Tripathy, A. [VIT University, School of Biotechnology, Chemical and Biomedical Engineering (India); Raichur, Ashok M. [Indian Institute of Science, Department of Materials Engineering (India); Chandrasekaran, N.; Prathna, T. C.; Mukherjee, Amitava, E-mail: amit.mookerjea@gmail.co [VIT University, School of Biotechnology, Chemical and Biomedical Engineering (India)

    2010-01-15

    Owing to widespread applications, synthesis and characterization of silver nanoparticles is recently attracting considerable attention. Increasing environmental concerns over chemical synthesis routes have resulted in attempts to develop biomimetic approaches. One of them is synthesis using plant parts, which eliminates the elaborate process of maintaining the microbial culture and often found to be kinetically favourable than other bioprocesses. The present study deals with investigating the effect of process variables like reductant concentrations, reaction pH, mixing ratio of the reactants and interaction time on the morphology and size of silver nanoparticles synthesized using aqueous extract of Azadirachta indica (Neem) leaves. The formation of crystalline silver nanoparticles was confirmed using X-ray diffraction analysis. By means of UV spectroscopy, Scanning and Transmission Electron Microscopy techniques, it was observed that the morphology and size of the nanoparticles were strongly dependent on the process parameters. Within 4 h interaction period, nanoparticles below 20-nm-size with nearly spherical shape were produced. On increasing interaction time (ageing) to 66 days, both aggregation and shape anisotropy (ellipsoidal, polyhedral and capsular) of the particles increased. In alkaline pH range, the stability of cluster distribution increased with a declined tendency for aggregation of the particles. It can be inferred from the study that fine tuning the bioprocess parameters will enhance possibilities of desired nano-product tailor made for particular applications.

  19. Perylene Nanoparticles Prepared by Reprecipitation Method

    Institute of Scientific and Technical Information of China (English)

    JI,Xue-Hai(纪学海); FU,Hong-Bing(付红兵); XIE,Rui-Min(谢锐敏); XIAO,De-Bao(肖德宝); YAO,Jian-Nian(姚建年)

    2002-01-01

    Perylene nanoparticles with different sizes were prepared by reprecipitation method. It is found that the nanoparticles show size-dependent optical property. Electron diffraction patterns indicate that all the nanoparticles of different sizes are in crystalline state. The rapid growth of the nanoparticles during the agingg process could be slowed down effectively by the addition of cationic or anionic surfactants.

  20. Biomimetic nanoparticles with polynucleotide and PEG mixed-monolayers enhance calcium phosphate mineralization

    Energy Technology Data Exchange (ETDEWEB)

    Vasconcellos, Kayla B.; McHugh, Sean M.; Dapsis, Katherine J.; Petty, Alexander R.; Gerdon, Aren E., E-mail: gerdoar@emmanuel.edu [Emmanuel College (United States)

    2013-09-15

    Biomineralization of hydroxyapatite (Ca{sub 10}(PO{sub 4}){sub 6}(OH){sub 2}) is of significant importance in biomedical applications such as bone and dental repair, and biomimetic control of mineral formation may lead to more effective restorative procedures. Gold nanoparticles are functional scaffolds on which to assemble multi-component monolayers capable of mimicking protein activity in the templated synthesis of calcium phosphate. The goal of this research was to explore nanoparticle templates with mixed-monolayers of uncharged polar polyethylene glycol (PEG) molecules and highly charged polynucleotide and amino acid molecules in their ability to influence mineralization rates and mineral particle size and morphology. This research demonstrates through time-resolved optical density and dynamic light scattering measurements that the combination of tiopronin, PEG, and DNA presented on a nanoparticle surface decreases nanoparticle aggregation from 59 to 21 nm solvated radius, increases mineralization kinetics from 1.5 Multiplication-Sign 10{sup -3} to 3.1 Multiplication-Sign 10{sup -3} OD/min, and decreases mineral particle size from 685 to 442 nm average radius. FT-IR and TEM data demonstrate that mineralized material, while initially amorphous, transforms to a semi-crystalline material when guided by template interactions. This demonstrates that surface-tailored monolayer protected cluster scaffolds are successful and controllable mineralization templates with further potential for biomedical applications involving calcium phosphate and other biomaterials.

  1. Biomimetic nanoparticles with polynucleotide and PEG mixed-monolayers enhance calcium phosphate mineralization

    Science.gov (United States)

    Vasconcellos, Kayla B.; McHugh, Sean M.; Dapsis, Katherine J.; Petty, Alexander R.; Gerdon, Aren E.

    2013-09-01

    Biomineralization of hydroxyapatite (Ca10(PO4)6(OH)2) is of significant importance in biomedical applications such as bone and dental repair, and biomimetic control of mineral formation may lead to more effective restorative procedures. Gold nanoparticles are functional scaffolds on which to assemble multi-component monolayers capable of mimicking protein activity in the templated synthesis of calcium phosphate. The goal of this research was to explore nanoparticle templates with mixed-monolayers of uncharged polar polyethylene glycol (PEG) molecules and highly charged polynucleotide and amino acid molecules in their ability to influence mineralization rates and mineral particle size and morphology. This research demonstrates through time-resolved optical density and dynamic light scattering measurements that the combination of tiopronin, PEG, and DNA presented on a nanoparticle surface decreases nanoparticle aggregation from 59 to 21 nm solvated radius, increases mineralization kinetics from 1.5 × 10-3 to 3.1 × 10-3 OD/min, and decreases mineral particle size from 685 to 442 nm average radius. FT-IR and TEM data demonstrate that mineralized material, while initially amorphous, transforms to a semi-crystalline material when guided by template interactions. This demonstrates that surface-tailored monolayer protected cluster scaffolds are successful and controllable mineralization templates with further potential for biomedical applications involving calcium phosphate and other biomaterials.

  2. PREPARATION OF POLYALKYLCYANOACRYLATE NANOPARTICLES WITH VARIOUS MORPHOLOGIES

    Institute of Scientific and Technical Information of China (English)

    Qing-lin Xu; He-xian Li; Guo-chang Wang

    2011-01-01

    The effects of various reaction conditions on the preparation of polyalkylcyanoacrylate (PACA) nanoparticles are studied. The PACA nanoparticles with different crosslinking degrees and morphology are prepared. Addition of crosslinkers can not only adjust the particle size, but also change the morphology of PACA nanoparticles. Moreover, the loose network structure of the PACA nanoparticles with “core/shell-like” morphology is investigated by AFM and TEM in detail.

  3. Nanomedicine: Interaction of biomimetic apatite colloidal nanoparticles with human blood components.

    Science.gov (United States)

    Choimet, Maëla; Hyoung-Mi, Kim; Jae-Min, Oh; Tourrette, Audrey; Drouet, Christophe

    2016-09-01

    This contribution investigates the interaction of two types of biomimetic-apatite colloidal nanoparticles (negatively-charged 47nm, and positively-charged 190nm NPs) with blood components, namely red blood cells (RBC) and plasma proteins, with the view to inspect their hemocompatibility. The NPs, preliminarily characterized by XRD, FTIR and DLS, showed low hemolysis ratio (typically lower than 5%) illustrating the high compatibility of such NPs with respect to RBC, even at high concentration (up to 10mg/ml). The presence of glucose as water-soluble matrix for freeze-dried and re-dispersed colloids led to slightly increased hemolysis as compared to glucose-free formulations. NPs/plasma protein interaction was then followed, via non-specific protein fluorescence quenching assays, by contact with whole human blood plasma. The amount of plasma proteins in interaction with the NPs was evaluated experimentally, and the data were fitted with the Hill plot and Stern-Volmer models. In all cases, binding constants of the order of 10(1)-10(2) were found. These values, significantly lower than those reported for other types of nanoparticles or molecular interactions, illustrate the fairly inert character of these colloidal NPs with respect to plasma proteins, which is desirable for circulating injectable suspensions. Results were discussed in relation with particle surface charge and mean particle hydrodynamic diameter (HD). On the basis of these hemocompatibility data, this study significantly complements previous results relative to the development and nontoxicity of biomimetic-apatite-based colloids stabilized by non-drug biocompatible organic molecules, intended for use in nanomedicine.

  4. Chitosan-mediated formation of biomimetic silica nanoparticles: an effective method for manganese peroxidase immobilization and stabilization.

    Science.gov (United States)

    Luan, Pan-Pan; Jiang, Yan-Jun; Zhang, Song-Ping; Gao, Jing; Su, Zhi-Guo; Ma, Guang-Hui; Zhang, Yu-Fei

    2014-11-01

    Our work here, for the first time, reported the use of chitosan-mediated biomimetic silica nanoparticles in enzyme immobilization. In order to make clear the relationship among silicification process, silica nanoparticle structure and immobilized enzyme activity, a mechanism of chitosan-mediated silicification using sodium silicate as the silica source was primarily evaluated. Chitosan was demonstrated effectively to promote the silicification not only in accelerating the aggregation rate of sodium silicate, but also in templating the formation of silica nanoparticles. Although the whole biomimetic silicification process contained polycondensation-aggregation-precipitation three stages, the elemental unit in precipitated silica was confirmed to be nanoparticles with 100 nm diameter regardless of the chitosan and silicate concentration used. Furthermore, the effect of enzyme on silicification process was also investigated. The introducing of manganese peroxidase (MnP) to silica precursor solution had no obvious effect on the silicification rate and nanoparticle morphology. The residual activity and embedding rate of immobilized MnP were 64.2% and 36.4% respectively under the optimum conditions. In addition, compared to native MnP, the MnP embedded in chitosan/silica nanoparticles exhibited improved stability against organic solvent and ultrasonic wave. After ultrasonic treatment for 20 min, 77% of the initial activity was remained due to the protective effect of chitosan/silica nanoparticles, while native MnP lost almost all of its original activity.

  5. WO3/Pt nanoparticles are NADPH oxidase biomimetics that mimic effector cells in vitro and in vivo.

    Science.gov (United States)

    Clark, Andrea J; Coury, Emma L; Meilhac, Alexandra M; Petty, Howard R

    2016-02-12

    To provide a means of delivering an artificial immune effector cell-like attack on tumor cells, we report the tumoricidal ability of inorganic WO3/Pt nanoparticles that mimic a leukocyte's functional abilities. These nanoparticles route electrons from organic structures and electron carriers to form hydroxyl radicals within tumor cells. During visible light exposure, WO3/Pt nanoparticles manufacture hydroxyl radicals, degrade organic compounds, use NADPH, trigger lipid peroxidation, promote lysosomal membrane disruption, promote the loss of reduced glutathione, and activate apoptosis. In a model of advanced breast cancer metastasis to the eye's anterior chamber, we show that WO3/Pt nanoparticles prolong the survival of 4T1 tumor-bearing Balb/c mice. This new generation of inorganic photosensitizers do not photobleach, and therefore should provide an important therapeutic advance in photodynamic therapy. As biomimetic nanoparticles destroy targeted cells, they may be useful in treating ocular and other forms of cancer.

  6. Investigation of biomimetic shear stress on cellular uptake and mechanism of polystyrene nanoparticles in various cancer cell lines.

    Science.gov (United States)

    Kang, Taehee; Park, Chulhun; Lee, Beom-Jin

    2016-12-01

    Cancer cells in the tumor microenvironment are affected by fluid shear stress generated by blood flow in the vascular microenvironment and interstitial flows in the tumor microenvironment. Thus, we investigated how fluidic shear stress affects cellular uptake as well as the endocytosis mechanism of nanoparticles using a biomimetic microfluidic system that mimics the human dynamic environment. Positively charged amino-modified polystyrene nanoparticles (PSNs) at 100 μg/mL were delivered to cancer cells under static and biomimetic dynamic conditions (0.5 dyne/cm(2)). Additionally, the experiment was done in the presence of endocytosis inhibitors specific for one of the endocytosis pathways. To evaluate cellular uptake of cationic PSNs, the fluorescence intensity of cationic PSNs in cancer cells was measured by flow cytometer and fluorescence images were taken using confocal laser scanning microscopy. Cancer cells in dynamic conditions exhibited higher cellular uptake of PSNs and showed different cellular uptake mechanisms compared with those in static conditions. From these results, it suggested that biomimetic dynamic conditions stimulated specific endocytosis and prompted cellular uptake. It was also important to consider fluidic shear stress as one of the critical factors because cellular uptake and drug delivery could play a key role in cancer cells and metastasis.

  7. Studies on the biomimetic membrane interaction between liposome and realsar nanoparticles

    Institute of Scientific and Technical Information of China (English)

    SHEN XingCan; JIN Tao; XIE Jun; LIANG Hong; YAN Yu

    2009-01-01

    Chemical Engineering,Guangxi Normal University,Guilin 541004,ChinaThe liposome of small unilamellar vesicles (SUV) made from phosphatidylcholine-cholesterol mixtures was used as a simple model for biomimetic membranes.The studies on the interaction between the liposome and realgar nanoparticles (NPs) demonstrate that the phospholipid is one of the key targeted molecules of realgar NPs,used by surface plasmon resonance (SPR) technology,fluorescence polarization,Raman spectroscopy,nuclear magnetic resonance (NMR) and atom force microscope (AFM).It was observed that the relative viscosity (ηr) of the membrane increased and the membrane fluidity decreased as realgar NPs bound to SUV.Calculations of Raman intensity ratios detected the increase of longitudinal order parameters (Strans) and lateral order parameters (Stat) of the lipid bilayer,indicating a rise in the proportion of trans conformations of alkyl chains,and the decrease of membrane's fluidity attributed to the interaction of realgar NPs.Results of Raman spectra and 31p NMR suggest that the polar headgroup of phospholipid is the interacted target site of realgar NPs.Moreover,time-lapse AFM images show that realgar NPs compromise the phospholipid membrane integrity to result in the formation of "pore" or "hole".

  8. Studies on the biomimetic membrane interaction between liposome and realgar nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The liposome of small unilamellar vesicles (SUV) made from phosphatidylcholine-cholesterol mixtures was used as a simple model for biomimetic membranes. The studies on the interaction between the liposome and realgar nanoparticles (NPs) demonstrate that the phospholipid is one of the key targeted molecules of realgar NPs, used by surface plasmon resonance (SPR) technology, fluorescence polarization, Raman spectroscopy, nuclear magnetic resonance (NMR) and atom force microscope (AFM). It was observed that the relative viscosity (ηr) of the membrane increased and the membrane fluidity decreased as realgar NPs bound to SUV. Calculations of Raman intensity ratios detected the increase of longitudinal order parameters (Strans) and lateral order parameters (Slat) of the lipid bilayer, indicating a rise in the proportion of trans conformations of alkyl chains, and the decrease of membrane’s fluidity attributed to the interaction of realgar NPs. Results of Raman spectra and 31P NMR suggest that the polar headgroup of phospholipid is the interacted target site of realgar NPs. Moreover, time-lapse AFM images show that realgar NPs compromise the phospholipid membrane integrity to result in the formation of "pore" or "hole".

  9. Oriented and Ordered Biomimetic Remineralization of the Surface of Demineralized Dental Enamel Using HAP@ACP Nanoparticles Guided by Glycine

    Science.gov (United States)

    Wang, Haorong; Xiao, Zuohui; Yang, Jie; Lu, Danyang; Kishen, Anil; Li, Yanqiu; Chen, Zhen; Que, Kehua; Zhang, Qian; Deng, Xuliang; Yang, Xiaoping; Cai, Qing; Chen, Ning; Cong, Changhong; Guan, Binbin; Li, Ting; Zhang, Xu

    2017-01-01

    Achieving oriented and ordered remineralization on the surface of demineralized dental enamel, thereby restoring the satisfactory mechanical properties approaching those of sound enamel, is still a challenge for dentists. To mimic the natural biomineralization approach for enamel remineralization, the biological process of enamel development proteins, such as amelogenin, was simulated in this study. In this work, carboxymethyl chitosan (CMC) conjugated with alendronate (ALN) was applied to stabilize amorphous calcium phosphate (ACP) to form CMC/ACP nanoparticles. Sodium hypochlorite (NaClO) functioned as the protease which decompose amelogenin in vivo to degrade the CMC-ALN matrix and generate HAP@ACP core-shell nanoparticles. Finally, when guided by 10 mM glycine (Gly), HAP@ACP nanoparticles can arrange orderly and subsequently transform from an amorphous phase to well-ordered rod-like apatite crystals to achieve oriented and ordered biomimetic remineralization on acid-etched enamel surfaces. This biomimetic remineralization process is achieved through the oriented attachment (OA) of nanoparticles based on non-classical crystallization theory. These results indicate that finding and developing analogues of natural proteins such as amelogenin involved in the biomineralization by natural macromolecular polymers and imitating the process of biomineralization would be an effective strategy for enamel remineralization. Furthermore, this method represents a promising method for the management of early caries in minimal invasive dentistry (MID).

  10. Oriented and Ordered Biomimetic Remineralization of the Surface of Demineralized Dental Enamel Using HAP@ACP Nanoparticles Guided by Glycine

    Science.gov (United States)

    Wang, Haorong; Xiao, Zuohui; Yang, Jie; Lu, Danyang; Kishen, Anil; Li, Yanqiu; Chen, Zhen; Que, Kehua; Zhang, Qian; Deng, Xuliang; Yang, Xiaoping; Cai, Qing; Chen, Ning; Cong, Changhong; Guan, Binbin; Li, Ting; Zhang, Xu

    2017-01-01

    Achieving oriented and ordered remineralization on the surface of demineralized dental enamel, thereby restoring the satisfactory mechanical properties approaching those of sound enamel, is still a challenge for dentists. To mimic the natural biomineralization approach for enamel remineralization, the biological process of enamel development proteins, such as amelogenin, was simulated in this study. In this work, carboxymethyl chitosan (CMC) conjugated with alendronate (ALN) was applied to stabilize amorphous calcium phosphate (ACP) to form CMC/ACP nanoparticles. Sodium hypochlorite (NaClO) functioned as the protease which decompose amelogenin in vivo to degrade the CMC-ALN matrix and generate HAP@ACP core-shell nanoparticles. Finally, when guided by 10 mM glycine (Gly), HAP@ACP nanoparticles can arrange orderly and subsequently transform from an amorphous phase to well-ordered rod-like apatite crystals to achieve oriented and ordered biomimetic remineralization on acid-etched enamel surfaces. This biomimetic remineralization process is achieved through the oriented attachment (OA) of nanoparticles based on non-classical crystallization theory. These results indicate that finding and developing analogues of natural proteins such as amelogenin involved in the biomineralization by natural macromolecular polymers and imitating the process of biomineralization would be an effective strategy for enamel remineralization. Furthermore, this method represents a promising method for the management of early caries in minimal invasive dentistry (MID). PMID:28079165

  11. Preparation of DPPE-Stabilized Gold Nanoparticles

    Science.gov (United States)

    Dungey, Keenan E.; Muller, David P.; Gunter, Tammy

    2005-01-01

    An experiment is presented that introduces students to nanotechnology through the preparation of nanoparticles and their visualization using transmission electron microscopy (TEM). The experiment familiarizes the students with nonaqueous solvents, biphasic reactions, phase-transfer agents, ligands to stabilize growing nanoparticles, and bidentate…

  12. Biomimetic preparation and multi-scale microstructures of nano-silica/polyurethane elastomeric fibers

    Institute of Scientific and Technical Information of China (English)

    Quanyong Liu; Li Gao; Lei Jiang

    2013-01-01

    Bioinspired by the spinning of spider silks, the biomimetic preparation of nano-silica/polyurethane (nano-SiO2/TPU) elastomeric fibers with distinctive multi-scale microstructures was successfully implemented. The formation mechanism of the nano-SiO2/TPU fibers was considered as the integrated mechanism of diffusion, coagulation, self-assembly, and microphase separation, same as that of the native spider silks. The mass ratio of nano-SiO2 to TPU greatly influenced the external and inner microstructures of the nano-SiO2/TPU fibers. The formation process of the nano-SiO2/TPU fibers was simply described as three main stages, and the second stage, such as the adding of the ethanol solvents and nano-SiO2 in different diameters, was thought to be very crucial for the final external and inner microstructures of the prepared fibers. For example, the adding of the ethanol and the nano-SiO2 spheres in diameter of 10 nm resulted in the existence of many TPU-self-assembled microspheres mostly spaced apart by the nano-SiO2 aggregates in the nano-SiO2/TPU fibers, while the adding of the ethanol and the nano-SiO2 spheres in diameter of 100 nm resulted in the existence of the nano-SiO2 spheres, instead of the TPU-self-assembled microspheres, distributed in the nano-SiO2/TPU fibers.

  13. Synthesis of biomimetic poly[2-(methacryloyloxy)ethyl phosphorycholine]-coated magnetite nanoparticles via surface-initiated atom transfer radical polymerization.

    Science.gov (United States)

    Sui, Jie-He; Cao, Chang-Yan; Cai, Wei

    2011-10-01

    Modification of magnetite nanoparticles with biomimetic poly[2-(methacryloyloxy)ethyl phosphorycholine] (poly(MPC)) via surface-initiated atom transfer radical polymerization (ATRP) was carried out. Fourier transform infrared (FT-IR) spectroscopy, thermogravimetric analyses (TGA) and zeta potential studies indicated that well defined poly (MPC) was successfully grafted on the surface of magnetite nanoparticles. X-ray diffraction results showed the structure of magnetite nanoparticles after surface modification was not changed. The poly (MPC)-coated magnetite nanoparticles had a mean transmission electron microscopy (TEM) diameter of 11 +/- 1.5 nm. The resulting nanomaterials were superparamagnetic at room temperature, exhibited good colloidal stability in aqueous media and good responsibility to magnetic field. Such magnetite nanoparticles with biomimetic surface have potential application in prolonging circulation time in vivo.

  14. Preparation and characterization of bioactive glass nanoparticles prepared by sol-gel for biomedical applications

    Science.gov (United States)

    Luz, Gisela M.; Mano, João F.

    2011-12-01

    Bioactive glass nanoparticles (BG-NPs), based on both ternary (SiO2-CaO-P2O5) and binary (SiO2-CaO) systems, were prepared via an optimized sol-gel method. The pH of preparation and the effect of heat treatment temperature were evaluated, as well as the effect of suppressing P in the bioactivity ability of the materials. The morphology and composition of the BG-NPs were studied using FTIR, XRD and SEM. The bioactive character of these materials was accessed in vitro by analyzing the ability for apatite formation onto the surface after being immersed in simulated body fluid (SBF). XRD, EDX and SEM were used to confirm the bioactivity of the materials. The BG-NP effect on cell metabolic activity was assessed by seeding L929 cells with their leachables, proving the non-cytotoxicity of the materials. Finally the most bioactive BG-NPs developed (ternary system prepared at pH 11.5 and treated at 700 °C) were successfully combined with chitosan in the production of biomimetic nanocomposite osteoconductive membranes that could have the potential to be used in guided tissue regeneration.

  15. Method to prepare nanoparticles on porous mediums

    Science.gov (United States)

    Vieth, Gabriel M [Knoxville, TN; Dudney, Nancy J [Oak Ridge, TN; Dai, Sheng [Knoxville, TN

    2010-08-10

    A method to prepare porous medium decorated with nanoparticles involves contacting a suspension of nanoparticles in an ionic liquid with a porous medium such that the particles diffuse into the pores of the medium followed by heating the resulting composition to a temperature equal to or greater than the thermal decomposition temperature of the ionic liquid resulting in the removal of the liquid portion of the suspension. The nanoparticles can be a metal, an alloy, or a metal compound. The resulting compositions can be used as catalysts, sensors, or separators.

  16. Preparation of Hydrochlorothiazide Nanoparticles for Solubility Enhancement

    Directory of Open Access Journals (Sweden)

    Eliska Vaculikova

    2016-08-01

    Full Text Available Nanoparticles can be considered as a useful tool for improving properties of poorly soluble active ingredients. Hydrochlorothiazide (Class IV of the Biopharmaceutical Classification System was chosen as a model compound. Antisolvent precipitation-solvent evaporation and emulsion solvent evaporation methods were used for preparation of 18 samples containing hydrochlorothiazide nanoparticles. Water solutions of surfactants sodium dodecyl sulfate, Tween 80 and carboxymethyl dextran were used in mass concentrations of 1%, 3% and 5%. Acetone and dichloromethane were used as solvents of the model compound. The particle size of the prepared samples was measured by dynamic light scattering. The selected sample of hydrochlorothiazide nanoparticles stabilized with carboxymethyl dextran sodium salt with particle size 2.6 nm was characterized additionally by Fourier transform mid-infrared spectroscopy and scanning electron microscopy. It was found that the solubility of this sample was 6.5-fold higher than that of bulk hydrochlorothiazide.

  17. Synthesis, characterization and antibacterial activity against Gram positive and Gram negative bacteria of biomimetically coated silver nanoparticles.

    Science.gov (United States)

    Amato, Elvio; Diaz-Fernandez, Yuri A; Taglietti, Angelo; Pallavicini, Piersandro; Pasotti, Luca; Cucca, Lucia; Milanese, Chiara; Grisoli, Pietro; Dacarro, Cesare; Fernandez-Hechavarria, Jose M; Necchi, Vittorio

    2011-08-02

    In the present work, we describe a simple procedure to produce biomimetically coated silver nanoparticles (Ag NPs), based on the postfunctionalization and purification of colloidal silver stabilized by citrate. Two biological capping agents have been used (cysteine Cys and glutathione GSH). The composition of the capped colloids has been ascertained by different techniques and antibacterial tests on GSH-capped Ag NPs have been conducted under physiological conditions, obtaining values of Minimum Inhibitory Concentration (MIC) of 180 and 15 μg/mL for Staphylococcus aureus and Escherichia coli, respectively. The antibacterial activity of these GSH capped NPs can be ascribed to the direct action of metallic silver NPs, rather than to the bulk release of Ag(+).

  18. Preparation of Bone-Like Apatite Coating on Surface of Ti-25Nb-2Zr Alloy by Biomimetic Growth Method

    Institute of Scientific and Technical Information of China (English)

    ZHOU Yu; HUANG Runmin; CUI Zhenduo; YANG Xianjin

    2009-01-01

    A bone-like apatite layer consisting of nano-crystals of apatite phase was prepared on the surface of Ti-25Nb-2Zr alloy by chemical biomimetic growth method. TiNbZr alloy specimens were first oxidized at 500℃ for 2 h in the air. Then, they were immersed in 40℃ saturated Na2HPO4 solution for 15 h and 25 ℃ saturated Ca(OH)2 solution for 8 h in turn for pre-calcification. The pre-calcified specimens were immersed in modified simulated body fluid up to 15 d for biomimetic growth. After common oxidization, amorphous titania and anatase were detected on the specimen surface. Except for the substantial amount of calcium and phosphorus, no new phase appeared on the pre-calcified specimens. After the coating process, it was found that the (002) orientation was the preferred orientation during the growing period of hydroxyapatite. The inorganic composition and structure of the coating are very similar to those of human thigh bone, which will be advantageous for its application as biomedical material.

  19. Biomimetic scaffolds containing nanofibers coated with willemite nanoparticles for improvement of stem cell osteogenesis

    Energy Technology Data Exchange (ETDEWEB)

    Ramezanifard, Rouhallah [Department of Biotechnology, College of Science, University of Tehran, Tehran (Iran, Islamic Republic of); Seyedjafari, Ehsan, E-mail: seyedjafari@ut.ac.ir [Department of Biotechnology, College of Science, University of Tehran, Tehran (Iran, Islamic Republic of); Ardeshirylajimi, Abdolreza [Department of Stem Cell Biology, Stem Cell Technology Research Center, Tehran (Iran, Islamic Republic of); Soleimani, Masoud [Department of Hematology, Faculty of Medical Science, Tarbiat Modares University, Tehran (Iran, Islamic Republic of)

    2016-05-01

    Nowadays, discovering osteogenesis stimulating effectors is one of the major topics in bone tissue engineering and regenerative medicine. In this study, the proliferation rate and osteogenic differentiation potency of adipose-derived mesenchymal stem cells (AT-MSCs) cultured on poly (L-lactide acid) (PLLA) and willemite-coated PLLA were investigated by MTT assay and common osteogenic markers such as alkaline phosphatase (ALP) activity, calcium mineral deposition and bone-related genes expression. Willemite-coated PLLA showed a higher proliferation support to AT-MSCs in comparison to PLLA and TCPS. During the period of study, AT-MSCs cultured on willemite-coated PLLA scaffolds exhibited the greatest ALP activity and mineralization. Gene expression analysis demonstrated that the highest expression of four important osteogenic-related genes, osteonectin, Runx2, collagen type 1 and osteocalcin was observed in stem cells cultured on willemite-coated PLLA nanofibrous scaffolds. According to the results, willemite-coated PLLA could be a suitable substrate to support the proliferation and osteogenic differentiation of stem cells and holds promising potential for bone tissue engineering and regenerative medicine applications. - Highlights: • Biodegradable PLLA eletrospun nanofibrous scaffold was prepared. • PLLA nanofibers were treated with plasma and coated with willemite nanoparticles. • MSC on willemite-coated PLLA showed greater osteogenic differentiation than those on uncoated PLLA and TCPS. • Willemite-coated nanofibers hold promising potential for bone tissue engineering application.

  20. Biomimetic fat cell (BFC) preparation and for lindane removal from aqueous solution.

    Science.gov (United States)

    Liyan, Song; Youcai, Zhao; Guojian, Wang; Bing, Li; Dongjie, Niu; Xiaoli, Chai

    2007-07-19

    Fat tissue of organism can accumulate hydrophobic chemicals efficiently and the accumulation level has a positive correlation with fat quantity. In this work, based on this characteristic, an innovative agent, that is, biomimetic fat cell (BFC) has been synthesized with interfacial polymerization. BFC has a hydrophobic nucleolus-triolein and hydrophilic membrane-polyamide, through which water, carrying hydrophobic organic contaminants (HOCs), can pass. This process is followed by the accumulation of HOCs. BFC has 97.39% lindane removal ability. This is close to 98.12% lindane removal by powder active carbon (PAC) in aqueous solution and 7 mg/L initial concentration of lindane. BFC can be regenerated easily by organic solvent dialysis in comparison with high temperature or pressure used for PAC regeneration. Lindane removal by BFC may occur through two mechanisms: bioaccumulation by BFC nucleolus-triolein; and adsorption by BFC membrane. Bioaccumulation is the prevailing mechanism.

  1. Adhesion enhancement of biomimetic dry adhesives by nanoparticle in situ synthesis

    Science.gov (United States)

    Díaz Téllez, J. P.; Harirchian-Saei, S.; Li, Y.; Menon, C.

    2013-10-01

    A novel method to increase the adhesion strength of a gecko-inspired dry adhesive is presented. Gold nanoparticles are synthesized on the tips of the microfibrils of a polymeric dry adhesive to increase its Hamaker constant. Formation of the gold nanoparticles is qualitatively studied through a colour change in the originally transparent substance and quantitatively analysed using ultraviolet-visible spectrophotometry. A pull-off force test is employed to quantify the adhesion enhancement. Specifically, adhesion forces of samples with and without embedded gold nanoparticles are measured and compared. The experimental results indicate that an adhesion improvement of 135% can be achieved.

  2. Preparation and application of various nanoparticles in biology and medicine

    Directory of Open Access Journals (Sweden)

    Vardan Gasparyan

    2013-02-01

    Full Text Available The present paper considers prospects for application of various nanoparticles in biology and medicine. Here are presented data on preparation of gold and silver nanoparticles, and effects of shape of these nanoparticles on their optical properties. Application of these nanoparticles in diagnostics, for drug delivery and therapy, and preparation of magnetic nanoparticles from iron and cobalt salts are also discussed. Application of these nanoparticles as magnetic resonance imaging (MRI contrast agents and as vehicles for drug delivery, and preparation of quantum dots and their application as prospective nanoparticles for multiplex analysis and for visualization of cellular processes will be tackled. Finally, prospects for new types of nanocomposites (metallic nano-shells will be not overlooked.

  3. Preparation and Characterization of Calcium Carbonate Nanoparticles

    Science.gov (United States)

    Hassim, Aqilah; Rachmawati, Heni

    2010-10-01

    Taking calcium supplements can reduce the risk of developing osteoporosis, but they are not readily absorbed in the gastrointestinal tract. Nanotechnology is expected to resolve this problem. In this study, we prepared and characterized calcium carbonate nanoparticle to improve the solubility by using bottom-up method. The experiment was done by titrating calcium chloride with sodium carbonate with the addition of polyvinylpyrrolidone (PVP) as stabilizer, using ultra-turrax. Various concentrations of calcium chloride and sodium carbonate as well as various speed of stirring were used to prepare the calcium carbonate nanoparticles. Evaluations studied were including particle size, polydispersity index (PI) and zeta potential with particle analyzer, surface morphology with scanning electron microscope, and saturated solubility. In addition, to test the ability of PVP to prevent particles growth, short stability study was performed by storing nano CaCO3 suspension at room temperature for 2 weeks. Results show that using 8000 rpm speed of stirring, the particle size tends to be bigger with the range of 500-600 nm (PI between 0.2-0.4) whereas with stirring speed of 4000 rpm, the particle size tends to be smaller with 300-400 nm (PI between 0.2-0.4). Stirring speed of 6000 rpm produced particle size within the range of 400-500 nm (PI between 0.2-0.4). SEM photograph shows that particles are monodisperse confirming that particles were physically stable without any agglomeration within 2 weeks storage. Taken together, nano CaCO3 is successfully prepared by bottom-up method and PVP is a good stabilizer to prevent the particle growth.

  4. Synthesis of robust and high-performance aquaporin-based biomimetic membranes by interfacial polymerization-membrane preparation and RO performance characterization

    DEFF Research Database (Denmark)

    Zhao, Yang; Qiu, Changquan; Li, Xuesong;

    2012-01-01

    %) at an applied pressure of 5bar. Its permeability was ∼40% higher compared to a commercial brackish water RO membrane (BW30) and an order of magnitude higher compared to a seawater RO membrane (SW30HR), which clearly demonstrates the great potential of the TFC ABM for desalination applications.......Aquaporins are water channel proteins with excellent water permeability and solute rejection, which makes them promising for preparing high-performance biomimetic membranes. Despite the growing interest in aquaporin-based biomimetic membranes (ABMs), it is challenging to produce robust and defect...... or with inactive (mutant) aquaporins, were also similarly prepared. The separation performance of these membranes was evaluated by cross-flow reverse osmosis (RO) tests. Compared to the controls, the active ABM achieved significantly higher water permeability (∼4L/m2hbar) with comparable NaCl rejection (∼97...

  5. Single-Nanoparticle Resolved Biomimetic Long-Range Electron Transfer and Electrocatalysis of Mixed-Valence Nanoparticles

    DEFF Research Database (Denmark)

    Zhu, Nan; Hao, Xian; Ulstrup, Jens;

    2016-01-01

    their enzyme-mimicking catalytic properties and controlled LRET to single-nanoparticle resolution. PBNPs show high substrate binding affinity and tunable electrocatalytic efficiency toward hydrogen peroxide reduction, resembling the patterns for similar size redox metalloenzymes. We have further disclosed...

  6. Preparation of nickel nanoparticles in emulsion

    Institute of Scientific and Technical Information of China (English)

    ZHANG You-xian; FU Wen-jie; AN Xue-qin

    2008-01-01

    The nickel nanoparticles with different sizes and spherical shape were prepared by the reduction of nickel sulfate with sodium borohydride in the water-in-oil emulsions of water/SDBS(sodium dodecylbenzene sulfonate)/n-pentanol/n-heptane. The effects of aging time, molar ratio of water to SDBS(R) and the concentration of nickel sulfate on the size of particles were studied. The samples were characterized by transmission electron microscopy(TEM) and inductively coupled plasma spectrometry(ICP). The results show that the average particle size changes from 20 to 40 nm by adjusting aging time (15-30 min) and R (9-11.5). The concentration of nickel sulfate of 1.0 mol/L is the favorite condition.

  7. Preparations, characterizations and applications of chitosan-based nanoparticles

    Science.gov (United States)

    Liu, Chenguang; Tan, Yulong; Liu, Chengsheng; Chen, Xiguang; Yu, Lejun

    2007-07-01

    Chitosan is a natural polysaccharide prepared by the N-deacetylation of chitin. In this paper we have reviewed the methods of preparation of chitosan-based nanoparticles and their pharmaceutical applications. There are five methods of their preparations: emulsion cross-linking, emulsion-droplet coalescence, ionic gelation, reverse micellar method and chemically modified chitosan method. Chitosan nanoparticles are used as carriers for low molecular weight drug, vaccines and DNA. Releasing characteristics, biodistribution and applications are also summarized.

  8. Preparations, Characterizations and Applications of Chitosan-based Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Chitosan is a natural polysaccharide prepared by the N-deacetylation of chitin. In this paper we have reviewed the methods of preparation of chitosan-based nanoparticles and their pharmaceutical applications. There are five methods of their preparations: emulsion cross-linking, emulsion-droplet coalescence, ionic gelation, reverse micellar method and chemically modified chitosan method. Chitosan nanoparticles are used as carriers for low molecular weight drug, vaccines and DNA. Releasing characteristics, biodistribution and applications are also summarized.

  9. Preparation of drug nanoparticles by emulsion evaporation method

    Energy Technology Data Exchange (ETDEWEB)

    Le Thi Mai Hoa; Dang Mau Chien [Laboratory for Nanotechnology, Vietnam National University of Ho Chi Minh City, 6 Community, Linh Trung Ward, Thu Duc District, Ho Chi Minh City (Viet Nam); Nguyen Tai Chi; Nguyen Minh Triet; Le Ngoc Thanh Nhan [Faculty of Pharmacy, University of Medicine and Pharmacy at Ho Chi Minh City, 41 Dinh Tien Hoang, Ben Nghe Ward, 1 District, Ho Chi Minh City (Viet Nam)], E-mail: ltmhoa@vnuhcm.edu.vn

    2009-09-01

    Polymeric drug nanoparticles were prepared by emulsion solvent evaporation method. In this study, prepared the polymeric drug nanoparticles consist of ketoprofen and Eudragit E 100. The morphology structure was investigated by scanning electron microscopy (SEM). The interactions between the drug and polymer were investigated by Fourier transform infrared spectroscopy (FTIR). The size distribution was measured by means of Dynamic Light Scattering. The nanoparticles have an average size of about 150 nm. The incorporation ability of drugs in the polymeric nanoparticles depended on the integration between polymer and drug as well as the glass transition temperature of the polymer.

  10. Biomimetic synthesis of antimicrobial silver nanoparticles using in vitro-propagated plantlets of a medicinally important endangered species: Phlomis bracteosa

    Science.gov (United States)

    Anjum, Sumaira; Abbasi, Bilal Haider

    2016-01-01

    In vitro-derived cultures of plants offer a great potential for rapid biosynthesis of chemical-free antimicrobial silver nanoparticles (AgNPs) by enhancing their phytochemical reducing potential. Here, we developed an efficient protocol for in vitro micropropagation of a high-value endangered medicinal plant species, Phlomis bracteosa, in order to explore its biogenic potential in biomimetic synthesis of antimicrobial AgNPs. Murashige and Skoog medium supplemented with 2.0 mg/L thidiazuron was found to be more efficient in inducing optimum in vitro shoot regeneration (78%±4.09%), and 2.0 mg/L indole-3-butyric acid was used for maximum root induction (86%±4.457%). Antimicrobial AgNPs were successfully synthesized by using aqueous extract (rich in total phenolics and flavonoids content) of in vitro derived plantlets of P. bracteosa. Ultraviolet–visible spectroscopy of synthesized AgNPs showed characteristic surface plasmon band in the range of 420–429 nm. The crystallinity, size, and shape of the AgNPs were characterized by X-ray diffraction and scanning electron microscopy. Face-centered cubic AgNPs of almost uniform spherical size (22.41 nm) were synthesized within a short time (1 hour) at room temperature. Fourier-transform infrared spectroscopy revealed that the polyphenols were mainly responsible for reduction and capping of synthesized AgNPs. Energy dispersive X-ray analysis further endorsed the presence of elemental silver in synthesized AgNPs. These biosynthesized AgNPs displayed significantly higher bactericidal activity against multiple drug-resistant human pathogens. The present work highlighted the potent role of in vitro-derived plantlets of P. bracteosa for feasible biosynthesis of antimicrobial AgNPs, which can be used as nanomedicines in many biomedical applications. PMID:27217745

  11. Optimization of a Biomimetic Apatite Nanoparticle Delivery System for Non-viral Gene Transfection---a Simulated Body Fluid Approach

    Science.gov (United States)

    Das, Debobrato

    Current methods for gene delivery utilize nanocarriers such as liposomes and viral vectors that may produce in vivo toxicity, immunogenicity, or mutagenesis. Moreover, these common high-cost systems have a low efficacy of gene-vehicle transport across the cell plasma membrane followed by inadequate release and weak intracellular stability of the genetic sequence. Thus, this study aims to maximize gene transfection while minimizing cytotoxicity by utilizing supersaturated blood-plasma ions derived from simulated body fluids (SBF). With favorable electrostatic interactions to create biocompatible calcium-phosphate nanoparticles (NPs) derived from biomimetic apatite (BA), results suggest that the SBF system, though naturally sensitive to reaction conditions, after optimization can serve as a tunable and versatile platform for the delivery of various types of nucleic acids. From a systematic exploration of the effects of nucleation pH, incubation temperature, and time on transfection efficiency, the study proposes distinct characteristic trends in SBF BA-NP morphology, cellular uptake, cell viability, and gene modulation. Specifically, with aggressive nucleation and growth of BA-NPs in solution (observed via scanning electron microscopy), the ensuing microenvironment imposes a more toxic cellular interaction (indicated by alamarBlue and BCA assays), limiting particle uptake (fluorescence experiments) and subsequent gene knockdown (quantitative loss of function assays). Controlled precipitation of BA-NPs function to increase particle accessibility by surrounding cells, and subsequently enhance uptake and transfection efficiency. By closely examining such trends, an optimal fabrication condition of pH 6.5-37C can be observed where particle growth is more tamed and less chaotic, providing improved, favorable cellular interactions that increase cell uptake and consequently maximize gene transfection, without compromising cellular viability.

  12. Preparation of Gold Nanoparticles Protected with Polyelectrolyte

    Institute of Scientific and Technical Information of China (English)

    Xu Ping SUN; Zhe Ling ZHANG; Bai Lin ZHANG; Xian Dui DONG; Shao Jun DONG; Er Kang WANG

    2003-01-01

    Gold nanoparticles were synthesized through the reduction of tetrachlorauric acid (HAuCl4) by NaBH4, with polyethyleneimine(PEI) as stabilizer. The nanoparticles were characterized by UV-vis spectroscopy and atomic force microscopy(AFM).

  13. Photochemical preparation and application research of Au nanoparticles

    Institute of Scientific and Technical Information of China (English)

    DONG; Shou-an; SUN; Jia-lin

    2005-01-01

    Gold nanoparticles protected by organic small molecular compounds or macromolecule have attracted considerable attention and their preparation is one of hotspots in the nano-chemical material field due to their ongoing and potential applications in optics, electronics, catalysts and biosensors. In recent years there are many liquid phase chemistry methods to prepare monodispersed gold particles. Among them, the photochemical method is quite attractive because of its some important advantages for size-controlled synthesis of gold nanoparticles. Therefore, in this paper the recert progress of the photochemical preparing Au nanoparticle materials was briefly introduced and mainly emphasized authors' own works of this area.

  14. Preparation of a biomimetic composite scaffold from gelatin/collagen and bioactive glass fibers for bone tissue engineering

    Energy Technology Data Exchange (ETDEWEB)

    Sharifi, Esmaeel; Azami, Mahmoud [Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Kajbafzadeh, Abdol-Mohammad [Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Pediatric Urology Research Center, Section of Tissue Engineering and Stem Cells Therapy, Department of Pediatric Urology, Children' s Hospital Medical Center, Tehran, Iran (IRI) (Iran, Islamic Republic of); Moztarzadeh, Fatollah [Department of Biomedical Engineering, Amirkabir University of Technology (Tehran Polytechnic), Tehran (Iran, Islamic Republic of); Faridi-Majidi, Reza [Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Shamousi, Atefeh; Karimi, Roya [Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Ai, Jafar, E-mail: jafar_ai@tums.ac.ir [Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Brain and Spinal Injury Research Center (BASIR), Imam Khomeini Hospital, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of)

    2016-02-01

    Bone tissue is a composite material made of organic and inorganic components. Bone tissue engineering requires scaffolds that mimic bone nature in chemical and mechanical properties. This study proposes a novel method for preparing composite scaffolds that uses sub-micron bioglass fibers as the organic phase and gelatin/collagen as the inorganic phase. The scaffolds were constructed by using freeze drying and electro spinning methods and their mechanical properties were enhanced by using genipin crosslinking agent. Electron microscopy micrographs showed that the structure of composite scaffolds were porous with pore diameters of approximately 70–200 μm, this was again confirmed by mercury porosimetery. These pores are suitable for osteoblast growth. The diameters of the fibers were approximately 150–450 nm. Structural analysis confirmed the formation of desirable phases of sub-micron bioglass fibers. Cellular biocompatibility tests illustrated that scaffolds containing copper ion in the bioglass structure had more cell growth and osteoblast attachment in comparison to copper-free scaffolds. - Highlights: • Fabrication of 45S5 sub-micron bioglass fiber using electrospinning method. • Production of copper doped submicron bioglass fibers on 45S5 bioglass base by electrospinning sol gel route method. • Incorporation of bioglass/Cu-bioglass sub-micron fibers into gelatin/collagen matrix to form biomimetic composite scaffold which were non-cytotoxic according to MTT assay. • Discovering that copper can decrease the glass transition temperatures and enhance osteoblast cell adhesion and viability.

  15. Preparation and Characterization of Nateglinide Loaded Hydrophobic Biocompatible Polymer Nanoparticles

    Science.gov (United States)

    Naik, Jitendra; Lokhande, Amolkumar; Mishra, Satyendra; Kulkarni, Ravindra

    2016-09-01

    The aim of the present study was to develop sustained release Nateglinide loaded Ethylcellulose nanoparticles and characterize the properties of recovered nanoparticles. The sustained release nanoparticles were prepared by oil in water single emulsion solvent evaporation method. The developed nanoparticles were characterised for their particle size, morphology, encapsulation efficiency, drug polymer compatibility and in vitro drug release. The drug polymer compatibility was investigated by XRPD. Imaging of particles was performed by field emission scanning electron microscopy. The highest particle size and encapsulation efficiency of recovered nanoparticles were 248.37 nm and 91.16 % respectively. The recovered nanoparticles are spherical in nature and uniform in size. Developed nanoparticles have low crystallinity than the pure Nateglinide. The highest drug-polymer ratio formulation showed drug release 61.1 ± 1.76 % up to 24 h.

  16. Influence of formulation factors on the preparation of zein nanoparticles.

    Science.gov (United States)

    Podaralla, Satheesh; Perumal, Omathanu

    2012-09-01

    The main objective of the present study was to investigate the influence of various formulation parameters on the preparation of zein nanoparticles. 6,7-dihydroxycoumarin (DHC) was used as a model hydrophobic compound. The influence of pH of the aqueous phase, buffer type, ionic strength, surfactant, and zein concentration on particle size, polydispersity index, and zeta potential of DHC-loaded zein nanoparticles were studied. Smaller nanoparticles were formed when the pH was close to the isoelectric point of zein. DHC-loaded zein nanoparticles prepared using citrate buffer (pH 7.4) was better than phosphate buffer in preventing particle aggregation during lyophilization. The ionic strength did not have a significant influence on the particle size of DHC-loaded zein nanoparticles. A combination of Pluronic F68 and lecithin in 2:1 ratio stabilized the zein nanoparticles. An increase in zein concentration led to increase in particle size of DHC-loaded zein nanoparticles. The use of optimal conditions produced DHC-loaded nanoparticles of 256 ± 30 nm and an encapsulation efficiency of 78 ± 7%. Overall, the study demonstrated the optimal conditions to prepare zein nanoparticles for drug encapsulation.

  17. Biomimetic synthesis of silver nanoparticles using microalgal secretory carbohydrates as a novel anticancer and antimicrobial

    Science.gov (United States)

    Ebrahiminezhad, Alireza; Bagheri, Mahboobeh; Taghizadeh, Seyedeh-Masoumeh; Berenjian, Aydin; Ghasemi, Younes

    2016-03-01

    Secreted carbohydrates by Chlorella vulgaris cells were used for reducing and capping Silver nanoparticles (AgNPs). Oxygen-bearing functional groups on the carbohydrates found to be the main biochemical groups responsible for anchoring the metal nanoparticles. Transmission electron microscopy (TEM) micrographs showed that isotropic small particles with mean particles size of 7 nm were synthesized. Comparing the TEM results with DLS analysis revealed that the thickness of carbohydrate capping was about 2 nm. A zeta potential of +26 mV made the particles colloidally stable and desirable for anticancer and antimicrobial applications. The MIC against gram positive (Staphylococcus aureus) and gram negative bacteria (Escherichia coli) were determined to be 37.5 μg ml-1 and 9.4 μg ml-1, respectively. Treatment of Hep-G2 cells with 4.7 μg ml-1 AgNPs for 24 h reduced the cell viability to 61%. This concentration was also reduced the cell viability to 37% after 48 h of exposure.

  18. Preparation and crystallization control of nanoparticle hydroxyapatite

    Institute of Scientific and Technical Information of China (English)

    Lianfeng Guo; Wenguang Zhang; Chengtao Wang

    2004-01-01

    Nanoparticle hydroxyapatite was prepared by a wet chemical precipitation method. The effects of different synthesis conditions, I.e. Contents of reagents (0.2, 0.5 and 0.8 mol/L), reaction temperatures (20, 37, 55 and 75℃) and reaction time (0-24 h),were studied based on crystallization process analysis and the effects of washing methods (with water or alcohol) were also studied.Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), electron diffraction (ED) and inductively coupled plasma spectroscopy (ICP) were used to characterize the powders. Chemical analysis shows that the purity of the precipitated hydroxyapatite largely depends on reaction time. X-ray diffraction and TEM micrographs results show that reaction temperature is a key factor affecting crystallinity, morphology and particle size. Degree of supersaturation and stirring also affects the crystallization. Particles are in a shape of short rod and have a size of 20-40 nm in length at 20℃ and 37℃,but acicular morphology and a size of 150-170 nm in length at 75C. Particles are monocrystalline at 20℃ and 37℃, and are polycrystalline at 55℃ and 75℃. The results show that stoichiometry hydroxyapatite with controlled particle size, morphology and crystallinity can be obtained by carefully controlling the reaction conditions.

  19. Preparation of P(St-BA-VBT)/dye Colored Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    HAN Dong-mei; FANG Kuan-jun

    2015-01-01

    P (St-BA-VBT)/dye colored nanoparticles were prepared by staining P (Styrene-Butyl Acrylate-VinylBenzyl Trimethylammonium chloride) nanoparticles synthesized by soap free cationic emulsion polymerization with reactive dyes. The effects of reactive dyes dosage, dyeing temperature and time on amounts of dyes adsorbed on the nanoparticles were analysed. Results showed that when Reactive Red 195 dosage was 5.25%, the adsorption amounts of dyes on the nanoparticles reached a maximum value of 18.64 mg/g at 65℃for 90 min.

  20. Preparation and Storage of Silver Nanoparticles in Aqueons Polymers

    Institute of Scientific and Technical Information of China (English)

    SONG,Weihong; ZHANG,Xiaoxiao; YIN,Hongzong; SA,Panpan; LIU,Xiaoyan

    2009-01-01

    Silver nanoparticles were obtained by a chemical reduction method using aqueous polymers as dispersant and characterized by UV-Vis spectroscopy,transmission electron microscopy (TEM) and light-scattering spectroscopy.Solid polymer films containing the silver nanoparticles were also prepared after evaporating the solvent,and then dried with existing polymer.The stability of the silver nanoparticles was compared between primary fresh silver nanoparticle solution and redissolved solid polymer films by UV-Vis spectroscopy.The particle size ranged from 5 to l0 rim,and no obvious differences were found.Therefore,preparing solid nano-Ag/polymer was a novel and useful method in storage of silver nanoparticles.

  1. Zero-valent iron nanoparticles preparation

    Energy Technology Data Exchange (ETDEWEB)

    Oropeza, S. [Instituto Politécnico Nacional, ESIQIE, UPALM, Edificio Z-6, Primer Piso, C.P. 07738, Col. San Pedro Zacatenco, México D.F. (Mexico); Corea, M., E-mail: mcoreat@yahoo.com.mx [Instituto Politécnico Nacional, ESIQIE, UPALM, Edificio Z-6, Primer Piso, C.P. 07738, Col. San Pedro Zacatenco, México D.F. (Mexico); Gómez-Yáñez, C. [Instituto Politécnico Nacional, ESIQIE, UPALM, Edificio Z-6, Primer Piso, C.P. 07738, Col. San Pedro Zacatenco, México D.F. (Mexico); Cruz-Rivera, J.J. [Universidad Autónoma de San Luis Potosí, Instituto de Metalurgia, Sierra Leona 550, San Luis Potosí, C.P. 78210 (Mexico); Navarro-Clemente, M.E., E-mail: mnavarroc@ipn.mx [Instituto Politécnico Nacional, ESIQIE, UPALM, Edificio Z-6, Primer Piso, C.P. 07738, Col. San Pedro Zacatenco, México D.F. (Mexico)

    2012-06-15

    Graphical abstract: Zero-valent iron nanoparticles were synthesized by hydrogenating [Fe[N(Si(CH{sub 3}){sub 3}){sub 2}]{sub 2}] at room temperature and a pressure of 3 atm. The synthesized nanoparticles were spherical and had diameters less than 5 nm. Highlights: ► Zero-valent iron nanoparticles were synthesized by hydrogenating [Fe[N(Si(CH{sub 3}){sub 3}){sub 2}]{sub 2}]. ► The conditions of reaction were at room temperature and a pressure of 3 atm. ► The synthesized nanoparticles were spherical and had diameters less than 5 nm. -- Abstract: Zero-valent iron nanoparticles were synthesized by hydrogenating [Fe[N(Si(CH{sub 3}){sub 3}){sub 2}]{sub 2}] at room temperature and a pressure of 3 atm. To monitor the reaction, a stainless steel pressure reactor lined with PTFE and mechanically stirred was designed. This design allowed the extraction of samples at different times, minimizing the perturbation in the system. In this way, the shape and the diameter of the nanoparticles produced during the reaction were also monitored. The results showed the production of zero-valent iron nanoparticles that were approximately 5 nm in diameter arranged in agglomerates. The agglomerates grew to 900 nm when the reaction time increased up to 12 h; however, the diameter of the individual nanoparticles remained almost the same. During the reaction, some byproducts constituted by amino species acted as surfactants; therefore, no other surfactants were necessary.

  2. Preparation and Nonlinearity properties of Pd Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Pd nanoparticles less than 8 nm were photoinduced by a near-IR femtosecond laser. The sign of the refraction nonlinearity is negative for the Pd nanoparticles with TiO2, while it is positive for those without TiO2.

  3. Antifungal activity of gold nanoparticles prepared by solvothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, Tokeer, E-mail: tahmad3@jmi.ac.in [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi 110025 (India); Wani, Irshad A.; Lone, Irfan H.; Ganguly, Aparna [Nanochemistry Laboratory, Department of Chemistry, Jamia Millia Islamia, New Delhi 110025 (India); Manzoor, Nikhat; Ahmad, Aijaz [Department of Biosciences, Jamia Millia Islamia, New Delhi 110025 (India); Ahmed, Jahangeer [Department of Chemistry, Michigan State University, East Lansing, MI 48824 (United States); Al-Shihri, Ayed S. [Department of Chemistry, Faculty of Science, King Khalid University, Abha 61413, P.O. Box 9004 (Saudi Arabia)

    2013-01-15

    Graphical abstract: Gold nanoparticles (7 and 15 nm) of very high surface area (329 and 269 m{sup 2}/g) have been successfully synthesized through solvothermal method by using tin chloride and sodium borohydride as reducing agents. As-prepared gold nanoparticles shows very excellent antifungal activity against Candida isolates and activity increases with decrease in the particle size. Display Omitted Highlights: ► Effect of reducing agents on the morphology of gold nanoparticles. ► Highly uniform and monodisperse gold nanoparticles (7 nm). ► Highest surface area of gold nanoparticles (329 m{sup 2/}g). ► Excellent antifungal activity of gold nanoparticles against Candida strains. -- Abstract: Gold nanoparticles have been successfully synthesized by solvothermal method using SnCl{sub 2} and NaBH{sub 4} as reducing agents. X-ray diffraction studies show highly crystalline and monophasic nature of the gold nanoparticles with face centred cubic structure. The transmission electron microscopic studies show the formation of nearly spherical gold nanoparticles of average size of 15 nm using SnCl{sub 2}, however, NaBH{sub 4} produced highly uniform, monodispersed and spherical gold nanoparticles of average grain size of 7 nm. A high surface area of 329 m{sup 2}/g for 7 nm and 269 m{sup 2}/g for 15 nm gold nanoparticles was observed. UV–vis studies assert the excitations over the visible region due to transverse and longitudinal surface plasmon modes. The gold nanoparticles exhibit excellent size dependant antifungal activity and greater biocidal action against Candida isolates for 7 nm sized gold nanoparticles restricting the transmembrane H{sup +} efflux of the Candida species than 15 nm sized gold nanoparticles.

  4. Preparation of Si-containing oxide coating and biomimetic apatite induction on magnesium alloy

    Science.gov (United States)

    Yu, Huijun; Dong, Qing; Dou, Jinhe; Pan, Yaokun; Chen, Chuanzhong

    2016-12-01

    Magnesium and its alloys are recently found important in the field of bone repairing for their ideal mechanical performance and excellent biocompatibility. Micro-arc oxidation (MAO) is a simple, controllable and efficient electrochemistry method that can prepare protective ceramic coatings on magnesium alloys. The properties of the MAO coating, such as thickness, microstructure, roughness and composition, can easily be controlled by adjusting the voltage, current density, duration or the electrolyte concentration. In this work, MAO coatings are prepared on ZK61 magnesium alloy at different voltages. The structure characteristics and element distributions of the coating are investigated by XRD, TEM, SEM and EPMA. The MAO samples are immersed in SBF for 7, 14 and 28 days respectively. The corrosion behaviors of the samples in SBF were also investigated by potentiodynamic polarization curves. The corrosion products were characterized by EDS and FT-IR. The MAO coated ZK61 alloy samples showed excellent corrosion resistance and bioactivity. The MAO method demonstrates a great potential in the preparation of degradable and bioactive orthopedic magnesium-based implants.

  5. Antimicrobial activity and cytocompatibility of silver nanoparticles coated catheters via a biomimetic surface functionalization strategy

    Directory of Open Access Journals (Sweden)

    Wu K

    2015-12-01

    Full Text Available Ke Wu,1 Yun Yang,2,3 Yanmei Zhang,2,3 Jiexi Deng,1 Changjian Lin2,31Department of Cardiology, The Affiliated Dongnan Hospital of Xiamen University, Zhangzhou, 2Department of Medical Materials, Beijing Medical Implant Engineering Research Center, Beijing Naton Technology Group, Beijing, 3State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, People’s Republic of ChinaAbstract: Catheter-related bloodstream infections are a significant problem in the clinic and may result in a serious infection. Here, we developed a facile and green procedure for buildup of silver nanoparticles (AgNPs on the central venous catheters (CVCs surface. Inspired by mussel adhesive proteins, dopamine was used to form a thin polydopamine layer and induce AgNPs formation without additional reductants or stabilizers. The chemical and physicochemical properties of AgNPs coated CVCs were characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, and water contact angle. The Staphylococcus aureus culture experiment was used to study the antibacterial properties. The cytocompatibility was assessed by water soluble tetrazolium salts (WST-1 assay, fluorescence staining, and scanning electron microscopy analysis. The results indicated that the CVCs surface was successfully coated with compact AgNPs. AgNPs were significantly well separated and spherical with a size of 30–50 nm. The density of AgNPs could be modulated by the concentration of silver nitrate solution. The antibacterial activity was dependent on the AgNPs dose. The high dose of AgNPs showed excellent antibacterial activity while associated with increased cytotoxicity. The appropriate density of AgNPs coated CVCs could exhibit improved biocompatibility and maintained evident sterilization effect. It is promising to design mussel-inspired silver releasing CVCs with both

  6. Preparation and bactericide activity of gallic acid stabilized gold nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Moreno-Alvarez, S. A. [UASLP, Doctorado Institucional en Ingenieria y Ciencia de Materiales (Mexico); Martinez-Castanon, G. A., E-mail: mtzcastanon@fciencias.uaslp.m [UASLP, Maestria en Ciencias Odontologicas, Facultad de Estomatologia (Mexico); Nino-Martinez, N. [UASLP, Facultad de Ciencias (Mexico); Reyes-Macias, J. F.; Patino-Marin, N.; Loyola-Rodriguez, J. P. [UASLP, Maestria en Ciencias Odontologicas, Facultad de Estomatologia (Mexico); Ruiz, Facundo [UASLP, Facultad de Ciencias (Mexico)

    2010-10-15

    In this work, gold nanoparticles with three different sizes (13.7, 39.4, and 76.7 nm) were prepared using a simple aqueous method with gallic acid as the reducing and stabilizing agent, the different sizes were obtained varying some experimental parameters as the pH of the reaction and the amount of the gallic acid. The prepared nanoparticles were characterized using X-ray diffraction, transmission electron microscopy, dynamic light scattering, and UV-Vis spectroscopy. Samples were identified as elemental gold and present spherical morphology, a narrow size distribution and good stabilization according to TEM and DLS results. The antibacterial activity of this gallic acid stabilized gold nanoparticles against S. mutans (the etiologic agent of dental caries) was assessed using a microdilution method obtaining a minimum inhibitory concentration of 12.31, 12.31, and 49.25 {mu}g/mL for 13.7, 39.4, and 76.7 nm gold nanoparticles, respectively. The antibacterial assay showed that gold nanoparticles prepared in this work present a bactericide activity by a synergistic action with gallic acid. The MIC found for this nanoparticles are much lower than those reported for mixtures of gold nanoparticles and antibiotics.

  7. Preparation and bactericide activity of gallic acid stabilized gold nanoparticles

    Science.gov (United States)

    Moreno-Álvarez, S. A.; Martínez-Castañón, G. A.; Niño-Martínez, N.; Reyes-Macías, J. F.; Patiño-Marín, N.; Loyola-Rodríguez, J. P.; Ruiz, Facundo

    2010-10-01

    In this work, gold nanoparticles with three different sizes (13.7, 39.4, and 76.7 nm) were prepared using a simple aqueous method with gallic acid as the reducing and stabilizing agent, the different sizes were obtained varying some experimental parameters as the pH of the reaction and the amount of the gallic acid. The prepared nanoparticles were characterized using X-ray diffraction, transmission electron microscopy, dynamic light scattering, and UV-Vis spectroscopy. Samples were identified as elemental gold and present spherical morphology, a narrow size distribution and good stabilization according to TEM and DLS results. The antibacterial activity of this gallic acid stabilized gold nanoparticles against S. mutans (the etiologic agent of dental caries) was assessed using a microdilution method obtaining a minimum inhibitory concentration of 12.31, 12.31, and 49.25 μg/mL for 13.7, 39.4, and 76.7 nm gold nanoparticles, respectively. The antibacterial assay showed that gold nanoparticles prepared in this work present a bactericide activity by a synergistic action with gallic acid. The MIC found for this nanoparticles are much lower than those reported for mixtures of gold nanoparticles and antibiotics.

  8. Preparation of silver nanoparticles at low temperature

    Science.gov (United States)

    Mishra, Mini; Chauhan, Pratima

    2016-04-01

    Silver from ancient time is used as antimicrobial agent in the bulk form but now with the advancement in nanotechnology silver in the form of nanoparticles shown potential effect against microbes which make us easy to fight with many diseases plants and animals. In this work silver nanoparticles were synthesized by chemical routes using sodium borohydride as reducing agent at low temperature. The particles were characterized through UV-Visible spectroscopy as well as X-Ray Diffraction. The UV-visible spectra of silver nanoparticles exhibited absorption at 425 cm; the crystallite size of the particles is between 19nm to 39nm. EDAX graph shows two peaks of silver and oxygen. Water absorbed by silver nanoparticles was removed by the calcinations.

  9. Characterization and Preparation of Bimetallic Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Bing; Joe; Hwang; Ching; Hsiang; Chen; Loka; Subramanyam; Sarma; Din-gao; Liu; Jyh; Fu; Lee

    2007-01-01

    1 Results Bimetallic particles in the nanometer size range are of substantial interest due to their vast applications in catalysis[1].The synthesis of bimetallic nanoparticles with definite size with a well-control over their nanostructure remains a challenging problem.Thus there exists a great demand for both synthesis and atomic level characterization of nanostructure of bimetallic nanoparticles (NPs).With the recent advent of high-intensity tunable sources of X-rays,now available at synchrotron radia...

  10. BIOMIMETIC SURFACE PREPARATION OF INERT POLYMER FILMS VIA GRAFTING LONG MONOALKYL CHAIN PHOSPHATIDYLCHOLINE

    Institute of Scientific and Technical Information of China (English)

    Peng-jun Wan; Dong-sheng Tan; Zheng-sheng Li; Xiao-qing Zhang; Jie-hua Li; Hong Tan

    2012-01-01

    To explore construction of novel mimicking biomembrane on biomaterials surfaces,a new polymerizable phosphatidylcholine containing a long monoalkyl chain ended with acryl group (AASOPC) was designed and synthesized,which was easily derived from the terminal amino group of 9-(2-amino-ethylcarbamoyl)-nonyl-l-phosphatidyl-choline (ASOPC) reacting with acryloyl chloride.The obtained AASOPC was grafted on poly(ethylene terephthalate) (PET) via surface-initiated atom-transfer radical polymerization (SI-ATRP) to form mimicking biomembrane.These modified surface structures of PET were investigated using water contact angle (WAC),X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM).The results indicated that the new mimicking phosphatidylcholine biomembrane could be prepared on inert polymer surfaces by using the acryloyl phosphatidylcholine (AASOPC) via surface-initiated atom transfer radical polymerization (SI-ATRP).

  11. Preparation of a biomimetic polyphosphorylcholine monolithic column for immobilized artificial membrane chromatography.

    Science.gov (United States)

    Zhao, XiangLong; Chen, WeiJia; Zhou, ZhengYin; Wang, QiQin; Liu, ZhengHua; Moaddel, Ruin; Jiang, ZhengJin

    2015-08-14

    The present work aims to prepare a novel phosphatidylcholine functionalized monolithic stationary phase by in situ co-polymerization of 12-methacryloyl dodecylphosphocholine (MDPC) and ethylene dimethacrylate (EDMA) for immobilized artificial membrane chromatography. Scanning electron microscopy, energy dispersive X-ray spectroscopy, FT-IR spectroscopy, pore size distribution analysis, ζ-potential analysis and micro-HPLC were used to evaluate the monolithic structure and physicochemical properties. Satisfactory morphology, high mechanical stability, good permeability and chromatographic performance were obtained on the optimized monolithic columns. A typical reverse-phase retention mechanism was observed over a wide range of organic solvent content (acetonitrilecolumn (IAM.PC.DD2) and poly(MDPC-co-EDMA) monolith. This novel poly(MDPC-co-EDMA) monolith exhibited good potential for studying the drug-membrane interaction.

  12. Preparation of nanoparticles with an environment-friendly approach

    Institute of Scientific and Technical Information of China (English)

    YAO Kefu; PENG Zhen; FAN Xiaolin

    2009-01-01

    Developing various approaches for preparing high performance materials has long been topics and tasks both for scientists and for engineers.Despite that many methods have been developed for preparing nanomaterials,developing simple and environment-friendly ways for preparing nanomaterials is very attractive.A simple approach of synthesizing Fe3O4 nanoparticles by arc-discharge submerging in water was reported.The results showed that by this method Fe3O4 nanoparticles can be synthesized in large scale.The as-prepared Fe3O4 nanoparticles exhibit uniform spherical shape and their diameters varied with arc-discharging parameters.The experimental results showed that the size of the synthesized Fe3O4 nanoparticles can be controlled through adjusting the processing parameters.Since no vacuum system has been used,the synthesizing process is greatly simplified.In addition,only cheap deionized water and industrial iron bar are used and no pollution or harmful by-products are found in the synthesis process.It indicated that the present approach is a simple,low-cost and environment-friendly for preparing nanoparticles.

  13. Preparation and evaluations in vitro of oxaliplatin polylactic acid nanoparticles.

    Science.gov (United States)

    Cui, Zhaoyuan; Sun, Yong; Liu, Xiaohong; Ju, Fang; Chen, Qian; Gao, Wen; Wei, Haitian

    2013-08-01

    The oxaliplatin nanoparticles were prepared with polylactic acid matrix, orthogonal test was applied to optimize the prescriptions, and the qualities of oxaliplatin nanoparticles were characterized by the shape, particle size, encapsulation efficiency (EE), and drug loading (DL). Oxaliplatin nanoparticle was prepared by solution replacement method. The formation of 0.25% Tween80, DMF-water 1:8 (v/v), oxaliplatin-polylactic acid 1:5 (w/w), and 20 mg/ml polylactic acid showed the suitable EE (17.4 ± 0.47%), DL (3.52 ± 0.07%). We observed the shape of oxaliplatin nanoparticles through SEM. The average size of the particles was 120.5 ± 8.7 nm, which was detected by N5 submicron particle size analyzer.

  14. Universal biomimetic preparation and immobilization of layered double hydroxide films and adsorption behavior

    Science.gov (United States)

    Zhou, Wei; Zhang, Wenpeng; Chen, Zilin

    2017-01-01

    Preparation and immobilization of layered double hydroxides (LDHs) film onto multiple substrates is important and challenging in functional materials fields by date. In this work, a simple and universal polydopamine (PD)-based layer-by-layer assembly strategy was developed for the immobilization of LDHs film onto surfaces such as polypropylene chip, glass slides and metal coins. The surface of substrates was firstly modified by polydopamine functionalization, and then LDHs film was synthesized via urea method and directly immobilized on the PD layer by in situ growing strategy in one step. The PD layer as well as the final LDHs film was characterized by energy dispersive X-ray spectroscopy, scanning electron microscope, infrared spectroscopy, X-ray diffraction pattern and X-ray photoelectron spectra. It has been demonstrated the formation of the dense and homogeneous nanoscaled LDHs film with 400 nm thickness. Adsorption behavior of the fabricated NiAl-LDHs film toward anionic dyes and pharmaceuticals was further assessed. To demonstrate their extensive application, fast and high efficient adsorption of anionic dyes and pharmaceuticals was achieved by NiAl-LDHs-modified polypropylene centrifugal tube.

  15. Nacre biomimetic design--a possible approach to prepare low infrared emissivity composite coatings.

    Science.gov (United States)

    Zhang, Weigang; Xu, Guoyue; Ding, Ruya; Duan, Kaige; Qiao, Jialiang

    2013-01-01

    Mimicking the highly organized brick-and-mortar structure of nacre, a kind of nacre-like organic-inorganic composite material of polyurethane (PU)/flaky bronze composite coatings with low infrared emissivity was successfully designed and prepared by using PU and flaky bronze powders as adhesives and pigments, respectively. The infrared emissivity and microstructure of the coatings were systematically investigated by infrared emissometer and scanning electron microscopy, respectively, and the cause of low infrared emissivity of the coatings was discussed by using the theories of one-dimensional photonic structure. The results show that the infrared emissivity of the nacre-like PU/flaky bronze composite coatings can be as low as 0.206 at the bronze content of 60 wt. %, and it is significantly lower than the value of PU/sphere bronze composite coatings. Microstructure observation illustrated that the nacre-like PU/flaky bronze composite coatings have similar one-dimensional photonic structural characteristics. The low infrared emissivity of PU/flaky bronze composite coatings is derived from the similar one-dimensional photonic structure in the coatings.

  16. Metal Nanoparticles Preparation In Supercritical Carbon Dioxide Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Harry W. Rollins

    2004-04-01

    The novel optical, electronic, and/or magnetic properties of metal and semiconductor nanoparticles have resulted in extensive research on new methods for their preparation. An ideal preparation method would allow the particle size, size distribution, crystallinity, and particle shape to be easily controlled, and would be applicable to a wide variety of material systems. Numerous preparation methods have been reported, each with its inherent advantages and disadvantages; however, an ideal method has yet to emerge. The most widely applied methods for nanoparticle preparation include the sonochemical reduction of organometallic reagents,(1&2) the solvothermal method of Alivisatos,(3) reactions in microemulsions,(4-6) the polyol method (reduction by alcohols),(7-9) and the use of polymer and solgel materials as hosts.(10-13) In addition to these methods, there are a variety of methods that take advantage of the unique properties of a supercritical fluid.(14&15) Through simple variations of temperature and pressure, the properties of a supercritical fluid can be continuously tuned from gas-like to liquid-like without undergoing a phase change. Nanoparticle preparation methods that utilize supercritical fluids are briefly reviewed below using the following categories: Rapid Expansion of Supercritical Solutions (RESS), Reactive Supercritical Fluid Processing, and Supercritical Fluid Microemulsions. Because of its easily accessible critical temperature and pressure and environmentally benign nature, carbon dioxide is the most widely used supercritical solvent. Supercritical CO2 is unfortunately a poor solvent for many polar or ionic species, which has impeded its use in the preparation of metal and semiconductor nanoparticles. We have developed a reactive supercritical fluid processing method using supercritical carbon dioxide for the preparation of metal and metal sulfide particles and used it to prepare narrowly distributed nanoparticles of silver (Ag) and silver sulfide

  17. Preparation of amine coated silver nanoparticles using triethylenetetramine

    Indian Academy of Sciences (India)

    L Ramajo; R Parra; M Reboredo; M Castro

    2009-01-01

    This article presents a simple method towards the preparation of functionalized silver nanoparticles in a continuous medium. Silver nanoparticles were obtained through AgNO3 chemical reduction in ethanol and triethylenetetramine was used to stabilize and functionalize the metal. The product was characterized with X-ray diffraction (XRD), Fourier-transformed infrared spectroscopy (FTIR), UVvisible spectroscopy, thermal gravimetric analysis (TGA) and transmission electron microscopy (TEM). Monocrystalline silver particles with cubic structure and an average size of 20 nm were obtained. The results reveal that it is possible to synthesize Ag nanoparticles functionalized with amine groups and that particle size is influenced by the processing route.

  18. Peptide-Loaded Solid Lipid Nanoparticles Prepared through Coacervation Technique

    Directory of Open Access Journals (Sweden)

    Marina Gallarate

    2011-01-01

    Full Text Available Stearic acid solid lipid nanoparticles were prepared according to a new technique, called coacervation. The main goal of this experimental work was the entrapment of peptide drugs into SLN, which is a difficult task, since their chemical characteristics (molecular weight, hydrophilicity, and stability hamper peptide-containing formulations. Insulin and leuprolide, chosen as model peptide drugs, were encapsulated within nanoparticles after hydrophobic ion pairing with anionic surfactants. Peptide integrity was maintained after encapsulation, and nanoparticles can act in vitro as a sustained release system for peptide.

  19. Preparation and Characterization of Biomimetic Hydroxyapatite-Resorbable Polymer Composites for Hard Tissue Repair

    Science.gov (United States)

    Hiebner, Kristopher Robert

    Autografts are the orthopedic "gold standard" for repairing bone voids. Autografts are osteoconductive and do not elicit an immune response, but they are in short supply and require a second surgery to harvest the bone graft. Allografts are currently the most common materials used for the repair of segmental defects in hard tissue. Unlike autografts, allografts can cause an undesirable immune response and the possibility of disease transmission is a major concern. As an alternative to the above approaches, recent research efforts have focused on the use of composite materials made from hydroxyapatite (HA) and bioresorbable polymers, such as poly-L-lactide (PLLA). Recent results have shown that the surface hydroxides on HA can initiate the ring opening polymerization (ROP) of L-lactide and other lactones creating a composite with superior interfacial strength. This thesis demonstrates that the surface of porous biologically derived HA substrates, such as coralline HA and trabecular bone, can be used to initiate the ROP of L-lactide and other lactones from the vapor phase. This process increases the strength of the porous scaffold through the deposition of a thin, uniform polymer coating, while maintaining the porous structure. The kinetics of the chemical vapor deposition polymerization (CVDP) are described using a quartz crystal microbalance (QCM). The reaction temperature and monomer vapor pressure are found to affect the rate of the polymerization. Also described in this thesis is the preparation of a porous polymer scaffold that mimics the structure of demineralized bone matrix (DBM). This demineralized bone matrix simulant (DBMS) is created using anorganic bovine bone as a template to initiate the polymerization of various lactones, followed by the removal of the HA scaffold. This material retained its shape and exhibits mechanical properties superior to DBM. Finally it is shown that HA can be used to initiate the ROP of a-caprolactam and the biocompatibility

  20. Preparation and evaluation of a biomimetic scaffold with porosity gradients in vitro

    Directory of Open Access Journals (Sweden)

    Qianbin Wang

    2012-03-01

    Full Text Available A novel biodegradable scaffold based on mimetic a natural bone tissue morphology with a porosity gradient structure was prepared in this paper. The result of surface morphology indicated that a graded porous structure was formed in the fabricated scaffold, where the dense layer (0% was connected with the most porous layer (60% by a middling porous layer (30%. To evaluate the degradability, graded porous scaffolds compared with homogeneous scaffolds were placed into a Tris-HCl buffer solution (pH = 7.4 for 28 days. It was found that both scaffolds presented the same degradation trend, and the graded porous structure did not change the original degradability of the scaffold. Moreover, the compressive strength of the graded porous scaffold was better than that of conventional homogeneous scaffold with the increase of degradation time, and the graded porous structure can enhanced the mechanical property of the scaffold. These findings suggest that this biodegradable and porosity-graded scaffold may be a new promising scaffold for loaded bone implant.Um novo esqueleto mimetizando a morfologia de tecido ósseo e com uma estrutura de porosidade gradiente foi preparado e é descrito neste artigo. O resultado da avaliação da morfologia da superfície indicou que uma estrutura porosa gradiente se formou no esqueleto fabricado no qual uma camada densa (0% foi conectada com a camada mais porosa (60% por uma camada porosa média (30%. Para avaliar a degradabilidade, esqueletos de porosidade gradiente e esqueletos homogêneos foram colocados em uma solução tampão Tris-HCL (pH = 7,4 durante 28 dias. Observou-se que ambos os esqueletos apresentaram a mesma tendência de degradação e a estrutura de porosidade gradiente não modificou a degradabilidade original do esqueleto. Além disso, a força compressiva do esqueleto de porosidade gradiente foi melhor do que aquela do esqueleto homogêneo convencional, com aumento do tempo de degradação, e que a

  1. Preparation of Chitosan Nanoparticles: A Study of Influencing Factors

    Science.gov (United States)

    Thakur, Anupama; Taranjit

    2011-12-01

    Chitosan (CS), a cationic polysaccharide, offers great advantages for ionic interactions with negatively charged species such as sodium tripolyphosphate (STPP) leading to the formation of biocompatible crosslinked chitosan nanoparticles In the present work, an attempt has been made to systematically study the following factors influencing the ionotropic gelation of chitosan with STPP to produce CS nanoparticles: effect of pH of solution, CS concentration, STPP concentration and CS/STPP ratio. The results show that with the increase in CS concentration, the yield of the nanoparticle decreases whereas size increases. The mean size of the prepared nanoparticles varied between 120 to 720 nm and zeta potential between +14 mV to +53 mV . Nanoparticle size and yield was found to be strongly dependent on solution pH. Nanoparticle size decreased with increase in solution pH from 4 to 5 and yield was found to be maximum at pH = 5. With increase in STPP concentration, the size and yield of the nanoparticle increased. The potential of CS nanoparticles to trap amoxicillin trihydrate, taken as the model drug, was also studied. The maximum drug loading capacity was found to be 35% at a solution pH = 5 for 0.2% CS and 0.086% STPP.

  2. Preparation and characterization of free-standing pure porphyrin nanoparticles

    Indian Academy of Sciences (India)

    Arun Kumar Perepogu; Prakriti Ranjan Bangal

    2008-09-01

    Preparation and characterization of absolutely pure and stable nanoparticles of 5,10,15,20-meso-tetrakis phenyl porphyrin (TPP) and catalytically repute 5,10,15,20-meso-tetrakis pentaflurophenyl porphyrin (H2F20TPP) by improved ‘reprecipitation method’ is described. The innovation of this modified `reprecipitation method’ lies on the judicial selection of organic solvent and amount of porphyrin solution to be injected in the aqueous media. Exactly similar process produces relatively small nanoparticles for TPP than that of H2F20TPP while the stability of the H2F20TPP nanoparticles is bit higher than nanoparticles of TPP. Absorption and emission spectra reveal that the formation of nanoparticles for both the cases is induced by J- and H-type aggregation. DFT calculations predict the optimized geometries and frontier molecular orbital, which favours the strength of face-to-face interaction with neighbour molecules to be more facile for TPP than that of H2F20TPP helping the latter to form bigger and relatively more stable and free-standing nanoparticles. The use of no other compounds except dichloromethane, a highly volatile organic solvent and respective porphyrins give absolutely pure nanoparticles. This improved method will lead to produce organic nanoparticles of -conjugated systems easily and efficiently.

  3. PREPARATION AND CHARACTERIZATION OF DOXORUBICIN-LOADED MAGNETIC ANTICANCER NANOPARTICLES

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Doxorubicin(ADM)-loaded magnetic anticancer nanoparticles,using Fe3O4 as core, doxorubicin as model drug and polyvinylpyrrolidone (PVP) as matrix, were prepared by inverse emulsion polymerization. The experimental results showed that the average diameter of Fe3O4 particles was 19.8nm. The X-ray diffraction indicated that the prepared Fe3O4 particle was pure cubic Fe3O4. The results obtained by SEM showed the magnetic nanoparticles under optimal operating condition had a smooth spherical surface , LLS showed an average size of 78.7nm. And IR results demonstrated that they consisted of ADM, PVP and Fe3O4.

  4. Improved nanoparticles preparation and drug release for liver targeted delivery

    Directory of Open Access Journals (Sweden)

    Qiao Weili

    2009-05-01

    Full Text Available "nTargeted delivery of drugs and proteins to liver can be achieved via asialoglycoprotein receptor, which can recognize and combine the galactose- and N-acetygalatosamine-terminated glycoproteins. Glycosyl is usually conjugated with drugs directly to fabricate prodrugs or with nanoparticles encapsulated drugs via forming covalent bonds, while the covalent bonds may lead to some shortages for drug release. Therefore, we have a hypothesis that we can prepare nanoparticles for efficient targeting by glycosylation using galactosylated poly (L-glutamic acid (Gal-PLGA as a carrier to entrap the model drugs in nanoparticles core physically rather than forming covalent drug conjugation. The means of incorporation of drug in nanoparticles may improve drug release to maintain its activity, raise its therapeutic index and diminish the adverse effect. Based on previous researches, it is achievable to obtain nanoparticles that we hypothesize to prepare. Due to their nanometer-size and galactosyl, the nanoparticles may be a potential delivery system for passive and active targeting to liver parenchymal cells for therapy of hepatitis and liver cancer.

  5. Preparation of Candesartan and Atorvastatin Nanoparticles by Solvent Evaporation

    Directory of Open Access Journals (Sweden)

    Josef Jampilek

    2012-11-01

    Full Text Available The solubility, absorption and distribution of a drug are involved in the basic aspects of oral bioavailability Solubility is an essential characteristic and influences the efficiency of the drug. Over the last ten years, the number of poorly soluble drugs has steadily increased. One of the progressive ways for increasing oral bioavaibility is the technique of nanoparticle preparation, which allows many drugs to thus reach the intended site of action. Candesartan cilexetil and atorvastatin, belonging to class II of the biopharmaceutical classification system, were chosen as model active pharmaceutical ingredients in this study. Forty samples were prepared either by antisolvent precipitation/solvent evaporation method or by the emulsion/solvent evaporation technique with various commonly used surface-active excipients as nanoparticle stabilizers. All samples were analyzed by means of dynamic light scattering. The particle size of the determined 36 nanoparticle samples was to 574 nm, whereas 32 samples contained nanoparticles of less than 200 nm. Relationships between solvents and excipients used and their amount are discussed. Based on the results the investigated solvent evaporation methods can be used as an effective and an affordable technique for the preparation of nanoparticles.

  6. Loading technique for preparing radionuclide containing nanoparticles

    DEFF Research Database (Denmark)

    2011-01-01

    Source: US2012213698A The present invention relates to a novel composition and method for loading delivery systems such as liposome compositions with radionuclides useful in targeted diagnostic and/or therapy of target site, such as cancerous tissue and, in general, pathological conditions associ...... of positron emission tomography (PET) imaging technique. One specific aspect of the invention is directed to a method of producing nanoparticles with desired targeting properties for diagnostic and/or radio-therapeutic applications....

  7. Holmium nanoparticles : preparation and in vitro characterization of a new device for radioablation of solid malignancies

    NARCIS (Netherlands)

    Bult, Wouter; Varkevisser, Rosanne; Soulimani, Fouad; Seevinck, Peter R; de Leeuw, Hendrik; Bakker, Chris J G; Luijten, Peter R; van Het Schip, Alfred D; Hennink, Wim E; Nijsen, J Frank W

    2010-01-01

    PURPOSE: The present study introduces the preparation and in vitro characterization of a nanoparticle device comprising holmium acetylacetonate for radioablation of unresectable solid malignancies. METHODS: HoAcAc nanoparticles were prepared by dissolving holmium acetylacetonate in chloroform, follo

  8. Facile Preparation of Silver Halide Nanoparticles as Visible Light Photocatalysts

    Directory of Open Access Journals (Sweden)

    Linfan Cui

    2015-07-01

    Full Text Available In this study, highly efficient silver halide (AgX-based photocatalysts were successfully fabricated using a facile and template-free direct-precipitation method. AgX nanoparticles, which included silver chloride (AgCl, silver bromide (AgBr and silver iodide (AgI, were synthesized using different potassium halides and silver acetate as reactive sources. The size distribution of the AgX nanopar‐ ticles was determined by the reaction time and ratio of the reagents, which were monitored by UV-vis spectra. The as- prepared AgX nanoparticles exhibited different photoca‐ talytic properties. This shows the differences for the photodegradation of methyl orange and Congo red dyes. In addition, the AgCl nanoparticle-based photocatalyst exhibited the best photocatalytic property among all three types of AgX nanoparticles that are discussed in this study. Therefore, it is a good candidate for removing organic pollutants.

  9. The preparation and fluorescence properties of europium nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A new structured metallic nanomaterial of europium nanoparticle was prepared using tannic acid as the reductive agent, and nanoeuropium protein conjugates were synthesized by the method of lipoic acid modification on the surface of nanoparticle, which opens a new field of application of lanthanides in nanotechniques. Their properties were also characterized by UV-vis absorption spectroscopy, transmission electron microscopy (TEM), and fluorescence spectroscopy. The europium nanoparticle and its protein conjugates solution were stable and water-soluble. The fluorescence intensity of the composite europium nanoparticles was significantly increased in the presence of trace protein, and was linear proportional to the concentration of proteins under optimum conditions. According to this, a fluorimetric method for the determination of protein was developed in this paper.

  10. Platinum adlayered ruthenium nanoparticles, method for preparing, and uses thereof

    Energy Technology Data Exchange (ETDEWEB)

    Tong, YuYe; Du, Bingchen

    2015-08-11

    A superior, industrially scalable one-pot ethylene glycol-based wet chemistry method to prepare platinum-adlayered ruthenium nanoparticles has been developed that offers an exquisite control of the platinum packing density of the adlayers and effectively prevents sintering of the nanoparticles during the deposition process. The wet chemistry based method for the controlled deposition of submonolayer platinum is advantageous in terms of processing and maximizing the use of platinum and can, in principle, be scaled up straightforwardly to an industrial level. The reactivity of the Pt(31)-Ru sample was about 150% higher than that of the industrial benchmark PtRu (1:1) alloy sample but with 3.5 times less platinum loading. Using the Pt(31)-Ru nanoparticles would lower the electrode material cost compared to using the industrial benchmark alloy nanoparticles for direct methanol fuel cell applications.

  11. The Intelligent Properties of Micro-reactors for Preparating Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Gang WEI; Hai Yan HUANG; Rong Chun XIONG

    2003-01-01

    TiO2 nanoparticles were synthesized by using micro-reactors. The shape and size of the nanoparticles produced from the original micro-reactors and the five times recycled micro-reactors mother liquor were investigated on transmission electron microscopy (TEM) by using the original sample, freeze prepared sample, and dyeing treated sample, respectively. UV-VIS spectrometry was used to study the growth process of TiO2 nanoparticles in main reactors. The results showed that micro-reactors with nanometer magnitude had spherical or oval structures, and could restore to their original structure after they were destroyed. The products prepared in the original micro-reactors were similar to that in the micro-reactors recycled for many times, suggesting that the micro-reactors had memory function.

  12. Preparation and Characterization of Polymeric Nanoparticles: An Interdisciplinary Experiment

    Science.gov (United States)

    Ramalho, Maria J.; Pereira, M. Carmo

    2016-01-01

    In this work, a laboratory experiment to introduce graduate students to nanotechnology is described. Students prepared poly(lactic-"co"-glycolic acid) (PLGA) nanoparticles using two different synthesis procedures, a single and a double emulsion-solvent evaporation method. The students also performed a physicochemical characterization of…

  13. Control-release microcapsule of famotidine loaded biomimetic synthesized mesoporous silica nanoparticles: Controlled release effect and enhanced stomach adhesion in vitro.

    Science.gov (United States)

    Li, Jing; Wang, Hongyu; Yang, Baixue; Xu, Lu; Zheng, Nan; Chen, Hongtao; Li, Sanming

    2016-01-01

    In the present work, control-release microcapsule of famotidine (FMT) loaded biomimetic synthesized mesoporous silica nanoparticles (B-MSNs) was developed, and controlled release effect and stomach adhesion of this formulation in vitro were mainly investigated. B-MSN was previously synthesized and it was amorphous mesoporous nanoparticles with helical channels. Cytotoxicity of B-MSN was studied using human breast cancer cells (MCF-7) and the result indicated that cytotoxicity of B-MSN can be neglected. After loading FMT into B-MSN, specific surface area, pore volume and pore diameter of B-MSN were obviously reduced. In vitro dissolution test showed that B-MSN had the ability to slow down FMT release for 15 min. In order to prolong controlled release effect and remained the advantage of B-MSN (improve drug stability due to its rigid silica framework), the combined application of control-release microcapsule (using cellulose and hydroxypropyl methylcellulose K15M as excipients) with B-MSN was designed. It was obvious that newly designed formulation significantly controlled FMT release with Fickian diffusion mechanism and showed enhanced stomach adhesion in vitro, which has significant value in widening the application of B-MSN in formulation design.

  14. Preparation of metal oxide nanoparticles in ionic liquid medium

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez-Cabo, Borja; Rodil, Eva; Soto, Ana; Arce, Alberto, E-mail: alberto.arce@usc.es [University of Santiago de Compostela, Department of Chemical Engineering, School of Engineering (Spain)

    2012-07-15

    In the present study, a facile, rapid, and environmentally friendly method was used for the preparation of metal oxide nanoparticles in an ionic liquid medium. This technique involves mixing and heating the corresponding powder material (cadmium oxide, anatase, and hematite) and the selected ionic liquid (trihexyl(tetradecyl)phosphonium chloride, [P{sub 6,6,6,14}]Cl), without any other precursors or solvents. The confirmation of the existence of nanoparticles in the ionic liquid was carried out using UV-Vis absorption spectroscopy, and its concentration was determined by X-ray fluorescence. In order to analyze the shape and size distribution, transmission electron microscopy and a ZetaSizer (DLS technique) were used; finding out that the size of the hematite nanoparticles was 10-55 nm. Nevertheless, for the cadmium oxide and the anatase nanoparticles, the size was between 2 and 15 nm. The composition of the prepared nanoparticles was studied by Raman spectroscopy. The structure of solids did not suffer any modification in their transformation to the nanoscale, as concluded from the X-ray powder diffraction analysis.

  15. Preparation of Risedronate Nanoparticles by Solvent Evaporation Technique

    Directory of Open Access Journals (Sweden)

    Eliska Vaculikova

    2014-11-01

    Full Text Available One approach for the enhancement of oral drug bioavailability is the technique of nanoparticle preparation. Risedronate sodium (Biopharmaceutical Classification System Class III was chosen as a model compound with high water solubility and low intestinal permeability. Eighteen samples of risedronate sodium were prepared by the solvent evaporation technique with sodium dodecyl sulfate, polysorbate, macrogol, sodium carboxymethyl cellulose and sodium carboxymethyl dextran as nanoparticle stabilizers applied in three concentrations. The prepared samples were characterized by dynamic light scattering and scanning electron microscopy. Fourier transform mid-infrared spectroscopy was used for verification of the composition of the samples. The particle size of sixteen samples was less than 200 nm. Polysorbate, sodium carboxymethyl dextran and macrogol were determined as the most favourable excipients; the particle size of the samples of risedronate with these excipients ranged from 2.8 to 10.5 nm.

  16. Systematic study on the preparation of BSA nanoparticles.

    Science.gov (United States)

    Galisteo-González, F; Molina-Bolívar, J A

    2014-11-01

    Albumins, in the form of nanoparticles, are increasingly used as drug carriers in the medical field, and the size effect of these nanomaterials is of major importance since it may affect their bioavailability and the in vivo behaviour after intravenous injection. This research provides a comprehensive study on the preparation of BSA nanoparticles, based on a simple coacervation method, with suitable size, size distribution, and surface charge for drug-delivery applications. Numerous experimental variables were examined in order to characterize their impact on nanoparticle size, distribution, electrophoretic mobility, and yield. Particle size was controlled by adjusting self-assembly phenomena of the protein molecules, which was affected by preparation conditions including BSA content, pH, and ionic strength (a parameter that strongly influences nanoparticle formation but surprisingly has not been previously studied in detail). Small particles with a narrow size distribution were obtained under experimental conditions where the repulsion between BSA molecules was high, i.e. at pH values far from the isoelectric point of the protein and low salt concentration. Changes in temperature, volume, and rate of addition of the dehydrating agent (ethanol) also affect nanoparticle characteristics, as they influence the nucleation rate and particle growth. The effect of these experimental conditions on the quantity of protein still dissolved in the aqueous phase after desolvation (i.e. the yield of BSA nanoparticles) was also studied. Nanoparticles surface charge was modulated with the extension of cross-linking. Finally, long-term colloidal stability of samples was evaluated after 2 months of storage.

  17. The optical nonlinearity of gold nanoparticles prepared by bioreduction method

    Science.gov (United States)

    Balbuena Ortega, A.; Arroyo Carrasco, M. L.; Gayou, V. L.; Orduña Díaz, A.; Delgado Macuil, R.; Rojas López, Marlon

    2013-11-01

    Nonlinear optical and electronic properties of nanosized metal particles have drawn considerable attention because of their strong and size-dependent plasmon resonance absorption. In a metal nanoparticle system such as gold dispersed in a transparent matrix, an absorption peak due to surface plasmon resonance is usually observed in the visible spectral region. Metal nanoparticles are of special interest as nonlinear materials for optical switching and computing because of their relatively large third-order nonlinearity (χ3) and ultrafast response time. The purpose of this study was to analyze the nonlinear optical properties of biosynthesized gold nanoparticles. The samples were prepared by biosynthesis method using yeast extract as reducing agent and the nonlinear optical properties of the nanoparticles were investigated using a single beam Z-scan technique with a beam power of 20 mW and operated at wavelength of 514 nm. The reaction between metal ions and yeast extracts were monitored by UV-visible spectra of Au nanoparticles in aqueous solution with different pH (3-6). The surface plasmon peak position was shifted from 528 nm to 573 nm, according to of pH variation 4 to 6. The average particle size was calculated by the absorption peak position using the Fernig method, from 42 to 103 nm. The z-scan curves showed a negative nonlocal nonlinear refractive index with a magnitude dependent on the nanoparticle size.

  18. Preparation of novel core-shell nanoparticles by electrochemical synthesis

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Nanostructural gold/polyaniline core/shell composite particles on conducting electrode ITO were successfully prepared via electrochemical polymerization of aniline based on 4-aminothiophenol (4-ATP) capped Au nanoparticles. The new approach to the fabrication included three steps: preparation of gold nanoparticles as core by pulse electrodeposition; formation of ATP monolayer on the gold particle surface, which served as a binder and an initiator; polymerization of aniline monomer initiated by ATP molecules under controlled voltage lower than the voltammetric threshold of aniline polymerization, which assured the formation of polyaniline shell film occurred on gold particles selectively. Topographic images were also studied by AFM, which indicated the diameter of gold nanoparticles were around 250 nm. Coulometry characterization confirmed the shell thickness of polyaniline film was about 30 nm.A possible formation mechanism of the Au/polyaniline core-shell nanocomposites was also proposed. The novel as-prepared core-shell nanoparticles have potential application in constructing biosensor when bioactive enzymes are absorbed or embedded in polyaniline shell film.

  19. Preparation of DNA/Gold Nanoparticle Encapsulated in Calcium Phosphate

    Directory of Open Access Journals (Sweden)

    Tomoko Ito

    2011-01-01

    Full Text Available Biocompatible DNA/gold nanoparticle complex with a protective calcium phosphate (CaP coating was prepared by incubating DNA/gold nanoparticle complex coated by hyaluronic acid in SBF (simulated body fluid with a Ca concentration above 2 mM. The CaP-coated DNA complex was revealed to have high compatibility with cells and resistance against enzymatic degradation. By immersion in acetate buffer (pH 4.5, the CaP capsule released the contained DNA complex. This CaP capsule including a DNA complex is promising as a sustained-release system of DNA complexes for gene therapy.

  20. Preparation, Characterization and Antibacterial Property of Cerium Substituted Hydroxyapatite Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Lin Yingguang; Yang Zhuoru; Cheng Jiang

    2007-01-01

    Nanoparticles of hydroxyapatite (HAP) and cerium substituted hydroxyapatite (CeHAP) with the atomic ratio of Ce/[Ca+Ce] (xCe) from 0 to 0.2 were prepared by sol-gel-supercritical fluid drying (SCFD) method. The nanoparticles were characterized by TEM, XRD, and FT-IR, and the effects of cerium on crystal structure, crystallinity, and particle shape were discussed. With the tests of bacterial inhibition zone and antibacterial ratio, the antibacterial property of HAP and CeHAP nanoparticles on Escherichia coli, Staphylococcus aureus, Lactobacillus were researched. Results showed that the nanoparticles of HAP and CeHAP could be made by sol-gel-SCFD, cerium could partially substitute for calcium and enter the structure of HAP. After substitution, the crystallinity, the IR wavenumbers of bonds in CeHAP decreased gradually with increase of cerium substitution, and the morphology of the nanoparticles changed from the short rod-shaped HAP to the needle-shaped CeHAP. The nanoparticles of HAP and CeHAP with xCe below 0.08 had antibacterial property only forcibly contacting with the test bacteria at the test concentration of 0.1 g·ml-1, however, the CeHAP nanoparticles had antibacterial ability at that concentration no matter statically or dynamically contacting with the test bacteria when xCe was above 0.08, and the antibacterial ability gets better with the increase of xCe, indicating that the antibacterial property was improved after calcium was partially substituted by cerium. The improved antibacterial effects of CeHAP nanoparticle on Lactobacillus showed its potential ability to anticaries.

  1. Research Progress of Biomimetic Material Prepared by Bacterial Cellulose%细菌纤维素制备生物医用材料的研究进展

    Institute of Scientific and Technical Information of China (English)

    蔡锐波; 陈海宏; 陈向标

    2012-01-01

    Bacterial cellulose(BC) is a potential versatile biomaterial. Research progress of medical dressing, vascular prosthesis and artificial skeleton prepared by bacterial cellulose were introduced at home and abroad. In addition, the hot spots and the main development direction of bacterial cellulose composite biomimetic materials were discussed.%细菌纤维素是一种很有潜力的新型生物纤维材料.重点介绍了国内外关于细菌纤维素在制备医用敷料、人造血管及人造骨骼等医用材料方面的研究进展,并指出今后的研究热点及主要发展方向.

  2. Preparation of Boron Suboxide Nanoparticles and Their Processing

    Directory of Open Access Journals (Sweden)

    Jānis GRABIS

    2012-03-01

    Full Text Available Crystalline boron suboxide B6O particles with size in the range of 1.5 µm – 2 µm and crystallite size in the range of 32 nm – 40 nm were prepared by calcination at 1400 °C for one or two hours of precursors obtained by mixing X-ray amorphous boron with water solution of B2O3 followed by evaporation and drying. Decrease of molar ratio B/B2O3 from 16 to 14 in the precursor mixture reduced nonstoichiometry of prepared B6O although simultaneously it increased admixture of B2O3. Particulate composites of B6O with TiN or Ni nanoparticles were prepared by mechanical mixing. The spark plasma sintering process intensified the densification of prepared boron suboxide nanoparticles at 1900 °C and allowed manufacturing of fully dense bodies (98 % during five minutes. Additives of TiN or Ni nanoparticles reduced sintering temperature to 1700 °C and their promoted formation of Ti or Ni borides.DOI: http://dx.doi.org/10.5755/j01.ms.18.1.1345

  3. Template preparation of twisted nanoparticles of mesoporous silica

    Institute of Scientific and Technical Information of China (English)

    Kui Niu; Zhongbin Ni; Chengwu Fu; Tatsuo Kaneko; Mingqing Chen

    2011-01-01

    Optical isomers of N-lauroyl-L-(or-D-) alanine sodium salt {C12-L-(or-D-)AlaS} surfactants were used for the preparation of mesoporous silica nanoparticles with a twisted hexagonal rod-like morphology. Thermogravimetric analysis (TGA) was used to determine the temperature for template removal. Circular dichroism (CD) spectra of the surfactant solution with various compositions illustrated the formation and supramolecular assembly of protein-like molecular architecture leading to formation of twisted nanoparticles. Scanning electron microscopy (SEM),high-resolution transmission electron microscopy (HRTEM)and X-ray powder diffraction (XRD) patterns of these as-synthesized mesoporous silica confirmed that the twisted morphology of these nanoparticles was closely related to the supramolecular-assembled complex of amino acid surfactants.

  4. Preparation, structural and morphological studies of Ni doped titania nanoparticles.

    Science.gov (United States)

    Rajamannan, B; Mugundan, S; Viruthagiri, G; Shanmugam, N; Gobi, R; Praveen, P

    2014-07-15

    TiO2 nanoparticles doped with different weight percentages (4%, 8%, 12% and 16%) of nickel contents were prepared by a modified sol-gel method using Titanium tetra iso propoxide and nickel nitrate as precursors and 2-propanol as a solvent. X-ray diffraction studies show that the as prepared and annealed products show anatase structure with average particle sizes running between of 8 and 16 nm. FTIR results demonstrate the presence of strong chemical bonding at the interface of TiO2 nanoparticles. The optical properties of bare and doped samples were carried out using UV-DRS and photoluminescence measurements. The surface morphology and the element constitution of the nickel doped TiO2 nanoparticles were studied by scanning electron microscope attached with energy dispersive X-ray spectrometer arrangement. The non linear optical properties of the products were confirmed by Kurtz second harmonic generation (SHG) test and the output power generated by the nanoparticle was compared with that of potassium di hydrogen phosphate (KDP).

  5. Preparation of Magnetic Chitosan Nanoparticles and Immobilization of Laccase

    Institute of Scientific and Technical Information of China (English)

    FANG Hua; HUANG Jun; DING Liyun; LI Mingtian; CHEN Zhao

    2009-01-01

    The magnetic chitosan nanoparticles were prepared by reversed-phase suspension method using Span-80 as an emulsifier, glutaraldehyde as cross-linking reagent. And the nanoparticles were characterized by TEM, FT-IR and hysteresis loop. The results show that the nanoparticles are spherical and almost superparamagnetic. The laccase was immobilized on nanoparticles by adsorption and subsequently by cross-linking with glutaraldehyde. The immobilization conditions and charac-terizations of the immobilized laccase were investigated. The optimal immobilization conditions were as follows: 10 mL of phosphate buffer (0.1 M, pH 7.0) containing 50 mg of magnetic chitosan nanoparticles, 1.0 mg·mL-1 of laccase and 1% (v/v) glutaraldehyde, immobilization temperature of 4 ℃ and immobilization time of 4 h. The immobilized laccase exhibited an appreciable catalytic capability (480 units·g-1 support) and had good storage stability and operation stability. The Km of immobilized and free laccase for ABTS were 140.6 and 31.1 μM in phosphate buffer (0.1 M, pH 3.0) at 37 ℃, respectively. The immobilized laccase is a good candidate for the research and development of biosensors based on laccase catalysis.

  6. Facile preparation of superhydrophobic surfaces based on metal oxide nanoparticles

    Science.gov (United States)

    Bao, Xue-Mei; Cui, Jin-Feng; Sun, Han-Xue; Liang, Wei-Dong; Zhu, Zhao-Qi; An, Jin; Yang, Bao-Ping; La, Pei-Qing; Li, An

    2014-06-01

    A novel method for fabrication of superhydrophobic surfaces was developed by facile coating various metal oxide nanoparticles, including ZnO, Al2O3 and Fe3O4, on various substrates followed by treatment with polydimethylsiloxane (PDMS) via chemical vapor deposition (CVD) method. Using ZnO nanoparticles as a model, the changes in the surface chemical composition and crystalline structures of the metal oxide nanoparticles by PDMS treatment were investigated by X-ray photoelectron spectroscopy (XPS), X-ray powder diffraction (XRD) and Fourier transform infrared (FTIR) analysis. The results show that the combination of the improved surface roughness generated from of the nanoparticles aggregation with the low surface-energy of silicon-coating originated from the thermal pyrolysis of PDMS would be responsible for the surface superhydrophobicity. By a simple dip-coating method, we show that the metal oxide nanoparticles can be easily coated onto the surfaces of various textural and dimensional substrates, including glass slide, paper, fabric or sponge, for preparation of superhydrophobic surfaces for different purpose. The present strategy may provide an inexpensive and new route to surperhydrophobic surfaces, which would be of technological significance for various practical applications especially for separation of oils or organic contaminates from water.

  7. Facile preparation of superhydrophobic surfaces based on metal oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Bao, Xue-Mei; Cui, Jin-Feng; Sun, Han-Xue; Liang, Wei-Dong; Zhu, Zhao-Qi; An, Jin; Yang, Bao-Ping; La, Pei-Qing; Li, An, E-mail: lian2010@lut.cn

    2014-06-01

    A novel method for fabrication of superhydrophobic surfaces was developed by facile coating various metal oxide nanoparticles, including ZnO, Al{sub 2}O{sub 3} and Fe{sub 3}O{sub 4}, on various substrates followed by treatment with polydimethylsiloxane (PDMS) via chemical vapor deposition (CVD) method. Using ZnO nanoparticles as a model, the changes in the surface chemical composition and crystalline structures of the metal oxide nanoparticles by PDMS treatment were investigated by X-ray photoelectron spectroscopy (XPS), X-ray powder diffraction (XRD) and Fourier transform infrared (FTIR) analysis. The results show that the combination of the improved surface roughness generated from of the nanoparticles aggregation with the low surface-energy of silicon-coating originated from the thermal pyrolysis of PDMS would be responsible for the surface superhydrophobicity. By a simple dip-coating method, we show that the metal oxide nanoparticles can be easily coated onto the surfaces of various textural and dimensional substrates, including glass slide, paper, fabric or sponge, for preparation of superhydrophobic surfaces for different purpose. The present strategy may provide an inexpensive and new route to surperhydrophobic surfaces, which would be of technological significance for various practical applications especially for separation of oils or organic contaminates from water.

  8. Preparation of nanoporous titania spherical nanoparticles

    Science.gov (United States)

    Shiba, Kota; Sato, Soh; Matsushita, Takayuki; Ogawa, Makoto

    2013-03-01

    Preparation of nanoporous titania particles from well-defined titania-octadecylamine (titania-ODA) hybrid spherical particles with 450 nm in size, which were prepared by the method reported previously (Chem. Commun., 2009, pp. 6851-6853 [39]; RSC Adv., 2012, vol. 2, pp. 1343-1349 [40]), was studied. ODA was removed by solvent extraction with acidic ethanol to obtain nanoporous titania particles and subsequent calcination led to the formation of nanoporous titania particles with the nanopore size ranging from 2 to 4 nm depending on the calcination temperature. The as-synthesized titania was amorphous and was transformed into anatase (at around 300 °C) and rutile (at around 600 °C) by the heat treatment. The phase transition behavior was discussed in comparison with that of as-synthesized titania-ODA particles without ODA removal. Spherical particles of titania-ODA hybrids with 70 nm in size were also transformed into nanoporous titania particles composed of anatase crystallites by the washing and calcination at 500 °C for 1 h.

  9. Preparation of paclitaxel-loaded microspheres with magnetic nanoparticles

    Institute of Scientific and Technical Information of China (English)

    CUI Sheng; SHEN Xiaodong; SHI Ruihua; LIN Benlan; CHEN Ping

    2007-01-01

    The objective of this paper was to prepare paclitaxel-loaded microspheres,a kind of target-orientation anticancer drug.The paclitaxel-loaded microspheres were prepared with magnetic Fe3O4 nanoparticles and taxo1.The morphology was characterized by scanning electron microscopy(SEM),and the average size and the size distribution were determined by a laser-size distributing instrument.High performance liquid chromatography(HPLC)was used to measure the paclitaxel content.Experimental results indicated that the effective drug loading and the entrapment ratio of paclitaxel-loaded microspheres were 1.83% and 92,62%,respectively.

  10. Preparation of uniform nanoparticles of ultra-high purity metal oxides, mixed metal oxides, metals, and metal alloys

    Science.gov (United States)

    Woodfield, Brian F.; Liu, Shengfeng; Boerio-Goates, Juliana; Liu, Qingyuan; Smith, Stacey Janel

    2012-07-03

    In preferred embodiments, metal nanoparticles, mixed-metal (alloy) nanoparticles, metal oxide nanoparticles and mixed-metal oxide nanoparticles are provided. According to embodiments, the nanoparticles may possess narrow size distributions and high purities. In certain preferred embodiments, methods of preparing metal nanoparticles, mixed-metal nanoparticles, metal oxide nanoparticles and mixed-metal nanoparticles are provided. These methods may provide tight control of particle size, size distribution, and oxidation state. Other preferred embodiments relate to a precursor material that may be used to form nanoparticles. In addition, products prepared from such nanoparticles are disclosed.

  11. Magnetic properties of iron nanoparticles prepared by exploding wire technique.

    Science.gov (United States)

    Alqudami, Abdullah; Annapoorni, S; Lamba, Subhalakshmi; Kothari, P C; Kotnala, R K

    2007-06-01

    Nanoparticles of iron were prepared in distilled water using very thin iron wires and sheets, by the electro-exploding wire technique. Transmission electron microscopy reveals the size of the nanoparticles to be in the range 10 to 50 nm. However, particles of different sizes can be segregated by using ultrahigh centrifuge. X-ray diffraction studies confirm the presence of the cubic phase of iron. These iron nanoparticles were found to exhibit fluorescence in the visible region in contrast to the normal bulk material. The room temperature hysteresis measurements upto a field of 1.0 tesla were performed on a suspension of iron particles in the solution as well as in the powders obtained by filtration. The hysteresis loops indicate that the particles are superparamagnetic in nature. The saturation magnetizations was approximately 60 emu/gm. As these iron particles are very sensitive to oxygen a coating of non-magnetic iron oxide tends to form around the particles giving it a core-shell structure. The core particle size is estimated theoretically from the magnetization measurements. Suspensions of iron nanoparticles in water have been proposed to be used as an effective decontaminant for ground water.

  12. Preparation and applications of ZnSe nanoparticles

    Science.gov (United States)

    Ravindranadh, K.; Shekhawat, M. S.; Rao, M. C.

    2013-06-01

    Semiconductor nanoparticles have been attracting widespread scientific and technological interest due to their unique size-tunable optical and electronic properties. The ZnSe nanoparticles have wide-ranging applications in laser, optical instruments, etc. because it has a wide band gap and transmittance range, high luminescence efficiency, low absorption coefficient, and excellent transparency to infrared. ZnSe nanoparticles have been prepared at room temperature. Zinc chloride 99 mM of 4 mL is added to 2.2g PVA. Volume of the solution is made up to 50 mL by bidistilled water. The Solution is left for 24 h at room temperature to swell. After that the solution is warmed up to 60°C and stirred for 4 h until viscous transparent solution was obtained. One milliliter of Sodium Hydrogen Selenide was dropped into the solution with gentle stirring. Solution is casted on flat glass plate dishes. After the solvent evaporation, a thin film containing ZnSe nanoparticles are obtained. The film is washed with de-ionized water to remove other soluble salts before measurements.

  13. Nanoparticle preparation of Mefenamic acid by electrospray drying

    Energy Technology Data Exchange (ETDEWEB)

    Zolkepali, Nurul Karimah, E-mail: fitrah@salam.uitm.edu.my; Bakar, Noor Fitrah Abu, E-mail: fitrah@salam.uitm.edu.my; Anuar, Nornizar [Faculty Of Chemical Engineering, Universiti Teknologi Mara (UiTM), 40450 Shah Alam, Selangor (Malaysia); Naim, M. Nazli [Food and Process Department, Faculty of Engineering, Universiti Putra Malaysia (UPM), 43400 UPM Serdang, Selangor (Malaysia); Bakar, Mohd Rushdi Abu [Kulliyyah of Pharmacy, International Islamic University Malaysia, P.O Box 141, 25710, Kuantan, Pahang (Malaysia)

    2014-02-24

    Nanoparticles preparation of Mefenamic acid (MA) by using an electrospray drying method was conducted in this study. Electrospray drying is a process that uses electrostatic force to disperse a conductive liquid stream into fine charged droplets through the coulomb fission of charges in the liquid and finally dry into fine particles. Electrospray drying modes operation usually in Taylor cone jet, and it was formed by controlling applied voltage and liquid flow rate. A conductive liquid (2.77–8.55μScm{sup −1}) which is MA solution was prepared by using acetone with concentration 0.041 and 0.055 M before pumping at a flow rate of 3–6ml/h. By applying the applied voltage at 1.3–1.5 kV, Taylor cone jet mode was formed prior to the electrospray. During electrospray drying process, solvent evaporation from the droplet was occurring that leads to coulomb disruption and may generate to nanoparticles. The dried nanoparticles were collected on a grounded substrate that was placed at varying distance from the electrospray. MA particle with size range of 100–400 nm were produced by electrospray drying process. Characterization of particles by using X-ray diffractometry (XRD) and differential scanning calorimetry (DSC) show that particles formed into polymorph I.

  14. Enhancing CaP biomimetic growth on TiO2 cuboids nanoparticles via highly reactive facets.

    Science.gov (United States)

    Ruso, Juan M; Verdinelli, Valeria; Hassan, Natalia; Pieroni, Olga; Messina, Paula V

    2013-02-19

    Pure decahedral anatase TiO(2) particles with high content of reactive {001} facets were obtained from titanium(IV) tetrachloride (TiCl(4)) using a microemulsions droplet system at specific conditions as chemical microreactor. The product was systematically characterized by X-ray diffraction, field-emission scanning and transmission electron microscopy (FE-SEM, TEM), N(2) adsorption-desorption isotherms, FT-IR and UV-vis spectroscopy, and photoluminescence studies. The obtained cuboids around 90 nm in size have a uniform and dense surface morphology with a BET specific surface area of 11.91 m(2) g(-1) and a band gap energy (3.18 eV) slightly inferior to the anatase dominated by the less-reactive {101} surface (3.20 eV). The presence of reactive facets on titania anatase favors the biomimetic growth of amorphous tricalcium phosphate after the first day of immersion in simulated human plasma. The results presented here can facilitate and improve the integration of anchored implants and enhance the biological responses to the soft tissues.

  15. Preparation and characterization of hexagonal close-packed Ni nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Hexagonal close-packed Ni nanoparticles were synthesized using a heat-treating technique with the precursors prepared by the sol-gel method.The synthesis condition,structure,and morphology of the samples were characterized and analysed by thermogravimetric analysis (TG),differential thermal analysis (DTA),X-ray diffraction (XRD) and transmission electron microscopy (TEM).Results indicate that the hexagonal close packed Ni nanoparticles were synthesized at a heat-treating temperature of 300℃.The cell constants are calculated at a=0.2652 nm and c=0.4334 nm.The average grain size of the hexagonal close-packed Ni particles evaluated by Scherrer equation is about 12 nm.The phase transformation from a hexagonal close-packed Ni to a face-centered cubic Ni structure occurred when the heat-treating temperature was increased.

  16. The improved stability of enzyme encapsulated in biomimetic titania particles

    Energy Technology Data Exchange (ETDEWEB)

    Jiang Yanjun; Sun Qianyun [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Jiang Zhongyi [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China)], E-mail: zhyjiang@tju.edu.cn; Zhang Lei; Li Jian; Li Lin; Sun Xiaohui [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China)

    2009-01-01

    This study demonstrates a novel biomimetic approach for the entrapment of yeast alcohol dehydrogenase (YADH) within titania nanoparticles to improve its stability. Protamine was as the template and catalyst for the condensation of titanium (IV) bis(ammonium lactato) dihydroxide (Ti-BALDH) into titania nanoparticles in which YADH was trapped. The as-prepared titania/protamine/YADH composites were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), dynamic light scattering (DLS), X-ray powder diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The mechanism of YADH encapsulation was tentatively proposed from a series of experimental results. The preliminary investigation showed that encapsulated YADH could retain most of its initial activity. Compared to free YADH, encapsulated YADH exhibited significantly improved thermal, pH and recycling stability. After 5 weeks storage, no substantial loss of catalytic activity for encapsulated YADH was observed.

  17. Biomimetic synthesis of silver nanoparticles by Citrus limon (lemon) aqueous extract and theoretical prediction of particle size.

    Science.gov (United States)

    Prathna, T C; Chandrasekaran, N; Raichur, Ashok M; Mukherjee, Amitava

    2011-01-01

    In the present study, silver nanoparticles were rapidly synthesized at room temperature by treating silver ions with the Citrus limon (lemon) extract. The effect of various process parameters like the reductant concentration, mixing ratio of the reactants and the concentration of silver nitrate were studied in detail. In the standardized process, 10(-2)M silver nitrate solution was interacted for 4h with lemon juice (2% citric acid concentration and 0.5% ascorbic acid concentration) in the ratio of 1:4 (vol:vol). The formation of silver nanoparticles was confirmed by Surface Plasmon Resonance as determined by UV-Visible spectra in the range of 400-500 nm. X-ray diffraction analysis revealed the distinctive facets (111, 200, 220, 222 and 311 planes) of silver nanoparticles. We found that citric acid was the principal reducing agent for the nanosynthesis process. FT-IR spectral studies demonstrated citric acid as the probable stabilizing agent. Silver nanoparticles below 50 nm with spherical and spheroidal shape were observed from transmission electron microscopy. The correlation between absorption maxima and particle sizes were derived for different UV-Visible absorption maxima (corresponding to different citric acid concentrations) employing "MiePlot v. 3.4". The theoretical particle size corresponding to 2% citric acid concentration was compared to those obtained by various experimental techniques like X-ray diffraction analysis, atomic force microscopy, and transmission electron microscopy.

  18. Preparation of Aromatic Polycarbonate Nanoparticles using Supercritical Carbon Dioxide

    Science.gov (United States)

    Lee, Jun-Young; Song, Cheong-Hun; Kim, Joong-In; Kim, Jung-Hyun

    2002-04-01

    A novel synthetic process for producing aromatic polycarbonate (PC) nanoparticles using supercritical CO2 was developed. The objective of the present research work was to synthesize high molecular weight PC nanoparticles using transesterification between bisphenol-A (BPA) and diphenyl carbonate (DPC) in supercritical CO2 which is an excellent plasticizing agent and a good solvent for phenol, a by-product of the reaction. Poly(propylene oxide)-poly(ethylene oxide)-poly(propylene oxide) tri-block copolymer with CO2-phobic anchor and CO2-philic tail group was used as a stabilizer for the preparation of stable dispersions of BPA-DPC mixture in a CO2 continuous phase. As the reaction was proceeding, phenol formed from the reaction was dissolved and diffused into supercritical CO2 phase. The PC nanoparticles were isolated by simple venting of the supercritical CO2 from the reactor. Spherical morphology of PC particles was confirmed by scanning electron microscopy. Particle size and morphology of PC particles were modified upon variation of the process conditions. The resulting PC particles with a nano-size of 30-140 nm have a high molecular weight ( M w) of 3.1×105 (g/mol).

  19. Synthesis and Characterization of Sol-Gel Prepared Silver Nanoparticles

    Science.gov (United States)

    Ahlawat, Dharamvir Singh; Kumari, Rekha; Rachna; Yadav, Indu

    2014-03-01

    Silver nanoparticles (SNPs) have been successfully prepared using sol-gel method by annealing the sample at 550°C for 30 min. The SNPs were not confirmed by X-ray diffraction (XRD) analysis when the annealing temperature was considered at 450°C. They were also not confirmed without calcination of the sample. The physical mechanism of silver clusters formation in the densified silica matrix with respect to thermal treatment has been understood. The presence of silver metal in the silica matrix was confirmed by XRD analysis and TEM image of the samples. The average size of nanoparticles dispersed in silica matrix was determined as 10.2 nm by the XRD technique. The synthesized nanocomposites were also characterized by UV-Visible spectroscopy with a peak in the absorption spectra at around 375 nm. The distribution of particle size has been reported here in the range from 8 nm to 25 nm by TEM observations of the sample prepared at 550°C. The spherically smaller size (≈10 nm) SNPs have reported the surface plasmons resonance (SPR) peak less than or near to 400 nm due to blue-shifting and effect of local refractive index. Without annealing the silica samples the absorption spectra does not show any peak around 375 nm. The FTIR spectroscopy of the three types of samples prepared at different temperatures (room temperature, 450°C and 550°C) has also been reported. This spectra have provided the identification of different chemical groups in the prepared samples. It has been predicted that the size of SNPs by XRD, UV-Visible and TEM results have agreed well with each other. It may be concluded that formation of SNPs is a function of annealing temperature.

  20. Preparation and characterization of Biochanin A loaded solid lipid nanoparticles

    Directory of Open Access Journals (Sweden)

    Chunlei Tao

    2012-01-01

    Full Text Available Biochanin A, the predominant isoflavones found in plants, had proved its human health benefits. The purpose of this research was to study whether Biochanin A (BCA loaded solid lipid nanoparticles (SLN could improve solution and prolong the half-life of BCA. BCA-SLN was prepared by emulsion evaporation and low temperature solidification technique, and freeze-dried powders were developed to improve stability. The mean particle sizes, zeta potential, entrapment efficiency (EE, and drug loading capacity (DL of BCA was 176.0 nm, −18.7 ± 0.26, 97.15 ± 0.28%, and 6.38 ± 0.04%, respectively. The results of differential scanning calorimetry (DSC and X-ray diffraction analysis (XRD indicated that the BCA was wrapped and absorbed in the nanoparticles. The solution of preparation is much higher than the untreated BCA. Results of stability of SLN showed a relatively short-term stability after storage at 4°C and 25°C for 15 days. Drug release of untreated BCA and BCA-SLN was fit into the Biexponential equations and Weibull equations, respectively, and SLN showed sustained release properties. But after freeze-dried, stability was improved, and the EE and DL had a slightly decrease. The mean particle size was slightly increased, but the structure was not changed. In conclusion, SLN systems can represent an effective strategy to change the poor aqueous solubility and prolong the half-time of BCA.

  1. Sonochemical synthesis of cobalt aluminate nanoparticles under various preparation parameters.

    Science.gov (United States)

    Lv, Weizhong; Qiu, Qi; Wang, Fang; Wei, Shaohui; Liu, Bo; Luo, Zhongkuan

    2010-06-01

    Cobalt aluminate (CoAl(2)O(4)) nanoparticles were synthesized using a precursor method with the aid of ultrasound irradiation under various preparation parameters. The effects of the preparation parameters, such as the sonochemical reaction time and temperature, precipitation agents, calcination temperature and time on the formation of CoAl(2)O(4) were investigated. The precursor on heating yields nanosized CoAl(2)O(4) particles and both these nanoparticles and the precursor were characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and atomic force microscopy (AFM). The use of ultrasound irradiation during the homogeneous precipitation of the precursor reduces the duration of the precipitation reaction. The mechanism of the formation of cobalt aluminate was investigated by means of Fourier transformation infrared spectroscopy (FT-IR) and EDX (energy dispersive X-ray). The thermal decomposition process and kinetics of the precursor of nanosized CoAl(2)O(4) were investigated by means of differential scanning calorimetry (DSC) and thermogravimetry (TG). The apparent activation energy (E) and the pre-exponential constant (A) were 304.26 kJ/mol and 6.441 x 10(14)s(-1), respectively. Specific surface area was investigated by means of Brunauer Emmett Teller (BET) surface area measurements.

  2. Nanoparticle-assisted laser desorption/ionization mass spectrometry: Novel sample preparation methods and nanoparticle screening for plant metabolite imaging

    Energy Technology Data Exchange (ETDEWEB)

    Yagnik, Gargey B. [Iowa State Univ., Ames, IA (United States)

    2016-02-19

    The main goal of the presented research is development of nanoparticle based matrix-assisted laser desorption ionization-mass spectrometry (MALDI-MS). This dissertation includes the application of previously developed data acquisition methods, development of novel sample preparation methods, application and comparison of novel nanoparticle matrices, and comparison of two nanoparticle matrix application methods for MALDI-MS and MALDI-MS imaging.

  3. Flexible Aluminum Nanobowls for Alternative Preparation of Individual or a Small Number of Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    SUN Yan; CHEN Xin; YUE Yang; ZHANG Rong-jun; DAI Ning

    2009-01-01

    The nanoscale aluminum bowls were derived from the porous alumina and were used as the flexible nanoscale reactors for the preparation of nanoparticles.Both single source precursor and preprepared nanoparticles were induced in the nanobowls by melting the precursor/polymer films spin-coated on aluminum nanobowis for the formation of nanostructural composites in the nanobowls.We have prepared a single nanoparticle or just a small number of metal(e.g.Pt) nanoparticles or semiconductor nanoparticles(e.g.CdSe or CdSe/ZnS core-shell nanostructures) in the nanobowls.

  4. Effect of retrogradation time on preparation and characterization of proso millet starch nanoparticles.

    Science.gov (United States)

    Sun, Qingjie; Gong, Min; Li, Ying; Xiong, Liu

    2014-10-13

    Starch nanoparticles were prepared from proso millet starch using a green and facile method combined with enzymolysis and recrystallization. Scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimeter (DSC) and thermal gravimetric analysis (TGA) were used to characterize the morphology and crystal structure of the starch nanoparticles prepared with different retrogradation time (0.5, 4, 12, and 24h). The results showed that the sizes of the starch nanoparticles were between 20 nm and 100 nm. The crystal pattern changed from A-type (native starch) to B-type (nanoparticles), and the relative crystallinity of the nanoparticles increased obviously, as compared with the native starch. The nanoparticles prepared with the 12h retrogradation time had the highest degree of crystallinity (47.04%). Compared to conventional acid hydrolysis to make starch nanoparticles, the present approach has the advantage of being quite rapid and presenting a higher yield (about 55%).

  5. Preparation of polymeric nanoparticles containing corticosteroid by a novel aerosol flow reactor method.

    Science.gov (United States)

    Eerikäinen, Hannele; Kauppinen, Esko I

    2003-09-16

    Polymeric drug-containing nanoparticles were prepared using a novel aerosol flow reactor method. The polymeric drug-containing nanoparticles prepared consist of a poorly water soluble corticosteroid, beclomethasone dipropionate, and polymeric materials Eudragit E 100 or Eudragit L 100. The novel method used in this study allows synthesis of nanoparticles directly as dry powders. The nanoparticles can contain various ratios of drug and polymer, and the use of any additional stabilisation materials is avoided. In this study, nanoparticles with different drug-to-polymer ratios were prepared. Particle size and morphology, crystallinity, and thermal behaviour were determined as a function of particle composition. It was found that all the nanoparticles produced, regardless of particle composition, had geometric number mean diameters of approximately 90 nm, and were spherical showing smooth surfaces. The drug was molecularly dispersed in the amorphous polymeric matrix of the nanoparticles, and drug crystallisation was not observed when the ambient temperature was below the glass transition temperature of the polymer.

  6. Silver confined within zeolite EMT nanoparticles: preparation and antibacterial properties

    Science.gov (United States)

    Dong, B.; Belkhair, S.; Zaarour, M.; Fisher, L.; Verran, J.; Tosheva, L.; Retoux, R.; Gilson, J.-P.; Mintova, S.

    2014-08-01

    The preparation of pure zeolite nanocrystals (EMT-type framework) and their silver ion-exchanged (Ag+-EMT) and reduced silver (Ag0-EMT) forms is reported. The template-free zeolite nanocrystals are stabilized in water suspensions and used directly for silver ion-exchange and subsequent chemical reduction under microwave irradiation. The high porosity, low Si/Al ratio, high concentration of sodium and ultrasmall crystal size of the EMT-type zeolite permitted the introduction of a high amount of silver using short ion-exchange times in the range of 2-6 h. The killing efficacy of pure EMT, Ag+-EMT and Ag0-EMT against Escherichia coli was studied semi-quantitatively. The antibacterial activity increased with increasing Ag content for both types of samples (Ag+-EMT and Ag0-EMT). The Ag0-EMT samples show slightly enhanced antimicrobial efficacy compared to that of Ag+-EMT, however, the differences are not substantial and the preparation of Ag nanoparticles is not viable considering the complexity of preparation steps.The preparation of pure zeolite nanocrystals (EMT-type framework) and their silver ion-exchanged (Ag+-EMT) and reduced silver (Ag0-EMT) forms is reported. The template-free zeolite nanocrystals are stabilized in water suspensions and used directly for silver ion-exchange and subsequent chemical reduction under microwave irradiation. The high porosity, low Si/Al ratio, high concentration of sodium and ultrasmall crystal size of the EMT-type zeolite permitted the introduction of a high amount of silver using short ion-exchange times in the range of 2-6 h. The killing efficacy of pure EMT, Ag+-EMT and Ag0-EMT against Escherichia coli was studied semi-quantitatively. The antibacterial activity increased with increasing Ag content for both types of samples (Ag+-EMT and Ag0-EMT). The Ag0-EMT samples show slightly enhanced antimicrobial efficacy compared to that of Ag+-EMT, however, the differences are not substantial and the preparation of Ag nanoparticles is not

  7. Effects of PVP on the preparation and growth mechanism of monodispersed Ni nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Monodispersed Ni nanoparticles were successfully prepared by chemical reduction with hydrazine hydrate in ethylene glycol.The effect of the amount of polyvinylpyrrolidone (PVP-K30) on the preparation of Ni nanoparticles was investigated.X-ray diffraction (XRD),transmission electron microscopy (TEM),and high resolution transmission electron microscopy (HRTEM) were employed to characterize the nickel particles are spherical in shape and are not agglomerated.A possible extensive mechanism of nickel nanoparticle formation has been suggested.

  8. CO responses of sensors based on cerium oxide thick films prepared from clustered spherical nanoparticles.

    Science.gov (United States)

    Izu, Noriya; Matsubara, Ichiro; Itoh, Toshio; Akamatsu, Takafumi; Shin, Woosuck

    2013-03-08

    Various types of CO sensors based on cerium oxide (ceria) have been reported recently. It has also been reported that the response speed of CO sensors fabricated from porous ceria thick films comprising nanoparticles is extremely high. However, the response value of such sensors is not suitably high. In this study, we investigated methods of improving the response values of CO sensors based on ceria and prepared gas sensors from core-shell ceria polymer hybrid nanoparticles. These hybrid nanoparticles have been reported to have a unique structure: The core consists of a cluster of ceria crystallites several nanometers in size. We compared the characteristics of the sensors based on thick films prepared from core-shell nanoparticles with those of sensors based on thick films prepared from conventionally used precipitated nanoparticles. The sensors prepared from the core-shell nanoparticles exhibited a resistance that was ten times greater than that of the sensors prepared from the precipitated nanoparticles. The response values of the gas sensors based on the core-shell nanoparticles also was higher than that of the sensors based on the precipitated nanoparticles. Finally, improvements in sensor response were also noticed after the addition of Au nanoparticles to the thick films used to fabricate the two types of sensors.

  9. Histidine-functionalized water-soluble nanoparticles for biomimetic nucleophilic/general-base catalysis under acidic conditions.

    Science.gov (United States)

    Chadha, Geetika; Zhao, Yan

    2013-10-21

    Cross-linking the micelles of 4-dodecyloxybenzyltripropargylammonium bromide by 1,4-diazidobutane-2,3-diol in the presence of azide-functionalized imidazole derivatives yielded surface-cross-linked micelles (SCMs) with imidazole groups on the surface. The resulting water-soluble nanoparticles were found, by fluorescence spectroscopy, to contain hydrophobic binding sites. The imidazole groups promoted the photo-deprotonation of 2-naphthol at pH 6 and catalyzed the hydrolysis of p-nitrophenylacetate (PNPA) in aqueous solution at pH ≥ 4. Although the overall hydrolysis rate slowed down with decreasing solution pH, the catalytic effect of the imidazole became stronger because the reactions catalyzed by unfunctionalized SCMs slowed down much more. The unusual ability of the imidazole–SCMs to catalyze the hydrolysis of PNPA under acidic conditions was attributed to the local hydrophobicity and the positive nature of the SCMs.

  10. Direct Preparation and Characterization of Copper Pentacyanonitrosylferrate Nanoparticles

    Directory of Open Access Journals (Sweden)

    D. R. Do Carmo

    2015-01-01

    Full Text Available The present work describes the preparation of nanoparticles of copper pentacyanonitrosyl complexes starting from the compound sodium nitroprusside. Copper pentacyanonitrosylferrate (NCuNP nanoparticles were successfully synthesized by using deionized water and formamide as solvent. The material was characterized by Fourier-transforming infrared spectroscopy (FT-IR, X-ray diffraction (XRD, ultraviolet-visible (UV-Vis spectroscopy, scanning electron microscopy (SEM, energy dispersive X-ray spectroscopy (EDX, and cyclic voltammetry (CV. The results revealed that the electronic spectra of NCuNP exhibited a broad intervalence charge transfer band at 685 nm. An XRD peak broadening pattern of the NCuNP was verified, indicating a particle decrease when formamide is used. The particle size of NCuNP is estimated to be 80 nm. The cyclic voltammogram of the modified graphite paste electrode with NCuNP showed two redox pairs with formal potentials Eθ′=0.36 V and Eθ′=0.78 V (ν=20 mV s−1; KCl 1.0 M, attributed to the redox process CuI/ CuII and [FeII(CN5NO]/[FeIII(CN5NO], respectively. The graphite paste electrode with NCuNP presents electrocatalytic response for Sulfite determination.

  11. A novel method for preparing monodispersed polystyrene nanoparticles

    Institute of Scientific and Technical Information of China (English)

    LIU Kaiyi; WANG Zhaoqun

    2007-01-01

    A preparation manner for monodispersed polystyrene(PS)nanoparticles polymerized by using a novel addition procedure of a monomer is suggested.In systems containing a smaller amount of surfactant compared with conventional microemulsion polymerization,the polymerization processes consists of three stages:adding dropwise the first part of the monomer for a few minutes at 80℃ and polymerizing for 1 h;adding collectively the residual part of the monomer and polymerizing at the same temperature for another 1 h;and then polymerizing at 85℃ for another 1 h.Based on discussions on the nucleation mechanism of particles in the polymerization system,the influences of monomer weight added dropwise,and amounts of initiator and emulsifier on the size and distribution of PS particles were investigated.PS nanoparticles with smaller diameter such as a number-average diameter of 18.7 nm and better monodispersity were obtained since the dropped styrene amount was suitable under 20wt-% emulsifier amount and 3wt-% initiator amount based on the monomer.

  12. Dialdehyde starch nanoparticles: Preparation and application in drug carrier

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Dialdehyde starch nanoparticles (DASNP) were prepared by the redox reaction of NaIO4 and starch in water-in-oil microemulsion. IR spectrum showed that DASNP had aldehyde groups, and quantitative alkali consumption showed that its dialdehyde content was about (50±5)%. The average diameter of DASNP determined by SEM was about 100 nm. TGA-DTA showed that its thermal stability was better than starch nanoparticle (StNP) and dialdehyde starch (DAS). Its low biological toxicity was detected by cell experiment. Also the best mass ratio of doxorubicin (DOX) to combined DASNP detected by UV-VIS was 15 : 1, and the product was effective for controlled release of DOX. The cell experiment showed that the drug-carrier particle (DOX-DASNP) can release DOX for a long time and strengthened the effect of the anticancer drug. This work demonstrates that the DASNP, which has good thermal stability, small particle size, low biological toxicity, and slowly anticancer drug-releasing to strengthen drug effect, is a potentially useful carrier for anticancer drug.

  13. Phytotoxicity of Ag nanoparticles prepared by biogenic and chemical methods

    Science.gov (United States)

    Choudhury, Rupasree; Majumder, Manna; Roy, Dijendra Nath; Basumallick, Srijita; Misra, Tarun Kumar

    2016-06-01

    Silver nanoparticles (Ag NPs) are now widely used as antibacterial and antifungal materials in different consumer products. We report here the preparation of Ag NPs by neem leaves extract ( Azadirachta) reduction and trisodium citrate-sodium borohydride reduction methods, and study of their phytotoxicity. The nanoparticles were characterized by UV-Vis spectroscopy, FTIR, and atomic force microscopy (AFM) techniques. Both neem-coated and citrate-coated Ag NPs exhibit surface plasmon around 400 nm, and their average sizes measured by AFM are about 100 and 20 nm, respectively. Antibacterial and antifungal activities of these nanomaterials have been studied by simple pea seed germination and disk diffusion methods. It has been observed from the growth of root and shoot, citrate-coated Ag NPs significantly affect seedling growth, but neem-coated Ag NPs exhibit somehow mild toxicity toward germination process due to the nutrient supplements from neem. On the other hand, antifungal activity of neem-coated Ag NPs has been found much higher than that of citrate-coated Ag NPs due to the combined effects of antifungal activity of neem and Ag NPs. Present research primarily indicates a possible application of neem-coated Ag NPs as a potential fungicide.

  14. Preparation of silver nanoparticles fabrics against multidrug-resistant bacteria

    Science.gov (United States)

    Hanh, Truong Thi; Thu, Nguyen Thi; Hien, Nguyen Quoc; An, Pham Ngoc; Loan, Truong Thi Kieu; Hoa, Phan Thi

    2016-04-01

    The silver nanoparticles (AgNPs)/peco fabrics were prepared by immobilization of AgNPs on fabrics in which AgNPs were synthesized by γ-irradiation of the 10 mM AgNO3 chitosan solution at the dose of 17.6 kGy. The AgNPs size has been estimated to be about 11 nm from TEM image. The AgNPs content onto peco fabrics was of 143±6 mg/kg at the initial AgNPs concentration of 100 ppm. The AgNPs colloidal solution was characterized by UV-vis spectroscopy and TEM image. The antibacterial activity of AgNPs/peco fabrics after 60 washings against Staphylococcus aureus and Klebsiella pneumoniae was found to be over 99%. Effects of AgNPs fabics on multidrug-resistant pathogens from the clinical specimens were also tested.

  15. Preparation of controlled gold nanoparticle aggregates using a dendronization strategy.

    Science.gov (United States)

    Paez, Julieta I; Coronado, Eduardo A; Strumia, Miriam C

    2012-10-15

    In this work, a dendronization strategy was used to control interparticle spacing and the optical properties of gold nanoparticle (NP) aggregates in aqueous media. To achieve this goal, two dendritic disulfides bearing different functionalities on their periphery were synthesized and used as ligands to dendronize gold NPs. The dendronized NPs then undergo aggregation; this process was followed by UV-vis spectroscopy, dynamic light scattering (DLS), and transmission electronic microscopy (TEM) measurements and correlated with Generalized Mie Theory electrodynamics calculations. For comparison, NP functionalization was also studied using a nondendritic ligand. It was found that the use of dendritic disulfides allows for the preparation of controlled NP aggregates. This study demonstrates how different dendronization parameters, such as disulfide concentration, temperature, time and nature of the ligand (dendritic vs nondendritic), determine the control exerted over the size and stability of the NP aggregates.

  16. Preparation of anionic polyurethane nanoparticles and blood compatible behaviors.

    Science.gov (United States)

    Zhu, Qinshu; Wang, Yan; Zhou, Min; Mao, Chun; Huang, Xiaohua; Bao, Jianchun; Shen, Jian

    2012-05-01

    The anionic polyurethane nanoparticles (APU-NPs) were obtained by an emulsion polymerization method. It was found that the average size of the prepared APU-NPs is about 84 nm, and the APU-NPs have zeta-potential of -38.9 mV. The bulk characterization of synthesized APU-NPs was investigated by FTIR. The blood compatibility of APU-NPs was characterized by in vitro for coagulation tests, complement activation, platelet activation, cytotoxicity experiments, and hemolysis assay. The results showed that the APU-NPs synthesized in this paper are blood compatible with low level of cell cytotoxicity, and the results were significant for their potential use in vivo.

  17. Nanoparticles containing ketoprofen and acrylic polymers prepared by an aerosol flow reactor method.

    Science.gov (United States)

    Eerikäinen, Hannele; Peltonen, Leena; Raula, Janne; Hirvonen, Jouni; Kauppinen, Esko I

    2004-09-23

    The purpose of this study was to outline the effects of interactions between a model drug and various acrylic polymers on the physical properties of nanoparticles prepared by an aerosol flow reactor method. The amount of model drug, ketoprofen, in the nanoparticles was varied, and the nanoparticles were analyzed for particle size distribution, particle morphology, thermal properties, IR spectroscopy, and drug release. The nanoparticles produced were spherical, amorphous, and had a matrix-type structure. Ketoprofen crystallization was observed when the amount of drug in Eudragit L nanoparticles was more than 33% (wt/wt). For Eudragit E and Eudragit RS nanoparticles, the drug acted as an effective plasticizer resulting in lowering of the glass transition of the polymer. Two factors affected the preparation of nanoparticles by the aerosol flow reactor method, namely, the solubility of the drug in the polymer matrix and the thermal properties of the resulting drug-polymer matrix.

  18. Green preparation and spectroscopic characterization of plasmonic silver nanoparticles using fruits as reducing agents

    DEFF Research Database (Denmark)

    Hyllested, Jes Ærøe; Espina Palanco, Marta; Hagen, Nicolai;

    2015-01-01

    Chemicals typically available in plants have the capability to reduce silver and gold salts and to create silver and gold nanoparticles. We report the preparation of silver nanoparticles with sizes between 10 and 300 nm from silver nitrate using fruit extract collected from pineapples and oranges...... as reducing agents. The evolvement of a characteristic surface plasmon extinction spectrum in the range of 420 nm to 480 nm indicates the formation of silver nanoparticles after mixing silver nitrate solution and fruit extract. Shifts in plasmon peaks over time indicate the growth of nanoparticles. Electron...... microscopy shows that the shapes of the nanoparticles are different depending on the fruit used for preparation. The green preparation process results mainly in individual nanoparticles with a very poor tendency to form aggregates with narrow gaps even when aggregation is forced by the addition of Na...

  19. Green preparation and spectroscopic characterization of plasmonic silver nanoparticles using fruits as reducing agents

    DEFF Research Database (Denmark)

    Hyllested, Jes Ærøe; Espina Palanco, Marta; Hagen, Nicolai

    2015-01-01

    Chemicals typically available in plants have the capability to reduce silver and gold salts and to create silver and gold nanoparticles. We report the preparation of silver nanoparticles with sizes between 10 and 300 nm from silver nitrate using fruit extract collected from pineapples and oranges...... microscopy shows that the shapes of the nanoparticles are different depending on the fruit used for preparation. The green preparation process results mainly in individual nanoparticles with a very poor tendency to form aggregates with narrow gaps even when aggregation is forced by the addition of Na...... absorption correlates with the decrease of absorption band in the UV. This confirms the evolution of silver nanoparticles from silver clusters. The presence of various silver clusters on the surface of the “green” plasmonic silver nanoparticles is also supported by a strong multi-color luminesce signal...

  20. Pulsed electric field assisted sol-gel preparation of TiO2 nanoparticles

    Science.gov (United States)

    Mani, Rajaboopathi; Han, Bing; Louhi-Kultanen, Marjatta

    2016-10-01

    This work studies the effect of a pulsed electric field (PEF) on the precipitation and properties of TiO2 nanoparticles. TiO2 nanoparticles were prepared using pulsed DC electric field assisted sol-gel method. The duration of the PEF treatment was varied to investigate its effect on the particle size of TiO2 nanoparticles. The nanoparticles were characterized by X-ray powder diffraction (XRD), Raman spectroscopy, UV diffuse reflectance spectroscopy (UV-DRS) and transmission electron microscopy (TEM). It was found that TiO2 particles prepared with pulsed electric field assisted sol-gel method had enhanced average crystallite size due to the effect of the pulsed electric field on primary nucleation. The effect of electric field on nanoparticle preparation is interesting which can be used to control the grain and crystallite size of nanoparticle.

  1. Preparation and characterization of PEG-albumin-curcumin nanoparticles intended to treat breast cancer

    Directory of Open Access Journals (Sweden)

    R Thadakapally

    2016-01-01

    Full Text Available The aim of present research was to prepare novel serum stable long circulating polymeric nanoparticles for curcumin with a modification to the well known and novel nanoparticle albumin bound technology. polyethylene glycol-albumin-curcumin nanoparticles were prepared using serum albumin and poly ethylene glycol using desolvation technique. Nanoparticles were characterized for encapsulation efficiency, particle size and surface morphology. Drug excipient compatibility was determined using fourier transform infrared spectroscopy. Physical state of the drug in the formulations was known by differential scanning colorimetry. In vitrorelease and solubility of the drug from nanoparticles were determined. In vivo Drug release, tissue uptake and kupffer cell uptake was determined with optimized nanoformulation in rats after intravenous administration. Cell viability assay was determined using breast cancer cell line MD-MB-231. Entrapment efficiency for prepared nanoparticle was above 95%. The polyethylene glycol-albumin-curcumin nanoparticles exhibited an interesting release profile with small initial burst followed by slower and controlled release. Solubility of the drug from the formulation was increased. A sustained release of drug from nanoparticles was observed for 35 days in both in vitro and in vivo studies with the optimized formulation. Polyethylene glycol-albumin-curcumin nanoparticles showed lesser liver and kupffer cell uptake as compared to that of curcumin-albumin nanoparticles suggesting the bestowment of stealthness to nanoparticles with pegylation. Also, the antiproliferative activity of polyethylene glycol-albumin-curcumin nanoparticle formulation was more as compared to native curcumin. Polyethylene glycol-albumin-curcumin nanoparticles thus developed can be conveniently used in breast cancer with improved efficacy compared to conventional therapies and as an alternate to nanoparticle albumin bound technology which is used in

  2. Control of Colloid Surface Chemistry through Matrix Confinement: Facile Preparation of Stable Antibody Functionalized Silver Nanoparticles

    Science.gov (United States)

    Skewis, Lynell R.; Reinhard, Björn M.

    2010-01-01

    Here we describe a simple yet efficient gel matrix assisted preparation method which improves synthetic control over the interface between inorganic nanomaterials and biopolymers and yields stable biofunctionalized silver nanoparticles. Covalent functionalization of the noble metal surface is aided by the confinement of polyethylene glycol acetate functionalized silver nanoparticles in thin slabs of a 1% agarose gel. The gel confined nanoparticles can be transferred between reaction and washing media simply by immersing the gel slab in the solution of interest. The agarose matrix retains nanoparticles but is swiftly penetrated by the antibodies of interest. The antibodies are covalently anchored to the nanoparticles using conventional crosslinking strategies, and the resulting antibody functionalized nanoparticles are recovered from the gel through electroelution. We demonstrate the efficacy of this nanoparticle functionalization approach by labeling specific receptors on cellular surfaces with functionalized silver nanoparticles that are stable under physiological conditions. PMID:20161660

  3. Preparation of Chitosan nanoparticles and its effect on detached rice leaves infected with Pyricularia grisea.

    Science.gov (United States)

    Manikandan, Appu; Sathiyabama, Muthukrishnan

    2016-03-01

    The aim of the present study was to prepare chitosan nanoparticles to evaluate their effect on protection of rice plants from blast fungus. Nanoparticles were prepared using the ionic gelation method by the interaction of Chitosan and sodium tripolyphosphate. The particle size, polydispersity index, zetapotential and structure was confirmed by DLS, FTIR, TEM and XRD. The Chitosan nanoparticle was evaluated for suppression of rice blast fungus (Pyricularia grisea) under the detached leaf condition. It is evident from our results that chitosan nanoparticle have potential in suppressing blast disease of rice which can be used further under field condition to protect rice plants from the devastating fungus.

  4. Preparation and UV-light Absorption Property of Oleic Acid Surface Modified ZnO Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    KANG Jong-hun; GUO Yu-peng; CHEN Yue; WANG Zi-chen

    2011-01-01

    Syntheses of zince oxide(ZnO) nanoparticles by direct precipitation and surface modification with oleic acid were reported. ZnO nanoparticles were characterized via X-ray diffractometry(XRD), transmission electron microscopy(TEM), infrared spectroscopy(IR) and UV-Vis spectroscopy. The prepared ZnO nanoparticles were nearly spherical and highly crystalline with an average size of 29 nm. In addition, high UV-light absorption properties of oleic acid surface modified ZnO nanoparticles were successfully obtained for a dispersion of ZnO nanoparticles in ethanol.

  5. Thiolated chitosan nanoparticles for enhancing oral absorption of docetaxel: preparation, in vitro and ex vivo evaluation

    Science.gov (United States)

    Saremi, Shahrooz; Atyabi, Fatemeh; Akhlaghi, Seyedeh Parinaz; Ostad, Seyed Nasser; Dinarvand, Rassoul

    2011-01-01

    The aim of this study was to prepare and evaluate mucoadhesive core-shell nanoparticles based on copolymerization of thiolated chitosan coated on poly methyl methacrylate cores as a carrier for oral delivery of docetaxel. Docetaxel-loaded nanoparticles with various concentrations were prepared via a radical emulsion polymerization method using cerium ammonium nitrate as an initiator. The physicochemical properties of the obtained nanoparticles were characterized by: dynamic light-scattering analysis for their mean size, size distribution, and zeta potential; scanning electron microscopy and transmission electron microscopy for surface morphology; and differential scanning calorimetry analysis for confirmation of molecular dispersity of docetaxel in the nanoparticles. Nanoparticles were spherical with mean diameter below 200 nm, polydispersity of below 0.15, and positive zeta potential values. The entrapment efficiency of the nanoparticles was approximately 90%. In vitro release studies showed a sustained release characteristic for 10 days after a burst release at the beginning. Ex vivo studies showed a significant increase in the transportation of docetaxel from intestinal membrane of rat when formulated as nanoparticles. Cellular uptake of nanoparticles was investigated using fluoresceinamine-loaded nanoparticles. Docetaxel nanoparticles showed a high cytotoxicity effect in the Caco-2 and MCF-7 cell lines after 72 hours. It can be concluded that by combining the advantages of both thiolated polymers and colloidal particles, these nanoparticles can be proposed as a drug carrier system for mucosal delivery of hydrophobic drugs. PMID:21289989

  6. Investigation of antibacterial properties silver nanoparticles prepared via green method

    Directory of Open Access Journals (Sweden)

    Shameli Kamyar

    2012-07-01

    Full Text Available Abstract Background This study aims to investigate the influence of different stirring times on antibacterial activity of silver nanoparticles in polyethylene glycol (PEG suspension. The silver nanoparticles (Ag-NPs were prepared by green synthesis method using green agents, polyethylene glycol (PEG under moderate temperature at different stirring times. Silver nitrate (AgNO3 was taken as the metal precursor while PEG was used as the solid support and polymeric stabilizer. The antibacterial activity of different sizes of nanosilver was investigated against Gram–positive [Staphylococcus aureus] and Gram–negative bacteria [Salmonella typhimurium SL1344] by the disk diffusion method using Müeller–Hinton Agar. Results Formation of Ag-NPs was determined by UV–vis spectroscopy where surface plasmon absorption maxima can be observed at 412–437 nm from the UV–vis spectrum. The synthesized nanoparticles were also characterized by X-ray diffraction (XRD. The peaks in the XRD pattern confirmed that the Ag-NPs possessed a face-centered cubic and peaks of contaminated crystalline phases were unable to be located. Transmission electron microscopy (TEM revealed that Ag-NPs synthesized were in spherical shape. The optimum stirring time to synthesize smallest particle size was 6 hours with mean diameter of 11.23 nm. Zeta potential results indicate that the stability of the Ag-NPs is increases at the 6 h stirring time of reaction. The Fourier transform infrared (FT-IR spectrum suggested the complexation present between PEG and Ag-NPs. The Ag-NPs in PEG were effective against all bacteria tested. Higher antibacterial activity was observed for Ag-NPs with smaller size. These suggest that Ag-NPs can be employed as an effective bacteria inhibitor and can be applied in medical field. Conclusions Ag-NPs were successfully synthesized in PEG suspension under moderate temperature at different stirring times. The study clearly showed that the Ag-NPs with

  7. Magnetic properties of Fe-Ni nanoparticles prepared by co-precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Davarpanah, A M; Sargazi, M [Department of Physics, University of Sistan and Baluchestan, Zahedan (Iran, Islamic Republic of); Mirzae, A A; Feizi, M [Department of Chemistry, University of Sistan and Baluchestan, Zahedan (Iran, Islamic Republic of)], E-mail: A.M.DAVARPANAH@hamoon.usb.ac.ir

    2008-08-15

    Many methods have been extended for the preparation of nanoparticles. One of the most important methods is the chemical wet process, e.g. the co-precipitation method that has been used for the preparation of Fe-Ni nanoparticles by the authors. XRD patterns show that the nanoparticles are amorphous before calcination and crystallized after calcination. SEM images show that the grain size of the Fe-Ni particles is in 50-300 nanometre range and that the texture of the nanoparticles after calcination was smoother than before calcination. Hysteresis loops show that the Fe-Ni nanoparticles are superparamagnetic before calcination, because the carbonate phase still exists in the sample, and that they are ferromagnetic materials after calcination. For 40Fe-60Ni nanoparticles after calcination, H{sub c} = 0.12 and B{sub s} = 4800 Oe, being very different in respect to the bulk 40Fe-60Ni alloy.

  8. Magnetic properties of Fe-Ni nanoparticles prepared by co-precipitation method

    Science.gov (United States)

    Davarpanah, A. M.; Mirzae, A. A.; Sargazi, M.; Feizi, M.

    2008-08-01

    Many methods have been extended for the preparation of nanoparticles. One of the most important methods is the chemical wet process, e.g. the co-precipitation method that has been used for the preparation of Fe-Ni nanoparticles by the authors. XRD patterns show that the nanoparticles are amorphous before calcination and crystallized after calcination. SEM images show that the grain size of the Fe-Ni particles is in 50-300 nanometre range and that the texture of the nanoparticles after calcination was smoother than before calcination. Hysteresis loops show that the Fe-Ni nanoparticles are superparamagnetic before calcination, because the carbonate phase still exists in the sample, and that they are ferromagnetic materials after calcination. For 40Fe-60Ni nanoparticles after calcination, Hc = 0.12 and Bs = 4800 Oe, being very different in respect to the bulk 40Fe-60Ni alloy.

  9. Preparation and characterization of PEG-Mentha oil nanoparticles for housefly control.

    Science.gov (United States)

    Kumar, Peeyush; Mishra, Sapna; Malik, Anushree; Satya, Santosh

    2014-04-01

    Nanoparticles of Mentha × piperita essential oil were prepared by melt-dispersion method. The nanoparticles prepared at varying oil doses (5-10%, w/v) showed an encapsulation efficiency of 78.2-83.4%, while the oil load was observed to range between 3.64 and 7.46%. The average particle size of the nanoparticles varied between 226 and 331 nm, while polydispersity index showed variation between 0.547 and 1.000. DSC analysis indicated endothermic reaction during formation of nanoparticles, while a 2-term exponential kinetic model was followed during oil release. Nanoparticles showed considerable mortality against housefly larvae in lab (100%) as well as simulated field condition after first week (93%) and 6th week (57%) of application. This was the first study utilizing controlled release property of nanoparticles to formulate a cost effective product for breeding site application against housefly.

  10. Preparation and characterization of hybrid nanoparticles based on chitosan and poly(methacryloylglycylglycine)

    Science.gov (United States)

    Ferri, Marcella; Dash, Mamoni; Cometa, Stefania; De Giglio, Elvira; Sabbatini, Luigia; Chiellini, Federica

    2014-05-01

    The present work investigated the possibility of preparing nanoparticles based on methacryloylglycylglycine (MAGG) and chitosan (CS) by in situ polymerization. The study revealed that nanoparticle formation was strictly dependent on ionic interactions between NH3 + groups from CS and COO- groups arising from the anionic monomer MAGG. The subsequent in situ polymerizations of MAGG in the presence of CS led to the formation of nanoparticles with homogeneous morphology, a uniform particle size distribution, and a good spherical shape as confirmed by laser diffraction granulometry and scanning electron microscopy analyses. Nanoparticle formulations with different amounts of CS and MAGG were prepared, and their chemical compositions were investigated by X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. The obtained results showed that the polymerization of MAGG in the presence of CS appears to be a very promising approach in the preparation of nanoparticles for drug delivery applications.

  11. Preparation of CdS nanoparticles by hydrothermal method in microemulsion

    Institute of Scientific and Technical Information of China (English)

    ZANG Jinxin; ZHAO Gaoling; HAN Gaorong

    2007-01-01

    CdS nanoparticles with good crystallinity were prepared by hydrothermal method in microemulsion composed of polyoxyethylene laurylether/water/cyclohexane/butanol.The structure and the size of the CdS nanoparticles were analyzed by TEM and XRD.The UV-Vis optical absorption of the samples was also investigated.The results show that hydrothermal treatment is an effective method to prepare CdS nanoparticles of hexagonal structure at lower temperature.The particles were in dimensional uniformity.The diameter of the CdS nanoparticles decreased with the increase of the molar ratio of water to surfactant.The minimum diameter of the CdS nanoparticles prepared in this work was about 10 nm.Obvious blue shift appeared in the UV-Vis absorption spectra.

  12. Preparation and characterization of carboxymethyl guar gum nanoparticles.

    Science.gov (United States)

    Gupta, Anek Pal; Verma, Devendra Kumar

    2014-07-01

    Carboxymethyl guar gum nanoparticles (CMGGNPs) were synthesized by nanoprecipitation and sonication method. This method was used for the first time for the synthesis of carboxymethyl guar gum nanoparticles. It was found that the formation of nanoparticles might depend upon the sonication time, solvent, and stirring time. Nanoparticles were characterized by SEM, TEM, XRD and FTIR. The sizes of the particles in suspension have been found in the range 12-30nm. It was concluded that such type of nanoparticles may be used in pharmaceutical and drug delivery.

  13. Preparation, characterization and in vitro antiviral activity evaluation of foscarnet-chitosan nanoparticles.

    Science.gov (United States)

    Russo, E; Gaglianone, N; Baldassari, S; Parodi, B; Cafaggi, S; Zibana, C; Donalisio, M; Cagno, V; Lembo, D; Caviglioli, G

    2014-06-01

    A new nanoparticulate system for foscarnet delivery was prepared and evaluated. Nanoparticles were obtained by ionotropic gelation of chitosan induced by foscarnet itself, acting as an ionotropic agent in a manner similar to tripolyphosphate anion. A Doehlert design allowed finding the suitable experimental conditions. Nanoparticles were between 200 and 300nm in diameter (around 450nm after redispersion). Nanoparticle size increased after 5h, but no size increase was observed after 48h when nanoparticles were crosslinked with glutaraldehyde. Zeta potential values of noncrosslinked and crosslinked nanoparticles were between 20 and 25mV, while drug loading of noncrosslinked nanoparticles was about 40% w/w (55% w/w for crosslinked nanoparticles). Nanoparticle yield was around 25% w/w. Crosslinked nanoparticles showed a controlled drug release. Foscarnet released from nanoparticles maintained the antiviral activity of the free drug when tested in vitro against lung fibroblasts (HELF) cells infected with HCMV strain AD-169. Moreover, nanoparticles showed no toxicity on non-infected HELF cells. These nanoparticles may represent a delivery system that could improve the therapeutic effect of foscarnet.

  14. Optimizing coverage of metal oxide nanoparticle prepared by pulsed laser deposition on nonenzymatic glucose detection.

    Science.gov (United States)

    Kaneko, Satoru; Ito, Takeshi; Hirabayashi, Yasuo; Ozawa, Takeshi; Okuda, Tetsuya; Motoizumi, Yu; Hirai, Kiyohito; Naganuma, Yasuhiro; Soga, Masayasu; Yoshimoto, Mamoru; Suzuki, Koji

    2011-04-15

    Metal oxide nanoparticles prepared by pulsed laser deposition (PLD) were applied to nonenzymatic glucose detection. NiO nanoparticles with size of 3 nm were deposited on glassy carbon (GC) and silicon substrates at room temperature in an oxygen atmosphere. Transmission electron microscope (TEM) image showed nanoparticles with the size of 3 nm uniformly scattered on the Si(001) substrate. Unlike co-sputtering nanoparticle and carbon simultaneously, the PLD method can easily control the surface coverage of nanoparticles on the surface of substrate by deposition time. Cyclic voltammetry was performed on the samples deposited on the GC substrates for electrochemical detection of glucose. The differences between peak currents with and without glucose was used to optimize the coverage of nanoparticles on carbon electrode. The results indicated that optimal coverage of nanoparticles on carbon electrode.

  15. Biomimetic nanocrystalline apatites: Emerging perspectives in cancer diagnosis and treatment.

    Science.gov (United States)

    Al-Kattan, Ahmed; Girod-Fullana, Sophie; Charvillat, Cédric; Ternet-Fontebasso, Hélène; Dufour, Pascal; Dexpert-Ghys, Jeannette; Santran, Véronique; Bordère, Julie; Pipy, Bernard; Bernad, José; Drouet, Christophe

    2012-02-14

    Nanocrystalline calcium phosphate apatites constitute the mineral part of hard tissues, and the synthesis of biomimetic analogs is now well-mastered at the lab-scale. Recent advances in the fine physico-chemical characterization of these phases enable one to envision original applications in the medical field along with a better understanding of the underlying chemistry and related pharmacological features. In this contribution, we specifically focused on applications of biomimetic apatites in the field of cancer diagnosis or treatment. We first report on the production and first biological evaluations (cytotoxicity, pro-inflammatory potential, internalization by ZR-75-1 breast cancer cells) of individualized luminescent nanoparticles based on Eu-doped apatites, eventually associated with folic acid, for medical imaging purposes. We then detail, in a first approach, the preparation of tridimensional constructs associating nanocrystalline apatite aqueous gels and drug-loaded pectin microspheres. Sustained releases of a fluorescein analog (erythrosin) used as model molecule were obtained over 7 days, in comparison with the ceramic or microsphere reference compounds. Such systems could constitute original bone-filling materials for in situ delivery of anticancer drugs.

  16. Metal nanoparticle deposited inorganic nanostructure hybrids, uses thereof and processes for their preparation

    Science.gov (United States)

    Tenne, Reshef; Tsverin, Yulia; Burghaus, Uwe; Komarneni, Mallikharjuna Rao

    2016-01-26

    This invention relates to a hybrid component comprising at least one nanoparticle of inorganic layered compound (in the form of fullerene-like structure or nanotube), and at least one metal nanoparticle, uses thereof as a catalyst, (e.g. photocatalysis) and processes for its preparation.

  17. The Salts of Fatty Acids as Precursors for Preparation of Silver Nanoparticles in Organic Solvents

    Directory of Open Access Journals (Sweden)

    V. N. Glushko

    2016-08-01

    Full Text Available The silver salts of fatty acids were studied as precursors for the preparation of colloidal dispersions of silver nanoparticles and UHMWPE (ultra-high-molecular-weight polyethylene composite with silver nanoparticles, as well as the composition, the spectra and SEM (scanning electron microscopy results.

  18. Biomimetic Flow Sensors

    NARCIS (Netherlands)

    Casas, J.; Liu, Chang; Krijnen, G.J.M.

    2012-01-01

    Biomimetic flow sensors are biologically inspired devices that measure the speed and direction of fluids. This survey starts by describing the role and functioning of airflow-sensing hairs in arthropods and in fishes, carries on with the biomimetic MEMS implementations, both for air and water flow s

  19. In situ preparation of Nanoparticles/polymer composites

    Institute of Scientific and Technical Information of China (English)

    SUN HaiZhu; YANG Bai

    2008-01-01

    Nanoparticle (NP) is the matter between molecule and bulk material. It has attracted much attention in catalysis, optoelectronics and biology due to its unique physical and chemical properties. Incorporation of these NPs into the polymer matrix is one of the best methods to display their special functions, which not only stabilize the NPs but also realize the functional assembly of NPs and polymers. However, reali-zation of this idea depends largely on the compatibility of NPs and polymers as well as the interaction between them. Therefore, many methods have been developed to prepare the composites of NPs and polymers in order to obtain the function ex-pected. In this review, we mainly focus on the combination of in situ method with other methods to synthesize different functional one-dimension, two-dimension as well as bulk composites, which has been recently developed by our group. The most striking character of our method is the excellent compatibility between NPs and polymers which ensures a homogeneous distribution of NPs in the polymer matrix. The existence of the polymer network makes the NPs more stable, and is significant for displaying their functions.

  20. In situ preparation of Nanoparticles/polymer composites

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Nanoparticle (NP) is the matter between molecule and bulk material. It has attracted much attention in catalysis, optoelectronics and biology due to its unique physical and chemical properties. Incorporation of these NPs into the polymer matrix is one of the best methods to display their special functions, which not only stabilize the NPs but also realize the functional assembly of NPs and polymers. However, reali- zation of this idea depends largely on the compatibility of NPs and polymers as well as the interaction between them. Therefore, many methods have been developed to prepare the composites of NPs and polymers in order to obtain the function ex- pected. In this review, we mainly focus on the combination of in situ method with other methods to synthesize different functional one-dimension, two-dimension as well as bulk composites, which has been recently developed by our group. The most striking character of our method is the excellent compatibility between NPs and polymers which ensures a homogeneous distribution of NPs in the polymer matrix. The existence of the polymer network makes the NPs more stable, and is significant for displaying their functions.

  1. Fluorescence of silicon nanoparticles prepared by nanosecond pulsed laser

    Directory of Open Access Journals (Sweden)

    Chunyang Liu

    2014-03-01

    Full Text Available A pulsed laser fabrication method is used to prepare fluorescent microstructures on silicon substrates in this paper. A 355 nm nanosecond pulsed laser micromachining system was designed, and the performance was verified and optimized. Fluorescence microscopy was used to analyze the photoluminescence of the microstructures which were formed using the pulsed laser processing technique. Photoluminescence spectra of the microstructure reveal a peak emission around 500 nm, from 370 nm laser irradiation. The light intensity also shows an exponential decay with irradiation time, which is similar to attenuation processes seen in porous silicon. The surface morphology and chemical composition of the microstructure in the fabricated region was also analyzed with multifunction scanning electron microscopy. Spherical particles are produced with diameters around 100 nm. The structure is compared with porous silicon. It is likely that these nanoparticles act as luminescence recombination centers on the silicon surface. The small diameter of the particles modifies the band gap of silicon by quantum confinement effects. Electron-hole pairs recombine and the fluorescence emission shifts into the visible range. The chemical elements of the processed region are also changed during the interaction between laser and silicon. Oxidation and carbonization play an important role in the enhancement of fluorescence emission.

  2. Fluorescence of silicon nanoparticles prepared by nanosecond pulsed laser

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Chunyang, E-mail: chunyangliu@126.com; Sui, Xin; Yang, Fang; Ma, Wei; Li, Jishun; Xue, Yujun [Henan University of Science and Technology, Luoyang, 471003 (China); Fu, Xing [Tianjin University, Tianjin, 300072 (China)

    2014-03-15

    A pulsed laser fabrication method is used to prepare fluorescent microstructures on silicon substrates in this paper. A 355 nm nanosecond pulsed laser micromachining system was designed, and the performance was verified and optimized. Fluorescence microscopy was used to analyze the photoluminescence of the microstructures which were formed using the pulsed laser processing technique. Photoluminescence spectra of the microstructure reveal a peak emission around 500 nm, from 370 nm laser irradiation. The light intensity also shows an exponential decay with irradiation time, which is similar to attenuation processes seen in porous silicon. The surface morphology and chemical composition of the microstructure in the fabricated region was also analyzed with multifunction scanning electron microscopy. Spherical particles are produced with diameters around 100 nm. The structure is compared with porous silicon. It is likely that these nanoparticles act as luminescence recombination centers on the silicon surface. The small diameter of the particles modifies the band gap of silicon by quantum confinement effects. Electron-hole pairs recombine and the fluorescence emission shifts into the visible range. The chemical elements of the processed region are also changed during the interaction between laser and silicon. Oxidation and carbonization play an important role in the enhancement of fluorescence emission.

  3. PREPARATION AND CHARACTERIZATION OF IRON OXIDE NANOPARTICLES ON DISACCHARIDE TEMPLATES

    Directory of Open Access Journals (Sweden)

    B ANILREDDY

    2013-09-01

    Full Text Available We report here the preparation of nanoparticles of iron oxide in the presence of polysaccharidetemplates. Interaction between iron sulfate and template has been carried out in aqueous phase,followed by the selective and controlled removal of the template to achieve narrow distribution ofparticle size. Particles of iron oxide obtained have been characterized for their stability in solventmedia, size, size distribution and crystallinity and it was found that when the negative value of thezeta potential increases, particle size decreases. A narrow particle size distribution with D100 = 275nm was obtained with chitosan and starch templates. SEM measurements further confirm the particlesize measurement. Diffuse reflectance UV–VIS spectra values show that the template is completelyremoved from the final iron oxide particles and powder XRD measurements show that the peaks ofthe diffractogram are in agreement with the theoretical data of hematite. The salient observations ofour study shows that there occurs a direct correlation between zeta potential, polydispersity index,band gap energy and particle size. The crystallite size of the particles was found to be 30–35 nm. Alarge negative zeta potential was found to be advantageous for achieving lower particle sizes, as theparticles remained discrete without agglomeration.

  4. Size-Controlled Pd Nanoparticle Catalysts Prepared by Galvanic Displacement into a Porous Si-Iron Oxide Nanoparticle Host.

    Science.gov (United States)

    Kim, Taeho; Fu, Xin; Warther, David; Sailor, Michael J

    2017-02-21

    Porous silicon nanoparticles containing both Pd and iron oxide nanoparticles are prepared and studied as magnetically recoverable catalysts for organic reductions. The Pd nanoparticles are generated in situ by electroless deposition of Pd(NH3)4(2+), where the porous Si skeleton acts as both a template and as a reducing agent and the released ammonia ligands raise the local pH to exert control over the size of the Pd nanoparticles. The nanocomposites are characterized by transmission electron microscopy, energy-dispersive X-ray spectroscopy, nitrogen adsorption, X-ray diffraction, superconducting quantum interference device magnetization, and dynamic light scattering. The nanocomposite consists of a porous Si nanoparticle (150 nm mean diameter) containing ∼20 nm pores, uniformly decorated with a high loading of surfactant-free Pd nanoparticles (12 nm mean diameter) and superparamagnetic γ-Fe2O3 nanoparticles (∼7 nm mean diameter). The reduction of 4-nitrophenol to 4-aminophenol by sodium borohydride is catalyzed by the nanocomposite, which is stable through the course of the reaction. Catalytic reduction of the organic dyes methylene blue and rhodamine B is also demonstrated. The conversion efficiency and catalytic activity are found to be superior to a commercial Pd/C catalyst compared under comparable reaction conditions. The composite catalyst can be recovered from the reaction mixture by applying an external magnetic field due to the existence of the superparamagnetic iron oxide nanoparticles in the construct. The recovered particles retain their catalytic activity.

  5. Studies on the Preparation Properties and Drug Loading of theStarch Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    WangJin; HouXinpu

    2001-01-01

    On the basis of studies of starch microspheres, we carried out the research program of starch nanoparticles(SNP)which included preparation, physical and chemical properties and drug loading. The SNP was prepared using reversedphase-microemulsion polymerization method, with soluble starch as raw material. The particle size, quantity ofphosphorous, degradability, scanning electron microgragh, IR spectra and stability of SNP were investigated. Thepharmacodynamics and concentration-time curve of insulin starch nanoparticles were determined.

  6. Preparation and Characterization of Monodisperse Nickel Nanoparticles by Polyol Process

    Institute of Scientific and Technical Information of China (English)

    LI Peng; GUAN Jianguo; ZHANG Qingjie; ZHAO Wenyu

    2005-01-01

    Polymer-protected monodisperse nickel nanoparticles were synthesized by a modified polyol reduction method in the presence of poly ( N-vinyl- 2-pyrrolidone ). These nanoparticles were characterized by transmission electron microscopy (TEM), X- ray diffraction ( XRD ), selected area electron diffraction ( SAED ), as well as vibrating sample magnetometer (VSM). The experimental results show that the addition of PVP and the concentration of NaOH have strong influences on the size, agglomeration and uniformity of nanoparticles. In the presence of PVP and NaOH with low concentrations, monodisperse nickel nanoparticles with average diameters about 42 nm were obtained and characterized to be pure nickel crystalline with fcc structure. Secondary structures such as clusters, loops, and strings resulted from magnetic interactions between particles were observed. The chemical interaction between the PVP and nickel nanoparticles was found by FTIR. The saturation magnetization ( Ms ), remanent magnetization (Mr) and coercivity ( Hc ) of these nickel nanoparticles are lower than those of bulk nickel.

  7. Preparation and Characterization of Rare Earth Doped Fluoride Nanoparticles

    Directory of Open Access Journals (Sweden)

    Timothy A. DeVol

    2010-03-01

    Full Text Available This paper reviews the synthesis, structure and applications of metal fluoride nanoparticles, with particular focus on rare earth (RE doped fluoride nanoparticles obtained by our research group. Nanoparticles were produced by precipitation methods using the ligand ammonium di-n-octadecyldithiophosphate (ADDP that allows the growth of shells around a core particle while simultaneously avoiding particle aggregation. Nanoparticles were characterized on their structure, morphology, and luminescent properties. We discuss the synthesis, properties, and application of heavy metal fluorides; specifically LaF3:RE and PbF2, and group IIA fluorides. Particular attention is given to the synthesis of core/shell nanoparticles, including selectively RE-doped LaF3/LaF3, and CaF2/CaF2 core/(multi-shell nanoparticles, and the CaF2-LaF3 system.

  8. Methods for Preparing Nanoparticle-Containing Thermoplastic Composite Laminates

    Science.gov (United States)

    Gruber, Mark B. (Inventor); Jensen, Brian J. (Inventor); Cano, Roberto J. (Inventor)

    2016-01-01

    High quality thermoplastic composites and composite laminates containing nanoparticles and/or nanofibers, and methods of producing such composites and laminates are disclosed. The composites comprise a thermoplastic polymer and a plurality of nanoparticles, and may include a fibrous structural reinforcement. The composite laminates are formed from a plurality of nanoparticle-containing composite layers and may be fused to one another via an automated process.

  9. Preparation and in vitro evaluation of hydrophilic fenretinide nanoparticles.

    Science.gov (United States)

    Ledet, Grace A; Graves, Richard A; Glotser, Elena Y; Mandal, Tarun K; Bostanian, Levon A

    2015-02-20

    Fenretinide is an effective anti-cancer drug with high in vitro cytotoxicity and low in vivo systemic toxicity. In clinical trials, fenretinide has shown poor therapeutic efficacy following oral administration - attributed to its low bioavailability and solubility. The long term goal of this project is to develop a formulation for the oral delivery of fenretinide. The purpose of this part of the study was to prepare and characterize hydrophilic nanoparticle formulations of fenretinide. Three different ratios of polyvinyl pyrrolidone (PVP) to fenretinide were used, namely, 3:1, 4:1, and 5:1. Both drug and polymer were dissolved in a mixture of methanol and dichloromethane (2:23 v/v). Rotary evaporation was used to remove the solvents, and, following reconstitution with water, a high pressure homogenizer was used to form nanoparticles. The particle size and polydispersity index were measured before and after lyophilization. The formulations were studied by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and X-ray powder diffraction (XRPD). The effectiveness of the formulations was assessed by release studies and Caco-2 cell permeability assays. As the PVP content increased, the recovered particle size following lyophilization became more consistent with the pre-lyophilization particle size, especially for those formulations with less lactose. The DSC scans of the formulations did not show any fenretinide melting endotherms, indicating that the drug was either present in an amorphous form in the formulation or that a solid solution of the drug in PVP had formed. For the release studies, the highest drug release among the formulations was 249.2±35.5ng/mL for the formulation with 4:1 polymer-to-drug. When the permeability of the formulations was evaluated in a Caco-2 cell model, the mean normalized flux for each treatment group was significantly higher (p<0.05) from the fenretinide control. The formulation containing 4:1 polymer

  10. Preparation and characterization of Ag nanoparticle-embedded polymer electrospun nanofibers

    Energy Technology Data Exchange (ETDEWEB)

    Dong Guoping, E-mail: guoping_dong@163.com; Xiao Xiudi; Liu, Xiaofeng; Qian Bin [Chinese Academy of Sciences, Shanghai Institute of Optics and Fine Mechanics (China); Ma Zhijun; Ye Song [Zhejiang University, State Key Laboratory of Silicon Materials (China); Chen Danping [Chinese Academy of Sciences, Shanghai Institute of Optics and Fine Mechanics (China); Qiu Jianrong, E-mail: jrqiu@zju.edu.c [Zhejiang University, State Key Laboratory of Silicon Materials (China)

    2010-05-15

    Poly (vinyl alcohol) (PVA) and poly (vinyl pyrrolidone) (PVP) nanofibers embedding Ag nanoparticles (5-18 nm) have been prepared successfully by electrospinning at room temperature. Scanning electron microscope (SEM), X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), Fourier transform IR spectra (FTIR), and Raman scattering were used to characterize the structure and properties of Ag nanoparticle-embedded PVA and PVP nanofibers before and after heat treatment at different temperature. The antibacterial activity of Ag nanoparticle-embedded PVP nanofibers after heat treatment was also tested, which indicated that the biological activity of yeast cells was effectively inhibited by these Ag nanoparticle-embedded PVP nanofibers.

  11. Preparation and characterization of graphene oxide encapsulated gold nanoparticles.

    Science.gov (United States)

    Yun, Yong Ju; Song, Ki-Bong

    2013-11-01

    We present a simple approach for the fabrication of graphene oxide-encapsulated gold nanoparticles using graphene oxide sheet-wrapping via electrostatic self-assembly. By mixing bovine serum albumin molecule-functionalized gold nanoparticles with graphene oxide dispersion, positively charged bovine serum albumin/gold nanoparticles easily assembled with negatively charged graphene oxide sheets through electrostatic interaction. Transmittance electron microscopy, scanning electron microscopy, atomic force microscopy, and Raman spectroscopy were used to confirm the encapsulation of graphene oxide on gold nanoparticles. Interestingly, graphene oxide sheets wrapping mainly occurs along the main body of single or a few gold nanoparticles. Additionally, by measuring the ultraviolet-visible spectroscopy spectrum, we found that the surface plasmon resonances band of the graphene oxide-encapsulated gold nanoparticles was found to become red-shifted compared to that of pristine gold nanoparticles, whereas similar to that of bovine serum albumin-coated gold nanoparticles. These results indicating that most of graphene oxide-encapsulated gold nanoparticles have good monodispersity and spherical shape. These resulting materials may potentially serve as a platform for plasmon resonance electron transfer spectroscopy or a probe for low level biosensing.

  12. Hollow nanoparticles of metal oxides and sulfides: fast preparation via laser ablation in liquid.

    Science.gov (United States)

    Niu, K Y; Yang, J; Kulinich, S A; Sun, J; Du, X W

    2010-11-16

    In this work, diverse hollow nanoparticles of metal oxides and sulfides were prepared by simply laser ablating metal targets in properly chosen liquids. The Kirkendall voiding and the selective heating with an infrared laser were shown to work as two independent mechanisms for the formation of such hollow nanoparticles in only one- or two-step synthesis approaches. One of the prepared materials, ZnS hollow nanoparticles, showed high performance in gas sensing. The simple, fast, inexpensive technique that is proposed demonstrates very promising perspectives.

  13. Preparation and characterization of aligned carbon nanotubes coated with titania nanoparticles

    Institute of Scientific and Technical Information of China (English)

    YU Hongtao; ZHAO Huimin; QUAN Xie; CHEN Shuo

    2006-01-01

    Well-aligned carbon nanotubes coated with titania (TiO2) were prepared by atmospheric pressure chemical vapor deposition (APCVD), and the sequential experiments including carbon nanotubes preparation, air-oxidation purification and titania nanoparticles coating were performed at different temperatures in the same reactor. Scanning electron microscopy (SEM), transmission electron microscope (TEM), X-ray diffraction patterns (XRD), and energy- dispersive X-ray spectra (EDX) demonstrated the well-aligned nanotubes and TiO2 nanoparticles in close proximity and the average diameter of TiO2 nanoparticles was 11.5 nm.

  14. Green preparation and spectroscopic characterization of plasmonic silver nanoparticles using fruits as reducing agents

    Directory of Open Access Journals (Sweden)

    Jes Ærøe Hyllested

    2015-01-01

    Full Text Available Chemicals typically available in plants have the capability to reduce silver and gold salts and to create silver and gold nanoparticles. We report the preparation of silver nanoparticles with sizes between 10 and 300 nm from silver nitrate using fruit extract collected from pineapples and oranges as reducing agents. The evolvement of a characteristic surface plasmon extinction spectrum in the range of 420 nm to 480 nm indicates the formation of silver nanoparticles after mixing silver nitrate solution and fruit extract. Shifts in plasmon peaks over time indicate the growth of nanoparticles. Electron microscopy shows that the shapes of the nanoparticles are different depending on the fruit used for preparation. The green preparation process can result in individual nanoparticles with a very poor tendency to form aggregates with narrow gaps even when aggregation is forced by the addition of NaCl. This explains only modest enhancement factors for near-infrared-excited surface enhanced Raman scattering. In addition to the surface plasmon band, UV–visible absorption spectra show features in the UV range which indicates also the presence of small silver clusters, such as Ag42+. The increase of the plasmon absorption correlates with the decrease of absorption band in the UV. This confirms the evolution of silver nanoparticles from silver clusters. The presence of various silver clusters on the surface of the “green” plasmonic silver nanoparticles is also supported by a strong multicolor luminesce signal emitted by the plasmonic particles during 473 nm excitation.

  15. Preparing and Characterizing Chitosan Nanoparticles Containing Hemiscorpius lepturus Scorpion Venom as an Antigen Delivery System

    Directory of Open Access Journals (Sweden)

    Mohammadpour Dounighi, N.

    2012-11-01

    Full Text Available In recent years, chitosan nanoparticles have been studied widely for protein delivery. In this study, Hemiscorpius lepturus (HL venom was encapsulated in chitosan nanoparticles. The aim of the present work was to carry out a systematic study for preparing biocompatible and biodegradable nanoparticles for loading HL scorpion venom and to evaluate their potential as an antigen delivery system. In this study, HL venom loaded chitosan nanoparticles fabricated by ionic gelation of chitosan and tripolyphosphate and the factors which may be influenced in the preparation of nanoparticles were analyzed. Also, their physicochemical properties and in vitro release behavior were studied. The optimum encapsulation efficiency and capacity were observed when the chitosan concentration and HL venom were 2mg/ml and 500µg/ml, respectively. The HL venom loaded nanoparticles were in the size range of 130-160nm (polydispersity index values of 0.423 and exhibited the positive zeta potential. Transmission electron microscope imaging showed spherical and smooth surface of nanoparticles. The profiles of the release exhibited a burst releases about 50% in the first 4 hr and then slowed down at a constant rate. The obtained results suggested that the chitosan nanoparticles prepared in this work had the potential for antigen delivery.

  16. Comparison of schemes for preparing magnetic Fe3O4 nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Ruoyu Hong; Jianhua Li; Jian Wang; Hongzhong Li

    2007-01-01

    Magnetic Fe3O4 nanoparticles were prepared by means of coprecipitation using NH3·H2O in water and in alcohol, and using NaOH in water. A series of instruments such as SEM, TEM, HRTEM, FT-IR, XRD and VSM were used to characterize the properties of the magnetic nanoparticles.was the longest. The process using NaOH in water was the simplest and the reaction time was the shortest, but the particle characteristics were inferior to those of the other two methods. The mean size of magnetic Fe3O4 nanoparticles prepared by coprecipitation in alcohol was the smallest among the three, but the nanoparticles aggregated severely. The magnetic Fe3O4 nanoparticles were coated with oleic acid using saturated sodium coated successfully and thoroughly.

  17. Preparation and drug releasing property of magnetic chitosan-5-fluorouracil nano-particles

    Institute of Scientific and Technical Information of China (English)

    WANG Dong-sheng; LI Jian-guo; LI He-ping; TANG Fa-qing

    2009-01-01

    In order to synthesize the targeting drug carrier system, magnetic chitosan-5-fluorouracil nano-particles were prepared by using 5-fluorouracil (5-Fu) as model drug, Fe_3O_4 nano-particles as kernel, chitosan as enveloping material and glutaraldehyde as cross linking agent through ultrasonic technique. The morphology of the magnetic chitosan-5-Fu nano-particles was observed with a transmission electron microscope(TEM). The results showed that magnetic chitosan-5-Fu nano-particles were prepared in spherical structure with a size range of 50-60 nm. The delivering capacity and drug releasing properties of magnetic chitosan-5-Fu nano-particles were investigated by UV-vis spectrum analysis. The results showed that the loading capacity was 13.4% and the cumulative release percentage in the phosphate buffer (pH=7.2) solutions was 68% in 30 h. These data indicate that the wrapped drug of magnetic chitosan-5-Fu nano-particles was slowly-released. The magnetic response of magnetic chitosan-5-Fu nano-particles was studied by UV-vis spectrometer to detect the changes of solution absorbance. Without external magnetic field, the nano-particle deposition rate was slow. When being subjected to 8 mT magnetic field, the particle sedimentation rate was increased rapidly. The results showed that magnetic chitosan-5-Fu nano-particles have a magnetic stability and strong targeting characteristics.

  18. Polymeric nanoparticles containing diazepam: preparation, optimization, characterization, in-vitro drug release and release kinetic study

    Science.gov (United States)

    Bohrey, Sarvesh; Chourasiya, Vibha; Pandey, Archna

    2016-03-01

    Nanoparticles formulated from biodegradable polymers like poly(lactic-co-glycolic acid) (PLGA) are being extensively investigated as drug delivery systems due to their two important properties such as biocompatibility and controlled drug release characteristics. The aim of this work to formulated diazepam loaded PLGA nanoparticles by using emulsion solvent evaporation technique. Polyvinyl alcohol (PVA) is used as stabilizing agent. Diazepam is a benzodiazepine derivative drug, and widely used as an anticonvulsant in the treatment of various types of epilepsy, insomnia and anxiety. This work investigates the effects of some preparation variables on the size and shape of nanoparticles prepared by emulsion solvent evaporation method. These nanoparticles were characterized by photon correlation spectroscopy (PCS), transmission electron microscopy (TEM). Zeta potential study was also performed to understand the surface charge of nanoparticles. The drug release from drug loaded nanoparticles was studied by dialysis bag method and the in vitro drug release data was also studied by various kinetic models. The results show that sonication time, polymer content, surfactant concentration, ratio of organic to aqueous phase volume, and the amount of drug have an important effect on the size of nanoparticles. Hopefully we produced spherical shape Diazepam loaded PLGA nanoparticles with a size range under 250 nm with zeta potential -23.3 mV. The in vitro drug release analysis shows sustained release of drug from nanoparticles and follow Korsmeyer-Peppas model.

  19. Gold core@silver semishell Janus nanoparticles prepared by interfacial etching

    Science.gov (United States)

    Chen, Limei; Deming, Christopher P.; Peng, Yi; Hu, Peiguang; Stofan, Jake; Chen, Shaowei

    2016-07-01

    Gold core@silver semishell Janus nanoparticles were prepared by chemical etching of Au@Ag core-shell nanoparticles at the air/water interface. Au@Ag core-shell nanoparticles were synthesized by chemical deposition of a silver shell onto gold seed colloids followed by the self-assembly of 1-dodecanethiol onto the nanoparticle surface. The nanoparticles then formed a monolayer on the water surface of a Langmuir-Blodgett trough, and part of the silver shell was selectively etched away by the mixture of hydrogen peroxide and ammonia in the water subphase, where the etching was limited to the side of the nanoparticles that was in direct contact with water. The resulting Janus nanoparticles exhibited an asymmetrical distribution of silver on the surface of the gold cores, as manifested in transmission electron microscopy, UV-vis absorption, and X-ray photoelectron spectroscopy measurements. Interestingly, the Au@Ag semishell Janus nanoparticles exhibited enhanced electrocatalytic activity in oxygen reduction reactions, as compared to their Au@Ag and Ag@Au core-shell counterparts, likely due to a synergistic effect between the gold cores and silver semishells that optimized oxygen binding to the nanoparticle surface.Gold core@silver semishell Janus nanoparticles were prepared by chemical etching of Au@Ag core-shell nanoparticles at the air/water interface. Au@Ag core-shell nanoparticles were synthesized by chemical deposition of a silver shell onto gold seed colloids followed by the self-assembly of 1-dodecanethiol onto the nanoparticle surface. The nanoparticles then formed a monolayer on the water surface of a Langmuir-Blodgett trough, and part of the silver shell was selectively etched away by the mixture of hydrogen peroxide and ammonia in the water subphase, where the etching was limited to the side of the nanoparticles that was in direct contact with water. The resulting Janus nanoparticles exhibited an asymmetrical distribution of silver on the surface of the gold

  20. Gold nanoparticles: preparation, functionalisation and applications in biochemistry and immunochemistry

    Energy Technology Data Exchange (ETDEWEB)

    Dykman, Lev A; Bogatyrev, Vladimir A [Institute of Biochemistry and Physiology of Plants and Microorganisms, Russian Academy of Sciences (Russian Federation)

    2007-02-28

    The review summarises data on the synthesis and functionalisation of gold nanoparticles and their applications in biological investigations. Particular attention is given to applications of colloidal gold in solid-phase assays, immunoassay and studies of biologically active compounds by vibrational spectroscopy. A special section deals with the use of gold nanoparticles as antigen carriers in immunisation.

  1. [Preparation, characterization and surface-enhanced Raman properties of agarose gel/gold nanoparticles hybrid].

    Science.gov (United States)

    Ma, Xiao-yuan; Liu, Ying; Wang, Zhou-ping

    2014-08-01

    Agarose gel/gold nanoparticles hybrid was prepared by adding gold nanoparticles to preformed agarose gel. Naniocomposite structures and properties were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and UV-Vis-NIR absorption spectroscopy. Experimental data indicated a uniform distribution of gold nanoparticles adsorbed on agarose gel network And the excellent optical absorption properties were shown. Based on the swelling-contraction characteristics of agarose gel and the adjustable localized surface plasmon resonance (LSPR) of the gold nanoparticles, the nano-composites were used as surface enhanced Raman scattering (SERS) substrate to detect the Raman signal molecules Nile blue A. Results revealed that the porous structure of the agarose gel provided a good carrier for the enrichment of the gold nanoparticles. The gold nanoparticles dynamic hot-spot effect arising from the agarose gel contraction loss of water in the air greatly enhanced the Raman signal.

  2. INFRARED PHOTOLUMINESCENCE SPECTRA OF PBS NANOPARTICLES PREPARED BY LANGMUIR–BLODGETT AND LASER ABLATION METHODS

    Directory of Open Access Journals (Sweden)

    Zdeněk Remes

    2014-12-01

    Full Text Available We optimized the optical setup originally designed for the photoluminescence measurements in the spectral range 400‒1100 nm. New design extends the spectral range into the near infrared region 900‒1700 nm and allows the colloidal solutions measurements in cuvettes as well as the measurements of nanoparticles deposited in the form of thin films on glass substrates. The infrared photoluminescence spectra of the PbS nanoparticles prepared by the Langmuir–Blodgett technique show the higher photoluminescence intensity and the shift to the shorter wavelengths compared to the infrared photoluminescence spectra of the PbS nanoparticles prepared by the laser ablation from PbS target. We aslo proved the high stability of PbS nanoparticles prepared in the form of thin layers.

  3. A moderate method for preparation DMSA coated Fe3O4 nanoparticles

    Science.gov (United States)

    Song, L. N.; Gu, N.; Zhang, Y.

    2017-01-01

    A moderate way to prepare water soluble magnetic Fe3O4 nanoparticles has been developed. Firstly, oleic acid coated Fe3O4 is prepared by coprecipitation. Second, oleic acid were replaced by 2,3-dimercaptosuccinnic acid (DMSA) to prepare DMSA/Fe3O4 in the mixed solution of n-hexane and acetone. After dialysis and filtration the DMSA/Fe3O4 can be transferred into distilled water to form stable Fe3O4 nanoparticle solutions. The TEM images indicated that the particles had spherical shape and the nanoparticles were found to be 12 nm with a relatively narrow size distribution with the hydrodynamic size of 30 nm. And the result of VSM shows that DMSA/Fe3O4 nanoparticles have a saturation magnetization of 31 emu/g. The IR spectra indicated that the iron oxide was located by carboxyl matrix.

  4. Preparation and Characterization of ZrO2 Nanoparticles Capped by Trioctylphosphine Oxide(TOPO)

    Institute of Scientific and Technical Information of China (English)

    MA Jianqi

    2011-01-01

    Monodisperse ZrO2 nanoparticles capped by trioctylphosphine oxide(TOPO)were prepared in non-aqueous solvent using in-situ synthesis method.Transmission electron microscopy(TEM),X-ray diffraction(XRD),X-ray photoelectron spectrometer(XPS),Fourier transformation infrared spectroscopy (FTIR),and thermogravimetric analysis(TGA)were adopted to characterize and investigate the size,structure,composition,and the binding manners between organic capping agent TOPO and inorganic ZrO2 nanocores of the as-prepared nanoparticles.In addition,the nanoparticles were also studied to determine their solubility and relative stability.The experimental results show that the prepared nanoparticles contain about 25% organic capping shell TOPO,75% inorganic ZrO2 nanocores,and can be easily dissolved and be stably disersed in nonpolar organic solvents.

  5. A simple improved desolvation method for the rapid preparation of albumin nanoparticles.

    Science.gov (United States)

    Jahanban-Esfahlan, Ali; Dastmalchi, Siavoush; Davaran, Soodabeh

    2016-10-01

    The current study tried to establish a simple and fast method for the preparation of BSA and HSA nanoparticles, based on an improved desolvation procedure under the aspect of a controllable particle size around 100nm for drug delivery applications. The Procedure used for the nanoparticles preparation was simplified by using a designed apparatus for controlling the addition of ethanol and it was used instead of conventional tubing pump which enabled the preparation of nanoparticles under defined conditions. By using EDC as cross-linker instead of glutharaldehyde, the time of nanoparticles preparation procedure was reduced to 3h. Several factors of the preparation process, such as the volume of the albumin solution, desolvating agent volume, the amount of cross-linker, the presence of salts and protein concentration were evaluated. Nanoparticles with smaller size were obtained under experimental conditions without the presence of salts or the use of buffers, 250mg of protein/4ml water, 5mg cross-linker, the addition of 4 and 8ml ethanol by using the designed apparatus to the HSA and BSA solution, respectively. By using this improved method, BSA and HSA nanoparticles of the size around 100nm and polydispersity below 0.2 were obtained.

  6. Biomimetic thin film synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Graff, G.L.; Campbell, A.A.; Gordon, N.R.

    1995-05-01

    The purpose of this program is to develop a new process for forming thin film coatings and to demonstrate that the biomimetic thin film technology developed at PNL is useful for industrial applications. In the biomimetic process, mineral deposition from aqueous solution is controlled by organic functional groups attached to the underlying substrate surface. The coatings process is simple, benign, inexpensive, energy efficient, and particularly suited for temperature sensitive substrate materials (such as polymers). In addition, biomimetic thin films can be deposited uniformly on complex shaped and porous substrates providing a unique capability over more traditional line-of-sight methods.

  7. Facile fabrication of organic-inorganic hybrid beads by aminated alginate enabled gelation and biomimetic mineralization.

    Science.gov (United States)

    Li, Jian; Wu, Hong; Liang, Yanpeng; Jiang, Zhongyi; Jiang, Yanjun; Zhang, Lei

    2013-01-01

    Inspired by biomineralization, design and preparation of biomimetic organic-inorganic composites have become a hot issue and a research frontier in many areas, including enzyme engineering. In this research, a unique and facile method for fabricating organic-inorganic hybrid beads is proposed. Modified alginate with a dual function of gelation and mineralization was synthesized for fabrication of hybrid carriers for enzyme immobilization. With the aid of EDC/NHS conjugation chemistry, the amine groups from diethylene triamine were grafted onto alginate in a controllable way. The resultant aminated alginate served manifold functions: forming a hydrogel via Ca(2+)-cross-linking, inducing the biomimetic silicification and manipulating the distribution of silica nanoparticles. Owing to the compact polymer network structure and the homogeneous silica nanoparticle dispersion, the as-prepared NH2-alginate/silica hybrid beads displayed superior swelling resistance and mechanical stability to pure alginate beads. The hybrid beads were subsequently utilized for encapsulation of yeast alcohol dehydrogenase (YADH). It was found that the thermal stability, pH tolerance and storage stability of the immobilized enzyme were all improved without significantly lowering the catalytic activity.

  8. Preparation of poly (Vinyl Alcohol) nanofibers containing silver nanoparticles by gamma-ray irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Yun Hye [AMOTECH Co., Ltd., Kimpo (Korea, Republic of); Shin, Jun Wha; An, Sung Jun; Youn, Min Ho; Lim, Youn Mook; Gwon, Hui Jeong; Nho, Young Chang [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, Jeongeup (Korea, Republic of)

    2008-08-15

    PVA nanofibers containing silver nanoparticles were prepared by two methods. The first method was electrospinning of irradiated solution. The prepared PVA/AgNO{sub 3} solution was irradiated by gamma-rays. And then the irradiated solution was electrospun. The second method was irradiation of electrospun nanofibers. Nanofibers prepared by electrospinning of unirradiated PVA/AgNO{sub 3} solution. The morphology of the nanofibers was observed with a SEM, TEM. When the irradiated PVA/AgNO{sub 3} solution were electrospun, the average size of the Ag nanoparticles was increased, but their number was decreased.

  9. Chitosan Nanoparticles Prepared by Ionotropic Gelation: An Overview of Recent Advances.

    Science.gov (United States)

    Desai, Kashappa Goud

    2016-01-01

    The objective of this review is to summarize recent advances in chitosan nanoparticles prepared by ionotropic gelation. Significant progress has occurred in this area since the method was first reported. The gelation technique has been improved through a number of creative methodological modifications. Ionotropic gelation via electrospraying and spinning disc processing produces nanoparticles with a more uniform size distribution. Large-scale manufacturing of the nanoparticles can be achieved with the latter approach. Hydrophobic and hydrophilic drugs can be simultaneously encapsulated with high efficiency by emulsification followed by ionic gelation. The turbulent mixing approach facilitates nanoparticle formation at a relatively high polymer concentration (5 mg/mL). The technique can be easily tuned to achieve the desired polymer/surface modifications (e.g., blending, coating, and surface conjugation). Using factorial-design-based approaches, optimal conditions for nanoparticle formation can be determined with a minimum number of experiments. New insights have been gained into the mechanism of chitosan-tripolyphosphate nanoparticle formation. Chitosan nanoparticles prepared by ionotropic gelation tend to aggregate/agglomerate in unfavorable environments. Factors influencing this phenomenon and strategies that can be adopted to minimize the instability are discussed. Ionically cross-linked nanoparticles based on native chitosan and modified chitosan have shown excellent efficacy for controlled and targeted drug-delivery applications.

  10. Progress in the preparation of magnetic nanoparticles for applications in biomedicine

    Energy Technology Data Exchange (ETDEWEB)

    Roca, A G; Costo, R; Rebolledo, A F; Veintemillas-Verdaguer, S; Tartaj, P; Gonzalez-Carreno, T; Morales, M P; Serna, C J, E-mail: puerto@icmm.csic.e [Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, 28049 Madrid (Spain)

    2009-11-21

    This review summarizes recent advances in synthesis routes for quickly and reliably making and functionalizing magnetic nanoparticles for applications in biomedicine. We put special emphasis on describing synthetic strategies that result in the production of nanosized materials with well-defined physical and crystallochemical characteristics as well as colloidal and magnetic properties. Rather than grouping the information according to the synthetic route, we have described methods to prepare water-dispersible equiaxial magnetic nanoparticles with sizes below about 10 nm, sizes between 10 and 30 nm and sizes around the monodomain-multidomain magnetic transition. We have also described some recent examples reporting the preparation of anisometric nanoparticles as well as methods to prepare magnetic nanosized materials other than iron oxide ferrites, for example Co and Mn ferrite, FePt and manganites. Finally, we have described examples of the preparation of multicomponent systems with purely inorganic or organic-inorganic characteristics. (topical review)

  11. Proliferation and differentiation of osteoblast-like MC3T3-E1 cells on biomimetically and electrolytically deposited calcium phosphate coatings

    NARCIS (Netherlands)

    Wang, Jiawei; Boer, de Jan; Groot, de Klaas

    2008-01-01

    Biomimetic and electrolytic deposition are versatile methods to prepare calcium phosphate coatings. In this article, we compared the effects of biomimetically deposited octacalcium phosphate and carbonate apatite coatings as well as electrolytically deposited carbonate apatite coating on the prolife

  12. BiVO4 nanoparticles: Preparation, characterization and photocatalytic activity

    Directory of Open Access Journals (Sweden)

    Venkataraman Sivakumar

    2015-12-01

    Full Text Available Bismuth vanadate (BiVO4 nanoparticles were synthesized by a simple thermal decomposition method. The synthesized bismuth vanadate nanoparticles were characterized by X-ray diffraction analysis, it is found that the synthesized sample belongs to monoclinic BiVO4. Fourier transform infrared spectroscopy confirms the formation of Bi-O bond in the sample. Ultraviolet–Visible (DRS-UV–Visible spectroscopy and photoluminescence spectroscopy reveal the optical property of the BiVO4 nanoparticles. The morphology was identified by both scanning electron microscopy and high-resolution transmission electron microscopy. Further, the photocatalytic activity of BiVO4 nanoparticles was investigated by photodegradation of methylene blue as a model organic pollutant.

  13. MgO nanoparticles as antibacterial agent: preparation and activity

    Energy Technology Data Exchange (ETDEWEB)

    Tang, Zhen-Xing, E-mail: tangzhenxing@126.com [Department of Food Science, Anqing, Vocational and Technical College, Anqing, Anhui (China); Lv, Bin-Feng [Date Palm Research Center, King Faisal University, (Saudi Arabia)

    2014-07-15

    Bacterial pollution is a great risk for human health. Nanotechnology offers a way to develop new inorganic antibacterial agents. Nano-inorganic metal oxide has a potential to reduce bacterial contamination. MgO is an important inorganic oxide and has been widely used in many fields. Many studies have shown that MgO nanoparticles have good antibacterial activity. Therefore, in this paper, the main synthesis methods, antibacterial activity and antibacterial mechanisms of MgO nanoparticles are reviewed. (author)

  14. MgO nanoparticles as antibacterial agent: preparation and activity

    OpenAIRE

    Zhen-Xing Tang; Bin-Feng Lv

    2014-01-01

    Bacterial pollution is a great risk for human health. Nanotechnology offers a way to develop new inorganic antibacterial agents. Nano-inorganic metal oxide has a potential to reduce bacterial contamination. MgO is an important inorganic oxide and has been widely used in many fields. Many studies have shown that MgO nanoparticles have good antibacterial activity. Therefore, in this paper, the main synthesis methods, antibacterial activity and antibacterial mechanisms of MgO nanoparticles are r...

  15. Preparation of gold nanoparticle dimers via streptavidin-induced interlinking

    Energy Technology Data Exchange (ETDEWEB)

    Zon, Vera B.; Sachsenhauser, Matthias; Rant, Ulrich, E-mail: rant@wsi.tum.de [Technische Universitaet Muenchen, Walter Schottky Institut (Germany)

    2013-10-15

    There is great interest in establishing efficient means of organizing nanoparticles into complex structures, especially in fields like nano-optical devices. One of the demonstrated routes uses biomolecular scaffolds, like the streptavidin-biotin system, to deterministically separate and structure particle complexes. However, controlled formation of streptavidin-linked nanoparticle dimers or trimers is challenging, and large aggregates are often formed under conditions that are difficult to regulate. Here, we studied the aggregates and interlinking kinetics of biotin-functionalized 20 nm gold nanoparticles in the presence of the interlinking protein, streptavidin. We found two different protein-linker concentration regions where small stable particle aggregates are formed: when the protein and nanoparticle concentrations are similar and when the protein to nanoparticle concentration ratio exceeds intermediate concentrations (10:1-100:1) that promote precipitation of large aggregates. We attribute this behavior to the limited availability of free-linker molecules and the limited availability of free ligand (biotin) on the particle surface for low and high protein concentrations, respectively. Furthermore, we show that the product can be additionally enriched up to 25 % through either centrifugation in sucrose or size-exclusion chromatography. These results provide additional understanding into the assembly of ligand-functionalized nanoparticles with water-soluble linkers and provide a facile way to produce well-defined small aggregates for potential use in, for instance, surface-enhanced spectroscopy.

  16. Microbial mediated preparation, characterization and optimization of gold nanoparticles.

    Science.gov (United States)

    Barabadi, Hamed; Honary, Soheila; Ebrahimi, Pouneh; Mohammadi, Milad Ali; Alizadeh, Ahad; Naghibi, Farzaneh

    2014-01-01

    The need for eco-friendly and cost effective methods for nanoparticles synthesis is developing interest in biological approaches which are free from the use of toxic chemicals as byproducts. This study aimed to biosynthesize and optimize the size of gold nanoparticles which produced by biotechnological method using Penicillium crustosum isolated from soil. Initially, Penicillium crustosum was grown in fluid czapek dox broth on shaker at 28 °C and 200 rpm for ten days and then the supernatant was separated from the mycelia to convert AuCl₄ solution into gold nanoparticles. The synthesized nanoparticles in the optimum conditions were formed with fairly well-defined dimensions and good monodispersity. The characterizations were done by using different methods (UV-Visible Spectroscopy, Fluorescence, FT-IR, AFM (Atomic Force Microscopy) and DLS (Dynamic Light Scattering). The bioconversion was optimized by Box-Behnken experimental design. The results show that the effective factors in this process were concentration of AuCl₄, pH of medium and temperature of shaker incubator. The R(2) value was calculated to be 0.9999 indicating the accuracy and ability of the polynomial model. It can be concluded that the use of multivariate analysis facilitated to find out the optimum conditions for the biosynthesis of gold nanoparticles induced by Penicillium crustosum in a time and cost effective process. The current approach suggested that rapid synthesis of gold nanoparticles would be suitable for developing a biological process for mass scale production of formulations.

  17. Chitosan–Pluronic nanoparticles as oral delivery of anticancer gemcitabine: preparation and in vitro study

    Directory of Open Access Journals (Sweden)

    Ostad SN

    2012-04-01

    Full Text Available Hosniyeh Hosseinzadeh1, Fatemeh Atyabi1, Rassoul Dinarvand1, Seyed Naser Ostad21Nanotechnology Research Centre, 2Department of Toxicology and Pharmacology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, IranAbstract: Nanoparticles have proven to be an effective delivery system with few side effects for anticancer drugs. In this study, gemcitabine-loaded nanoparticles have been prepared by an ionic gelation method using chitosan and Pluronic® F-127 as a carrier. Prepared nanoparticles were characterized using dynamic light scattering, Fourier transform infrared spectroscopy (FT-IR, differential scanning calorimetry (DSC, scanning electron microscopy, and transmission electron microscopy. Different parameters such as concentration of sodium tripolyphosphate, chitosan, Pluronic, and drug on the properties of the prepared nanoparticles were evaluated. In vitro drug release was studied in phosphate-buffered saline (PBS; pH = 7.4. The cytotoxicity of the nanoparticles was assayed in the HT-29 colon cancer cell line. The mucoadhesion behavior of the nanoparticles was also studied by mucus glycoprotein assay. The prepared nanoparticles had a spherical shape with positive charge and a mean diameter ranging between 80 to 170 nm. FT-IR and DSC studies found that the drug was dispersed in its amorphous form due to its potent interaction with nanoparticle matrix. Maximum drug encapsulation efficiency was achieved at 0.4 mg/mL gemcitabine while maximum drug loading was 6% obtained from 0.6 mg/mL gemcitabine. An in vitro drug release study at 37°C in PBS (pH = 7.4 exhibited a controlled release profile for chitosan–Pluronic® F-127 nanoparticles. A cytotoxicity assay of gemcitabine-loaded nanoparticles showed an increase in the cytotoxicity of gemcitabine embedded in the nanoparticles in comparison with drug alone. The mucoadhesion study results suggest that nanoparticles could be considered as an efficient oral formulation for colon

  18. Preparation and characterization of ketoprofen loaded eudragit RS polymeric nanoparticles for controlled release

    Science.gov (United States)

    Anh, Nguyen Tuan; Chi, Nguyen T.; Khai Tran, T.; Tuyen Dao, T. P.; Nhan Le, N. T.; Mau Chien, Dang; Hoai, Nguyen To

    2012-12-01

    Nanospheres containing ketoprofen (Keto) and polymer eudragit RS were prepared using an emulsion solvent evaporation method. The ultrasonic probe (VCX500, vibracell) was used as a tool to disperse oil phase into aqueous phase leading to water/oil emulsion. Nanoparticles were successfully prepared and their morphologies and diameters were confirmed by transmission electron microscope (TEM) and dynamic light scattering (DLS), respectively. The result showed that particles were spherical with submicron size. The particle size was dependent on the RS concentration, emulsification tools and the types of organic solvents. For the encapsulation ability, Keto-loaded RS nanoparticle showed 9.8% of Keto in nanoparticle, which was evaluated by high-performance liquid chromatography (HPLC). Moreover, the drug release behavior of Keto-loaded eudragit RS nanoparticle was also investigated in vitro at pH 7.4 and compared to referential profenid.

  19. Metal nanoparticles (other than gold or silver) prepared using plant extracts for medical applications

    Science.gov (United States)

    Pasca, Roxana-Diana; Santa, Szabolcs; Racz, Levente Zsolt; Racz, Csaba Pal

    2016-12-01

    There are many modalities to prepare metal nanoparticles, but the reducing of the metal ions with plant extracts is one of the most promising because it is considerate less toxic for the environment, suitable for the use of those nanoparticles in vivo and not very expensive. Various metal ions have been already studied such as: cobalt, copper, iron, platinum, palladium, zinc, indium, manganese and mercury and the number of plant extracts used is continuously increasing. The prepared systems were characterized afterwards with a great number of methods of investigation: both spectroscopic (especially UV-Vis spectroscopy) and microscopic (in principal, electron microscopy-TEM) methods. The applications of the metal nanoparticles obtained are diverse and not completely known, but the medical applications of such nanoparticles occupy a central place, due to their nontoxic components, but some diverse industrial applications do not have to be forgotten.

  20. Green preparation and spectroscopic characterization of plasmonic silver nanoparticles using fruits as reducing agents

    DEFF Research Database (Denmark)

    Hyllested, Jes Ærøe; Espina Palanco, Marta; Hagen, Nicolai;

    2015-01-01

    microscopy shows that the shapes of the nanoparticles are different depending on the fruit used for preparation. The green preparation process results mainly in individual nanoparticles with a very poor tendency to form aggregates with narrow gaps even when aggregation is forced by the addition of Na......Cl. This explains only modest enhancement factors for near-infrared-excited surface enhanced Raman scattering. In addition to the surface plasmon band, UV-visible absorption spectra show features in the UV range which indicates also the presence of small silver clusters, such as Ag42+. The increase of the plasmon...... absorption correlates with the decrease of absorption band in the UV. This confirms the evolution of silver nanoparticles from silver clusters. The presence of various silver clusters on the surface of the “green” plasmonic silver nanoparticles is also supported by a strong multi-color luminesce signal...

  1. Nanoprecipitation versus two step desolvation technique for the preparation of gelatin nanoparticles

    Science.gov (United States)

    Khan, Saeed Ahmad; Schneider, Marc

    2013-02-01

    Various techniques have been used for preparation of gelatin nanoparticles, such as coacervation, emulsion/solvent evaporation, reverse phase preparation, inverse miniemulsion and two step desolvation. Both methods are based on different mechanisms of nanoparticle formation. The main goal of this study was to systematically compare the performance of nanoprecipitation and the most widely utilized two step desolvation methods with respect to effect of gelatin concentration on nanoparticle size and polydispersity index. Particles size was determined by dynamic light scattering, and the morphology by atomic force microscopy. It was observed that gelatin concentration 20 mg/ml yielded nanoparticles of around 60 nm size by two step desolvation, on the other hand nanoprecipitation produced 210 nm particles with the same gelatin concentration.

  2. Influence of PVP in magnetic properties of NiSn nanoparticles prepared by polyol method

    Energy Technology Data Exchange (ETDEWEB)

    Bobadilla, L.F., E-mail: lbobadilla@iciq.es [Departamento de Quimica Inorganica e Instituto de Ciencia de Materiales, Centro mixto Universidad de Sevilla-CSIC, Av. Americo Vespucio, 41092 Sevilla (Spain); Garcia, C. [Physics Department, Bogazici University, North Campus KB 331-O, Bebek/Istambul (Turkey); Delgado, J.J. [Departamento de Ciencia de los Materiales e Ingenieria Metalurgica y Quimica Inorganica, Facultad de Ciencias, Universidad de Cadiz, Campus Rio San Pedro, E-11510 Puerto Real, Cadiz (Spain); Sanz, O. [Grupo de Ingenieria Quimica, Departamento de Quimica Aplicada, Facultad de Ciencias Quimicas, UPV/EHU, Paseo Manuel de Lardizabal, 3, 20018 San Sebastian (Spain); Romero-Sarria, F.; Centeno, M.A.; Odriozola, J.A. [Departamento de Quimica Inorganica e Instituto de Ciencia de Materiales, Centro mixto Universidad de Sevilla-CSIC, Av. Americo Vespucio, 41092 Sevilla (Spain)

    2012-11-15

    The influence of PVP on the magnetic properties of NiSn nanoparticles prepared by polyol method has been studied. NiSn nanoparticles exhibit superparamagnetic behavior although there is a ferromagnetic contribution due to particles agglomerated below the blocking temperature. The particle size is controlled by the addiction of PVP in varying amounts. The addition of PVP also favours the particles isolation, narrow the particle size distribution and decrease the interparticle interaction strength increasing the superparamagnetic contribution. - Highlights: Black-Right-Pointing-Pointer Ni{sub x}Sn{sub y} alloys nanoparticles have been prepared by polyol method. Black-Right-Pointing-Pointer NiSn nanoparticles exhibit superparamagnetic behavior. Black-Right-Pointing-Pointer The PVP addition favours the particles isolation.

  3. Preparation of cobalt nanoparticles from polymorphic bacterial templates: A novel platform for biocatalysis.

    Science.gov (United States)

    Jang, Eunjin; Shim, Hyun-Woo; Ryu, Bum Han; An, Deu Rae; Yoo, Wan Ki; Kim, Kyeong Kyu; Kim, Dong-Wan; Kim, T Doohun

    2015-11-01

    Nanoparticles have gathered significant research attention as materials for enzyme immobilization due to their advantageous properties such as low diffusion rates, ease of manipulation, and large surface areas. Here, polymorphic cobalt nanoparticles of varied sizes and shapes were prepared using Micrococcus lylae, Bacillus subtilis, Escherichia coli, Paracoccus sp., and Haloarcula vallismortis as bacterial templates. Furthermore, nine lipases/carboxylesterases were successfully immobilized on these cobalt nanoparticles. Especially, immobilized forms of Est-Y29, LmH, and Sm23 were characterized in more detail for potential industrial applications. Immobilization of enzymes onto cobalt oxide nanoparticles prepared from polymorphic bacterial templates may have potential for efficient hydrolysis on an industrial-scale, with several advantages such as high retention of enzymatic activity, increased stability, and strong reusability.

  4. A Novel Preparation Method for 5-Aminosalicylic Acid Loaded Eudragit S100 Nanoparticles

    Directory of Open Access Journals (Sweden)

    Sining Li

    2012-05-01

    Full Text Available In this study, solution enhanced dispersion by supercritical fluids (SEDS technique was applied for the preparation of 5-aminosalicylic acid (5-ASA loaded Eudragit S100 (EU S100 nanoparticles. The effects of various process variables including pressure, temperature, 5-ASA concentration and solution flow rate on morphology, particle size, 5-ASA loading and entrapment efficiency of nanoparticles were investigated. Under the appropriate conditions, drug-loaded nanoparticles exhibited a spherical shape and small particle size with narrow particle size distribution. In addition, the nanoparticles prepared were characterized by X-ray diffraction, Differential scanning calorimetry and Fourier transform infrared spectroscopy analyses. The results showed that 5-ASA was imbedded into EU S100 in an amorphous state after SEDS processing and the SEDS process did not induce degradation of 5-ASA.

  5. Preparation of low-crystalline apatite nanoparticles and their coating onto quartz substrates.

    Science.gov (United States)

    Kawashita, Masakazu; Taninai, Koji; Li, Zhixia; Ishikawa, Kunio; Yoshida, Yasuhiro

    2012-06-01

    We prepared low-crystalline apatite nanoparticles and coated them onto a surface of a Au/Cr-plated quartz substrate by the electrophoretic deposition (EPD) method or by using a self-assembled monolayer of 11-mercaptoundecanoic acid (SAM method). Low-crystalline apatite nanoparticles around 10 nm in size with extremely low contents of undesirable residual products were obtained by adding (NH(4))(2)HPO(4) aqueous droplets into a modified synthetic body fluid solution that contained Ca(CH(3)COO)(2). The apatite nanoparticles were successfully coated by either the EPD method or the SAM method; the nanoparticle coating achieved by the SAM method was more uniform than that achieved by the EPD method. The present SAM method is expected to be a promising technique for obtaining a quartz substrate coated with apatite nanoparticles, which can be used as a quartz crystal microbalance device.

  6. Preparation and formation mechanism of Al2O3 nanoparticles by reverse microemulsion

    Institute of Scientific and Technical Information of China (English)

    HUANG Ke-long; YIN Liang-guo; LIU Su-qin; LI Chao-jian

    2007-01-01

    Al2O3 nanoparticles were prepared by polyethylene glycol octylphenyl ether(Triton X-100)/n-butyl alcohol/cyclohexane/ water W/O reverse microemulsion. The proper calcination temperature was determined at 1 150 ℃ by thermal analysis of the precursor products. The structures and morphologies of Al2O3 nanoparticles were characterized by X-ray diffraction, transmission electron microscopy and UV-Vis spectra. The influences of mole ratio of water to surfactant on the morphologies and the sizes of the Al2O3 nanoparticles were studied. With the increase of surfactant content, the particles size becomes larger. The agglomeration of nanoparticles was solved successfully. And the formation mechanisms of Al2O3 nanoparticles in the reverse microemulsion were also discussed.

  7. The preparation of highly active antimicrobial silver nanoparticles by an organometallic approach

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez, Eduardo J; Garcia-Barrasa, Jorge; Lopez-de-Luzuriaga, Jose M; Monge, Miguel [Departamento de Quimica Grupo de SIntesis Quimica de La Rioja, UA-CSIC, Universidad de La Rioja, Complejo CientIfico-Tecnologico, E-26004 Logrono (Spain); Laguna, Antonio [Departamento de Quimica Inorganica, Instituto de Ciencia de Materiales de Aragon, Universidad de Zaragoza-CSIC, E-50009 Zaragoza (Spain); Torres, Carmen [Departamento de Agricultura y Alimentacion, Universidad de La Rioja, Complejo Cientifico-Tecnologico, E-26004 Logrono (Spain)], E-mail: eduardo.fernandez@unirioja.es

    2008-05-07

    Silver nanoparticles of small size with a high surface to volume ratio have been prepared using an organometallic approach. For this, the complex NBu{sub 4}[Ag(C{sub 6}F{sub 5}){sub 2}] has been treated with AgClO{sub 4} in a 1:1 molar ratio, giving rise to the nanoparticle precursor [Ag(C{sub 6}F{sub 5})] in solution. Addition of one equivalent of hexadecylamine (HDA) and 5 h of reflux in toluene leads to a deep yellow solution containing monodisperse silver nanoparticles (Ag NPs) of ca. 10 nm. This approach leads to nanoparticles with almost uncontaminated surfaces which make them very reactive. Antimicrobial studies show that these nanoparticles are very active as antimicrobial agents. Very low concentrations between 12 and 25 {mu}g ml{sup -1} of Ag NPs are enough to produce bacteriostatic and bactericidal effectiveness.

  8. One-Step Method for Preparation of Magnetic Nanoparticles Coated with Chitosan

    Directory of Open Access Journals (Sweden)

    Karla M. Gregorio-Jauregui

    2012-01-01

    Full Text Available Preparation of magnetic nanoparticles coated with chitosan in one step by the coprecipitation method in the presence of different chitosan concentrations is reported here. Obtaining of magnetic superparamagnetic nanoparticles was confirmed by X-ray diffraction and magnetic measurements. Scanning transmission electron microscopy allowed to identify spheroidal nanoparticles with around 10-11 nm in average diameter. Characterization of the products by Fourier transform infrared spectroscopy demonstrated that composite chitosan-magnetic nanoparticles were obtained. Chitosan content in obtained nanocomposites was estimated by thermogravimetric analysis. The nanocomposites were tested in Pb2+ removal from a PbCl2 aqueous solution, showing a removal efficacy up to 53.6%. This work provides a simple method for chitosan-coated nanoparticles obtaining, which could be useful for heavy metal ions removal from water.

  9. CO Responses of Sensors Based on Cerium Oxide Thick Films Prepared from Clustered Spherical Nanoparticles

    OpenAIRE

    Woosuck Shin; Takafumi Akamatsu; Toshio Itoh; Ichiro Matsubara; Noriya Izu

    2013-01-01

    Various types of CO sensors based on cerium oxide (ceria) have been reported recently. It has also been reported that the response speed of CO sensors fabricated from porous ceria thick films comprising nanoparticles is extremely high. However, the response value of such sensors is not suitably high. In this study, we investigated methods of improving the response values of CO sensors based on ceria and prepared gas sensors from core-shell ceria polymer hybrid nanoparticles. These hybrid nano...

  10. Preparation and Self-assembly of Zirconia Nanoparticles via Hydrothermal Method

    Institute of Scientific and Technical Information of China (English)

    LI Guang-Hui; HONG Zhang-Lian; YANG Hui

    2008-01-01

    Zirconia nanoparticles were synthesized via hydrothermal method without any additives. This work focuses on the effect of preparation conditions such as the precursor preparation condition and crystallization time of nanocrystallite in autoclave on the properties of as-prepared products. The results indicated that the amount of tetragonal zirconia varied with the preparation conditions. It increased with the increase of the concentration of KOH solution in precursor producing process and reduced with the prolongation of crystallization time. At the same time, the particle size and morphology were also affected by the preparation conditions. In addition,the self-assembled spindle- like aggregates were observed in present works.

  11. Preparation of novel magnetic fluorescent nanoparticles using amino acids.

    Science.gov (United States)

    Ebrahiminezhad, Alireza; Ghasemi, Younes; Rasoul-Amini, Sara; Barar, Jaleh; Davaran, Soodabeh

    2013-02-01

    Nanotechnology has opened new gates to pharmaceutical sciences and medicine from the aspect of drug delivery and imaging systems. Currently, bimodal fluorescent-magnetic nanoparticles are of great interest to biomedical scientists. In order to constructing these kinds of nanoparticles, fluorescent molecules should be linked to a magnetic core, while luminescence quenching is prevented. In order to alleviate this effect, usually fluorescent molecules are attached to a magnetic core after a multistep hydrocarbon, polymer or silica coating, which significantly increases the particle's size and reduces its magnetic saturation value. In this study, for the first time, amino acids (L-lysine and L-arginine) have been used as a linker and spacer between a fluorescent molecule (FITC) and a magnetic nanoparticle (Fe(3)O(4)) in a simple, two-step synthesis. Also, 3-aminopropyltriethoxysilane (APTES) was used without any previous silica coating for fluorescent magnetic nanoparticles construction. Routinely APTES is used after silica coating by tetraethoxysilane (TEOS). Either of L-lysine, L-arginine and APTES coating provides surface functional groups which interact with the isothiocyanate group of FITC. According to the obtained results, amino acids could be used for successful construction of fluorescent magnetic nanoparticles in a simple synthesis pathway, without any significant impact on the excitation and emission properties of fluorescent molecule.

  12. Preparation, Physicochemical Characterization and Performance Evaluation of Gold Nanoparticles in Radiotherapy

    Directory of Open Access Journals (Sweden)

    Ali Kamiar

    2013-08-01

    Full Text Available Purpose: The aim of the present study was preparation, physicochemical characterization and performance evaluation of gold nanoparticles (GNPs in radiotherapy. Another objective was the investigation of anti-bacterial efficacy of gold nanoparticle against E. coli clinical strains. Methods: Gold nanoparticles prepared by controlled reduction of an aqueous HAuCl4 solution using Tri sodium citrate. Particle size analysis and Transmission electron microscopy were used for physicochemical characterization. Polymer gel dosimetry was used for evaluation of the enhancement of absorbed dose. Diffusion method in agar media was used for investigation of anti-bacterial effect. Results: Gold nanoparticles synthesized in size range from 57 nm to 346 nm by planning different formulation. Gold nanoparticle in 57 nm size increased radiation dose effectiveness with the magnitude of about 21 %. At the concentration of 400 ppm, Nano gold exhibited significant anti-bacterial effect against E. coli clinical strains. Conclusion: It is concluded that gold nanoparticles can be applied as dose enhancer in radiotherapy. The Investigation of anti-bacterial efficacy showed that gold nanoparticle had significant effect against E. coli clinical strains.

  13. Study on fluorouracil–chitosan nanoparticle preparation and its antitumor effect

    Directory of Open Access Journals (Sweden)

    Gaimin Chen

    2016-05-01

    Full Text Available To successfully prepare fluorouracil–chitosan nanoparticles, and further analyze its anti-tumor activity mechanism, this paper makes a comprehensive study of existing preparation prescription and makes a detailed analysis of fluorouracil–chitosan in vitro release and pharmacodynamic behavior of animals. Two-step synthesis method is adopted to prepare 5-FU–CS–mPEG prodrugs, and infrared, 1H NMR and differential thermal analysis are adopted to analyze characterization synthetic products of prepared drugs. To ensure clinical efficacy of prepared drugs, UV spectrophotometry is adopted for determination of drug loading capacity of prepared drugs, transmission electron microscopy is adopted to observe the appearance, dynamic dialysis method is used to observe in vitro drug release of prepared drugs and fitting of various release models is done. Anti-tumor effect is studied via level of animal pharmacodynamics. After the end of the experiment, tumor inhibition rate, spleen index and thymus index of drugs are calculated. Experimental results show that the prepared drugs are qualified in terms of regular shape, dispersion, drug content, etc. Animal pharmacodynamics experiments have shown that concentration level of drug loading capacity of prepared drugs has a direct impact on anti-tumor rate. The higher the concentration, the higher the anti-tumor rate. Results of pathological tissue sections of mice show that the prepared drugs cause varying degrees of damage to receptor cells, resulting in cell necrosis or apoptosis problem. It can thus be concluded that ion gel method is an effective method to prepare drug-loading nanoparticles, with prepared nanoparticles evenly distributed in regular shape which demonstrate good slow-release characteristics in receptor vitro and vivo. At the same time, after completion of drug preparation, relatively strong anti-tumor activity can be generated for the receptor, so this mode of preparation enjoys broad

  14. Synthesis and preparation of biocompatible and pH-responsive cyclodextrin-based nanoparticle

    Science.gov (United States)

    Hu, Xiaohong; Chen, Shangneng; Gong, Xiao; Gao, Ziyu; Wang, Xin; Chen, Pin

    2017-03-01

    As a temporarily protective reaction for active hydrogen group, acetylation is reversible and responsive to low pH value. According to the reaction, pH-sensitive β-cyclodextrin (β-CD) was synthesized in the first step of our research. During the synthesis, the acetal groups including linear acetal (LA) groups and cyclic acetal (CA) groups were successfully modified onto β-CD. Particularly, the structural details of acetalated β-CD (Ac-β-CD) were greatly influenced by reaction time. Furthermore, in respect to water solubility, Ac-β-CDs exhibited different pH response properties due to their different structure. In the second step, Ac-β-CD1 nanoparticles were prepared by a single oil-in-water (O/W) emulsion technique using a biocompatible emulsifier, gelatin. Meanwhile, gelatin was absorbed onto the surface of nanoparticle, which was confirmed by FTIR spectra. The formed nanoparticles showed monodispersion and nearly spherical morphology. In order to obtain optimal preparing conditions, the effects of preparative parameters such as gelatin concentration, Ac-β-CD concentration, and water/oil ratio on properties including diameters and zeta potential as well as gelatin content were investigated. Moreover, the pH response properties of nanoparticle were characterized by transparency of nanoparticle solution. Finally, in vitro cell culture confirmed that Ac-β-CD nanoparticle could support cell survival and enhance cell viability.

  15. Preparation and characterization of polymeric nanoparticles from Gadong starch

    Energy Technology Data Exchange (ETDEWEB)

    Sisika, Regina; Ahmad, Wan Yaacob Wan; Lazim, Azwan Mat [School of Chemical Sciences and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia 43600 Bangi, Selangor (Malaysia); Fazry, Shazrul [School of Biosciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia 43600 Bangi, Selangor (Malaysia)

    2015-09-25

    Dioscorea hispida (Gadong tuber) was seldom used and forgotten as a food source due to their toxicity. In contrast to that, the Gadong tuber can be a source of polysaccharides which can be manipulated as an alternative source for industrial applications. This research reported on how to synthesize starch nanoparticles from Gadong tuber by using a simple acid hydrolysis process. The yield of starch nanoparticles obtained from seven days of acid hydrolysis was reduced to 13%. The X-ray diffraction measurements showed that the native Gadong starch particle is of the C-crystalline type, and that the synthesized nanoparticles showed an increase in crystallinity compared to the native particles. Transmission electron microscopy results demonstrated that the starch particle morphologies were either round or irregular shape, with diameters ranging from 96-110 nm.

  16. Preparation and characterization of polymeric nanoparticles from Gadong starch

    Science.gov (United States)

    Sisika, Regina; Ahmad, Wan Yaacob Wan; Fazry, Shazrul; Lazim, Azwan Mat

    2015-09-01

    Dioscorea hispida (Gadong tuber) was seldom used and forgotten as a food source due to their toxicity. In contrast to that, the Gadong tuber can be a source of polysaccharides which can be manipulated as an alternative source for industrial applications. This research reported on how to synthesize starch nanoparticles from Gadong tuber by using a simple acid hydrolysis process. The yield of starch nanoparticles obtained from seven days of acid hydrolysis was reduced to 13%. The X-ray diffraction measurements showed that the native Gadong starch particle is of the C-crystalline type, and that the synthesized nanoparticles showed an increase in crystallinity compared to the native particles. Transmission electron microscopy results demonstrated that the starch particle morphologies were either round or irregular shape, with diameters ranging from 96-110 nm.

  17. Effect of Preparation Methods of Bi2O3 Nanoparticles on their Photocatalytic Activity

    Institute of Scientific and Technical Information of China (English)

    DING Peng; DU Yao-guo; XU Zi-li

    2004-01-01

    Bi2O3 nanoparticles were prepared by means of ammonia precipitation, polyol mediated methods and microemulsion chemical method. The structure and properties of the as-prepared nanoparticles, having been submitted to a heat-treatment test at 750 ℃, were characterized by means of XRD, BET, XPS and UV-Vis absorption techniques. The photocatalytic oxidation reactions of benzene, toluene and xylene were used as the model reaction to measure the photocatalytic activity of Bi2O3 nanoparticles, respectively. The results show that the crystallite size of Bi2O3 prepared with different methods and calcined at 750 ℃ were 50.6, 38.5 and 31.5 nm, respectively. The photocatalytic activity of Bi2O3 nanoparticles prepared with the microemulsion chemical method was higher than that of the particles prepared with the polyol mediated method; and that of the particles prepared with the micromulsion chemical method was the highest among the three. The degradation rates of the three pollutants xylene, toluene and benzene decreased in sequence.

  18. Photodynamic therapy using upconversion nanoparticles prepared by laser ablation in liquid

    Energy Technology Data Exchange (ETDEWEB)

    Ikehata, Tomohiro; Onodera, Yuji; Nunokawa, Takashi [Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8502 (Japan); Hirano, Tomohisa; Ogura, Shun-ichiro; Kamachi, Toshiaki [Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8502 (Japan); Odawara, Osamu [Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8502 (Japan); Wada, Hiroyuki, E-mail: wada.h.ac@m.titech.ac.jp [Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8502 (Japan)

    2015-09-01

    Highlights: • Highly crystalline upconversion nanoparticles were prepared by laser ablation in liquid. • Highly transparent near-IR irradiation generated singlet oxygen. • Viability of cancer cells was significantly decreased by near-IR irradiation. - Abstract: Upconversion nanoparticles were prepared by laser ablation in liquid, and the potential use of the nanoparticles for cancer treatment was investigated. A Nd:YAG/SHG laser (532 nm, 13 ns, 10 Hz) was used for ablation, and the cancer treatment studied was photodynamic therapy (PDT). Morphology and crystallinity of prepared nanoparticles were examined by transmission electron microscopy and X-ray diffraction. Red and green emissions resulting from near-infrared excitation were observed by a fluorescence spectrophotometer. Generation of singlet oxygen was confirmed by a photochemical method using 1,3-diphenylisobenzofuran (DPBF). In vitro experiments using cultivated cancer cells were conducted to investigate PDT effects. Uptake of the photosensitizer by cancer cells and cytotoxicities of cancer cells were also examined. We conclude that the combination of PDT and highly crystalline nanoparticles, which were prepared by laser ablation in liquid, is an effective cancer treatment.

  19. Preparation and characterization of chitosan/β-cyclodextrin nanoparticles containing plasmid DNA encoding interleukin-12.

    Science.gov (United States)

    Nahaei, M; Valizadeh, H; Baradaran, B; Nahaei, M R; Asgari, D; Hallaj-Nezhadi, S; Dastmalchi, S; Lotfipour, F

    2013-01-01

    Interleukin-12 (IL-12) as a cytokine has been proved to possess antitumor effects via stimulating the immune system. Non-viral gene delivery systems offer several advantages, including easiness in production, low cost, safety; low immunogenicity and can carry higher amounts of genetic material without limitation on their sizes.pUMVC3-hIL12 loaded Low Molecular Weight chitosan/β-cyclodextrin (LMW CS/CD) nanoparticles were prepared using ionotropic gelation method and characterized in terms of size, zeta potential, polydispersity index, morphology, loading efficiency and cytotoxicity against the CT-26 colon carcinoma cell line.All prepared particles were spherical in shape and nano-sized (171.3±2.165 nm, PdI: 0.231±0.014) and exhibited a positive zeta potential (34.3±1.55). The nanoparticles demonstrated good DNA encapsulation efficiencies (83.315%±2.067). Prepared pUMVC3-hIL12 loaded LMW CS/CD nanoparticles showed no cell toxicity in murine CT-26 colon carcinoma cells. At the concentration of 0.1 µg/ml of nanoparticles, the transfection ability was obviously higher than that of the naked DNA.LMW CS/CD-plasmid DNA nanoparticles encoding IL-12 prepared using ionotropic gelation method with no toxic effect on the tested cells can be considered as a basis for further gene delivery studies both in vitro and in vivo to enhance the expression of IL-12.

  20. Streptomycin-loaded PLGA-alginate nanoparticles: preparation, characterization, and assessment

    Science.gov (United States)

    Asadi, Asadollah

    2014-04-01

    The aim of this study was to formulate and characterize streptomycin-loaded PLGA-alginate nanoparticles for their potential therapeutic use in Salmonella subsp. enterica ATCC 14028 infections. The streptomycin nanoparticle was prepared by solvent diffusion method, and the other properties such as size, zeta potential, loading efficacy, release kinetics, and antimicrobial strength were evaluated. The survey shows that nanoparticles may serve as a carrier of streptomycin and may provide localized antibacterial activity in the treatment of Salmonellosis. Electron microscopy showed spherical particles with indentations. The average size of the nanoparticles was 90 nm. At pH 7.2, the release kinetics of streptomycin from the nanoparticles was successfully illustrated as an initial burst defined by a first order equation that after this stage, it has a drastic tendency to obtain steady state. Nevertheless, nanoparticles showed loading efficacy nearly about 70-75 %. In addition, the tendency of concentration of streptomycin released from nanoparticles to reach antibacterial activity was similar to that of free streptomycin against PLGA-alginate, but it had threefold more antimicrobial strength in comparison with free streptomycin. This work shows the potential use of streptomycin-loaded PLGA-alginate nanoparticles and its capability.

  1. Preparation of Gold Nanoparticles Using Tea: A Green Chemistry Experiment

    Science.gov (United States)

    Sharma, R. K.; Gulati, Shikha; Mehta, Shilpa

    2012-01-01

    Assimilating green chemistry principles in nanotechnology is a developing area of nanoscience research nowadays. Thus, there is a growing demand to develop environmentally friendly and sustainable methods for the synthesis of nanoparticles that utilize nontoxic chemicals, environmentally benign solvents, and renewable materials to avoid their…

  2. Lamellar metal-organic complex and its rod-like nanoparticles prepared with ultrasonic technique

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Metal-organic complex (H3NCH2CH2NH2)3[MoO2(OC6H4O)2] with a lamellar morphology has been syn- thesized. Its crystal structure was confirmed by single-crystal X-ray diffraction. The morphology of the crystal was observed by scanning electron microscopy (SEM). The metal-organic nanoparticles have been prepared by using an ultrasonic method. The morphology of the as-prepared nanoparticles was observed by transmission electron microscopy (TEM). The possible formation mechanism has also been proposed.

  3. Preparation of niobium nanoparticles by sodiothermic reduction of Nb_2O_5 in molten salts

    Institute of Scientific and Technical Information of China (English)

    2012-01-01

    Niobium nanoparticles with high purity were prepared by a sodiothermic reduction process using Nb2O5 as the raw material, LiCl, NaCl, KCl and CaCl2 as the diluents and sodium as the reducing reagent. The effects of the different molten salt systems, CaCl2 content, reaction time, excessive sodium and reaction temperature on the characteristics of the obtained niobium powder were discussed. The as-prepared niobium nanoparticles under the optimum experimental conditions were obtained by sodiothermic reduction ...

  4. Preparation and characterization of curcumin-piperine dual drug loaded nanoparticles

    Institute of Scientific and Technical Information of China (English)

    C Moorthi; Kiran Krishnan; R Manavalan; K Kathiresan

    2012-01-01

    Objective: To prepare curcumin-piperine (Cu-Pi) nanoparticles by various methods and to study the effect of various manufacturing parameters on Cu-Pi nanoparticles and to identify a suitable method for the preparation of Cu-Pi nanoparticles to overcome oral bioavailability and cancer cell targeting limitations in the treatment of cancer. Methods: Cu-Pi nanoparticles were prepared by thin film hydration method, solid dispersion method, emulsion polymerization method and Fessi method. Optimization was carried out to study the effect of various manufacturing parameter on the Cu-Pi nanoparticles. Results: Out of four methods, Fessi method produced a minimum average particle size of 85.43 nm with a polydispersity index of 0.183 and zeta potential of 29.7 mV. Change of organic solvent (acetone or ethanol) did not have any significant effect on Cu-Pi nanoparticles. However, increase in sonication time, stirring speed, viscosity, use of 1:10:10 ratio of drug/polymer/surfactant, and use of anionic surfactant or combination of anionic surfactant with cationic polymer or combination of non-ionic surfactant with cationic polymer had a significant effect on Cu-Pi nanoparticles. Conclusions: Cu-Pi nanoparticles coated with PEG containing copolymer produced by Fessi method had a minimum average particle size, excellent polydispersity index and optimal zeta potential which fall within the acceptable limits of the study. This dual nanoparticulate drug delivery system appears to be promising to overcome oral bioavailability and cancer cell targeting limitations in the treatment of cancer.

  5. Enhanced bioavailability of sirolimus via preparation of solid dispersion nanoparticles using a supercritical antisolvent process

    Directory of Open Access Journals (Sweden)

    Kim MS

    2011-11-01

    Full Text Available Min-Soo Kim1, Jeong-Soo Kim1, Hee Jun Park1, Won Kyung Cho1,3, Kwang-Ho Cha1,3, Sung-Joo Hwang2,31College of Pharmacy, Chungnam National University, Daejeon, Republic of Korea, 2College of Pharmacy, 3Yonsei Institute of Pharmaceutical Sciences, Yonsei University, Incheon, Republic of KoreaBackground: The aim of this study was to improve the physicochemical properties and bioavailability of poorly water-soluble sirolimus via preparation of a solid dispersion of nanoparticles using a supercritical antisolvent (SAS process.Methods: First, excipients for enhancing the stability and solubility of sirolimus were screened. Second, using the SAS process, solid dispersions of sirolimus-polyvinylpyrrolidone (PVP K30 nanoparticles were prepared with or without surfactants such as sodium lauryl sulfate (SLS, tocopheryl propylene glycol succinate, Sucroester 15, Gelucire 50/13, and Myrj 52. A mean particle size of approximately 250 nm was obtained for PVP K30-sirolimus nanoparticles. Solid state characterization, kinetic solubility, powder dissolution, stability, and pharmacokinetics were analyzed in rats.Results: X-ray diffraction, differential scanning calorimetry, and high-pressure liquid chromatography indicated that sirolimus existed in an anhydrous amorphous form within a solid dispersion of nanoparticles and that no degradation occurred after SAS processing. The improved supersaturation and dissolution of sirolimus as a solid dispersion of nanoparticles appeared to be well correlated with enhanced bioavailability of oral sirolimus in rats. With oral administration of a solid dispersion of PVP K30-SLS-sirolimus nanoparticles, the peak concentration and AUC0→12h of sirolimus were increased by approximately 18.3-fold and 15.2-fold, respectively.Conclusion: The results of this study suggest that preparation of PVP K30-sirolimus-surfactant nanoparticles using the SAS process may be a promising approach for improving the bioavailability of sirolimus

  6. Preparation of PLA and PLGA nanoparticles by binary organic solvent diffusion method

    Institute of Scientific and Technical Information of China (English)

    蒋新宇; 周春山; 唐课文

    2003-01-01

    The nanoparticles of polylactide (PLA) and poly(lactide-co-glycolide) (PLGA) were prepared by the bi-nary organic solvent diffusion method. The yield, particle size and size distribution of these nanoparticles wereevaluated. The yield of nanoparticles prepared by this method is over 90%, and the average size of the nanoparticlesis between 130-180 nm. In order to clarify the effect of the organic solvent used in the system on nanoparticle yieldand size, the cloud points of PLA and PLGA were examined by cloud point titration. The results indicate that theyields of nanoparticles increase with the increase of ethanol in the acetone solution and attain the maximum at thecloud point of ethanol, while the size of nanoparticles decreases with the increase of ethanol in the acetone solutionand attains the minimum at the cloud point of ethanol. The optimal composition ratio of binary organic solvents coin-cides to that near the cloud point and the optimal condition of binary organic solvents can be predicted.

  7. Physical and Chemical Transformation of Hydroxyapatite Nanoparticles in Aqueous Sol after Preparation and in vitro

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    The co-precipitation method followed by ultrasound and heat treatment is a common way to prepare below 100 nm sized hydroxyapatite nanoparticles for biomedical studies and applications. The size and pH value of the obtained calcium phosphate nanoparticles in aqueous sol have a strong impact on the interactions with cells and tissue. The physical and chemical properties of material samples for in vitro and in vivo studies are often assumed to remain constant from the time after fabrication to the actual use. Only little attention is paid to eventual changes of the material over time or due to the different in vitro conditions. In this study, the physical and chemical transformation of calcium phosphate nanoparticles after preparation and in vitro was investigated. As the result showed, dispersed nano sized amorphous calcium phosphate precipitation as well as crystallized hydroxyapatite nanoparticles continue to crystallize even when kept at 4 ℃ leading to declining pH values and particle sizes.Due to the pH buffer in the medium the pH value of the cell culture remained stable after adding 20% nanoparticle sol in vitro. However, hydroxyapatite nanoparticles immediately became unstable in the presents of cell culture medium. The resulting loose agglomerations showed a size of above 500 nm.

  8. Biophysical inhibition of synthetic vs. naturally-derived pulmonary surfactant preparations by polymeric nanoparticles.

    Science.gov (United States)

    Beck-Broichsitter, Moritz; Ruppert, Clemens; Schmehl, Thomas; Günther, Andreas; Seeger, Werner

    2014-01-01

    Reasonable suspicion has accumulated that inhaled nano-scale particulate matter influences the biophysical function of the pulmonary surfactant system. Hence, it is evident to provide novel insights into the extent and mechanisms of nanoparticle-surfactant interactions in order to facilitate the fabrication of safe nanomedicines suitable for pulmonary applications. Negatively- and positively-charged poly(styrene) nanoparticles (diameters of ~100nm) served as model carriers. Nanoparticles were incubated with several synthetic and naturally-derived pulmonary surfactants to characterize the sensitivity of each preparation to biophysical inactivation. Changes in surface properties (i.e. adsorption and dynamic surface tension behavior) were monitored in a pulsating bubble surfactometer. Both nanoparticle formulations revealed a dose-dependent influence on the biophysical behavior of all investigated pulmonary surfactants. However, the surfactant sensitivity towards inhibition depended on both the carrier type, where negatively-charged nanoparticles showed increased inactivation potency compared to their positively-charged counterparts, and surfactant composition. Among the surfactants tested, synthetic mixtures (i.e. phospholipids, phospholipids supplemented with surfactant protein B, and Venticute®) were more susceptible to surface-activity inhibition as the more complex naturally-derived preparations (i.e. Alveofact® and large surfactant aggregates isolated from rabbit bronchoalveolar lavage fluid). Overall, nanoparticle characteristics and surfactant constitution both influence the extent of biophysical inhibition of pulmonary surfactants.

  9. Preparation and Evaluation of Contact Lenses Embedded with Polycaprolactone-Based Nanoparticles for Ocular Drug Delivery.

    Science.gov (United States)

    Nasr, Farzaneh Hashemi; Khoee, Sepideh; Dehghan, Mohammad Mehdi; Chaleshtori, Sirous Sadeghian; Shafiee, Abbas

    2016-02-08

    To improve the efficiency of topical ocular drug administration, we focused on development of a nanoparticles loaded contact lens to deliver the hydrophobic drug over a prolonged period of time. The cross-linked nanoparticles based on PCL (poly ε-caprolactone), 2-hydroxy ethyl methacrylate (HEMA), and poly ethylene glycol diacrylate (PEG-DA) were prepared by surfactant-free miniemulsion polymerization. The lens material was prepared through photopolymerization of HEMA and N-vinylpyrrolidone (NVP) using PEG-DA as the cross-linker. Effects of nanoparticles loading on critical contact lens properties such as transparency, water content, modulus and ion and oxygen permeabilities were studied. Nanoparticles and hydrogel showed high viability, indicating the absence of cytotoxicity and stimulatory effect. Drug release studies revealed that the hydrogel embedded with nanoparticles released the drug for a period of 12 days. The results of this study provide evidence that nanoparticles loaded hydrogels could be used for extended delivery of loteprednol etabonate and perhaps other drugs.

  10. Scalable manufacturing of biomimetic moldable hydrogels for industrial applications

    Science.gov (United States)

    Yu, Anthony C.; Chen, Haoxuan; Chan, Doreen; Agmon, Gillie; Stapleton, Lyndsay M.; Sevit, Alex M.; Tibbitt, Mark W.; Acosta, Jesse D.; Zhang, Tony; Franzia, Paul W.; Langer, Robert; Appel, Eric A.

    2016-12-01

    Hydrogels are a class of soft material that is exploited in many, often completely disparate, industrial applications, on account of their unique and tunable properties. Advances in soft material design are yielding next-generation moldable hydrogels that address engineering criteria in several industrial settings such as complex viscosity modifiers, hydraulic or injection fluids, and sprayable carriers. Industrial implementation of these viscoelastic materials requires extreme volumes of material, upwards of several hundred million gallons per year. Here, we demonstrate a paradigm for the scalable fabrication of self-assembled moldable hydrogels using rationally engineered, biomimetic polymer–nanoparticle interactions. Cellulose derivatives are linked together by selective adsorption to silica nanoparticles via dynamic and multivalent interactions. We show that the self-assembly process for gel formation is easily scaled in a linear fashion from 0.5 mL to over 15 L without alteration of the mechanical properties of the resultant materials. The facile and scalable preparation of these materials leveraging self-assembly of inexpensive, renewable, and environmentally benign starting materials, coupled with the tunability of their properties, make them amenable to a range of industrial applications. In particular, we demonstrate their utility as injectable materials for pipeline maintenance and product recovery in industrial food manufacturing as well as their use as sprayable carriers for robust application of fire retardants in preventing wildland fires.

  11. Preparation and Characterization of Cationic PLA-PEG Nanoparticles for Delivery of Plasmid DNA

    Directory of Open Access Journals (Sweden)

    Zou Weiwei

    2009-01-01

    Full Text Available Abstract The purpose of the present work was to formulate and evaluate cationic poly(lactic acid-poly(ethylene glycol (PLA-PEG nanoparticles as novel non-viral gene delivery nano-device. Cationic PLA-PEG nanoparticles were prepared by nanoprecipitation method. The gene loaded nanoparticles were obtained by incubating the report gene pEGFP with cationic PLA-PEG nanoparticles. The physicochemical properties (e.g., morphology, particle size, surface charge, DNA binding efficiency and biological properties (e.g., integrity of the released DNA, protection from nuclease degradation, plasma stability, in vitro cytotoxicity, and in vitro transfection ability in Hela cells of the gene loaded PLA-PEG nanoparticles were evaluated, respectively. The obtained cationic PLA-PEG nanoparticles and gene loaded nanoparticles were both spherical in shape with average particle size of 89.7 and 128.9 nm, polydispersity index of 0.185 and 0.161, zeta potentials of +28.9 and +16.8 mV, respectively. The obtained cationic PLA-PEG nanoparticles with high binding efficiency (>95% could protect the loaded DNA from the degradation by nuclease and plasma. The nanoparticles displayed sustained-release properties in vitro and the released DNA maintained its structural and functional integrity. It also showed lower cytotoxicity than Lipofectamine 2000 and could successfully transfect gene into Hela cells even in presence of serum. It could be concluded that the established gene loaded cationic PLA-PEG nanoparticles with excellent properties were promising non-viral nano-device, which had potential to make cancer gene therapy achievable.

  12. Preparation and Characterization of Cationic PLA-PEG Nanoparticles for Delivery of Plasmid DNA

    Science.gov (United States)

    Zou, Weiwei; Liu, Chunxi; Chen, Zhijin; Zhang, Na

    2009-09-01

    The purpose of the present work was to formulate and evaluate cationic poly(lactic acid)-poly(ethylene glycol) (PLA-PEG) nanoparticles as novel non-viral gene delivery nano-device. Cationic PLA-PEG nanoparticles were prepared by nanoprecipitation method. The gene loaded nanoparticles were obtained by incubating the report gene pEGFP with cationic PLA-PEG nanoparticles. The physicochemical properties (e.g., morphology, particle size, surface charge, DNA binding efficiency) and biological properties (e.g., integrity of the released DNA, protection from nuclease degradation, plasma stability, in vitro cytotoxicity, and in vitro transfection ability in Hela cells) of the gene loaded PLA-PEG nanoparticles were evaluated, respectively. The obtained cationic PLA-PEG nanoparticles and gene loaded nanoparticles were both spherical in shape with average particle size of 89.7 and 128.9 nm, polydispersity index of 0.185 and 0.161, zeta potentials of +28.9 and +16.8 mV, respectively. The obtained cationic PLA-PEG nanoparticles with high binding efficiency (>95%) could protect the loaded DNA from the degradation by nuclease and plasma. The nanoparticles displayed sustained-release properties in vitro and the released DNA maintained its structural and functional integrity. It also showed lower cytotoxicity than Lipofectamine 2000 and could successfully transfect gene into Hela cells even in presence of serum. It could be concluded that the established gene loaded cationic PLA-PEG nanoparticles with excellent properties were promising non-viral nano-device, which had potential to make cancer gene therapy achievable.

  13. Preparation and characterization of functional silica hybrid magnetic nanoparticles

    Science.gov (United States)

    Digigow, Reinaldo G.; Dechézelles, Jean-François; Dietsch, Hervé; Geissbühler, Isabelle; Vanhecke, Dimitri; Geers, Christoph; Hirt, Ann M.; Rothen-Rutishauser, Barbara; Petri-Fink, Alke

    2014-08-01

    We report on the synthesis and characterization of functional silica hybrid magnetic nanoparticles (SHMNPs). The co-condensation of 3-aminopropyltriethoxysilane (APTES) and tetraethyl orthosilicate (TEOS) in presence of superparamagnetic iron oxide nanoparticles (SPIONs) leads to hybrid magnetic silica particles that are surface-functionalized with primary amino groups. In this work, a comprehensive synthetic study is carried out and completed by a detailed characterization of hybrid particles' size and morphology, surface properties, and magnetic responses using different techniques. Depending on the mass ratio of SPIONs and the two silanes (TEOS and APTES), we were able to adjust the number of surface amino groups and tune the magnetic properties of the superparamagnetic hybrid particles.

  14. Porous silicon nanoparticles for nanomedicine: preparation and biomedical applications.

    Science.gov (United States)

    Santos, Hélder A; Mäkilä, Ermei; Airaksinen, Anu J; Bimbo, Luis M; Hirvonen, Jouni

    2014-04-01

    The research on porous silicon (PSi) materials for biomedical applications has expanded greatly since the early studies of Leigh Canham more than 25 years ago. Currently, PSi nanoparticles are receiving growing attention from the scientific biomedical community. These nanostructured materials have emerged as promising multifunctional and versatile platforms for nanomedicine in drug delivery, diagnostics and therapy. The outstanding properties of PSi, including excellent in vivo biocompatibility and biodegradability, have led to many applications of PSi for delivery of therapeutic agents. In this review, we highlight current advances and recent efforts on PSi nanoparticles regarding the production properties, efficient drug delivery, multidrug delivery, permeation across biological barriers, biosafety and in vivo tracking for biomedical applications. The constant boost on successful preclinical in vivo data reported so far makes this the 'golden age' for PSi, which is expected to finally be translated into the clinic in the near future.

  15. Epigallocatechin-3-gallate-capped Ag nanoparticles: preparation and characterization.

    Science.gov (United States)

    Hussain, Shokit; Khan, Zaheer

    2014-07-01

    We used an aqueous leaf extract of Camellia sinensis to synthesize Ag nanoparticles (AgNPs). A layer of ca. 6 nm around a group of the AgNPs in which the inner layer is bound to the AgNPs surface via the hydroxyl groups of catechin has been observed. TEM analysis of AgNPs showed the formation of truncated triangular nanoplates and/or nanodisks and spherical with some irregular-shaped polydispersed nanoparticles in absence and presence of shape-directing cetyltrimethylammonium bromide. The polyphenolic groups of epigallocatechin-3-gallate (EGCG) are responsible for the rapid reduction of Ag(+) ions into metallic Ag(0). The free -OH groups are able to stabilize AgNPs by the interaction between the surface Ag atoms of AgNPs and oxygen atoms of EGCG molecules.

  16. Preparation and characteristics of DNA-nanoparticles targeting to hepatocarcinoma cells

    Institute of Scientific and Technical Information of China (English)

    Qin He; Ji Liu; Xun Sun; Zhi-Rong Zhang

    2004-01-01

    AIM: To prepare thymidine kinase gene (TK gene) nanopartuckes and to investigate the expression of TK gene.METHODS: Poly(D,L-lactic-co-glycolic acid) (PLGA), a biodegradable and biocompatible polymer, was used to prepare recombinant plasmid pEGFP-AFP nanoparticles by a double-emulsion evaporation technique. Characteristics of the nanoparticles were investigated in this study, including morphology, entrapment efficiency, and tissue distribution.The expression of TK gene was also investigated by MTT assay, by which the viable cells were determined after the addition of ganciclovir (GCV). The enhanced green fluorescent protein (EGFP) expression in human hepatocellular carcinoma 5MMC-7721 cells and normal parenchymal Chang liver cells were assessed by flow cytometry.RESUITS: The prepared plasmid-nanoparticles had regular spherical surface and narrow particle size span with a mean diameter of 72±12 nm. The mean entrapment efficiency was 91.25%. A total of 80.14% DNA was found to be localized in the livers after 1-h injection with 32P-DNA-PLGA nanoparticles in mouse caudal vein. The expression of DNA encapsulated in nanopartides was much higher than that in naked DNA, and human hepatocellular carcinoma SMMC7721 cells were more sensitive to GCV than human normal parenchymal Chang liver cells.CONCLUSION: The enhanced transfection efficiency and stronger ability to protect plasmid DNA from being degraded by nucleases are due to nanoparticles encapsulation.

  17. Preparation of anatase/rutile mixed-phase titania nanoparticles for dye-sensitized solar cells.

    Science.gov (United States)

    Hwang, Yong-Kyung; Park, Sung Soo; Lim, Jun-Heok; Won, Yong Sun; Huh, Seong

    2013-03-01

    Acid-labile high surface mesoporous ZnO/Zn(OH)2 composite material is used as a novel hard template for the preparation of mesoporous amorphous TiO2. The template-free amorphous TiO2 material is then thermally crystallized at suitable temperature to control the relative ratio of anatase and rutile phases in a particle. Four different anatase/rutile (AR) mixed-phase TiO2 nanoparticles (AR-3, AR-15, AR-20, and AR-23 denoted for the samples of 3%, 15%, 20%, and 23% rutile phase, respectively) are prepared and characterized by powder X-ray diffraction (PXRD) and transmission electron microscopy (TEM). The coexistence of anatase and rutile phases in a TiO2 nanoparticle is visually confirmed by HRTEM analysis. These mixed-phase TiO2 nanoparticles are examined as candidates for photoelectrodes of dye-sensitized solar cells (DSSCs). The J-V curves and IPCE spectra for the DSSCs prepared from the mixed-phase TiO2 nanoparticles are obtained, and their photovoltaic properties are investigated. The photo-conversion efficiency (eta) indicates the highest value of 5.07% for AR-20. The synergistic effect of coexisting anatase and rutile phases with an optimal ratio in a TiO2 nanoparticle of AR-20 for an efficient interfacial transfer of photo-generated electrons is likely to lead to the highest efficiency among the AR-n samples.

  18. Preparation and characterization of Ce-doped HfO{sub 2} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Gálvez-Barboza, S. [Centro de Investigación en Química Aplicada, Departamento de Materiales Avanzados, Blvd. Enrique Reyna Hermosillo #140, C.P. 25294 Saltillo, Coahuila (Mexico); Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Av. Industria Metalúrgica # 1062 Parque Industrial, C.P. 25900 Ramos Arizpe, Coahuila (Mexico); González, L.A. [Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Av. Industria Metalúrgica # 1062 Parque Industrial, C.P. 25900 Ramos Arizpe, Coahuila (Mexico); Puente-Urbina, B.A.; Saucedo-Salazar, E.M. [Centro de Investigación en Química Aplicada, Departamento de Materiales Avanzados, Blvd. Enrique Reyna Hermosillo #140, C.P. 25294 Saltillo, Coahuila (Mexico); García-Cerda, L.A., E-mail: luis.garcia@ciqa.edu.mx [Centro de Investigación en Química Aplicada, Departamento de Materiales Avanzados, Blvd. Enrique Reyna Hermosillo #140, C.P. 25294 Saltillo, Coahuila (Mexico)

    2015-09-15

    Highlights: • Ce-doped HfO{sub 2} nanoparticles were prepared by a modified solgel method. • Ce-doped HfO{sub 2} nanoparticles have a semispherical shape with sizes between 6 and 11.5 nm. • The samples doped with 10% in weight of Ce directly crystallized in a cubic structure. • A quick, straightforward and effective route for the preparation of Ce-doped nanoparticles. - Abstract: A modified solgel method to synthesize Ce-doped HfO{sub 2} nanoparticles was carried out using a precursor material prepared with cerium nitrate, hafnium chloride, citric acid and ethylene glycol. The obtained precursor material was calcined at 500 and 700 °C for 2 h in air. The influence of the concentration of Ce and the calcination temperature was studied to observe the structural and morphological changes of the obtained materials. For the characterization, X-ray diffraction (XRD), transmission electron microscopy (TEM) and Raman scattering (RS) were employed. The XRD patterns shown that the Ce-doped HfO{sub 2} undergoes a structural transformation from monoclinic to cubic phase, which is significantly dependent on the Ce content and calcination temperature. TEM images have also confirmed the existence of semispherical nanoparticles with sizes between 6 and 11.5 nm.

  19. Preparation and immobilization of noble metal nanoparticles for plasmonic solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Ruoli; Pitzer, Martin; Hu, DongZhi; Schaadt, Daniel M. [Institut fuer Angewandte Physik, Karlsruher Institut fuer Technologie (KIT), Karlsruhe (Germany); DFG Centrum fuer Funktionelle Nanostrukturen (CFN), KIT (Germany); Fruk, Ljiljana [DFG Centrum fuer Funktionelle Nanostrukturen (CFN), KIT (Germany)

    2011-07-01

    Thin-film solar cells are of high interest due to good electrical properties and low material consumption. Traditional thin-film cells, however, have considerable transmission losses because of the reduced absorption volume. A promising way to enhance absorption in the active layer is the light-trapping by plasmonic nanostructures. Metallic nanoparticles have in particular shown large enhancement of the photocurrent in thin-film devices. In this poster, we present preparation of Au,Ag and Pt nanoparticles by polyol method and seed mediated methods for use in plasmonic solar cells. Polyol method typically uses ethylene glycol as the solvent and reducing agent,and in seed-mediated synthesis small nanoparticle seeds are first prepared and then used to promote the growth of different shapes of nanoparticles. We particularly focus on the use of nanocubes and nanospheres for solar cell design. Following the nanoparticle preparation, a new method to immobilize particles on GaAs surfaces via covalent chemical bonds has been developed which prevents agglomerations and allows control of the surface density. Photocurrent spectra of GaAs pin solar cells with and without particles have been recorded. These measurements show the dependence of the photocurrent enhancement on particle material, shape and density.

  20. Preparation of PbSe nanoparticles by electron beam irradiation method

    Indian Academy of Sciences (India)

    Zhen Li; Chao Wu; Yanyan Liu; Tiebing Liu; Zheng Jiao; Minghong Wu

    2008-11-01

    A novel method has been developed by electron beam irradiation to prepare PbSe nanoparticles. 2 MeV 10mA GJ-2-II electronic accelerator was used as radiation source. Nanocrystalline PbSe was prepared rapidly at room temperature under atmospheric pressure without any kind of toxic reagents. The structure and morphology of prepared PbSe nanoparticles were analysed by X-ray diffraction, transmission electron microscope and atomic force microscope. The results indicated that the obtained materials were cubic nanocrystalline PbSe with an average grain size of 30 nm. The optical properties of prepared PbSe nanocrystalline were characterized by using photoluminescence spectroscopy. The possible mechanism of the PbSe grain growth by electron beam irradiation method is proposed.

  1. Preparation of silver nanoparticle via active template under ultrasonic

    Institute of Scientific and Technical Information of China (English)

    ZHENG Min; WANG Zuo-shan; ZHU Ya-wei

    2006-01-01

    A novel method was described for the production of silver nanoparticle by using nano-carbon as active template. Special ultrasonic condition was used to assure the active effect of the template and achieve an even and stable micro-reactor system,therefore yield uniform silver nanoparticle without obvious agglomeration. By laser granularity instrument measurement, the silver nanoparticles show a mean diameter of 20.4 nm and narrow distribution between 18.7 nm and 23.0 nm according to the optimum technology. Regular spherical morphology can be observed by transmission electron microscopy(TEM). X-ray diffraction analysis indicates that Ag+ is deoxidized to form metal Ag during producing precursor, subsequent calcinations promote phase transformation from nonholonomic crystal to complete cubic crystal, which is consistent with the standard JCPDS card of silver. The results reveal that the nano-carbon in active template system not only exerts micro-reactor and steric stabilization effect, but also acts as reducing agent during the reaction.

  2. Microwave Absorption Properties of Iron Nanoparticles Prepared by Ball-Milling

    Science.gov (United States)

    Chu, Xuan T. A.; Ta, Bach N.; Ngo, Le T. H.; Do, Manh H.; Nguyen, Phuc X.; Nam, Dao N. H.

    2016-05-01

    A nanopowder of iron was prepared using a high-energy ball milling method, which is capable of producing nanoparticles at a reasonably larger scale compared to conventional chemical methods. Analyses using x-ray diffraction and magnetic measurements indicate that the iron nanoparticles are a single phase of a body-centered cubic structure and have quite stable magnetic characteristics in the air. The iron nanoparticles were then mixed with paraffin and pressed into flat square plates for free-space microwave transmission and reflection measurements in the 4-8 GHz range. Without an Al backing plate, the Fe nanoparticles seem to only weakly absorb microwave radiation. The reflected signal S 11 drops to zero and a very large negative value of reflection loss ( RL) are observed for Al-backed samples, suggesting the existence of a phase matching resonance near frequency f ˜ 6 GHz.

  3. Preparation and up-conversion luminescence of 8 nm rare-earth doped fluoride nanoparticles.

    Science.gov (United States)

    Tikhomirov, V K; Mortier, M; Gredin, P; Patriarche, G; Görller-Walrand, C; Moshchalkov, V V

    2008-09-15

    Free-standing, 8 nm diameter, rare-earth doped nanoparticles Re(10)Pb(25)F(65) have been prepared, where Re stands for either single rare-earth ion, such as Er(3+), Yb(3+), Eu(3+), Dy(3+), Ho(3+), Tm(3+) or combinations of those ions. The nanoparticles have been extracted by chemical etching from the oxyfluoride nano-glass-ceramics template and analyzed by transmission electron microscope with energy dispersion spectroscopy. The nanoparticles show durable up-conversion photoluminescence, which is neither concentration nor impurity quenched after 6 months ageing in ambient atmosphere. High doping levels in these nanoparticles ensure high, up to 15%, quantum yield of up-conversion luminescence.

  4. Preparation of silver nanoparticles in virgin coconut oil using laser ablation

    Science.gov (United States)

    Zamiri, Reza; Azmi, B Z; Sadrolhosseini, Amir Reza; Ahangar, Hossein Abbastabar; Zaidan, A W; Mahdi, M A

    2011-01-01

    Laser ablation of a silver plate immersed in virgin coconut oil was carried out for fabrication of silver nanoparticles. A Nd:YAG laser at wavelengths of 1064 nm was used for ablation of the plate at different times. The virgin coconut oil allowed formation of nanoparticles with well-dispersed, uniform particle diameters that were stable for a reasonable length of time. The particle sizes and volume fraction of nanoparticles inside the solutions obtained at 15, 30, 45 min ablation times were 4.84, 5.18, 6.33 nm and 1.0 × 10−8, 1.6 × 10−8, 2.4 × 10−8, respectively. The presented method for preparation of silver nanoparticles in virgin coconut oil is environmentally friendly and may be considered a green method. PMID:21289983

  5. pH-responsive lyotropic liquid crystals for the preparation of pure cubic zirconia nanoparticles

    Science.gov (United States)

    He, Wei Yan; Liu, Jin Rong; He, Zhang; Cao, Zhen Zhu; Li, Cai Hong; Gao, Yan Fang

    2016-07-01

    We present a lyotropic liquid crystal system consisting of SDS/Triton X-100/water at 25 °C. This system is respond to pH variations with a phase switch. When pH is altered from alkaline (pH 13) to acidic (pH 2) conditions, phase change occurs from a bicontinuous hexagonal phase to a partially hexagonal phase until it disappears. The hexagonal phase under alkaline conditions is stable. Thus, this system is an ideal candidate for the preparation of pure cubic ZrO2 nanoparticles. XRD results confirm that the as-synthesized powder is composed of pure cubic ZrO2. These nanoparticles also exhibit a thermal stability of up to 800 °C. The size and morphological characteristics of the nanoparticles are greatly affected by ZrOCl2 concentration. The mechanism of zirconia nanoparticle synthesis in a lyotropic hexagonal phase was proposed.

  6. Preparation of AgX (X = Cl, I) nanoparticles using ionic liquids

    Science.gov (United States)

    Rodil, Eva; Aldous, Leigh; Hardacre, Christopher; Lagunas, M. Cristina

    2008-03-01

    Nanoparticles of silver halides have been prepared by mixing silver halide powder with a single liquid phase consisting of an ionic liquid, isooctane, n-decanol and water. Much higher nanoparticle concentrations may be formed with ionic liquids using this new simple method than are found with conventionally applied surfactants. This method also emphasizes the applicability of ionic liquids as versatile components in microemulsions and as solvents for the synthesis of nanomaterials. The effect on the nanoparticles of changing the composition of the liquid mixtures and the nature of the ionic liquid is analysed. High nanoparticle concentrations were only found with chloride based ionic liquids, indicating the importance of the ionic liquid anion in the mechanism of the reaction.

  7. pH-responsive lyotropic liquid crystals for the preparation of pure cubic zirconia nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    He, Wei Yan; Liu, Jin Rong; He, Zhang; Cao, Zhen Zhu; Li, Cai Hong; Gao, Yan Fang [Inner Mongolia University of Technology, School of Chemical Engineering, Hohhot (China)

    2016-07-15

    We present a lyotropic liquid crystal system consisting of SDS/Triton X-100/water at 25 C. This system is respond to pH variations with a phase switch. When pH is altered from alkaline (pH 13) to acidic (pH 2) conditions, phase change occurs from a bicontinuous hexagonal phase to a partially hexagonal phase until it disappears. The hexagonal phase under alkaline conditions is stable. Thus, this system is an ideal candidate for the preparation of pure cubic ZrO{sub 2} nanoparticles. XRD results confirm that the as-synthesized powder is composed of pure cubic ZrO{sub 2}. These nanoparticles also exhibit a thermal stability of up to 800 C. The size and morphological characteristics of the nanoparticles are greatly affected by ZrOCl{sub 2} concentration. The mechanism of zirconia nanoparticle synthesis in a lyotropic hexagonal phase was proposed. (orig.)

  8. Preparation of silver nanoparticles in virgin coconut oil using laser ablation.

    Science.gov (United States)

    Zamiri, Reza; Azmi, B Z; Sadrolhosseini, Amir Reza; Ahangar, Hossein Abbastabar; Zaidan, A W; Mahdi, M A

    2011-01-07

    Laser ablation of a silver plate immersed in virgin coconut oil was carried out for fabrication of silver nanoparticles. A Nd:YAG laser at wavelengths of 1064 nm was used for ablation of the plate at different times. The virgin coconut oil allowed formation of nanoparticles with well-dispersed, uniform particle diameters that were stable for a reasonable length of time. The particle sizes and volume fraction of nanoparticles inside the solutions obtained at 15, 30, 45 min ablation times were 4.84, 5.18, 6.33 nm and 1.0 × 10(-8), 1.6 × 10(-8), 2.4 × 10(-8), respectively. The presented method for preparation of silver nanoparticles in virgin coconut oil is environmentally friendly and may be considered a green method.

  9. Biocompatible branched copolymer nanoparticles prepared by RAFT polymerization as MRI/PET bimodal tracers

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Chang-Tong [Lee Kong Chian School of Medicine, Nanyang Technological University (Singapore); Tao, He; Jackson, Alexander W [Institute of Chemical and Engineering Sciences, Agency for Science Technology and Research (Singapore); Chandrasekharan, Prashant [Laboratory of Molecular Imaging, Singapore Bioimaging Consortium, Agency for Science Technology and Research (Singapore); Padmanabhan, Parasuraman [Lee Kong Chian School of Medicine, Nanyang Technological University (Singapore); Gulyás, Balázs; Halldin, Christer [Lee Kong Chian School of Medicine, Nanyang Technological University (Singapore); Karolinska Institutet, Department of Clinical Neuroscience, Stockholm (Sweden)

    2015-05-18

    Stable branched copolymer nanoparticles of varying size (Dh = 20 – 35 nm) have been developed and employed as MRI nano-sized contrast agents. RAFT polymerization has been employed to prepare these novel nanoparticles possessing DO3A macrocycles within their cores and succinimidyl ester benzoate functionalities within their coronas. It has been demonstrated that these nanoparticles can chelate gadolinium and in vitro cytotoxicity studies using HK-2 cells established their negligible toxicity profile. In vivo MRI experiments showed that these nanoparticles have a high relaxivity and a long blood retention time. Xenograft experiments further illustrated the ability of these nanoparticles to perfuse and passively accumulate in tumor cells, presumably through the enhanced EPR effect. The presence of the succinimidyl ester benzoate functionalities within the nanoparticle coronas will permit future surface modification with fluorophores or targeting moieties to generate nanoparticles to study opportunities for bimodal imaging nano-probes or active cell targeting contrast agents. The chelation with PET radioisotopes (68Ga(III) or 64Cu(II)) can afford various PET tracers.

  10. Preparation and antibacterial activity of Fe{sub 3}O{sub 4}-Ag nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Gong Ping [State Key Laboratory of Chemo/Biosensing and Chemometrics, Biomedical Engineering Centre, College of Chemistry and Chemical Engineering, Hunan University, Research Centre for Bio-Nanotechnology Engineering of Hunan Province, Changsha 410082 (China); Li Huimin [Biomedical Engineering Center, College of Material Science and Technology, Hunan University, Changsha, 410082 (China); He Xiaoxiao [State Key Laboratory of Chemo/Biosensing and Chemometrics, Biomedical Engineering Centre, College of Chemistry and Chemical Engineering, Hunan University, Research Centre for Bio-Nanotechnology Engineering of Hunan Province, Changsha 410082 (China)] (and others)

    2007-07-18

    Bifunctional Fe{sub 3}O{sub 4}-Ag nanoparticles with both superparamagnetic and antibacterial properties were prepared by reducing silver nitrate on the surface of Fe{sub 3}O{sub 4} nanoparticles using the water-in-oil microemulsion method. Formation of well-dispersed nanoparticles with sizes of 60 {+-} 20 nm was confirmed by transmission electron microscopy and dynamic light scattering. X-ray diffraction patterns and UV-visible spectroscopy indicated that both Fe{sub 3}O{sub 4} and silver are present in the same particle. The superparamagnetism of Fe{sub 3}O{sub 4}-Ag nanoparticles was confirmed with a vibrating sample magnetometer. Their antibacterial activity was evaluated by means of minimum inhibitory concentration value, flow cytometry, and antibacterial rate assays. The results showed that Fe{sub 3}O{sub 4}-Ag nanoparticles presented good antibacterial performance against Escherichia coli (gram-negative bacteria), Staphylococcus epidermidis (gram-positive bacteria) and Bacillus subtilis (spore bacteria). Furthermore, Fe{sub 3}O{sub 4}-Ag nanoparticles can be easily removed from water by using a magnetic field to avoid contamination of surroundings. Reclaimed Fe{sub 3}O{sub 4}-Ag nanoparticles can still have antibacterial capability and can be reused.

  11. Electrochemical characterization of platinum-ruthenium nanoparticles prepared by water-in-oil microemulsion

    Energy Technology Data Exchange (ETDEWEB)

    Solla-Gullon, J.; Vidal-Iglesias, F.J.; Montiel, V.; Aldaz, A. [Universidad de Alicante (Spain). Instituto Universitario de Electroquimica, Departamento de Quimica-Fisica

    2004-11-01

    The synthesis, physical characterization, decontamination and some electrocatalytic properties of PtRu nanoparticles prepared using the microemulsion method are reported. The nanoparticles are synthesized by reduction with sodium borohydride of H{sub 2}PtCl{sub 6} and RuCl{sub 3} in a water-in-oil microemulsion of water/polyethylenglycol-dodecylether (BRIJ(Registered Trademark) 30)/n-heptane. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and energy dispersive analysis by X-rays (EDAX) experiments were carried out to characterize the single and bimetallic nanoparticles obtained. Cyclic voltammograms (CV) of clean nanoparticles were obtained after a controlled decontamination procedure of their surfaces. CO adsorption-oxidation and methanol electrooxidation were tested as test reactions to check the electrocatalytic behaviour of the bimetallic nanoparticles. Pt{sub 80}Ru{sub 20} (nominal atomic composition) nanoparticles are the best electrocatalyst for both CO{sub ad} and methanol oxidation. All these results show that the microemulsion method can be used to produce bimetallic nanoparticles in a very easy way. The method can be very easily scaled-up for industrial use. (author)

  12. Preparation of Monodisperse Nanoparticle of Layered Double Hydroxides and Polyoxyethylene Sulfate

    Institute of Scientific and Technical Information of China (English)

    XU Huizhong; QIN Lianjie; ZHANG Hong; YANG Qinzheng; YANG Jing

    2005-01-01

    In order to obtain the bio-molecule/ LDHs nanocomposites having regular crystal structure,three nanocomposites of layered double hydroxides and polyoxyethylene sulfates were prepared by ion-exchange method. TEM analysis reveals that the monodisperse rigid .sphere of approximately 200 nm in diameter could be gotten when the intergallery anion was PEGS-400. Such monodisperse nanoparticle could be used as a promising precursor for preparing bio-molecule/LDHs nanocomposites.

  13. Preparation of superparamagnetic sodium alginate nanoparticles for covalent immobilization of Candida rugosa lipase

    Energy Technology Data Exchange (ETDEWEB)

    Liu Xiao; Chen Xia; Li Yanfeng, E-mail: liyf@lzu.edu.cn; Cui Yanjun; Zhu Hao; Zhu Weiwei [Lanzhou University, State Key Laboratory of Applied Organic Chemistry, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, College of Chemistry and Chemical Engineering, Institute of Biochemical Engineering and Environmental Technology (China)

    2012-03-15

    Superparamagnetic sodium alginate nanoparticles with diameter around 25-30 nm were prepared with a water-in-oil emulsion method. The resulted magnetic SA nanoparticle was activated with glutaraldehyde and epichlorohydrin to form nanoscale support. Candida rugosa lipase (CRL), hereby chosen as a model enzyme, was covalently immobilized on the resulted magnetic support. The structure and magnetic behavior of the magnetic nanoparticles were confirmed by transmission electron microscopy, Fourier transform infrared spectroscopy, and vibrating sample magnetometer. Based on the structural character of enzyme (containing functional residues that are ideal reaction sites for the immobilization of enzyme repeatedly), the regeneration of support was investigated by reactivating the deactivated immobilized lipase with glutaraldehyde. And the results indicated that these regenerated supports remained to be efficient for lipase immobilization. Finally, all of the immobilized CRL prepared by different generations of supports displayed excellent reusability and applicability.

  14. Effective preparation of graphite nanoparticles using mechanochemical solid-state reactions

    Science.gov (United States)

    Motozuka, S.; Tagaya, M.; Ogawa, N.; Fukui, K.; Nishikawa, M.; Shiba, K.; Uehara, T.; Kobayashi, T.

    2014-07-01

    The mechanochemical milling was utilized to control the nanostructures of plate-like graphite (Gp) microparticles in an argon atmosphere and at room temperature. The aggregated Gp nanoparticles were prepared by the simple solid-state process without organic solvent. Electron microscope observations, X-ray diffraction patterns and Raman spectra revealed the fractured plate-like Gp microparticles as well as the Gp microparticles agglomerated to each other through the dissociative edge surfaces by the milling process to finally generate the Gp nanoparticle aggregates. In the process, the ratio of the edge plane surfaces with the dangling bondings to layered internal surfaces clearly increased with the milling. Therefore, the low environmental burden process for preparing the Gp nanoparticle aggregation was achieved.

  15. Preparation of AZO Nanoparticles, Ceramic Targets and Thin Films by a Co-precipitaition Method

    Institute of Scientific and Technical Information of China (English)

    XIU Sanmu; WEI Tiefeng; YANG Ye; ZHANG Ting; LI Jia; SONG Weijie

    2015-01-01

    We comprehensively study the co-precipitation preparation of aluminum doped zinc oxide (AZO) nanoparticles, ceramic target and thin iflm deposition. The nanoparticles calcined below 700℃possessed pure wurtzite structure of ZnO. When the calcination temperature exceeded 700℃, ZnAl2O4 phase appeared. The resistivity and relative density of the AZO target pressed from nanoparticles were 3×10-3Ω∙cm and 99.1%, respectively. The minimum resistivity of AZO thin films prepared by DC sputtering of the ceramic target reached 4.1×10–4Ω∙cm with the mobility of 33 cm2/v∙s and the carrier concentration of 4.5 ×1020 cm-3. The average optical transmittance of the AZO thin iflms in the visible wavelength range (400-800 nm) was more than 80%.

  16. A method for top down preparation of chitosan nanoparticles and nanofibers.

    Science.gov (United States)

    Wijesena, Ruchira N; Tissera, Nadeeka; Kannangara, Yasun Y; Lin, Yuan; Amaratunga, Gehan A J; de Silva, K M Nalin

    2015-03-01

    A method of top down preparation of chitosan nanoparticles and nanofibers is proposed. Chitin nanofibrils (chitin NFs) were prepared using ultrasonic assisted method from crab shells with an average diameter of 5 nm and the length less than 3 μm as analyzed by atomic force microscopy and transmission electron microscopy. These chitin nanofibers were used as the precursor material for the preparation of chitosan nanoparticles and nanofibers. The degree of deacetylation of these prepared chitosan nanostructures were found to be approximately 98%. In addition these chitosan nanostructures showed amorphous crystallinity. Transmission electron microscopic studies revealed that chitosan nanoparticles were roughly spherical in nature and had diameters less than 300 nm. These larger particles formed through self-assembly of much smaller 25 nm particles as evidenced by the TEM imaging. The diameter and the length of the chitosan nanofibers were found to be less than 100 nm and 3 μm respectively. It is envisaged that due to the cavitation effect, the deacetylated chitin nanofibers were broken down to small pieces to form seed particles. These seed particles can then be self-assembled to form larger chitosan nanoparticles.

  17. Surface characterisation of dextran-coated iron oxide nanoparticles prepared by laser pyrolysis and coprecipitation

    Energy Technology Data Exchange (ETDEWEB)

    Carmen Bautista, M. [Instituto de Ciencia de Materiales de Madrid, CSIC, C Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Bomati-Miguel, Oscar [Instituto de Ciencia de Materiales de Madrid, CSIC, C Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Puerto Morales, Maria del [Instituto de Ciencia de Materiales de Madrid, CSIC, C Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Serna, Carlos J. [Instituto de Ciencia de Materiales de Madrid, CSIC, C Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Veintemillas-Verdaguer, Sabino [Instituto de Ciencia de Materiales de Madrid, CSIC, C Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain)]. E-mail: sabino@icmm.csic.es

    2005-05-15

    The favoured mechanism of adsorption of dextran on the surface of maghemite nanoparticles (5 nm) prepared by laser pyrolysis seems to be the collective hydrogen bonding between dextran hydroxyl groups and iron oxide particle surface. After heating, the formation of a surface complex between the polysaccharide oxygen atoms and the surface iron atoms gave rise to a stronger bonding.

  18. Pickering emulsions stabilized by whey protein nanoparticles prepared by thermal cross-linking

    NARCIS (Netherlands)

    Wu, Jiande; Shi, Mengxuan; Li, Wei; Zhao, Luhai; Wang, Ze; Yan, Xinzhong; Norde, Willem; Li, Yuan

    2015-01-01

    A Pickering (o/w) emulsion was formed and stabilized by whey protein isolate nanoparticles (WPI NPs). Those WPI NPs were prepared by thermal cross-linking of denatured WPI proteins within w/o emulsion droplets at 80. °C for 15. min. During heating of w/o emulsions containing 10% (w/v) WPI protein

  19. Cell Interactions within Biomimetic Apatite Microenvironments

    OpenAIRE

    Tsang, Eric

    2014-01-01

    Bioactive ceramics, such as calcium phosphate-based materials, have been studied extensively for the regeneration of bone tissue. Accelerated apatite coatings prepared from biomimetic methods is one approach that has had a history of success in both in vitro and in vivo studies for bone regeneration [1]-[4]. However, how cells interact within the apatite microenvironment remains largely unclear, despite the vast literature available today. In response, this thesis evaluates the in vitro i...

  20. Preparation of magnetic polymer particles with nanoparticles of Fe(0).

    Science.gov (United States)

    Buendía, S; Cabañas, G; Alvarez-Lucio, G; Montiel-Sánchez, H; Navarro-Clemente, M E; Corea, M

    2011-02-01

    Iron nanoparticles (Fe(0)), were encapsulated into polymethyl methacrylate (PMMA), by means of emulsion polymerization techniques in a semicontinuous process. The final average diameter of the composite particle was calculated until three times of average particle of iron particles and were stabilized with a non-ionic surfactant. They were then characterized by scanning electron microscopy and dynamic light scattering. Their magnetic properties were determined by parallel field vibrating-sample magnetometry method. The results indicated that the magnetic properties are a function of polymer concentration in the nanocomposite particle.

  1. Preparation and Evaluation of Vancomycin-Loaded N-trimethyl Chitosan Nanoparticles

    Directory of Open Access Journals (Sweden)

    Jiaojiao Xu

    2015-09-01

    Full Text Available Chronic intracellular infections caused by drug-resistant pathogens pose a challenge to the treatment of chronic osteomyelitis. Such treatment requires an intracellular delivery system for the sustained release of antibiotics such as vancomycin (VCM, which is an antibiotic of last resort used against many clinically resistant bacteria. In this work, we report VCM-loaded N-trimethyl chitosan (TMC nanoparticles and their potential application for drug delivery. The results showed that the prepared nanoparticles were predominantly spherical in shape with an average particle diameter of 220 nm, a positive zeta potential, and a loading efficiency of 73.65% ± 1.83%. Furthermore, their drug release profile followed the Higuchi model for sustained release, with non-Fickian diffusion. Over a 24-h period, 6.51% ± 0.58% of the drug within the optimized nanoparticles was released. In vitro cytology showed that osteoblasts (OBs exhibited higher alkaline phosphatase activity (ALP after exposure to TMC nanoparticle material. Furthermore, TMC nanoparticles increased the uptake of water-soluble quantum dots (QDs by OBs, and both nanoparticles and VCM/TMC mixtures improved OB proliferative activity. We also investigated the minimum inhibitory concentration (MIC, 60 μg/mL, half maximal inhibitory concentration (IC50, 48.47 μg/mL, diameter of inhibition zone (DIZ, 1.050 cm, and turbidimetric (TB assay of nanoparticles. All data demonstrated that VCM/TMC nanoparticles had excellent antibacterial activity against the Gram-positive bacterium Staphylococcus aureus. These findings suggest that VCM-loaded TMC nanoparticles have good potential for the sustained delivery of antibiotics to bone infections.

  2. Preparation and properties of amorphous titania-coated zinc oxide nanoparticles

    Science.gov (United States)

    Liao, Min-Hung; Hsu, Chih-Hsiung; Chen, Dong-Hwang

    2006-07-01

    Amorphous TiO 2-coated ZnO nanoparticles were prepared by the solvothermal synthesis of ZnO nanoparticles in ethanol and the followed by sol-gel coating of TiO 2 nanolayer. The analyses of X-ray diffraction (XRD) and transmission electron microscopy (TEM) revealed that the resultant ZnO nanoparticles were hexagonal with a wurtzite structure and a mean diameter of about 60 nm. Also, after TiO 2 coating, the TEM images clearly indicated the darker ZnO nanoparticles being surrounded by the lighter amorphous TiO 2 layers. The zeta potential analysis revealed the pH dependence of zeta potentials for ZnO nanoparticles shifted completely to that for TiO 2 nanoparticles after TiO 2 coating, confirming the formation of core-shell structure and suggesting the coating of TiO 2 was achieved via the adhesion of the hydrolyzed species Ti-O - to the positively charged surface of ZnO nanoparticles. Furthermore, the analyses of Fourier transform infrared (FTIR) and Raman spectra were also conducted to confirm that amorphous TiO 2 were indeed coated on the surface of ZnO nanoparticles. In addition, the analyses of ultraviolet-visible (UV-VIS) and photoluminescence (PL) spectra revealed that the absorbance of amorphous TiO 2-coated ZnO nanoparticles at 375 nm gradually decreased with an increase in the Ti/Zn molar ratio and the time for TiO 2 coating, and the emission intensity of ZnO cores could be significantly enhanced by the amorphous TiO 2 shell.

  3. Biomimetic synthesis of raspberry-like hybrid polymer-silica core-shell nanoparticles by templating colloidal particles with hairy polyamine shell.

    Science.gov (United States)

    Pi, Mengwei; Yang, Tingting; Yuan, Jianjun; Fujii, Syuji; Kakigi, Yuichi; Nakamura, Yoshinobu; Cheng, Shiyuan

    2010-07-01

    The nanoparticles composed of polystyrene core and poly[2-(diethylamino)ethyl methacrylate] (PDEA) hairy shell were used as colloidal templates for in situ silica mineralization, allowing the well-controlled synthesis of hybrid silica core-shell nanoparticles with raspberry-like morphology and hollow silica nanoparticles by subsequent calcination. Silica deposition was performed by simply stirring a mixture of the polymeric core-shell particles in isopropanol, tetramethyl orthosilicate (TMOS) and water at 25 degrees C for 2.5h. No experimental evidence was found for nontemplated silica formation, which indicated that silica deposition occurred exclusively in the PDEA shell and formed PDEA-silica hybrid shell. The resulting hybrid silica core-shell particles were characterized by transmission electron microscopy (TEM), thermogravimetry, aqueous electrophoresis, and X-ray photoelectron spectroscopy. TEM studies indicated that the hybrid particles have well-defined core-shell structure with raspberry morphology after silica deposition. We found that the surface nanostructure of hybrid nanoparticles and the composition distribution of PDEA-silica hybrid shell could be well controlled by adjusting the silicification conditions. These new hybrid core-shell nanoparticles and hollow silica nanoparticles would have potential applications for high-performance coatings, encapsulation and delivery of active organic molecules.

  4. Preparation of Au and Ag nanoparticles using Artemisia annua and their in vitro antibacterial and tyrosinase inhibitory activities

    Energy Technology Data Exchange (ETDEWEB)

    Basavegowda, Nagaraj; Idhayadhulla, Akber; Lee, Yong Rok, E-mail: yrlee@yu.ac.kr

    2014-10-01

    This work describes a plant-mediated approach to the preparation of metal nanoparticles using leaf extract of Artemisia annua (A. annua), an ethno-medicinal plant widely found in Asia, which was used as reducing and stabilizing agent. A. annua is used in traditional Chinese medicine to alleviate fever. Au and Ag nanoparticles were prepared using a one-step aqueous method at room temperature without any toxic chemicals. The formation of Au and Ag nanoparticles was monitored by UV–vis spectroscopy. Synthesized nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX), Fourier transform infrared (FT-IR) spectroscopy, and thermogravimetric analysis (TGA). TEM analysis of Au nanoparticles showed that they had triangular and spherical shapes with sizes ranging from 15 to 40 nm. The silver nanoparticles were predominantly spherical and uniformly sized (30–50 nm). The Au and Ag nanoparticles produced showed significant tyrosinase inhibitory and antibacterial effects. These results suggest that the synthesized nanoparticles provide good alternatives in varied medical and industrial applications. - Highlights: • Au and Ag nanoparticles were synthesized using Artemisia annua leaf aqueous extract. • Nanoparticles were characterized by UV–vis spectroscopy, FT-IR, TEM, EDX, XRD, and TGA. • Au and Ag nanoparticles were of size 25 and 30 nm respectively, in spherical forms. • Nanoparticles showed significant tyrosinase inhibitory and antibacterial activities.

  5. Microbial preparation of metal-substituted magnetite nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Moon, Ji Won [ORNL; Roh, Yul [Chonnam National University, Gwangju; Lauf, Robert J [ORNL; Vali, Hojatollah [McGill University, Montreal, Quebec; Yeary, Lucas W [ORNL; Phelps, Tommy Joe [ORNL

    2007-01-01

    A microbial process that exploits the ability of iron-reducing microorganisms to produce copious amounts of extra-cellular metal (M)-substituted magnetite nanoparticles using akaganeite and dopants of dissolved form has previously been reported. The objectives of this study were to develop methods for producing M-substituted magnetite nanoparticles with a high rate of metal substitution by biological processes and to identify factors affecting the production of nano crystals. The thermophilic and psychrotolerant iron-reducing bacteria had the ability to form M substituted magnetite nano-crystals (MyFe3-yO4) from a doped precursor, mixed-M iron oxyhydroxide, (MxFe1-xOOH, x 0.5, M is Mn, Zn, Ni, Co, and Cr). Within the range of 0.01 x 0.3, using the mixed precursor material enabled the microbial synthesis of more heavily substituted magnetite compared to the previous method, in which the precursor was pure akaganeite and the dopants were present as soluble metal salts. The mixed precursor method was especially advantageous in the case of toxic metals such as Cr and Ni. Also this new method increased the production rate and magnetic properties of the product, while improving crystallinity, size control and scalability.

  6. Preparation of Antibacterial Nanofibre/Nanoparticle Covered Composite Yarns

    Directory of Open Access Journals (Sweden)

    Fatma Yalcinkaya

    2016-01-01

    Full Text Available The antibacterial efficiency of nanofibre composite yarns with an immobilized antibacterial agent was tested. This novel type of nanofibrous composite material combines the good mechanical properties of the core yarn with the high specific surface of the nanofibre shell to gain specific targeted qualities. The main advantages of nanofibre covered composite yarns over the standard planar nanofibre membranes include high tensile strength, a high production rate, and their ability to be processed by standard textile techniques. The presented paper describes a study of the immobilization of an antibacterial agent and its interaction with two types of bacterial colonies. The aim of the study is to assess the applicability of the new composite nanomaterial in antibacterial filtration. During the experimental tests copper(II oxide particles were immobilized in the polyurethane and polyvinyl butyral nanofibre components of a composite yarn. The antibacterial efficiency was evaluated by using both Gram-negative Escherichia coli and Gram-positive Staphylococcus gallinarum bacteria. The results showed that the composite yarn with polyvinyl butyral nanofibres incorporating copper(II oxide nanoparticles exhibited better antibacterial efficiency compared to the yarn containing the polyurethane nanofibres. The nanofibre/nanoparticle covered composite yarns displayed good antibacterial activity against a number of bacteria.

  7. Exploring the Preparation of Albendazole-Loaded Chitosan-Tripolyphosphate Nanoparticles

    Directory of Open Access Journals (Sweden)

    Bong-Seok Kang

    2015-02-01

    Full Text Available The objective of this study was to improve the solubility of albendazole and optimize the preparation of an oral nanoparticle formulation, using β-cyclodextrin (βCD and chitosan-tripolyphosphate (TPP nanoparticles. The solubility of albendazole in buffers, surfactants, and various concentrations of acetic acid solution was investigated. To determine drug loading, the cytotoxic effects of the albendazole concentration in human hepatocellular carcinoma cells (HepG2 were investigated. The formulations were prepared by mixing the drug solution in Tween 20 with the chitosan solution. TPP solution was added dropwise with sonication to produce a nanoparticle through ionic crosslinking. Then the particle size, polydispersity index, and zeta potential of the nanoparticles were investigated to obtain an optimal composition. The solubility of albendazole was greater in pH 2 buffer, Tween 20, and βCD depending on the concentration of acetic acid. Drug loading was determined as 100 µg/mL based on the results of cell viability. The optimized ratio of Tween 20, chitosan/hydroxypropyl βCD, and TPP was 2:5:1, which resulted in smaller particle size and proper zeta positive values of the zeta potential. The chitosan-TPP nanoparticles increased the drug solubility and had a small particle size with homogeneity in formulating albendazole as a potential anticancer agent.

  8. PREPARATION, CHARACTERIZATION AND ADHESIVE PROPERTIES OF DI-AND TRI-HYDROXY BENZOYL CHITOSAN NANOPARTICLES

    Institute of Scientific and Technical Information of China (English)

    Mohamad Taghi Taghizadeh; Ali Bahadori

    2013-01-01

    Modified chitosans with 3,4-di-hydroxy benzoyl groups (CS-DHBA) and 3,4,5-tri-hydroxy benzoyl groups (CSTHBA) were synthesized and their nanoparticles were prepared via ionic crosslinking by tripolyphosphate (TPP).The chemical structure and degree of substitution (DS) of di-and tri-hydroxy benzoyl chitosans are determined by FTIR and 1HNMR spectroscopy.The morphology of particles,size distribution and zeta potential of nanoparticles were studied using transmission electron microscopy (TEM) and dynamic light scattering (DLS),respectively.The mean diameters of particles of CS-DHBA and CS-THBA nanoparticles were 144 nm and 112 nm,respectively.It was found that the particles size decreased slightly with decreasing the degree of substitution and increasing degree of deacetylation (DD),due to increasing of ionic crosslinking of ammonium ions and polyanions of tripolyphosphate.The TEM photographs of CS-DHBA show that these particles are spherical in shape,but the particles of CS-THBA show some aggregation.In addition,the solubility and the mechanical properties of the prepared modified chitosans and their nanoparticles were evaluated for bio-adhesive and biomedical application.The results of solubility tests indicated that,the CS-DHBA and CS-THBA have higher solubility at pH > 7 comparing to CS.Also the CS-DHBA,CS-THBA and their nanoparticles showed a significant adhesive capacity and enhanced tensile strength and tensile modulus.

  9. Preparation and optical properties of composite thin films with embedded InP nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    InP nanoparticles embedded in SiO2 thin films were prepared by radio-frequency magnetron co-sputtering. We analyzed the structure and growth behavior of the composite films under different preparation conditions. X-ray diffraction and Raman spectroscopy analyses indicate that InP nanoparticles have a polycrystalline structure. The aver-age size of InP nanoparticles is in the range of 3-10 nm. The broadening and red shift of the Raman peaks were observed,which can be interpreted by the phonon confinement model. Optical transmission spectra indicate that the optical absorp-tion edges of the films can be modulated in the visible light range. The marked blue shift of the absorption edge with respect to that of bulk InP is explained by the quantum con-finement effect. The theoretical values of the blue shift pre-dicted by the effective mass approximation model are differ-ent from the experimental results for the InP-SiO2 system. Analyses indicate that the exciton effective mass of the InP nanoparticles is not constant and is inverse relative to the particles radius,which may be the main reason that results in the discrepancy between the theoretical and the experi-mental result. We discussed the possible transition of the direct band gap to the indirect band gap for InP nanoparti-cles embedded in SiO2 thin films.

  10. Preparation of starch nanoparticles in water in oil microemulsion system and their drug delivery properties.

    Science.gov (United States)

    Wang, Xinge; Chen, Haiming; Luo, Zhigang; Fu, Xiong

    2016-03-15

    In this research, 1-hexadecyl-3-methylimidazolium bromide C16mimBr/butan-1-ol/cyclohexane/water ionic liquid microemulsion was prepared. The effects of n-alkyl alcohols, alkanes, water content and temperature on the properties of microemulsion were studied by dilution experiment. The microregion of microemulsion was identified by pseudo-ternary phase diagram and conductivity measurement. Then starch nanoparticles were prepared by water in oil (W/O) microemulsion-cross-linking methods with C16mimBr as surfactant. Starch nanoparticles with a mean diameter of 94.3nm and narrow size distribution (SD=3.3) were confirmed by dynamic light scattering (DLS). Scanning electron microscope (SEM) data revealed that starch nanoparticles were spherical granules with the size about 60nm. Moreover the results of Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) demonstrated the formation of cross-linking bonds in starch molecules. Finally, the drug loading and releasing properties of starch nanoparticles were investigated with methylene blue (MB) as drug model. This work may provide an efficient pathway to synthesis starch nanoparticles.

  11. Preparation and Biocompatible Surface Modification of Redox Altered Cerium Oxide Nanoparticle Promising for Nanobiology and Medicine

    KAUST Repository

    Nanda, Himansu

    2016-11-03

    The biocompatible surface modification of metal oxide nanoparticles via surface functionalization technique has been used as an important tool in nanotechnology and medicine. In this report, we have prepared aqueous dispersible, trivalent metal ion (samarium)-doped cerium oxide nanoparticles (SmCNPs) as model redox altered CNPs of biological relevance. SmCNP surface modified with hydrophilic biocompatible (6-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-hexyl) triethoxysilane (MEEETES) were prepared using ammonia-induced ethylene glycol-assisted precipitation method and were characterized using a variety of complementary characterization techniques. The chemical interaction of functional moieties with the surface of doped nanoparticle was studied using powerful 13C cross polarization magic angle sample spinning nuclear magnetic resonance spectroscopy. The results demonstrated the production of the extremely small size MEEETES surface modified doped nanoparticles with significant reduction in aggregation compared to their unmodified state. Moreover, the functional moieties had strong chemical interaction with the surface of the doped nanoparticles. The biocompatible surface modification using MEEETES should also be extended to several other transition metal ion doped and co-doped CNPs for the production of aqueous dispersible redox altered CNPs that are promising for nanobiology and medicine.

  12. Preparation of ultrafine Ce-based oxide nanoparticles and their catalytic performances for diesel soot combustion

    Institute of Scientific and Technical Information of China (English)

    韦岳长; 赵震; 焦金庆; 刘坚; 段爱军; 姜桂元

    2014-01-01

    The ultrafine Ce-based oxide nanoparticles with different element dopings (Zr, Y) were synthesized by the method of mi-cropores-diffused coprecipitation (MDC) using ammonia solution as the precipitation agent. The activities of the catalysts for soot oxidation were evaluated by the temperature-programmed oxidation (TPO) reaction. Ce-based oxides prepared in this study exhibited high catalytic activity for soot oxidation under the condition of loose contact between soot particles and catalysts, and the catalytic ac-tivity of ultrafine Ce0.9Zr0.1O2 nanoparticle for soot combustion was the highest, whose T10, T50 and SCO2m was 364, 442 ºC and 98.3%, respectively. All catalysts were systematically characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brumauer-Emett-Teller (BET), Fourier transform infrared spectroscopy (FT-IR) and UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS). It was indicated that the MDC method could prepare the ultrafine Ce-based oxide nanoparticles whose the crystal lattice were perfect, and the BET surface area and average crystal size of the ultrafine nanoparticles changed with the different element dopings (Zr, Y). The H2-TPR measurements showed that the ultrafine Ce-based ox-ide nanoparticles with the doping-Zr cation could be favorable for improving the redox property of the catalysts.

  13. Paraquat-loaded alginate/chitosan nanoparticles: Preparation, characterization and soil sorption studies

    Energy Technology Data Exchange (ETDEWEB)

    Santos Silva, Mariana dos; Sgarbi Cocenza, Daniela [Department of Environmental Engineering, Sao Paulo State University - UNESP, Avenida Tres de Marco, No. 511, CEP 18087-180, Sorocaba, SP (Brazil); Grillo, Renato; Silva de Melo, Nathalie Ferreira [Department of Environmental Engineering, Sao Paulo State University - UNESP, Avenida Tres de Marco, No. 511, CEP 18087-180, Sorocaba, SP (Brazil); Department of Biochemistry, Institute of Biology, State University of Campinas - UNICAMP, Campinas, SP (Brazil); Tonello, Paulo Sergio [Department of Environmental Engineering, Sao Paulo State University - UNESP, Avenida Tres de Marco, No. 511, CEP 18087-180, Sorocaba, SP (Brazil); Camargo de Oliveira, Luciana [Department of Chemistry, UFSCAr, Campus Sorocaba, SP (Brazil); Lopes Cassimiro, Douglas [Institute of Chemistry, Sao Paulo State University - UNESP, Araraquara, SP (Brazil); Rosa, Andre Henrique [Department of Environmental Engineering, Sao Paulo State University - UNESP, Avenida Tres de Marco, No. 511, CEP 18087-180, Sorocaba, SP (Brazil); Fernandes Fraceto, Leonardo, E-mail: leonardo@sorocaba.unesp.br [Department of Environmental Engineering, Sao Paulo State University - UNESP, Avenida Tres de Marco, No. 511, CEP 18087-180, Sorocaba, SP (Brazil); Department of Biochemistry, Institute of Biology, State University of Campinas - UNICAMP, Campinas, SP (Brazil)

    2011-06-15

    Agrochemicals are amongst the contaminants most widely encountered in surface and subterranean hydrological systems. They comprise a variety of molecules, with properties that confer differing degrees of persistence and mobility in the environment, as well as different toxic, carcinogenic, mutagenic and teratogenic potentials, which can affect non-target organisms including man. In this work, alginate/chitosan nanoparticles were prepared as a carrier system for the herbicide paraquat. The preparation and physico-chemical characterization of the nanoparticles was followed by evaluation of zeta potential, pH, size and polydispersion. The techniques employed included transmission electron microscopy, differential scanning calorimetry and Fourier transform infrared spectroscopy. The formulation presented a size distribution of 635 {+-} 12 nm, polydispersion of 0.518, zeta potential of -22.8 {+-} 2.3 mV and association efficiency of 74.2%. There were significant differences between the release profiles of free paraquat and the herbicide associated with the alginate/chitosan nanoparticles. Tests showed that soil sorption of paraquat, either free or associated with the nanoparticles, was dependent on the quantity of organic matter present. The results presented in this work show that association of paraquat with alginate/chitosan nanoparticles alters the release profile of the herbicide, as well as its interaction with the soil, indicating that this system could be an effective means of reducing negative impacts caused by paraquat.

  14. Enhanced Oral Delivery of Docetaxel Using Thiolated Chitosan Nanoparticles: Preparation, In Vitro and In Vivo Studies

    Science.gov (United States)

    Saremi, Shahrooz; Kebriaeezadeh, Abbas; Ostad, Seyed Nasser; Atyabi, Fatemeh

    2013-01-01

    The aim of this study was to evaluate a nanoparticulate system with mucoadhesion properties composed of a core of polymethyl methacrylate surrounded by a shell of thiolated chitosan (Ch-GSH-pMMA) for enhancing oral bioavailability of docetaxel (DTX), an anticancer drug. DTX-loaded nanoparticles were prepared by emulsion polymerization method using cerium ammonium nitrate as an initiator. Physicochemical properties of the nanoparticles such as particle size, size distribution, morphology, drug loading, and entrapment efficiency were characterized. The pharmacokinetic study was carried out in vivo using wistar rats. The half-life of DTX-loaded NPs was about 9 times longer than oral DTX used as positive control. The oral bioavailability of DTX was increased to 68.9% for DTX-loaded nanoparticles compared to 6.5% for positive control. The nanoparticles showed stronger effect on the reduction of the transepithelial electrical resistance (TEER) of Caco-2 cell monolayer by opening the tight junctions. According to apparent permeability coefficient (Papp) results, the DTX-loaded NPs showed more specific permeation across the Caco-2 cell monolayer in comparison to the DTX. In conclusion, the nanoparticles prepared in this study showed promising results for the development of an oral drug delivery system for anticancer drugs. PMID:23971023

  15. Enhanced Oral Delivery of Docetaxel Using Thiolated Chitosan Nanoparticles: Preparation, In Vitro and In Vivo Studies

    Directory of Open Access Journals (Sweden)

    Shahrooz Saremi

    2013-01-01

    Full Text Available The aim of this study was to evaluate a nanoparticulate system with mucoadhesion properties composed of a core of polymethyl methacrylate surrounded by a shell of thiolated chitosan (Ch-GSH-pMMA for enhancing oral bioavailability of docetaxel (DTX, an anticancer drug. DTX-loaded nanoparticles were prepared by emulsion polymerization method using cerium ammonium nitrate as an initiator. Physicochemical properties of the nanoparticles such as particle size, size distribution, morphology, drug loading, and entrapment efficiency were characterized. The pharmacokinetic study was carried out in vivo using wistar rats. The half-life of DTX-loaded NPs was about 9 times longer than oral DTX used as positive control. The oral bioavailability of DTX was increased to 68.9% for DTX-loaded nanoparticles compared to 6.5% for positive control. The nanoparticles showed stronger effect on the reduction of the transepithelial electrical resistance (TEER of Caco-2 cell monolayer by opening the tight junctions. According to apparent permeability coefficient (Papp results, the DTX-loaded NPs showed more specific permeation across the Caco-2 cell monolayer in comparison to the DTX. In conclusion, the nanoparticles prepared in this study showed promising results for the development of an oral drug delivery system for anticancer drugs.

  16. Preparation and characterization of polymer nanocomposites coated magnetic nanoparticles for drug delivery applications

    Science.gov (United States)

    Prabha, G.; Raj, V.

    2016-06-01

    In the present research work, the anticancer drug 'curcumin' is loaded with Chitosan (CS)-polyethylene glycol (PEG)-polyvinylpyrrolidone (PVP) (CS-PEG-PVP) polymer nanocomposites coated with superparamagnetic iron oxide (Fe3O4) nanoparticles. The system can be used for targeted and controlled drug delivery of anticancer drugs with reduced side effects and greater efficiency. The prepared nanoparticles were characterized by Fourier transmission infrared spectroscopy (FTIR), vibrating sample magnetometry (VSM), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Curcumin drug loaded Fe3O4-CS, Fe3O4-CS-PEG and Fe3O4-CS-PEG-PVP nanoparticles exhibited the mean particle size in the range of 183-390 nm with a zeta potential value of 26-41 mV as measured using Malvern Zetasizer. The encapsulation efficiency, loading capacity and in-vitro drug release behavior of curcumin drug loaded Fe3O4-CS, Fe3O4-CS-PEG and Fe3O4-CS-PEG-PVP nanoparticles were studied using UV spectrophotometer. Besides, the cytotoxicity of the prepared nanoparticles using MTT assay was also studied. The curcumin drug release was examined at different pH medium and it was proved that the drug release depends upon the pH medium in addition to the nature of matrix.

  17. A convenient method to prepare emulsified polyacrylate nanoparticles from powders [corrected] for drug delivery applications.

    Science.gov (United States)

    Garay-Jimenez, Julio C; Turos, Edward

    2011-08-01

    We describe a method to obtain purified, polyacrylate nanoparticles in a homogeneous powdered form that can be readily reconstituted in aqueous media for in vivo applications. Polyacrylate-based nanoparticles can be easily prepared by emulsion polymerization using a 7:3 mixture of butyl acrylate and styrene in water containing sodium dodecyl sulfate as a surfactant and potassium persulfate as a water-soluble radical initiator. The resulting emulsions contain nanoparticles measuring 40-50 nm in diameter with uniform morphology, and can be purified by centrifugation and dialysis to remove larger coagulants as well as residual surfactant and monomers associated with toxicity. These purified emulsions can be lyophilized in the presence of maltose (a non-toxic cryoprotectant) to provide a homogeneous dried powder, which can be reconstituted as an emulsion by addition of an aqueous diluent. Dynamic light scattering and microbiological experiments were carried out on the reconstituted nanoparticles. This procedure allows for ready preparation of nanoparticle emulsions for drug delivery applications.

  18. Tailored antireflective biomimetic nanostructures for UV applications

    Energy Technology Data Exchange (ETDEWEB)

    Morhard, Christoph; Pacholski, Claudia; Spatz, Joachim P [Department of New Materials and Biosystems, Max Planck Institute for Metals Research, Heisenbergstrasse 3, D-70569 Stuttgart (Germany); Lehr, Dennis; Brunner, Robert; Helgert, Michael [Carl Zeiss Jena GmbH, Technology Center, Carl-Zeiss-Promenade 10, D-07745 Jena (Germany); Sundermann, Michael, E-mail: Pacholski@mf.mpg.de [Carl Zeiss Jena GmbH, Technology Center, Carl-Zeiss-Strasse 56, D-73447 Oberkochen (Germany)

    2010-10-22

    Antireflective surfaces composed of biomimetic sub-wavelength structures that employ the 'moth eye principle' for reflectance reduction are highly desirable in many optical applications such as solar cells, photodetectors and laser optics. We report an efficient approach for the fabrication of antireflective surfaces based on a two-step process consisting of gold nanoparticle mask generation by micellar block copolymer nanolithography and a multi-step reactive ion etching process. Depending on the RIE process parameters nanostructured surfaces with tailored antireflective properties can easily be fabricated that show optimum performance for specific applications.

  19. Structural and optical properties of silicon nanoparticles prepared by pulsed laser ablation in hydrogen background gas

    Science.gov (United States)

    Makino, T.; Inada, M.; Yoshida, K.; Umezu, I.; Sugimura, A.

    We studied the structural and optical properties of silicon (Si) nanoparticles (np-Si) prepared by pulsed laser ablation (PLA) in hydrogen (H2) background gas. The mean diameter of the np-Si was estimated to be approximately 5 nm. The infrared absorption corresponding to Si-Hn (n=1,2,3) bonds was observed at around 2100 cm-1, and a Raman scattering peak corresponding to crystalline Si was observed at around 520 cm-1. These results indicate that nanoparticles are not an alloy of Si and hydrogen but Si nanocrystal covered by hydrogen or hydrogenated silicon. This means that surface passivated Si nanoparticles can be prepared by PLA in H2 gas. The band-gap energy of np-Si prepared in H2 gas (1.9 eV) was larger than that of np-Si prepared in He gas (1.6 eV) even though they are almost the same diameter. After decreasing the hydrogen content in np-Si by thermal annealing, the band-gap energy decreased, and reached the same energy level as np-Si prepared in He gas. Thus, the optical properties of np-Si were affected by the hydrogenation of the surface of np-Si.

  20. Biomimetics: process, tools and practice.

    Science.gov (United States)

    Fayemi, P E; Wanieck, K; Zollfrank, C; Maranzana, N; Aoussat, A

    2017-01-23

    Biomimetics applies principles and strategies abstracted from biological systems to engineering and technological design. With a huge potential for innovation, biomimetics could evolve into a key process in businesses. Yet challenges remain within the process of biomimetics, especially from the perspective of potential users. We work to clarify the understanding of the process of biomimetics. Therefore, we briefly summarize the terminology of biomimetics and bioinspiration. The implementation of biomimetics requires a stated process. Therefore, we present a model of the problem-driven process of biomimetics that can be used for problem-solving activity. The process of biomimetics can be facilitated by existing tools and creative methods. We mapped a set of tools to the biomimetic process model and set up assessment sheets to evaluate the theoretical and practical value of these tools. We analyzed the tools in interdisciplinary research workshops and present the characteristics of the tools. We also present the attempt of a utility tree which, once finalized, could be used to guide users through the process by choosing appropriate tools respective to their own expertize. The aim of this paper is to foster the dialogue and facilitate a closer collaboration within the field of biomimetics.

  1. Poly(vinylpyrrolidone)/silver nanoparticles: preparation and characterization; Nanoparticulas de prata/poli(vinilpirrolidona): obtencao e caracterizacao

    Energy Technology Data Exchange (ETDEWEB)

    Andrade, P.F.; Goncalves, M.C. [Instituto de Quimica - UNICAMP, Campinas, SP (Brazil)], e-mail: patandrade@iqm.unicamp.br

    2010-07-01

    In this work silver nanoparticles were prepared by chemical reduction method using PVP as dispersant agent. The formation of silver nanoparticles was investigated by UV-vis optical spectroscopy and X-ray diffraction. FT-IR spectroscopy confirmed the formation of Ag/PVP complex. The transmission electron microscopy images indicated that the concentration of Ag{sup +} precursor influenced the nanoparticles dispersion and size distribution significantly. The results indicated that dispersed nanoparticles with uniform size distribution can be prepared by this methodology to obtain polymeric nano composites. (author)

  2. Studies of poly-L-lysine-starch nanoparticle preparation and its application as gene carrier

    Institute of Scientific and Technical Information of China (English)

    XIAO; Suyao; LIU; Xuanming; TONG; Chunyi; LIU; Jun; TANG; D

    2005-01-01

    Anion starch nanoparticle (StNP) with a diameter of 50 nm was prepared in water-in-oil microemulsion, with soluble starch as raw materials and POCl3 as crosslinking agent. PLL-StNP was prepared by linking poly-L-lysine (PLL) on the surface of StNP. At the same time, the size of PLL-StNP and its stability in aqueous solution were checked by AFM. The analysis of plasmid DNA binding, DNase I enzymatic degradation, toxicity and transfection were done. We discovered that PLL-StNP may be used as non-virus nanoparticle gene carrier. And we developed the method of preparing PLL-StNP gene carrier and used it in cell transfection. As non-virus gene carrier, PLL-StNP has some advantages, such as large load of DNA, high transfection efficiency, low cell toxicity and biodegradability.

  3. Preparation and characterization of n-dodecyl-ferulate-loaded solid lipid nanoparticles (SLN).

    Science.gov (United States)

    Souto, E B; Anselmi, C; Centini, M; Müller, R H

    2005-05-13

    Solid lipid nanoparticles (SLN) containing a novel potential sunscreen n-dodecyl-ferulate (ester of ferulic acid) were developed. The preparation and stability parameters of n-dodecyl-ferulate-loaded SLN have been investigated concerning particle size, surface electrical charge (zeta potential) and matrix crystallinity. The chemical stability of n-dodecyl-ferulate at high temperatures was also assessed by thermal gravimetry analysis. For the selection of the appropriated lipid matrix, chemically different lipids were melted with 4% (m/m) of active and lipid nanoparticles were prepared by the so-called high pressure homogenization technique. n-Dodecyl-ferulate-loaded SLN prepared with cetyl palmitate showed the lowest mean particle size and polydispersity index, as well as the highest physical stability during storage time of 21 days at 4, 20 and 40 degrees C. These colloidal dispersions containing the sunscreen also exhibited the common melting behaviour of aqueous SLN dispersions.

  4. Titanium dioxide nanoparticles prepared by laser pyrolysis: Synthesis and photocatalytic properties

    Science.gov (United States)

    Figgemeier, E.; Kylberg, W.; Constable, E.; Scarisoreanu, M.; Alexandrescu, R.; Morjan, I.; Soare, I.; Birjega, R.; Popovici, E.; Fleaca, C.; Gavrila-Florescu, L.; Prodan, G.

    2007-12-01

    TiO 2 nanoparticles were synthesized via the laser pyrolysis of titanium tetrachloride-based gas-phase mixtures. In the obtained nanopowders, a mixture of anatase and rutile phases with mean particle size of about 14 nm was identified. Using the thermal heated laser nanopowders, mechanically stable films were produced by immobilizing titania nanopowders on glass substrates (the doctor blading method followed by compression). The photocatalytic activity of the prepared films was tested by the degradation of 4-chlorophenol in an aqueous solution under UV-illumination. By referring to known commercial samples (Degussa P25) similarly prepared, higher photocatalytic efficiency was found for the laser-prepared samples.

  5. Preparation, stability and two-dimensional ordered arrangement of gold nanoparticles capped by surfactants with different chain lengths

    Institute of Scientific and Technical Information of China (English)

    周学华; 李津如; 刘春艳; 江龙

    2002-01-01

    Gold nanoparticles modified with C10NH2, C12NH2, C16NH2 and C18NH2 respectively have been prepared by the reverse micelle method. Nanoparticles stability and their two-dimensional (2D) ordered arrangement were studied by UV-Vis absorption spectra and LB technique. The factors, such as the chain length and the size distribution of particles, which affect the 2D ordered arrangement formation, are discussed. Experimental results show that the longer the chain length of surfactants capping the gold nanoparticles, the more stable the nanoparticles, and the more ordered 2D arrangement of gold nanoparticles.

  6. Preparation and Comparison of Chitosan Nanoparticles with Different Degrees of Glutathione Thiolation

    Directory of Open Access Journals (Sweden)

    R Dinarvand

    2011-12-01

    Full Text Available Background: Chitosan has gained considerable attentions as a biocompatible carrier to improve delivery of active agents. Application of this vehicle in the form of nanoparticle could profit advantages of nanotechnology to increase efficacy of active agents. The purpose of this study was to provide detailed information about chitosan-glutathione (Cht-GSHnanoparticles which are gaining popularity because of their high mucoadhesive and extended drug release properties. Methods: Depolymerization of chitosan was carried out using sodium nitrite method.Glutathione was covalently attached to chitosan and the solubility of the resulting conjugates was evaluated. Nanoparticles were prepared by ionic gelation method and then the effect of glutathione immobilization on properties of nanoparticles was investigated. Results: Thiolation efficiency was higher in lower molecular weight chitosan polymers compared to unmodified chitosan nanoparticles. Cht-GSH conjugates of the same molecular weight but with different degrees of thiolation had the same hydrodynamic diameter (995± nm and surface charge (102± mV as unmodified chitosan, but comprised of a denser network structure and lower concentration. Cht-GSH nanoparticles also exhibited greater mucoadhesive strength which was less affected by ionic strength and pH of the environment. Conclusion:Thiolation improves the solubility of chitosan without any significant changes in size and charge of nanoparticles, but affects the nanogel structure.

  7. Preparation and in vitro-in vivo evaluation of salmon calcitonin-loaded polymeric nanoparticles.

    Science.gov (United States)

    Glowka, Eliza; Sapin-Minet, Anne; Leroy, Pierre; Lulek, Janina; Maincent, Philippe

    2010-01-01

    The aim of the study was to develop and characterize polymeric nanoparticles as a sustained release system for salmon calcitonin (sCT). Nanoparticles were prepared by a double emulsion solvent evaporation method using Eudragit RS and two types of a biodegradable poly(lactic-co-glycolic) copolymer (PLGA). It was demonstrated that sCT was incorporated into nanoparticles with encapsulation efficiencies in the range 69-83%. In vitro release studies, unconventionally conducted in 5% acetic acid, showed great differences in sCT release time profiles. Nanoparticles with fast release profile (Eudragit RS, PLGA/Eudragit RS) released 80-100% of the encapsulated drug within a few hours. In contrast, the sCT release from pure PLGA nanoparticles was very slow, incomplete and reached only 20% after 4 weeks. In vivo study, conducted in Wistar rats, proved that elevated serum sCT levels could be sustained for 3 days after subcutaneous administration of PLGA nanoparticles and the achieved bioavailability was increased compared to sCT solution.

  8. Preparation and evaluation of oleoyl-carboxymethy-chitosan (OCMCS) nanoparticles as oral protein carriers.

    Science.gov (United States)

    Liu, Ya; Cheng, Xiao Jie; Dang, Qi Feng; Ma, Fang Kui; Chen, Xi Guang; Park, Hyun Jin; Kim, Bum Keun

    2012-02-01

    Oleoyl-carboxymethy chitosan (OCMCS) nanoparticles based on chitosan with different molecular weights (50, 170 and 820 kDa) were prepared by self-assembled method. The nanoparticles had spherical shape, positive surface charges and the mean diameters were 157.4, 274.1 and 396.7 nm, respectively. FITC-labeled OCMCS nanoparticles were internalized via the intestinal mucosa and observed in liver, spleen, intestine and heart following oral deliverance to carps (Cyprinus carpio). Extracellular products (ECPs) of Aeromonas hydrophila as microbial antigen was efficiently loaded to form OCMCS-ECPs nanoparticles and shown to be sustained release in PBS. Significantly higher (P < 0.05) antigen-specific antibodies were detected in serum after orally immunized with OCMCS-ECPs nanoparticles than that immunized with ECPs alone and non-immunized in control group in carps. These results implied that amphiphilic modified chitosan nanoparticles had great potential to be applied as carriers for the oral administration of protein drugs.

  9. Preparation of porous polymer monoliths featuring enhanced surface coverage with gold nanoparticles

    KAUST Repository

    Lv, Yongqin

    2012-10-01

    A new approach to the preparation of porous polymer monoliths with enhanced coverage of pore surface with gold nanoparticles has been developed. First, a generic poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith was reacted with cystamine followed by the cleavage of its disulfide bonds with tris(2-carboxylethyl)phosphine, which liberated the desired thiol groups. Dispersions of gold nanoparticles with sizes varying from 5 to 40. nm were then pumped through the functionalized monoliths. The materials were then analyzed using both energy dispersive X-ray spectroscopy and thermogravimetric analysis. We found that the quantity of attached gold was dependent on the size of nanoparticles, with the maximum attachment of more than 60. wt% being achieved with 40. nm nanoparticles. Scanning electron micrographs of the cross sections of all the monoliths revealed the formation of a non-aggregated, homogenous monolayer of nanoparticles. The surface of the bound gold was functionalized with 1-octanethiol and 1-octadecanethiol, and these monolithic columns were used successfully for the separations of proteins in reversed phase mode. The best separations were obtained using monoliths modified with 15, 20, and 30. nm nanoparticles since these sizes produced the most dense coverage of pore surface with gold. © 2012 Elsevier B.V.

  10. Catalase-only nanoparticles prepared by shear alone: Characteristics, activity and stability evaluation.

    Science.gov (United States)

    Huang, Xiao-Nan; Du, Xin-Ying; Xing, Jin-Feng; Ge, Zhi-Qiang

    2016-09-01

    Catalase is a promising therapeutic enzyme; however, it carries risks of inactivation and rapid degradation when it is used in practical bioprocess, such as delivery in vivo. To overcome the issue, we made catalase-only nanoparticles using shear stress alone at a moderate shear rate of 217s(-1) in a coaxial cylinder flow cell. Properties of nanoparticles, including particle size, polydispersity index and zeta potential, were characterized. The conformational changes of pre- and post-sheared catalase were determined using spectroscopy techniques. The results indicated that the conformational changes of catalase and reduction in α-helical content caused by shear alone were less significant than that by desolvation method. Catalase-only nanoparticles prepared by single shear retained over 90% of its initial activity when compared with the native catalase. Catalase nanoparticles lost only 20% of the activity when stored in phosphate buffer solution for 72h at 4°C, whereas native catalase lost 53% under the same condition. Especially, the activity of nanogranulated catalase was decreased only slightly in the simulated intestinal fluid containing α-chymotrypsin during 4h incubation at 37°C, implying that the catalase nanoparticle was more resistant to the degradation of proteases than native catalase molecules. Overall, catalase-only nanoparticles offered a great potential to stabilize enzymes for various pharmaceutical applications.

  11. Cationic Albumin Nanoparticles for Enhanced Drug Delivery to Treat Breast Cancer: Preparation and In Vitro Assessment

    Directory of Open Access Journals (Sweden)

    Sana Abbasi

    2012-01-01

    Full Text Available Most anticancer drugs are greatly limited by the serious side effects that they cause. Doxorubicin (DOX is an antineoplastic agent, commonly used against breast cancer. However, it may lead to irreversible cardiotoxicity, which could even result in congestive heart failure. In order to avoid these harmful side effects to the patients and to improve the therapeutic efficacy of doxorubicin, we developed DOX-loaded polyethylenimine- (PEI- enhanced human serum albumin (HSA nanoparticles. The formed nanoparticles were ~137 nm in size with a surface zeta potential of ~+15 mV, prepared using 20 μg of PEI added per mg of HSA. Cytotoxicity was not observed with empty PEI-enhanced HSA nanoparticles, formed with low-molecular weight (25 kDa PEI, indicating biocompatibility and safety of the nanoparticle formulation. Under optimized transfection conditions, approximately 80% of cells were transfected with HSA nanoparticles containing tetramethylrhodamine-conjugated bovine serum albumin. Conclusively, PEI-enhanced HSA nanoparticles show potential for developing into an effective carrier for anticancer drugs.

  12. Homogeneous nanoparticle dispersion prepared with impurity-free dispersant by the ball mill technique

    Institute of Scientific and Technical Information of China (English)

    Lingyun Zhou; Hui Zhang; Hui Zhang; Zhong Zhang

    2013-01-01

    The homogeneous dispersion of nanoparticles in solvents or polymer matrices is essential tor prac tical application of nanocomposites.In this study,the planetary ball milling technique was used to de-agglomerate silica nanoparticles in butyl acetate.The size of the nanosilica aggregates was evaluated by TEM and SEM.With the addition of polyacrylate polymer to the organic solvent,the nanoparticle agglomerates were effectively broken up by planetary ball milling at the proper milling time; however,re-agglomeration occurred after a longer milling time.The results of TGA and FTIR indicated that the polyacrylate molecules could be adsorbed in situ onto the nanoparticles.Behaving similar to a dispersant,the adsorbed polyacrylate reduced the blend viscosity significantly and prevented re-agglomeration of the nanoparticles.Utilizing the polyacrylate polymer both as the dispersant and the polymer matrix,the polyacrylate-based nanocoatings were further prepared.The optical transmittance and haze value of the nanocoatings were found to be sensitive to the dispersion level of the nanoparticles,and the elastic modulus and hardness of the nanocoatings were improved in comparison with those of the neat polymer coating.

  13. Surface-Enhanced Raman Scattering Study of Silver Nanoparticles Prepared by Using MC as a Template

    Directory of Open Access Journals (Sweden)

    Yudong Lu

    2013-01-01

    Full Text Available A good Ag-based SERS substrate has been prepared by one-pot reaction using methyl cellulose as a template. Effects of methyl cellulose concentration, silver ammonia chloride solution concentration, reaction duration, and reducing agent on silver nanoparticles were discussed in this paper. The performance of the obtained Ag nanoparticles was characterized by UV-visible spectroscopy, transmission electron microscopy, and surface-enhanced Raman spectroscopy. Results show that the reducing agent plays a crucial role in the performance of silver nanoparticles. Optimum preparation conditions of synthesis of SERS substrates were as follows: 10 mM silver ammonia chloride and 0.2% MC at 75°C, reducing in 0.2% reducing agent at 120 min. TEM studies reveal that particles are mostly spherical and rod in shape with an average size of 80 nm. Silver nanoparticles prepared with MC as a template have been shown to provide strong SERS enhancement signals of R6G, which can be used as a good Ag-based SERS substrate in the analytical environment for routine measurements.

  14. Preparation of albumin based nanoparticles for delivery of fisetin and evaluation of its cytotoxic activity.

    Science.gov (United States)

    Ghosh, Pooja; Singha Roy, Atanu; Chaudhury, Susmitnarayan; Jana, Saikat Kumar; Chaudhury, Koel; Dasgupta, Swagata

    2016-05-01

    Fisetin is a well known flavonoid that shows several properties such as antioxidant, antiviral and anticancer activities. Its use in the pharmaceutical field is limited due to its poor aqueous solubility which results in poor bioavailability and poor permeability. The aim of our present study is to prepare fisetin loaded human serum albumin nanoparticles to improve its bioavailability. The nanoparticles were prepared by a desolvation method and characterized by spectroscopic and microscopic techniques. The particles were smooth and spherical in nature with an average size of 220 ± 8 nm. The encapsulation efficiency was found to be 84%. The in vitro release profile showed a biphasic pattern and the release rate increases with increase in ionic strength of solution. We have also confirmed the antioxidant activity of the prepared nanoparticles by a DPPH (2,2-diphenyl-1-picrylhydrazyl) assay. Further its anticancer activity was evaluated using MCF-7 breast cancer cell lines. Our findings suggest that fisetin loaded HSA nanoparticles could be used to transfer fisetin to target areas under specific conditions and thus may find use as a delivery vehicle for the flavonoid.

  15. Practical preparation procedures for docetaxel-loaded nanoparticles using polylactic acid-co-glycolic acid

    Directory of Open Access Journals (Sweden)

    Keum CG

    2011-10-01

    Full Text Available Chang-Gu Keum1*, Young-Wook Noh1*, Jong-Suep Baek1, Ji-Ho Lim1, Chan-Ju Hwang1, Young-Guk Na1, Sang-Chul Shin2, Cheong-Weon Cho11College of Pharmacy and Institute of Drug Research and Development, Chungnam National University, Gungdong, Yuseonggu, Daejeon, South Korea; 2College of Pharmacy, Chonnam National University, Yongbongdong, Buggu, Gwangju, South Korea *These authors contributed equally to this work Background: Nanoparticles fabricated from the biodegradable and biocompatible polymer, polylactic-co-glycolic acid (PLGA, are the most intensively investigated polymers for drug delivery systems. The objective of this study was to explore fully the development of a PLGA nanoparticle drug delivery system for alternative preparation of a commercial formulation. In our nanoparticle fabrication, our purpose was to compare various preparation parameters. Methods: Docetaxel-loaded PLGA nanoparticles were prepared by a single emulsion technique and solvent evaporation. The nanoparticles were characterized by various techniques, including scanning electron microscopy for surface morphology, dynamic light scattering for size and zeta potential, x-ray photoelectron spectroscopy for surface chemistry, and high-performance liquid chromatography for in vitro drug release kinetics. To obtain a smaller particle, 0.2% polyvinyl alcohol, 0.03% D-α-tocopheryl polyethylene glycol 1000 succinate (TPGS, 2% Poloxamer 188, a five-minute sonication time, 130 W sonication power, evaporation with magnetic stirring, and centrifugation at 8000 rpm were selected. To increase encapsulation efficiency in the nanoparticles, certain factors were varied, ie, 2–5 minutes of sonication time, 70–130 W sonication power, and 5–25 mg drug loading. Results: A five-minute sonication time, 130 W sonication power, and a 10 mg drug loading amount were selected. Under these conditions, the nanoparticles reached over 90% encapsulation efficiency. Release kinetics showed that 20

  16. Preparation of ITO Nanoparticles by Liquid Phase Coprecipitation Method

    Directory of Open Access Journals (Sweden)

    Zhanlai Ding

    2010-01-01

    Full Text Available The nanoscale indium tin oxide (ITO particles are synthesied by liquid phase coprecipitation method under given conditions with solution of indium chloride, tin chloride, and ammonia. The absolute ethyl alcohol or deionized water was used as solvent and the dodecylamine or hexadecylamine surfactant was used as a dispersant in the reaction system. The sample powder was characterized by X-ray diffraction (XRD, transmission electron microscopy (TEM, and high-resolution electron microscopy (HRTEM. Based on the transmission electron micrograph, the influences of the two different solvents and the two different dispersants on the nanoparticle size and dispersion were studied, respectively. The results showed that the ITO particles are finely crystallized body-centered cubic structure. The particle size has distributed in 30 nm to 90 nm.

  17. Mechanochemical Preparation of Cobalt Nanoparticles through a Novel Intramolecular Reaction in Cobalt(II) Complexes

    OpenAIRE

    2015-01-01

    A novel solid state reaction involving a series of cobalt(II) hydrazine-azides has been used to prepare metallic cobalt nanoparticles. The reactions of [Co(N2H4)(N3)2], [Co(N2H4)2(N3)2], and [Co(N2H4)(N3)Cl]·H2O via NaOH, KOH as reactants were carried out in the solid state. These complexes undergo an intramolecular two-electron oxidation-reduction reaction at room temperature, producing metallic cobalt nanoparticles (Co1–Co6). The aforementioned complexes contain cobalt(II) that is an oxidiz...

  18. Preparation of dextran immunological magnetic nanoparticles and their application to combined targeting carrier

    Institute of Scientific and Technical Information of China (English)

    李民勤; 徐慧显; 左榘; 姬昂; 何炳林; 庞雁; 黄建英; 牛瑞芳

    1996-01-01

    Superparamagnetic dextran nanoparticles were prepared by coprecipitation. Effects of concentration of dextran, amount of ironic salts, stirring speed, concentration of ammonium hydroxide and mole ratio of Fe3+/Fe2+ on the effective diameter of dextran magnetic nanopartides (DMNP) were studied. Dextran immunological magnetic nanoparticles (DIMNP) were formed by the reaction of the monoclonal anti-human mammary cancer antibody with DMNP oxidized by sodium periodate, and the properties of magnetic susceptibility, shape and retention of antibody activity were investigated. The in vitro cancer antigen binding ability of DIMNP was demonstrated by radioimmunoassay, and the in vivo magnetic localization and antibody targeting ability of radiolabeled DIMNP were studied.

  19. PREPARATION,COMPLEX MECHANISM AND STRUCTURE MODEL OF METALLOPHTHALOC- YANINE-Fe3O4 NANOPARTICLES COMPOSITE

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    MPc-Fe3O4-nanoparticles composite(M=Co, Cu, Ni, Mn) have been prepared and the factors that influence their mean size have been studied. The mean size of the nanoparticles composite increase with the increase of complex temperature. The interaction of MPc with Fe3O4 nanoparticles has been studied. There are M-O covalent bonding and ionic bonding between MPc and Fe3O4 nanoparticles. The intensities of M-O bonding and ionic bonding are in vestigated .The complex mechanism of MPc with Fe3O4 nanoparticles have been studied. First, there are complex between MPc and all Fe3O4 nanoparticles. Then, Fe3O4 nanoparticles accumulate together to form the accumulators, MPc have the function of cohering Fe3O4 nanoparticles. A considerable number of MPc combine with Fe3O4 nanoparticles on the surface of the accumulators to form MPc-Fe3O4 nanoparticles composite. All the above proesses take place spontaneously. The structure model of MPc-Fe3O4 nanoparticles composite has also been investigated. Inside the MPc-Fe3O4 nanoparticles composite, Fe3O4 nanoparticles accumulate together without order, on the surface of the composite, MPc form molecular dispersion layer. The threshold of molecular dispersion layer are also investigated.

  20. Nanostructures of functionalized gold nanoparticles prepared by particle lithography with organosilanes.

    Science.gov (United States)

    Lusker, Kathie L; Li, Jie-Ren; Garno, Jayne C

    2011-11-01

    Periodic arrays of organosilane nanostructures were prepared with particle lithography to define sites for selective adsorption of functionalized gold nanoparticles. Essentially, the approach for nanoparticle lithography consists of procedures with two masks. First, latex mesospheres were used as a surface mask for deposition of an organosilane vapor, to produce an array of holes within a covalently bonded, organic thin film. The latex particles were readily removed with solvent rinses to expose discrete patterns of nanosized holes of uncovered substrate. The nanostructured film of organosilanes was then used as a surface mask for a second patterning step, with immersion in a solution of functionalized nanoparticles. Patterned substrates were fully submerged in a solution of surface-active gold nanoparticles coated with 3-mercaptopropyltrimethoxysilane. Regularly shaped, nanoscopic areas of bare substrate produced by removal of the latex mask provided sites to bind silanol-terminated gold nanoparticles, and the methyl-terminated areas of the organosilane film served as an effective resist, preventing nonspecific adsorption on masked areas. Characterizations with atomic force microscopy demonstrate the steps for lithography with organosilanes and functionalized nanoparticles. Patterning was accomplished for both silicon and glass substrates, to generate nanostructures with periodicities of 200-300 nm that match the diameters of the latex mesospheres of the surface masks. Nanoparticles were shown to bind selectively to uncovered, exposed areas of the substrate and did not attach to the methyl-terminal groups of the organosilane mask. Billions of well-defined nanostructures of nanoparticles can be generated using this high-throughput approach of particle lithography, with exquisite control of surface density and periodicity at the nanoscale.

  1. Biomimetic mineral coatings in dental and orthopaedic implantology

    Institute of Scientific and Technical Information of China (English)

    Yue-lian LIU; Klaas de GROOT; Ernst B.HUNZIKER

    2009-01-01

    Biomimetic techniques are used to deposit coatings of calcium phosphate upon medical devices. The procedure is conducted under near-physiological, or "biomimetic", conditions of temperature and pH primarily to improve their biocompatibility and biodegradability of the materials. The inorganic layers genelated by biomi-metic methods resemble bone mineral, and can be degraded within a biological milieu.The biomimetic coating technique involves the nuclea-tion and growth of bone-like crystals upon a pretreated substrate by immersing this in a supersaturated solution of calcium phosphate under physiological conditions of temperature (37~C) and pH (7.4). The method, originally developed by Kokubo in 1990, has since undergone improvement and refinement by several groups of investigators.Biomimetic coatings are valuable in that they can serve as a vehicle for the slow and sustained release of osteogenic agents at the site of implantation. This attribute is rendered possible by the near-physiological conditions under which these coatings are prepared, which permits an incorporation of binactive agents into the inorganic crystal latticework rather than their nlere superficial adsorption onto preformed layers. In addition, the biomimetic coating technique can be applied to implants of an organic as well as of an inorganic nature and to those with irregular surface geometries, which is not possible using conventional methodologies.

  2. Multi criteria decision making to select the suitable method for the preparation of nanoparticles using an analytical hierarchy process.

    Science.gov (United States)

    Velmurugan, R; Selvamuthukumar, S; Manavalan, R

    2011-11-01

    Selecting the right method for the preparation of nanoparticles is a crucial decision. A wrong decision can result in the product having to be formulated and developed again. One tool that can be useful in determining the most appropriate method is the Analytical Hierarchy Process (AHP). AHP has been employed in almost all areas related to decision-making problems. In this paper, the results of a case study illustrate that the AHP concept can assist designers in the effective evaluation of various methods available for the preparation of nanoparticles. This paper presents the methodology of selecting the most suitable method for preparing nanoparticles using the analytical hierarchy process.

  3. The Preparation and Biocompatibility Study on Fe2O3 Magnetic Nanoparticles Used in Tumor Hyperthermia

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Objective:To evaluate the in vitro and in vivo toxicity of self-prepared nanosized Fe2 O3, which has the potential implication in tumor hyperthermia. Methods:Fe2O3 nanoparticles were prepared by improving co-precipitation, which characterization was detected by TEM, XRD, CMIAS, EDS. MTT assay was used to evaluate the in vitro cytotoxicity test; hemolytic test was carried out to estimate whether it has blood toxicity;Fe2O3 suspended in sterile 0.9% NaCl was intraperitoneally injected into Kunming mouse to calculate the LD50; micronucleus (MN) were reckoned to identify whether it is genotoxic. Results :The nanoparticles are brown spherical particles with diameter ranging from 8 to 15 nm, which have good decentralization and stability. The experiments also showed that the toxicity of the material on mouse fibroblast (L-929) cell lines was 0 - 1 degree; it has no hemolysis activity; LD50 arrived at 5.45 g/kg-1 after intraperitoneal injection of 1 ml suspension; micronucleus test showed that it has no genotoxic effects either. Conclusion:The results showed that the Fe2O3 nanoparticles are prepared successfully, the self-prepared nanosized Fe2O3 is a kind of high biocompatibility materials and perhaps it is suitable for further application in tumor hyperthermia.

  4. Biomimetic Membrane Arrays on Cast Hydrogel Supports

    DEFF Research Database (Denmark)

    Roerdink-Lander, Monique; Ibragimova, Sania; Rein Hansen, Christian;

    2011-01-01

    Lipid bilayers are intrinsically fragile and require mechanical support in technical applications based on biomimetic membranes. Tethering the lipid bilayer membranes to solid substrates, either directly through covalent or ionic substrate−lipid links or indirectly on substrate-supported cushions......, provides mechanical support but at the cost of small molecule transport through the membrane−support sandwich. To stabilize biomimetic membranes while allowing transport through a membrane−support sandwich, we have investigated the feasibility of using an ethylene tetrafluoroethylene (ETFE......)/hydrogel sandwich as the support. The sandwich is realized as a perforated surface-treated ETFE film onto which a hydrogel composite support structure is cast. We report a simple method to prepare arrays of lipid bilayer membranes with low intrinsic electrical conductance on the highly permeable, self...

  5. Green Tribology Biomimetics, Energy Conservation and Sustainability

    CERN Document Server

    Bhushan, Bharat

    2012-01-01

    Tribology is the study of friction, wear and lubrication. Recently, the concept of “green tribology” as “the science and technology of the tribological aspects of ecological balance and of environmental and biological impacts” was introduced. The field of green tribology includes tribological technology that mimics living nature (biomimetic surfaces) and thus is expected to be environmentally friendly, the control of friction and wear that is of importance for energy conservation and conversion, environmental aspects of lubrication and surface modification techniques, and tribological aspects of green applications such as wind-power turbines or solar panels. This book is the first comprehensive volume on green tribology. The chapters are prepared by leading experts in their fields and cover such topics as biomimetics, environmentally friendly lubrication, tribology of wind turbines and renewable sources of energy, and ecological impact of new technologies of surface treatment.

  6. Green tribology. Biomimetics, energy conservation and sustainability

    Energy Technology Data Exchange (ETDEWEB)

    Nosonovsky, Michael [Wisconsin Univ., Milwaukee, WI (United States). Dept. of Mechanical Engineering; Bhushan, Bharat (eds.) [Ohio State Univ., Columbus, OH (US). Nanoprobe Lab. for Bio- and Nanotechnology and Biomimetics (NLB2)

    2012-07-01

    Tribology is the study of friction, wear and lubrication. Recently, the concept of ''green tribology'' as ''the science and technology of the tribological aspects of ecological balance and of environmental and biological impacts'' was introduced. The field of green tribology includes tribological technology that mimics living nature (biomimetic surfaces) and thus is expected to be environmentally friendly, the control of friction and wear that is of importance for energy conservation and conversion, environmental aspects of lubrication and surface modification techniques, and tribological aspects of green applications such as wind-power turbines or solar panels. This book is the first comprehensive volume on green tribology. The chapters are prepared by leading experts in their fields and cover such topics as biomimetics, environmentally friendly lubrication, tribology of wind turbines and renewable sources of energy, and ecological impact of new technologies of surface treatment. (orig.)

  7. Compaction of Chemically Prepared Amorphous Fe-B nanoparticles

    DEFF Research Database (Denmark)

    Hendriksen, P.V.; Bødker, Franz; Mørup, Steen

    1997-01-01

    We report on attempts to compact chemically prepared amorphous iron-boron particles. The praticles have a size of about 100 nm and are pyrophoric. We have made a special die for uniaxial pressing in which the compaction can be performed at elevated temperature without exposing the powder to air. ....... Densities of up to 75% of that of bulk Fe-B have been obtained. Coercivity measurements show that the material is not magnetically soft....

  8. An experimental assessment of toxic potential of nanoparticle preparation of heavy metals in streptozotocin induced diabetes.

    Science.gov (United States)

    Gandhi, Sonia; Srinivasan, B P; Akarte, Atul Sureshrao

    2013-11-01

    Nanoparticle preparations of heavy metals have attracted enormous scientific and technological interest. Biologically produced nanoparticle preparations of heavy metals are elaborately described in traditional texts and being widely prescribed. The underlying interactions of nano preparations within the physiological fluids are key feature to understand their biological impact. In this perspective, we performed an experimental assessment of the toxicity potential of a marketed metallic preparation named Vasant Kusumakar Ras (VKR), wherein different heavy metals in composite form are reduced to nanoparticle size to produce the desired effect in diabetes and its complications. VKR (50mg/kg) was administered to Albino Wistar rats rendered diabetic using streptozotocin (90mg/kg) in 2 days old neonates. Anti-hyperglycemic effect was observed with VKR along with increased levels of plasma insulin. Renal variables including total proteins and albumin along with glomerular filtration rate were found to improve biochemically. The results were supplemented by effects on different inflammatory and growth factors like TNF-α, nitric oxide, TGF-β and VEGF. However, the results observed in kidney histopathology were not in accordance with the biochemical parameters. Inflammation observed in kidney was confirmed by immunostaining metallothionein, which was due to the accumulation of heavy metals. Furthermore, mercury accumulation in kidney further confirmed by autometallography, which activated mononuclear phagocyte system, which generated an immune response. This was further supported by increase in the extent of apoptosis in kidney tissues. In conclusion, nanoparticle preparations of heavy metals can be toxic to kidney if it is not regulated with respect to its surface chemistry and dosage.

  9. Design, preparation and preliminary use of a novel biomimetic agent rFN/CAD%一种仿生修饰分子rFN/CAD的设计、制备及初步应用

    Institute of Scientific and Technical Information of China (English)

    匡红; 张瑗; 张聪; 贾淑芳; 孙薏; 李静; 呼永河

    2012-01-01

    Objective To prepare a novel biomimetic agent with adhesive and osteoinduction capabilities, and provide a new approach for improving seeding cell adhesion and osteoblastic differentiation on a scaffold surface. Methods A novel bi-functional recombinant protein was engineered and prepared by bioinformatics, standard molecular cloning, protein expression and purification techniques. A centrifugal cell adhesive assay and an osteoinduction assay were employed to determine the biofunction ex vivo. Results A 1954bp long DNA chimera of FN 17-10/CAD11 EC1-2 and recombinant FN 17-10/CAD11 EC1-2 of 641 amino acids were obtained. Polystyrene surface coated with this protein significantly increased the adhesive property and osteodifferentiation of human bone marrow mesenchymal stem cells. Conclusion rFN/CAD possesses dual biofunctions of osteoblastic adhesion and differentiation, which can be further applied as an ideal biomimetic molecule for surface modification.%目的 制备一种具有黏附和成骨双重功能的仿生分子,为种子细胞在支架材料界面的高效黏附和靶向分化提供新途径.方法 筛选纤维连接蛋白和钙黏附蛋白前体分子,通过分子模拟、基因克隆、蛋白表达纯化等技术设计并进行制备.通过离心促黏附实验和成骨诱导分化实验检测其体外活性.结果 成功获得长1954bp的FNⅢ7-10/CAD11 EC1-2重组基因和由641个氨基酸组成的融合蛋白.体外功能研究发现聚苯乙烯表面的融合蛋白涂层可显著提高人骨髓间质干细胞的黏附和成骨分化能力.结论 rFN/CAD具有促黏附和促成骨的双重生物活性,可作为一种理想的仿生修饰分子用于生物界面的构建.

  10. Glycyrrhetinic acid-modified nanoparticles for drug delivery:Preparation and characterization

    Institute of Scientific and Technical Information of China (English)

    TIAN Qin; WANG Wei; HE XiaoTing; ZHU XiaoCui; HUANG Wei; ZHANG ChuangNian; YUAN Zhi; CHEN XueSi

    2009-01-01

    In this work,glycyrrhetinic acid-modified chitosan (mGA-suc-CTS) used as liver targeted carrier for drug delivery,was prepared via hemisuccinate as a bridged group. The structure of the product was confirmed by IR and NMR methods and the degree of substitution (DS) of glycyrrhetinic acid groups was estimated via elemental analysis. Nanoparticles were formed by ionic gelation methold. The drug-loading and release behavior of the nanoparticles were investigated using BSA as the model drug.The results indicated that the carrier with a highest DS of 5.19% could be got and the DS was controlled by changing reaction temperature or feed ratio. BSA could be entrapped into the nanoparticles with the drug-loading ratio of 26.3% and the encapsulation efficiency of 81.5%. A sustained release over an 11-day period was observed in pH 7.4 in vitro.

  11. Preparation and performance of CeO2 hollow spheres and nanoparticles

    Institute of Scientific and Technical Information of China (English)

    ZHANG Wenwen; CHEN Donghui

    2016-01-01

    CeO2 hollow spheres were synthesized by polystryrene sphere (PS) templates and CeO2 nanoparticles were prepared by a facile method. The as-obtained products were characterized by scanning electron microscopy (SEM), N2 adsorption-desorption, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and UV-vis diffuse reflectance spectra. The results showed that the structure of the obtained CeO2 hollow spheres was hollow microsphere with a diameter of 380 nm and the average particle size of CeO2 nanoparticles was about 1700 nm. The two samples' Brunauer-Emmett-Teller (BET) surface area was 67.1 and 37.2 m2/g. The CeO2 hollow spheres had a better performance than nanoparticles at UV-shielding because of higher surface area and the structure of hollow sphere.

  12. Preparation of Hard Coating Films with High Refractive Index from Titania Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Nam Woo; Ahn, Chi Yong; Song, Ki Chang [Konyang University, 121 Daehak-ro, Nonsan (Korea, Republic of)

    2015-12-15

    The titania (TiO{sub 2}) nanoparticles with a diameter 2-3 nm were synthesized by controlling hydrolysis of titanium tetraisopropoxide (TTIP) in acid solution. Organic-inorganic hybrid coating solutions were prepared by reacting the titania nanoparticles with 3-glycidoxypropyl trimethoxysilane (GPTMS) by the sol-gel method. The hard coating films with high refractive index were obtained by curing thermally at 120 .deg. C after spin-coating the coating solutions on the polycarbonate (PC) sheets. The coating films showed high optical transparency of 90% in the visible range and exhibited a pencil hardness of 2H. Also, the refractive index at 633 nm wavelength of coating films enhanced from 1.502 to 1.584 as the weight content of titania nanoparticles in the coating solutions increased from 4% to 25%.

  13. Preparation of bicontinuous mesoporous silica and organosilica materials containing gold nanoparticles by co-synthesis method

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Byunghwan [Korea Institute of Industrial Technology, ChonAn, Korea; Zhu, Haoguo [ORNL; Zhang, Zongtao [ORNL; Overbury, Steven {Steve} H [ORNL; Dai, Sheng [ORNL

    2004-01-01

    Catalytic activities of gold strongly depend on its particle size. It is necessary to have homogeneous distributions of small gold nanoparticles with diameters between 2 and 5 nm for excellent catalytic activities. In this study, gold-containing mesoporous silica materials were prepared by a co-synthesis method. The essence of this sol-gel co-synthesis method is to combine together neutral surfactant template synthesis of mesoporous silica materials with the introduction of metal ions via bifunctional silane ligands, so that the formation of mesostructures and metal-ion doping occur simultaneously. The formation of gold nanoparticles with size less than 5 nm inside mesoporous materials (HMS, MSU, and PMO) has been achieved by this co-synthesis sol-gel process. In addition, the effects of post-treatments, such as calcination and reduction, on pore structures and nanoparticle size distributions were also investigated.

  14. Liquid antisolvent preparation of amorphous cefuroxime axetil nanoparticles in a tube-in-tube microchannel reactor.

    Science.gov (United States)

    Zhu, Wen-Zhen; Wang, Jie-Xin; Shao, Lei; Zhang, Hai-xia; Zhang, Qian-xia; Chen, Jian-Feng

    2010-08-16

    This article presents the preparation of nanoparticles of amorphous cefuroxime axetil (CFA) in a microporous tube-in-tube microchannel reactor (MTMCR). The experimental results indicated that CFA particle with a tunable size of 400-1400 nm could be achieved under a high throughput in the range of 1.5-6L/min. The average particle size decreased with increasing overall volumetric flow rate and decreasing CFA concentration, micropore size, and annular channel width. The produced CFA nanoparticles were characterized by SEM, XRD, FT-IR, DSC and a dissolution test, which indicated that the nanosized CFA was amorphous and exhibited higher dissolution rate compared to the raw CFA. The MTMCR might offer a general and facile pathway for mass production of the nanoparticles of hydrophobic pharmaceuticals thanks to its high throughput capacity and excellent micromixing performance.

  15. A novel route to prepare and characterize Sn-Bi nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Chen Hongjie [Key Laboratory of Special Functional Materials, Henan University, Kaifeng 475001 (China)]. E-mail: chjhenan@yahoo.com.cn; Li Zhiwei [Key Laboratory of Special Functional Materials, Henan University, Kaifeng 475001 (China); Wu Zhishen [Key Laboratory of Special Functional Materials, Henan University, Kaifeng 475001 (China); Zhang Zhijun [Key Laboratory of Special Functional Materials, Henan University, Kaifeng 475001 (China)

    2005-05-17

    A sonochemical method of synthesis for Sn-Bi nanoalloy directly from bulk Sn-Bi alloy is introduced in this paper. The nanoparticles were found to be monodispersed and the size distribution was influenced by the ultrasonic power. The formation and composition of the as-prepared Sn-Bi nanoparticles were revealed by X-ray diffraction (XRD), differential thermal analysis (DTA) and thermogravimetry (TG), transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM). It was found that the Sn-Bi eutectic alloy nanoparticles consisted of the tetragonal phase of tin and the rhombohedral phase of bismuth. In addition, we also found the powder had excellent antiwear properties through tribological test results.

  16. Preparation and Characterization of NiO Nanoparticles by Anodic Arc Plasma Method

    Directory of Open Access Journals (Sweden)

    Hongxia Qiao

    2009-01-01

    Full Text Available NiO nanoparticles with average particle size of 25 nm were successfully prepared by anodic arc plasma method. The composition, morphology, crystal microstructure, specific surface area, infrared spectra, and particle size distribution of product were analyzed by using X-ray diffraction (XRD, transmission electron microscopy (TEM and the corresponding selected area electron diffraction (SAED, Fourier transform infrared (FTIR spectrum, and Brunauer-Emmett-Teller (BET N2 adsorption. The experiment results show that the NiO nanoparticles are bcc structure with spherical shape and well dispersed, the particle size distribution ranging from 15 to 45 nm with the average particle size is about 25 nm, and the specific surface area is 33 m2/g. The infrared absorption band of NiO nanoparticles shows blue shifts compared with that of bulk NiO.

  17. Pt nanoparticles on titania nanotubes prepared by vapor-phase impregnation-decomposition method

    Energy Technology Data Exchange (ETDEWEB)

    Encarnacion Gomez, C. [National Polytechnic Institute, Dept. of Metallurgical Eng., Mexico 07300 DF, AP 75-874 (Mexico); Vargas Garcia, J.R., E-mail: rvargasga@ipn.m [National Polytechnic Institute, Dept. of Metallurgical Eng., Mexico 07300 DF, AP 75-874 (Mexico); Toledo Antonio, J.A.; Cortes Jacome, M.A.; Angeles Chavez, C. [Petroleum Mexican Institute, Eje Central Lazaro Cardenas No. 152, Mexico 07730 DF (Mexico)

    2010-04-16

    Platinum (Pt) nanoparticles were prepared on titania nanotubes (TNTs) by vapor-phase impregnation-decomposition method using platinum acetylacetonate as precursor. TNTs and Pt precursor were mixed in 3:1 weight ratio before vapor-phase impregnation. The mixed powders were heated at 453 K for 10 min to evaporate the precursor in a horizontal tube quartz reactor at a total pressure of 66.6 kPa. Then, the impregnated TNTs were moved to a higher temperature zone (673 K) inside the tube reactor to achieve the precursor decomposition. HAADF-STEM observations, AAS and XPS results revealed that this method allows the formation of uniformly distributed Pt nanoparticles on the surface of TNTs with a narrow distribution of particle size (2.1 nm mean size). Pt nanoparticles remain mainly as Pt{sup 0} oxidation state with a Pt{sup 0}/Pt{sup 2+} atomic ratio of 3.9.

  18. Polymeric Nanoparticles of Brazilian Red Propolis Extract: Preparation, Characterization, Antioxidant and Leishmanicidal Activity.

    Science.gov (United States)

    do Nascimento, Ticiano Gomes; da Silva, Priscilla Fonseca; Azevedo, Lais Farias; da Rocha, Louisianny Guerra; de Moraes Porto, Isabel Cristina Celerino; Lima E Moura, Túlio Flávio Accioly; Basílio-Júnior, Irinaldo Diniz; Grillo, Luciano Aparecido Meireles; Dornelas, Camila Braga; Fonseca, Eduardo Jorge da Silva; de Jesus Oliveira, Eduardo; Zhang, Alex Tong; Watson, David G

    2016-12-01

    The ever-increasing demand for natural products and biotechnology derived from bees and ultra-modernization of various analytical devices has facilitated the rational and planned development of biotechnology products with a focus on human health to treat chronic and neglected diseases. The aim of the present study was to prepare and characterize polymeric nanoparticles loaded with Brazilian red propolis extract and evaluate the cytotoxic activity of "multiple-constituent extract in co-delivery system" for antileishmanial therapies. The polymeric nanoparticles loaded with red propolis extract were prepared with a combination of poly-ε-caprolactone and pluronic using nanoprecipitation method and characterized by different analytical techniques, antioxidant and leishmanicidal assay. The red propolis nanoparticles in aqueous medium presented particle size (200-280 nm) in nanometric scale and zeta analysis (-20 to -26 mV) revealed stability of the nanoparticles without aggregation phenomenon during 1 month. After freeze-drying method using cryoprotectant (sodium starch glycolate), it was possible to observe particles with smooth and spherical shape and apparent size of 200 to 400 nm. Attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and thermal analysis revealed the encapsulation of the flavonoids from the red propolis extract into the polymeric matrix. Ultra performance liquid chromatography coupled with diode array detector (UPLC-DAD) identified the flavonoids liquiritigenin, pinobanksin, isoliquiritigenin, formononetin and biochanin A in ethanolic extract of propolis (EEP) and nanoparticles of red propolis extract (NRPE). The efficiency of encapsulation was determinate, and median values (75.0 %) were calculated using UPLC-DAD. 2,2-Diphenyl-1-picryhydrazyl method showed antioxidant activity to EEP and red propolis nanoparticles. Compared to negative control, EEP and NRPE exhibited leishmanicidal activity with an IC50 value of ≅38

  19. Polymeric Nanoparticles of Brazilian Red Propolis Extract: Preparation, Characterization, Antioxidant and Leishmanicidal Activity

    Science.gov (United States)

    do Nascimento, Ticiano Gomes; da Silva, Priscilla Fonseca; Azevedo, Lais Farias; da Rocha, Louisianny Guerra; de Moraes Porto, Isabel Cristina Celerino; Lima e Moura, Túlio Flávio Accioly; Basílio-Júnior, Irinaldo Diniz; Grillo, Luciano Aparecido Meireles; Dornelas, Camila Braga; Fonseca, Eduardo Jorge da Silva; de Jesus Oliveira, Eduardo; Zhang, Alex Tong; Watson, David G.

    2016-06-01

    The ever-increasing demand for natural products and biotechnology derived from bees and ultra-modernization of various analytical devices has facilitated the rational and planned development of biotechnology products with a focus on human health to treat chronic and neglected diseases. The aim of the present study was to prepare and characterize polymeric nanoparticles loaded with Brazilian red propolis extract and evaluate the cytotoxic activity of "multiple-constituent extract in co-delivery system" for antileishmanial therapies. The polymeric nanoparticles loaded with red propolis extract were prepared with a combination of poly-ɛ-caprolactone and pluronic using nanoprecipitation method and characterized by different analytical techniques, antioxidant and leishmanicidal assay. The red propolis nanoparticles in aqueous medium presented particle size (200-280 nm) in nanometric scale and zeta analysis (-20 to -26 mV) revealed stability of the nanoparticles without aggregation phenomenon during 1 month. After freeze-drying method using cryoprotectant (sodium starch glycolate), it was possible to observe particles with smooth and spherical shape and apparent size of 200 to 400 nm. Attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and thermal analysis revealed the encapsulation of the flavonoids from the red propolis extract into the polymeric matrix. Ultra performance liquid chromatography coupled with diode array detector (UPLC-DAD) identified the flavonoids liquiritigenin, pinobanksin, isoliquiritigenin, formononetin and biochanin A in ethanolic extract of propolis (EEP) and nanoparticles of red propolis extract (NRPE). The efficiency of encapsulation was determinate, and median values (75.0 %) were calculated using UPLC-DAD. 2,2-Diphenyl-1-picryhydrazyl method showed antioxidant activity to EEP and red propolis nanoparticles. Compared to negative control, EEP and NRPE exhibited leishmanicidal activity with an IC50 value of ≅38.0

  20. PREPARATION AND EVALUATION OF MUCOADHESIVE NANOPARTICLE OF AN ANTIHYPERTENSIVE AGENT

    Directory of Open Access Journals (Sweden)

    Vaibhav Shukla

    2012-02-01

    Full Text Available Diltiazem HCl (DTZ is an antihypertensive agent that antagonizes the action of beta-1 receptor. DTZ when given orally is well absorbed from the gastrointestinal tract and is subject to an extensive first-pass effect. DTZ undergoes extensive metabolism in which only 2% to 4% of the unchanged drug appears in the urine. Drugs which induce or inhibit hepatic microsomal enzymes may alter DTZ disposition. It has been reported that the absolute bioavailability of DTZ when given orally is 30-40%. The biological half-life of DTZ is 4-6 hour and the main site of absorption is proximal small intestine.The reduced bioavailability of DTZ may be because of transportation of dosage form from the region of absorption window to site where it is less absorbed. Therefore there was a need to increase gastroretention time of dosage form so that drug would be available at the site of absorption and results in improved bioavailability. A mucoadhesive nanoparticle delivery system was envisioned for DTZ as such a system when administered would adhere on the gastric mucosa for a prolong period of time and the drug would be available at the main site of absorption i.e. proximal small intestine resulting in enhanced bioavailability.

  1. Preparation of fluorescent polyaniline nanoparticles in aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Alves, Kleber G. B. [Universidade Federal de Pernambuco, Departamento de Engenharia Mecanica (Brazil); Melo, Etelino F. de [Universidade Federal de Pernambuco, Departamento de Quimica Fundamental (Brazil); Andrade, Cesar A. S. [Universidade Federal de Pernambuco, Departamento de Bioquimica (Brazil); Melo, Celso P. de, E-mail: celso@df.ufpe.br [Universidade Federal de Pernambuco, Departamento de Fisica (Brazil)

    2013-01-15

    We report the synthesis of stable polyaniline nanoparticles (PANI{sub N}Ps) based on the chemical oxidative polymerization of aniline in aqueous solutions of surfactants. Surfactants of three different types-cationic (dodecyltrimethylammonium bromide-DTAB), anionic (sodium dodecyl sulfate-SDS), and non-ionic (Triton X-405-TX-405)-were used. The resulting PANI{sub N}Ps{sub s}urfactant samples were characterized through UV-Vis, fluorescence and Fourier transform infrared spectroscopies, and scanning electronic microscopy (SEM). We have verified that the color of the PANI{sub N}Ps{sub s}urfactant dispersions is affected by a change in the pH of the solution. The PANI-NPs{sub s}urfactant colloidal suspensions in aqueous solution present a surprising high fluorescence quantum yield value (ranging from 1.9 Multiplication-Sign 10{sup -3} to 6.9 Multiplication-Sign 10{sup -3}) that can be controlled as a function of the pH, a fact that we associate to the corresponding protonation degree of the PANI polymeric chains. We suggest that these fluorescent nanocomposites can find important technological applications in different areas such as organic light emitting devices, biosensors, and pigments for coatings.

  2. Organic/hybrid nanoparticles and single-walled carbon nanotubes: preparation methods and chiral applications.

    Science.gov (United States)

    Alhassen, Haysem; Antony, Vijy; Ghanem, Ashraf; Yajadda, Mir Massoud Aghili; Han, Zhao Jun; Ostrikov, Kostya Ken

    2014-11-01

    Nanoparticles are molecular-sized solids with at least one dimension measuring between 1-100 nm or 10-1000 nm depending on the individual discipline's perspective. They are aggregates of anywhere from a few hundreds to tens of thousands of atoms which render them larger than molecules but smaller than bulk solids. Consequently, they frequently exhibit physical and chemical properties somewhere between. On the other hand, nanocrystals are a special class of nanoparticles which have started gaining attention recently owing to their unique crystalline structures which provide a larger surface area and promising applications including chiral separations. Hybrid nanoparticles are supported by the growing interest of chemists, physicists, and biologists, who are researching to fully exploit them. These materials can be defined as molecular or nano-composites with mixed (organic or bio) and inorganic components, where at least one of the component domain has a dimension ranging from a few Å to several nanometers. Similarly, and due to their extraordinary physical, chemical, and electrical properties, single-walled carbon nanotubes have been the subject of intense research. In this short review, the focus is mainly on the current well-established simple preparation techniques of chiral organic and hybrid nanoparticles as well as single-walled carbon nanotubes and their applications in separation science. Of particular interest, cinchonidine, chitosan, and β-CD-modified gold nanoparticles (GNPs) are discussed as model examples for organic and hybrid nanoparticles. Likewise, the chemical vapor deposition method, used in the preparation of single-walled carbon nanotubes, is discussed. The enantioseparation applications of these model nanomaterials is also presented.

  3. Preparation and characterization of 6-mercaptopurine-coated magnetite nanoparticles as a drug delivery system

    Directory of Open Access Journals (Sweden)

    Dorniani D

    2013-09-01

    Full Text Available Dena Dorniani,1 Mohd Zobir bin Hussein,1 Aminu Umar Kura,2 Sharida Fakurazi,2 Abdul Halim Shaari,3 Zalinah Ahmad4 1Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology, 2Vaccines and Immunotherapeutics Laboratory, 3Physics Department, Faculty of Science, 4Chemical Pathology Unit, Department of Pathology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Selangor, Malaysia Background: Iron oxide nanoparticles are of considerable interest because of their use in magnetic recording tape, ferrofluid, magnetic resonance imaging, drug delivery, and treatment of cancer. The specific morphology of nanoparticles confers an ability to load, carry, and release different types of drugs. Methods and results: We synthesized superparamagnetic nanoparticles containing pure iron oxide with a cubic inverse spinal structure. Fourier transform infrared spectra confirmed that these Fe3O4 nanoparticles could be successfully coated with active drug, and thermogravimetric and differential thermogravimetric analyses showed that the thermal stability of iron oxide nanoparticles coated with chitosan and 6-mercaptopurine (FCMP was markedly enhanced. The synthesized Fe3O4 nanoparticles and the FCMP nanocomposite were generally spherical, with an average diameter of 9 nm and 19 nm, respectively. The release of 6-mercaptopurine from the FCMP nanocomposite was found to be sustained and governed by pseudo-second order kinetics. In order to improve drug loading and release behavior, we prepared a novel nanocomposite (FCMP-D, ie, Fe3O4 nanoparticles containing the same amounts of chitosan and 6-mercaptopurine but using a different solvent for the drug. The results for FCMP-D did not demonstrate “burst release” and the maximum percentage release of 6-mercaptopurine from the FCMP-D nanocomposite reached about 97.7% and 55.4% within approximately 2,500 and 6,300 minutes when exposed to pH 4.8 and pH 7.4 solutions, respectively

  4. Preparation and optimization of N-trimethyl-O-carboxymethyl chitosan nanoparticles for delivery of low-molecular-weight heparin.

    Science.gov (United States)

    Mahjub, Reza; Heidari Shayesteh, Tavakol; Radmehr, Moojan; Vafaei, Seyed Yaser; Amini, Mohsen; Dinarvand, Rasoul; Dorkoosh, Farid Abedin

    2016-01-01

    The aim of this study was preparation, optimization and in vitro characterization of nanoparticles composed of 6-[O-carboxymethyl]-[N,N,N-trimethyl] (TMCMC) for oral delivery of low-molecular-weight heparin. The chitosan derivative was synthesized. Nanoparticles were prepared using the polyelectrolyte complexation method. Box-Behnken response surface experimental design methodology was used for optimization of nanoparticles. The morphology of nanoparticles was studied using transmission electron microscopy. In vitro release of enoxaparin from nanoparticles was determined under simulated intestinal fluid. The cytotoxicity of nanoparticles on a Caco-2 cell line was determined, and finally the transport of prepared nanoparticles across Caco-2 cell monolayer was defined. Optimized nanoparticles with proper physico-chemical properties were obtained. The size, zeta potential, poly-dispersity index, entrapment efficiency and loading efficiency of nanoparticles were reported as 235 ± 24.3 nm, +18.6 ± 2.57 mV, 0.230 ± 0.03, 76.4 ± 5.43% and 12.6 ± 1.37%, respectively. Morphological studies revealed spherical nanoparticles with no sign of aggregation. In vitro release studies demonstrated that 93.6 ± 1.17% of enoxaparin released from nanoparticles after 600 min of incubation. MTT cell cytotoxicity studies showed no cytotoxicity at 3 h post-incubation, while the study demonstrated concentration-dependent cytotoxicity after 24 h of exposure. The obtained data had shown that the nanoparticles prepared from trimethylcarboxymethyl chitosan may be considered as a good candidate for oral delivery of enoxaparin.

  5. Preparation of Bovine Serum Albumin (BSA) nanoparticles by desolvation using a membrane contactor: a new tool for large scale production.

    Science.gov (United States)

    Yedomon, B; Fessi, H; Charcosset, C

    2013-11-01

    Albumin nanoparticles are attractive drug delivery systems as they can be prepared under soft conditions and incorporate several kinds of molecules. The aim of this study was to upscale the desolvation process for preparing Bovine Serum Albumin (BSA) nanoparticles using a membrane contactor. At a first step, the BSA nanoparticles were prepared at small scale using a syringe pump. BSA nanoparticles of 139 nm in size, with a polydispersity index of 0.046, were obtained at the optimal conditions: pH 8.2, 100 mg mL(-1) BSA albumin solution (2 mL), and 1 mL min(-1) flow rate of ethanol addition (8 mL). The upscaling with a membrane contactor was achieved by permeating ethanol through the pores of a Shirasu Porous Glass (SPG Technology Co., Japan) membrane and circulating the aqueous phase tangentially to the membrane surface. By increasing the pressure of the ethanol from 1 to 2.7 bars, a progressive decrease in nanoparticle size was obtained with a high nanoparticles yield (around 94-96%). In addition, the flow rate of the circulating phase did not affect the BSA nanoparticle characteristics. At the optimal conditions (pH 8.2, 100 mg mL(-1) BSA albumin solution, pressure of ethanol 2.7 bars, flow rate of the circulating phase 30.7 mL s(-1)), the BSA nanoparticles showed similar characteristics to those obtained with the syringe pump. Large batches of BSA nanoparticles were prepared up to 10 g BSA. The BSA nanoparticles were stable at least during 2 months at 4 °C, and their characteristics were reproducible. It was then concluded that the membrane contactor technique could be a suitable method for the preparation of albumin nanoparticles at large scale with properties similar to that obtained at small scale.

  6. Melting of iron nanoparticles embedded in silica prepared by mechanical milling

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Peng; Ma, Ji [Institute of Materials Science and Engineering, School of Physical Science and Technology, Lanzhou University, Lanzhou 730000 (China); Cao, Hui, E-mail: caoh@lzu.edu.cn [Institute of Materials Science and Engineering, School of Physical Science and Technology, Lanzhou University, Lanzhou 730000 (China); Liu, Yi [Department of Biology Science, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201203 (China); Wang, Lianwen, E-mail: lwwang@lzu.edu.cn [Institute of Materials Science and Engineering, School of Physical Science and Technology, Lanzhou University, Lanzhou 730000 (China); Li, Jiangong [Institute of Materials Science and Engineering, School of Physical Science and Technology, Lanzhou University, Lanzhou 730000 (China)

    2013-08-20

    Highlights: • Melting of metallic nanoparticles was studied for some eight elements. • This slim range of materials is successfully expanded to iron. • A mechanical-milled iron–silica composite is employed. • For iron particles of 15 nm in diameter, the melting point depression is 30 K. • The measured data is in agreement with our theoretical calculations. -- Abstract: For decades, experimental studies on the size-dependent melting of metals are regretfully limited to some eight archetypal examples. In this work, to expand this slim range of materials, the melting behavior of Fe nanoparticles embedded in SiO{sub 2} prepared by using mechanical milling are investigated. Effects of factors in sample preparation on the size, isolation and thermal stability of Fe nanoparticles are systematically studied. On this basis, the size-dependent melting of Fe is successfully traced: for Fe nanoparticles with a diameter of about 15 nm, the melting point depression is 30 °C in comparison with bulk Fe, in accordance with our recent theoretical prediction.

  7. TiO2 nanoparticles prepared without harmful organics: A biosafe and economical approach

    KAUST Repository

    Shah, M.A.

    2011-06-01

    Growth of titanium oxide (TiO2) nanoparticles of varying size, ranging from 20-60 nms through a versatile and an economic route, is being reported. The approach is based on a simple reaction of titanium powder and De-Ionized (DI) water at ∼180 °C, without use of any harmful additives. Field Emission Scanning Electron Microscopy (FESEM) reveals the well defined morphology of nanoparticles, whereas X-ray Diffraction (XRD) studies reveal that the, as prepared, nanoparticles are in a mixed phase, with a dominance of a stable rutile phase. Since only water, which is regarded as a benign solvent, is used during the preparation of nanoparticles, we believe that the products so produced are biocompatible and bio-safe and can be readily used for medical applications. The biocompatibility tests are yet to be carried out and shall be reported in forthcoming publications. © 2011 Sharif University of Technology. Production and hosting by Elsevier B.V. All rights reserved.

  8. Preparation and characterization of oligochitosan-tragacanth nanoparticles as a novel gene carrier.

    Science.gov (United States)

    Fattahi, Ali; Sadrjavadi, Komail; Golozar, Mohammad Ali; Varshosaz, Jaleh; Fathi, Mohammad-Hossein; Mirmohammad-Sadeghi, Hamid

    2013-09-12

    The nanoparticles of oligochitosan-water soluble tragacanth (OCH-WST) as novel gene carriers have been prepared and their transfection efficiency has been investigated on Hela and HepG2 cell lines. Different OCH:WST weight ratios were prepared to obtain particles with low size distribution and high surface charge, and also in range of below 200 nm. Nanoparticles with 132.5 ± 6.77 nm size, polydispersity index 1.92 ± 0.061, surface charge 30.45 ± 1.84 and spherical morphology, have been chosen as gene carrier. Nanoparticle-DNA complexes (nanoplexes) showed better transfection efficiency in both Hela and HepG2 cells than chitosan polyplexes, with 1.26 × 10(6) versus 9.05 × 10(5) and 7.76 × 10(5) versus 2.16 × 10(5), respectively. Higher transfection efficiency of nanoplexes could be attributed to their weaker complexation. Decreasing of transfection in presence of galactose in HepG2 cells, indicated receptor mediated endocytosis of nanoplexes. These properties all together, make OCH-WST nanoparticles as potential gene carrier for active gene delivery into cells containing sugar receptors.

  9. Preparation and characterization of chondroitin‐sulfate‐A‐coated magnetite nanoparticles for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Tóth, Ildikó Y., E-mail: Ildiko.Toth@chem.u-szeged.hu; Illés, Erzsébet; Szekeres, Márta; Tombácz, Etelka, E-mail: tombacz@chem.u-szeged.hu

    2015-04-15

    Polysaccharides are promising candidates for manufacturing biocompatible core–shell nanoparticles with potential in vivo use. Superparamagnetic magnetite nanoparticles (MNPs) have prospective application in both diagnosis and therapy, and so developing a novel polysaccharide shell on MNP core is of great challenge. MNPs were prepared by co-precipitation, then the surface of purified MNPs was coated with chondroitin-sulfate-A (CSA) to obtain core–shell structured magnetite nanoparticles (CSA@MNP). The effect of the added amount of CSA on the surface charging and the aggregation state of MNPs at various pHs and 10 mM NaCl was measured by electrophoresis and dynamic light scattering. The amphoteric behavior of MNPs was fundamentally modified by adsorption of CSA polyanions. A very low CSA-loading induces the aggregation of MNPs, while four times more stabilizes the dispersions over the whole pH-range studied. The coagulation kinetics experiments measured at pH=6.3±0.3 showed that salt tolerance of CSA@MNPs rises up to ~150 mM NaCl. - Highlights: • Novel CSA-coated core–shell magnetite nanoparticles were prepared successfully. • The aggregation range of MNPs was shifted gradually to the lower pHs by CSA-loading. • CSA stabilizes electrosterically the MNPs over wide pH-range relevant to biosystems. • The salt tolerance of CSA@MNP enables them to use under physiological condition.

  10. Preparation of nanoparticles of Magnolia bark extract by rapid expansion from supercritical solution into aqueous solutions.

    Science.gov (United States)

    He, Shuai; Zhou, Benjie; Zhang, Shouyao; Lei, Zhengjie; Zhang, Zhongyi

    2011-01-01

    A rapid expansion from supercritical solution into aqueous solution (RESSAS) technology was presented for the micronization of Chinese medicinal material. Magnolia bark extract (MBE) obtained by supercritical carbon dioxide (scCO₂) extraction technology was chosen as the experimental material. RESSAS process produced 303.0 nm nanoparticles (size distribution, 243.6-320.5 nm), which was significantly smaller than the 55.3 µm particles (size distribution, 8.3-102.4 µm) prepared by conventional mechanical milling. The effect of process parameters, including extraction temperature (30 °C, 40 °C, 50 °C), extraction pressure (200, 250, 300 bar) and nozzle size (50, 100, 200 µm), on the size distribution of nanoparticles was investigated. The characteristics of nanoparticles and materials were also studied by scanning electron microscopy (SEM) and laser light scattering (LLS). This study demonstrates that RESSAS is applicable for preparing nanoparticles of MBE at low operating temperature; the process is simple without any residual solvent.

  11. Preparation of multi-functionalized Fe3O4/Au nanoparticles for medical purposes.

    Science.gov (United States)

    del Mar Ramos-Tejada, María; Viota, Julian L; Rudzka, Katarzyna; Delgado, Angel V

    2015-04-01

    In this work, we investigate a route towards the synthesis of multi-functionalized nanoparticles for medical purposes. The aim is to produce magnetite/gold (Fe3O4/Au) nanoparticles combining several complementary properties, specifically, being able to carry simultaneously an antitumor drug and a selected antibody chosen so as to improve specificity of the drug vehicle. The procedure included, firstly, the preparation of Fe3O4 cores coated with Au nanoparticles: this was achieved by using initially the layer-by-layer technique in order to coat the magnetite particles with a three polyelectrolyte (cationic-anionic-cationic) layer. With this, the particles became a good substrate for the growth of the gold layer in a well-defined core-shell structure. The resulting nanoparticles benefit from the magnetic properties of the magnetite and the robust chemistry and the biostability of gold surfaces. Subsequently, the Fe3O4/Au nanoparticles were functionalized with a humanized monoclonal antibody, bevacizumab, and a chemotherapy drug, doxorubicin. Taken together, bevacizumab enhances the therapeutic effect of chemotherapy agents on some kinds of tumors. In this work we first discuss the morphology of the particles and the electrical characteristics of their surface in the successive synthesis stages. Special attention is paid to the chemical stability of the final coating, and the physical stability of the suspensions of the nanoparticles in aqueous solutions and phosphate buffer. We describe how optical absorbance and electrokinetic data provide a follow up of the progress of the nanostructure formation. Additionally, the same techniques are employed to demonstrate that the composite nanoparticles are capable of loading/releasing doxorubicin and/or bevacizumab.

  12. Preparation of porous chitosan-poly(acrylic acid)-calcium phosphate hybrid nanoparticles via mineralization

    Institute of Scientific and Technical Information of China (English)

    CHEN ChangJing; DENG Yu; YAN ErYun; HU Yong; JIANG XiQun

    2009-01-01

    In this work,the preparation of chitosan-poly(acrylic acid)-calcium phosphate hybrid nanoparticles (CS-PAA-CaP NP) based on the mineralization of calcium phosphate (CAP) on the surface of chitosan-poly (acrylic acid) nanoparticles (CS-PAA NPs) was reported. CS-PAA-CaP NPs were achieved by directly adding ammonia to the aqueous solution of CS-PAA nanoparticles or by thermal decomposition of urea in the aqueous solution of CS-PAA nanoparticles,resulting in the mineralization of CaP on the surface of CS-PAA NPs. Through these two routes,especially using urea as a pH-regulator,the precipitation of CS-PAA NPs,a common occurrence in basic environment,was avoided. The size,morphology and ingredient of CS-PAA-CaP hybrid nanoparticles were characterized by dynamic light scattering (DLS),transmission electron microscope (TEM),scanning electron microscope (SEM),thermogravimetry analysis (TGA) and X-ray diffractometer (XRD). When urea was used as the pH regulator to facilitate the mineralization during the thermal urea decomposition procedure,regular CS-PAA-CaP hybrid nanoparticles with a porosity-structural CaP shells and 400-600 nm size were obtained. TGA result revealed that the hybrid NPs contained approximately 23% inorganic component,which was consistent with the ratio of starting materials. The XRD spectra of hybrid nanoparticles indicated that dicalcium phosphate (DCP:CaHPO4) crystal was a dominant component of mineralization.The porous structure of the CS-PAA-CaP hybrid NPs might be greatly useful in pharmaceutical and other medical applications.

  13. Preparation, characterisation and antibacterial activity of a florfenicol-loaded solid lipid nanoparticle suspension.

    Science.gov (United States)

    Wang, Ting; Chen, Xiaojin; Lu, Mengmeng; Li, Xihe; Zhou, WenZhong

    2015-12-01

    A florfenicol-loaded solid lipid nanoparticle (FFC-SLN) suspension was prepared by hot homogenisation and ultrasonic technique. The suspension was characterised for its release profile, stability, toxicity, and the physicochemical properties of the nanoparticles. Antibacterial activity of the suspension was evaluated in vitro and in vivo. The results showed that the mean diameter, polydispersity index and zeta potential of the nanoparticles were 253 ± 3 nm, 0.409 ± 0.022 and 47.5 ± 0.21 mV, respectively. In vitro release profile showed the FFC-SLN suspension had sustained release effect. The minimum inhibition concentration values of the FFC-SLN suspension were 6 and 3 µg/mL against Staphylococcus aureus and Escherichia coli respectively, compared with 3.5 and 2 µg/mL of native florfenicol. The suspension was relatively stable at 4°C and less stable at room temperature during 9 months storage. Although the nanoparticle carriers exhibited cytotoxicity in cell cultures, the LD50 of the lyophilised dry power of the suspension was higher than 5 g/kg body weight. Mortality protection against E. coli lethal infection in mice showed that the nanoparticle suspension had much better efficacy (6/10) than native drug (1/10). These results indicate that FFC-SLN suspension could be a promising formulation in veterinary medicine.

  14. Colloidally stable surface-modified iron oxide nanoparticles: Preparation, characterization and anti-tumor activity

    Energy Technology Data Exchange (ETDEWEB)

    Macková, Hana [Institute of Macromolecular Chemistry, AS CR, Heyrovsky Sq. 2, 162 06 Prague 6 (Czech Republic); Horák, Daniel, E-mail: horak@imc.cas.cz [Institute of Macromolecular Chemistry, AS CR, Heyrovsky Sq. 2, 162 06 Prague 6 (Czech Republic); Donchenko, Georgiy Viktorovich; Andriyaka, Vadim Ivanovich; Palyvoda, Olga Mikhailovna; Chernishov, Vladimir Ivanovich [Palladin Institute of Biochemistry, NASU, 9 Leontovich St., 01601 Kiev (Ukraine); Chekhun, Vasyl Fedorovich; Todor, Igor Nikolaevich [R. E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology, NASU, 45 Vasylkivska St., 03022 Kiev (Ukraine); Kuzmenko, Oleksandr Ivanovich [Palladin Institute of Biochemistry, NASU, 9 Leontovich St., 01601 Kiev (Ukraine)

    2015-04-15

    Maghemite (γ-Fe{sub 2}O{sub 3}) nanoparticles were obtained by co-precipitation of Fe(II) and Fe(III) chlorides and subsequent oxidation with sodium hypochlorite and coated with poly(N,N-dimethylacrylamide-co-acrylic acid) [P(DMAAm-AA)]. They were characterized by a range of methods including transmission electron microscopy (TEM), elemental analysis, dynamic light scattering (DLS) and zeta potential measurements. The effect of superparamagnetic P(DMAAm-AA)-γ-Fe{sub 2}O{sub 3} nanoparticles on oxidation of blood lipids, glutathione and proteins in blood serum was detected using 2-thiobarbituric acid and the ThioGlo fluorophore. Finally, mice received magnetic nanoparticles administered per os and the antitumor activity of the particles was tested on Lewis lung carcinoma (LLC) in male mice line C57BL/6 as an experimental in vivo metastatic tumor model; the tumor size was measured and the number of metastases in lungs was determined. Surface-modified γ-Fe{sub 2}O{sub 3} nanoparticles showed higher antitumor and antimetastatic activities than commercial CuFe{sub 2}O{sub 4} particles and the conventional antitumor agent cisplatin. - Highlights: • Maghemite nanoparticles were prepared and characterized. • Poly(N,N-dimethylacrylamide-co-acrylic acid) coating was synthetized. • Blood lipid, glutathione and protein peroxidation/oxidation was determined. • Antitumor effect of coated particles on Lewis lung carcinoma in mice was observed.

  15. Preparation of amino acid nanoparticles at varying saturation conditions in an aerosol flow reactor

    Energy Technology Data Exchange (ETDEWEB)

    Raula, Janne, E-mail: janne.raula@aalto.fi [Aalto University School of Science, Department of Applied Physics (Finland); Lehtimaeki, Matti; Karppinen, Maarit [Aalto University School of Chemical Technology, Department of Chemistry (Finland); Antopolsky, Maxim [University of Helsinki, Drug Discovery and Development Technology Center (Finland); Jiang Hua; Rahikkala, Antti; Kauppinen, Esko I. [Aalto University School of Science, Department of Applied Physics (Finland)

    2012-07-15

    Nanoparticle formation of five amino acids, glycine, l-proline, l-valine, l-phenylalanine, and l-leucine was studied. The aim was to explore factors determining nanoparticle formation and crystallinity. The amino acid nanoparticles have been prepared at different saturation conditions in the aerosol reactor. In a condensed state, the particles were formed by droplet drying. The raise in temperature induced the sublimation of amino acids from the aerosol particles. The amino acid vapor was condensed by physical vapor deposition in a rapid cooling process. The diffusion coefficients and nucleation rates of amino acids have been calculated to understand particle formation. Upon the vapor deposition, amino acids formed crystalline nanoparticles except in the case l-phenylalanine according to X-ray diffraction. The crystal polymorph of glycine in the nanoparticles depended on the applied reactor temperature. The preference of crystallographic orientation varied in both the particle formations from condensed and vapor phase. l-Valine, l-phenylalanine, and l-leucine formed leafy-looking particles. These results could be utilized in the fabrication of nano-sized asperities on drug particle surfaces to reduce forces between particles and accordingly increase particle dispersion in dry powder inhalers.

  16. Preparation of silver nanoparticles in virgin coconut oil using laser ablation

    Directory of Open Access Journals (Sweden)

    Reza Zamiri,B Z Azmi. Amir Reza Sadrolhosseini

    2011-01-01

    Full Text Available Reza Zamiri1, B Z Azmi1,2, Amir Reza Sadrolhosseini1, Hossein Abbastabar Ahangar3, A W Zaidan1, M A Mahdi41Department of Physics, 2Advanced Materials and Nanotechnology Laboratory, 3Department of Chemistry, 4Wireless and Photonics Networks Research Center, Universiti Putra Malaysia, Serdang, Selangor, MalaysiaAbstract: Laser ablation of a silver plate immersed in virgin coconut oil was carried out for fabrication of silver nanoparticles. A Nd:YAG laser at wavelengths of 1064 nm was used for ablation of the plate at different times. The virgin coconut oil allowed formation of nanoparticles with well-dispersed, uniform particle diameters that were stable for a reasonable length of time. The particle sizes and volume fraction of nanoparticles inside the solutions obtained at 15, 30, 45 min ablation times were 4.84, 5.18, 6.33 nm and 1.0 × 10-8, 1.6 × 10-8, 2.4 × 10-8, respectively. The presented method for preparation of silver nanoparticles in virgin coconut oil is environmentally friendly and may be considered a green method.Keywords: silver nanoparticles, laser ablation, virgin coconut oil

  17. Preparation of Zirconia Nanoparticles with Different Morphology Using Lyotropic Liquid Crystal Template

    Directory of Open Access Journals (Sweden)

    HE Wei-yan

    2016-06-01

    Full Text Available Zirconia nanoparticles were prepared using ZrOCl2·8H2O and NH3·H2O as raw materials in the lyotropic hexagonal phase consisting of SDS/TritonX-100/H2O. Effects of pH on the phase structure stability of the template were determined. Effect of ZrOCl2 concentration on the size and morphology of zirconia were discussed. Polarizing optical microscopy was applied to investigate the stability of the hexagonal phase. The size and morphology of the nanoparticles were characterized by SEM, TEM and particle size analyzer. The crystalline structure and purity of the sample were characterized by XRD. In addition, the synthetic mechanism of zirconia nanoparticles in the lyotropic hexagonal phase were proposed by FT-IR. The results show that the hexagonal phase is stable in the condition of alkalinity and the hexagonal phase texture disappear in the conditions of acid; the size and morphology of the nanoparticles obtained are greatly affected by concentration of ZrOCl2. Morphology of samples changes from spherical-like particle to cotton-like particle with the increase of the concentration of ZrOCl2; the mechanism analysisresults show that complexation reaction between the precursor of the sample and the template does not occur, and crystal growth and nucleation of the zirconia nanoparticles are limited by a direct template route in the hexagonal phase lyotropic liquid crystal.

  18. Preparation and characterization of TiO 2-cationic hybrid nanoparticles as electrophoretic particles

    Science.gov (United States)

    Li, Jingjing; Deng, Liandong; Xing, Jinfeng; Dong, Anjie; Li, Xianggao

    2012-01-01

    The hybrid nanoparticles (TiO2-HNPs) with TiO2 nanoparticles as core and with poly(N,N-dimethylaminoethyl methacrylate-co-methyl methacrylate) by using triallylamine as cross-linking agent as shell were firstly prepared via atom transfer radical polymerization (ATRP) in methanol. Then the hybrid nanoparticles with positive charge were produced by the quaternization with methyl iodide as quaternization reagent so as to endow them with greater electrophoretic mobility. The cationic hybrid nanoparticles (TiO2-CHNPs) were studied by means of transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) spectroscopy and dynamic light scattering (DLS) measurements. The results indicate that the cationic polymer is successfully grafted on the surface of the TiO2 nanoparticles. The particle size of TiO2-CHNPs is about 150 nm and the polydispersity index (PDI) is 0.307. The zeta potential, the contrast ratio of white state to dark state and response time of TiO2-CHNPs are +16.8 mV, 30 and 3 s, respectively, which show the potential application prospect in the development of electrophoretic ink.

  19. Chitosan-lignosulfonates sono-chemically prepared nanoparticles: characterisation and potential applications.

    Science.gov (United States)

    Kim, Suyeon; Fernandes, Margarida M; Matamá, Teresa; Loureiro, Ana; Gomes, Andreia C; Cavaco-Paulo, Artur

    2013-03-01

    Due to their recognised properties of biocompatibility, biodegradability and sustainability, chitosan nanocarriers have been successfully used as new delivery systems. In this work, nanoparticles combining chitosan and lignosulfonates were developed for the first time for cosmetic and biomedical applications. The ability of lignosulfonates to act as a counter polyion for stabilisation of chitosan particles, generated using high intensity ultrasound, was investigated. Several conditions for particles preparation were tested and optimised and the resulting nanoparticles were comprehensively characterised by measuring particle size, zeta potential and polydispersity index. The pH of chitosan solution, sonication time and the presence of an adequate surfactant, poloxamer 407, were determinant factors on the development of smaller particles with low polydispersity index (an average particle size of 230 nm was obtained at pH 5 after 8 min of sonication). The beneficial effects of lignosulfonates complex on chitosan nanoparticles were further characterised. Greater stability to lysozyme degradation, biocompatibility with human cells and antimicrobial activity was found upon lignosulfonates incorporation into chitosan nanoparticles. Furthermore, these particles were able to incorporate a hydrophilic model protein - RNase A. A burst release was observed when nanoparticles were loaded with low amount of protein while with high protein content, a sustained release was found, suggesting that the protein cargo maybe loaded both at the surface as in the bulk of the particle, depending on the concentration of drug incorporated.

  20. Carboxymethyl guar gum nanoparticles for drug delivery applications: Preparation and preliminary in-vitro investigations

    Energy Technology Data Exchange (ETDEWEB)

    Dodi, G., E-mail: gianina.dodi@yahoo.co.uk [“Gheorghe Asachi” Technical University of Iasi (Romania); SCIENT — Research Centre for Instrumental Analysis, Bucharest (Romania); Pala, A. [University of Sassari, Sassari (Italy); Barbu, E. [University of Portsmouth, Portsmouth (United Kingdom); Peptanariu, D. [“Petru Poni” Institute of Macromolecular Chemistry, Iasi (Romania); Hritcu, D.; Popa, M.I. [“Gheorghe Asachi” Technical University of Iasi (Romania); Tamba, B.I. [“Gr. T. Popa” University of Medicine and Pharmacy, Iasi (Romania)

    2016-06-01

    Carboxymethyl guar gum (CMGG) synthesized from commercially available polysaccharide was formulated into nanoparticles via ionic gelation using trisodium trimetaphosphate (STMP) as cross-linking agent. Characterisation using a range of analytical techniques (FTIR, NMR, GPC, TGA and DLS) confirmed the CMGG structure and revealed the effect of the CMGG and STMP concentration on the main characteristics of the obtained nanoformulations. The average nanoparticle diameter was found to be around 208 nm, as determined by dynamic light scattering (DLS) and confirmed by scanning electron microscopy (SEM) and nanoparticle tracking analysis (NTA). Experiments using simulated gastric and intestinal fluids evidenced significant pH-dependent drug release behaviour of the nanoformulations loaded with Rhodamine B (RhB) as a model drug (loading capacity in excess of 83%), as monitored by UV–Vis. While dose-dependent cytotoxicity was observed, the nanoformulations appeared completely non-toxic at concentrations below 0.3 mg/mL. Results obtained so far suggest that carboxymethylated guar gum nanoparticles formulated with STMP warrant further investigations as polysaccharide based biocompatible drug nanocarriers. - Highlights: • Carboxymethyl guar gum nanoparticles preparation by ionic gelation • The optimum synthesis system designed particles around 200 nm • The nanoformulations appeared completely non-toxic at specific concentrations • The loaded formulations evidenced significant pH-dependent drug release behaviour • The results encourage further investigations as polysaccharidic drug nanocarriers.

  1. Photoluminescence properties of LaF3: Eu3+ nanoparticles prepared byrefluxing method

    Institute of Scientific and Technical Information of China (English)

    WANG Zhenling; LI Min; WANG Chang; CHANG Jiazhong; SHI Hengzhen; LIN Jun

    2009-01-01

    The europium-doped LaF3 nanoparticles were prepared by refluxing method in glycerol/water mixture and characterized with X-ray diffraction(XRD), field emission scanning electron microscopy(FE-SEM), UV-vis diffuse reflectance spectrum, and photoluminescence spectra. The results of XRD indicated that the obtained LaF3: Eu3+ nanoparticles were well crystallized with a hexagonal structure. The FE-SEM image illustrated that the LaF3: Eu3+ nanoparticles were spherical with an average size around 30 nm. Under irradiation of UV light, the emission spectrum of LaF3: Eu3+ nanoparticles exhibited the characteristic line emissions arising from the 5D0→7FJ (J=1, 2, 3, 4) transitions of the Eu3+ ions, with the dominating emission centered at 590 nm. In addition, the emissions from the 5D1 level could be clearly observed due to the low phonon energies (-350 cm-1) of LaF3 matrix. The optimum doping concentration for LaF3: Eu3+ nanoparticles was determined to be 20mol.%.

  2. Preparation of silica coated cobalt ferrite magnetic nanoparticles for the purification of histidine-tagged proteins

    Science.gov (United States)

    Aygar, Gülfem; Kaya, Murat; Özkan, Necati; Kocabıyık, Semra; Volkan, Mürvet

    2015-12-01

    Surface modified cobalt ferrite (CoFe2O4) nanoparticles containing Ni-NTA affinity group were synthesized and used for the separation of histidine tag proteins from the complex matrices through the use of imidazole side chains of histidine molecules. Firstly, CoFe2O4 nanoparticles with a narrow size distribution were prepared in an aqueous solution using the controlled co-precipitation method. In order to obtain small CoFe2O4 agglomerates, oleic acid and sodium chloride were used as dispersants. The CoFe2O4 particles were coated with silica and subsequently the surface of these silica coated particles (SiO2-CoFe2O4) was modified by amine (NH2) groups in order to add further functional groups on the silica shell. Then, carboxyl (-COOH) functional groups were added to the SiO2-CoFe2O4 magnetic nanoparticles through the NH2 groups. After that Nα,Nα-Bis(carboxymethyl)-L-lysine hydrate (NTA) was attached to carboxyl ends of the structure. Finally, the surface modified nanoparticles were labeled with nickel (Ni) (II) ions. Furthermore, the modified SiO2-CoFe2O4 magnetic nanoparticles were utilized as a new system that allows purification of the N-terminal His-tagged recombinant small heat shock protein, Tpv-sHSP 14.3.

  3. Silk sericin loaded alginate nanoparticles: Preparation and anti-inflammatory efficacy.

    Science.gov (United States)

    Khampieng, Thitikan; Aramwit, Pornanong; Supaphol, Pitt

    2015-09-01

    In this study, silk sericin loaded alginate nanoparticles were prepared by the emulsification method followed by internal crosslinking. The effects of various silk sericin loading concentration on particle size, shape, thermal properties, and release characteristics were investigated. The initial silk sericin loadings of 20, 40, and 80% w/w to polymer were incorporated into these alginate nanoparticles. SEM images showed a spherical shape and small particles of about 71.30-89.50 nm. TGA analysis showed that thermal stability slightly increased with increasing silk sericin loadings. FTIR analysis suggested interactions between alginate and silk sericin in the nanoparticles. The release study was performed in acetate buffer at normal skin conditions (pH 5.5; 32 °C). The release profiles of silk sericin exhibited initial rapid release, consequently with sustained release. These silk sericin loaded alginate nanoparticles were further incorporated into topical hydrogel and their anti-inflammatory properties were studied using carrageenan-induced paw edema assay. The current study confirms the hypothesis that the application of silk sericin loaded alginate nanoparticle gel can inhibit inflammation induced by carrageenan.

  4. Characterization of boron carbide nanoparticles prepared by a solid state thermal reaction

    Science.gov (United States)

    Chang, B.; Gersten, B. L.; Szewczyk, S. T.; Adams, J. W.

    2007-01-01

    The production of boron carbide (B4C) nanoparticles was investigated in a conventional high temperature furnace reactor. The reaction was carried out by heating a mixture of amorphous carbon and amorphous boron at 1550 °C to efficiently obtain a quantity of B4C. Scanning electron microscopy studies showed the average size of B4C particles was 200 nm, ranging from 50 nm to 350 nm. X-ray diffraction transmission electron microscopy and electron diffraction studies indicated that the prepared nanoparticles were crystalline B4C with a high density twin structure. High resolution transmission electron microscopy and selected area diffraction were also used to further characterize the structure of the prepared B4C particles, while energy dispersive spectroscopy and electron energy loss spectroscopy were used to determine the stoichiometry of the product. A solid state diffusion reaction mechanism is proposed.

  5. Sonochemical preparation and characterization of photochromic MoO3 nanoparticles

    Institute of Scientific and Technical Information of China (English)

    CHEN Jiu-ju; YANG Hai-bin; CHANG Lian-xia; FU Wu-you; ZENG Yi; ZHU Hong-yang; ZOU Guang-tian

    2007-01-01

    The effect of ultrasound irradiation on molybdenum trioxide has been investigated. Under ultrasonic irradiation, spherical-like MoO3 nanoparticles were obtained, while bulk-like MoO3 nanoparticles were prepared without ultrasonic irradiation. The changes in the physicochemical properties of MoO3 have been investigated using techniques such as X-ray powder diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and ultraviolet and visible spectroscopy (UV-vis). The physicochemical changes of MoO3 due to ultrasound irradiation have been attributed to the sonochemical cavity collapse onto the molybdenum trioxide particles. The ultrasonically prepared particles can also greatly improve the photochromism efficiency.

  6. The novel albumin-chitosan core-shell nanoparticles for gene delivery: preparation, optimization and cell uptake investigation

    Science.gov (United States)

    Karimi, Mahdi; Avci, Pinar; Mobasseri, Rezvan; Hamblin, Michael R.; Naderi-Manesh, Hossein

    2013-05-01

    Natural polymers and proteins such as chitosan (CS) and albumin (Alb) have recently attracted much attention both in drug delivery and gene delivery. The underlying rationale is their unique properties such as biodegradability, biocompatibility and controlled release. This study aimed to prepare novel albumin-chitosan-DNA (Alb-CS-DNA) core-shell nanoparticles as a plasmid delivery system and find the best conditions for their preparation. Phase separation method and ionic interaction were used for preparation of Alb nanoparticles and Alb-CS-DNA core-shell nanoparticles, respectively. The effects of three important independent variables (1) CS/Alb mass ratio, (2) the ratios of moles of the amine groups of cationic polymers to those of the phosphate groups of DNA (N/P ratio), and (3) Alb concentration, on the nanoparticle size and loading efficiency of the plasmid were investigated and optimized through Box-Behnken design of response surface methodology (RSM). The optimum conditions were found to be CS/Alb mass ratio = 3, N/P ratio = 8.24 and Alb concentration = 0.1 mg/mL. The most critical factors for the size of nanoparticles and loading efficiency were Alb concentration and N/P ratio. The optimized nanoparticles had an average size of 176 ± 3.4 nm and loading efficiency of 80 ± 3.9 %. Cytotoxicity experiments demonstrated that the prepared nanoparticles were not toxic. The high cellular uptake of nanoparticles ( 85 %) was shown by flow cytometry and fluorescent microscopy.

  7. The novel albumin-chitosan core-shell nanoparticles for gene delivery: preparation, optimization and cell uptake investigation

    Energy Technology Data Exchange (ETDEWEB)

    Karimi, Mahdi [Tarbiat Modares University, Department of Nanobiotechnology, Faculty of Biological Sciences (Iran, Islamic Republic of); Avci, Pinar [Massachusetts General Hospital, Wellman Center for Photomedicine (United States); Mobasseri, Rezvan [Tarbiat Modares University, Department of Nanobiotechnology, Faculty of Biological Sciences (Iran, Islamic Republic of); Hamblin, Michael R. [Massachusetts General Hospital, Wellman Center for Photomedicine (United States); Naderi-Manesh, Hossein, E-mail: naderman@modares.ac.ir [Tarbiat Modares University, Department of Nanobiotechnology, Faculty of Biological Sciences (Iran, Islamic Republic of)

    2013-05-15

    Natural polymers and proteins such as chitosan (CS) and albumin (Alb) have recently attracted much attention both in drug delivery and gene delivery. The underlying rationale is their unique properties such as biodegradability, biocompatibility and controlled release. This study aimed to prepare novel albumin-chitosan-DNA (Alb-CS-DNA) core-shell nanoparticles as a plasmid delivery system and find the best conditions for their preparation. Phase separation method and ionic interaction were used for preparation of Alb nanoparticles and Alb-CS-DNA core-shell nanoparticles, respectively. The effects of three important independent variables (1) CS/Alb mass ratio, (2) the ratios of moles of the amine groups of cationic polymers to those of the phosphate groups of DNA (N/P ratio), and (3) Alb concentration, on the nanoparticle size and loading efficiency of the plasmid were investigated and optimized through Box-Behnken design of response surface methodology (RSM). The optimum conditions were found to be CS/Alb mass ratio = 3, N/P ratio = 8.24 and Alb concentration = 0.1 mg/mL. The most critical factors for the size of nanoparticles and loading efficiency were Alb concentration and N/P ratio. The optimized nanoparticles had an average size of 176 {+-} 3.4 nm and loading efficiency of 80 {+-} 3.9 %. Cytotoxicity experiments demonstrated that the prepared nanoparticles were not toxic. The high cellular uptake of nanoparticles ({approx}85 %) was shown by flow cytometry and fluorescent microscopy.

  8. Preparation and Characterization of Nano-particle Substituted Barium Hexaferrite

    CERN Document Server

    Atassi, Yomen; Tally, Mohammad

    2014-01-01

    High density magnetic recording requires high coercivity magnetic media and small particle size. Barium hexaferrite has been considered as a leading candidate material because of its chemical stability, fairly large crystal anisotropy and suitable magnetic characteristics. In this work, we present the preparation of the hexagonal ferrite BaFe12O19 and one of its derivative; the Zn-Sn substituted hexaferrite by the chemical co-precipitation method. The main advantage of this method on the conventional glass-ceramic one, resides in providing a small enough particle size for magnetic recording. We demonstrate using the X-ray diffraction patterns that the particle size decreases when substituting the hexaferrite by the Zn-Sn combination. This may improve the magnetic properties of the hexaferrite as a medium for HD magnetic recording

  9. Preparation of poly (alkylcyanoacrylate) nanoparticles by polymerization of water-free microemulsions

    DEFF Research Database (Denmark)

    Krauel, Karen; Graf, Anja; Hook, Sarah M;

    2006-01-01

    Phase diagrams of the pseudoternary systems ethyloleate, polyoxyethylene 20 sorbitan mono-oleate/sorbitan monolaurate and propylene glycol with and without butanol as a co-surfactant were prepared. Areas containing optically isotropic, one-phase systems were identified and samples therein...... that polymerization is expected to occur at a water-oil interface by base-catalysed polymerization. It would appear that propylene glycol is sufficiently nucleophilic to initiate the polymerization. The use of water-free microemulsions as templates for the preparation of poly (alkylcyanoacrylate) nanoparticles opens...

  10. Preparation of hydroxyapatite nanoparticles by sol-gel method with optimum processing parameters

    Energy Technology Data Exchange (ETDEWEB)

    Yusoff, Yusriha Mohd; Salimi, Midhat Nabil Ahmad; Anuar, Adilah [Universiti Malaysia Perlis, Kompleks Pusat Pengajian Jejawi 3, 02600 Arau, Perlis (Malaysia)

    2015-05-15

    Many studies have been carried out in order to prepare hydroxyapatite (HAp) by various methods. In this study, we focused on the preparation of HAp nanoparticles by using sol-gel technique in which few parameters are optimized which were stirring rate, aging time and sintering temperature. HAp nanoparticles were prepared by using precursors of calcium nitrate tetrahydrate, Ca(NO{sub 3}){sub 2}.4H{sub 2}O and phosphorous pentoxide, P{sub 2}O{sub 5}. Both precursors are mixed in ethanol respectively before they were mixed together in which it formed a stable sol. Fourier transform infrared (FTIR), X-ray diffraction (XRD) and Scanning electron microscopy (SEM) were used for its characterization in terms of functional group, phase composition, crystallite size and morphology of the nanoparticles produced. FTIR spectra showed that the functional groups that present in all five samples were corresponding to the formation of HAp. Besides, XRD shows that only one phase was formed which was hydroxyapatite. Meanwhile, SEM shows that the small particles combine together to form agglomeration.

  11. Effect of preparation parameters on ultra low molecular weight chitosan/hyaluronic acid nanoparticles.

    Science.gov (United States)

    Nazeri, Niloofar; Avadi, Mohammad Reza; Faramarzi, Mohammad Ali; Safarian, Shahrokh; Tavoosidana, Gholamreza; Khoshayand, Mohammad Reza; Amani, Amir

    2013-11-01

    Nanoparticles of ultra low molecular weight chitosan (ULMWCS)/hyaluronic acid (HA) were prepared by ion gelation. Three independent variables, namely, ratio of concentration of ULMWCS to HA (CS/HA), pH of solution and stirring time were studied to identify their effects on size, polydispersity and zeta potential of prepared nanoparticles using a Box-Behnken design. Results showed that pH and CS/HA have a direct effect on size, while increase of stirring time decreases the size of nanoparticles. Additionally, it was shown that all the independent parameters have direct effects on zeta potential. Also, the minimum polydispersity index was observed at lowest values of CS/HA. The model also predicted that the optimum values are 4.15, 4.14 and 180 (min) for the CS/HA, solution pH and stirring time, respectively. The obtained preparation had a size of 200 nm, polydispersity index of 0.37, and zeta potential of 13.0 mV.

  12. Ferrocenyl branched poly (ethylene imine) micelles as reductive templates for the preparation of silver nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zhu Leize; Zhou Wenbo; Ji Jian, E-mail: jijian@zju.edu.c [Zhejiang University, Department of Polymer Science, Key Laboratory of Macromolecule Synthesis and Functionalization of Minister of Education (China)

    2010-08-15

    Polymeric micelles with a branched poly (ethylene imine) shell and a reductive ferrocene core were prepared via self-assembly of ferrocene modified branched poly (ethylene imine) (BPEI-Fc). The well-controlled polymeric micelles with a reductive core were used as templates to prepare core-shell-structured silver nanoparticles (AgNPs) in aqueous solution. The as-prepared nanoparticles were characterized by UV-Vis spectrophotometer, transmission electron microscope (TEM), selected-area electron diffraction (SAED), thermogravimetry analyzer (TGA), and dynamic light scattering (DLS). The AgNPs of 39 {+-} 9 nm with a 39-nm BPEI layer were obtained. It is demonstrated that ferrocene, which is a neutral, chemically stable, and nontoxic molecule, plays a dual role as the hydrophobe and as the electron donating group. Moreover, the formation of these particles was monitored in situ by UV-Vis spectrophotometer. It is found that the growth of AgNPs through reductive templates is much slower than that reduced by NaBH{sub 4}. Meanwhile, the size distribution of AgNPs becomes narrower during the reaction. BPEI-covered AgNPs (Ag-BPEI) are stable up to 3 months and carry amino groups, which can further be bioconjugated. These core-shell-structured nanoparticles may enable them to be used for wide applications in aqueous solution.

  13. Application of Box-Behnken design to prepare gentamicin-loaded calcium carbonate nanoparticles.

    Science.gov (United States)

    Maleki Dizaj, Solmaz; Lotfipour, Farzaneh; Barzegar-Jalali, Mohammad; Zarrintan, Mohammad-Hossein; Adibkia, Khosro

    2016-09-01

    The aim of this research was to prepare and optimize calcium carbonate (CaCO3) nanoparticles as carriers for gentamicin sulfate. A chemical precipitation method was used to prepare the gentamicin sulfate-loaded CaCO3 nanoparticles. A 3-factor, 3-level Box-Behnken design was used for the optimization procedure, with the molar ratio of CaCl2: Na2CO3 (X1), the concentration of drug (X2), and the speed of homogenization (X3) as the independent variables. The particle size and entrapment efficiency were considered as response variables. Mathematical equations and response surface plots were used, along with the counter plots, to relate the dependent and independent variables. The results indicated that the speed of homogenization was the main variable contributing to particle size and entrapment efficiency. The combined effect of all three independent variables was also evaluated. Using the response optimization design, the optimized Xl-X3 levels were predicted. An optimized formulation was then prepared according to these levels, resulting in a particle size of 80.23 nm and an entrapment efficiency of 30.80%. It was concluded that the chemical precipitation technique, together with the Box-Behnken experimental design methodology, could be successfully used to optimize the formulation of drug-incorporated calcium carbonate nanoparticles.

  14. Flame spray synthesis under a non-oxidizing atmosphere: Preparation of metallic bismuth nanoparticles and nanocrystalline bulk bismuth metal

    Energy Technology Data Exchange (ETDEWEB)

    Grass, Robert N.; Stark, Wendelin J. [Institute for Chemical and Bioengineering, ETH Zuerich (Switzerland)], E-mail: wendelin.stark@chem.ethz.ch

    2006-10-15

    Metallic bismuth nanoparticles of over 98% purity were prepared by a modified flame spray synthesis method in an inert atmosphere by oxygen-deficient combustion of a bismuth-carboxylate based precursor. The samples were characterized by X-ray diffraction, thermal analysis and scanning electron microscopy confirming the formation of pure, crystalline metallic bismuth nanoparticles. Compression of the as-prepared powder resulted in highly dense, nanocrystalline pills with strong electrical conductivity and bright metallic gloss.

  15. Magnetic hyperthermia heating of cobalt ferrite nanoparticles prepared by low temperature ferrous sulfate based method

    Directory of Open Access Journals (Sweden)

    Tejabhiram Yadavalli

    2016-05-01

    Full Text Available A facile low temperature co-precipitation method for the synthesis of crystalline cobalt ferrite nanostructures using ferrous sulfate salt as the precursor has been discussed. The prepared samples were compared with nanoparticles prepared by conventional co-precipitation and hydrothermal methods using ferric nitrate as the precursor. X-ray diffraction studies confirmed the formation of cubic spinel cobalt ferrites when dried at 110 °C as opposed to conventional methods which required higher temperatures/pressure for the formation of the same. Field emission scanning electron microscope studies of these powders revealed the formation of nearly spherical nanostructures in the size range of 20-30 nm which were comparable to those prepared by conventional methods. Magnetic measurements confirmed the ferromagnetic nature of the cobalt ferrites with low magnetic remanance. Further magnetic hyperthermia studies of nanostructures prepared by low temperature method showed a rise in temperature to 50 °C in 600 s.

  16. Preparation and characterization of Tamoxifen citrate loaded nanoparticles for breast cancer therapy

    Directory of Open Access Journals (Sweden)

    Maji R

    2014-06-01

    Full Text Available Ruma Maji, Niladri Shekhar Dey, Bhabani Sankar Satapathy, Biswajit Mukherjee, Subhasish MondalDepartment of Pharmaceutical Technology, Jadavpur University, Kolkata (Calcutta, IndiaBackground: Four formulations of Tamoxifen citrate loaded polylactide-co-glycolide (PLGA based nanoparticles (TNPs were developed and characterized. Their internalization by Michigan Cancer Foundation-7 (MCF-7 breast cancer cells was also investigated.Methods: Nanoparticles were prepared by a multiple emulsion solvent evaporation method. Then the following studies were carried out: drug-excipients interaction using Fourier transform infrared spectroscopy (FTIR, surface morphology by field emission scanning electron micro­scopy (FESEM, zeta potential and size distribution using a Zetasizer Nano ZS90 and particle size analyzer, and in vitro drug release. In vitro cellular uptake of nanoparticles was assessed by confocal microscopy and their cell viability (% was studied.Results: No chemical interaction was observed between the drug and the selected excipients. TNPs had a smooth surface, and a nanosize range (250–380 nm with a negative surface charge. Drug loadings of the prepared particles were 1.5%±0.02% weight/weight (w/w, 2.68%±0.5% w/w, 4.09%±0.2% w/w, 27.16%±2.08% w/w for NP1–NP4, respectively. A sustained drug release pattern from the nanoparticles was observed for the entire period of study, ie, up to 60 days. Further, nanoparticles were internalized well by the MCF-7 breast cancer cells on a concentration dependent manner and were present in the cytoplasm. The nucleus was free from nanoparticle entry. Drug loaded nanoparticles were found to be more cytotoxic than the free drug.Conclusion: TNPs (NP4 showed the highest drug loading, released the drug in a sustained manner for a prolonged period of time and were taken up well by the MCF-7 breast cancer cell line in vitro. Thus the formulation may be suitable for breast cancer treatment due to the

  17. Synthesis of nanogranular Fe3O4/biomimetic hydroxyapatite for potential applications in nanomedicine: structural and magnetic characterization

    Science.gov (United States)

    Del Bianco, L.; Lesci, I. G.; Fracasso, G.; Barucca, G.; Spizzo, F.; Tamisari, M.; Scotti, R.; Ciocca, L.

    2015-06-01

    We realized the synthesis of a novel nanogranular system consisting of magnetite nanoparticles embedded in biomimetic carbonate hydroxyapatite (HA), for prospective uses in bone tissue engineering. An original two-step method was implemented: in the first step, magnetite nanoparticles are prepared by refluxing an aqueous solution of Fe(SO4) and Fe2(SO4)3 in an excess of tetrabutilammonium hydroxide acting as surfactant; then, the magnetite nanoparticles are coated with a Ca(OH)2 layer, to induce the growth of HA directly on their surface, by reaction of Ca(OH)2 with HPO42-. Two nanogranular samples were collected with magnetite content ˜0.8 and ˜4 wt%. The magnetite nanoparticles and the composite material were investigated by x-ray diffraction, Fourier transform infrared spectroscopy and transmission electron microscopy. These analyses provided information on the structure of the nanoparticles (mean size ˜6 nm) and revealed the presence of surface hydroxyl groups, which promoted the subsequent growth of the HA phase, featuring a nanocrystalline lamellar structure. The magnetic study, by a superconducting quantum interference device magnetometer, has shown that both the as-prepared and the HA-coated magnetite nanoparticles are superparamagnetic at T = 300 K, but the magnetization relaxation process is dominated by dipolar magnetic interactions of comparable strength. In the three samples, a collective frozen magnetic regime is established below T ˜ 20 K. These results indicate that the magnetite nanoparticles tend to form agglomerates in the as-prepared state, which are not substantially altered by the HA growth, coherently with the creation of electrostatic hydrogen bonds among the surface hydroxyl groups.

  18. Biomimetic Composite Structural T-joints

    Institute of Scientific and Technical Information of China (English)

    Vimal Kumar Thummalapalli; Steven L.Donaldson

    2012-01-01

    Biological structural fixed joints exhibit unique attributes,including highly optimized fiber paths which minimize stress concentrations.In addition,since the joints consist of continuous,uncut fiber architectures,the joints enable the organism to transport information and chemicals from one part of the body to the other.To the contrary,sections of man-made composite material structures are often joined using bolted or bonded joints,which involve low strength and high stress concentrations.These methods are also expensive to achieve.Additional functions such as fluid transport,electrical signal delivery,and thermal conductivity across the joints typically require parasitic tubes,wires,and attachment clips.By using the biomimetic methods,we seek to overcome the limitations which are present in the conventional methods. In the present work,biomimetic co-cured composite sandwich T-joints were constructed using unidirectional glass fiber,epoxy resin,and structural foam.The joints were fabricated using the wet lay-up vacuum bag resin infusion method.Foam sandwich T-joints with multiple continuous fiber architectures and sandwich foam thickness were prepared.The designs were tested in quasi-static bending using a mechanical load frame.The significantweight savings using the biomimetic approaches is discussed,as well as a comparison of failure modes versus architecture is described.

  19. The Optical Nonlinearity of Au and Ag Nanoparticle Prepared by the Γ-Radiation Method

    Directory of Open Access Journals (Sweden)

    Esmaeil Shahriari

    2010-01-01

    Full Text Available Problem statement: The third order nonlinear optical properties of metal nanoparticles have been of interest in physical chemistry, medical diagnostics and optical devices. Gold colloidal nanoparticles are responsible for the brilliant reds seen in stained glass windows and silver particles are typically yellow. The purpose of the study was to determine the nonlinear refraction and absorption coefficient of the Au and Ag nanoparticles in PVP solution. Approach: The samples were prepared by Γ-radiation method and the nonlinear optical properties of the composites were investigated using a single beam Z-scan technique with a beam power of 40 mW and operated at wavelength of 532 nm. The measurements were carried out for both Open and closed aperture Z-scan arrangements. Results: For both Au/PVP and Ag/PVP samples the results exhibited reverse saturable absorption. The closed aperture Z-scan of the nano-fluid samples revealed self-defocusing effect while the open aperture Z-scan of the samples show a reversible saturable absorption. Conclusion: The Z-scan measurement showed that silver and gold nano-fluid prepared by gamma radiation exhibited large thermal nonlinear refractive index n2 as -8.78×10-7 and -2.478×10-6 cm2/W, respectively. We have also investigated nonlinear absorption of these samples and we found a large value of nonlinear absorption for Ag nanoparticle and a weak absorption for Au nanoparticle. In conclusion, the experimental result shows a good nonlinear refractive index at low laser power in which encouraging for possible applications in nonlinear optical devices.

  20. Preparation of luminescent CdTe quantum dots doped core-shell nanoparticles and their application in cell recognition

    Institute of Scientific and Technical Information of China (English)

    LI Zhaohui; WANG Kemin; TAN Weihong; LI Jun; FU Zhiying; WANG Yilin; LIU Jianbo; YANG Xiaohai

    2005-01-01

    Based on the reverse microemulsion technique, luminescent quantum dots doped core-shell nanoparticles have been prepared by employing silica as the shell and CdTe quantum dots as the core of the nanoparticles, which have an excellent solubility and dispersibility, especially amine and phosphonate groups have been modified on their surface synchronously. In comparison with CdTe quantum dots, these nanoparticles show superiority in chemical and photochemical stability. The quantum dots doped core-shell nanoparticles were successfully linked with lactobionic acid by amine group on it, which was used to recognize living liver cells.

  1. Preparation and evaluation of alginate nanoparticles containing pertussis toxin as a particulate delivery system

    Directory of Open Access Journals (Sweden)

    Hamid Reza Goudarzi

    2016-04-01

    Full Text Available During the last decades, research on different kinds of nanoparticles (NPs has been increased to prepare various medical applications, for instance in vaccine and gene delivery and as new generation of adjuvant candidates. The aim of the present study was to prepare sodium alginate nanoparticles (Alg-NPs containing pertussis toxin (PTX as an candidate acellular vaccine. Formulation of antigen loaded Alg-NPs were assessed for immunological activities and their role as potential immunological adjuvant. Alg-Nps were prepared using mild ionic gelation method. Optimal formulation was obtained by concentration of 0.2%w/v sodium alginate, 0.1%w/v CaCl2 solution and magnetically homogenization condition of 45 min and rate of 2000 rpm. Obtained Alg-NPs showed average size of 88 nm and zeta potential of -32mV in blank and 72 nm and -29 mV in PTX entrapped nanoparticles, respectively. A Loading efficiency of more than 90% was determined for PTX. The antigen loaded nanoparticles showed 75.3% of release within 144 h in in vitro release studies. The immunological evaluation in female Balb/c mice groups revealed that the Alg-NPs formulation induced significantly higher serum antibody titers (p < 0.01 as compared with commercial acellular pertussis vaccine and conventional alum-adjuvanted antigen administered by subcutaneous route. The results showed the potential of Alg-NPS to be a simplex and efficient delivery system. This study also indicated the potential of Alg-NPs as new generation of immunostimulant adjuvant to boost the antigenecity of the antigens in a cellular pertussis vaccines.

  2. Preparation, Characterization of Hydrophobic Drug in Combine Loaded Chitosan/Cyclodextrin/Trisodium Citrate Nanoparticles and in vitro Release Study

    Institute of Scientific and Technical Information of China (English)

    JI Jin-gou; ZHANG Jing-fen; HAO Shi-lei; WU Dan-jun; LIU Li; XU Yi

    2012-01-01

    Chitosan/cyclodextrin/trisodium citrate(CS/CD/TSC) nanoparticles with ibuprofen(IBU) loaded were prepared via the ionic cross-linking method,with trisodium citrate selected as the cross-linking agent.The drug-loading capacity,particle size,zeta potential and surface morphology of the obtained nanoparticles were investigated.The results show a good drug-loading capacity.The prepared nanoparticles were spherical in shape with an average size of 293.7 nm and a zeta potential of +30.72 mV.The in vitro release studies show that the controlled release of IBU from the nanoparticles was followed.The drug release from CS/β-CD/TSC nanoparticles followed non-Fickian or anomalous diffusion.

  3. One-Step Self-Assembling Method to Prepare Dual-Functional Transferrin Nanoparticles for Antitumor Drug Delivery.

    Science.gov (United States)

    Wang, Kaikai; Yuan, Ahu; Yu, Jiaqian; Wu, Jinhui; Hu, Yiqiao

    2016-03-01

    Protein-based nanoparticles hold great promise in both preclinical and clinical practices due to their high biocompatibility and biodegradability. However, the complicated preparations often denature proteins, which subsequently diminish their bioactivity. To overcome these drawbacks, we developed a one-step self-assembling method for preparing protein-based nanoparticles. Transferrin (Tf), a targeting protein, was mixed with 2-mercaptoethanol to break disulfide bonds. Using this method, Tf-PTX-NPs (paclitaxel-loaded Tf nanoparticles) could be readily obtained. Tf-PTX-NPs were round and their diameter could be controlled in the range of 5-200 nm. The bioactivity of Tf to its receptor after forming nanoparticles was also confirmed in vitro. Tf-PTX-NPs also could inhibit the tumor growth to some extent in a mice tumor xenograft model. Therefore, using this self-assembling method, we fabricated this antitumor Tf-based nanoparticle, in which Tf acted as both the targeting moiety and drug carrier.

  4. Facile preparation of TiO{sub 2}–polyvinyl alcohol hybrid nanoparticles with improved visible light photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Filippo, Emanuela [Department of Innovation Engineering, University of Salento, Monteroni Street, 73100, Lecce (Italy); Carlucci, Claudia; Capodilupo, Agostina Lina [National Nanotechnology Laboratory (NNL), Nanoscience Institure – CNR, Arnesano Street, 73100 Lecce (Italy); Perulli, Patrizia [Department of Innovation Engineering, University of Salento, Monteroni Street, 73100, Lecce (Italy); Conciauro, Francesca [National Nanotechnology Laboratory (NNL), Nanoscience Institure – CNR, Arnesano Street, 73100 Lecce (Italy); Corrente, Giuseppina Anna [University of Calabria, Pietro Bucci Street, 87036 Arcavacata di Rende, Cosenza (Italy); Gigli, Giuseppe [National Nanotechnology Laboratory (NNL), Nanoscience Institure – CNR, Arnesano Street, 73100 Lecce (Italy); Center for Biomolecular Nanotechnologies (CBN) of Italian Institute of Technology (IIT), Barsanti Street 1, 73010 Arnesano (Italy); Department of Physics, University of Salento, Monteroni Street, 73100, Lecce (Italy); Ciccarella, Giuseppe, E-mail: giuseppe.ciccarella@unisalento.it [Department of Innovation Engineering, University of Salento, Monteroni Street, 73100, Lecce (Italy); National Nanotechnology Laboratory (NNL), Nanoscience Institure – CNR, Arnesano Street, 73100 Lecce (Italy)

    2015-03-15

    Graphical abstract: - Highlights: • Hybrid TiO{sub 2}/PVA core/shell nanoparticles were prepared through a two step procedure. • TiO{sub 2}–PVA samples were prepared based on different TiO{sub 2}–PVA weight ratios. • All samples were characterized using XRD, TEM, FT-IR and BET analysis. • The photocatalytic performance was evaluated. - Abstract: Hybrid inorganic/organic core/shell nanoparticles were prepared through a two step synthesis procedure. In the first step, pure anatase TiO{sub 2} nanoparticles were synthesized though a rapid microwave assisted non-aqueous route. Then, the obtained titania nanoparticles were coated with polyvinyl alcohol (PVA) using a simple solution method followed by relatively low temperature treatment. The PVA-coated titania nanoparticles samples were prepared at different TiO{sub 2}–PVA weight ratio and they were characterized using X-Ray diffraction, transmission electron microscopy, infrared spectroscopy and Brunauer–Emmett–Teller (BET) analysis. Photocatalytic performance was also evaluated for all samples and the results indicated that TiO{sub 2}:PVA weight ratio was a key factor to obtain an improvement of the photocatalytic activity with respect to bare TiO{sub 2} nanoparticles, since PVA concentration influenced the surface area and the aggregation of nanoparticles and the thickness of the coating layer. This inexpensive system provides a simple, quick and effective approach which allows to obtain core/shell hybrid nanostructures.

  5. Preparation, characterization and scale-up of sesamol loaded solid lipid nanoparticles

    Directory of Open Access Journals (Sweden)

    Vandita Kakkar

    2012-01-01

    Full Text Available Sesamol loaded solid lipid nanoparticles (SSLNs were prepared with the aim of minimizing its distribution to tissues and achieving its targeting to the brain. Three scale-up batches (100x1 L of S-SLNs were prepared using a microemulsification technique and all parameters were statistically compared with the small batch (1x;10 mL. S-SLNs with a particle size of less than 106 nm with a spherical shape (transmission electron microscopy were successfully prepared with a total drug content and entrapment efficiency of 94.26±2.71% and 72.57±5.20%, respectively. Differential scanning calorimetry and infrared spectroscopy confirmed the formation of lipidic nanoparticles while powder X-ray diffraction revealed their amorphous profile. S-SLNs were found to be stable for three months at 5±3°C in accordance with International Conference on Harmonisation guidelines. The SLN preparation process was successfully scaled-up to a 100x batch on a laboratory scale. The procedure was easy to perform and allowed reproducible SLN dispersions to be obtained.

  6. Biomimetic synthesis of silver nanoparticles using the fish scales of Labeo rohita and their application as catalysts for the reduction of aromatic nitro compounds.

    Science.gov (United States)

    Sinha, Tanur; Ahmaruzzaman, M; Sil, A K; Bhattacharjee, Archita

    2014-10-15

    In this article, a cleaner, greener, cheaper and environment friendly method for the generation of self assembled silver nanoparticles (Ag NPs) applying a simple irradiation technique using the aqueous extract of the fish scales (which is considered as a waste material) of Labeo rohita is described. Gelatin is considered as the major ingredient responsible for the reduction as well as stabilisation of the self assembled Ag NPs. The size and morphology of the individual Ag NPs can be tuned by controlling the various reaction parameters, such as temperature, concentration, and pH. Studies showed that on increasing concentration and pH Ag NPs size decreases, while on increasing temperature, Ag NPs size increases. The present process does not need any external reducing agent, like sodium borohydride or hydrazine or others and gelatin itself can play a dual role: a 'reducing agent' and 'stabilisation agent' for the formation of gelatin-Ag NPs colloidal dispersion. The synthesized Ag NPs were characterised by Ultraviolet-Visible spectroscopy (UV-Vis), Transmission electron microscopy (TEM) and Selected area electron diffraction (SAED) analyses. The synthesized Ag NPs was used to study the catalytic reduction of various aromatic nitro compounds in aqueous and three different micellar media. The hydrophobic and electrostatic interaction between the micelle and the substrate is responsible for the catalytic activity of the nanoparticles in micelle.

  7. Preparation of photoreactive phospholipid polymer nanoparticles to immobilize and release protein by photoirradiation.

    Science.gov (United States)

    Chen, Weixin; Inoue, Yuuki; Ishihara, Kazuhiko

    2015-11-01

    Photoreactive and cytocompatible polymer nanoparticles for immobilizing and releasing proteins were prepared. A water-soluble and amphiphilic phospholipid polymer, poly(2-methacryloyloxyethyl phosphorylcholine (MPC)-co-n-butyl methacrylate (BMA)-co-4-(4-(1-methacryloyloxyethyl)-2-methoxy-5-nitrophenoxy) butyric acid (PL)) (PMB-PL) was synthesized. The PMB-PL underwent a cleavage reaction at the PL unit with photoirradiation at a wavelength of 365 nm. Additionally, the PMB-PL took polymer aggregate in aqueous medium and was used to modify the surface of biodegradable poly(L-lactic acid) (PLA) nanoparticle as an emulsifier. The morphology of the PMB-PL/PLA nanoparticle was spherical and approximately 130 nm in diameter. The carboxylic acid group in the PL unit could immobilize proteins by covalent bonding. The bound proteins were released by a photoinduced cleavage reaction. Within 60s, up to 90% of the immobilized proteins was released by photoirradiation. From these results and with an understanding of the fundamental properties of MPC polymers, we concluded that PMB-PL/PLA nanoparticles have the potential to be used as smart carriers to deliver proteins to biological systems, such as the inside of living cells.

  8. Preparation and Characterization of Modified Polyethyleneimine Magnetic Nanoparticles for Cancer Drug Delivery

    Directory of Open Access Journals (Sweden)

    Sedighe Arabi

    2016-01-01

    Full Text Available Magnetic nanoparticles with polymeric coating have great significance in drug delivery purpose. We intended to prepare a modified amphiphilic polymer with targeting susceptibility to reduce side effects to normal cells. In this study polyethyleneimine (PEI as a polycationic polymer reacted with sebacoyl chloride to make a new amphiphilic polymer and folic acid as a targeting agent to reduce cytotoxicity of polymer and increase specific entrance of nanoparticles to cancerous cells. The obtained polymer (PEI-Sb-FA was then coated on magnetic nanoparticles (MNPs to stabilize them. The core-shell nanoparticles were characterized by different methods such as scanning electron microscopy (SEM, X-ray diffraction (XRD, thermogravimetric analysis (TGA, and vibrating sample magnetometer (VSM. Curcumin was finally loaded on PEI-Sb-FA-MNPs and the release behavior was studied in different pH. Curcumin loading of 28.2% was obtained and released drug in acidic pH = 4.5 was more than pH = 7.4, showing drug release sensitivity toward pH of media.

  9. Magnetic Properties of FePt Nanoparticles Prepared by a Micellar Method

    Directory of Open Access Journals (Sweden)

    Gao Y

    2009-01-01

    Full Text Available Abstract FePt nanoparticles with average size of 9 nm were synthesized using a diblock polymer micellar method combined with plasma treatment. To prevent from oxidation under ambient conditions, immediately after plasma treatment, the FePt nanoparticle arrays were in situ transferred into the film-growth chamber where they were covered by an SiO2 overlayer. A nearly complete transformation of L10 FePt was achieved for samples annealed at temperatures above 700 °C. The well control on the FePt stoichiometry and avoidance from surface oxidation largely enhanced the coercivity, and a value as high as 10 kOe was obtained in this study. An evaluation of magnetic interactions was made using the so-called isothermal remanence (IRM and dc-demagnetization (DCD remanence curves and Kelly–Henkel plots (ΔM measurement. The ΔM measurement reveals that the resultant FePt nanoparticles exhibit a rather weak interparticle dipolar coupling, and the absence of interparticle exchange interaction suggests no significant particle agglomeration occurred during the post-annealing. Additionally, a slight parallel magnetic anisotropy was also observed. The results indicate the micellar method has a high potential in preparing FePt nanoparticle arrays used for ultrahigh density recording media.

  10. Magnetic Properties of γ-Fe2O3 Nanoparticles Prepared by Laser Ablation

    Institute of Scientific and Technical Information of China (English)

    WANG Zemin; ZENG Xiaoyan

    2006-01-01

    A new method of preparing nanoparticles by pulsed-laser ablation of a tiny wire was reported, and pure maghemite ( γ-Fe2O3 ) nanoparticles were synthesized by this method in a mixed gas flux of N2 and O2 at atmospheric pressure. The obtainedγ- Fe2O3 nanopartiles were in the range of 5 to 80 nm in diameter and largely spherical in shape. Structural characteristics and morphologies of the nanoparticles were characterized by XRD and TEM, respectively. Moreover, magnetic properties of the obtained γ- Fe2O3 nanopartiles in the temperature range of 300 to 773 K were investigated. The experimental results demonstrate that the squareness value of the hysteresis loop decreases with increasing temperature. Both the coercivity and the saturation magnetization of the γ- Fe2O3 nanoparticles show a constantly decreasing trend with increasing temperature up to the occurrence of the transformation from γ- Fe2O3 to α- Fe2O3. Especially, at the temperature of 773 K, the γ- Fe2O3 begins to transform to the α-Fe2O3 phase and the hysteresis loop becomes unclosed.

  11. Preparation and application of hydroxyapatite(HA) nanoparticles/NR2B-siRNA complex

    Institute of Scientific and Technical Information of China (English)

    YANG Hui; HUANG Dong; ZHU Shai-hong; YAN Xue-bin; GU Yong-hong; YAN Hui; WU Li-xiang

    2008-01-01

    Hydroxyapatite(HA) nanoparticles were prepared by coprecipitation-hydrothermal synthesis and their exosyndrome was estimated via transmission electron microscopy. Agarose gel electrophoresis and ultraviolet spectrophotometry were used to evaluate the ability of HA to bind NR2B-siRNA at different pH values and at different HA-NR2B-siRNA ratios. And the stability of the complex in saline was also evaluated. The effect of HA/NR2B-siRNA complex on chronic inflammatory pain was evaluated in vivo in mice. Transmission electron microscopy(TEM) reveals that HA nanoparticles are thin strips or short rod in shape and the one-dimensional particle size of HA nanoparticles is 40-50 nm. Under the acid or neutral condition, the Zeta potential of HA is positive; nanoparticles can completely bind NR2B-siRNA when the HA:NR2B-siRNA ratio is at or larger than 35-1; while under the alkaline condition, the affinity of HA to NR2B-siRNA is rather weak. HA/NR2B-siRNA complex is not dissociated when being resuspended in saline. The nociception of the tonic phase induced by formalin is significantly reduced in the HA/NR2B-siRNA treated mice as compared with the controls. Therefore, HA may be a new siRNA nano-vector material.

  12. Preparation and antibacterial properties of hybrid-zirconia films with silver nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Azocar, Ignacio, E-mail: manuel.azocar@usach.cl [Departamento de Quimica de los Materiales, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACH, Avenida Bernardo O' Higgins 3363, Casilla 40, Correo 33, Santiago (Chile); Vargas, Esteban [Facultad de Ingenieria, Departamento de Metalurgia, Universidad de Santiago de Chile, USACH (Chile); Duran, Nicole [Departamento de Quimica de los Materiales, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACH, Avenida Bernardo O' Higgins 3363, Casilla 40, Correo 33, Santiago (Chile); Arrieta, Abel [Departamento de Biologia, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACH (Chile); Gonzalez, Evelyn [Departamento de Quimica de los Materiales, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACH, Avenida Bernardo O' Higgins 3363, Casilla 40, Correo 33, Santiago (Chile); Facultad de Ingenieria, Departamento de Metalurgia, Universidad de Santiago de Chile, USACH (Chile); Departamento de Biologia, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACH (Chile); Departamento de Quimica Farmacologica y Toxicologica, Facultad de Ciencias Quimicas, Universidad de Chile, Sergio Livingstone Polhammer 1007, Santiago (Chile); and others

    2012-11-15

    The antimicrobial effect of incorporating silver nanoparticles (AgNps) into zirconia matrix-polyether glycol was studied. AgNps of 4-6 nm in size were synthesized using the inverse micelles method, and different doses of metallic nanoparticles were incorporated into zirconia-polyether glycol mixtures during the ageing procedure. Atomic force microscopy (AFM) of the modified hybrid film showed a homogenous distribution of 20-80 nm diameter AgNps, indicating agglomeration of these structures during film modification; such agglomerations were greater when increasing the dosage of the colloidal system. The AgNps-hybrid films showed higher antimicrobial activity against Gram-positive bacteria than for Gram-negative bacteria. Hybrid films prepared with dioctyl sodium sulfosuccinate (AOT) stabilized AgNps presented enhanced antibacterial activity compared to that obtained through the addition of a high AgNO{sub 3} concentration (0.3 wt%). -- Graphical abstract: Atomic Force Micrographs, top and cross section view, showing silver nanoparticles embedded in a zirconia-polyether glycol hybrid film. Highlights: Black-Right-Pointing-Pointer Antibacterial activity of films (zirconia-polyether glycol) modified with silver nanoparticles. Black-Right-Pointing-Pointer Biofilm formation is prevented. Black-Right-Pointing-Pointer High sensibility against gram positive bacteria.

  13. Preparation of carbon nanoparticles by plasma arc discharge under fluidized dynamic equilibrium

    Science.gov (United States)

    Wang, F.; Sun, D. L.; Hong, R. Y.; Kumar, M. R.

    2016-06-01

    Continuous preparation of carbon nanoparticles by dielectric barrier discharge (DBD)-induced non-thermal plasma arc discharge with large spacing in a modified fluidized bed is presented. Discharge arc is generated via the inducement of DBD which provides conductive media in order to realize a large spacing arc discharge. Three kinds of flow conditions defined as full circulation, fluidized dynamic equilibrium, and full collection are determined by the relationship of critical fluidized velocity and the real gas velocity after some modification of the fluidized bed. Movement model of carbon nanoparticles has been proposed to illustrate the flow conditions. A visualized and comprehensive refinement of aggregating processes has been exhibited and proved by high-resolution transmission electron microscopy. Simplified equivalent electrical conductive model of the arc discharge system is successful to generally and perspicuously figure out the discharge process which is impeded by the generated carbon nanoparticles. Effects of flow conditions and flow ratio of carrier gas/carbon source on morphology and yield of nanoparticles have been analyzed by morphology observation and yield calculation along with modeling the process.

  14. Preparation and Characterization of CuO Nanoparticles by Novel Sol-Gel Technique

    Directory of Open Access Journals (Sweden)

    Y. Aparna

    2012-10-01

    Full Text Available Recent developments of nanosize materials of metal and metal oxide particles are intensively pursued because of their prominence in different fields of applications. Among all the transition metal oxides, CuO is a potential candidate for the application of magnetic storage devices, solar energy transfer, sensors, and super capacitors etc. Moreover CuO nanoparticles act as a good catalyst in some of the chemical reactions. CuO nanoparticles were prepared by novel sol-gel method. In this technique CuCl2.6H2O is added with acetic acid and heated to 100 °C with continuous stirring. To control the ph of the above solution, NaOH is added to the solution till ph reached desired value. The color of the solution changed from blue to black with precipitation. The black precipitation was washed 3 – 4 times with distilled water. Finally the solution was centrifuged and dried in air for one day. The CuO nanoparticles were characterized by studying their structure with X-ray diffraction and composition by energy dispersive X-ray analysis. The size of the nanoparticles is estimated by particle size analyzer and transmission electron microscopy. The optical studies were carried out with Uv-Vis spectrophotometer.

  15. Preparation and characterization of nanoparticles of carboxymethyl cellulose acetate butyrate containing acyclovir

    Science.gov (United States)

    Vedula, Venkata Bharadwaz; Chopra, Maulick; Joseph, Emil; Mazumder, Sonal

    2016-02-01

    Nanoparticles of carboxymethyl cellulose acetate butyrate complexed with the poorly soluble antiviral drug acyclovir (ACV) were produced by precipitation process and the formulation process and properties of nanoparticles were investigated. Two different particle synthesis methods were explored—a conventional precipitation method and a rapid precipitation in a multi-inlet vortex mixer. The particles were processed by rotavap followed by freeze-drying. Particle diameters as measured by dynamic light scattering were dependent on the synthesis method used. The conventional precipitation method did not show desired particle size distribution, whereas particles prepared by the mixer showed well-defined particle size ~125-450 nm before and after freeze-drying, respectively, with narrow polydispersity indices. Fourier transform infrared spectroscopy showed chemical stability and intactness of entrapped drug in the nanoparticles. Differential scanning calorimetry showed that the drug was in amorphous state in the polymer matrix. ACV drug loading was around 10 wt%. The release studies showed increase in solution concentration of drug from the nanoparticles compared to the as-received crystalline drug.

  16. Mechanochemical Preparation of Cobalt Nanoparticles through a Novel Intramolecular Reaction in Cobalt(II Complexes

    Directory of Open Access Journals (Sweden)

    Seyed Abolghasem Kahani

    2015-01-01

    Full Text Available A novel solid state reaction involving a series of cobalt(II hydrazine-azides has been used to prepare metallic cobalt nanoparticles. The reactions of [Co(N2H4(N32], [Co(N2H42(N32], and [Co(N2H4(N3Cl]·H2O via NaOH, KOH as reactants were carried out in the solid state. These complexes undergo an intramolecular two-electron oxidation-reduction reaction at room temperature, producing metallic cobalt nanoparticles (Co1–Co6. The aforementioned complexes contain cobalt(II that is an oxidizing agent and also hydrazine ligand as a reducing agent. Other products produced include sodium azide and ammonia gas. The cobalt metal nanoparticles were characterized using X-ray powder diffraction (XRD, scanning electron microscopy (SEM, and vibrating sample magnetometer (VSM. The synthesized cobalt nanoparticles have similar morphologies; however, their particle size distributions are different.

  17. Sol-gel preparation and spectroscopic study of the pyrophanite MnTiO3 nanoparticles

    Institute of Scientific and Technical Information of China (English)

    ZHOU; Guowei; KANG; Youngsoo; LI; Tianduo; XU; Guiying

    2005-01-01

    The nanosized xerogel of titanium dioxide (TiO2) and manganese oxides (MnO2, Mn2O3, Mn3O4) was prepared by the sol-gel method using manganese chloride (MnCl2·4H2O) and titanium isopropoxide (Ti(O-iPr)4) as precursors in cetyltrimethylammonium bromide (CTAB)/ ethanol/H2O/HCl micelle solutions, following the calcinations of the produced powders at difference temperatures. The nanostructure and phase composition of these nanoparticles were characterized with X-ray powder diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS). The spectroscopic characterizations of these nanoparticles were also done with UV-Vis spectroscopy and laser Raman spectroscopy (LRS). XRD patterns show that the pyrophanite MnTiO3 phase was formed at the calcinations temperature of 900℃. The TEM images show that the nanoparticles are almost spherical or slight ellipose and the sizes are 50 nm on average. The UV-Vis spectra show that the nanosized MnTiO3 have significant absorption bands in the visible region. There are new absorption peaks of MnTiO3 nanoparticles in LRS compared with the pure TiO2 powder.

  18. Preparation of Titanium Nitride Nanoparticles from a Novel Refiuxing Derived Precursor

    Institute of Scientific and Technical Information of China (English)

    LIU Fei; LIANG Xiaofeng; LI Yongdi; YAO Yadong; ZHANG Hao; SHAO Wei; KANG Yunqing; YIN Guangfu; HUANG Zhongbing; LIAO Xiaoming

    2011-01-01

    Titanium nitride (TiN) nanoparticles were prepared from a novel refiuxing-derived precursor.The organic/inorganic hybrid precursor was prepared by a two-stage refluxing method using hydrous TiO2 as titania source and n-dodecane as carbon source. The precursor was heat-treated to 1 200 ℃ in flowing ammonia (NH3) to get TiN nanoparticles. The phase and chemical compositions were investigated by means of XRD,Raman spectroscopy and XPS. Samples microstructure was studied by means of SEM, TEM and SEAD. XRD pattern indicated that the product was face-centered cubic TiN with a lattice constant a = 4.236(A) and average crystallite sizes of 35.2 nm. Raman spectra indicated that long time refluxing results in Alkane dehydrogenation and the formation of coke on TiO2 nanoparticles. Oxygen presence in TiN lattice was confirmed by XPS investigation. The particle size that was showed by Electron microscopy photographs ranged from 20 to 60 nm.

  19. Preparation of antimony sulfide semiconductor nanoparticles by pulsed laser ablation in liquid

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Ren-De, E-mail: son003@sekisui.com [Research & Development Institute, High Performance Plastics Company, Sekisui Chemical Co., Ltd. 2-1 Hyakuyama, Shimamoto-Cho, Mishima-Gun, Osaka, 618-0021 (Japan); Tsuji, Takeshi [Interdisciplinary Graduate School of Science and Engineering, Shimane University, 1060 Nishikawatsu-Cho, Matsue, 690-8504 (Japan)

    2015-09-01

    Highlights: • Pulsed laser ablation in liquid (LAL) was applied to prepare antimony sulfide nanoparticles (Sb{sub 2}S{sub 3} NPs). • Sb{sub 2}S{sub 3} NPs with a stoichiometric composition were successfully prepared by LAL in water without using any surfactants or capping agents. • Thus-prepared Sb{sub 2}S{sub 3} NPs showed low-temperature crystallization and melting at a temperature low as 200 °C. • The NPs-coated Sb{sub 2}S{sub 3} thin film showed comparable semiconductor properties (carrier mobility and carrier density) to the vacuum deposited one. • Byproducts such as CS{sub 2}, CH{sub 4} and CO were detected by GC-MS analysis when LAL was performed in organic solvent. • The LAL-induced decomposition mechanism of Sb{sub 2}S{sub 3} and organic solvents was discussed based on the GC-MS results. - Abstract: In this paper, we report on the synthesis of antimony sulfide (Sb{sub 2}S{sub 3}) semiconductor nanoparticles by pulsed laser ablation in liquid without using any surfactants or capping agents. Different results were obtained in water and organic solvents. In the case of water, Sb{sub 2}S{sub 3} nanoparticles with chemical compositions of stoichiometry were successfully prepared when laser irradiation was performed under the condition with the dissolved oxygen removed by argon gas bubbling. It was shown that thus-obtained Sb{sub 2}S{sub 3} nanoparticles exhibit features of not only low-temperature crystallization but also low-temperature melting at a temperature as low as 200 °C. Nanoparticle-coated Sb{sub 2}S{sub 3} thin films were found to show good visible light absorption and satisfying semiconductor properties (i.e., carrier mobility and density), which are essential for photovoltaic application. On the other hand, in the case of organic solvents (e.g., acetone, ethanol), such unexpected byproducts as CS{sub 2}, CO and CH{sub 4} were detected from the reaction system by GC-MS analysis, which suggests that both Sb{sub 2}S{sub 3} and organic

  20. Development of olmesartan medoxomil lipid-based nanoparticles and nanosuspension: preparation, characterization and comparative pharmacokinetic evaluation.

    Science.gov (United States)

    B, Arun; D, Narendar; Veerabrahma, Kishan

    2017-03-14

    The aim was to enhance the oral bioavailability of olmesartan medoxomil (OM) by preparing solid lipid nanoparticles (SLNs) and comparing with nanosuspension (OM-NS). OM-SLNs and OM-NS were prepared by known methods. Prepared SLNs were evaluated for physical characters and in vivo pharmacokinetic (PK) performance in rats. OM-NS showed more than four-fold increase in the solubility. During DSC and XRD studies, drug incorporated in SLNs was found to be in amorphous form. The relative bioavailability of OM-SLN and OM-NS was 7.21- and 3.52-fold when compared with that of coarse suspension. Further, OM-SLNs also increased the oral bioavailability by two-fold over that of OM-NS.

  1. Preparation of Hierarchical Mesoporous Silica Nanoparticles through a Single-Templating Approach

    Institute of Scientific and Technical Information of China (English)

    陈媛丽; 肖敏; 庄伟; 李艺; 李宝宗; 杨永刚

    2012-01-01

    Silicas with hierarchical porous architectures attracted much attention, due to their potential applications in catalysis and separation. Generally, they were prepared through dualor triple-templating approaches. Herein, mesoporous silica nanoparticles with rod-like pore channels inside and lamellar mesopores on the surfaces were prepared using the self-assemblies of a chiral low-molecular-weight amphiphile as templates through a single-templating approach. The formation of the lamellar mesopores was studied by taking field-emission scanning electron microscopy and transmission electron microscopy images after different reaction times. The lamellar pores were proposed to be formed by merging rod-like micelles during the sol-gel process. Moreover, helical nanofibers with rod-like pore channels inside and lamellar mesopores on the surfaces were prepared with the addition of n-octanol as a co-structure-directing agent.

  2. Preparation and characterization of silver nanoparticles in natural polymers using laser ablation

    Indian Academy of Sciences (India)

    Reza Zamiri; B Z Azmi; Hossein Abbastabar Ahangar; Golnoosh Zamiri; M Shahril Husin; Z A Wahab

    2012-10-01

    In this paper we have done a comparative study on efficiency of natural polymers for stabilizing silver nanoparticles (Ag-NPs) prepared by laser ablation technique. The selected polymers are starch (St), gelatin (Gt) and chitosan (Ct). The fabrication process was carried out through ablation of a pure Ag plate by nanosecond Q-switched Nd–Yg pulsed laser ( = 532 nm, 360 mJ/pulse). The stability of the samples was studied by measuring UV-visible absorption spectra of the samples one month after preparation. The result showed that the formation efficiency of NPs in St were highest and also the prepared NPs in St solution were more stable than other polymers during one month storage.

  3. Biomimetic Receptors and Sensors

    Directory of Open Access Journals (Sweden)

    Franz L. Dickert

    2014-11-01

    Full Text Available In biomimetics, living systems are imitated to develop receptors for ions, molecules and bioparticles. The most pertinent idea is self-organization in analogy to evolution in nature, which created the key-lock principle. Today, modern science has been developing host-guest chemistry, a strategy of supramolecular chemistry for designing interactions of analytes with synthetic receptors. This can be realized, e.g., by self-assembled monolayers (SAMs or molecular imprinting. The strategies are used for solid phase extraction (SPE, but preferably in developing recognition layers of chemical sensors.

  4. Preparation of Silver Nanoparticle and Its Application to the Determination of ct-DNA

    Directory of Open Access Journals (Sweden)

    Dan Xiao

    2007-05-01

    Full Text Available A new method to prepare silver nanoparticles was reported in this paper, whichbased on aqueous-gaseous phase reaction of silver nitrate solution and ammonia gas. Theproposed method is effective, rapid, and convenient. Transmission electron microscope(TEM and X-ray diffraction (XRD were used to characterize the structure of the particles,respectively. It was found that the average diameter of the particles was about 10 nm and theshape was spherical. And the strong fluorescence signal of the silver nanoparticles solutioncan be quenched after the adding of the calf thymus DNA (ct-DNA solution. Thequenched fluorescence intensity was linear with the concentration of ct-DNA in the range of0.5 to 5.0 Ã��— 104 ng mL-1 with a detection limit of 0.3 ng mL-1.

  5. Emulsification-Induced Homohelicity in Racemic Helical Polymer for Preparing Optically Active Helical Polymer Nanoparticles.

    Science.gov (United States)

    Zhao, Biao; Deng, Jinrui; Deng, Jianping

    2016-04-01

    Optically active nano- and microparticles have constituted a significant category of advanced functional materials. However, constructing optically active particles derived from synthetic helical polymers still remains as a big challenge. In the present study, it is attempted to induce a racemic helical polymer (containing right- and left-handed helices in equal amount) to prefer one predominant helicity in aqueous media by using emulsifier in the presence of chiral additive (emulsification process). Excitingly, the emulsification process promotes the racemic helical polymer to unify the helicity and directly provides optically active nanoparticles constructed by chirally helical polymer. A possible mechanism is proposed to explain the emulsification-induced homohelicity effect. The present study establishes a novel strategy for preparing chirally helical polymer-derived optically active nanoparticles based on racemic helical polymers.

  6. Study on the preparation and formation mechanism of barium sulphate nanoparticles modified by different organic acids

    Indian Academy of Sciences (India)

    Yuhua Shen; Chuanhao Li; Xuemei Zhu; Anjian Xie; Lingguang Qiu; Jinmiao Zhu

    2007-07-01

    This paper reports a simple method to prepare barium sulphate nanoparticles by use of tetradecanoic acid, hexadecanoic acid and stearic acid as modifier. The barium sulphate nanoparticles obtained are characterized by using Fourier transform infra-red spectroscopy (FT-IR), powder X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic laser light scatter (DLLS) and thermogravimetric analysis (TGA), respectively. The results show that the BaSO4 particles are all spherical and in the nano-scale. Our method has a better dispersion and controllable diameter dependent on the length of the chain of organic acid and the pH value of the system. A possible mechanism is also discussed.

  7. Influence of preparation method on structural and magnetic properties of nickel ferrite nanoparticles

    Indian Academy of Sciences (India)

    Binu P Jacob; Ashok Kumar; R P Pant; Sukhvir Singh; E M Mohammed

    2011-12-01

    Nickel ferrite nanoparticles of very small size were prepared by sol–gel combustion and co-precipitation techniques. At the same annealing temperature sol–gel derived particles had bigger crystallite size. In both methods, crystallite size of the particles increased with annealing temperature. Sol–gel derived nickel ferrite particles were found to be of almost spherical shape and moderate particle size with a narrow size distribution; while co-precipitation derived particles had irregular shape and very small particle size with a wide size distribution. Nickel ferrite particles produced by sol–gel method exhibited more purity. Sol–gel synthesized nanoparticles were found to be of high saturation magnetization and hysteresis. Co-precipitation derived nickel ferrite particles, annealed at 400°C exhibited superparamagnetic nature with small saturation magnetization. Saturation magnetization increased with annealing temperature in both the methods. At the annealing temperature of 600°C, co-precipitation derived particles also became ferrimagnetic.

  8. Preparation of iron oxides using ammonium iron citrate precursor: Thin films and nanoparticles

    Science.gov (United States)

    Park, Sangmoon

    2009-09-01

    Ammonium iron citrate (C 6H 8O 7·nFe ·nH 3N) was used as a precursor for preparing both iron-oxide thin films and nanoparticles. Thin films of iron oxides were fabricated on silicon (111) substrate using a successive-ionic-layer-adsorption-and-reaction (SILAR) method and subsequent hydrothermal or furnace annealing. Atomic force microscopy (AFM) images of the iron-oxide films obtained under various annealing conditions show the changes of the micro-scale surface structures and the magnetic properties. Homogenous Fe 3O 4 nanoparticles around 4 nm in diameter were synthesized by hydrothermal reduction method at low temperature and investigated using transmission electron microscopy (TEM).

  9. Preparation and characterization of conductive antimony-doped tin oxide (ATO) nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    In this paper, conductive antimony-doped tin oxide (ATO) composite particles is prepared by hydroxylation method of metal alcoxides. This method has many advantages such as little pollution, low cost, simple sheet and equipment. The synthesis processing and the ATO nanoparticles are characterized by means of transmission electron microscope (TEM), X-ray diffraction (XRD), thermal gravimetric and differential thermal analysis, and BET. The results show that the ATO nanoparticles is tetragonal rutile crystal structure. TEM show that the particles are monodispersed with weak aggromation. The size of the particles calcinated at 700 is about 8nm. The specific areas are 153 m2 · g-1. In addition to, ATO nanop articles have good electric properties

  10. Study on the interaction between bovine serum albumin and starch nanoparticles prepared by isoamylolysis and recrystallization.

    Science.gov (United States)

    Ji, Na; Qiu, Chao; Li, Xiaojing; Xiong, Liu; Sun, Qingjie

    2015-04-01

    The current study primarily investigated the interaction of bovine serum albumin (BSA) with starch nanoparticles (SNPs) prepared by isoamylolysis and recrystallization using UV-vis, fluorescence, transmission electron microscopy (TEM), Fourier transform infrared (FTIR) and circular dichroism (CD). The enhanced absorbance observed by UV-vis spectroscopy and decreased intensity of fluorescence spectroscopy suggested that BSA could bind to SNPs and form a BSA-SNP complex. The synchronous fluorescence spectra revealed that the emission maximum of Tyr residue (at Δλ=15nm) was red-shifted at the investigated concentrations range, indicating that the conformation of BSA was changed. Quenching parameters showed that the quenching effect of SNPs was static quenching. TEM images showed that the SNPs were surrounded by protein coronae, indicating that nanoparticle-protein complexes had formed. The FTIR and CD characterization indicated that the SNPs induced structural changes in the secondary structure of BSA.

  11. Third-order nonlinear optical response of colloidal gold nanoparticles prepared by sputtering deposition

    Energy Technology Data Exchange (ETDEWEB)

    Castro, Hemerson P. S.; Alencar, Márcio A. R. C.; Hickmann, Jandir M. [Optics and Materials Group–OPTMA, Universidade Federal de Alagoas, CAIXA POSTAL 2051, 57061-970 Maceió (Brazil); Wender, Heberton [Brazilian Synchrotron National Laboratory (LNLS), CNPEM, Rua Giuseppe Máximo Scolfaro 10.000, 13083-970 Campinas (Brazil); Department of Physics, Universidade Federal do Mato Grosso do Sul, 79070-900, Campo Grande (Brazil); Teixeira, Sergio R. [Institute of Physics, Universidade Federal do Rio Grande do Sul, 91501-970, Porto Alegre (Brazil); Dupont, Jairton [Laboratory of Molecular Catalysis, Institute of Chemistry, Universidade Federal do Rio Grande do Sul, 91501-970, Porto Alegre (Brazil)

    2013-11-14

    The nonlinear optical responses of gold nanoparticles dispersed in castor oil produced by sputtering deposition were investigated, using the thermally managed Z-scan technique. Particles with spherical shape and 2.6 nm of average diameter were obtained and characterized by transmission electron microscopy and small angle X-ray scattering. This colloid was highly stable, without the presence of chemical impurities, neither stabilizers. It was observed that this system presents a large refractive third-order nonlinear response and a negligible nonlinear absorption. Moreover, the evaluation of the all-optical switching figures of merit demonstrated that the colloidal nanoparticles prepared by sputtering deposition have a good potential for the development of ultrafast photonic devices.

  12. Surface engineered nanoparticles for improved surface enhanced Raman scattering applications and method for preparing same

    Science.gov (United States)

    Simmons, Blake A.; Talin, Albert Alec

    2009-11-27

    A method for producing metal nanoparticles that when associated with an analyte material will generate an amplified SERS spectrum when the analyte material is illuminated by a light source and a spectrum is recorded. The method for preparing the metal nanoparticles comprises the steps of (i) forming a water-in-oil microemulsion comprising a bulk oil phase, a dilute water phase, and one or more surfactants, wherein the water phase comprises a transition metal ion; (ii) adding an aqueous solution comprising a mild reducing agent to the water-in-oil microemulsion; (iii) stirring the water-in-oil microemulsion and aqueous solution to initiate a reduction reaction resulting in the formation of a fine precipitate dispersed in the water-in-oil microemulsion; and (iv) separating the precipitate from the water-in-oil microemulsion.

  13. Desalination by biomimetic aquaporin membranes: Review of status and prospects

    DEFF Research Database (Denmark)

    Tang, C.Y.; Zhao, Y.; Wang, R.;

    2013-01-01

    Based on their unique combination of offering high water permeability and high solute rejection aquaporin proteins have attracted considerable interest over the last years as functional building blocks of biomimetic membranes for water desalination and reuse. The purpose of this review is to prov......Based on their unique combination of offering high water permeability and high solute rejection aquaporin proteins have attracted considerable interest over the last years as functional building blocks of biomimetic membranes for water desalination and reuse. The purpose of this review...... is to provide an overview of the properties of aquaporins, their preparation and characterization. We discuss the challenges in exploiting the remarkable properties of aquaporin proteins for membrane separation processes and we present various attempts to construct aquaporin in membranes for desalination......; including an overview of our own recent developments in aquaporin-based membranes. Finally we outline future prospects of aquaporin based biomimetic membrane for desalination and water reuse....

  14. Preparation, in vitro release, and pharmacokinetics in rabbits of lyophilized injection of sorafenib solid lipid nanoparticles

    Directory of Open Access Journals (Sweden)

    Zhang H

    2012-06-01

    Full Text Available Hong Zhang, Fu-Ming Zhang, Shi-Jun YanDepartment of Pharmacy, Renmin Hospital of Wuhan University, Wuhan, People’s Republic of ChinaAbstract: Sorafenib solid lipid nanoparticles (S-SLN were prepared by emulsion evaporation–solidification at low temperature. Morphology was examined by transmission electron microscope. Particle size and zeta potential were determined by laser granularity equipment. Encapsulation efficiency (EE was detected by Sephadex gel chromatography and high-performance liquid chromatography (HPLC. The in vitro release profile of S-SLN was studied with dialysis technology. The lyophilized injection of S-SLN was prepared by freeze drying and analyzed by differential scanning calorimetry. The plasma concentration of sorafenib in blood was determined by HPLC. The solid lipid nanoparticles assumed a spherical shape with an even distribution of diameter and particle size 108.23 ± 7.01 nm (n = 3. The polydispersity index, zeta potential, and EE were determined to be 0.25 ± 0.02, -16.37 ± 0.65 mV, and 93.49% ± 1.87%, respectively (n = 3. The in vitro release accorded with the Weibull distribution model. An equal volume of 15% (w/v mannitol performed better as the protective agent for a lyophilized injection of S-SLN with a new material phase formation. The pharmacokinetic processes of sorafenib solution and lyophilized injection of S-SLN in vivo were in accordance with the two-compartment and one-compartment models, respectively. S-SLN nanoparticles are thus considered a promising drug-delivery system.Keywords: sorafenib, solid lipid nanoparticles, material phase analysis, HPLC, release profile, pharmacokinetics

  15. New Method to Prepare Mitomycin C Loaded PLA-Nanoparticles with High Drug Entrapment Efficiency

    Science.gov (United States)

    Hou, Zhenqing; Wei, Heng; Wang, Qian; Sun, Qian; Zhou, Chunxiao; Zhan, Chuanming; Tang, Xiaolong; Zhang, Qiqing

    2009-07-01

    The classical utilized double emulsion solvent diffusion technique for encapsulating water soluble Mitomycin C (MMC) in PLA nanoparticles suffers from low encapsulation efficiency because of the drug rapid partitioning to the external aqueous phase. In this paper, MMC loaded PLA nanoparticles were prepared by a new single emulsion solvent evaporation method, in which soybean phosphatidylcholine (SPC) was employed to improve the liposolubility of MMC by formation of MMC-SPC complex. Four main influential factors based on the results of a single-factor test, namely, PLA molecular weight, ratio of PLA to SPC (wt/wt) and MMC to SPC (wt/wt), volume ratio of oil phase to water phase, were evaluated using an orthogonal design with respect to drug entrapment efficiency. The drug release study was performed in pH 7.2 PBS at 37 °C with drug analysis using UV/vis spectrometer at 365 nm. MMC-PLA particles prepared by classical method were used as comparison. The formulated MMC-SPC-PLA nanoparticles under optimized condition are found to be relatively uniform in size (594 nm) with up to 94.8% of drug entrapment efficiency compared to 6.44 μm of PLA-MMC microparticles with 34.5% of drug entrapment efficiency. The release of MMC shows biphasic with an initial burst effect, followed by a cumulated drug release over 30 days is 50.17% for PLA-MMC-SPC nanoparticles, and 74.1% for PLA-MMC particles. The IR analysis of MMC-SPC complex shows that their high liposolubility may be attributed to some weak physical interaction between MMC and SPC during the formation of the complex. It is concluded that the new method is advantageous in terms of smaller size, lower size distribution, higher encapsulation yield, and longer sustained drug release in comparison to classical method.

  16. Preparation, statistical optimization, and in vitro characterization of insulin nanoparticles composed of quaternized aromatic derivatives of chitosan.

    Science.gov (United States)

    Mahjub, Reza; Dorkoosh, Farid Abedin; Amini, Mohsen; Khoshayand, Mohammad Reza; Rafiee-Tehrani, Morteza

    2011-12-01

    The aim of this study was the preparation, optimization, and in vitro characterization of insulin nanoparticles composed of methylated N-(4-N,N-dimethylaminobenzyl), methylated N-(4-pyridinyl), and methylated N-(benzyl) chitosan. Three types of derivatives were synthesized by the Schiff base reaction followed by quaternization. Nanoparticles were prepared by the polyelectrolyte complexation method. Experimental design D-optimal response surface methodology was used for the optimization of the nanoparticles. Independent variables were pH of polymer solution, concentration ratio of polymer/insulin, and also polymer type. Dependent variables include size, zeta potential, polydispersity index (PdI), and entrapment efficiency (EE%). Optimized nanoparticles were studied morphologically by transmission electron microscopy (TEM), and in vitro release of insulin from nanoparticles were determined under phosphate buffer (pH = 6.8) condition. Although a quadratic model has been chosen to fit the responses for size, PdI, and EE%, the zeta potential of the particles has been best fitted to 2-FI model. The optimized nanoparticles were characterized. The size of the particles were found to be 346, 318, and 289 nm; zeta potentials were 28.5, 27.7, and 22.2 mV; PdI of particles were 0.305, 0.333, and 0.437; and calculated EE% were 70.3%, 84.5%, and 69.2%, for methylated (aminobenzyl), methylated (pyridinyl), and methylated (benzyl) chitosan nanoparticles, respectively. TEM images show separated and non-aggregated nanoparticles with sub-spherical shapes and smooth surfaces. An in vitro release study of the prepared nanoparticles showed that the cumulative percentage of insulin released from the nanoparticles were 47.1%, 38%, and 68.7% for (aminobenzyl), (pyridinyl), and (benzyl) chitosan, respectively, within 300 min.

  17. Preparation, characterization, and transport of dexamethasone-loaded polymeric nanoparticles across a human placental in vitro model.

    Science.gov (United States)

    Ali, Hazem; Kalashnikova, Irina; White, Mark Andrew; Sherman, Michael; Rytting, Erik

    2013-09-15

    The purpose of this study was to prepare dexamethasone-loaded polymeric nanoparticles and evaluate their potential for transport across human placenta. Statistical modeling and factorial design was applied to investigate the influence of process parameters on the following nanoparticle characteristics: particle size, polydispersity index, zeta potential, and drug encapsulation efficiency. Dexamethasone and nanoparticle transport was subsequently investigated using the BeWo b30 cell line, an in vitro model of human placental trophoblast cells, which represent the rate-limiting barrier for maternal-fetal transfer. Encapsulation efficiency and drug transport were determined using a validated high performance liquid chromatography method. Nanoparticle morphology and drug encapsulation were further characterized by cryo-transmission electron microscopy and X-ray diffraction, respectively. Nanoparticles prepared from poly(lactic-co-glycolic acid) were spherical, with particle sizes ranging from 140 to 298 nm, and encapsulation efficiency ranging from 52 to 89%. Nanoencapsulation enhanced the apparent permeability of dexamethasone from the maternal compartment to the fetal compartment more than 10-fold in this model. Particle size was shown to be inversely correlated with drug and nanoparticle permeability, as confirmed with fluorescently labeled nanoparticles. These results highlight the feasibility of designing nanoparticles capable of delivering medication to the fetus, in particular, potential dexamethasone therapy for the prenatal treatment of congenital adrenal hyperplasia.

  18. Preparation of Au and Ag nanoparticles using Artemisia annua and their in vitro antibacterial and tyrosinase inhibitory activities.

    Science.gov (United States)

    Basavegowda, Nagaraj; Idhayadhulla, Akber; Lee, Yong Rok

    2014-10-01

    This work describes a plant-mediated approach to the preparation of metal nanoparticles using leaf extract of Artemisia annua (A. annua), an ethno-medicinal plant widely found in Asia, which was used as reducing and stabilizing agent. A. annua is used in traditional Chinese medicine to alleviate fever. Au and Ag nanoparticles were prepared using a one-step aqueous method at room temperature without any toxic chemicals. The formation of Au and Ag nanoparticles was monitored by UV-vis spectroscopy. Synthesized nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX), Fourier transform infrared (FT-IR) spectroscopy, and thermogravimetric analysis (TGA). TEM analysis of Au nanoparticles showed that they had triangular and spherical shapes with sizes ranging from 15 to 40 nm. The silver nanoparticles were predominantly spherical and uniformly sized (30-50 nm). The Au and Ag nanoparticles produced showed significant tyrosinase inhibitory and antibacterial effects. These results suggest that the synthesized nanoparticles provide good alternatives in varied medical and industrial applications.

  19. NOVEL PREPARATION AND MAGNETO CHEMICAL CHARACTERIZATION OF NANO-PARTICLE MIXED ALCOHOL CATALYSTS

    Energy Technology Data Exchange (ETDEWEB)

    Setala V. Naidu

    2003-01-01

    We have produced Co, Cu, and Fe nano-particles by Laser-induced solution deposition (LISD) as evidenced by TEM investigations. Sizes of the nano-particles created are in the order of 5 nm. The LISD system could generate nano-particles in quantities only in the order of a milligram. This may be mainly due to the limited photo induced reactions taking place on the surface of the solutions. We have designed experiments to use drop flow technique with LISD for nano-particle deposition on microreactors. Preliminary work has been done on Co and Fe thin film deposited microreactors. We are also investigating the catalytic properties of nano-particles of FeO and CoO prepared by ball milling and dispersed into sol-gel prepared alumina granules. We have continued our investigation of catalytic reactions of Cu, Co, Fe, Cu/Co, Cu/Fe and Co/Fe on alumina support. The metal oxides were first reduced with hydrogen and used for the conversion of CO/H{sub 2}. The surface area of the catalysts has been determined by nitrogen disorption. They are in the range of 200-300 m{sup 2}/g. Cu, Co, Fe, Co/Fe, Cu/Co and Cu/Fe showed increasing order of catalytic activity for CO/H{sub 2} conversion. We are also studying catalytic conversion rates for CO{sub 2}/H{sub 2} and CO/CO{sub 2}/H{sub 2} mixtures using these catalysts. Our investigations of Co and Fe thin film deposited microreactors showed higher CO/H{sub 2} conversion for Fe compared to Co. We have used vibrating sample magnetometer (VSM) to study the magnetic characteristics of as prepared, reduced, post-reaction catalysts. Comparative study of the ferromagnetic component of these samples gives the reduction efficiency and the changes in metal centers during catalytic reactions. Magnetic studies of post-reaction Co and Fe micro-reactors show that more carbide formation occurs for iron compared to cobalt.

  20. Preparation of Ultrafine Fe-Pt Alloy and Au Nanoparticle Colloids by KrF Excimer Laser Solution Photolysis.

    Science.gov (United States)

    Watanabe, Masato; Takamura, Hitoshi; Sugai, Hiroshi

    2009-03-10

    We prepared ultrafine Fe-Pt alloy nanoparticle colloids by UV laser solution photolysis (KrF excimer laser of 248 nm wavelength) using precursors of methanol solutions into which iron and platinum complexes were dissolved together with PVP dispersant to prevent aggregations. From TEM observations, the Fe-Pt nanoparticles were found to be composed of disordered FCC A1 phase with average diameters of 0.5-3 nm regardless of the preparation conditions. Higher iron compositions of nanoparticles require irradiations of higher laser pulse energies typically more than 350 mJ, which is considered to be due to the difficulty in dissociation of Fe(III) acetylacetonate compared with Pt(II) acetylacetonate. Au colloid preparation by the same method was also attempted, resulting in Au nanoparticle colloids with over 10 times larger diameters than the Fe-Pt nanoparticles and UV-visible absorption peaks around 530 nm that originate from the surface plasmon resonance. Differences between the Fe-Pt and Au nanoparticles prepared by the KrF excimer laser solution photolysis are also discussed.

  1. Preparation of Ultrafine Fe–Pt Alloy and Au Nanoparticle Colloids by KrF Excimer Laser Solution Photolysis

    Directory of Open Access Journals (Sweden)

    Sugai Hiroshi

    2009-01-01

    Full Text Available Abstract We prepared ultrafine Fe–Pt alloy nanoparticle colloids by UV laser solution photolysis (KrF excimer laser of 248 nm wavelength using precursors of methanol solutions into which iron and platinum complexes were dissolved together with PVP dispersant to prevent aggregations. From TEM observations, the Fe–Pt nanoparticles were found to be composed of disordered FCC A1 phase with average diameters of 0.5–3 nm regardless of the preparation conditions. Higher iron compositions of nanoparticles require irradiations of higher laser pulse energies typically more than 350 mJ, which is considered to be due to the difficulty in dissociation of Fe(III acetylacetonate compared with Pt(II acetylacetonate. Au colloid preparation by the same method was also attempted, resulting in Au nanoparticle colloids with over 10 times larger diameters than the Fe–Pt nanoparticles and UV–visible absorption peaks around 530 nm that originate from the surface plasmon resonance. Differences between the Fe–Pt and Au nanoparticles prepared by the KrF excimer laser solution photolysis are also discussed.

  2. Preparation of Ibuprofen-loaded Eudragit S100 nanoparticles by Solvent evaporation technique.

    Directory of Open Access Journals (Sweden)

    VINEELA CH

    2014-07-01

    Full Text Available Aim The aim of the present study is to prepare Ibuprofen loaded Eudragit-S100 nanoparticles by means of Solvent evaporation method. Span 80 is used as surfactant. The model drug, Ibuprofen is a non-steroidal antiinflammatory drug (NSAID commonly used for the relief of symptoms of arthritis, primary dysmenorrheal, alleviating fever and reducing inflammation. It also has an analgesic effect, anti-platelet effect and vasodilation effect. Ibuprofen is available in the form of extended release tablets, chewable tablets, sustained release capsules, liquid filled capsules, syrup and suspension. Methodology Solvent evaporation technique was adapted for the preparation of Ibuprofen loaded Eudragit S100 nanoparticles. Preformed polymeric and drug solution was used as internal phase and mineral oil with 1% span 80 is used as external phase and allowed for stirring resulting in the formation of nanoparticles. Parameters like stirring rate, polymer to drug concentration and organic solvent quantity were optimized. Results and Conclusion In order to optimize the concentration of drug, polymer and organic solvent, three formulations were prepared by varying the concentration of polymer and solvents. The results obtained were compared. On comparision formulation 3(1:2 was showing particles in nanorange (345nm, higher stability (-26.9mV and better entrapment efficiency (96.47. Invitro drug release studies were performed for a period of 10hrs and 46.02% of the drug has been released from the formulation. Conclusion It was observed that as the polymer ratio increases the release rate is sustained and encapsulation efficiency also increased.

  3. Preparation of nanoparticles of poorly water-soluble antioxidant curcumin by antisolvent precipitation methods

    Science.gov (United States)

    Kakran, Mitali; Sahoo, Nanda Gopal; Tan, I.-Lin; Li, Lin

    2012-03-01

    The objective of this study was to enhance the solubility and dissolution rate of a poorly water-soluble antioxidant, curcumin, by fabricating its nanoparticles with two methods: antisolvent precipitation with a syringe pump (APSP) and evaporative precipitation of nanosuspension (EPN). For APSP, process parameters like flow rate, stirring speed, solvent to antisolvent (SAS) ratio, and drug concentration were investigated to obtain the smallest particle size. For EPN, factors like drug concentration and the SAS ratio were examined. The effects of these process parameters on the supersaturation, nucleation, and growth rate were studied and optimized to obtain the smallest particle size of curcumin by both the methods. The average particle size of the original drug was about 10-12 μm and it was decreased to a mean diameter of 330 nm for the APSP method and to 150 nm for the EPN method. Overall, decreasing the drug concentration or increasing the flow rate, stirring rate, and antisolvent amount resulted in smaller particle sizes. Differential scanning calorimetry studies suggested lower crystallinity of curcumin particles fabricated. The solubility and dissolution rates of the prepared curcumin particles were significantly higher than those the original curcumin. The antioxidant activity, studied by the DPPH free radical-scavenging assay, was greater for the curcumin nanoparticles than the original curcumin. This study demonstrated that both the methods can successfully prepare curcumin into submicro to nanoparticles. However, drug particles prepared by EPN were smaller than those by APSP and hence, showed the slightly better solubility, dissolution rate, and antioxidant activity than the latter.

  4. Preparation of nanoparticles of poorly water-soluble antioxidant curcumin by antisolvent precipitation methods

    Energy Technology Data Exchange (ETDEWEB)

    Kakran, Mitali; Sahoo, Nanda Gopal; Tan, I-Lin; Li Lin, E-mail: mlli@ntu.edu.sg [Nanyang Technological University, School of Mechanical and Aerospace Engineering (Singapore)

    2012-03-15

    The objective of this study was to enhance the solubility and dissolution rate of a poorly water-soluble antioxidant, curcumin, by fabricating its nanoparticles with two methods: antisolvent precipitation with a syringe pump (APSP) and evaporative precipitation of nanosuspension (EPN). For APSP, process parameters like flow rate, stirring speed, solvent to antisolvent (SAS) ratio, and drug concentration were investigated to obtain the smallest particle size. For EPN, factors like drug concentration and the SAS ratio were examined. The effects of these process parameters on the supersaturation, nucleation, and growth rate were studied and optimized to obtain the smallest particle size of curcumin by both the methods. The average particle size of the original drug was about 10-12 {mu}m and it was decreased to a mean diameter of 330 nm for the APSP method and to 150 nm for the EPN method. Overall, decreasing the drug concentration or increasing the flow rate, stirring rate, and antisolvent amount resulted in smaller particle sizes. Differential scanning calorimetry studies suggested lower crystallinity of curcumin particles fabricated. The solubility and dissolution rates of the prepared curcumin particles were significantly higher than those the original curcumin. The antioxidant activity, studied by the DPPH free radical-scavenging assay, was greater for the curcumin nanoparticles than the original curcumin. This study demonstrated that both the methods can successfully prepare curcumin into submicro to nanoparticles. However, drug particles prepared by EPN were smaller than those by APSP and hence, showed the slightly better solubility, dissolution rate, and antioxidant activity than the latter.

  5. Preparation and in vitro/in vivo evaluation of resveratrol-loaded carboxymethyl chitosan nanoparticles.

    Science.gov (United States)

    Zu, Yuangang; Zhang, Yin; Wang, Weiguo; Zhao, Xiuhua; Han, Xue; Wang, Kunlun; Ge, Yunlong

    2016-01-01

    Resveratrol (RES) is natural polyphenol with a strong biological activity, but its disadvantages, such as poor water solubility, susceptibility to oxidative decomposition and rapid metabolism in the body, which substantially restricts in vivo bioavailability, need to be resolved. This study used carboxymethyl chitosan (CMCS) as a drug carrier and utilized emulsion cross-linking to prepare RES-loaded CMCS nanoparticles (RES-CMCSNPs). A single-factor experiment was performed to optimize the preparation of these particles; in vitro and in vivo characteristics were evaluated. Spherical RES-CMCSNPs were prepared under optimal conditions, in which average particle size, potential, drug loading and encapsulation efficiency were (155.3 ± 15.2) nm, (-10.28 ± 6.4) mV, (5.1 ± 0.8)% and (44.5 ± 2.2)%, respectively. FTIR, DSC and XRD showed that RES molecules were wrapped in the nanoparticles. In vitro DPPH radical scavenging abilities showed RES-CMCSNPs were better than RES raw powder. The nanoparticles improved the solubility of RES, thereby greatly improving the antioxidant activity of the drug. In vitro release experiments of RES and RES-CMCSNPs by simulating the human gastrointestinal tract were performed, in which RES-CMCSNPs rendered better releasing effects than raw RES. Raw RES and RES-CMCSNPs results were in line with those obtained for the single-chamber model for pharmacokinetic studies in rats. Compared with the bulk drugs, the RES-CMCSNPs exhibited increased in vivo absorption, prolonged duration of action and increased relative bioavailability by 3.516 times more than those of the raw RES. In addition, the residual chloroform is less than the ICH limit for class 2 solvents.

  6. Biomimetic Cilia Based on MEMS Technology

    Institute of Scientific and Technical Information of China (English)

    Zhi-guo Zhou; Zhi-wen Liu

    2008-01-01

    A review on the research of Micro Electromechanical Systems (MEMS) technology based biomimetic cilia is presented. Biomimetic cilia, enabled by the advancement of MEMS technology, have been under dynamic development for the past decade. After a brief description of the background of cilia and MEMS technology, different biomimetic cilia applications are reviewed. Biomimetic cilia micro-actuators, including micromachined polyimide bimorph biomimetic cilia micro-actuator, electro-statically actuated polymer biomimetic cilia micro-actuator, and magnetically actuated nanorod array biomimetic cilia micro-actuator, are presented. Subsequently micromachined underwater flow biomimetic cilia micro-sensor is studied, followed by acoustic flow micro-sensor. The fabrication of these MEMS-based biomimetic cilia devices, characterization of their physical properties, and the results of their application experiments are discussed.

  7. Intercalated carbon nanotubes as a template for the preparation of supported heteroatomic nanoparticles.

    Science.gov (United States)

    Schouler, Marie-Claude; Chamssedine, Fadel; Claves, Daniel

    2011-03-01

    Chemistry in confined conditions is explored at the level of the interlayer space of multiwall carbon nanotubes. Starting from preliminary intercalated tubes, a ligand exchange reaction has been successfully conducted within the former Van der Waals gap, resulting in a final dispersion of heteroatomic particles, around 2 nm large and nearly homogeneous in size, on the outer surface of the tubes. Intercalated tubular carbon architectures thus prove to be interesting templates for a bottom-up preparation of chemically complex supported nanoparticles, with potential activities for versatile applications.

  8. Preparation of glucose oxidase electrode containing hydrophobic silica nanoparticles by the sol-gel method

    Institute of Scientific and Technical Information of China (English)

    张琳; 唐芳琼; 袁金锁; 江龙

    1995-01-01

    The influences of hydrophobic SiO2 nanoparticles and the contents of glucose oxidase(GOD)upon the response current of enzyme electrode have been investigated by using the sol-gel method,in whichpolyvinylbutyryl(PVB)was used as a matrix.The influenoe of enzymatic activity was measured byelectrochemical method.Experimental data demonstrated that hydrophobic SiO2 particles can immobilizeenzyme well,providing a good and simple method for preparing high quality GOD biosensor.The mechanismhas been discussed.

  9. Dendrimer-Capped Nanoparticles Prepared by Picosecond Laser Ablation in Liquid Environment

    Directory of Open Access Journals (Sweden)

    Paolo Marsili

    2009-09-01

    Full Text Available Fifth generation ethylendiamine-core poly(amidoamine (PAMAM G5 is presented as an efficient capping agent for the preparation of metal and semiconductor nanoparticles by ps laser ablation in water. In particular, we describe results obtained with the fundamental, second and third harmonic of a ps Nd:YAG laser and the influence of laser wavelength and pulse energy on gold particle production and subsequent photofragmentation. In this framework, the role of the dendrimer and, in particular, its interactions with gold clusters and cations are accounted.

  10. A novel preparation method of Sn-modified Pt nanoparticles and application for methanol oxidation

    Science.gov (United States)

    Du, Yongling; Su, Biquan; Zhang, Nuo; Wang, Chunming

    2008-12-01

    With polystyrene latex spheres self-assembled on ITO glass as templates, highly ordered two-dimensional (2D) Pt nanoparticles (PtNPs) were prepared by electrochemical deposition. The morphology and element composition of PtNPs were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The electrocatalytic properties of PtNPs/ITO and Sn underpotential deposition (UPD) modified PtNPs/ITO for methanol oxidation has been investigated by cyclic voltammetry (CV) and chronoamperometry (CA). The excellent electrocatalytic activity can be observed for these catalytic systems.

  11. Aqueous Solution Preparation of Ruthenium Nanoparticles Using Ammonium Formate as the Reducing Agent

    Institute of Scientific and Technical Information of China (English)

    LIU Shaohong; CHEN Jialin; GUAN Weiming; BI Jun; CHEN Nanguang; CHEN Dengquan; LIU Manmen; SUN Xudong

    2012-01-01

    Ruthenium,one of the platinum group metals,has drawn much attention due to its catalytic behavior,hardness,electrical conductivity and density.Ruthenium particles are usually prepared on a small scale by the polyol process,however,the size of the obtained ruthenium nanoparticles is most below 10 nm.In this work,ruthenium particles about 200 nm in diameter were obtained in aqueous solution by using ammonium formate as the reducing agent.Tohave a better control of particle's size and shape,the effects of PVP,mixing mode,reaction temperature,solution pH and calcination temperature were investigated.

  12. Influences of surfactants on the preparation of copper nanoparticles by electron beam irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Zhou Ruimin [Shanghai Applied Radiation Institute, Shanghai University, Shanghai 201800 (China)], E-mail: zhourm47@staff.shu.edu.cn; Wu Xinfeng; Hao Xufeng; Zhou Fei [Shanghai Applied Radiation Institute, Shanghai University, Shanghai 201800 (China); Li Hongbin [Department of Chemical Engineering and Technology, Shanghai University, Shanghai 201800 (China); Rao Weihong [Shenzhen Tianding Fine Chemical Engineering Manufacturing Co., Ltd., Shenzhen, Guangdong 518057 (China)

    2008-02-15

    Electron beam radiation was applied to prepare nano-size copper in water system using polyvinyl alcohol, sodium dodecyl benzene sulfonate, gluten and polyethylene glycol as the surfactants, respectively. The irradiated products were characterized by XRD, TEM and LSPSDA. The XRD and TEM showed that relative pure copper products with an average size of 20 nm, 40 nm and 20 nm can be obtained by using gluten, PEG and SDBS as surfactant, respectively. An admixture of copper and cuprous oxide was obtained in PVA system. The LSPSDA showed that the size of the Cu nanoparticles decreased with increasing the glutin concentration.

  13. Preparation of CuS nanoparticles embedded in poly(vinyl alcohol) nanofibre via electrospinning

    Indian Academy of Sciences (India)

    Jia Xu; Xuejun Cui; Jinhui Zhang; Hongwei Liang; Hongyan Wang; Junfeng Li

    2008-04-01

    Poly(vinyl alcohol) (PVA)/CuS composite nanofibres were successfully prepared by electrospinning technique and gas–solid reaction. Scanning electron microscopic (SEM) images showed that the average diameter of PVA/CuS fibres was about 150–200 nm. Transmission electron microscopy (TEM) proved that a majority of CuS nanoparticles with an average diameter of about 15–25 nm are incorporated in the PVA fibres. Xray diffraction (XRD) analyses and electron diffraction pattern also revealed the forming of CuS crystal structure in the PVA fibres.

  14. Preparation and Photodynamic Anti-tumor Activity of Magnetic Polylactic Acid Nanoparticles Loaded with Photosensitizer

    Institute of Scientific and Technical Information of China (English)

    YANG Xiao-xia; HUANG Hui; CHEN Zhi-long; HUANG Peng; SUN Yun; ZHOU Xing-ping

    2010-01-01

    A novel magnetic nanocarrier was strategically designed and successfully prepared. Photosensitizer 2, 7,12, 18-tetramethyl-3, 8-di-(1-propoxyethyl)-13, 17-bis-( 3-hydroxypropyl ) porphyrin ( PHPP ) wasencapsulated into polylactic acid (PLA)-coated Fe3O4nanoparticles. The diameter of nanocarrier is 30-50 nm by transmission electron micrograph ( TEM ). The encapsulation efficiency of photosensitizer is 27.98% calculated from UV-vis absorption spectra. The nanocarrier shows obvious photocytotoxic activity to Hela299 tumor cells in vitro.

  15. Preparation of mixed matrix PES-based nanofiltration membrane filled with PANI-co-MWCNT composite nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Bagheripour, Ehsan; Moghadassi, Abdolreza; Hosseini, Sayed Mohsen [Faculty of Engineering, Arak University, Arak (Iran, Islamic Republic of)

    2016-04-15

    Mixed matrix polyethersulfone/PANI-co-MWCNTs composite nanoparticle nanofiltration membrane was prepared by casting solution technique. Polyvinylpyrrolidone was also used as membrane pore former in membrane fabrication. The effect of polyaniline-co-multi walled carbon nanotubes composite nanoparticle concentration in the casting solution on membrane structure and performance was investigated. Scanning optical microscopy and scanning electron microscopy, FTIR analysis, porosity, mean pore size, contact angle, water content, NaCl/Na2SO4 rejection, water flux, tensile strength measurements and 3D surface image were also carried out in membrane characterization. SOM images showed nanoparticle agglomeration at high additive loading ratio. SEM images showed the membrane sub-layer porosity and thickness were changed by use of nanoparticles in membrane matrix. The membrane water content, porosity and pore size were increased by increase of nanoparticle concentration, except for 1%wt. Use of PANI-co- MWCNT nanoparticles in the membrane matrix caused a decrease of membrane contact angle from 63.43 to 46.76o. Salt rejection and water flux were improved initially by increase of nanoparticle concentration up to 0.1%wt and then decreased by more additive concentration. In addition, the membranes tensile strength was reduced by increase of PANI-co-MWCNTs composite nanoparticle concentration. 3D surface images showed a smoother surface for mixed matrix membrane filled with 0.1wt% PANI-co-MWCNTs. Modified membrane containing 0.1wt% composite nanoparticles showed better performance compared to others.

  16. PEGylated PLGA Nanoparticles as Tumor Ecrosis Factor-α Receptor Blocking Peptide Carriers: Preparation,Characterization and Release in vitro

    Institute of Scientific and Technical Information of China (English)

    LIU Wei; YANG Anshu; LI Zhuoya; XU Huibi; YANG Xiangliang

    2007-01-01

    To assess the merits of PEGylated poly (lactic-co-glycolic acid) (PEG-PLGA) nanoparticles as drug carriers for tumor necrosis factor-α receptor blocking peptide (TNFR-BP), PEG-PLGA copolymer,which could be used to prepare the stealth nanoparticles, was synthesized with methoxypolyethyleneglycol,DL-lactide and glycolide. The structure of PEG-PLGA was confirmed with 1H-NMR and FT-IR spectroscopy,and the molecular weight (MW) was determined by gel permeation chromatography. Fluorescent FITC-TNFR-BP was chosen as model protein and encapsulated within PEG-PLGA nanoparticles using the double emulsion method. Atomic force microscopy and photon correlation spectroscopy were employed to characterize the stealth nanoparticles fabricated for morphology, size with polydispersity index and zeta potential. Encapsulation efficiency (EE) and the release of FITC-TNFR-BP in nanoparticles in vitro were measured by the fluorescence measurement. The stealth nanoparticles were found to have the mean diameter less than 270 nm and zeta potential less than-20 mV. In all nanoparticle formulations, more than 45% of EE were obtained. FITC-TNFR-BP release from the PEG-PLGA nanoparticles exhibited a biphasic pattern, initial burst release and consequently sustained release. The experimental results show that PEG-PLGA nanoparticles possess the potential to develop as drug carriers for controlled release applications of TNFR-BP.

  17. Preparation of Multifunctional Fe@Au Core-Shell Nanoparticles with Surface Grafting as a Potential Treatment for Magnetic Hyperthermia

    Directory of Open Access Journals (Sweden)

    Ren-Jei Chung

    2014-01-01

    Full Text Available Iron core gold shell nanoparticles grafted with Methotrexate (MTX and indocyanine green (ICG were synthesized for the first time in this study, and preliminarily evaluated for their potential in magnetic hyperthermia treatment. The core-shell Fe@Au nanoparticles were prepared via the microemulsion process and then grafted with MTX and ICG using hydrolyzed poly(styrene-alt-maleic acid (PSMA to obtain core-shell Fe@Au-PSMA-ICG/MTX nanoparticles. MTX is an anti-cancer therapeutic, and ICG is a fluorescent dye. XRD, TEM, FTIR and UV-Vis spectrometry were performed to characterize the nanoparticles. The data indicated that the average size of the nanoparticles was 6.4 ± 09 nm and that the Au coating protected the Fe core from oxidation. MTX and ICG were successfully grafted onto the surface of the nanoparticles. Under exposure to high frequency induction waves, the superparamagnetic nanoparticles elevated the temperature of a solution in a few minutes, which suggested the potential for an application in magnetic hyperthermia treatment. The in vitro studies verified that the nanoparticles were biocompatible; nonetheless, the Fe@Au-PSMA-ICG/MTX nanoparticles killed cancer cells (Hep-G2 via the magnetic hyperthermia mechanism and the release of MTX.

  18. Comparative studies of salinomycin-loaded nanoparticles prepared by nanoprecipitation and single emulsion method

    Science.gov (United States)

    Wang, Qin; Wu, Puyuan; Ren, Wei; Xin, Kai; Yang, Yang; Xie, Chen; Yang, Chenchen; Liu, Qin; Yu, Lixia; Jiang, Xiqun; Liu, Baorui; Li, Rutain; Wang, Lifeng

    2014-07-01

    To establish a satisfactory delivery system for the delivery of salinomycin (Sal), a novel, selective cancer stem cell inhibitor with prominent toxicity, gelatinase-responsive core-shell nanoparticles (NPs), were prepared by nanoprecipitation method (NR-NPs) and single emulsion method (SE-NPs). The gelatinase-responsive copolymer was prepared by carboxylation and double amination method. We studied the stability of NPs prepared by nanoprecipitation method with different proportions of F68 in aqueous phase to determine the best proportion used in our study. Then, the NPs were prepared by nanoprecipitation method with the best proportion of F68 and single emulsion method, and their physiochemical traits including morphology, particle size, zeta potential, drug loading content, stability, and in vitro release profiles were studied. The SE-NPs showed significant differences in particle size, drug loading content, stability, and in vitro release profiles compared to NR-NPs. The SE-NPs presented higher drug entrapment efficiency and superior stability than the NR-NPs. The drug release rate of SE-NPs was more sustainable than that of the NR-NPs, and in vivo experiment indicated that NPs could prominently reduce the toxicity of Sal. Our study demonstrates that the SE-NPs could be a satisfactory method for the preparation of gelatinase-responsive NPs for intelligent delivery of Sal.

  19. Engineering nanomaterials with a combined electrochemical and molecular biomimetic approach

    Science.gov (United States)

    Dai, Haixia

    Biocomposite materials, such as bones, teeth, and shells, are created using mild aqueous solution-based processes near room temperature. Proteins add flexibility to these processes by facilitating the nucleation, growth, and ordering of specific inorganic materials into hierarchical structures. We aim to develop a biomimetic strategy for engineering technologically relevant inorganic materials with controlled compositions and structures, as Nature does, using proteins to orchestrate material formation and assembly. This approach involves three basic steps: (i) preparation of inorganic substrates compatible with combinatorial polypeptide screening; (ii) identification of inorganic-binding polypeptides and their engineering into inorganic-binding proteins; and (iii) protein-mediated inorganic nucleation and organization. Cuprous oxide (Cu2O), a p-type semiconductor, has been used to demonstrate all three steps. Zinc oxide (ZnO), an n-type semiconductor, has been used to show the generality of selected steps. Step (i), preparation of high quality inorganic substrates to select inorganic-binding polypeptides, was accomplished using electrochemical microfabrication to grow and pattern Cu2O and ZnO. Raman spectroscopy and x-ray photoelectron spectroscopy were used to verify phase purity and compositional stability of these surfaces during polypeptide screening. Step (ii), accomplished in collaboration with personnel in Prof Baneyx' lab at the University of Washington, involved incubating the inorganic substrates with the FliTrx(TM) random peptide library to identify cysteine-constrained dodecapeptides that bind the targeted inorganic. Insertion of a Cu2O-binding dodecapeptide into the DNA-binding protein TraI endowed the engineered TraI with strong affinity for Cu2O (Kd ≈ 10 -8 M). Finally, step (iii) involved nonequilibrium synthesis and organization of Cu2O nanoparticles, taking advantage of the inorganic and DNA recognition properties of the engineered TraI. The

  20. Water- and organo-dispersible gold nanoparticles supported by using ammonium salts of hyperbranched polystyrene: preparation and catalysis.

    Science.gov (United States)

    Gao, Lei; Nishikata, Takashi; Kojima, Keisuke; Chikama, Katsumi; Nagashima, Hideo

    2013-12-01

    Gold nanoparticles (1 nm in size) stabilized by ammonium salts of hyperbranched polystyrene are prepared. Selection of the R groups provides access to both water- and organo-dispersible gold nanoparticles. The resulting gold nanoparticles are subjected to studies on catalysis in solution, which include reduction of 4-nitrophenol with sodium borohydride, aerobic oxidation of alcohols, and homocoupling of phenylboronic acid. In the reduction of 4-nitrophenol, the catalytic activity is clearly dependent on the size of the gold nanoparticles. For the aerobic oxidation of alcohols, two types of biphasic oxidation are achieved: one is the catalyst dispersing in the aqueous phase, whereas the other is in the organic phase. The catalysts are reusable more than four times without loss of the catalytic activity. Selective synthesis of biphenyl is achieved by the homocoupling of phenylboronic acid catalyzed by organo-dispersible gold nanoparticles.

  1. Preparation of manganese-based perovskite nanoparticles using a reverse microemulsion method: biomedical applications

    Indian Academy of Sciences (India)

    MEYSAM SOLEYMANI; MOHAMMAD EDRISSI

    2016-04-01

    In this study, La$_{0.7}Sr$_{0.3}Mn$_{0.98}$Ti$_{0.02}$O$_{3}$ (LSMTO) nanoparticles with a perovskite structure and an average particle size of 23.5 nm were synthesized using a reverse microemulsion method. In this method, cetyltrimethylammonium bromide (CTAB) was used as a surfactant, 1-butanol as a co-surfactant, $n$-hexane as a continuous oil phase, and an aqueous solution containing metal cations or precipitating agent as a dispersed aqueousphase. The aqueous nanodroplets of microemulsions were used for the formation of perovskite precursor. The obtained precursor was then calcined at 700$^{\\circ}$C for 4 h to convert the precursor to the perovskite phase. In addition, the heating ability of the LSMTO nanoparticles was evaluated under a safe alternating magnetic field used in magnetic hyperthermia therapy. The results showed the fast magneto-temperature response of the prepared samplewith sufficient heat loss at the therapeutic temperature range, indicating the LSMTO nanoparticles can be used as a self-regulated heating agent in the magnetic hyperthermia therapy.

  2. Preparation of crystalline starch nanoparticles using cold acid hydrolysis and ultrasonication.

    Science.gov (United States)

    Kim, Hee-Young; Park, Dong June; Kim, Jong-Yea; Lim, Seung-Taik

    2013-10-15

    Waxy maize starch in an aqueous sulfuric acid solution (3.16 M, 14.7% solids) was hydrolyzed for 2-6 days, either isothermally at 40 °C or 4 °C, or at cycled temperatures of 4 and 40 °C (1 day each). The starch hydrolyzates were recovered as precipitates after centrifuging the dispersion (10,000 rpm, 10 min). The yield of starch hydrolyzates depended on the hydrolysis temperature and time, which varied from 6.8% to 78%. The starch hydrolyzed at 40 °C or 4/40 °C exhibited increased crystallinity determined by X-ray diffraction analysis, but melted in broader temperature range (from 60 °C to 110 °C). However, the starch hydrolyzed at 4 °C displayed the crystallinity and melting endotherm similar to those of native starch. The starch hydrolyzates recovered by centrifugation were re-dispersed in water (15% solids), and the dispersion was treated by an ultrasonic treatment (60% amplitude, 3min). The ultrasonication effectively fragmented the starch hydrolyzates to nanoparticles. The hydrolyzates obtained after 6 days of hydrolysis were more resistant to the ultrasonication than those after 2 or 4 days, regardless of hydrolysis temperatures. The starch nanoparticles could be prepared with high yield (78%) and crystallinity by 4 °C hydrolysis for 6 days followed by ultrasonication. Scanning electron microscopy revealed that the starch nanoparticles had globular shapes with diameters ranging from 50 to 90 nm.

  3. Preparation of silver nanoparticle containing silica micro beads and investigation of their antibacterial activity

    Science.gov (United States)

    Quang, Dang Viet; Sarawade, Pradip B.; Hilonga, Askwar; Kim, Jong-Kil; Chai, Young Gyu; Kim, Sang Hoon; Ryu, Jae-Yong; Kim, Hee Taik

    2011-05-01

    Silver nanoparticle containing silica micro beads (Ag-NPBs) were successfully prepared by using sodium silicate, a cheap precursor, involving chemical reductive method. First, silica gel was synthesized and crushed into micro beads which have sizes ranging from 0.5 to 1 mm. Silica micro beads were then modified with 3-aminopropyltriethoxysilane to graft amino functional groups onto their surface. Silver ions were loaded onto the surface of the modified silica and reduced to silver crystal by adding NaBH 4. The presence of silver nanoparticles as well as structure of materials was characterized with FT-IR, XRD, BET, FE-SEM, TEM, UV-vis spectrophotometer, and optical microscope. Silver nanoparticles with an average size about 5 nm were found in the pore and on the surface of amino functionalized silica beads. Ag-NPBs samples were tested for their antibacterial activity against Escherichia coli ( E. coli). The antibacterial activity was examined by both zone inhibition and test tube test method. Biological results indicated that the synthesized materials have an excellent antibacterial performance against E. coli which was completely inhibited after 5 min contact with Ag-NPBs.

  4. Preparation and characterization of Chinese yam polysaccharide PLGA nanoparticles and their immunological activity.

    Science.gov (United States)

    Luo, Li; Zheng, Sisi; Huang, Yifan; Qin, Tao; Xing, Jie; Niu, Yale; Bo, Ruonan; Liu, Zhenguang; Huang, Yee; Hu, Yuanliang; Liu, Jiaguo; Wu, Yi; Wang, Deyun

    2016-09-10

    This paper first provides that Chinese yam polysaccharide (CYP) is encapsulated by PLGA using a double emulsion solvent evaporation method and aims to screen the optimal preparation of CYP-PLGA nanoparticles (CYPP) using response surface methodology (RSM). The volume ratio of the internal water phase to the organic phase (W1:O), the volume ratio of the primary emulsion to the external water phase (PE:W2) and the concentration of Poloxamer 188 (F68) are deemed key variables for the encapsulation efficiency of CYPP. The results demonstrated that the data were accurately fitted into the RSM model. According to the RSM, the optimal scheme was a volume ratio of W1:O of 1:9, a volume ratio of PE: W2 of 1:10 and a concentration of F68 (W/V) of 0.7%. TEM and SEM images demonstrated that the nanoparticles had a spherical shape and smooth surface. The CYP and CYPP in vitro release studies demonstrated that the CYPP showed a release rate 53.41% lower than the release rate of CYP after 48h. The result of pro-proliferation and flow cytometry emerged that the CYPP were more effective compared with the free CYP and blank PLGA nanoparticles in promoting lymphocyte proliferation and triggering the transformation of T lymphocytes into Th cells.

  5. Preparation and characterization of ketoprofen-loaded solid lipid nanoparticles made from beeswax and carnauba wax.

    Science.gov (United States)

    Kheradmandnia, Soheila; Vasheghani-Farahani, Ebrahim; Nosrati, Mohsen; Atyabi, Fatemeh

    2010-12-01

    Solid lipid nanoparticles (SLNs) have been proposed as suitable colloidal carriers for delivery of drugs with limited solubility. Ketoprofen as a model drug was incorporated into SLNs prepared from a mixture of beeswax and carnauba wax using Tween 80 and egg lecithin as emulsifiers. The characteristics of the SLNs with various lipid and surfactant composition were investigated. The mean particle size of drug-loaded SLNs decreased upon mixing with Tween 80 and egg lecithin as well as upon increasing total surfactant concentration. SLNs of 75 ± 4 nm with a polydispersity index of 0.2 ± 0.02 were obtained using 1% (vol/vol) mixed surfactant at a ratio of 60:40 Tween 80 to egg lecithin. The zeta potential of these SLNs varied in the range of -15 to -17 (mV), suggesting the presence of similar interface properties. High drug entrapment efficiency of 97% revealed the ability of SLNs to incorporate a poorly water-soluble drug such as ketoprofen. Differential scanning calorimetry thermograms and high-performance liquid chromatographic analysis indicated the stability of nanoparticles with negligible drug leakage after 45 days of storage. It was also found that nanoparticles with more beeswax content in their core exhibited faster drug release as compared with those containing more carnauba wax in their structure.

  6. Facile route for preparation of silver nanoparticle-coated precipitated silica

    Science.gov (United States)

    Quang, Dang Viet; Sarawade, Pradip B.; Hilonga, Askwar; Park, Sung Dae; Kim, Jong-Kil; Kim, Hee Taik

    2011-02-01

    In this research, a facile route was used to prepare silver nanoparticle-coated precipitated silica using sodium silicate, a cheap precursor. Precipitated silica (PS) was synthesized by dropping 8% H2SO4 into a mixed solution of sodium silicate 24% (Na2O·3.4SiO2) and NaCl 4%; under constant stirring. The precipitated silica was then modified by simultaneous addition of 3-aminopropyltriethoxysilane (3-APTES) and 8% H2SO4. The resulting material was aged at 80 °C for 1 h to produce amino-functionalized precipitated silica (AFPS). Silver nanoparticle-coated precipitated silica (Ag-NPS) was synthesized by adding silver nitrate (AgNO3). The synthesis procedure also involved mixing for 2 h and dropping 0.05 M sodium borohydride (NaBH4). The final products, namely, PS, AFPS, and Ag-NPS were characterized using BET analyzer, FE-SEM, TEM and XRD. Silver nanoparticles with an average size ranging from 18 to 25 nm were found mostly coated on the exterior layer of the precipitated silica. The synthesis method reported in this work is facile and might be used for large-scale industrial production of inexpensive Ag-NPS.

  7. Preparation of platinum-iridium nanoparticles on titania nanotubes by MOCVD and their catalytic evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Colindres, S. Capula [National Polytechnic Institute, Department of Metallurgical Eng., Mexico 07300 D.F., AP 75-874 (Mexico); Garcia, J.R. Vargas, E-mail: rvargasga@ipn.m [National Polytechnic Institute, Department of Metallurgical Eng., Mexico 07300 D.F., AP 75-874 (Mexico); Antonio, J.A. Toledo; Chavez, C. Angeles [Petroleum Mexican Institute, Eje Central Lazaro Cardenas No.152, Mexico 07730 D.F. (Mexico)

    2009-08-26

    Pt based catalysts are commonly used in several industrial processes involving hydrogenation and dehydrogenation reactions. New deposition methods as well as support materials are being investigated to generate new catalysts with superior catalytic activity. In this work, platinum-iridium (Pt-Ir) nanoparticles of about 5 nm in size were supported on titania (TiO{sub 2}) nanotubes by metal organic chemical vapor deposition (MOCVD). The TiO{sub 2} nanotubes were prepared by an alkali hydrothermal method using sodium hydroxide solution at 100 deg. C, during 64.8 ks. Pt-Ir nanoparticles were obtained by controlling the MOCVD conditions at 400 deg. C and 66.6 kPa. Textural properties and particle size were investigated by nitrogen physisorption (BET method), X-ray diffraction, Raman spectroscopy and high resolution transmission electron microscopy. Catalytic activity was measured in cyclohexene disproportion as the test molecule for hydrogenation/dehydrogenation reactions. The TiO{sub 2} nanotubes exhibit a considerable high surface area of about 425,000 m{sup 2}/kg, however, after calcination at 400 deg. C their nanotubular morphology was partially transformed. In spite of this change, the 5 nm Pt-Ir nanoparticles supported on TiO{sub 2} nanotubes were more active in the cyclohexene disproportion reaction than conventional Pt-Ir/alumina catalysts in the whole range of temperatures investigated (50-250 deg. C). Hydrogenation reactions (high selectivity to cyclohexane) predominate at temperatures below 150 deg. C.

  8. Preparation of hydroxyapatite nanoparticles facilitated by the presence of {beta}-cyclodextrin

    Energy Technology Data Exchange (ETDEWEB)

    Martinez-Perez, Carlos A., E-mail: camartin@uacj.mx [Institute of Engineering and Technology, Autonomous University of Juarez, UACJ, Ave. del Charro 610 norte, C.P. 32320, Cd. Juarez, Chihuahua (Mexico); Garcia-Montelongo, Jorge; Garcia Casillas, Perla E.; Farias-Mancilla, Jose R. [Institute of Engineering and Technology, Autonomous University of Juarez, UACJ, Ave. del Charro 610 norte, C.P. 32320, Cd. Juarez, Chihuahua (Mexico); Monreal Romero, Humberto [School of Odontology, Autonomous University of Chihuahua, UACH, Ave. Universidad s/n Campus Universitario I, C.P. 31170, Chihuahua (Mexico)

    2012-09-25

    Highlights: Black-Right-Pointing-Pointer It was found that {beta}-cyclodextrin can control the particle size in the production of nanohydroxyapatite. Black-Right-Pointing-Pointer Particle size in the range of 30-50 nm was obtained. Black-Right-Pointing-Pointer A new simple methodology for the preparation of hydroxyapatite nanoparticles with a well controlled size and narrow particles size distribution was developed. - Abstract: Hydroxyapatite nanoparticles with uniform morphology have been successfully synthesized by a chemical coprecipitation method and facilitated by the presence of the {beta}-cyclodextrin. X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM); and Fourier Transformed Infrared Spectroscopy (FT-IR) were used in order to characterize the hydroxyapatite samples. The experimental results indicate that the obtained HA is in the range of 20-50 nm. Also it was found that the content of {beta}-CD has an impact on the purity of the HA as well in the particle size of the hydroxyapatite nanoparticles.

  9. Preparation and characterization of chondroitin-sulfate-A-coated magnetite nanoparticles for biomedical applications

    Science.gov (United States)

    Tóth, Ildikó Y.; Illés, Erzsébet; Szekeres, Márta; Tombácz, Etelka

    2015-04-01

    Polysaccharides are promising candidates for manufacturing biocompatible core-shell nanoparticles with potential in vivo use. Superparamagnetic magnetite nanoparticles (MNPs) have prospective application in both diagnosis and therapy, and so developing a novel polysaccharide shell on MNP core is of great challenge. MNPs were prepared by co-precipitation, then the surface of purified MNPs was coated with chondroitin-sulfate-A (CSA) to obtain core-shell structured magnetite nanoparticles (CSA@MNP). The effect of the added amount of CSA on the surface charging and the aggregation state of MNPs at various pHs and 10 mM NaCl was measured by electrophoresis and dynamic light scattering. The amphoteric behavior of MNPs was fundamentally modified by adsorption of CSA polyanions. A very low CSA-loading induces the aggregation of MNPs, while four times more stabilizes the dispersions over the whole pH-range studied. The coagulation kinetics experiments measured at pH=6.3±0.3 showed that salt tolerance of CSA@MNPs rises up to ~150 mM NaCl.

  10. Preparation of tungsten carbide nanoparticles by ion implantation and electrochemical etching

    Energy Technology Data Exchange (ETDEWEB)

    Kato, S. [Department of Nuclear Engineering and Management, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan); Quantum Beam Science Directorate, Japan Atomic Energy Agency, 1233 Watanuki, Takasaki, Gunma 370-1292 (Japan); Yamaki, T., E-mail: yamaki.tetsuya@jaea.go.jp [Quantum Beam Science Directorate, Japan Atomic Energy Agency, 1233 Watanuki, Takasaki, Gunma 370-1292 (Japan); Yamamoto, S.; Hakoda, T. [Quantum Beam Science Directorate, Japan Atomic Energy Agency, 1233 Watanuki, Takasaki, Gunma 370-1292 (Japan); Kawaguchi, K. [Department of Chemistry and Materials Technology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585 (Japan); Kobayashi, T. [RIKEN, 2-1 Hirosawa, Wako-shi, Saitama 350-0198 (Japan); Suzuki, A.; Terai, T. [Department of Nuclear Engineering and Management, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan)

    2013-11-01

    Glassy carbon (GC) substrates were implanted with 100 keV tungsten ions at retained fluences of 4 × 10{sup 16} and 6 × 10{sup 16} ions/cm{sup 2} and surface-etched electrochemically in order to prepare tungsten-carbide (WC) nanoparticles on their topmost layers. The calculated current efficiency for the electrochemical etching was nearly the same for the two samples implanted at different fluences, suggesting the controllability of the etched depth using the consumed electric charge. The etching front reached the buried tungsten-implanted layer and increased the tungsten concentration at the surface. No oxidation of WC was observed, even under anodic potential application during electrochemical etching. The voltammogram response of the topmost nanoparticle layer was too small to be observed, probably due to the limited activity of the WC itself and the remaining low concentration. It was demonstrated that this technique could, in principle, be applied to various types of nanoparticle catalysts implanted in GC substrates.

  11. Antibacterial, Structural and Optical Characterization of Mechano-Chemically Prepared ZnO Nanoparticles.

    Directory of Open Access Journals (Sweden)

    Umair Manzoor

    Full Text Available Structural investigations, optical properties and antibacterial performance of the pure Zinc Oxide (ZnO nanoparticles (NPs synthesized by mechano-chemical method are presented. The morphology, dimensions and crystallinity of the ZnO NPs were controlled by tweaking the mechanical agitation of the mixture and subsequent thermal treatment. ZnO nanoparticles in small (< 20 nm dimensions with spherical morphology and narrow size distribution were successfully obtained after treating the mechano-chemically prepared samples at 250°C. However, higher temperature treatments produced larger particles. TEM, XRD and UV-Vis spectroscopy results suggested crystalline and phase pure ZnO. The NPs demonstrated promising antibacterial activity against Gram negative foodborne and waterborne bacterial pathogens i.e. Enteropathogenic E. coli (EPEC, Campylobacter jejuni and Vibrio cholerae as well as Gram positive methicillin resistant Staphylococcus aureus (MRSA, thus potential for medical applications. Scanning electron microscopy and survival assay indicated that most probably ZnO nanoparticles cause changes in cellular morphology which eventually causes bacterial cell death.

  12. Facile Route to Prepare TaC,NbC and WC Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    DU Yinxiao; LEI Ming; YANG Hui; WANG Xuefei

    2008-01-01

    By a novel solid-state reaction process using amorphous C3N4 (a-C3N4) and transition metal oxides as starting reagents,cubic TaC,NbC and hexagonal WC nanoparticles were successfully synthesized at 1150 ℃.The products were characterized by power X-ray diffraction (XRD),field-emission scanning electron microscope (FE-SEM),energy-dispersive X-ray spectroscopy (EDX),transmission electron microscopy (TEM) and high-resolution TEM (HRTEM).The experimental resuits show that a-C3N4 obtained by the reaction between C3N3Cl3 and Li3N is a highly efficient carburation reagent and the transition metal oxides are completely transformed into the corresponding metal carbide nanoparticles at 1150 ℃,respectively,which is significantly lower than that reported for the traditional preparation of carbides,typically> 1600 ℃.The TaC,NbC and WC nanoparticles are found to have an average particle size of 10 nm,15 nm and 8 nm by TEM observation,respectively.

  13. Study on the effect of electrostatic interaction on core-shell nanoparticles preparation with microemulsion technique

    Institute of Scientific and Technical Information of China (English)

    HE Xiaoxiao; WANG Kemin; TAN Weihong; CHEN Jiyun; DUAN Jinghua; YUAN Yin; LIN Xia

    2005-01-01

    The routine method for preparation of silica core-shell nanoparticles (NPs) is to carry out nucleation and shell coating through the hydrolysis of silane in water in oil (W/O) microemulsion to form three-dimensional netted silica shell. We found that electrostatic interaction of the core materials with shell materials would determine whether the stable core-shell silica NPs formed or not. The traditional important factors such as molecular weight of core materials or the thickness of the shell have no obvious relationship with it. And the stability of the core-shell silica NPs can be improved after changing the electric charge polarity by regulating the experiment condition of relevant materials if some core materials cannot be doped inside to form the stable core-shell silica NPs based on the traditional method, which provided experimental and theoretic foundation for preparation and application of the core-shell silica NPs.

  14. Preparation of curcumin-loaded pluronic F127/chitosan nanoparticles for cancer therapy

    Science.gov (United States)

    Phuc Le, Thi Minh; Phuc Pham, Van; Lua Dang, Thi Minh; Huyen La, Thi; Hanh Le, Thi; Huan Le, Quang

    2013-06-01

    Nanoparticles (NPs) have been proven to be an effective delivery system with few side effects for anticancer drugs. In this study, curcumin-loaded NPs have been prepared by an ionic gelation method using chitosan (Chi) and pluronic®F-127 (PF) as carriers to deliver curcumin to the target cancer cells. Prepared NPs were characterized using Zetasizer, fluorescence microscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Our results showed that the encapsulation efficiency of curcumin was approximately 50%. The average size of curcumin-loaded PF/Chi NPs was 150.9 nm, while the zeta potential was 5.09 mV. Cellular uptake of curcumin-loaded NPs into HEK293 cells was confirmed by fluorescence microscopy.

  15. Preparation and Evaluation in vitro of Salicylic Acid-pachyman Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    ZHANG Junbo; SHAO Huili; XIAO Yuling; ZHU Yuanchun; LIANG Shucai

    2011-01-01

    Pachyman based nanoparticles loading salicylic acid as model drug(SA-PNPs)were prepared by an inverse microemulsion crosslinking approach using epichlorohydrin(ECH)as crosslinker.The effects of crosslinking reaction time,initial volume ratio of oil to aqueous phase and dosage of crosslinker on the particle size of SA-PNPs were optimized by orthogonal experimental design.SA-PNPs prepared under the optimal conditions had the average size of 230 nm and high encapsulation efficiency of 90%.The in vitro drug release was also investigated and the release data were analyzed using zero order,first order and Higuchi's kinetics model.According to the determined coefficients,release data fitted to Higuchi's model,which suggested that the release of SA from SA-PNPs in phosphate buffer(pH 7.4)was diffusion controlled release.The experimental results indicated that pachyman possesses a promising potential to be applied as nanocarriers for controlled drug release.

  16. Facile preparation of Bi nanoparticles by novel cathodic dispersion of bulk bismuth electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Chen Xin [Zhejiang Key Laboratory for Reactive Chemistry on Solid Surfaces, Institute of Physical Chemistry, Zhejiang Normal University, Jinhua 321004 (China); Chen Shu; Huang Wei [Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research (Ministry of Education of China), College of Chemistry and Chemical Engineering, Hunan Normal University, Lushan Road, Changsha 410081 (China); Zheng Jufang [Zhejiang Key Laboratory for Reactive Chemistry on Solid Surfaces, Institute of Physical Chemistry, Zhejiang Normal University, Jinhua 321004 (China); Li Zelin, E-mail: lizelin@zjnu.c [Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research (Ministry of Education of China), College of Chemistry and Chemical Engineering, Hunan Normal University, Lushan Road, Changsha 410081 (China)

    2009-12-01

    A novel electrochemical approach has been developed to prepare clean bismuth nanoparticles (NPs) with a bulk Bi electrode in a 0.5 mol dm{sup -3} NaOH solution under highly cathodic polarization of -8 V versus a saturated mercurous sulfate electrode, requiring no any precursor ions and organic protective agents. The bulk Bi electrode can be facilely dispersed into Bi NPs at the condition of intensive hydrogen evolution. This cathodic dispersion of the bulk Bi electrode involves the formation and decomposition of unstable bismuth hydrides and the aggregation of atomic bismuth from the decomposition. Moreover, Bi{sub 2}O{sub 3} NPs have also been achieved by heating the precursor Bi NPs. Field-emission scanning electron microscopy, transmission electron microscope and X-ray diffraction were used to characterize these NPs. The as-prepared Bi NPs mainly existed in rhombohedral phase.

  17. Raman spectroscopic studies on bismuth nanoparticles prepared by laser ablation technique

    Science.gov (United States)

    Onari, Seinosuke; Miura, Masaaki; Matsuishi, Kiyoto

    2002-09-01

    Bi nanoparticles are prepared by means of laser ablation in Ar atmosphere (0.2-10 Torr) with KrF (248 nm) excimer laser of the power 200 mJ. The size of the Bi particles estimated by TEM measurements is in the range 3-10 nm. Raman active E g mode shifts to a higher frequency and becomes broader for a sample prepared in a lower pressure of Ar atmosphere. However, the peak frequency and the bandwidth of A 1g mode show almost no change with the change of the particle size. These experimental results can be well explained by a phonon confinement model of Campbell and Fauchet by taking the phonon dispersion properties that the E g mode of the crystal has a large dependence on the wave numbers near the Γ point, but the A 1g mode is rather independent of the phonon wave numbers.

  18. Nanoparticles prepared from porous silicon nanowires for bio-imaging and sonodynamic therapy.

    Science.gov (United States)

    Osminkina, Liubov A; Sivakov, Vladimir A; Mysov, Grigory A; Georgobiani, Veronika A; Natashina, Ulyana А; Talkenberg, Florian; Solovyev, Valery V; Kudryavtsev, Andrew A; Timoshenko, Victor Yu

    2014-01-01

    Evaluation of cytotoxicity, photoluminescence, bio-imaging, and sonosensitizing properties of silicon nanoparticles (SiNPs) prepared by ultrasound grinding of porous silicon nanowires (SiNWs) have been investigated. SiNWs were formed by metal (silver)-assisted wet chemical etching of heavily boron-doped (100)-oriented single crystalline silicon wafers. The prepared SiNWs and aqueous suspensions of SiNPs exhibit efficient room temperature photoluminescence (PL) in the spectral region of 600 to 1,000 nm that is explained by the radiative recombination of excitons confined in small silicon nanocrystals, from which SiNWs and SiNPs consist of. On the one hand, in vitro studies have demonstrated low cytotoxicity of SiNPs and possibilities of their bio-imaging applications. On the other hand, it has been found that SiNPs can act as efficient sensitizers of ultrasound-induced suppression of the viability of Hep-2 cancer cells.

  19. Iron oxide nanoparticles embedded in activated carbons prepared from hydrothermally treated waste biomass.

    Science.gov (United States)

    Hao, Wenming; Björkman, Eva; Yun, Yifeng; Lilliestråle, Malte; Hedin, Niklas

    2014-03-01

    Particles of iron oxide (Fe3O4 ; 20–40 nm) were embedded within activated carbons during the activation of hydrothermally carbonized (HTC) biomasses in a flow of CO2. Four different HTC biomass samples (horse manure, grass cuttings, beer production waste, and biosludge) were used as precursors for the activated carbons. Nanoparticles of iron oxide formed from iron catalyst included in the HTC biomasses. After systematic optimization, the activated carbons had specific surface areas of about 800 m2g1. The pore size distributions of the activated carbons depended strongly on the degree of carbonization of the precursors. Activated carbons prepared from highly carbonized precursors had mainly micropores, whereas those prepared from less carbonized precursors contained mainly mesopores. Given the strong magnetism of the activated carbon–nano-Fe3O4 composites, they could be particularly useful for water purification.

  20. Ferromagnetism of Mn-doped ZnO nanoparticles prepared by sol-gel process at room temperature

    Institute of Scientific and Technical Information of China (English)

    HUANG Gui-jun; WANG Jin-bin; ZHONG Xiang-li; ZHOU Gong-cheng; YAN Hai-long

    2006-01-01

    Mn-doped ZnO diluted magnetic semiconductor nanoparticles are prepared by an ultrasonic assisted sol gel process. Transmission electron microscopy shows pseudo-hexagonal nanoparticles with an average size of about 24 nm. From the analysis of X-ray diffraction,the Mn-doped ZnO nanoparticles are identified to be a wurtzite structure without any impurity phases. The magnetic properties are measured by using su perconducting quantum interference device. For the ZnO with 2 % Mn doping concentration, a good hyster esis loop indicates fine ferromagnetism with a Curie temperature higher than 350 K.

  1. Preparation of polyelectrolyte complex nanoparticles of chitosan and poly(2-acry1amido-2-methylpropanesulfonic acid) for doxorubicin release.

    Science.gov (United States)

    Zhang, Liping; Wang, Jie; Ni, Caihua; Zhang, Yanan; Shi, Gang

    2016-01-01

    A new kind of polyelectrolyte complex (PEC) based on cationic chitosan (CS) and anionic poly(2-acry1amido-2-methylpropanesulfonic acid) (PAMPS) was prepared using a polymer-monomer pair reaction system. Chitosan was mixed with 2-acry1amido-2-methylpropanesulfonic acid) (AMPS) in an aqueous solution, followed by polymerization of AMPS. The complex was formed by electrostatic interaction of NH3(+) groups of CS and SO3(-) groups of AMPS, leading to a formation of complex nanoparticles of CS-PAMPS. A series of nanoparticles were obtained by changing the weight ratio of CS to AMPS, the structure and properties of nanoparticles were investigated. It was observed that the nanoparticles possessed spherical morphologies with average diameters from 255 nm to 390 nm varied with compositions of the nanoparticles. The nanoparticles were used as drug vehicles for doxorubicin, displaying relative high drug loading rate and encapsulation rate. The vitro release profiles revealed that the drug release could be controlled by adjusting pH of the release media. The nanoparticles demonstrated apparent advantages such as simple preparation process, free of organic solvents, size controllable, good biodegradability and biocompatibility, and they could be potentially used in drug controlled release field.

  2. Structural and magnetic properties of cobalt-doped iron oxide nanoparticles prepared by solution combustion method for biomedical applications.

    Science.gov (United States)

    Venkatesan, Kaliyamoorthy; Rajan Babu, Dhanakotti; Kavya Bai, Mane Prabhu; Supriya, Ravi; Vidya, Radhakrishnan; Madeswaran, Saminathan; Anandan, Pandurangan; Arivanandhan, Mukannan; Hayakawa, Yasuhiro

    2015-01-01

    Cobalt-doped iron oxide nanoparticles were prepared by solution combustion technique. The structural and magnetic properties of the prepared samples were also investigated. The average crystallite size of cobalt ferrite (CoFe2O4) magnetic nanoparticle was calculated using Scherrer equation, and it was found to be 16±5 nm. The particle size was measured by transmission electron microscope. This value was found to match with the crystallite size calculated by Scherrer equation corresponding to the prominent intensity peak (311) of X-ray diffraction. The high-resolution transmission electron microscope image shows clear lattice fringes and high crystallinity of cobalt ferrite magnetic nanoparticles. The synthesized magnetic nanoparticles exhibited the saturation magnetization value of 47 emu/g and coercivity of 947 Oe. The anti-microbial activity of cobalt ferrite nanoparticles showed better results as an anti-bacterial agent. The affinity constant was determined for the nanoparticles, and the cytotoxicity studies were conducted for the cobalt ferrite nanoparticles at different concentrations and the results are discussed.

  3. Potential exposure to silver nanoparticles during spraying preparation for air-conditioning cleaning

    Directory of Open Access Journals (Sweden)

    Elżbieta Jankowska

    2013-02-01

    Full Text Available Background: Unique properties of engineered nanomaterials (ENMs and products made of them have contributed to a rapid progress in the production and application of ENMs in different branches of industry and in factories with different production scale. Bearing in mind that nano-objects (nanoplates, nanofibres, nanoparticles, emitted during ENM production and application, can cause many diseases, even those not yet recognized, extensive studies have been carried all over the world to assess the extent of exposure to nano-objects at workstations and related health effects in workers employed in ENM manufacture and application processes. Material and Methods: The study of potential exposure to silver nanoparticles contained in the preparation for airconditioning cleaning (Nano Silver from Amtra Sp. z o.o. involved the determination of concentrations and size distribution of particles, using different devices, allowing for tracing changes in a wide range of dimensions, from nano-size (10 nm to micrometrsize (10 µm, of the particles which are usually inhaled by humans. Results and Conclusions: The results of the study shows that even during a short-term spraying of Nano Silver preparation (for 10 s at the distance of 52 cm from the place of preparation spraying - particles of 10 nm-10 µm can be emitted into in the air. During a three-fold preparation spraying in similar conditions differences in concentration increase were observed, but in each case the particles remained in the air for a relatively long time. Med Pr 2013;64(1:57–67

  4. Recent Trends in Preparation of Poly(lactide-co-glycolide Nanoparticles by Mixing Polymeric Organic Solution with Antisolvent

    Directory of Open Access Journals (Sweden)

    Edel Sah

    2015-01-01

    Full Text Available In recent years, there have been a plethora of nanoengineering approaches for the development of poly(lactide-co-glycolide (PLGA nanoparticulate carrier systems. However, overlooking the multifaceted issues in the preparation and characterization of PLGA-based nanoparticles, many reports have been focused on their in vivo behaviors. It is imperative to fully assess technological aspects of a nanoencapsulation method of choice and to carefully evaluate the nanoparticle quality. The selection of a nanoencapsulation technique should consider drug property, nanoparticle quality, scale-up feasibility, manufacturing costs, personnel safety, environmental impact, waste disposal, and the like. Made in this review are the fundamentals of classical emulsion-templated nanoencapsulation methods used to prepare PLGA nanoparticles. More specifically, this review provides insight into emulsion solvent evaporation/extraction, salting-out, nanoprecipitation, membrane emulsification, microfluidic technology, and flow focusing. Innovative nanoencapsulation techniques are being developed to address many challenges existing in the production of PLGA-based nanoparticles. In addition, there are various out-of-the-box approaches for the development of novel PLGA hybrid systems that could deliver multiple drugs. Latest trends in these areas are also dealt with in this review. Relevant information might be helpful to those who prepare and develop PLGA-based nanoparticles that meet their specific demands.

  5. Preparation, characterization, and in vivo evaluation of tanshinone IIA solid dispersions with silica nanoparticles

    Directory of Open Access Journals (Sweden)

    Jiang YR

    2013-06-01

    Full Text Available Yan-rong Jiang,1,2 Zhen-hai Zhang,1 Qi-yuan Liu,1,2 Shao-ying Hu,1,2 Xiao-yun Chen,1,2 Xiao-bin Jia11Key Laboratory of New Drug Delivery System of Chinese Materia Medica, Jiangsu Provincial Academy of Chinese Medicine, Nanjing, Jiangsu, People’s Republic of China; 2College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, People’s Republic of ChinaAbstract: We prepared solid dispersions (SDs of tanshinone IIA (TSIIA with silica nanoparticles, which function as dispersing carriers, using a spray-drying method and evaluated their in vitro dissolution and in vivo performance. The extent of TSIIA dissolution in the silica nanoparticles/TSIIA system (weight ratio, 5:1 was approximately 92% higher than that of the pure drug after 60 minutes. However, increasing the content of silica nanoparticles from 5:1 to 7:1 in this system did not significantly increase the rate or extent of TSIIA dissolution. The physicochemical properties of SDs were investigated using scanning electron microscopy, differential scanning calorimetry, X-ray powder diffraction, and Fourier transforms infrared spectroscopy. Studying the stability of the SDs of TSIIA revealed that the drug content of the formulation and dissolution behavior was unchanged under the applied storage conditions. In vivo tests showed that SDs of the silica nanoparticles/TSIIA had a significantly larger area under the concentration-time curve, which was 1.27 times more than that of TSIIA (P < 0.01. Additionally, the values of maximum plasma concentration and the time to reach maximum plasma concentration of the SDs were higher than those of TSIIA and the physical mixing system. Based on these results, we conclude that the silica nanoparticle based SDs achieved complete dissolution, increased absorption rate, maintained drug stability, and showed improved oral bioavailability compared to TSIIA alone.Keywords: tanshinone IIA, solid dispersions, silica nanoparticles, in vitro

  6. Preparation and testing of quaternized chitosan nanoparticles as gene delivery vehicles.

    Science.gov (United States)

    Li, Guang-Feng; Wang, Jing-Cheng; Feng, Xin-Min; Liu, Zhen-Dong; Jiang, Chao-Yong; Yang, Jian-Dong

    2015-04-01

    The aim of this study was to synthesize a chitosan (CS) derivative, a quaternary ammonium salt crystal called N-2-hydroxypropyl trimethyl ammonium chloride chitosan (HACC), and test a series of HACC and pEGFP-DNA complexes at different weight ratios for their efficiency of gene delivery into human cells. CS was modified with cationic etherifying agent to obtain the CS derivative. Fourier transform infrared spectra were recorded on KBr pellets with a spectrometer. (1)H nuclear magnetic resonance (NMR) spectra of HACC were obtained using a spectrometer. HACC was subsequently used to prepare HACC/DNA complexes at different weight ratios by coacervation method. The resulting particle size and surface charge were assessed by laser light scattering using a zeta potential analyzer. The HACC/DNA complex formation and DNA protection in the nanoparticle complex was investigated by gel mobility shift assay and DNase I protection assay, respectively. The cytotoxicity of HACC and HACC/DNA nanoparticles was evaluated by MTT assay using (mesenchymal stem cell) MSC lines. The nanoscale structure of the particles was obtained by transmission electron microscope (TEM). The FTIR spectrum of HACC showed the characteristic quaternary ammonium group absorption band at 1475 cm(-1), which indicated the presence of quaternary ammonium group. The successful synthesis of HACC was also confirmed by (1)H NMR spectrum. HACC showed good solubility in water and was electropositive. HACC efficiently packed and protected pEGFP-DNA at a weight ratio of 10. With increased weight ratios, the surface charge of the composite particle increased from negative to positive, the average particle size increased, and HACC nanoparticle had a higher carrying efficiency. The nanoparticles released DNA in two distinct phases, and 55 % was released within the first 20 h of solubilization. The nanoparticles under TEM showed circular or oval shapes. The particles exhibited no cytotoxicity against human cells. No

  7. Preparation and evaluation of ofloxacin-loaded palmitic acid solid lipid nanoparticles

    Directory of Open Access Journals (Sweden)

    Shuyu Xie

    2011-03-01

    Full Text Available Shuyu Xie, Luyan Zhu, Zhao Dong, Yan Wang, Xiaofang Wang, WenZhong ZhouDepartment of Preventive Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing, People’s Republic of ChinaAbstract: The purpose of this study was to use solid lipid nanoparticles (SLN to improve the pharmacological activity of ofloxacin. Ofloxacin-loaded SLN were prepared using palmitic acid as lipid matrix and poly vinyl alcohol (PVA as emulsifier by a hot homogenization and ultrasonication method. The physicochemical characteristics of SLN were investigated by optical microscope, scanning electron microscopy, and photon correlation spectroscopy. Pharmacokinetics was studied after oral administration in mice. In vitro antibacterial activity and in vivo antibacterial efficacy of the SLN were investigated using minimal inhibitory concentrations (MIC and a mouse protection model. The results demonstrated that the encapsulation efficiency, loading capacity, diameter, polydispersivity index, and zeta potential of the nanoparticles were 41.36% ± 1.50%, 4.40% ± 0.16%, 156.33 ± 7.51 nm, 0.26 ± 0.04, and –22.70 ± 1.40 mv, respectively. The SLN showed sustained release and enhanced antibacterial activity in vitro. Pharmacokinetic results demonstrated that SLN increased the bioavailability of ofloxacin by 2.27-fold, and extended the mean residence time of the drug from 10.50 to 43.44 hours. Single oral administrations of ofloxacin-loaded nanoparticles at 3 drug doses, 5 mg/kg, 10 mg/kg, and 20 mg/kg, all produced higher survival rates of lethal infected mice compared with native ofloxacin. These results indicate that SLN might be a promising delivery system to enhance the pharmacological activity of ofloxacin.Keywords: ofloxacin, pharmacological activity, solid lipid nanoparticles, antibacterial activity

  8. Preparation and photoelectric property of TiO{sub 2} nanoparticles with controllable phase junctions

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Hongmei [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); Tan, Xin [School of Science, Tibet University, Lhasa 850000, Tibet (China); Yu, Tao, E-mail: yutao@tju.edu.cn [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Tianjin University-National Institute for Materials Science (TU-NIMS) Joint Research Center, Tianjin University, Tianjin 300072 (China)

    2014-12-01

    Graphical abstract: - Highlights: • A series of bicrystalline TiO{sub 2} nanoparticles with different ratio of controllable phase junctions between anatase and rutile were synthesized successfully using ionic liquid-assisted method by hydrolysis of TiCl{sub 4}. • The spatial separation capacity of photogenerated charge carriers and photocatalytic activities of the samples with different ratio of controllable phase junctions were evaluated systemically. • The best photocatalytic activity for MO degradation can reach above 99% at the sample with 27.4% rutile which also has the best photoelectric property compared with other samples. - Abstract: To explore the effect of phase composition on the photoelectric property of anatase–rutile mixed crystal nanoparticles, a series of TiO{sub 2} nanoparticles with phase junctions controlling were synthetized by hydrolysis of TiCl{sub 4} in hydrochloric acid, an ionic liquid-assisted method was used during this process. Crystalline size and the ratio of anatase to rutile of as-prepared samples were calculated by the XRD. The surface area was measured by nitrogen sorption measurements using the BET method. The micro-structure of phase junctions was characterized by TEM. Optical transmittance properties of TiO{sub 2} with controllable phase junctions were examined via ultraviolet–visible diffuse reflection spectroscopy (UV–vis DRS). The particles were manufactured into films using the doctor-blade technique on FTO glasses. To test photocurrent density, and spatial separation capacity of electron–holes pairs, photo-electro method was employed. The photocatalytic activities of the resulting samples were examined in the degradation of methyl orange (MO) under artificial solar light irradiation. Mechanisms of separation and transfer of photogenerated charge and the effect of phase composition on photoelectric property of anatase–rutile nanoparticles were discussed.

  9. Synthesis, Characterization and Catalytic Activity of Cu/Cu2O Nanoparticles Prepared in Aqueous Medium

    Directory of Open Access Journals (Sweden)

    Sayed M. Badawy

    2015-07-01

    Full Text Available Copper/Copper oxide (Cu/Cu2O nanoparticles were synthesized by modified chemical reduction method in an aqueous medium using hydrazine as reducing agent and copper sulfate pentahydrate as precursor. The Cu/Cu2O nanoparticles were characterized by X-ray Diffraction (XRD, Energy Dispersive X-ray Fluorescence (EDXRF, Scanning Electron Microscope (SEM, and Transmission Electron Microscope (TEM. The analysis revealed the pattern of face-centered cubic (fcc crystal structure of copper Cu metal and cubic cuprites structure for Cu2O. The SEM result showed monodispersed and agglomerated particles with two micron sizes of about 180 nm and 800 nm, respectively. The TEM result showed few single crystal particles of face-centered cubic structures with average particle size about 11-14 nm. The catalytic activity of Cu/Cu2O nanoparticles for the decomposition of hydrogen peroxide was investigated and compared with manganese oxide MnO2. The results showed that the second-order equation provides the best correlation for the catalytic decomposition of H2O2 on Cu/Cu2O. The catalytic activity of hydrogen peroxide by Cu/Cu2O is less than the catalytic activity of MnO2 due to the presence of copper metal Cu with cuprous oxide Cu2O. © 2015 BCREC UNDIP. All rights reservedReceived: 6th January 2015; Revised: 14th March 2015; Accepted: 15th March 2015How to Cite: Badawy, S.M., El-Khashab, R.A., Nayl, A.A. (2015. Synthesis, Characterization and Catalytic Activity of Cu/Cu2O Nanoparticles Prepared in Aqueous Medium. Bulletin of Chemical Reaction Engineering & Catalysis, 10 (2: 169-174. (doi:10.9767/bcrec.10.2.7984.169-174 Permalink/DOI: http://dx.doi.org/10.9767/bcrec.10.2.7984.169-174  

  10. Biomimetic thin film deposition

    Energy Technology Data Exchange (ETDEWEB)

    Rieke, P.R.; Graff, G.E.; Campbell, A.A.; Bunker, B.C.; Baskaran, S.; Song, L.; Tarasevich, B.J.; Fryxell, G.E.

    1995-09-01

    Biological mineral deposition for the formation of bone, mollusk shell and other hard tissues provides materials scientists with illustrative materials processing strategies. This presentation will review the key features of biomineralization and how these features can be of technical importance. We have adapted existing knowledge of biomineralization to develop a unique method of depositing inorganic thin films and coating. Our approach to thin film deposition is to modify substrate surfaces to imitate the proteins found in nature that are responsible for controlling mineral deposition. These biomimetic surfaces control the nucleation and growth of the mineral from a supersaturated aqueous solution. This has many processing advantages including simple processing equipment, environmentally benign reagents, uniform coating of highly complex shapes, and enhanced adherence of coating. Many different types of metal oxide, hydroxide, sulfide and phosphate materials with useful mechanical, optical, electronic and biomedical properties can be deposited.

  11. A Biomimetic Haptic Sensor

    Directory of Open Access Journals (Sweden)

    Ben Mitchinson

    2008-11-01

    Full Text Available The design and implementation of the periphery of an artificial whisker sensory system is presented. It has been developed by adopting a biomimetic approach to model the structure and function of rodent facial vibrissae. The artificial vibrissae have been formed using composite materials and have the ability to be actively moved or whisked. The sensory structures at the root of real vibrissae has been modelled and implemented using micro strain gauges and Digital Signal Processors. The primary afferents and vibrissal trigeminal ganglion have been modelled using empirical data taken from electrophysiological measurements, and implemented in real-time using a Field Programmable Gate Array. Pipelining techniques were employed to maximise the utility of the FPGA hardware. The system is to be integrated into a more complete whisker sensory model, including neural structures within the central nervous system, which can be used to orient a mobile robot.

  12. Preparation of an agar-silver nanoparticles (A-AgNp) film for increasing the shelf-life of fruits.

    Science.gov (United States)

    Gudadhe, Janhavi A; Yadav, Alka; Gade, Aniket; Marcato, Priscyla D; Durán, Nelson; Rai, Mahendra

    2014-12-01

    Preparation of protective coating possessing antimicrobial properties is present day need as they increase the shelf life of fruits and vegetables. In the present study, preparation of agar-silver nanoparticle film for increasing the shelf life of fruits is reported. Silver nanoparticles (Ag-NPs) biosynthesised using an extract of Ocimum sanctum leaves, were mixed with agar-agar to prepare an agar-silver nanoparticles (A-AgNp) film. This film was surface-coated over the fruits, Citrus aurantifolium (Thornless lime) and Pyrus malus (Apple), and evaluated for the determination of antimicrobial activity of A-AgNp films using disc diffusion method, weight loss and shelf life of fruits. This study demonstrates that these A-AgNp films possess antimicrobial activity and also increase the shelf life of fruits.

  13. Microwave-Assisted Preparation of CdS Nanoparticles in a Halide-Free Ionic Liquid and Their Photocatalytic Activities

    Institute of Scientific and Technical Information of China (English)

    M. ESMAILI, A; HABIBI-YANGJEH

    2011-01-01

    A microwave-assisted (4-6 min) method was used for the preparation ofCdS nanoparticles in 1-ethyl-3-methylimidazolium ethyl sulfate, a halide-free room-temperature ionic liquid (RTIL). The samples were characterized by powder X-ray diffraction, energy dispersive X-ray spectroscopy, and scanning electron microscopy. Diffuse reflectance spectra showed a 1.33 eV blue shift relative to bulk CdS. The photocatalytic activities of the nanoparticles for photodegradation of methylene blue (MB) using UV and visible light were measured. The photodegradation of MB decreased with calcination temperature. First order rate constants for the reaction under visible and UV irradiations over the nanoparticles prepared in the RTIL rich media were 5.4 and 2.5 higher, respectively, than the sample prepared in water.

  14. Biomimetic Preparation of Magnetite/Chitosan Nanocomposite via In Situ Composite Method——Potential Use in Magnetic Tissue Repair Domain

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    This study focused on the preparation of magnetic chitosan nanocomposite that has a potential application to bone repair and regeneration using an in situ composite method where chitosan membrane was used as the template and NaOH was used as the precipitant. X-ray diffraction analysis results show the formation of magnetite in the chitosan matrix. From the magnetic measurement, it could be concluded that the magnetic chitosan rods were superparamagnetic,and that this is the unique property of nanomagnetite. Macroscopical layer structure of the magnetic chitosan rods was observed from the photographs after mechanical test, and the microlayer structure of the rods was observed from the images of scanning electron microscopy. The mechanism for preparing the rods was discussed in detail. Transmission electron microscope was used to investigate the magnetite particles in the chitosan matrix and from the images it was concluded that the magnetite particles dispersed well in chitosan matrix with particle size of about 10 nm. The mechanical properties of the magnetic chitosan rods were measured and the blending strength was found to be 98.8 MPa. The mechanical properties did not decline when compared with those of the pure chitosan materials.

  15. Optimized Preparation of Levofloxacin-loaded Chitosan Nanoparticles by Ionotropic Gelation

    Science.gov (United States)

    Guan, J.; Cheng, P.; Huang, S. J.; Wu, J. M.; Li, Z. H.; You, X. D.; Hao, L. M.; Guo, Y.; Li, R. X.; Zhang, H.

    The present work investigates the feasibility of fabricating chitosan (CS)-levofloxacin (LOF) nanoparticles by ionotropic gelation technology. An orthogonal experiment was designed to optimize its preparing parameters and multi-index comprehensive weighed score analysis method was used to study the effects of various factors including concentration of CS, concentration of tripolyphosphate (TPP), mass ratio of CS to TPP, and mass ratio of CS to LOF on the properties of nanoparticles. The particles prepared under optimal condition of 2 mg/ml CS concentration, 2 mg/ml TPP concentration, 0.5:1 mass ratio of oil to water and 4:1 mass ratio of CS to TPP had 140 nm diameter, 0.95 span, 6.13% loading capacity (LC) and 24.91% encapsulation efficiency (EE). In vitro release profile showed that LOF released fast initially and then slowly with T90 occurring at 76.5 h. Future studies should focus on antibacterial and biocompatible properties in order to evaluate its potential as sustainable delivery system.

  16. Preparation of platinum modified titanium dioxide nanoparticles with the use of laser ablation in water.

    Science.gov (United States)

    Siuzdak, K; Sawczak, M; Klein, M; Nowaczyk, G; Jurga, S; Cenian, A

    2014-08-07

    We report on the preparation method of nanocrystalline titanium dioxide modified with platinum by using nanosecond laser ablation in liquid (LAL). Titania in the form of anatase crystals has been prepared in a two-stage process. Initially, irradiation by laser beam of a titanium metal plate fixed in a glass container filled with deionized water was conducted. After that, the ablation process was continued, with the use of a platinum target placed in a freshly obtained titania colloid. In this work, characterization of the obtained nanoparticles, based on spectroscopic techniques--Raman, X-ray photoelectron and UV-vis reflectance spectroscopy--is given. High resolution transmission electron microscopy was used to describe particle morphology. On the basis of photocatalytic studies we observed the rate of degradation process of methylene blue (MB) (a model organic pollution) in the presence of Pt modified titania in comparison to pure TiO2--as a reference case. Physical and chemical mechanisms of the formation of platinum modified titania are also discussed here. Stable colloidal suspensions containing Pt modified titanium dioxide crystalline anatase particles show an almost perfect spherical shape with diameters ranging from 5 to 30 nm. The TiO2 nanoparticles decorated with platinum exhibit much higher (up to 30%) photocatalytic activity towards the degradation of MB under UV illumination than pure titania.

  17. Preparation and antioxidant capacity of element selenium nanoparticles sol-gel compounds.

    Science.gov (United States)

    Bai, Yan; Qin, Biyin; Zhou, Yanhui; Wang, Yudong; Wang, Zi; Zheng, Wenjie

    2011-06-01

    This paper reported the preparation and antioxidant capacities of element selenium nanoparticles (nanoSe(0))-ascorbic acid (Vc) sol and nanSe(0)/Vc/selenocystine (SeCys) sol-gel compounds. NanoSe(0)-Vc sol was prepared by reduction of selenious dioxide (SeO2) with Vc. In the nanoSe(0)-Vc sol, highly concentrated Vc was also used as a modifier to modulate the diameter of Se(0) nanoparticles in the liquid phase. Then excellent nanoSe(0) sol-gel compounds were obtained by adding SeCys into the nanoSe(0)-Vc sol. The structure of the nanoSe(0)/Vc/SeCys sol-gel compounds was defined, which was constructed via C-Se, Se-H and O=C-Se valences and by interaction between SeCys and Vc via peptide bonds, esterification and dehydration. The antioxidant capacities of the nanoSe(0)-Vc sol and the nanoSe(0)Vc/SeCys sol-gel compounds were estimated by oxygen radical absorption capacity (ORAC) assay. The nanoSe(0)/Vc/SeCys sol-gel compounds possessed a strong antioxidant capacity due to forming the perfect three-dimensional (3D) frameworks structure. The results suggested that the nanoSe(0)-Vc sol and the nanoSe(0)Vc/SeCys sol-gel compounds might be potential medicine, especially antioxidant.

  18. Preparation and efficacy of Newcastle disease virus DNA vaccine encapsulated in chitosan nanoparticles.

    Science.gov (United States)

    Zhao, Kai; Zhang, Yang; Zhang, Xiaoyan; Li, Wei; Shi, Ci; Guo, Chen; Dai, Chunxiao; Chen, Qian; Jin, Zheng; Zhao, Yan; Cui, Hongyu; Wang, Yunfeng

    2014-01-01

    Optimal preparation conditions of Newcastle disease virus (NDV) F gene deoxyribonucleic acid (DNA) vaccine encapsulated in chitosan nanoparticles (pFNDV-CS-NPs) were determined. The pFNDV-CS-NPs were prepared according to a complex coacervation method. The pFNDV-CS-NPs were produced with good morphology, high stability, a mean diameter of 199.5 nm, encapsulation efficiency of 98.37% ± 0.87%, loading capacity of 36.12% ± 0.19%, and a zeta potential of +12.11 mV. The in vitro release assay showed that the plasmid DNA was sustainably released from the pFNDV-CS-NPs, up to 82.9% ± 2.9% of the total amount. Cell transfection test indicated that the vaccine expressed the F gene in cells and maintained good bioactivity. Additionally, the safety of mucosal immunity delivery system of the pFNDV-CS-NPs was also tested in vitro by cell cytotoxicity and in vivo by safety test in chickens. In vivo immunization showed that better immune responses of specific pathogen-free chickens immunized with the pFNDV-CS-NPs were induced, and prolonged release of the plasmid DNA was achieved compared to the chickens immunized with the control plasmid. This study lays the foundation for the further development of mucosal vaccines and drugs encapsulated in chitosan nanoparticles.

  19. One-step preparation of antimicrobial silver nanoparticles in polymer matrix

    Energy Technology Data Exchange (ETDEWEB)

    Lyutakov, O., E-mail: lyutakoo@vscht.cz; Kalachyova, Y. [Institute of Chemical Technology, Department of Solid State Engineering (Czech Republic); Solovyev, A. [Institute of Chemical Process Fundamentals of the ASCR (Czech Republic); Vytykacova, S. [Institute of Chemical Technology, Department of Glass and Ceramics (Czech Republic); Svanda, J.; Siegel, J. [Institute of Chemical Technology, Department of Solid State Engineering (Czech Republic); Ulbrich, P. [Institute of Chemical Technology, Department of Biochemistry and Microbiology (Czech Republic); Svorcik, V. [Institute of Chemical Technology, Department of Solid State Engineering (Czech Republic)

    2015-03-15

    Simple one-step procedure for in situ preparation of silver nanoparticles (AgNPs) in the polymer thin films is described. Nanoparticles (NPs) were prepared by reaction of N-methyl pyrrolidone with silver salt in semi-dry polymer film and characterized by transmission electron microscopy, XPS, and UV–Vis spectroscopy techniques. Direct synthesis of NPs in polymer has several advantages; even though it avoids time-consuming NPs mixing with polymer matrix, uniform silver distribution in polymethylmethacrylate (PMMA) films is achieved without necessity of additional stabilization. The influence of the silver concentration, reaction temperature and time on reaction conversion rate, and the size and size-distribution of the AgNPs was investigated. Polymer films doped with AgNPs were tested for their antibacterial activity on Gram-negative bacteria. Antimicrobial properties of AgNPs/PMMA films were found to be depended on NPs concentration, their size and distribution. Proposed one-step synthesis of functional polymer containing AgNPs is environmentally friendly, experimentally simple and extremely quick. It opens up new possibilities in development of antimicrobial coatings with medical and sanitation applications.

  20. Antibacterial continuous nanofibrous hybrid yarn through in situ synthesis of silver nanoparticles: Preparation and characterization

    Energy Technology Data Exchange (ETDEWEB)

    Barani, Hossein, E-mail: barani@birjand.ac.ir

    2014-10-01

    Nanofibrous hybrid yarns of polyvinyl alcohol (PVA) and poly-L-lactide acid (PLLA) with the antibacterial activity were prepared that contains 0, 5, 10, 20, and 30 wt.% of silver nanoparticles according to the PVA polymer content. This was performed by electrospinning using distilled water and 2, 2, 2-trifluoroethanol as a solvent for PVA and PLLA respectively, and sodium borohydride was used as a reducing agent. The scanning electron microscope observation confirmed the formation of AgNPs into the PVA nanofiber structure, and they were uniform, bead free, cylindrical and smooth. The diameter of hybrid yarns and their nanofiber component was decreased as the silver nitrate concentration in electrospinning solutions was increased. The differential scanning calorimetry results indicated that the silver nanoparticles can form interactions with polymer chains and decrease the melting enthalpy. The mechanical analysis showed a lower stress and strain at break of the AgNP-loaded nanofibrous hybrid yarns than the unloaded hybrid yarn. However, there wasn't a statistically significant difference between the strain at break of electrospun nanofibrous hybrid yarns. Moreover, the bactericidal efficiency of all loaded samples was over 99.99%. - Highlights: • Nanofibrous hybrid yarns of PVA/PLLA with antibacterial activity were prepared. • The diameter of nanofibers was decreased as the AgNP concentration was increased. • AgNPs make interactions with amorphous phase of polymer and increase the Tg. • All loaded samples presented a good bactericidal and bacteriostatic efficiency.

  1. Preparation of lithium ferrite nanoparticles by high energy ball milling and characterizations

    Directory of Open Access Journals (Sweden)

    J. Touthang

    2016-11-01

    Full Text Available Ferrites are ferrimagnetic ceramic materials with inherent useful electromagnetic properties. Of them, spinelstructured ferrites are promising materials for microwave device applications; stress/torsion sensors and energy storage applications like anode materials in lithium batteries, fuel cells, solar cells etc. Nanostructured spinels further have high and wide scope of potential applications. In the present study, two different types of varied sized ferrimagnetic lithium ferrite spinel nanoparticles prepared using chemical sol-gel auto-combustion method were chosen. The prepared spinel particles were heated at 300°C for 1h. After heating the powders were milled using a High Energy Ball Mill for 30 minutes to further grind the particles and then subjected to various characterizations. Structural characterization was done using X-Ray Diffraction Method (XRD. The study revealed the spinel structure of these samples. Structural parameter such as lattice constant was determined using XRD data and found that the lattice parameter agrees with the standard data. DLS study found the agglomerations of the nanoparticles. The synthesized nanospinel particles were also characterized by the UVVis Spectroscopy, the Fourier Transform Infrared Spectroscopy (FTIR. Finally the magnetic hysteresis properties were studied using a Vibrating Sample Magnetometer (VSM.

  2. Biotemplated preparation of CdS nanoparticles/bacterial cellulose hybrid nanofibers for photocatalysis application.

    Science.gov (United States)

    Yang, Jiazhi; Yu, Junwei; Fan, Jun; Sun, Dongping; Tang, Weihua; Yang, Xuejie

    2011-05-15

    In this work, we describe a novel facile and effective strategy to prepare micrometer-long hybrid nanofibers by deposition of CdS nanoparticles onto the substrate of hydrated bacterial cellulose nanofibers (BCF). Hexagonal phase CdS nanocrystals were achieved via a simple hydrothermal reaction between CdCl(2) and thiourea at relatively low temperature. The prepared pristine BCF and the CdS/BCF hybrid nanofibers were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), UV-vis absorption spectroscopy (UV-vis), and X-ray photoelectron spectroscopy (XPS). The results reveal that the CdS nanoparticles were homogeneously deposited on the BCF surface and stabilized via coordination effect. The CdS/BCF hybrid nanofibers demonstrated high-efficiency photocatalysis with 82% methyl orange (MO) degradation after 90 min irradiation and good recyclability. The results indicate that the CdS/BCF hybrid nanofibers are promising candidate as robust visible light responsive photocatalysts.

  3. A solid control strategy for preparation of silver nanoparticles in aqueous medium

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Daechul [Soonchunhyang University, Asan (Korea, Republic of); Kwon, Sung-Hyun [Gyeongsang National University, Tongyong (Korea, Republic of)

    2015-12-15

    Uniformly distributed, spherically shaped, mild concentrated silver nanoparticles with single-digit to hundreds nm size have been prepared by reducing silver nitrate with popular reducers like sodium borohydride or hydrazine in the presence of ordinary stabilizers such as SDS, PVP, Polysorbates and ultrasonication. Uv-visble spectroscopic analysis, particle size analysis, and particle-imaging through transmission electron microscopy (TEM) were used for nanoparticle characterization. Higher temperature accelerated the reduction rates, which follows the typical autocatalytic kinetics. Particularly, ultrasonication helped to facilitate the crucial stage of reduction phase to result in excellent quality of nanosolution, such as narrow distribution of particles and size uniformity. We found that initial location or arrangement of silver ions in clouds of stabilizers and 'effectve mixing' in the stage of reduction were vital for successful preparation of silver nanosolution. Also, reagent/stabilizer ratio, reducer input, solution environment such as pH, temperature, and stabilizer properties were optimized and discussed in detail. Proper selection of stabilizer and molar ratio to reagent and effective 'mixing' for preventing grain growth needs to be investigated more in the future work.

  4. Preparation and evaluation of tilmicosin-loaded hydrogenated castor oil nanoparticle suspensions of different particle sizes.

    Science.gov (United States)

    Chen, Xiaojin; Wang, Ting; Lu, Mengmeng; Zhu, Luyan; Wang, Yan; Zhou, WenZhong

    2014-01-01

    Three tilmicosin-loaded hydrogenated castor oil nanoparticle (TMS-HCO-NP) suspensions of different particle sizes were prepared with different polyvinyl alcohol surfactant concentrations using a hot homogenization and ultrasonic technique. The in vitro release, in vitro antibacterial activity, mammalian cytotoxicity, acute toxicity in mice, and stability study were conducted to evaluate the characteristics of the suspensions. The in vitro tilmicosin release rate, antibacterial activity, mammalian cytotoxicity, acute toxicity in mice, and stability of the suspensions were evaluated. When prepared with polyvinyl alcohol concentrations of 0.2%, 1%, and 5%, the mean diameters of the nanoparticles in the three suspensions were 920±35 nm, 452±10 nm, and 151±4 nm, respectively. The three suspensions displayed biphasic release profiles similar to that of freeze-dried TMS-HCO-NP powders, with the exception of having a faster initial release. Moreover, suspensions of smaller-sized particles showed faster initial release, and lower minimum inhibitory concentrations and minimum bactericidal concentrations. Time-kill curves showed that within 12 hours, the suspension with the 151 nm particles had the most potent bactericidal activity, but later, the suspensions with larger-sized particles showed increased antibacterial activity. None of the three suspensions were cytotoxic at clinical dosage levels. At higher drug concentrations, all three suspensions showed similar concentration-dependent cytotoxicity. The suspension with the smallest-sized particle showed significantly more acute toxicity in mice, perhaps due to faster drug release. All three suspensions exhibited good stability at 4°C and at room temperature for at least 6 months. These results demonstrate that TMS-HCO-NP suspensions can be a promising formulation for tilmicosin, and that nanoparticle size can be an important consideration for formulation development.

  5. Preparation of 5-fluorouracil nanoparticles by supercritical antisolvents for pulmonary delivery

    Directory of Open Access Journals (Sweden)

    Pardis Kalantarian

    2010-09-01

    Full Text Available Pardis Kalantarian1,2, Abdolhosein Rouholamini Najafabadi1, Ismaeil Haririan2, Alireza Vatanara1, Yadollah Yamini3, Majid Darabi1, Kambiz Gilani11Aerosol Research Laboratory and 2Pharmaceutical Laboratory, School of Pharmacy, Tehran University of Medical Sciences, 3Department of Chemistry, Tarbiat Modarres University, Tehran, IranAbstract: This study concerns the supercritical antisolvent process which allows single-step production of 5-fluorouracil (5-FU nanoparticles. This process enhances the physical characteristics of 5-FU in order to deliver it directly to the respiratory tract. Several mixtures of methanol with dichloromethane, acetone, or ethanol were used for particle preparation, and their effects on the physical characteristics of the final products were studied. The conditions of the experiment included pressures of 100 and 150 bar, temperature of 40°C, and a flow rate of 1 mL/min. The particles were characterized physicochemically before and after the process for their morphology and crystallinity. In spite of differences in size, the particles were not very different regarding their morphology. The resulting particles were of a regular shape, partly spherical, and appeared to have a smooth surface, whereas the mechanically milled particles showed less uniformity, had surface irregularities and a high particle size distribution, and seemed aggregated. Particles of 5-FU precipitated from methanol-dichloromethane 50:50 had a mean particle size of 248 nm. In order to evaluate the aerodynamic behavior of the nanoparticles, six 5-FU dry powder formulations containing mixtures of coarse and fine lactose of different percentages were prepared. Deposition of 5-FU was measured using a twin-stage liquid impinger and analyzed using a validated high pressure liquid chromatography method. Addition of fine lactose improved the aerodynamic performance of the drug, as determined by the fine particle fraction.Keywords: supercritical antisolvent, 5

  6. Preparation and optical properties of sodium borosilicate glasses containing Sb nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zhong, Jiasong, E-mail: jiasongzhong@hdu.edu.cn [College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Ma, Xin [College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035 (China); Lu, Hongwei; Wang, Xin; Zhang, Suling [College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Xiang, Weidong, E-mail: xiangweidong001@126.com [College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035 (China)

    2014-09-01

    Highlights: • The Sb nanoparticles doped in Na{sub 2}O–B{sub 2}O{sub 3}–SiO{sub 2} glass were prepared by sol–gel methods. • Obtained glass was investigated by structural and optical measurements. • The glass was crystalline with a rhombohedral structure of Sb. • An absorption peak centered on 566 nm has been observed in doping glass. • The third-order optical nonlinearity was investigated by femtosecond Z-scan technique. - Abstract: Sb nanoparticles have been successfully prepared from SbCl{sub 3} in sodium borosilicate (Na{sub 2}O–B{sub 2}O{sub 3}–SiO{sub 2}) glass matrix by sol–gel method, involving metallic sodium as sodium source, boric acid as boron source and SiO{sub 2} come from hydrolysis of tetraethoxysilane. The feasibility of process conditions were analyzed by using Fourier Transform Infrared (FT-IR), thermal gravimetric (TG), and nuclear magnetic resonance (NMR). X-ray diffraction (XRD) study revealed that the rhombohedral structure of metal Sb have formed in the glass. The particle was found to be spherical shaped and highly monodispersed with an average size of about 32.63 nm as analyzed from transmission electron microscopy (TEM). The surface plasmon resonance (SPR) of Sb nanoparticle was studied from the UV–Vis absorption. The nonlinear optical properties were studied by using the Z-scan technique with a Ti:sapphire laser at 800 nm. Results showed that the third-order optical nonlinear susceptibility χ{sup (3)} of the glass was determined to be 4.85 × 10{sup −11} esu.

  7. Magnetite nanoparticles prepared by co-precipitation method in different conditions

    Energy Technology Data Exchange (ETDEWEB)

    Aphesteguy, J.C., E-mail: caphestegu@fi.uba.ar [LAFMACEL-INTECIN, Facultad de Ingeniería, UBA, Paseo Colón 850, C1063EHA Buenos Aires (Argentina); Kurlyandskaya, G.V. [Universidad del País Vasco UPV-EHU, Dept. Electricidad y Electronica, 48940 Leioa (Spain); Ural Federal University, Dept. Magnetism and Magnetic Nanomaterials, 620000 Ekaterinburg (Russian Federation); Celis, J.P. de [National Technology University (UTN), Facultad Regional Avellaneda, Department of Chemistry (Argentina); Safronov, A.P. [Ural Federal University, Dept. Magnetism and Magnetic Nanomaterials, 620000 Ekaterinburg (Russian Federation); Institute of Electrophysics UD RAS, Ekaterinburg 620016 (Russian Federation); Schegoleva, N.N. [Institute of Metal Physics UD RAS, Ekaterinburg 620044 (Russian Federation)

    2015-07-01

    Magnetic nanoparticles (MNPs) of pure magnetite (Fe{sub 3}O{sub 4}) were prepared in an aqueous solution (sample M−I) and in a water-ethyl alcohol mixture (sample M−II) by the co-precipitation method. The structure and magnetic properties of both samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), magnetic (M−H) and microwave measurements (FMR). The mean average particle diameter and particle size distribution was evaluated by the Dynamic Light Scattering (DLS) and Brunauer- Emmett-Teller techniques (BET). The Quantitative chemical analysis of iron was performed by Inductively Coupled Plasma (ICP)- Atomic Emission Spectroscopy (AES) technique. The MNPs prepared in aqueous solution show a higher grain than those prepared in the water-ethyl alcohol mixture. The type of phase structure in both cases can be defined as “defective spinel”. The shape of the majority of M−I MNPs is octahedral. The shape of the majority of M−II MNPs is cubic. The specific surface area of MNPs was as high as 14.4 m{sup 2}/g for M−I sample and 77.8 m{sup 2}/g for sample M–II. The obtained saturation magnetization values of 75 emu/g (M−I) and 68 emu/g (M−II) are consistent with expected values for magnetite MNPs of observed sizes. Ferromagnetic resonance (FMR) measurements confirmed that MNPs of both types are magnetically homogeneous materials. FMR lines' position and line widths can be understood by invoking the local dipolar fields, deviations from sphericity, magnetocrystalline anisotropy and stresses. M−I sample shows sizeable zero field microwave absorption which is absent in the M−II case. The differences in microwave behaviour of M−I and M−II MNPs can be used in the design of microwave radiation absorbing multilayers. - Highlights: • Magnetite nanoparticles were prepared in two different conditions. • Specific surface area of sample prepared in water- ethanol mix is

  8. NOVEL PREPARATION AND MAGNETO CHEMICAL CHARACTERIZATION OF NANOPARTICLE MIXED ALCOHOL CATALYSTS

    Energy Technology Data Exchange (ETDEWEB)

    Seetala V. Naidu; Upali Siriwardane

    2005-05-24

    We have developed and streamlined the experimental systems: (a) Laser-induced solution deposition (LISD) photosynthesis, ball-milling, and chemical synthesis of Fe, Co, and Cu nanoparticle catalysts; (b) Sol-gel method for mesoporous {gamma}-Al{sub 2}O{sub 3}, SiO{sub 2}, hybrid alumina/silica granular supports; (c) Three sol-gel/oil-drop catalyst preparation methods to incorporate metal nanoparticles into mesoporous 1 mm granular supports; (d) Low-cost GC-TCD system with hydrogen as carrier gas for the determination of wide spectrum of alkanes produced during the F-T reactions; and (e) Gas-flow reactor and microchannel reactor for fast screening of catalysts. The LISD method could produce Co, Cu, and Fe (5 nm) nanoparticles, but in milligram quantities. We could produce nanoparticles in gram quantities using high-energy ball milling and chemical synthesis methods. Ball milling gave wide particle size distribution compared to the chemical synthesis method that gave almost uniform size ({approx}5 nm) particles. Metal nanoparticles Cu, Co, Fe, Cu/Co, Cu/Fe and Co/Fe were loaded (2-12 wt%) uniformly into {gamma}-Al{sub 2}O{sub 3}, SiO{sub 2}, or alumina/silica hybrid supports by combined sol-gel/oil-drop methods followed by calcination and hydrogenation steps, prior to syngas FT reaction studies. The properties of metal loaded {gamma}-Al{sub 2}O{sub 3} granules were compared for the two precursors: aluminum tri-sec-butoxide (ALTSB) and aluminum tri-iso-propoxide (ALTIP). The effect of solgel supports alumina, silica, and alumina/silica hybrid were examined on catalytic properties. Metal loading efficiencies for pure metal catalysts increased in the order Co, Cu and Fe in agreement with solubility of metal hydroxides. In case of mixed metals, Co and Cu seams to interfere and reduce Fe metal loading when metal nitrate solutions are used. The solubility differences of metal hydroxides would not allow precise control of metal loading. We have overcome this problem by

  9. Preparation, characterization, and potential application of chitosan, chitosan derivatives, and chitosan metal nanoparticles in pharmaceutical drug delivery

    Directory of Open Access Journals (Sweden)

    Ahmed TA

    2016-01-01

    Full Text Available Tarek A Ahmed1,2 Bader M Aljaeid11Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia; 2Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Al-Azhar University, Cairo, EgyptAbstract: Naturally occurring polymers, particularly of the polysaccharide type, have been used pharmaceutically for the delivery of a wide variety of therapeutic agents. Chitosan, the second abundant naturally occurring polysaccharide next to cellulose, is a biocompatible and biodegradable mucoadhesive polymer that has been extensively used in the preparation of micro- as well as nanoparticles. The prepared particles have been exploited as a potential carrier for different therapeutic agents such as peptides, proteins, vaccines, DNA, and drugs for parenteral and nonparenteral administration. Therapeutic agent-loaded chitosan micro- or nanoparticles were found to be more stable, permeable, and bioactive. In this review, we are highlighting the different methods of preparation and characterization of chitosan micro- and nanoparticles, while reviewing the pharmaceutical applications of these particles in drug delivery. Moreover, the roles of chitosan derivatives and chitosan metal nanoparticles in drug delivery have been illustrated.Keywords: nanoparticles, microparticles, preparation, characterization, pharmaceutical application

  10. Inverse supercritical fluid extraction as a sample preparation method for the analysis of the nanoparticle content in sunscreen agents.

    Science.gov (United States)

    Müller, David; Cattaneo, Stefano; Meier, Florian; Welz, Roland; de Vries, Tjerk; Portugal-Cohen, Meital; Antonio, Diana C; Cascio, Claudia; Calzolai, Luigi; Gilliland, Douglas; de Mello, Andrew

    2016-04-01

    We demonstrate the use of inverse supercritical carbon dioxide (scCO2) extraction as a novel method of sample preparation for the analysis of complex nanoparticle-containing samples, in our case a model sunscreen agent with titanium dioxide nanoparticles. The sample was prepared for analysis in a simplified process using a lab scale supercritical fluid extraction system. The residual material was easily dispersed in an aqueous solution and analyzed by Asymmetrical Flow Field-Flow Fractionation (AF4) hyphenated with UV- and Multi-Angle Light Scattering detection. The obtained results allowed an unambiguous determination of the presence of nanoparticles within the sample, with almost no background from the matrix itself, and showed that the size distribution of the nanoparticles is essentially maintained. These results are especially relevant in view of recently introduced regulatory requirements concerning the labeling of nanoparticle-containing products. The novel sample preparation method is potentially applicable to commercial sunscreens or other emulsion-based cosmetic products and has important ecological advantages over currently used sample preparation techniques involving organic solvents.

  11. Transmetallation as an effective strategy for the preparation of bimetallic CoPd and CuPd nanoparticles

    Science.gov (United States)

    Bersani, Marco; Conte, Luca; Martucci, Alessandro; Guglielmi, Massimo; Mattei, Giovanni; Bello, Valentina; Rosei, Renzo; Centazzo, Massimo

    2014-01-01

    The preparation of palladium alloy nanoparticles is of great interest for many applications, especially in catalysis. Starting from presynthesized nanoparticles of a less noble metal, a transmetallation reaction involving a redox process at the nanoparticle surface can be exploited to modify the nanoparticle composition and crystalline phase. As an example, monodispersed ε-cobalt and face-centered cubic copper nanoparticles were synthesized in organic solvents at high temperature and the as-formed nanoparticles were reacted with palladium(ii) hexafluoroacetylacetonate resulting in the formation of alloyed nanoparticles whose composition closely follows the reactant ratio. The oxidative state of the nanoparticle surface greatly affects the success of the transmetallation reaction and a reduction treatment was necessary to achieve the desired final product. Electron microscopy and X-ray diffraction showed that for cobalt a limiting palladium content for the ε-phase alloy is found, above which an fcc alloy nucleates, while for copper the fcc crystalline phase is preserved throughout the whole composition range.

  12. Preparation and in vitro characterization of chitosan nanoparticles containing Mesobuthus eupeus scorpion venom as an antigen delivery system

    Directory of Open Access Journals (Sweden)

    N Mohammadpour Dounighi

    2012-01-01

    Full Text Available Hydrophilic nanoparticles have been widely investigated in recent years as delivery systems for therapeutic macromolecules such as antigens. In the present study Mesobuthus eupeus venom-loaded chitosan nanoparticles were prepared via ionic gelation of tripolyphosphate (TPP and chitosan. The optimum encapsulation efficiency (91.1% and loading capacity (76.3% were obtained by a chitosan concentration of 2 mg/mL, chitosan-to-TPP mass ratio of 2 and M. eupeus venom concentration of 500 µg/mL. The average nanoparticle size at optimum conditions was determined by Zetasizer (Malvern Instruments, UK. The nanoparticle size was about 370 nm (polydispersity index: 0.429 while the zeta potential was positive. Transmission electron microscope (TEM imaging showed a spherical, smooth and almost homogenous structure for nanoparticles. Fourier transform infrared (FTIR spectroscopy confirmed tripolyphosphoric groups of TPP linked with ammonium groups of chitosan in the nanoparticles. The in vitro release of nanoparticles showed an initial burst release of approximately 60% in the first ten hours, followed by a slow and much reduced additional release for about 60 hours. It is suggested that the chitosan nanoparticles fabricated in our study may provide a suitable alternative to traditional adjuvant systems.

  13. One-pot solventless preparation of PEGylated black phosphorus nanoparticles for photoacoustic imaging and photothermal therapy of cancer.

    Science.gov (United States)

    Sun, Caixia; Wen, Ling; Zeng, Jianfeng; Wang, Yong; Sun, Qiao; Deng, Lijuan; Zhao, Chongjun; Li, Zhen

    2016-06-01

    Black phosphorus (BP) nanostructures such as nanosheets and nanoparticles have attracted considerable attention in recent years due to their unique properties and great potential in various physical, chemical, and biological fields. In this article, water-soluble and biocompatible PEGylated BP nanoparticles with a high yield were prepared by one-pot solventless high energy mechanical milling technique. The resultant BP nanoparticles can efficiently convert near infrared (NIR) light into heat, and exhibit excellent photostability, which makes them suitable as a novel nanotheranostic agent for photoacoustic (PA) imaging and photothermal therapy of cancer. The in-vitro results demonstrate the excellent biocompatibility of PEGylated BP nanoparticles, which can be used for photothermal ablation of cancer cells under irradiation with NIR light. The in-vivo PA images demonstrate that these BP nanoparticles can be efficiently accumulated in tumors through the enhanced permeability retention effect. The resultant BP nanoparticles can be further utilized for photothermal ablation of tumors by irradiation with NIR light. The tumor-bearing mice were completely recovered after photothermal treatment with BP nanoparticles, in comparison with mice from control groups. Our research highlights the great potential of PEGylated BP nanoparticles in detection and treatment of cancer.

  14. Preparation of Concanavalin A-Chelating Magnetic Nanoparticles for Selective Enrichment of Glycoproteins.

    Science.gov (United States)

    Dong, Liping; Feng, Shun; Li, Shanshan; Song, Peipei; Wang, Jide

    2015-07-07

    In this work, a soft and nondestructive approach was developed to prepare concanavalin A-chelating magnetic nanoparticles (Con A-MNPs) for selective enrichment of glycoproteins. Ethylenediamine tetraacetic acid-modified-MNPs (EDTA-MNPs) were prepared by a one-pot chemical coprecipitation method first, and then, Cu(II) cations were used as bridge groups to immobilize Con A on EDTA-MNPs. The as-prepared absorbents with a mean diameter of 15 nm showed a strong magnetic response to an externally applied magnetic field. The results of thermogravimetric analysis showed the content of immobilized Con A was up to 28 wt %. For glycoprotein ovalbumin, the maximum capacity and equilibrium constant were 72.41 mg/g and 0.6035 L/mg, respectively. The as-prepared nanocomposites exhibited a remarkable selectivity for glycoproteins and can enrich glycoproteins specifically from a mixture of glycoprotein and nonglycoprotein even at a molar ratio of 1:600. It was also successfully applied for the enrichment of glycoproteins from real egg white samples. We expect that our finding will serve as a helpful template for others to design new adsorbents for enriching glycoproteins.

  15. Preparation of CNC-dispersed Fe3O4 nanoparticles and their application in conductive paper.

    Science.gov (United States)

    Liu, Kai; Nasrallah, Joseph; Chen, Lihui; Huang, Liulian; Ni, Yonghao

    2015-08-01

    Well-dispersed Fe3O4 nanoparticles (NPs) were synthesized by a co-precipitation method in the presence of cellulose nano-crystals (CNC) as the template. The thus prepared Fe3O4 NPs were then used as a coating agent for the preparation of conductive paper. Fourier transform infrared spectroscopy (FTIR) results revealed that the Fe3O4 NPs were immobilized on the CNC through interactions between the hydroxyl groups of CNC and Fe3O4. Scanning transmission electron microscopy (STEM) images showed that the Fe3O4 NPs prepared in the presence of CNC can be dispersed in the CNC network, while the Fe3O4 NPs prepared in the absence of CNC tended to aggregate in aqueous solutions. The conductivity of the Fe3O4 NPs coated paper can reach to 0.0269 S/m at the coating amount of 14.75 g/m(2) Fe3O4/CNC nanocomposites. Therefore, the thus obtained coated paper can be potentially used as anti-static packaging material in the packaging field.

  16. A simple method to prepare titania nanomaterials of core-shell structure, hollow nanospheres and mesoporous nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    A simple method to prepare titania nanomaterials of core-shell structure, hollow nanospheres and mesoporous nanoparticles has been developed. The core-shell nanostructures with NH4Cl as core and TiO2·xH2O-NH4Cl as shell were prepared in nonaqueous system by the deposition on the surface of the aggregated NH4Cl crystals, which could be transformed into mesoporous anatase nanoparticles or hollow nanospheres by calcination at 500℃ or extraction with methanol, respectively. The hierarchical mesoporous nanostructures benefited the photocatalytic activities of the resultant titania nanomateri-als, demonstrated by the UV light photodegradation of Methyl Orange.

  17. Composite Materials with Magnetically Aligned Carbon Nanoparticles Having Enhanced Electrical Properties and Methods of Preparation

    Science.gov (United States)

    Hong, Haiping (Inventor); Peterson, G.P. (Bud) (Inventor); Salem, David R. (Inventor)

    2016-01-01

    Magnetically aligned carbon nanoparticle composites have enhanced electrical properties. The composites comprise carbon nanoparticles, a host material, magnetically sensitive nanoparticles and a surfactant. In addition to enhanced electrical properties, the composites can have enhanced mechanical and thermal properties.

  18. Amino acid mediated synthesis of silver nanoparticles and preparation of antimicrobial agar/silver nanoparticles composite films.

    Science.gov (United States)

    Shankar, Shiv; Rhim, Jong-Whan

    2015-10-05

    Silver nanoparticles (AgNPs) were synthesized using amino acids (tyrosine and tryptophan) as reducing and capping agents, and they were incorporated into the agar to prepare antimicrobial composite films. The AgNPs solutions exhibited characteristic absorption peak at 420 nm that showed a red shift to ∼434 nm after forming composite with agar. XRD data demonstrated the crystalline structure of AgNPs with dominant (111) facet. Apparent surface color and transmittance of agar films were greatly influenced by the AgNPs. The incorporation of AgNPs into agar did not exhibit any change in chemical structure, thermal stability, moisture content, and water vapor permeability. The water contact angle, tensile strength, and modulus decreased slightly, but elongation at break increased after AgNPs incorporation. The agar/AgNPs nanocomposite films possessed strong antibacterial activity against Listeria monocytogenes and Escherichia coli. The agar/AgNPs film could be applied to the active food packaging by controlling the food-borne pathogens.

  19. Preparation and Properties of Nanoparticles of Calcium Phosphates With Various Ca/P Ratios.

    Science.gov (United States)

    Sun, Limin; Chow, Laurence C; Frukhtbeyn, Stanislav A; Bonevich, John E

    2010-01-01

    This study aimed at preparing and studying the properties of nanoparticles of calcium phosphate (nCaP) with Ca/P ratios ranging from 1.0 to 1.67 using a spray-drying technique. Micro-structural analyses suggested that the nCaPs with Ca/P ratios of 1.67 to 1.33 were nano-sized amorphous calcium phosphate (ACP) containing varying amounts of acid phosphate and carbonate. The nCaP with Ca/P ratio of 1 contained only nano-sized low crystalline dicalcium phosphate (DCP). BET measurements of the nCaPs showed specific surface areas of (12 ± 2 to 50 ± 1) m(2)/g, corresponding to estimated equivalent spherical diameters of (38 to 172) nm. However, dynamic light scattering measurements revealed much larger particles of (380 ± 49 to 768 ± 111) nm, owing to agglomeration of the smaller primary nano particles as revealed by Scanning Electron Microscopy (SEM). Thermodynamic solubility measurements showed that the nCaPs with Ca/P ratio of 1.33 - 1.67 all have similar solubility behavior. The materials were more soluble than the crystalline hydroxyapatite (HA) at pH greater than about 4.7, and more soluble than β-tricalcium phosphate (β-TCP), octacalcium phosphate (OCP) and DCP at pH above 5.5. Their solubility approached that of α-tricalcium phosphate (α-TCP) at about pH 7. These nCaPs, which cannot be readily prepared by other currently available methods for nanoparticle preparation, have potential biomedical applications.

  20. Negatively charged silver nanoparticles with potent antibacterial activity and reduced toxicity for pharmaceutical preparations

    Directory of Open Access Journals (Sweden)

    Salvioni L

    2017-03-01

    Full Text Available Lucia Salvioni,1 Elisabetta Galbiati,1 Veronica Collico,1 Giulia Alessio,1 Svetlana Avvakumova,1 Fabio Corsi,2,3 Paolo Tortora,1 Davide Prosperi,1 Miriam Colombo1 1Nanobiolab, Department of Biotechnology and Bioscience, University of Milano-Bicocca, 2Biological and Clinical Science Department, University of Milan, Milano, 3Surgery Department, Breast Unit, IRCCS S Maugeri Foundation, Pavia, Italy Background: The discovery of new solutions with antibacterial activity as efficient and safe alternatives to common preservatives (such as parabens and to combat emerging infections and drug-resistant bacterial pathogens is highly expected in cosmetics and pharmaceutics. Colloidal silver nanoparticles (NPs are attracting interest as novel effective antimicrobial agents for the prevention of several infectious diseases.Methods: Water-soluble, negatively charged silver nanoparticles (AgNPs were synthesized by reduction with citric and tannic acid and characterized by transmission electron microscopy, dynamic light scattering, zeta potential, differential centrifuge sedimentation, and ultraviolet–visible spectroscopy. AgNPs were tested with model Gram-negative and Gram-positive bacteria in comparison to two different kinds of commercially available AgNPs.Results: In this work, AgNPs with higher antibacterial activity compared to the commercially available colloidal silver solutions were prepared and investigated. Bacteria were plated and the antibacterial activity was tested at the same concentration of silver ions in all samples. The AgNPs did not show any significant reduction in the antibacterial activity for an acceptable time period. In addition, AgNPs were transferred to organic phase and retained their antibacterial efficacy in both aqueous and nonaqueous media and exhibited no toxicity in eukaryotic cells.Conclusion: We developed AgNPs with a 20 nm diameter and negative zeta potential with powerful antibacterial activity and low toxicity compared

  1. Preparation and evaluation of SiO2-deposited stearic acid-g-chitosan nanoparticles for doxorubicin delivery

    Directory of Open Access Journals (Sweden)

    Yuan H

    2012-09-01

    Full Text Available Hong Yuan, Xin Bao, Yong-Zhong Du, Jian You, Fu-Qiang HuCollege of Pharmaceutical Sciences, Zhejiang University, Hangzhou, PR ChinaPurpose: Both polymer micelles and mesoporous silica nanoparticles have been widely researched as vectors for small molecular insoluble drugs. To combine the advantages of copolymers and silica, studies on the preparation of copolymer-silica composites and cellular evaluation were carried out.Methods: First, a stearic acid-g-chitosan (CS-SA copolymer was synthesized through a coupling reaction, and then silicone oxide (SiO2-deposited doxorubicin (DOX-loaded stearic acid-g-chitosan (CS-SA/SiO2/DOX nanoparticles were prepared through the sol-gel reaction. Physical and chemical properties such as particle size, zeta potential, and morphologies were examined, and small-angle X-ray scattering (SAXS analysis was employed to identify the mesoporous structures of the generated nanoparticles. Cellular uptake and cytotoxicity studies were also conducted.Results: CS-SA/SiO2/DOX nanoparticles with different amounts of SiO2 deposited were obtained, and SAXS studies showed that mesoporous structures existed in the CS-SA/SiO2/DOX nanoparticles. The mesoporous size of middle-ratio and high-ratio deposited CS-SA/SiO2/DOX nanoparticles were 4–5 nm and 8–10 nm, respectively. Based on transmission electron microscopy images of CS-SA/SiO2/DOX nanoparticles, dark rings around the nanoparticles could be observed in contrast with CS-SA/DOX micelles. Furthermore, CS-SA/SiO2/DOX nanoparticles exhibited faster release behavior in vitro than CS-SA/DOX micelles; cellular uptake research in A549 indicated that the CS-SA/SiO2/DOX nanoparticles were taken up by A549 cells more rapidly, and that CS-SA/SiO2/DOX nanoparticles entered the cell more easily when the amount of SiO2 was higher. IC50 values of CS-SA/DOX micelles, CS-SA/SiO2/DOX-4, CS-SA/SiO2/DOX-8, and CS-SA/SiO2/DOX-16 nanoparticles against A549 cells measured using the MTT assay were

  2. Preparation and characterization of magnetic Fe{sub 3}O{sub 4}–chitosan nanoparticles loaded with isoniazid

    Energy Technology Data Exchange (ETDEWEB)

    Qin, H.; Wang, C.M.; Dong, Q.Q. [School of Chemistry and Materials Science, Nanjing Normal University Nanjing, Jiangsu 210097 (China); Zhang, L.; Zhang, X. [Nanjing Chest Hospital, Jiangsu 210097 (China); Ma, Z.Y., E-mail: 07197@njnu.edu.cn [School of Chemistry and Materials Science, Nanjing Normal University Nanjing, Jiangsu 210097 (China); Han, Q.R. [School of Chemistry and Materials Science, Nanjing Normal University Nanjing, Jiangsu 210097 (China)

    2015-05-01

    A novel and simple method has been proposed to prepare magnetic Fe{sub 3}O{sub 4}–chitosan nanoparticles loaded with isoniazid (Fe{sub 3}O{sub 4}/CS/INH nanocomposites). Efforts have been made to develop isoniazid (INH) loaded chitosan (CS) nanoparticles by ionic gelation of chitosan with tripolyphosphate (TPP). The factors that influence the preparation of chitosan nanoparticles, including the TPP concentration, the chitosan/TPP weight ratio and the chitosan concentration on loading capacity and encapsulation efficiency of chitosan nanoparticles were studied. The magnetic Fe{sub 3}O{sub 4} nanoparticles were prepared by co-precipitation method of Fe{sup 2+} and Fe{sup 3+}. Then the magnetic Fe{sub 3}O{sub 4}/CS/INH nanocomposites were prepared by ionic gelation method. The magnetic Fe{sub 3}O{sub 4} nanoparticles and magnetic Fe{sub 3}O{sub 4}/CS/INH nanocomposites were characterized by XRD, TEM, FTIR and SQUID magnetometry. The in vitro release of Fe{sub 3}O{sub 4}/CS/INH nanocomposites showed an initial burst release in the first 10 h, followed by a more gradual and sustained release for 48 h. It is suggested that the magnetic Fe{sub 3}O{sub 4}/CS/INH nanocomposites may be exploited as potential drug carriers for controlled-release applications in magnetic targeted drugs delivery system. - Highlights: • A novel and simple method for preparation of nanocomposites for biomedicine. • All the materials are non-toxic and biocompatibility. • This paper gives systematic study of the nanocomposites in biomedicine.

  3. Studies on Preparation of Photosensitizer Loaded Magnetic Silica Nanoparticles and Their Anti-Tumor Effects for Targeting Photodynamic Therapy

    Directory of Open Access Journals (Sweden)

    Chen Zhi-Long

    2009-01-01

    Full Text Available Abstract As a fast developing alternative of traditional therapeutics, photodynamic therapy (PDT is an effective, noninvasive, nontoxic therapeutics for cancer, senile macular degeneration, and so on. But the efficacy of PDT was compromised by insufficient selectivity and low solubility. In this study, novel multifunctional silica-based magnetic nanoparticles (SMNPs were strategically designed and prepared as targeting drug delivery system to achieve higher specificity and better solubility. 2,7,12,18-Tetramethyl-3,8-di-(1-propoxyethyl-13,17-bis-(3-hydroxypropyl porphyrin, shorted as PHPP, was used as photosensitizer, which was first synthesized by our lab with good PDT effects. Magnetite nanoparticles (Fe3O4 and PHPP were incorporated into silica nanoparticles by microemulsion and sol–gel methods. The prepared nanoparticles were characterized by transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy and fluorescence spectroscopy. The nanoparticles were approximately spherical with 20–30 nm diameter. Intense fluorescence of PHPP was monitored in the cytoplasm of SW480 cells. The nanoparticles possessed good biocompatibility and could generate singlet oxygen to cause remarkable photodynamic anti-tumor effects. These suggested that PHPP-SMNPs had great potential as effective drug delivery system in targeting photodynamic therapy, diagnostic magnetic resonance imaging and magnetic hyperthermia therapy.

  4. Facile preparation of TiO2-polyvinyl alcohol hybrid nanoparticles with improved visible light photocatalytic activity

    Science.gov (United States)

    Filippo, Emanuela; Carlucci, Claudia; Capodilupo, Agostina Lina; Perulli, Patrizia; Conciauro, Francesca; Corrente, Giuseppina Anna; Gigli, Giuseppe; Ciccarella, Giuseppe

    2015-03-01

    Hybrid inorganic/organic core/shell nanoparticles were prepared through a two step synthesis procedure. In the first step, pure anatase TiO2 nanoparticles were synthesized though a rapid microwave assisted non-aqueous route. Then, the obtained titania nanoparticles were coated with polyvinyl alcohol (PVA) using a simple solution method followed by relatively low temperature treatment. The PVA-coated titania nanoparticles samples were prepared at different TiO2-PVA weight ratio and they were characterized using X-Ray diffraction, transmission electron microscopy, infrared spectroscopy and Brunauer-Emmett-Teller (BET) analysis. Photocatalytic performance was also evaluated for all samples and the results indicated that TiO2:PVA weight ratio was a key factor to obtain an improvement of the photocatalytic activity with respect to bare TiO2 nanoparticles, since PVA concentration influenced the surface area and the aggregation of nanoparticles and the thickness of the coating layer. This inexpensive system provides a simple, quick and effective approach which allows to obtain core/shell hybrid nanostructures.

  5. Biomimetic Production of Hydrogen

    Science.gov (United States)

    Gust, Devens

    2004-03-01

    The basic reaction for hydrogen generation is formation of molecular hydrogen from two electrons and two protons. Although there are many possible sources for the protons and electrons, and a variety of mechanisms for providing the requisite energy for hydrogen synthesis, the most abundant and readily available source of protons and electrons is water, and the most attractive source of energy for powering the process is sunlight. Not surprisingly, living systems have evolved to take advantage of these sources for materials and energy. Thus, biology provides paradigms for carrying out the reactions necessary for hydrogen production. Photosynthesis in green plants uses sunlight as the source of energy for the oxidation of water to give molecular oxygen, protons, and reduction potential. Some photosynthetic organisms are capable of using this reduction potential, in the form of the reduced redox protein ferredoxin, to reduce protons and produce molecular hydrogen via the action of an hydrogenase enzyme. A variety of other organisms metabolize the reduced carbon compounds that are ultimately the major products of photosynthesis to produce molecular hydrogen. These facts suggest that it might be possible to use light energy to make molecular hydrogen via biomimetic constructs that employ principles similar to those used by natural organisms, or perhaps with hybrid "bionic" systems that combine biomimetic materials with natural enzymes. It is now possible to construct artificial photosynthetic systems that mimic some of the major steps in the natural process.(1) Artificial antennas based on porphyrins, carotenoids and other chromophores absorb light at various wavelengths in the solar spectrum and transfer the harvested excitation energy to artificial photosynthetic reaction centers.(2) In these centers, photoinduced electron transfer uses the energy from light to move an electron from a donor to an acceptor moiety, generating a high-energy charge-separated state

  6. Research progress and preparation methods of biomimetic functional superhydrophobic wood surfaces%木材仿生超疏水功能化制备方法

    Institute of Scientific and Technical Information of China (English)

    刘峰; 王成毓

    2016-01-01

    The superhydrophobic surfaces with the water contact angle greater than 150° and the contact angle hysteresis less than 10° have aroused a considerable interest in the scientific and industrial community due to their great importance in the fundamental research and the potential industrial applications.Generally speaking,the superhydrophobic surfaces can be fabricated by creating a rough structure on a hydrophobic material surface or modifying a rough surface with a special low surface energy material.This paper reviews the preparation methods based on superhydrophobic wood sciences,as well as the applications of the sol-gel processing,the hydrothermal synthesis processing,the wet chemical method,the surface coating technology and the solution-immersion process,and some suggestions about how the field is likely to advance in future are made.Some problems in the present stage,and the development in the future are discussed.%超疏水表面是一类与水的接触角大干150°且接触角滞后小于10°的固体表面,其在基础研究和工业应用方面具有重大的研究和实用价值.通常情况下,超疏水表面可通过在疏水材料表面构建一定尺寸的粗糙结构或利用低表面能的物质对粗糙表面进行修饰而获得.本文综述木材超疏水表面的制备方法,主要概括了溶胶-凝胶法、水热合成法、湿化学方法、表面涂覆和溶液浸泡法等的应用情况,讨论了超疏水木质基表面研发中存在的问题,探讨了该研究领域的发展趋势.