WorldWideScience

Sample records for determining radioactive substances

  1. Analysis of determination modalities concerning the exposure and emission limits values of chemical and radioactive substances; Analyse des modalites de fixation des valeurs limites d'exposition et d'emission pour les substances chimiques et radioactives

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, C.; Schneider, T

    2002-08-01

    This document presents the generic approach adopted by various organizations for the determination of the public exposure limits values to chemical and radioactive substances and for the determination of limits values of chemical products emissions by some installations. (A.L.B.)

  2. Transport of radioactive substances; Der Transport radioaktiver Stoffe

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2014-12-15

    The report on the transport of radioactive substances covers the following topics: facts on radioactive materials transport, safety of the transport of radioactive substances, legal regulations and guidelines: a multiform but consistent system, transport of nuclear fuels, safety during the transport of nuclear fuel, future transport of spent fuel elements and high-level radioactive wastes in Germany.

  3. Measurement and analysis of radioactive substances; Mesure et analyse de substances radioactives

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-07-01

    Here are gathered the abstracts presented to the 3. summer university of the year 2001 whose main themes were the destructive (5 conferences) and nondestructive (8 conferences) analyses applied to nuclear industry. The points of view of different organisms (as DSIN: Directorate for the Safety of Nuclear Installations, IPSN: Institute of Nuclear Protection and Safety, OPRI: Office of Protection against Ionizing Radiations, TUI: Institute for Transuranium Elements, COGEMA, EDF: Electric Utilities, ANDRA: French National Agency for Radioactive Waste Management, CRLC Val d'Aurelle, France) concerning the needs involved in nuclear facilities control, the methods of radionuclide speciation in use internationally, the measurements and analyses of radioactive substances are given too as well as some general concepts concerning 1)the laser-matter interaction 2)the ions production 3)the quality applied to the measurements and analyses 4)the standard in activity metrology. (O.M.)

  4. Process for the Production of Radioactive Substances

    Science.gov (United States)

    Fermi, Enrico; Amaldi, Edoardo; Pontecorvo, Bruno; Rasetti, Franco; Segré, Emilio

    In this Patent, a very detailed description of the experimental results, obtained by studying the radioactivity induced in a number of chemical elements by irradiation with slow neutrons, is reported, along with a corresponding theoretical interpretation. It is here emphasized, in order to achieve better efficiencies, the use of neutrons instead of charged particles, as considered in previous works on nuclear reactions. Moreover, since neutrons produced by bombardment of atomic nuclei with artificially accelerated particles have high average energies, a method for slowing down fast neutrons is described, by passing the neutrons through a screen of hydrogenous materials, like water or paraffin. The reduction of the energy of the neutrons is interpreted as due to their collisions against the nuclei or the entire atoms of energy reducing materials. An interpretation is provided for the experimental observations: in the case of a strong induced radio-activity following the absorption of the slow neutrons, the formation of an unstable isotope is assumed, while the formation of a stable nucleus is assumed in case no activation or, at least, no strong activation follows an anomalously large absorption. Particularly interesting is the mention of the possible discovery of "transuranic" elements given in the present Patent. Even here, some caution was adopted about its interpretation, as well as the theoretical interpretation of the effects induced by slow neutrons considered in the paper: "The theoretical statements and explanations are, of course, not conclusive and our invention is in no way dependent upon their correctness. We have found them helpful and give them for the aid of others, but our invention will be equally useful if it should prove that our theoretical conclusions are not altogether correct."1 The original Patent application, Metodo per accrescere il rendimento dei procedimenti per la produzione di radioattività artificiali mediante il bombardamento con

  5. [Determination of radioactivity by smartphones].

    Science.gov (United States)

    Hartmann, H; Freudenberg, R; Andreeff, M; Kotzerke, J

    2013-01-01

    The interest in the detection of radioactive materials has strongly increased after the accident in the nuclear power plant Fukushima and has led to a bottleneck of suitable measuring instruments. Smartphones equipped with a commercially available software tool could be used for dose rate measurements following a calibration according to the specific camera module. We examined whether such measurements provide reliable data for typical activities and radionuclides in nuclear medicine. For the nuclides 99mTc (10 - 1000 MBq), 131I (3.7 - 1800 MBq, therapy capsule) and 68Ga (50 - 600 MBq) radioactivity with defined geometry in different distances was measured. The smartphones Milestone Droid 1 (Motorola) and HTC Desire (HTC Corporation) were compared with the standard instruments AD6 (automess) and DoseGUARD (AEA Technology). Measurements with the smartphones and the other devices show a good agreement: linear signal increase with rising activity and dose rate. The long time measurement (131I, 729 MBq, 0.5 m, 60 min) demonstrates a considerably higher variation (by 20%) of the measured smartphone data values compared with the AD6. For low dose rates (rates resulting from typical nuclear medicine procedures can be measured reliably (e. g., dismissal dose after radioiodine therapy). The signal shows a high correlation to measured values of conventional dose measurement devices.

  6. Dynamic uptake of radioactive substance in rat salivary gland following /sup 3/H-melatonin administration

    Energy Technology Data Exchange (ETDEWEB)

    Withyachumnarnkul, B.; Wongprapairot, P.; Trakulrungsi, W.

    1987-01-01

    Dynamics of radioactive accumulation in rat greater salivary gland following systemic administration of /sup 3/H-melatonin was studied to determine a possible action of the hormone in the gland. Progressive decline of /sup 3/H-melatonin concentrations was found in the serum, lung, skeletal muscle, liver, kidney, and salivary gland during 60 min following the administration. On the contrary, there was a progressive accumulation of radioactive substance other than /sup 3/H-melatonin in the salivary gland but not in other tissues mentioned. The radioactivity was also progressively and preferentially localized in the nuclear fraction of the gland cells. These results suggest a possible direct action of melatonin derivative in rat salivary gland.

  7. [The main directions of improving the system of state accounting and control of radioactive substances and radioactive waste products].

    Science.gov (United States)

    2012-01-01

    This paper describes a modification of the basic directions of state accounting and control of radioactive substances and radioactive waste products, whose implementation will significantly improve the efficiency of its operation at the regional level. Selected areas are designed to improve accounting and control system for the submission of the enterprises established by the reporting forms, the quality of the information contained in them, as well as structures of information and process for collecting, analyzing and data processing concerning radioactive substances and waste products.

  8. Radioactive substances in foodstuffs and drinking water in Finland

    Energy Technology Data Exchange (ETDEWEB)

    Vaaramaa, K.; Vesterbacka, P.; Solatie, D. [STUK - Radiation and Nuclear Safety Authority (Finland)

    2014-07-01

    The concentrations of radioactive substances in the environment and foodstuffs are continuously monitored in Finland. Radiation and Nuclear Safety Authority (STUK) publishes the annual report of Surveillance of Environmental Radiation which shows the activity levels of artificial radionuclides in Finland. Based on the results the radiation dose to Finnish people is estimated. Natural radioactive elements will be included in the surveillance program in future years. The aim of the foodstuffs monitoring program is to obtain information from the intake of radionuclides through ingestion. The radioactivity in foodstuffs is monitored by collecting foodstuffs on market, drinking water and daily meals offered at hospitals over one week. The sampling sites are located in southern, central and northern Finland, representing the main population centres and areal differences in the consumption of foodstuffs. One of these sampling sites is located in the highest {sup 137}Cs deposition area in Finland originating from the Chernobyl accident. The foodstuff samples on market are, for example, wild game, wild berries, wild mushrooms and fish. {sup 137}Cs and {sup 90}Sr are analysed from mixed diet samples and {sup 137}Cs from foodstuffs samples on market. The concentrations of {sup 137}Cs and {sup 90}Sr in daily meals are low because the agricultural products used as raw material are almost free of artificial radionuclides. The small variation in the results is caused by the differences in the types of meals that were prepared on the sampling dates and in the areal origins of raw materials. {sup 137}Cs concentration is remarkably higher in such food which contains a lot of natural products like wild berries, freshwater fish, wild mushrooms and game. As an example, the concentrations of {sup 137}Cs in the solid food in 2012 ranged from 0.06 - 1.0 Bq/kg, and in the drinks from 0.27 - 0.40 Bq/l, respectively. The radiation dose to Finnish people is estimated based on an analysis of

  9. Methodological guide: management of industrial sites potentially contaminated by radioactive substances; Guide methodologique: gestion des sites industriels potentiellement contamines par des substances radioactives

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-07-01

    At the request of the Ministries of Health and the Environment, IPSN is preparing and publishing the first version of the methodological guide devoted to managing industrial sites potentially contaminated by radioactive substances. This guide describes a procedure for defining and choosing strategies for rehabilitating such industrial sites. (author)

  10. Guideline for the assessment of radioactive substances in drinking water in the frame of the implementation of the drinking water regulation. Recommendation by BMUB, BfS, UBA and the responsible state authorities and DVGW and BDFW; Leitfaden zur Untersuchung und Bewertung von radioaktiven Stoffen im Trinkwasser bei der Umsetzung der Trinkwasserverordnung. Empfehlung von BMUB, BMG, BfS, UBA und den zustaendigen Landesbehoerden sowie DVGW und BDEW

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2017-01-15

    The guidelines on the assessment of radioactive substances in drinking water cover the following issues: terms, symbols and units concerning radioactivity, radioactivity in the drinking water and radiation exposure, requirements for drinking water with respect to radioactive substances, fundamentals of the assessment concept according to the drinking water regulation, practical application of the assessment concept, analytical determination of radioactivity related parameters.

  11. Hazardous and radioactive substances in Danish marine waters. Status and temporal trends

    Energy Technology Data Exchange (ETDEWEB)

    Dahlloef, I.; Andersen, Jesper H.

    2009-07-15

    This book fulfils the Danish reporting obligations in relation to the OSPAR Trend Assessment on Dangerous Substances, and describes the degree of contamination from hazardous and radioactive substances and their temporal trends, as well as the effects of some of these hazardous substances, in the Danish marine environment. The assessment is based on existing information, primarily data collected via national and regional Danish monitoring activities until 2004. (author)

  12. A kinematic model to estimate effective dose of radioactive substances in a human body

    Science.gov (United States)

    Sasaki, S.; Yamada, T.

    2013-05-01

    The great earthquake occurred in the north-east area in Japan in March 11, 2011. Facility system to control Fukushima Daiichi nuclear power station was completely destroyed by the following giant tsunami. From the damaged reactor containment vessels, an amount of radioactive substances had leaked and diffused in the vicinity of this station. Radiological internal exposure became a serious social issue both in Japan and all over the world. The present study provides an easily understandable, kinematic-based model to estimate the effective dose of radioactive substances in a human body by simplifying the complicated mechanism of metabolism. International Commission on Radiological Protection (ICRP) has developed a sophisticated model, which is well-known as a standard method to calculate the effective dose for radiological protection. However, owing to that ICRP method is fine, it is rather difficult for non-professional people of radiology to gasp the whole images of the movement and the influences of radioactive substances in a human body. Therefore, in the present paper we propose a newly-derived and easily-understandable model to estimate the effective dose. The present method is very similar with the traditional and conventional tank model in hydrology. Ingestion flux of radioactive substances corresponds to rain intensity and the storage of radioactive substances to the water storage in a basin in runoff analysis. The key of the present method is to estimate the energy radiated in the radioactive nuclear disintegration of an atom by using classical theory of β decay and special relativity for various kinds of radioactive atoms. The parameters used in this model are only physical half-time and biological half-time, and there are no operational parameters or coefficients to adjust our theoretical runoff to ICRP. Figure shows the time-varying effective dose with ingestion duration, and we can confirm the validity of our model. The time-varying effective dose with

  13. Releases of radioactive substances from Swedish nuclear power plants (RAKU)

    Energy Technology Data Exchange (ETDEWEB)

    Ingemansson, T.; Bergstroem, C. [ALARA Engineering AB, Skultuna (Sweden)

    1997-04-01

    Releases of radioactivity to air and water from Swedish nuclear power plants have been studied and compared with those from foreign reactors. Averaged over the years from commissioning of the reactors to the last year data are available, the release of radioactive noble gas from the Swedish BWRs has been about the same as from comparable foreign reactors. The oldest Swedish BWRs, Oskarshamn 1 and 2 (O1 and O2) and Ringhals 1 (R1), have simple off-gas systems with only one delay volume. All BWRs in US, Germany, Japan and Switzerland are equipped with more sophisticated off-gas systems. It can be expected that O1, O2 and R1 therefore will have the highest release of noble gas activity at an international comparison if they do not modernize their off-gas system. BWRs in US, Germany and Japan are today equipped with recombiners and with one exception also charcoal columns. Japanese BWRs report zero releases to air. Releases of radioactivity to water after commissioning was about the same for most of the studied reactors. Some of the newest German plants have had low annual releases already at commissioning. Improvements of the treatment systems at old German, Swiss and US reactors have significantly lowered the releases. For most of the Swedish plants the annual releases to water have remained at the initial level. Forsmark 3 has succeeded in decreasing the release of radionuclides to water by a factor of almost one hundred compared to other Swedish reactors. Also O3 has managed to decrease the liquid effluents. Japanese plants have zero release of radioactivity excluding tritium to water. The release of tritium is about the same for all reactors of the same type in the world. 35 refs, 31 figs, 24 tabs.

  14. 29 CFR 570.57 - Exposure to radioactive substances and to ionizing radiations (Order 6).

    Science.gov (United States)

    2010-07-01

    ... 29 Labor 3 2010-07-01 2010-07-01 false Exposure to radioactive substances and to ionizing radiations (Order 6). 570.57 Section 570.57 Labor Regulations Relating to Labor (Continued) WAGE AND HOUR... walls of solid material and extending from floor to ceiling; (3) The term ionizing radiations shall mean...

  15. Management of sites potentially polluted by radioactive substances - Methodological guidebook; Gestion des sites potentiellement pollues par des substances radioactives - Guide methodologique

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2011-12-15

    This document is the update of the 'methodological guidelines for the management of industrial areas potentially contaminated by radioactive substances', published in 2001 by IRSN. Revisions intended to bring coherence between management of areas polluted by radioactive substances and the general policy applied to polluted sites described in a document published in Feb. 2007 by the French Ministry in charge of Environment. Requirements introduced both by the law relative to waste management of June 28, 2006 and the ministerial order of 17 November 2008 were introduced. The involvement of all stakeholders during the process was stressed. The updating mainly lead to introduce a clear distinction between polluted areas where uses are established and those without use or at redevelopment stage. When the uses are established, an 'Interpretation of the condition of environment' is conducted. Alternatively, the remediation process follows a 'management plan'. The revision also led to the disappearance of the 'doubt removal' phase which has been incorporated as an entire part in the site characterisation. Among other significant changes, it may be noted the evolution of the 'risk assessment' tools from simplified risk assessment and detailed risk assessment to a single tool allowing the quantitative assessment of exposure (EQER). Finally, the guidelines highlight stakeholder involvement in identifying the different participants and in reminding the benefits of a consultative approach. Whatever the remediation process: interpretation of the condition of environment or management plan; site characterisation is required as soon as a pollution is suspected. It includes literature reviews and field investigations primarily to confirm or deny the presence of pollution and, where appropriate, to determine its location, nature and level. The effort accorded to site characterisation must be proportionate to identified issues. The

  16. Determination of lead and radioactivity in cosmetics products: Hazard assessment

    OpenAIRE

    Medhat Moustafa E.; Singh Vishwanath P.; Shirmardi Seyed P.

    2015-01-01

    In the proposed work, an investigation on hazard assessment by lead element and natural radioactivity in cosmetic samples collected from various countries is presented. These samples were face powder, eyebrow paint and henna. The lead element in cosmetic samples was determined using particle-induced X-ray emission. Maximum natural radioactivity concentrations of 226Ra and 40K were found in khol and make-up cosmetic samples, respectively. The qualitative ana...

  17. Models for environmental impact assessments of releases of radioactive substances from CERN facilities

    CERN Document Server

    Vojtyla, P

    2005-01-01

    The document describes generic models for environmental impact assessments of releases of radioactive substances from CERN facilities. Except for few models developed in the Safety Commission, the models are based on the 1997 Swiss directive HSK-R-41 and on the 2001 IAEA Safety Report No. 19. The writing style is descriptive, facilitating the practical implementation of the models at CERN. There are four scenarios assumed for airborne releases: (1) short-term releases for release limit calculations, (2) actual short-term releases, (3) short-term releases during incidents/accidents, and (4) chronic long-term releases during the normal operation of a facility. For water releases, two scenarios are considered: (1) a release into a river, and (2) a release into a water treatment plant. The document shall be understood as a reference for specific environmental studies involving radioactive releases and as a recommendation of the Safety Commission.

  18. Determination of lead and radioactivity in cosmetics products: Hazard assessment

    Directory of Open Access Journals (Sweden)

    Medhat Moustafa E.

    2015-01-01

    Full Text Available In the proposed work, an investigation on hazard assessment by lead element and natural radioactivity in cosmetic samples collected from various countries is presented. These samples were face powder, eyebrow paint and henna. The lead element in cosmetic samples was determined using particle-induced X-ray emission. Maximum natural radioactivity concentrations of 226Ra and 40K were found in khol and make-up cosmetic samples, respectively. The qualitative analysis of cosmetic samples showed that lead is the most toxic element found in eyebrow paint samples.

  19. [Medical and hygienic aspects of instrumental supervision system over nuclear materials and radioactive substances transport on Russian Federation territory].

    Science.gov (United States)

    Grabskiĭ, Iu V; Gavrish, N N; Shevchenko, G T; Viaz'min, S O; Pertsev, V S; Kirillov, V F; Tsov'ianov, A G

    2014-01-01

    Hygienic evaluation of radiation situation in operation of mobile and stationery elements within a project of national system for instrumental supervision over nuclear materials and radioactive substances transport, created with a Global initiative against nuclear terrorism. Levels of exposure to ionizing radiation of the screening complexes appeared to match requirements on radiation safety for service personnel and general population.

  20. 10 CFR 20.1203 - Determination of external dose from airborne radioactive material.

    Science.gov (United States)

    2010-01-01

    ... material. Licensees shall, when determining the dose from airborne radioactive material, include the... equivalent when the airborne radioactive material includes radionuclides other than noble gases or if the cloud of airborne radioactive material is not relatively uniform. The determination of the...

  1. Development of an ASIC for Si/CdTe detectors in a radioactive substance visualizing system

    Science.gov (United States)

    Harayama, Atsushi; Takeda, Shin`ichiro; Sato, Goro; Ikeda, Hirokazu; Watanabe, Shin; Takahashi, Tadayuki

    2014-11-01

    We report on the recent development of a 64-channel analog front-end ASIC for a new gamma-ray imaging system designed to visualize radioactive substances. The imaging system employs a novel Compton camera which consists of silicon (Si) and cadmium telluride (CdTe) detectors. The ASIC is intended for the readout of pixel/pad detectors utilizing Si/CdTe as detector materials, and covers a dynamic range up to 1.4 MeV. The readout chip consists of 64 identical signal channels and was implemented with X-FAB 0.35 μm CMOS technology. Each channel contains a charge-sensitive amplifier, a pole-zero cancellation circuit, a low-pass filter, a comparator, and a sample-hold circuit, along with a Wilkinson-type A-to-D converter. We observed an equivalent noise charge of 500 e- and a noise slope of 5 e-/pF (r.m.s.) with a power consumption of 2.1 mW per channel. The chip works well when connected to Schottky CdTe diodes, and delivers spectra with good energy resolution, such as 12 keV (FWHM) at 662 keV and 24 keV (FWHM) at 1.33 MeV.

  2. Development of an ASIC for Si/CdTe detectors in a radioactive substance visualizing system

    Energy Technology Data Exchange (ETDEWEB)

    Harayama, Atsushi, E-mail: harayama@astro.isas.jaxa.jp [Institute of Space and Astronautical Science, Japan Aerospace Exploration Agency, Sagamihara, Kanagawa 229-8510 (Japan); Takeda, Shin' ichiro [Institute of Space and Astronautical Science, Japan Aerospace Exploration Agency, Sagamihara, Kanagawa 229-8510 (Japan); Sato, Goro [RIKEN Nishina Center, 2-1 Hirosawa, Wako, Saitama 351-0198 (Japan); Institute of Space and Astronautical Science, Japan Aerospace Exploration Agency, Sagamihara, Kanagawa 229-8510 (Japan); Ikeda, Hirokazu; Watanabe, Shin; Takahashi, Tadayuki [Institute of Space and Astronautical Science, Japan Aerospace Exploration Agency, Sagamihara, Kanagawa 229-8510 (Japan)

    2014-11-21

    We report on the recent development of a 64-channel analog front-end ASIC for a new gamma-ray imaging system designed to visualize radioactive substances. The imaging system employs a novel Compton camera which consists of silicon (Si) and cadmium telluride (CdTe) detectors. The ASIC is intended for the readout of pixel/pad detectors utilizing Si/CdTe as detector materials, and covers a dynamic range up to 1.4 MeV. The readout chip consists of 64 identical signal channels and was implemented with X-FAB 0.35μm CMOS technology. Each channel contains a charge-sensitive amplifier, a pole-zero cancellation circuit, a low-pass filter, a comparator, and a sample-hold circuit, along with a Wilkinson-type A-to-D converter. We observed an equivalent noise charge of ∼500 e{sup −} and a noise slope of ∼5 e{sup −}/pF (r.m.s.) with a power consumption of 2.1 mW per channel. The chip works well when connected to Schottky CdTe diodes, and delivers spectra with good energy resolution, such as ∼12 keV (FWHM) at 662 keV and ∼24 keV (FWHM) at 1.33 MeV.

  3. Smuggling of radioactive substances. Swedish capacity to detect and analyze; Smuggling av radioaktivt material. Sveriges foermaaga till detektion och analys

    Energy Technology Data Exchange (ETDEWEB)

    Ringbom, A.; Spjuth, L. [Swedish Defence Research Agency (FOI), Stockholm (Sweden)

    2001-04-01

    This report is the result of a survey of the existing Swedish national capability to detect an attempt to smuggle nuclear material or other radioactive substances. The capacity to perform a more thorough analysis of a seized sample has also been investigated. The study shows that Sweden today has a small capacity to disclose a smuggling attempt of such materials. The limited detection capacity that exists is not sensitive enough for this purpose, and is not used in an optimal way. Furthermore, relevant education of the custom officers is needed. Today, a national capability for an initial analysis of seized material exists, but action plans describing the handling of the material should be resolved. The high number of seizures of radioactive material in countries having a better detection capability indicates that illicit trafficking of radioactive materials is still a problem. In Sweden, we so far do not have many reported incidents of illicit trafficking - partly due to our limited capacity to detect radioactive material - however, we do not know how many incidents that really have occurred. Fixed installations for detection at the border controls are the most efficient way to improve our capacity for detecting nuclear material. An initial pilot study is suggested to be able to estimate the need. Increased education of the custom officers, establishment of formal routines for handling and analysis of seized materials, and to formalise the contacts with international analysis laboratories are also identified as important factors to be improved.

  4. Determining radioactive aerosol concentrations using a surface radioactive contamination measurement device.

    Science.gov (United States)

    Cerny, R; Johnova, K; Kozlovska, M; Otahal, P; Vosahlikova, I

    2015-06-01

    For experiments with dispersed radioactive aerosols in a radon-aerosol chamber (RAC), it is desirable to know the activity of the radioactive aerosols applied in the RAC. A COLIBRI TTC survey metre with an SABG-15+ probe (Canberra, USA) was purchased for this purpose. The probe is designed for surface contamination measurements, and it is intended to measure the activity of aerosols deposited on the filters during experiments in the RAC. Since the probe is calibrated in a different geometry, its response in the authors' experimental geometry was simulated by a Monte Carlo method. The authors present a Monte Carlo model using MCNPX and an experimental verification of this probe model.

  5. Sensitive determination of specific radioactivity of positron emission tomography radiopharmaceuticals by radio high-performance liquid chromatography with fluorescence detection

    Energy Technology Data Exchange (ETDEWEB)

    Nakao, Ryuji [Molecular Imaging Center, National Institute of Radiological Sciences, Chiba 263-8555 (Japan)], E-mail: nakaor@nirs.go.jp; Furutsuka, Kenji [Molecular Imaging Center, National Institute of Radiological Sciences, Chiba 263-8555 (Japan); Sumitomo Accelerator Service, Tokyo 141-8686 (Japan); Yamaguchi, Masatoshi [Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka 814-0180 (Japan); Suzuki, Kazutoshi [Molecular Imaging Center, National Institute of Radiological Sciences, Chiba 263-8555 (Japan)

    2008-10-15

    A sensitive quality control method is often required in positron emission tomography (PET) radiopharmaceutical analysis due to the high specific radioactivity of synthetic products. The applicability of a radio high-performance liquid chromatography (HPLC) method with fluorescence detection was evaluated for a wide variety of PET radiopharmaceuticals. In 29 different radiopharmaceuticals studied, 20 compounds exhibited native fluorescence. These properties enabled sensitive determination of their chemical masses by direct fluorimetric detection after separation by HPLC. For some substances, detection limits were below nanograms per milliliter level, at least 40 times better than current UV absorbance detection. Sufficient reproducibility and linearity were obtained for the analysis of pharmaceutical fluid. Post-column fluorimetric derivatization was also established for the quantitative determination of FDG and ClDG in [{sup 18}F]FDG samples. These methods could be applied successfully to the analysis of PET radiopharmaceuticals with ultra-high specific radioactivity.

  6. Toxic Substances Control Act (TSCA) Polychlorinated Biphenyl (PCB)/Radioactive Waste Annual Inventory for Calendar Year 2013

    Energy Technology Data Exchange (ETDEWEB)

    no author on report

    2014-06-01

    The Toxic Substances Control Act, 40 CFR 761.65(a)(1) provides an exemption from the one year storage time limit for PCB/radioactive waste. PCB/radioactive waste may exceed the one year time limit provided that the provisions at 40 CFR 761.65(a)(2)(ii) and 40 CFR 761.65(a)(2)(iii) are followed. These two subsections require, (ii) "A written record documenting all continuing attempts to secure disposal is maintained until the waste is disposed of" and (iii) "The written record required by subsection (ii) of this section is available for inspection or submission if requested by EPA." EPA Region 10 has requested the Department of Energy (DOE) to submit an inventory of radioactive-contaminated PCB waste in storage at the Idaho National Laboratory (INL) for the previous calendar year. The annual inventory is separated into two parts, INL without Advanced Mixed Waste Treatment Project (AMWTP) (this includes Battelle Energy Alliance, LLC, CH2M-WG Idaho, LLC, and the Naval Reactors Facility), and AMWTP.

  7. Toxic Substances Control Act (TSCA) Polychlorinated Biphenyl (PCB)/Radioactive Waste Annual Inventory for Calendar Year 2014

    Energy Technology Data Exchange (ETDEWEB)

    Layton, Deborah L. [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2015-06-01

    The Toxic Substances Control Act, 40 CFR 761.65(a)(1) provides an exemption from the one year storage time limit for PCB/radioactive waste. PCB/radioactive waste may exceed the one year time limit provided that the provisions at 40 CFR 761.65(a)(2)(ii) and 40 CFR 761.65(a)(2)(iii) are followed. These two subsections require, (ii) "A written record documenting all continuing attempts to secure disposal is maintained until the waste is disposed of" and (iii) "The written record required by subsection (ii) of this section is available for inspection or submission if requested by EPA." EPA Region 10 has requested the Department of Energy (DOE) to submit an inventory of radioactive-contaminated PCB waste in storage at the Idaho National Laboratory (INL) for the previous calendar year. The annual inventory is separated into two parts, INL without Advanced Mixed Waste Treatment Project (AMWTP) (this includes Battelle Energy Alliance, LLC, CH2M-WG Idaho, LLC, and the Naval Reactors Facility), and AMWTP.

  8. Radioactivity

    Energy Technology Data Exchange (ETDEWEB)

    Baratta, E.J. [Winchester Engineering and Analytical Center, Winchester, MA (United States)

    1997-01-01

    Cesium-134 and -137 in Foods, Gamma-Ray Spectrophotometric Methods. The method entitled {open_quotes}Cs-134 and Cs-137 in Foods, Gamma-Ray Spectrophotometric Method{close_quotes} has been adopted official first action, with minor revisions. Iodine 131: The method {open_quotes}Iodine-131 in Milk, Radiochemical Separation Method{close_quotes} has been accepted by the Committee on Residues and Related Topics and has been recommended to the Methods Committee for adoption first action. Search is continuing for a new Associated Referee. Plutonium-239: The Associate Referee is doing a literature search for a method for the determination of plutonium in foods. When one is selected, she will prepared a protocol for a collaborative study and submit it for approval. Radium-228: Search is ongoing for a new Associate Referee. When one is appointed, a method should be selected and tested. Strontium-89 and -90: The Associate Referee is investigating methods using resin discs and/or resin columns for these radionuclides. These methods are now being used in analyses for strontium-89 and -90 in water. She will now attempt to apply it to milk. If successful, she will prepare a protocol for a collaborative study and submit it for approval. Tritium: Search is continuing for a new Associate Referee for this topic.

  9. Illustrative assessment of human health issues arising from the potential release of chemotoxic substances from a generic geological disposal facility for radioactive waste.

    Science.gov (United States)

    Wilson, James C; Thorne, Michael C; Towler, George; Norris, Simon

    2011-12-01

    Many countries have a programme for developing an underground geological disposal facility for radioactive waste. A case study is provided herein on the illustrative assessment of human health issues arising from the potential release of chemotoxic and radioactive substances from a generic geological disposal facility (GDF) for radioactive waste. The illustrative assessment uses a source-pathway-receptor methodology and considers a number of human exposure pathways. Estimated exposures are compared with authoritative toxicological assessment criteria. The possibility of additive and synergistic effects resulting from exposures to mixtures of chemical contaminants or a combination of radiotoxic and chemotoxic substances is considered. The case study provides an illustration of how to assess human health issues arising from chemotoxic species released from a GDF for radioactive waste and highlights potential difficulties associated with a lack of data being available with which to assess synergistic effects. It also highlights how such difficulties can be addressed.

  10. [HPLC determination of the related substances in erdosteine].

    Science.gov (United States)

    Ma, Li; Zhang, Ling-di; Wang, Wen-na; Yao, Tong-wei

    2012-08-01

    An HPLC method was established for the determination of the related substance in erdosteine. Waters ODS-SunFire (250 mm x 4.6 mm ID, 5 microm) column was used, the mobile phase was composed of methanol-acetonitrile-0.01 mol x L(-1) citric acid (20:4:76, the pH value was adjusted by triethylamine to 2.5). The flow rate was 1 mL x min(-1). The detection wavelength was 254 nm. The related substances in the sample of erdosteine taken were calculated by self control with or without the response factor of impurity relative to that of erdosteine. Under the chromatographic condition developed, the impurities in erdosteine were isolated well. The detection limit was 0.2 microg x mL(-1) (signal/noise = 3) by principal component calculated. The method can be adopted to control the related substances in erdosteine.

  11. A Historical Note about how the Property was Discovered that Hydrogenated Substances Increase the Radioactivity Induced by Neutrons

    CERN Document Server

    De Gregorio, A

    2003-01-01

    At the "Domus Galilaeana" in Pisa, many original documents and records are kept, which belong to the scientific activity carried out by Enrico Fermi until 1938. I compared those documentary sources with the supported evidences, the personal recollections, concerning the discovery that hydrogenated substances increase the radioactivity induced by neutrons: such a comparison leads to the conclusion that the discovery occurred on October 20th 1934, i.e., two days before the date that all the accounts that have been supported so far report. That suggests that any historical study to come, and regarding the experiments carried out by Fermi and his group on neutrons, cannot neglect to analyse carefully the accounts regarding those experiments and to compare them with the archive records.

  12. Evaluation of the adsorptive behavior of cesium and strontium on hydroxyapatite and zeolite for decontamination of radioactive substances.

    Science.gov (United States)

    Ozeki, K; Aoki, H

    2016-08-12

    Removal of radioactive substances, such as cesium (Cs) and strontium (Sr), has become an emerging issue after the Fukushima Daiichi Nuclear Power Plant Disaster. To assess the possibility that hydroxyapatite (HA) and zeolites can be used for removal of radioactive substances, the adsorption capacities of Cs and Sr on the HA and a zeolite were investigated. The influence of Fe ions on Cs and Sr adsorption on the HA and the zeolite was also evaluated, because Fe ions are the most effective inhibitor of Cs adsorption on the zeolite.In the Cs adsorption process on the HA and the zeolite, the zeolite showed a higher adsorption ratio than the HA, and the maximum sorption capacity of the zeolite was calculated as 196 mg/g, whereas the HA showed a higher Sr adsorption ratio than the zeolite. The maximum sorption capacity of Sr on the HA was 123 mg/g. Under coexistence with Fe, Cs adsorption on the zeolite decreased with increasing Fe concentration, reaching 2.0 ± 0.8% at 0.1 M Fe concentration. In contrast, Cs adsorption on the zeolite was improved by adding the HA. In the case of coexistence of the HA, the Cs adsorption on the mixture of the HA and the zeolite was 52.4% ± 3.6 % at 0.1 M Fe concentration, although Cs adsorption on the HA alone was quite low. In the Fe adsorption processes of the HA and the zeolite, the HA exhibited a maximum sorption capacity of 256 mg/g, which was much higher than that of the zeolite (111 mg/g). The high affinity of Fe on the HA contributes to the improvement of the deteriorated Cs adsorption on the zeolite due to Fe ions.

  13. Small WEEE: determining recyclables and hazardous substances in plastics.

    Science.gov (United States)

    Dimitrakakis, Emmanouil; Janz, Alexander; Bilitewski, Bernd; Gidarakos, Evangelos

    2009-01-30

    An examination regarding the determination of recyclables and hazardous substances in small waste electrical and electronic equipment (WEEE) found in the residual household waste stream of the city of Dresden, Germany, is described. Firstly, attitudes towards the disposal of small WEEE in the latter are assessed, and product types and categories which mostly contribute to its composition are identified. Physical parameters which could be used as mechanical sorting criteria are measured, and the material composition of the small WEEE found is determined. The hazardous substances' "base" charge in the residual waste is established by means of atomic absorption spectrometry and ionic chromatography, as a first step in estimating the contribution of small WEEE to its pollutant load. Consequently, the content of small WEEE plastics in key heavy metals and halogens is determined. Key conclusions are drawn concerning the future strategic development and practical implementation of the 2002/96/EC Directive, in relation to small WEEE management and recycling.

  14. Studies on deposition, adhesion and resuspension of radioactive substances on the ground surface and ground cover

    Energy Technology Data Exchange (ETDEWEB)

    Kurita, Susumu; Kurihara, Kazuo [Meteorological Research Inst., Tsukuba, Ibaraki (Japan)

    1999-03-01

    After the Chernobyl` nuclear power plant accident, resuspension of radioactive nuclei into the atmosphere is recognized as the one of the important processes that must be considered in the estimation of inhalation doses to humans. In this study, resuspensions of particles from soil and grass have been studied. The resuspension of particles from bare soil was modelized by using Shao`s method. The resuspension of particles from grass was studied by a wind tunnel and a field experiment. Dependencies of the resuspension rate on time and on friction velocity were obtained clearly. And it was also found that the other meteorological parameters, such as temperature, relative humidity, solar radiation and condensation, affected the resuspension rate in the field. (author)

  15. Modelling migration in the marine environment of radioactive substances from Fukushima Daiichi with the use of computer code POMRad

    Energy Technology Data Exchange (ETDEWEB)

    Krylov, A.L.; Nossov, A.V.; Kisselev, V.P. [Nuclear Safety Institute of Russian Academy of Sciences, 52, B. Tulskaya, Moscow (Russian Federation)

    2014-07-01

    Fukushima accident proved once more the necessity of computer codes for modelling of radioactive substances migration in the marine environment. Radionuclides were discharged (and leaked) into the sea with contaminated waters and fell-out from the atmosphere. Unfortunately assessments of the radioactivity sources differ significantly. The uncertainty is significant as for contamination that took place in months following the disaster as for leakages that took place in 2013. According to most researches, in the spring of 2011 the most important sources of radioactive pollution of the sea were direct inflows of contaminated water. In the long-term, due to contamination of river basins, the inflow of radioactivity with river waters may become the most significant source. Strontium, iodine and cesium tend to migrate in seas in dissolved state due to small values of K{sub d} (distribution factor water - suspended sediments). However distribution factor of Cs in fresh water is high. Thus it can be assumed that most of cesium entering the sea with a river flow will be sorbed on suspended particles. Sedimentation of the particles can lead to development of contaminated areas of bottom sediments. Thus modelling migration and transformation of radionuclides in water bodies is an important radioecological problem. The three-dimensional dynamic computer code POMRad is a tool for solution of the problem. It can be used to implement full cycle of modelling: - hydrological modelling - computation of fields of currents (and other important hydrological characteristics); - sediment transport modelling (cohesive, non-cohesive and 'hot particles' if necessary); - radioactivity transport modelling (taking into account decay, sorption, desorption, etc). The article is aimed to give a brief description of the computer code and examples of its use for modelling of migration in the sea of radionuclides from Fukushima Daiichi nuclear power plant (NPP). The base of POMRad is the

  16. Four methods for determining the composition of trace radioactive surface contamination of low-radioactivity metal

    CERN Document Server

    O'Keeffe, H M; Cleveland, B T; Doucas, G; Gagnon, N; Jelley, N A; Kraus, C; Lawson, I T; Majerus, S; McGee, S R; Myers, A W; Poon, A W P; Rielage, K; Robertson, R G H; Rosten, R C; Stonehill, L C; VanDevender, B A; Van Wechel, T D

    2011-01-01

    Four methods for determining the composition of low-level uranium- and thorium-chain surface contamination are presented. One method is the observation of Cherenkov light production in water. In two additional methods a position-sensitive proportional counter surrounding the surface is used to make both a measurement of the energy spectrum of alpha particle emissions and also coincidence measurements to derive the thorium-chain content based on the presence of short-lived isotopes in that decay chain. The fourth method is a radiochemical technique in which the surface is eluted with a weak acid, the eluate is concentrated, added to liquid scintillator and assayed by recording beta-alpha coincidences. These methods were used to characterize two `hotspots' on the outer surface of one of the He-3 proportional counters in the Neutral Current Detection array of the Sudbury Neutrino Observatory experiment. The methods have similar sensitivities, of order tens of ng, to both thorium- and uranium-chain contamination.

  17. Four methods for determining the composition of trace radioactive surface contamination of low-radioactivity metal

    Energy Technology Data Exchange (ETDEWEB)

    O' Keeffe, H.M. [Department of Physics, University of Oxford, Denys Wilkinson Building, Oxford OX1 3RH (United Kingdom); Burritt, T.H. [Center for Experimental Nuclear Physics and Astrophysics and Department of Physics, University of Washington, Seattle, WA 98195 (United States); Cleveland, B.T. [SNOLAB, Lively, Ontario, P3Y 1M3 (Canada); Doucas, G. [Department of Physics, University of Oxford, Denys Wilkinson Building, Oxford OX1 3RH (United Kingdom); Gagnon, N. [SNOLAB, Lively, Ontario, P3Y 1M3 (Canada); Jelley, N.A. [Department of Physics, University of Oxford, Denys Wilkinson Building, Oxford OX1 3RH (United Kingdom); Kraus, C. [Department of Physics and Astronomy, Laurentian University, Sudbury, Ontario, P3E 2C6 (Canada); Lawson, I.T. [SNOLAB, Lively, Ontario, P3Y 1M3 (Canada); Majerus, S. [Department of Physics, University of Oxford, Denys Wilkinson Building, Oxford OX1 3RH (United Kingdom); McGee, S.R.; Myers, A.W. [Center for Experimental Nuclear Physics and Astrophysics and Department of Physics, University of Washington, Seattle, WA 98195 (United States); Poon, A.W.P. [Institute for Nuclear and Particle Astrophysics, and Nuclear Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States); Rielage, K. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Center for Experimental Nuclear Physics and Astrophysics and Department of Physics, University of Washington, Seattle, WA 98195 (United States); Robertson, R.G.H., E-mail: rghr@u.washington.edu [Center for Experimental Nuclear Physics and Astrophysics and Department of Physics, University of Washington, Seattle, WA 98195 (United States); Rosten, R.C. [Center for Experimental Nuclear Physics and Astrophysics and Department of Physics, University of Washington, Seattle, WA 98195 (United States); and others

    2011-12-11

    Four methods for determining the composition of low-level uranium- and thorium-chain surface contamination are presented. One method is the observation of Cherenkov light production in water. In two additional methods a position-sensitive proportional counter surrounding the surface is used to make both a measurement of the energy spectrum of alpha particle emissions and also coincidence measurements to derive the thorium-chain content based on the presence of short-lived isotopes in that decay chain. The fourth method is a radiochemical technique in which the surface is eluted with a weak acid, the eluate is concentrated, added to liquid scintillator and assayed by recording beta-alpha coincidences. These methods were used to characterize two 'hotspots' on the outer surface of one of the {sup 3}He proportional counters in the Neutral Current Detection array of the Sudbury Neutrino Observatory experiment. The methods have similar sensitivities, of order tens of ng, to both thorium- and uranium-chain contamination.

  18. Quantitative radiochemical methods for determination of the sources of natural radioactivity

    Science.gov (United States)

    Rosholt, J.N.

    1957-01-01

    Study of the state of equilibrium of any natural radioactive source requires determination of several key nuclides or groups of nuclides to find their contribution to the total amount of radioactivity. Alpha activity measured by scintillation counting is used for determination of protactinium-231, thorium-232, thorium-230, and radium-226. The chemical procedures for the separations of the specific elements are described, as well as the measurement techniques used to determine the abundances of the individual isotopes. To correct for deviations in the ore standards, an independent means of evaluating the efficiencies of the individual separations and measurements is used. The development of these methods of radiochemical analysis facilitates detailed investigation of the major sources of natural radioactivity.

  19. Determining the Knowledge Level of Pre-Service Teachers' on Radioactivity and Radiation

    Science.gov (United States)

    Ergul, N. Remziye

    2012-01-01

    This study investigated the basic knowledge levels of teacher candidates from different branches regarding the subjects of radiation and radioactivity. 42 variables were determined in relation to the specified titles. In the preparation stage of determining the variables, all the related programs were examined, and attention was paid to include…

  20. Determining the Knowledge Level of Pre-Service Teachers' on Radioactivity and Radiation

    Science.gov (United States)

    Ergul, N. Remziye

    2012-01-01

    This study investigated the basic knowledge levels of teacher candidates' from different branches regarding the subjects of radiation and radioactivity. 42 variables were determined in relation to the specified titles. In the preparation stage of determining the variables, all the related programs were examined, and attention was paid to include…

  1. Study of casks shielded with heavy metal to transport highly radioactive substances; Estudo de embalados com blindagem em metal pesado para transporte de substancias altamente radioativas

    Energy Technology Data Exchange (ETDEWEB)

    Lucchesi, R.F.; Hara, D.H.S.; Martinez, L.G.; Mucsi, C.S.; Rossi, J.L., E-mail: rflguimaraes@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2014-07-01

    Nowadays, Brazil relies on casks produced abroad for transportation in its territory of substances that are sources of high radioactivity, especially the Mo-99. The product of the radioactive decay of the Mo-99 is the Tc-99m, which is used in nuclear medicine for administration to humans in the form of injectable radioactive drugs for the image diagnosis of numerous pathologies. This paper aims to study the existing casks in order to propose materials for the construction of the core part as shielding against gamma radiation. To this purpose, the existing literature on the subject was studied, as well as evaluation of existing and available casks. The study was focused on the core of which is made of heavy metals, especially depleted uranium for shielding the emitted radiation. (author)

  2. Study on Water—Soluble Organic Reducing Substances.I.Determination of Organic Reducing Substances by Differential Pulse Voltammetry

    Institute of Scientific and Technical Information of China (English)

    WUYOU-XIAN; DINGCHANG-PU

    1991-01-01

    A new method was proposed for study of organic reducing substances in soils.According to the theoretical relationship between the voltammetric behaviors and reduction-oxidation reaction of reducing substances,the working conditions of differential pulse voltammetry (d.p.v.)for determining the organic reducing substances produced during the processes of the anaerobic decomposition of plant materials were established with a glass carbon electrode as working electrode,1M Ag-AgCl electrode with large area as reference electrode,0.2M NH4Ac as supporting from -0.5 to +1.2 voltage(vs.M Ag-AgCl).The peak current proportional to the concentration of reducing substances,and the characteristic peak potential of each organic reducing substance were regarded as the quantitative and qualitative base,respectively.These results obtained under the conditions mentioned above directly reflect both the reducing intensity and capacity of the organic reducing system in soils.

  3. Mapping the social determinants of substance use for pregnant-involved young Aboriginal women.

    Science.gov (United States)

    Shahram, Sana Z; Bottorff, Joan L; Oelke, Nelly D; Kurtz, Donna L M; Thomas, Victoria; Spittal, Patricia M; And For The Cedar Project Partnership

    2017-12-01

    There is a dearth of knowledge about the social determinants of substance use among young pregnant-involved Indigenous women in Canada from their perspectives. As part of life history interviews, 17 young pregnant-involved Indigenous women with experiences with substances completed a participant-generated mapping activity CIRCLES (Charting Intersectional Relationships in the Context of Life Experiences with Substances). As women created their maps, they discussed how different social determinants impacted their experiences with pregnancy and substance use. The social determinants identified and used by women to explain determinants of their substance use were grouped into 10 themes: traumatic life histories; socioeconomic status; culture, identity and spirituality; shame and guilt; mental wellness; family connections; romantic and platonic relationships; strength and hope; mothering; and the intersections of determinants. We conclude that understanding the context and social determinants of substance use from a woman-informed perspective is paramount to informing effective and appropriate programs to support young Indigenous women who use substances.

  4. Nondestructive NMR technique for moisture determination in radioactive materials.

    Energy Technology Data Exchange (ETDEWEB)

    Aumeier, S.; Gerald, R.E. II; Growney, E.; Nunez, L.; Kaminski, M.

    1998-12-04

    This progress report focuses on experimental and computational studies used to evaluate nuclear magnetic resonance (NMR) spectroscopy and magnetic resonance imaging (MRI) for detecting, quantifying, and monitoring hydrogen and other magnetically active nuclei ({sup 3}H, {sup 3}He, {sup 239}Pu, {sup 241}Pu) in Spent nuclear fuels and packaging materials. The detection of moisture by using a toroid cavity NMR imager has been demonstrated in SiO{sub 2} and UO{sub 2} systems. The total moisture was quantified by means of {sup 1}H NMR detection of H{sub 2}O with a sensitivity of 100 ppm. In addition, an MRI technique that was used to determine the moisture distribution also enabled investigators to discriminate between bulk and stationary water sorbed on the particles. This imaging feature is unavailable in any other nondestructive assay (NDA) technique. Following the initial success of this program, the NMR detector volume was scaled up from the original design by a factor of 2000. The capacity of this detector exceeds the size specified by DOE-STD-3013-96.

  5. Laser photodetachment of radioactive ions: towards the determination of the electronegativity of astatine

    CERN Multimedia

    Rothe, Sebastian; Welander, Jakob Emanuel; Chrysalidis, Katerina; Day Goodacre, Thomas; Fedosseev, Valentine; Fiotakis, Spyridon; Forstner, Oliver; Heinke, Reinhard Matthias; Johnston, Karl; Kron, Tobias; Koester, Ulli; Liu, Yuan; Marsh, Bruce; Ringvall Moberg, Annie; Rossel, Ralf Erik; Seiffert, Christoph; Studer, Dominik; Wendt, Klaus; Hanstorp, Dag

    2017-01-01

    Negatively charged ions are mainly stabilized through the electron correlation effect. A measure of the stability of a negative ion is the electron affinity, which the energy gain by attaching an electron to a neutral atom. This fundamental quantity is, due to the almost general lack of bound excited states, the only atomic property that can be determined with high accuracy for negative ions. We will present the results of the first laser photodetachment studies of radioactive negative ions at CERN-ISOLDE. The photodetachment threshold for the radiogenic iodine isotope 128I was measured successfully, demonstrating the performance of the upgraded GANDALPH experimental beam line. The first detection of photo-detached astatine atoms marks a milestone towards the determination of the EA of this radioactive element.

  6. A portable Si/CdTe Compton camera and its applications to the visualization of radioactive substances

    Energy Technology Data Exchange (ETDEWEB)

    Takeda, Shin' ichiro, E-mail: takeda@astro.isas.jaxa.jp [Institute of Space and Astronautical Science (ISAS)/JAXA, 3-1-1 Yoshinodai, Chuo-ku, Sagamihara, Kanagawa 252-5210 (Japan); Harayama, Atsushi [Institute of Space and Astronautical Science (ISAS)/JAXA, 3-1-1 Yoshinodai, Chuo-ku, Sagamihara, Kanagawa 252-5210 (Japan); Ichinohe, Yuto [Institute of Space and Astronautical Science (ISAS)/JAXA, 3-1-1 Yoshinodai, Chuo-ku, Sagamihara, Kanagawa 252-5210 (Japan); University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo 113-0033 (Japan); Odaka, Hirokazu [Institute of Space and Astronautical Science (ISAS)/JAXA, 3-1-1 Yoshinodai, Chuo-ku, Sagamihara, Kanagawa 252-5210 (Japan); Watanabe, Shin; Takahashi, Tadayuki [Institute of Space and Astronautical Science (ISAS)/JAXA, 3-1-1 Yoshinodai, Chuo-ku, Sagamihara, Kanagawa 252-5210 (Japan); University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo 113-0033 (Japan); Tajima, Hiroyasu [Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8601 (Japan); Genba, Kei; Matsuura, Daisuke; Ikebuchi, Hiroshi; Kuroda, Yoshikatsu [Mitsubishi Heavy Industries, 1200 Higashi-Tanaka, Komaki, Aichi 485-8561 (Japan); Tomonaka, Tetsuya [Mitsubishi Heavy Industry, 2-1-1 Shinhama, Arai-cho, Takasago, Hyogo 676-8686 (Japan)

    2015-07-01

    Gamma-ray imagers with the potential for visualizing the distribution of radioactive materials are required in the fields of astrophysics, medicine, nuclear applications, and homeland security. Based on the technology of the Si/CdTe Compton camera, we have manufactured the first commercial Compton camera for practical use. Through field tests in Fukushima, we demonstrated that the camera is capable of hot spot detection and the evaluation of radioactive decontamination.

  7. Determination of radioactivity levels and hazards of soil and sediment samples in Firtina Valley (Rize, Turkey)

    Energy Technology Data Exchange (ETDEWEB)

    Kurnaz, A.; Kuecuekoemeroglu, B. [Department of Physics, Faculty of Arts and Sciences, Karadeniz Technical University, Trabzon, TR 61080 (Turkey); Keser, R.; Okumusoglu, N.T.; Korkmaz, F. [Department of Physics, University of Rize, Rize, TR 53100 (Turkey); Karahan, G. [Cekmece Nuclear Research and Training Center P.O. Box 1, Atatuerk Airport, Istanbul, TR 34381 (Turkey); Cevik, U. [Department of Physics, Faculty of Arts and Sciences, Karadeniz Technical University, Trabzon, TR 61080 (Turkey)], E-mail: ugurc@ktu.edu.tr

    2007-11-15

    The natural radioactivity levels in soil and sediment samples of Firtina Valley have been determined. To our knowledge, there seems to be no information about radioactivity level in the Firtina Valley soils and sediments so far. For this reason, soil and sediment samples were collected along the Firtina Valley and analysis on the collected samples were carried out to determine {sup 238}U, {sup 232}Th, {sup 40}K and {sup 137}Cs radioisotopes using high purity germanium detector. The activity concentrations obtained for {sup 226}Ra, {sup 214}Pb, {sup 214}Bi, {sup 228}Ac, {sup 208}Tl, {sup 40}K and {sup 137}Cs are given in the unit of Bq/kg. The results have been compared with other radioactivity measurements in different country's soils and sediments. The radium equivalent activity (Ra{sub eq}), the absorbed dose rate (D), the external hazard index (H{sub ex}), the annual gonadal dose equivalent (AGDE) and the annual effective dose equivalent (AEDE) were also calculated and compared with the international recommended values.

  8. Sensitive non-radioactive determination of aminotransferase stereospecificity for C-4' hydrogen transfer on the coenzyme

    Energy Technology Data Exchange (ETDEWEB)

    Jomrit, Juntratip [Department of Biotechnology, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok 10400 (Thailand); Center of Excellence for Agricultural Biotechnology: (AG-BIO/PERDO-CHE), Bangkok (Thailand); Summpunn, Pijug [Department of Biotechnology, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok 10400 (Thailand); Meevootisom, Vithaya [Department of Microbiology, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok 10400 (Thailand); Center of Excellence for Agricultural Biotechnology: (AG-BIO/PERDO-CHE), Bangkok (Thailand); Wiyakrutta, Suthep, E-mail: scsvy@mahidol.ac.th [Department of Microbiology, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok 10400 (Thailand); Center of Excellence for Agricultural Biotechnology: (AG-BIO/PERDO-CHE), Bangkok (Thailand)

    2011-02-25

    Research highlights: {yields} Stereochemical mechanism of PLP enzymes is important but difficult to determine. {yields} This new method is significantly less complicated than the previous ones. {yields} This assay is as sensitive as the radioactive based method. {yields} LC-MS/MS positively identify the analyte coenzyme. {yields} The method can be used with enzyme whose apo form is unstable. -- Abstract: A sensitive non-radioactive method for determination of the stereospecificity of the C-4' hydrogen transfer on the coenzymes (pyridoxal phosphate, PLP; and pyridoxamine phosphate, PMP) of aminotransferases has been developed. Aminotransferase of unknown stereospecificity in its PLP form was incubated in {sup 2}H{sub 2}O with a substrate amino acid resulted in PMP labeled with deuterium at C-4' in the pro-S or pro-R configuration according to the stereospecificity of the aminotransferase tested. The [4'-{sup 2}H]PMP was isolated from the enzyme protein and divided into two portions. The first portion was incubated in aqueous buffer with apo-aspartate aminotransferase (a reference si-face specific enzyme), and the other was incubated with apo-branched-chain amino acid aminotransferase (a reference re-face specific enzyme) in the presence of a substrate 2-oxo acid. The {sup 2}H at C-4' is retained with the PLP if the aminotransferase in question transfers C-4' hydrogen on the opposite face of the coenzyme compared with the reference aminotransferase, but the {sup 2}H is removed if the test and reference aminotransferases catalyze hydrogen transfer on the same face. PLP formed in the final reactions was analyzed by LC-MS/MS for the presence or absence of {sup 2}H. The method was highly sensitive that for the aminotransferase with ca. 50 kDa subunit molecular weight, only 2 mg of the enzyme was sufficient for the whole test. With this method, the use of radioactive substances could be avoided without compromising the sensitivity of the assay.

  9. Background radioactivity of construction materials, raw substance and ready-made CaMoO4 crystals

    CERN Document Server

    Busanov, O A; Gavriljuk, Yu M; Gezhaev, A M; Kazalov, V V; Kornoukhov, V N; Kuzminov, V V; Moseev, P S; Panasenko, S I; Ratkevich, S S; Yakimenko, S P

    2013-01-01

    The results of measurements of natural radioactive isotopes content in different source materials of natural and enriched composition used for CaMoO4 scintillation crystal growing are presented. The crystals are to be used in the experiment to search for double neutrinoless betas-decay of Mo-100.

  10. Background radioactivity of construction materials, raw substance and ready-made CaMoO4 crystals

    Directory of Open Access Journals (Sweden)

    Busanov O.A.

    2014-01-01

    Full Text Available The results of measurements of natural radioactive isotopes content in different source materials of natural and enriched composition used for CaMoO4 scintillation crystal growing are presented. The crystals are to be used in the experiment to search for neutrinoless double beta decay of 100Mo.

  11. Gross alpha determination in radioactive wastes from nuclear power plants using the track registration technique

    Energy Technology Data Exchange (ETDEWEB)

    Suarez-Navarro, M.J. [Universidad Politecnica de Madrid (UPM) E.T.S.I de Caminos, Canales y Puertos, Profesor Aranguren, s/n, 28040 Madrid (Spain)]. E-mail: he04@caminos.upm.es; Pujol, Ll. [Centro de Estudios y Experimentacion de Obras Publicas (CEDEX), Alfonso XII, 3, 28014 Madrid (Spain); Gonzalez-Gonzalez, J.A. [Universidad Politecnica de Madrid (UPM) E.T.S.I de Caminos, Canales y Puertos, Profesor Aranguren, s/n, 28040 Madrid (Spain)

    2007-03-15

    Low and intermediate level nuclear wastes (ion-exchange resins and evaporator concentrates) essentially contain beta and gamma emitters, with very few alpha emitters. Several techniques may be used to determine gross alpha activity but, in this case, solid-state nuclear track detectors (SSNTDs) are a suitable technique for gross alpha determination because track detectors are not sensitive to beta and gamma emitters. Also, this technique is simple and inexpensive. In this paper, we studied the parameters (background, efficiency and self-absorption) that could affect the gross alpha determination using SSNTDs for both sample preparation methods, the 'dry method' with tensioactives and the 'wet method'. For the 'dry method', a self-absorption curve for {sup 241}Am standard was prepared using a set of varying thickness of sodium salt and for two different tensioactives: Tween{sup (R)}20 and Teg. The results showed that, below 1mg/cm{sup 2}, the self-absorption factor can be considered similar for both tensioactives and equal to unity. Several detectors for gross alpha determination were compared and we found that the most suitable techniques were ZnS(Ag) solid scintillator and track detectors. Both detectors were used to compare radioactive waste samples. Finally, the proposed methods ('dry method' with Teg tensioactive and 'wet method') using track detectors were tested by analysing the gross alpha activity of several radioactive wastes.

  12. Factors Influencing the HPLC Determination for Related Substances of Azithromycin.

    Science.gov (United States)

    Chang, Yan; Wang, Li-Xin; Li, Ya-Ping; Hu, Chang-Qin

    2016-02-01

    The European Pharmacopoeia, the U.S. Pharmacopoeia, and the Pharmacopoeia of the People's Republic of China all prescribe a high-performance liquid chromatography-ultraviolet method within a C18 column system for the separation of Azithromycin (AZT) and its related substances. The identification of impurities in the AZT complex was performed according to the relative retention time (RRT) between each impurity and AZT. However, the RRT values of impurities often vary on different types of C18 packing materials and at different column temperatures, which could affect the accurate and fast identification of impurities. In our study, five different commonly used C18 columns as well as nine different column temperature set points were assessed for the analysis of AZT and its related substances. A factorial design was applied to analysis the relationships between column types/column temperatures and RRT value of each impurity. The results showed that the change rates of the RRT values of impurities were different on different columns and at different column temperature set points. Therefore, the current method adopted by the three Pharmacopeias, in which the RRT values were used to identify the related substances, is not suitable to identify the ones in the AZT chromatographic system.

  13. A Study to Determine Clearance Levels of Radioactive Wastes in Kenya

    Energy Technology Data Exchange (ETDEWEB)

    Mukakaa, Zaphania O. [KAIST, Daejeon (Korea, Republic of); Kim, Sung Il [KINS, Daejeon (Korea, Republic of)

    2015-10-15

    Due to lack of a radioactive waste disposal facility in Kenya, radioactive wastes are stored in a bonded warehouse until such a time when their activity is low and they meet the criterion for clearance. The International Atomic Energy Agency (IAEA) has established activity concentrations of radionuclides to act as a universal guideline or standard for clearance in member countries. Radioactive wastes whose activity would yield a trivial risk to the people and environment, i.e. with an annual dose below 10 µSv are usually cleared from regulatory control with no further regulatory control mechanisms being taken. The Radiation Protection Board currently depends on the IAEA's generic clearance level activity concentrations for purposes of clearing the radiation wastes within its inventory. This study aims to determine activity concentrations of radionuclides in the Kenyan inventory that correspond to the clearance level dose of 10 µSv/a as set by the IAEA. The RESidual RADioactivity (RESRAD) computer code, an important tool developed in 1989 to aid in evaluation of sites with radioactive contamination, will aid in modeling these clearance level values using a pathways analysis method and available site-specific data from Kenya. Afterwards, the obtained clearance level values will be compared with the IAEA's generic clearance level values of the corresponding radionuclides. The results modeled using the RESRAD code are conservative. For most of the radionuclides in the Kenyan inventory, the values do correspond with the IAEA standard generic clearance level values, albeit with minor differences. For most of the radionuclides, the difference is within the acceptable uncertainty limit. For these low probability events the effective dose resulting from them should not exceed 1 mSv per year. Thus, consideration was given to doses to the skin and an equivalent dose to the skin of 50 mSv per year was duly used in estimating the clearance level activities. The

  14. Rapid and simple determination of delivery after iontophoretic and pressure injections of radiolabeled tracer substances

    Energy Technology Data Exchange (ETDEWEB)

    Imai, H.; Steindler, D.A.; Kitai, S.T. (Michigan State Univ., East Lansing (USA))

    1983-04-01

    A fluorographic method is described using X-ray film analysis for the determination of delivery of radiolabeled tracer substances both in Agar plates and in tissue sections. This method is most useful in neuroanatomical autoradiographic studies for providing rapid identification of delivery, placement and extent of an injection site after iontophoresis or pressure injections of radiolabeled axonal tracer substances.

  15. Sedimentological study of a lagoon through natural radioactivity and 137Cs determinations

    Science.gov (United States)

    San Miguel, E. G.; Pérez-Moreno, J. P.; Aguado, J. L.; Bolívar, J. P.; García-Tenorio, R.

    2003-01-01

    Profiles of artificial fallout (such as 137Cs) and natural radioactivity radionuclides in sediment cores are useful tools to study sedimentological properties of different aquatic environments as well as to evaluate average sedimentation rates. In the Portil lagoon, a small natural reservoir located in Huelva province (southwest of Spain), and through the analysis of 210Pb, 226Ra, 137Cs, 238U and 210Po vertical profiles in sediment cores, it is shown how the accumulative or transport character of the collection zones may be inferred. In the accumulation zone of the lagoon the influence of focusing effects has been analysed and an average sedimentation rate has been determined through 210Pb in one sediment core. This 210Pb-sedimentation rate is consistent with sediment dating based on the 137Cs data.

  16. Monitoring of radioactive substances in foods distributed in Kyoto, Japan (1991-2011). - Comparison of detection rates and concentrations before and after the Fukushima Daiichi Nuclear Power Plant accident - .

    Science.gov (United States)

    Banno, Yukinori; Namikawa, Mikio; Miwa, Mariko; Ban, Soichirou; Orito, Taichi; Semura, Shunsuke; Kawakami, Masahiro; Doi, Naoya; Miyake, Shiro; Ishikawa, Yasuhiro

    2013-01-01

    Since the Chernobyl Nuclear Power Plant accident, radioactive substances have been continually monitored in foods collected in the city of Kyoto, Japan. The importance of the monitoring was increased by the Fukushima Daiichi Nuclear Power Plant accident in March 2011. Here, the detection rates and concentrations of radioactive substances were compared among food samples collected before and after the accident in Fukushima prefecture. Before the accident, (137)Cs was the only radioactive substance detected in foods. The detection rate was 70% for fish and shellfish samples and the highest concentration was 1.7 Bq/kg. It was also 83% for fresh mushroom samples and the highest concentration was 7.5 Bq/kg. In contrast, the detection rate was low for vegetables and the concentrations were also lower than those of the above samples. On the other hand, after the accident, (131)I was detected in food produced in the Tohoku and Kanto areas. Actually, (131)I (3,400 Bq/kg), (134)Cs (280 Bq/kg), and (137)Cs (280 Bq/kg) were detected in mizuna, a leaf vegetable, on March 23, 2011. These radioactive substances were detected in all leaf vegetable samples examined in March and April 2011, but they were not detected in samples examined in November 2011. (131)I was not detected in any food sample examined after May 2011. However, (137)Cs (average=7.9 Bq/kg) was consistently detected in fish and shellfish samples until November, although the concentrations were less than the regulatory limits. It appears unlikely that foods containing radioactive substances over the regulatory limits are currently being distributed in Kyoto.

  17. [An evaluation of methods for the quantitative determination of praziquantel as a substance].

    Science.gov (United States)

    Lopatin, B V; Bebris, N K; Lopatina, N B

    1989-01-01

    Feasibility of quantitative determination of a new helminthicide prasiquantel as a substance by spectral and chemical analytic procedures has been investigated. Chemical methods based on nitrogen measurement in the samples were shown to lack precision which is obligatory for drug analysis. The quantitative analytic procedures based on UV spectrophotometry are of low precision and selectivity. Infrared spectroscopy is the only method of prasiquantel assay that meets the requirements for drug substance measurement.

  18. Determination of the depth of localized radioactive contamination by 137Cs and 60Co in sand with principal component analysis.

    Science.gov (United States)

    Adams, Jamie C; Mellor, Matthew; Joyce, Malcolm J

    2011-10-01

    A method to determine the depth of buried localized radioactive contamination nonintrusively and nondestructively using principal component analysis is described. The γ-ray spectra from two radionuclides, cesium-137 and cobalt-60, have been analyzed to derive the two principal components that change most significantly as a result of varying the depth of the sources in a bespoke sand-filled phantom. The relationship between depth (d) and the angle (θ) between the first two principal component coefficients has been derived for both cases, viz. d(Φ) = x + y log(e) Φ where x and y are constants dependent on the shielding material and the γ-ray energy spectrum of the radioactivity in question, and φ is a function of θ. The technique enables the depth of a localized radioactive source to be determined nonintrusively in the range 5 to 50 mm with an accuracy of ±1 mm.

  19. Development of quantitative radioactive methodologies on paper to determine important lateral-flow immunoassay parameters.

    Science.gov (United States)

    Mosley, Garrett L; Nguyen, Phuong; Wu, Benjamin M; Kamei, Daniel T

    2016-08-01

    The lateral-flow immunoassay (LFA) is a well-established diagnostic technology that has recently seen significant advancements due in part to the rapidly expanding fields of paper diagnostics and paper-fluidics. As LFA-based diagnostics become more complex, it becomes increasingly important to quantitatively determine important parameters during the design and evaluation process. However, current experimental methods for determining these parameters have certain limitations when applied to LFA systems. In this work, we describe our novel methods of combining paper and radioactive measurements to determine nanoprobe molarity, the number of antibodies per nanoprobe, and the forward and reverse rate constants for nanoprobe binding to immobilized target on the LFA test line. Using a model LFA system that detects for the presence of the protein transferrin (Tf), we demonstrate the application of our methods, which involve quantitative experimentation and mathematical modeling. We also compare the results of our rate constant experiments with traditional experiments to demonstrate how our methods more appropriately capture the influence of the LFA environment on the binding interaction. Our novel experimental approaches can therefore more efficiently guide the research process for LFA design, leading to more rapid advancement of the field of paper-based diagnostics.

  20. Exact method for determining subsurface radioactivity depth profiles from gamma spectroscopy measurements

    CERN Document Server

    Van Siclen, Clinton DeW

    2011-01-01

    Subsurface radioactivity may be due to transport of radionuclides from a contaminated surface into the solid volume, as occurs for radioactive fallout deposited on soil, or from fast neutron activation of a solid volume, as occurs in concrete blocks used for radiation shielding. For purposes including fate and transport studies of radionuclides in the environment, decommissioning and decontamination of radiation facilities, and nuclear forensics, an in situ, nondestructive method for ascertaining the subsurface distribution of radioactivity is desired. The method developed here obtains a polynomial expression for the radioactivity depth profile, using a small set of gamma-ray count rates measured by a collimated detector directed towards the surface at a variety of angles with respect to the surface normal. To demonstrate its capabilities, this polynomial method is applied to the simple case where the radioactivity is maximal at the surface and decreases exponentially with depth below the surface, and to the ...

  1. Determination of plutonium resent in highly radioactive irradiated fuel solution by spectrophotometric method

    Energy Technology Data Exchange (ETDEWEB)

    Dhamodharam, Krishnan [Reprocessing Group, Indira Gandhi Centre for Atomic Research, Kalpakkam (India); Pius, Anitha [The Gandhigram Rural Institute - Deemed University, Gandhigram (India)

    2016-06-15

    A simple and rapid spectrophotometric method has been developed to enable the determination of plutonium concentration in an irradiated fuel solution in the presence of all fission products. An excess of ceric ammonium nitrate solution was employed to oxidize all the valence states of plutonium to +6 oxidation state. Interference due to the presence of fission products such as ruthenium and zirconium, and corrosion products such as iron in the envisaged concentration range, as in the irradiated fuel solution, was studied in the determination of plutonium concentration by the direct spectrophotometric method. The stability of plutonium in +6 oxidation state was monitored under experimental conditions as a function of time. Results obtained are reproducible, and this method is applicable to radioactive samples resulting before the solvent extraction process during the reprocessing of fast reactor spent fuel. An analysis of the concentration of plutonium shows a relative standard deviation of <1.2% in standard as well as in simulated conditions. This reflects the fast reactor fuel composition with respect to uranium, plutonium, fission products such as ruthenium and zirconium, and corrosion products such as iron.

  2. Imaging plant leaves to determine changes in radioactive contamination status in Fukushima, Japan.

    Science.gov (United States)

    Nakajima, Hiroo; Fujiwara, Mamoru; Tanihata, Isao; Saito, Tadashi; Matsuda, Norihiro; Todo, Takeshi

    2014-05-01

    The chemical composition of plant leaves often reflects environmental contamination. The authors analyzed images of plant leaves to investigate the regional radioactivity ecology resulting from the 2011 accident at the Fukushima No. 1 nuclear power plant, Japan. The present study is not an evaluation of the macro radiation dose per weight, which has been performed previously, but rather an image analysis of the radioactive dose per leaf, allowing the capture of various gradual changes in radioactive contamination as a function of elapsed time. In addition, the leaf analysis method has potential applications in the decontamination of food plants or other materials.

  3. Radioactive chromium-ethylenediaminetetraacetic acid for determination of glomerular filtration rate in rabbits

    Energy Technology Data Exchange (ETDEWEB)

    Tvedegaard, E.; Kamstrup, O.

    1981-12-01

    Simultaneous determination of the glomerular filtration rate was made by the insulin clearance technique and by analysis of the plasma disappearance curve of radioactive chromium-ethylenediaminetetraacetic acid (/sup 51/Cr-EDTA) following an intravenous injection in 28 anaesthetized rabbits. In some rabbits, the renal function was reduced by previous surgery. The insulin clearances ranged from 2.7 to 17 ml/minute. By a double-exponential analysis of the plasma disappearance curve, the total plasma clearance of /sup 51/Cr-EDTA was found to exceed the inulin clearance by 12%. By the simpler slope-intercept analysis requiring only two blood samples, this value was 32%. The renal clearance of /sup 51/Cr-EDTA was 97% of inulin clearance. In nephrectomized rabbits, plasma clearance of /sup 51/Cr-EDTA was 0.7 ml/minute. At all levels of renal function, measurement of the plasma clearance rate of /sup 51/Cr-EDTA by the single injection technique allowed a fairly reliable estimate of the glomerular filtration rate.

  4. Determination of {sup 129}I in simulated radioactive wastes using distillation technique

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Ke Chon; Song, Byung Cheol; Han, Sun Ho; Park, Yong Joon; Song, Kyu Seok [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2011-09-15

    It is clarified in the radioactive waste transfer regulation that the concentration of radioactive waste for the major radio nuclide has to be examined when radioactive waste is guided to the radioactive waste stores. In case of the low level radioactive waste sample, the analytical results of radioactive waste concentration frequently show a value lower than minimum detectable activity (MDA). Since the MDA value basically depends on the amount of a sample, background value, measurement time, counting efficiency, and etc, it would be necessary to increase a sample amount with a intention of minimizing MDA. In order to measure a concentration of {sup 129}I in low and medium level radioactive waste, {sup 129}I was collected by using a distillation technique after leaching the simulated radioactive waste sample with a non-volatile acid. The recovery of {sup 129}I measured was compared with that measured with column elution technique which is a conventional method using an anion-exchange resin. The recovery of inactive iodide by using the distillation method and column elution were found as 86.5 {+-} 0.9% and 87.3 {+-}2.7%, respectively. The recovery and MDA value calculated for distillation technique when 100 g of extracted solution of {sup 129}I was taken,were found to be 84.6 {+-} 1.6% and 1.2 X 10{sup -4} Bq/g, respectively. Consequently, the proposed technique with simplified process lowered the MDA value more than 10 times compared to the column elution technique that has a disadvantage of limited sampling amount.

  5. Determination of {sup 226}Ra, {sup 228}Ra, and {sup 210}Pb in mushroom from a naturally high radioactive region

    Energy Technology Data Exchange (ETDEWEB)

    Rosa, Mychelle M.L.; Custodio, Luis Gustavo; Cheberle, Luan T.V.; Taddei, Maria Helena T., E-mail: mychelle@cnen.gov.br, E-mail: lgcustodio@hotmail.com, E-mail: lt.cheberle@bol.com.br, E-mail: mhtaddei@cnen.gov.br [Comissao Nacional de Energia Nuclear (LAPOC/CNEN-MG), Pocos de Caldas, MG (Brazil). Laboratorio de Pocos de Caldas; Maihara, Vera A., E-mail: vmaihara@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (CNEN/IPEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    Many studies have shown that mushrooms are organisms which efficiently accumulate radionuclides and can be used as indicators of environmental contamination and ecosystem quality. The Pocos de Caldas plateau, in Minas Gerais, is a region that has elevated natural radioactivity due to the presence of radiological anomalies of volcanic origin. Seventy areas of radioactive anomalies have been identified in this region. From the radiological point of view the determination of {sup 226}Ra, {sup 228}Ra, and {sup 210}Pb is relevant because they are decay products of the natural series of {sup 238}U and {sup 232}Th, mainly responsible for natural radioactive exposures of man. The present paper is part of a broader study conducted in the Pocos de Caldas plateau, in which the concentration activities of {sup 226}Ra, {sup 228}Ra, and {sup 210}Pb in mushroom samples were determined. The mushrooms were collected at different points of the plateau under the influence of radioactive anomalies and away from the influence of anomalies. From statistical studies a correlation between the accumulation of radionuclides in mushrooms and anomalies was established and it was possible to confirm the efficiency that the mushrooms present as environmental contamination indicators. (author)

  6. Determination of Tc-99 in radioactive wastes; Determinacion de Tc-99 en desechos radiactivos

    Energy Technology Data Exchange (ETDEWEB)

    Rivera S, A. A.

    2015-07-01

    Tc-99 is a fission product and one of the most important radionuclides from the view point of safety assessment for the disposal of radioactive waste because of its long half-life (2.1 x 10{sup 5} years) and high mobility in soil-water systems, if this is released into the environment in significant quantities can concentrate on plants and animals. Tc-99 is a pure beta emitter with a maximum energy of 292 KeV, so their quantification imposes destructive methods to be analyzed by liquid scintillation. Therefore the quantification of Tc-99 in ion exchange resins requires of the mineralization of these and separation of Tc-99 of other radioisotopes present in the resin. Therefore the object of this thesis is to develop a quantification method of Tc-99 content in spent exchange resins. So in order to track the behavior of technetium during digestion exchange resins and radiochemical separation, given its high volatility, in this work the {sup 99m}Tc is used. To determine the degree of mineralization of the resins, an analysis was performed by chromatography. Subsequently the method used to determine the percentage of {sup 99m}Tc aerosolized during mineralization of resin is described. After the method for the radiochemical separation of {sup 99m}Tc is presented by liquid-liquid extraction using crown ether as extractant; for this testing was performed by varying the molarity of the extractant, the ratio of solvent extractant, type of digestion of the resin and the presence of Sr-85, in order to study the behavior of {sup 99m}Tc in the presence of this radioisotope. Finally, a track beta spectra of a sample of {sup 99m}Tc eluted from a generator {sup 99}Mo/{sup 99m}Tc function of time was performed. (Author)

  7. Methods for the Determination of Chemical Substances in Marine and Estuarine Environmental Matrices - 2nd Edition

    Science.gov (United States)

    This NERL-Cincinnati publication, “Methods for the Determination of Chemical Substances in Marine and Estuarine Environmental Matrices - 2nd Edition” was prepared as the continuation of an initiative to gather together under a single cover a compendium of standardized laborato...

  8. Methods for the Determination of Chemical Substances in Marine and Estuarine Environmental Matrices - 2nd Edition

    Science.gov (United States)

    This NERL-Cincinnati publication, “Methods for the Determination of Chemical Substances in Marine and Estuarine Environmental Matrices - 2nd Edition” was prepared as the continuation of an initiative to gather together under a single cover a compendium of standardized laborato...

  9. Determination of the fission barrier height in fission of heavy radioactive beams induced by the (d,p)-transfer

    CERN Multimedia

    A theoretical framework is described, allowing to determine the fission barrier height using the observed cross sections of fission induced by the (d,p)-transfer with accuracy, which is not achievable in another type of low-energy fission of neutron-deficient nuclei, the $\\beta$-delayed fission. The primary goal is to directly determine the fission barrier height of proton-rich fissile nuclei, preferably using the radio-active beams of isotopes of odd elements, and thus confirm or exclude the low values of fission barrier heights, typically extracted using statistical calculations in the compound nucleus reactions at higher excitation energies. Calculated fission cross sections in transfer reactions of the radioactive beams show sufficient sensitivity to fission barrier height. In the probable case that fission rates will be high enough, mass asymmetry of fission fragments can be determined. Results will be relevant for nuclear astrophysics and for production of super-heavy nuclei. Transfer induced fission of...

  10. Determination of natural radioactivity in irrigation water of drilled wells in northwestern Saudi Arabia.

    Science.gov (United States)

    Alkhomashi, N; Al-Hamarneh, Ibrahim F; Almasoud, Fahad I

    2016-02-01

    The levels of natural radiation in bedrock groundwater extracted from drilled wells in selected farms in the northwestern part of Saudi Arabia were addressed. The investigated waters form a source of irrigation for vegetables, agricultural crops, wheat, and alfalfa to feed livestock consumed by the general public. Information about water radioactivity in this area is not available yet. Therefore, this study strives to contribute to the quality assessment of the groundwater of these wells that are drilled into the non-renewable Saq sandstone aquifer. Hence, gross alpha and beta activities as well as the concentrations of (224)Ra, (226)Ra, (228)Ra, (234)U, (238)U, and U(total) were measured, compared to national and international limits and contrasted with data quoted from the literature. Correlations between the activities of the analyzed radionuclides were discussed. The concentrations of gross alpha and beta activities as well as (228)Ra were identified by liquid scintillation counting whereas alpha spectrometry was used to determine (224)Ra, (226)Ra, (234)U and (238)U after separation from the matrix by extraction chromatography. The mean activity concentrations of gross α and β were 3.15 ± 0.26 Bq L(-1) and 5.39 ± 0.44 Bq L(-1), respectively. Radium isotopes ((228)Ra and (226)Ra) showed mean concentrations of 3.16 ± 0.17 Bq L(-1) and 1.12 ± 0.07 Bq L(-1), respectively, whereas lower levels of uranium isotopes ((234)U and (238)U) were obtained.

  11. Evaluation of natural substances from Evolvulus alsinoides L. with the purpose of determining their antioxidant potency.

    Science.gov (United States)

    Cervenka, Frantisek; Koleckar, Vit; Rehakova, Zuzana; Jahodar, Ludek; Kunes, Jiri; Opletal, Lubomir; Hyspler, Radomir; Jun, Daniel; Kuca, Kamil

    2008-08-01

    In recent years, great attention has been given to the search for natural compounds or extracts with the purpose of medical use. Evolvulus alsinoides L. (Convolvulaceae) is a plant used in traditional medicine of East Asia in many indications and has known nootropic and anti-inflammatory activity. However, the bioactive constituents have been described poorly in the literature. Four substances isolated from the ethanol extract of E. alsinoides by means of polyamide and Silica-gel chromatography are reported here. Their molecular structures were determined using NMR analyses. There were identified as scopoletin, umbelliferone, scopolin and 2-methyl-1,2,3,4-butanetetrol. The quantity of these substances was determined using HPLC-UV and GC-FID detection. Antioxidant activity of the isolated substances was measured by DPPH assay using the SIA method. Antioxidant activity and total phenolic content of the prepared fractions are also described. The prepared fractions and isolated substances did not exhibit any significant activity in DPPH test.

  12. Method to determine the activity concentration and total activity of radioactive waste; Metodo para determinar la concentracion de actividad y actividad total de desechos radiactivos

    Energy Technology Data Exchange (ETDEWEB)

    Angeles C, A

    2001-02-15

    A characteristic system of radioactive waste is described to determine the concentration of radionuclides activity and the total activity of bundles of radioactive waste. The system this integrated by three subsystems: - Elevator of drums. - Electromechanics. - Gamma spectroscopy. In the system it is analyzed waste of issuing gamma specifically, and this designed for materials of relative low density and it analyzes materials of cylindrical recipients.

  13. Method to determine the activity concentration and total activity of radioactive waste; Metodo para determinar la concentracion de actividad y actividad total de desechos radiactivos

    Energy Technology Data Exchange (ETDEWEB)

    Angeles C, A

    2001-02-15

    A characteristic system of radioactive waste is described to determine the concentration of radionuclides activity and the total activity of bundles of radioactive waste. The system this integrated by three subsystems: - Elevator of drums. - Electromechanics. - Gamma spectroscopy. In the system it is analyzed waste of issuing gamma specifically, and this designed for materials of relative low density and it analyzes materials of cylindrical recipients.

  14. Stability-indicating UPLC method for determining related substances and degradants in dronedarone.

    Science.gov (United States)

    Pydimarry, Surya Prakash Rao; Cholleti, Vijay Kumar; Vangala, Ranga Reddy

    2014-08-01

    A simple, sensitive and reproducible method was developed on ultra-performance liquid chromatography coupled with photodiode array detection for the quantitative determination of dronedarone hydrochloride (DRO) in drug substance and pharmaceutical dosage forms. The method is applicable for the quantification of related substances and assays of drug substances. Chromatographic separation was achieved on Acquity UPLC BEH C8 100 mm, 2.1 mm and 1.7 µm columns, using gradient elution within a short run time of 10.0 min. The eluted compounds were monitored at 288 nm, the flow rate was 0.5 mL/min and the column oven temperature was maintained at 40°C. The resolution of DRO and 11 impurities (potentials and by-products) was greater than 2.0 for all pairs of components. The high correlation coefficient value (>0.9995) indicates the clear correlations between the concentrations of investigated compound and their peak areas within the test ranges. The repeatability and intermediate precision, expressed by the relative standard deviation, were less than 2.5%. The accuracy and validity of the method were further ascertained by performing recovery studies via a spike method. The accuracy of the method, expressed as relative error, was satisfactory. No interference was observed from concomitant substances normally added to the tablets. DRO was subjected to the stress conditions of oxidative, acid, base, hydrolytic, thermal and photolytic degradation. DRO was found to degrade significantly in acid and base stress conditions and to remain stable in thermal, photolytic degradation, oxidative and hydrolytic conditions. The degradation products were well resolved from primary peak and its impurities, proving that the method is stability indicating. The developed method was validated as per International Conference on Harmonization guidelines with respect to specificity, limit of detection, limit of quantification, linearity, accuracy, precision, solution stability and robustness

  15. Determination of the isomeric fraction in a postaccelerated radioactive ion beam using the coupled decay-chain equations

    CERN Document Server

    Ekstrom, A; Dijulio, D D; Cederkall, J; Van de Walle, J

    2010-01-01

    A method based on the coupled decay-chain equations for extracting the isotopic and the isomeric composition of a postaccelerated radioactive ion beam is presented and demonstrated on a data set from a Coulomb excitation experiment. This is the first attempt of analyzing the content of a postaccelerated radioactive ion beam using this technique. The beam composition is required for an absolute normalization of the measurement. The strength of the method, as compared to present online-based methods, lies in the determination of the isomeric fraction of a partially isomeric beam using all data accumulated during the experiment. We discuss the limitations and sensitivity of the method with respect to the gamma-ray detection efficiency and the accumulated flux. (C) 2010 Elsevier B.V. All rights reserved.

  16. Simple Electrochemical Determination of Surface-Active Substances in Natural Waters

    Directory of Open Access Journals (Sweden)

    Željka Cvrković-Karloci

    2011-01-01

    Full Text Available A simple electrochemical determination of surface-active substances by using time-dependent variation of the capacitive current in a.c. voltammetry at the HMDE is described. Surface-active substances were accumulated by stirring solution at the deposition potential of −0.6 V versus Ag/AgCl (sat. NaCl. The capacitive current was recorded for different deposition times in the range 0–120 s, wherefrom the linear calibration plot is constructed. The proposed method was verified for model surfactant TritonX-100 in the concentration range 0.02–0.25 mg/L and for humic acid in the concentration range 1.65–20 mg/L. The application of the method was demonstrated for freshwater samples of the Drava river, Danube river, and the wetland Kopački Rit, Croatia. The shape of the i ac -E curves as well as the obtained concentrations of surface-active substances by using humic acid as the calibration substance are quite well describing the type and the nature of organic matter in the freshwater samples.

  17. RADIOACTIVE OR NATURAL TRACER。TECHNIQUES FOR LEAK DETERMINING OF DAM ABUTMENT

    Institute of Scientific and Technical Information of China (English)

    陈建生; 杜国平; 等

    1995-01-01

    Infiltration and localization of preferential infiltration zones at the dam abutment are measured using radioactive tracer tests of flow in boreholes,meanwhile interconnection between boreholes and the energing water points is analysed.The theory and practice of radioactive tracer synthetic detective method are described to give methods and calculation formulae used under the condition of stable flow in single well to measure permeability coefficient and hydrostatic heads.Major single hole techniques including measurement for seepage line,velocity,rate of seepage flow and relationship of recharge of groundwater in aquifers are introduced briefly.The possibilities offered by natureal tracers are analysed,uincluding electric-conduct,pH-value and temperature of water as well as stable isotopes(D,18O) and tritium.Furthermore,the sensibilities of this theory and methods were confirmed by detecting seepage flow field of Xinanjiang Dam.

  18. DETERMINATION OF THE HABITS OF ASTHMATIC PATIENTS ABOUT USING SUBSTANCE CONTAINING PERFUME

    Directory of Open Access Journals (Sweden)

    Ercan GOCGELDI

    2005-06-01

    Full Text Available Introduction: Air pollution, perfume, aerosol substances, odors of paint and detergent are the most important non-specific irritants stimulating the asthmatic attack. The odors of these substances exist for long time and form the serious risk for the asthmatic patients. This study was planned to determine the frequency of using perfume and substance containing perfume and the sensitivities to the substances among the asthmatic patients using inhaling steroid and b2-mimetic ant asthmatic drugs. Methods: This is a descriptive study and conducted among patients who applied to the Allergic Diseases outpatient service of Gulhane Military Medical Academia in October-December 2004. 83 asthmatic patients who accepted to participate to the study filled out a questionnaire that including patients habits relating perfume, cleaners with perfume, perfume for living room, toilets and bathrooms, and having dyspnea or not when exposed any kind of perfumes and using any b2-mimetik or not. Results: 73.5% (n=61 of participants were male, and 26.5 % (n=22 were women. Their ages were from 18 to 57 years. 79.5% (n=66 of participants expressed that they were sensitive to the odors mentioned and experienced the respiratory problems when they were at the surroundings by odour and 26.5% (n=22 of participants sometimes used the B2-mimetic antiasthmatic drugs for this reason. On the other hand; It was found that 68.7% (n=57 of participants regularly used the perfume for themselves everyday, 85.5% (n=71 of participants washed their clothings by using cleaners and/or softeners with perfume, 44.6% (n=37 of participants used the perfume for their rooms frequently, 62.7% (n=52 of participants used substance with perfume in their toilets and bathrooms. Conclusion: We conclude that the asthmatic patients have not sufficient knowledge about non-spesific irritants stimulating the asthmatic attack, and don’t behave sensitive. It’s important to plan properly the medical

  19. Determination and validation of zonisamide and its four related substances by HPLC and UV-spectrophotometry

    Directory of Open Access Journals (Sweden)

    Hosseini Maryam

    2010-01-01

    Full Text Available A selective and sensitive liquid chromatographic method has been developed for simultaneous determination of zonisamide and its four related substances in pharmaceutical dosage forms. The assay involved an isocratic elution in perfectsil Target C18 column using a mobile phase composition of disodium hydrogen phosphate buffer, acetonitrile and methanol (650:150:200 v/v, pH adjusted to 3±0.05 with flow rate 1.2 ml/min and analyte monitored at 240 nm. Also a simple and precise spectrophotometric method was developed for dissolution studies. These proposed methods are sensitive, accurate, reproducible and useful for the routine determination of zonisamide in pharmacy.

  20. Determination of related substances in lisinopril and amlodipine tablets by HPLC

    Institute of Scientific and Technical Information of China (English)

    Dao-Rui Yu; Gui-Fang Yang; Wen-Li Xiao; Jun Wang; Qi-Bing Liu

    2016-01-01

    Objective:To establish an HPLC method for determining the related substances in lisinopril and amlodipine tablets.Methods:An Inertsil Thermo BDS HYPERSIL C18 (4.6 mmí250 mm, 5 μm) column was used with the Acetonitrile-water-phosphoric acid (10:90:0.1) as mobile phase A and Acetonitrile-water-phosphoric acid (90:10:0.1) as mobile phase B by gradient elution at the detection wavelength of 215 nm. The flow rate was 1.0 mL/min and the column temperature was 30℃.Results: The separation of the impurity peak and peak was good. Besides, all the impurities could be detected effectively.Conclusions:The method is sensitive, accurate and selective. It is suitable for control the related substances in lisinopril and Amlodipine tablets.

  1. Substance Use, Depression and Sociodemographic Determinants of HIV Sexual Risk Behavior in Outpatient Substance Abuse Treatment Patients.

    Science.gov (United States)

    Tross, Susan; Feaster, Daniel J; Thorens, Gabriel; Duan, Rui; Gomez, Zoilyn; Pavlicova, Martina; Hu, Mei Chen; Kyle, Tiffany; Erickson, Sarah; Spector, Anya; Haynes, Louise; Metsch, Lisa R

    2015-01-01

    The NIDA Clinical Trials Network trial of rapid HIV testing/counseling in 1281 patients was a unique opportunity to examine relationships among substance use, depressive symptoms, and sex risk behavior. Past 6-month substance use; substance use severity (Drug Abuse Screening Test - 10); depressive symptoms (Quick Inventory of Depressive Symptomatology); and three types of sex risk behavior (unprotected sex occasions [USOs] with primary partners; USOs with nonprimary partners; and USOs while high/drunk) were assessed. Zero-inflated negative binomial analyses provided: probability and rate of sex risk behavior (in risk behavior subsample). Levels of sexual risk behavior were high, while variable across the three types of sex risk behaviors. Among the patients, 50.4% had engaged in USOs with primary partners, 42% in sex while drunk or high, and 23.8% in USOs with nonprimary partners. Similar factors were significantly associated with all three types of sex risk behaviors. For all types, problem drinking, cocaine use, and substance use severity had an exacerbating effect. Older age was associated with lower risk behavior; other relationship categories (eg, married, separated/divorced, cohabitating) were associated with greater risk behavior than was single status. Depressive symptoms were associated with decreased likelihood of USOs with a primary partner. Sexual risk behavior is common among individuals in outpatient substance abuse treatment. Results highlight problem drinking (eg, up to three-fold) and cocaine (eg, up to twice) in increasing sex risk behavior. They demonstrate the utility of distinguishing between partner types and presence/absence of alcohol/drugs during sex. Findings argue for the need to integrate sex risk reduction into drug treatment.

  2. Experimental determination of the shipboard fire environment for simulated radioactive material packages

    Energy Technology Data Exchange (ETDEWEB)

    Koski, J.A.; Bobbe, J.G.; Arviso, M. [and others

    1997-03-01

    A series of eight fire tests with simulated radioactive material shipping containers aboard the test ship Mayo Lykes, a break-bulk freighter, is described. The tests simulate three basic types of fires: engine room fires, cargo fires and open pool fires. Detailed results from the tests include temperatures, heat fluxes and air flows measured during the fires. The first examination of the results indicates that shipboard fires are not significantly different from fires encountered in land transport. 13 refs., 15 figs., 11 tabs.

  3. [Evaluation of pharmacopoeia methods for determination of antimicrobial agents, especially of natural substances].

    Science.gov (United States)

    Brantner, A

    1997-01-01

    Microbiological assays referring to antibiotics were first mentioned in 1955 in the US Pharmacopedia XV and in the Pharmacopedia of India I. In the pharmacopedias two general methods are employed: The first group of methods is grounded on diffusion (disc assay, cylinder-plate and hole-plate assay), the second one is based on the determination of optical density (turbidimetric method). Both methods involve certain problems, particularly with respect to the testing of low-active natural substances. In the course of our investigations those test methods were evaluated and the advantages and disadvantages discussed. The methods were compared to test systems not being described in the pharmacopedias (microdilution test, bioautographic TLC assay). In addition to that we examined spectrophotometrically (OD580nm) the influence of an antimicrobial substance and of a solutizer on the bacterial growth. Tetracycline hydrochloride was used as reference and naringenin as test substance. The results were analyzed with statistical methods cited in the pharmacopedias, e.g. straight-line method and compared to other common methods, e.g. analysis of variance.

  4. Review of international normatives for natural radioactivity determination in building materials

    Directory of Open Access Journals (Sweden)

    Mossini Eros

    2015-09-01

    Full Text Available Anthropogenic activities, such as high-altitude flights and living in buildings, have enhanced the public exposure to natural radiation. In particular, 40K and radionuclides belonging to 232Th and 238U decay chains are present even in building materials, and they may be considered as partially responsible for the effective dose coming from natural radioactivity. Scientists and governments have devoted great attention to the evaluation of the effects produced on the public by naturally occurring radionuclides. In this context, to evaluate the building materials acceptability, accurate and reliable methods for the measurement of the specific activity of natural radioactive isotopes in building materials have been developed. This paper aims to provide a clear and exhaustive review on natural radionuclide measurement procedures. Several standard national normatives (Dutch NEN 5697, Italian UNI 10797, Polish ITB 455, based on gamma spectrometry, have been considered and some critical issues were identified regarding the preparation and the radiometric measuring of the samples. Therefore, the direct measurement of 238U and 232Th by ICP-MS spectrometry as well as the extrapolation of the specific activities without waiting for secular equilibrium have been considered as two promising alternative approaches.

  5. A Simple Spectrophotometric Method for the Determination of Thiobarbituric Acid Reactive Substances in Fried Fast Foods

    Directory of Open Access Journals (Sweden)

    Alam Zeb

    2016-01-01

    Full Text Available A simple and highly sensitive spectrophotometric method was developed for the determination of thiobarbituric acid reactive substances (TBARS as a marker for lipid peroxidation in fried fast foods. The method uses the reaction of malondialdehyde (MDA and TBA in the glacial acetic acid medium. The method was precise, sensitive, and highly reproducible for quantitative determination of TBARS. The precision of extractions and analytical procedure was very high as compared to the reported methods. The method was used to determine the TBARS contents in the fried fast foods such as Shami kebab, samosa, fried bread, and potato chips. Shami kebab, samosa, and potato chips have higher amount of TBARS in glacial acetic acid-water extraction system than their corresponding pure glacial acetic acid and vice versa in fried bread samples. The method can successfully be used for the determination of TBARS in other food matrices, especially in quality control of food industries.

  6. Quality analysis of Iranian crack referred to Forensic Department of Khuzestan to determine substances affecting dementia

    Directory of Open Access Journals (Sweden)

    Ali Hassan Rahmani

    2016-12-01

    Full Text Available Pharmaceutical drug abuse refers to conscious consumption of drugs for non-medical purposes such as changing the mood, and fitness, etc. Iranian crack (street crock is one of the most abused drugs in Iran. This crack has different medicinal compounds, synthetic, adulterants that have pharmacological structure. Determining type and amount of compounds of Iranian crack and its impact on individuals’ performance, creation of dementia and abnormal behavior, and crime rate are considered as objectives of this study. In this cross-sectional study, 61 crock sampleswere analyzed in forensic toxicology laboratory of Khuzestan. Samples were evaluated usingthin layer chromatography (TLC. Verification tests and identification of pharmaceutical substances were performed qualitatively by HPLC and GC / MS methods. Statistical examination of data by SPSS (V22 (p value <0.05 indicated that 93. 4 % of crack samples contained morphine, 83,6% of them contained caffeine, noscapine and dextromethorphan, 27.9% of them contained heroin and codeine, 37.7 of them contained monoacetyl morphine, 34.4% of them contained acetyl codeine, and 13.1% of them contained narceine and acetaminophen. Other compounds included methyl amphetamines, diphenhydramine, lidocaine, thebaine, amoxicillin, amitriptyline, and nortriptyline. In addition, 6.6% of samples were combination of methyl amphetamine, diphenhydramine and acetaminophen, playing an important role in dementia and mental illness similar to schizophrenia due to presence of amphetamine. Iranian crack not only differs from real crack (cocaine, but also they differ in terms of variety and amount of adulterants, opioid, and diluent substances. In fact, crack has different amounts of substances affecting central nervous system, and other drugs and substances play important role with their pharmacological and non-pharmacological properties in this regard.

  7. Penetration studies of topically applied substances: Optical determination of the amount of stratum corneum removed by tape stripping.

    Science.gov (United States)

    Lademann, J; Ilgevicius, A; Zurbau, O; Liess, H D; Schanzer, S; Weigmann, H J; Antoniou, C; Pelchrzim, R V; Sterry, W

    2006-01-01

    Tape stripping is a standard measuring method for the investigation of the dermatopharmacokinetics of topically applied substances using adhesive films. These tape strips are successively applied and removed from the skin after application and penetration of topically applied substances. Thus, layers of corneocytes and some amount of topical applied substances are removed. The amount of substances and the amount of stratum corneum removed with a single tape strip has to be determined for the calculation of the penetration profile. The topically applied substances removed from the skin can be determined by classical analytical methods like high-pressure liquid chromatography, mass spectroscopy, and spectroscopic measurements. The amount of corneocytes on the tape strips can be easily detected by their pseudoabsorption. In the present paper, an easy and cheap corneocyte density analyzer is presented that is based on a slide projector. Comparing the results of the measurements obtained by the corneocyte density analyzer and by uv-visible spectrometry, identical results were obtained.

  8. Determination of Heavy Metal and Radioactivity in Agaricus campestris Mushroom Collected from Kahramanmaraş and Erzurum Proviences

    Directory of Open Access Journals (Sweden)

    Aysenur Yilmaz

    2016-03-01

    Full Text Available In this study, radioactivity and heavy metals accumulations in Agaricus campestris mushroom collected from Kahramanmaraş and Erzurum provinces was determined. HPGe gamma detector was used for the determination of radioactivity concentrations. Heavy metal content was measured using a ICP-MS. As radioactive element; natural (238U, 232Th 40K and artificial radionuclide (137Cs concentrations were determined. The values of the committed effective dose were calculated. Same measurements were made in soils. Absorbed dose and excess lifetime cancer risk were calculated. Amount of Mg, Al, Ca, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Cd, Pb206, Pb207 and Pb208 as heavy metals of mushrooms were determined. 238U, 232Th, 40K activity concentrations of mushroom collected from Erzurum was determined as 12.1 ± 0.8, 11.7 ± 0.9, 497.7 ± 17.8 Bq/kg, respectively and 137Cs was not detected by system. 232Th and 40K activity concentrations of mushroom collected from Kahramanmaraş was determined as 13.4 ± 0.5, 134.9 ± 6.3 Bq/kg, respectively, 238U and 137Cs was not detected by system similarly. The value of the committed effective dose collected from Erzurum and Kahramanmaraş were calculated as 75 and 29 μSv respectively and these values were found lower than 290 μSv accepted as world average. Absorbed dose and risk of lifetime cancer for Erzurum was determined as 37.39 nGy/h, 16.5 x 10-5; absorbed dose and excess lifetime cancer risk for Kahramanmaraş was determined as 30.92 nGy/h, 13.3 x 10-5 respectively. Amount of daily intake for each heavy metal was calculated. Radionuclide activity concentrations and accumulations of heavy metal were not founded threaten level to healthy, except from arsenic As (0.025 and 0.039 mg/kg in mushroom collected from both provinces. They were found a bit higher than upper limit (0.015 mg/kg in report which is prepared World Health Organization (WHO and Food and Agriculture Organization of the United Nations (FAO jointly.

  9. Radioactivity measurements principles and practice

    CERN Document Server

    Mann, W B; Spernol, A

    2012-01-01

    The authors have addressed the basic need for internationally consistent standards and methods demanded by the new and increasing use of radioactive materials, radiopharmaceuticals and labelled compounds. Particular emphasis is given to the basic and practical problems that may be encountered in measuring radioactivity. The text provides information and recommendations in the areas of radiation protection, focusing on quality control and the precautions necessary for the preparation and handling of radioactive substances. New information is also presented on the applications of both traditiona

  10. Determination of Medronic Acid and Its Related Substances by Reversed-Phase High-Performance Liquid Chromatography

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    An isocratic liquid chromatographic method with evaporative light scattering detection (ELSD) was developed for the determination of medronic acid and its related substance. Volatile pentylamine was used as ion-pairing agent. Separations were performend

  11. Using Geographic Information Systems to Determine Site Suitability for a Low-Level Radioactive Waste Storage Facility.

    Science.gov (United States)

    Wilson, Charles A; Matthews, Kennith; Pulsipher, Allan; Wang, Wei-Hsung

    2016-02-01

    Radioactive waste is an inevitable product of using radioactive material in education and research activities, medical applications, energy generation, and weapons production. Low-level radioactive waste (LLW) makes up a majority of the radioactive waste produced in the United States. In 2010, over two million cubic feet of LLW were shipped to disposal sites. Despite efforts from several states and compacts as well as from private industry, the options for proper disposal of LLW remain limited. New methods for quickly identifying potential storage locations could alleviate current challenges and eventually provide additional sites and allow for adequate regional disposal of LLW. Furthermore, these methods need to be designed so that they are easily communicated to the public. A Geographic Information Systems (GIS) based method was developed to determine suitability of potential LLW disposal (or storage) sites. Criteria and other parameters of suitability were based on the Code of Federal Regulation (CFR) requirements as well as supporting literature and reports. The resultant method was used to assess areas suitable for further evaluation as prospective disposal sites in Louisiana. Criteria were derived from the 10 minimum requirements in 10 CFR Part 61.50, the Nuclear Regulatory Commission's Regulatory Guide 0902, and studies at existing disposal sites. A suitability formula was developed permitting the use of weighting factors and normalization of all criteria. Data were compiled into GIS data sets and analyzed on a cell grid of approximately 14,000 cells (covering 181,300 square kilometers) using the suitability formula. Requirements were analyzed for each cell using multiple criteria/sub-criteria as well as surrogates for unavailable datasets. Additional criteria were also added when appropriate. The method designed in this project proved to be sufficient for initial screening tests in determining the most suitable areas for prospective disposal (or storage

  12. Determination of radon concentration in soil air and in the radioactive spring's bathroom air by passive method

    Energy Technology Data Exchange (ETDEWEB)

    Horiuchi, Kimiko [Otsuma Women' s Univ., School of Social Information Studies, Tama, Tokyo (Japan); Ishii, Tadashi [Yamanashi Medical Univ., Radioisotope Lab., Tamaho, Yamanashi (Japan)

    2002-06-01

    There are many kind of passive methods such as open vial method, {alpha}-track method and active carbon method (PICO-RAD detector) or so. The open vial method can determine radon in soil air, which dissolves easily into toluene and afterwards can be measured by the integral counting with a liquid scintillation counter. The {alpha}-track method can record {alpha} ray tracks of radon on thin cellulose nitrate film which can be rendered visible for counting after NaOH solution treatment. The PICO-RAD detectors are passive devices requiring no power. They are integrating detectors used to determine the average radon concentration in air where they are placed. The detectors consist of a plastic liquid scintillation vial which consists a porous canister held securely near the top of the vial. The porous canister contains a bed of a controlled weight of charcoal covered by a layer of desiccant. The securely capped canister has and indefinite shelf life. The {alpha} radioactivity of radon gas adsorbed in fine active charcoal exposed in the air is measured with a liquid scintillation counter. Using of those simple detectors, we have measured distribution of radon concentration in soil air and in the radioactive spring's bathroom air. (author)

  13. [Simultaneous determination of four common nonprotein nitrogen substances in urine by high performance liquid chromatography].

    Science.gov (United States)

    Ma, Yuhua; Huang, Dongqun; Zhang, Rui; Xu, Shiru; Feng, Shun

    2013-11-01

    A high performance liquid chromatographic (HPLC) method was proposed to simultaneously determine four common nonprotein nitrogen substances, including creatine (Cr), creatinine (Cn), uric acid (Ua) and pseudouridine (Pu) in urine. After proteins being removed by acetone precipitation method, freeze drying and redissolving, the urine samples were analyzed by HPLC. Chromatographic separation was performed on a Waters RP18 Column (150 mm x 4.60 mm, 3.5 microm) in gradient elution mode using 10.0 mmol/L KH2PO4 solution (pH 4.78) and acetonitrile as mobile phases at a flow rate of 0.8 mL/min. The samples were detected at 220 nm. Rapid separation was achieved within 7 min. Under the optimized conditions, good linearities of four common nonprotein nitrogen substances were obtained in the range of 0.1-250 mg/L. The detection limits were 9.31 (Cr), 26.19 (Cn), 4.70 (Ua), an 6.30 (Pu) microg/L and the recoveries were in the range of 81%-111% with the relative standar deviations of 0.23%-2.78% (n = 3). The results demonstrate that this method is simple, rapid and accurate with good reproducibility, and can provide early diagnosis and preliminary judgment for type 2 diabetes mellitus (T2DM) patients with renal damage.

  14. Determination of Erosion/Corrosion Rates in Hanford Tank Farms Radioactive Waste Transfer System Pipelines

    Energy Technology Data Exchange (ETDEWEB)

    Washenfelder, D. J.; Girardot, C. L.; Wilson, E. R.; Page, J. A.; Engeman, J. K.; Gunter, J. R.; Johnson, J. M.; Baide, D. G.; Cooke, G. A.; Larson, J. D.; Castleberry, J. L.; Boomer, K. D.

    2015-11-05

    The twenty-eight double-shell underground radioactive waste storage tanks at the U. S. Department of Energy’s Hanford Site near Richland, WA are interconnected by the Waste Transfer System network of buried steel encased pipelines and pipe jumpers in below-grade pits. The pipeline material is stainless steel or carbon steel in 51 mm to 152 mm (2 in. to 6 in.) sizes. The pipelines carry slurries ranging up to 20 volume percent solids and supernatants with less than one volume percent solids at velocities necessary to prevent settling. The pipelines, installed between 1976 and 2011, were originally intended to last until the 2028 completion of the double-shell tank storage mission. The mission has been subsequently extended. In 2010 the Tank Operating Contractor began a systematic evaluation of the Waste Transfer System pipeline conditions applying guidelines from API 579-1/ASME FFS-1 (2007), Fitness-For-Service. Between 2010 and 2014 Fitness-for-Service examinations of the Waste Transfer System pipeline materials, sizes, and components were completed. In parallel, waste throughput histories were prepared allowing side-by-side pipeline wall thinning rate comparisons between carbon and stainless steel, slurries and supernatants and throughput volumes. The work showed that for transfer volumes up to 6.1E+05 m3 (161 million gallons), the highest throughput of any pipeline segment examined, there has been no detectable wall thinning in either stainless or carbon steel pipeline material regardless of waste fluid characteristics or throughput. The paper describes the field and laboratory evaluation methods used for the Fitness-for-Service examinations, the results of the examinations, and the data reduction methodologies used to support Hanford Waste Transfer System pipeline wall thinning conclusions.

  15. Management of radioactive waste: A review

    Directory of Open Access Journals (Sweden)

    Luis Paulo Sant'ana

    2016-06-01

    Full Text Available The issue of disposal of radioactive waste around the world is not solved by now and the principal reason is the lack of an efficient technologic system. The fact that radioactive waste decays of radioactivity with time are the main reasons for setting nuclear or radioactive waste apart from the other common hazardous wastes management. Radioactive waste can be classified according to the state of matter and level of radioactivity and this classification can be differently interpreted from country to country. Furthermore, microbiological procedures, plasma vitrification process, chemical precipitation, ion exchange, evaporation and reverse osmosis are strategies used for the treatment of radioactive wastes. The major challenge is to manage these radioactive substances after being used and discharged. This report brings data from the literature published worldwide from 2009 to 2014 on radioactive waste management studies and it covers production, classification and management of radioactive solid, liquid and gas waste.

  16. Determination of strontium in drinking water and consequences of radioactive elements present in drinking water for human health

    Directory of Open Access Journals (Sweden)

    Rajković Miloš B.

    2006-01-01

    Full Text Available In this paper the analysis of strontium and uranium content in drinking water has been done, indirectly, according to the scale which originates from drinking water in water-supply system of the city of Belgrade. Gamaspectrometric analysis showed the presence of free natural radionuclide in low activities. The activity of 90Sr in scale which is 0.72±0.11 Bq/kg was determined by radiochemical. Because of the small quantities of fur in the house heater this activity can be considered as irrelevant, but the accumulation of scale can have intensified influence. In this paper, the analysis of effects of the radioactive isotopes presence (first of all 238U and 235U in drinking water on human health has been done. .

  17. Study on radioactive material management plan and environmental analysis of water (I) study of radioactive substance in water management and analyse to eat of the US environmental protection agency (environmental protection agency)

    Energy Technology Data Exchange (ETDEWEB)

    Her, Jae; Min, Hye Lim; Han, Seong Gyu; Lim, Hyun Jong; Jo, Han Byeol; Noh, Young Hoon; Lee, Ho Sun [Dept. of Bio-convergence Engineering, Graduate School of Korea University, Seoul (Korea, Republic of); Kim, Jung Min [Dept. of Radiological Science, Korea University, Seoul (Korea, Republic of); Park, Min Suk [Korea Institute of Radiological and Medical Sciences, Seoul (Korea, Republic of)

    2015-06-15

    The interest of the people in the radioactive contamination of the water has increased significantly and the study about analysis and management of radioactive materials are being actively conducted. And monitoring spots have been expanded to the range of public water as well as drinking water by publishing the rule of drinking water quality standards and examination in the Environmental Enforcement Ordinance No. 553 of Korea. In this study, US EPA was investigated as the foreign advanced cases and the way that is appropriate for the Korea was sought by analyzing investigate radionuclide, interval and management. As a result, in the selection part of investigate radionuclide, geological survey, status of nuclear power plants and the presence of the use of artificial radionuclides of the Korea should be investigated and additionally after the selection of a few radionuclides, the systems should be extended to cover all possible radionuclides by considering radioactive pollution levels in humans may be exposed due to the annual drinking water. In the part of the investigate interval, the concept(MCL, DL) should be set up for preventing concentration detection of above MCL and it needs to the maintenance and management. For example, when the concentration is more than MCL, it should be investigated on a quarterly and when the concentration is lower than MCL, it should be investigated to each different interval and management. And the US EPA divided the management area and make the road map for managing drinking water. The each classified area has been organized to match the state budget and labor force and the individual data have been managed effectively by HPGe, the NaI, TLD and so on.

  18. Recent trends in analytical methods to determine new psychoactive substances in hair.

    Science.gov (United States)

    Kyriakou, Chrystalla; Pellegrini, Manuela; García-Algar, Oscar; Marinelli, Enrico; Zaami, Simona

    2016-11-11

    New Psychoactive Substances (NPS) belong to several chemical classes, including phenethylamines, piperazines, synthetic cathinones and synthetic cannabinoids. Development and validation of analytical methods for the determination of NPS both in traditional and alternative matrices is of crucial importance to study drug metabolism and to associate consumption to clinical outcomes and eventual intoxication symptoms. Among different biological matrices, hair is the one with the widest time window to investigate drug-related history and demonstrate past intake. The aim of this paper was to overview the trends of the rapidly evolving analytical methods for the determination of NPS in hair and the usefulness of these methods when applied to real cases. A number of rapid and sensitive methods for the determination of NPS in hair matrix has been recently published, most of them using liquid chromatography coupled to mass spectrometry. Hair digestion and subsequent solid phase extraction or liquid-liquid extraction were described as well as extraction in organic solvents. For most of the methods limits of quantification at picogram per milligram hair were obtained. The measured concentrations for most of the NPS in real samples were in the range of picograms of drug per milligram of hair. Interpretation of the results and lack of cut-off values for the discrimination between chronic consumption and occasional use or external contamination are still challenging. Methods for the determination of NPS in hair are continually emerging to include as many NPS as possible due to the great demand for their detection.

  19. Advance in radioactive decontamination; Avances en descontaminacion radiactiva

    Energy Technology Data Exchange (ETDEWEB)

    Basteris M, J. A. [Universidad Autonoma de Yucatan, Facultad de Medicina, Departamento de Diagnostico por Laboratorio y Gabinete, Av. Cupules No. 232, Col. Garcia Gineres, 97070 Merida, Yucatan (Mexico); Farrera V, R., E-mail: basteris@prodigy.net.m [Hospital de Especialidades de la UMAE, Centro Medico Nacional Ignacio Garcia Tellez, Departamento de Medicina Nuclear, Calle 34 x 41, Exterrenos el Fenix s/n, Col. Industrial, 91750 Merida, Yucatan (Mexico)

    2010-09-15

    The objective of the present work was to determine if the application of the Na hypochlorite has some utility in the radioactive decontamination, in comparison with the water, detergent and alcohol. Several methods were compared for decontaminate the iodine 131 and technetium 99, the work table and the skin it was carried out an initial count with the Geiger Muller. Later on, in a single occasion, the areas were washed with abundant water, alcohol, clothes detergent and sodium hypochlorite (used commercially as domestic bleacher) without diluting. Observing that the percentage in the decrease of the counted radioactivity by the Geiger Muller, decreased in the following way: It was demonstrated that the Na hypochlorite presents the highest index of radioactive decontamination with 100% of effectiveness. The Na hypochlorite is an excellent substance that can be used with effectiveness and efficiency like decontamination element in the accident cases of radioactive contamination in the clinical laboratories of nuclear medicine. (Author)

  20. Determination of Critical Parameters of Drug Substance Influencing Dissolution: A Case Study

    Directory of Open Access Journals (Sweden)

    Erika Bojnanska

    2014-01-01

    Full Text Available The purpose of this study was to specify critical parameters (physicochemical characteristics of drug substance that can affect dissolution profile/dissolution rate of the final drug product manufactured by validated procedure from various batches of the same drug substance received from different suppliers. The target was to design a sufficiently robust drug substance specification allowing to obtain a satisfactory drug product. For this reason, five batches of the drug substance and five samples of the final peroral drug products were analysed with the use of solid state analysis methods on the bulk level. Besides polymorphism, particle size distribution, surface area, zeta potential, and water content were identified as important parameters, and the zeta potential and the particle size distribution of the drug substance seem to be critical quality attributes affecting the dissolution rate of the drug substance released from the final peroral drug formulation.

  1. Prevalence and Socio-Demographic Determinants of Tobacco, Alcohol, Substance Use and Drug Misuse in General Population in Turkey.

    Science.gov (United States)

    Ilhan, Mustafa Necmi; Arikan, Zehra; Kotan, Zeynep; Tunçoğlu, Tolga; Pinarci, Mustafa; Taşdemir, Ahmet; Ay, Bülent; Koçak, Nadir

    2016-09-01

    The aim of the current study is to determine prevalence ratios of tobacco, alcohol, substance use and drug misuse in a large scale sample of general population and recognize related socio-demographic factors. The study was based on a cross-sectional survey conducted with a nationally representative sample of 8045 individuals with face-to-face, in-house interviews implemented by a trained team of interviewers. Life-time prevalences of tobacco, alcohol, substance use and drug misuse are 51.8%, 28.3%, 2.8% and 10.5% respectively. Age, gender, education level and marital status are important socio-demographic determinants for tobacco, alcohol use and drug misuse. Income level is an important determinant for alcohol and substance use. Tobacco, alcohol, substance use and drug misuse are significant health concerns in Turkey. Socio-demographic status is an important determinant of several aspects of tobacco, alcohol, substance use and drug misuse and should therefore be evaluated carefully to develop effective protective and preventive strategies.

  2. Radioactivity determination of sealed pure beta-sources by surface dose measurements and Monte Carlo simulations

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Chang Heon [Interdisciplinary Program in Radiation Applied Life Science, Seoul National University College of Medicine, Seoul (Korea, Republic of); Jung, Seongmoon [Program in Biomedical Radiation Sciences, Department of Transdisciplinary Studies, Graduate School of Convergence Science and Technology, Seoul National University, Seoul (Korea, Republic of); Choi, Kanghyuk; Son, Kwang-Jae; Lee, Jun Sig [Hanaro Applications Research, Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of); Ye, Sung-Joon, E-mail: sye@snu.ac.kr [Interdisciplinary Program in Radiation Applied Life Science, Seoul National University College of Medicine, Seoul (Korea, Republic of); Program in Biomedical Radiation Sciences, Department of Transdisciplinary Studies, Graduate School of Convergence Science and Technology, Seoul National University, Seoul (Korea, Republic of); Center for Convergence Research on Robotics, Advance Institutes of Convergence Technology, Seoul National University, Suwon (Korea, Republic of)

    2016-04-21

    This study aims to determine the activity of a sealed pure beta-source by measuring the surface dose rate using an extrapolation chamber. A conversion factor (cGy s{sup −1} Bq{sup −1}), which was defined as the ratio of surface dose rate to activity, can be calculated by Monte Carlo simulations of the extrapolation chamber measurement. To validate this hypothesis the certified activities of two standard pure beta-sources of Sr/Y-90 and Si/P-32 were compared with those determined by this method. In addition, a sealed test source of Sr/Y-90 was manufactured by the HANARO reactor group of KAERI (Korea Atomic Energy Research Institute) and used to further validate this method. The measured surface dose rates of the Sr/Y-90 and Si/P-32 standard sources were 4.615×10{sup −5} cGy s{sup −1} and 2.259×10{sup −5} cGy s{sup −1}, respectively. The calculated conversion factors of the two sources were 1.213×10{sup −8} cGy s{sup −1} Bq{sup −1} and 1.071×10{sup −8} cGy s{sup −1} Bq{sup −1}, respectively. Therefore, the activity of the standard Sr/Y-90 source was determined to be 3.995 kBq, which was 2.0% less than the certified value (4.077 kBq). For Si/P-32 the determined activity was 2.102 kBq, which was 6.6% larger than the certified activity (1.971 kBq). The activity of the Sr/Y-90 test source was determined to be 4.166 kBq, while the apparent activity reported by KAERI was 5.803 kBq. This large difference might be due to evaporation and diffusion of the source liquid during preparation and uncertainty in the amount of weighed aliquot of source liquid. The overall uncertainty involved in this method was determined to be 7.3%. We demonstrated that the activity of a sealed pure beta-source could be conveniently determined by complementary combination of measuring the surface dose rate and Monte Carlo simulations.

  3. Cluster Radioactivity

    Science.gov (United States)

    Poenaru, Dorin N.; Greiner, Walter

    One of the rare examples of phenomena predicted before experimental discovery, offers the opportunity to introduce fission theory based on the asymmetric two center shell model. The valleys within the potential energy surfaces are due to the shell effects and are clearly showing why cluster radioactivity was mostly detected in parent nuclei leading to a doubly magic lead daughter. Saddle point shapes can be determined by solving an integro-differential equation. Nuclear dynamics allows us to calculate the half-lives. The following cluster decay modes (or heavy particle radioactivities) have been experimentally confirmed: 14C, 20O, 23F, 22,24-26Ne, 28,30Mg, 32,34Si with half-lives in good agreement with predicted values within our analytical superasymmetric fission model. The preformation probability is calculated as the internal barrier penetrability. An universal curve is described and used as an alternative for the estimation of the half-lives. The macroscopic-microscopic method was extended to investigate two-alpha accompanied fission and true ternary fission. The methods developed in nuclear physics are also adapted to study the stability of deposited atomic clusters on the planar surfaces.

  4. Clinical implications of reinforcement as a determinant of substance use disorders.

    Science.gov (United States)

    Higgins, Stephen T; Heil, Sarah H; Lussier, Jennifer Plebani

    2004-01-01

    Extensive scientific evidence indicates that reinforcement plays an important role in the genesis, maintenance, and recovery from substance use disorders. In this chapter, we review recent clinical research from laboratory, clinic, and naturalistic settings examining the role of reinforcement in substance use disorders. Well-controlled human laboratory studies are reviewed characterizing orderly interactions between the reinforcing effects of drugs and environmental context that have important implications for understanding risk factors for substance use disorders and for the development of efficacious interventions. Recent treatment-outcome studies on voucher-based contingency management and community reinforcement therapy are reviewed demonstrating how reinforcement and related principles can be used to improve outcomes across a wide range of different substance use disorders and populations. Overall, the chapter characterizes a vigorous area of clinical research that has much to contribute to a scientific analysis of substance use disorders.

  5. The evaluation of an analytical protocol for the determination of substances in waste for hazard classification

    Energy Technology Data Exchange (ETDEWEB)

    Hennebert, Pierre, E-mail: pierre.hennebert@ineris.fr [INERIS – Institut National de l’Environnement Industriel et des Risques, Domaine du Petit Arbois BP33, F-13545 Aix-en-Provence (France); Papin, Arnaud [INERIS, Parc Technologique ALATA, BP No. 2, 60550 Verneuil en Halatte (France); Padox, Jean-Marie [INERIS – Institut National de l’Environnement Industriel et des Risques, Domaine du Petit Arbois BP33, F-13545 Aix-en-Provence (France); Hasebrouck, Benoît [INERIS, Parc Technologique ALATA, BP No. 2, 60550 Verneuil en Halatte (France)

    2013-07-15

    Highlights: • Knowledge of wastes in substances will be necessary to assess HP1–HP15 hazard properties. • A new analytical protocol is proposed for this and tested by two service laboratories on 32 samples. • Sixty-three percentage of the samples have a satisfactory analytical balance between 90% and 110%. • Eighty-four percentage of the samples were classified identically (Seveso Directive) for their hazardousness by the two laboratories. • The method, in progress, is being normalized in France and is be proposed to CEN. - Abstract: The classification of waste as hazardous could soon be assessed in Europe using largely the hazard properties of its constituents, according to the the Classification, Labelling and Packaging (CLP) regulation. Comprehensive knowledge of the component constituents of a given waste will therefore be necessary. An analytical protocol for determining waste composition is proposed, which includes using inductively coupled plasma (ICP) screening methods to identify major elements and gas chromatography/mass spectrometry (GC–MS) screening techniques to measure organic compounds. The method includes a gross or indicator measure of ‘pools’ of higher molecular weight organic substances that are taken to be less bioactive and less hazardous, and of unresolved ‘mass’ during the chromatography of volatile and semi-volatile compounds. The concentration of some elements and specific compounds that are linked to specific hazard properties and are subject to specific regulation (examples include: heavy metals, chromium(VI), cyanides, organo-halogens, and PCBs) are determined by classical quantitative analysis. To check the consistency of the analysis, the sum of the concentrations (including unresolved ‘pools’) should give a mass balance between 90% and 110%. Thirty-two laboratory samples comprising different industrial wastes (liquids and solids) were tested by two routine service laboratories, to give circa 7000 parameter

  6. Determination of environmental radioactivity (238U, 232Th and 40K) and indoor natural background radiation level in Chennai city (Tamilnadu State), India.

    Science.gov (United States)

    Babai, K S; Poongothai, S; Punniyakotti, J

    2013-01-01

    An extensive study on the determination of the natural radioactivity ((238)U, (232)Th and (40)K) levels in soil samples of Chennai city, India has been undertaken and the results of the same are compared with the levels reported in other Indian cities as well as other parts of the world. The radioactivity content in the soil samples, the absorbed dose rate, annual effective dose equivalent, radium equivalent activity, internal and external hazard indices were calculated and compared with UNSCEAR 2000 recommended values. In addition to the above, mapping of indoor natural background gamma radiation levels has been made using thermo luminescent dosemeters throughout Chennai city and the same are reported.

  7. Analitical determination of substances subject to authorization or restriction in detergents and cleaning products

    Directory of Open Access Journals (Sweden)

    Pedro José Úbeda Ruiz

    2015-12-01

    Full Text Available The presence of the phthalates di-n-dibutyl phthalate, bis(2-ethylhexyl phthalate and benzyl butyl phthalate, the alkylphenols nonylphenol and nonylphenol ethoxylates, and 2-(2-Methoxyethoxyethanol (DEGME was determined and quanti ed in 26 detergents and cleaning products for domestic use. These chemicals are subject to authorization and restriction (REACH Regulation. Chromatography was used for separation (reverse-phase liquid chromatography for phthalates and alkylphenols, and gas chromatography for glycol ethers, and mass spectrometry for detection. Phthalates were detected in all samples. Phthalate concentrations were below the authorization limit for mixtures. Nonylphenol was present in a concentration that was relatively lower than those of nonylphenol ethoxylates. Alkylphenol concentrations were below the restriction level on the sale and use of domestic cleaning products. DEGME concentrations were below the restriction level on the sale of cleaning products to the general public. In sum, the concentrations of the di erent analyzed substances were below the concentration levels requiring authorization or restriction under the REACH Regulation.

  8. Determination of humic substances in natural waters by cathodic stripping voltammetry of their complexes with iron.

    Science.gov (United States)

    Laglera, Luis M; Battaglia, Gianluca; van den Berg, Constant M G

    2007-09-05

    A new voltammetric method is presented for the measurement of humic substances (HS) in natural waters. The method is based on catalytic cathodic stripping voltammetry (CSV) and makes use of adsorptive properties of iron-HS complexes on the mercury drop electrode at natural pH. A fulvic acid standard (IHSS) was used to confirm the voltammetric response (peak potential and sensitivity) for the HS for natural water samples. Optimized conditions included the linear-sweep mode, deposition at -0.1 V, pH buffered at 8 and a scan rate of 50 mV s(-1). At a deposition time of 240 s in the presence of 10 nM iron and 30 mM bromate, the detection limit was 5 microg L(-1) HS in seawater, which could be lowered further by an increase in the bromate concentration, or in the adsorption time. The method was used to determine HS in the Irish Sea which were found to occur at levels between 60 and 600 microg L(-1). The new method is sufficiently sensitive to detect the low HS content in oceanic samples and has implications to the study of iron speciation.

  9. Radioactive Substances Act 1993 - annex document. To accompany the explanatory document and draft authorisation prepared by the Environment Agency to assist public consultation on the application by Devonport Royal Dockyard Limited to dispose of radioactive wastes from Devonport Royal Dockyard Plymouth

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2000-07-01

    This document constitutes Devonport Royal Dockyard Limited' s (DML) application to vary its authorisations to dispose of radioactive wastes from Devonport Royal Dockyard (DRD). The document describes the radioactive waste arisings from existing and future facilities at DRD and the way these wastes are handled and treated on site from generation to disposal. It also serves to present to a wider audience DML's activities and plans for radioactive waste management, and the 'benefits and detriments of the activities giving rise to radioactive wastes. DML's current Authorisations, granted in 1997, cover its refuelling, refitting and general maintenance activities on the so-called 'Hunter-killer' nuclear powered submarines. Following Ministerial approval, DRD is being modernised and enhanced. This will bring existing dock structures, refuelling facilities, and services in line with latest standards, and also provide new facilities to support the refit and refuel of the new Vanguard class ballistic missile carrying nuclear powered submarines. To cover these additional activities, revised authorisations - which in some cases include increased disposal limits - are being requested tinder the Radioactive Substances Act 1993. The current DML Authorisations were also due for review and so this Application covers both continuing and new operations and facilities. It is Government policy that the UK should maintain and operate a fleet of nuclear powered submarines. It is also Government policy to have a single dockyard for the refitting of nuclear powered submarines at DRD. DML owns the DRD site, and carries out work for the Ministry of Defence (MoD) and other customers. The radiation from the operation of a submarine's nuclear reactor causes some of the materials of the reactor core - and the Water used to cool it - to become radioactive. As a consequence of DML's work on these submarines, radioactive wastes are generated; these wastes

  10. IFCC reference measurement procedure for substance concentration determination of total carbon dioxide in blood, plasma or serum

    NARCIS (Netherlands)

    Burnett, RW; Covington, AK; Fogh-Andersen, N; Kulpmann, WR; Lewenstam, A; Mas, AHJ; VanKessel, AL; Zijlstra, WG

    2001-01-01

    A reference measurement procedure for substance concentration determination of total CO, in blood, plasma (the anticoagulant is usually heparin) or serum is described. The document covers the principle of the method, the materials and equipment needed and essential aspects of the procedure. The subs

  11. A simplified method for determination of radioactive iron in whole-blood samples

    DEFF Research Database (Denmark)

    Bukhave, Klaus; Sørensen, Anne Dorthe; Hansen, M.

    2001-01-01

    For studies on iron absorption in man radioisotopes represent an easy and simple tool. However, measurement of the orbital electron emitting radioiron, Fe-55, in blood is difficult and insufficiently described in the literature. The present study describes a relatively simple method for simultane...... a sensitive method for studying the intestinal absorption of Fe-55 and Fe-59 in man and at the same time allows estimation of the amount of radioiron Located in the vascular compartment.......For studies on iron absorption in man radioisotopes represent an easy and simple tool. However, measurement of the orbital electron emitting radioiron, Fe-55, in blood is difficult and insufficiently described in the literature. The present study describes a relatively simple method...... for simultaneous determination of Fe-55 and Fe-59 in blood, using a dry-ashing procedure and recrystallization of the remaining iron. The detection Limit of the method permits measurements of 0.1 Bq/ml blood thus allowing detection of Less than 1% absorption from a 40 kBq dose, which is ethically acceptable...

  12. Presence of a radioactive gas in archaeological excavations, determination and mitigation.

    Science.gov (United States)

    Balcázar, M; Gómez, S; Peña, P; Zavala Arredondo, J; Gazzola, J; Villamares, A

    2014-01-01

    During recent archaeological discovery and excavation of a tunnel build approximately 2000 years ago by the Teotihuacans under the feathered serpent temple, in Mexico, abnormal radon concentrations up to 700 Bq m(-3) were measured at several excavation stages. The tunnel is at 15m below the earth surface with a vertical rectangular entrance of 4×4 m(2), a semi cylindrical shape of 3m in diameter, with a probable length of 100 m. This study supports the assumption that at the opening of the tunnel radon concentration was around 5500 Bq m(-3); however, although natural convection in the tunnel atmosphere naturally pups radon out, it build up to a maximum concentration of 2000 Bq m(-3). This paper presents the identification of the radon problem in this archaeological site, dose determination, and the mitigation actions that reduced the radon concentration down to 40 Bq m(-3) that ensure a negligible radon risk for archaeologist. Copyright © 2013 Elsevier Ltd. All rights reserved.

  13. Determination of {sup 93}Zr in medium and low level radioactive wastes from Brazilian nuclear power plants

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Thiago C.; Oliveira, Arno H., E-mail: oliveiratco2010@gmail.com, E-mail: heeren@nuclear.ufmg.br [Universidade Federal de Minas Gerais (DEN/UFMG), Belo Horizonte, MG (Brazil). Departamento de Engenharia Nuclear; Kastner, Geraldo F.; Monteiro, Roberto Pellacani G., E-mail: rpgm@cdtn.br, E-mail: gfk@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2015-07-01

    The majority of long-lived radionuclides produced in the nuclear power plants can be regarded as difficult-to-measure radionuclides (RDM), hence chemical separation is necessary before the nuclear measurement of them. The zirconium isotope {sup 93}Zr is a long-lived pure β-particle-emitting radionuclide produced from {sup 235}U fission and from neutron activation of the stable isotope {sup 92}Zr and thus occurring as one of the radionuclides found in nuclear reactors. Due to its long half-life, {sup 93}Zr is one of the radionuclides of interest for the performance of assessment studies of waste storage or disposal. Two different methodologies based on extractive resins and LSC and ICP-MS techniques that enables the {sup 93}Zr determination in medium (ILW) and low level (LLW) radioactive wastes samples from Brazilian nuclear power plants has been developed in our laboratory. Analyzing real samples 65% and 75% chemical yields for {sup 93}Zr recovery were achieved for ICP-MS and LSC techniques, respectively. The detection limits were 0.045 μg.L{sup -1} for ICP-MS and 0.05 Bq.L{sup -1} for LSC techniques. (author)

  14. Radioactive Material

    CERN Multimedia

    2004-01-01

    The Radiation Protection Group of the Safety Commission is responsible for shipping of radioactive material from CERN to any external institute or organisation. The RP group is equally responsible for the reception of radioactive material shipped to any of the CERN sites. Anyone who needs to ship from or import into CERN radioactive material must contact the Radioactive Shipping Service of the RP group in advance. Instructions are available at: http://cern.ch/rp-shipping or in the Radiation Protection Procedure PRP13: https://edms.cern.ch/document/346823 Radiation Protection Group

  15. Radioactive Material

    CERN Multimedia

    2004-01-01

    The Radiation Protection Group of the Safety Commission is responsible for shipping of radioactive material from CERN to any external institute or organisation. The RP group is equally responsible for the reception of radioactive material shipped to any of the CERN sites. Anyone who needs to ship from or import into CERN radioactive material must contact the Radioactive Shipping Service of the RP group in advance. Instructions are available at: http://cern.ch/rp-shipping or in the Radiation Protection Procedure PRP13: https://edms.cern.ch/document/346823 Radiation Protection Group

  16. Development and validation of a stability-indicating high performance liquid chromatographic (HPLC) method for the determination of related substances of micafungin sodium in drug substances.

    Science.gov (United States)

    Zhu, Shengsheng; Meng, Xiang; Su, Xin; Luo, Yongwei; Sun, Zuyue

    2013-10-24

    An isocratic, sensitive and stability-indicating high performance liquid chromatographic (HPLC) method for separation and determination of the related substances of micafungin sodium was developed. The chromatographic separation was achieved on Agilent Zorbax SB-C18 column (250 × 4.6 mm, 5 μm). Forced degradation study confirmed that the newly developed method was specific and selective to the degradation products. The performance of the method was validated according to the present ICH guidelines for specificity, linearity, accuracy, precision and robustness. Regression analysis showed correlation coefficient value greater than 0.999 for micafungin sodium and its six impurities. Limit of detection of impurities was in the range of 0.006%-0.013% indicating the high sensitivity of the newly developed method. Accuracy of the method was established based on the recovery obtained between 98.2% and 102.0% for all impurities. RSD obtained for the repeatability and intermediate precision experiments, was less than 1.0%. The method was successfully applied to quantify related substances of micafungin sodium in bulk drugs.

  17. HPLC-MS/MS methods for the determination of 52 perfluoroalkyl and polyfluoroalkyl substances in aqueous samples.

    Science.gov (United States)

    Gremmel, Christoph; Frömel, Tobias; Knepper, Thomas P

    2017-02-01

    Two quantitative methods using high-performance liquid chromatography (HPLC) combined with triple quadrupole tandem mass spectrometry (MS/MS) were developed to determine perfluoroalkyl and polyfluoroalkyl substances (PFASs) in aqueous samples. The first HPLC-MS/MS method was applied to 47 PFASs of 12 different substance classes with acidic characteristics such as perfluoroalkyl carboxylic acids (PFCAs) and perfluoroalkane sulfonic acids (PFSAs), as well as precursor substances and biotransformation intermediates (e.g., unsaturated fluorotelomer carboxylic acids). In addition, 25 (13)C-, (18)O-, and (2)H-labeled PFASs were used as internal standards in this method. The second HPLC-MS/MS method was applied to fluorotelomer alcohols (FTOHs) and perfluorooctane sulfonamidoethanols as these compounds have physicochemical properties different from those of the previous ones. Accuracy between 82% and 110% and a standard deviation in the range from 2% to 22% depending on the substances were determined during the evaluation of repeatability and precision. The method quantification limit after solid-phase extraction ranged from 0.3 to 199 ng/L depending on the analyte and matrix. The HPLC-MS/MS methods developed were suitable for the determination of PFASs in aqueous samples (e.g., wastewater treatment plant effluents or influents after solid-phase extraction). These methods will be helpful in monitoring campaigns to evaluate the relevance of precursor substances as indirect sources of perfluorinated substances in the environment. In one exemplary application in an industrial wastewater treatment plant, FTOHs were found to be the major substance class in the influent; in particular, 6:2-FTOH was the predominant compound in the industrial samples and accounted for 74% of the total PFAS concentration. The increase in the concentration of the transformation products of FTOHs in the corresponding effluent, such as fluorotelomer carboxylic acids, unsaturated fluorotelomer

  18. Anatomic-physiological schema of the gastrointestinal tract, to be taken in account in determining the levels of radioactive contamination; Schema anatomo-physiologique du tractus gastro-intestinal a prendre en consideration pour le calcul des niveaux de contamination Radioactive

    Energy Technology Data Exchange (ETDEWEB)

    Fabry, C. [Commissariat a l' Energie Atomique, Cadarache, Association EURATOM-CEA, Niveaux de Contamination (France). Centre d' Etudes Nucleaires

    1964-07-01

    Anatomical and physiological data of the gastrointestinal tract of adults and children were summarized in a standard schema, to be used in calculating the levels of radioactive contamination, in the food chain. (author) [French] Cette note a pour objet de rassembler les donnees anatomiques et physiologiques du tractus gastrointestinal, chez l'adulte et chez l'enfant, et d'en deduire un schema standard qui puisse servir de base au calcul des niveaux de contamination de la chaine alimentaire par les substances radioactives. (auteur)

  19. Determination of Other Related Carotenoids Substances in Astaxanthin Crystals Extracted from Adonis amurensis.

    Science.gov (United States)

    Zhang, Li-hua; Peng, Yong-jian; Xu, Xin-de; Wang, Sheng-nan; Yu, Lei-ming; Hong, Yi-min; Ma, Jin-ping

    2015-01-01

    Astaxanthin is a kind of important carotenoids with powerful antioxidation capacity and other health functions. Extracting from Adonis amurensis is a promising way to obtain natural astaxanthin. However, how to ensure the high purity and to investigate related substances in astaxanthin crystals are necessary issues. In this study, to identify possible impurities, astaxanthin crystal was first extracted from Adonis amurensis, then purified by saponification and separation. The concentration of total carotenoids in purified astaxanthin crystals was as high as 97% by weight when analyzed by UV-visible absorption spectra. After identified with TLC, HPLC and MS, besides free astaxanthin as main ingredient in the crystals, there existed four other unknown related substances, which were further investigated by HPLC/ESI/MS with the positive ion mode combining with other auxiliary reference data obtained in stress tests, at last it was confirmed that four related carotenoids substances were three structural isomers of semi-astacene and adonirubin.

  20. Determinants of substance use amongst Brazilians residing in the UK: The role of acculturation.

    Science.gov (United States)

    Canfield, Martha; Worrell, Marcia; Gilvarry, Catherine

    2017-04-10

    Evidence suggests that patterns of substance use are changing amongst some members of migrant groups in the UK. This study explored the extent to which residing in the UK has an impact on substance use behaviours amongst Brazilian migrants. A mixed methods approach was adopted comparing Brazilians residing in the UK (n = 164) and Brazilians residing in Brazil (n = 161), age 27.82 (SD = 5.65) average. Participants' socio-demographic characteristics, resilience, personality traits, drinking motives, psychological distress, frequency of alcohol intake, smoking and other drugs used (Brazil and UK), acculturation outcomes and length of residence (UK) were explored. Six in-depth interviews were conducted with Brazilian residents in the UK and analysed using thematic analysis. Participants from the UK reported higher prevalence of substance use; however, significant country differences were only found in binge drinking and poly drug use. While in Brazil, substance use was associated with being male, no religious practices, having resided in another country and higher scores in drinking for social motives and sensation seeking, in the UK it was associated with elementary occupations, higher scores in drinking for social and enhancement motives, threat to cultural identity and lower length of residence in the UK. Interview data suggested that living in the UK was stressful. Country differences in patterns of substance use were associated with changes resulting from the migratory process to the UK. The stresses associated with the process of acculturation presents a promising path for addressing substance use problems in migrant populations. © 2017 Australasian Professional Society on Alcohol and other Drugs.

  1. Temporary Personal Radioactivity

    Science.gov (United States)

    Myers, Fred

    2012-01-01

    As part of a bone scan procedure to look for the spread of prostate cancer, I was injected with radioactive technetium. In an effort to occupy/distract my mind, I used a Geiger counter to determine if the radioactive count obeyed the inverse-square law as a sensor was moved away from my bladder by incremental distances. (Contains 1 table and 2…

  2. Substance Use: Determinants and Opportunities for Prevention in the Family and School Context

    Science.gov (United States)

    Kleinjan, Marloes; Engels, Rutger C. M. E.

    2014-01-01

    During adolescence, teenagers try a range of risk behaviors including smoking, drinking, and the use of soft drugs. Because substance use contributes to an unhealthy lifestyle of teenagers on the short term and can lead to serious health problems on the longer term, prevention in this target group is important. This chapter provides an overview of…

  3. Determination of perfluoroalkylated substances (PFASs) in drinking water from the Netherlands and Greece

    NARCIS (Netherlands)

    Zafeiraki, Effrosyni; Costopoulou, Danae; Vassiliadou, Irene; Leondiadis, Leondios; Dassenakis, Emmanouil; Traag, Wim; Hoogenboom, Ron L.A.P.; Leeuwen, van Stefan P.J.

    2015-01-01

    In the present study 11 perfluoroalkylated substances (PFASs) were analysed in drinking tap water samples from the Netherlands (n = 37) and from Greece (n = 43) by applying LC-MS/MS and isotope dilution. PFASs concentrations above the limit of quantification, LOQ (0.6 ng/l) were detected in 20.9%

  4. Substance Use: Determinants and Opportunities for Prevention in the Family and School Context

    Science.gov (United States)

    Kleinjan, Marloes; Engels, Rutger C. M. E.

    2014-01-01

    During adolescence, teenagers try a range of risk behaviors including smoking, drinking, and the use of soft drugs. Because substance use contributes to an unhealthy lifestyle of teenagers on the short term and can lead to serious health problems on the longer term, prevention in this target group is important. This chapter provides an overview of…

  5. Determination of perfluoroalkylated substances (PFASs) in drinking water from the Netherlands and Greece

    NARCIS (Netherlands)

    Zafeiraki, Effrosyni; Costopoulou, Danae; Vassiliadou, Irene; Leondiadis, Leondios; Dassenakis, Emmanouil; Traag, Wim; Hoogenboom, Ron L.A.P.; Leeuwen, van Stefan P.J.

    2015-01-01

    In the present study 11 perfluoroalkylated substances (PFASs) were analysed in drinking tap water samples from the Netherlands (n = 37) and from Greece (n = 43) by applying LC-MS/MS and isotope dilution. PFASs concentrations above the limit of quantification, LOQ (0.6 ng/l) were detected in 20.9%

  6. Determination of residual isobutylene oxide--a genotoxic starting material in a drug substance by static headspace gas chromatography.

    Science.gov (United States)

    Han, Jun; Yeung, David; Wang, Fang; Semin, David

    2008-08-01

    A sensitive static headspace gas chromatography (sHS-GC) method is developed and validated for the determination of residual isobutylene oxide (IBO)-a genotoxic starting material in a drug substance for Phase I clinical trial studies. The experimental parameters, such as headspace vial pressure, headspace oven temperature, vial equilibration time, column flow rate, and GC oven temperature programs are optimized. Under the optimal conditions, the recovery is between 89.3% and 102.4% for spiked samples at three levels of IBO concentration in triplicates in sample preparations. Limits of quantitation (LOQ) and detection (LOD) of the standard solutions are 0.048 and 0.018 microg/mL, respectively. Linear range from 0.018 to 6 microg/mL is obtained with a correlation coefficient of 0.9999. The method is applied to determine residual IBO in drug substance samples from different batches.

  7. DETERMINING PARAMETERS OF THE DIELECTRIC FUNCTION OF A SUBSTANCE IN AQUEOUS SOLUTION BY SELF-REFERENCED REFLECTION THZ SPECTROSCOPY

    DEFF Research Database (Denmark)

    2008-01-01

    Method and apparatus for determining dielectric function of liquid solutions and thereby concentrations of substances in aqueous solution or the volatile/non-volatile nature of the liquid by self-referenced reflection THz spectroscopy. Having the aqueous solution in any container with a window...... allows irradiating coherent THz radiation with frequencies within the range 0.05 - 2 THz on the front of the window, and recording both a reference signal reflected from the front of the window and a sample signal reflected from the back of the window in contact with the aqueous solution. From...... these signals, the complex index of refraction, (I) or the complex reflection coefficient (II), can be calculated. The calculated components are compared with previously determined components from samples with known concentrations, whereby a concentration of the substance in the mixture can be estimated...

  8. Research on Calibration of Radioactive Aerosol Monitor

    Institute of Scientific and Technical Information of China (English)

    CHEN; Xi-lin; WU; Chang-ping; ZHANG; Xi; MENG; Jun; DIAO; Li-jun; CHEN; Ke-sheng

    2015-01-01

    Radioactive aerosol monitors were used to monitor the radioactive substance concentration or the total amounts in effluents from the nuclear facilities,in according to which evaluation was done if the national regulated discharged limitations or the designated object amounts were met

  9. Optimisation, validation and application of a capillary electrophoresis method for the determination of ranitidine hydrochloride and related substances.

    Science.gov (United States)

    Kelly, M A; Altria, K D; Grace, C; Clark, B J

    1998-03-06

    Ranitidine hydrochloride is an H2-antagonist which is widely prescribed for the treatment of peptic ulcers. The drug is marketed in a variety of dosage forms including tablets, syrups and injection solutions. A range of synthetic and degradative impurities of ranitidine are known and currently, these impurities are routinely determined using thin-layer chromatography (TLC). Alternatively a high-performance liquid chromatography (HPLC) method has also been employed in the assay of the pharmaceutical preparation. Unlike TLC, capillary electrophoresis (CE) offers the capability to quantify simultaneously both the active drug content and the levels of the related substances. The advantages of simplicity, selectivity, versatility and ease of use of CE offers a complementary separation technique to the established methods of HPLC and TLC in the determination of ranitidine and its related substances. This work represents a comprehensive evaluation of the performance of a developed CE method in the determination of drug-related impurities in both drug substance and various pharmaceutical formulations. The data obtained clearly shows that the performance of an optimised CE method can be equivalent in terms of sensitivity and precision to that of a HPLC method employed for a similar purpose and offers better selectivity against TLC and HPLC.

  10. Simultaneous and group determination methods for designated substances by HPLC with multi-channel electrochemical detection and their application to real samples.

    Science.gov (United States)

    Min, Jun Zhe; Yamashita, Kazuhide; Toyo'oka, Toshimasa; Inagaki, Shinsuke; Higashi, Tatsuya; Kikura-Hanajiri, Ruri; Goda, Yukihiro

    2010-12-01

    Many psychotropic substances are illegally available on the streets and/or via the Internet. This wide distribution has become a serious social problem. To control this problem, many substances have been controlled as 'designated substances' (Shitei-Yakubutsu) in Japan since April 2007 by the Pharmaceutical Affairs Law, including tryptamines, phenethylamines and piperazines. In the present study, simultaneous determination methods using HPLC with multi-channel electrochemical detection (MECD) were developed for the designated substances. The proposed methods utilizing online electrochemical oxidation are the first report on the simultaneous determination of various designated substances. The methods involve direct determination and require no complicated pretreatments such as fluorescence labeling. The designated substances were separated by reversed-phase chromatography using a TSK-gel ODS-100V (4.6 × 250 mm, i.d., 3 µm) and gradient elution by a mixture of potassium phosphate buffer, methanol and acetonitrile. The total separation of 31 designated substances was successfully performed but required long chromatographic run times. Thus, the designated substances were divided into three groups: (1) tryptamines, (2) phenethylamines and (3) piperazines and others. They were then analyzed by HPLC-MECD as another separation method. The suitable applied voltages for each designated substance were determined based upon the hydrodynamic voltammogram. The limits of detection (signal-to-noise ratio of 3) of the designated substances for the most suitable voltages were in the range of 17.1 pg (5-MeO-MIPT) to 117 ng (indan-2-amine). The calibration curves based on the peak heights were linearly related to the amounts of the designated substances (R(2) > 0.999). Good accuracy and precision by intra-day assay and inter-day assay were also obtained using the present procedures. The proposed methods were applied to the analyses of the designated substance in several real

  11. Simulated Radioactivity

    Science.gov (United States)

    Boettler, James L.

    1972-01-01

    Describes the errors in the sugar-cube experiment related to radioactivity as described in Project Physics course. The discussion considers some of the steps overlooked in the experiment and generalizes the theory beyond the sugar-cube stage. (PS)

  12. Radioactivity Calculations

    Science.gov (United States)

    Onega, Ronald J.

    1969-01-01

    Three problems in radioactive buildup and decay are presented and solved. Matrix algebra is used to solve the second problem. The third problem deals with flux depression and is solved by the use of differential equations. (LC)

  13. Concentrating Radioactivity

    Science.gov (United States)

    Herrmann, Richard A.

    1974-01-01

    By concentrating radioactivity contained on luminous dials, a teacher can make a high reading source for classroom experiments on radiation. The preparation of the source and its uses are described. (DT)

  14. HPLC测定阿苯达唑有关物质%Determination of Related Substances in Albendazole by HPLC

    Institute of Scientific and Technical Information of China (English)

    孙春艳; 赵亚萍; 郭江红

    2012-01-01

    目的 建立高效液相色谱法测定阿笨达唑有关物质.方法 采用资生堂MGⅡC18柱(250 mm×4.6mm,5 μm)色谱柱;流动相:磷酸二氢铵溶液(1.67 mg·mL-1)-甲醇(40∶60);检测波长:290nm.结果 样品中的杂质均能很好检出,各杂质与主峰之间的分离度良好,检测限为0.2286 ng.结论 该方法简单快速,专属性强,结果准确,可用作阿苯达唑有关物质检查.%OBJECTIVE To establish an HPLC method for determination of related substances in albendazole. METHODS PAK C18 HPLC packed column(MG Ⅱ, 250 mm × 4.6 mm, 5 μm)was used, the mobile phase was ammonium dihydrogen phosphate-methanol(40 : 60) and the determination wavelength was 290 nm. RESULTS Albendazole and related substances could be well isolated. The detection limit was 0.228 6 ng. CONCLUSION The method is simple, rapid, accurate and suitable for examinating the related substances of albendazole.

  15. DETERMINATION OF SATURATION VAPOR PRESSURE OF LOW VOLATILE SUBSTANCES THROUGH THE STUDY OF EVAPORATION RATE BY THERMOGRAVIMETRIC ANALYSIS

    Directory of Open Access Journals (Sweden)

    R. V. Ralys

    2015-11-01

    Full Text Available Subject of Study.Research of vapor pressure of low volatile substances is a complicated problem due to both direct experimental implementation complexity and, most significantly, the issues faced correctness of the analysis and processing of experimental data. That is why it is usually required engaging the reference substances (with vapor pressures well studied. The latter drastically reduces the effectiveness of the experimental methods used and narrows their applicability. The paper deals with an approach to the evaporation process description (sublimation of low volatile substances based on molecular kinetic description in view of diffusive and convection processes. The proposed approach relies on experimental thermogravimetricfindingsina wide range of temperatures, flow rates ofthe purge gas and time. Method. A new approach is based on the calculation of the vapor pressure and uses the data about the speed of evaporation by thermogravimetric analysis depending on the temperature, the flow rate of the purge gas, and the evaporation time. The basis for calculation is the diffusion-kinetic description of the process of evaporation (mass loss of the substance from the exposed surface. The method is applicable to determine the thermodynamic characteristics for both the evaporation (the equilibrium liquid - vapor and sublimation (the equilibrium solid - vapor. We proposed the appropriate method of the experiment and analysis of its data in order to find the saturated vapor pressure of individual substances of low volatility. Main Results. The method has been tested on substances with insufficiently reliable and complete study of the thermodynamic characteristics but, despite this, are often used (because of the other data limitations as reference ones. The vaporization process (liquid-vapor has been studied for di-n-butyl phthalate C16H22O4 at 323,15–443,15 К, and sublimation for benzoic acid C7H6O2at 303,15–183,15 К. Both processes have

  16. Calibration with MCNP of NaI detector for the determination of natural radioactivity levels in the field.

    Science.gov (United States)

    Cinelli, Giorgia; Tositti, Laura; Mostacci, Domiziano; Baré, Jonathan

    2016-05-01

    In view of assessing natural radioactivity with on-site quantitative gamma spectrometry, efficiency calibration of NaI(Tl) detectors is investigated. A calibration based on Monte Carlo simulation of detector response is proposed, to render reliable quantitative analysis practicable in field campaigns. The method is developed with reference to contact geometry, in which measurements are taken placing the NaI(Tl) probe directly against the solid source to be analyzed. The Monte Carlo code used for the simulations was MCNP. Experimental verification of the calibration goodness is obtained by comparison with appropriate standards, as reported. On-site measurements yield a quick quantitative assessment of natural radioactivity levels present ((40)K, (238)U and (232)Th). On-site gamma spectrometry can prove particularly useful insofar as it provides information on materials from which samples cannot be taken.

  17. A novel reverse phase stability indicating RP-UPLC method for the quantitative determination of fifteen related substances in Ranolazine drug substance and drug product.

    Science.gov (United States)

    Malati, Vakamulla; Reddy, Anumala Raghupati; Mukkanti, K; Suryanarayana, M V

    2012-08-15

    A gradient reverse-phase ultra performance liquid chromatographic (RP-UPLC) method was developed for the quantitative determination of Ranolazine and potential process-related impurities (starting materials, positional isomers, degradants and byproducts) at the level of 0.1 μg mL(-1) to 0.3 μg mL(-1). Fifteen potential impurities were identified in the crude samples during the process development. Tentative structures for all the impurities were assigned based on m/z values from LC-MS/MS analysis. This method can be used for the quality control of both drug substance and drug product. All these impurities were separated with a gradient UPLC method by using a polar embedded Waters Acquity BEH RP18 100 mm × 2.1 mm,1.7 μm column, monobasic sodium buffer, a basic organic modifier and acetonitrile in the mobile phase. Further, this method is also capable of separating a major oxidative degradant Di-N-oxide. Impurities having electron donating groups(+I effect) on the phenyl ring increased the retention by improved п-п interactions. The drug was subjected to the International Conference on Harmonization (ICH)-prescribed hydrolytic, oxidative, photolytic and thermal stress conditions. The performance of the method was validated according to the present ICH guidelines for specificity, limit of detection, limit of quantification, linearity, accuracy, precision, ruggedness and robustness.

  18. Development of a validated liquid chromatographic method for determination of related substances of telmisartan in bulk drugs and formulations.

    Science.gov (United States)

    Rao, R Nageswara; Guru Prasad, K; Gangu Naidu, Ch; Maurya, Pawan K

    2011-11-01

    A simple and rapid reversed phase liquid chromatographic method for separation and determination of the related substances of telmisartan (TLM) was developed and validated. The chromatographic separation was achieved on Lichrospher RP-18 column (250 × 4.6 mm, 5 μm), using 20 mM ammonium acetate containing 0.1% (v/v) triethylamine (pH adjusted to 3.0 with trifluoroacetic acid) and acetonitrile as mobile phase at 25°C. The detection was performed at 254 nm. The method was validated and found to be robust, precise, specific and linear between 0.37 and 500 μg/mL. The limits of detection and quantification of telmisartan were 0.11 and 0.37 μg/mL, respectively. The method was successfully applied to quantify related substances and assay of TLM in bulk drugs and commercial tablets. The related substances relate to a novel synthetic route and different from those A-H impurities reported by European Pharmacopeia.

  19. Determination of substance overdose in two Iranian centers: comparison between opioids and non-opioids.

    Science.gov (United States)

    Taghaddosinejad, Fakhreddin; Arefi, Mohammad; Fayaz, Amir Farshid; Tanhaeivash, Roozbeh

    2013-04-01

    Recently, new trend toward non-opioid substances is observed in Iran. This is, therefore, to compare overdose of opioids and non-opioids origin. We performed this investigation to provide more detailed information so that preventive actions are taken in future. Over 18 month, 1876 individuals with opioid (opium, heroin, compact-heroin, buprenorphine and opiates) or non-opioid (MDMA (ecstasy), LSD, hashish and cocaine) overdose were selected. They have been compared regarding sex, age, reason of overdose, method of substance use, occupation, marital status, history of addiction in parents/siblings, duration of hospital admission and educational level. There were 1782 and 94 persons with opioid and non-opioid, respectively. Inhalation was the method of choice and women were found to have more tendencies to hallucinogens rather opioids. Moreover, use of non-opioids was observed more in individuals with university education and moreover in whom none of whose parents/siblings was addict. Policies should be planned by the governments to prevent further addictions especially to non-opioids. Copyright © 2012 Elsevier Ltd and Faculty of Forensic and Legal Medicine. All rights reserved.

  20. Determination of caffeine and identification of undeclared substances in dietary supplements and caffeine dietary exposure assessment.

    Science.gov (United States)

    Neves, Diana Brito da Justa; Caldas, Eloisa Dutra

    2017-07-01

    Caffeine is one of the most consumed stimulants in the world, and is a frequent ingredient of dietary supplements. The aims of this work were to validate a GC-MS method for the quantitation of caffeine and identification of other substances in supplements, mainly weight loss products, and to estimate the caffeine intake by consumers. Sample preparation included extraction with chloroform:water in ultrasonic bath, centrifugation and analysis of the organic layer for caffeine quantitation, and extraction with methanol for identification of other substances. A total of 213 samples of 52 supplement products not registered in Brazil and seized by the Brazilian Federal Police were analyzed. From the 109 samples that declared the amount of caffeine present, 26.6% contained more than 120% of the specified content. Considering the maximum recommended dose stated on the product labels, the consumption of 47.9% of the samples would lead to a daily intake of caffeine above the safe limit of 400 mg. Undeclared drugs, including sibutramine, phenolphthalein, amphepramone and femproporex were found in 28 samples. These results show that consumers of dietary supplements should be aware that these products might contain caffeine at levels that could represent potential health risks, in addition to undeclared pharmaceutical drugs. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. HPLC测定多司马酯的有关物质%Determination of Related Substances of Dosmalfate by HPLC

    Institute of Scientific and Technical Information of China (English)

    张广洲; 马玉贞; 赵仁永; 张岱州

    2012-01-01

    Objective To establish an RP-HPLC method for the determination of the related substances of dosmalfate. Methods The separation was performed with ODS C18 column. Glacial acetic acid 0.4mL and triethylamine 1.6 mL was dissolved with 400 mL water, adjusting pH to 7.5 with phosphoric acid. The mobile phase consisted of this solution-methanol(72:28). The detection wavelength was set at 330 nm. Results In this chromatography system, the related substances had a good separation and a good linear relation over the determination concentration. Conclusion This method is simple, accurate and applicable for the determination of related substances of dosmalfate.%目的 建立测定多司马酯中有关物质的HPLC方法.方法 采用ODS C18柱;流动相为缓冲液(冰醋酸0.4 mL,三乙胺1.6 mL,加水400 mL,用磷酸调pH至7.5)-甲醇(72∶28);检测波长330nm.结果 样品在本色谱条件下,有关物质均能较好分离,在测定范围内有较好的线性关系及精密度.结论 测定方法简便、准确可靠,可用于多司马酯有关物质的测定.

  2. Radioactive Waste.

    Science.gov (United States)

    Blaylock, B. G.

    1978-01-01

    Presents a literature review of radioactive waste disposal, covering publications of 1976-77. Some of the studies included are: (1) high-level and long-lived wastes, and (2) release and burial of low-level wastes. A list of 42 references is also presented. (HM)

  3. Predictive Models for the Determination of Pitting Corrosion Versus Inhibitor Concentrations and Temperature for Radioactive Sludge in Carbon Steel Waste Tanks

    Energy Technology Data Exchange (ETDEWEB)

    Mickalonis, J.I.

    1998-10-06

    Statistical models have been developed to predict the occurrence of pitting corrosion in carbon steel waste storage tanks exposed to radioactive nuclear waste. The levels of nitrite concentrations necessary to inhibit pitting at various temperatures and nitrate concentrations were experimentally determined via electrochemical polarization and coupon immersion corrosion tests. Models for the pitting behavior were developed based on various statistical analyses of the experimental data. Feed-forward Artificial Neural Network (ANN) models, trained using the Back-Propagation of Error Algorithm, more accurately predicted conditions at which pitting occurred than the logistic regression models developed using the same data.

  4. Method development and validation study for quantitative determination of nifedipine and related substances by ultra-high-performance liquid chromatography.

    Science.gov (United States)

    Galan-Rodriguez, Cristobal; González-Álvarez, Jaime; Valls-Remolí, Màrius

    2015-02-01

    A novel stability-indicating reversed phase ultra-high performance liquid chromatography (UPLC) coupled photodiode array gradient method was developed for determination of the nifedipine and related compounds. Furthermore, based on the chromatographic conditions and forced degradation studies performed through the development of the related substances method a UPLC isocratic method was validated for the determination of the assay of this active substance. An Acquity Shield RP18 (50 × 3.0 mm 1.7 µm) column was used for separation of nifedipine and its five potential impurities within 11 min, which is 5-fold less than the official method. A mobile phase consisting of 10 mm ammonium formate (pH 4.5) and methanol, delivered at a flow rate 0.5 mL/min, was employed to achieve a minimum resolution of 2.0 for all consecutive pairs of compounds. The precision value expressed as percentage relative standard deviation for method repeatability and reproducibility was <5.0%. The recoveries for all the related compounds were in the range of 99-105.0%. Linearity was found to be acceptable over the concentration range of 0.25-1.5 µg/mL for nifedipine and its impurities. The limit of quantification for nifedipine was 0.05 µg/mL, which is much less than the European Pharmacopoeia method.

  5. SHIPPING OF RADIOACTIVE ITEMS

    CERN Multimedia

    TIS/RP Group

    2001-01-01

    The TIS-RP group informs users that shipping of small radioactive items is normally guaranteed within 24 hours from the time the material is handed in at the TIS-RP service. This time is imposed by the necessary procedures (identification of the radionuclides, determination of dose rate and massive objects require a longer procedure and will therefore take longer.

  6. Determination of Erythromycin Ethylsuccinate and its Related Substances by Ion Suppression Chromatography

    Institute of Scientific and Technical Information of China (English)

    LEIJia-chuan; LUOShun-de; Guo-lin; YuJian-qing

    2003-01-01

    Aim:Method for the deternination of erythromycin ethylsuccinale(EES) by ion suppression chromatography(ISC) was developed and the influenc factors on ISC were investigated.Methods:A Zorbax SB-C18 column was used with 0.02mol.L-1 potassium dihydrogen phosphate-acetonitrile(45:55) as mobile phase,The pH and proportion of the mobile phase showed the greatest influences on retention and selectivity.Therefore,the pH of mobile was adjusted to 6.8,the bhest acetonitrile proportion was 55%.The column temperature was maintained at (300±0.5)℃.Acetonitrile was used as solvent for the sample preparation because EES is more stable in it.The flow rate was 1.2mL.min-1 and UV detection was performed at 210nm.Results :Under these chromatographic conditions,the main component (erythromycin A ethylsuccinate)and its related substances were separated.The calibration curve showed good linearity over the range of 0.1-1.0mg.mL-1,and its correlation coefficient was 0.9998.Conclusion:The method is very suitable for the analysis of erythromycin ethylsuccinate.

  7. Systematic determination of perfluoroalkyl and polyfluoroalkyl substances (PFASs) in outdoor jackets.

    Science.gov (United States)

    Gremmel, Christoph; Frömel, Tobias; Knepper, Thomas P

    2016-10-01

    Sixteen outdoor jackets were purchased in 2011/12 and analyzed for 23 different perfluoroalkyl and polyfluoroalkyl substances (PFASs). The jackets were selected based on their origin of production, price, market, and textile, such as polyester, nylon, polyamide, and content of poly(tetrafluoroethylene) membranes. Two robust analytical methods based on high pressure liquid chromatography combined with tandem mass spectrometry, as well as two liquid extractions, were developed enabling the analysis of PFASs with widely different physico-chemical properties. The jackets were found to contain PFASs in a range between 0.03 and 719 μg/m(2). Perfluorooctanoic acid (PFOA) was omnipresent (0.02-171 μg/m(2)), although at lower concentrations compared to the precursors of perfluoroalkyl carboxylic acids (PFCAs), namely fluorotelomer alcohols (FTOHs) (dark at room temperature and re-analyzed after 3.5 years. Only 10%-20% of the initial concentration of 8:2-FTOH and 20%-50% of 10:2-FTOH were found, whereas the concentrations of PFOA and perfluorodecanoic acid increased significantly. This supports the hypothesis that PFAS concentrations in textiles are also strongly dependent on age, and conditions of transport and storage.

  8. Development and validation of a novel stability-indicating HPLC method for the quantitative determination of eleven related substances in ezetimibe drug substance and drug product.

    Science.gov (United States)

    Luo, Zhiqiang; Deng, Zhongqing; Liu, Yang; Wang, Guopeng; Yang, Wenning; Hou, Chengbo; Tang, Minming; Yang, Ruirui; Zhou, Huaming

    2015-07-01

    Ezetimibe is a novel lipid-lowering agent that inhibits intestinal absorption of dietary and biliary cholesterol. In the present work, a simple, sensitive and reproducible gradient reverse phase high performance liquid chromatographic (RP-HPLC) method for separation and determination of the related substances of ezetimibe was developed and validated. Eleven potential process-related impurities (starting materials, (3S,4S,3'S)-isomer, degradants and byproducts) were identified in the crude samples. Tentative structures for all the impurities were assigned primarily based on comparison of their retention time and mass spectrometric data with that of available standards and references. This method can be applied to routine analysis in quality control of both bulk drugs and commercial tablets. Separation of all these compounds was performed on a Phenomenex Luna Phenyl-Hexyl (100mm×4.6mm, 5μm) analytical column. The mobile phase-A consists of acetonitrile-water (pH adjusted to 4.0 with phosphoric acid)-methanol at 15:75:10 (v/v/v), and mobile phase-B contains acetonitrile. The eluted compounds were monitored at 210nm. Ezetimibe was subjected to hydrolytic, acid, base, oxidative, photolytic and thermal stress conditions as per ICH serves to generate degradation products that can be used as a worst case to assess the analytical method performance. The drug showed extensive degradation in thermal, acid, oxidative, base and hydrolytic stress conditions, while it was stable to photolytic degradation conditions. The main degradation product formed under thermal, acid, oxidative, base and hydrolytic stress conditions corresponding to (2R,3R,6S)-N, 6-bis(4-fluorophenyl)-2-(4-hydroxyphenyl)-oxane-3-carboxamide (Ezetimibe tetrahydropyran impurity) was characterized by LC-MS/MS analysis. The degradation products were well resolved from the main peak and its impurities, thus proved the stability-indicating power of the method. The developed method was validated as per

  9. Report of radioactivity survey research in fiscal year 1996

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-12-01

    In National Institute of Radiological Sciences, a survey was made on radioactivities in the environment due to the substances released from nuclear installations and radioactive fall-out brought out by nuclear explosion tests since 1959. As the marked progress of non-military utilization of nuclear energy the national concern on environmental radioactivity has been increasing in Japan and thus it has become more and more important to make a survey research of radioactivities, which might affect the environment and human health. In these situations, the institute attempted to make the following six surveys in the fiscal year of 1996; `a survey on radioactive levels in environment, foods and human bodies`, `survey on the radioactive level in the regions around nuclear installations`, `works in radioactive data center`, `fundamental survey on the evaluation of the results from radioactivity survey`, `workshop for technical experts of environmental radioactivity monitoring` and `survey research on the measurement and countermeasures for emergency exposure`. (M.N.)

  10. Report of radioactivity survey research in fiscal year 1997

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-12-01

    In National Institute of Radiological Sciences, a survey was made on radioactivities in the environment due to the substances released from nuclear installations and radioactive fall-out brought out by nuclear explosion tests since 1959. As the marked progress of non-military utilization of nuclear energy the national concern on environmental radioactivity has been increasing in Japan and thus it has become more and more important to make a survey research of radioactivities, which might affect the environment and human health. In these situations, the institute attempted to make the following six surveys in the fiscal year of 1997; `a survey on radioactive levels in environment, foods and human bodies`, `survey on the radioactive level in the regions around nuclear installations`, `works in radioactive data center`, `fundamental survey on the evaluation of the results from radioactivity survey`, `workshop for technical experts of environmental radioactivity monitoring` and `survey research on the measurement and countermeasures for emergency exposure`. (J.P.N.)

  11. Goadsporin, a chemical substance which promotes secondary metabolism and Morphogenesis in streptomycetes. II. Structure determination.

    Science.gov (United States)

    Igarashi, Y; Kan, Y; Fujii, K; Fujita, T; Harada, K; Naoki, H; Tabata, H; Onaka, H; Furumai, T

    2001-12-01

    The structure of goadsporin was determined by using spectroscopic techniques. NMR analysis revealed that goadsporin consists of 19 amino acids, two of which are dehydroalanines (Deala), and six of which are cyclized to oxazoles (Oxz) and thiazoles (Thz) by dehydrative cyclization and dehydrogenation from serine, threonine and cysteine. NMR analysis established seven partial structures, and their sequence was determined by CID-MS/MS. Negative mode FAB-MS/MS gave product ions arising from charge-remote fragmentation that allowed determination of the sequence of the amino acid components as AcNH-Ala-MeOxz-Val-Deala-MeOxz-Ile-Leu-Thz-Ser-Gly-Gly-MeOxz-Leu-Deala-Oxz-Ala-Gly-Thz-Val-OH. The chiral amino acids were determined by the advanced Marfey's method to have L-configurations.

  12. HPLC determination of related substance in emtricitabine%HPLC法测定恩曲他滨中有关物质

    Institute of Scientific and Technical Information of China (English)

    房桂珍; 安庆军; 霍明山; 王丽丽

    2011-01-01

    Objective:To establish an HPLC method for determining the related substance of emtricitabine. Methods:Used Inertsil C8 chromatographic column(250 mm x4. 6 mm,5μm) ;flow liquid was buffer solution( 10% tet-rabutylammonium hydroxide solution 2. 0 g,adding 0. 013 mol·L-1 sodium dihydrogen phosphate solution to 1000 mL) -acetonitrile(85:15) (pH value adjusted to 5. 0 with phosphoric acid) ;flow rate:l. 0 mL·min-1,determination wavelength was 220 nm. Results:Impurity peak and sample peak can be effectively separated. Conclusions:The method shows good separating degree and stable result which can be used determining the related substance of emtricitabine.%目的:建立高效液相色谱测定恩曲他滨中有关物质的方法.方法:采用Inertsil Cs色谱柱(250mm×4.6mm,5μm),以缓冲液(取10%四丁基氢氧化铵溶液2.0g,用0.013 mol·L-1磷酸二氢钠溶液稀释至1000 mL) -乙腈(85∶15)为流动相(用磷酸调节pH至5.0),流速为1.0mL· min-1,检测波长为220nm.结果:杂质峰与主峰均分离良好.结论:该法专属性强、准确、灵敏,可用于恩曲他滨原料中有关物质的检查.

  13. Determination of active substances in multicomponent veterinary preparations of antiparasitic action by HPLC method.

    Science.gov (United States)

    Białecka, Wanda; Kulik, Anna

    2010-01-01

    The study aimed at the development of an HPLC method enabling the identification and determination of the content of selected compounds occurring in multicomponent veterinary preparations used in parasitic diseases. The studied compounds included: pyrantel embonate, fenbendazole, praziquantel, epsiprantel and febantel. Using the developed HPLC method, a good separation of the above compounds was achieved. The regression analysis has shown linearity of the method in the required concentration range. The determination of the compounds mentioned and statistical evaluation of the results have demonstrated that the method is characterized by a good selectivity and high precision.

  14. Metabolic relationships of the isolated fractions of the pectic substances of actively growing sycamore cells.

    Science.gov (United States)

    Stoddart, R W; Northcote, D H

    1967-10-01

    1. d-Glucose and l-arabinose serve as precursors of the pectic polysaccharides of sycamore suspension-callus tissue. 2. The rates and characteristics of the incorporation of radioactive sucrose, glucose and mesoinositol by sycamore callus tissue have been compared and shown to be different. 3. The time-course of the incorporation of radioactive glucose into the major fractions within the cells has been determined. Approx. 7-10% of the radioactivity incorporated is present in the whole pectin of the cells. 4. A study of the continuous incorporation of radioactive glucose showed that the neutral arabinan-galactan fraction of the pectin quickly became saturated with the radioactive label. During the incorporation of radioactivity from a pulse of radioactive glucose the neutral fraction became progressively less labelled, with a corresponding increase in the radioactivity of the weakly acidic pectinic acid, which is known to contain neutral sugars. 5. When the cells were exposed to a pulse of radioactive l-arabinose, the label accumulated first in the neutral fraction and then after 4hr. it passed to the weakly acidic pectinic acid with a corresponding decrease in the radioactivity of the neutral fraction. 6. The product that was initially labelled during the first hour of exposure of the cells in the stationary phase to radioactive glucose was identified as an incompletely methylated galacturonan in which the radioactivity was present in the anhydrogalacturonide residues. This polysaccharide probably acts as the precursor of the polyuronide portions of both the strongly acidic and weakly acidic pectinic acids. 7. The observations are discussed in relation to the structure of the pectic substances and their function in cell growth and development. A tentative model for their metabolic relationship is put forward.

  15. Using geologic conditions and multiattribute decision analysis to determine the relative favorability of selected areas for siting a high-level radioactive waste repository

    Energy Technology Data Exchange (ETDEWEB)

    Harrison, W.; Edgar, D.E.; Baker, C.H.; Buehring, W.A.; Whitfield, R.G.; Van Luik, A.E.J.; Sood, M.K.; Flower, M.F.J.; Warren, M.F.; Jusko, M.J.; Peerenboom, J.P.; Bogner, J.E.

    1988-05-01

    A method is presented for determining the relative favorability of geologically complex areas for isolating high-level radioactive wastes. In applying the method to the northeastern region of the United States, seismicity and tectonic activity were the screening criteria used to divide the region into three areas of increasing seismotectonic risk. Criteria were then used to subdivide the area of lowest seismotectonic risk into six geologically distinct subareas including characteristics, surface-water and groundwater hydrology, potential human intrusion, site geometry, surface characteristics, and tectonic environment. Decision analysis was then used to identify the subareas most favorable from a geologic standpoint for further investigation, with a view to selecting a site for a repository. Three subareas (parts of northeastern Vermont, northern New Hampshire, and western Maine) were found to be the most favorable, using this method and existing data. However, because this study assessed relative geologic favorability, no conclusions should be drawn concerning the absolute suitability of individual subareas for high-level radioactive waste isolation. 34 refs., 7 figs., 20 tabs.

  16. Determination of (241)Pu by the method of disturbed radioactive equilibrium using 2πα-counting and precision gamma-spectrometry.

    Science.gov (United States)

    Alekseev, I; Kuzmina, T

    2016-04-01

    A simple technique is proposed for the determination of the content of (241)Pu, which is based on disturbance of radioactive equilibrium in the genetically related (237)U←(241)Pu→(241)Am decay chain of radionuclides, with the subsequent use of 2πα-counting and precision gamma-spectroscopy for monitoring the process of restoration of that equilibrium. It has been shown that the data on dynamics of accumulation of the daughter (241)Am, which were obtained from the results of measurements of α- and γ-spectra of the samples, correspond to the estimates calculated for the chain of two genetically related radionuclides, the differences in the estimates of (241)Pu radioactivity not exceeding 2%. Combining the different methods of registration (2πα-counting, semiconductor alpha- and gamma-spectrometry) enables the proposed method to be efficiently applied both for calibration of (241)Pu-sources (from several hundreds of kBq and higher) and for radioisotopic analysis of plutonium mixtures. In doing so, there is a deep purification of (241)Pu from its daughter decay products required due to unavailability of commercial detectors that could make it possible, based only on analysis of alpha-spectra, to conduct quantitative analysis of the content of (238)Pu and (241)Am.

  17. A straightforward method to determine flavouring substances in food by GC-MS

    NARCIS (Netherlands)

    Lopez Sanchez, P.; Sisseren, van M.; Marco, De S.; Jekel, A.A.; Nijs, de W.C.M.; Mol, J.G.J.

    2015-01-01

    A straightforward GC–MS method was developed to determine the occurrence of fourteen flavouring compounds in food. It was successfully validated for four generic types of food (liquids, semi-solids, dry solids and fatty solids) in terms of limit of quantification, linearity, selectivity, matrix

  18. A straightforward method to determine flavouring substances in food by GC-MS

    NARCIS (Netherlands)

    Lopez Sanchez, P.; Sisseren, van M.; Marco, De S.; Jekel, A.A.; Nijs, de W.C.M.; Mol, J.G.J.

    2015-01-01

    A straightforward GC–MS method was developed to determine the occurrence of fourteen flavouring compounds in food. It was successfully validated for four generic types of food (liquids, semi-solids, dry solids and fatty solids) in terms of limit of quantification, linearity, selectivity, matrix effe

  19. 40 CFR 720.25 - Determining whether a chemical substance is on the Inventory.

    Science.gov (United States)

    2010-07-01

    ... portion of the Inventory by a specific chemical name (either a Chemical Abstracts (CA) Index Name or a CA Preferred Name) and a Chemical Abstracts Service (CAS) Registry Number if its identity is not confidential... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Determining whether a chemical...

  20. HPLC测定氟他胺有关物质%Determination of Related Substances of Flutamide by HPLC

    Institute of Scientific and Technical Information of China (English)

    崔正华

    2013-01-01

    目的 建立高效液相色谱法(HPLC)测定氟他胺中有关物质的含量.方法 采用HPLC,用Diamonsil C18色谱柱(250 mm×4.6 mm,5μm);流动相:甲醇-水(60∶40);检测波长:230 nm;进样量:20 μL;流速:1.0 mL/min;柱温:25℃.结果 氟他胺与各杂质能得到有效分离,各杂质在0.04~2.0 μg/mL范围内线性良好.结论 本测定方法操作方便,灵敏度高,准确可靠,可用于氟他胺中有关物质的测定.%Objective To establish an HPLC for determination of related substances in flutamide.Methods The chromatographic procedure was carried out with Diamonsil C18 (250 mm × 4.6 mm,5 μm) as an analytical column and methanol-water (60∶40) as mobile phase at a flow rate of 1.0 mL/min.The detection wavelength was 230 nm and the column temperature was 25 ℃.Results Flutamide could be completely separated from the other impurities with a linear range of 0.04~2.0 μg/mL.Conclusion A sensitive and accurate method for determination of related substances in flutamide was established.

  1. Optimization of separation and determination of moxifloxacin and its related substances by RP-HPLC.

    Science.gov (United States)

    Djurdjevic, Predrag; Ciric, Andrija; Djurdjevic, Aleksandra; Stankov, Milena Jelikic

    2009-09-01

    A RP-HPLC method for the separation and determination of impurities of moxifloxacin, in its pharmaceutical forms as well as moxifloxacin degradation products, was developed with the aid of DryLab software and chemometric (response surface) approach. The separation of four synthesis-related impurities was achieved on a Waters C(18) XTerra column using a mobile phase of (water+triethylamine (2%, v/v)): acetonitrile=90:10 (v/v%); the pH of water phase being adjusted with phosphoric acid to 6.0. Flow rate of the mobile phase was 1.5 ml/min and UV detection at 290 nm was employed. The column was thermostated at 45 degrees C. The resolution between the two least resolved impurity peaks was in average, R(s,min) > 1.5. Method validation parameters indicate linear dynamic range 0.2-2.0 microg/ml with LOQ ca. 0.20 microg/ml and LOD ca. 0.05 microg/ml for all analytes. The method was applied for the impurities determination in drug tablets and infusion (Avelox), Bayer AG) and for degradation products determination in a stability study of moxifloxacin. The impurity content in the tablets and infusion was quantified as 0.1% of total drug. Two degradation products were noted under hydrolytic conditions. The method can also be used for rapid and accurate quantification of moxifloxacin hydrochloride in its tablets during stability testing.

  2. Determination of morphine, codeine and 6-monoacetylmorphine in saliva of substance-abuse patients using HPLC/MS methods

    Directory of Open Access Journals (Sweden)

    Milovanović Vesna

    2012-01-01

    Full Text Available Background/Aim. Saliva represents an alternative specimen for substances abuse determination in toxicology. Hence, the aim of this study was to optimize a method for saliva specimen preparation for heroin metabolites, morphine and 6-monoacetylmorphine (6-mam, and codeine determination by liquid chromatography-mass spectrometry (LC/MS, and to apply this method on saliva samples taken from the patients. Methods. Saliva specimen was prepared using liqiud/liquid extraction of morphine, codeine and 6- mam by mixture of chloroform and isopropanol (9 : 1; v/v. Extracts were analysed by HPLC/MS technique: separation column Waters Spherisorb® 5 μm, ODS2, 4.6 × 100 mm; mobile phase: ammonium acetate : acetonitile (80 : 20; v/v, mobile phase flow rate 0.3 mL/min; mass detection range: 100-400 m/z. Regression and correlation analyses were performed with the probalility level of 0.05. Concentrations of morphine, codeine and 6-mam were determined in saliva samples of the patients with “opiates” in urine identified by the test strips. Results. Calibration for each analysed substance was done in the concentration range from 0.1 to 1 mg/L and the coefficient of correlation was R2 > 0.99. We obtained following calibration curves: y = 385531x + 14584; y = 398036x + 31542; and y = 524162x - 27105, for morphine, codeine and 6-mam, respectively. Recovery for morphine and codeine determination was 99%, while for 6- mam it was 94%. Limits of detection and quantification of a proposed method were 0.01 mg/L and 0.05 mg/L, respectively. Concentration of morphine in the saliva of the heroin users ranged between 0.54 and 5.82 mg/L, concentration of codeine between 0.05 and 5.33, and 6-mam between 0.01 and 0.68 mg/L. A statistically significant correlation between codeine and 6-mam concentrations was obtained. Conclusion. A proposed HPLC/MS method for morphine, codeine and 6-mam determination in saliva is accurate, simple, cheap and suitable for routine analysis and

  3. Determination of true optical absorption and scattering coefficient of wooden cell wall substance by time-of-flight near infrared spectroscopy.

    Science.gov (United States)

    Kitamura, Ryunosuke; Inagaki, Tetsuya; Tsuchikawa, Satoru

    2016-02-22

    The true absorption coefficient (μa) and reduced scattering coefficient (μ´s) of the cell wall substance in Douglas fir were determined using time-of-flight near infrared spectroscopy. Samples were saturated with hexane, toluene or quinolone to minimize the multiple reflections of light on the boundary between pore-cell wall substance in wood. μ´s exhibited its minimum value when the wood was saturated with toluene because the refractive index of toluene is close to that of the wood cell wall substance. The optical parameters of the wood cell wall substance calculated were μa = 0.030 mm(-1) and μ´s= 18.4 mm(-1). Monte Carlo simulations using these values were in good agreement with the measured time-resolved transmittance profiles.

  4. IFCC recommended reference method for the determination of the substance concentration of ionized calcium in undiluted serum, plasma or whole blood

    NARCIS (Netherlands)

    Burnett, RW; Christiansen, TF; Covington, AK; Fogh-Andersen, N; Kulpmann, WR; Lewenstam, A; Maas, AHJ; Muller-Plathe, O; Sachs, C; Siggaard-Andersen, O; VanKessel, AL; Zijlstra, WG

    2000-01-01

    A reference method is described for the determination of the substance concentration of ionized calcium in plasma by which ionized calcium (free or unbound) may be reliably determined on the basis of calibration with aqueous solutions with known concentration of ionized calcium. The composition of t

  5. Environmental radioactive intercomparison program and radioactive standards program

    Energy Technology Data Exchange (ETDEWEB)

    Dilbeck, G. [Environmental Monitoring Systems Laboratory, Las Vegas, NV (United States)

    1993-12-31

    The Environmental Radioactivity Intercomparison Program described herein provides quality assurance support for laboratories involved in analyzing public drinking water under the Safe Drinking Water Act (SDWA) Regulations, and to the environmental radiation monitoring activities of various agencies. More than 300 federal and state nuclear facilities and private laboratories participate in some phase of the program. This presentation describes the Intercomparison Program studies and matrices involved, summarizes the precision and accuracy requirements of various radioactive analytes, and describes the traceability determinations involved with radioactive calibration standards distributed to the participants. A summary of program participants, sample and report distributions, and additional responsibilities of this program are discussed.

  6. Removal of radioactive contaminants by polymeric microspheres.

    Science.gov (United States)

    Osmanlioglu, Ahmet Erdal

    2016-11-01

    Radionuclide removal from radioactive liquid waste by adsorption on polymeric microspheres is the latest application of polymers in waste management. Polymeric microspheres have significant immobilization capacity for ionic substances. A laboratory study was carried out by using poly(N-isopropylacrylamide) for encapsulation of radionuclide in the liquid radioactive waste. There are numbers of advantages to use an encapsulation technology in radioactive waste management. Results show that polymerization step of radionuclide increases integrity of solidified waste form. Test results showed that adding the appropriate polymer into the liquid waste at an appropriate pH and temperature level, radionuclide was encapsulated into polymer. This technology may provide barriers between hazardous radioactive ions and the environment. By this method, solidification techniques became easier and safer in nuclear waste management. By using polymer microspheres as dust form, contamination risks were decreased in the nuclear industry and radioactive waste operations.

  7. Method Validation for the Gamma-ray Spectrometric Determination of Natural Radioactive Nuclides in NORM Samples - Method Validation for the Gamma-ray Spectrometric Determination of Natural Radionuclides in raw materials and by-products

    Energy Technology Data Exchange (ETDEWEB)

    Ji, Young-Yong; Lim, Jong-Myoung; Jang, Mee; Kim, Chang-Jong; Chung, Kun Ho; Kang, Mun Ja; Choi, Geun-Sik [Environmental Radioactivity Assessment Team, Korea Atomic Energy Research Institute, 111, Daedeok-daero 989, Yuseong, Daejeon, 305-353 (Korea, Republic of)

    2014-07-01

    It has established the 'Act on safety control of radioactive rays around living environment' in Korea, since 2011, to protect the public from natural occurring radioactive materials (NORM) and their by-products. The increasing concerns regarding the radioactivity of those materials therefore dictate many demands for the radioactive analysis for them. There are several methods to determine the concentration of natural radionuclides, such as {sup 235}U, {sup 238}U, {sup 226}Ra, {sup 232}Th, and so on, through a radiochemical analysis using an alpha spectrometer, mass spectrometer and liquid scintillation counter. However, gamma-ray spectroscopy still has an effect on the assessment of radioactive concentration for these nuclides and their progenies. To adapt a gamma spectrometer to the determination of natural radionuclides, the feasibility of their analysis methods should be first verified and validated with respect to accuracy and time and cost constraints. In general, one of the well-known processes in analyzing uranium with a gamma spectrometer is an indirect measurement using the secular equilibrium state with their progenies in a sample. This method, however, demands the time elapsed about 3 weeks to reach the equilibrium state between {sup 226}Ra and {sup 222}Rn and the sufficient integrity of a sample bottle to prevent the leakage of radon isotopes which is a form of noble gas. The simple and quick method is to directly measure a full energy absorption peak of 186.2 keV from {sup 226}Ra without the secular equilibrium state between {sup 226}Ra and {sup 222}Rn in the common sample bottle. However, this direct measurement also has difficulties about the interference with a full energy absorption peak of 185.7 keV from {sup 235}U. In this study, direct measurement with the interference correction technique, which uses several reference peaks for gamma-rays from {sup 235}U and {sup 234}Th, and indirect measurement, which means the identification of {sup

  8. Determination of natural radioactivity, 222Rn and 220Rn exhalation rates and radiation hazards of fly ash and fly ash brick used in Baotou, China

    Directory of Open Access Journals (Sweden)

    Li Yuxin

    2016-01-01

    Full Text Available Natural radioactivity levels, 222Rn and 220Rn exhalation rates and radiation hazards of fly ash and fly ash brick used in Baotou, China were determined. The activity concentrations of 226Ra, 232Th, and 40K in fly ash samples ranged from 38.81 to 93.73, 40.34 to 135.17, and 66.92 to 290.86 Bq/kg with an average of 76.52, 109.95, and 170.72 Bq/kg, respectively; while in fly ash brick samples, these radionuclides ranged from 42.43 to 71.60, 76.65 to 208.37, and 94.32 to 489.42 Bq/kg with an average of 53.83, 101.93, and 266.48 Bq/kg, respectively. The exhalation rates of 222Rn and 220Rn in all determined samples were in the range of 1.13-20.50 and 15.60-113.00 mBq/m2s, respectively. The calculated results of the radium equivalent activity, external hazard index, internal hazard index, indoor annual effective dose and outdoor annual effective dose indicated that fly ashes and fly ash bricks collected from some brick factories of Baotou would pose excessive radiation risks to inhabitants and that they are not suitable for use in building construction. The natural radioactivity level of fly ash and fly ash brick needs to be constantly monitored considering the radiation safety of the local residents.

  9. Separation and determination of nimesulide related substances for quality control purposes by micellar electrokinetic chromatography.

    Science.gov (United States)

    Zacharis, Constantinos K; Tzanavaras, Paraskevas D; Notou, Maria; Zotou, Anastasia; Themelis, Demetrius G

    2009-02-20

    A micellar electrokinetic chromatography (MEKC) method has been developed and validated for the determination of nimesulide related compounds in pharmaceutical formulations. Electrophoretic separation of six European Pharmacopoeia (EP) impurities (A-F) was performed using a fused silica capillary (L(eff.)=50 cm, L(tot.)=57 cm, 50 microm i.d.) with a background electrolyte (BGE) containing 25 mM borate buffer (pH 9.5), 30 mM sodium dodecyl sulphate and phi=3% (v/v) acetonitrile. The influence of several factors (surfactant and buffer concentration, pH, organic modifier, applied voltage, capillary temperature and injection time) was studied. The method was suitably validated with respect to linearity, limit of detection and quantification, accuracy, precision and selectivity. The calibration curves obtained for the six compounds were linear over the range 5-12 microgml(-1) (0.05-0.12%). The relative standard deviations (s(r)) of intra- and inter-day experiments were less than 5.0%. The detection limits ranged between 0.7 and 1.6 microgml(-1) depending on the impurity. The proposed method was applied successfully to the quantification of nimesulide impurities in its pharmaceutical formulation.

  10. A quantitative radiochemical method for the determination of the major sources of natural radioactivity in ores and minerals

    Science.gov (United States)

    Rosholt, John Nicholas

    1953-01-01

    The determination of Th232, Rn222, and Pb210 by isolation and subsequent activity analysis of some of their short-lived daughter products is described. The sulfides of bismuth and polonium are precipitated out of solutions of thorium or uranium ores, and the alpha particle activity of PO214. PO212 and PO210 is determined by scintillation counting techniques. PO214 activity is used to determine Rn222, PO212 activity for Th232, and PO210 for Pb210.

  11. Theoretical Purge Factor Determination as a Control Strategy for Potential Mutagenic Impurities in the Synthesis of Drug Substances.

    Science.gov (United States)

    Kragelj Lapanja, Nevenka; Toplak Časar, Renata; Jurca, Sabina; Doljak, Bojan

    Mutagenic impurities (MIs) are of serious concern for pharmaceutical industry, regulatory agencies and public health. The first guideline addressing the control of genotoxic impurities (GTIs) dates back to 2006. Since then there have been several updates and refinements, which eventually resulted in the guideline, published by the International Conference on Harmonisation (ICH) in June 2014. The ICH M7 guideline, compared to previous ones, offers greater flexibility in terms of control strategies for GTIs in drug substances. More specifically, it describes a control strategy that relies on process controls in lieu of analytical testing which is based on understanding the process chemistry and process parameters that impact the levels of GTIs. This principle is adopted in the theoretical purge factor determination tool proposed by Teasdale et al. Several case studies applying the proposed theoretical purge factor determination tool were published in recent years. The results confirm the tool's good predictability of the extent to which the impurity is removed by the process. Hopefully, this approach will soon be released as an in-silico tool, generally accepted by the regulatory agencies.

  12. SHIPPING OF RADIOACTIVE ITEMS

    CERN Multimedia

    TIS/RP Group

    2001-01-01

    The TIS-RP group informs users that shipping of small radioactive items is normally guaranteed within 24 hours from the time the material is handed in at the TIS-RP service. This time is imposed by the necessary procedures (identification of the radionuclides, determination of dose rate, preparation of the package and related paperwork). Large and massive objects require a longer procedure and will therefore take longer.

  13. Determination of neomycin and related substances in pharmaceutical preparations by reversed-phase high performance liquid chromatography with mass spectrometry and charged aerosol detection.

    Science.gov (United States)

    Stypulkowska, K; Blazewicz, A; Fijalek, Z; Warowna-Grzeskiewicz, M; Srebrzynska, K

    2013-03-25

    A new, simple and repeatable liquid chromatographic method with charged aerosol detection (LC-CAD) for determination of neomycin and related substances has been developed. Analysis of neomycin or other aminoglycosides is problematic due to a lack of chromophores. Universal response of CAD enables direct quantification of neomycin and related substances, for which no reference standard are available. Separation was performed on C18 Hypersil(®) Gold aQ column using water, methanol and heptaflurobutyric acid as mobile phase. Under developed chromatographic conditions all impurities were well separated from neomycin B. Peaks identification was evaluated by electrospray ionization mass spectrometry. The proposed method was validated according to ICH guidelines and applied to the content determination of neomycin and related substances in pharmaceutical preparations.

  14. Determination of {sup 228}Th, {sup 232}Th, and{sup 228}Ra in wild mushroom from a naturally high radioactive region in Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Rosa, Mychelle M.L.; Taddei, Maria Helena T.; Silva, Marco A.; Ferreira, Marcelo T., E-mail: mychelle@cnen.gov.b, E-mail: mhtaddei@cnen.gov.b, E-mail: masilva@cnen.gov.b, E-mail: ferreira@cnen.gov.b [Brazilian Nuclear Energy Commission (LAPOC/CNEN-MG), Pocos de Caldas, MG (Brazil). Lab. of Pocos de Caldas; Maihara, Vera A., E-mail: vmaihara@ipen.gov.b [Nuclear and Energy Research Institute (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-07-01

    Mushrooms are fungi which efficiently accumulate radionuclides, as verified by radiochemistry analyses of specimens collected in contaminated areas, specifically after the Chernobyl nuclear accident. Many studies have demonstrated that mushrooms can be used in monitoring of ecosystem contamination and quality. The present paper is part of a broader study conducted in the Pocos de Caldas plateau region in Minas Gerais, Brazil, investigating assimilation of natural Uranium and Thorium radionuclide series by mushrooms. This region has elevated natural radioactivity due to the presence of radiological anomalies of volcanic origin. These anomalies are ore bodies containing Uranium and Thorium, the later being highly predominant. Many researchers have been conducted concerning radionuclide incorporation by agricultural products on the plateau. The present paper aims to determine {sup 232}Th, {sup 228}Th, and {sup 228}Ra radionuclides in wild mushrooms collected at different locations in the plateau region. {sup 228}Ra was determined by radiochemical separation using sulphate coprecipitation followed by beta radiometry. {sup 232}Th and {sup 228}Th were determined using anion exchange resin purification followed by alpha spectrometry. Higher values were obtained to {sup 228}Th than to {sup 232}Th. This is due to higher {sup 228}Ra mobility, which decays to {sup 228}Th. The accuracy of the analytical methods employed was evaluated using the reference sample IAEA Soil 327. These methods had high chemical recovery and high sensitivity. It was possible to confirm that mushrooms accumulate radionuclide and so can be used in environmental contamination and quality assessment. (author)

  15. Simultaneous separation and determination of process-related substances and degradation products of venlafaxine by reversed-phase HPLC.

    Science.gov (United States)

    Nageswara Rao, R; Narasa Raju, A

    2006-12-01

    A simple and rapid gradient RP HPLC method for simultaneous separation and determination of venlafaxine and its related substances in bulk drugs and pharmaceutical formulations has been developed. As many as four process impurities and one degradation product of venlafaxine have been separated on a Kromasil KR100-5C18 (4.6 mm x 250 mm; particle size 5 microm) column with gradient elution using 0.3% diethylamine buffer (pH 3.0) and ACN/methanol (90:10 v/v) as a mobile phase. The column was maintained at 40 degrees C and the eluents were monitored with photo diode array detection at 225 nm. The chromatographic behaviour of all the compounds was examined under variable compositions of different solvents, temperatures, buffer concentrations and pH. The method was validated in terms of accuracy, precision and linearity as per ICH guidelines. The inter- and intraday assay precision was method was successfully applied to the analysis of commercial formulations and the recoveries of venlafaxine were in the range of 99.32-100.67 with %RSD method could be of use not only for rapid and routine evaluation of the quality of venlafaxine in bulk drug manufacturing units but also for the detection of its impurities in pharmaceutical formulations. Forced degradation of venlafaxine was carried out under thermal, photo, acidic, basic and peroxide conditions and the acid degradation products were characterized by ESI-MS/MS, 1H NMR and FT-IR spectral data.

  16. Development of stability-indicating UHPLC method for the quantitative determination of silodosin and its related substances.

    Science.gov (United States)

    Shaik, Jafer Vali; Saladi, Shantikumar; Sait, Shakil S

    2014-08-01

    A novel, specific and stability-indicating reversed-phase (RP) ultra-high-performance liquid chromatography (UHPLC) method, which is mass compatible, was developed and validated for the quantitative determination of silodosin and its related substances. Silodosin was subjected to stress conditions like hydrolysis (acid and basic), oxidation, photolysis and thermal degradation, as per the guidelines of the International Conference Harmonization, to show that the method is stability-indicating. The proposed UHPLC method has a resolution of greater than 2.0 between silodosin and its process-related impurities. The chromatographic separation was achieved on an Agilent Poroshell 120 EC-C18 column (50 × 4.6mm i.d.; particle size, 2.7 µm). The method employed a linear gradient elution using a mobile phase consisting of acetonitrile and 10 mM ammonium acetate buffer with 0.1% triethyl amine, with pH adjusted to 6.0, monitored at 273 nm. The developed RP-LC method was validated with respect to linearity, accuracy, precision and robustness. The known process impurities were separated and their structure was confirmed by using liquid chromatography-mass spectrometry and direct mass analysis.

  17. Isolation of iron and strontium from liquid samples and determination of {sup 55}Fe and {sup 89,90}Sr in liquid radioactive waste

    Energy Technology Data Exchange (ETDEWEB)

    Grahek, Zeljko; Macefat, Martina Rozmaric

    2004-05-31

    This paper describes the method of isolating iron and strontium from liquid samples with a low concentration of ions that enables simple and rapid determination of {sup 55}Fe and {sup 89,90}Sr. The method consists of binding (concentrating) Fe and Sr at the cation exchanger Amberlite IR-120, their elution from cation exchanger with 4 M HCl or 8 M HNO{sub 3}, isolating Fe on the TRU extraction chromatographic column with 4 M HCl or 8 M HNO{sub 3}, and isolating Sr on the Sr.spec column with the mixture of 8 M HNO{sub 3}+2 M HCl or 5 M HNO{sub 3}. After the isolation, {sup 55}Fe is determined by liquid scintillation counting with scintillation solution, while activity of {sup 89,90}Sr is obtained by Cherenkov counting in 5 M HNO{sub 3}. It was shown that successive counting can be used for simultaneous determination of {sup 89,90}Sr activity. The activity ratio of {sup 89}Sr/{sup 90}Sr (up to 20:1) and vice versa does not impact the determination. {sup 55}Fe is also determined immediately after isolation. The measurements in {alpha},{beta} mode can be used to verify any presence of {alpha}-emitter (americium) in the fraction of iron and to correct the result. The method was tested by determining {sup 55}Fe and {sup 89,90}Sr in model samples and radioactive waste samples. The paper also shows that Fe and Zn can be bound to the TEVA and TRU resins from the solutions of HCl, HNO{sub 3}, and mixture of HCl+HNO{sub 3}. The binding strength depends on the type of resin and the concentration of the acid or the concentration of acids in the mixture. These resin and acids can be used for mutual separation of Fe and Zn and their separation from other elements.

  18. A simultaneous determination of related substances by high performance liquid chromatography in a drug product using quality by design approach.

    Science.gov (United States)

    Tol, Trupti; Kadam, Nilesh; Raotole, Nilesh; Desai, Anita; Samanta, Gautam

    2016-02-05

    The combination of Abacavir, Lamivudine and Dolutegravir is an anti-retroviral formulation that displays high efficacy and superiority in comparison to other anti-retroviral combinations. Analysis of related substances in this combination drug product was very challenging due to the presence of nearly thirty peaks including the three active pharmaceutical ingredients (APIs), eleven known impurities and other pharmaceutical excipients. Objective of this study was to develop a single, selective, and robust high performance liquid chromatography method for the efficient separation of all peaks. Initially, one-factor-at-a-time (OFAT) approach was adopted to develop the method. But, it could not resolve all the critical peaks in such complex matrix. This led to the advent of two different HPLC methods for the determination of related substances, one for Abacavir and Lamivudine and the other for Dolutegravir. But, since analysis of a single sample using two methods instead of one is time and resource consuming and thus expensive, an attempt was made to develop a single and robust method by adopting quality by design (QbD) principles. Design of Experiments (DoE) was applied as a tool to achieve the optimum conditions through Response surface methodology with three method variables, pH, temperature, and mobile phase composition. As the study progressed, it was discovered that establishment of the design space was not viable due to the completely distant pH requirements of the two responses, i.e. (i) retention time for Lamivudine carboxylic acid and (ii) resolution between Abacavir impurity B and unknown impurity. Eventually, neglecting one of these two responses each time, two distinguished design spaces have been established and verified. Edge of failures at both design spaces indicate high probability of failure. It therefore, becomes very important to identify the most robust zone or normal operating range (NOR) within the design space with low risk of failure and high

  19. Determination of the correlation between elemental and organic carbons to trace elemental substances and anions in DPM samples

    CSIR Research Space (South Africa)

    Mahlangu, Vusi J

    2016-09-01

    Full Text Available improvements and analysis techniques. Samples investigated were received from different mine commodities and were initially characterised for their diesel particulate matter content and trace elemental substances on a thermo-optical analyser and an inductively...

  20. Determination and mapping the spatial distribution of radioactivity of natural spring water in the Eastern Black Sea Region by using artificial neural network method.

    Science.gov (United States)

    Yeşilkanat, Cafer Mert; Kobya, Yaşar

    2015-09-01

    In this study, radiological distribution of gross alpha, gross beta, (226)Ra, (232)Th, (40)K, and (137)Cs for a total of 40 natural spring water samples obtained from seven cities of the Eastern Black Sea Region was determined by artificial neural network (ANN) method. In the ANN method employed, the backpropagation algorithm, which estimates the backpropagation of the errors and results, was used. In the structure of ANN, five input parameters (latitude, longitude, altitude, major soil groups, and rainfall) were used for natural radionuclides and four input parameters (latitude, longitude, altitude, and rainfall) were used for artificial radionuclides, respectively. In addition, 75 % of the total data were used as the data of training and 25 % of them were used as test data in order to reveal the structure of each radionuclide. It has been seen that the results obtained explain the radiographic structure of the region very well. Spatial interpolation maps covering the whole region were created for each radionuclide including spots not measured by using these results. It has been determined that artificial neural network method can be used for mapping the spatial distribution of radioactivity with this study, which is conducted for the first time for the Black Sea Region.

  1. Determination of the priority substances regulated by 2000/60/EC and 2008/105/EC Directives in the surface waters supplying water treatment plants of Athens, Greece.

    Science.gov (United States)

    Golfinopoulos, Spyros K; Nikolaou, Anastasia D; Thomaidis, Nikolaos S; Kotrikla, Anna Maria; Vagi, Maria C; Petsas, Andreas S; Lekkas, Demetris F; Lekkas, Themistokles D

    2017-03-21

    An investigation into the occurrence of priority substances regulated by 2000/60/EC Water Framework Directive and 2008/105/EC Directive was conducted for a period of one year in the surface water sources supplying the water treatment plants (WTPs) of Athens and in the raw water of WTPs. Samples from four reservoirs and four water treatment plants of Athens were taken seasonally. The substances are divided into seven specific groups, including eight volatile organic compounds (VOCs), diethylhexylphthalate, four organochlorine pesticides (OCPs), three organophosphorus/organonitrogen pesticides (OPPs/ONPs), four triazines and phenylurea herbicides, pentachlorophenol, and four metals. The aforementioned substances belong to different chemical categories, and different analytical methods were performed for their determination. The results showed that the surface waters that feed the WTPs of Athens are not burdened with significant levels of toxic substances identified as European Union (EU) priority substances. Atrazine, hexachlorocyclohexane, endosulfan, trifluralin, anthracene and 4-nonylphenol were occasionally observed at very low concentrations. Their presence in a limited number of cases could be attributed to waste disposal, agricultural activities, and to a limited industrial activity in the area nearby the water bodies.

  2. A model for determination of screening level for radioactive elements in soil; Modelo para o estabelecimento de valores orientadores para elementos radioativos no solo

    Energy Technology Data Exchange (ETDEWEB)

    Peres, Ana Claudia

    2007-07-01

    At the present, decision about clean-up of Brazilian sites contaminated with radioactive isotopes is addressed on a case-by-case basis, since there is no general guidance or recommendation to support actions in early phases of the problem identification. For chemicals, CETESB - the governmental organization responsible for preventing and controlling environmental pollution in Sao Paulo State - established background values, prevention and intervention, as the first step to implement a remediation actions based on human health risk assessment. The aim of this study was to develop a methodology for the establishment of target values for radioactive soil contamination, as far as possible consistent and compatible with the approach adopted by CETESB for sites contaminated with chemicals. The following steps have been addressed in this study: conceptual scenario and model development; codification of the equations in an electronic spreadsheet; selection of proper range and statistical distribution of the input values; derivation of the intervention levels for selected radionuclides using Monte Carlo methods. The mathematical model developed was mainly based on the equations used by the U.S. Environmental Protection Agency (EPA) and by the National Council on Radiation Protection and Measurements (NCRP) for soil screening purposes. Intervention and prevention values are presented for adult and 10 years old child, for each 3 exposure scenarios: agricultural, residential and industrial; the following radionuclides were considered: {sup 3}H, {sup 14}C, {sup 32}P, {sup 35}S, {sup 45}Ca, {sup 51}Cr, {sup 90}Sr, {sup 125}I, {sup 131}I, {sup 134}Cs, {sup 137}Cs, {sup 210}Pb, {sup 226}Ra, {sup 228}Ra, {sup 232}Th, {sup 238}U, {sup 239}Pu and {sup 241} Am. Quality reference values were determined for {sup 40}K, {sup 137}Cs, {sup 210}Pb, {sup 226}Ra, {sup 228}Ra, {sup 228}Th, Th-nat e U-nat. Results obtained in this study showed a good agreement with those reported by NCRP

  3. Optimisation of spectrometric gamma-gamma probe configuration using very low radioactivity sources for lead and zinc grade determination in borehole logging

    CERN Document Server

    Asfahani, J

    1999-01-01

    The suitability of spectrometric backscattered gamma-gamma well logging measurements to predict lead and zinc metal equivalent content is demonstrated. A centralised tool employing a gamma-ray source of very low radioactivity (1.8 MBq) is used. The logging tool is tested using sup 1 sup 3 sup 3 Ba and sup 1 sup 3 sup 7 Cs sources with a 37 mm (diameter)x75 mm NaI (TI) scintillation detector. Five source-to-detector configurations were analysed for 18 geophysical models, 13 of which had a borehole diameter of 130 mm and the other 5 had a borehole diameter of 160 mm. Regression analysis on the laboratory logging data for each configuration in order to establish the calibration equation for a lead (Pb) and zinc metal equivalent (ZME) prediction is carried out. The optimum configuration for the logging probe using a sup 1 sup 3 sup 3 Ba source was determined to be 52 mm source-to-detector spacing. This configuration gives the best results for both Pb and ZME grade. The rms deviations for Pb and ZME were 0.33 and ...

  4. Determination of {sup 238}Pu, {sup 239+240}Pu, {sup 241}Pu and {sup 241}Am in radioactive waste from IPEN reactor

    Energy Technology Data Exchange (ETDEWEB)

    Geraldo, Bianca; Taddei, Maria Helena T.; Cheberle, Sandra M.; Ferreira, Marcelo T., E-mail: bgeraldo@cnen.gov.b, E-mail: mhtaddei@cnen.gov.b, E-mail: scsantos@cnen.gov.b, E-mail: ferreira@cnen.gov.b [Brazilian Nuclear Energy Commission (LAPOC/CNEN-MG), Pocos de Caldas, MG (Brazil). Lab. of Pocos de Caldas; Marumo, Julio T., E-mail: jtmarumo@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-07-01

    Ion exchange resin is a common type of radioactive waste arising from treatment of coolant water of the main circuit of research and nuclear power reactors. This waste contains high concentrations of fission and activation products. The management of this waste includes its characterization in order to determine and quantify specific radionuclides including those known as difficult-to-measure radionuclides (RDM). The analysis of RDMs generally involves expensive and time-consuming complex radiochemical analysis for purification and separation of the radionuclides. The objective of this work is to show an easy methodology for quantifying plutonium and americium isotopes in spent ion exchange resin, used for purification of the cooling water of the IEA-R1 reactor located at the Nuclear and Energy Research Institute, IPEN-CNEN/SP. The resins were destroyed by acid digestion, followed by purification and separation of the Pu and Am isotopes with anionic and chromatographic resins. {sup 238}Pu, {sup 239}+{sup 24}'0Pu, and {sup 24}'1Am isotopes were analyzed in an alpha spectrometer equipped with surface barrier detectors. {sup 241}Pu isotope was analyzed by liquid scintillation counting. Chemical recovery yield ranged from 73 to 98% for Pu and 77 to 98% for Am, demonstrating that the methodology is suitable for identification and quantification of the isotopes studied in spent resins. (author)

  5. Structural determination of a highly stable metal-organic framework with possible application to interim radioactive waste scavenging: Hf-UiO-66

    Science.gov (United States)

    Jakobsen, Søren; Gianolio, Diego; Wragg, David S.; Nilsen, Merete Hellner; Emerich, Hermann; Bordiga, Silvia; Lamberti, Carlo; Olsbye, Unni; Tilset, Mats; Lillerud, Karl Petter

    2012-09-01

    High-resolution synchrotron radiation x-ray powder diffraction (HR-XRPD) combined with Hf L3-edge extended x-ray absorption fine structure allowed us to determine the structure of a Hf-UiO-66 metal-organic framework (MOF) showing that it is isoreticular to Zr-UiO-66 MOF [Cavka , J. Am. Chem. Soc.JACSAT0002-786310.1021/ja8057953 130, 13850 (2008).]. Thermal gravimetric measurements (coupled with mass spectroscopy) and temperature-dependent synchrotron radiation XRPD proved the high thermal stability of the Hf-UiO-66 MOF. The Langmuir surface area (849 m2/g) combined with the high stability of the UiO-66 framework and with the high neutron absorption cross section of Hf suggest that among all microporous crystalline materials the Hf-UiO-66 MOF possesses the physical and chemical requirements for the interim storage of radioactive waste in a much safer way than is currently available. The first results proving the synthesis of a MOF material with UiO-66 topology realized by a B-containing linker are also reported, allowing a further improvement of the neutron shielding power of this class of materials.

  6. Experience with local lymph node assay performance standards using standard radioactivity and nonradioactive cell count measurements.

    Science.gov (United States)

    Basketter, David; Kolle, Susanne N; Schrage, Arnhild; Honarvar, Naveed; Gamer, Armin O; van Ravenzwaay, Bennard; Landsiedel, Robert

    2012-08-01

    The local lymph node assay (LLNA) is the preferred test for identification of skin-sensitizing substances by measuring radioactive thymidine incorporation into the lymph node. To facilitate acceptance of nonradioactive variants, validation authorities have published harmonized minimum performance standards (PS) that the alternative endpoint assay must meet. In the present work, these standards were applied to a variant of the LLNA based on lymph node cell counts (LNCC) run in parallel as a control with the standard LLNA with radioactivity measurements, with threshold concentrations (EC3) being determined for the sensitizers. Of the 22 PS chemicals tested in this study, 21 yielded the same results from standard radioactivity and cell count measurements; only 2-mercaptobenzothiazole was positive by LLNA but negative by LNCC. Of the 16 PS positives, 15 were positive by LLNA and 14 by LNCC; methylmethacrylate was not identified as sensitizer by either of the measurements. Two of the six PS negatives tested negative in our study by both LLNA and LNCC. Of the four PS negatives which were positive in our study, chlorobenzene and methyl salicylate were tested at higher concentrations than the published PS, whereas the corresponding concentrations resulted in consistent negative results. Methylmethacrylate and nickel chloride tested positive within the concentration range used for the published PS. The results indicate cell counts and radioactive measurements are in good accordance within the same LLNA using the 22 PS test substances. Comparisons with the published PS results may, however, require balanced analysis rather than a simple checklist approach.

  7. Determination of small halogenated carboxylic acid residues in drug substances by high performance liquid chromatography-diode array detection following derivatization with nitro-substituted phenylhydrazines.

    Science.gov (United States)

    Hou, Desheng; Fan, Jingjing; Han, Lingfei; Ruan, Xiaoling; Feng, Feng; Liu, Wenyuan; Zheng, Feng

    2016-03-18

    A method for the determination of small halogenated carboxylic acid (HCA) residues in drug substances is urgently needed because of the potential of HCAs for genotoxicity and carcinogenicity in humans. We have now developed a simple method, involving derivatization followed by high performance liquid chromatography-diode array detection (HPLC-DAD), for the determination of six likely residual HCAs (monochloroacetic acid, monobromoacetic acid, dichloroacetic acid, 2-chloropropionic acid, 2-bromopropionic acid and 3-chloropropionic acid) in drug substances. Different nitro-substituted phenylhydrazines (NPHs) derivatization reagents were systematically compared and evaluated. 2-Nitrophenylhydrazine hydrochloride (2-NPH·HCl) was selected as the most suitable choice since its derivatives absorb strongly at 392 nm, a region of the spectrum where most drug substances and impurities absorb very weakly. During the derivatization process, the commonly used catalyst, pyridine, caused rapid dechlorination or chlorine substitution of α-halogenated derivatives. To avoid these unwanted side reactions, a reliable derivatization method that did not use pyridine was developed. Reaction with 2-NPH·HCl using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride as coupling agent in acetonitrile-water (70:30) at room temperature for 2h gave complete reaction and avoided degradation products. The derivatives were analyzed, without any pretreatment, using gradient HPLC with detection in the near visible region. Organic acids commonly found in drug substances and other impurities did not interfere with the analysis. Good linearity (r>0.999) and low limits of quantitation (0.05-0.12 μg mL(-1)) were obtained. The mean recoveries were in the range of 80-115% with RSD <5.81% except for 3-CPA in ibuprofen which was 78.5%. The intra- and inter-day precisions were expressed as RSD <1.98% and <4.39%, respectively. Finally, the proposed method was successfully used for the residue

  8. Determination of the biologically active flavour substances thujone and camphor in foods and medicines containing sage (Salvia officinalis L.

    Directory of Open Access Journals (Sweden)

    Stühlinger Wolf

    2011-07-01

    Full Text Available Abstract Background The sage plant Salvia officinalis L. is used as ingredient in foods and beverages as well as in herbal medicinal products. A major use is in the form of aqueous infusions as sage tea, which is legal to be sold as either food or medicine. Sage may contain two health relevant substances, thujone and camphor. The aim of this study was to develop and validate an analytical methodology to determine these active principles of sage and give a first overview of their concentrations in a wide variety of sage foods and medicines. Results A GC/MS procedure was applied for the analysis of α- and β-thujone and camphor with cyclodecanone as internal standard. The precision was between 0.8 and 12.6%, linearity was obtained from 0.1 - 80 mg/L. The recoveries of spiked samples were between 93.7 and 104.0% (average 99.1%. The time of infusion had a considerable influence on the content of analytes found in the teas. During the brewing time, thujone and camphor show an increase up to about 5 min, after which saturation is reached. No effect was found for preparation with or without a lid on the pot used for brewing the infusion. Compared to extracts with ethanol (60% vol, which provide a maximum yield, an average of 30% thujone are recovered in the aqueous tea preparations. The average thujone and camphor contents were 4.4 mg/L and 16.7 mg/L in food tea infusions and 11.3 mg/L and 25.4 mg/L in medicinal tea infusions. Conclusions The developed methodology allows the efficient determination of thujone and camphor in a wide variety of sage food and medicine matrices and can be applied to conduct surveys for exposure assessment. The current results suggest that on average between 3 and 6 cups of sage tea could be daily consumed without reaching toxicological thresholds.

  9. Determination of "new psychoactive substances" in postmortem matrices using microwave derivatization and gas chromatography-mass spectrometry.

    Science.gov (United States)

    Margalho, Cláudia; Castanheira, Alice; Real, Francisco Corte; Gallardo, Eugenia; López-Rivadulla, Manuel

    2016-05-01

    Despite worldwide efforts aiming to ban the marketing and subsequent abuse of psychoactive substances such as synthetic cathinones and phenethylamines, there has been an alarming growth of both in recent years. Different compounds similar to those already existing are continuously appearing in the market in order to circumvent the legislation. An analytical methodology has been validated for qualitative and quantitative determinations of D-cathine (D-norpseudoehedrine), ephedrine, methcathinone, 1-(4-methoxyphenyl)-propan-2-amine (PMA), mephedrone, methedrone, 2,5-dimethoxy-4-methylamphetamine (DOM), 4-bromo-2,5-dimethoxyamphetamine (DOB), 2,5-dimethoxyphenethylamine (2C-H), 4-bromo-2,5-dimethoxyphenethylamine (2C-B), 4-iodo-2,5-dimethoxyphenethylamine (2C-I), 2-[2,5-dimethoxy-4-(ethylthio)phenyl]ethanamine (2C-T-2), 2,5-dimethoxy-4-isopropylthiophenethylamine (2C-T-4) and 2-[2,5-dimethoxy-4-(propylthio)phenyl]ethanamine (2C-T-7), in low volumes of vitreous humor (100 μL), pericardial fluid (250 μL) and whole blood (250 μL), using deutered amphetamine, ephedrine and mephedrone as internal standards. The validation parameters included selectivity, linearity and limits of detection and quantification, intra- and interday precision and trueness, recovery and stability. The method included mixed-mode solid phase extraction, followed by microwave fast derivatization and analysis by gas chromatography-mass spectrometry operated in selected ion monitoring mode. The procedure was linear between 5 and 600 ng/mL, with determination coefficients higher than 0.99 for all analytes. Intra- and interday precision ranged from 0.1 to 13.6%, while accuracy variability was within 80-120% interval from the nominal concentration at all studied levels. The extraction efficiencies ranged from 76.6 to 112.8%. Stability was considered acceptable for all compounds in the studied matrices. The developed assay was applied to authentic samples of the Laboratory of Chemistry and Forensic

  10. HPLC determination of substance and related substances for the preparation of ibuprofen%HPLC法测定布洛芬原料及制剂的有关物质

    Institute of Scientific and Technical Information of China (English)

    刘芳; 柳小秦; 徐长根; 孟新芳

    2011-01-01

    Objective : To perfect the determination method of the related substances in ibuprofen, for its adaptability to our country. Methods: Three related substances of' ibuprofen are determinated by HPLC. Waters Symmetry ShieldTM C18 (4. 6 mm × 250 mm,5 μm) was used with mobile phase consisted of acetonitrile - water ( adjusted pH to 3. 0 with phosphoric acid) (1: 1). The detective wavelength was set at 254 nm. Results : In the determination of related substances by HPLC,the linearity were good within the range 2 - 50 μg · mL -1 , and the regression coefficient were 0. 9999 , 1. 0000 ,0. 9999 , respectively , while the recoveries were 99. 7% ,99. 5 % , 100. 1% , respectively.Conclusion: This method is operated easily, and it can be used to accurately determinate the related substances contend in ibuprofen.%目的:为了完善布洛芬的有关物质检查方法,使其更适用于中国的实际生产情况.方法:采用高效液相色谱法,紫外检测器,十八烷基硅烷键合硅胶柱,固定相:phenomenex C18(4.6mmx250mm,5μm),流动相:乙腈-水(用磷酸调节pH为3.0)(1:1),检测波长:254nm.结果:3种已知杂质和布洛芬及其他未知杂质均能得到有效分离;;3种已知杂质在2-50μg·ML-1范围内线性关系良好,r分别为0.9999,1.0000,0.9999,平均回收率分别为99.7%,99.5%,100.1%.结论:本方法灵敏、准确、可靠,能够准确测定布洛芬原料及制剂的有关物质.

  11. RADIO-ACTIVE TRANSDUCER

    Science.gov (United States)

    Wanetick, S.

    1962-03-01

    ABS>ure the change in velocity of a moving object. The transducer includes a radioactive source having a collimated beam of radioactive particles, a shield which can block the passage of the radioactive beam, and a scintillation detector to measure the number of radioactive particles in the beam which are not blocked by the shield. The shield is operatively placed across the radioactive beam so that any motion normal to the beam will cause the shield to move in the opposite direction thereby allowing more radioactive particles to reach the detector. The number of particles detected indicates the acceleration. (AEC)

  12. Determinants of Substance Abuse in a Population of Children and Adolescents Involved with the Child Welfare System

    Science.gov (United States)

    Singh, Veeran-Anne S.; Thornton, Tiffany; Tonmyr, Lil

    2011-01-01

    Substance abuse is an important health issue facing children involved with child welfare, but little is known about the associated factors. The purpose of this study was to build on findings from the "Canadian Incidence Study of Reported Child Abuse and Neglect-2003" and use a national sample of 10-15 year old children to examine the factors…

  13. Validation of analytical procedure for determination of recidual organic solvents for standardization the substance of 5,7-bis-meta-nitrophenylamino-4,6-dinitrobenzofuroxan

    Directory of Open Access Journals (Sweden)

    R. Sh. Markhabullina

    2014-01-01

    Full Text Available The aim of this study was to develop and validate a gas chromatography methods of quantitative determination of residual organic solvents in substance of 5,7-bis-(meta-nitrophenylamino-4,6-dinitrobenzofuroxan. Validation of elaborating methods of quantitative determination of residual organic solvents - ethyl alcohol and acetonitrile in substance of 5,7-bis-(meta-nitrophenylamino-4,6-dinitrobenzofuroxan using gas chromatography method allowed to evaluate their metrology parameters. All parameters of validation characteristics met their acceptance criteria's. Specificity was demonstrated by a complete chromatographic separation of peaks of ethyl alcohol and acetonitrile, and lack of peaks of ethyl alcohol and acetonitrile in the chromatogram of solvent. The linearity was proven in the range of quantitation limit to 120 % of the test concentrations. Precision of the methods comply with the requirement defined - the relative standard deviation for of ethyl alcohol and acetonitrile below 3 %. The results of this validation study prove the suitability of the gas chromatography method for quantitative determination of residual organic solvents in substance of 5,7-bis-(meta-nitrophenylamino-4,6-dinitrobenzofuroxan.

  14. An analytical model for radioactive pollutant release simulation in the atmospheric boundary layer

    Energy Technology Data Exchange (ETDEWEB)

    Weymar, Guilherme J.; Vilhena, Marco T.; Bodmann, Bardo E.J., E-mail: guicefetrs@gmail.com, E-mail: mtmbvilhena@gmail.com, E-mail: bejbodmann@gmail.com [Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS (Brazil). Programa de Pos-Graduacao em Engenharia Mecanica; Buske, Daniela; Quadros, Regis, E-mail: danielabuske@gmail.com, E-mail: quadros99@gmail.com [Universidade Federal de Pelotas (UFPel), Capao do Leao, RS (Brazil). Programa de Pos-Graduacao em Modelagem Matematica

    2013-07-01

    Simulations of emission of radioactive substances in the atmosphere from the Brazilian nuclear power plant Angra 1 are a necessary tool for control and elaboration of emergency plans as a preventive action for possible accidents. In the present work we present an analytical solution for radioactive pollutant dispersion in the atmosphere, solving the time-dependent three-dimensional advection-diffusion equation. The experiment here used as a reference in the simulations consisted of the controlled releases of radioactive tritiated water vapor from the meteorological tower close to the power plant at Itaorna Beach. The wind profile was determined using experimental meteorological data and the micrometeorological parameters were calculated from empirical equations obtained in the literature. We report on a novel analytical formulation for the concentration of products of a radioactive chain released in the atmospheric boundary layer and solve the set of coupled equations for each chain radionuclide by the GILTT solution, assuming the decay of all progenitors radionuclide for each equation as source term. Further we report on numerical simulations, as an explicit but fictitious example and consider three radionuclides in the radioactive chain of Uranium 235. (author)

  15. Radioactivity in consumer products

    Energy Technology Data Exchange (ETDEWEB)

    Moghissi, A.A.; Paras, P.; Carter, M.W.; Barker, R.F. (eds.)

    1978-08-01

    Papers presented at the conference dealt with regulations and standards; general and biological risks; radioluminous materials; mining, agricultural, and construction materials containing radioactivity; and various products containing radioactive sources.

  16. Comparative Study on Determination Methods of Lansoprazole Related Substances%兰索拉唑有关物质测定方法的比较研究

    Institute of Scientific and Technical Information of China (English)

    陈苑; 宋粉云

    2015-01-01

    目的:比较不同国家药典中兰索拉唑有关物质的检测方法。方法采用2010年版《中国药典·第一增本》(以下简称ChP2010)、35版《美国药典》(以下简称USP35)、7.0版《欧洲药典》(以下简称EP7.0)所收载的兰索拉唑有关物质质量标准中的方法,分别对兰索拉唑有关物质进行测定,对其色谱行为、分离效能、已知杂质方法学、有关物质测定结果等进行比较。结果 USP35中兰索拉唑有关物质的流动相系统较EP7.0和ChP2010收载的流相系统对兰索拉唑杂质的分离效能更好,而采用EP7.0有关物质方法中收载的溶剂对杂质的溶解力更强。结论 ChP2010兰索拉唑有关物质的测定方法与欧美药典相比尚存在较大差距,建议ChP2010在以后的修订中,将兰索拉唑有关物质的测定方法改为USP35的流动相系统,溶剂则采用EP7.0的溶剂,并借鉴欧美药典制定限度。%Objective To compare the determination methods of lansoprazole related substances in the pharmacopoeias of difference coun-tries. Methods The lansoprazole related substances were determined by adopting the methods of lansoprazole related substances quality standard contained in Chinese Pharmacopeia version 2010 ( Chp2010 ) , US Pharmacopeia edition 35 ( USP35 ) and European Pharmacopeia edition 7. 0 ( EP7. 0 ) . Their chromatographic behavior, separation efficiency, known impurities methodology and related substances determi-nation results were performed the comparison and research. Results The mobile phase system for the determination of lansoprazole re-lated substances in USP35 was better for the lansoprazole impurities separation than that in Chp2010 and EP7. 0, while adopting the solvent contained in the related substances methods of EP7. 0 had stronger dissolving capacity on impurity. Conclusion The determina-tion methods of lansoprazole related substances have large difference between Chp2010 with USP35 and EP

  17. Implementation in laboratories of Latin America of procedures of harmonized essay for the determination of the radioactive contamination of food; Implementacion en laboratorios de Latinoamerica de procedimientos de ensayo armonizados para la determinacion de la contaminacion radiactiva de alimentos

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez G, I.M. [CPHR (Cuba); Iglicki, F.A. [CNEA (Argentina); Aguirre G, J. [CNSNS, (Mexico); Melo F, A.C. de [Instituto de Radioprotecao e Dosimetria, (Brazil); Tomicic M, I.J. [Comision Chilena de Energia Nuclear, (Chile); Loria M, L.G. [Centro de Investigacion en Ciencias Atomicas Nucleares y Moleculares, (Costa Rica); Diodati, J.M. [ARN, Av. Del Libertador 8250, Buenos Aires (1429), (Argentina); Vasquez B, L.R. [Comision Ecuatoriana de Energia Atomica, (Ecuador); Alarcon S, F.A. [Centro de Investigaciones y Aplicaciones Nucleares, El Salvador (El Salvador); Civil, M. [Laboratoire Veterinaire et de Controle de Qualite des Aliments, (Haiti); Naut M, B.C. [Universidad Autonoma de Santo Domingo, Republica Dominicana (Dominican Republic); Odino M, M.R. [Direccion Nacional de Energia y Tecnologia Nuclear (Uruguay); Flores M, Y.R. [Direccion General de Energia Atomica, (Venezuela); Rossbach, M. [International Atomic Energy Agency, (Austria)]. e-mail: isis@cphr.edu.cu

    2006-07-01

    In Latin America, nowadays, it is not had harmonized essay procedures for the determination of radioactive contaminants in foods. Equally, the great diversity of institutions that in each country are devoted to carry out this control and the difference in the level that its possess the same ones in quality matter, its impose the necessity to implant a Quality Management System on the base of harmonized technical criteria that its help to obtain reliable analytical results. With this end, it was proposed and it was approved the ARCAL LXXIX regional project: 'Harmonization of the technical and specific requirements of quality for the control of the radioactive contamination of foods'. In this work the aspects more significant of the design and content of the Manual of technical procedures for the determination of radioactive contaminants in foods, elaborated in the marks of the one referred project are presented. The same one includes eight procedures for the previous treatment of the samples, the spectrometric determination of gamma emitters radionuclides, the determination of the alpha activity indexes and total beta, of {sup 131} I, {sup 89,90} Sr, {sup 226} Ra, {sup 238,} {sup 239} Pu and {sup 3} H, using different methodologies validated in the region. The actions carried out to implement this Manual are also exposed. (Author)

  18. Determination of total alpha activity index in samples of radioactive wastes; Determinacion del indice de actividad alfa total en muestras de desechos radiactivos

    Energy Technology Data Exchange (ETDEWEB)

    Galicia C, F. J.

    2015-07-01

    This study aimed to develop a methodology of preparation and quantification of samples containing radionuclides beta and/or alpha emitters, to determine the rates of alpha and beta total activity of radioactive waste samples. For this, a device of planchettes preparer was designed, to assist the planchettes preparation in a controlled environment and free of corrosive vapors. Planchettes were prepared in three means: nitrate, carbonate and sulfate, to different mass thickness, natural uranium (alpha and beta emitter) and in case of Sr-90 (beta emitter pure) only in half nitrate; and these planchettes were quantified in an alpha/beta counter, in order to construct the self-absorption curves for alpha and beta particles. These curves are necessary to determine the rate of alpha-beta activity of any sample because they provide the self-absorption correction factor to be applied in calculating the index. Samples with U were prepared with the help of the device of planchettes preparer and subsequently were analyzed in the proportional counter Mpc-100 Pic brand. Samples with Sr-90 were prepared without the device to see if there was a different behavior with respect to obtaining mass thickness. Similarly they were calcined and carried out count in the Mpc-100. To perform the count, first the parameters of counter operating were determined: operating voltages for alpha and beta particles 630 and 1500 V respectively, a count routine was generated where the time and count type were adjusted, and counting efficiencies for alpha and beta particles, with the aid of calibration sources of {sup 210}Po for alphas and {sup 90}Sr for betas. According to the results, the counts per minute will decrease as increasing the mass thickness of the sample (self-absorption curve), adjusting this behavior to an exponential function in all cases studied. The minor self-absorption of alpha and beta particles in the case of U was obtained in sulfate medium. The self-absorption curves of Sr-90

  19. Development and validation of a micellar electrokinetic capillary chromatography method for the determination of goserelin and related substances.

    Science.gov (United States)

    Gong, Feifei; Yang, Huaxin; Sun, Wen; Cao, Junzi; Liu, Wanhui

    2016-02-01

    An MEKC method for the analysis of goserelin and related substances has been developed using a combination of additives including CTAB, β-CD, and sodium hexanesulfonate. For this assay, the running buffer (pH and additives) and separation conditions (voltage and temperature) were optimized. The optimized system was the following: 200 mM 6-aminocaproic acid buffer (pH 4.2) supplemented with 175 mM CTAB, 3.0% w/v β-CD, and 20 mM sodium hexanesulfonate; the voltage was 10 kV in reverse polarity mode, the temperature was 20°C, and UV detection was measured at 220 nm. The method was qualified by evaluating the specificity, precision, linearity, accuracy, LOD, and LOQ. According to validation experiments, the optimized method was specific, accurate, and repeatable and satisfied the requirements for the analysis of goserelin and related substances. Compared with the RP-HPLC method, the MEKC method better solved the problem of overlapping impurity signals, and the migration time required was shorter. This method can be used for quality control and for the analysis of goserelin and its related substances.

  20. Study of proton radioactivities

    Energy Technology Data Exchange (ETDEWEB)

    Davids, C.N.; Back, B.B.; Henderson, D.J. [and others

    1995-08-01

    About a dozen nuclei are currently known to accomplish their radioactive decay by emitting a proton. These nuclei are situated far from the valley of stability, and mark the very limits of existence for proton-rich nuclei: the proton drip line. A new 39-ms proton radioactivity was observed following the bombardment of a {sup 96}Ru target by a beam of 420-MeV {sup 78}Kr. Using the double-sided Si strip detector implantation system at the FMA, a proton group having an energy of 1.05 MeV was observed, correlated with the implantation of ions having mass 167. The subsequent daughter decay was identified as {sup 166}Os by its characteristic alpha decay, and therefore the proton emitter is assigned to the {sup 167}Ir nucleus. Further analysis showed that a second weak proton group from the same nucleus is present, indicating an isomeric state. Two other proton emitters were discovered recently at the FMA: {sup 171}Au and {sup 185}Bi, which is the heaviest known proton radioactivity. The measured decay energies and half-lives will enable the angular momentum of the emitted protons to be determined, thus providing spectroscopic information on nuclei that are beyond the proton drip line. In addition, the decay energy yields the mass of the nucleus, providing a sensitive test of mass models in this extremely proton-rich region of the chart of the nuclides. Additional searches for proton emitters will be conducted in the future, in order to extend our knowledge of the location of the proton drip line.

  1. 茴拉西坦有关物质测定方法的改进%Improved HPLC Method for Determination of Related Substances in Aniracetam

    Institute of Scientific and Technical Information of China (English)

    郭志渊; 傅萍; 谢华; 张悦杨

    2013-01-01

    OBJECTIVE To improve an HPLC method for determination of the related substances in aniracetam. METHODS The column was C18 colum. Mobile phase was acetonitrile-water(35 : 65). The detection wavelength was 254 nm. RESULTS Aniracetam and its related substances can be separated effectively by this method. CONCLUSION The method is accurate and reliable. It can be used for the related substances determination in aniracetam.%目的 改进茴拉西坦的有关物质测定方法.方法 采用高效液相色谱法,以C18为色谱柱,流动相为乙腈-水(35:65),检测波长为254 nm.结果 茴拉西坦与其降解产物在该色谱条件下能够有效分离.结论 该方法准确可靠,可用于测定茴拉西坦的有关物质测定.

  2. Determination of related substance in duloxetine hydrochloride by HPLC%HPLC法测定盐酸度洛西汀的有关物质

    Institute of Scientific and Technical Information of China (English)

    黄文姝; 董爱军; 金红雨; 刘心

    2011-01-01

    Objective To establish an HPLC method for determining related substances of duloxetine hydrochloride. Methods An Inertsil CN-3 ( 4.6 mm × 250 mm, 5 μm ) column was used with 0.05 mol/L potassium dihyduogen phosphate solution( adjusted to pH 6. 0 with triethanolamine)and acetonitrile (30: 70)as the mobile phase, the flow rate was 1.0 mL/min, the detection wavelength was 228 nm. Results The related substances were separated from duloxetine hydrochloride. Conclusion The method is convenient,sensitive and accurate for determination of its related substance.%目的 建立HPLC法,测定盐酸度洛西汀的有关物质.方法 色谱柱为Inertsil CN-3(4.6mm×250mm,5μm),流动相为0.05mol/L磷酸二氢钾溶液(用三乙胺调节pH值为6.0)-乙腈(30:70),流速为1.0mL/min,检测波长为228nm.结果 盐酸度洛西汀与杂质能完全分离.结论 本方法可准确、快速、简便地测定盐酸度洛西汀中的有关物质.

  3. Induced radioactivity in LDEF components

    Science.gov (United States)

    Harmon, B. A.; Fishman, G. J.; Parnell, T. A.; Laird, C. E.

    1992-01-01

    A systematic study of the induced radioactivity of the Long Duration Exposure Facility (LDEF) is being carried out in order to gather information about the low earth orbit radiation environment and its effects on materials. The large mass of the LDEF spacecraft, its stabilized configuration, and long mission duration have presented an opportunity to determine space radiation-induced radioactivities with a precision not possible before. Data presented include preliminary activities for steel and aluminum structural samples, and activation subexperiment foils. Effects seen in the data show a clear indication of the trapped proton anisotropy in the South Atlantic Anomaly and suggest contributions from different sources of external radiation fluxes.

  4. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory; determination of methylene blue active substances by spectrophotometry

    Science.gov (United States)

    Burkhardt, Mark R.; Cinotto, Pete J.; Frahm, Galen W.; Woodworth, Mark T.; Pritt, Jeffrey W.

    1995-01-01

    A method for the determination of methylene blue active substances in whole-water samples by liquid-liquid extraction and spectrophotometric detection is described. Sulfate and sulfonate-based surfectants are reacted with methylene blue to form a blue-colored complex. The complex is extracted into chloroform, back-washed with an acidified phosphate-based buffer solution, and measured against external standards with a probe spectrophotometer. The method detection limt for routine analysis is 0.02 milligram per liter. The precision is plus/minus 10 percent relative standard deviation. The positive bias from nitrate and chloride and U.S. Geological Survey method O-3111-83 for methylene blue active substances is minized by adding a back-washing step.

  5. Determining redox properties of clay-rich sedimentary deposits in the context of performance assessment of radioactive waste repositories : Conceptual and practical aspects

    NARCIS (Netherlands)

    Behrends, T.; Bruggeman, Christophe

    2016-01-01

    Redox reactions play a key factor controlling the mobility of redox sensitive radionuclides in clay-rich sediments which might serve as host formations for radioactive waste repositories. Assessing the redox speciation of radionuclides requires information about the redox conditions in the formation

  6. Determination of related substances in Zolmitriptan by HPLC%HPLC测定佐米曲普坦中的有关物质

    Institute of Scientific and Technical Information of China (English)

    张姮婕; 江燕; 袁军; 张丹

    2012-01-01

    OBJECTIVE To establish an HPLC method for determination of related substances of Zolmitriptan. METHODS The Waters Symmetry shieldTM C18 column( 250 mm × 4. 6 mm ,5 μm) was adopted. The mobile phase consisted of phosphate buffer( containing 6. 8 g of potassium dihydrogen phosphate and 1. 01 g of sodium heptanesulfonate in 1 litre of water,adjusted to pH6 with triethyl-amine) - acetonitrile (82 : 18). The flow rate was 1.0 mL·min-1.The related substances of Zolmitriptan could be determined by the self contrast method with no correction factors by UV detection at 224 nm. RESULTS The limit of detection of Zolmitriptan was 0. 109 ng( S/N = 3 ) . Zolmitriptan could be separated from all related substances completely. The contents of all related substance was lower than 0. 5% . CONCLUSION The method is specific,accurate,simple and quick for determination of related substances of Zolmitriptan.%目的 采用HPLC法测定佐米曲普坦中的有关物质.方法 采用Waters Symmetry shieldTM C18色谱柱(250 mm×4.6mm,5μm),流动相为磷酸二氢钾缓冲溶液(取6.8g磷酸二氢钾、1.01 g庚烷磺酸钠,加水溶解并稀释至1L,用三乙胺调pH6)-乙腈(82∶18),流速1.0 mL·min-1,在波长224 nm处采用不加校正因子的主成分自身对照法对其有关物质进行检查.结果 佐米曲普坦的检测限为0.109 ng(S/N =3),杂质与主成分能完全分离,有关物质的限量控制在0.5%以下.结论 所用方法专属性强、准确、简便、快速,适用于佐米曲普坦中有关物质的检查.

  7. Substance use

    Science.gov (United States)

    Substance abuse; Illicit drug abuse; Narcotic abuse; Hallucinogen abuse ... Arlington, VA: American Psychiatric Publishing. 2013. Weiss RD. Drugs of abuse. In: Goldman L, Schafer AI, eds. Goldman's Cecil ...

  8. Determination of the related substance of Carvedilol by HPLC%HPLC测定卡维地洛中的有关物质

    Institute of Scientific and Technical Information of China (English)

    谢华; 江燕; 刘峰

    2012-01-01

    目的 采用HPLC法研究卡维地洛的有关物质.方法 采用C18色谱柱,流动相为乙腈- 0.02 mol·L-1磷酸二氢钾溶液(磷酸调pH3.5)(35∶65),检测波长241 nm.结果 卡维地洛最低检测限为0.52 ng.结论 各有关物质的峰与卡维地洛的均能达到有效分离,方法简便、稳定、专属性强,可以有效地控制卡维地洛的有关物质.%OBJECTIVE To establish a method for examining the related substances of Carvedilol. METHODS Use C18 column as the analytical column. The mobile phase was acetonitrile -0. 02 mol·L‐1 potassium dihydrogen phosphate solution(adjust to pH3. 5 with phosphoric acid ) (35 : 65 ) , and the detective wavelength was 241 nm. RESUILS The LOD of Carvedilol was 0. 52 ng. CONCLUSION The peak of related substances vs Carvedilol can be separated effectively. The method is simple, stable, reliable and specific. It can be used as an effective determination of the related substances of Carvedilol.

  9. 头孢尼西钠有关物质检测方法再研究%Research on Determination Method of Cefonicid sodium Related Substance

    Institute of Scientific and Technical Information of China (English)

    贾金焕

    2012-01-01

    To determine the cefonicid sodium related substances in 7-ACA of the peak position. Using HPLC,to test related substances, prepare the different concentration of 7-ACA standard solution for retention time confirmation. At lower concentrations, 7-ACA peak and one can distinctly separated peaks of impurities. The method can accurately detect cefonicid sodium related substance in the presence of 7-ACA impurities.%确定头孢尼西钠有关物质中7-氨基头孢烷酸(7-ACA)的出峰位置。采用高效液相色谱法(HPLC)进行有关物质检测,配制不同浓度7-ACA对照品溶液进行保留时间确认。在较低浓度下,7-ACA峰与其中-杂质峰能明显分开。该方法能够准确检测头孢尼西钠有关物质中是否存在7-ACA杂质。

  10. Determination of related substance in hydrochloride fluoxetine capsules by HPLC%测定盐酸氟西汀胶囊有关物质的HPLC法

    Institute of Scientific and Technical Information of China (English)

    郝桂彤; 孔令钰; 王倩

    2013-01-01

    [Objective] To establish the method for determination of related substance in hydrochloride fluoxetine capsules by HPLC.[Methods] C-18 column was used,mobile phase was methanol:tetrahydrofuran:triethylamine phosphate buffer (pH 6.0)(32 ∶ 15 ∶ 53),the flow rate was 1.0 ml/min,detection wavelength was 215 nm,and column temperature was 25 ℃.[Results]In this chromatography condition,hydrochloride fluoxetine had a good separation from intermediates and impurity substance(R > 1.5),besides,excipients didn't interfere the results of related substance.The linear range of hydrochloride fluoxetine was 0.235 5-23.55 μg/ml (r =0.999 98),and the detection limit was 23.55 ng/ml.[Conclusion] The method for the determination of related substance in hydrochloride fluoxetine capsules is sensitive and reliable.%目的 建立用反相高效液相色谱法测定盐酸氟西汀胶囊的有关物质的方法.方法 采用C18色谱柱,以甲醇-四氢呋喃-三乙胺缓冲液(pH 6.0) (32∶15∶53)为流动相,流速1.0 ml/min,检测波长为215 nm,柱温为25℃.结果 在该色谱条件下,盐酸氟西汀与各中间体、杂质分离良好(R>1.5),辅料对有关物质检测无干扰.盐酸氟西汀在0.235 5~23.55μg/ml范围内浓度与峰面积线性关系良好(r=0.999 98).盐酸氟西汀的检测限为23.55 ng/ml.结论 所建立用反相高效液相色谱法测定盐酸氟西汀胶囊的有关物质的方法灵敏,可靠.

  11. Radioactive anomaly discrimination from spectral ratios

    Science.gov (United States)

    Maniscalco, James; Sjoden, Glenn; Chapman, Mac Clements

    2013-08-20

    A method for discriminating a radioactive anomaly from naturally occurring radioactive materials includes detecting a first number of gamma photons having energies in a first range of energy values within a predetermined period of time and detecting a second number of gamma photons having energies in a second range of energy values within the predetermined period of time. The method further includes determining, in a controller, a ratio of the first number of gamma photons having energies in the first range and the second number of gamma photons having energies in the second range, and determining that a radioactive anomaly is present when the ratio exceeds a threshold value.

  12. Radioactivity of drinking water in Finland - basis for quality requirements; Talousveden radioaktiivisuus - perusteita laatuvaatimuksille

    Energy Technology Data Exchange (ETDEWEB)

    Maekelaeinen, I.; Huikuri, P.; Salonen, L.; Markkanen, M.; Arvela, H

    2001-07-01

    Several natural radioactive substances occur in drinking water in Finland, among which radon-222 is the most harmful from radiation protection viewpoint. Also long-lived alpha-active substances like uranium-238, uranium-234, polonium-210 and radium-226, as well as beta-active lead-210 and radium-228 occur in drinking water. Elevated concentrations are found only in ground water, those originating from bedrock being clearly higher than those from soil. Assessments based on dosimetry indicate that radioactivity in drinking water causes annually 20 fatal cancers. About 40% of cases is due to inhaled waterborn radon, 40% is due to ingested radon and 20% is due to other natural radioactive substances than radon. This report gives motivation for a proposition to restrict and monitor the radiation exposure from radioactive substances in drinking water, delivered by STUK to the Ministry of Social Affairs and Health in March 1999. The proposition introduces an action level of 300 Bq/l for radon concerning the waterworks. For other radionuclides except radon the action level proposed is 0.1 millisieverts per year (mSv/a), collectively. This new proposition does not bring in notable changes in the monitoring practice, although the calculated doses will change slightly. The proposed guideline for radon in private wells is 1000 Bq/l. According to the present monitoring data, less than 200 Finns served by waterworks use drinking water with radon concentration exceeding 300 Bq/l. Approximately 1000 waterworks consumers receive an annual dose that exceeds 0.1 mSv from other radionuclides than radon. About 20 000 Finns served by private wells use drinking water with radon concentration exceeding the STUK guideline 1 000 Bq/l. Radon can be removed from drinking water using aeration or granular activated carbon filtration (GAC), whereas uranium and radium can be effectively removed by ion exchange resins and lead and polonium using reverse osmosis. There are two methods to determine

  13. Radioactivity of drinking water in Finland - basis for quality requirements; Talousveden radioaktiivisuus - perusteita laatuvaatimuksille

    Energy Technology Data Exchange (ETDEWEB)

    Maekelaeinen, I.; Huikuri, P.; Salonen, L.; Markkanen, M.; Arvela, H

    2001-07-01

    Several natural radioactive substances occur in drinking water in Finland, among which radon-222 is the most harmful from radiation protection viewpoint. Also long-lived alpha-active substances like uranium-238, uranium-234, polonium-210 and radium-226, as well as beta-active lead-210 and radium-228 occur in drinking water. Elevated concentrations are found only in ground water, those originating from bedrock being clearly higher than those from soil. Assessments based on dosimetry indicate that radioactivity in drinking water causes annually 20 fatal cancers. About 40% of cases is due to inhaled waterborn radon, 40% is due to ingested radon and 20% is due to other natural radioactive substances than radon. This report gives motivation for a proposition to restrict and monitor the radiation exposure from radioactive substances in drinking water, delivered by STUK to the Ministry of Social Affairs and Health in March 1999. The proposition introduces an action level of 300 Bq/l for radon concerning the waterworks. For other radionuclides except radon the action level proposed is 0.1 millisieverts per year (mSv/a), collectively. This new proposition does not bring in notable changes in the monitoring practice, although the calculated doses will change slightly. The proposed guideline for radon in private wells is 1000 Bq/l. According to the present monitoring data, less than 200 Finns served by waterworks use drinking water with radon concentration exceeding 300 Bq/l. Approximately 1000 waterworks consumers receive an annual dose that exceeds 0.1 mSv from other radionuclides than radon. About 20 000 Finns served by private wells use drinking water with radon concentration exceeding the STUK guideline 1 000 Bq/l. Radon can be removed from drinking water using aeration or granular activated carbon filtration (GAC), whereas uranium and radium can be effectively removed by ion exchange resins and lead and polonium using reverse osmosis. There are two methods to determine

  14. [Examination of radioactive contamination in foods].

    Science.gov (United States)

    Miyazaki, Hitoshi; Tsuchiyama, Tomoyuki; Terada, Hisaya

    2013-01-01

    Following the Fukushima nuclear plant accident in Mar. 2011, the examination of radioactive contamination in foods is being carried out in Nagoya. During the period between 30 Mar. 2011 and 31 Oct. 2012, a total of 300 food samples were collected and the concentrations of radioactive nuclides were determined by means of γ-ray spectrometry using a high-purity germanium semiconductor detector. The results of analysis indicate that the concentrations of radioactive iodine (I) and cesium (Cs) were below the regulatory limits. Radioactive I ((131)I) was detected in 7 samples which belonged to the categories of green and yellow vegetables and other vegetables. Radioactive Cs ((134)Cs and (137)Cs) was detected in 60 samples which belonged to the categories of rice and its processed products, potatoes and its processed products, nuts and seeds, green and yellow vegetables, other vegetables, fruits, mushrooms, fishes and shellfishes, processed sea foods, meat, milk and dairy products and other beverages.

  15. A New Approach for the Determination of Dose Rate and Radioactivity for Detected Gamma Nuclides Using an Environmental Radiation Monitor Based on an NaI(Tl) Detector.

    Science.gov (United States)

    Ji, Young-Yong; Kim, Chang-Jong; Lim, Kyo-Sun; Lee, Wanno; Chang, Hyon-Sock; Chung, Kun Ho

    2017-10-01

    To expand the application of dose rate spectroscopy to the environment, the method using an environmental radiation monitor (ERM) based on a 3' × 3' NaI(Tl) detector was used to perform real-time monitoring of the dose rate and radioactivity for detected gamma nuclides in the ground around an ERM. Full-energy absorption peaks in the energy spectrum for dose rate were first identified to calculate the individual dose rates of Bi, Ac, Tl, and K distributed in the ground through interference correction because of the finite energy resolution of the NaI(Tl) detector used in an ERM. The radioactivity of the four natural radionuclides was then calculated from the in situ calibration factor-that is, the dose rate per unit curie-of the used ERM for the geometry of the ground in infinite half-space, which was theoretically estimated by Monte Carlo simulation. By an intercomparison using a portable HPGe and samples taken from the ground around an ERM, this method to calculate the dose rate and radioactivity of four nuclides using an ERM was experimentally verified and finally applied to remotely monitor them in real-time in the area in which the ERM had been installed.

  16. Effect of humic substances aggregation on the determination of fluoride in water using an ion selective electrode.

    Science.gov (United States)

    Shen, Junjie; Gagliardi, Simona; McCoustra, Martin R S; Arrighi, Valeria

    2016-09-01

    The control of drinking water quality is critical in preventing fluorosis. In this study humic substances (HS) are considered as representative of natural organic matter (NOM) in water. We show that when HS aggregate the response of fluoride ion selective electrodes (ISE) may be perturbed. Dynamic light scattering (DLS) results of both synthetic solutions and natural water sample suggest that low pH and high ionic strength induce HS aggregation. In the presence of HS aggregates, fluoride concentration measured by ISE has a reduction up to 19%. A new "open cage" concept has been developed to explain this reversible phenomenon. The interference of HS aggregation on fluoride measurement can be effectively removed by centrifugation pretreatment.

  17. Management of radioactive waste generated in nuclear medicine; Gestion de los residuos radiactivos generados en medicina nuclear

    Energy Technology Data Exchange (ETDEWEB)

    Lorenz Perez, P.

    2015-07-01

    Nuclear medicine is a clinical specialty in which radioactive material is used in non-encapsulated form, for the diagnosis and treatment of patients. Nuclear medicine involves administering to a patient a radioactive substance, usually liquid, both diagnostic and therapeutic purposes. This process generates solid radioactive waste (syringes, vials, gloves) and liquid (mainly the patient's urine). (Author)

  18. Radioactive air sampling methods

    CERN Document Server

    Maiello, Mark L

    2010-01-01

    Although the field of radioactive air sampling has matured and evolved over decades, it has lacked a single resource that assimilates technical and background information on its many facets. Edited by experts and with contributions from top practitioners and researchers, Radioactive Air Sampling Methods provides authoritative guidance on measuring airborne radioactivity from industrial, research, and nuclear power operations, as well as naturally occuring radioactivity in the environment. Designed for industrial hygienists, air quality experts, and heath physicists, the book delves into the applied research advancing and transforming practice with improvements to measurement equipment, human dose modeling of inhaled radioactivity, and radiation safety regulations. To present a wide picture of the field, it covers the international and national standards that guide the quality of air sampling measurements and equipment. It discusses emergency response issues, including radioactive fallout and the assets used ...

  19. Comparisons between radioactive and non-radioactive gas lantern mantles.

    Science.gov (United States)

    Furuta, E; Yoshizawa, Y; Aburai, T

    2000-12-01

    Gas lantern mantles containing radioactive thorium have been used for more than 100 years. Although thorium was once believed to be indispensable for giving a bright light, non-radioactive mantles are now available. From the radioactivities of the daughter nuclides, we estimated the levels of radioactivity of 232Th and 228Th in 11 mantles. The mantles contained various levels of radioactivity from background levels to 1410 +/- 140 Bq. Our finding that radioactive and non-radioactive mantles are equally bright suggests that there is no advantage in using radioactive mantles. A remaining problem is that gas lantern mantles are sold without any information about radioactivity.

  20. Rapid Determination of Perfluoroalkylated Substances in Oral Liquid%口服液中全氟烷基类化合物的快速测定

    Institute of Scientific and Technical Information of China (English)

    肖锋; 卞学海; 沈金灿; 岳振峰; 陈沛金; 肖陈贵

    2016-01-01

    A method of high-performance liquid chromatography-tandem mass spectrom-etry (HPLC-MS/MS)was developed for the simultaneous determination of 1 6 perflu-oroalkylated substances (PFASs)in oral liquid products.The residual of perfluoroalky-lated substances in samples were extracted using methanol acidified with 2% hydrochlo-ric acid solution as the extraction solvent,then enriched by N-propylethylenediamine (PSA)and PestiCarb (GCB)absorbent after adjusting extract's pH to neutral.Next, the compounds were eluted with 50 mmol/L triethylamine-methanol solution.At last, the exact was analyzed by HPLC-MS/MS in negative mode with multiple reaction moni-toring (MRM).All the analyte were calibrated by the internal method.Good linearities were established for the 1 6 perfluoroalkylated substances in the range from 0.2 g/L to 20 g/L.For all of 1 6 perfluoroalkylated substances,the limit of detection is less than 0.15 g/L,while the limit of quantitation is less than 0.43 g/L.The average recoveries of 1 6 perfluoroalkylated substances are between 80.8% and 1 1 9% in the spiking levels of 0.5,1.0,2.0 and 5.0 g/L.The relative standard deviation (RSD)of 1 6 perfluoroal-kylated substances is less than 10.5%.The method is simple,rapid and sensitive, which suits for determination of 1 6 perfluoroalkylated substances in oral liquid samples.%建立了高效液相色谱-串联质谱法(HPLC-MS/MS)检测口服液中16种全氟烷基类化合物(PFASs)。样品采用2%盐酸酸化甲醇溶液提取,用 NaOH 溶液将提取液的 pH 值调至中性后,加入PSA 和 GCB 粉末吸附剂分散固相萃取富集净化,用50 mmol/L 三乙胺-甲醇溶液洗脱,HPLC-MS/MS负离子多反应监测模式测定,同位素内标法定量。结果表明:在0.2~20μg/L 浓度范围内,16种全氟烷基类化合物具有良好的线性关系,线性相关系数(r)大于0.996,方法的检出限均小于0.15μg/L,定量限均小于0.43μg/L;在0.5、1.0、2.0和5.0μg/L 添加水平下,

  1. Radioactivity and its measurement

    CERN Document Server

    Mann, W B; Garfinkel, S B

    1980-01-01

    Begins with a description of the discovery of radioactivity and the historic research of such pioneers as the Curies and Rutherford. After a discussion of the interactions of &agr;, &bgr; and &ggr; rays with matter, the energetics of the different modes of nuclear disintegration are considered in relation to the Einstein mass-energy relationship as applied to radioactive transformations. Radiation detectors and radioactivity measurements are also discussed

  2. Uranium Glass: A Glowing Alternative to Conventional Sources of Radioactivity

    Science.gov (United States)

    Boot, Roeland

    2017-02-01

    There is a relatively simple way of using radioactive material in classroom experiments: uranium glass, which provides teachers with a suitable substance. By using the right computer software and a radiation sensor, it can be demonstrated that uranium glass emits radiation at a greater rate than the background radiation and with the aid of UV light a bright green luster appears. Therefore, with two pieces of uranium glass, students can learn about two different physical phenomena: fluorescence and radioactivity.

  3. 氟康唑原料药有关物质的研究%Determination of Related Substances in Fluconazole Bulk Drug

    Institute of Scientific and Technical Information of China (English)

    严小红; 李春盈; 陈安丽; 江英桥; 霍秀敏; 邵颖

    2012-01-01

    目的 建立高效液相色谱梯度法测定氟康唑原料药的有关物质.方法 采用十八烷基硅烷键合硅胶为填充剂,流动相A为0.01 mol · L-1甲酸铵,流动相B为乙腈,梯度洗脱,流速为0.5 mL·min-1,检测波长为261 nm,进样量为20 μL.结果 降解产物和杂质在该色谱条件分离良好,氟康唑与杂质B~D在2.632~21.06、2.688 ~ 53.76、0.853 6 ~ 21.34、2.595 ~20.76μg·mL-1之间线性关系良好,检测限分别为0.20、0.005 2、0.0073、0.13 μg·mL-1,对来自9个厂家17批氟康唑原料药(含国外5批)进行了测定,各杂质能有效检出.结论 该方法简便、快速、灵敏、准确,可用于测定氟康唑原料药的有关物质.%OBJECTIVE To establish an HPLC gradient elution method for the determination of related substances in fluconazole bulk drug. METHODS The separation was achieved by using an ODS column with gradient elution of mobile phase composed of 0. 01 mol·L-1 ammonium formate and acetonitrile. The flow rate was 0.5 mL·min-1. The UV detection wavelength was 261 nm,injection volume is 20 μL. RESULTS Fluconazole and its related substances can be separated effectively by this method, linear relation of fluconazole and impurity B - D were good, the detection limit were 0. 20, 0. 005 2, 0. 007 3, 0. 13 μg·mL-1, seventeen batches sample from nine manufacturers were determined. The related substances in fluconazole bulk drug were effectively determined. CONCLUSION The HPLC method is rapid and accurate which may be used for the inspection of related substances in fluconazole bulk drug.

  4. Determination of antimicrobial substances by microbial turbidimetry%分光光度计比浊法测定抗菌物质效价

    Institute of Scientific and Technical Information of China (English)

    王凯旋; 卫兰兰; 洪婷; 付瑞燕

    2015-01-01

    Agar diffusion method is widely used for determine the antimicrobial activities,but errors due to human factors always influence the accuracy of the results.The objective of this study was to set up a spectrophotometer turbidimetry with characteristics of accuracy,simpleness,and no special requirement for equipments to determine the potency of all kinds of antimicrobial substances.Results revealed that the calibration curves of three antimicrobial substances,including bacteriocin nisin,bacteriocin-like substance NFL and antibiotic gentamycin sulfate,were linear in the experimental range at the sampling time point which corresponded to the maximal inhibitory rate with middle inoculum size (R2 > 0.99).This method is suitable for precise determination of all kinds of antimicrobial substances under simple laboratory conditions.%琼脂扩散法是测定抗菌物质效价常用的方法,但人为操作因素常常影响实验结果的准确性.实验旨在建立一种测定准确、操作简单、无需特殊设备的分光光度计比浊法来测定各种抗菌物质的效价.研究发现,以抑菌率最高时对应的培养时间为取样时间点,在中等接种量下,在实验浓度范围内,细菌素nisin、类细菌素NFL和抗生素硫酸庆大霉素这3种抗菌物质的浓度与抑菌率之间的线性关系良好,R2值均高于0.99,标准曲线成立.该法适用于设备条件简单的实验室准确测定各类抗菌物质效价.

  5. HPLC测定长春西汀注射液的有关物质%Determination of Related Substances in Vinpocetine Injection by HPLC

    Institute of Scientific and Technical Information of China (English)

    刘加元; 何胜利

    2013-01-01

    Objective: To determine the related substances of Vinpocetine Injection by HPLC. Method: The separation was performed on Hypersil ODS C18 column (4.6 mm × 150 mm, 5 μm). The mobile phase consisted of methanol-1. 75 g·L-1 ammonium carbonate solution-acetic acid (80:25:3) , the flow rate was set at 1.0 mL·min-1 with detection at 273 nm. Result: Under the established chromatographic conditions, the related substances and vinpocetine were separated completely. The detective limit was 20 ng. The precision in a day was good (RSD 0. 52% ). Conclusion: The method is simple, accurate, specific and sensitive for the determination Vinpocetine Injection related substances.%目的:应用高效液相色谱法测定长春西汀注射液的有关物质.方法:采用Hypersil ODS C18色谱柱(4.6 mm×150 mm,5μm),甲醇-1·75 g·L-1碳酸铵溶液-乙酸(80∶25∶3)为流动相,流速1.0 mL· min-1,检测波长273 nm.结果:在选定的色谱条件下,长春西汀与有关物质分离完全,最低检测限为20 ng,精密度良好(RSD 0.52%).结论:方法简便、准确、专属性好、灵敏度高,可用于长春西汀注射液的有关物质测定.

  6. HPLC 测定利鲁唑片的有关物质%HPLC determination of riluzole tablets and related substances

    Institute of Scientific and Technical Information of China (English)

    姚丹丹; 李华; 黄艳山

    2013-01-01

    目的:建立高效液相色谱测定利鲁唑必利片有关物质的方法。方法采用 C18柱(250mm×4.6mm),以甲醇-水(70:30)为流动相,流速1.0 ml·min-1,检测波长为254nm,自身对照法测定。结果线性范围为0.5O2~4.016μg·ml-1, R2=0.9978,最低检测限为0.33 ng。结论该方法准确、简便,可以用于利鲁唑必利片有关物质的测定。%Objective To establish an HPLC method for the determination of related substances in Riluzole Tablets. Methods The separation was performed on C18 Column (250mm×4.6mm) with mobile phase consisted of methanol-water (70:30)and the flow rate was 1.0mL·m in- 1. The detection wave length was set at 274 nm. The content of related substance was calculated by self-control with main component. Results The standard curve was linear within the range of 0.502 ~ 4.016 μg·ml-1 (R2=0.9978) and the limit of detection was 0.33 ng. Conclusion The method is accurate and simple for the determination of the related substances in Riluzole Tablets.

  7. Determination of related substance in Ritodrine hydrochloride tablets by HPLC%HPLC测定盐酸利托君片的有关物质

    Institute of Scientific and Technical Information of China (English)

    刘加元; 何胜利

    2013-01-01

    目的 应用HPLC测定盐酸利托君片的有关物质.方法 采用Apollo C8色谱柱(250 mm×4.6 mm,5μm),甲醇-磷酸氢二铵和庚烷磺酸钠混合溶液(30∶70)为流动相,流速1.0 mL· min-1,检测波长214 nm.结果 盐酸利托君与有关物质分离完全,最低检测限为3×10-5 μg,RSD=0.52%.结论 方法简便、准确、灵敏,可用于盐酸利托君片有关物质的测定.%OBJECTIVE To determine the related substances of Ritodrine hydrochloride tablets by HPLC.METHOD The separation was performed on Apollo C8 column(250 mm× 4.6 mm,5 μm).The mobile phase consisted of methanol-mixture of diammonium hydrogen phosphate and heptane mahogany acid sodium(30:70),and the flow rate was set at 1.0 mL·min-1 with detection wave at 214 nm.RESULTS Under the established chromatographic condition,the related substances and Ritodrine hydrochloride were separated completely,the limit of detection was 3 × 10-5 μg.The precision was good (RSD =0.52%).CONCLUSION The method is simple,accurate,specific and sensitive for the determination of Ritodrine hydrochloride tablets and its related substance.

  8. Determination of related substances of Vitamin B4 Tablets by HPLC%HPLC法测定维生素B4片的有关物质

    Institute of Scientific and Technical Information of China (English)

    顾秋琴

    2014-01-01

    OBJECTIVE To establish a HPLC method to determine the related substances in Vitamin B 4 Tab-lets.METHODS The HPLC column was Waters SunFireTM C 18 (250mm ×4.6mm,5μm);the mobile phase was methanol-0.05mol· L-1 potassium dihydrogen phosphate solution-triethylamine (10∶90∶0.25 );the flow rate was 0.8 mL· min-1 ,the detection wavelength was 261 nm.RESULTS Vitamin B4 was separated well from the related substances;The reproducibility and precision of the method were good.CONCLUSION The method is simple ,ac-curate and sensitive.It can be used for the determination of the related substances of Vitamin B 4 Tablets.%目的:建立高效液相色谱法测定维生素B4片的有关物质。方法采用Waters SunFireTM C18柱(250mm ×4.6mm,5μm),流动相为甲醇-0.05mol· L-1磷酸二氢钾溶液-三乙胺(10∶90∶0.25),流速0.8mL· min -1,检测波长261nm。结果主峰与各降解产物峰的分离良好,方法的精密度良好。结论本方法简便、准确、灵敏度高,可用于维生素B4片的有关物质检查。

  9. HPLC Determination of Related Substances of Sodium Ferulate Granules%HPLC法测定阿魏酸钠颗粒中有关物质

    Institute of Scientific and Technical Information of China (English)

    冯彩丽; 张丹; 卜越浜; 隋峰

    2013-01-01

    目的 建立阿魏酸钠颗粒有关物质的HPLC测定方法.方法 色谱柱为C18柱(4.6 mm×250 mm,5μm),流动相:甲醇-0.05 mol·L-1磷酸二氢钾水溶液(38:62)(磷酸调pH至2.5);流速:1.0 ml ·min-1;检测波长:322 nm.结果 阿魏酸钠最低检测限为0.1 ng,与杂质的分离度符合要求,有关物质检查重复性试验符合要求.结论 本法简便、准确、快速、专属性强,可用于阿魏酸钠制剂有关物质的控制.%Objective To develop a method for determination of related substances of sodium ferulate granules by HPLC.Methods The separation was performed on a C18 (4.6 mm × 250 mm,5 μm) column with methanol0.05 mol ·L-1 potassium dihydrogen phosphate (38:62) at pH of 2.5 adjusted with phosphoric acid on 322 nm at 1.0 ml ·min-1.Results The detection limit was 0.1 ng,meeting the need of impurity resolution and repeatability for related substances of podophyllotoxin.Conclusion This method is simple,accurate,quick,specific and thus can be applied to the determination of related substances of sodium ferulate granules.

  10. Determination of Related Substances in Dienestrol Tablets by HPLC%HPLC法测定己二烯雌酚片的有关物质

    Institute of Scientific and Technical Information of China (English)

    海川; 何胜利

    2014-01-01

    目的::建立高效液相色谱法测定己二烯雌酚片的有关物质。方法:采用Hypersil C18色谱柱(250 mm ×4.6 mm,5μm),甲醇-乙腈(76∶24)为流动相,流速:0.8 ml·min-1,检测波长:229 nm,进样量:10μl。结果:在选定的色谱条件下,己二烯雌酚与有关物质分离完全,最低检测限为2 ng。结论:该方法简便、准确、专属性好、灵敏度高,可用于己二烯雌酚片的有关物质测定。%Objective:To determine the related substances in dienestrol tablets by HPLC. Methods:The separation was performed on a C18 column(250 mm × 4. 6 mm,5μm). The mobile phase consisted of methanol-acetonitrile(76∶24), the flow rate was set at 0. 8 ml·min-1 with the detection wavelength at 229 nm, and the sample size was 10 μl. Results:Under the established chromatographic conditions, the related substances and dienestrol were separated completely. The limit of detection was 2 ng. Conclusion:The method is simple, accurate, specific and sensitive in the determination of related substances in dienestrol tablets.

  11. Simultaneous determination of related substances of telmisartan and hydrochlorothiazide in tablet dosage form by using reversed phase high performance liquid chromatographic method

    Directory of Open Access Journals (Sweden)

    Sutirtho Mukhopadhyay

    2011-01-01

    Full Text Available Objective : Telmisartan is a potent, long-lasting, nonpeptide antagonist of the angiotensin II type-1 (AT 1 receptor that is indicated for the treatment of essential hypertension. Hydrochlorothiazide is a widely prescribed diuretic and it is indicated for the treatment of edema, control of essential hypertension and management of diabetes insipidus. In the current article a new, accurate, sensitive, precise, rapid, reversed phase high performance liquid chromatography (RP-HPLC method was developed for determination of related substances of Telmisartan and Hydrochlorthiazide in tablet dosage form. Materials and Methods : Simultaneous determination of related substances was performed on Kromasil C 18 analytical column (250 × 4.6 mm; 5΅m pertical size column at 40°C employing a gradient elution. Mobile phase consisting of solvent A (solution containing 2.0 g of potassium dihydrogen phosphate anhydrous and 1.04 g of Sodium 1- Hexane sulphonic acid monohydrate per liter of water, adjusted to pH 3.0 with orthophosphoric acid and solvent B (mixture of Acetonitrile: Methanol in the ratio 80:20 v/v was used at a flow rate of 1.0 ml min−1 . UV detection was performed at 270 nm. Results : During method validation parameter such as precision, linearity, accuracy, specificity, limit of detection and quantification were evaluated, which remained within acceptable limits. Conclusions : HPLC analytical method is linear, accurate, precise, robust and specific, being able to separate the main drug from its degradation products. It may find application for the routine analysis of the related substances of both Telmisartan and Hydrochlorthiazide in this combination tablets.

  12. Radioactivity in Dutch consumer products

    CERN Document Server

    Janssen, M P M

    2002-01-01

    This study took place within the framework of a general update of the average radiation dose for the Dutch population. It focuses on consumer products in which radionuclides have been intentionally incorporated and on radiation-emitting devices that can be supplied to members of the public without special surveillance. Eleven consumer products were studied in more detail. The radiation from these products determined 90% of the total collective dose due to consumer products in the Netherlands in 1988. Individual and collective doses are presented here for each product. The total collective dose has decreased from 130 personSv in 1988 to 4.6 personSv at present. This reduction was attributed to: a decrease in the number of radioactive products (gas mantles), lower estimates of the number of radioactive products present in the Netherlands thanks to new information (camera lenses, smoke detectors containing Ra-226), replacement of radioactive by non-radioactive products (gas mantles, dental protheses), and a lowe...

  13. Development and validation of a reversed-phase HPLC method for separation and simultaneous determination of process-related substances of mirtazapine in bulk drugs and formulations.

    Science.gov (United States)

    Rao, R Nageswara; Raju, A Narasa

    2009-03-01

    A simple and rapid reversed-phase high-performance liquid chromatographic method has been developed for the separation and simultaneous determination of related substances of mirtazapine in bulk drugs and pharmaceutical formulations. Six impurities, including one degradation product of mirtazapine, have been separated on a BDS Hypersil (4.6 x 250 mm; particle size 5 microm) column with a mobile phase consisting of 0.3% triethylamine (pH 3.0)-acetonitrile (78:22 v/v) eluted in an isocratic mode and monitored with a photo diode array detector at 215 nm. The chromatographic behavior of all the analytes was studied under variable compositions of different solvent systems, temperatures, buffer concentrations, and pH values. The method was validated in terms of accuracy, precision, and linearity. The inter- and intra-day assay precision was found to be method was successfully applied to the analysis of commercial formulations and the recoveries of mirtazapine were in the range of 99.38-100.73% with method is useful not only for rapid evaluation of the purity of mirtazapine, but also for the simultaneous determination of related substances in bulk drugs and pharmaceutical formulations.

  14. Novel spectrophotometric determination of chloramphenicol and dexamethasone in the presence of non labeled interfering substances using univariate methods and multivariate regression model updating

    Science.gov (United States)

    Hegazy, Maha A.; Lotfy, Hayam M.; Rezk, Mamdouh R.; Omran, Yasmin Rostom

    2015-04-01

    Smart and novel spectrophotometric and chemometric methods have been developed and validated for the simultaneous determination of a binary mixture of chloramphenicol (CPL) and dexamethasone sodium phosphate (DSP) in presence of interfering substances without prior separation. The first method depends upon derivative subtraction coupled with constant multiplication. The second one is ratio difference method at optimum wavelengths which were selected after applying derivative transformation method via multiplying by a decoding spectrum in order to cancel the contribution of non labeled interfering substances. The third method relies on partial least squares with regression model updating. They are so simple that they do not require any preliminary separation steps. Accuracy, precision and linearity ranges of these methods were determined. Moreover, specificity was assessed by analyzing synthetic mixtures of both drugs. The proposed methods were successfully applied for analysis of both drugs in their pharmaceutical formulation. The obtained results have been statistically compared to that of an official spectrophotometric method to give a conclusion that there is no significant difference between the proposed methods and the official ones with respect to accuracy and precision.

  15. HPLC测定司帕沙星及其制剂中的有关物质%Determination of the related substance of Sparfloxacin and Sparfloxacin preparation

    Institute of Scientific and Technical Information of China (English)

    杨淑先; 王立萍

    2011-01-01

    OBJECTIVE To establish a gradient elution HPLC method to determine the related substances of Sparfloxacin and Spar-floxacin preparation. METHODS C18 column was adopted. The mobile phase consisted of a mixture of sodium citrate buffer solution -acetonitrile. Gradient elution was used with flow rate of 1.0 mL·min-1. The detection wavelength was 290 run,and the column temperature was 30℃. RESULTS A good separation for Sparfloxacin and other impurities was achieved. CONCLUSION This method is simple and accurate for determination of related substances in Sparfloxacin and Sparfloxacin preparation.%采用HPLC法测定司帕沙星及其制剂中的有关物质.方法用C18为填充剂;流动相为枸橼酸钠缓冲液-乙腈,梯度洗脱;流速1.0 mL·min-1;检测波长290 nm,柱温30℃.结果司帕沙星峰与各杂质峰分离良好.结论所建方法简便、准确,可测定司帕沙星及其制剂中的有关物质.

  16. Selective determination of dimenhydrinate in presence of six of its related substances and potential impurities using a direct GC/MS method

    Directory of Open Access Journals (Sweden)

    Tarek S. Belal

    2016-01-01

    Full Text Available A novel simple, direct and selective gas chromatography–mass spectrometry (GC/MS procedure was developed for the determination of the antihistamine drug dimenhydrinate (DMH in presence of six of its related substances and potential impurities, namely, diphenylmethane, diphenylmethanol, benzophenone, orphenadrine, caffeine and 8-chlorocaffeine. The method involved resolution of the underivatized compounds using a trifluoropropylmethyl polysiloxane (Rtx-200 capillary column and the mass spectrometric detection was carried out in the electron-impact (EI mode. Excellent baseline separation of DMH and the cited related substances was achieved in less than 15 min. Quantification of the parent drug DMH was based on measuring its peak area. The reliability and analytical performance of the proposed method were validated with respect to linearity, range, precision, accuracy, specificity, robustness, detection and quantification limits. Calibration curve of DMH was linear over the range 50–500 μg/mL with determination coefficient (R2 = 0.9982. The proposed method was successfully applied for the assay of DMH in tablets dosage form with recoveries >96.80%.

  17. Application of a comprehensive extraction technique for the determination of poly- and perfluoroalkyl substances (PFASs) in Great Lakes Region sediments.

    Science.gov (United States)

    Guo, Rui; Megson, David; Myers, Anne L; Helm, Paul A; Marvin, Chris; Crozier, Patrick; Mabury, Scott; Bhavsar, Satyendra P; Tomy, Gregg; Simcik, Matt; McCarry, Brian; Reiner, Eric J

    2016-12-01

    A comprehensive method to extract perfluoroalkane sulfonic acids (PFSAs), perfluoroalkyl carboxylic acids (PFCAs), polyfluoroalkyl phosphoric acid diesters (diPAPs), perfluoroalkyl phosphinic acids (PFPiAs) and perfluoroalkyl phosphonic acids (PFPAs) from sediment and analysis by liquid chromatography tandem mass spectrometry (LC-MS/MS) was developed and applied to sediment cores from three small isolated lakes (Plastic Lake, Lake 442, Lake Tettegouche) and Lake Ontario in the Great Lakes Region. Recoveries of the target compounds using the optimized acetonitrile/sodium hydroxide extraction ranged from 73% to 120%. The greatest concentrations of per- and polyfluorinated alkyl substances (PFASs) were recorded in sediment from Lake Ontario (ΣPFASs 13.1 ng/g), where perfluorooctane sulfonic acid (PFOS) contributed over 80% of the total. Concentrations in Lake Ontario were approximately 1-2 orders of magnitude greater than the more remote lakes subject to primarily atmospheric inputs. Whilst the PFAS contribution in Lake Ontario was dominated by PFOS, the more remote lakes contained sediment with higher proportions of PFCAs. Trace amounts of emerging PFASs (diPAPs and PFPiAs) were found in very recent surface Lake Ontario and remote lake sediments.

  18. Development of a liquid chromatographic method for the determination of related substances and assay of d-cycloserine.

    Science.gov (United States)

    Pendela, Murali; Dragovic, Sanja; Bockx, Lien; Hoogmartens, Jos; Van Schepdael, Ann; Adams, Erwin

    2008-08-05

    d-cycloserine or d-4-amino-3-isoxazolidinone is an antibiotic produced by Streptomyces garyphalus and Streptomyces orchidaceus. d-Cycloserine is used in the second line treatment of tuberculosis and is often used in developing countries. Therefore, expensive high-tech techniques are not recommended for analysis. Here, a liquid chromatography method with ultraviolet detection (LC-UV) is described using a base deactivated column (Hypersil BDS column; 25 cm x 4.6 mm I.D.) kept at 45 degrees C. The gradient method uses mobile phases containing acetonitrile (ACN), 20mM sodium octane sulphonate (SOS), 0.2M potassium dihydrogen phosphate buffer pH 2.8, water: A: (4:70:10:16v/v/v/v) and B: (17:70:10:3v/v/v/v). The method proved to be robust, linear, repeatable, sensitive, selective and easy to perform. For the related substances test 50 microl of a 0.5 mg/ml d-cycloserine solution is injected. For assay, a concentration of 0.1 mg/ml is proposed to avoid overloading of the detector.

  19. A Multidisciplinary Investigation to Determine the Structure and Source of Dimeric Impurities in AMG 517 Drug Substance

    Directory of Open Access Journals (Sweden)

    Maria Victoria Silva Elipe

    2009-01-01

    Full Text Available In the initial scale-up batches of the experimental drug substance AMG 517, a pair of unexpected impurities was observed by HPLC. Analysis of data from initial LC-MS experiments indicated the presence of two dimer-like molecules. One impurity had an additional sulfur atom incorporated into its structure relative to the other impurity. Isolation of the impurities was performed, and further structural elucidation experiments were conducted with high-resolution LC-MS and 2D NMR. The dimeric structures were confirmed, with one of the impurities having an unexpected C-S-C linkage. Based on the synthetic route of AMG 517, it was unlikely that these impurities were generated during the last two steps of the process. Stress studies on the enriched impurities were carried out to further confirm the existence of the C-S-C linkage in the benzothiazole portion of AMG 517. Further investigation revealed that these two dimeric impurities originated from existing impurities in the AMG 517 starting material, N-acetyl benzothiazole. The characterization of these two dimeric impurities allowed for better quality control of new batches of the N-acetyl benzothiazole starting material. As a result, subsequent batches of AMG 517 contained no reportable levels of these two impurities

  20. HPLC法测定地夫可特的含量及有关物质%HPLC determination of deflazacort and its related substances

    Institute of Scientific and Technical Information of China (English)

    方滢芝; 郑国钢

    2012-01-01

    目的:建立测定地夫可特含量及有关物质的高效液相色谱方法.方法:采用VP - ODS色谱柱(250 mm×4.6 mm,5μm),以水-乙腈(60:40)为流动相,流速1.0 mL·min-1,检测波长244 nm.结果:在上述色谱条件下,各中间体及降解产物均可与地夫可特主峰良好分离.地夫可特与有关物质测定的线性范围分别为50.2 ~ 201.0μg·mL-1(r=0.9999)与2.0~15.1 μg·mL-1(r =0.9993);方法的重复性与中间精密度RSD分别为0.43%和0.68%.结论:本文方法简便,可用于测定地夫可特的含量及有关物质.%Objective: To establish a RP - HPLC method for content determination of deflazacort and its related substances. Methods:The separation was performed on a Shimadzu VP - ODS column(250 mm ×4. 6 mm,5μm) with the mobile phase consisting of water - acetontrile(60: 40) at a flow rate of 1. 0 mL · min-1 ,and the detection wavelength was set at 244 nm. Results; An excellent separation was achieved for deflazacort and its related substances. The linear ranges of deflazacort and its related substances were 50. 2 -201. 0 μg · mL (r =0. 9999)and 2. 0 - 15. 1 μg · mL-1 ( r = 0. 9993 ) , respectively. The repeatability and intermediate precision were 0. 43% and 0. 68%. Conclusion; The method is simple and can be successfully applied in the determination of deflazacort and its related substances.

  1. Nuclear power in space. Use of reactors and radioactive substances as power sources in satellites and space probes; Kaernkraft i rymden. Anvaendningen av reaktorer och radioaktiva aemnen som kraftkaellor i satelliter och rymdsonder

    Energy Technology Data Exchange (ETDEWEB)

    Hoestbaeck, Lars

    2008-11-15

    Today solar panels are the most common technique to supply power to satellites. Solar panels will work as long as the power demand of the satellite is limited and the satellite can be equipped with enough panels, and kept in an orbit that allows enough sunlight to hit the panels. There are various types of space missions that do not fulfil these criteria. With nuclear power these types of missions can be powered regardless of the sunlight and as early as 1961 the first satellite with a nuclear power source was placed in orbit. Out of seventy known space missions that has made use of nuclear power, ten have had some kind of failure. In no case has the failure been associated with the nuclear technology used. This report discusses to what degree satellites with nuclear power are a source for potential radioactive contamination of Swedish territory. It is not a discussion for or against nuclear power in space. Neither is it an assessment of consequences if radioactive material from a satellite would reach the earth's surface. Historically two different kinds of Nuclear Power Sources (NPS) have been used to generate electric power in space. The first is the reactor where the energy is derived from nuclear fission of 235U and the second is the Radioisotope Thermoelectric Generator (RTG) where electricity is generated from the heat of naturally decaying radionuclides. NPS has historically only been used in space by United States and the Soviet Union (and in one failing operation Russia). Nuclear Power Sources have been used in three types of space objects: satellites, space probes and moon/Mars vehicles. USA has launched one experimental reactor into orbit, all other use of NPS by the USA has been RTG:s. The Soviet Union, in contrast, only launched a few RTG:s but nearly forty reactors. The Soviet use of NPS is less transparent than the use in USA and some data published on Soviet systems are more or less well substantiated assessments. It is likely that also future

  2. Bioactive substances

    Digital Repository Service at National Institute of Oceanography (India)

    Wahidullah, S.

    Chemistry related to certain bioactive molecules, from Indian Ocean Region, developed into drugs or which served as models for the synthesis of more effective bioactive substances or in use in fundamental studies of physiological and biochemical...

  3. Radioactive Wastes. Revised.

    Science.gov (United States)

    Fox, Charles H.

    This publication is one of a series of information booklets for the general public published by the United States Atomic Energy Commission. This booklet deals with the handling, processing and disposal of radioactive wastes. Among the topics discussed are: The Nature of Radioactive Wastes; Waste Management; and Research and Development. There are…

  4. Induced radioactivity at CERN

    CERN Multimedia

    1970-01-01

    A description of some of the problems and some of the advantages associated with the phenomenon of induced radioactivity at accelerator centres such as CERN. The author has worked in this field for several years and has recently written a book 'Induced Radioactivity' published by North-Holland.

  5. A Remote Radioactivity Experiment

    Science.gov (United States)

    Jona, Kemi; Vondracek, Mark

    2013-01-01

    Imagine a high school with very few experimental resources and limited budgets that prevent the purchase of even basic laboratory equipment. For example, many high schools do not have the means of experimentally studying radioactivity because they lack Geiger counters and/or good radioactive sources. This was the case at the first high school one…

  6. Determination of Cefixime by a Validated Stability-Indicating HPLC Method and Identification of its Related Substances by LC-MS/MS Studies.

    Science.gov (United States)

    Talebpour, Zahra; Pourabdollahi, Hakimeh; Rafati, Hasan; Abdollahpour, Asem; Bashour, Yusef; Aboul-Enein, Hassan Y

    2013-01-01

    Cefixime is an important cephalosporin antibiotic that easily decomposes and releases different related substances in preparation and storage steps. The objective of the current study was to develop a simple, precise, and accurate isocratic liquid chromatography (LC) method for the determination of cefixime in the presence of its related substances generated from thermal stress in the bulk drug. The chromatographic conditions were comprised of a reversed-phase C18 column (4.6 × 250 mm, 5 μm) with a mobile phase composed of water: acetonitrile (85:15 v/v, with 0.5% formic acid) and ultraviolet detection (UV). Some thermal degradation products were identified using a proposed liquid chromatography-mass spectrometry method. Five peaks (A, B, C, D, and E impurities based on British Pharmacopoeia) were known and a few unknown peaks appeared in the thermal stress solution of cefixime. The linear regression analysis data for the calibration plot of the LC-UV method showed a good linear relationship in the concentration range 0.9-1000.0 μg mL(-1). The recovery of the optimized method was between 94.6 and 98.4% and the inter- and intra-day relative standard deviations were less than 3.3%. The obtained results shown in the LC-UV proposed method can be conveniently used in a quality control laboratory for routine analysis of cefixime for the assay and related substances, as well as for the evaluation of stability samples of bulk drugs.

  7. 溶剂萃取GC-MS法测定纺织衣物中的异味物%DETERMINATION OF ODOROUS SUBSTANCES IN TEXTILE BY SOLVENT EXTRACTION GC- MS

    Institute of Scientific and Technical Information of China (English)

    李竹英; 韦顺文; 朱艳俊; 金江岚

    2011-01-01

    2-isopropyl-3-methoxypyrazine, 2-methylisoborneol and geosmin in textile were extracted by solvent hexane and dichloromethane, respectively, and determined by GC - MS. Effects of solvent, temperature and extracted time on the recovery of odorous substances were investigated. The results showed that the recovery of odorous substances extracted by solvent hexane was higher than by solvent dichloromethane, and more than 85% of odorous substances were recovered when extraction was carried out by solvent hexane at 60 -80℃ for 15 min and the RSD was less than 5% (n =5).%采用溶剂萃取法提取纺织品中的土腥霉味化合物二甲萘炕醇(GSM)、2-异丁基-3.甲氧基吡嗪(IBMP)和2-甲基异茨醇(MIB),用气相色谱-质谱法测定其含量.考察了溶剂二氯甲烷和正己烷的提取效果以及提取时间、温度、溶盐因素对提取回收率的影响.结果表明:正己烷的提取效果优于二氯甲烷,采用正己烷提取剂.温度控制在60-80℃、振荡提取时间15 min,回收率大于85%,相对偏差小于5%(n=6).

  8. A mechanistic approach to link biological effects of radioactive substances from molecules to populations in wildlife species - A mechanistic approach to link biological effects of radionuclides from molecules to populations in wildlife species

    Energy Technology Data Exchange (ETDEWEB)

    Alonzo, Frederic; Parisot, Florian; Plaire, Delphine; Adam-Guillermin, Christelle; Garnier- Laplace, Jacqueline [Institut de Radioprotection et de Surete Nucleaire (IRSN), PRP-ENV, SERIS, LECO, Cadarache, Saint-Paul- Lez-Durance, 13115 (France)

    2014-07-01

    Understanding how toxic contaminants affect wildlife species at various levels of biological organisation (sub-cellular, histological, physiological, organism, population levels) is a major research goal in both ecotoxicology and radioecology. A mechanistic understanding of the links between the different observed perturbations is necessary to predict consequences for survival, growth and reproduction which are critical for population dynamics. However, time scales at which such links are established in the laboratory are rarely relevant for natural populations. With a small size and short life cycle, the cladoceran micro-crustacean Daphnia magna is a particularly suitable biological model for studying effects of radioactive contaminants over several generations. Multi-generational exposures are much more representative of the environmental context of field populations for which contaminations can last for durations which largely exceed individual longevity and involve exposure of many successive generations. Over the last decade, multi-generational investigations of toxic effects were conducted under controlled conditions in D. magna exposed to various radionuclides including depleted uranium, americium-241 and cesium-137, representing respectively a dominantly chemo-toxic metal, an alpha internal contamination and a gamma external radiation. Results showed in all cases that toxic effects on physiology and life history (survival, body size, fecundity) increased in severity across generations. These observations demonstrated that measured effects in one generation might not be representative of toxicity in the following offspring generations, and ultimately of the population response. Reduction in somatic growth and reproduction induced by uranium were analysed using the mechanistic modelling approach known as DEBtox (model of dynamic energy budget applied to toxicology). Modelling results suggested that uranium primarily affects assimilation. This metabolic mode

  9. Determination of degradation rates of organic substances in the unsaturated soil zone depending on the grain size fractions of various soil types

    Science.gov (United States)

    Fichtner, Thomas; Stefan, Catalin; Goersmeyer, Nora

    2015-04-01

    Rate and extent of the biological degradation of organic substances during transport through the unsaturated soil zone is decisively influenced by the chemical and physical properties of the pollutants such as water solubility, toxicity and molecular structure. Furthermore microbial degradation processes are also influenced by soil-specific properties. An important parameter is the soil grain size distribution on which the pore volume and the pore size depends. Changes lead to changes in air and water circulation as well as preferred flow paths. Transport capacity of water inclusive nutrients is lower in existing bad-drainable fine pores in soils with small grain size fractions than in well-drainable coarse pores in a soil with bigger grain size fractions. Because fine pores are saturated with water for a longer time than the coarse pores and oxygen diffusion in water is ten thousand times slower than in air, oxygen is replenished much slower in soils with small grain size fractions. As a result life and growth conditions of the microorganisms are negatively affected. This leads to less biological activity, restricted degradation/mineralization of pollutants or altered microbial processes. The aim of conducted laboratory column experiments was to study the correlation between the grain size fractions respectively pore sizes, the oxygen content and the biodegradation rate of infiltrated organic substances. Therefore two columns (active + sterile control) were filled with different grain size fractions (0,063-0,125 mm, 0,2-0,63 mm and 1-2 mm) of soils. The sterile soil was inoculated with a defined amount of a special bacteria culture (sphingobium yanoikuae). A solution with organic substances glucose, oxalic acid, sinaphylic alcohol and nutrients was infiltrated from the top in intervals. The degradation of organic substances was controlled by the measurement of dissolved organic carbon in the in- and outflow of the column. The control of different pore volumes

  10. Determination of the Content and Related Substances Pirfenidone Tablets and its Related Substances by HPLC%HPLC法测定吡菲尼酮片的含量及有关物质

    Institute of Scientific and Technical Information of China (English)

    刘和凤; 高嵩

    2011-01-01

    Objective: To establish an HPLC method for the determination of pirfenidone and the related substances in pirfenidone tablets. Method: The analysis was performed on a column of Kromasil C18 (250 mm ×4. 6 mm,5 μm). The mobile phase consisted of acetonitrile-phosphate buffer (34: 66) ( NaOH adjusting pH to 6. 8 ). The flow rate was 1.0 ml ·min -1. The detection wavelength was set at 220 nm. The column temperature was 30 ℃. Result: Good linearity was obtained over the range of 36.00-180.00 μg·ml-1 for pirfenidone (r =0. 999 9). The limit of detection was 0. 72 ng. The average recovery was 98.75% (RSD =0. 50% ). A good separation for pirfenidone and the related substances was achieved. Conclusion: The method is simple, sensitive and accurate,and can be used in the quality control for pirfenidone tablets.%目的:建立HPLC法测定吡菲尼酮片的含量及有关物质.方法:色谱柱为Kromasil C18柱(250 mm×4.6 mm,5μm);流动相为乙腈-0.1 mol·L-1磷酸二氢钾缓冲液(34:66)(氢氧化钠调pH至6.8);流速为1.0 ml·min-1;检测波长为220 nm;柱温为30℃.结果:吡菲尼酮在36.00~180.00μg·ml-1浓度范围线性关系良好(r=0.999 9),最低检测限0.72 ng,平均回收率为98.75%,RSD=0.50%,各杂质峰与主峰分离良好.结论:本方法简单方便,专属性强,准确可靠,可用于测定吡菲尼酮片的含量及有关物质.

  11. Determination of Fenazinel Dihydrochloride and Its Related Substances by HPLC%盐酸非那嗪奈含量及有关物质的HPLC法测定

    Institute of Scientific and Technical Information of China (English)

    周一萌; 周斌

    2012-01-01

    An HPLC method was established for the determination of fenazinel dihydrochloride and its related substances. A LiChroCART RP-18 column was used with the mobile phase of 0.3% triethylamine (adjusted to pH 7.0 with phosphoric acid) -methanol (37 : 63) at the detection wavelength of 246 nm. Fenazinel dihydrochloride and its related substances were separated successfully. The calibration curve was linear in the concentration range of 0.01 - 2 mg/ml. The average recovery was 100.1 %, with RSD of 0.13 %.%建立了高效液相色谱法测定盐酸非那嗪奈的含量及有关物质.使用LiChroCART RP-18色谱柱,流动相为0.3%三乙胺溶液(用磷酸调至pH 7.0)-甲醇(37∶63),检测波长246 nm.盐酸非那嗪奈与有关物质的分离度良好.线性范围为0.01~2 mg/ml,平均回收率为100.1%,RSD为0.13%.

  12. Development and Validation of a Stability-Indicating RP-UPLC Method for Determination of Rosuvastatin and Related Substances in Pharmaceutical Dosage Form.

    Science.gov (United States)

    Trivedi, Harshal Kanubhai; Patel, Mukesh C

    2012-01-01

    A stability-indicating reversed phase ultra performance liquid chromatographic (RP-UPLC) method was developed for the determination of related substances in rosuvastatin calcium (ROSV) tablet dosage form. The chromatographic separation was achieved on an Acquity BEH C18 (100 mm × 2.1 mm, 1.7 μm) column with mobile phase containing a gradient mixture of solvent-A (0.1% trifluoroacetic acid) and solvent-B (methanol). The eluted compounds were monitored at 240 nm and the run time was 10.0 min. Degradation behavior of the ROSV was studied under various degradation stress conditions. Four major unknown degradation products (late eluting impurities) were found in acid stress condition and two unknown degradation products were found in oxidative stress condition. The developed method separates (six) unknown impurities, (three) known impurities and ROSV substance from each other, providing the stability-indicating power of the method. The developed RP-UPLC method was validated according to the International Conference on Harmonization (ICH) guidelines. The developed and validated RP-UPLC method is LC-MS compatible and can be applied for identification of eluted unknown impurities of ROSV.

  13. Determination of the Related Substances of Cefazedone Sodium%头孢西酮钠有关物质的 HPLC 测定

    Institute of Scientific and Technical Information of China (English)

    何雅官; 郭中明; 柴倩

    2013-01-01

    An HPLC method was established for the determination of the related substances of cefazedone sodium. A C18 column was used, with the mobile phase of 0.02 mol/L ammonium dihydrogen phosphate buffer (adjusted to pH 5.0 by 0.1mol/L NaOH solution)-acetonitrile by gradient elution. The flow rate was 1ml/min. The detection wavelength was 278 nm. The result showed that cefazedone sodium and its related substances were isolated well.%建立了高效液相色谱法测定头孢西酮钠的有关物质。采用十八烷基键合硅胶,流动相为0.02 mol/L 磷酸二氢铵缓冲液(0.1 mol/L 氢氧化钠溶液调至 pH 5.0)-乙腈,梯度洗脱,流速为1 ml/min,检测波长278 nm。结果显示,头孢西酮钠与各杂质分离良好。

  14. Simple and sensitive stability-indicating ion chromatography method for the determination of cyclopropylamine in nevirapine and moxifloxacin hydrochloride drug substances.

    Science.gov (United States)

    Kothapalli, Pavan Kumar S R; Khagga, Mukkanti; Mekala, Nageswara Rao; Sigamani, John Prasanna; Vundavilli, Jagadeesh Kumar; Masani, Narendra Kumar; Sharma, Hemant Kumar

    2012-01-01

    A simple and sensitive ion chromatography method has been developed for the determination of cyclopropylamine (CPA) in nevirapine (NEV) and moxifloxacin HCl (MOX) pharmaceutical drug substances. Efficient chromatographic separation was achieved on a Metrosep C4, 5 μm (250 mm × 4.0 mm) column. The mobile phase consists of 5 mM hydrochloric acid containing 10% (v/v) acetonitrile and was delivered in an isocratic mode at a flow rate of 0.9 mL min(-1) at 27°C. A conductometric detector was used for the detection of the analyte. The drug substances were subjected to stress conditions including oxidation, thermal, photolytic and humidity for the evaluation of the stability-indicating nature of the method. The method was validated for specificity, precision, linearity, accuracy and solution stability. The limit of detection (LOD) and limit of quantification (LOQ) values are 0.10 μg mL(-1) and 0.37 μg mL(-1) respectively. The linearity range of the method is between 0.37 μg mL(-1) and 1.5 μg mL(-1) and the correlation coefficient is found to be 0.9971. The average recoveries of CPA in NEV and MOX are 97.0% and 98.0%, respectively.

  15. HPLC法测定特非那定片中有关物质含量%Content Determination of Related Substances in Terfenadine Tablets by HPLC

    Institute of Scientific and Technical Information of China (English)

    龙娜

    2013-01-01

    OBJECTIVE:To establish a method for the content determination of related substances in Terfenadine tablets.METHODS:HPLC method was adopted.The determination was performed on Hypersil Phenyl 2 column with mobile phase consisted of acetonitrile-phosphate buffer (50∶50) at the flow rate of 1.5 ml/min.The detection wavelength was set at 220 nm and the column temperature was maintained at room temperature.RESULTS:Under this condition,the impurity could be completely separated from main components (R>8).The RSD of repeatability test was 0.27% (n=6).The limit of detection was 0.005 μg/ml and the contents of related substances were 0.3% in 3 batches of samples.CONCLUSIONS:The method is simple,sensitive and suitable for the content determination of related substances in Terfenadine tablets.%目的:建立测定特非那定片中有关物质含量的方法.方法:采用高效液相色谱法.色谱柱为Hypersil Phenyl 2,流动相为乙腈-磷酸盐缓冲液(50∶50),流速为1.5 ml/min,检测波长为220nm,柱温为室温.结果:该色谱条件下,杂质与主成分能完全分离(分离度>8),重复性试验RSD=0.27%(n=6),检测限为0.005 μg/ml.3批样品中有关物质含量均为0.3%.结论:建立的方法简便、灵敏度高,可用于特非那定片中有关物质的含量测定.

  16. Natural radioactivity in groundwater--a review.

    Science.gov (United States)

    Dinh Chau, Nguyen; Dulinski, Marek; Jodlowski, Pawel; Nowak, Jakub; Rozanski, Kazimierz; Sleziak, Monika; Wachniew, Przemyslaw

    2011-12-01

    The issue of natural radioactivity in groundwater is reviewed, with emphasis on those radioisotopes which contribute in a significant way to the overall effective dose received by members of the public due to the intake of drinking water originating from groundwater systems. The term 'natural radioactivity' is used in this context to cover all radioactivity present in the environment, including man-made (anthropogenic) radioactivity. Comprehensive discussion of radiological aspects of the presence of natural radionuclides in groundwater, including an overview of current regulations dealing with radioactivity in drinking water, is provided. The presented data indicate that thorough assessments of the committed doses resulting from the presence of natural radioactivity in groundwater are needed, particularly when such water is envisaged for regular intake by infants. They should be based on a precise determination of radioactivity concentration levels of the whole suite of radionuclides, including characterisation of their temporal variability. Equally important is a realistic assessment of water intake values for specific age groups. Only such an evaluation may provide the basis for possible remedial actions.

  17. QUANTITATIVE DETERMINATION OF MAIN GROUPS OF SUBSTANCES IN GRANULES ON THE BASIS OF MEDICINAL VEGETABLE RAW MATERIAL FOR TREATING GASTROINTESTINAL DISEASES

    Directory of Open Access Journals (Sweden)

    Spiridonov S.V.

    2014-12-01

    Full Text Available In the last time a significant increasing of gastrointestinal tract diseases has been observed. The poor quality and irrational feeding, environmental pollution, psychological and other factors is the causes of this. Very often the gastrointestinal tract has a multifactorial pathological effects, also affecting the hepatosphere organs and urogenital system. Also a great importance have accompanying disorders of the central nervous system. Thus we must to require a comprehensive approach to the creation of drugs for use in gastroenterology, the assortment range of which should be expanded. Advantageous position in this case takes a phytotherapy using drugs based on medicinal plant raw material, which acting on the main areas of the pathological process. For this purpose the scientists from the National University of Pharmacy (Kharkov, Ukraine was created a complex herbal drug in the form of granules under the code name "Poligerbagastrin", includes the following types of medicinal plant raw material powders: helichrysum arenarium flowers, corn stigmas, horsetail grass, knotweed grass, horse chestnut seeds, licorice roots and wheat bran. Materials and methods To determine the quantity of biologically active substances the method of spectrophotometry in the visible and UV spectral region was used. This method is well studied and available, equipped with high-precision hardware. He also described in the Ukrainian normative documents and contained in the world's leading pharmacopoeias. For determination was used the unifieds methods, which shown in pharmacopoeia monographs and other reference literature. Determination was carried out with a spectrophotometer HP 8543 UV-VIZ of «Hewlett Packard» company, USA. Results and discussion For the quantitative determination of flavonoids was used a methodology, which based on the complexation reaction of isolated by acid hydrolysis and extraction with ethylacetate hydrolysis products with aluminum chloride in

  18. Radioactivity; La radioactivite

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2002-07-01

    This pedagogical document presents the origin, effects and uses of radioactivity: where does radioactivity comes from, effects on the body, measurement, protection against radiations, uses in the medical field, in the electric power industry, in the food (ionization, radio-mutagenesis, irradiations) and other industries (radiography, gauges, detectors, irradiations, tracers), and in research activities (dating, preservation of cultural objects). The document ends with some examples of irradiation levels (examples of natural radioactivity, distribution of the various sources of exposure in France). (J.S.)

  19. Development and Validation of a Stability Indicating LC Method for the Assay and Related Substances Determination of a Proteasome Inhibitor Bortezomib

    Directory of Open Access Journals (Sweden)

    Kasa Srinivasulu

    2012-01-01

    Full Text Available A novel, simple, sensitive, stability indicating HPLC method was developed and validated for quantification of impurities (process related and degradants and assay determination of bortezomib. Stability indicating power of the method was established by forced degradation experiments and mass balance study. The chromatographic separation was achieved with Waters SymmetryShield RP18 column using gradient elution using the mobile phase-A consists of a mixture of water-acetonitrile-formic acid (715 : 285 : 1, v/v/v and the mobile phase-B consists a mixture of methanol-water-formic acid (800 : 200 : 1, v/v/v, respectively. The developed method is validated for parameters like precision, accuracy, linearity, LOD, LOQ, and ruggedness. Central composite experimental design (CCD was applied to check the robustness of the method. The stability tests were also performed on drug substances as per ICH norms.

  20. Radioactive isotopes in Danish drinking water

    Energy Technology Data Exchange (ETDEWEB)

    Nielsen, Sven P. [Risoe National Lab., Roskilde (Denmark)

    2006-08-31

    A screening investigation of radioactivity in Danish drinking water has been carried out during 2001-2003. Samples of drinking water were collected from 296 water supplies representing more than 40% of the water delivered from water works in the country. Total alpha and total beta radioactivity was determined in the samples and compared with screening levels of 0.1 Bq/l total alpha and 1 Bq/l total beta radioactivity. The levels for total beta radioactivity were met in all the water works while total alpha radioactivity exceeded the screening levels for 13 water supplies. Further investigations were carried out for the water works with concentrations of alpha radioactivity above the screening levels in Ebeltoft, Grenae and Frederikssund to estimate the total indicative dose from the water. The elevated levels were found to be due to uranium in the water from individual boreholes. Radiation doses from consumption of water at these uranium levels are estimated to be well below the total indicative dose of 0.1 mSv/y specified in the Drinking Water Directive Groundwater used for drinking water was collected from different types of geological structures including bed rock and areas with potentially elevated levels of natural radioactivity. Also in these cases the concentrations of radioactivity were sufficiently low to meet the requirements in the Drinking Water Directive. In view of the results it seems probable that the risk of finding drinking water in Denmark with unacceptable concentrations of radioactivity is very small. Therefore there is no need for further radiological investigations of the Danish water supply based on natural groundwaters. (au)

  1. DETERMINATION OF CONTENTS OF NICOUSAMIDE AND RELATED SUBSTANCES BY HPLC%HPLC法测定硝克柳胺的含量及有关物质

    Institute of Scientific and Technical Information of China (English)

    王乐; 王娅莉; 赵玉; 牛长群; 郭丽

    2013-01-01

    Objective To establish an high performance liquid chromatography(HPLC) method for determination of nicousamide and its related substances. Methods The separation was performed on an Inertsil C8(250mm ×4. 6mm,5μm,GL Sciences Inc.) column with the mobile phase consisting of water-acetonitrile-tetrahydrofuran (50:50:1) (including 0. 1% phosphoric acid) at the flow rate of 1.0mL/min. The detection wavelength was set at 330nm. The column temperature was 30℃. Results Under the above conditions, the main peak and the peaks of the related substances were separated quite well. Nicousamide had a good linear relationship (r =0. 999 6) within the range of 0. 02-1.0g/L. The average recovery (n =9) was 100. 1%. The limit of detection was 0. Ing. Conclusion The method is sensitive, specific and simple. It can be used for determinating nicousamide and its related substances.%目的 建立硝克柳胺含量和有关物质的高效液相色谱(high performance liquid chromatography,HPLC)测定方法.方法 采用Inertsil C8柱(250mm×4.6mm,5μm,GL Sciences Inc.);流动相为水-乙腈-四氢呋喃(50∶50∶1)(内含0.1%磷酸);流速为1.0mL/min;检测波长为330nm;柱温为30℃.结果 在选定色谱条件下,主峰与有关物质峰分离度良好,硝克柳胺在0.02~1.0g/L浓度范围内线性关系良好(r=0.999 6);平均回收率为100.1%(n=9);检测限为0.1ng.结论 该方法 专属性强、灵敏度高、操作简便,可用于测定硝克柳胺的含量及有关物质.

  2. HPLC法测定硝唑尼特中的3种有关物质%Determination of Three Related Substances in Nitazoxanide by HPLC

    Institute of Scientific and Technical Information of China (English)

    谢宜名; 张燕; 杨钊; 李新荣; 楚敏

    2012-01-01

    Objective: To establish an HPLC method for the determination of three related substances in nitazoxanide. Method: The separation was performed on an Alltima C8( 250 mm ×4. 6 mm,5 μm )column with the mobile phase of acetonitrile-water ( adjusting pH to 2. 5 with phosphoric acid ) with gradient elution at a flow rate of 1. 0 ml ? Min-1. The column temperature was 25℃ and the detection wavelength was 210 nm. Result: The quantification limit of the three related substances in nitazoxanide was 0.087 6, 0. 050 4 and 0.013 5 μg ? Ml-1 , respectively. The theoretical plate number was above 7 000 with the resolution of the impurities over 1.5. Conclusion: The method is specific, sensitive and accurate, which can be used in the determination of related substances in nitazoxanide.%目的:建立HPLC法测定药物硝唑尼特中三种有关物质的方法.方法:色谱柱:Alltima C8(250 mm×4.6 mm,5 μm);流动相为乙腈-水(磷酸调节pH至2.5)梯度洗脱;流速:1.0 ml·min-1;柱温:25 ℃;检测波长210 nm.结果:硝唑尼特三种有关物质定量限分别为0.087 6,0.050 4,0.013 5 μg·ml-1,硝唑尼特峰的理论塔板数大于7 000,且与杂质峰的分离度大于1.5.结论:本方法专属性强、灵敏度高、准确性高,适宜分析硝唑尼特中的有关物质.

  3. HPLC测定枸橼酸莫沙必利片的有关物质%HPLC determination of related substances in mosapride citrate tablets

    Institute of Scientific and Technical Information of China (English)

    王守箐

    2011-01-01

    目的:建立高效液相色谱测定枸橼酸莫沙必利片有关物质的方法.方法:采用C18柱(250 mm×4.6 mm,5μm),以0.05mol·L-1枸橼酸溶液(用氢氧化钠溶液调节pH至4.0) -乙腈(65∶35)为流动相,流速1.0 mL·min-1,检测波长为274 nm,自身对照法测定.结果:线性范围为0.502 ~4.016 μg·mL-1,r2=0.9978,最低检测限为0.33 ng.结论:该方法准确、简便,可以用于枸橼酸莫沙必利片有关物质的测定.%Objective:To establish an HPLC method for the determination of related substances in mosapride citrate tablets. Methods:The separation was performed on C18 Column (250 mm x4. 6 mm,5μm) with mobile phase consisted of 0.05 mol·L-1 citric acid (adjusted pH =4. 0 with sodium hydroxide solution) -acetonitrile(65:35)and the flow rate was 1. 0 mL·min-1. The detection wave length was set at 274 nm. The content of related substance was calculated by self - control with main component. Results:The standard curve was linear within the range of 0. 502 -4. 016 μg@mL-1 (r2 =0. 9978) and the limit of detection was 0. 33 ng. Conclusion;The method is accurate and simple for the determination of the related substances in mosapride citrate tablets.

  4. HPLC determination of related substances of phenylbutazone tablets%高效液相色谱法测定保泰松片的有关物质

    Institute of Scientific and Technical Information of China (English)

    李玲; 姜燕; 陈乃江

    2015-01-01

    目的:建立测定保泰松片有关物质的高效液相色谱法。方法采用Phenomenex Luna C18(250mm×4.6mm,5μm)色谱柱,流动相为乙腈-水(磷酸调pH至3.0)(50∶50),检测波长为239nm,流速1.0mL/min,柱温为30℃,进样体积为10μL。结果在选定的色谱条件下,主成分能与杂质峰之间分离度良好;方法的检测限为0.2μg/mL;供试品溶液在8h内稳定性良好。结论本方法简单,准确,重现性好,可用于保泰松片的有关物质检查。%Objective To establish a HPLC method for the determination of related substances of phenylbutazone tablets.MethodsA Phenomenex LunaC18 column(250mm×4.6mm,5μm) was used, and the mobile phase was acetonitrile–water[adjusting pH to 3.0 with phosphoric acid] (50:50).The flow rate was 1.0 mL/min and the detection wavelength was set at 239nm.The column temperature was set at 30℃ and the injection volume was 10 μL. Results Related substances were completely separated from the main constituent.The limit of detection was 0.2μg/mL.The sample solution was stable within 8h.Conclusion The method wsa simple,accurate with good reproducibility,and can be used in the determination of related substances of phenylbutazone tablets.

  5. 氯芬黄敏片的有关物质检查%Determination of related substances concentration of compound diclofenac aodium and chlorphenamine maleate tablets

    Institute of Scientific and Technical Information of China (English)

    龙敏玲; 陈禧翎

    2012-01-01

    目的 采用高效液相色谱法对氯芬黄敏片进行有关物质检查.方法 色谱柱:HyperClone 5 μ m BDSC18(4.60 mm×150 mm);流动相:庚烷磺酸钠溶液(庚烷磺酸钠15.2 mg,加三乙胺0.8ml,加水800 ml,用冰醋酸调pH至3.3±0.1,加水至1000ml)甲醇-乙腈(25∶ 30∶ 18);检测波长:262 nm;进样体积:20μl;流速:1.0 ml/min.结果 马来酸氯苯钠敏、双氯芬酸钠与其它有关物质均达到基线分离,最小检测浓度为1.18 μg/ml.结论 该法专属性强,操作方便,结果准确,重现性好,可用于氯芬黄敏片的有关物质检查.%Objective To establish a high performance liquid chromatogra (HPLC) method for determining the related substances concentration ofcompound diclofenac sodium and chlorphenamine maleate tablets.Methods Diclofenac sodium and chlorphenamine maleate can be separated on HyperClone 5 μ BDS C18(4.60 mm x 150 mm )column with a mixture of (CH3)(CH2)6SO3Na 15.2mg,(C2H5)3N 0.8 ml,and distilled water 800 ml,pH adjusted to 3.3 ± 0.1 with CH3COOH,then add distilled water to 1000 ml)-CH3OH-CH3CN (25∶ 30∶ 18) as mobile phase and detected at 262 nm.Injection volume:20 μ 1.Flow rate:1.0 ml/min.Results Diclofenac sodium and chlorphenamine maleate were separated from reference substances in base-line.The dection limits were 1.18 μ g/ml.Conclusion The method has strong specificity,and is simple,accurate and reproducible.It is adapted to determine the felsted substances concentration of compound diclofenac sodium and chlorphenamine maleate tablets.

  6. Elimination of interferences from surface active substances in voltammetric determination of trace amounts of titanium in environmental water samples

    Directory of Open Access Journals (Sweden)

    Grabarczyk M.

    2013-04-01

    Full Text Available A cathodic stripping voltammetric method for determination of Ti(IV in water samples containing high concentrations of surfactants is described. The linear calibration plot for Ti(IV was achieved in the simultaneous presence of 5 mg L-1 anionic, 1 mg L-1 cationic and 2 mg L-1 nonionic surfactants for an accumulation time of 30 s in the range 2.5 × 10-8 to 5 × 10-7 mol L-1, the detection limit for accumulation time of 30 s was about 8.4 × 10-9 mol L-1. The developed method was successfully applied to Ti(IV determination in environmental waters, such as river water (Bystrzyca, Czerniejówka, stagnant water (Lake Zemborzyce and rain water (collected from eastern areas of Poland with satisfactory results.

  7. Understanding radioactive waste

    Energy Technology Data Exchange (ETDEWEB)

    Murray, R.L.

    1981-12-01

    This document contains information on all aspects of radioactive wastes. Facts are presented about radioactive wastes simply, clearly and in an unbiased manner which makes the information readily accessible to the interested public. The contents are as follows: questions and concerns about wastes; atoms and chemistry; radioactivity; kinds of radiation; biological effects of radiation; radiation standards and protection; fission and fission products; the Manhattan Project; defense and development; uses of isotopes and radiation; classification of wastes; spent fuels from nuclear reactors; storage of spent fuel; reprocessing, recycling, and resources; uranium mill tailings; low-level wastes; transportation; methods of handling high-level nuclear wastes; project salt vault; multiple barrier approach; research on waste isolation; legal requiremnts; the national waste management program; societal aspects of radioactive wastes; perspectives; glossary; appendix A (scientific American articles); appendix B (reference material on wastes). (ATT)

  8. Electro-analytical Chemistry and Chemo-metrics for Meat Products in the Quantitative Determination of Hazardous Substances

    Directory of Open Access Journals (Sweden)

    Cheng Hao

    2014-10-01

    Full Text Available In this study, differential pulse stripping voltammetry meat tissues examined three drug residues salbutamol and ractopamine hydrochloride oxidation peak on the glassy carbon electrode serious overlapping and partially overlapping with clenbuterol, among the three components there is a strong interaction, the mixture is difficult to determine the content of each single component directly. Based on the optimization of the experimental conditions and based on the introduction Chemometrics mixing its components resolved to avoid the tedious separation and purification steps, simplifying the measurement process.

  9. Uranium Glass: A Glowing Alternative to Conventional Sources of Radioactivity

    Science.gov (United States)

    Boot, Roeland

    2017-01-01

    There is a relatively simple way of using radioactive material in classroom experiments: uranium glass, which provides teachers with a suitable substance. By using the right computer software and a radiation sensor, it can be demonstrated that uranium glass emits radiation at a greater rate than the background radiation and with the aid of UV…

  10. Shared Substance

    DEFF Research Database (Denmark)

    Gjerlufsen, Tony; Klokmose, Clemens Nylandsted; Eagan, James

    2011-01-01

    This paper presents a novel middleware for developing flexible interactive multi-surface applications. Using a scenario-based approach, we identify the requirements for this type of applications. We then introduce Substance, a data- oriented framework that decouples functionality from data, and S...

  11. Determination of diets for the populations of eleven regions of the European community to be used for obtaining radioactive contamination levels. First results concerning the food consumption of individuals classified in nine age-groups; Determination des regimes alimentaires des populations de onze regions de la Communaute Europenne et vue de l'etude des niveaux de contamination radioactive. Premiere serie de resultats concernant la consommation alimentaire des individus groupes en neuf classes d'ages

    Energy Technology Data Exchange (ETDEWEB)

    Ledermann, S.; Lacourly, G.; Garnier, A.; Cresta, M.; Lombardo, E. [Commissariat a l' Energie Atomique, 92 - Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1968-07-01

    The present document continues the report CEA-R--2979 - EUR--2768-f. The processing of the data given by the family food enquiry carried out in eleven regions of the European Community, has permitted to determine the food consumption of individuals classified in nine age-groups, in order to study the radioactive contamination levels in the food-chain. The used statistical method is described, and the obtained results are presented in form of double-entry tables giving for each region and for each age-group the mean weekly food-consumption and the contribution of each diet in nutrition principles, in minerals, vitamins, trace elements and calories. (authors) [French] Ce rapport fait suite au rapport CEA-R--2979 - EUR--2768-f. Le traitement de l'information apportee par les enquetes alimentaires familiales realisees dans onze regions de la Communaute Europeenne a permis de determiner les consommations alimentaires des individus groupes en neuf classes d'age, en vue de l'etude des niveaux de contamination radioactive dans les chaines alimentaires. La methode statistique employee est decrite et les resultats obtenus sont presentes sous forme de tableaux a double entree donnant pour chacune des regions etudiees et pour chacune des neuf classes d'age, les consommations moyennes hebdomadaires, ainsi que les apports en principes nutritifs, mineraux, vitamines et oligo-elements, et calories de chaque regime. (auteurs)

  12. Thermodynamic stability of radioactivity standard solutions

    Energy Technology Data Exchange (ETDEWEB)

    Iroulard, M.G

    2007-04-15

    The basic requirement when preparing radioactivity standard solutions is to guarantee the concentration of a radionuclide or a radioelement, expressed in the form of activity concentration (Ac = A/m (Bq/g), with A: activity and m: mass of solution). Knowledge of the law of radioactive decay and the half-life of a radionuclide or radioelement makes it possible to determine the activity concentration at any time, and this must be confirmed subsequently by measurement. Furthermore, when radioactivity standard solutions are prepared, it is necessary to establish optimal conditions of thermodynamic stability of the standard solutions. Radioactivity standard solutions are prepared by metrology laboratories from original solutions obtained from a range of suppliers. These radioactivity standard solutions must enable preparation of liquid and/or solid radioactivity standard sources of which measurement by different methods can determine, at a given instant, the activity concentration of the radionuclide or radioelement present in the solution. There are a number of constraints associated with the preparation of such sources. Here only those that relate to the physical and chemical properties of the standard solution are considered, and therefore need to be taken into account when preparing a radioactivity standard solution. These issues are considered in this document in accordance with the following plan: - A first part devoted to the chemical properties of the solutions: - the solubilization media: ultra-pure water and acid media, - the carriers: concentration, oxidation state of the radioactive element and the carrier element. - A second part describing the methodology of the preparation, packaging and storage of standard solutions: - glass ampoules: the structure of glasses, the mechanisms of their dissolution, the sorption phenomenon at the solid-solution interface, - quartz ampoules, - cleaning and packaging: cleaning solutions, internal surface coatings and

  13. Development and validation of an ultra high-performance liquid chromatographic method for the determination of a diastereomeric impurity in (+)-pinoresinol diglucoside chemical reference substance.

    Science.gov (United States)

    Song, Jing-Zheng; Cheung, Lok Man; Liu, Xin; Qiao, Chun-Feng; Zhou, Yan; Li, Song-Lin; Chen, Shi-Lin; Xu, Hong-Xi

    2010-07-01

    (+)-Pinoresinol 4,4'-di-O-beta-D-glucopyranoside ((+)-PDG) is one of the major lignans with various pharmacological activities which could be isolated from Duzhong and other plant species. In this study, a diastereomeric impurity, (-)-pinoresinol 4,4'-di-O-beta-D-glucopyranoside ((-)-PDG), the main impurity was identified in (+)-PDG chemical reference substance (CRS) and a reliable chromatographic method for rapid purity determination of (+)-PDG CRS was firstly developed. The optimal chromatographic condition was found to be using ACN/1,4-dioxane-water (2.5:6:91.5, v/v/v) as mobile phase on a Waters Acquity UPLC HSS T3 column (2.1 mm x 100 mm, 1.8 microm) with column temperature of 37 degrees C. The method was validated and applied to determine the chromatographic purity of five (+)-PDG CRS samples. The content of (-)-PDG in four commercial (+)-PDG CRS was 8.47-20.30%, whereas no (-)-PDG was detected in our in-house prepared (+)-PDG CRS in which purity was confirmed to be 99.80%. The above results confirmed that this method is fast and highly efficient for purity determination of the (+)-PDG CRS.

  14. HPLC determination of related substances of salicylic acid%HPLC法测定水杨酸原料药的有关物质

    Institute of Scientific and Technical Information of China (English)

    黄洁; 李锋武; 刘鹏鸣; 范菲; 单敏

    2011-01-01

    目的:建立RP- HPLC法测定水杨酸原料药的有关物质.方法:采用Phenomenex Luna C18柱(4.6 mm×150 mm,5μm),流动相为甲醇-水-冰醋酸(60:40:1),流速1.0 mL · min-1,检测波长270 nm.结果:水杨酸与4-羟基苯甲酸、4-羟基间苯二甲酸和苯酚分离度良好,3种杂质在0.958 ~ 19.16 μg·mL-1、0.4912 ~9.824μg·mL-1、0.214~4.28 μg·mL-1之间线性关系良好,检测限分别为0.025 μg·mL-1、0.025 μg·mL-1、0.04 μg·mL-1.结论:本方法简便、准确,专属性好,灵敏度高,可作为水杨酸原料药有关物质的检查方法.%Objective:To establish an HPLC method for determination of relater substances of salicylic acid. Methods; Phenomenex Luna C18 (4. 6 mm × 150 mm ,5 μm) was adopted with methanol - water - acetic acid (60: 40= 1) as mobile phase at the flow rate of 1.0 mL · Min-1,detection was set at 270 nm. Results;Good separation of salicylic acid and other substance could be achieved. Three kinds of material and linear relationship was good,The detection limits were 0.025 μg · mL-1,0.025 μg · mL-1 and 0. 04μg · mL-1. Conclusion; This method is simple,sensitive , selective and repetitive, accurate for analysis of related substances of salicylic acid.

  15. Development and optimization the method for determination the related substances of azithromycin%阿奇霉素有关物质测定方法的优化

    Institute of Scientific and Technical Information of China (English)

    寇晋萍; 王国兰; 王俊秋; 周立春

    2011-01-01

    目的 对阿奇霉素有关物质测定方法进行优化.方法 采用SHISEIDO CAPCELL PAK C18 MG Ⅱ(51μm,4.6mm×250mm)色谱柱;磷酸盐缓冲液(0.05mol/L磷酸氢二钾溶液,用20%的磷酸调节pH值至8.2):乙腈(45:55)为流动相;柱温30℃;流速1.0mL/min;检测波长210nm.结果 阿奇霉素在10~1000μg/mL范围内浓度与峰面积呈良好线性关系,r=0.9999;最低检测限为100ng,与其已知杂质分离度良好.结论 本方法可用于测定阿奇霉素及制剂的有关物质.%Objective To optimize the method to determination the related substances of azithromycin.Methods A SHISEIDO CAPCELL PAK C18 MG Ⅱ (5μm, 4.6mm×250mm) column was used. The mobile phase consisted of 0.05mol/L K2HPO4 solution (pH8.2, adjust with 20% phosphate acid): acetonitrile (45: 55), the flow rate was 1.0mL/min, the detection wavelength was 210nm. The column temperature was 30℃. Results The calibration curves were linear in the range of 10~1000μg/mL(r=0.9996) for azithromycin, The minimal detection limit was 100ng, and its related substance can be well separated. Conclusion The selective and reliable method can be used for related substances in azithromycin.

  16. Determination of the related substances in Mometasone Furoate Cream by HPLC%HPLC法测定糠酸莫米松乳膏中的有关物质

    Institute of Scientific and Technical Information of China (English)

    曹玉明

    2016-01-01

    Objective To develop a method for the related substances in mometasone furoate cream(Eloson).Methods HPLC was a-dopted for the limits determination of the related substances.An Amethyst C18 -P column(250 mm ×4.6 mm,5 μm)was used as the stationary phase,with a mobile phase of acetonitrile-water solution(53∶47),the flow rate was 1 mL·min-1 ,the detection wavelength was 254 nm and the injection volume was 20 μL.Results For each impurity was not more than 1 .0%,the total was not more than 2.0%.Five batches of Eloson were analyzed under the established method,all of results were that for each impurity was not more than 1.0% and the total was not more than 2.0%.Conclusion The developed method is accurate and reliable,which could be used for the limit control of the related substances in Eloson.%目的:建立糠酸莫米松乳膏(艾洛松)中有关物质的检测方法。方法采用HPLC法对艾洛松中的有关物质进行测定。以Amethyst C18-P(250 mm ×4.6 mm,5μm)色谱柱为固定相;乙腈-水(53∶47)为流动相;流速为1 mL·min-1;检测波长为254 nm;进样量为20μL。结果各单个杂质不超过1.0%,总杂质不超过2.0%。该方法对5个批次糠酸莫米松乳膏中的有关物质进行了测定,其限度均为单个杂质不超过1.0%,总杂质不超过2.0%。结论该方法准确可靠,可作为糠酸莫米松乳膏(艾洛松)中有关物质的测定方法。

  17. HPLC determination of the related substances in erdosteine%厄多司坦原料药中有关物质的测定方法

    Institute of Scientific and Technical Information of China (English)

    马丽; 张玲娣; 王文娜; 姚彤炜

    2012-01-01

    建立厄多司坦原料药中有关物质的反相高效液相色谱测定方法.以ODS-SunFire (250 mm×4.6 mm ID,5 μm)为分析柱;甲醇-乙腈-0.01 mol·L-1枸橼酸溶液(pH 2.5) (20∶4∶76)为流动相,流速为1 mL·min-1;检测波长254 nm.采用加或不加校正因子的主成分自身对照法控制原料药中有关物质.在选定的色谱条件下,厄多司坦与有关杂质分离良好.以主成分计,检测限为0.2 μg·mL-1(S/N=3).该方法能够有效地控制厄多司坦原料药中的有关物质.%An HPLC method was established for the determination of the related substance in erdosteine. Waters ODS-SunFire (250 mm × 4.6 mm ID, 5 (μm) column was used, the mobile phase was composed of methanol-acetonitrile-0.01 mol·L-1 citric acid (20 : 4 : 76, the pH value was adjusted by triethylamine to 2.5). The flow rate was 1 mL·min-1. The detection wavelength was 254 nm. The related substances in the sample of erdosteine taken were calculated by self control with or without the response factor of impurity relative to that of erdosteine. Under the chromatographic condition developed, the impurities in erdosteine were isolated well. The detection limit was 0.2 ng·mL-1 (Signal/Noise = 3) by principal component calculated. The method can be adopted to control the related substances in erdosteine.

  18. High-performance liquid chromatographic methods for the determination of ranitidine and related substances in raw materials and tablets.

    Science.gov (United States)

    Beaulieu, N; Lacroix, P M; Sears, R W; Lovering, E G

    1988-10-01

    High-performance liquid chromatographic methods have been developed for the determination of ranitidine and related compounds in drug raw material and tablets. The method has been shown to resolve at least nine related compounds from the drug. The sensitivity of the method to related compounds is better than 0.01%. Eight raw material samples and 11 tablet samples were examined for related compounds. Total impurities found ranged from 0.31 to 0.79% in raw materials and from 0.40 to 1.75% in tablets. Drug raw materials and tablets were assayed by HPLC; results for raw materials were between 98.2 and 101.1%, and those for tablets were between 96.1 and 102.2%, with a relative standard deviation for the assay of less than 1%. Raw material assay results were confirmed by nonaqueous titration.

  19. HPLC测定醋酸泼尼松片中的有关物质%Determination of the related substances in Prednisone acetate tablet by HPLC

    Institute of Scientific and Technical Information of China (English)

    韩学静; 刘红莉; 闫凯

    2011-01-01

    目的 采用HPLC法测定醋酸泼尼松片的有关物质.方法 采用DIONEX Acclaim C18色谱柱(250 mm ×4.6 mm,5μm),流动相为乙腈-水(42∶58),检测波长240 nm.结果 泼尼松0.5~30 μg·mL-1与峰面积呈良好线性关系(r=0.9999),最低检测限为0.25 ng;醋酸可的松0.5 ~30 μg·mL-1与峰面积呈良好线性关系(r =0.9999),最低检测限为0.25 ng.结论 所建方法准确、简便、快速,适用于醋酸泼尼松片的质量控制.%OBJECTIVE To determine the related substances in Prednisone acetate tablet by HPLC. METHODS The separation was performed on a DIONEX Acclaim C18 column(250 mm ×4.6 mm,5 μm). The mobile phase was acetonitrile -water(42 : 58). The detection wavelength was set at 240 nm. RESULTS The calibration curve of prednisone showed a good linearity over the range of 0. 5 -30.0 μg-mL-1 (r =0.9999) and the LOD was 0.25 ng. The calibration curve of cortisone acetate showed a good linearity over the range of 0.5 - 30.0 μg · mL-1 ( r = 0. 9999 ) and the LOD was 0. 25 ng. CONCLUSION The method is simple, rapid, accurate and suitable for testing the related substances in Prednisone acetate tablets.

  20. Intergenerational ethics of high level radioactive waste

    Energy Technology Data Exchange (ETDEWEB)

    Takeda, Kunihiko [Nagoya Univ., Graduate School of Engineering, Nagoya, Aichi (Japan); Nasu, Akiko; Maruyama, Yoshihiro [Shibaura Inst. of Tech., Tokyo (Japan)

    2003-03-01

    The validity of intergenerational ethics on the geological disposal of high level radioactive waste originating from nuclear power plants was studied. The result of the study on geological disposal technology showed that the current method of disposal can be judged to be scientifically reliable for several hundred years and the radioactivity level will be less than one tenth of the tolerable amount after 1,000 years or more. This implies that the consideration of intergenerational ethics of geological disposal is meaningless. Ethics developed in western society states that the consent of people in the future is necessary if the disposal has influence on them. Moreover, the ethics depends on generally accepted ideas in western society and preconceptions based on racism and sexism. The irrationality becomes clearer by comparing the dangers of the exhaustion of natural resources and pollution from harmful substances in a recycling society. (author)

  1. Use of radioanalytical methods for determination of uranium, neptunium, plutonium, americium and curium isotopes in radioactive wastes; Utilizacao de metodos radioanaliticos para a determinacao de isotopos de uranio, plutonio, americio e curio em rejeitos radioativos

    Energy Technology Data Exchange (ETDEWEB)

    Geraldo, Bianca

    2012-07-01

    Activated charcoal is a common type of radioactive waste that contains high concentrations of fission and activation products. The management of this waste includes its characterization aiming the determination and quantification of the specific radionuclides including those known as Difficult-to-Measure Radionuclides (RDM). The analysis of the RDM's generally involves complex radiochemical analysis for purification and separation of the radionuclides, which are expensive and time-consuming. The objective of this work was to define a methodology for sequential analysis of the isotopes of uranium, neptunium, plutonium, americium and curium present in a type of radioactive waste, evaluating chemical yield, analysis of time spent, amount of secondary waste generated and cost. Three methodologies were compared and validated that employ ion exchange (TI + EC), extraction chromatography (EC) and extraction with polymers (ECP). The waste chosen was the activated charcoal from the purification system of primary circuit water cooling the reactor IEA-R1. The charcoal samples were dissolved by acid digestion followed by purification and separation of isotopes with ion exchange resins, extraction and chromatographic extraction polymers. Isotopes were analyzed on an alpha spectrometer, equipped with surface barrier detectors. The chemical yields were satisfactory for the methods TI + EC and EC. ECP method was comparable with those methods only for uranium. Statistical analysis as well the analysis of time spent, amount of secondary waste generated and cost revealed that EC method is the most effective for identifying and quantifying U, Np, Pu, Am and Cm present in charcoal. (author)

  2. Assessment of radioactivity in the drinking water of state of Goias, Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Eliane E.; Costa, Heliana F.; Mignote, Raquel M., E-mail: mingote@cnen.gov.br, E-mail: heliana@cnen.gov.br, E-mail: esantos@cnen.gov.br [Centro Regional de Ciencias Nucleares do Centro-Oeste (CRCN-CO/CNEN-GO), Abadias de Goias, GO (Brazil); Thome Filho, Jamilo J., E-mail: jamilothome@gmail.com [Geological Consultant, Cuiaba, MT (Brazil); Bakker, Alexandre P. de [Instituto Nacional do Semiarido (INSA/MCTI), Campina Grande, PB (Brazil)

    2013-07-01

    The demand for drinking water is supplied by surface and underground sources such as rivers and streams. However, there is an increasing worldwide concern about the quality of drinking water. As a result, it is a major goal of governments throughout the world to ensure that water is safe for human consumption through the control of microorganisms, chemicals and radioactive substances. The Brazilian Ministry of Health has issued guidelines designed to protect the quality of drinking water. The use of screening measurements for gross alpha and beta radioactivity is recommend since it maximizes cost-effectiveness of assessing the individual radionuclide content of drinking water. In order to do so tests were carried out to determine of gross alpha and beta radioactivity concentrations in drinking water samples from 44 water supply wells within the State of Goias. The technique used was thermal preconcentration and radiometric determination by liquid scintillation spectrometry. The concentrations for gross alpha ranged from < LD at 0.19 ± 0.05 Bq/L. As for gross beta they ranged from < LD at 0.2 ± 0.1 Bq/L. The results were also related with the geological and hydrological data. (author)

  3. Determination of levels of naturally occurring radioactive materials in lagoon samples containing produced water from the Minagish oil field in the state of Kuwait

    Science.gov (United States)

    Shams, H. M.; Bradley, D. A.; Regan, P. H.

    2017-08-01

    An evaluation of the activity concentration (Ac) associated with naturally occurring radioactive materials has been undertaken as part of a systematic study to provide a radiological map of the ground materials from a produced wastewater lagoon located in the Minagish oil field in the south west of the State of Kuwait. This lagoon contains material from the discharge of produced water which is a by-product of oil production in the region. Samples of surface materials have been collected, prepared and placed into sealed, Marinelli beakers for a full gamma-ray spectrometric analysis using a high-resolution, low-background, high-purity germanium detection system. This short conference paper presents a summary of results for an initial selection of sixteen surface samples from the edges of the Minagish oil lagoon which have been analysed to obtain Ac values for members of the 226Ra (214Bi and 214Pb) and 232Th (228Ac, 212Pb and 208Tl) decay chains and for 40K. These are compared with other studies for the same geographical region.

  4. Improvement of Determination Method for Related Substances in Cefuroxime Sodium by HPLC%HPLC法测定头孢呋辛钠有关物质的改进

    Institute of Scientific and Technical Information of China (English)

    周劲康

    2013-01-01

    Objective: To improve the: determination method for the related substances in ecfiiroximc sodium by HPLC. Method: A Phenomenex Luna C18( 250 mm ×4. 6 mm, 5 μm ) column was used, the mobile phase was composed of methanol-0. 1% phosphoric acid with linear gradient clution, the detection wavelength was 273 nm and the flow rate was 1. 0 ml · mill-1 . Result: The method was suitable for the determination of the related substances in cefuroxime sodium, the drug peak and the impurity peaks could be separated efficiently, cefuroxime showed a good linearity within the range of 0. 101 4-2.028 μg( r =0.999 9), and LOD and LOQ was 0. 105 ng and 0.351 ng, respectively. Conclusion: The improved method is simple, accurate and reproducible, and the determination result of the method is the same as that of the described method in China Pharmacopoeia ( 2010 ).%目的:改进用于头孢呋辛钠有关物质检测的HPLC方法.方法:选用Phenomenex Luna C18(250 mm×4.6 mm,5 μm)色谱柱,流动相为甲醇-0.1%磷酸溶液,梯度洗脱,检测波长为273 nm;流速为1.0 ml·min-1.结果:头孢呋辛与相邻杂质峰分离度符合要求,在0.101 4~2.028 μg范围内线性关系良好(r=0.999 9),检测限和定量限分别为0.105 ng和0.351 ng.结论:改进后的方法更快速、准确、专属性好,检测结果与2010版方法所得结果基本相同.

  5. Determination method of related substances in risedronate sodium tablets%利塞膦酸钠片有关物质的方法学研究

    Institute of Scientific and Technical Information of China (English)

    张秀立; 张宇佳; 王璐璐; 方夏琴; 陈少华; 郑稳生

    2015-01-01

    Objective To establish a HPLC method for determination of related substances of risedronate sodium tab‐lets .Methods The C18 column ,5 μm ,150 mm × 4 .6 mm ,the buffer solution (3 .22 g tetrabutyl ammonium bromide was added to a buffer solution of 1 000 ml 0 .05 mol/L ammonium chloride ,then adjusted pH to 7 .8 ± 0 .05 by ammonia)‐methanol‐aceto‐nitrile =250:50:25 as mobile phase ,column temperature:room temperature ,flow rate:1 .0 ml/min ,detection length:254 nm . Results Determined by HPLC at high temperature ,acid ,alkali degradation ,the main peak and the impurity peaks were separa‐ted well ,and the peaks had a linear relationship ,Y=1 .28 × 107 X-1 .62 × 105 (r=0 .999 9) .Conclusion The method was rap‐id ,simple ,accurate and sensitive ,and suitable for determination of risedronate sodium tablets related substances .%目的:建立测定利塞膦酸钠片有关物质的高效液相色谱法。方法采用ODS C18色谱柱(5μm ,150 mm ×4.6mm),以缓冲液(取四丁基溴化铵3.22g 加入1000ml0.05mol/L氯化铵缓冲液中,用氨水调pH至7.8±0.05)‐甲醇‐乙腈(250:50:25)为流动相;柱温:室温;流速:1.0 ml/min;检测波长:254 nm。结果在高温、酸、碱、氧化、强光降解下用HPLC测定,各杂质峰和主峰均有较好的分离效果,线性关系为Y=1.28×107 X-1.62×105(r=0.9999),线性良好,稳定性良好。结论该方法测定快速、简单、准确,灵敏度高,适用于利塞膦酸钠片有关物质的测定。

  6. Disposal of radioactive waste. Some ethical aspects

    Energy Technology Data Exchange (ETDEWEB)

    Streffer, Christian

    2014-07-01

    The threat posed to humans and nature by radioactive material is a result of the ionizing radiation released during the radioactive decay. The present use of radioactivity in medicine research and technologies produces steadily radioactive waste. It is therefore necessary to safely store this waste, particularly high level waste from nuclear facilities. The decisive factors determining the necessary duration of isolation or confinement are the physical half-life times ranging with some radionuclides up to many million years. It has therefore been accepted worldwide that the radioactive material needs to be confined isolated from the biosphere, the habitat of humans and all other organisms, for very long time periods. Although it is generally accepted that repositories for the waste are necessary, strong public emotions have been built up against the strategies to erect such installations. Apparently transparent information and public participation has been insufficient or even lacking. These problems have led to endeavours to achieve public acceptance and to consider ethical acceptability. Some aspects of such discussions and possibilities will be taken up in this contribution. This article is based on the work of an interdisciplinary group. The results have been published in 'Radioactive Waste - Technical and Normative Aspects of its Disposal' by C. Streffer, C.F. Gethmann, G. Kamp et al. in 'Ethics of Sciences and Technology Assessment', Volume 38, Springer-Verlag Berlin Heidelberg 2011.

  7. Comparison of reversed-phase enantioselective HPLC methods for determining the enantiomeric purity of (S-omeprazole in the presence of its related substances

    Directory of Open Access Journals (Sweden)

    Bruno Gallinella

    2016-04-01

    Full Text Available A simple analytical high-performance liquid chromatography (HPLC method was applied for the enantiomeric excess determination of esomeprazole ((S-OME, the enantiopure active ingredient contained in drug products, in the presence of its potential organic impurities A-E. The enantioselective separation was accomplished on the immobilized-type Chiralpak ID-3 chiral stationary phase (CSP under reversed-phase conditions. The results were evaluated and compared with those obtained by the official enantioselective method of European Pharmacopoeia used as the reference for checking the enantiomeric excess of (S-OME. It has been established that the use of the Chiralpak ID-3 CSP allows the determination of the enantiomeric purity of (S-OME without any interference coming from its chiral and achiral related substances. The analytical procedure of the drug regulatory agencies based on the AGP CSP suffered instead from poor specificity due to overlap of the peaks pertinent to the achiral impurity A and the chiral impurity (R-OME (impurity F.

  8. Comparison of reversed-phase enantioselective HPLC methods for determining the enantiomeric purity of (S)-omeprazole in the presence of its related substances$

    Institute of Scientific and Technical Information of China (English)

    Bruno Gallinella; Rosella Ferretti; Leo Zanitti; Isabella Sestili; Antonina Mosca; Roberto Cirilli n

    2016-01-01

    A simple analytical high-performance liquid chromatography (HPLC) method was applied for the en-antiomeric excess determination of esomeprazole ((S)-OME), the enantiopure active ingredient con-tained in drug products, in the presence of its potential organic impurities A-E. The enantioselective separation was accomplished on the immobilized-type Chiralpak ID-3 chiral stationary phase (CSP) under reversed-phase conditions. The results were evaluated and compared with those obtained by the official enantioselective method of European Pharmacopoeia used as the reference for checking the enantiomeric excess of (S)-OME. It has been established that the use of the Chiralpak ID-3 CSP allows the determination of the enantiomeric purity of (S)-OME without any interference coming from its chiral and achiral related substances. The analytical procedure of the drug regulatory agencies based on the AGP CSP suffered instead from poor specificity due to overlap of the peaks pertinent to the achiral impurity A and the chiral impurity (R)-OME (impurity F).

  9. Multiresidue method for the determination of pharmacologically active substances in egg and honey using a continuous solid-phase extraction system and gas chromatography-mass spectrometry.

    Science.gov (United States)

    Azzouz, Abdelmonaim; Ballesteros, Evaristo

    2015-07-01

    A sensitive, selective, efficient gas chromatography-mass spectrometry method for the simultaneous determination of 22 pharmacologically active substances (antibacterials, nonsteroidal antiinflammatories, antiseptics, antiepileptics, lipid regulators, β-blockers and hormones) in eggs and honey was developed. The sample pretreatment includes precipitation of proteins and lipids with acetonitrile:water (3:2, v/v), centrifugation and continuous solid-phase extraction for cleanup and preconcentration. The proposed method was validated with quite good analytical results including limits of detection of 0.4-3.3 ng/kg for 2g of sample and good linearity (r(2)>0.995) throughout the studied concentration ranges. The recoveries of analytes from real honey and egg samples spiked at concentrations of 15-2,000 ng/kg fell in the range 87-102%, with relative standard deviations from 2.6% to 7.0%. The method was successfully used to determine the target compounds in various types of eggs (hen, quail and duck) and honey samples (flower, forest, acacia, sunflower, clover and pine tree). Two samples of hen eggs bought at supermarkets and one of quail eggs were found to contain florfenicol, pyrimethamine, estrone and 17β-estradiol at levels from 0.095 to 2.7 μg/kg.

  10. Optimization of matrix solid-phase dispersion for the rapid determination of salicylate and benzophenone-type UV absorbing substances in marketed fish.

    Science.gov (United States)

    Tsai, Dung-Ying; Chen, Chien-Liang; Ding, Wang-Hsien

    2014-07-01

    A simple and effective method for the rapid determination of five salicylate and benzophenone-type UV absorbing substances in marketed fish is described. The method involves the use of matrix solid-phase dispersion (MSPD) prior to their determination by on-line silylation gas chromatography tandem mass spectrometry (GC-MS/MS). The parameters that affect the extraction efficiency were optimized using a Box-Behnken design method. The optimal extraction conditions involved dispersing 0.5g of freeze-dried powdered fish with 1.0g of Florisil using a mortar and pestle. This blend was then transferred to a solid-phase extraction (SPE) cartridge containing 1.0g of octadecyl bonded silica (C18), as the clean-up co-sorbent. The target analytes were then eluted with 7mL of acetonitrile. The extract was derivatized on-line in the GC injection-port by reaction with a trimethylsilylating (TMS) reagent. The TMS-derivatives were then identified and quantitated by GC-MS/MS. The limits of quantitation (LOQs) were less than 0.1ng/g. Copyright © 2014 Elsevier Ltd. All rights reserved.

  11. Determination of Content and Related Substances of Tadalafil Tablets by HPLC%HPLC法测定他达拉非片含量和有关物质

    Institute of Scientific and Technical Information of China (English)

    郭兴辉

    2015-01-01

    Objective:To establish a determination method for the content and related substances of tadalafil tablets. Methods:An HPLC method was adopted. The determination was performed on a ZORBAX Eclipse XDB C8 (250 mm × 4. 6 mm,5μm) column with the mobile phase consisting of 0.1% trifluoroacetic acid-acetonitrile(65∶35)at a flow rate of 1.0 ml· min-1,the column temperature was controlled at 35℃, the detection wavelength was 285 nm and the injection volume was 20 μl. Results:The related substances could be completely separated from the maln component under the selected chromatographic conditions. A good linear relationship was found be-tween the peak area and the concentration of tadalafil within the range of 20. 13-201. 30μg·ml-1(r=0. 999 3) with the average recover-y of 99. 5% (RSD=1. 1%, n= 9). The limit of detection was 0. 6 ng and the limit of quantification was 2 ng. Conclusion:The method is specific and sensitive, and can be used in the determination of content and related substances of tadalafil tablets.%目的::建立他达拉非片含量测定及有关物质检查的方法。方法:采用高效液相色谱法。色谱柱:安捷伦ZORBAX E-clipse XDB C8(250 mm ×4.6 mm,5μm);流动相:0.1%三氟乙酸溶液-乙腈(65∶35);流速:1.0 ml·min-1;柱温:35℃;检测波长:285 nm,进样量20μl。结果:在选定的色谱条件下,主成分与各杂质峰分离度良好。他达拉非质量浓度在20.13~201.30μg ·ml-1范围内与峰面积有良好的线性关系(r=0.9993);平均回收率为99.5%(RSD=1.1%,n=9);检出限为0.6 ng,定量限为2 ng。结论:该方法专属性强、灵敏度高,可用于他达拉非片含量和有关物质测定。

  12. Radioactivity in food crops

    Energy Technology Data Exchange (ETDEWEB)

    Drury, J.S.; Baldauf, M.F.; Daniel, E.W.; Fore, C.S.; Uziel, M.S.

    1983-05-01

    Published levels of radioactivity in food crops from 21 countries and 4 island chains of Oceania are listed. The tabulation includes more than 3000 examples of 100 different crops. Data are arranged alphabetically by food crop and geographical origin. The sampling date, nuclide measured, mean radioactivity, range of radioactivities, sample basis, number of samples analyzed, and bibliographic citation are given for each entry, when available. Analyses were reported most frequently for /sup 137/Cs, /sup 40/K, /sup 90/Sr, /sup 226/Ra, /sup 228/Ra, plutonium, uranium, total alpha, and total beta, but a few authors also reported data for /sup 241/Am, /sup 7/Be, /sup 60/Co, /sup 55/Fe, /sup 3/H, /sup 131/I, /sup 54/Mn, /sup 95/Nb, /sup 210/Pb, /sup 210/Po, /sup 106/Ru, /sup 125/Sb, /sup 228/Th, /sup 232/Th, and /sup 95/Zr. Based on the reported data it appears that radioactivity from alpha emitters in food crops is usually low, on the order of 0.1 Bq.g/sup -1/ (wet weight) or less. Reported values of beta radiation in a given crop generally appear to be several orders of magnitude greater than those of alpha emitters. The most striking aspect of the data is the great range of radioactivity reported for a given nuclide in similar food crops with different geographical origins.

  13. Radioactivity measurement of radioactive contaminated soil by using a fiber-optic radiation sensor

    Science.gov (United States)

    Joo, Hanyoung; Kim, Rinah; Moon, Joo Hyun

    2016-06-01

    A fiber-optic radiation sensor (FORS) was developed to measure the gamma radiation from radioactive contaminated soil. The FORS was fabricated using an inorganic scintillator (Lu,Y)2SiO5:Ce (LYSO:Ce), a mixture of epoxy resin and hardener, aluminum foil, and a plastic optical fiber. Before its real application, the FORS was tested to determine if it performed adequately. The test result showed that the measurements by the FORS adequately followed the theoretically estimated values. Then, the FORS was applied to measure the gamma radiation from radioactive contaminated soil. For comparison, a commercial radiation detector was also applied to measure the same soil samples. The measurement data were analyzed by using a statistical parameter, the critical level to determine if net radioactivity statistically different from background was present in the soil sample. The analysis showed that the soil sample had radioactivity distinguishable from background.

  14. Determination of Related Substances in Levamisole Hydrochloride by HPLC%HPLC法测定盐酸左旋咪唑中有关物质

    Institute of Scientific and Technical Information of China (English)

    郭江红; 赵亚萍; 吴蔚

    2012-01-01

    Objective: To establish an HPLC method for the determination of the related substances in levamisole hydrochloride. Method: The column was Aichrombond C18( 250 mm ×4. 6 mm,5 μm ), the mobile phase consisted of 0. 5% ammonium dihydrogen phosphate ( adjusting pH to 6. 5 with triethylamine )-acetone( 70: 30 ) at the flow rate of 1. 0 ml · min-1 , the detection wavelength was 215 nm and the injection volume was 10 μl. Result: The linear range of 2,3-dihydrogen-6-phenylimidazol[ 2,1 - b ] thiazoli hydro-chloride was 1.11-11. 10 μg · ml-1(r = 0. 998 5 ), and the detection limit was 0. 6 ng. Conclusion: The method is specific and reproducible for the determination of the related substances in levamisole hydrochloride.%目的:建立高效液相色谱法测定盐酸左旋咪唑中的有关物质.方法:色谱柱为Aichrombond C18(250 mm×4.6 mm,5 μm);流动相为0.5%磷酸二氢铵(用三乙胺调节pH至6.5)-乙腈(70:30);流速为1.0 ml·min-1;检测波长为215 nm;进样量为10 μl.结果:有关物质各杂质峰与主峰之间分离良好,杂质2,3-二氢-6-苯基咪唑[2,1-b]噻唑盐酸盐的线性范围为1.11~11.10 μg·ml-1(r=0.998 5),最低检测限为0.6 ng.结论:该方法专属性强、重复性好,可用于盐酸左旋咪唑的有关物质测定.

  15. Determination of related substances in Glucosamine Hydrochloride Capsules%盐酸氨基葡萄糖胶囊有关物质测定方法研究

    Institute of Scientific and Technical Information of China (English)

    张德柱; 宋愿智; 沈登林

    2014-01-01

    Objective To establish an HPLC method for the determination of related substances in Glucosamine Hydrochloride Cap-sules .Methods The separation was performed on a C18 (250 mm × 4 .6 mm ,5 μm) column at room temperature .The mobile phase was a mixture of sodium 1-heptanesulfonate solution and acetonitrile at a flow-rate of 1 .0 mL · min-1 .The detection wave-length was at 195 nm .Results The Glucosamine Hydrochloride Capsules was stable with acid destruction ,but unstable with alka-li ,high temperature and strong oxidative destruction .The linear range was 6 .32-31 .60 μg · mL -1 .Conclusion This method is simple ,accurate ,and rapid with high specificity .It is applicable for the determination of related substances in Glucosamine Hydro-chloride Capsules .%目的:建立测定盐酸氨基葡萄糖胶囊有关物质的高效液相色谱方法。方法采用C18柱(250mm×4.6mm,5μm);以庚烷磺酸钠溶液(0.5g庚烷磺酸钠溶解在水中,加0.5mL磷酸,再加0.224g氢氧化钾,加水稀释至1000mL,摇匀)-乙腈(1000∶50)为流动相;流速1.0mL·min-1;检测波长:195nm;柱温:室温。结果盐酸氨基葡萄糖胶囊对酸稳定,对碱、高温、强氧化破坏不稳定,其线性范围为6.32~31.60μg·mL-1。结论此方法简便,准确,快速,专属性强,可用于该制剂的有关物质检查。

  16. 瑞格列奈片有关物质的HPLC测定%Determination of Related Substances in Repaglinide Tablets by HPLC

    Institute of Scientific and Technical Information of China (English)

    胡士现; 蒋成猛; 张华州

    2015-01-01

    Objective:To establish an HPLC method for the determination of related substances in Repaglinide Tablets.Methods:The separation was performed on an Agilent ZORBAX SB-Aq column(4.6 mm ×150 mm, 5 μm ) with phosphate buffer(4.0 g· L-1 po-tassium dihydrogen phosphate solution, adjusted to pH 3.2 with dilute phosphoric acid) as mobile phase A, mobile phase A-acetonitrile (30∶70) as mobile phase B, gradient elution fiow rate was 1.5 mL· min-1.The detection wavelength was 240 nm and the column temperature was 45 ℃.Results:The prominent peak was well separated from other impurities.Conclusion:The method is specific, accurate and reliable, It can be used to determine the related substances in Repaglinide Tablets.%目的:建立高效液相色谱法测定瑞格列奈片中有关物质的方法。方法:色谱柱为Agilent ZORBAX SB-Aq(4.6 mm ×150 mm,5μm),以磷酸盐缓冲液(取磷酸二氢钾4.0 g,加水1000 mL溶解后,用磷酸调节pH值至3.2)为流动相A,以流动相A-乙腈(30∶70)为流动相B,进行梯度洗脱;流量为1.5 mL· min-1,检测波长240 nm,柱温为45℃。结果:各相邻杂质峰之间、杂质峰与主峰之间能有效分离且物料平衡。结论:该方法专属性好,灵敏度高,结果准确,可用于瑞格列奈片有关物质的测定。

  17. RP-HPLC测定盐酸奈必洛尔含量和有关物质%RP-HPLC determination of nebivolol hydrochloride and its related substances

    Institute of Scientific and Technical Information of China (English)

    张士洋

    2012-01-01

    目的 建立反相高效液相色谱法测定盐酸奈必洛尔含量和有关物质.方法 采用的色谱柱为ODS色谱柱(250mm×4.6 mm,5 μm);以甲醇为溶剂,进样浓度:0.5 g·L-1,0.05 mol·的磷酸盐缓冲液(2%三乙胺,pH=3.5):乙腈:甲醇=200:115:40为流动相;检测波长为280 nm.结果 盐酸奈必洛尔峰与杂质峰分离良好,盐酸奈必洛尔浓度在31.71~158.55 mg·L-1与峰面积呈良好的线性关系(r=0.999 7),最低检检测限为5 ng.方法 精密度RSD为0.35%.结论 采用反相高效液相色谱法测定盐酸奈必洛尔含量及其有关物质方法 快速简便,结果 准确.也可用于该品制剂中有关物质和含量的测定.%Objective To establish an RP-HPLC method for the determination of content of nebivolol hydrochloride and its related substances in raw material. Methods An ODS column(250 mm × 4. 6 mm,5μm) was used with the mobile phase of 0. 05 mol · L-1 NaH2PO4 buffer solution(6.8 g potassium dihydrogen phosphate, and add water to 1 000 ml dissolving, and 2 ml triethylamine,adjusted pH to 3.5 with phosphoric acid)-acetonitrile-methanol (200:115:40) at a flow rate of 1.0 ml · min-1 and the detection wavelength of 280 run. Results The nebivolol hydrochloride and the related substances could be base line separated. The calibration curve was linear in the range of 31.71 ~ 158.55 mg · L-1 with r = 0.999 7. The detection limit was 5 ng. The precision( RSD) was 0. 35%. Conclusion The method is simple,accurate and rapid to operate and the results of the determination can be used for the quality control of nebivolol hydrochloride.

  18. Investigation of the complexation and the migration of actinides and non-radioactive substances with humic acids under geogenic conditions. Complexation of humic acids with actinides in the ocidation state IV Th, U, Np

    Energy Technology Data Exchange (ETDEWEB)

    Sachs, S.; Schmeide, K.; Brendler, V.; Krepelova, A.; Mibus, J.; Geipel, G.; Heise, K.H.; Bernhard, G.

    2004-03-01

    Objective of this project was the study of basic interaction and migration processes of actinides in the environment in presence of humic acids (HA). To obtain more basic knowledge on these interaction processes synthetic HA with specific functional properties as well as {sup 14}C-labeled HA were synthesized and applied in comparison to the natural HA Aldrich. One focus of the work was on the synthesis of HA with distinct redox functionalities. The obtained synthetic products that are characterized by significantly higher Fe(III) redox capacities than Aldrich HA were applied to study the redox properties of HA and the redox stability of U(VI) humate complexes. It was confirmed that phenolic OH groups play an important role for the redox properties of HA. However, the results indicate that there are also other processes than the single oxidation of phenolic OH groups and/or other functional groups contributing to the redox behavior of HA. A first direct-spectroscopic proof for the reduction of U(VI) by synthetic HA with distinct redox functionality was obtained. The complexation behavior of synthetic and natural HA with actinides (Th, Np, Pu) was studied. Structural parameters of Pu(III), Th(IV), Np(IV) and Np(V) humates were determined by X-ray absorption spectroscopy (XAS). The results show that carboxylate groups dominate the interaction between HA and actinide ions. These are predominant monodentately bound. The influence of phenolic OH groups on the Np(V) complexation by HA was studied with modified HA (blocked phenolic OH groups). The blocking of phenolic OH groups induces a decrease of the number of maximal available complexing sites of HA, whereas complex stability constant and Np(V) near-neighbor surrounding are not affected. The effects of HA on the sorption and migration behavior of actinides was studied in batch and column experiments. Th(IV) sorption onto quartz and Np(V) sorption onto granite and its mineral constituents are affected by the pH value

  19. Structure and dynamics of humic substances and model poly-electrolytes in solution; Structure et dynamique de substances humiques et polyelectrolytes modeles en solution

    Energy Technology Data Exchange (ETDEWEB)

    Roger, G.

    2010-09-15

    In the frame of a study about the feasibility of an underground storage of radioactive wastes, we focused on the role of degraded natural organic matter in the eventual transport of radionuclides in the environment. We are more interested by the determination of electro kinetic properties of these humic substances rather than the description of speciation reaction already widely discussed in the literature. We chose to determine the size and the charge of these humic substances thanks to an original method: high precision conductometry. This technique, associated to a suited transport theory, allows to describe the mobility of charged species in solution when taking into account the pairs interactions. We have participated in the development of this transport theory and we use it in order to determine the size and the charge of humic substances and a reference polyelectrolyte in different conditions of pH and ionic strength. All these experimental results obtained by conductometry were correlated with other experimental and theoretical methods: Atomic Force Microscopy, dynamic light scattering, laser zeta-metry and Monte-Carlo simulations. The obtained results confirm the generally admitted idea that humic substances are nano-metric entities having complexing properties towards cations and that can aggregate to form supra molecular structures. The effect of the ions present in the environment (sodium, calcium, magnesium) has been investigated. Finally the complexation of europium (which is considered as a good analogue of americium 241) has also been analysed by square wave voltammetry. (author)

  20. Trapping radioactive ions

    CERN Document Server

    Kluge, Heinz-Jürgen

    2004-01-01

    Trapping devices for atomic and nuclear physics experiments with radioactive ions are becoming more and more important at accelerator facilities. While about ten years ago only one online Penning trap experiment existed, namely ISOLTRAP at ISOLDE/CERN, meanwhile almost every radioactive beam facility has installed or plans an ion trap setup. This article gives an overview on ion traps in the operation, construction or planing phase which will be used for fundamental studies with short-lived radioactive nuclides such as mass spectrometry, laser spectroscopy and nuclear decay spectroscopy. In addition, this article summarizes the use of gas cells and radiofrequency quadrupole (Paul) traps at different facilities as a versatile tool for ion beam manipulation like retardation, cooling, bunching, and cleaning.

  1. Radioactivity of Consumer Products

    Science.gov (United States)

    Peterson, David; Jokisch, Derek; Fulmer, Philip

    2006-11-01

    A variety of consumer products and household items contain varying amounts of radioactivity. Examples of these items include: FiestaWare and similar glazed china, salt substitute, bananas, brazil nuts, lantern mantles, smoke detectors and depression glass. Many of these items contain natural sources of radioactivity such as Uranium, Thorium, Radium and Potassium. A few contain man-made sources like Americium. This presentation will detail the sources and relative radioactivity of these items (including demonstrations). Further, measurements of the isotopic ratios of Uranium-235 and Uranium-238 in several pieces of china will be compared to historical uses of natural and depleted Uranium. Finally, the presenters will discuss radiation safety as it pertains to the use of these items.

  2. Improved determination of the position and activity of a radioactive point source inside a bulky medium using several detectors. The special case of a lung counter-A general view

    Energy Technology Data Exchange (ETDEWEB)

    Pelled, Omer [NRC-Negev, P.O.Box 9001, Beer-Sheva 84190 (Israel); Bonardi, Mauro L. [Universita degli Studi and INFN-Milano, LASA, Radiochemistry Laboratory Via F.lli Cervi 201, 20090 Segrate, Milan (Italy); German, Uzi [NRC-Negev, P.O.Box 9001, Beer-Sheva 84190 (Israel); Groppi, Flavia [Universita degli Studi and INFN-Milano, LASA, Radiochemistry Laboratory Via F.lli Cervi 201, 20090 Segrate, Milan (Italy); Alfassi, Zeev B. [Department of Nuclear Engineering, Ben Gurion University, Beer Sheva 84105 (Israel)]. E-mail: alfassi@bgumail.bgu.ac.il

    2007-02-15

    A method is described to locate a radioactive point source in a lung using a commercial array of lung detectors. The method takes advantage of the fact that modern commercial systems consist of several Ge detectors, each connected to a multi-channel analyzer, and the information from each detector can be analyzed separately. The system is calibrated with point sources placed in various locations in the lungs of a phantom. A vector method is presented for determining which of the calibration locations in the phantom is closest to the location of the unknown point source. It has been shown that the accuracy of the method increases with increasing number of the vector dimensions. A higher dimensionality can be achieved by analyzing counts of several gamma lines or by using more detectors.

  3. Measurement and Monte Carlo Calculation of Waste Drum Filled With Radioactive Aqueous Solution

    Institute of Scientific and Technical Information of China (English)

    XU; Li-jun; ZHANG; Wei-dong; YE; Hong-sheng; LIN; Min; CHEN; Xi-lin; GUO; Xiao-qing

    2012-01-01

    <正>Theoretically the best calibrating source of gamma scan system (SGS) is a waste drum filled with uniform distribution of medium and radioactive nuclides. However, in reality, waste drums usually full of solid substance, which are difficult to be prepared in a completely uniformly distributed state. To reduce measurement uncertainty of the radioactivity of waste drums prepared using the method of shell source, a waste drum filled with radioactive aqueous solution was prepared. Besides, its radioactivity was measured by a SGS device and calculated using Monte Carlo method to verify the exact geometric model, which

  4. The Development and Validation of a Stability-Indicating UHPLC-DAD Method for Determination of Perindopril l-Arginine in Bulk Substance and Pharmaceutical Dosage Form.

    Science.gov (United States)

    Paczkowska, Magdalena; Zalewski, Przemysław; Garbacki, Piotr; Talaczyńska, Alicja; Krause, Anna; Cielecka-Piontek, Judyta

    2014-01-01

    A stability-indicating ultra-high-performance liquid chromatography (UHPLC) method with a diode array detector was developed and validated for the determination of cis/trans isomers of perindopril l-arginine in bulk substance and pharmaceutical dosage form. The separation was achieved on a Poroshell 120 Hilic (4.6 × 150 mm, 2.7 µm) column using a mobile phase composed of acetonitrile-0.1 % formic acid (20:80 v/v) at a flow rate of 1 mL min(-1). The injection volume was 5.0 µL and the wavelength of detection was controlled at 230 nm. The selectivity of the UHPLC-DAD method was confirmed by determining perindopril l-arginine in the presence of degradation products formed during acid-base hydrolysis and oxidation as well as degradation in the solid state, at an increased relative air humidity and in dry air. The method's linearity was investigated in the ranges 0.40-1.40 µg mL(-1) for isomer I and 0.40-2.40 µg mL(-1) for isomer II of perindopril l-arginine. The UHPLC-DAD method met the precision and accuracy criteria for the determination of the isomers of perindopril l-arginine. The limits of detection and quantitation were 0.1503 and 0.4555 µg mL(-1) for isomer I and 0.0356 and 0.1078 µg mL(-1) for isomer II, respectively.

  5. Radioactivity doubles up

    Science.gov (United States)

    Blank, Bertram

    2008-05-01

    More than a century after Henri Becquerel discovered radioactivity, there is still much that physicists do not understand about this spontaneous natural phenomenon. Through Becquerel's use of simple photographic plates to the sophisticated nuclear experiments carried out in today's laboratories, researchers have unearthed a total of nine different ways in which an atomic nucleus can decay. The most well known of these decay modes - alpha (α), beta (β) and gamma (γ) radioactivity - are widely used in applications ranging from medicine to archaeology; the others are much rarer.

  6. Simple and rapid method on High Performance Liquid Chromatography for simultaneous determination of benzylpenicillin potassium, streptomycin sulphate and related substances in Ascomicin – a veterinary use ointment

    Directory of Open Access Journals (Sweden)

    Neagu Maria

    2015-06-01

    Full Text Available A new simple, rapid, accurate and precise High – Performance Liquid Chromatography (HPLC method for determination of benzylpenicillin potassium and streptomycin sulphate in Ascomicin ointment was developed and validated. The method can be used for the detection and quantification of known and unknown impurities and degradation products in this pharmaceutical product during routine analysis and also for stability studies in view of its capability to separate degradation products. The method was validated for accuracy, precision, specificity, robustness and quantification limits according to ICH Guidelines. The estimation of benzylpenicillin potassium and streptomycin sulphate was done by Waters HPLC 2695. The chromatographic conditions comprised a reverse-phased C18 column (5 µm particle size, 250 mm×4.6 mm i.d. with a mobile phase consisting of a mixture of solution in water containing 0.025 M of sodium phosphate dibasic and 0.02 of sodium hexansulfonate adjusted to pH 6.0 with 22.5 g/lsolution of phosphoric acid and acetonitrile in gradient elution. The flow rate was 0.8 ml/min. Standard curves were linear over the concentration range of 5.00 µg/ml to 5.00 mg/ml for streptomycin sulphate and 3.26 µg/ml to 3.26 mg/ml for benzylpenicillin potassium. Statistical analyses proved the method was precise, reproducible, selective, specific and accurate for analysis of benzylpenicillin potassium, streptomycin sulphate and related substances.

  7. The determination of the absolute bioavailability for drug substances with long elimination half-lives (with PC-programs for the method of truncated areas).

    Science.gov (United States)

    Wijnand, H P

    1992-01-01

    A survey is given of the methods for the determination of the absolute bioavailability for drug substances with long elimination half-lives. All methods depend on the assumption of linear pharmacokinetics. Emphasis is laid on Urso and Aarons' regression method of truncated areas-under-the-curve (AUC) to obtain estimates of the absolute bioavailability, F, and the absorption rate constant, ka, without obeying the otherwise general rule of following blood or plasma levels for at least three times the terminal half-life. It is shown by simulation when the linear and when the logarithmic trapezoidal rule is to be used for the calculation of the AUC. Two PC-programs for the regression method of truncated areas are presented: one program (SIMF&KA.EXE) simulates, based on tentative pharmacokinetic parameters, whether a blood sampling scheme, together with the precision of the analytical assay, is adequate to obtain accurate and precise estimates of F and ka; the method is insensitive to large variations in the tentative value of the elimination half-life. The other program (ESTF&KA.EXE) provides estimates of F and ka, with standard deviations of the estimates, from empirical data.

  8. Psychotoxic Substances

    Science.gov (United States)

    1964-11-16

    began an in- tensive research for the clarification of the mechanism of the effect of psychotomimetic substances. In addition to the semi-synthetically...Dibenamine i.v. 200,000 ... 6oo,000 Ethyl ether p.o. 200,000 ... 400,000 Cocaine s.c. 80,000 ... 300,000 Mescaline p.o. 10,000 ... 20,000 Morphia s.c. 5,000...Autonomic functions Excitement, mood Pyramidal and extra- Meso-diencephalic changes: pyramidal effects: effects: Euphoria , depres- Ataxia, spastic

  9. Determination of related substances in Candesartan Cilexetil Tablets%HPLC法测定坎地沙坦酯片中有关物质

    Institute of Scientific and Technical Information of China (English)

    房思萌; 苏慕君; 臧可昕

    2014-01-01

    目的:分析对比多国药典改进HPLC法测定坎地沙坦酯及其片剂中有关物质的方法。方法采用HPLC法对坎地沙坦酯及其片剂中9个杂质进行测定。Waters Symmetry C18色谱柱(150 mm×4.6 mm,5μm);流动相:[乙腈-水-冰醋酸(57∶43∶1)]-[乙腈-水-冰醋酸(90∶10∶1)],梯度洗脱;体积流量:0.9 mL/min;柱温:35℃;样品仓温度:10℃;进样量:20μL;检测波长:254 nm。结果在选定的色谱条件下,坎地沙坦酯与有关物质分离良好。试验专属性、线性、耐用性良好。结论本研究可为坎地沙坦酯片的质量标准的制订和提高提供参考和依据。%Objective To optimize the HPLC method to determinate the related substances in candesartan cilexetil and its tablets compared with the national pharmacopoeias.Methods Nine impurities in Candesartan Cilexetil Tablets were separated and identified by HPLC. Chromatographic separation was carried out on an Waters Symmetry C18 column (150 mm × 4.6 mm, 5μm) at a flow rate of 0.9 mL/min. [Acetonitrile - water - acetic acid glacial (57∶43∶1)]-[acetonitrile - water - acetic acid glacial (90∶10∶1)] was used as mobile phase. It was monitored at a wavelength of 254 nm, the temperatures of column and sample chamber were 35 and 10℃, and the injection volume was 20μL..Results There was good separation among candesartan cilexetil and related substances under the chromatographic conditions. The method had good specificity, linearity, and durability.Conclusion It provides reference and basis to develop and improve the quality control of Candesartan Cilexetil Tablets.

  10. Determination of the Related Substances in Nimesulide Granules by HPLC%HPLC测定尼美舒利颗粒中的有关物质

    Institute of Scientific and Technical Information of China (English)

    高武

    2015-01-01

    Objective:To establish an HPLC method for the determination of the related substances in nimesulide granules. Meth-ods:An Agilent HC-C18(250 mm ×4.6 mm,5 μm)column was used, the mobile phase was composed of acetonitrile-0.01 mol ·L-1 ammonium dihydrogen phosphate (adjusting pH to 7. 0 with ammonia) (40:60) and the detection wavelength was 230 nm, the flow rate was 1. 0 ml·min-1 ,the column temperature was 30℃, and the injection volume was 20μl. Results:The linear range of nimesu-lide was 0. 10-0. 30 mg·ml-1(r=0. 999 9). Nimesulide and its related substances could be well separated with the peak separation degree above 2. 0. The limit of detection and the limit of quantification was 0. 3 ng and 1. 0 ng, respectively. Conclusion:The method is simple, accurate and reproducible, which can be used for the quality control of nimesulide granules.%目的:建立尼美舒利颗粒有关物质的HPLC测定方法.方法:采用Agilent HC-C18 (250 mm × 4. 6 mm,5 μm)色谱柱;流动相:乙腈-0. 01 mol·L-1磷酸二氢铵溶液(氨水调pH至7. 0) (40:60);检测波长:230 nm;流速:1. 0 ml·min-1;柱温:30℃;进样量:20 μl. 结果:尼美舒利在0.10~0.30 mg·ml-1(r=0.999 9)浓度范围内线性关系良好,各杂质峰与主峰分离度均大于2. 0,检测限为0. 3 ng,定量限为1. 0 ng. 结论:本方法专属性强,准确度高,重现性良好,可用于尼美舒利颗粒的质量控制.

  11. Rapid, sensitive and simultaneous determination of fluorescence-labeled designated substances controlled by the Pharmaceutical Affairs Law in Japan by ultra-performance liquid chromatography coupled with electrospray-ionization time-of-flight mass spectrometry.

    Science.gov (United States)

    Min, Jun Zhe; Hatanaka, Suguru; Toyo'oka, Toshimasa; Inagaki, Shinsuke; Kikura-Hanajiri, Ruri; Goda, Yukihiro

    2009-11-01

    A simultaneous determination method based on ultra-performance liquid chromatography (UPLC) with fluorescence (FL) detection and electrospray-ionization time-of-flight mass spectrometry (ESI-TOF-MS) was developed for 16 "designated substances" (Shitei-Yakubutsu) controlled by the Pharmaceutical Affairs Law in Japan. These substances were first labeled with 4-(N,N-dimethylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole at 60 degrees C for 2 h in 0.1 M borax (pH 9.3). The resulting fluorophores were well separated by reversed-phase chromatography using an Acquity UPLC BEH C(18) column (1.7 microm, 100 mm x 2.1 mm i.d.) by isocratic elution with a mixture of water and acetonitrile-methanol (20:80) containing 0.1% formic acid. The separated derivatives were sensitively detected by both FL and TOF-MS. However, the determination of several designated substances by FL detection showed interference from endogenous substances in biological samples. Therefore, the determination in real samples was carried out by a combination of UPLC separation and ESI-TOF-MS detection. The structures of the designated substances were identified from the protonated-molecular ions [M+H](+) obtained from the TOF-MS measurement. The calibration curves obtained from the peak area ratios of the internal standard (I.S.), i.e., 3-phenyl-1-propylamine, and the designated substances versus the injection amounts showed good linearity. The limits of detection (S/N = 3) and the limits of quantification (S/N = 10) in 0.1 mL of human plasma and urine for the present method were 0.30-150 pmol and 1.0-500 pmol, respectively. Good accuracy and precision (according to intraday and interday assays) were also obtained with the present procedure. This method was applied to analyses of human plasma, urine and real products.

  12. Disposal of radioactive waste

    Science.gov (United States)

    Van Dorp, Frits; Grogan, Helen; McCombie, Charles

    The aim of radioactive and non-radioactive waste management is to protect man and the environment from unacceptable risks. Protection criteria for both should therefore be based on similar considerations. From overall protection criteria, performance criteria for subsystems in waste management can be derived, for example for waste disposal. International developments in this field are summarized. A brief overview of radioactive waste sorts and disposal concepts is given. Currently being implemented are trench disposal and engineered near-surface facilities for low-level wastes. For low-and intermediate-level waste underground facilities are under construction. For high-level waste site selection and investigation is being carried out in several countries. In all countries with nuclear programmes, the predicted performance of waste disposal systems is being assessed in scenario and consequence analyses. The influences of variability and uncertainty of parameter values are increasingly being treated by probabilistic methods. Results of selected performance assessments show that radioactive waste disposal sites can be found and suitable repositories can be designed so that defined radioprotection limits are not exceeded.

  13. Radioactivity: A Natural Phenomenon.

    Science.gov (United States)

    Ronneau, C.

    1990-01-01

    Discussed is misinformation people have on the subject of radiation. The importance of comparing artificial source levels of radiation to natural levels is emphasized. Measurements of radioactivity, its consequences, and comparisons between the risks induced by radiation in the environment and from artificial sources are included. (KR)

  14. Viewer Makes Radioactivity "Visible"

    Science.gov (United States)

    Yin, L. I.

    1983-01-01

    Battery operated viewer demonstrates feasibility of generating threedimensional visible light simulations of objects that emit X-ray or gamma rays. Ray paths are traced for two pinhold positions to show location of reconstructed image. Images formed by pinholes are converted to intensified visible-light images. Applications range from radioactivity contamination surveys to monitoring radioisotope absorption in tumors.

  15. AIR RADIOACTIVITY MONITOR

    Science.gov (United States)

    Bradshaw, R.L.; Thomas, J.W.

    1961-04-11

    The monitor is designed to minimize undesirable background buildup. It consists of an elongated column containing peripheral electrodes in a central portion of the column, and conduits directing an axial flow of radioactively contaminated air through the center of the column and pure air through the annular portion of the column about the electrodes. (AEC)

  16. Radioactive Sources Service

    CERN Multimedia

    2007-01-01

    Please note that the radioactive sources service will be open by appointment only every Monday, Wednesday and Friday during CERN working hours (instead of alternate weeks). In addition, please note that our 2007 schedule is available on our web site: http://cern.ch/service-rp-sources

  17. Radioactive Sources Service

    CERN Multimedia

    2007-01-01

    Please note that the radioactive sources service will be open by appointment only every Monday, Wednesday and Friday during CERN working hours (instead of alternate weeks). In addition, please note that our 2007 schedule is available on our web site. http://cern.ch/service-rp-sources

  18. Determination of water and alkaline extractable atmospheric humic-like substances with the TU Vienna HULIS analyzer in samples from six background sites in Europe

    Science.gov (United States)

    Feczko, T.; Puxbaum, H.; Kasper-Giebl, A.; Handler, M.; Limbeck, A.; GelencséR, A.; Pio, C.; Preunkert, S.; Legrand, M.

    2007-12-01

    With a newly developed method based on the combination of two separation steps (by polarity and by acidity) with a universal detector for organic carbon, efficient isolation of humic-like substances (HULIS) from the matrix and quantitative determination of the isolated organic carbon is achieved. This new method was applied to determine the water extractable (HULISWS) and, in sequence, the 0.1 M NaOH alkaline extractable HULIS (HULISAS) fractions in aerosol from six sites situated at a transect from west to east across Europe. The sum of the two HULIS fractions is here defined as total HULIS (HULIST). The lowest 12-month average concentrations of HULIST ranged from 0.075 μgC/m3 the Azores (Portugal) to 1.7 μgC/m3 at the continental background site K-puszta (Hungary). On the continent, the HULIST concentration decreases exponentially with elevation. The relative amounts of water extractable and alkaline soluble HULIS were relatively similar at the six sites. Dramatic differences were observed for the seasonal variations of the HULIS fractions at the different sites. At the Azores, as well as at the higher mountain sites (1450 and 3100 m), a summer maximum of the HULIST concentration was observed, while at the continental low-level sites (Aveiro and K-puszta), winter maxima dominated the seasonal variation. The summer/winter ratio of the HULIST concentration varied from 7.1 at Sonnblick to 0.36 at Aveiro. The seasonal variation at the two continental lower-level sites with winter maxima might be explained by overlapping of a weaker summer source and a stronger winter source.

  19. [Determination of migration of 15 N-nitrosamines and N-nitrosatable substances from children's latex articles by gas chromatography-tandem mass spectrometry using solid phase extraction].

    Science.gov (United States)

    Li, Pi; Bai, Hua; Li, Haiyu; Chen, Ming; Lu, Qing; Zhang, Qing

    2014-01-01

    A method based on gas chromatography-tandem mass spectrometry (GC-MS/MS) using solid phase extraction (SPE) has been developed for the determination of 15 N-nitrosamines from children's latex articles. Artificial saliva was used as the migration solution to extract N-nitrosamines in children' s latex articles. And then a polar modified polystyrene-divinylbenzene copolymer (Chromabond Easy) was used for the selective SPE of the analytes in the migration solution. The analytes were then separated on an HP-5MS UI GC column and determined by MS/MS in multiple reaction monitoring mode for qualitative and quantitative analysis. Good linearity ranged from 5 microg/L to 2 000 microg/L was observed for all the compounds (R2 > 0.998) and the limits of quantification for the 15 N-nitrosamines were 0.625 - 12.50 microg/kg (S/N = 10), which were lower than the limits required by the EU 2009/48/EC Directive. The average recoveries of the target analytes at low, medium, and high spiked levels were in the ranges of 53.8% - 116.2%, 52.7% - 105.1% and 49.5% - 102.9%, respectively. The average within-day and between-day RSDs were from 1.3% to 14.0% (n = 6) and from 1.6% to 7.6% (n = 4), respectively. The proposed method was used to monitor N-nitrosamines in baby nipples and balloons, and N-nitrosamines were found in some samples. The total contents of the 15 N-nitrosamines in the analyzed nipples and balloons samples ranged from 0.049 9 mg/kg to 41.2 mg/kg. And the total contents of the N-nitrosatable substances in the analyzed samples ranged from 0.026 4 mg/kg to 12.5 mg/kg.

  20. Determination of radioactive materials in men. Applications and techniques, in the past and today; Bestimmung radioaktiver Stoffe im Menschen. Anwendungen und Technik, damals und heute

    Energy Technology Data Exchange (ETDEWEB)

    Gerstmann, U.C. [Bundesamt fuer Strahlenschutz (Germany). Fachbereich Strahlenschutz und Gesundheit

    2016-07-01

    The development of the two main applications of the determination of radionuclides in men - diagnostic nuclear medicine and incorporation monitoring since their beginnings are reviewed. Some less known applications are presented too.

  1. Public involvement in radioactive waste management decisions

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1994-04-01

    Current repository siting efforts focus on Yucca Mountain, Nevada, where DOE`s Office of Civilian Radioactive Waste Management (OCRWM) is conducting exploratory studies to determine if the site is suitable. The state of Nevada has resisted these efforts: it has denied permits, brought suit against DOE, and publicly denounced the federal government`s decision to study Yucca Mountain. The state`s opposition reflects public opinion in Nevada, and has considerably slowed DOE`s progress in studying the site. The Yucca Mountain controversy demonstrates the importance of understanding public attitudes and their potential influence as DOE develops a program to manage radioactive waste. The strength and nature of Nevada`s opposition -- its ability to thwart if not outright derail DOE`s activities -- indicate a need to develop alternative methods for making decisions that affect the public. This report analyzes public participation as a key component of this openness, one that provides a means of garnering acceptance of, or reducing public opposition to, DOE`s radioactive waste management activities, including facility siting and transportation. The first section, Public Perceptions: Attitudes, Trust, and Theory, reviews the risk-perception literature to identify how the public perceives the risks associated with radioactivity. DOE and the Public discusses DOE`s low level of credibility among the general public as the product, in part, of the department`s past actions. This section looks at the three components of the radioactive waste management program -- disposal, storage, and transportation -- and the different ways DOE has approached the problem of public confidence in each case. Midwestern Radioactive Waste Management Histories focuses on selected Midwestern facility-siting and transportation activities involving radioactive materials.

  2. Family Characteristics and Adolescent Substance Use.

    Science.gov (United States)

    Stephenson, Andy L.; And Others

    1996-01-01

    Study used self-report questionnaire data from high school students to determine the relation between adolescents' perception of family characteristics and adolescent substance use patterns. Results indicate adolescents' perception of maternal substance use, family hardiness, and age of the adolescent were significant predictors of substance use.…

  3. The radioactive fallout of Chernobylsk accident on the French territory; Les retombees radioactives de l'accident de Tchernobyl sur le territoire francais

    Energy Technology Data Exchange (ETDEWEB)

    Renaud, Ph.; Champion, D.; Brenot, J

    2008-07-01

    The twentieth anniversary of the Chernobylsk disaster was the opportunity, for the I.R.S.N., to to draw up a new assessment of radioactive fallout due to the accident on the French territory. This new publishing gives the knowledge and the most current interpretations on the radioactive substances transfer released by the accident, in grounds and in food. This inventory allows to explain the levels of radioactive contamination observed in France from 1986 till 2006, then to estimate the exposure of the French population at the fallout from the accident. The analysis of the Chernobylsk accident illustrates the multitude and the complexity of the contamination phenomena and radioactive substances transfer in the environment to the man.The book presents finally the lessons pulled by the disaster in terms of scientific knowledge and program development, of radiological surveillance and management of a nuclear crisis in France. (N.C.)

  4. Environmental Pathway Models-Ground-Water Modeling in Support of Remedial Decision Making at Sites Contaminated with Radioactive Material

    Science.gov (United States)

    The Joint Interagency Environmental Pathway Modeling Working Group wrote this report to promote appropriate and consistent use of mathematical environmental models in the remediation and restoration of sites contaminated by radioactive substances.

  5. Accumulation of radioactive cesium released from Fukushima Daiichi Nuclear Power Plant in terrestrial cyanobacteria Nostoc commune.

    Science.gov (United States)

    Sasaki, Hideaki; Shirato, Susumu; Tahara, Tomoya; Sato, Kenji; Takenaka, Hiroyuki

    2013-01-01

    The Fukushima Daiichi Nuclear Power Plant accident released large amounts of radioactive substances into the environment and contaminated the soil of Tohoku and Kanto districts in Japan. Removal of radioactive material from the environment is an urgent problem, and soil purification using plants is being considered. In this study, we investigated the ability of 12 seed plant species and a cyanobacterium to accumulate radioactive material. The plants did not accumulate radioactive material at high levels, but high accumulation was observed in the terrestrial cyanobacterium Nostoc commune. In Nihonmatsu City, Fukushima Prefecture, N. commune accumulated 415,000 Bq/kg dry weight (134)Cs and 607,000 Bq kg(-1) dry weight (137)Cs. The concentration of cesium in N. commune tended to be high in areas where soil radioactivity was high. A cultivation experiment confirmed that N. commune absorbed radioactive cesium from polluted soil. These data demonstrated that radiological absorption using N. commune might be suitable for decontaminating polluted soil.

  6. Proton Radioactivity Within a Hybrid Metho d

    Institute of Scientific and Technical Information of China (English)

    张鸿飞

    2016-01-01

    The proton radioactivity half-lives are investigated theoretically within a hybrid method. The potential barriers preventing the emission of protons are determined in the quasimolecular shape path within a generalized liquid drop model (GLDM). The penetrability is calculated with the Wentzel-Kramers-Brillouin (WKB) approximation. The spectroscopic factor has been taken into account in half-life calculation, which is obtained by employing the relativistic mean field (RMF) theory combined with the Bardeen-Cooper-Schrieffer (BCS) method. The half-lives within the present hybrid method repro-duced the experimental data very well. Some predictions for proton radioactivity are made for future experiments.

  7. HPLC法测定布洛芬钠有关物质%Determination of the related substances in ibuprofen sodium by HPLC

    Institute of Scientific and Technical Information of China (English)

    齐勇; 聂磊

    2014-01-01

    目的:采用高效液相色谱法测定布洛芬钠有关物质。方法仪器:高效液相色谱仪(紫外检测器);色谱柱:SuPelco discovery C18(4.0 mm ×150 mm,5μm);流动相:水(用H3 PO4调PH为2.5)-乙腈(66:34);检测波长:214 nm;柱温:(30±0.5)℃;流速:2 mL·min-1;进样体积:5μL。结果布洛芬钠主峰与杂质B主峰分离度为3.0,分离良好;布洛芬钠盐检测限为0.1006μg·mL-1,定量限为0.503μg·mL-1;杂质B检测限为0.06μg· mL-1,定量限为0.24μg·mL-1;精密度:样品杂质含量测试结果的RSD=0<2.0%。结论该方法灵敏、简单、准确,适用于布洛芬钠有关物质的测定。%Objective To establish an HPLC method for the determination of the related substances in ibuProfen sodi-um. Methods Instrument:HPLC(UV detector),column:SuPelco discovery C18(4. 0 mm × 150 mm,5 μm),mobile Phase:water(adjusted PH to 2. 5 with PhosPhoric acid)-acetonitrile(66:34),the detection wavelength was 214 nm,the column temPerature was(30 ± 0. 5)℃;The flow rate was 2 mL·min-1 and the inject volume was 5μL. Results The main Peak of ibuProfen sodium was seParated from imPurity B comPletely,the resolution was 3. 0;The limit of detection( LOD)of ibuProfen sodium was 0. 100 6μg·mL-1 ,and its limit of quantitation( LOQ)was 0. 503μg·mL-1;The LOD of imPurity B was 0. 06 μg·mL-1 ,and its LOQ was 0. 24 μg·mL-1;Precision:the RSD of test results of samPle imPurities was 0<2. 0%. Conclusion The method was highly selective,simPle and accurate,and was suitable for the determination of related substances in ibuProfen sodium.

  8. Development of In-situation radioactivity Inspection system

    Energy Technology Data Exchange (ETDEWEB)

    Min, Sujung; Lee, Sanghun; Kim, Miyoung; Kim, Myungjin; Lee, Unjang [ORIONENC Co., Seoul (Korea, Republic of); Park, Jungkyun [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2015-05-15

    Many Korean people worry about radioactive contamination of Japanese and Korean marine products. Radioactive contamination of processed foodstuffs, livestock, marine products, farm products imported from Japan and fishes caught in coastal waters of Korea has become an important social issue. Radioactivity inspections of those foods are executed manually with portable measuring instruments or at labs using their samples. In consequence, there are some problem of time delay and low reliability. To protect the health of citizens from radioactivity contained in Japanese marine products imported to Korea, a system to inspect radioactivity in real time will be developed. The system is to measure the radioactivity level of farm and marine products continuously and automatically at inspection sites of an agency checking radiation of imported foodstuffs to determine radioactive contamination. Product performance assessment and tests will be conducted later. When the system develops and its commercialization begins, people's anxiety about radioactive contamination of foods after the Fukushima nuclear accident will be eased and people will be able to trust the radioactive inspection.

  9. Stability indicating LC method for rapid determination of related substances of O-desmethyl venlafaxine in active pharmaceutical ingredients and pharmaceutical formulations.

    Science.gov (United States)

    Rao, Karri Visweswara; Reddy, Kesareddy Padmaja; Kumar, Yelavarthi Ravindra

    2014-01-01

    A simple, precise and accurate stability-indicating reversed phase-high performance liquid chromatography method was developed for the quantitative determination of O-desmethyl venlafaxine (ODV) and its related substances in active pharmaceutical ingredient and pharmaceutical formulation. The method was developed using YMC-pack ODS-A (150 × 4.6 mm, 3 μm) column with mobile phase containing a gradient mixture of solvents A and B. Solvent A contained a mixture of buffer and acetonitrile in the ratio of 85:15 (v/v). The buffer consisted of 10 mM potassium dihydrogen phosphate and 2 mM 1-octane sulfonic acid sodium salt (pH adjusted to 6.0 by using diluted potassium hydroxide solution). Solvent B contained a mixture of water and acetonitrile in the ratio of 20:80 (v/v). The eluted compounds were monitored at 230 nm. ODV and its six impurities were well separated within 14 min run time. It was subjected under the stress conditions of oxidative, acid, base, water, thermal and photolytic degradation. It was sensitive towards acidic, basic, oxidative and water stress conditions, stable in photolytic and thermal degradation conditions. The degradation products were well resolved from main peak and its impurities, the mass balance in each case was >99.0%, proving the stability-indicating power of the method. The developed method was validated as per International Conference on Harmonization (ICH) guidelines with respect to its specificity, linearity (correlation coefficient >0.9996), limit of detection, limit of quantification, accuracy (recovery range 97.1-103.2%), precision (% relative standard deviation ≤1.9%) and robustness.

  10. 纺织品中易挥发土腥霉味组分分析%Determination of Odorous Substances in Textile

    Institute of Scientific and Technical Information of China (English)

    李竹英; 韦顺文; 王正林

    2011-01-01

    Analysis of 2-isopropyl-3-methoxypyrazine,2-methylisoborneol and geosmin in textile by HS/GC/MS,and the effect of heat time and temperature on the recovery were investigated.The result showed that the limit of detection for 2-isopropyl-3-methoxypyrazine,2-methylisoborneol and geosmin were 0.01 mg/kg,0.005 mg/kg and 0.003 mg/kg,respectively,the recoveries were 81%,95% and 84%,respectively and relative deviation was less than 7%.This method for determination of odorous substances in textile was simple,quickly and reliable,with satisfactory result.%采用直接顶空进样气相色谱-质谱法测定纺织品中二甲萘烷醇(GSM)、2-异丁基-3-甲氧基吡嗪(IBMP)和2-甲基异茨醇(M IB)异味物质,考察了顶空加热时间、温度等因素对异味化合物回收率的影响,结果表明:2-异丁基-3-甲氧基吡嗪、2-甲基异茨醇和二甲萘烷醇检出限分别为0.01 mg/kg、0.005 mg/kg、0.003 mg/kg。加标回收率依次为在81%、95%、84%,相对标准偏差均小于7%,该测试方法简单、快捷、可靠,结果令人满意。

  11. Radioactive waste management; Gerencia de rejeitos radioativos

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2013-11-15

    This eighth chapter presents the radioactive wastes and waste disposal; classification of radioactive wastes; basis requests of the radioactive waste management; conditions for a radioactive waste disposal; registers and inventories; transport of radioactive wastes from a facility to another and the radioactive waste management plan.

  12. Handbook of radioactivity analysis

    CERN Document Server

    2012-01-01

    The updated and much expanded Third Edition of the "Handbook of Radioactivity Analysis" is an authoritative reference providing the principles, practical techniques, and procedures for the accurate measurement of radioactivity from the very low levels encountered in the environment to higher levels measured in radioisotope research, clinical laboratories, biological sciences, radionuclide standardization, nuclear medicine, nuclear power, fuel cycle facilities and in the implementation of nuclear forensic analysis and nuclear safeguards. The Third Edition contains seven new chapters providing a reference text much broader in scope than the previous Second Edition, and all of the other chapters have been updated and expanded many with new authors. The book describes the basic principles of radiation detection and measurement, the preparation of samples from a wide variety of matrices, assists the investigator or technician in the selection and use of appropriate radiation detectors, and presents state-of-the-ar...

  13. White sea radioactivity assessment

    Energy Technology Data Exchange (ETDEWEB)

    Aliev, R.A. [Lomonosov Moscow State Univ. (Russian Federation). Skobeltsyn Inst. of Nuclear Physics]|[Lomonosov Moscow State Univ. (Russian Federation). Chemistry Dept.]|[Russian Academy of Sciences, Moscow (Russian Federation). Shirshov Inst. of Oceanology; Kalmykov, S.N.; Lisitzin, A.P. [Lomonosov Moscow State Univ. (Russian Federation). Chemistry Dept.

    2004-07-01

    The aim of the present work is to estimate potential sources and chronology of pollution of the White Sea (Russia) by artificial radionuclides. White Sea is semi-closed water body connected with Barents Sea by a narrow strait. Thus, pollution of White Sea may be caused by highly polluted Barents waters and river (mainly Northern Dvina) run-off. This is the first detailed investigation of radioactivity of White Sea sediment records. (orig.)

  14. Impact of the Fukushima Daiichi Nuclear Power Plant accident on hemodialysis facilities: an evaluation of radioactive contaminants in water used for hemodialysis.

    Science.gov (United States)

    Kamei, Daigo; Kuno, Tsutomu; Sato, Sumihiko; Nitta, Kosaku; Akiba, Takashi

    2012-02-01

    Following the crisis at the Fukushima Daiichi Nuclear Power Plant caused by the 2011 Tohoku earthquake and tsunami, radioactive substances ((131) I, (134) Cs, (137) Cs) were detected in tap water throughout eastern Japan. There is now concern that internal exposure to radioactive substances in the dialysate could pose a danger to hemodialysis patients. Radioactive substances were measured in three hemodialysis facilities before and after purification of tap water for use in hemodialysis. Radioactive iodine was detected at levels between 13 and 15 Bq/kg in tap water from the three facilities, but was not detected by reverse osmosis membrane at any of the facilities. We confirmed that the amount of radioactive substances in dialysate fell below the limit of detection (7-8 Bq/kg) by reverse osmosis membrane. It is now necessary to clarify the maximum safe level of radiation in dialysate for chronic hemodialysis patients.

  15. Radioactive waste storage issues

    Energy Technology Data Exchange (ETDEWEB)

    Kunz, Daniel E. [Colorado Christian Univ., Lakewood, CO (United States)

    1994-08-15

    In the United States we generate greater than 500 million tons of toxic waste per year which pose a threat to human health and the environment. Some of the most toxic of these wastes are those that are radioactively contaminated. This thesis explores the need for permanent disposal facilities to isolate radioactive waste materials that are being stored temporarily, and therefore potentially unsafely, at generating facilities. Because of current controversies involving the interstate transfer of toxic waste, more states are restricting the flow of wastes into - their borders with the resultant outcome of requiring the management (storage and disposal) of wastes generated solely within a state`s boundary to remain there. The purpose of this project is to study nuclear waste storage issues and public perceptions of this important matter. Temporary storage at generating facilities is a cause for safety concerns and underscores, the need for the opening of permanent disposal sites. Political controversies and public concern are forcing states to look within their own borders to find solutions to this difficult problem. Permanent disposal or retrievable storage for radioactive waste may become a necessity in the near future in Colorado. Suitable areas that could support - a nuclear storage/disposal site need to be explored to make certain the health, safety and environment of our citizens now, and that of future generations, will be protected.

  16. A kinematic-based methodology for radiological protection: Runoff analysis to calculate the effective dose for internal exposure caused by ingestion of radioactive isotopes

    Science.gov (United States)

    Sasaki, Syota; Yamada, Tadashi; Yamada, Tomohito J.

    2014-05-01

    We aim to propose a kinematic-based methodology similar with runoff analysis for readily understandable radiological protection. A merit of this methodology is to produce sufficiently accurate effective doses by basic analysis. The great earthquake attacked the north-east area in Japan on March 11, 2011. The system of electrical facilities to control Fukushima Daiichi nuclear power plant was completely destroyed by the following tsunamis. From the damaged reactor containment vessels, an amount of radioactive isotopes had leaked and been diffused in the vicinity of the plant. Radiological internal exposure caused by ingestion of food containing radioactive isotopes has become an issue of great interest to the public, and has caused excessive anxiety because of a deficiency of fundamental knowledge concerning radioactivity. Concentrations of radioactivity in the human body and internal exposure have been studied extensively. Previous radiologic studies, for example, studies by International Commission on Radiological Protection(ICRP), employ a large-scale computational simulation including actual mechanism of metabolism in the human body. While computational simulation is a standard method for calculating exposure doses among radiology specialists, these methods, although exact, are too difficult for non-specialists to grasp the whole image owing to the sophistication. In this study, the human body is treated as a vessel. The number of radioactive atoms in the human body can be described by an equation of continuity, which is the only governing equation. Half-life, the period of time required for the amount of a substance decreases by half, is only parameter to calculate the number of radioactive isotopes in the human body. Half-life depends only on the kinds of nuclides, there are no arbitrary parameters. It is known that the number of radioactive isotopes decrease exponentially by radioactive decay (physical outflow). It is also known that radioactive isotopes

  17. Natural radioactivity in petroleum residues

    Energy Technology Data Exchange (ETDEWEB)

    Gazineu, M.H.P. [UNICAP, Dept. de Quimica, Recife (Brazil); Gazineu, M.H.P.; Hazin, C.A. [UFPE, Dept. de Energia Nuclear, Recife (Brazil); Hazin, C.A. [Centro Regional de Ciencias Nucleares/ CNEN, Recife (Brazil)

    2006-07-01

    The oil extraction and production industry generates several types of solid and liquid wastes. Scales, sludge and water are typical residues that can be found in such facilities and that can be contaminated with Naturally Occurring Radioactive Material (N.O.R.M.). As a result of oil processing, the natural radionuclides can be concentrated in such residues, forming the so called Technologically Enhanced Naturally Occurring Radioactive Material, or T.E.N.O.R.M.. Most of the radionuclides that appear in oil and gas streams belong to the {sup 238}U and {sup 232}Th natural series, besides 40 K. The present work was developed to determine the radionuclide content of scales and sludge generated during oil extraction and production operations. Emphasis was given to the quantification of {sup 226}Ra, {sup 228}Ra and 40 K since these radionuclides,are responsible for most of the external exposure in such facilities. Samples were taken from the P.E.T.R.O.B.R.A.S. unity in the State of Sergipe, in Northeastern Brazil. They were collected directly from the inner surface of water pipes and storage tanks, or from barrels stored in the waste storage area of the E and P unit. The activity concentrations for {sup 226}Ra, {sup 228}Ra and 40 K were determined by using an HP Ge gamma spectrometric system. The results showed concentrations ranging from 42.7 to 2,110.0 kBq/kg for {sup 226}Ra, 40.5 to 1,550.0 kBq/kg for {sup 228}Ra, and 20.6 to 186.6 kBq/kg for 40 K. The results highlight the importance of determining the activity concentration of those radionuclides in oil residues before deciding whether they should be stored or discarded to the environment. (authors)

  18. MONITORING OF RADIOACTIVITY AT DNURT CAMPUS

    Directory of Open Access Journals (Sweden)

    L. F. Dolina

    2016-06-01

    Full Text Available Purpose. The research paper aims to determine radioactive contamination on the territory of campus of Dnipropetrovsk National University of Railway Transport named after Academician V. Lazaryan (DNURT. Methodology. The dosimeters measured the radioactive contamination in different places (points of DNURT campus, focusing on public places. The centres of measurements became dormitories, monuments, stops, main entrances of the new and the old buildings, classrooms, basements, a swimming pool, boiler room and others. Findings. The conducted radiation monitoring for the first time in the history of the University discovered the source of radioactive contamination on DNURT territory and campus. The highest radiation background is observed on three points, namely: the pedestal of the monument, the monument to students-soldiers, the main entrance of the new building (columns. This can be explained by granite materials, which the pedestals and the stairs are made of. Originality. The largest contribution to the total value of annual effective dose of human exposure is made by ionizing radiation sources (IRS of building materials (65 - 70%. The radioactivity level of building materials is determined by the content of natural radionuclides that are included in uranium-radium and thorium decay series (18 and 12 radionuclides as well as potassium-40. Radioactivity of building materials is evaluated by the content of dominant radionuclides radium-226, thorium-232 and potassium-40. Their dominant role is explained by the fact that these long-lived high-energy - emitters are the products of decay of radium-226 in uranium series of and radium-224 in thorium series, exposing radioactive gases (radon-222 and radon-220. Radioactive gases are accumulated in the basements of educational buildings; their decay is accompanied by 100% alpha radiation, which is the most dangerous. Practical value. It is necessary to set radioactivity signs near the objects with high

  19. Substance Identification Information from EPA's Substance Registry

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Substance Registry Services (SRS) is the authoritative resource for basic information about substances of interest to the U.S. EPA and its state and tribal...

  20. The Radium Terrors. Science Fiction and Radioactivity before the Bomb.

    Science.gov (United States)

    Candela, Andrea

    2015-01-01

    At the beginning of the 20th century the collective imagination was fascinated and terrified by the discovery of radium. A scientific imagery sprang up around radioactivity and was disseminated by public lectures and newspaper articles discussing the ambiguous power of this strange substance. It was claimed that radium could be used to treat cholera, typhus and tuberculosis, but at the same time there were warnings that it could be used for military purposes. The media and the scientists themselves employed a rich vocabulary influenced by religion, alchemy and magic. The ambivalent power of radioactive elements exerted a great influence on science fiction novelists. This paper will examine some significant works published in Europe, America and Russia during the first decades of the 20th century and their role in the creation of the complex imagery of radioactivity that seized the public imagination long before the invention of the atomic bomb.

  1. Assessments of natural radioactivity and determination of heavy metals in soil around industrial dumpsites in Sango-Ota, Ogun state, Nigeria

    Directory of Open Access Journals (Sweden)

    Augustine Kolapo Ademola

    2014-01-01

    Full Text Available The activity concentration of natural radionuclides in soil samples from industrial dumpsites in Sango-Ota were determined using gamma-ray spectrometry with NaI(Tl detector. The mean activity concentration of 226 Ra, 232 Th and 40 K was 3.0 ± 1.2, 33.3 ± 9.8 and 122.1 ± 20.6 Bqkg−1 , respectively. Radium equivalent activities were calculated to assess the hazards arising from the use of the soil sample in agriculture. All the calculated values were lower than the world average. The mean concentration of heavy metals in the soil samples were 33.6, 2.9, 3.8, 2.7, 48.9, 1,5, 34.5 and 0.8 mg l -1 for Cu, Mg, Ca, P, Fe, Pb, Zn and Cd, respectively. The concentrations of Cd, Cu and Pb were higher than the natural permissible range in soil. Therefore, the government should discourage the use of the soil around dumpsites for planting because of the presence of heavy metals in the sites.

  2. Environmental Radioactivity Study in Surface Sediments of Guacanayabo Gulf (Cuba)

    Science.gov (United States)

    Reyes, H.; López-Pino, N.; Rizo, O. Díaz; Bernal, J. L.; D'Alessandro, K.; Padilla, F.; Corrales, Y.; Casanova, O. A.; Gelen, A.; Martínez, Y.; Aguilar, J.; Arado, J. O.; Maidana, N. L.

    2009-06-01

    Sediment samples have been collected in the Guacanayabo gulf located in the southeast Cuba, to determinate the radioactivity levels of 210Pb, 234Th, 214Pb, 137Cs, 232Th and 40K using Low-Background Gamma Spectrometry and to evaluate its impact in the habitat of important marine species for fishery industry. The obtained results show the lowest radioactivity levels determined in Cuban marine environments. The species capture declination in the last years is not originated by radioactive pollution of the zone.

  3. Determination of the Content Related Substances of Mesna Injection%美司钠注射液有关物质及其含量测定

    Institute of Scientific and Technical Information of China (English)

    周征; 章燕

    2012-01-01

    目的 建立测定美司钠注射液有关物质及其含量的高效液相色谱法.方法 采用CAPCELL PAK C18柱(4.6 mm×250 mm,5μm),流动相为甲醇-磷酸盐缓冲液(磷酸二氢钾、磷酸氢二钾各2.94g,四丁基硫酸氢铵2.6g,溶于水660 mL,用磷酸调节pH至2.3)(35:65),流速1.0 mL·min-1,检测波长235 nm.结果 美司钠和双硫化合物的线性范围分别为0.002~7.4(r=1.000 0)和0.003 ~0.300 mg·mL-1(r=1.000 0);平均加样回收率分别为99.8%(RSD=0.6%)和99.8% (RSD=0.7%).结论 该方法操作简便,专属性强,定量准确,可用于该制剂的质量控制.%Objective To establish a method for determining content and related substances of mesna injection by HPLC. Methods A CAPCELL PAK C18(4.6 mm×250 mm,5 μm) column was used with methanol-phosphate buffered solution(2. 94 g of potassium dihydrogen phosphate,2. 94 g of dipotassium hydrogen phosphate and 2.6 g of tetrabutylammonium hydrogen sulfale dissolved in about 660 mL water:pH adjusted to 2.3 with phosphoric acid) (35 : 65) as mobile phase. The flow rale was 1.0 mL·min-1 and the detection wavelength was at 235 nm. Results The linear ranges of mesna and dimlsna were within 0.002-7.4 mg·mL-1 (r= 1. 000 0)and 0.003-0.300 mg ·mL-1(r = 1. 000 0),respectively. The average recoveries of mesna and dimlsna were 99. 8% (RSD=0.6% )and 99. 8% ( RSD = 0.1% ) (n=6) .respectively. Conclusion The method is simple,reliable,accurate and can be applied to the quality control of the preparation.

  4. The radioactive equilibrium and determination methods for ratio e Ra/U; Desequilibrio Radiactivos-1. Metodo {sub {beta}}-{gamma}. Determinacion de la razon eRa/U. Valoracion del contenido en U{sub 3}O{sub 8}

    Energy Technology Data Exchange (ETDEWEB)

    Mingarro, E.

    1966-07-01

    The main problems concerning the radioactive non-equilibrium on minerals and a simultaneous counting procedure for {beta}- and {gamma}- activities developed to solve those problems, are described. (Author)

  5. Determining the isotopic compositions of uranium and fission products in radioactive environmental microsamples using laser ablation ICP-MS with multiple ion counters.

    Science.gov (United States)

    Boulyga, Sergei F; Prohaska, Thomas

    2008-01-01

    This paper presents the application of a multicollector inductively coupled plasma mass spectrometer (MC-ICP-MS)--a Nu Plasma HR--equipped with three ion-counting multipliers and coupled to a laser ablation system (LA) for the rapid and sensitive determination of the 235U/238U, 236U/238U, 145Nd/143Nd, 146Nd/143Nd, 101Ru/(99Ru+99Tc) and 102Ru/(99Ru+99Tc) isotope ratios in microsamples collected in the vicinity of Chernobyl. Microsamples with dimensions ranging from a hundred mum to about 1 mm and with surface alpha activities of 3-38 mBq were first identified using nuclear track radiography. U, Nd and Ru isotope systems were then measured sequentially for the same microsample by LA-MC-ICP-MS. The application of a zoom ion optic for aligning the ion beams into the ion counters allows fast switching between different isotope systems, which enables all of the abovementioned isotope ratios to be measured for the same microsample within a total analysis time of 15-20 min (excluding MC-ICP-MS optimization and calibration). The 101Ru/(99Ru+99Tc) and 102Ru/(99Ru+99Tc) isotope ratios were measured for four microsamples and were found to be significantly lower than the natural ratios, indicating that the microsamples were contaminated with the corresponding fission products (Ru and Tc). A slight depletion in 146Nd of about 3-5% was observed in the contaminated samples, but the Nd isotopic ratios measured in the contaminated samples coincided with natural isotopic composition within the measurement uncertainty, as most of the Nd in the analyzed samples originates from the natural soil load of this element. The 235U/238U and 236U/238U isotope ratios were the most sensitive indicators of irradiated uranium. The present work yielded a significant variation in uranium isotope ratios in microsamples, in contrast with previously published results from the bulk analysis of contaminated samples originating from the vicinity of Chernobyl. Thus, the 235U/238U ratios measured in ten

  6. Determining the isotopic compositions of uranium and fission products in radioactive environmental microsamples using laser ablation ICP-MS with multiple ion counters

    Energy Technology Data Exchange (ETDEWEB)

    Boulyga, Sergei F.; Prohaska, Thomas [University of Natural Resources and Applied Life Sciences, Department of Chemistry, Division of Analytical Chemistry-VIRIS Laboratory, Vienna (Austria)

    2008-01-15

    This paper presents the application of a multicollector inductively coupled plasma mass spectrometer (MC-ICP-MS) - a Nu Plasma HR - equipped with three ion-counting multipliers and coupled to a laser ablation system (LA) for the rapid and sensitive determination of the {sup 235}U/{sup 238}U, {sup 236}U/{sup 238}U, {sup 145}Nd/{sup 143}Nd, {sup 146}Nd/{sup 143}Nd, {sup 101}Ru/({sup 99}Ru+{sup 99}Tc) and {sup 102}Ru/({sup 99}Ru+{sup 99}Tc) isotope ratios in microsamples collected in the vicinity of Chernobyl. Microsamples with dimensions ranging from a hundred {mu}m to about 1 mm and with surface alpha activities of 3-38 mBq were first identified using nuclear track radiography. U, Nd and Ru isotope systems were then measured sequentially for the same microsample by LA-MC-ICP-MS. The application of a zoom ion optic for aligning the ion beams into the ion counters allows fast switching between different isotope systems, which enables all of the abovementioned isotope ratios to be measured for the same microsample within a total analysis time of 15-20 min (excluding MC-ICP-MS optimization and calibration). The {sup 101}Ru/({sup 99}Ru+{sup 99}Tc) and {sup 102}Ru/({sup 99}Ru+{sup 99}Tc) isotope ratios were measured for four microsamples and were found to be significantly lower than the natural ratios, indicating that the microsamples were contaminated with the corresponding fission products (Ru and Tc). A slight depletion in {sup 146}Nd of about 3-5% was observed in the contaminated samples, but the Nd isotopic ratios measured in the contaminated samples coincided with natural isotopic composition within the measurement uncertainty, as most of the Nd in the analyzed samples originates from the natural soil load of this element. The {sup 235}U/{sup 238}U and {sup 236}U/{sup 238}U isotope ratios were the most sensitive indicators of irradiated uranium. The present work yielded a significant variation in uranium isotope ratios in microsamples, in contrast with previously

  7. Radioactive Materials Analytical Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Laing, W.R.; Corbin, L.T.

    1979-01-01

    The Radioactive Materials Analytical Laboratory was completed 15 years ago and has been used since as an analytical chemistry support lab for reactor, fuel development, and reprocessing programs. Additions have been made to the building on two occasions, and a third addition is planned for the future. Major maintenance items include replacement of ZnBr/sub 2/ windows, cleanup of lead glass windows, and servicing of the intercell conveyor. An upgrading program, now in progress, includes construction of new hot-cell instrumentation and the installation of new equipment such as an x-ray fluorescence analyzer and a spark source mass spectrometer.

  8. 5He radioactivity

    OpenAIRE

    Poenaru, D.N.; Ivaşcu, M.

    1984-01-01

    The disintegration of a metastable nuclear state by emission of a light particle can be considered to be a very asymmetric fission process. An approximation of the potential barrier in the overlapping region of the two fragments leads to an analytic relationship for the life-time, allowing us to handle a large number of cases to search for new kinds of radioactivities. In this way, it is predicted that some nuclei with Z = 83-92, N = 127-137 and 97-105,145-157 are able to decay spontaneously ...

  9. Radioactive isotope uptake in a grass-legume association

    Energy Technology Data Exchange (ETDEWEB)

    Douka, C.E.; Xenoulis, A.C. (National Centre for Scientific Research, Demokritos (Greece))

    1991-01-01

    The radioactive uptake of Medicago sativa and Rye grass in a pasture exposed to the fallout from the Chernobyl reactor accident, was determined in four consecutive harvests covering a period of one year after the accident. In plants of Medicago sativa, inoculated with an effective Rhizobia meliloti strain isolated from Greek soils, a high degree of biological nitrogen fixation was observed at all harvests using N-15 techniques. At the second and third harvests, the percentage nitrogen derived from fixation (%NdfF), the percentage nitrogen derived from soil (%NdfS), as well as the radioactive uptake from the soil remained stable. At the fourth harvest, however, the %NdfF decreased while the %NdfS and the radioactive uptake from soil significantly increased. At the first harvest the radioactivity in both plants, caused mainly by direct fallout contamination, was considerably higher than that observed at the later harvests. Medicago sativa contained significantly less radioactivity than the grass at all harvests, although both plants were grown under the same environmental conditions. Even at the fourth harvest, almost one year after the initial contamination, the radioactivity of grass remained at high levels (20 Bq g{sup -1} of protein) while in Medicago sativa it assumed considerably lower values (3.6 Bq g{sup -1} of protein). A possible involvement of biological nitrogen fixation in the reduction of radioactive uptake is discussed. Finally, certain practical conclusions are drawn with respect to a safer management of pastures exposed to radioactivity. (author).

  10. What factors determine Belgian general practitioners' approaches to detecting and managing substance abuse? A qualitative study based on the I-Change Model.

    Science.gov (United States)

    Ketterer, Frederic; Symons, Linda; Lambrechts, Marie-Claire; Mairiaux, Philippe; Godderis, Lode; Peremans, Lieve; Remmen, Roy; Vanmeerbeek, Marc

    2014-06-14

    General practitioners (GPs) are considered to play a major role in detecting and managing substance abuse. However, little is known about how or why they decide to manage it. This study investigated the factors that influence GP behaviours with regard to the abuse of alcohol, illegal drugs, hypnotics, and tranquilisers among working Belgians. Twenty Belgian GPs were interviewed. De Vries' Integrated Change Model was used to guide the interviews and qualitative data analyses. GPs perceived higher levels of substance abuse in urban locations and among lower socioeconomic groups. Guidelines, if they existed, were primarily used in Flanders. Specific training was unevenly applied but considered useful. GPs who accepted abuse management cited strong interpersonal skills and available multidisciplinary networks as facilitators.GPs relied on their clinical common sense to detect abuse or initiate management. Specific patients' situations and their social, psychological, or professional dysfunctions were cited as cues to action.GPs were strongly influenced by their personal representations of abuse, which included the balance between their professional responsibilities toward their patients and the patients' responsibilities in managing their own health as well the GPs' abilities to cope with unsatisfying patient outcomes without reaching professional exhaustion. GPs perceived substance abuse along a continuum ranging from a chronic disease (whose management was part of their responsibility) to a moral failing of untrustworthy people. Alcohol and cannabis were more socially acceptable than other drugs. Personal experiences of emotional burdens (including those regarding substance abuse) increased feelings of empathy or rejection toward patients.Multidisciplinary practices and professional experiences were cited as important factors with regard to engaging GPs in substance abuse management. Time constraints and personal investments were cited as important barriers

  11. Radioactivity a very short introduction

    CERN Document Server

    Tuniz, Claudio

    2012-01-01

    Radioactivity: A Very Short Introduction explains radioactivity and discusses its fundamental role in nature. Radioactivity remains misunderstood and feared perhaps because nuclear radiation cannot be detected by human senses, and can undoubtedly do great harm if appropriate precautions are not taken. Radioactivity in the stars and in the Earth and its wide range of applications in biomedicine, science, industry, agriculture are described, as well as the mechanisms of nuclear fission and fusion, and the harnessing of nuclear power. The issues surrounding safety and security and the increasing concerns about nuclear terrorism are also considered.

  12. Determination of 9-Deoxo-9a-Aza-9a-Homoerythromycin A and Related Substances by High-Performance Liquid Chromatography

    Institute of Scientific and Technical Information of China (English)

    SHI Ying; YAO Guo-wei; OU Yu-xiang; MA Min

    2005-01-01

    A high-performance liquid chromatography(HPLC) method was developed and validated for the assay of 9-deoxo-9a-aza-9a-homoerythromycin A and related substances that might coexist in products as impurities that originate from the synthesis processes. A chromatographic system comprising an ODS 150 mm ×4.6 mm I.D. column, a mobile phase of cetonitrile monobasic potassium phosphate buffer (25/75), a flow rate of 1.2 mL/min, a temperature of 30 ℃ and a UV detector set at 205 nm has shown good chromatographic separation for 9-deoxo-9a-aza-9a-homoerythromycin A and other related substances. The linearity of the calibration curves, the precision, expressed as relative standard deviations, of the HPLC method have been studied. The HPLC method under study was found to be specific, precise, accurate and reproducible, indicating stability.

  13. Some observations indicating a low brain uptake of (/sup 3/H)Nle/sup 11/-Substance P

    Energy Technology Data Exchange (ETDEWEB)

    Landgraf, R.; Klauschenz, E.; Bienert, M.; Ermisch, A.; Oehme, P. (Akademie der Wissenschaften der DDR, Berlin. Inst. fuer Wirkstofforschung; Karl-Marx-Universitaet, Leipzig (German Democratic Republic). Sektion Biowissenschaften; Deutsche Hochschule fuer Koerperkultur, Leipzig (German Democratic Republic))

    1983-02-01

    The studies concerning the problem of whether an exogenous neuropeptide is able to enter the brain tissue were extended to the undecapeptide Substance P (SP). The amount of radioactivity 15 s after intracarotid injection of (/sup 3/H)Nle/sup 11/-SP or (/sup 14/C)inulin was determined in 18 brain regions and the anterior pituitary of male rats. As compared to the reference (/sup 14/C)inulin, the amount of radioactivity was higher after (/sup 3/H)Nle/sup 11/-SP injection (0.233 +- 0.039%, p < 0.001). Statistically significant differences could be found particularly in cortical and caudal areas as well as in the circumventricular organs studied. These observations do not refute the assumption that a low brain uptake of the labelled neuropeptide occurred due to an accumulation within structures of the blood-brain barrier and/or a penetration of the barrier system.

  14. Laser photodetachment of radioactive 128I‑

    Science.gov (United States)

    Rothe, Sebastian; Sundberg, Julia; Welander, Jakob; Chrysalidis, Katerina; Day Goodacre, Thomas; Fedosseev, Valentin; Fiotakis, Spyridon; Forstner, Oliver; Heinke, Reinhard; Johnston, Karl; Kron, Tobias; Köster, Ulli; Liu, Yuan; Marsh, Bruce; Ringvall-Moberg, Annie; Rossel, Ralf Erik; Seiffert, Christoph; Studer, Dominik; Wendt, Klaus; Hanstorp, Dag

    2017-10-01

    The first experimental investigation of the electron affinity (EA) of a radioactive isotope has been conducted at the CERN-ISOLDE radioactive ion beam facility. The EA of the radioactive iodine isotope 128I (t 1/2 = 25 min) was determined to be 3.059 052(38) eV. The experiment was conducted using the newly developed Gothenburg ANion Detector for Affinity measurements by Laser PHotodetachment (GANDALPH) apparatus, connected to a CERN-ISOLDE experimental beamline. 128I was produced in fission induced by 1.4 GeV protons striking a thorium/tantalum foil target and then extracted as singly charged negative ions at a beam energy of 20 keV. Laser photodetachment of the fast ion beam was performed in a collinear geometry inside the GANDALPH chamber. Neutral atoms produced in the photodetachment process were detected by allowing them to impinge on a glass surface, creating secondary electrons which were then detected using a channel electron multiplier. The photon energy of the laser was tuned across the threshold of the photodetachment process and the detachment threshold data were fitted to a Wigner law function in order to extract the EA. This first successful demonstration of photodetachment at an isotope separator on line facility opens up the opportunity for future studies of the fundamental properties of negatively charged radioactive isotopes such as the EA of astatine and polonium.

  15. Preliminary Estimation of Radioactive Cesium Concentration due to Hypothetical Accident in East Sea

    Energy Technology Data Exchange (ETDEWEB)

    Min, Byung-Il; Kim, Sora; Park, Kihyun; Suh, Kyung-suk [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2015-10-15

    The sea has no large islands, bays or capes. Its water balance is mostly determined by the inflow (Korea Strait) and outflow (Tsugaru Strait and Soya Strait) through the straits connecting it to the neighboring seas and Pacific Ocean. All of the Korean nuclear power plants are located in the coastal area, 3 sites in the east coast and 1 site in the west coast. So the Korean nuclear power plants there may be possibility that such dangerous substances spread out of the East Sea. The East Sea is a fertile fishing ground for surrounding counties. The environmental radionuclides concentration estimation is important for fish and sea plants may be contaminated by those radioactive materials. In order to simplify the problem, the experiment has been considered the many simplifying assumptions. The bed sediments are uniform over all the model domain, using the monthly mean ocean current data set and ignored effect of the facilities for damage preventions.

  16. 缩宫素注射液的有关物质研究%HPLC determination of oxytocin injection and its related substances

    Institute of Scientific and Technical Information of China (English)

    黄青; 陆益红; 史清水; 金卫红; 汪玉馨; 张玫

    2011-01-01

    Objective: A selective gradient liquid chromatographic method for the determination of oxytocin and its related substances has been developed and applied to analyze 178 batches of commercial oxytocin injection samples. Methods: An Agilent ZORBAX SB - C18 column (250 mm ×4. 6 mm,5 μm) was used for the gradient elution. The mobile phases consisted of 0. 1 mol · L-1 dihydrogen phosphate solution (adjust to pH 6. 0) - acetonitrile (50:50). The flow rate was 1. 0 mL · min-1. UV detection was performed at 220 nm,and the column temperature was set to 40 t. Results; Oxytocin and its related substances were successfully detected by the established method. The method showed good resolution and linearity between peak area and oxytocin concentration at the range of 0. 36 -23. 04 IU · mL-1 with r =0. 9999. The average recoveries (n =9) was 99. 1%. In 178 batchs of commercial oxytocin injection samples,the total content of impurity range from 25. 9% to 36. 0% ,the largest content of single impurity range from 6. 1% to 13. 0% . Conclusion: The method is proved to be specific, sensitive and accurately and could be used to control the quality of oxytocin injection. Furthermore, the method proved to be successful when applied to analyze 178 batches of commercial oxytocin injection samples. The research suggests that the existing standards is in deficiencies, and need to be improved immediately by using more proprietary methods such as HPLC to control and check the quality of drugs. Most of the impurities in the oxytocin injections are related to the raw materials and the raw materials produced by solid - phase peptide synthesis method should be used by guiding the enterprises.%目的:针对缩宫素注射液现行标准中未对注射液中有关物质进行控制的情况,建立了缩宫素注射液有关物质的HPLC测定法,并对2010年国家评价性抽验中178批缩宫素注射液样品进行了测定.方法:采用Agilent ZORBAX SB -C18色谱柱(250 mm×4.6 mm,5

  17. Age determination of meteorites using radioactive nuclides

    Energy Technology Data Exchange (ETDEWEB)

    Tanimizu, Masaharu [Tokyo Institute of Technology, Graduate School of Science and Engineering, Department of Earth and Planetary Sciences, Tokyo (Japan)

    2002-07-01

    Recently, the precise isotope ratios of some refractory elements in meteorites have been reported using inductively coupled plasma mass spectrometry. The in situ decay of {sup 182}Hf (T{sub 1/2}=9 Myr), which was produced at the latest nucleosynthesis, is recognized in many meteorites as isotopic anomalies of its daughter isotope, {sup 182}W. The degrees of relative {sup 182}W isotopic deviation in extra-terrestrial and terrestrial silicate samples vary from +0.3% to {+-}0% related to the size of their parent bodies. One ready interpretation of its correlation is the difference in timing of metal-silicate separation in the parent bodies. Between the earth and meteorite parent bodies, the difference is calculated to be about four times of the half-life of {sup 182}Hf, equivalent to 36 Myr. (author)

  18. [The history of radioactivity and its applications in hygiene and therapy].

    Science.gov (United States)

    Corrao, Carmela Romana Natalina; Serarcangeli, Carla

    2011-01-01

    Since Antiquity, the observation of matter and its composition has been fascinating for the human mind. It represented the core of philosophical studies since the atomistic theory by Leucippus and Democritus, as well as of the opposed theory of elements by Empedocles, Plato and Aristoteles. Research on the atom, on its spontaneous or artificial disgregation, on the practical application of radioactive substances has strongly influenced daily life and the development of knowledge. Products containing radioactive substances have been used, often without regulation or control, in many scientific fields, as well as in medicine and cosmetics.

  19. Radioactivity in the Baltic Sea, 1999-2006 HELCOM thematic assessment

    Energy Technology Data Exchange (ETDEWEB)

    Herrmann, J.; Ikaeheimonen, T.K.; Ilus, E.; Kanisch, G.; Luning, M.; Mattila, J.; Nielsen, S.P.; Osvath, I.; Outola, I.

    2009-07-01

    The report describes work carried out by HELCOM's (Helsinki Commission, Baltic Marine Environment Commission) project on the Monitoring of Radioactive Substances in the Baltic Sea (MORS-PRO) during the period 1999-2006. The main topics include: sources of man-made radioactivity in the Baltic Sea; levels of man-made radionuclides in seawater, sediments and biota; work on modelling and evaluations of the riks to man caused by radioactivity in the Baltic Sea; comparison of man-made radionuclides in the Baltic Sea with levels in other sea regions. The concequent recommendations and work on data quality are presented in the Appendix

  20. Determination of L-Carnosine and Its Related Substances by HPLC%高效液相色谱法测定L-肌肽原料药的含量及其有关物质

    Institute of Scientific and Technical Information of China (English)

    韩木南; 陈晓辉; 其其格; 纪晓影; 毕开顺

    2009-01-01

    目的 建立HPLC测定L-帆肽原料药的含量并进行有关物质检查.方法 采用Kromasil NH2色谱柱(4.6 mm×200 mm,5μm),流动相为乙腈-40 mmol·L-1磷酸氢二钾溶液(44:56,磷酸调pH 6.3),流速1.0 mL·min-1,检测波长为210 nm,柱温35℃.结果 L-肌肽在9.93~99.3 mg·L-1内线性关系良好(r=-0.999 8),平均回收率为100.5%(RSD=1.0%),检测限为1 ng(S/N=3).L-肌肽与有关物质分离良好.结论 该方法操作简便、重复性好,专属性强,可用作L-肌肽原料药的含量测定和有关物质检查.%OBJECTIVE To establish a HPLC method for determining the content of L-camosine and its related substances. METHODS The determination of L-carnosine and the separation of its related substances was performed on a Kromasil NH2 average recovery was 100.5% with RSD of 1.0%. The related substances of L-carnosine were completely separated from L-carnosine. The limit of detection (LOD) was 1 ng (S/N=3) . CONCLUSION A reproducible and specific method is provided for thedetermination of L-carnosine and its related substances.

  1. Contra-expertise on determination of radioactivity of waste water and ventilation air of Urenco Nederland B.V. Period 2011; Contra-expertise op bepalingen van radioactiviteit van afvalwater en ventilatielucht van Urenco Nederland BV. Periode 2011

    Energy Technology Data Exchange (ETDEWEB)

    Kwakman, P.J.M.; Overwater, R.M.W.

    2012-08-15

    Within the framework of a monitoring programme, RIVM measures the release of radioactivity into the waste water and atmosphere of the Urenco uranium enrichment plant in Almelo, Netherlands. Measurements are carried out eight times per year. This form of counter-expertise is aimed at verifying and supporting the reliability of the analyses carried out by the Urenco plant. As a rule, the waste water contains very low levels of gross alpha and gross beta activity. The two different sets of measurements of gross alpha and gross beta in waste water are generally in agreement, as is also the case in 2011. Radioactivity levels in the ventilation air are very close to those levels expected due to the natural presence of radon in the outside atmosphere. For gross alpha 0,007 - 0,13 mBq.m{sup -3} was found and for gross beta 0,026 - 0,5 mBq.m{sup -3}. The agreement with the measurement results of Urenco was mostly good. Taking into account the natural gross-beta activity, and the ratio gross alpha / gross beta it is possible that at SP4 in two cases a small release of uranium may have occurred. The RIVM determined the gross alpha and gross beta activity in eight waste water samples and 40 samples of ventilation air. The samples were taken by Urenco at time points dispersed throughout 2011. This procedure provides the RIVM with a method for determining the release of artificial alpha emitters into the environment. The analyses were carried out on behalf of the Department of Nuclear Safety, Security and Safeguards of the Human Environment and Transport Inspectorate from the Ministry of Infrastructure and Environment [Dutch] Het RIVM controleert achtmaal per jaar de metingen van de verrijkingsfabriek Urenco te Almelo. Het gaat hierbij om lozingen van radioactiviteit in water en lucht. De contra-expertise onderbouwt de betrouwbaarheid van de analyses die Urenco uitvoert. Uit de metingen blijkt dat er in het afvalwater doorgaans een (zeer) lage totaal {alpha} en totaal {beta

  2. Radioactivity, radionuclides, radiation

    CERN Document Server

    Magill, Joseph

    2005-01-01

    RADIOACTIVITY – RADIONUCLIDES – RADIATION is suitable for a general audience interested in topical environmental and human health radiological issues such as radiation exposure in aircraft, food sterilisation, nuclear medicine, radon gas, radiation dispersion devices ("dirty bombs")… It leads the interested reader through the three Rs of nuclear science, to the forefront of research and developments in the field. The book is also suitable for students and professionals in the related disciplines of nuclear and radiochemistry, health physics, environmental sciences, nuclear and astrophysics. Recent developments in the areas of exotic decay modes (bound beta decay of ‘bare’ or fully ionized nuclei), laser transmutation, nuclear forensics, radiation hormesis and the LNT hypothesis are covered. Atomic mass data for over 3000 nuclides from the most recent (2003) evaluation are included.

  3. Radioactive waste: show time?

    Energy Technology Data Exchange (ETDEWEB)

    Verhoef, E.V. [COVRA N.V., Spanjeweg 1, 4455 TW Nieuwdorp (Netherlands); McCombie, Charles; Chapman, Neil [Arius Association, Taefernstrasse 1, CH-4050 Baden (Switzerland)

    2010-07-01

    The basic concept within both EC funded SAPIERR I and SAPIERR II projects (FP6) is that of one or more geological repositories developed in collaboration by two or more European countries to accept spent nuclear fuel, vitrified high-level waste and other long-lived radioactive waste from those partner countries. The SAPIERR II project (Strategic Action Plan for Implementation of Regional European Repositories) examines in detail issues that directly influence the practicability and acceptability of such facilities. This paper describes the work in the SAPIERR II project (2006-2008) on the development of a possible practical implementation strategy for shared, regional repositories in Europe and lays out the first steps in implementing that strategy. (authors)

  4. Standardization of {sup 32}P radioactive solution

    Energy Technology Data Exchange (ETDEWEB)

    Marques, Caio Pinheiros; Koskinas, Marina Fallone; Almeida, Jamille da Silveira; Yamazaki, Ione M.; Dias, Mauro da Silva, E-mail: cpmarques@usp.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2016-07-01

    The standardization of {sup 32}P radioactive solution using three different methods is presented. The disintegration rate was determined by the CIEMAT/NIST and TDCR methods in liquid scintillator systems and self-absorption extrapolation method using 4π(PC)-β system. The results obtained for the activity of the {sup 32}P solution were compared and they agree within the experimental uncertainties. (author)

  5. Airborne Chernobyl radioactivity in College Park, Maryland

    Energy Technology Data Exchange (ETDEWEB)

    Kitto, M.E. (Dept. of Chemistry, Univ. of Maryland, College Park, MD (USA) New York State Dept. of Health, Wadsworth Center for Laboratories and Research, Albany, NY (USA)); Faller, S.H. (Dept. of Chemistry, Univ. of Maryland, College Park, MD (USA) Environmental Monitoring Systems Lab., U.S. Environmental Protection Agency, Las Vegas, NV (USA)); Anderson, D.L. (Dept. of Chemistry, Univ. of Maryland, College Park, MD (USA) Food and Drug Administration Lab., National Inst. of Standards and Technology, Gaithersburg, MD (USA)); McCarthy, L.E. (Dept. of Chemistry, Univ. of Maryland, College Park, MD (USA) Gerghty and Miller, Inc., Plainview, NY (USA))

    1991-01-01

    Atmospheric concentrations of Chernobyl-derived radionuclides collected on filters in College Park, Maryland during May, 1986 have been determined by gamma-ray analysis. Measurements indicate that following an extensive wash-out of radioactivity, {sup 103}Ru was enriched in the upper atmosphere relative to {sup 137}Cs and {sup 131}I. Absolute concentrations of particulate and gas-phase radionuclides and the observed enrichment of {sup 103}Ru are in agreement with other studies. (orig.).

  6. Arduino based radioactive tracking system

    Science.gov (United States)

    Rahman, Nur Aira Abd; Rashid, Mohd Fazlie Bin Abdul; Rahman, Anwar Bin Abdul; Ramlan, Atikah

    2017-01-01

    There is a clear need to strengthen security measures to prevent any malevolent use or accidental misuse of radioactive sources. Some of these radioactive sources are regularly transported outside of office or laboratory premises for work and consultation purposes. This paper present the initial development of radioactive source tracking system, which combined Arduino microcontroller, Global Positioning System (GPS) and Global System for Mobile communication (GSM) technologies. The tracking system will help the owner to monitor the movement of the radioactive sources. Currently, the system is capable of tracking the movement of radioactive source through the GPS satellite signals. The GPS co-ordinate could either be transmitted to headquarters at fixed interval via Short Messaging Service (SMS) to enable real time monitoring, or stored in a memory card for offline monitoring and data logging.

  7. Introduction to Astronomy with Radioactivity

    CERN Document Server

    Diehl, Roland

    2010-01-01

    In the late nineteenth century, Antoine Henri Becquerel discovered radioactivity and thus the physics of weak interactions, well before atomic and quantum physics was known. The different types of radioactive decay, alpha, beta, and gamma decay, all are different types of interactions causing the same, spontaneous, and time-independent decay of an unstable nucleus into another and more stable nucleus. Nuclear reactions in cosmic sites re-arrange the basic constituents of atomic nuclei (neutrons and protons) among the different configurations which are allowed by Nature, thus producing radioactive isotopes as a by-product. Throughout cosmic history, such reactions occur in different sites, and lead to rearrangements of the relative abundances of cosmic nuclei, a process called cosmic chemical evolution, which can be studied through the observations of radioactivity. The special role of radioactivity in such studies is contributed by the intrinsic decay of such material after it has been produced in cosmic site...

  8. PERSPECTIVE: Fireworks and radioactivity

    Science.gov (United States)

    Breitenecker, Katharina

    2009-09-01

    both reaction products and unburnt constituents of a pyrotechnic mixture. One major environmental concern in pyrotechnics focuses on the emission of heavy metals. This is the topic discussed in the article by Georg Steinhauser and Andreas Musilek in this issue [4]. A possible interrelationship between respiratory effects and fireworks emissions of barium-rich aerosols was also raised last year [5]. In recent years the potential hazard of naturally occurring radioactive material has become of importance to the scientific community. Naturally occurring radionuclides can be of terrestrial or cosmological origin. Terrestrial radionuclides were present in the presolar cloud that later contracted in order to build our solar system. These radionuclides—mainly heavy metals—and their non-radioactive isotopes are nowadays fixed in the matrix of the Earth's structure. Usually, their percentage is quite small compared to their respective stable isotopes—though there are exceptions like in the case of radium. The problem with environmental pollution due to naturally occurring radioactive material begins when this material is concentrated due to mining and milling, and later further processed [6]. Environmental pollution due to radioactive material goes back as far as the Copper and Iron Ages, when the first mines were erected in order to mine ores (gold, silver, copper, iron, etc), resulting in naturally occurring radioactive material being set free with other dusts into the atmosphere. So where is the link between pyrotechnics and radioactivity? In this article presented by Georg Steinhauser and Andreas Musilek [4], the pyrotechnic ingredients barium nitrate and strontium nitrate are explored with respect to their chemical similarities to radium. The fundamental question, therefore, was whether radium can be processed together with barium and strontium. If so, the production and ignition of these pyrotechnic ingredients could cause atmospheric pollution with radium aerosols

  9. Accelerated radioactive beams from REX-ISOLDE

    Energy Technology Data Exchange (ETDEWEB)

    Kester, O. E-mail: oliver.kester@physik.uni-muenchen.de; Sieber, T.; Emhofer, S.; Ames, F.; Reisinger, K.; Reiter, P.; Thirolf, P.G.; Lutter, R.; Habs, D.; Wolf, B.H.; Huber, G.; Schmidt, P.; Ostrowski, A.N.; Hahn, R. von; Repnow, R.; Fitting, J.; Lauer, M.; Scheit, H.; Schwalm, D.; Podlech, H.; Schempp, A.; Ratzinger, U.; Forstner, O.; Wenander, F.; Cederkaell, J.; Nilsson, T.; Lindroos, M.; Fynbo, H.; Franchoo, S.; Bergmann, U.; Oinonen, M.; Aeystoe, J.; Den Bergh, P. Van; Duppen, P. Van; Huyse, M.; Warr, N.; Weisshaar, D.; Eberth, J.; Jonson, B.; Nyman, G.; Pantea, M.; Simon, H.; Shrieder, G.; Richter, A.; Tengblad, O.; Davinson, T.; Woods, P.J.; Bollen, G.; Weissmann, L.; Liljeby, L.; Rensfelt, K.G

    2003-05-01

    In 2001 the linear accelerator of the Radioactive beam EXperiment (REX-ISOLDE) delivered for the first time accelerated radioactive ion beams, at a beam energy of 2 MeV/u. REX-ISOLDE uses the method of charge-state breeding, in order to enhance the charge state of the ions before injection into the LINAC. Radioactive singly-charged ions from the on-line mass separator ISOLDE are first accumulated in a Penning trap, then charge bred to an A/q<4.5 in an electron beam ion source (EBIS) and finally accelerated in a LINAC from 5 keV/u to energies between 0.8 and 2.2 MeV/u. Dedicated measurements with REXTRAP, the transfer line and the EBIS have been carried out in conjunction with the first commissioning of the accelerator. Thus the properties of the different elements could be determined for further optimization of the system. In two test beam times in 2001 stable and radioactive Na isotopes ({sup 23}Na-{sup 26}Na) have been accelerated and transmitted to a preliminary target station. There {sup 58}Ni- and {sup 9}Be- and {sup 2}H-targets have been used to study exited states via Coulomb excitation and neutron transfer reactions. One MINIBALL triple cluster detector was used together with a double sided silicon strip detector to detect scattered particles in coincidence with {gamma}-rays. The aim was to study the operation of the detector under realistic conditions with {gamma}-background from the {beta}-decay of the radioactive ions and from the cavities. Recently for efficient detection eight tripple Ge-detectors of MINIBALL and a double sided silicon strip detector have been installed. We will present the first results obtained in the commissioning experiments and will give an overview of realistic beam parameters for future experiments to be started in the spring 2002.

  10. Count rate balance method of measuring sediment transport of sand beds by radioactive tracers; Methode du bilan des taux de comptage d'indicateurs radioactifs pour la determination du debit de charriage des lits sableux

    Energy Technology Data Exchange (ETDEWEB)

    Sauzay, G. [Commissariat a l' Energie Atomique, 91 - Saclay (France). Centre d' Etudes Nucleaires

    1967-11-01

    Radioactive tracers are applied to the direct measurement of the sediment transport rate of sand beds. The theoretical measurement formula is derived: the variation of the count rate balance is inverse of that of the transport thickness. Simultaneously the representativeness of the tracer is critically studied. The minimum quantity of tracer which has to be injected in order to obtain a correct statistical definition of count rate given by a low number of grains 'seen' by the detector is then studied. A field experiment was made and has let to study the technological conditions for applying this method: only the treatment of results is new, the experiment itself is carried out with conventional techniques applied with great care. (author) [French] Les indicateurs radioactifs sont appliques a la mesure directe du debit de charriage des lits sableux. On etablit la formule theorique de mesure: le bilan des taux de comptage varie en sens inverse de l'epaisseur de charriage. Parallelement on fait une etude critique de la representativite de l'indicateur, puis on determine la quantite minimale de traceur qu'il faut immerger pour que les taux de comptage fournis pour un faible nombre de grains 'vus' par le detecteur aient une definition statistique correcte. Une experience de terrain a permis d'etudier les conditions technologiques de cette methode: seul le depouillement des resultats est nouveau. L'experimentation in-situ se fait suivant les procedes classiques avec un tres grand soin. (auteur)

  11. Analysis of {sup 14}CO{sub 2} trapped {sup 14}C Sorbent, and {sup 14}C and {sup 3}H Radioactivity Determination in Resins and Oils from Nuclear Power Plants Using a Combustion Method

    Energy Technology Data Exchange (ETDEWEB)

    Ko, Young Gun; Kim, Chang Jong; Choi, Geun Sik; Chung, Kun Ho; Kang, Mun Ja [KAERI, Daejeon (Korea, Republic of)

    2016-05-15

    Tritium ({sup 3}H, T) generated in the heavy water and C fourteen ({sup 14}C) originated from the graphite moderator or structural materials of the nuclear power plant can cause acute and/or chronic harmful effects by inhalation and ingestion of these radionuclides owing to their binding affinity toward biomolecules and gas phase. {sup 3}H and {sup 14}C radioactivity in ion exchange resins and oils from nuclear power plants were determined by an oxidation (combustion) method. The 0.1 M HNO{sub 3} solution and the {sup 14}C sorbent trapped the {sub 3}H and {sup 14}C respectively in the gas from the combustion of samples. All samples were burned without ash in the combustion system. The reaction of CO{sub 2} and {sup 14}C sorbent was investigated by FT-IR analysis. The study demonstrated the different reaction mechanism according to the CO{sub 2} concentration. In the FT-IR study, it is clearly confirmed that CO{sub 2} from the burned 1 g of sample can be trapped in the {sup 14}C sorbent completely. During the reaction of CO{sub 2} and {sup 14}C sorbent, the temperature and the viscosity of {sup 14}C sorbent increased due to the decrease of enthalpy change and the bonding between each molecules of the sorbent. We expect that our FT-IR study could motivate the development of {sup 14}C sorbent and confirm the {sup 14}C trapping performance of the {sup 14}C sorbent.

  12. Progress on Radioactive Waste Treatment Facilities Construction

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    In 2011, five projects were undertaken by radioactive waste projects management department, which are "Cold Commissioning of the Pilot Project on Radioactive Waste Retrieval and Conditioning (abbreviation 'Pilot Project')", "Radioactive Ventilation Project Construction (abbreviation 'Ventilation

  13. Development and validation of a capillary electrophoresis method for determination of enantiomeric purity and related substances of esomeprazole in raw material and pellets.

    Science.gov (United States)

    Estevez, Pablo; Flor, Sabrina; Boscolo, Oriana; Tripodi, Valeria; Lucangioli, Silvia

    2014-03-01

    A capillary electrophoresis method using CDs for quality control of esomeprazole (ESO) in terms of enantiomeric purity and related substances in raw material and pellets was developed. ESO is the S-enantiomer of omeprazole (OMZ). Several parameters were evaluated, including type and concentration of buffer and CD, concentration of additives and electrolyte pH. Resolution between the enantiomers of OMZ obtained for each parameter tested was calculated and the presence of the main related substance such as OMZ sulfone was carefully monitored. The optimized system consisted of 100 mM Tris-phosphate buffer pH 2.5 with 20 mM 2-hydroxypropyl-β-CD, 1 mM sodium dithionite, temperature at 15°C, voltage at 28 kV, and UV detection at 301 nm. Once optimized, the electrophoretic system was validated according to ICH guidelines. The limits of detection and quantification for R-OMZ were 0.6 μg/mL (0.06% w/w of ESO) and 2.0 μg/mL (0.2% w/w of ESO), respectively. A mean concentration of R-OMZ pellet samples of ESO. No other impurities were found in the samples under these conditions. Therefore, the developed method was found to be appropriate not only for enantiomeric quality control of ESO but also for the analysis of ESO and the main related substance in raw material and pharmaceutical formulations as well as for stability indicating studies.

  14. Radioactive particles in the 234-5 Building ventilation exhaust

    Energy Technology Data Exchange (ETDEWEB)

    Postma, A.K.; Schwendiman, L.C.

    1959-07-13

    The 234-5 Building ventilation exhaust is continuously sampled for the purpose of estimating the amount of radioactive (alpha emitting) material discharged to the atmosphere. Although a record is kept of the gross amount of radioactive material discharged, few data are available concerning the size and kind of active particles in the exhaust air. Knowledge of the particle size permits: (1) an estimate of the validity of samples drawn through the sampling system, (2) a better knowledge of what the active particle ground deposition pattern might be, and (3) may provide information relating to filter performance. The kind of radioactive material discharged is important in determining relative health hazards. The object of this work was to determine the size and kind of radioactive particles in the 234-5 Building ventilation exhaust. A secondary objective was to review present routine sampling of the stream with particular regard to the particulates to be sampled.

  15. A Simple and Sensitive RP-UPLC Method for the Simultaneous Determination of N-Hydroxybenzotriazole, Cinchonidine and 1,3-Dicyclohexyl Urea Contents in Fosinopril Sodium Drug Substance

    Directory of Open Access Journals (Sweden)

    M. Narendra Kumar

    2012-01-01

    Full Text Available A simple and sensitive reverse phase ultra performance liquid chromatography (RP-UPLC method has been developed, optimized and validated for the simultaneous determination of N-Hydroxybenzotriazole (HOBt, Cinchonidine and 1,3-Dicyclohexyl urea (DCU contents at low levels in fosinopril sodium drug substance. Efficient chromatographic separation was achieved on Acquity UPLC HSS C18 column, 100 mm long with 2.1 mm i.d., 1.8 µm particle diameter, thermo stated at 30°C. Gradient elution involving binary mixture of potassium dihydrogen orthophosphate (0.01M, pH:3.0±0.05 with ortho-phosphoric acid and acetonitrile at a flow rate of 0.10 mL min-1 has been used. The analytes were monitored by photodiode array (PDA detector set at 205 nm. The drug substance was subjected to stress conditions of hydrolysis, oxidation, photolysis, thermal and humidity degradation. The method was validated for specificity, sensitivity, linearity, precision, accuracy and solution stability. The limit of detection (LOD and limit of quantification (LOQ for HOBt, Cinchonidine and DCU were in the range of 0.85-3.52 ppm and 2.57-10.67 ppm, respectively. The average recoveries for HOBt, Cinchonidine and DCU are in the range of 98.1% to 102.6%. The method can be used for the routine quality control analysis of fosinopril sodium drug substance.

  16. 固体219Rn 源的γ能谱法放射性纯度检验%Determination of Radioactivity Purity of Solid 219 Rn Source by γ-ray Spectrometry

    Institute of Scientific and Technical Information of China (English)

    唐泉; 安小刚; 丘寿康

    2014-01-01

    对利用从铀矿石中提取得到的227 Ac制备的固体219 Rn源进行了γ能谱分析,确定了227 Ac的4个子体核素227 T h、223 Ra、219 Rn和211 Bi的活度,并分析了能对219 Rn造成干扰的222 Rn、220 Rn母体核素226 Ra、224 Ra的活度。待227 Ac及其子体达到放射性平衡后,通过测量227 Th的235.97、256.25 keV ,223 Ra的154.21 keV ,219 Rn的401.81 keV ,211 Bi的351.059 keV共5条γ射线,最终确定固体219 Rn源中227 T h、223 Ra、219 Rn和211 Bi的活度为(1069±3)、(1079±5)、(1095±13)、(1096±14)和(11089±4) Bq ,固体219 Rn源的平均活度为(1093±8) Bq;通过测量224 Ra子体212 Pb的238.632 keV、208 T l的583.191 keVγ射线以及226 Ra子体214 Bi的609.312、1120.287 keV γ射线得到226 Ra与224 Ra的平均活度分别为5.12 Bq及0.433 Bq ,远低于固体219 Rn源的平均活度,说明固体219 Rn源放射性纯度较高。以上结果表明,此源有望制成标准固体219 Rn源以用于延迟符合法测223 Ra、227 Ac装置的刻度。%Radioactivity purity of the solid 219 Rn source made using 227 Ac extracted from uranium ore were determined by γ‐spectrometry .The activities of 227 Th ,223 Ra ,219 Rn and 211 Bi produced by the decay of 227 Ac and the contents of 226 Ra ,224 Ra w hich generates 222 Rn ,220 Rn to affect the purity of actinide in this source were analyzed after 227 Ac in radioactive equilibrium with its daughter nuclides . The γ‐ray energy used for the determination of these daughter nuclides of 227 Ac are 235.97 ,256.25 keV for 227 Th , 154.21 keV for 223Ra ,401.81 keV for 219Rn ,and 351.059 keV for 211Bi .Through the analysis ,the results are acquired that their activities are (1 069 ± 3 ) , (1 079 ± 5 ) , (1 095 ± 13) ,(1 096 ± 14) and (11 089 ± 4) Bq respectively ,and the average activity of solid 219 Rn source is (1 093 ± 8) Bq .The activities of 226 Ra and 224 Ra in this source are 5.12 Bq and 0.433 Bq respectively

  17. Acupuncture meridians demythified. A study using the radioactive tracer method

    Energy Technology Data Exchange (ETDEWEB)

    Simon, J.; Esquerre, J.P.; Guiraud, R.; Guiraud, G.; Lazorthes, Y.

    1988-07-01

    Radioactive trajectories can be visualized by injecting a radioactive tracer, technetium 99 m, at the site of acupuncture points. To determine the exact nature of these trajectories we performed several experiments on healthy volunteers, and our results may be summarized as follows. The target organs of technetium 99 m, and notably the thyroid gland, were always visualized. The circulating radioactivity, visible on scintiscans and confirmed by venous blood counts, was not negligible. The radioactive trajectories we observed were often divided at their starting point and did not extend along the whole length of the acupuncture meridians they might have made visible. The radioactive trajectories disappeared after venous blockade to reappear when the blockade was lifted. Finally, the radioactive trajectories obtained were very similar after injection at the acupuncture point and at a control point. These findings indicate a lymphatic and venous drainage of the radioactive tracer at the site of injection followed by transportation through the veins, rather than visualization of acupuncture meridians as suggested by some authors.

  18. [Polonium: the radioactive killer from tobacco smoke].

    Science.gov (United States)

    Zagà, Vincenzo; Gattavecchia, Enrico

    2008-01-01

    Among all carcinogenic substances contained in tobacco smoke, Polonium 210 (Po-210), with a half-life of 138 days, is one of the most dangerous, by exerting a devastating, chronic, slow and progressive carcinogenesis activity. The main source of Po-210 in tobacco is represented by fertilizers (polyphosphates) containing radium-226 (Ra-222) which decades to plumb 210 (Pb-210). Through the thricomes Pb-210 is concentrated in the tobacco leaves, where it turns to Po-210, which at the cigarette combustion temperature (800-900 degrees C) reaches the gaseous state and it is absorbed by the micro particles released into tobacco smoke. Thus, smoke becomes radioactive in both its gaseous and corpuscular components and reaches the airways, where, particularly at the branches level and together with other substances, it exerts its carcinogenic activity, especially in those subjects with impaired respiratory mucosal clearance. The carcinogenic risk/one year lifetime of a smoker of 20 cigarettes per day is equivalent to that of undertaking 300 chest x-rays. It is calculated that Po-210 may be independently responsible of 4 lung cancers every 10,000 smokers. During cigarette's combustion, tobacco smoke is also released in the air, contributing to serious health risks for those exposed to passive smoke.

  19. HPLC determination of related substances in clemastine fumarate and its tablets*%HPLC法测定富马酸氯马斯汀及富马酸氯马斯汀片的有关物质

    Institute of Scientific and Technical Information of China (English)

    刘德胜; 徐玉文; 李玉梅

    2011-01-01

    Objective:High performance liquid chromatography method was established to determine the related substances and the degradation substances in clemastine fumarate ant its tablets. Methods:An ODS -3 C18 column (250 mm x4. 6 mm,5 μm)with UV detection at 210 nm,and acetonitrile -sodium octanesulfonate solution (50:50) as the mobile phase were used in HPLC. The flow rate was 1. 0 mL·min-1 ,and the temperature of the column was 35 t. Results; An excellent separation was achieved for clemastine fumarate, excipient and its related substances. The reproducibility and precision of the method were good( RSD <0. 3% ). Conclusion:This method was accurate, simple, quick and effective for determination of related substances and the degradation substances in clemastine fumarate tablets. It was also suitable for the quality control for clemastine fumarate and its tablets.%目的:采用高效液相色谱法测定富马酸氯马斯汀及片剂中的有关物质和降解产物.方法:采用ODS -3 C18色谱柱(250mm ×4.6 mm,5μm);柱温为35℃;流动相为乙腈-辛烷磺酸钠溶液(50∶50);流速为1.0 mL·min-1;检测波长为210 nm;进样量为10μL.结果:各降解产物、辅料均可与富马酸氯马斯汀主峰良好分离,方法的精密度和重复性良好(RSD<0.3%).结论:经方法学验证,该法灵敏、准确,适用于富马酸氯马斯汀及片剂中有关物质的测定.

  20. Determination of natural radioactivity of groundwater and surface of Brumadinho and Nova Lima, Brazil; Determinacao da radioatividade natural de agua subterranea e superficial de Brumadinho e Nova Lima, Brasil

    Energy Technology Data Exchange (ETDEWEB)

    Faria, Ligia Santana de

    2013-07-01

    The municipalities of Brumadinho and Nova Lima are located in the metropolitan area of Belo Horizonte city. They are of ecological interest since they belong to an Environmental Protection Area, which is located on a very important deposit of iron ore. In addition of mineral wealth, the region has a geological characteristic that includes quartzitic conglomerates associated with uranium and significant potential underground water with hydrogeological characteristics very particular and complex, as the Quartzite Aquifer, which belongs to a geological formation called the 'Moeda Formation'. In the present work radiometric measurements were performed for 44 water samples. The samples were collected in four geographical points, three of them situated in Brumadinho (surface water) and one point situated in Nova Lima municipality (underground water). The period of sampling extended for a thirteen months period. Some of these locations was used as an alternative sampling point. Uranium and thorium concentrations of the samples were determined using an Inductively Coupled Plasma Mass Spectrometer. The content of gross alpha and gross beta activity, and the concentration of the radionuclides {sup 226}Ra, {sup 228}Ra e {sup 210}Pb were determinate by using Spectrometer Liquid Scintillation. In this case was necessary to calibrate the spectrometer using {sup 241}Am e {sup 90}Sr/{sup 90}Y standards. The resultants values were compared with those recommended by the World Health Organization, Ministry of Health and the National Council of the Environment. The maximum level of water natural radioactivity found was 0,275 ± 0,052 Bq.L{sup -1} for gross alpha radiation, 0,130 ± 0,046 Bq.L{sup -1} for {sup 226}Ra and 0,096 ± 0,005 Bq.L-1 for {sup 228}Ra. The levels of gross beta activity and {sup 210}Pb were below the detection limit. The maximum concentrations of uranium and thorium found were 0,068 μg.L{sup -1} and 0.027 μg.L{sup -1} respectively. (author)

  1. Consensus evaluation of radioactivity-in-soil reference materials in the context of an NPL Environmental Radioactivity Proficiency Test Exercise.

    Science.gov (United States)

    Dean, Julian; Collins, Sean; Garcia Miranda, Maria; Ivanov, Peter; Larijani, Cyrus; Woods, Selina

    2017-01-25

    The development of two radioactivity-in-soil reference materials is described - one for peat and one for soil with high sand content. Each bulk material was processed, subdivided and measured before being sent to participants in an NPL Environmental Radioactivity Proficiency Test Exercise. Activity concentrations of radionuclides in each material were determined by 'consensus' evaluations of participants' results using two weighted mean methods. The project demonstrated the use of such exercises in delivering reference materials to the user community.

  2. Sampling procedure, receipt and conservation of water samples to determine environmental radioactivity; Procedimiento para el muestreo, recepcion y conservacion de muestras de agua para la determinacion de la radiactividad ambiental

    Energy Technology Data Exchange (ETDEWEB)

    Herranz, M.; Navarro, E.; Payeras, J. (and others)

    2009-07-01

    The present document informs about essential goals, processes and contents that the subgroups Samling and Samples Preparation and Conservation believe they should be part of the procedure to obtain a correct sampling, receipt, conservation and preparation of samples of continental, marine and waste water before qualifying its radioactive content.

  3. SELF SINTERING OF RADIOACTIVE WASTES

    Science.gov (United States)

    McVay, T.N.; Johnson, J.R.; Struxness, E.G.; Morgan, K.Z.

    1959-12-29

    A method is described for disposal of radioactive liquid waste materials. The wastes are mixed with clays and fluxes to form a ceramic slip and disposed in a thermally insulated container in a layer. The temperature of the layer rises due to conversion of the energy of radioactivity to heat boillng off the liquid to fomn a dry mass. The dry mass is then covered with thermal insulation, and the mass is self-sintered into a leach-resistant ceramic cake by further conversion of the energy of radioactivity to heat.

  4. Final disposal of radioactive waste

    Science.gov (United States)

    Freiesleben, H.

    2013-06-01

    In this paper the origin and properties of radioactive waste as well as its classification scheme (low-level waste - LLW, intermediate-level waste - ILW, high-level waste - HLW) are presented. The various options for conditioning of waste of different levels of radioactivity are reviewed. The composition, radiotoxicity and reprocessing of spent fuel and their effect on storage and options for final disposal are discussed. The current situation of final waste disposal in a selected number of countries is mentioned. Also, the role of the International Atomic Energy Agency with regard to the development and monitoring of international safety standards for both spent nuclear fuel and radioactive waste management is described.

  5. Fields of View for Environmental Radioactivity

    CERN Document Server

    Malins, Alex; Machida, Masahiko; Takemiya, Hiroshi; Saito, Kimiaki

    2015-01-01

    The gamma component of air radiation dose rates is a function of the amount and spread of radioactive nuclides in the environment. These radionuclides can be natural or anthropogenic in origin. The field of view describes the area of radionuclides on, or below, the ground that is responsible for determining the air dose rate, and hence correspondingly the external radiation exposure. This work describes Monte Carlo radiation transport calculations for the field of view under a variety of situations. Presented first are results for natural 40K and thorium and uranium series radionuclides distributed homogeneously within the ground. Results are then described for atmospheric radioactive caesium fallout, such as from the Fukushima Daiichi Nuclear Power Plant accident. Various stages of fallout evolution are considered through the depth distribution of 134Cs and 137Cs in soil. The fields of view for the natural radionuclides and radiocaesium are different. This can affect the responses of radiation monitors to th...

  6. Nuclear astrophysics with radioactive ions at FAIR

    Science.gov (United States)

    Reifarth, R.; Altstadt, S.; Göbel, K.; Heftrich, T.; Heil, M.; Koloczek, A.; Langer, C.; Plag, R.; Pohl, M.; Sonnabend, K.; Weigand, M.; Adachi, T.; Aksouh, F.; Al-Khalili, J.; AlGarawi, M.; AlGhamdi, S.; Alkhazov, G.; Alkhomashi, N.; Alvarez-Pol, H.; Alvarez-Rodriguez, R.; Andreev, V.; Andrei, B.; Atar, L.; Aumann, T.; Avdeichikov, V.; Bacri, C.; Bagchi, S.; Barbieri, C.; Beceiro, S.; Beck, C.; Beinrucker, C.; Belier, G.; Bemmerer, D.; Bendel, M.; Benlliure, J.; Benzoni, G.; Berjillos, R.; Bertini, D.; Bertulani, C.; Bishop, S.; Blasi, N.; Bloch, T.; Blumenfeld, Y.; Bonaccorso, A.; Boretzky, K.; Botvina, A.; Boudard, A.; Boutachkov, P.; Boztosun, I.; Bracco, A.; Brambilla, S.; Briz Monago, J.; Caamano, M.; Caesar, C.; Camera, F.; Casarejos, E.; Catford, W.; Cederkall, J.; Cederwall, B.; Chartier, M.; Chatillon, A.; Cherciu, M.; Chulkov, L.; Coleman-Smith, P.; Cortina-Gil, D.; Crespi, F.; Crespo, R.; Cresswell, J.; Csatlós, M.; Déchery, F.; Davids, B.; Davinson, T.; Derya, V.; Detistov, P.; Diaz Fernandez, P.; DiJulio, D.; Dmitry, S.; Doré, D.; Dueñas, J.; Dupont, E.; Egelhof, P.; Egorova, I.; Elekes, Z.; Enders, J.; Endres, J.; Ershov, S.; Ershova, O.; Fernandez-Dominguez, B.; Fetisov, A.; Fiori, E.; Fomichev, A.; Fonseca, M.; Fraile, L.; Freer, M.; Friese, J.; Borge, M. G.; Galaviz Redondo, D.; Gannon, S.; Garg, U.; Gasparic, I.; Gasques, L.; Gastineau, B.; Geissel, H.; Gernhäuser, R.; Ghosh, T.; Gilbert, M.; Glorius, J.; Golubev, P.; Gorshkov, A.; Gourishetty, A.; Grigorenko, L.; Gulyas, J.; Haiduc, M.; Hammache, F.; Harakeh, M.; Hass, M.; Heine, M.; Hennig, A.; Henriques, A.; Herzberg, R.; Holl, M.; Ignatov, A.; Ignatyuk, A.; Ilieva, S.; Ivanov, M.; Iwasa, N.; Jakobsson, B.; Johansson, H.; Jonson, B.; Joshi, P.; Junghans, A.; Jurado, B.; Körner, G.; Kalantar, N.; Kanungo, R.; Kelic-Heil, A.; Kezzar, K.; Khan, E.; Khanzadeev, A.; Kiselev, O.; Kogimtzis, M.; Körper, D.; Kräckmann, S.; Kröll, T.; Krücken, R.; Krasznahorkay, A.; Kratz, J.; Kresan, D.; Krings, T.; Krumbholz, A.; Krupko, S.; Kulessa, R.; Kumar, S.; Kurz, N.; Kuzmin, E.; Labiche, M.; Langanke, K.; Lazarus, I.; Le Bleis, T.; Lederer, C.; Lemasson, A.; Lemmon, R.; Liberati, V.; Litvinov, Y.; Löher, B.; Lopez Herraiz, J.; Münzenberg, G.; Machado, J.; Maev, E.; Mahata, K.; Mancusi, D.; Marganiec, J.; Martinez Perez, M.; Marusov, V.; Mengoni, D.; Million, B.; Morcelle, V.; Moreno, O.; Movsesyan, A.; Nacher, E.; Najafi, M.; Nakamura, T.; Naqvi, F.; Nikolski, E.; Nilsson, T.; Nociforo, C.; Nolan, P.; Novatsky, B.; Nyman, G.; Ornelas, A.; Palit, R.; Pandit, S.; Panin, V.; Paradela, C.; Parkar, V.; Paschalis, S.; Pawłowski, P.; Perea, A.; Pereira, J.; Petrache, C.; Petri, M.; Pickstone, S.; Pietralla, N.; Pietri, S.; Pivovarov, Y.; Potlog, P.; Prokofiev, A.; Rastrepina, G.; Rauscher, T.; Ribeiro, G.; Ricciardi, M.; Richter, A.; Rigollet, C.; Riisager, K.; Rios, A.; Ritter, C.; Rodriguez Frutos, T.; Rodriguez Vignote, J.; Röder, M.; Romig, C.; Rossi, D.; Roussel-Chomaz, P.; Rout, P.; Roy, S.; Söderström, P.; Saha Sarkar, M.; Sakuta, S.; Salsac, M.; Sampson, J.; Sanchez, J.; Rio Saez, del; Sanchez Rosado, J.; Sanjari, S.; Sarriguren, P.; Sauerwein, A.; Savran, D.; Scheidenberger, C.; Scheit, H.; Schmidt, S.; Schmitt, C.; Schnorrenberger, L.; Schrock, P.; Schwengner, R.; Seddon, D.; Sherrill, B.; Shrivastava, A.; Sidorchuk, S.; Silva, J.; Simon, H.; Simpson, E.; Singh, P.; Slobodan, D.; Sohler, D.; Spieker, M.; Stach, D.; Stan, E.; Stanoiu, M.; Stepantsov, S.; Stevenson, P.; Strieder, F.; Stuhl, L.; Suda, T.; Sümmerer, K.; Streicher, B.; Taieb, J.; Takechi, M.; Tanihata, I.; Taylor, J.; Tengblad, O.; Ter-Akopian, G.; Terashima, S.; Teubig, P.; Thies, R.; Thoennessen, M.; Thomas, T.; Thornhill, J.; Thungstrom, G.; Timar, J.; Togano, Y.; Tomohiro, U.; Tornyi, T.; Tostevin, J.; Townsley, C.; Trautmann, W.; Trivedi, T.; Typel, S.; Uberseder, E.; Udias, J.; Uesaka, T.; Uvarov, L.; Vajta, Z.; Velho, P.; Vikhrov, V.; Volknandt, M.; Volkov, V.; von Neumann-Cosel, P.; von Schmid, M.; Wagner, A.; Wamers, F.; Weick, H.; Wells, D.; Westerberg, L.; Wieland, O.; Wiescher, M.; Wimmer, C.; Wimmer, K.; Winfield, J. S.; Winkel, M.; Woods, P.; Wyss, R.; Yakorev, D.; Yavor, M.; Zamora Cardona, J.; Zartova, I.; Zerguerras, T.; Zgura, M.; Zhdanov, A.; Zhukov, M.; Zieblinski, M.; Zilges, A.; Zuber, K.

    2016-01-01

    The nucleosynthesis of elements beyond iron is dominated by neutron captures in the s and r processes. However, 32 stable, proton-rich isotopes cannot be formed during those processes, because they are shielded from the s-process flow and r-process, β-decay chains. These nuclei are attributed to the p and rp process. For all those processes, current research in nuclear astrophysics addresses the need for more precise reaction data involving radioactive isotopes. Depending on the particular reaction, direct or inverse kinematics, forward or time-reversed direction are investigated to determine or at least to constrain the desired reaction cross sections. The Facility for Antiproton and Ion Research (FAIR) will offer unique, unprecedented opportunities to investigate many of the important reactions. The high yield of radioactive isotopes, even far away from the valley of stability, allows the investigation of isotopes involved in processes as exotic as the r or rp processes.

  7. Development of synthetic environmental radioactivity reference materials.

    Science.gov (United States)

    Harms, Arvic; Gilligan, Chris

    2012-09-01

    In this paper, a novel way of developing synthetic environmental radioactivity reference materials via the sol-gel process is described. Two solid reference materials (both having a SiO(2) matrix) were synthesised by hydrolysing a liquid mixture of tetraethyl orthosilicate (TEOS), ethanol and standardised mixed radionuclide solutions. The certified values, which were in the Bqg(-1) range, for the radionuclides in the material were determined by NPL and compared with results from measurements made by 36 organisations from 17 countries using a 'consensus' approach. The measurements were made within two wider test exercises (the NPL Environmental Radioactivity Proficiency Test Exercises 2009 and 2010). Certified activity concentration values were obtained for (60)Co, (133)Ba, (134)Cs, (137)Cs, (152)Eu, (154)Eu and (241)Am and indicative values were obtained for (55)Fe and (90)Sr.

  8. Nuclear astrophysics with radioactive ions at FAIR

    CERN Document Server

    Reifarth, R; Göbel, K; Heftrich, T; Heil, M; Koloczek, A; Langer, C; Plag, R; Pohl, M; Sonnabend, K; Weigand, M; Adachi, T; Aksouh, F; Al-Khalili, J; AlGarawi, M; AlGhamdi, S; Alkhazov, G; Alkhomashi, N; Alvarez-Pol, H; Alvarez-Rodriguez, R; Andreev, V; Andrei, B; Atar, L; Aumann, T; Avdeichikov, V; Bacri, C; Bagchi, S; Barbieri, C; Beceiro, S; Beck, C; Beinrucker, C; Belier, G; Bemmerer, D; Bendel, M; Benlliure, J; Benzoni, G; Berjillos, R; Bertini, D; Bertulani, C; Bishop, S; Blasi, N; Bloch, T; Blumenfeld, Y; Bonaccorso, A; Boretzky, K; Botvina, A; Boudard, A; Boutachkov, P; Boztosun, I; Bracco, A; Brambilla, S; Monago, J Briz; Caamano, M; Caesar, C; Camera, F; Casarejos, E; Catford, W; Cederkall, J; Cederwall, B; Chartier, M; Chatillon, A; Cherciu, M; Chulkov, L; Coleman-Smith, P; Cortina-Gil, D; Crespi, F; Crespo, R; Cresswell, J; Csatlós, M; Déchery, F; Davids, B; Davinson, T; Derya, V; Detistov, P; Fernandez, P Diaz; DiJulio, D; Dmitry, S; Doré, D; nas, J Due\\; Dupont, E; Egelhof, P; Egorova, I; Elekes, Z; Enders, J; Endres, J; Ershov, S; Ershova, O; Fernandez-Dominguez, B; Fetisov, A; Fiori, E; Fomichev, A; Fonseca, M; Fraile, L; Freer, M; Friese, J; Borge, M G; Redondo, D Galaviz; Gannon, S; Garg, U; Gasparic, I; Gasques, L; Gastineau, B; Geissel, H; Gernhäuser, R; Ghosh, T; Gilbert, M; Glorius, J; Golubev, P; Gorshkov, A; Gourishetty, A; Grigorenko, L; Gulyas, J; Haiduc, M; Hammache, F; Harakeh, M; Hass, M; Heine, M; Hennig, A; Henriques, A; Herzberg, R; Holl, M; Ignatov, A; Ignatyuk, A; Ilieva, S; Ivanov, M; Iwasa, N; Jakobsson, B; Johansson, H; Jonson, B; Joshi, P; Junghans, A; Jurado, B; Körner, G; Kalantar, N; Kanungo, R; Kelic-Heil, A; Kezzar, K; Khan, E; Khanzadeev, A; Kiselev, O; Kogimtzis, M; Körper, D; Kräckmann, S; Kröll, T; Krücken, R; Krasznahorkay, A; Kratz, J; Kresan, D; Krings, T; Krumbholz, A; Krupko, S; Kulessa, R; Kumar, S; Kurz, N; Kuzmin, E; Labiche, M; Langanke, K; Lazarus, I; Bleis, T Le; Lederer, C; Lemasson, A; Lemmon, R; Liberati, V; Litvinov, Y; Löher, B; Herraiz, J Lopez; Münzenberg, G; Machado, J; Maev, E; Mahata, K; Mancusi, D; Marganiec, J; Perez, M Martinez; Marusov, V; Mengoni, D; Million, B; Morcelle, V; Moreno, O; Movsesyan, A; Nacher, E; Najafi, M; Nakamura, T; Naqvi, F; Nikolski, E; Nilsson, T; Nociforo, C; Nolan, P; Novatsky, B; Nyman, G; Ornelas, A; Palit, R; Pandit, S; Panin, V; Paradela, C; Parkar, V; Paschalis, S; Paw\\lowski, P; Perea, A; Pereira, J; Petrache, C; Petri, M; Pickstone, S; Pietralla, N; Pietri, S; Pivovarov, Y; Potlog, P; Prokofiev, A; Rastrepina, G; Rauscher, T; Ribeiro, G; Ricciardi, M; Richter, A; Rigollet, C; Riisager, K; Rios, A; Ritter, C; Frutos, T Rodríguez; Vignote, J Rodriguez; Röder, M; Romig, C; Rossi, D; Roussel-Chomaz, P; Rout, P; Roy, S; Söderström, P; Sarkar, M Saha; Sakuta, S; Salsac, M; Sampson, J; Saez, J Sanchez del Rio; Rosado, J Sanchez; Sanjari, S; Sarriguren, P; Sauerwein, A; Savran, D; Scheidenberger, C; Scheit, H; Schmidt, S; Schmitt, C; Schnorrenberger, L; Schrock, P; Schwengner, R; Seddon, D; Sherrill, B; Shrivastava, A; Sidorchuk, S; Silva, J; Simon, H; Simpson, E; Singh, P; Slobodan, D; Sohler, D; Spieker, M; Stach, D; Stan, E; Stanoiu, M; Stepantsov, S; Stevenson, P; Strieder, F; Stuhl, L; Suda, T; Sümmerer, K; Streicher, B; Taieb, J; Takechi, M; Tanihata, I; Taylor, J; Tengblad, O; Ter-Akopian, G; Terashima, S; Teubig, P; Thies, R; Thoennessen, M; Thomas, T; Thornhill, J; Thungstrom, G; Timar, J; Togano, Y; Tomohiro, U; Tornyi, T; Tostevin, J; Townsley, C; Trautmann, W; Trivedi, T; Typel, S; Uberseder, E; Udias, J; Uesaka, T; Uvarov, L; Vajta, Z; Velho, P; Vikhrov, V; Volknandt, M; Volkov, V; von Neumann-Cosel, P; von Schmid, M; Wagner, A; Wamers, F; Weick, H; Wells, D; Westerberg, L; Wieland, O; Wiescher, M; Wimmer, C; Wimmer, K; Winfield, J S; Winkel, M; Woods, P; Wyss, R; Yakorev, D; Yavor, M; Cardona, J Zamora; Zartova, I; Zerguerras, T; Zgura, I; Zhdanov, A; Zhukov, M; Zieblinski, M; Zilges, A; Zuber, K

    2016-01-01

    The nucleosynthesis of elements beyond iron is dominated by neutron captures in the s and r processes. However, 32 stable, proton-rich isotopes cannot be formed during those processes, because they are shielded from the s-process flow and r-process beta-decay chains. These nuclei are attributed to the p and rp process. For all those processes, current research in nuclear astrophysics addresses the need for more precise reaction data involving radioactive isotopes. Depending on the particular reaction, direct or inverse kinematics, forward or time-reversed direction are investigated to determine or at least to constrain the desired reaction cross sections. The Facility for Antiproton and Ion Research (FAIR) will offer unique, unprecedented opportunities to investigate many of the important reactions. The high yield of radioactive isotopes, even far away from the valley of stability, allows the investigation of isotopes involved in processes as exotic as the r or rp processes.

  9. Radioactive decay data tables

    Energy Technology Data Exchange (ETDEWEB)

    Kocher, D.C.

    1981-01-01

    The estimation of radiation dose to man from either external or internal exposure to radionuclides requires a knowledge of the energies and intensities of the atomic and nuclear radiations emitted during the radioactive decay process. The availability of evaluated decay data for the large number of radionuclides of interest is thus of fundamental importance for radiation dosimetry. This handbook contains a compilation of decay data for approximately 500 radionuclides. These data constitute an evaluated data file constructed for use in the radiological assessment activities of the Technology Assessments Section of the Health and Safety Research Division at Oak Ridge National Laboratory. The radionuclides selected for this handbook include those occurring naturally in the environment, those of potential importance in routine or accidental releases from the nuclear fuel cycle, those of current interest in nuclear medicine and fusion reactor technology, and some of those of interest to Committee 2 of the International Commission on Radiological Protection for the estimation of annual limits on intake via inhalation and ingestion for occupationally exposed individuals.

  10. /sup 5/He radioactivity

    Energy Technology Data Exchange (ETDEWEB)

    Poenaru, D.N.; Ivascu, M. (Institute for Physics and Nuclear Engineering, Bucharest (Romania))

    1984-07-01

    The disintegration of a metastable nuclear state by emission of a light particle can be considered to be a very asymmetric fission process. An approximation of the potential barrier in the overlapping region of the two fragments leads to an analytic relationship for the life-time, allowing us to handle a large number of cases to search for new kinds of radioactivities. In this way, it is predicted that some nuclei with Z=83-92, N=127-137 and 97-105, 145-157 are able to decay spontaneously by emission of /sup 5/He particles. A tentative optimistic estimation leads to the result that only 15 radionuclides should have partial life-times in the range 10/sup 14/-10/sup 38/ years; all others, except some superheavies, are longer lived. The best candidate is /sup 213/Po for which the daughter is a double magic nucleus. Smaller life-times, with a better chance to be experimentally confirmed have some ..beta..-delayed /sup 5/He emitters, as for example /sup 155/Yb, /sup 175/Pt, /sup 209 -217/Ra, /sup 9 -11/Be, /sup 13 -14/B, /sup 13 -17/C and /sup 19 -21/O.

  11. Substance use and multiculturalism.

    Science.gov (United States)

    Adrian, M

    1996-01-01

    This paper reviews intercultural variability of substance use behaviors, including availability of international statistics on consumption of alcohol and other drugs, as well as the use of drugs available locally only. Within a conceptual framework of intercultural relations, it considers the history of transcultural spread of substance use behaviors and possible reactions to the introduction of new drugs within a culture or jurisdiction, including illustrations of the "law of alien poisons." Although intercultural views of substance use have generally concentrated on majority groups' views of substance use in minority groups, minority and non-Western views of substance use need to be considered in the context of increasing international and intercultural communications that increase the rate at which substance use behaviors spread. Both Western and non-Western experiences with substance use and misuse must be taken into account so that better interventions can be developed to deal with addictions and other substance-related problems.

  12. Substance Use in Women

    Science.gov (United States)

    ... emergency room or die from overdose or other effects of certain substances. Women who are victims of domestic violence are at increased risk of substance use. Divorce, loss of child custody, or the death of ...

  13. Plasma substance P levels in fibrositis.

    Science.gov (United States)

    Reynolds, W J; Chiu, B; Inman, R D

    1988-12-01

    The mechanism of pain in the fibrositis syndrome is unknown. We measured plasma levels of substance P in 32 patients with fibrositis and 26 sex and age matched controls using a radioimmunoassay. The mean plasma level of substance P in the patients with fibrositis was 371 +/- 91 pg/ml and in controls 397 +/- 84 pg/ml (p = NS). We conclude that determination of plasma levels of substance P in fibrositis is of no diagnostic value. This does not exclude the possible role of substance P as a neurotransmitter in the fibrositis syndrome.

  14. Molecular size of aquatic humic substances

    Science.gov (United States)

    Thurman, E.M.; Wershaw, R. L.; Malcolm, R.L.; Pinckney, D.J.

    1982-01-01

    Aquatic humic substances, which account for 30 to 50% of the organic carbon in water, are a principal component of aquatic organic matter. The molecular size of aquatic humic substances, determined by small-angle X-ray scattering, varies from 4.7 to 33 A?? in their radius of gyration, corresponding to a molecular weight range of 500 to greater than 10,000. The aquatic fulvic acid fraction contains substances with molecular weights ranging from 500 to 2000 and is monodisperse, whereas the aquatic humic acid fraction contains substances with molecular weights ranging from 1000 to greater than 10,000 and is generally polydisperse. ?? 1982.

  15. Substance Abuse and Trauma.

    Science.gov (United States)

    Simmons, Shannon; Suárez, Liza

    2016-10-01

    There is a strong, bidirectional link between substance abuse and traumatic experiences. Teens with cooccurring substance use disorders (SUDs) and posttraumatic stress disorder (PTSD) have significant functional and psychosocial impairment. Common neurobiological foundations point to the reinforcing cycle of trauma symptoms, substance withdrawal, and substance use. Treatment of teens with these issues should include a systemic and integrated approach to both the SUD and the PTSD.

  16. Low-Activity Radioactive Wastes

    Science.gov (United States)

    In 2003 EPA published an Advance Notice of Proposed Rulemaking (ANPR) to collect public comment on alternatives for disposal of waste containing low concentrations of radioactive material ('low-activity' waste).

  17. Radioactivity standardization in South Africa

    CSIR Research Space (South Africa)

    Simpson, BRS

    2002-01-01

    Full Text Available South Africa's national radioactivity measurement standard is maintained at a satellite laboratory in Cape Town by the National Metrology Laboratory (NML) of the Council-for Scientific and Industrial Research. Standardizations are undertaken by a...

  18. Consumer Products Containing Radioactive Materials

    Science.gov (United States)

    ... 2010 Health Physics Society Specialists in Radiation Safety Consumer Products Containing Radioactive Materials Everything we encounter in ... eat, the ground we walk upon, and the consumer products we purchase and use. Although many might ...

  19. Environmental radioactivity survey in Suwon

    Energy Technology Data Exchange (ETDEWEB)

    Park, Won Keun; Park, Jong Mi [Kyunghee Univ., Suwon (Korea, Republic of)

    2003-12-15

    The project is carried out to monitor the change of environmental radioactivity in Suwon, and to provide a systematic data for radiation monitoring and counter measurement at a radiological emergency situation. Also the survey of natural environmental radioactivities in the samples was conducted to make the reliable data base for evaluation of internal exposure and environmental contamination of radiation. This report contains the data of gamma exposure rates and radioactivities of airborne dust, fallout, precipitation and tap water which were analyzed periodically by Suwon regional monitoring station m 2003. Also it contains the data of natural radioactivity levels of environmental samples such as soil, drinking water, indicator plant(mugwort, pine-needle), agricultural and forest products, and processed food(tea)

  20. Radioactive waste material melter apparatus

    Science.gov (United States)

    Newman, D.F.; Ross, W.A.

    1990-04-24

    An apparatus for preparing metallic radioactive waste material for storage is disclosed. The radioactive waste material is placed in a radiation shielded enclosure. The waste material is then melted with a plasma torch and cast into a plurality of successive horizontal layers in a mold to form a radioactive ingot in the shape of a spent nuclear fuel rod storage canister. The apparatus comprises a radiation shielded enclosure having an opening adapted for receiving a conventional transfer cask within which radioactive waste material is transferred to the apparatus. A plasma torch is mounted within the enclosure. A mold is also received within the enclosure for receiving the melted waste material and cooling it to form an ingot. The enclosure is preferably constructed in at least two parts to enable easy transport of the apparatus from one nuclear site to another. 8 figs.

  1. Naturally Occurring Radioactive Materials (NORM)

    Energy Technology Data Exchange (ETDEWEB)

    Gray, P. [ed.

    1997-02-01

    This paper discusses the broad problems presented by Naturally Occuring Radioactive Materials (NORM). Technologically Enhanced naturally occuring radioactive material includes any radionuclides whose physical, chemical, radiological properties or radionuclide concentration have been altered from their natural state. With regard to NORM in particular, radioactive contamination is radioactive material in an undesired location. This is a concern in a range of industries: petroleum; uranium mining; phosphorus and phosphates; fertilizers; fossil fuels; forestry products; water treatment; metal mining and processing; geothermal energy. The author discusses in more detail the problem in the petroleum industry, including the isotopes of concern, the hazards they present, the contamination which they cause, ways to dispose of contaminated materials, and regulatory issues. He points out there are three key programs to reduce legal exposure and problems due to these contaminants: waste minimization; NORM assesment (surveys); NORM compliance (training).

  2. Radioactive waste engineering and management

    CERN Document Server

    Nakayama, Shinichi

    2015-01-01

    This book describes essential and effective management for reliably ensuring public safety from radioactive wastes in Japan. This is the first book to cover many aspects of wastes from the nuclear fuel cycle to research and medical use, allowing readers to understand the characterization, treatment and final disposal of generated wastes, performance assessment, institutional systems, and social issues such as intergenerational ethics. Exercises at the end of each chapter help to understand radioactive waste management in context.

  3. Radioactivity of the Cooling Water

    Science.gov (United States)

    Wigner, E. P.

    1943-03-01

    The most important source of radioactivity at the exit manifold of the pile will be due to O{sup 19}, formed by neutron absorption of O{sup 18}. A recent measurement of Fermi and Weil permits to estimate that it will be safe to stay about 80 minutes daily close to the exit manifolds without any shield. Estimates are given for the radioactivities from other sources both in the neighborhood and farther away from the pile.

  4. Atomic Batteries: Energy from Radioactivity

    OpenAIRE

    Kumar, Suhas

    2015-01-01

    With alternate, sustainable, natural sources of energy being sought after, there is new interest in energy from radioactivity, including natural and waste radioactive materials. A study of various atomic batteries is presented with perspectives of development and comparisons of performance parameters and cost. We discuss radioisotope thermal generators, indirect conversion batteries, direct conversion batteries, and direct charge batteries. We qualitatively describe their principles of operat...

  5. Final disposal of radioactive waste

    OpenAIRE

    Freiesleben H.

    2013-01-01

    In this paper the origin and properties of radioactive waste as well as its classification scheme (low-level waste – LLW, intermediate-level waste – ILW, high-level waste – HLW) are presented. The various options for conditioning of waste of different levels of radioactivity are reviewed. The composition, radiotoxicity and reprocessing of spent fuel and their effect on storage and options for final disposal are discussed. The current situation of final waste disposal in a selected number of c...

  6. Predicted halflives for cluster radioactivities

    Science.gov (United States)

    Poenaru, D. N.; Greiner, W.; Ivascu, M.

    1989-10-01

    The main results of the analytical superasymmetric fission model, describing in a unified manner cluster radioactivities, alpha-decay and cold fission processes, are briefly reviewed. Predicted halflives for 14C, 24, 25, 26Ne, 28, 30Mg and 32Si radioactivities in the range 10 11-10 26 s and the corresponding branching ratios relative to α-decay 10 -16 - 10 -9 have been experimentally confirmed within 1.5 orders of magnitude.

  7. Determination of related substance in methenamine hippurate tablets by HPLC%高效液相色谱法测定马尿酸乌洛托品片的有关物质

    Institute of Scientific and Technical Information of China (English)

    海川; 何胜利

    2013-01-01

    目的:应用高效液相色谱法测定马尿酸乌洛托品片的有关物质。方法采用C18色谱柱(4.6mm×250mm,5μm),甲醇-乙腈-0.1%磷酸溶液(40∶25∶35)为流动相,流速:0.9mL/min,检测波长:217nm。结果在选定的色谱条件下,马尿酸乌洛托品与有关物质分离完全.最低检测限为30ng,精密度良好(RSD=0.78%)。结论该方法简便、准确、专属性好、灵敏度高,可用于马尿酸乌洛托品片的有关物质测定。%Objective To determine the related substances of Methenamine hippurate Tablets by HPLC.Methods The separation was performed on C18 column(4.6mm×250mm,5μm),The mobile phase consisted of methanol and acetonitrile-0.1%phosphoric acid solution(40:25:35),the flow rate was set at 0.9mL/min with detection at 217nm. Results Under tlle established chromatographic conditions, the related substances and methenamine hippurate were separated completely.The least detective range was 30ng.The precision in a day is good(RSD=0.78%). Conclusion The method is simple,accurate,specific and sensitiveness for the determination methenamine hippurate Tablets related substance.

  8. Determination of relavant substances of oxacillin sodium for injection by RP-HPLC%反相高效液相色谱法测定注射用苯唑西林钠有关物质

    Institute of Scientific and Technical Information of China (English)

    吴琦琦; 刘雁鸣; 倪孟祥

    2011-01-01

    Objective To establish an RP-HPLC method for the determination of relavant substance of oxacillin sodium for injection. Methods The chromatographic analysis was performed on C1s column with 0. 01 mol · L-1 ammonium acetate (pH 5.0) - acetonitrile (75∶25) as the mobile phase, the tenperature was 30C, flow rate was 1.0 mL·min-1, and detection wavelength was 225 nm. Results The linear range was 1. 171-28. 114μg · mL-1 (r=0.999 8), and the detection limit was 0. 036μg·mL-1. The relavant substances were separated from oxacillin sodium. Conclusion The method is rapid, simple and accurate to determine the relavant substances of oxacillin sodium.%目的 建立RP-HPLC法测定苯唑西林钠的有关物质.方法 采用C18色谱柱;流动相:0.01 mol·L-1醋酸铵溶液(醋酸调pH至5.0)-乙腈(75:25);流速:1.0 mL·min-1;检测波长:225nm;柱A:30℃.结果 苯唑西林钠线性范围为1.171~28.11 μg·mL-1,r=0.999 8,检测限:0.036 μg·mL-1,笨唑西林钠能与各杂质完全分离.结论 建立的苯唑西林钠有关物质的测定方法简单、快速、重现性好.

  9. Determination of relevant substances of diclofenac diethylamine emulgel by HPLC%高效液相色谱法测定双氯芬酸二乙胺乳胶剂有关物质

    Institute of Scientific and Technical Information of China (English)

    王勇; 张海龙; 周彦彬; 刘廷艳; 丁劲松

    2011-01-01

    目的 建立HPLC法测定双氯芬酸二乙胺乳胶的有关物质.方法 采用Ultimate C18色谱柱,以0.2%乙酸溶液(pH=3.0)-甲醇(34∶66)为流动相,检测波长为254 nm.结果 辅料不干扰各杂质的检出,双氯芬酸二乙胺能与各杂质完全分离,检测限为0.02 μg·mL-1,在杂质的吸收系数等于或大于双氯芬酸二乙胺的情况下,最低杂质检出量为0.002%.结论 建立的双氯芬酸二乙胺有关物质测定方法简单,灵敏度高,能用于该制剂的质量控制.%Objective To establish an HPLC method for the determination of relevant substances of diclofenac diethyl-amine emulgel. Methods An Utimate C18 column was used with the mobile phase of 0. 2% acetic acid (pH = 3. 0) -methanol (34:66). The detection wavelength was 254 ran. Results Blank adjuvant didn't interfere with the detection of impurities. The relevant substances were separated from diclofenac diethylamine, and the detection limit was 0. 02 ug·mL-1. When the absorption coefficient of the impurities was equal to or greater than that of diclofenac diethylamine, the minimum detectable quantity of impurities was 0. 002%. Conclusion The method is simple and sensitive, which is suitable for the determination of relevant substances of diclofenac diethylamine emulgel.

  10. Content Determination and Extraction Technology Optimization of Total Fluorescent Substances from Ligusticum chuanxiong%川芎中总荧光物质的含量测定及提取工艺优化

    Institute of Scientific and Technical Information of China (English)

    银玲; 陈鸿平; 彭月; 刘荣; 樊丹青; 刘友平

    2013-01-01

    目的:建立川芎中总荧光物质的含量测定方法,优化总荧光物质的超声提取工艺.方法:采用荧光分光光度法测定川芎中总荧光物质的含量.通过单因素试验考察料液比、超声时间、提取溶剂种类与浓度对总荧光物质提取工艺的影响,采用星点设计对总荧光物质超声提取工艺的参数进行优选,通过对自变量各水平的多元线性回归及二项式拟合,选用效应面法选取最佳工艺,并进行预测分析.结果:确定的最佳工艺条件为乙醇体积分数63%,液固比350∶1,超声53 min.川芎中总荧光物质提取率的预测值达3.444%,预测值与验证值偏差2.70%.二项式拟合R2=0.9532.结论:优选的提取工艺具有简便、精密度高、可预测性好的优点;建立的含量测定方法稳定可行,为川芎药材的质量控制提供理论依据.%Objective:To establish content determination method of total fluorescent substances from Ligusticum chuanxiong, and optimize ultrasonic extraction technology of total fluorescent substances. Method:Fluorescence spectrophotometric method was adopted for determining the content of total fluorescent substances from. L. chuanxiong. Influence of solid-liquid ratio, extraction time, kind and concentration of extraction solvent on extraction technology of total fluorescent substances was investigated by single factor test, ultrasound extraction technology parameters of total fluorescent substances were optimized by composite design, multiple linear regression and binomial fitting were used to evaluate relationship between independent and dependent variables, response surface methodology was used to optimize extraction process, prediction analysis was carried out by comparing the observed value and the predicted value. Result:Optimal technology conditions of ultrasonic extraction process were as followings; ultrasound extracted 53 min with 350 times the amount of 63% ethanol. The predictive extraction rate

  11. Endangered and Extinct Radioactivity

    Science.gov (United States)

    Leising, M. D.

    1993-07-01

    Gamma ray spectroscopy holds great promise for probing nucleosynthesis in individual nucleosynthesis events, via observations of short-lived radioactivity, and for measuring global galactic nucleosynthesis today with detections of longer-lived radioactivity. Many of the astrophysical issues addressed by these observations are precisely those that must be understood in order to interpret observations of extinct radioactivity in meteorites. It was somewhat surprising that the former case was realized first for a Type II supernova, when both 56Co [1] and 57Co [2] were detected in SN 1987A. These provide unprecedented constraints on models of Type II explosions. Live 26Al in the galaxy might come from Type II supernovae and their progenitors, and if this is eventually shown to be the case, can constrain massive star evolution, supernova nucleosynthesis, the galactic Type II supernova rate, and even models of the chemical evolution of the galaxy [3]. Titanium-44 is produced primarily in the alpha-rich freezeout from nuclear statistical equilibrium, possibly in Type Ia [4] and almost certainly in Type II supernovae [5]. The galactic recurrence time of these events is comparable to the 44Ti lifetime, so we expect to be able to see at most a few otherwise unseen 44Ti remnants at any given time. No such remnants have been detected yet [6]. Very simple arguments lead to the expectation that about 4 x 10^-4 M(sub)solar mass of 44Ca are produced per century. The product of the supernova frequency times the 44Ti yield per event must equal this number. Even assuming that only the latest event would be seen, rates in excess of 2 century^-1 are ruled out at >=99% confidence by the gamma ray limits. Only rates less than 0.3 century^-1 are acceptable at >5% confidence, and this means that the yield per event must be >10^-3 M(sub)solar mass to produce the requisite 44Ca. Rates this low are incompatible with current estimates for Type II supernovae and yields this high are also very

  12. Substance, Reality, and Distinctness

    Directory of Open Access Journals (Sweden)

    Boris Hennig

    2008-04-01

    Full Text Available Descartes claims that God is a substance, and that mind and body are two different and separable substances. This paper provides some background that renders these claims intelligible. For Descartes, that something is real means it can exist in separation, and something is a substance if it does not depend on other substances for its existence. Further, separable objects are correlates of distinct ideas, for an idea is distinct (in an objective sense if its object may be easily and clearly separated from everything that is not its object. It follows that if our idea of God is our most distinct idea, as Descartes claims, then God must be a substance in the Cartesian sense of the term. Also, if we can have an idea of a thinking subject which does not in any sense refer to bodily things, and if bodily things are substances, then mind and body must be two different substances.

  13. Decoding Environmental Processes Using Radioactive Isotopes for the Post-Radioactive Contamination Recovery Assessment

    Science.gov (United States)

    Yasumiishi, Misa; Nishimura, Taku; Osawa, Kazutoshi; Renschler, Chris

    2017-04-01

    The continual monitoring of environmental radioactive levels in Fukushima, Japan following the nuclear plant accident in March 2011 provides our society with valuable information in two ways. First, the collected data can be used as an indicator to assess the progress of decontamination efforts. Secondly, the collected data also can be used to understand the behavior of radioactive isotopes in the environment which leads to further understanding of the landform processes. These two aspects are inseparable for us to understand the effects of radioactive contamination in a dynamic environmental system. During the summer of 2016, 27 soil core samples were collected on a farmer's land (rice paddies and forest) in Fukushima, about 20 km northwest of the nuclear plant. Each core was divided into 2.0 - 3.0 cm slices for the Cs-134, Cs-137, and I-131 level measurement. The collected data is being analyzed from multiple perspectives: temporal, spatial, and geophysical. In the forest area, even on the same hillslope, multiple soil types and horizon depths were observed which indicates the challenges in assessing the subsurface radioactive isotope movements. It appears that although highly humic soils show higher or about the same level of radioactivity in the surface layers, as the depth increased, the radioactivity decreased more in those samples compared with more sandy soils. With regard to the direction a slope faces and the sampling altitudes, the correlation between those attributes and radioactivity levels is inconclusive at this moment. The altitude might have affected the fallout level on a single hillslope-basis. However, to determine the correlation, further sampling and the detailed analysis of vegetation and topography might be necessary. Where the surface soil was scraped and new soil was brought in, former rice paddy surface layers did show three-magnitude levels lower of radioactivity in the top layer when compared with forest soils. At the foot of forest

  14. Determination of Contents and Related Substances of Ecabet Sodium Granules by HPLC%HPLC测定依卡倍特钠颗粒有关物质及其含量

    Institute of Scientific and Technical Information of China (English)

    刘广娟; 裴志东; 张镓小; 张慧

    2012-01-01

    OBJECTIVE To establish the HPLC method for determining the contents and related substances in Ecabet sodium granules. METHODS C18 column (250 mm× 4.6 mm, S urn) was used. The mobile phase consisted of acetonitrile-1.36% potassium dihydrogen phosphate (27 : 73), and the detective wavelength was 271 nm. RESULTS The linearity was obtained over the range of 0.010 26-0.153 9 mg·mL-1, (r=0.999 8). The average recovery was 99.8%. The related substances were well separated in the degradation test. CONCLUSION The method is simple, convenient, accurate and can be employed to assay the contents and related substances in Ecabet sodium granules for its quality control.%目的 建立HPLC测定依卡倍特钠颗粒的含量及有关物质的方法.方法 采用美国热电公司C18色谱柱(250 min×4.6 mm,5μm);流动相为乙腈-1.36%磷酸二氢钾溶液(27:73);柱温为室温;检测波长为271 nm.结果 依卡倍特钠在0.010 26~0.153 9 mg·mL-1浓度范围内呈良好的线性关系(r=0.999 8),平均回收率为99.8%;有关物质的破坏性试验中杂质与主峰分离度符合规定.结论 该方法简便、准确、专属性强,可用于控制依卡倍特钠颗粒的质量.

  15. Validated Densitometric TLC-Method for the Simultaneous Analysis of (R)- and (S)-Citalopram and its Related Substances Using Macrocyclic Antibiotic as a Chiral Selector: Application to the Determination of Enantiomeric Purity of Escitalopram.

    Science.gov (United States)

    Soliman, Suzan Mahmoud

    2012-03-01

    A novel economic procedure for the simultaneous stereospecific separation and analysis of (R)- and (S)-citalopram and its related substances or impurities has been developed and validated. Chromatography was performed on silica gel 60 F254 plates with acetonitrile: methanol: water (15:2.5:2.5: v/v/v) as a mobile phase containing 1.5 mM norvancomycin or 2.5 mM vancomycin as a selector at ambient temperature. (R)- and (S)-citalopram enantiomers in presence of its related substances; citalopram citadiol and citalopram N-oxide were well separated with significant Rf values of 0.33 ± 0.02, 0.85 ± 0.02, 0.45 ± 0.02 and 0.22 ± 0.02, respectively. The spots were detected with either iodine vapor, or by use of a UV lamp followed by densitometric measurement at 239 nm. All variables affecting the resolution, such as concentration of chiral selectors, mobile phase system at different temperatures and pH-values were investigated and the conditions were optimized. Calibration plots for analysis of (R)- and (S)-enantiomers were linear in the range of 0.2-16.8 μg/10 μl (R≥0.9994, n=6) with acceptable precision (%RSDescitalopram, respectively). The limit of detection and quantification were 0.08 μg/10 μl and 0.25 μg/10 μl, respectively, for (R)- and (S)-citalopram. The proposed method is simple, selective, and robust and can be applied for quantitative determination of enantiomeric purity of (R)- and (S)-citalopram (escitalopram) as well as the related impurities in drug substances and pharmaceutical preparations. The method can be useful to investigate adulteration of pure isomer with the cheep racemic form.

  16. Regulation of Transportation of Radioactive Material in Indonesia

    Energy Technology Data Exchange (ETDEWEB)

    Nirwono, Muttaqin Margo; Choi, Kwang Sik [KAIST, Daejeon (Korea, Republic of)

    2011-05-15

    1.1. Background Indonesia is a biggest archipelago country with 17,508 islands in 33 provinces. In transportation Indonesia has large number of airports, railways, roadways, waterways, and merchant marines. Since nuclear and radiation utilizations are expanding on whole country, the mobilization of these is usually placed outside of controlled facilities, in the public domain, and often entails movement between countries. The Indonesian Nuclear Energy Regulatory Agency (BAPETEN) is responsible for supervision and also authorization of the transport of radioactive material (TRM). TRM is the specific movement of a radioactive material consignment from origin to destination by public transportation (road or rail, water and air). This study aims to determine whether national regulation is harmonized with international practice in ensuring safety and security of TRM. The finding of this study will provide recommendation for enhancement of regulation on TRM. 1.2. Regulation of TRM in Indonesia Government Regulation (GR) No. 26, 2002 on the Safe Transport of Radioactive Material is implemented pursuant to Act 10, 1997 on Nuclear Energy. This GR was repealed GR 13, 1975 on TRM. The GR 26 consist of 16 chapters and 39 articles, included licensing: authority and responsibilities: packaging: radiation protection programme; training: quality assurance programme: type and activity limit of radioactive materials: radioactive materials with other dangerous properties: emergency preparedness: administrative sanction: and penal provisions. Principally, this GR adopted IAEA-TS-R-1, 'Regulations for the Safe Transport of Radioactive Material', 1996's Edition

  17. 苏云金芽胞杆菌挥发性物质的测定%Determination of Bacillus thuringiensis volatile substances

    Institute of Scientific and Technical Information of China (English)

    郑梅霞; 潘志针; 刘波; 陈峥; 车建美; 唐建阳; 朱育菁; 陈梅春

    2014-01-01

    目的:分析、鉴定苏云金芽胞杆菌(Bacillus thuringiensis, Bt)的挥发性成分。方法采用顶空固相微萃取技术(HS-SPME)对 Bt 的挥发性成分进行捕集,再通过气相色谱-质谱联用(GC-MS)技术对挥发性成分进行鉴定。以本实验室分离的高效苏云金芽胞杆菌 FJAT-12菌株为实验菌株,探索 Bt 菌株的不同培养方式、不同固相微萃取吸附方式及不同萃取头的选择对挥发性成分鉴定结果的影响,确定 Bt 菌株挥发性物质测定的最优方法。结果采用NA液体培养基培养,选择水浴至气-液平衡再吸附的吸附方式,采用65µm PDMS/DVB萃取头的萃取效果最佳。Bt菌株的挥发性成分主要为6-甲基-2-庚酮、2,4-二氨基甲苯、苯甲醇、2,3-二乙基-5-甲基吡嗪、2-甲基萘、2,3-Dimethyl-5-isopentylpyrazine、十四烷、正十二烷、2-甲硫基苯并噻唑。结论 HS-SPME/GC-MS效果好,方法实用,便于操作,适用于对Bt挥发性成分进行分析,从而为食品安全评估提供理论依据。%Objective To analyze and identify the volatile substances of Bacillus thuringiensis. Methods The volatile constituents of Bacillus thuringiensis were captured by headspace solid phase micro-extraction technology (HS-SPME) and identified by gas chromatography-mass spectrometry (GC-MS) tech-nology. The optimal method was used to analyze the volatile constituents of Bacillus thuringiensis FJAT-12, which was a high efficient strain separated by our lab, investigated from the culture way, adsorption pattern and fibers type. Results Bacillus thuringiensis FJAT-12 was better cultured by NA liquid medium, and volatile vial was maintained in a water bath at 50 ℃ for equilibrating (180 min) and then extracted by 65 µm PDMS/DVB fibers for 60 min. The mainly volatile constituents of Bt were 6-methyl-2-Heptanone, 4-methyl-1,3-Benzenediamine, Benzyl Alcohol, 3,5-diethyl-2-methyl-Pyrazine, 2-methyl-Naphthalene, 2,3-Dimethyl-5-isopentylpyrazine

  18. Enzymic synthesis of labelled chiral substances.

    Science.gov (United States)

    Battersby, A R

    1985-01-01

    The enzymic synthesis of chiral substances in which one hydrogen atom of a methylene group has been replaced by deuterium or tritium is illustrated. Such labelled products can be used to determine the stereochemistry of other enzyme-catalysed reactions.

  19. HPLC法测定注射用阿奇霉素枸橼酸二氢钠的含量及有关物质%Content Determination and Related Substances of Azithromycin Sodium Dihydrogen Citrate for Injection by HPLC

    Institute of Scientific and Technical Information of China (English)

    柏大为; 陈佳

    2013-01-01

    OBJECTIVE: To establish a method for the content determination of azithromycin and its related substances in Azithromycin sodium dihydrogen citrate for injection. METHODS: HPLC method was adopted and compared with the results of standard method for content determination of the preparation (antibiotic microbiological assay) and TLC for related substances. The determination was performed on C18 MG II column with mobile phase consisted of phosphate buffer (pH 8.2)-acetonitrile (45 : 55, VIV) at flow rate of 1.0 ml/min. The detection wavelength was set at 215 nm and column temperature was 35 ℃. RESULTS: The linear range for azithromycin was 0.5-3.0 mg/ml (r=0.999 9) with average recovery of 100.2% (RSD=0.7%, n=9). The results of content determination of main component are concordant with those of standard method. The method for the determination of related substance was better than previous method. CONCLUSIONS: The method is simple, accurate, specific and reproducible, and suitable for the content determination of azithromycin and its related substances in Azithromycin sodium dihydrogen citrate for injection.%目的:建立注射用阿奇霉素枸橼酸二氢钠含量和有关物质的测定方法.方法:采用高效液相色谱法,并与该制剂标准采用的含量测定方法(抗生素微生物检定法)及有关物质检查方法(薄层色谱法)测定结果进行比较.色谱柱为资生堂C18MGⅡ柱,流动相为磷酸盐缓冲液(pn 8.2)-乙腈(45∶55,Ⅴ/Ⅴ),流速为1.0 ml/min,检测波长为215 nm,柱温为35℃.结果:阿奇霉素检测质量浓度线性范围为0.5~3.0 mg/ml(r=0.999 9),平均回收率为100.2%,RSD=0.7%(n=9).本方法主药含量测定结果与原标准方法结果一致,有关物质检查方法优于原标准方法.结论:建立的方法简便、准确、专属性强、重复性好,可用于注射用阿奇霉素枸橼酸二氢钠含量及有关物质的测定.

  20. Development and Validation of Stability-Indicating RP-UPLC Method for Simultaneous Determination of Related Substances of S(−Amlodipine and S(−Metoprolol Succinate in Fixed Dose Combination Tablet Dosage Form

    Directory of Open Access Journals (Sweden)

    Suresh Shitole

    2014-01-01

    Full Text Available A novel, rapid, accurate, sensitive, precise, and stability-indicating reverse-phase ultra-performance liquid chromatographic (RP-UPLC method was developed and validated for determination of related substances of S(−Amlodipine and S(−Metoprolol Succinate in fixed dose combination tablet dosage form. The chromatographic separation was achieved with the use of Acquity UPLC HSS T3, 1.8 μm, 2.1 × 100 mm analytical column at 45°C employing a gradient elution. Mobile phase consisting of mobile phase-A (solution containing 5.0 gm of sodium dihydrogen phosphate monohydrate per liter of water and Acetonitrile in the ratio of 95 : 5 and mobile phase-B (Acetonitrile was used at a flow rate of 0.5 mL min−1 with injection volume of 10 μL and the detection was done at 232 nm using UV detector. The retention times of S(−Metoprolol Succinate and S(−Amlodipine were found to be 2.8 minutes and 8.1 minutes, respectively. During method validation all the parameters were evaluated as per ICH guidelines, which remained well within acceptable limits. This method can be used for the estimation of related substances of S(−Amlodipine and S(−Metoprolol Succinate in fixed dose combination tablet dosage form.

  1. Radioactivity in French bottled waters

    Energy Technology Data Exchange (ETDEWEB)

    Loyen, J.; Brassac, A.; Augeray, C.; Fayolle, C.; Gleizes, M. [Institut de Radioprotection et de Surete Nucleaire - IRSN (France)

    2014-07-01

    As IRSN is considered as a reference laboratory for radioactivity measurements, French health ministry and French nuclear safety authority asked IRSN to carry out a study in order to get a fresh and complete status of radiological water quality of French bottled waters. The study was carried out during 12 months in 2012. A total of 142 bottled waters samples were analyzed (75 spring waters and 67 natural mineral waters). The laboratories of IRSN were in charge of: - systematic measurement of radioactivity following requirements of the French health ministry (Circulaire du 13/06/2007) regarding the monitoring and management of sanitary risk linked to the presence of radionuclides in drinking waters (natural mineral waters excepted). - systematic uranium mass concentration determination; - a few radon-222 gas measurements for waters in glass bottles. This study is a flash assessment of radiological characteristics of French bottled waters, at the analysis date for the sample received. It was done in informative way and was not done for regulatory control purposes.. This study has shown that: - all bottled waters analyzed have a tritium activity concentration lower than the quality reference value of 100 Bq/l of the French regulation; - More than 105 bottled waters analyzed (80% of the springs waters and 70% of natural mineral waters received) have a gross alpha activity concentration lower than the guideline value of 0,1 Bq/l of the French regulation; - All bottled waters analyzed have a residual gross beta activity concentration lower than the guideline value of 1 Bq/l of the French regulation; - All bottled waters analyzed have a uranium mass concentration lower than the provisory guideline value of 30 μg/l of the WHO for drinking waters; - radon-222 was only significantly measured once upon 6 glass bottled waters with a value far below the reference value of 100 Bq/l of the future European Directive on drinking waters. For 32 bottled waters with gross alpha

  2. Characterization of low energy radioactive beams using direct reactions

    DEFF Research Database (Denmark)

    Johansen, J.G.; Fraser, M.A.; Bildstein, V.

    2013-01-01

    We demonstrate a new technique to determine the beam structure of low energy radioactive beams using coincidence events from a direct reaction. The technique will be described and tested using Geant4 simulations. We use the technique to determine for the first time the width, divergence and energy...... of an accelerated radioactive beam produced at ISOLDE. We use data from an experiment with an 11Be beam incident on a deuteron target producing 10Be from a (d,t) reaction. The T-REX Si detector array was used for particle detection, but the technique is applicable for other setups....

  3. Environmental radioactivity survey in Andong

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, Zi Hong; Jo, Kum Ju [Andong Regional Radioactivity Monitoring Station, Andong National Univ., Andong (Korea, Republic of)

    2002-12-15

    The objectives of the project are to monitor an abnormal level in Andong area and to provide a base-line data on environmental radiation/radioactivity levels in case of any radiological emergency situation. The project is important in view of protecting the public health from the potential hazards of radiation and keeping up the clean environment. This report summarizes and interprets environmental radiation/radioactivity monitoring samples Gamma exposure rates, airborne dust, precipitation, fall-out and drinking-water. Environmental samples 2 kinds of indicator plant, 4 kinds of mushroom, 7 kinds of nut and seeds, and drinking waters. Among the all 2002 radiological monitoring and environmental data in Andong area were not found the extraordinary data. And a nation-wide environmental radiation/radioactivity level survey results were all background levels attributed to terrestrial and cosmic radiation.

  4. Final disposal of radioactive waste

    Directory of Open Access Journals (Sweden)

    Freiesleben H.

    2013-06-01

    Full Text Available In this paper the origin and properties of radioactive waste as well as its classification scheme (low-level waste – LLW, intermediate-level waste – ILW, high-level waste – HLW are presented. The various options for conditioning of waste of different levels of radioactivity are reviewed. The composition, radiotoxicity and reprocessing of spent fuel and their effect on storage and options for final disposal are discussed. The current situation of final waste disposal in a selected number of countries is mentioned. Also, the role of the International Atomic Energy Agency with regard to the development and monitoring of international safety standards for both spent nuclear fuel and radioactive waste management is described.

  5. Low-level Radioactivity Measurements

    Energy Technology Data Exchange (ETDEWEB)

    Hurtgen, C

    2001-04-01

    The objectives of the research performed in the area of low-level radioactivity measurements are (1) to maintain and develop techniques for the measurement of low-level environmental and biological samples, (2) to measure these samples by means of low-background counters (liquid scintillators, proportional counters, ZnS counters, alpha spectrometry), (3) to support and advice the nuclear and non-nuclear industry in matters concerning radioactive contamination and/or low-level radioactivity measurements; (4) to maintain the quality assurance system according to the EN45001/ISO17025 standard; and (5) to assess the internal dose from occupational intakes of radionuclides of workers of the nuclear industry. Progress and achievements in these areas in 2000 are reported.

  6. Low-level Radioactivity Measurements

    Energy Technology Data Exchange (ETDEWEB)

    Hurtgen, C

    2002-04-01

    The objectives of the research performed in the area of low-level radioactivity measurements are (1) to maintain and develop techniques for the measurement of low-level environmental and biological samples, (2) to measure these samples by means of low-background counters (liquid scintillators, proportional counters, ZnS counters, alpha spectrometry), (3) to support and advise the nuclear and non-nuclear industry on problems of radioactive contamination and low-level radioactivity measurements; (4) to maintain and improve the quality assurance system according to the ISO17025 standard; and (5) to assess the internal dose from occupational intakes of radionuclides of workers of the nuclear industry. Progress and achievements in these areas in 2001 are reported.

  7. RP-HPLC法测定抗癌新药WF210的含量和有关物质%Determination of New Anticancer Drug WF210 and Its Related Substances by RP-HPLC

    Institute of Scientific and Technical Information of China (English)

    王曼曼; 霍艳双; 李清; 崔红霞; 陈晓辉; 毕开顺

    2012-01-01

    OBJECTIVE: To establish a method for the content determination of new anticancer drug WF210 and its related substances. METHODS: RP-HPLC method was adopted. The determination was performed on Diamonsil C18 column with mobile phase consisted of acetonitrile-methanol-water(60:20:20)at the flow rate of 1.0 mL·min-1. UV detection wavelength was set at 238 nm and column temperature was 30 ℃. RESULTS: The linear range of WF210 was 5.045~50.45 μg·mL-1 (r=0.999 8) with an average recovery of 100.0% (RSD=0.5%). The related substances of WF210 could be completely separated from WF210. The limit of detection was 0.8 ng. CONCLUSION: The method is simple, accurate and reproducible for the content determination of WF210 and its related substances.%目的:建立测定抗癌新药乙酰肼类化合物WF210的含量及有关物质的方法.方法:采用反相高效液相色谱法.色谱柱为DiamonsilC18,流动相为乙腈-甲醇-水(60:20:20),流速为1.0mL·min-1,紫外检测波长为238nm,柱温为30℃.结果:WF210检测浓度线性范围为5.045~50.45 μg·mL-1(r=0.9998),平均回收率为100.0% (RSD=0.5%);主成分与其有关物质分离良好,检测限为0.8 ng.结论:该方法简便、准确、重复性好,可用于WF210的含量测定和有关物质的检查.

  8. Content Determination of Related Substance in Cefpodoxime Proxetil Dispersible Tablet by HPLC%HPLC法测定头孢泊肟酯分散片中有关物质的含量

    Institute of Scientific and Technical Information of China (English)

    俞平

    2011-01-01

    目的:建立测定头孢泊肟酯分散片中有关物质含量的方法.方法:采用高效液相色谱法.色谱柱为ODS(C18)柱,流动相为水-甲醇(55∶45),流速为2.0 mL· min-1,检测波长为240nm,柱温为25℃,进样量为20μL.结果:头孢泊肟酯A、头孢泊肟酯B与杂质能完全分离;头孢泊肟酯A最小检测限为1.6 ng,头孢泊肟酯B最小检测限为1.2 ng,其有关物质含量均<4.0%.结论:该方法简便、准确,灵敏度高,专属性强,可用于头孢泊肟酯分散片有关物质含量的测定.%OBJECTIVE: To establish the method for the content determination of the related substances in Cefpodoxime prox-etil tablet. METHODS: HPLC method was adopted. The determination was performed on ODS(C18) column with water-methanol (55:45) as mobile phase at the flow rate of 2.0 mL -min-1. The detection wavelength was set at 240 am and column temperature was 25 X. Injection volume was 20 nL. RESULTS: Cefpodoxime proxetil A and cefpodoxime proxetil B could be separated from impurity completely. The lowest detectable limit of cefpodoxime proxetil A was 1.6 ng and that of cefpodoxime proxetil B was 1.2 ng. The contents of the related substances were less than 4.0%. CONCLUSION: The method is convenient, accurate, sensitive and specific. It is suitable for the content determination of the related substances in Cefpodoxime proxetil dispersible tablet.

  9. Radioactive Ion Beams and Radiopharmaceuticals

    Science.gov (United States)

    Laxdal, R. E.; Morton, A. C.; Schaffer, P.

    2014-02-01

    Experiments performed at radioactive ion beam facilities shed new light on nuclear physics and nuclear structure, as well as nuclear astrophysics, materials science and medical science. The many existing facilities, as well as the new generation of facilities being built and those proposed for the future, are a testament to the high interest in this rapidly expanding field. The opportunities inherent in radioactive beam facilities have enabled the search for radioisotopes suitable for medical diagnosis or therapy. In this article, an overview of the production techniques and the current status of RIB facilities and proposals will be presented. In addition, accelerator-generated radiopharmaceuticals will be reviewed.

  10. Predicted halflives for cluster radioactivities

    Energy Technology Data Exchange (ETDEWEB)

    Poenaru, D.N. (Institutul Central de Fizica, Bucharest (Romania); Frankfurt Univ. (Germany, F.R.). Inst. fuer Theoretische Physik); Greiner, W. (Frankfurt Univ. (Germany, F.R.). Inst. fuer Theoretische Physik); Ivascu, M. (Institutul Central de Fizica, Bucharest (Romania))

    1989-10-09

    The main results of the analytical superasymmetric fission model, describing in a unified manner cluster radioactivities, alpha-decay and cold fission processes, are briefly reviewed. Predicted halflives for {sup 14}C, {sup 24,25,26}Ne, {sup 28,30}Mg and {sup 32}Si radioactivities in the range 10{sup 11}-10{sup 26} s and the corresponding branching ratios relative to {alpha}-decay 10{sup -16}-10{sup -9} have been experimentally confirmed within 1.5 orders of magnitude. (orig.).

  11. Simultaneous Determination of a Variety of Related Substances in Clotri-mazole Tablets by HPLC%HPLC法同时测定克霉唑片中多种有关物质

    Institute of Scientific and Technical Information of China (English)

    何淑旺; 王雪敏; 谢晓燕; 郑娣; 岳德仁

    2016-01-01

    目的:建立HPLC法同时检测克霉唑片中多种有关物质。方法:采用InertSustain-C18色谱柱(4.6 mm×150 mm,5μm),以磷酸二氢钾-四丁基硫酸氢铵溶液为流动相A、乙腈为流动相B,按梯度进行洗脱,流速为1.0 mL·min-1,检测波长为210 nm。结果:克霉唑与有关物质A、B、E、F在该色谱条件下均完全分离,在0.08~3.03μg·mL-1浓度范围内克霉唑与峰面积线性关系良好(r=0.9998);有关物质A在0.04~3.42μg·mL-1范围内与峰面积线性关系良好(r=0.9999),平均回收率为99.43%,RSD=1.72%(n=9);有关物质E在0.42~3.58μg·mL-1范围内与峰面积线性关系良好(r=0.9997),平均回收率为100.10%,RSD=1.17%(n=9)。结论:HPLC方法准确、简便、快速,适用于同时测定克霉唑片中多种有关物质。%Obje ctive: To develop an HPLC method for simultaneous determining a variety of related substances in clotrimazole tablets. Methods: The separation was carried out on an InertSustain-C18 (4.6 mm ×150 mm, 5μm) column with a mobile phase of potassium dihydrogen phosphate-tetrabutylammonium hydrogen sulfate solvent (A) and acetonitrile (B) in gradient, at a flow rate of 1.0 mL·min-1. The detection wave was set at 210 nm. Results: Clotrimazole was well separated with related substances A, B, E and F under the above chromatographic conditions. The calibration curve was linear (r=0.9998) within the range of 0.08-3.03 μg·mL-1 for clotrimazole. The calibration curve was linear (r=0.9999) within the range of 0.04-3.42 μg·mL-1 for related substance A, the average recovery rate was 99.43% with RSD at 1.72% (n=9). The calibration curve was linear (r=0.9997) within the range of 0.42-3.58 μg·mL-1 for related substance E, the average recovery rate was 100.10% with RSD at 1.17% (n=9). Conclusion: This method can be used to simultaneously separate and determine clotrimazole and a variety of related substances in clotrimazole

  12. Development of monitoring technology for environmental radioactivity

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Chang Woo; Cho, Young Hyun; Lee, M. H.; Choi, K. S.; Hong, K. H.; Sin, H. S.; Kim, M. K.; Pak, J. H

    2000-05-01

    The accurate and reliable determination techniques of the radioactive isotopes in environmental samples are very important to protect public health from the potential hazards of radiation. Isolation and purification of radiostrontium from environmental aqueous sample was performed by using strontium selectively binding resin (Sr-spec) and strontium selectively permeable liquid membrane. Radioactivity of radiostrontium was measured by liquid scintillation counter coupled with dual counting window and spectrum unfolding method. With combustion apparatus a new determination of Tc-99 in the environmental samples was developed for overcoming demerits of conventional TBP extraction method. An optimized method for determining beta-emitting {sup 2}41Pu in the presence of alpha-emitting nuclides was developed using a liquid scintillation counting system. A method for measuring Rn-222 and Ra-226 in aqueous sample using liquid scintillation counting technique has studied. On-line measurement system coupled with ion chromatography and portable liquid scintillation detector was developed. U and Th measured by inductively coupled plasma mass spectrometry (ICP-MS). The mehtod of flow-injection preconcentration for the analysis of U and Th in seawater was developed. A new electrodeposition method for alpha spectrometry was developed.

  13. Is It the Music? Peer Substance Use as a Mediator of the Link between Music Preferences and Adolescent Substance Use

    Science.gov (United States)

    Mulder, Juul; Ter Bogt, Tom F. M.; Raaijmakers, Quinten A. W.; Gabhainn, Saoirse Nic; Monshouwer, Karin; Vollebergh, Wilma A. M.

    2010-01-01

    Both music preferences and the substance use behavior of peers are important elements in explaining adolescent substance use. The extent to which music preference and peer use overlap in explaining adolescent substance use remains to be determined. A nationally representative sample of 7324 Dutch school-going adolescents (aged 12-16) provided data…

  14. Environmental radioactivity assessment for Bayburt, Turkey

    Energy Technology Data Exchange (ETDEWEB)

    Kucukomeroglu, B; Kurnaz, A; Cevik, U [Department of Physics, Karadeniz Technical University, Trabzon (Turkey); Damla, N [Department of Physics, Batman University, Batman (Turkey); Celebi, N; Ataksor, B; Taskin, H [Cekmece Nuclear Research and Training Centre, Altinsehir Yolu, Halkali, Istanbul (Turkey)], E-mail: ndamla@ktu.edu.tr

    2009-09-01

    This study assesses the results of environmental radioactivity measurements for Bayburt Province in the Eastern Black Sea area of Turkey. Using {gamma}-ray spectrometry, activity concentrations of the natural radionuclides {sup 226}Ra, {sup 232}Th and {sup 40}K and a fission product {sup 137}Cs were investigated in soil samples. The activity concentrations of {sup 226}Ra, {sup 232}Th and {sup 40}K in various building materials such as sand, cement and marble and in drinking waters were determined. The activity concentrations vary from 16 to 54 Bq kg{sup -1} for {sup 226}Ra, from 10 to 21 Bq kg{sup -1} for {sup 232}Th and from 113 to 542 Bq kg{sup -1} for {sup 40}K in building materials. The mean specific activity concentrations of {sup 226}Ra, {sup 232}Th and {sup 40}K in drinking waters were 93, 30 and 504 mBq l{sup -1}, respectively. The concentrations of gross {alpha} and {beta} radioactivity in drinking water samples collected from four different sampling stations have been determined. The results show that the gross {alpha} and {beta} activities are lower than the screening levels given by the World Health Organization (WHO), which are a maximum contaminant level of 0.5 Bq l{sup -1} and 1.0 Bq l{sup -1} gross {alpha} and {beta} radioactivity, respectively, in drinking water. Indoor radon measurements were made in 44 dwellings in Bayburt by using Cr-39 detectors. Radon concentrations in dwellings in Bayburt varied from 17 to 125 Bq m{sup -3} and the average value was 56 Bq m{sup -3}. The results obtained in this study indicate that the region has a background radiation level that is within the typical natural range and shows no significant departures from other parts of the country.

  15. Measurement of natural and 137Cs radioactivity concentrations at Izmit Bay (Marmara Sea), Turkey

    Science.gov (United States)

    Öksüz, I.; Güray, R. T.; Özkan, N.; Yalçin, C.; Ergül, H. A.; Aksan, S.

    2016-03-01

    In order to determine the radioactivity level at Izmit Bay Marmara Sea, marine sediment samples were collected from five different locations. The radioactivity concentrations of naturally occurring 238U, 232Th and 40K isotopes and also that of an artificial isotope 137Cs were measured by using gamma-ray spectroscopy. Preliminary results show that the radioactivity concentrations of 238U and 232Th isotopes are lower than the average worldwide values while the radioactivity concentrations of the 40K are higher than the average worldwide value. A small amount of 137Cs contamination, which might be caused by the Chernobyl accident, was also detected.

  16. Purification of the off-gases of the process of radioactive waste vitrification in induction melter

    Energy Technology Data Exchange (ETDEWEB)

    Gorbunov, V. A.; Katannikov, I. S.; Knyasev, O. A.; Kornev, V. I.; Lifanov, F. A.; Polkanov, M. A.; Savkin, A. E. [Moscow Scientific and Inndustrial Association RADON, Moscow (Russian Federation)

    1999-07-01

    Moscow SIA RADON has developed the method of vitrifying both radioactive ashes, arising from radioactive waste incineration, and liquid radioactive waste in induction melter. In the experimental plant the characteristics of off-gases were determined and various constructions of filters and filtering materials for dust trapping were tested. On the base of test results the plant for liquid radioactive waste vitrification has been constructed on the base of induction melter {sup c}old crucible{sup ,} equipped with modern effective dust and gas purification system, consisting of filtration unit, absorption unit and unit for nitrogen oxide catalytic reduction. (author). 3 refs., 9 tabs., 3 figs.

  17. Determination of Contents 3-amide-indole Derivative and Related Substances%3-酰胺基-吲哚类衍生物及其有关物质含量测定

    Institute of Scientific and Technical Information of China (English)

    申冬妮; 杨建云; 肖炳坤; 黄荣清

    2014-01-01

    Objective To establish a RP-HPLC method for the determination of 3-amide-indole derivative and its related substances. Methods Diamonsil C18(250 mmí4. 6 mm,5 μm) column was adopted. The mobile phase consisted of a mixture of methanol-acetonitrile-water(431245) at the flow rate of 1. 0 mL·min-1 . The wavelength for ultraviolet detection was 224 nm. The injection volume was 20 μL and the column temperature was room temperature. Results 3-amide-indole derivative and related substances could be well separated. The linearity of the 3-amide-indole derivative curve was well correlated (r=0. 999 7) within the range of 0. 04-0. 16 mg·mL-1. The RSD was 0. 52%with good repeatability. The detection limit was 2. 65 ng. Conclusion The method is accurate,reliable,sensitive and specific,which could be used for the determination of 3-amide-indolederivative and related substances.%目的:建立反相高效液相色谱法测定3-酰胺基-吲哚类衍生物及其有关物质含量。方法采用Diamonsil C18(250 mm×4.6 mm,5μm)色谱柱,流动相为甲醇乙腈水(431245),流速1.0 mL·min-1;检测波长224 nm;进样量20μL;柱温:室温。结果3-酰胺基-吲哚类衍生物与有关物质能达到较好分离,在0.04~0.16 mg·mL-1浓度范围内与峰面积线性关系良好,r=0.9997;方法重复性RSD为0.52%;检测限为2.65 ng。结论该方法准确可靠,灵敏度高,专属性好,可用于3-酰胺基-吲哚类衍生物及其有关物质含量测定。

  18. HPLC法测定双氯芬酸钠盐酸利多卡因注射液的有关物质%Determination of Diclofenac sodium and Lidocaine Hydrochloride Injection related substances by HPLC

    Institute of Scientific and Technical Information of China (English)

    李春盈; 张玉英

    2016-01-01

    Objective: To establish a HPLC method for the determination of Diclofenac sodium and Lidocaine Hydrochloride Injection related substances. Methods:The sample was analyzed on a C18(250mm×4.6mm,5μm)column with mobile phase consisting of methonal-4% Acetic Acid (65∶35). The flow rate was 1.0mL/min and the detection wavelength was 245nm. Results: The peaks of Diclofenac, Lidocaine and its impurities were completely separated. The regression equation for related substances was A=22.139 ×C+2.3422,r=0.9995 (n=5). The detection limit was 0.0089%. Conclusions: This method is convenient, quick and reproducible for the quantitative determination of Diclofenac sodium and Lidocaine Hydrochloride Injection in the related substances.%目的:建立HPLC法测定复方制剂双氯芬酸钠盐酸利多卡因注射液中的有关物质。方法:采用反相高效液相色谱法,以自身对照法计算双氯芬酸钠盐酸利多卡因注射液有关物质的量。用C18(250mm×4.6mm,5μm)色谱柱,以甲醇-4%冰醋酸溶液(65∶35)为流动相,流速1.0mL/min,于波长为245nm处检测。结果:双氯芬酸钠与利多卡因杂质完全分离,有关物质的线性回归方程为A=22.139×C+2.3422,相关系数为r=0.9995(n=5);方法的最低检出限为0.0089%。结论:实验证明该法简便快捷,能准确地测定样品的有关物质。

  19. Determination of Related Substances of Citicoline Sodium Injection by High Performance Liquid Chromatography%高效液相色谱法测定胞磷胆碱钠注射液中的有关物质

    Institute of Scientific and Technical Information of China (English)

    赵明; 高锦; 嵇扬; 沈娟; 刘俊; 祁冰洁; 程洋; 赵春杰

    2011-01-01

    Objective To establish an high performance liquid chromatography method for the determination of related substances of citicoline sodium injection. Methods Seperation was performed on a C18 column(250 mm x 4.6 mm,5 μm)and the mobile phase was phosphate buffer (potassium dihydrogen phosphate solution (0.1 mol/L) was mixed with the same amount of tetrabutylammonium hydroxide solution (0.01 mol/L) ,with the pH value of the mixture adjusted to 5.2 by phosphate]-methanol (96:4) at a folw rate of 0.8 ml/min. The column temperature was set at 30℃ and the detection wavelength was 276 nm. Results A good separation was achieved for citicoline sodium and its related substances. The limit of detection was 0.006 ng. Conclusion The method is simple, specific, sensitive and applicable to the determination of related substances of citicoline sodium injection.%目的 建立胞磷胆碱钠注射液中有关物质的高效液相色谱测定方法.方法 采用C18柱(250 mm ×4.6 mm,5μm),以磷酸盐缓冲液(0.1 mol/L磷酸二氢钾与0.01 mol/L四丁基氢氧化铵等量混合,用磷酸调节pH值至5.2)-甲醇(96:4)为流动相,流速:0.8 ml/min,检测波长:276 nm,柱温:30℃.结果 经破坏性试验后的胞磷胆碱钠注射液中各有关物质与胞磷胆碱分离良好;最低检测限为0.006 ng.结论 该方法简便、专属性及灵敏度好,可用于胞磷胆碱钠注射液中有关物质的检查.

  20. 梯度洗脱HPLC法测定苄星青霉素中的有关物质%Determination of related substances of benzathine benzylpenicillin by gradient elution HPLC method

    Institute of Scientific and Technical Information of China (English)

    陈汝红

    2012-01-01

    目的 建立测定苄星青霉素有关物质的梯度洗脱HPLC法.方法 采用端基封尾的C18柱,流动相A为0.05mol/L磷酸二氢钾溶液(用磷酸调节pH值至3.1),流动相B为甲醇,流速1.0mL/min,线性梯度洗脱,检测波长220nm,柱温40℃.结果 二苄基乙二胺和青霉素分别与相邻杂质峰分离完全,二苄基乙二胺的检测限为2.5ng,青霉素的检测限为0.6ng.结论 本法专属、灵敏,可作为苄星青霉素有关物质的测定方法.%Objective To develop gradient elution HPLC method for the determination of related substances in benzathine benzylpenicillin. Methods The HPLC method was carried on a column packed with end-capped octadecylsilance bonded silica gel, 0.05mol/L potassium dihydrogen solution (adjust pH to 3.1 with phosphoric acid ) as mobile phase A and methanol as mobile phase B, the flow rate was 1.0 mL per minute, linear gradient elution. The column temperature was 40°C. The detection wavelength was 220 nm. Results Benzathine and benzylpenicillin could be completely separated from the other impurities respectively. Limit of detection for benzathine was 2.5ng. Limit of detection for benzylpenicillin was 0.6ng. Conclusion The proposed HPLC method was specific and sensitive. The method could be used for the determination of related substances in benzathine benzylpenicillin.

  1. High-Level Radioactive Waste.

    Science.gov (United States)

    Hayden, Howard C.

    1995-01-01

    Presents a method to calculate the amount of high-level radioactive waste by taking into consideration the following factors: the fission process that yields the waste, identification of the waste, the energy required to run a 1-GWe plant for one year, and the uranium mass required to produce that energy. Briefly discusses waste disposal and…

  2. Traps for neutral radioactive atoms

    CERN Document Server

    Sprouse, G D; Grossman, J S; Orozco, L A; Pearson, M R

    2002-01-01

    We describe several methods for efficiently injecting a small number of radioactive atoms into a laser trap. The characteristics of laser traps that make them desirable for physics experiments are discussed and several different experimental directions are described. We describe recent experiments with the alkali element Fr and point to future directions of the neutral atom trapping program.

  3. Keeping an Eye on Radioactivity

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    China sets up a national testing system for levels of radiation from various sources Radioactive iodine had been detected in the air above several regions of China,said China’s National Nuclear Emergency Coordination Committee on March 29.The regions include Heilongjiang

  4. Mass measurement of radioactive isotopes

    CERN Document Server

    Kluge, H J; Scheidenberger, C

    2004-01-01

    The highest precision in mass measurements on short-lived radionuclides is obtained using trapping and cooling techniques. Here, the experimental storage ring (ESR) at GSI/Darmstadt and the tandem Penning trap mass spectrometer ISOLTRAP at ISOLDE/CERN play an important role. Status and recent results on mass measurements of radioactive nuclides with ESR and ISOLTRAP are summarized.

  5. Gradient HPLC determination of related substances of cefmenoxime hydrochloride drug substance and its sterillized powder for injection%梯度洗脱HPLC法测定盐酸头孢甲肟原料药及注射粉末的有关物质

    Institute of Scientific and Technical Information of China (English)

    阮丹; 王红波; 王建

    2012-01-01

    Objective To develop gradient HPLC method for the determination of related substances of cefmenoxime hydrochloride drug substance and its sterillized powder for injection. Methods The column was Alltima C18(250×4.6mm, 5μm). The mobile phase consisted of water-acetic acid acetonitrile(85:1.7:15)(A) and water-acetic acid-acetonitrile(50:1.7:50)(B) with gradient program. The flow rate was 1.0mL/min and the detection wavelength was 254nm. Results Good separation of cefmenoxime hydrochloride and four intermediates could be achieved. The RSD of precision was 2.9%. The detection limit was 0.01~0.1ug/mL. Conclusion The method is simple, sensitive and reproducible, and can be used for quality control of cefmenoxime hydrochloride.%目的 建立梯度洗脱HPLC法,测定盐酸头孢甲肟原料药及其注射粉末的有关物质.方法 采用Alltima C18(250×4.6mm,5μm)柱,流动相A为水-冰醋酸-乙腈(85:1.7:15),流动相B为水-冰醋酸-乙腈(50:1.7:50),流速为1.0mL/min,线性梯度洗脱,检测波长为254nm.结果 盐酸头孢甲肟与4种中间体、副产物完全分离.重复性RSD为2.9%,检测限为0.01~0.1 μg/mL.结论 方法简便、灵敏、重复性好,可用于本品的质量控制.

  6. Research on the Effects of the Contents of Radioactive Elements on Granularity and Climate Change: An Example of SZK1 and SZK2 Drill Holes Strata in the Fuzhou Basin

    Institute of Scientific and Technical Information of China (English)

    Zheng Rongzhang; Xu Xiwei; Li Jianping

    2006-01-01

    Based on the content of radioactive elements (U, Th, K) of strata in two drill holes in the Fuzhou basin, and combined with the result of spore-pollen analysis, the relationship between radioactivity and lithology and deposit environments is discussed and the results show that the content of radioactive substances is related to the granularity and lithology in sediment, and it is higher in argillaceous sediment (e.g. silt and clay), lower in sand sediment and in the middle in gravels between the above two kinds of sediment. The content of radioactive substances is also related to paleoclimate. A warm and humid environment is propitious to the deposition of radioactive substances, while a cool and dry climate is just the reverse.

  7. Indian programme on radioactive waste management

    Indian Academy of Sciences (India)

    P K Wattal

    2013-10-01

    The primary objective of radioactive waste management is protection of human health, environment and future generation. This article describes, briefly, the Indian programme on management of different radioactive wastes arising in the entire nuclear fuel cycle adhering to this objective.

  8. Radioactive content in aerosols and rainwater; Contenido radiactivo en aerosoles y agua de lluvia

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez Perestelo, N.; Lopez Perez, M.; Rodriguez, S.; Duarte, X.; Catalan, A.; Fernandez de Aldecoa, J. C.; Hernandez, J.

    2013-07-01

    The environmental radiological characterization of a place requires knowledge of the radioactive contents of its components, such as air (aerosol), rain, soil, etc ... Inhalation of radioactive aerosols in the air remains the main component of the total dose to the world population. This work focuses on its determination. (Author)

  9. Radioactive releases at the Savannah River Site, 1954--1988

    Energy Technology Data Exchange (ETDEWEB)

    Hetrick, C.S.; Martin, D.K.

    1988-01-01

    Radioactive Releases at the Savannah River Site, 1954--1988 (WSRC-RP-89-737) is the continuation of a series of reports, previously titled Releases of Radioactivity at the Savannah River Plant (DPSU-1-YR-25). The series reflects the use of air and liquid effluent sample analyses in determining the amount of radioactivity released from Savannah River Site (SRS) operations. The identification and characterization of these source terms since plant startup in 1954 have aided Site personnel in confining and limiting the amount of radioactivity released to the environment from SRS facilities. Data contained in this report are used for a variety of purposes, including the calculation of offsite dose estimates and aiding special environmental studies. This document is an effluent/source term report. The report is divided into four summary sections. Summary A details volumes of air and water released from emission sources since plant startup. Summary B lists annual radioactive release data from these emission sources, grouped by nuclide and area. Summary C provides yearly totals of radioactive releases by radionuclide, under the headings Atmospheric,'' Liquid to streams,'' or Liquid to Seepage Basins'' accordingly. Monthly radioactive releases from each emission source from 1986 to 1988 are found in Summary D. Where appropriate, headings in the summary tables have been changed to clarify and simplify emission data (see Appendix B). Additionally, any new discharge points, such as the liquid discharge from the Effluent Treatment Facility (ETF), are included in this report. A listing of 1988 source term and onsite discharge designations is provided in Appendix C. 36 refs.

  10. Rapid and simultaneous determination of sulfonate ester genotoxic impurities in drug substance by liquid chromatography coupled to tandem mass spectrometry: comparison of different ionization modes.

    Science.gov (United States)

    Guo, Tian; Shi, Yuanyuan; Zheng, Li; Feng, Feng; Zheng, Feng; Liu, Wenyuan

    2014-08-15

    Two ionization techniques for liquid chromatography-mass spectrometry (LC-MS) determination of sulfonate ester potentially genotoxic impurities (PGIs) were evaluated. Twelve PGIs including methyl, ethyl, propyl and isopropyl esters of methanesulfonate, benzenesulfonate and p-toluenesulfonate were studied in this research. Electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) sources were compared in terms of performance and quality parameters for detection of the twelve PGIs. Their mass spectra obtained by APCI and ESI were very different in both fragment ions and relative abundances. In APCI negative ion mode the twelve sulfonate esters showed their stable precursor ions of [M-alkyl](-), which readily yielded product ions of [M-alkyl-CH3](-) (for aliphatic sulfonate esters) or [M-alkyl-SO2](-) (for aromatic sulfonate esters) with collision-induced dissociation (CID) applied; and working in selected reaction monitoring (SRM) mode has allowed limits of detection to be decreased. In the case of ESI ionization, these compounds showed their precursor ions [M+H](+), but their abundance was easily competed by formation of ions [M+NH4](+) and/or [M+Na](+), which led to poor analytical sensitivity and reproducibility. Although mobile phase additives could enhance the responses of adduct ions like [M+NH4](+) and [M+Na](+), no improvement was obtained when using SRM mode. Twelve sulfonate esters were systematically compared and APCI was shown to be a better ionization technique for rapid and sensitive determination of these PGIs. Performance of the developed approach for rapid determination of 12 PGIs was also evaluated. Quality parameters were established and good precision (relative standard deviations <8%) and very low limits (2-4ng/mL) of detection were obtained, mainly when using APCI in SRM mode.

  11. Environmental aspects of commercial radioactive waste management

    Energy Technology Data Exchange (ETDEWEB)

    1979-05-01

    Volume 2 contains chapters 6 through 10: environmental effects related to radioactive waste management associated with LWR fuel reprocessing - mixed-oxide fuel fabrication plant; environmental effects related to transporting radioactive wastes associated with LWR fuel reprocessing and fabrication; environmental effects related to radioactive waste management associated with LWR fuel reprocessing - retrievable waste storage facility; environmental effects related to geologic isolation of LWR fuel reprocessing wastes; and integrated systems for commercial radioactive waste management. (LK)

  12. Radioactive waste caracterisation by neutron activation

    OpenAIRE

    Nicol, Tangi

    2016-01-01

    Nuclear activities produce radioactive wastes classified following their radioactive level and decay time. An accurate characterization is necessary for efficient classification and management. Medium and high level wastes containing long lived radioactive isotopes will be stored in deep geological storage for hundreds of thousands years. At the end of this period, it is essential to ensure that the wastes do not represent any risk for humans and environment, not only from radioactive point o...

  13. HPLC法测定胆维丁原料药的含量和有关物质%Determination of the Content of Cholecalciferol Cholesterol and Related Substances by HPLC

    Institute of Scientific and Technical Information of China (English)

    何丹; 杨林

    2012-01-01

    OBJECTIVE: To establish a method for the content determination of cholecalciferol cholesterol and related substances. METHODS: HPLC method was adopted to determine the contents of cholecalciferol cholesterol and related substances, referring to the determination method of vitamin D3 and cholesterol stated in Chinese Pharmacopeia (2010 edition). UV detector replaced ELSD detector for the determination of cholesterol stated in Chinese Pharmacopeia. Phenomenex Luna 5 μm Silica (2) was used for the content determination of vitamin D5 and related substances, the mobile phase was hexanes-pentanol (997:3) at a flow rate of 2.5 mL·min-1 and the detection wavelength was set at 254 nm. Waters Sunfire C18 column was used for the determination of cholesterol, the mobile phase was menthol at a flow rate of 1.0 mL·min-1 and detection wavelength was set at 205 nm. RESULTS: The linear range of cholesterol was 51.15-511.5 μg·mL-1 (r=0.999 9) with an average recovery of 98.75% (RSD=0.94%). CONCLUSION: The method is accurate, reliable and suitable for the quality control of cholecalciferol cholesterol.%目的:建立测定胆维丁原料药及其有关物质含量的方法.方法:采用高效液相色谱法,参照《中国药典》2010年版二部中维生素D3和胆固醇的含量测定项下方法测定胆维丁中2种成分的含量,其中胆固醇测定时由《中国药典》的蒸发光散射检测器改为二极管阵列检测器,并进行方法学考察.维生素D3和有关物质含量测定的色谱柱为Phenomenex Luna5 μm Silica(2),流动相为正己烷-正戊醇(997:3),测定波长为254nm,流速为2.5 mL·min-1;胆固醇测定的色谱柱为Waters Sunfire C18,流动相为甲醇,检测波长205nm,流速为1.0 mL·min-1.结果:胆固醇检测浓度线性范围为51.15~511.5μg·mL-1 (r=0.999 9),平均回收率为98.75%(RSD=0.94%).结论:建立的方法准确、可靠,能有效控制胆维丁原料药的质量.

  14. Development and validation of chromatographic methods for simultaneous determination of ibuprofen and famotidine in presence of related substances in pharmaceutical formulations.

    Science.gov (United States)

    Elzanfaly, Eman S; Zaazaa, Hala E; Soudi, Aya T; Salem, Maissa Y

    2015-01-01

    Two validated methods for the simultaneous determination of ibuprofen and famotidine in the presence of ibuprofen impurity (4-isobutylacetophenone) and or famotidine degradation products were described. The first method was a simple TLC method where separation was performed on silica gel platesusing ethyl acetate: methanol: ammonia (9:2:1, by volume) as a mobile phase. Rf values were found to be 0.40, 0.94, 0.66, 0.27, 0.83 for ibuprofen, 4-isobutylacetophenone, famotidine, famotidine acid and basic degradation products, respectively. The second method is by HPLC on C18 column using methanol: phosphate buffer pH 3 (80:20, v/v) as a mobile phase. Retention times were found to be 2.2, 9.9, and 8.6 for famotidine, ibuprofen, and 4-isobutylacetophenone, respectively. Both methods were validated according to the ICH guidelines and applied for the determination of the two drugs in pure powder and combined dosage form without interference from the excipients.

  15. Development and validation of a liquid chromatographic method for the simultaneous determination of aniracetam and its related substances in the bulk drug and a tablet formulation.

    Science.gov (United States)

    Papandreou, Georgios; Zorpas, Kostas; Archontaki, Helen

    2011-11-01

    Simultaneous determination of aniracetam and its related impurities (2-pyrrolidinone, p-anisic acid, 4-p-anisamidobutyric acid and (p-anisoyl)-4-methyl-2-pyrrolidinone) was accomplished in the bulk drug and in a tablet formulation using a high performance liquid chromatographic method with UV detection. Separation was achieved on a Hypersil BDS-CN column (150 mm × 4.0 mm, 5 μm) using a gradient elution program with solvent A composed of phosphate buffer (pH 4.0; 0.010 M) and solvent B of acetonitrile-phosphate buffer (pH 4.0; 0.010 M) (90:10, v/v). The flow rate of the mobile phase was 1.0 mL min(-1) and the total elution time, including the column re-equilibration, was approximately 20 min. The UV detection wavelength was varied appropriately among 210, 250 and 280 nm. Injection volume was 20 μL and experiments were conducted at ambient temperature. The developed method was validated in terms of system suitability, selectivity, linearity, range, precision, accuracy, limits of detection and quantification for the impurities, short term and long term stability of the analytes in the prepared solutions and robustness, following the ICH guidelines. Therefore, the proposed method was suitable for the simultaneous determination of aniracetam and its studied related impurities.

  16. Environmentally safe management of radioactive and toxic sludges

    Energy Technology Data Exchange (ETDEWEB)

    Shingarev, N.E.; Mukhin, I.V.; Polyakov, A.S.; Raginsky, L.S.; Semenov, B.A. [SSC RF, A.A. Bochvar All-Russia, Research Institute of Inorganic Materials, VNIINM (Russian Federation)

    2000-07-01

    Toxic industrial wastes constitute a significant part of Russian natural environment. The most reliable route to provide the long-term ecologic safety involves removal of toxicants or radioactive substances from polluted sites. With a view of processing toxic and radioactive sludges available in reservoirs, a process flowsheet is suggested that comprises the operations of sludge concentration, dehydration and granulation.Flocculation is an operation required to concentrate a solid phase. Polyacrylamide (PAA) and hydrolyzed PAA (HPAA) are standard flocculating agents used in the processing of sludges coming from storage facilities of radioactive wastes. HPAA is less efficient and it is shown that the optimized concentration of PAA is 4 mg/g solid. Flotation agents are used to extract the solid phase of sludges, it is shown that the process of extraction has to be carried out in 2 stages, the first flotation cycle with a Ph value between 7.5 and 9.5 and the second with a Ph adjustment to 3.5-6.0.The cake resulting from the sludge filtration has poor technological properties, it is advisable to produce a granular material. Hydro-granulation using hydrophobic flocculating agents may be implemented immediately after sludge concentration. The other granulation technique involves the sol-gel process used to incorporate sludge into a ceramic (aluminium oxide) matrix.

  17. Decree no 2007-1557 from November 2, 2007, relative to basic nuclear facilities and to the nuclear safety control of nuclear materials transport; Decret no 2007-1557 du 2 novembre 2007 relatif aux installations nucleaires de base et au controle, en matiere de surete nucleaire, du transport de substances radioactives

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2007-11-15

    This decree concerns the enforcement of articles 5, 17 and 36 of the law 2006-686 from June 13, 2006, relative to the transparency and safety in the nuclear domain. A consultative commission of basic nuclear facilities is established. The decree presents the general dispositions relative to basic nuclear facilities, the dispositions relative to their creation and operation, to their shutdown and dismantling. It precises the dispositions in the domain of public utility services, administrative procedures and sanctions. It stipulates also the particular dispositions relative to other facilities located in the vicinity of nuclear facilities, relative to the use of pressure systems, and relative to the transport of radioactive materials. (J.S.)

  18. 49 CFR 175.705 - Radioactive contamination.

    Science.gov (United States)

    2010-10-01

    ... 49 Transportation 2 2010-10-01 2010-10-01 false Radioactive contamination. 175.705 Section 175.705... Regulations Applicable According to Classification of Material § 175.705 Radioactive contamination. (a) A... (radioactive) materials that may have been released from their packagings. (b) When contamination is present...

  19. Radioactive Waste Material From Tapping Natural Resources ...

    Science.gov (United States)

    2017-08-07

    Rocks around oil and gas and mineral deposits may contain natural radioactivity. Drilling through these rocks and bringing them to the surface creates radioactive waste materials. Once desired minerals have been removed from ore, the radionuclides left in the waste are more concentrated. Scientists call this waste Technologically Enhanced Naturally Occurring Radioactive Material or simply TENORM.

  20. 46 CFR 147.100 - Radioactive materials.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Radioactive materials. 147.100 Section 147.100 Shipping... Stowage and Other Special Requirements for Particular Materials § 147.100 Radioactive materials. (a) Radioactive materials must not be brought on board, used in any manner, or stored on the vessel, unless the...

  1. Determination of Related Substances in PentoXifylline for Injection by HPLC%高效液相色谱法测定注射用己酮可可碱中有关物质

    Institute of Scientific and Technical Information of China (English)

    杜碧莹

    2015-01-01

    目的 建立测定注射用己酮可可碱中有关物质的高效液相色谱(HPLC)法.方法 色谱柱为Agilent Zorbax Eclipse plus C8柱(250 mm × 4. 6 mm,5μm),流动相A为甲醇-0. 544%磷酸二氢钾溶液(3:7),流动相B为甲醇-0. 544%磷酸二氢钾溶液(7:3)梯度洗脱,流速为1. 0 mL/min,,检测波长为272 nm.结果 己酮可可碱与各杂质分离良好,与可可碱、茶碱、咖啡因在质量浓度0. 4~5. 0μg/mL范围内与峰面积呈良好线性关系,定量限分别为8. 5,11. 1,28. 8,12. 6 ng.结论 该法专属性强、灵敏、准确,可用于注射用己酮可可碱有关物质的测定.%Objective To establish an HPLC gradient elution method for the determination of related substances in pentoxifylline for in-jection. Methods Agilent Zorbax Eclipse plus C8 column ( 250 mm × 4. 6 mm, 5 μm ) was used, the methanol-0. 544% solution of potassium dihydrogen phosphate ( 3:7 ) as mobile phase A, and a mixture of methanol-0. 544% solution of potassium dihydrogen phos-phate-( 7:3 ) as mobile phase B. The detection wavelength was 272 nm and the flow rate 1. 0 mL/min for the gradient elute. Results Pentoxifylline and its related substances can be separated effectively by this method. The concentration-response relationship was linear over the range of 0. 4-5. 0 μg/mL and the limit of detection were 8. 5, 11. 1, 28. 8, 12. 6 ng. Conclusion The HPLC method is spe-cific, accurate and sensitive which may be used for the inspection of related substances in pentoxifylline for injection.

  2. Determination of Related Substances in Zofenopril Calcium by RP-HPLC%反相高效液相色谱法测定佐芬普利钙原料的有关物质

    Institute of Scientific and Technical Information of China (English)

    吴亚利; 毛士龙; 苗积康; 季爱玲; 朱建民

    2011-01-01

    目的 建立测定佐芬普利钙原料中有关物质的反相高效液相色谱法.方法 采用Zorbax Eclipse Plus C18色谱柱(250 mm×4.6 mm,5μm),以甲醇-水-冰醋酸(76:24:1)为流动相,检测波长220 nm,柱温40℃,流速1 mL/min.结果 佐芬普利钙质量浓度在1.02~6.12 μg/mL范围内与峰面积线性关系良好(r=0.999 9),最低检测限为0.204 ng,佐芬普利钙主峰与有关物质峰分离良好.结论 所用方法专属性强,适用于佐芬普利钙原料有关物质的测定.%Objective To determine the related substances in the raw material of zofenopril calcium by RP- HPLC method. Methods The Zorbax Eclipse Plus C18 column(250 mm×4. 6mm, 5 μm) was used with the mobile phase of methanol-water-glacial acetic acid(76:24: 1)at the detection wavelength of 220 nm, the temperature of the column was 40 ℃, the flow rate was 1 mL/min. Results The linearity relation was in the range of 1.02-6.12 μg/mL(r=0.999 9) and the limit of detection (LOD) was 0.204 ng. The related substances could be well separated from the zofenopril. Conclusion This method is simple, accurate, sensitive and suitable for the assay on the related substances in the raw material of zofenopril calcium.

  3. 离子对高效液相色谱法测定舒必利片的含量及有关物质%Determination of Sulpiride Tablets′ content and related substances by ion-pair HPLC

    Institute of Scientific and Technical Information of China (English)

    马晓金

    2012-01-01

    目的 建立反相离子对高效液相色谱法测定舒必利片的含量及有关物质.方法 采用反相离子对高效液相色谱法.色谱柱:Agilengt ZORBAX SB-C18(150 mm×4.6 mm,5 μm);流动相:磷酸二氢钾缓冲液(取磷酸二氢钾6.8 g,辛烷磺酸钠1 g,加水1 000 mL使溶解,用磷酸调节pH至3.3)-乙腈-甲醇(80∶10∶10);流速:1.4 mL· min-1;柱温:35 ℃;含量检测波长均为291 nm;有关物质检测波长为240 nm.结果 在2.4~611.6 μg·mL-1范围内线性关系良好,平均回收率为100.01%,RSD为1.03%.结论 该方法专属性强,灵敏度高,操作简便、准确,可作为舒必利片的质量控制与评价方法.%Objective To establish an ion-pair reversed-phase HPLC method for the determination of Sulpiride Tablets content and related substances. Methods The analysis was performed on an Agilent ZORBAX SB- C18 column(150 mm×4. 6 mm,5 μm) with the potassium dihydrogen phosphate buffer (dissolving monopotassium phosphate 6. 8 g and sodium 1-octane sulfonate 1 g with water to 1 000 mL,and adjusted to pH 3. 3 with phosphoric acid)-acetonitrile-methanol(80 : 10 : 10) as the mobile phase at flow rate of 1. 4 mL o min-1 , detected at 291 nm for Sulpiride Tablets content and 240 nm for Sulpiride Tablets related substances. The column temperature was at 35℃. Results The calibration curves showed good linear response ranged from 2. 4 to 611. 6 μtg o mL-1 for Sulpiride Tablets' content and it' s related substances. Conclusion This method with strong specificity and high sensitivity is simple and accurate,and can be used for the quality control and evaluation of Sulpiride Tablets.

  4. Determination of Related Substances in Salbutamol Sulfate Nebules Inhalation Solution by HPLC%HPLC测定硫酸沙丁胺醇雾化吸入溶液有关物质方法的研究

    Institute of Scientific and Technical Information of China (English)

    张冬梅; 牛冲; 冷佳蔚

    2012-01-01

    目的 研究建立测定硫酸沙丁胺醇雾化吸入溶液中有关物质的HPLC方法.方法 采用Agilent ZORBAX SB-C8柱(250mm×4.6 mm,5μm);柱温:35℃;流动相:庚烷磺酸钠溶液-乙腈(78∶22);流速:1.5 mL/min;检测波长:220 nm.结果 硫酸沙丁胺醇主峰与各分解产物峰分离良好,硫酸沙丁胺醇的检出限为1.0 ng.结论 此方法准确、简便、快速,适用于硫酸沙丁胺醇雾化吸入溶液的质量控制.%Objective To establish a HPLC method for the determination of related substances in Salbutamol Sulfate Nebules Inhalation Solution. Methods The HPLC was performed on an Agilent ZORBAX SB-C8 column(250 mm × 4.6 mm, 5 μrn) with the mixture of 22 volumes of acetonitrile and 78 volumes of the solution containing 2.87 g/L of sodium heptanesulfonate and 2.5 g/L of potassium dihydrogen phosphate R previously adjusted to pH 3.65 with dilute phosphoric acid solution as the mobile phase. The detection wavelength was 220 nm. The flow rate was 1.5mL·min. The temperature of the column was 35 ℃. Results An excellent separation was achieved for salbutamol sulfate and its related substances. The LOD of salbutamol sulfate was l.Ong. Conclusion This method is accurate, simple, quick and effective for testing related substances in Salbutamol Sulfate Nebules Inhalation Solution. It is suitable for the quality control of Salbutamol Sulfate Nebules Inhalation Solution.

  5. HPLC法测定加巴喷丁胶囊的含量及有关物质%Determination of Gabapentin and Related Substances in Gabapentin Capsules by HPLC

    Institute of Scientific and Technical Information of China (English)

    董莉; 窦佳; 王书玉; 栾爽; 赵迎春

    2015-01-01

    目的::用高效液相色谱法测定加巴喷丁胶囊的含量及有关物质。方法:采用Kromasil C8柱(250 mm ×4.6 mm,5μm);流动相:甲醇-0.01 mol·L-1磷酸二氢钾溶液(用2 mol·L-1氢氧化钾溶液调pH 6.9)(40∶60);检测波长:210 nm;柱温:40℃;进样量:20μl。采用外标法测定主成分和已知杂质的含量,自身对照法测定未知杂质的含量。结果:加巴喷丁浓度在2.5~20.0 mg·ml-1范围内与峰面积呈良好的线性关系(r=0.9999)。平均加样回收率为100.74%(RSD=0.24%, n=5)。结论:本方法快速、准确、专属性好,可用于加巴喷丁胶囊的含量及有关物质测定。%Objective:To establish an HPLC method for the determination of gabapentin and the related substances in gabapentin capsules. Methods:A Kromasil C8 column (250 mm × 4. 6 mm,5μm)was used. The mobile phase was methanol-0. 01 mol·L-1 po-tassium dihydrogen phosphate solution (adjusting pH to 6. 9 with 2 mol·L-1 potassium hydroxide) (40∶60). The detection wave-length was 210 nm. The column temperature was 40℃ and the injection volume was 20μl. The main component and the known impuri-ty were determined by an external standard method. The unknown impurities were determined by a self-control method. Results: The calibration curve of gabapentin was linear within the range of 2.5-20.0 mg·ml-1(r=0.999 9). The average sample recovery was 100. 74% with RSD of 0. 24%(n=5). Conclusion:The method is simple, accurate,specific and applicable in the determination of gabapentin and the related substances in gabapentin capsules.

  6. 刚果红法测定乳酸发酵液中的β-葡聚糖类物质%Determination of β-glucan substances in L-lactic acid fermentation broth by Congo red method

    Institute of Scientific and Technical Information of China (English)

    韩玉杰; 马建卢; 寇永磊; 樊伟丽; 常文耀; 吴健

    2011-01-01

    在利用凝结芽孢杆菌(Bacillus coagulans)进行以葡萄糖为基质的乳酸发酵过程中通过外加商品纤维素酶可以显著增加乳酸产量。为探讨其中原因,用羧甲基纤维素(CMC)作为β-葡聚糖标品,建立了刚果红分光光度法测定乳酸发酵提取液中β-葡聚糖的稳定体系,用以测定乳酸发酵液中的β-葡聚糖含量。实验证明当Na+浓度为0.025~0.175mol/L,Ca2+浓度为0.001~0.005mol/L,蛋白质质量浓度为0~40mg/L时,这几种杂质对β-葡聚糖测定的干扰可以忽略。刚果红法测定β-葡聚糖的最佳条件为:最大吸收波长550nm、pH8.0磷酸缓冲液、测定时间15min。实验结果显示乳酸发酵液中β-葡聚糖含量很低,纤维素酶水解发酵液中的β-葡聚糖类物质不足于显著增加乳酸产量,其增产作用一定另有原因。%In the process of L-lactic acid fermentation by Bacillus coagulans using glucose as the feedstock,the yield of L-lactic acid could be increased through adding cellulases.To investigate the reason,a stable system of spectrophotometric determination of β-glucan substance was established to measure the content of β-glucan substance in the L-lactic acid fermentation broth,using carboxymethyl cellulose(CMC) as the standard substance of β-glucan.It was illustrated that the potential influence might be omitted when the concentration of sodium ions in 0.025~0.175 mol/L,calcium ions in 0.001~0.005 mol/L,and the concentration of proteins in 0~40 mg/L.The optimal condition for determination by Congo red method is the maximum absorption wavelength 550 nm,pH 8.0 with phosphate buffer and the reaction time 15 minutes.The experiments reveal that the content of β-glucan substance in L-lactic acid fermentation broth is rather low,and the reason why cellulases could enhance the yield of L-lactic acid needs further investigation.

  7. Quantitative determination of two polymorphic forms of imatinib mesylate in a drug substance and tablet formulation by X-ray powder diffraction, differential scanning calorimetry and attenuated total reflectance Fourier transform infrared spectroscopy.

    Science.gov (United States)

    Bellur Atici, Esen; Karlığa, Bekir

    2015-10-10

    Imatinib has been identified as a tyrosine kinase inhibitor that selectively inhibits the Abl tyrosine kinases, including Bcr-Abl. The active substance used in drug product is the mesylate salt form of imatinib, a phenylaminopyrimidine derivative and chemically named as N-(3-(4-(pyridin-3-yl) pyrimidin-2-ylamino)-4-methylphenyl)-4-((4-methylpiperazin-1-yl) methyl)-benzamide methanesulfonic acid salt. It exhibits many polymorphic forms and most stable and commercialized polymorphs are known as α and β forms. Molecules in α and β polymorphic forms exhibit significant conformational differences due to their different intra- and intermolecular interactions, which stabilize their molecular conformations and affect their physicochemical properties such as bulk density, melting point, solubility, stability, and processability. The manufacturing process of a drug tablet included granulation, compression, coating, and drying may cause polymorphic conversions. Therefore, polymorphic content of the drug substance should be controlled during quality control and stability testing. Attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy, differential scanning calorimetry (DSC), and powder X-ray diffraction (PXRD) methods were evaluated for determination of the polymorphic content of the drug substance and drug product; and PXRD was the most accurate technique and selected as preferred method and validated. Prior to development of a quantification method, pure α and β polymorphs were characterized and used throughout the method development and validation studies. Mixtures with different ratios of α and β forms were scanned using X-ray diffractometer with a scan rate of 0.250°/min over an angular range of 19.5-21.0° 2θ and the peak heights for characteristic peak of β form at 20.5 ± 0.2° 2θ diffraction angle were used to generate a calibration curve. The detection limit of β polymorph in α form imatinib mesylate tablets was found as 4% and

  8. Experimental determination of re-suspension data of particle-bound radioactive materials of relevant contaminated surfaces in case of radiological emergencies for the radioactive exposure assessment of the emergency staff and affected persons due to re-suspension; Experimentelle Bestimmung von Resuspensionsdaten partikelgebundener radioaktiver Stoffe von relevanten kontaminierten Oberflaechen bei radiologischen Notfaellen zur Beurteilung einer Exposition von Einsatzpersonal und betroffenen Personen durch Resuspension

    Energy Technology Data Exchange (ETDEWEB)

    Koch, Wolfgang; Loedding, Hubert; Lange, Florentin

    2012-01-15

    Accidental and intentional release of radioactive materials, for example in the wake of a nuclear accident, causes contamination of surfaces in the outdoor environment, in buildings and the clothing of humans. Resuspension of radioactive material from contaminated surfaces is the dominant source of radioactive inhalation exposure of first responders and emergency personnel at the accident site as well as in emergency care centres during the time period following the event. The assessment of the aerosol borne activity concentration is based on reasonable assumptions or measurements of the surface contamination and a quantitative understanding of the resuspension process. In this project the resuspension rate of respirable particles (< 10 {mu}m) and its dependence on time and influencing parameters was measured. Special emphasis was directed to the early phase after the release event. Using a versatile, small scale flow channel set-up, wind resuspension and resuspension caused by transient or continuous mechanical forces impacting on the surfaces was investigated. The flux of particles resuspended from small test surfaces was detected by an optical particle size spectrometer. Influencing parameters such properties of contaminated surfaces, wind speed, type of particle etc. could be easily varied. Well defined contaminations of the test surfaces were prepared in a settling chamber by dry and wet deposition using aerosolized dry powders of spherical (silver) and agglomerated (cerium oxide) particles, and sprays of aqueous solutions of cesium chloride, respectively. In the latter case the surface was dried after deposition of the liquid droplets leading to a surface contamination of CsCl crystals adhering stronger to the surface than particulates. The resuspension rate for surfaces contaminated by wet deposition is 2-3 orders of magnitude lower compared to the situation for dry deposition, irrespective of the resuspension mechanism. The air flow induced resuspension

  9. Development and validation of a selective, sensitive and stability indicating UPLC-MS/MS method for rapid, simultaneous determination of six process related impurities in darunavir drug substance.

    Science.gov (United States)

    A, Vijaya Bhaskar Reddy; Yusop, Zulkifli; Jaafar, Jafariah; Aris, Azmi B; Majid, Zaiton A; Umar, Khalid; Talib, Juhaizah

    2016-09-05

    In this study a sensitive and selective gradient reverse phase UPLC-MS/MS method was developed for the simultaneous determination of six process related impurities viz., Imp-I, Imp-II, Imp-III, Imp-IV, Imp-V and Imp-VI in darunavir. The chromatographic separation was performed on Acquity UPLC BEH C18 (50 mm×2.1mm, 1.7μm) column using gradient elution of acetonitrile-methanol (80:20, v/v) and 5.0mM ammonium acetate containing 0.01% formic acid at a flow rate of 0.4mL/min. Both negative and positive electrospray ionization (ESI) modes were operated simultaneously using multiple reaction monitoring (MRM) for the quantification of all six impurities in darunavir. The developed method was fully validated following ICH guidelines with respect to specificity, linearity, limit of detection (LOD), limit of quantification (LOQ), accuracy, precision, robustness and sample solution stability. The method was able to quantitate Imp-I, Imp-IV, Imp-V at 0.3ppm and Imp-II, Imp-III, and Imp-VI at 0.2ppm with respect to 5.0mg/mL of darunavir. The calibration curves showed good linearity over the concentration range of LOQ to 250% for all six impurities. The correlation coefficient obtained was >0.9989 in all the cases. The accuracy of the method lies between 89.90% and 104.60% for all six impurities. Finally, the method has been successfully applied for three formulation batches of darunavir to determine the above mentioned impurities, however no impurity was found beyond the LOQ. This method is a good quality control tool for the trace level quantification of six process related impurities in darunavir during its synthesis.

  10. [Radioactive contamination of foods marketed in saitama prefecture].

    Science.gov (United States)

    Yoshida, Terumitsu; Nagahama, Yoshiyuki; Takekuma, Mikiko; Miyake, Sadaaki; Nomoto, Kahoru; Takano, Mariko

    2013-01-01

    Up to October 31, 2012, a total of 170 food samples marketed in Saitama Prefecture were examined following the setting of provisional regulatory limits for radioactivity in drinking water and foodstuffs by the Ministry of Health, Labour and Welfare on 1 April 2012. No sample exceeded the regulatory limits as determined by gamma ray spectrometry with a germanium semiconductor detector. However the radioactive cesium concentrations of food samples such as raw wood-shiitake and maccha (powdered green tea) produced in Saitama were nearly at the regulatory limits, being 74 Bq/kg and 84 Bq/kg, respectively.

  11. Radioactivity survey data in Japan. Pt. 1. Environmental materials

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-02-01

    This is a report on radioactivity survey in Japan issued by National Institute of Radiological Sciences, Chiba on February, 1996. This data relates to radioactive materials such as Strontium-90 and Cesium-137 in environmental materials such as rain and dry fallout, airborne dust, service water, freshwater, soil, seawater, and sea sediments, which were collected at all over of Japan. In the survey report, followings are also contained; (1) Collection and pretreatment of samples, (2) Preparation of samples for analysis, (3) Separation of Strontium-90 and Cesium-137, (4) Determination of stable Strontium, Calcium and Potassium, (5) Counting, (6) Results, and (7) Contents of figure. (G.k.)

  12. Radioactivity survey data in Japan. Pt. 2. Dietary materials

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-02-01

    This is a report on radioactivity survey in Japan issued by National Institute of Radiological Sciences, Chiba on February, 1996. This data relates to radioactive materials such as total diet, rice, milk, vegetables, tea, sea fish, freshwater fish, shellfish, and seaweeds, which were collected at all over of Japan. In the survey report, followings are also contained; (1) Collection and pretreatment of samples, (2) Preparation of samples for analysis, (3) Separation of Strontium-90 and Cesium-137, (4) Determination of stable Strontium, Calcium and Potassium, (5) Counting, (6) Results, and (7) Contents of figure. (G.K.)

  13. Analysis of Radioactive Nuclide Impurities in Potassium Pertechnetate

    Institute of Scientific and Technical Information of China (English)

    WANG; Xiu-feng; CHEN; Ming; SUN; Hong-qing; SUN; Xiao-yi; MA; Peng; DING; You-qian

    2015-01-01

    99Tc is a pure beta radionuclide,its half-life is 2.111×105 a,and is widely used in nuclear medicine.Potassium pertechnetate is an important material of technetium(99Tc)methylene diphosphate injection.In order to determinate the radioactive impurity content,this study established

  14. Pricing hazardous substance emissions

    Energy Technology Data Exchange (ETDEWEB)

    Staring, Knut; Vennemo, Haakon

    1997-12-31

    This report discusses pricing of emissions to air of several harmful substances. It combines ranking indices for environmentally harmful substances with economic valuation data to yield price estimates. The ranking methods are discussed and a relative index established. Given the relative ranking of the substances, they all become valued by assigning a value to one of them, the `anchor` substance, for which lead is selected. Valuations are provided for 19 hazardous substances that are often subject to environmental regulations. They include dioxins, TBT, etc. The study concludes with a discussion of other categories of substances as well as uncertainties and possible refinements. When the valuations are related to CO, NOx, SOx and PM 10, the index system undervalues these pollutants as compared to other studies. The scope is limited to the outdoor environment and does not include global warming and eutrophication. The indices are based on toxicity and so do not apply to CO{sub 2} or other substances that are biologically harmless. The index values are not necessarily valid for all countries and should be considered as preliminary. 18 refs., 6 tabs.

  15. Method for radioactivity monitoring

    Science.gov (United States)

    Umbarger, C. John; Cowder, Leo R.

    1976-10-26

    The disclosure relates to a method for analyzing uranium and/or thorium contents of liquid effluents preferably utilizing a sample containing counting chamber. Basically, 185.7-keV gamma rays following .sup.235 U alpha decay to .sup.231 Th which indicate .sup.235 U content and a 63-keV gamma ray doublet found in the nucleus of .sup.234 Pa, a granddaughter of .sup.238 U, are monitored and the ratio thereof taken to derive uranium content and isotopic enrichment .sup.235 U/.sup.235 U + .sup.238 U) in the liquid effluent. Thorium content is determined by monitoring the intensity of 238-keV gamma rays from the nucleus of .sup.212 Bi in the decay chain of .sup.232 Th.

  16. Optimization of Determination System for Gallic Acid and Its Synthetic Related Substances in Pomegranate Fruit%石榴果实没食子酸及其合成相关物质HPLC 测定体系优化

    Institute of Scientific and Technical Information of China (English)

    冯立娟; 尹燕雷; 杨雪梅; 李英朋

    2015-01-01

    建立了‘泰山三白甜’石榴果实不同部位没食子酸及其合成相关物质的高效液相色谱(HPLC)定性和定量检测方法。色谱条件:色谱柱为 Agilent Zorbax XDB -C18(4.6 mm ×150 mm,5μm),没食子酸以乙腈-2%冰乙酸水溶液为流动相(20∶80),检测波长270 nm;莽草酸和3-脱氢莽草酸以甲醇-1%磷酸水溶液(5∶95)为流动相,检测波长214 nm;五没食子酰葡萄糖以乙腈-0.5%磷酸水溶液(20∶80)为流动相,检测波长275 nm,4种物质均等度洗脱,流速均为0.8 mL/min,柱温均为30℃。结果表明,4种物质在一定线性范围内的峰面积与质量浓度呈良好的线性关系,相关系数均大于0.99,检测限为0.12~0.24 mg/L;加标回收率为98.9%~102.5%,相对标准偏差(RSD)为1.2%~2.2%。‘泰山三白甜’石榴果实不同部位没食子酸、莽草酸、3-脱氢莽草酸和五没食子酰葡萄糖含量存在显著差异,果皮中含量最高,果汁次之,种子中最低。该方法操作简单,灵敏度高,重复性好,可用于没食子酸及其合成相关物质的快速鉴定及含量测定。%The qualitative and quantitative determination methods of gallic acid and its synthetic related substances in different parts of Taishansanbaitian pomegranate fruit were developed by high performance liquid chromatography (HPLC).The chromatographic column was Agilent Zorbax XDB -C1 8 (4.6 mm ×1 50 mm, 5 μm).The mobile phase of gallic acid was acetonitrile and 2% glacial acetic acid solution with the ratio of 20∶80.Its determine wavelength was 270 nm.The mobile phase of shikimic acid and 3 -dehydroshikimic acid was methanol and 1 % phosphoric acid with the ratio of 5∶95.Their determine wavelengths both were 21 4 nm.The mobile phase of pentagalloylglucose was acetonitrile and 0.5% phosphoric acid with the ratio of 20∶80.Its determine wavelength was 275 nm

  17. Radioactive standards and calibration methods for contamination monitoring instruments

    Energy Technology Data Exchange (ETDEWEB)

    Yoshida, Makoto [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    1997-06-01

    Contamination monitoring in the facilities for handling unsealed radioactive materials is one of the most important procedures for radiation protection as well as radiation dose monitoring. For implementation of the proper contamination monitoring, radiation measuring instruments should not only be suitable to the purpose of monitoring, but also be well calibrated for the objective qualities of measurement. In the calibration of contamination monitoring instruments, quality reference activities need to be used. They are supplied in different such as extended sources, radioactive solutions or radioactive gases. These reference activities must be traceable to the national standards or equivalent standards. On the other hand, the appropriate calibration methods must be applied for each type of contamination monitoring instruments. In this paper, the concepts of calibration for contamination monitoring instruments, reference sources, determination methods of reference quantities and practical calibration methods of contamination monitoring instruments, including the procedures carried out in Japan Atomic Energy Research Institute and some relevant experimental data. (G.K.)

  18. Environmental radioactivity in the Netherlands. Results in 2009

    Energy Technology Data Exchange (ETDEWEB)

    Knetsch, G.J.; Groot, M.C.E. (eds.)

    2011-11-15

    In 2009 the Netherlands fulfilled the European obligation to annually measure radioactivity in the environment and in food. According to the Euratom Treaty of 1957, all Member States of the European Union are obliged to perform these measurements each year. Euratom has provided guidelines for performing the measurements uniformly since 2000. However, Member States are not obliged to comply with these recommended guidelines. In the Netherlands, in 2009 strontium-90 was also determined (for the first time) in a mixed food package for which the above recommendations had been fulfilled. The National Institute for Public Health and the Environment (RIVM) reports on behalf of the Netherlands to the European Union about radioactivity in the environment. Moreover, this information provides background values and/or amounts of radioactivity that are present under normal circumstances. These background values can be used as reference values, for instance, during a disaster.

  19. Rapid Screening Method for New Psychoactive Substances of Forensic Interest: Electrochemistry and Analytical Determination of Phenethylamines Derivatives (NBOMe) via Cyclic and Differential Pulse Voltammetry.

    Science.gov (United States)

    Andrade, Ana Flávia B; Mamo, Samuel Kasahun; Gonzalez-Rodriguez, Jose

    2017-02-07

    The NBOMe derivatives are phenethylamines derived from the 2C class of hallucinogens. Only a few human pharmacologic studies have been conducted on these drugs, and several cases of intoxication and deaths have been reported. Presently, NBOMe are not a part of the routine drugs-of-abuse screening procedure for many police forces, and there are no rapid immunoassay screening tests that can detect the presence of those compounds. In this Article, the voltammetric behavior of 25B NBOMe and 25I NBOMe were investigated and their electroanalytical characteristics determined for the first time. A novel, fast, and sensitive screening method for the identification of the two most common NBOMes (25B-NBOMe and 25I-NBOMe) in real samples is reported. The method uses the electrochemical oxidation of these molecules to produce an analytical signal that can be related to the NBOMe concentration with an average lower limit of quantitation of 0.01 mg/mL for both of them. The method is selective enough to identify the two compounds individually, even given the great similarity in their structure.

  20. A Validated Stability-indicating Reverse Phase HPLC Assay Method for the Determination of Memantine Hydrochloride Drug Substance with UV-Detection Using Precolumn Derivatization Technique

    Directory of Open Access Journals (Sweden)

    Bhavil Narola

    2010-07-01

    Full Text Available This present paper deals with the development and validation of a stability indicating high performance liquid chromatographic method for the quantitative determination of Memantine hydrochloride. Memantine hydrochloride was derivatized with 0.015 M 9-fluorenylmethyl chloroformate (FMOC and 0.5 M borate buffer solution by keeping it at room temperature for about 20 minutes and the chromatographic separation achieved by injecting 10 µL of the derivatized mixture into a Waters HPLC system with photodiode array detector using a kromasil C18 column (150 × 4.6 mm, 5 µ. The mobile phase consisting of 80% acetonitrile and 20% phosphate buffer solution and a flow rate of 2 milliliter/minute. The Memantine was eluted at approximately 7.5 minutes. The volume of FMOC used in derivatization, concentration of FMOC and derivatization time was optimized and used. Forced degradation studies were performed on bulk sample of Memantine hydrochloride using acid (5.0 Normal (N hydrochloric acid, base (1.0 N sodium hydroxide, oxidation (30% hydrogen peroxide, thermal (105°C, photolytic and humidity conditions. The developed LC method was validated with respect to specificity, precision (% RSD about 0.70%, linearity (linearity of range about 70–130 µg/mL, ruggedness (Overall % RSD about 0.35%, stability in analytical solution (Cumulative % RSD about 0.11% after 1450 min. and robustness.

  1. Direct injection liquid chromatography/electrospray ionization mass spectrometric horse urine analysis for the quantification and confirmation of threshold substances for doping control. II. Determination of theobromine.

    Science.gov (United States)

    Vonaparti, A; Lyris, E; Panderi, I; Koupparis, M; Georgakopoulos, C

    2009-04-01

    In equine sport, theobromine is prohibited with a threshold level of 2 microg mL(-1) in urine, hence doping control laboratories have to establish quantitative and qualitative methods for its determination. Two simple liquid chromatography/mass spectrometry (LC/MS) methods for the identification and quantification of theobromine were developed and validated using the same sample preparation procedure but different mass spectrometric systems: ion trap mass spectrometry (ITMS) and time-of-flight mass spectrometry (TOFMS). Particle-free diluted urine samples were directly injected into the LC/MS systems, avoiding the time-consuming extraction step. 3-Propylxanthine was used as the internal standard. The tested linear range was 0.75-15 microg mL(-1). Matrix effects were evaluated analyzing calibration curves in water and different fortified horse urine samples. A great variation in the signal of theobromine and the internal standard was observed in different matrices. To overcome matrix effects, a standard additions calibration method was applied. The relative standard deviations of intra- and inter-day analysis were lower than 8.6 and 7.2%, respectively, for the LC/ITMS method and lower than 5.7 and 5.8%, respectively, for the LC/TOFMS method. The bias was less than 8.7% for both methods. The methods were applied to two case samples, demonstrating simplicity, accuracy and selectivity.

  2. Rapid separation and determination of process-related substances of paracetamol using reversed-phase HPLC with photo diode array as a detector.

    Science.gov (United States)

    Rao, R Nageswara; Narasaraju, A

    2006-02-01

    A simple and rapid gradient reversed-phase high-performance liquid chromatographic method for simultaneous separation and determination of paracetamol and its related compounds in bulk drugs and pharmaceutical formulations has been developed. As many as nine process impurities and one degradation product of paracetamol have been separated on a Symmetry C18 column (4.6 x 250 mm i.d., particle size 5 microm) with gradient elution using 0.01 M potassium dihydrogen phosphate buffer (pH 3.0) and acetonitrile as mobile phase and photo diode array detection at 215 nm. The chromatographic behavior of all the compounds was examined under variable compositions of different solvents, temperatures, buffer concentrations and pH values. The correlation coefficients for calibration curves for paracetamol as well as impurities were in the range of 0.9951 - 0.9994. The proposed RP-LC method was successfully applied to the analysis of commercial formulations; the recoveries of paracetamol were in the range of 99-101%. The method could be of use not only for rapid and routine evaluation of the quality of paracetamol in bulk drug manufacturing units but also for detection of its impurities in pharmaceutical formulations.

  3. Childhood Predictors of Adult Substance Abuse.

    Science.gov (United States)

    Arteaga, Irma; Chen, Chin-Chih; Reynolds, Arthur J

    2010-08-01

    Identification of the early determinants of substance abuse is a major focus of life course research. In this study, we investigated the child, family, and school-related antecedents of the onset and prevalence of substance abuse by age 26 for a cohort of 1,208 low-income minority children in the Chicago Longitudinal Study. Data onon well-being have been collected prospectively since birth from administrative records, parents, teachers, and children. Results indicated that the prevalence of substance abuse by age 26 was 32 percent (self reports or criminal justice system records) with a median age of first use of 17. Probit regression analysis indicated that substance abuse prevalence was primarily determined by gender (males had a higher rate), trouble making behavior by age 12, school mobility, and previous substance use. Family and peer predictors included involvement in the child welfare system by age 9, parent expectations for school success at age 9, parent substance abuse by children's age 15, and deviant peer affiliation by age 16. Age of first substance use was predicted by gender and race/ethnicity (males and Blacks had earlier incidence), involvement in the child welfare system, and family risk status at age 8. As with prevalence, the pattern of predictors for males was similar to the overall sample but the magnitude of effects was stronger.. The predictors of the timing of substance use dependency were gender, family conflict by age 5, involvement in the child welfare system, social maturity at age 9, adolescent school mobility, and school dropout by age 16. Findings indicate that the promotion of family involvement and positive school and social behavior can reduce the risk of substance abuse.

  4. CONTAMINACIÓN RADIACTIVA AMBIENTAL EN EL NEOTRÓPICO ENVIRONMENTAL RADIOACTIVE POLLUTION IN NEOTROPIC

    Directory of Open Access Journals (Sweden)

    Osores, J, M.

    2008-07-01

    Full Text Available Environmental radioactive pollution is produced mainly by the use of natural or artificial radioactive substances, the use of the nuclear power and nuclear weapons, constituting a great danger of contamination for the nature and the humanity; since many residues of these polluting materials have been scattered by all the earth. The risks of the radioactive contamination for the people and the environment depend on the nature of the radioactive contaminant, the pollution level and the extension of the contamination; since all the radiations are genotoxics, the probability of genetic alterations and production of mutations is going to depend on the exposure degree of the cells of an organism. In the last years, the environmental radioactive pollution hazards due to artificial radionuclides were reduced considerably, the scientific community has paid special interest in the contamination with natural radioactive elements like for example the radon released within the underground mines that the probability of occurrence of cancer of lung between the workers and the accumulation of different materials NORMS in mining activities increases, especially in the uranium zones of Pozo de Caldas (Brazil and Macusani (Peru, zones of phosphoric operation of rocks (Bayovar or polimetalic mining; the inadequate treatment of these materials is going to produce an important radiological impact and to alter to the habitat of different communities from plants and animals in the region.

  5. Radioactive sample effects on EDXRF spectra

    Energy Technology Data Exchange (ETDEWEB)

    Worley, Christopher G [Los Alamos National Laboratory

    2008-01-01

    Energy dispersive X-ray fluorescence (EDXRF) is a rapid, straightforward method to determine sample elemental composition. A spectrum can be collected in a few minutes or less, and elemental content can be determined easily if there is adequate energy resolution. Radioactive alpha emitters, however, emit X-rays during the alpha decay process that complicate spectral interpretation. This is particularly noticeable when using a portable instrument where the detector is located in close proximity to the instrument analysis window held against the sample. A portable EDXRF instrument was used to collect spectra from specimens containing plutonium-239 (a moderate alpha emitter) and americium-241 (a heavy alpha emitter). These specimens were then analyzed with a wavelength dispersive XRF (WDXRF) instrument to demonstrate the differences to which sample radiation-induced X-ray emission affects the detectors on these two types of XRF instruments.

  6. The safe transport of radioactive materials

    CERN Document Server

    Gibson, R

    1966-01-01

    The Safe Transport of Radioactive Materials is a handbook that details the safety guidelines in transporting radioactive materials. The title covers the various regulations and policies, along with the safety measures and procedures of radioactive material transport. The text first details the 1963 version of the IAEA regulation for the safe transport of radioactive materials; the regulation covers the classification of radionuclides for transport purposes and the control of external radiation hazards during the transport of radioactive materials. The next chapter deals with concerns in the im

  7. Determination of Related Substances and Content of Buprenorphine Hydrochloride Sublingual Tablet by HPLC%HPLC法测定盐酸丁丙诺啡舌下片的含量和有关物质

    Institute of Scientific and Technical Information of China (English)

    刘胜春; 赵学刚; 冯雅慧; 康海霞; 滑千里; 王乃浩

    2013-01-01

    OBJECTIVE:To establish a method for the determination of content and related substances in Buprenorphine hydrochloride sublingual tablets.METHODS:HPLC method was adopted.The determination was performed on Agilent Eclipse XDB C18 column with mobile phase consisted of 1% ammonium acetate (containing 0.1% acetic acid)-methanol (15∶85) at the flow rate of 1.0 ml/min.The column temperature was 40 ℃,and detection wavelength was 288 nm.RESULTS:Buprenorphine hydrochloride was separated with its impurities thoroughly,and its linear range were 0.004 04-0.040 4 mg/ml (r=0.999 9) with average recovery of 100.1% (RSD=0.33 %,n=9).The detection limit was 0.5 ng.CONCLUSIONS:The method is simple,sensitive and accurate.It could be applied for the determination of content and related substance in Buprenorphine hydrochloride sublingual tablets.%目的:建立同时测定盐酸丁丙诺啡舌下片含量和有关物质的方法.方法:采用高效液相色谱法.色谱柱为Agilent Eclipse XDB C18,流动相为1%醋酸铵溶液(含0.1%冰醋酸)-甲醇(15∶85),流速为1.0 ml/min,柱温为40℃,检测波长为288nm.结果:有关物质与主成分有较好的分离,盐酸丁丙诺啡检测质量浓度线性范围为0.004 04~0.040 4 mg/ml(r=0.999 9),检测限为0.5 ng,平均回收率为100.1%,RSD为0.33%(n=9).结论:本方法简便、灵敏度高、结果准确,可用于盐酸丁丙诺啡舌下片含量和有关物质测定.

  8. Radioactive waste management in Austria

    Directory of Open Access Journals (Sweden)

    Neubauer Josef

    2004-01-01

    Full Text Available At the Austrian Research Centers Seibersdorf, there are several facilities in stalled for treatment of waste of low and intermediate radioactivity level (radwaste. A separate company within Centers, Nuclear Engineering Seibersdorf, has been formed recently, acting as a centralized facility for treatment, conditioning and storing of such waste within the country. The relevant treatment technology is applied depending on the waste category. In total about 6900 m3 of solid waste of low and intermediate radioactivity level originating from Austria was treated in the period between 1976 and 2002. Presently, there exists no final repository for radwaste in Austria. A study is under way to identify the structure for a long term storage facility.

  9. DISSOLVED CONCENTRATION LIMITS OF RADIOACTIVE ELEMENTS

    Energy Technology Data Exchange (ETDEWEB)

    NA

    2004-11-22

    The purpose of this study is to evaluate dissolved concentration limits (also referred to as solubility limits) of elements with radioactive isotopes under probable repository conditions, based on geochemical modeling calculations using geochemical modeling tools, thermodynamic databases, field measurements, and laboratory experiments. The scope of this modeling activity is to predict dissolved concentrations or solubility limits for 14 elements with radioactive isotopes (actinium, americium, carbon, cesium, iodine, lead, neptunium, plutonium, protactinium, radium, strontium, technetium, thorium, and uranium) important to calculated dose. Model outputs for uranium, plutonium, neptunium, thorium, americium, and protactinium are in the form of tabulated functions with pH and log (line integral) CO{sub 2} as independent variables, plus one or more uncertainty terms. The solubility limits for the remaining elements are either in the form of distributions or single values. The output data from this report are fundamental inputs for Total System Performance Assessment for the License Application (TSPA-LA) to determine the estimated release of these elements from waste packages and the engineered barrier system. Consistent modeling approaches and environmental conditions were used to develop solubility models for all of the actinides. These models cover broad ranges of environmental conditions so that they are applicable to both waste packages and the invert. Uncertainties from thermodynamic data, water chemistry, temperature variation, and activity coefficients have been quantified or otherwise addressed.

  10. Management options for recycling radioactive scrap metals

    Energy Technology Data Exchange (ETDEWEB)

    Dehmel, J.C.; MacKinney, J.; Bartlett, J.

    1997-02-01

    The feasibility and advantages of recycling radioactive scrap metals (RSM) have yet to be assessed, given the unique technical, regulatory, safety, and cost-benefit issues that have already been raised by a concerned recycling industry. As is known, this industry has been repeatedly involved with the accidental recycling of radioactive sources and, in some cases, with costly consequences. If recycling were deemed to be a viable option, it might have to be implemented with regulatory monitoring and controls. Its implementation may have to consider various and complex issues and address the requirements and concerns of distinctly different industries. There are three basic options for the recycling of such scraps. They are: (1) recycling through the existing network of metal-scrap dealers and brokers, (2) recycling directly and only with specific steelmills, or (3) recycling through regional processing centers. Under the first option, scrap dealers and brokers would receive material from RSM generators and determine at which steelmills such scraps would be recycled. For the second option, RSM generators would deal directly with selected steelmills under specific agreements. For the third option, generators would ship scraps only to regional centers for processing and shipment to participating steelmills. This paper addresses the potential advantages of each option, identifies the types of arrangements that would need to be secured among all parties, and attempts to assess the receptivity of the recycling industry to each option.

  11. Nuclide radioactive decay data uncertainties library

    Science.gov (United States)

    Barabanova, D. S.; Zherdev, G. M.

    2017-01-01

    The results of the developing the library of uncertainties of radioactive decay data in the ABBN data library format are described. Different evaluations of uncertainties were compared and their effects on the results of calculations of residual energy release were determined using the test problems and experiment. Tables were generated in the ABBN format with the data obtained on the basis of libraries in ENDF-6 format. 3821 isotopes from the ENDF/B-7 data library, 3852 isotopes from the JEFF-3.11 data library and 1264 isotopes from the JENDL-4.0 data library were processed. It was revealed that the differences in the evaluations accepted in different decay data libraries are not so big, although they sometimes exceed the uncertainties assigned to the data in the ENDF/B-7 and JEFF-3.11 libraries, which as a rule, they agree with each other. On the basis of developed method it is supposed to create a library of data uncertainties for radioactive decay within the constant data system in FSUE RFNC-VNIIEF with its further connection with CRYSTAL module.

  12. Radioactive Waste Management BasisApril 2006

    Energy Technology Data Exchange (ETDEWEB)

    Perkins, B K

    2011-08-31

    This Radioactive Waste Management Basis (RWMB) documents radioactive waste management practices adopted at Lawrence Livermore National Laboratory (LLNL) pursuant to Department of Energy (DOE) Order 435.1, Radioactive Waste Management. The purpose of this Radioactive Waste Management Basis is to describe the systematic approach for planning, executing, and evaluating the management of radioactive waste at LLNL. The implementation of this document will ensure that waste management activities at LLNL are conducted in compliance with the requirements of DOE Order 435.1, Radioactive Waste Management, and the Implementation Guide for DOE Manual 435.1-1, Radioactive Waste Management Manual. Technical justification is provided where methods for meeting the requirements of DOE Order 435.1 deviate from the DOE Manual 435.1-1 and Implementation Guide.

  13. A rapid method for the determination of perfluoroalkyl substances including structural isomers of perfluorooctane sulfonic acid in human serum using 96-well plates and column-switching ultra-high performance liquid chromatography tandem mass spectrometry.

    Science.gov (United States)

    Salihovic, Samira; Kärrman, Anna; Lindström, Gunilla; Lind, P Monica; Lind, Lars; van Bavel, Bert

    2013-08-30

    To facilitate high-throughput analysis suitable for large epidemiological studies we developed an automated column-switching ultra-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method for determination of perfluorocarboxylic acids (PFCAs; C5, C6, C7, C8, C9, C10, C11, C12, and C13), perfluoroalkyl sulfonic acids (PFSAs; C4, C6, C8, and C10), perfluorooctane sulfonamide (PFOSA), and five groups of structural perfluorooctane sulfonic acid (PFOS) isomers in human serum or plasma. The analytical procedure involves rapid protein precipitation using 96-well plates followed by an automated sample clean-up using an on-line trap column removing many potentially interfering sample components while through the mobile phase gradient the target analytes are eluted onto the analytical column for further separation and subsequent mass detection. The method was linear (R(2)method detection limits ranging between 0.01 and 0.17ngmL(-1) depending on the analyte. The developed method was precise, with repeatability (n=7) and reproducibility (n=103) coefficients of variation between 2% and 20% for most compounds including PFOS (2% and 8%) and its structural isomers (2-6% and 4-8%). The method was in conformity with a standard reference material. The column-switching HPLC-MS/MS method has been successfully applied for the determination of perfluoroalkyl substances including structural PFOS isomers in human plasma from an epidemiological study.

  14. Study of the interfering substances in the dried meat floss starch content determination%肉松制品淀粉含量测定中干扰物质的研究

    Institute of Scientific and Technical Information of China (English)

    蔡志兴

    2013-01-01

    Starch in dried meat floss was determined by iodine-starch method, double enzymolysis-HPLC method and acid hydrolysis method. And the potentially interfering substances in acid hydrolysis method were also studied. The result shows that the double enzymolysis-HPLC method has high anti-reference ability to polysaccharide. The contents of starch in dried meat floss can accurately determined using iodine-starch method and double enzymolysis-HPLC method.%本文采用碘显色法、双酶水解-高效液相色谱法和酸水解法对13种肉松样、自制肉松样和加标样进行淀粉含量测定,分析结果,并进一步对肉松制品淀粉含量测定中多糖、抗性糊精等可能干扰物质进行研究。结果表明:采用双酶水解-高效液相色谱法和淀粉显色相结合,可以有效地排除多糖类物质的干扰,避免测定假阳性,从而真实准确地反应肉制品中淀粉含量。

  15. Analysis methods for airborne radioactivity

    OpenAIRE

    Ala-Heikkilä, Jarmo J

    2008-01-01

    High-resolution gamma-ray spectrometry is an analysis method well suitable for monitoring airborne radioactivity. Many of the natural radionuclides and a majority of anthropogenic nuclides are prominent gamma-ray emitters. With gamma-ray spectrometry different radionuclides are readily observed at minute concentrations that are far from health hazards. The gamma-ray spectrometric analyses applied in air monitoring programmes can be divided into particulate measurements and gas measurements. I...

  16. Clays in radioactive waste disposal

    OpenAIRE

    Delage, Pierre; Cui, Yu-Jun; Tang, Anh-Minh

    2010-01-01

    Clays and argillites are considered in some countries as possible host rocks for nuclear waste disposal at great depth. The use of compacted swelling clays as engineered barriers is also considered within the framework of the multi-barrier concept. In relation to these concepts, various research programs have been conducted to assess the thermo-hydro-mechanical properties of radioactive waste disposal at great depth. After introducing the concepts of waste isolation developed in Belgium, Fran...

  17. HMPT: Basic Radioactive Material Transportation

    Energy Technology Data Exchange (ETDEWEB)

    Hypes, Philip A. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-02-29

    Hazardous Materials and Packaging and Transportation (HMPT): Basic Radioactive Material Transportation Live (#30462, suggested one time) and Test (#30463, required initially and every 36 months) address the Department of Transportation’s (DOT’s) function-specific [required for hazardous material (HAZMAT) handlers, packagers, and shippers] training requirements of the HMPT Los Alamos National Laboratory (LANL) Labwide training. This course meets the requirements of 49 CFR 172, Subpart H, Section 172.704(a)(ii), Function-Specific Training.

  18. Radioactive waste management in Austria

    OpenAIRE

    Neubauer Josef

    2004-01-01

    At the Austrian Research Centers Seibersdorf, there are several facilities in stalled for treatment of waste of low and intermediate radioactivity level (radwaste). A separate company within Centers, Nuclear Engineering Seibersdorf, has been formed recently, acting as a centralized facility for treatment, conditioning and storing of such waste within the country. The relevant treatment technology is applied depending on the waste category. In total about 6900 m3 of solid waste of low and inte...

  19. Supervision: Substance and Style

    Science.gov (United States)

    Gellerman, Saul W.

    1976-01-01

    Argues that managerial style and substance are inextricably intertwined, illustrating the discussion with excerpts from an extensive study and job analysis of first-line supervisors in a food packaging plant. (JG)

  20. Radioactive materials transport accident analysis

    Energy Technology Data Exchange (ETDEWEB)

    McSweeney, T.I.; Maheras, S.J.; Ross, S.B. [Battelle Memorial Inst. (United States)

    2004-07-01

    Over the last 25 years, one of the major issues raised regarding radioactive material transportation has been the risk of severe accidents. While numerous studies have shown that traffic fatalities dominate the risk, modeling the risk of severe accidents has remained one of the most difficult analysis problems. This paper will show how models that were developed for nuclear spent fuel transport accident analysis can be adopted to obtain estimates of release fractions for other types of radioactive material such as vitrified highlevel radioactive waste. The paper will also show how some experimental results from fire experiments involving low level waste packaging can be used in modeling transport accident analysis with this waste form. The results of the analysis enable an analyst to clearly show the differences in the release fractions as a function of accident severity. The paper will also show that by placing the data in a database such as ACCESS trademark, it is possible to obtain risk measures for transporting the waste forms along proposed routes from the generator site to potential final disposal sites.