WorldWideScience

Sample records for antidotes

  1. [Antidote update].

    Science.gov (United States)

    Kiyota, Kazuya

    2016-02-01

    In Japan, several products of the antidote for poisoning have been authorized in clinical use from some recent years. For example, Hydroxcobalamin for cyanide poisoning was introduced in 2008. In 2009, Ministry of Health, Labour and Welfare invited suggestions of demand of pharmaceutical products which is high in the need in the medical care but yet unauthorized. Japanese Society for Clinical Toxicology and Japan Poison Information Center applied some candidates including methyleneblue (MB) and fomepizole, both of them were authorized in clinical market in 2015. MB is the medicine for methemoglobinemia, caused by variety of chemical products such as nitrogen oxide. Fomepizole is the antidote for methanol and ethyleneglycol, blocking alcohol dehydrogenase.

  2. Which cyanide antidote?

    Science.gov (United States)

    Hall, Alan H; Saiers, Jane; Baud, Frédéric

    2009-01-01

    Cyanide has several antidotes, with differing mechanisms of action and diverse toxicological, clinical, and risk-benefit profiles. The international medical community lacks consensus about the antidote or antidotes with the best risk-benefit ratio. Critical assessment of cyanide antidotes is needed to aid in therapeutic and administrative decisions that will improve care for victims of cyanide poisoning (particularly poisoning from enclosed-space fire-smoke inhalation), and enhance readiness for cyanide toxic terrorism and other mass-casualty incidents. This paper reviews preclinical and clinical data on available cyanide antidotes and considers the profiles of these antidotes relative to properties of a hypothetical ideal cyanide antidote. Each of the antidotes shows evidence of efficacy in animal studies and clinical experience. The data available to date do not suggest obvious differences in efficacy among antidotes, with the exception of a slower onset of action of sodium thiosulfate (administered alone) than of the other antidotes. The potential for serious toxicity limits or prevents the use of the Cyanide Antidote Kit, dicobalt edetate, and 4-dimethylaminophenol in prehospital empiric treatment of suspected cyanide poisoning. Hydroxocobalamin differs from these antidotes in that it has not been associated with clinically significant toxicity in antidotal doses. Hydroxocobalamin is an antidote that seems to have many of the characteristics of the ideal cyanide antidote: rapid onset of action, neutralizes cyanide without interfering with cellular oxygen use, tolerability and safety profiles conducive to prehospital use, safe for use with smoke-inhalation victims, not harmful when administered to non-poisoned patients, easy to administer.

  3. [Antidotes in clinical toxicology].

    Science.gov (United States)

    Hruby, K

    2013-09-01

    This overview describes antidotes, and their clinical pharmacology, that have an established significance in the currently practiced clinical toxicology because of their proven effectiveness in the treatment of serious poisonings. For the proper, efficient, and targeted use of an antidote, pharmacological knowledge is required, which is a central subject of this article. Current data from the literature are used as reference along with the accumulated experiences about possible adverse effects in order to include them in therapeutic considerations. The dosage of antidotes is the subject of several other review articles and is therefore not included in this synopsis.

  4. [New antidotes in toxicology].

    Science.gov (United States)

    Bédry, Régis

    2008-04-30

    New antidotes appeared in the French pharmacopoeia (fomepizole, Viperfav), and old drugs, usually unused in toxicology, saw their indications enlarged in an antidotic activity (glucose and insulin, L-carnitine, octreotide). Fomepizole is an antidote for toxic alcohol and glycol intoxications, which is much easier to handle than ethylic alcohol and as efficient as the classical antidote of this kind of intoxication. Octreotide improves the result of hypertonic glucose infusion in sulfonylurea derivatives intoxications, by blocking insulin release. The glucose-insulin association allows the myocardium to use the main energy substrate necessary for its action in the setting of beta-blocking and calcium channel blocking agents intoxications when they are associated to a cardiogenic shock. Viperfav is a polyvalent antivenom used in European adders envenomations, which showed its effectiveness and safety. Levocarnitine allows to correct the wrong metabolic pathway induced by a deficit in carnitine in valproïc acid intoxications.

  5. Graphene antidot lattice waveguides

    DEFF Research Database (Denmark)

    Pedersen, Jesper Goor; Gunst, Tue; Markussen, Troels

    2012-01-01

    We introduce graphene antidot lattice waveguides: nanostructured graphene where a region of pristine graphene is sandwiched between regions of graphene antidot lattices. The band gaps in the surrounding antidot lattices enable localized states to emerge in the central waveguide region. We model...... the waveguides via a position-dependent mass term in the Dirac approximation of graphene and arrive at analytical results for the dispersion relation and spinor eigenstates of the localized waveguide modes. To include atomistic details we also use a tight-binding model, which is in excellent agreement...... with the analytical results. The waveguides resemble graphene nanoribbons, but without the particular properties of ribbons that emerge due to the details of the edge. We show that electrons can be guided through kinks without additional resistance and that transport through the waveguides is robust against...

  6. Modifying toxicokinetics with antidotes.

    Science.gov (United States)

    Baud, F J; Borron, S W; Bismuth, C

    1995-12-01

    Five approaches may be described through which antidotes can modify toxicokinetics: (1) Decreased bioavailability of the toxins; (2) Cellular redistribution of the toxin in the organism; (3) Promotion of elimination in an unchanged form; (4) Slowing of metabolic activation pathways; (5) Acceleration of metabolic deactivation pathways. However, the ability to modify toxicokinetics with a new treatment, while demonstrating an understanding of the mechanism of action, must never be construed to be, in and of itself, the goal of therapy. The ultimate evaluation of an antidote modifying toxicokinetics is strictly clinical.

  7. The Antidote to Extremism

    Science.gov (United States)

    Jackson, Anthony

    2016-01-01

    For centuries, education has been seen as an antidote to intolerance and conflict. In a world rocked by violence, much of it across cultural borders, developing students' cultural understanding has become more important than ever. In this article, Asia Society vice president Anthony Jackson discusses how two high schools in the Society's…

  8. Antidotes for acute cyanide poisoning.

    Science.gov (United States)

    Borron, Stephen W; Baud, Frederic J

    2012-08-01

    Cyanide poisoning can present in multiple ways, given its widespread industrial use, presence in combustion products, multiple physical forms, and chemical structures. The primary target of toxicity is mitochondrial cytochrome oxidase. The onset and severity of poisoning depend on the route, dose, physicochemical structure and other variables. Common poisoning features include dyspnea, altered respiratory patterns, abnormal vital signs, altered mental status, seizures, and lactic acidosis. Our present knowledge supports cyanide poisoning treatment based on excellent supportive care with adjunctive antidotal therapy. Multiple antidotes exist and vary in regional availability. All currently marketed antidotes appear to be effective. Antidotal mechanisms include chelation, formation of stable, less toxic complexes, methemoglobin induction, and sulfane sulfur supplementation for detoxification by endogenous rhodanese. Each antidote has advantages and disadvantages. For example, hydroxocobalamin is safer than the methemoglobin inducers in patients with smoke inhalation. Research for new, safer and more effective cyanide antidotes continues.

  9. Spin qubits in antidot lattices

    DEFF Research Database (Denmark)

    Pedersen, Jesper Goor; Flindt, Christian; Mortensen, Niels Asger;

    2008-01-01

    and density of states for a periodic potential modulation, referred to as an antidot lattice, and find that localized states appear, when designed defects are introduced in the lattice. Such defect states may form the building blocks for quantum computing in a large antidot lattice, allowing for coherent...

  10. Where to find the antidote?

    Directory of Open Access Journals (Sweden)

    Carlo Locatelli

    2008-09-01

    Full Text Available In the last ten years, increasing attention has been paid to the unavailability of antidotes in hospital pharmacies and emergency setting. Essential antidotes are not adequately stocked in many European and extra-European countries. The Pavia Poison Center (PPC was charged by the National Institute of Health to conduct a survey in order to define the antidotes availability in emergency setting and to identify areas of possible improvement. Insufficient antidote stocking was defined as lack of the antidote or an amount inadequate to treat 1 seriously poisoned 70-kg patient for 24 hours. A national database (BaNdA accessible through our PC website (www.cavpavia.it that includes information on antidotes stocks of all hospital departments was created. The database information is available for all registered users and regularly updated: a simple query allows to identify hospitals provided with the antidote looked for at local, regional or national level. This database permit to optimize the antidotes procurement by EDs, through agreements with other hospitals serving the same area, to allow a more appropriate utilization of resources and to ameliorate the clinical management of the poisoned patient.

  11. 46 CFR 154.1440 - Antidotes.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Antidotes. 154.1440 Section 154.1440 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) CERTAIN BULK DANGEROUS CARGOES SAFETY STANDARDS FOR... Equipment § 154.1440 Antidotes. Each vessel must have the antidotes prescribed in the IMO Medical First...

  12. 46 CFR 153.930 - Cargo antidotes.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Cargo antidotes. 153.930 Section 153.930 Shipping COAST... Cargo antidotes. No person may operate a tankship that carries a cargo listed in Table 1 unless the tankship has on board the antidotes described for the cargo in the Medical First Aid Guide for Use...

  13. Polymer antidotes for toxin sequestration.

    Science.gov (United States)

    Weisman, Adam; Chou, Beverly; O'Brien, Jeffrey; Shea, Kenneth J

    2015-08-01

    Toxins delivered by envenomation, secreted by microorganisms, or unintentionally ingested can pose an immediate threat to life. Rapid intervention coupled with the appropriate antidote is required to mitigate the threat. Many antidotes are biological products and their cost, methods of production, potential for eliciting immunogenic responses, the time needed to generate them, and stability issues contribute to their limited availability and effectiveness. These factors exacerbate a world-wide challenge for providing treatment. In this review we evaluate a number of polymer constructs that may serve as alternative antidotes. The range of toxins investigated includes those from sources such as plants, animals and bacteria. The development of polymeric heavy metal sequestrants for use as antidotes to heavy metal poisoning faces similar challenges, thus recent findings in this area have also been included. Two general strategies have emerged for the development of polymeric antidotes. In one, the polymer acts as a scaffold for the presentation of ligands with a known affinity for the toxin. A second strategy is to generate polymers with an intrinsic affinity, and in some cases selectivity, to a range of toxins. Importantly, in vivo efficacy has been demonstrated for each of these strategies, which suggests that these approaches hold promise as an alternative to biological or small molecule based treatments.

  14. Antidote Stocking at Hospitals in North Palestine

    Directory of Open Access Journals (Sweden)

    Ansam F. Sawalha

    2007-03-01

    Full Text Available Objective: The purpose of this study was to determine the availability and adequacy of antidote stocking at hospitals in north Palestine based on published guidelines for antidote stocking.Methodology: This study is a cross sectional survey of all hospitals at north Palestine (n=11 using a questionnaire which was completed by the director of the pharmacy department at each hospital. The questionnaire was divided into 2 parts. The first part contained a list of 25 antidotes while the second part contained a list of 12 antidotes. This classification is based on the guideline proposed by the British Association for Emergency Medicine (BAEM. The net antidote stock results were compared with the American guidelines as well.Result: The overall availability of each antidote in the first list varied widely from zero for glucagon to 100% for atropine. The number antidotes of the first list that were stocked in the 11 hospitals ranged from 5 to 12 antidotes but none of the hospitals stocked all the 25 antidotes. Additionally, availability of antidotes in the second list varied widely from zero for polyethylene glycol to 100% for dobutamine. The number of antidotes stocked ranged from 5 to 9 but none of the hospitals stocked all the 12 antidotes.Discussion and Conclusion: hospitals in north Palestine do not have adequate stock of antidotes. Raising awareness of the importance of antidotes by education, regular review of antidote storage, distribution plans, and appropriate legislation might provide solutions. Coordination between Palestinian hospitals and the PCDIC at An-Najah National University is also important.

  15. Graphene antidot lattice transport measurements

    DEFF Research Database (Denmark)

    Mackenzie, David; Cagliani, Alberto; Gammelgaard, Lene

    2017-01-01

    We investigate graphene devices patterned with a narrow band of holes perpendicular to the current flow, a few-row graphene antidot lattice (FR-GAL). Theoretical reports suggest that a FR-GAL can have a bandgap with a relatively small reduction of the transmission compared to what is typical...... for antidot arrays devices. Graphene devices were fabricated using 100 keV electron beam lithography (EBL) for nanopatterning as well as for defining electrical contacts. Patterns with hole diameter and neck widths of order 30 nm were produced, which is the highest reported pattern density of antidot lattices...... in graphene reported defined by EBL. Electrical measurements showed that devices with one and five rows exhibited field effect mobility of ∼100 cm2/Vs, while a larger number of rows, around 40, led to a significant reduction of field effect mobility (

  16. Graphene on graphene antidot lattices

    DEFF Research Database (Denmark)

    Gregersen, Søren Schou; Pedersen, Jesper Goor; Power, Stephen

    2015-01-01

    Graphene bilayer systems are known to exhibit a band gap when the layer symmetry is broken by applying a perpendicular electric field. The resulting band structure resembles that of a conventional semiconductor with a parabolic dispersion. Here, we introduce a bilayer graphene heterostructure......, where single-layer graphene is placed on top of another layer of graphene with a regular lattice of antidots. We dub this class of graphene systems GOAL: graphene on graphene antidot lattice. By varying the structure geometry, band-structure engineering can be performed to obtain linearly dispersing...

  17. The dilemma of approving antidotes.

    Science.gov (United States)

    Steffen, Christian

    2007-04-20

    Clinical trials with antidotes are difficult to perform for a variety of practical, ethical, and financial reasons. As acute poisoning is a rare event, the commercial interest in basic and clinical research is low. Poisoned patients are usually not available for normal clinical trial procedures and, if they are, they cannot give informed consent. This situation results in a dilemma: antidotes are essential drugs. A resolution of the Council of Europe requests to guarantee the optimal availability of antidotes and the improvement of their use. As comprehensive data on the efficacy of antidotes are often missing, a marketing authorisation under exceptional circumstances according to Article 14(8) of Regulation (EC) No. 276/2004, will often be the only way to get an approval, as: (1) the indications for which the product in question is intended are encountered so rarely that the applicant cannot reasonably be expected to provide comprehensive evidence ("orphan drug"), (2) in the present state of scientific knowledge, comprehensive information cannot be provided, or (3) it would be contrary to generally accepted principles of medical ethics to collect such data. Typically, data on antidotes are obtained from a patchwork of studies with animals, human tissue and a few observations from human poisoning corroborated with data from clinical observations and biochemistry. Generalisations from chemical and mechanistic similarities between groups of poisons are usual, but often lack scientific evidence. Current standards of good clinical practice can rarely be observed. Therefore, public funding and other financial support are necessary incentives to initiate trials in this important area.

  18. Vesicant chemotherapy extravasation antidotes and treatments.

    Science.gov (United States)

    Schulmeister, Lisa

    2009-08-01

    Oncology nurses and pharmacists often are given the responsibility of developing or updating institutional policies to manage vesicant chemotherapy extravasations. Antidote and treatment recommendations of vesicant chemotherapy manufacturers, antidotes and treatments approved by the U.S. Food and Drug Administration (FDA), and guidelines and recommendations made by professional oncology organizations are useful resources in this process. This article describes manufacturers' recommendations, lists antidotes and treatments approved by the FDA, and reviews published guidelines and recommendations. Available antidote and treatment formulations and their preparation and administration also are discussed.

  19. Novel, orally effective cyanide antidotes.

    Science.gov (United States)

    Nagasawa, Herbert T; Goon, David J W; Crankshaw, Daune L; Vince, Robert; Patterson, Steven E

    2007-12-27

    A series of prodrugs of 3-mercaptopyruvate (3-MP), the substrate for the enzyme 3-mercaptopyruvate/cyanide sulfurtransferase (3-MPST) that converts cyanide to the nontoxic thiocyanate, which are highly effective cyanide antidotes, have been developed. These prodrugs of 3-MP are unique in being not only orally bioavailable, but may be administered up to an hour prior to cyanide as a prophylactic agent and are both rapid- or slow-acting when given parenterally.

  20. Screening in graphene antidot lattices

    DEFF Research Database (Denmark)

    Schultz, Marco Haller; Jauho, A. P.; Pedersen, T. G.

    2011-01-01

    We compute the dynamical polarization function for a graphene antidot lattice in the random-phase approximation. The computed polarization functions display a much more complicated structure than what is found for pristine graphene (even when evaluated beyond the Dirac-cone approximation...... the plasmon dispersion law and find an approximate square-root dependence with a suppressed plasmon frequency as compared to doped graphene. The plasmon dispersion is nearly isotropic and the developed approximation schemes agree well with the full calculation....

  1. Who gets antidotes? choosing the chosen few.

    Science.gov (United States)

    Buckley, Nicholas A; Dawson, Andrew H; Juurlink, David N; Isbister, Geoffrey K

    2016-03-01

    An understanding of mechanisms, potential benefits and risks of antidotes is essential for clinicians who manage poisoned patients. Of the dozens of antidotes currently available, only a few are regularly used. These include activated charcoal, acetylcysteine, naloxone, sodium bicarbonate, atropine, flumazenil, therapeutic antibodies and various vitamins. Even then, most are used in a minority of poisonings. There is little randomized trial evidence to support the use of most antidotes. Consequently, decisions about when to use them are often based on a mechanistic understanding of the poisoning and the expected influence of the antidote on the patient's clinical course. For some antidotes, such as atropine and insulin, the doses employed can be orders of magnitude higher than standard dosing. Importantly, most poisoned patients who reach hospital can recover with supportive care alone. In low risk patients, the routine use of even low risk antidotes such as activated charcoal is unwarranted. In more serious poisonings, decisions regarding antidote use are generally guided by a risk/benefit assessment based on low quality evidence.

  2. Electronic properties of graphene antidot lattices

    DEFF Research Database (Denmark)

    Fürst, Joachim Alexander; Pedersen, Jesper Goor; Flindt, C.;

    2009-01-01

    Graphene antidot lattices constitute a novel class of nano-engineered graphene devices with controllable electronic and optical properties. An antidot lattice consists of a periodic array of holes that causes a band gap to open up around the Fermi level, turning graphene from a semimetal...... into a semiconductor. We calculate the electronic band structure of graphene antidot lattices using three numerical approaches with different levels of computational complexity, efficiency and accuracy. Fast finite-element solutions of the Dirac equation capture qualitative features of the band structure, while full...

  3. THE HERBICIDES ANTIDOTES OF AGRICULTURAL CROPS (OVERVIEW

    Directory of Open Access Journals (Sweden)

    Yablonskaya Y. K.

    2013-12-01

    Full Text Available The extensive overview of the currently used herbicides antidotes of agricultural crops is reviewed in this article. The most important results are discussed and the technology of combined application is described

  4. Antidote to Controversy? Responses to Carolyn Henly.

    Science.gov (United States)

    Randall, Mary Ella; And Others

    1993-01-01

    Provides four practicing teachers' written responses to Carolyn Henly's article entitled "Reader Response Theory as Antidote to Controversy: Teaching "The Bluest Eye," which appears in the same issue. (HB)

  5. Rising Price of Opioid OD Antidote Could Cost Lives: Study

    Science.gov (United States)

    ... fullstory_162410.html Rising Price of Opioid OD Antidote Could Cost Lives: Study Investigators identify strategies for ... called attention to skyrocketing prices for the lifesaving antidote, noting: Hospira (a Pfizer Inc. company) charges $142 ...

  6. Antidotes for alcohol and glycol toxicity: translating mechanisms into treatments.

    Science.gov (United States)

    McMartin, K E

    2010-09-01

    Translational toxicology can be defined as the movement of potential antidotes for the treatment of poisonings from basic mechanistic research to the marketplace. Because poisonings are infrequent, the clinical development of antidotes is fraught with trials and tribulations. Academic scientists often conduct basic mechanistic work with antidotes but are infrequently involved in further drug development. This article presents the development of 4-methylpyrazole (4MP) (fomepizole) as an antidote against toxic alcohol poisonings, particularly by methanol and ethylene glycol (EG).

  7. Magnetic switching of nanoscale antidot lattices

    Directory of Open Access Journals (Sweden)

    Ulf Wiedwald

    2016-05-01

    Full Text Available We investigate the rich magnetic switching properties of nanoscale antidot lattices in the 200 nm regime. In-plane magnetized Fe, Co, and Permalloy (Py as well as out-of-plane magnetized GdFe antidot films are prepared by a modified nanosphere lithography allowing for non-close packed voids in a magnetic film. We present a magnetometry protocol based on magneto-optical Kerr microscopy elucidating the switching modes using first-order reversal curves. The combination of various magnetometry and magnetic microscopy techniques as well as micromagnetic simulations delivers a thorough understanding of the switching modes. While part of the investigations has been published before, we summarize these results and add significant new insights in the magnetism of exchange-coupled antidot lattices.

  8. Magnetic switching of nanoscale antidot lattices

    Science.gov (United States)

    Gräfe, Joachim; Lebecki, Kristof M; Skripnik, Maxim; Haering, Felix; Schütz, Gisela; Ziemann, Paul; Goering, Eberhard; Nowak, Ulrich

    2016-01-01

    Summary We investigate the rich magnetic switching properties of nanoscale antidot lattices in the 200 nm regime. In-plane magnetized Fe, Co, and Permalloy (Py) as well as out-of-plane magnetized GdFe antidot films are prepared by a modified nanosphere lithography allowing for non-close packed voids in a magnetic film. We present a magnetometry protocol based on magneto-optical Kerr microscopy elucidating the switching modes using first-order reversal curves. The combination of various magnetometry and magnetic microscopy techniques as well as micromagnetic simulations delivers a thorough understanding of the switching modes. While part of the investigations has been published before, we summarize these results and add significant new insights in the magnetism of exchange-coupled antidot lattices. PMID:27335762

  9. Electronic properties of disordered graphene antidot lattices

    DEFF Research Database (Denmark)

    Yuan, Shengjun; Roldán, Rafael; Jauho, Antti-Pekka

    2013-01-01

    Regular nanoscale perforations in graphene (graphene antidot lattices, GALs) are known to lead to a gap in the energy spectrum, thereby paving a possible way towards many applications. This theoretical prediction relies on a perfect placement of identical perforations, a situation not likely to o...

  10. Thermoelectric properties of finite graphene antidot lattices

    DEFF Research Database (Denmark)

    Gunst, Tue; Markussen, Troels; Jauho, Antti-Pekka

    2011-01-01

    We present calculations of the electronic and thermal transport properties of graphene antidot lattices with a finite length along the transport direction. The calculations are based on the π-tight-binding model and the Brenner potential. We show that both electronic and thermal transport...

  11. Development of antidotes for sodium monofluoroacetate (1080).

    Science.gov (United States)

    Cook, C J; Eason, C T; Wickstrom, M; Devine, C D

    2001-01-01

    Baits containing sodium monofluoroacetate (1080) are commonly used in New Zealand during feral pest control operations. However, each year, a number of domestic dogs are unintentionally killed during these control operations, and a suitable antidote to 1080 intoxication is required. The primary toxic mechanism of 1080 is well known. However, as with other pathologies where energy deprivation is the main effect of intoxication, the cascade of effects that arises from this primary mechanism is complex. At present, putative antidotes for 1080 are generally unable to address the primary mechanism of intoxication but such agents may be able to control the cascade of secondary effects, which can result during intoxication. Part of the reason for this is that targeting the cascade can provide a longer window of time for antidote success. We have undertaken studies that identified some of the central nervous system (CNS) and systemic pathophysiological cascades caused by 1080 intoxication. Using this information we designed antidotes, on the basis of preventing different steps in this cascade. In the chicken model targeting systemic changes, in particular reducing effects of nitric oxide derivatives generated in cardiac muscle, proved successful in reducing fatality associated with 1080. In rats and sheep, targeting the CNS with a number of compounds including: glutamate; calcium and dopamine antagonists; gamma amino butyric acid agonists, and astressin-like compounds reduced fatalaties. However, to be successful in the rat and sheep model a given antidote needed to move quickly from systemic circulation across the blood brain barrier and into the CNS. The work also suggests ways in which specific biomarkers of 1080 exposure may be developed with respect to different species.

  12. [Antidotes--often expensive and not always available].

    Science.gov (United States)

    Hoppu, Kalle; Pajarre-Sorsa, Suvi

    2012-01-01

    While there is seldom need for most anti-poisoning agents and antidotes, they should be quickly available, when needed. Local worst-case scenarios, regional staggering of the treatment, and distances must be taken into account at the health care unit level. Hospitals are fairly well equipped with the recommended antidotes. Replenishment of the stocks is complicated by continual disruptions in supply of antidotes. New antidotes in the updated recommendation include calcium folinate (leucovorin) for methanol poisoning and octreotide for the treatment of hypoglycemia caused by intoxications resulting from antidiabetics of the sulfonyl urea group.

  13. [Antidotes to novel direct oral anticoagulants].

    Science.gov (United States)

    Khorev, N G; Momot, A P; Kon'kova, V O

    During the last 10 years, several novel direct oral anticoagulants (NOACs) have entered the clinical arena and were registered in the Russian Federation for use in patients presenting with atrial fibrillation, venous thrombosis, and pulmonary artery thromboembolism. NOACs are classified into two groups: direct thrombin inhibitor (notably dabigatran) and factor Xa inhibitors (including rivaroxaban, apixaban, and edoxaban). Their disadvantage is lack of specific antidotes in case of an emergency situation (injury, infarction, stroke requiring thrombolysis, urgent operation). The review contains the data on the existing therapeutic regimens of treating haemorrhage on the background of taking these coagulants. This is followed by analysing the present-day results of clinical trials aimed at working out pharmaceutical agents (andexanet alpha, idarucizumab, aripazine) being antidotes to direct thrombin inhibitor and the factor Xa inhibitors. Administration of these agents makes it possible to reverse coagulation and minimize the aftermaths of haemorrhage in patients taking these drugs, in emergency situations.

  14. Critical phenomena in ferromagnetic antidot lattices

    Directory of Open Access Journals (Sweden)

    R. Zivieri

    2016-05-01

    Full Text Available In this paper a quantitative theoretical formulation of the critical behavior of soft mode frequencies as a function of an applied magnetic field in two-dimensional Permalloy square antidot lattices in the nanometric range is given according to micromagnetic simulations and simple analytical calculations. The degree of softening of the two lowest-frequency modes, namely the edge mode and the fundamental mode, corresponding to the field interval around the critical magnetic field, can be expressed via numerical exponents. For the antidot lattices studied we have found that: a the ratio between the critical magnetic field and the in-plane geometric aspect ratio and (b the ratio between the numerical exponents of the frequency power laws of the fundamental mode and of the edge mode do not depend on the geometry. The above definitions could be extended to other types of in-plane magnetized periodic magnetic systems exhibiting soft-mode dynamics and a fourfold anisotropy.

  15. Unilateral Antidotes to DNS Cache Poisoning

    OpenAIRE

    Herzberg, Amir; Shulman, Haya

    2012-01-01

    We investigate defenses against DNS cache poisoning focusing on mechanisms that can be readily deployed unilaterally by the resolving organisation, preferably in a single gateway or a proxy. DNS poisoning is (still) a major threat to Internet security; determined spoofing attackers are often able to circumvent currently deployed antidotes such as port randomisation. The adoption of DNSSEC, which would foil DNS poisoning, remains a long-term challenge. We discuss limitations of the prominent r...

  16. Newer clinically available antithrombotics and their antidotes.

    Science.gov (United States)

    Lévy, Samuel

    2014-09-01

    New oral anticoagulants (NOACs) have emerged as an alternative therapy to warfarin in the treatment of arterial and venous thromboembolism and in stroke prevention in patients with non-valvular atrial fibrillation (AF). Three of them, i.e., dabigatran, rivaroxaban, and apixaban, have been approved for clinical use in North America and in a number of European countries. In non-valvular AF, their approval was based on large randomized trials showing that they are non-inferior or even, in some instances, superior to warfarin. Dabigatran is a direct thrombin (factor IIa) inhibitor; rivaroxaban and apixaban are direct factor Xa inhibitors. Before using NOACs, it is recommended to become familiar with their pharmacological characteristics and their metabolism. The absence of specific antidotes is often cited as part of the possible weaknesses of NOACs. Antidotes are perceived to be useful in emergency situations such as life-threatening bleeding or non-elective major surgery. NOACs do not require blood monitoring, and therefore, patient compliance to the treatment is essential. For the present time, there are no specific antidotes available for the three NOACs approved for clinical use. However, phase I or phase II research studies in this area are ongoing. For dabigatran, a specific antidote has been tested in a rat model of anticoagulation, and a study in healthy male volunteers has been recently reported. For rivaroxaban, prothrombin complex concentrates (PCCs) have been found to completely reverse the prolongation of the prothrombin time induced by this NOAC. For apixaban, recombinant factor VII was found in an experimental study using human blood to be superior to activated PCC (aPCC) and PCC. More specific antidotes for rivaroxaban and apixaban are in phases I and II evaluation. The management of patients suffering from a major bleeding or requiring a non-elective major surgery includes non-specific reversal agents and is discussed in the light of a recent position

  17. Common reversal agents/antidotes in small animal poisoning.

    Science.gov (United States)

    Khan, Safdar A

    2012-03-01

    Different antidotes counteract the effect of a toxicant in several different ways. Antidotes can reverse, decrease, or prevent action of a toxicant. They can also help in achieving stabilization of vital signs, directly or indirectly, and promote excretion of a toxicant. However, overreliance on an antidote can be unrealistic and dangerous. While expectations of rapid recovery from antidotes are usually high, in a real life situation, there are many impediments in achieving this goal. The timing of its use, availability, cost, and sometimes adverse effects from the antidote itself can influence the results and outcome of a case. The majority of toxicants do not have a specific antidote therapy indicated and patients in these cases equally benefit from supportive care. In this chapter, commonly used antidotes and reversal agents in small animals are listed in a table form. The table lists generic name along with brand name of an antidote/reversal agent whenever available, main indications for their use, and provides comments or cautions in their use as needed. After stabilizing the patient and establishing the etiology, the clinicians must review more detailed management of that particular toxicant discussed here or in other references.

  18. [Bezoars in history--not only a perfect antidote].

    Science.gov (United States)

    Ryś, Anna; Siek, Bartłomiej; Sein Anand, Jacek

    2012-01-01

    Bezoar is a concretion found in gastrointestinal tract. The word "bezoar" is derived from the Arabic 'padzahr', and means antidote. Animal bezoars were widely used in medicine until the 18th century. Article presents European medieval and modern tradition about bezoar as an antidote. Ancient literary sources are compared with the medieval and modern medical and magical texts.

  19. Anisotropy engineering using exchange bias on antidot templates

    Directory of Open Access Journals (Sweden)

    F. J. T. Goncalves

    2015-06-01

    Full Text Available We explore an emerging device concept based on exchange bias used in conjunction with an antidot geometry to fine tune ferromagnetic resonances. Planar cavity ferromagnetic resonance is used to study the microwave response of NiO/NiFe bilayers with antidot structuring. A large frequency asymmetry with respect to an applied magnetic field is found across a broad field range whose underlying cause is linked to the distribution of magnetic poles at the antidot surfaces. This distribution is found to be particularly sensitive to the effects of exchange bias, and robust in regards to the quality of the antidot geometry. The template based antidot geometry we study offers advantages for practical device construction, and we show that it is suitable for broadband absorption and filtering applications, allowing tunable anisotropies via interface engineering.

  20. Nano-antidotes for drug overdose and poisoning.

    Science.gov (United States)

    Forster, Vincent; Leroux, Jean-Christophe

    2015-06-03

    The number of intoxications from xenobiotics--natural or synthetic foreign chemicals, or substances given in higher doses than typically present in humans--has risen tremendously in the last decade, placing poisoning as the leading external cause of death in the United States. This epidemic has fostered the development of antidotal nanomedicines, which we call "nano-antidotes," capable of efficiently neutralizing offending compounds in situ. Although prototype nano-antidotes have shown efficacy in proof-of-concept studies, the gap to clinical translation can only be filled if issues such as the clinical relevance of intoxication models and the safety profile of nano-antidotes are properly addressed. As the unmet medical needs in resuscitative care call for better treatments, this Perspective critically reviews the recent progress in antidotal medicine and emerging nanotechnologies.

  1. Development of universal antidotes to control aptamer activity.

    Science.gov (United States)

    Oney, Sabah; Lam, Ruby T S; Bompiani, Kristin M; Blake, Charlene M; Quick, George; Heidel, Jeremy D; Liu, Joanna Yi-Ching; Mack, Brendan C; Davis, Mark E; Leong, Kam W; Sullenger, Bruce A

    2009-10-01

    With an ever increasing number of people taking numerous medications, the need to safely administer drugs and limit unintended side effects has never been greater. Antidote control remains the most direct means to counteract acute side effects of drugs, but, unfortunately, it has been challenging and cost prohibitive to generate antidotes for most therapeutic agents. Here we describe the development of a set of antidote molecules that are capable of counteracting the effects of an entire class of therapeutic agents based upon aptamers. These universal antidotes exploit the fact that, when systemically administered, aptamers are the only free extracellular oligonucleotides found in circulation. We show that protein- and polymer-based molecules that capture oligonucleotides can reverse the activity of several aptamers in vitro and counteract aptamer activity in vivo. The availability of universal antidotes to control the activity of any aptamer suggests that aptamers may be a particularly safe class of therapeutics.

  2. Electronic transport in disordered graphene antidot lattice devices

    DEFF Research Database (Denmark)

    Power, Stephen; Jauho, Antti-Pekka

    2014-01-01

    Nanostructuring of graphene is in part motivated by the requirement to open a gap in the electronic band structure. In particular, a periodically perforated graphene sheet in the form of an antidot lattice may have such a gap. Such systems have been investigated with a view towards application...... in transistor or waveguiding devices. The desired properties have been predicted for atomically precise systems, but fabrication methods will introduce significant levels of disorder in the shape, position and edge configurations of individual antidots. We calculate the electronic transport properties of a wide...... range of finite graphene antidot devices to determine the effect of such disorders on their performance. Modest geometric disorder is seen to have a detrimental effect on devices containing small, tightly packed antidots, which have optimal performance in pristine lattices. Larger antidots display...

  3. Antidot effects on micromagnetic behavior of Py ferromagnetic samples

    Energy Technology Data Exchange (ETDEWEB)

    Yetis, Hakan, E-mail: yetis_h@ibu.edu.tr; Denizli, Haluk

    2016-09-01

    The coercivity and magnetic hysteresis behavior of permalloy (Py) samples have been studied in the presence of square arrays of the circular antidots. The open source OOMMF micromagnetic software is used to numerically solve the Landau–Lifshitz–Gilbert (LLG) equation. In calculations, Py samples are designed in such a way that they include a different number of antidot in an array which possess the same total surface area. In this way, the total Py region stayed unchanged despite the growing number of antidots in a fixed sample size. We found significant increase in the coercive field for the sample with the smallest antidot spacing. The results are discussed within the framework of superdomain (SD) and superdomain wall (SDW) formation. - Highlights: • The choice of antidot parameters in a finite sized Py film affects the magnetic reversal process. • The antidot pattern causes the formation of SDs and LE-SDWs at nano-meter scales. • A significant increase in the coercivity is found for the sample with the largest number of antidots.

  4. Magnetic edge states and magnetotransport in graphene antidot barriers

    DEFF Research Database (Denmark)

    Thomsen, M. R.; Power, Stephen; Jauho, Antti-Pekka;

    2016-01-01

    Magnetic fields are often used for characterizing transport in nanoscale materials. Recent magnetotransport experiments have demonstrated that ballistic transport is possible in graphene antidot lattices (GALs). These experiments have inspired the present theoretical study of GALs in a perpendicu......Magnetic fields are often used for characterizing transport in nanoscale materials. Recent magnetotransport experiments have demonstrated that ballistic transport is possible in graphene antidot lattices (GALs). These experiments have inspired the present theoretical study of GALs...... in a perpendicular magnetic field. We calculate magnetotransport through graphene antidot barriers (GABs), which are finite rows of antidots arranged periodically in a pristine graphene sheet, using a tight-binding model and the Landauer-Buttiker formula. We show that GABs behave as ideal Dirac mass barriers...... for antidots smaller than the magnetic length and demonstrate the presence of magnetic edge states, which are localized states on the periphery of the antidots due to successive reflections on the antidot edge in the presence of a magnetic field. We show that these states are robust against variations...

  5. Programmability of Co-antidot lattices of optimized geometry

    Science.gov (United States)

    Schneider, Tobias; Langer, Manuel; Alekhina, Julia; Kowalska, Ewa; Oelschlägel, Antje; Semisalova, Anna; Neudert, Andreas; Lenz, Kilian; Potzger, Kay; Kostylev, Mikhail P.; Fassbender, Jürgen; Adeyeye, Adekunle O.; Lindner, Jürgen; Bali, Rantej

    2017-02-01

    Programmability of stable magnetization configurations in a magnetic device is a highly desirable feature for a variety of applications, such as in magneto-transport and spin-wave logic. Periodic systems such as antidot lattices may exhibit programmability; however, to achieve multiple stable magnetization configurations the lattice geometry must be optimized. We consider the magnetization states in Co-antidot lattices of ≈50 nm thickness and ≈150 nm inter-antidot distance. Micromagnetic simulations were applied to investigate the magnetization states around individual antidots during the reversal process. The reversal processes predicted by micromagnetics were confirmed by experimental observations. Magnetization reversal in these antidots occurs via field driven transition between 3 elementary magnetization states – termed G, C and Q. These magnetization states can be described by vectors, and the reversal process proceeds via step-wise linear operations on these vector states. Rules governing the co-existence of the three magnetization states were empirically observed. It is shown that in an n × n antidot lattice, a variety of field switchable combinations of G, C and Q can occur, indicating programmability of the antidot lattices.

  6. Magnetic edge states and magnetotransport in graphene antidot barriers

    Science.gov (United States)

    Thomsen, M. R.; Power, S. R.; Jauho, A.-P.; Pedersen, T. G.

    2016-07-01

    Magnetic fields are often used for characterizing transport in nanoscale materials. Recent magnetotransport experiments have demonstrated that ballistic transport is possible in graphene antidot lattices (GALs). These experiments have inspired the present theoretical study of GALs in a perpendicular magnetic field. We calculate magnetotransport through graphene antidot barriers (GABs), which are finite rows of antidots arranged periodically in a pristine graphene sheet, using a tight-binding model and the Landauer-Büttiker formula. We show that GABs behave as ideal Dirac mass barriers for antidots smaller than the magnetic length and demonstrate the presence of magnetic edge states, which are localized states on the periphery of the antidots due to successive reflections on the antidot edge in the presence of a magnetic field. We show that these states are robust against variations in lattice configuration and antidot edge chirality. Moreover, we calculate the transmittance of disordered GABs and find that magnetic edge states survive a moderate degree of disorder. Due to the long phase-coherence length in graphene and the robustness of these states, we expect magnetic edge states to be observable in experiments as well.

  7. Low-Temperature Magnetic Properties of Co Antidot Array

    Institute of Scientific and Technical Information of China (English)

    LIU Qing-Fang; JIANG Chang-Jun; FAN Xiao-Long; WANG Jian-Bo; XUE De-Sheng

    2006-01-01

    Cobalt antidot arrays with different thicknesses are fabricated by rf magnetron sputtering onto porous alumina substrates. Scanning electron microscopy and grazing incidence x-ray diffraction are employed to characterize the morphology and crystal structure of the antidot array, respectively. The temperature dependence of magnetic properties shows that in the temperature range 5K-300K, coercivity and squareness increase firstly, reach their maximum values, then decrease. The anomalous temperature dependences of coercivity and squareness are discussed by considering the pinning effect of the antidot and the magnetocrystalline anisotropy.

  8. Graphene antidot lattices: Designed defects and spin qubits

    DEFF Research Database (Denmark)

    Pedersen, Thomas; Flindt, Christian; Pedersen, Jesper Goor;

    2008-01-01

    Antidot lattices, defined on a two-dimensional electron gas at a semiconductor heterostructure, are a well-studied class of man-made structures with intriguing physical properties. We point out that a closely related system, graphene sheets with regularly spaced holes ("antidots"), should display...... qubits. We present a detailed study of the energetics of periodic graphene antidot lattices, analyze the level structure of a single defect, calculate the exchange coupling between a pair of spin qubits, and identify possible avenues for further developments....

  9. Toxicology: pearls and pitfalls in the use of antidotes.

    Science.gov (United States)

    Smollin, Craig G

    2010-02-01

    Although most poisonings require only supportive care, the emergency physician must recognize when the use of an antidote is required, and understand the risks and benefits of the treatment rendered. Although the more commonly instituted specific therapy in acute poisoning is the administration of intravenous fluids followed by the administration of oxygen, in certain circumstances prompt administration of a specific antidote may be required, and failure to identify these circumstances may lead to significant morbidity or mortality. This article describes select antidotes, and discusses their indications and potential pitfalls.

  10. Interaction of nerve agent antidotes with cholinergic systems.

    Science.gov (United States)

    Soukup, O; Tobin, G; Kumar, U K; Binder, J; Proska, J; Jun, D; Fusek, J; Kuca, K

    2010-01-01

    The poisoning with organophosphorus compounds represents a life threatening danger especially in the time of terroristic menace. No universal antidote has been developed yet and other therapeutic approaches not related to reactivation of acetylcholinesterase are being investigated. This review describes the main features of the cholinergic system, cholinergic receptors, cholinesterases and their inhibitors. It also focuses on the organophosphorus nerve agents, their properties, effects and a large part describes various possibilities in treatments, mainly traditional oxime therapies based on reactivation of AChE. Furthermore, non-cholinesterase coupled antidotal effects of the oximes are thoroughly discussed. These antidotal effects principally include oxime interactions with muscarinic and nicotinic receptors.

  11. Antidot effects on micromagnetic behavior of Py ferromagnetic samples

    Science.gov (United States)

    Yetis, Hakan; Denizli, Haluk

    2016-09-01

    The coercivity and magnetic hysteresis behavior of permalloy (Py) samples have been studied in the presence of square arrays of the circular antidots. The open source OOMMF micromagnetic software is used to numerically solve the Landau-Lifshitz-Gilbert (LLG) equation. In calculations, Py samples are designed in such a way that they include a different number of antidot in an array which possess the same total surface area. In this way, the total Py region stayed unchanged despite the growing number of antidots in a fixed sample size. We found significant increase in the coercive field for the sample with the smallest antidot spacing. The results are discussed within the framework of superdomain (SD) and superdomain wall (SDW) formation.

  12. Band Gap Tuning of Armchair Graphene Nanoribbons by Using Antidotes

    Science.gov (United States)

    Zoghi, Milad; Goharrizi, Arash Yazdanpanah; Saremi, Mehdi

    2017-01-01

    The electronic properties of armchair graphene nanoribbons (AGNRs) can be changed by creating antidotes within the pristine ribbons and producing antidote super lattice AGNRs (ASL-AGNRs). In the present work, band gap tuning of ASL-AGNRs is investigated by varying the width of ribbons ( d W) and the distance between antidotes ( d L) for five different antidote topologies. Numerical tight-binding model is applied to obtain the band structure of the ribbons. Based on our results, it is found that the band gap of ASL-AGNRs can be increased or decreased in different cases. Furthermore, changing the width of ribbons generally results in more predictable␣band gap profiles compared to the variation of distance between antidotes. Consequently, by opting appropriate antidote topologies and dimensional parameters ( d W and d L), it is possible to gain a desired band gap size. This can be considered as an alternative solution in design of electronic and optoelectronic devices where tunable band gap values are needed.

  13. A specific antidote for dabigatran: functional and structural characterization.

    Science.gov (United States)

    Schiele, Felix; van Ryn, Joanne; Canada, Keith; Newsome, Corey; Sepulveda, Eliud; Park, John; Nar, Herbert; Litzenburger, Tobias

    2013-05-02

    Dabigatran etexilate is a direct thrombin inhibitor and used widely as an anticoagulant for the prevention of stroke in patients with atrial fibrillation. However, anticoagulation therapy can be associated with an increased risk of bleeding. Here, we present data on the identification, humanization, and in vitro pharmacology of an antidote for dabigatran (aDabi-Fab). The X-ray crystal structure of dabigatran in complex with the antidote reveals many structural similarities of dabigatran recognition compared with thrombin. By a tighter network of interactions, the antidote achieves an affinity for dabigatran that is ~350 times stronger than its affinity for thrombin. Despite the structural similarities in the mode of dabigatran binding, the antidote does not bind known thrombin substrates and has no activity in coagulation tests or platelet aggregation. In addition we demonstrate that the antidote rapidly reversed the anticoagulant activity of dabigatran in vivo in a rat model of anticoagulation. This is the first report of a specific antidote for a next-generation anticoagulant that may become a valuable tool in patients who require emergency procedures.

  14. 48 CFR 225.7005 - Restriction on certain chemical weapons antidote.

    Science.gov (United States)

    2010-10-01

    ... 48 Federal Acquisition Regulations System 3 2010-10-01 2010-10-01 false Restriction on certain chemical weapons antidote. 225.7005 Section 225.7005 Federal Acquisition Regulations System DEFENSE... on certain chemical weapons antidote....

  15. SYNTHESIS OF SUBSTITUTED ISOXAZOLO[5,4-b]PYRIDINE AND THEIR ANTIDOTE ACTIVITY

    Directory of Open Access Journals (Sweden)

    Dyadyuchenko L. V.

    2016-10-01

    Full Text Available To develop the novel herbicide antidotes for the sunflower vegetative plants, the group of chemical compounds, belonging to the derivatives of isoxalopyrazolopyridines was synthesized and their antidote activity both in the laboratory and field experiments was studied. The compounds with a high antidote effect were found

  16. Dynamics of Vortices in Nano-Structured Superconductors with Periodic Arrays of Various Antidots

    Science.gov (United States)

    Fujibayashi, David E.; Kato, Masaru

    2012-12-01

    Stable vortex configurations and its dynamics in superconductors with various types of antidotes are examined, using the molecular dynamics simulation. A pinning potential function, which parameterizes spatial shapes and pinning potential structure of the antidot, is introduced. Dependence of saturation number, which is a maximum number of vortices pinned in a single antidot, on these spatial shape and potential structure are investigated.

  17. Graphene antidot lattices as potential electrode materials for supercapacitors

    Science.gov (United States)

    Liu, Lizhao; Yue, Xin; Zhao, Jijun; Cheng, Qian; Tang, Jie

    2015-05-01

    Thermodynamic stabilities and electronic properties of graphene antidot lattices with hexagonal holes were examined using density functional theory calculations and several crucial factors related to the applications of supercapacitors were discussed. For the graphene antidot lattices with different hole sizes, the formation energy per edge length is about 0.50∼0.60 eV/nm, which is comparable to that of graphene nanoribbon edges. Within a hole density of 10%, the graphene antidot lattices can maintain the excellent electronic properties of perfect graphene due to negligible intervalley scattering. Further increasing the hole density will open a band gap. Taking the potassium chloride (KCl) electrolyte as an example, we further investigated the diffusion behaviors of potassium (K) and chlorine (Cl) atoms through the graphene antidot lattices. It was shown that K and Cl atoms can go through the holes with nearly no barrier at an appropriate hole size of 0.54 nm, which gives an optimum pore diameter of ∼0.86 nm. Therefore, the excellent graphene-like electronic properties and good penetrability for ions suggest promising applications of graphene antidot lattices in the field of supercapacitors.

  18. Transport and magnetic properties of CMR manganites with antidot arrays

    Science.gov (United States)

    Zhang, Kai; Du, Kai; Niu, Jiebin; Wei, Wengang; Chen, Jinjie; Yin, Lifeng; Shen, Jian

    2014-03-01

    We fabricated and characterized a series of manganites thin film samples with different densities of antidots. With increasing antidot density, the samples show higher MIT temperature and lower resistivity under zero and low magnetic fields. These differences become smaller and finally vanished when the magnetic field is large enough to melt the charge ordered phase in the system, which is expected in our theoretical explanations. We believe that emerging edge states at the ring of antidotes play a significant role for observed metal-insulator transition and electrical transport properties, which are of great importance of real storage and sensor device design. Magnetic property measurements and theoretical simulation also support the conclusion. These results open up new ways to control and tune the strongly correlated oxides without introduce any new material or field.

  19. [Antidotes availability in Emergency Departments of the Italian National Health System and development of a national data-bank on antidotes].

    Science.gov (United States)

    Locatelli, Carlo; Petrolini, Valeria; Lonati, Davide; Butera, Raffaella; Bove, Angelo; Mela, Lidia; Manzo, Luigi

    2006-01-01

    The availability of antidotes in Italian hospitals has been evaluated through the answers to a specific questionnaire sent to all Italian Emergency Departments, Intensive Care Units, 118 emergency response system, and Poison Centres. Five Poison Centres and, approximately, the 30% of the Emergency Departments and Intensive Care Units of all Italian emergency hospitals answered to the questionnaire. The results point out an insufficient availability of antidotes in the Italian emergency hospitals, with an almost total absence of those necessary for the treatment of less frequent and less known poisonings (e.g. digoxin, industrial agents), also when the antidote is a lifesaving drug. To improve the antidotes availability for the toxicological emergencies and to facilitate its supplying, a "national antidotes data-base" (BaNdA) has been realized, freely available to the hospital services which register themselves and make their antidotes stockpile available.

  20. Antidot shape dependence of switching mechanism in permalloy samples

    Science.gov (United States)

    Yetiş, Hakan; Denizli, Haluk

    2017-01-01

    We study antidot shape dependence of the switching magnetization for various permalloy samples with square and triangular arrays of nanometer scale antidots. The remnant magnetization, squareness ratio, and coercive fields of the samples are extracted from the hysteresis loops which are obtained by solving the Landau-Lifshitz-Gilbert (LLG) equation numerically. We find several different magnetic spin configurations which reveal the existence of superdomain wall structures. Our results are discussed in terms of the local shape anisotropy, array geometry, and symmetry properties in order to explain the formation of inhomogeneous domain structures.

  1. Screening and collective modes in disordered graphene antidot lattices

    DEFF Research Database (Denmark)

    Yuan, Shengjun; Jin, Fengping; Roldan, Rafael;

    2013-01-01

    The excitation spectrum and the collective modes of graphene antidot lattices (GALs) are studied in the context of a π-band tight-binding model. The dynamical polarizability and dielectric function are calculated within the random-phase approximation. The effect of different kinds of disorder, su...

  2. Creativity: Performativity's Poison or Its Antidote?

    Science.gov (United States)

    Munday, Ian

    2014-01-01

    A common move in the study of creativity and performativity is to present the former as an antidote to the latter. Might we, therefore, see work on creativity in education as heralding an era of post-performativity? In this paper I argue that the portrayal of performativity in the literature on creativity presents an overly simplistic (vulgar?)…

  3. Structural and functional characterization of a specific antidote for ticagrelor.

    Science.gov (United States)

    Buchanan, Andrew; Newton, Philip; Pehrsson, Susanne; Inghardt, Tord; Antonsson, Thomas; Svensson, Peder; Sjögren, Tove; Öster, Linda; Janefeldt, Annika; Sandinge, Ann-Sofie; Keyes, Feenagh; Austin, Mark; Spooner, Jennifer; Gennemark, Peter; Penney, Mark; Howells, Garnet; Vaughan, Tristan; Nylander, Sven

    2015-05-28

    Ticagrelor is a direct-acting reversibly binding P2Y12 antagonist and is widely used as an antiplatelet therapy for the prevention of cardiovascular events in acute coronary syndrome patients. However, antiplatelet therapy can be associated with an increased risk of bleeding. Here, we present data on the identification and the in vitro and in vivo pharmacology of an antigen-binding fragment (Fab) antidote for ticagrelor. The Fab has a 20 pM affinity for ticagrelor, which is 100 times stronger than ticagrelor's affinity for its target, P2Y12. Despite ticagrelor's structural similarities to adenosine, the Fab is highly specific and does not bind to adenosine, adenosine triphosphate, adenosine 5'-diphosphate, or structurally related drugs. The antidote concentration-dependently neutralized the free fraction of ticagrelor and reversed its antiplatelet activity both in vitro in human platelet-rich plasma and in vivo in mice. Lastly, the antidote proved effective in normalizing ticagrelor-dependent bleeding in a mouse model of acute surgery. This specific antidote for ticagrelor may prove valuable as an agent for patients who require emergency procedures.

  4. Sodium dimercaptopropane sulfonate as antidote against non-metallic pesticides

    Institute of Scientific and Technical Information of China (English)

    Zhi-kang CHEN; Zhong-qiu LU

    2004-01-01

    @@ INTRODUCTION With the advent of World War II, dimercaptol was first developed in England as an effective antidote against arsenical agents. In 1950' s, scientists from the Soviet Union developed a water-soluble compound, sodium dimercaptopropane sulfonate (Na-DMPS) named as Unithiol (or Unitiol), which was able to chelate heavy metals and metalloids.

  5. Drugs and pharmaceuticals: management of intoxication and antidotes.

    Science.gov (United States)

    Smith, Silas W

    2010-01-01

    The treatment of patients poisoned with drugs and pharmaceuticals can be quite challenging. Diverse exposure circumstances, varied clinical presentations, unique patient-specific factors, and inconsistent diagnostic and therapeutic infrastructure support, coupled with relatively few definitive antidotes, may complicate evaluation and management. The historical approach to poisoned patients (patient arousal, toxin elimination, and toxin identification) has given way to rigorous attention to the fundamental aspects of basic life support--airway management, oxygenation and ventilation, circulatory competence, thermoregulation, and substrate availability. Selected patients may benefit from methods to alter toxin pharmacokinetics to minimize systemic, target organ, or tissue compartment exposure (either by decreasing absorption or increasing elimination). These may include syrup of ipecac, orogastric lavage, activated single- or multi-dose charcoal, whole bowel irrigation, endoscopy and surgery, urinary alkalinization, saline diuresis, or extracorporeal methods (hemodialysis, charcoal hemoperfusion, continuous venovenous hemofiltration, and exchange transfusion). Pharmaceutical adjuncts and antidotes may be useful in toxicant-induced hyperthermias. In the context of analgesic, anti-inflammatory, anticholinergic, anticonvulsant, antihyperglycemic, antimicrobial, antineoplastic, cardiovascular, opioid, or sedative-hypnotic agents overdose, N-acetylcysteine, physostigmine, L-carnitine, dextrose, octreotide, pyridoxine, dexrazoxane, leucovorin, glucarpidase, atropine, calcium, digoxin-specific antibody fragments, glucagon, high-dose insulin euglycemia therapy, lipid emulsion, magnesium, sodium bicarbonate, naloxone, and flumazenil are specifically reviewed. In summary, patients generally benefit from aggressive support of vital functions, careful history and physical examination, specific laboratory analyses, a thoughtful consideration of the risks and benefits of

  6. [Modern approaches to the formation of antidote stocks at medical institutions in Russia and foreign countries].

    Science.gov (United States)

    Simonenko, V E; Sarmanaev, S Kh; Kovalev, E V; Sarmanaeva, R R; Kukhanov, A V

    2014-11-01

    This article analyses the approaches to the formation of specific treatment of acute poisoning in the various countries. The authors present a systematic review of scientific publications about the formation of reserves of antidote agents at medical institutions of the Russian Federation, the US, Canada, France, Spain, Greece, Norway, Czech Republic, Taiwan and Poland. A search for a variety of databases, as well as by reviewing reference lists of publications on the subject of "stockpiling antidote means". It is concluded that the antidote provision at health care institutions in different countries is insufficient. State of affairs with the formation of antidote stocks is better at hospitals of Czech Republic, France and Spain. To determine the range and volume of the stock of fixed assets necessary antidote coordination and approval of the list and the number of mandatory for every medical institution antidotes.

  7. Effect of Anti-dots on the Magnetic Susceptibility in a Superconducting Long Prism

    Science.gov (United States)

    Aguirre, C. A.; Joya, Miryam R.; Barba-Ortega, J.

    2017-02-01

    The magnetic susceptibility of a long mesoscopic superconducting square prism containing one/two (dot) anti-dots is calculated in the framework of the Ginzburg-Landau theoretical model. This magnetic susceptibility shows jumps at each of the vortex transition fields. We studied the influence of the number, size and geometry of the anti-dots on the magnetic susceptibility in a superconducting sample. We found interesting physical behavior when several kinds of materials filled into the anti-dot are considered.

  8. Acceleration of Advanced CN Antidote Agents for Mass Exposure Treatments: DMTS

    Science.gov (United States)

    2014-12-01

    AD_________________ Award Number: W81XWH-12-2-0098 TITLE: Acceleration of Advanced CN Antidote Agents for Mass Exposure Treatments: DMTS...26 Sept 2012 – 25 Sept 2014 4. TITLE AND SUBTITLE Acceleration of Advanced CN Antidote Agents for Mass Exposure Treatments: DMTS 5a. CONTRACT...gas values and blood pressure during CN treatment and reversal. In the first year of this work, stability and IM antidote administration studies were

  9. A specific antidote for reversal of anticoagulation by direct and indirect inhibitors of coagulation factor Xa.

    Science.gov (United States)

    Lu, Genmin; DeGuzman, Francis R; Hollenbach, Stanley J; Karbarz, Mark J; Abe, Keith; Lee, Gail; Luan, Peng; Hutchaleelaha, Athiwat; Inagaki, Mayuko; Conley, Pamela B; Phillips, David R; Sinha, Uma

    2013-04-01

    Inhibitors of coagulation factor Xa (fXa) have emerged as a new class of antithrombotics but lack effective antidotes for patients experiencing serious bleeding. We designed and expressed a modified form of fXa as an antidote for fXa inhibitors. This recombinant protein (r-Antidote, PRT064445) is catalytically inactive and lacks the membrane-binding γ-carboxyglutamic acid domain of native fXa but retains the ability of native fXa to bind direct fXa inhibitors as well as low molecular weight heparin-activated antithrombin III (ATIII). r-Antidote dose-dependently reversed the inhibition of fXa by direct fXa inhibitors and corrected the prolongation of ex vivo clotting times by such inhibitors. In rabbits treated with the direct fXa inhibitor rivaroxaban, r-Antidote restored hemostasis in a liver laceration model. The effect of r-Antidote was mediated by reducing plasma anti-fXa activity and the non-protein bound fraction of the fXa inhibitor in plasma. In rats, r-Antidote administration dose-dependently and completely corrected increases in blood loss resulting from ATIII-dependent anticoagulation by enoxaparin or fondaparinux. r-Antidote has the potential to be used as a universal antidote for a broad range of fXa inhibitors.

  10. Strengthening positive interpersonal relationships at work: An antidote for burnout

    Directory of Open Access Journals (Sweden)

    CORALIA SULEA

    2014-05-01

    Full Text Available Burnout is an important phenomenon for organizations and employees associated with negative outcomes. Key organizational areas, like fairness and workplace community, are responsible for employee burnout. This editorial argues for the importance of workplace community and presents the mechanisms through which dysfunctional relationships at work may contribute to burnout, as well as the processes that explain how healthy interpersonal relationships can be an antidote for burnout.

  11. Altshuler-Aronov-Spivak Oscillation in Graphene Antidot lattice

    Science.gov (United States)

    Yagi, Ryuta; Sakakibara, Ryoji; Onishi, Junpei; Yagi Lab. Team

    2015-03-01

    We have observed the Altshuler-Aronov-Spivac (AAS) oscillation in triangular antidot lattice of single layer graphene. Low temperature magnetoresistance exhibited h / 2 e periodic oscillations near zero magnetic field, negative magnetoresistance, and h / e periodic (AB-type) oscillations at higher magnetic fields. Phase of the AAS oscillation was the same as those for conventional 2D electrons with negligible spin orbit interaction, showing that inter-valley scattering averaged the Berry phase effect which results in anti-localization.

  12. Spatial confinement of ferromagnetic resonances in honeycomb antidot lattices

    Energy Technology Data Exchange (ETDEWEB)

    Krivoruchko, V.N., E-mail: krivoruc@gmail.com [Donetsk Physics and Technology Institute NAS of Ukraine, 72 R. Luxemburg Str., 83114 Donetsk (Ukraine); Marchenko, A.I., E-mail: marchalexx@gmail.com [Donetsk Physics and Technology Institute NAS of Ukraine, 72 R. Luxemburg Str., 83114 Donetsk (Ukraine)

    2012-09-15

    We report on a theoretical investigation of the magnetic static and dynamic properties of a thin ferromagnetic film with honeycomb lattice of circular antidots using micromagnetic simulations and analytical calculations. The theoretical model is based on the Landau-Lifshitz equations and directly accounts for the effects of the magnetic state nonuniformity. A direct calculation of local dynamic susceptibility tensor yields that the resonance spectra consist of four different quasi-uniform modes of the magnetization precession related to the confinement of magnetic domains by the hole mesh. Three of four resonant modes follow a two-fold variation with respect to the in-plane orientation of the applied magnetic field. The easy axes of these modes are mutually rotated by 60 Degree-Sign and combine to yield the apparent six-fold configurational anisotropy. Additionally, a mode with intrinsic six-fold symmetry behavior exists, as well. Micromagnetic calculations of the local dynamic susceptibility tensor allow identifying the magnetic unit cell areas/domains responsible for each resonance mode. - Highlights: Black-Right-Pointing-Pointer We study the magnetic static and dynamic properties of honeycomb antidot lattices. Black-Right-Pointing-Pointer Micromagnetic simulation and analytical calculation were used. Black-Right-Pointing-Pointer Four quasi-uniform precession modes exist in resonance spectra. Black-Right-Pointing-Pointer The antidot unit cell areas responsible for each resonance mode were identified.

  13. Photostability of antidotal oxime HI-6, impact on drug development.

    Science.gov (United States)

    Bogan, Reinhard; Worek, Franz; Koller, Marianne; Klaubert, Bernd

    2012-01-01

    HI-6 exhibits superior efficacy in the therapy of intoxication by different highly toxic organophosphorus nerve agents. Therefore HI-6 is a promising candidate for the development of new antidotes against nerve agents. For ethical and safety reasons antidotes containing HI-6 should get marketing authorization. Active pharmaceutical ingredients of medicinal products have to fulfil regulatory conditions in terms of purity and stability. Photostability is an essential parameter in this testing strategy. HI-6 was tested under conditions of ICH Q1B 'Photostability testing of new drug substances and products'. The data showed a marked degradation of HI-6 after exposure to daylight. The mechanism of degradation could be detected as photoisomerism. The light burden dependent rate of photoisomerism was followed quantitatively. Based on these quantitative results on the amount of light induced isomeric product a pharmacological qualification was made. A standardized in vitro test showed a decreased ability of light exposed HI-6 to reactivate sarin- and paraoxon-inhibited human acetylcholinesterase. These results have an impact on the further development of antidotes containing HI-6, as light protection will probably be necessary during handling, packaging, storage and application.

  14. Selection of an aptamer antidote to the anticoagulant drug bivalirudin.

    Science.gov (United States)

    Martin, Jennifer A; Parekh, Parag; Kim, Youngmi; Morey, Timothy E; Sefah, Kwame; Gravenstein, Nikolaus; Dennis, Donn M; Tan, Weihong

    2013-01-01

    Adverse drug reactions, including severe patient bleeding, may occur following the administration of anticoagulant drugs. Bivalirudin is a synthetic anticoagulant drug sometimes employed as a substitute for heparin, a commonly used anticoagulant that can cause a condition called heparin-induced thrombocytopenia (HIT). Although bivalrudin has the advantage of not causing HIT, a major concern is lack of an antidote for this drug. In contrast, medical professionals can quickly reverse the effects of heparin using protamine. This report details the selection of an aptamer to bivalirudin that functions as an antidote in buffer. This was accomplished by immobilizing the drug on a monolithic column to partition binding sequences from nonbinding sequences using a low-pressure chromatography system and salt gradient elution. The elution profile of binding sequences was compared to that of a blank column (no drug), and fractions with a chromatographic difference were analyzed via real-time PCR (polymerase chain reaction) and used for further selection. Sequences were identified by 454 sequencing and demonstrated low micromolar dissociation constants through fluorescence anisotropy after only two rounds of selection. One aptamer, JPB5, displayed a dose-dependent reduction of the clotting time in buffer, with a 20 µM aptamer achieving a nearly complete antidote effect. This work is expected to result in a superior safety profile for bivalirudin, resulting in enhanced patient care.

  15. Selection of an aptamer antidote to the anticoagulant drug bivalirudin.

    Directory of Open Access Journals (Sweden)

    Jennifer A Martin

    Full Text Available Adverse drug reactions, including severe patient bleeding, may occur following the administration of anticoagulant drugs. Bivalirudin is a synthetic anticoagulant drug sometimes employed as a substitute for heparin, a commonly used anticoagulant that can cause a condition called heparin-induced thrombocytopenia (HIT. Although bivalrudin has the advantage of not causing HIT, a major concern is lack of an antidote for this drug. In contrast, medical professionals can quickly reverse the effects of heparin using protamine. This report details the selection of an aptamer to bivalirudin that functions as an antidote in buffer. This was accomplished by immobilizing the drug on a monolithic column to partition binding sequences from nonbinding sequences using a low-pressure chromatography system and salt gradient elution. The elution profile of binding sequences was compared to that of a blank column (no drug, and fractions with a chromatographic difference were analyzed via real-time PCR (polymerase chain reaction and used for further selection. Sequences were identified by 454 sequencing and demonstrated low micromolar dissociation constants through fluorescence anisotropy after only two rounds of selection. One aptamer, JPB5, displayed a dose-dependent reduction of the clotting time in buffer, with a 20 µM aptamer achieving a nearly complete antidote effect. This work is expected to result in a superior safety profile for bivalirudin, resulting in enhanced patient care.

  16. Effects of antidot shape on the spin wave spectra of two-dimensional Ni{sub 80}Fe{sub 20} antidot lattices

    Energy Technology Data Exchange (ETDEWEB)

    Mandal, Ruma; Laha, Pinaki; Das, Kaustuv; Saha, Susmita; Barman, Saswati; Raychaudhuri, A. K.; Barman, Anjan, E-mail: abarman@bose.res.in [Thematic Unit of Excellence on Nanodevice Technology, Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700 098 (India)

    2013-12-23

    We show that the optically induced spin wave spectra of nanoscale Ni{sub 80}Fe{sub 20} (permalloy) antidot lattices can be tuned by changing the antidot shape. The spin wave spectra also show an anisotropy with the variation of the in-plane bias field orientation. Analyses show this is due to various quantized and extended modes, whose nature changes with the antidot shape and bias field orientation as a result of the variation of the internal magnetic field profile. The observed variation and anisotropy in the spin waves with the internal and external parameters are important for their applications in magnonic devices.

  17. Cyanide antidotes for mass casualties: water-soluble salts of the dithiane (sulfanegen) from 3-mercaptopyruvate for intramuscular administration.

    Science.gov (United States)

    Patterson, Steven E; Monteil, Alexandre R; Cohen, Jonathan F; Crankshaw, Daune L; Vince, Robert; Nagasawa, Herbert T

    2013-02-14

    Current cyanide antidotes are administered by IV infusion, which is suboptimal for mass casualties. Therefore, in a cyanide disaster, intramuscular (IM) injectable antidotes would be more appropriate. We report the discovery of the highly water-soluble sulfanegen triethanolamine as a promising lead for development as an IM injectable cyanide antidote.

  18. Temperature dependent nonlinear Hall effect in macroscopic Si-MOS antidot array

    OpenAIRE

    Kuntsevich, A. Yu.; Shupltetsov, A. V.; Nunuparov, M. S.

    2015-01-01

    By measuring magnetoresistance and Hall effect in classically moderate perpendicular magnetic field in Si-MOSFET-type macroscopic antidot array we found a novel effect: nonlinear with field, temperature- and density-dependent Hall resistivity. We discuss qualitative explanation of the phenomenon and suggest that it might originate from strong temperature dependence of the resistivity and mobility in the shells of the antidots.

  19. Meso- and racemic-DMSA as Antidotes in Heavy Metal Poisoning

    Science.gov (United States)

    2001-09-01

    UNCLASSIFIED Defense Technical Information Center Compilation Part Notice ADP013383 TITLE: Meso- and racemic-DMSA as Antidotes in Heavy Metal Poisoning...comprise the compilation report: ADP013371 thru ADP013468 UNCLASSIFIED 13. Meso- AND racemic-DMSA AS ANTIDOTES IN HEAVY METAL POISONING 1Maja Blanu~a

  20. Antidotes and treatments for chemical warfare/terrorism agents: an evidence-based review.

    Science.gov (United States)

    Rodgers, G C; Condurache, C T

    2010-09-01

    This article reviews the evidence supporting the efficacy of antidotes used or recommended for the potential chemical warfare agents of most concern. Chemical warfare agents considered include cyanide, vesicants, pulmonary irritants such as chlorine and phosgene, and nerve agents. The strength of evidence for most antidotes is weak, highlighting the need for additional research in this area.

  1. Monitoring the Effects and Antidotes of the Non-vitamin K Oral Anticoagulants

    DEFF Research Database (Denmark)

    Rahmat, Nur A; Lip, Gregory Y H

    2015-01-01

    major challenges: the need for reliable laboratory assays to assess their anticoagulation effect, and the lack of approved antidotes to reverse their action. This article provides an overview of monitoring the anticoagulant effect of NOACs and their potential specific antidotes in development....

  2. [Antidotes and medicines used to treat poisoning in Brazil: needs, availability and opportunities].

    Science.gov (United States)

    Galvão, Tais F; Bucaretchi, Fabio; De Capitani, Eduardo M; Pereira, Maurício G; Silva, Marcus T

    2013-11-01

    Antidotes and certain other drugs are essential for treating some types of poisoning. Failures in their supply can jeopardize the population's health and safety. The current study aimed to assess the availability of antidotes and other drugs used in the treatment of poisonings in Brazil. International guidelines were used as the basis for selecting 41 antidotes for analysis, none of which currently protected by patents. Of these, 27 are registered in Brazil, but 11 of these are available in inadequate forms for treating poisoning, leaving 16 commercially available antidotes. Only one-third of the drugs needed for treating poisoning are included in the country's list of essential drugs. The article also presents a proposal for supplying the demand for one of the antidotes, anti-digoxin antibody, considering Brazil's domestic capacity for manufacturing immunobiologicals. The study's results show the limitations to adequate treatment for poison victims in Brazil and reinforce the urgent need to strengthen public policies in this area.

  3. Antidote control of aptamer therapeutics: the road to a safer class of drug agents.

    Science.gov (United States)

    Bompiani, K M; Woodruff, R S; Becker, R C; Nimjee, S M; Sullenger, B A

    2012-08-01

    Aptamers, or nucleic acid ligands, have gained clinical interest over the past 20 years due to their unique characteristics, which are a combination of the best facets of small molecules and antibodies. The high binding affinity and specificity of aptamers allows for isolation of an artificial ligand for theoretically any therapeutic target of interest. Chemical manipulations of aptamers also allow for fine-tuning of their bioavailability, and antidote control greatly expands their clinical use. Here we review the various methods of antidote control of aptamer therapeutics--matched oligonucleotide antidotes and universal antidotes. We also describe the development, recent progress, and potential future therapeutic applications of these types of aptamer-antidote pairs.

  4. Magnetic Property in large array cobalt antidot thin film using polymer-assisted nanosphere lithography

    Science.gov (United States)

    Lee, Wei-Li; Ho, Chi-Chih; Hsieh, Yung-Wu; Juan, Wen-Tau; Lin, Keng-Hui

    2010-03-01

    We have developed a new method to prepare monolayer of close- packed nanospheres (NSs) over large area onto a substrate of any kind utilizing polymer bridging effect. The NSs packing domain can be as large as 1 cmx1 cm which is demonstrated from its diffraction pattern. It was then used as a template to fabricate series of cobalt antidot thin films with different antidot diameter ranging from 100nm to 180nm. Because of the good periodicity and less defects in our nanostructured samples, we would be able to not only qualitatively study their magnetic properties but also quantitatively. As the antidot diameter increases, the surface to bulk volume fraction increases and the surface magnetism becomes more prominent. We found a systematic increase in magnetic coercivity with the antidote diameter, while the saturation magnetization drops at large antidote diameter. Detailed analysis and their implication will be discussed.

  5. Resonant tunneling diode based on band gap engineered graphene antidot structures

    Science.gov (United States)

    Palla, Penchalaiah; Ethiraj, Anita S.; Raina, J. P.

    2016-04-01

    The present work demonstrates the operation and performance of double barrier Graphene Antidot Resonant Tunnel Diode (DBGA-RTD). Non-Equilibrium Green's Function (NEGF) frame work with tight-binding Hamiltonian and 2-D Poisson equations were solved self-consistently for device study. The interesting feature in this device is that it is an all graphene RTD with band gap engineered graphene antidot tunnel barriers. Another interesting new finding is that it shows negative differential resistance (NDR), which involves the resonant tunneling in the graphene quantum well through both the electron and hole bound states. The Graphene Antidot Lattice (GAL) barriers in this device efficiently improved the Peak to Valley Ratio to approximately 20 even at room temperature. A new fitting model is developed for the number of antidots and their corresponding effective barrier width, which will help in determining effective barrier width of any size of actual antidot geometry.

  6. Boron and nitrogen doping in graphene antidot lattices

    Science.gov (United States)

    Brun, Søren J.; Pereira, Vitor M.; Pedersen, Thomas G.

    2016-06-01

    Bottom-up fabrication of graphene antidot lattices (GALs) has previously yielded atomically precise structures with subnanometer periodicity. Focusing on this type of experimentally realized GAL, we perform density functional theory calculations on the pristine structure as well as GALs with edge carbon atoms substituted with boron or nitrogen. We show that p - and n -type doping levels emerge with activation energies that depend on the level of hydrogenation at the impurity. Furthermore, a tight-binding parametrization together with a Green's function method are used to describe more dilute doping. Finally, random configurations of impurities in moderately doped systems are considered to show that the doping properties are robust against disorder.

  7. Neuroprotective efficacy of pharmacological pretreatment and antidotal treatment in tabun-poisoned rats.

    Science.gov (United States)

    Krejcová, G; Kassa, J

    2003-03-14

    To study the influence of pharmacological pretreatment (PANPAL) and antidotal treatment (obidoxime plus atropine) on tabun-induced neurotoxicity, male albino rats were poisoned with a lethal dose of tabun (280 microg/kg i.m.; 100% of LD(50) value) and observed at 24 h and 7 days following tabun challenge. The neurotoxicity of tabun was evaluated using a functional observational battery (FOB) and an automatic measurement of motor activity. Pharmacological pretreatment as well as antidotal treatment were able to eliminate most of tabun-induced neurotoxic effects observed at 24 h following tabun poisoning. However, there was not significant difference between the efficacy of PANPAL and antidotal treatment to eliminate tabun-induced neurotoxicity in rats. The combination of PANPAL pretreatment and antidotal treatment seems to be slightly more effective in the elimination of tabun-induced neurotoxicity in rats at 24 h following tabun challenge in comparison with the administration of PANPAL pretreatment or antidotal treatment alone. At 7 days following tabun poisoning, very few neurotoxic signs in tabun-poisoned rats were observed regardless of administration of pharmacological pretreatment or antidotal treatment. Thus, our findings confirm that the combination of pharmacological pretreatment and antidotal treatment is not only able to protect the experimental animals from the lethal effects of tabun but also to eliminate most of tabun-induced signs of neurotoxicity in tabun-poisoned rats.

  8. Geometric control of the magnetization reversal in antidot lattices with perpendicular magnetic anisotropy

    Science.gov (United States)

    Gräfe, Joachim; Weigand, Markus; Träger, Nick; Schütz, Gisela; Goering, Eberhard J.; Skripnik, Maxim; Nowak, Ulrich; Haering, Felix; Ziemann, Paul; Wiedwald, Ulf

    2016-03-01

    While the magnetic properties of nanoscaled antidot lattices in in-plane magnetized materials have widely been investigated, much less is known about the microscopic effect of hexagonal antidot lattice patterning on materials with perpendicular magnetic anisotropy. By using a combination of first-order reversal curve measurements, magnetic x-ray microscopy, and micromagnetic simulations we elucidate the microscopic origins of the switching field distributions that arise from the introduction of antidot lattices into out-of-plane magnetized GdFe thin films. Depending on the geometric parameters of the antidot lattice we find two regimes with different magnetization reversal processes. For small antidots, the reversal process is dominated by the exchange interaction and domain wall pinning at the antidots drives up the coercivity of the system. On the other hand, for large antidots the dipolar interaction is dominating which leads to fragmentation of the system into very small domains that can be envisaged as a basis for a bit patterned media.

  9. [Decontamination and antidotes in acute cases of poisoning].

    Science.gov (United States)

    Kupferschmidt, Hugo; Züst, Ariane; Rauber-Lüthy, Christine

    2009-05-01

    In acute poisoning the maintenance or reconstitution of vital functions is the first and most critical action. All subsequent therapies and the prognosis depend on the identification of the causative agent and on information about substance-specific toxicity. Despite incomplete evidence the concept of harm reduction by decreased absorption of the toxicants and by shortening the course of illness is consistent with toxicokinetic-dynamic principles and is therefore still used by clinical toxicologists. All these treatment options have to be seen within the context of the prognosis and the time course of an individual case of poisoning. Treatment options of gastrointestinal decontamination are (in decreasing order of importance) single-dose activated charcoal, whole bowel irritation, and gastric lavage. Induced emesis by ipecac syrup is not practiced anymore. Enhanced elimination techniques are multiple-dose activated charcoal, urine alkalinization, and extracorporeal techniques such as hemodialysis and hemoperfusion. Enhanced elimination is only beneficial in toxicants with long half-life. Antidotes are directed against specific agents and therefore may be used only in a limited number of cases. The procurement of specific antidotes, often hardly available and not approved, is facilitated if the supply is organized in a transparent and standardized manner.

  10. Drugs of abuse: management of intoxication and antidotes.

    Science.gov (United States)

    Montoya, Ivan D; McCann, David J

    2010-01-01

    Illicit drug intoxications are an increasing public health problem for which, in most cases, no antidotes are clinically available. The diagnosis and treatment of these intoxications requires a trained clinician with experience in recognizing the specific signs and symptoms of intoxications to individual drugs as well as polydrug intoxications, which are more the rule than the exception. To make the diagnosis, the clinical observation and a urine toxicology test are often enough. Evaluating the blood levels of drugs is frequently not practical because the tests can be expensive and results may be delayed and unavailable to guide the establishment of a treatment plan. Other laboratory tests may be useful depending on the drug or drugs ingested and the presence of other medical complications. The treatment should be provided in a quiet, safe and reassuring environment. Vital signs should be closely monitored. Changes in blood pressure, respiratory frequency and temperature should be promptly treated, particularly respiratory depression (in cases of opiate intoxication) or hyperthermia (in cases of cocaine or amphetamine intoxication). Intravenous fluids should be administered as soon as possible. Other psychiatric and medical complication should receive appropriate symptomatic treatment. Research on immunotherapies, including vaccines, monoclonal and catalytic antibodies, seems to be a promising approach that may yield specific antidotes for drugs of abuse, helping to ameliorate the morbidity and mortality associated with illicit drug intoxications.

  11. Enhanced Spin Hall Effect by Single Antidot Potential

    Science.gov (United States)

    Eto, Mikio; Yokoyama, Tomohiro

    2009-03-01

    We theoretically investigate an extrinsic spin Hall effect in semiconductor heterostructures due to the scattering by an artificial potential created by a single antidot, STM tip, etc. The strength of the potential is electrically tunable. First, we formulate the spin Hall effect in terms of phase shifts in the partial wave expansion for two-dimensional electron gas. For scattered electrons in θ direction, we obtain a spin polarization P(θ) perpendicular to the two-dimensional plane [P(-θ)=-P (θ)]. The spin polarization P(θ) is significantly enhanced by an attractive potential when the resonant condition of a partial wave is satisfied by tuning the potential strength. Second, we study the spin Hall effect in a three-terminal device with an antidot at the junction. The conductance and spin polarization are evaluated numerically.ootnotetextM. Yamamoto and B. Kramer, J. Appl. Phys. 103, 123703 (2008), for repulsive potential. We obtain a spin polarization of more than 50% due to the resonant scattering when the attractive potential is properly tuned.

  12. Evaluation of oxime k203 as antidote in tabun poisoning.

    Science.gov (United States)

    Kovarik, Zrinka; Vrdoljak, Ana Lucić; Berend, Suzana; Katalinić, Maja; Kuc, Kamil; Musilek, Kamil; Radić, Bozica

    2009-03-01

    We studied bispyridinium oxime K203 [(E)-1-(4-carbamoylpyridinium)-4-(4-hydroxyiminomethylpyridinium)-but-2-ene dibromide] with tabun-inhibited human acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) in vitro, and its antidotal effect on tabun-poisoned mice and rats in vivo. We compared it with oximes K048 and TMB-4, which have proven the most efficient oxime antidotes in tabun poisoning by now. Tabun-inhibited AChE was completely reactivated by K203, with the overall reactivation rate constant of 1806 L mol(-1) min(-1). This means that K203 is a very potent reactivator of tabun-inhibited AChE. In addition, K203 reversibly inhibited AChE (Ki = 0.090 mmol L(-1)) and BChE (K(i) = 0.91 mmol L(-1)), and exhibited its protective effect against phosphorylation of AChE by tabun in vitro. In vivo, a quarter of the LD50 K203 dose insured survival of all mice after the application of as many as 8 LD50 doses of tabun, which is the highest dosage obtained compared to K048 and TMB-4. Moreover, K203 showed high therapeutic potency in tabun-poisoned rats, preserving cholinesterase activity in rat plasma up to 60 min after poisoning. This therapeutic improvement obtained by K203 in tabun-poisoning places this oxime in the spotlight for further development.

  13. A novel paradigm for assessing efficacies of potential antidotes against neurotoxins in mice.

    Science.gov (United States)

    Crankshaw, Daune L; Goon, David J W; Briggs, Jacquie E; DeLong, David; Kuskowski, Michael; Patterson, Steven E; Nagasawa, Herbert T

    2007-12-10

    Historically, antidotal potencies of cyanide antagonists were measured as increases in the experimental LD(50) for cyanide elicited by the antidotes. This required the use of high doses of cyanide following pre-treatment with the putative antidote. Since IACUC guidelines at our institutions strongly discourage LD(50) determinations: we developed a new test paradigm that allowed for maximal survival of cyanide-treated animals with greatly reduced numbers of animals. Symptoms of cyanide toxicity include disruption of neuromuscular coordination, i.e., the righting reflex. Therefore, to establish a dose-response curve, the times required for recovery of this righting reflex with increasing doses of cyanide were measured. A cyanide dose that disrupted this righting reflex for approximately 1h with minimal deaths was then selected. Using this paradigm, the current cyanide antidotes, viz., nitrite plus thiosulfate and hydroxocobalamin, as well as some potential cyanide antidotes that we developed, were evaluated pre- and post-cyanide. This allowed, for the first time, the assessment of the post-cyanide effectiveness of the current antidotes against cyanide poisoning in a live animal. In addition, some prototype compounds were found to exhibit antidotal efficacy not only when injected i.p. following cyanide, but also when administered orally 30 min before cyanide. Pre-cyanide oral efficacy suggests that such compounds have the potential of being administered prophylactically before exposure to cyanide. This new test paradigm was found to be a powerful tool for assessing the efficacies of some novel antidotes against cyanide and should be equally applicable for evaluating putative antidotes for other neurotoxins.

  14. Characterization and Magnetic Properties of Iron-Based Alloy Antidot Arrays

    Institute of Scientific and Technical Information of China (English)

    LIU Qing-Fang; JIANG Chang-Jun; WANG Jian-Bo; FAN Xiao-Long; XUE De-Sheng

    2007-01-01

    Fe29Co71 and Fe19Ni8 antidot arrays, with different dimensions, are prepared with the rf magnetron sputtering method onto the porous alumina substrate. The size and shape of antidot arrays are characterized by scanning electron microscopy. The glancing angle x-ray diffraction patterns of Fe29Co71 and Fe1gNis1 antidot arrays indicate the bcc and fcc structures, respectively. The coercivities of both the alloys show abnormal thickness dependence, which are discussed qualitatively by considering the pinning and the thickness effect to the films.

  15. Dispersions of the resonance frequencies in an antidot system in a magnetic field

    CERN Document Server

    Lee, Y S

    2000-01-01

    An analytical and quantum-mechanical method is developed to study the collective excitation spectrum of an antidot system in a normal magnetic field. The problem is solved within the single-particle picture within the framework of an anisotropic quantum wire or dot, taking into account the classical phenomenon of edge magneto-plasmons (EMP's) through the renormalization of the effective strength of the antidot potential at a hole. The resulting dispersions with magnetic fields explain quantitatively the main spectrum of the antidot system observed in recent experiments.

  16. Vortices trapped in the damaged surroundings of antidots in Nb films - Depinning transition

    Energy Technology Data Exchange (ETDEWEB)

    Nunes-Kapp, J.S. [Grupo de Supercondutividade e Magnetismo, Departamento de Fisica, Universidade Federal de Sao Carlos, Sao Carlos, SP (Brazil); Faculdade de Tecnologia SENAI ' Antonio Adolpho Lobbe' , Sao Carlos, SP (Brazil); Zadorosny, R.; Oliveira, A.A.M. [Grupo de Supercondutividade e Magnetismo, Departamento de Fisica, Universidade Federal de Sao Carlos, Sao Carlos, SP (Brazil); Vaz, A.R.; Moshkalev, S.A. [Centro de Componentes Semicondutores, UNICAMP, Campinas, SP (Brazil); Lepienski, M. [Departamento de Fisica, Universidade Federal do Parana, Curitiba, PR (Brazil); Ortiz, W.A., E-mail: wortiz@df.ufscar.b [Grupo de Supercondutividade e Magnetismo, Departamento de Fisica, Universidade Federal de Sao Carlos, Sao Carlos, SP (Brazil)

    2010-10-01

    The depinning transition of Vortex Matter in the presence of antidots in superconducting Nb films has been investigated. The antidots were fabricated using two different techniques, resulting in samples with arrays of diverse pinning efficiency. At low temperatures and fields, the spatial arrangement of Vortex Matter is governed by the presence of the antidots. Keeping the temperature fixed, an increase of the field induces a depinning transition. As the temperature approaches T{sub c}, the depinning frontier exhibits a characteristic kink at the temperature T{sub k}, above which the phase boundary exhibits a different regime. The lower-temperature regime is adequately described by a power-law expression, whose exponent n was observed to be inversely proportional to the pinning capability of the antidot, a feature that qualifies this parameter as a figure of merit to quantify the pinning strength of the defect.

  17. Density functional study of graphene antidot lattices: Roles of geometrical relaxation and spin

    DEFF Research Database (Denmark)

    Fürst, Joachim Alexander; Pedersen, Thomas Garm; Brandbyge, Mads;

    2009-01-01

    Graphene sheets with regular perforations, dubbed as antidot lattices, have theoretically been predicted to have a number of interesting properties. Their recent experimental realization with lattice constants below 100 nanometers stresses the urgency of a thorough understanding of their electron...

  18. A micromagnetic study of the hysteretic behavior of antidot Fe films

    Energy Technology Data Exchange (ETDEWEB)

    Torres Bruna, J.M. [Instituto de Ciencia de Materiales de Aragon (CSIC-Universidad de Zaragoza), Plaza de San Francisco s/n, 50009 Zaragoza (Spain); Bartolome, J. [Instituto de Ciencia de Materiales de Aragon (CSIC-Universidad de Zaragoza), Plaza de San Francisco s/n, 50009 Zaragoza (Spain); Garcia Vinuesa, L.M. [Instituto de Ciencia de Materiales de Aragon (CSIC-Universidad de Zaragoza), Plaza de San Francisco s/n, 50009 Zaragoza (Spain); Garcia Sanchez, F. [Instituto de Ciencia de Materiales de Madrid, CSIC Cantoblanco, 28049 Madrid (Spain); Gonzalez, J.M. [Unidad Asociada ICMM-IMA, Sor Juana Ines de la Cruz s/n, 28049 Madrid P.O. Box 155, 28230 Las Rozas, Madrid (Spain); Chubykalo-Fesenko, O.A. [Instituto de Ciencia de Materiales de Madrid, CSIC Cantoblanco, 28049 Madrid (Spain)]. E-mail: oksana@icmm.csic.es

    2005-04-15

    We report on the results of a micromagnetic study of the magnetization reversal process taking place in square arrays of antidots lithographed in Fe thin films. Our study focuses on the influence on the reversal process of the antidot diameter and the distance between adjacent antidots. It is shown that the minimization of the dipolar energy term of the total system energy originates inhomogeneous moment distributions at the antidot surfaces, and that these structures and their coupling rule the reversal process. We also show that the variation of the interantidot distance in the range of a few units of the exchange length allows varying the coercive force value by a factor of four approximately.

  19. Application of Conformal Mapping to the determination of Magnetic Moment Distributions in typical Antidot Film Nanostructures

    CERN Document Server

    Schilling, Osvaldo F

    2008-01-01

    There has been an increasing technological interest on magnetic thin films containing antidot arrays of hexagonal or square symmetry. Part of this interest is related to the possibility of domain formation and pinning at the antidots boundaries. In this paper, we develop a method for the calculation of the magnetic moment distribution for such arrays which concentrates on the immediate vicinity of each antidot. For each antidot distribution (square or hexagonal) a suitable system of coordinates is defined to exploit the shape of the unit-cells of the overall nanostructure. The Landau-Lifshitz-Gilbert-Brown equations that govern the distribution of moments are rewritten in terms of these coordinates. The equilibrium moments orientation is calculated for each position in a Cartesian grid defined for these new coordinate systems, and then a conformal transformation is applied to insert the moment vectors into the actual unit-cell. The resulting vector maps display quite clearly regions of different moment orient...

  20. Anticholinergic drugs--functional antidotes for the treatment of tabun intoxication.

    Science.gov (United States)

    Krejcová, Gabriela; Kassa, Jirí

    2004-01-01

    1. To study the influence of antidotes on tabun-induced neurotoxicity, the rats were injected intramuscularly with organophosphate tabun (LD50). The efficacy of choice antidotal treatment consisting of acetylcholinesterase reactivator obidoxime and one of four anticholinergic drugs (atropine, benactyzine, biperiden, scopolamine) was compared. 2. Testing of tabun-induced neurotoxicity progress was carried out using the method Functional observational battery. The experimental animals as well as controls were observed at 24 hours and 7 days following tabun or saline administration. 3. The results were compared to the condition of animals without anticholinergic drug (oxime alone) and control rats that received physiological solution instead of tabun and treatment. Antidotal treatment involving centrally acting anticholinergic drugs (benactyzine, biperiden, scopolamine) showed significantly higher neuroprotective efficacy compared to antidotal treatment containing atropine.

  1. Reprint of : Thermodynamic properties of a quantum Hall anti-dot interferometer

    Science.gov (United States)

    Levy Schreier, Sarah; Stern, Ady; Rosenow, Bernd; Halperin, Bertrand I.

    2016-08-01

    We study quantum Hall interferometers in which the interference loop encircles a quantum anti-dot. We base our study on thermodynamic considerations, which we believe reflect the essential aspects of interference transport phenomena. We find that similar to the more conventional Fabry-Perot quantum Hall interferometers, in which the interference loop forms a quantum dot, the anti-dot interferometer is affected by the electro-static Coulomb interaction between the edge modes defining the loop. We show that in the Aharonov-Bohm regime, in which effects of fractional statistics should be visible, is easier to access in interferometers based on anti-dots than in those based on dots. We discuss the relevance of our results to recent measurements on anti-dots interferometers.

  2. Designed defects in 2D antidot lattices for quantum information processing

    DEFF Research Database (Denmark)

    Pedersen, Jesper Goor; Flindt, Christian; Mortensen, Niels Asger

    2008-01-01

    We propose a new physical implementation of spin qubits for quantum information processing, namely defect states in antidot lattices defined in the two-dimensional electron gas (2DEG) at a semiconductor heterostructure. Calculations of the band structure of a periodic antidot lattice are presented....... We find results reminiscent of double quantum dot structures, indicating that the suggested structure is a feasible physical implementation of spin qubits....

  3. Preparation of Oxime HI-6 (Dichloride and DimethanesulphonateŒAntidote against Nerve Agents

    Directory of Open Access Journals (Sweden)

    Kamil Kuca

    2008-05-01

    Full Text Available Because of the threat of misuse of nerve agents as terroristic weapons by the terrorists, animmediate need is felt for the preparation of antidotes on large-scale basis.  HI-6 (dichloride anddimethanesulphonate salt are the most promising acetylcholinesterase reactivators used ascausal antidotes in nerve agents intoxication. In this study, rapid and large-scale preparationof oxime HI-6, the most promising reactivator has been described.

  4. Specific antidotes in development for reversal of novel anticoagulants: a review.

    Science.gov (United States)

    Gomez-Outes, Antonio; Suarez-Gea, M L; Lecumberri, Ramon; Terleira-Fernandez, Ana I; Vargas-Castrillon, Emilio

    2014-01-01

    In the last decade, several direct oral anticoagulants (DOAC; dabigatran, rivaroxaban, apixaban, edoxaban) have been marketed for prophylaxis and/or treatment of thromboembolism without having specific antidotes available for their reversal. Current management of bleeding associated to DOAC includes the removal of all antithrombotic medications and supportive care. Non-specific procoagulant agents (prothrombin complex concentrates and activated factor VIIa) have been used in case of serious bleeding. Currently, some specific antidotes for the DOAC are under development. Idarucizumab (BI 655075; Boehringer Ingelheim) is a fragment of an antibody (Fab), which is a specific antidote to the oral direct thrombin inhibitor dabigatran. Andexanet alfa (r-Antidote, PRT064445; Portola Pharmaceuticals) is a truncated form of enzymatically inactive factor Xa, which binds and reverses the anticoagulant action of the factor Xa inhibitors (e.g.: rivaroxaban, apixaban and edoxaban). Aripazine (PER-977, ciraparantag; Perosphere Inc.) is a synthetic small molecule (~500 Da) that reverses oral dabigatran, apixaban, rivaroxaban, as well as subcutaneous fondaparinux and LMWH in vivo. These antidotes could provide an alternative for management of life-threatening bleeding events occurring with the above-mentioned anticoagulants. In addition, the specific antidote anivamersen (RB007; Regado Biosciences Inc.) is an RNA aptamer in clinical development to reverse the anticoagulant effect of the parenteral factor IXa inhibitor pegnivacogin, which is also in development. This anticoagulant-antidote pair may provide an alternative in situations in which a fast onset and offset of anticoagulation is needed, like in patients undergoing cardiac surgery with extracorporeal circulation, as an alternative to the heparin/protamine pair. This patent review includes a description of the pharmacological characteristics of the novel specific antidotes, the available results from completed non

  5. Idarucizumab as Antidote to Intracerebral Hemorrhage under Treatment with Dabigatran

    Science.gov (United States)

    Held, Valentin; Eisele, Philipp; Eschenfelder, Christoph C.; Szabo, Kristina

    2016-01-01

    Background and Purpose Non-vitamin K anticoagulants (NOAC) such as dabigatran have become important therapeutic options for the prevention of stroke. Until recently, there were only nonspecific agents to reverse their anticoagulant effects in a case of emergency. Idarucizumab, an antibody fragment targeting dabigatran, is the first specific antidote for a NOAC to be approved, but real-world experience is limited. Methods We report two cases of patients on dabigatran with acute intracerebral hemorrhage who received idarucizumab. Results In both cases, idarucizumab promptly reversed the anticoagulant effect of dabigatran and there was no hematoma expansion in follow-up imaging. Conclusions In addition to clinical and preclinical studies, our cases add to the experience regarding the safety and efficacy of idarucizumab. They show that idarucizumab may be an important safety option for patients on dabigatran in emergency situations. PMID:27920714

  6. That's a Phat Antidote: Intravenous Fat Emulsions and Toxicological Emergencies.

    Science.gov (United States)

    Schultz, Amy E; Lewis, Temeka; Reed, Brittany S; Weant, Kyle A; Justice, Stephanie Baker

    2015-01-01

    Health care providers in the emergency department (ED) frequently find themselves caring for patients who may have overdosed on a medication(s) or other toxic substance. These patients can prove to be a challenge, as providers must try to determine the substance(s) involved so that the appropriate treatment can be initiated. For those patients who are hemodynamically unstable upon presentation, it is important to note that supportive care is of the utmost importance, as there are few substances that have antidotes available. In these situations, lipid emulsion can be considered. This is especially true in the setting of the following toxicities: local anesthetics, β-blockers, calcium channel blockers, and the tricyclic antidepressants. Even though lipid emulsion may not be used that frequently in the ED, it is important to be aware of its role in the setting of toxicological emergencies, how it should be dosed and administered, and the necessary safety precautions.

  7. Intralipid emulsion treatment as an antidote in lipophilic drug intoxications.

    Science.gov (United States)

    Eren Cevik, Sebnem; Tasyurek, Tanju; Guneysel, Ozlem

    2014-09-01

    Intravenous lipid emulsion (ILE) is a lifesaving treatment of lipophilic drug intoxications. Not only does ILE have demonstrable efficacy as an antidote to local anesthetic toxicity, it is also effective in lipophilic drug intoxications. Our case series involved 10 patients with ingestion of different types of lipophilic drugs. Intravenous lipid emulsion treatment improved Glasgow Coma Scale or blood pressure and pulse rate or both according to the drug type. Complications were observed in 2 patients (minimal change pancreatitis and probable ILE treatment-related fat infiltration in lungs). In our case series, ILE was used for different lipophilic drug intoxications to improve cardiovascular and neurologic symptoms. According to the results, it was found that ILE treatment is a lifesaving agent in lipophilic drug intoxications and it can be used in unconscious patients who have cardiac and/or neurologic symptoms but no history of a specific drug ingestion.

  8. Hydrogen sulfide poisoning: an antidotal role for sodium nitrite?

    Science.gov (United States)

    Hall, A H; Rumack, B H

    1997-06-01

    In 2 separate incidents, 6 patients were poisoned with hydrogen sulfide (H2S) in sewer gas. In the first incident, mixing acid- and sodium hydroxide-based drain cleaners in a confined space resulted in 4 poisonings and 2 deaths. Three would-be rescuers were seriously poisoned and 1 died. Two survivors had neurological sequelae. Sodium nitrite appeared to have some clinical efficacy in 1 case. The second incident involved 2 patients working on a pump in a sewage pond. A patient lying on a raft close to the pond surface was seriously poisoned; sodium nitrite was clinically efficacious and this patient survived without developing neurological sequelae. Sodium nitrite deserves further clinical study as a potential H2S antidote.

  9. A study of periodic and aperiodic ferromagnetic antidot lattices

    Science.gov (United States)

    Bhat, Vinayak S.

    This thesis reports our study of the effect of domain wall pinning by ferromagnetic (FM) metamaterials [1] in the form of periodic antidot lattices (ADL) on spin wave spectra in the reversible regime. This study was then extended to artificial quasicrystals in the form of Penrose P2 tilings (P2T). Our DC magnetization study of these metamaterials showed reproducible and temperature dependent knee anomalies in the hysteretic regime that are due to the isolated switching of the FM segments. Our dumbbell model analysis [2] of simulated magnetization maps indicates that FM switching in P2T is nonstochastic . We have also acquired the first direct, two-dimensional images of the magnetization of Permalloy films patterned into P2T using scanning electron microscopy with polarization analysis (SEMPA). Our SEMPA images demonstrate P2T behave as geometrically frustrated networks of narrow ferromagnetic film segments having near-uniform, bipolar (Ising-like) magnetization, similar to artificial spin ices (ASI). We find the unique aperiodic translational symmetry and diverse vertex coordination of multiply-connected P2T induce a more complex spin-ice behavior driven by exchange interactions in vertex domain walls, which differs markedly from the behavior of disconnected ASI governed only by dipolar interactions. Keywords: Ferromagnetic Antidot Lattices, Metamaterials, Ferromagnetic Resonance, Artificial Quasicrystal, Artificial Spin Ice. [1] VV Kruglyak et al. "Magnonic metamaterials". In: Metamaterial, edited by X.-Y. Jiang (InTech, 2012) (2012). [2] Claudio Castelnovo, Roderich Moessner, and Shivaji L Sondhi. "Magnetic monopoles in spin ice". In: Nature 451.7174 (2008), pp. 42--45.

  10. Crystal structure of the MazE/MazF complex: molecular bases of antidote-toxin recognition.

    Science.gov (United States)

    Kamada, Katsuhiko; Hanaoka, Fumio; Burley, Stephen K

    2003-04-01

    A structure of the Escherichia coli chromosomal MazE/MazF addiction module has been determined at 1.7 A resolution. Addiction modules consist of stable toxin and unstable antidote proteins that govern bacterial cell death. MazE (antidote) and MazF (toxin) form a linear heterohexamer composed of alternating toxin and antidote homodimers (MazF(2)-MazE(2)-MazF(2)). The MazE homodimer contains a beta barrel from which two extended C termini project, making interactions with flanking MazF homodimers that resemble the plasmid-encoded toxins CcdB and Kid. The MazE/MazF heterohexamer structure documents that the mechanism of antidote-toxin recognition is common to both chromosomal and plasmid-borne addiction modules, and provides general molecular insights into toxin function, antidote degradation in the absence of toxin, and promoter DNA binding by antidote/toxin complexes.

  11. Kind and estimated stocking amount of antidotes for initial treatment for acute poisoning at emergency medical centers in Korea.

    Science.gov (United States)

    Sohn, Chang Hwan; Ryoo, Seung Mok; Lim, Kyoung Soo; Kim, Won; Lim, Hoon; Oh, Bum Jin

    2014-11-01

    Antidotes for toxicological emergencies can be life-saving. However, there is no nationwide estimation of the antidotes stocking amount in Korea. This study tried to estimate the quantities of stocking antidotes at emergency department (ED). An expert panel of clinical toxicologists made a list of 18 emergency antidotes. The quantity was estimated by comparing the antidote utilization frequency in a multicenter epidemiological study and the nation-wide EDs' data of National Emergency Department Information System (NEDIS). In an epidemiological study of 11 nationwide EDs from January 2009 to December 2010, only 92 (1.9%) patients had been administered emergency antidotes except activated charcoal among 4,870 cases of acute adult poisoning patients. Comparing with NEDIS data, about 1,400,000 patients visited the 124 EDs nationwide due to acute poisoning and about 103,348 adult doses of the 18 emergency antidotes may be required considering poisoning severity score. Of these, 13,224 (1.9%) adult doses of emergency antidotes (575 of atropine, 144 of calcium gluconate or other calcium salts, 2,587 of flumazenil, 3,450 of N-acetylcysteine, 5,893 of pralidoxime, 287 of hydroxocobalamin, 144 of sodium nitrite, and 144 of sodium thiosulfate) would be needed for maintaining the present level of initial treatment with emergency antidotes at EDs in Korea.

  12. Benzylpenicillin, acetylcysteine and silibinin as antidotes in human hepatocytes intoxicated with alpha-amanitin.

    Science.gov (United States)

    Magdalan, Jan; Ostrowska, Alina; Piotrowska, Aleksandra; Gomułkiewicz, Agnieszka; Podhorska-Okołów, Marzena; Patrzałek, Dariusz; Szelag, Adam; Dziegiel, Piotr

    2010-07-01

    Fatalities due to mushroom poisonings are increasing worldwide, with high mortality rate resulting from ingestion of amanitin-producing species. Intoxications caused by amanitin-containing mushrooms represent an unresolved problem in clinical toxicology since no specific and fully efficient antidote is available. The objective of this study was a comparative evaluation of benzylpenicillin (BPCN), acetylcysteine (ACC) and silibinin (SIL) as an antidotes in human hepatocytes intoxicated with alpha-amanitin (alpha-AMA). All experiments were performed on cultured human hepatocytes. Cytotoxicity evaluation of cultured cells using MTT assay and measurement of lactate dehydrogenase (LDH) activity was performed at 12, 24 and 48h of exposure to alpha-AMA and/or antidotes. The significant decline of cell viability and significant increase of LDH activity were observed in all experimental hepatocyte cultures after 12, 24 and 36h exposure to alpha-AMA at concentration 2microM. Exposure of the cells to alpha-AMA resulted also in significant reduction of cell spreading and attachment. However, addition of tested antidotes to experimental cultures significantly stimulated cell proliferation and attachment. In cell cultures exposed simultaneously to alpha-AMA and tested antidotes cytotoxic parameters (MTT and LDH) were not significantly different from control incidences. The cytoprotective effect of all antidotes was not dose-related, which reflects a high efficacy of all these substances. Administration of studied antidotes was not associated with any adverse effects in hepatocytes. The administration of ACC, BPCN or SIL to human hepatocyte cultures showed a similar strong protective effect against cell damage in alpha-AMA toxicity.

  13. Universal rule on chirality-dependent bandgaps in graphene antidot lattices.

    Science.gov (United States)

    Liu, Xiaofei; Zhang, Zhuhua; Guo, Wanlin

    2013-04-22

    Graphene with periodically patterned antidots has attracted intense research attention as it represents a facile route to open a bandgap for graphene electronics. However, not all graphene antidot lattices (GALs) can open a bandgap and a guiding rule is missing. Here, through systematic first-principles calculations, it is found that bandgaps in triangular GALs are surprisingly well defined by a chirality vector R = n a1 + ma2 connecting two neighboring antidots, where a1 and a2 are the basis vectors of graphene. The bandgap opens in the GALs with (n-m)mod3 = 0 but remains closed in those with (n-m)mod3 = ±1, reminiscent of the gap-chirality rule in carbon nanotubes. Remarkably, the gap value in GALs allows ample modulation by adjusting the length of chirality vectors, shape and size of the antidots. The gap-chirality relation in GALs stems from the chirality-dependent atomic structures of GALs as revealed by a super-atom model as well as Clar sextet analyses. This chirality-dependent bandgap is further shown to be a generic behavior in any parallelogram GAL and thus serves as an essential stepping stone for experimenters to realize graphene devices by antidot engineering.

  14. Recent advances in the development of specific antidotes for target-specific oral anticoagulants.

    Science.gov (United States)

    Mo, Yoonsun; Yam, Felix K

    2015-02-01

    Warfarin, a vitamin K antagonist, has been the only orally available anticoagulant for > 60 years. During the past decade, the U.S. Food and Drug Administration has approved several target-specific oral anticoagulants (TSOACs) for the prophylaxis and treatment of arterial and venous thromboembolism and stroke prevention in patients with nonvalvular atrial fibrillation. These new agents have several advantages over warfarin including more predictable pharmacokinetics and pharmacodynamics, fewer food and drug interactions, and lack of need for routine coagulation monitoring. However, unlike warfarin, currently no antidotes are available to reverse the anticoagulant effect of TSOACs. Specific antidotes for TSOACs may not be needed in most situations due to their short half-life, yet the absence of antidotes for these agents is a concern, especially in emergent situations such as life-threatening major bleeding or nonelective major surgery. Several specific antidotes for TSOACs including idarucizumab, andexanet alfa, and aripazine have been developed and have shown promise in early clinical trials evaluating their efficacy and safety. In this narrative review, the progress made in developing specific antidotes for TSOACs is summarized based on the latest available preclinical and clinical data.

  15. An in vivo zebrafish screen identifies organophosphate antidotes with diverse mechanisms of action.

    Science.gov (United States)

    Jin, Shan; Sarkar, Kumar S; Jin, Youngnam N; Liu, Yan; Kokel, David; Van Ham, Tjakko J; Roberts, Lee D; Gerszten, Robert E; Macrae, Calum A; Peterson, Randall T

    2013-01-01

    Organophosphates are a class of highly toxic chemicals that includes many pesticides and chemical weapons. Exposure to organophosphates, either through accidents or acts of terrorism, poses a significant risk to human health and safety. Existing antidotes, in use for over 50 years, have modest efficacy and undesirable toxicities. Therefore, discovering new organophosphate antidotes is a high priority. Early life stage zebrafish exposed to organophosphates exhibit several phenotypes that parallel the human response to organophosphates, including behavioral deficits, paralysis, and eventual death. Here, we have developed a high-throughput zebrafish screen in a 96-well plate format to find new antidotes that counteract organophosphate-induced lethality. In a pilot screen of 1200 known drugs, we identified 16 compounds that suppress organophosphate toxicity in zebrafish. Several in vitro assays coupled with liquid chromatography/tandem mass spectrometry-based metabolite profiling enabled determination of mechanisms of action for several of the antidotes, including reversible acetylcholinesterase inhibition, cholinergic receptor antagonism, and inhibition of bioactivation. Therefore, the in vivo screen is capable of discovering organophosphate antidotes that intervene in distinct pathways. These findings suggest that zebrafish screens might be a broadly applicable approach for discovering compounds that counteract the toxic effects of accidental or malicious poisonous exposures.

  16. Evolution of microwave ferromagnetic resonance with magnetic domain structure in FeCoBSi antidot arrays

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Peiheng, E-mail: phzhou@uestc.edu.cn; Zhang, Nan; Liu, Tao; Xie, Jianliang; Deng, Longjiang

    2014-08-01

    Magnetic domain structure of FeCoBSi antidot array thin films of varying thickness were characterized using surface magneto-optic Kerr effect. Vibrating sample magnetometry and microstrip transmission line measurements helped to associate the microwave magnetic analysis of the antidot arrays with hysteresis studies. The domain structure evolution from quasi-continuous domains to strip domains induced by the competing exchange and dipolar interaction resulted in the change of ferromagnetic resonance from multi-band to single-band. Hence, the mechanisms of multi-resonance are proposed to be related to domain wall motion, natural resonance and spin wave modes. This phenomenon can be used to control the magnetization dynamics in spin wave devices. - Highlights: • A multiresonance mechanism for ferromagnetic antidot array is proposed. • The mechanism relies on the domain structure evolution of antidote arrays. • Domain structure of antidot arrays changes from quasi-continuous patterns to strip domains. • Resonance of domain wall motion is discriminated from the natural resonance and spin wave modes.

  17. Ethylene glycol or methanol intoxication: which antidote should be used, fomepizole or ethanol?

    Science.gov (United States)

    Rietjens, S J; de Lange, D W; Meulenbelt, J

    2014-02-01

    Ethylene glycol (EG) and methanol poisoning can cause life-threatening complications. Toxicity of EG and methanol is related to the production of toxic metabolites by the enzyme alcohol dehydrogenase (ADH), which can lead to metabolic acidosis, renal failure (in EG poisoning), blindness (in methanol poisoning) and death. Therapy consists of general supportive care (e.g. intravenous fluids, correction of electrolytes and acidaemia), the use of antidotes and haemodialysis. Haemodialysis is considered a key element in the treatment of severe EG and methanol intoxication and is aimed at removing both the parent compound and its toxic metabolites, reducing the duration of antidotal treatment and shortening the hospital observation period. Currently, there are two antidotes used to block ADH-mediated metabolism of EG and methanol: ethanol and fomepizole. In this review, the advantages and disadvantages of both antidotes in terms of efficacy, safety and costs are discussed in order to help the physician to decide which antidote is appropriate in a specific clinical setting.

  18. Antidotes for poisoning by alcohols that form toxic metabolites.

    Science.gov (United States)

    McMartin, Kenneth; Jacobsen, Dag; Hovda, Knut Erik

    2016-03-01

    The alcohols, methanol, ethylene glycol and diethylene glycol, have many features in common, the most important of which is the fact that the compounds themselves are relatively non-toxic but are metabolized, initially by alcohol dehydrogenase, to various toxic intermediates. These compounds are readily available worldwide in commercial products as well as in homemade alcoholic beverages, both of which lead to most of the poisoning cases, from either unintentional or intentional ingestion. Although relatively infrequent in overall occurrence, poisonings by metabolically-toxic alcohols do unfortunately occur in outbreaks and can result in severe morbidity and mortality. These poisonings have traditionally been treated with ethanol since it competes for the active site of alcohol dehydrogenase and decreases the formation of toxic metabolites. Although ethanol can be effective in these poisonings, there are substantial practical problems with its use and so fomepizole, a potent competitive inhibitor of alcohol dehydrogenase, was developed for a hopefully better treatment for metabolically-toxic alcohol poisonings. Fomepizole has few side effects and is easy to use in practice and it may obviate the need for haemodialysis in some, but not all, patients. Hence, fomepizole has largely replaced ethanol as the toxic alcohol antidote in many countries. Nevertheless, ethanol remains an important alternative because access to fomepizole can be limited, the cost may appear excessive, or the physician may prefer ethanol due to experience.

  19. Antidotal Efficacy of Antioxidants against Cyanide Poisoning in vitro.

    Directory of Open Access Journals (Sweden)

    R. Bhattacharya

    1999-01-01

    Full Text Available Cyanide is a potent homicidal, genocidal and chemical warfare agent. Besides, its known inhibitory effects on various enzyme Systems, its other pronounced toxic effects include lipid peroxidation (LPx, particularly in the central nervous system or neuronal cells in vitro. The present study assessed the cytotoxicity of potassium cyanide (KCN in two non-neuronal mammalian cell cultures, viz., human embryonic lung epithelium (L-132 and baby hamster kidney (BHK-21 cells. In addition, the cytoprotective potential of two antioxidant agents, namely, curcumin (CMN and N-acetylcysteine (NAC against KCN (2 and 4 mM in vitro was evaluated. In both the cell lines, KCN reduced cell viability as indicated by trypan blue dye exclusion, leakage of cytosolic lactate dehydrogenase and neutral red uptake. Protein content was unaffected in L-132 cells while cellular respiration determined by MTT assay was impaired in both the cells. A dose-dependent glutathione mediated LPx was observed in BHK-21 cells alone. The above cytotoxic changes produced by KCN were more effectively minimised by NAC as compared to CMN. Efficacy of CMN and NAC have therapeutic implications as adjuncts to existing cyanide antidotes.

  20. Properties of two-dimensional electron gas containing self-organized quantum antidots

    Science.gov (United States)

    Vasilyev, Yu.; Suchalkin, S.; Zundel, M.; Heisenberg, D.; Eberl, K.; von Klitzing, K.

    1999-11-01

    A nonuniform two-dimensional electron gas in a heterojunction with inserted self-organized electrically inactive dots (acting as antidots) has been fabricated by molecular-beam epitaxy of AlGaAs/AlInAs/GaAs layer sequences. Transport measurements give the ratio of the transport mobility to the quantum mobility less than four, which suggests that the dominant scattering at low magnetic fields is the short-range scattering from the lateral potential of the antidots. Far-infrared cyclotron resonance (CR) spectra show an absorption mode as narrow as 0.5 cm-1 at high magnetic fields associated with the high-mobility electron gas formed between the antidot islands and confined in the lateral directions. The confinement energy of 14 cm-1 is derived from the CR spectra.

  1. Detoxification of mercury species - an in vitro study with antidotes in human whole blood

    Energy Technology Data Exchange (ETDEWEB)

    Truempler, Stefan; Nowak, Sascha; Meermann, Bjoern; Buscher, Wolfgang; Karst, Uwe [University of Muenster, Institute of Inorganic and Analytical Chemistry, Muenster (Germany); Wiesmueller, Gerhard A. [University Hospital Muenster, Environmental Specimen Bank for Human Tissues, Muenster (Germany); Sperling, Michael [University of Muenster, Institute of Inorganic and Analytical Chemistry, Muenster (Germany); European Virtual Institute for Speciation Analysis, Muenster (Germany)

    2009-11-15

    To investigate the effects of mercury species intoxication and to test the efficiency of different commonly applied antidotes, human whole blood and plasma surrogate samples were spiked with inorganic mercury (Hg{sup 2+}) and methylmercury (MeHg{sup +}, CH{sub 3}Hg{sup +}) prior to treatment with the antidotes 2,3-dimercaptopropan-1-ol (British Anti Lewisite), 2,3-dimercaptosuccinic acid (DMSA), and N-acetylcysteine (NAC). For mercury speciation analysis in these samples, liquid chromatography was coupled to either inductively coupled plasma mass spectrometry (ICP-MS) or electrospray ionisation time-of-flight mass spectrometry (ESI-TOF-MS). Adduct formation between mercury species and physiological thiols (cysteine and glutathione) was observed as well as the release of glutathione under treatment with the antidotes DMSA and NAC. (orig.)

  2. Detoxification of mercury species--an in vitro study with antidotes in human whole blood.

    Science.gov (United States)

    Trümpler, Stefan; Nowak, Sascha; Meermann, Björn; Wiesmüller, Gerhard A; Buscher, Wolfgang; Sperling, Michael; Karst, Uwe

    2009-11-01

    To investigate the effects of mercury species intoxication and to test the efficiency of different commonly applied antidotes, human whole blood and plasma surrogate samples were spiked with inorganic mercury (Hg2+) and methylmercury (MeHg+, CH3Hg+) prior to treatment with the antidotes 2,3-dimercaptopropan-1-ol (British Anti Lewisite), 2,3-dimercaptosuccinic acid (DMSA), and N-acetylcysteine (NAC). For mercury speciation analysis in these samples, liquid chromatography was coupled to either inductively coupled plasma mass spectrometry (ICP-MS) or electrospray ionisation time-of-flight mass spectrometry (ESI-TOF-MS). Adduct formation between mercury species and physiological thiols (cysteine and glutathione) was observed as well as the release of glutathione under treatment with the antidotes DMSA and NAC.

  3. Generation of propagating spin waves from regions of increased dynamic demagnetising field near magnetic antidots

    Energy Technology Data Exchange (ETDEWEB)

    Davies, C. S., E-mail: csd203@exeter.ac.uk; Kruglyak, V. V. [School of Physics, University of Exeter, Stocker Road, Exeter EX4 4QL (United Kingdom); Sadovnikov, A. V.; Nikitov, S. A. [Laboratory “Metamaterials,” Saratov State University, Saratov 410012 (Russian Federation); Kotel' nikov Institute of Radioengineering and Electronics, Russian Academy of Sciences, Moscow 125009 (Russian Federation); Grishin, S. V.; Sharaevskii, Yu. P. [Laboratory “Metamaterials,” Saratov State University, Saratov 410012 (Russian Federation)

    2015-10-19

    We have used Brillouin Light Scattering and micromagnetic simulations to demonstrate a point-like source of spin waves created by the inherently nonuniform internal magnetic field in the vicinity of an isolated antidot formed in a continuous film of yttrium-iron-garnet. The field nonuniformity ensures that only well-defined regions near the antidot respond in resonance to a continuous excitation of the entire sample with a harmonic microwave field. The resonantly excited parts of the sample then served as reconfigurable sources of spin waves propagating (across the considered sample) in the form of caustic beams. Our findings are relevant to further development of magnonic circuits, in which point-like spin wave stimuli could be required, and as a building block for interpretation of spin wave behavior in magnonic crystals formed by antidot arrays.

  4. Homer's moly identified as Galanthus nivalis L.: physiologic antidote to stramonium poisoning.

    Science.gov (United States)

    Plaitakis, A; Duvoisin, R C

    1983-03-01

    The antidotal properties of certain naturally occurring medicinal plants against central nervous system intoxication appear to have been empirically established in ancient times. Homer, in his epic poem, the Odyssey, described a plant, "moly," used by Odysseus as an antidote against Circe's poisonous drugs. Centrally acting anticholinergic agents are thought to have been used by Circe to induce amnesia and a delusional state in Odysseus' crew. We present evidence to support the hypothesis that "moly" might have been the snowdrop, Galanthus nivalis, which contains galanthamine, a centrally acting anticholinesterase. Thus the description of "moly" as an antidote in Homer's Odyssey may represent the oldest recorded use of an anticholinesterase to reverse central anticholinergic intoxication.

  5. Quaternary and tertiary aldoxime antidotes for organophosphate exposure in a zebrafish model system.

    Science.gov (United States)

    Schmidt, Hayden R; Radić, Zoran; Taylor, Palmer; Fradinger, Erica A

    2015-04-15

    The zebrafish is rapidly becoming an important model system for screening of new therapeutics. Here we evaluated the zebrafish as a potential pharmacological model for screening novel oxime antidotes to organophosphate (OP)-inhibited acetylcholinesterase (AChE). The ki values determined for chlorpyrifos oxon (CPO) and dichlorvos (DDVP) showed that CPO was a more potent inhibitor of both human and zebrafish AChE, but overall zebrafish AChE was less sensitive to OP inhibition. In contrast, aldoxime antidotes, the quaternary ammonium 2-PAM and tertiary amine RS-194B, showed generally similar overall reactivation kinetics, kr, in both zebrafish and human AChE. However, differences between the Kox and k2 constants suggest that zebrafish AChE associates more tightly with oximes, but has a slower maximal reactivation rate than human AChE. Homology modeling suggests that these kinetic differences result from divergences in the amino acids lining the entrance to the active site gorge. Although 2-PAM had the more favorable in vitro reactivation kinetics, RS-194B was more effective antidote in vivo. In intact zebrafish embryos, antidotal treatment with RS-194B rescued embryos from OP toxicity, whereas 2-PAM had no effect. Dechorionation of the embryos prior to antidotal treatment allowed both 2-PAM and RS-194B to rescue zebrafish embryos from OP toxicity. Interestingly, RS-194B and 2-PAM alone increased cholinergic motor activity in dechorionated embryos possibly due to the reversible inhibition kinetics, Ki and αKi, of the oximes. Together these results demonstrate that the zebrafish at various developmental stages provides an excellent model for investigating membrane penetrant antidotes to OP exposure.

  6. Neuroprotective effects of currently used antidotes in tabun-poisoned rats.

    Science.gov (United States)

    Kassa, Jirí; Krejèová, Gabriela

    2003-06-01

    The neuroprotective effects of antidotes (atropine, pralidoxime/atropine, obidoxime/atropine and HI-6/atropine mixtures) on rats poisoned with tabun at a lethal dose (220 microg/kg intramuscularly; 100% of LD50 value) were studied. The tabun-induced neurotoxicity was monitored using a functional observational battery and an automatic measurement of motor activity. The neurotoxicity of tabun was monitored at 24 hr and 7 days after tabun challenge. The results indicate that atropine alone is not able to protect the rats from the lethal effects of tabun. Three non-treated tabun-poisoned rats and one tabun-poisoned rat treated with atropine alone died within 24 hr. On the other hand, atropine combined with all tested oximes allows all tabun-poisoned rats to survive at least 7 days following tabun challenge. Obidoxime combined with atropine seems to be the most effective antidotal treatment for the elimination of tabun-induced neurotoxicity in the case of lethal poisoning among tested antidotal mixtures. The antidotal mixture consisting of atropine and HI-6 is significantly less effective than the combination of atropine with obidoxime in the elimination of tabun-induced neurotoxicity in rats at 24 hr following tabun challenge. Pralidoxime in combination with atropine appears to be practically ineffective to decrease tabun-induced neurotoxicity at 24 hours as well as 7 days following tabun poisoning. Due to its neuroprotective effects, obidoxime seems to be the most effective and most suitable oxime for the antidotal treatment of acute tabun exposure among currently used oximes. Thus, the replacement of obidoxime by a more effective acetylcholinesterase reactivator for soman poisoning, the oxime HI-6, can to a small extent diminish the neuroprotective efficacy of antidotal treatment in the case of acute tabun poisonings.

  7. Enhanced spin Hall effect by tuning antidot potential: Proposal for a spin filter

    Science.gov (United States)

    Yokoyama, Tomohiro; Eto, Mikio

    2009-09-01

    We propose an efficient spin filter including an antidot fabricated on semiconductor heterostructures with strong spin-orbit interaction. The antidot creates a tunable potential on two-dimensional electron gas in the heterostructures, which may be attractive as well as repulsive. Our idea is based on the enhancement of extrinsic spin Hall effect by resonant scattering when the attractive potential is properly tuned. Numerical studies for three- and four-terminal devices indicate that the efficiency of the spin filter can be more than 50% by tuning the potential to the resonant condition.

  8. Multifunctional drugs as novel antidotes for organophosphates' poisoning.

    Science.gov (United States)

    Weissman, Ben Avi; Raveh, Lily

    2011-12-18

    Some organophosphorus compounds (OPs) are nerve agents that continue to concern military personnel and civilians as potential battlefield and terrorist threats. Additionally, OPs are used in agriculture where they are associated with numerous cases of intentional and accidental misuse. These toxicants induce an array of deleterious effects including respiratory distress, convulsions and ultimately death. A mechanism involving a rapid and potent inhibition of peripheral and central cholinesterases leading to a massive buildup of acetylcholine in synaptic clefts was suggested as the underlying trigger of the toxic events. Indeed, therapy comprised of an acetylcholinesterase reactivator (i.e., oxime) and a cholinergic antagonist (e.g., atropine) is the accepted major paradigm for protection. This approach yields a remarkable survival rate but fails to prevent neurological and behavioral deficits. Extensive research revealed a complex picture consisting of an early activation of several neurotransmitter systems, in which the glutamatergic plays a pivotal role., Data accumulated in recent years support the concept that multi-targeting of pathways including glutamatergic and cholinergic circuits is required for an effective treatment. Drugs that demonstrate the ability to interact with several systems (e.g., caramiphen) were found to afford a superior protection against OPs as compared to specific antimuscarinic ligands (e.g., scopolamine). Compounds that potently block muscarinic receptors, interact with the NMDA ion channel and in addition are able to modulate σ(1) sites and/or GABAergic transmission seem to represent the emerging backbone for novel antidotes against OP poisoning. Several multifunctional drugs are already used for complex diseases e.g., cancer and depression.

  9. N-acetylcysteine amide, a promising antidote for acetaminophen toxicity.

    Science.gov (United States)

    Khayyat, Ahdab; Tobwala, Shakila; Hart, Marcia; Ercal, Nuran

    2016-01-22

    Acetaminophen (N-acetyl-p-aminophenol, APAP) is one of the most widely used over the counter antipyretic and analgesic medications. It is safe at therapeutic doses, but its overdose can result in severe hepatotoxicity, a leading cause of drug-induced acute liver failure in the USA. Depletion of glutathione (GSH) is one of the initiating steps in APAP-induced hepatotoxicity; therefore, one strategy for restricting organ damage is to restore GSH levels by using GSH prodrugs. N-acetylcysteine (NAC), a GSH precursor, is the only currently approved antidote for an acetaminophen overdose. Unfortunately, fairly high doses and longer treatment times are required due to its poor bioavailability. In addition, oral and I.V. administration of NAC in a hospital setting are laborious and costly. Therefore, we studied the protective effects of N-acetylcysteine amide (NACA), a novel antioxidant with higher bioavailability, and compared it with NAC in APAP-induced hepatotoxicity in C57BL/6 mice. Our results showed that NACA is better than NAC at a low dose (106mg/kg) in preventing oxidative stress and protecting against APAP-induced damage. NACA significantly increased GSH levels and the GSH/GSSG ratio in the liver to 66.5% and 60.5% of the control, respectively; and it reduced the level of ALT by 30%. However, at the dose used, NAC was not effective in combating the oxidative stress induced by APAP. Thus, NACA appears to be better than NAC in reducing the oxidative stress induced by APAP. It would be of great value in the health care field to develop drugs like NACA as more effective and safer options for the prevention and therapeutic intervention in APAP-induced toxicity.

  10. The Copernican Revolution as Story: an Antidote for Scientific Illiteracy

    Science.gov (United States)

    Wallace, P. M.

    2005-08-01

    ``When a white-robed scientist, momentarily looking away from his microscope or cyclotron [or telescope], makes some pronouncement for the general public, he may not be understood but at least he is certain to be believed.'' The truth of this opening sentence of Anthony Standen's 1950 book Science is a Sacred Cow, as clear today as it was then, is the motivation for a new astronomy course at Berry College near Atlanta, GA, USA. To non-scientists, science is known by its products, not by what it is: a human progress. For this illiteracy an antidote is offered: the history of astronomy. In this course the story of the Copernican Revolution is told, for within this story the true nature of science can be found in its fullness. For example, Aristotle's uniform circular motion is used to emphasize the role of assumptions, and the occasional value of wrong ideas is evident in Tycho's theory and in Kepler's universe of perfect solids. Tycho's observations of Mars and Kepler's analysis illustrate the interplay of observation, theory, and technology. As a final example, the indirectness and often-unintentional nature of scientific advance can be seen in the work of Copernicus. The roles of personality and the intersections of science and society are themes throughout the course, as are the merging of disparate fields and the power of strong theories. There are other themes (e.g., coherence, the role of mathematics), but the emphasis is on the science and much of the work is quantitative. There is a laboratory component that features observations and experiments, and in order to bring the narrative to life the class spends two weeks in Poland, the Czech Republic, and Italy, touring sites that are relevant to the story of the Copernican Revolution.

  11. Novel nerve-agent antidote design based on crystallographic and mass spectrometric analyses of tabun-conjugated acetylcholinesterase in complex with antidotes.

    Science.gov (United States)

    Ekström, F J; Astot, C; Pang, Y-P

    2007-09-01

    Organophosphorus compound-based nerve agents inhibit the essential enzyme acetylcholinesterase (AChE) causing acute toxicity and death. Clinical treatment of nerve-agent poisoning is to use oxime-based antidotes to reactivate the inhibited AChE. However, the nerve agent tabun is resistant to oximes. To design improved oximes, crystal structures of a tabun-conjugated AChE in complex with different oximes are needed to guide the structural modifications of known antidotes. However, this type of structure is extremely challenging to obtain because both deamidation of the tabun conjugate and reactivation of AChE occur during crystallographic experiments. Here we report, for the first time, the crystal structures of Ortho-7 and HLö-7 in complex with AChE that is conjugated to an intact tabun. These structures were determined by our new strategy of combining crystallographic and mass spectrometric analyses of AChE crystals. The results explain the relative reactivation potencies of the two oximes and offer insights into improving known medical antidotes.

  12. Magnetization reversal mechanism in patterned (square to wave-like) Py antidot lattices

    Science.gov (United States)

    Tahir, N.; Zelent, M.; Gieniusz, R.; Krawczyk, M.; Maziewski, A.; Wojciechowski, T.; Ding, J.; Adeyeye, A. O.

    2017-01-01

    The effects of shape and geometry of antidot (square, bi-component, and wave-like) lattices (ADLs) on the magnetization reversal processes and magnetic anisotropy has been systematically investigated by magneto-optical Kerr effect based microscopy. Our experimental results were reproduced by micromagnetic simulations, which highlight the qualitative agreement with the experimental results. We have demonstrated that a small antidot in the center of a unit cell in the square ADL is sufficient to induce additional easy axes with large coercive fields. In wave-like patterns, narrow channels connecting smaller and larger antidots (bi-component ADL) further drastically change the anisotropy map, creating the high coercive fields along a wide angular range (90°) of directions parallel to the channels. In simulated results, we have observed formation of periodic domain structures in all ADLs, however, in the case of a wave-like pattern it is most regular and moreover two different periodic patterns are stabilized at different applied magnetic field values. The formation of 360° domain walls were also observed in wave-like ADL where these domains are formed along the lines connecting adjacent larger and smaller antidots, perpendicular to the channels. These findings point out the possibility of exploiting ADLs with complex unit cells in magnonic or spintronic applications.

  13. Chemical and metabolomic screens identify novel biomarkers and antidotes for cyanide exposure.

    Science.gov (United States)

    Nath, Anjali K; Roberts, Lee D; Liu, Yan; Mahon, Sari B; Kim, Sonia; Ryu, Justine H; Werdich, Andreas; Januzzi, James L; Boss, Gerry R; Rockwood, Gary A; MacRae, Calum A; Brenner, Matthew; Gerszten, Robert E; Peterson, Randall T

    2013-05-01

    Exposure to cyanide causes a spectrum of cardiac, neurological, and metabolic dysfunctions that can be fatal. Improved cyanide antidotes are needed, but the ideal biological pathways to target are not known. To understand better the metabolic effects of cyanide and to discover novel cyanide antidotes, we developed a zebrafish model of cyanide exposure and scaled it for high-throughput chemical screening. In a screen of 3120 small molecules, we discovered 4 novel antidotes that block cyanide toxicity. The most potent antidote was riboflavin. Metabolomic profiling of cyanide-treated zebrafish revealed changes in bile acid and purine metabolism, most notably by an increase in inosine levels. Riboflavin normalizes many of the cyanide-induced neurological and metabolic perturbations in zebrafish. The metabolic effects of cyanide observed in zebrafish were conserved in a rabbit model of cyanide toxicity. Further, humans treated with nitroprusside, a drug that releases nitric oxide and cyanide ions, display increased circulating bile acids and inosine. In summary, riboflavin may be a novel treatment for cyanide toxicity and prophylactic measure during nitroprusside treatment, inosine may serve as a biomarker of cyanide exposure, and metabolites in the bile acid and purine metabolism pathways may shed light on the pathways critical to reversing cyanide toxicity.

  14. Insufficient stocking of cyanide antidotes in US hospitals that provide emergency care

    Directory of Open Access Journals (Sweden)

    Lucas Gasco

    2013-01-01

    Full Text Available Objective: To identify the influence of catchment area, trauma center designation, hospital size, subspecialist employment, funding source, and other hospital characteristics on cyanide antidote stocking choice in US hospitals that provides emergency care. Materials and Methods: A web-based survey was sent out to pharmacy managers through two listservs; the American Society of Health-Systems Pharmacists and the American College of Clinical Pharmacy. A medical marketing company also broadcasted the survey to 2,659 individuals. We collected data on hospital characteristics (size, state, serving population, etc., to determine what influenced the hospital′s stocking choice. Results: The survey response rate was approximately 10% ( n = 286. Thirty-eight hospitals (16% stocked at least 4 antidote kits. Safety profile, recommendations from a poison control center, and ease of use had the strongest influence on stocking decisions. Conclusions: Survey of 286 US hospital pharmacy managers, 38/234 (16% hospitals had sufficient stocking of cyanide antidotes. Antidote preference was based on safety, ease of use, and recommendations by the local poison center, over cost.

  15. Development of a recombinant antithrombin variant as a potent antidote to fondaparinux and other heparin derivatives.

    Science.gov (United States)

    Bianchini, Elsa P; Fazavana, Judicael; Picard, Veronique; Borgel, Delphine

    2011-02-10

    Heparin derivative-based therapy has evolved from unfractionated heparin (UFH) to low-molecular-weight heparins (LMWHs) and now fondaparinux, a synthetic pentasaccharide. Contrary to UFH or LMWHs, fondaparinux is not neutralized by protamine sulfate, and no antidote is available to counteract bleeding disorders associated with overdosing. To make the use of fondaparinux safer, we developed an antithrombin (AT) variant as a potent antidote to heparin derivatives. This variant (AT-N135Q-Pro394) combines 2 mutations: substitution of Asn135 by a Gln to remove a glycosylation site and increase affinity for heparins, and the insertion of a Pro between Arg393 and Ser394 to abolish its anticoagulant activity. As expected, AT-N135Q-Pro394 anticoagulant activity was almost abolished, and it exhibited a 3-fold increase in fondaparinux affinity. AT-N135Q-Pro394 was shown to reverse fondaparinux overdosing in vitro in a dose-dependent manner through a competitive process with plasma AT for fondaparinux binding. This antidote effect was also observed in vivo: administration of AT-N135Q-Pro394 in 2.5-fold molar excess versus plasma AT neutralized 86% of the anti-Xa activity within 5 minutes in mice treated with fondaparinux. These results clearly demonstrate that AT-N135Q-Pro394 can reverse the anticoagulant activity of fondaparinux and thus could be used as an antidote for this drug.

  16. Hofstadter butterflies and magnetically induced band-gap quenching in graphene antidot lattices

    DEFF Research Database (Denmark)

    Pedersen, Jesper Goor; Pedersen, Thomas Garm

    2013-01-01

    We study graphene antidot lattices (GALs) in magnetic fields. Using a tight-binding model and a recursive Green's function technique that we extend to deal with periodic structures, we calculate Hofstadter butterflies of GALs. We compare the results to those obtained in a simpler gapped graphene...

  17. Observing Altshuler--Aronov--Spivak Oscillation in a Hexagonal Antidot Array of Monolayer Graphene

    Science.gov (United States)

    Yagi, Ryuta; Shimomura, Midori; Tahara, Fumiya; Kobara, Hiroaki; Fukada, Seiya

    2012-06-01

    We show that hexagonal antidot lattices of monolayer graphene exhibited the Altshuler--Aronov--Spivak (AAS) effect in low field magnetoresistance. In higher magnetic fields, Aharonov--Bohm-type oscillations were visible. The phase of AAS oscillation indicated that the chirality effect of graphene is suppressed because of inter-valley scattering due to boundary scatterings.

  18. Quantum computing via defect states in two-dimensional antidot lattices.

    Science.gov (United States)

    Flindt, Christian; Mortensen, Niels Asger; Jauho, Antti-Pekka

    2005-12-01

    We propose a new structure suitable for quantum computing in a solid-state environment: designed defect states in antidot lattices superimposed on a two-dimensional electron gas at a semiconductor heterostructure. State manipulation can be obtained with gate control. Model calculations indicate that it is feasible to fabricate structures whose energy level structure is robust against thermal dephasing.

  19. Thermodynamic modeling using BINGO-ANTIDOTE: A new strategy to investigate metamorphic rocks

    Science.gov (United States)

    Lanari, Pierre; Duesterhoeft, Erik

    2016-04-01

    BINGO-ANTIDOTE is a new program, combing the achievements of the two petrological software packages XMAPTOOLS[1] and THERIAK-DOMINO[2]. XMAPTOOLS affords information about compositional zoning in mineral and local bulk composition of domains at the thin sections scale. THERIAK-DOMINO calculates equilibrium phase assemblages from given bulk rock composition, temperature T and pressure P. Primarily BINGO-ANTIDOTE can be described as an inverse THERIAK-DOMINO, because it uses the information provided by XMAPTOOLS to calculate the probable P-T equilibrium conditions of metamorphic rocks. Consequently, the introduced program combines the strengths of forward Gibbs free energy minimization models with the intuitive output of inverse thermobarometry models. In order to get "best" P-T equilibrium conditions of a metamorphic rock sample and thus estimating the degree of agreement between the observed and calculated mineral assemblage, it is critical to define a reliable scoring strategy. BINGO uses the THERIAKD ADD-ON[3] (Duesterhoeft and de Capitani, 2013) and is a flexible model scorer with 3+1 evaluation criteria. These criteria are the statistical agreement between the observed and calculated mineral-assemblage, -proportions (vol%) and -composition (mol). Additionally, a total likelihood, consisting of the first three criteria, allows the user an evaluation of the most probable equilibrium P-T condition. ANTIDOTE is an interactive user interface, displaying the 3+1 evaluation criteria as probability P-T-maps. It can be used with and without XMAPTOOLS. As a stand-alone program, the user is able to give the program macroscopic observations (i.e., mineral names and proportions), which ANTIDOTE converts to a readable BINGO input. In this manner, the use of BINGO-ANTIDOTE opens up thermodynamics to students and people with only a basic knowledge of phase diagrams and thermodynamic modeling techniques. This presentation introduces BINGO-ANTIDOTE and includes typical examples

  20. Quaternary and tertiary aldoxime antidotes for organophosphate exposure in a zebrafish model system

    Energy Technology Data Exchange (ETDEWEB)

    Schmidt, Hayden R. [Department of Biology, Whittier College, Whittier, CA 90608 (United States); Radić, Zoran; Taylor, Palmer [Department of Pharmacology, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego, La Jolla, CA 92093-0650 (United States); Fradinger, Erica A., E-mail: efrading@whittier.edu [Department of Biology, Whittier College, Whittier, CA 90608 (United States)

    2015-04-15

    The zebrafish is rapidly becoming an important model system for screening of new therapeutics. Here we evaluated the zebrafish as a potential pharmacological model for screening novel oxime antidotes to organophosphate (OP)-inhibited acetylcholinesterase (AChE). The k{sub i} values determined for chlorpyrifos oxon (CPO) and dichlorvos (DDVP) showed that CPO was a more potent inhibitor of both human and zebrafish AChE, but overall zebrafish AChE was less sensitive to OP inhibition. In contrast, aldoxime antidotes, the quaternary ammonium 2-PAM and tertiary amine RS-194B, showed generally similar overall reactivation kinetics, k{sub r}, in both zebrafish and human AChE. However, differences between the K{sub ox} and k{sub 2} constants suggest that zebrafish AChE associates more tightly with oximes, but has a slower maximal reactivation rate than human AChE. Homology modeling suggests that these kinetic differences result from divergences in the amino acids lining the entrance to the active site gorge. Although 2-PAM had the more favorable in vitro reactivation kinetics, RS-194B was more effective antidote in vivo. In intact zebrafish embryos, antidotal treatment with RS-194B rescued embryos from OP toxicity, whereas 2-PAM had no effect. Dechorionation of the embryos prior to antidotal treatment allowed both 2-PAM and RS-194B to rescue zebrafish embryos from OP toxicity. Interestingly, RS-194B and 2-PAM alone increased cholinergic motor activity in dechorionated embryos possibly due to the reversible inhibition kinetics, K{sub i} and αK{sub i}, of the oximes. Together these results demonstrate that the zebrafish at various developmental stages provides an excellent model for investigating membrane penetrant antidotes to OP exposure. - Highlights: • Zebrafish AChE shares significant structural similarities with human AChE. • OP-inhibited zebrafish and human AChE exhibit similar reactivation kinetics. • The zebrafish chorion is permeable to BBB penetrant and not

  1. Organophosphate antidote auto-injectors vs. traditional administration: a time motion study.

    Science.gov (United States)

    Rebmann, Terri; Clements, Bruce W; Bailey, Jeffrey A; Evans, R Gregory

    2009-08-01

    Organophosphates may be used as weapons in chemical attacks on civilian or military populations. Antidotes are available to counter the effects of organophosphates, but they must be administered shortly after exposure. Timing required to administer organophosphate antidotes using traditional equipment vs. auto-injectors has not been studied. This study is intended to quantify and compare the time required to administer organophosphate antidotes using traditional equipment vs. auto-injectors in different treatment conditions. The study was a randomized, un-blinded design. There were 62 participants assigned to one of three groups: Mark I, ATNAA (antidote treatment nerve agent auto-injector), and traditional needle/syringe; however, the results from only 56 participants could be analyzed. Injection trials were videotaped. Subjects also completed a 14-item survey containing demographic questions, perceived ease of injection, receipt of prior training, and preferred training format for organophosphate treatment. Injection time differentials were compared using one-way analysis of variance; post hoc evaluation was performed using the Scheffe test with Bonferroni correction. Fifty-six subjects completed this study. The ATNAA required less time to administer than the Mark I or traditional needle/syringe devices (p antidote treatment. An ATNAA auto-injector can be administered in less than half the time it takes to administer a single injection using a needle and syringe or two injections using a Mark I. Mark I can be administered in approximately the same amount of time it takes to administer a single injection using a needle and syringe. The difference between injection time for the ATNAA and needle and syringe would have been even larger if two injections were given with the needle and syringe. The wearing or absence of personal protective equipment does not affect injection time.

  2. Energy Method of Finding Distribution Constants of an Antiferromagnetic Vector for an Antidot System in a Two-sublattice Antiferromagnet

    Directory of Open Access Journals (Sweden)

    V.V. Kulish

    2015-06-01

    Full Text Available The paper investigates the antiferromagnetic vector distribution in an antiferromagnetic film with a system of antidots. A static distribution of the antiferromagnetic vector is written and a method – based on the minimization of the antiferromagnet energy – that allows reducing the number of boundary conditions required for finding the constants of this distribution is proposed. Equations for the distribution constants are obtained for the both cases of minimizing the antiferromagnet energy by one and by two distribution constants that enter the expression for the antiferromagnet energy. The method is illustrated on a system of one isolated antidot. For such system, one additional condition – for the case when two boundary conditions on the surface of the antidot are given – and two additional conditions – for the case when one boundary condition on the surface of the antidot is given – on the distribution constants are written.

  3. Effect of antiferromagnetic layer thickness on exchange bias, training effect, and magnetotransport properties in ferromagnetic/antiferromagnetic antidot arrays

    Energy Technology Data Exchange (ETDEWEB)

    Gong, W. J.; Liu, W., E-mail: wliu@imr.ac.cn; Feng, J. N.; Zhang, Z. D. [Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016 (China); Kim, D. S.; Choi, C. J. [Functional Materials Division, Korea Institute of Materials Science, 531 Changwon- daero, Changwon 631-831 (Korea, Republic of)

    2014-04-07

    The effect of antiferromagnetic (AFM) layer on exchange bias (EB), training effect, and magnetotransport properties in ferromagnetic (FM) /AFM nanoscale antidot arrays and sheet films Ag(10 nm)/Co(8 nm)/NiO(t{sub NiO})/Ag(5 nm) at 10 K is studied. The AFM layer thickness dependence of the EB field shows a peak at t{sub NiO} = 2 nm that is explained by using the random field model. The misalignment of magnetic moments in the three-dimensional antidot arrays causes smaller decrease of EB field compared with that in the sheet films for training effect. The anomalous magnetotransport properties, in particular positive magnetoresistance (MR) for antidot arrays but negative MR for sheet films are found. The training effect and magnetotransport properties are strongly affected by the three-dimensional spin-alignment effects in the antidot arrays.

  4. New edge magnetoplasmon interference like photovoltage oscillations and their amplitude enhancement in the presence of an antidot lattice

    Energy Technology Data Exchange (ETDEWEB)

    Bisotto, I., E-mail: isabelle.bisotto@lncmi.cnrs.fr [LNCMI, UPR 3228, CNRS–INSA–UJF–UPS, BP 166, 38042 Grenoble, Cedex 9 (France); Portal, J.-C. [LNCMI, UPR 3228, CNRS–INSA–UJF–UPS, BP 166, 38042 Grenoble, Cedex 9 (France); Institut National des Sciences Appliquées, 31077 Toulouse Cedex 4 (France); Institut Universitaire de France, 75005 Paris (France); Brown, D. [Microelectronics Research Center Georgia Institute of Technology, 791 Atlantic Drive NW, Atlanta, GA 30332 (United States); Wieck, A. D. [Lehrstuhl für Angewandte Festkörperphysik, Ruhr-Universität Bochum, D-44780 Bochum (Germany)

    2015-11-15

    We present new photovoltage oscillation in a pure two dimensional electron gas (2DEG) and in the presence of circular or semicircular antidot lattices. Results were interpreted as EMPs-like photovoltage oscillations. We observed and explained the photovoltage oscillation amplitude enhancement in the presence of an antidot lattice with regard to the pure 2DEG. The microwave frequency excitation range is 139 – 350 GHz. The cyclotron and magnetoplasmon resonances take place in the magnetic field range 0.4 – 0.8 T. This original experimental condition allows edge magnetoplasmons EMPs interference like observation at low magnetic field, typically B < B{sub c} where B{sub c} is the magnetic field at which the cyclotron resonance takes place. The different oscillation periods observed and their microwave frequency dependence were discussed. For 139 and 158 GHz microwave excitation frequencies, a unique EMPs-like interference period was found in the presence of antidots whereas two periods were extracted for 295 or 350 GHz. An explanation of this effect is given taking account of strong electron interaction with antidot at low magnetic field. Indeed, electrons involved in EMPs like phenomenon interact strongly with antidots when electron cyclotron orbits are larger than or comparable to the antidot diameter.

  5. New edge magnetoplasmon interference like photovoltage oscillations and their amplitude enhancement in the presence of an antidot lattice

    Directory of Open Access Journals (Sweden)

    I. Bisotto

    2015-11-01

    Full Text Available We present new photovoltage oscillation in a pure two dimensional electron gas (2DEG and in the presence of circular or semicircular antidot lattices. Results were interpreted as EMPs-like photovoltage oscillations. We observed and explained the photovoltage oscillation amplitude enhancement in the presence of an antidot lattice with regard to the pure 2DEG. The microwave frequency excitation range is 139 – 350 GHz. The cyclotron and magnetoplasmon resonances take place in the magnetic field range 0.4 – 0.8 T. This original experimental condition allows edge magnetoplasmons EMPs interference like observation at low magnetic field, typically B < Bc where Bc is the magnetic field at which the cyclotron resonance takes place. The different oscillation periods observed and their microwave frequency dependence were discussed. For 139 and 158 GHz microwave excitation frequencies, a unique EMPs-like interference period was found in the presence of antidots whereas two periods were extracted for 295 or 350 GHz. An explanation of this effect is given taking account of strong electron interaction with antidot at low magnetic field. Indeed, electrons involved in EMPs like phenomenon interact strongly with antidots when electron cyclotron orbits are larger than or comparable to the antidot diameter.

  6. Magnetic properties of Fe{sub 20} Ni{sub 80} antidots: Pore size and array disorder

    Energy Technology Data Exchange (ETDEWEB)

    Palma, J.L., E-mail: juan.palma.s@usach.cl [Departamento de Física, Universidad de Santiago de Chile (USACH), Avda. Ecuador 3493, 917-0124 Santiago (Chile); Gallardo, C. [Departamento de Física, Universidad de Santiago de Chile (USACH), Avda. Ecuador 3493, 917-0124 Santiago (Chile); Spinu, L.; Vargas, J.M. [Advanced Material Research Institute (AMRI) and Department of Physics, University of New Orleans, New Orleans, LA 70148 (United States); Dorneles, L.S. [Departamento de Fisica, Universidade Federal de Santa Maria UFSM, Av. Roraima 1000, Camobi, Santa Maria, RS 97105-900 (Brazil); Denardin, J.C.; Escrig, J. [Departamento de Física, Universidad de Santiago de Chile (USACH), Avda. Ecuador 3493, 917-0124 Santiago (Chile); Center for the Development of Nanoscience and Nanotechnology (CEDENNA), Avda. Ecuador 3493, 917-0124 Santiago (Chile)

    2013-10-15

    Magnetic properties of nanoscale Fe{sub 20}Ni{sub 80} antidot arrays with different hole sizes prepared on top of nanoporous alumina membranes have been studied by means of magnetometry and micromagnetic simulations. The results show a significant increase of the coercivity as well as a reduction of the remanence of the antidot arrays, as compared with their parent continuous film, which depends on the hole size introduced in the Fe{sub 20}Ni{sub 80} thin film. When the external field is applied parallel to the antidots, the reversal of magnetization is achieved by free-core vortex propagation, whereas when the external field is applied perpendicular to the antidots, the reversal occurs through a process other than the coherent rotation (a maze-like pattern). Besides, in-plane hysteresis loops varying the angle show that the degree of disorder in the sample breaks the expected hexagonal symmetry. - Highlights: • Magnetic properties are strongly influenced by the pore diameter of the samples. • Coercive fields for antidots are higher than the values for the continuous film. • Disorder breaks the hexagonal symmetry of the sample. • Each hole acts as a vortex nucleation point. • Antidots have unique properties that allow them to be used in applications.

  7. Patterns of cyanide antidote use since regulatory approval of hydroxocobalamin in the United States.

    Science.gov (United States)

    Streitz, Matthew J; Bebarta, Vikhyat S; Borys, Douglas J; Morgan, David L

    2014-01-01

    Sodium nitrite and sodium thiosulfate are common cyanide antidotes. Hydroxocobalamin was approved for use in the United States in 2006. Our objective was to determine the frequency of antidote use as reported to the US poison centers from 2005 to 2009 and describe which antidotes were used in critically ill cyanide toxic patients. We performed a retrospective review over 5 years (2005-2009) from 61 US poison centers. We identified all cyanide-exposed cases that received a cyanide antidote. Variables collected included demographics, gastric decontamination, antidote used, predefined serious clinical effects (hypotension, cardiac arrest, respiratory arrest, and coma), and predefined serious therapies (cardiopulmonary resuscitation, vasopressors, atropine, anticonvulsant, antidysrhythmic, and intubation/ventilation). One trained abstractor abstracted each chart to a standardized electronic form. Another investigator audited 20% of the charts. Kappa values were calculated. One hundred sixty-five exposures were identified. Mean age was 42 years (range, 3-93 years). Seventy-one percent were male. Exposures were 27% ingestion and 53% inhalation. Thirty-two percent of the ingestions were suicide attempts. Twenty percent (32 of 157) of all cases died. Over all years reported, hydroxocobalamin was administered to 29% (45 of 157) of patients, sodium nitrite to 25%, and sodium thiosulfate to 46%. Hydroxocobalamin use increased from 24% to 54% from 2007 to 2009, respectively (P = 0.024). Sodium thiosulfate use decreased from 73% to 31% (P = 0.002) and sodium nitrite use decreased from 26% to 14% (P = 0.39). The proportion of cases with serious clinical effects that received hydroxocobalamin increased each year, and the proportion that received other antidotes decreased. Hydroxocobalamin was also administered more often in cases that required serious therapies and increased each year. Hydroxocobalamin use for cyanide toxicity increased each year as reported to the US poison

  8. Spin Waves in a Ferromagnetic Film with a Periodic System of Antidots

    Directory of Open Access Journals (Sweden)

    V.V. Kulish

    2015-03-01

    Full Text Available In the paper, spin waves in a thin film (composed of a uniaxial ferromagnet with a two-dimensional periodical system of antidots are studied. The film ferromagnet is considered to have the “easy axis” type. To describe such waves, the magnetostatic approximation with account for the magnetic dipole-dipole interaction, the exchange interaction and the anisotropy effects is used. For such waves, an equation for the magnetic potential is derived; for the case of remote antidots, the dispersion relation and the transverse wavenumber spectrum are found. For the case of a film thin compared to the exchange length and for the case of a film bounded by a high-conductivity metal, the longitudinal wavenumber spectrum and the frequency spectrum of such spin waves are also obtained.

  9. Acute ethanol administration reduces the antidote effect of N-acetylcysteine after acetaminophen overdose in mice

    DEFF Research Database (Denmark)

    Dalhoff, K; Hansen, P B; Ott, P;

    1991-01-01

    1. The combined antidote effect of N-acetylcysteine and ethanol on the toxicity of acetaminophen was investigated. 2. Fed male mice were given acetaminophen i.p. (600 mg kg-1) and after 5 min in addition ethanol i.p. (0.2 ml, 19% v/v), N-acetylcysteine i.p. (1.2 g kg-1, 0.2 ml), N-acetylcysteine ......1. The combined antidote effect of N-acetylcysteine and ethanol on the toxicity of acetaminophen was investigated. 2. Fed male mice were given acetaminophen i.p. (600 mg kg-1) and after 5 min in addition ethanol i.p. (0.2 ml, 19% v/v), N-acetylcysteine i.p. (1.2 g kg-1, 0.2 ml), N...

  10. Oral anticoagulants and status of antidotes for the reversal of bleeding risk.

    Science.gov (United States)

    Ebright, Joseph; Mousa, Shaker A

    2015-03-01

    Anticoagulants have been used in clinical practice for more than 50 years. Their indications expand, as more people are diagnosed each year with atrial fibrillation and venous thromboembolism. Vitamin K antagonists have been the most popular choice due to their effectiveness and their ability to reverse bleeding using a known antidote; oral and intravenous vitamin K have long been known to reverse the effects of warfarin. With new classes of anticoagulants making their way onto the market, such as factor Xa inhibitors (rivaroxaban, apixaban) and direct thrombin inhibitors (dabigatran), the need for new reversal agents is paramount. Patients tend to be more receptive to these medications because they do not require routine blood monitoring, can be used at fixed doses, and do not have major drug or food interactions. Antidotes for these medications have shown promise in animal models and are currently in clinical trials.

  11. Antidotes to coumarins, isoniazid, methotrexate and thyroxine, toxins that work via metabolic processes.

    Science.gov (United States)

    Bateman, D Nicholas; Page, Colin B

    2016-03-01

    Some toxins cause their effects by affecting physiological processes that are fundamental to cell function or cause systemic effects as a result of cellular interaction. This review focuses on four examples, coumarin anticoagulants, isoniazid, methotrexate and thyroxine from the context of management of overdose as seen in acute general hospitals. The current basic clinical pharmacology of the toxin, the clinical features in overdose and evidence base for specific antidotes are discussed. The treatment for this group is based on an understanding of the toxic mechanism, but studies to determine the optimum dose of antidote are still required in all these toxins except thyroxine, where treatment dose is based on symptoms resulting from the overdose.

  12. Nitrocobinamide, a new cyanide antidote that can be administered by intramuscular injection.

    Science.gov (United States)

    Chan, Adriano; Jiang, Jingjing; Fridman, Alla; Guo, Ling T; Shelton, G Diane; Liu, Ming-Tao; Green, Carol; Haushalter, Kristofer J; Patel, Hemal H; Lee, Jangwoen; Yoon, David; Burney, Tanya; Mukai, David; Mahon, Sari B; Brenner, Matthew; Pilz, Renate B; Boss, Gerry R

    2015-02-26

    Currently available cyanide antidotes must be given by intravenous injection over 5-10 min, making them ill-suited for treating many people in the field, as could occur in a major fire, an industrial accident, or a terrorist attack. These scenarios call for a drug that can be given quickly, e.g., by intramuscular injection. We have shown that aquohydroxocobinamide is a potent cyanide antidote in animal models of cyanide poisoning, but it is unstable in solution and poorly absorbed after intramuscular injection. Here we show that adding sodium nitrite to cobinamide yields a stable derivative (referred to as nitrocobinamide) that rescues cyanide-poisoned mice and rabbits when given by intramuscular injection. We also show that the efficacy of nitrocobinamide is markedly enhanced by coadministering sodium thiosulfate (reducing the total injected volume), and we calculate that ∼1.4 mL each of nitrocobinamide and sodium thiosulfate should rescue a human from a lethal cyanide exposure.

  13. Antidote treatment for cyanide poisoning with hydroxocobalamin causes bright pink discolouration and chemical-analytical interferences.

    Science.gov (United States)

    Brunel, C; Widmer, C; Augsburger, M; Dussy, F; Fracasso, T

    2012-11-30

    Here we report the case of a 70-year-old woman who committed suicide by cyanide poisoning. During resuscitation cares, she underwent an antidote treatment by hydroxocobalamin. Postmortem investigations showed marked bright pink discolouration of organs and fluids, and a lethal cyanide blood concentration of 43 mg/L was detected by toxicological investigation. Discolouration of hypostasis and organs has widely been studied in forensic literature. In our case, we interpreted the unusual pink coloration as the result of the presence of hydroxocobalamin. This substance is a known antidote against cyanide poisoning, indicated because of its efficiency and poor adverse effects. However, its main drawback is to interfere with measurements of many routine biochemical parameters. We have tested the potential influence of this molecule in some routine postmortem investigations. The results are discussed.

  14. The bezoar stone: a princely antidote, the Távora Sequeira Pinto Collection-Oporto.

    Science.gov (United States)

    Do Sameiro Barroso, Maria

    2014-01-01

    Bezoar stones, once used as universal antidotes and panaceas, but currently regarded as costly and useless medicines of the past, are a major milestone in the history of toxicology. Arabic physicians had been using bezoars in medicine from the 8th century onwards. In the 16th century, the Portuguese controlled bezoar trade from India, and the Portuguese doctors Garcia de Orta, Amatus Lusitanus, and Cristobal Acosta introduced the medicinal use of Oriental bezoars to European medical literature. Some criticism aside, leading European doctors prescribed bezoars mainly as powerful antidotes. Five bezoars that now adorn the Távora Sequeira Pinto Collection in Oporto testify to the allure and glory of bezoars at the height of their golden age, when they equalled the splendour of gems and noble minerals that dominated the Eastern and Western lithotherapy.The end of the 18th century marked the end of ancient panaceas. This article focuses on the therapeutic and apotropaic use of bezoars.

  15. Angle-resolved spin wave band diagrams of square antidot lattices studied by Brillouin light scattering

    Energy Technology Data Exchange (ETDEWEB)

    Gubbiotti, G.; Tacchi, S. [Istituto Officina dei Materiali del Consiglio Nazionale delle Ricerche (IOM-CNR), Sede di Perugia, c/o Dipartimento di Fisica e Geologia, Via A. Pascoli, I-06123 Perugia (Italy); Montoncello, F.; Giovannini, L. [Dipartimento di Fisica e Scienze della Terra, Università di Ferrara, Via G. Saragat 1, I-44122 Ferrara (Italy); Madami, M.; Carlotti, G. [Dipartimento di Fisica e Geologia, Università di Perugia, Via A. Pascoli, I-06123 Perugia (Italy); Ding, J.; Adeyeye, A. O. [Information Storage Materials Laboratory, Department of Electrical and Computer Engineering, National University of Singapore, Singapore 117576 (Singapore)

    2015-06-29

    The Brillouin light scattering technique has been exploited to study the angle-resolved spin wave band diagrams of squared Permalloy antidot lattice. Frequency dispersion of spin waves has been measured for a set of fixed wave vector magnitudes, while varying the wave vector in-plane orientation with respect to the applied magnetic field. The magnonic band gap between the two most dispersive modes exhibits a minimum value at an angular position, which exclusively depends on the product between the selected wave vector magnitude and the lattice constant of the array. The experimental data are in very good agreement with predictions obtained by dynamical matrix method calculations. The presented results are relevant for magnonic devices where the antidot lattice, acting as a diffraction grating, is exploited to achieve multidirectional spin wave emission.

  16. Edge structures and properties of triangular antidots in single-layer MoS2

    KAUST Repository

    Gan, Li Yong

    2016-08-30

    Density functional theory and experiments are employed to shed light on the edge structures of antidots in O etched single-layer MoS2. The equilibrium morphology is found to be the zigzag Mo edge with each Mo atom bonded to two O atoms, in a wide range of O chemical potentials. Scanning electron microscopy shows that the orientation of the created triangular antidots is opposite to the triangular shape of the single-layer MoS2 samples, in agreement with the theoretical predictions. Furthermore, edges induced by O etching turn out to be p-doped, suggesting an effective strategy to realize p-type MoS2 devices. Published by AIP Publishing.

  17. Molecular Modeling in Drug Design for the Development of Organophosphorous Antidotes/Prophylactics

    Science.gov (United States)

    1986-05-01

    5012 61102A 1102BS11 EB 025 11. TITLE (Include Security Classification) Molecular Modeling in Drug Design for the Development of Organophosphorous...t ....................................., ’ i.° AD MOLECULAR MODELING IN DRUG DESIGN FOR THE DEVELOPMENT OF ORGANOPHOSPHOROUS ANTIDOTES...Reed, W.J. Murray, E.B. Roche and L.N. Donelsmith, Gen. Pharmac., 12, 177-185 (1981). 5. L.B.Kier, "Molecular Orbital Theory in Drug Design ", Academic

  18. Acute liver acetaminophen toxicity in rabbits and the use of antidotes: a metabonomic approach in serum.

    Science.gov (United States)

    Zira, Athina; Mikros, Emmanuel; Giannioti, Konstantina; Galanopoulou, Panagiota; Papalois, Apostolos; Liapi, Charis; Theocharis, Stamatios

    2009-07-01

    The metabonomic approach has been widely used in toxicology to investigate mechanisms of toxicity. In the present study alterations in the metabolic profiles, monitored by (1)H-NMR spectroscopy, on serum samples in acetaminophen (APAP)-induced liver injury in rabbits were examined. Furthermore, the effect of the established antidote N-acetylcysteine (NAC) and the proposed antidotes silybinin (SIL), cimetidine (CIM) and SIL/CIM was also investigated. A single dose of APAP (2 g kg(-1) b.w., i.g.) was administered to rabbits and APAP combined with the antidotes SIL, CIM and NAC. Animals were sacrificed at 24 h post-APAP treatment. Healthy untreated animals served as controls. (1)H-NMR spectra of serum samples were acquired and underwent principal component analysis (PCA). Acute liver injury was verified by histopathological examination and the alterations of serum biochemical enzymes AST and ALT. (1)H-NMR spectroscopy revealed variations in the serum metabolic profile of APAP-intoxicated rabbits compared with controls. Co-administration of APAP with NAC, CIM and SIL + CIM seems to ameliorate the metabolic profile of animals compared with simply APAP-treated ones. In this study, the model of APAPinduced liver injury was successfully described using the (1)H-NMR based metabonomic approach in serum. Furthermore, the use of antidotes that reduced the toxic insult was also recorded using this technique. The combination of NMR spectroscopy and PCA is a rapid methodology, capable of detecting alterations in the metabolic profile, and produces adequate models that could be used for the characterization of unknown samples, both experimental and clinical, reinforcing its future use in clinical settings.

  19. Consolidarea relațiilor interpersonale pozitive la locul de muncă: antidot pentru burnout

    Directory of Open Access Journals (Sweden)

    CORALIA SULEA

    2014-05-01

    Full Text Available Burnout is an important phenomenon for organizations and employees associated with negative outcomes. Key organizational areas, like fairness and workplace community, are responsible for employee burnout. This editorial argues for the importance of workplace community and presents the mechanisms through which dysfunctional relationships at work may contribute to burnout, as well as the processes that explain how healthy interpersonal relationships can be an antidote for burnout.

  20. Nonclinical evaluation of novel cationically modified polysaccharide antidotes for unfractionated heparin.

    Directory of Open Access Journals (Sweden)

    Bartlomiej Kalaska

    Full Text Available Protamine, the only registered antidote of unfractionated heparin (UFH, may produce a number of adverse effects, such as anaphylactic shock or serious hypotension. We aimed to develop an alternative UFH antidote as efficient as protamine, but safer and easier to produce. As a starting material, we have chosen generally non-toxic, biocompatible, widely available, inexpensive, and easy to functionalize polysaccharides. Our approach was to synthesize, purify and characterize cationic derivatives of dextran, hydroxypropylcellulose, pullulan and γ-cyclodextrin, then to screen them for potential heparin-reversal activity using an in vitro assay and finally examine efficacy and safety of the most active polymers in Wistar rat and BALB/c mouse models of experimentally induced arterial and venous thrombosis. Efficacy studies included the measurement of thrombus formation, activated partial thromboplastin time, bleeding time, and anti-factor Xa activity; safety studies included the measurement of hemodynamic, hematologic and immunologic parameters. Linear, high molecular weight dextran substituted with glycidyltrimethylammonium chloride groups at a ratio of 0.65 per glucose unit (Dex40-GTMAC3 is the most potent and the safest UFH inhibitor showing activity comparable to that of protamine while possessing lower immunogenicity. Cationic polysaccharides of various structures neutralize UFH. Dex40-GTMAC3 is a promising and potentially better UFH antidote than protamine.

  1. Nonclinical evaluation of novel cationically modified polysaccharide antidotes for unfractionated heparin.

    Science.gov (United States)

    Kalaska, Bartlomiej; Kaminski, Kamil; Sokolowska, Emilia; Czaplicki, Dominik; Kujdowicz, Monika; Stalinska, Krystyna; Bereta, Joanna; Szczubialka, Krzysztof; Pawlak, Dariusz; Nowakowska, Maria; Mogielnicki, Andrzej

    2015-01-01

    Protamine, the only registered antidote of unfractionated heparin (UFH), may produce a number of adverse effects, such as anaphylactic shock or serious hypotension. We aimed to develop an alternative UFH antidote as efficient as protamine, but safer and easier to produce. As a starting material, we have chosen generally non-toxic, biocompatible, widely available, inexpensive, and easy to functionalize polysaccharides. Our approach was to synthesize, purify and characterize cationic derivatives of dextran, hydroxypropylcellulose, pullulan and γ-cyclodextrin, then to screen them for potential heparin-reversal activity using an in vitro assay and finally examine efficacy and safety of the most active polymers in Wistar rat and BALB/c mouse models of experimentally induced arterial and venous thrombosis. Efficacy studies included the measurement of thrombus formation, activated partial thromboplastin time, bleeding time, and anti-factor Xa activity; safety studies included the measurement of hemodynamic, hematologic and immunologic parameters. Linear, high molecular weight dextran substituted with glycidyltrimethylammonium chloride groups at a ratio of 0.65 per glucose unit (Dex40-GTMAC3) is the most potent and the safest UFH inhibitor showing activity comparable to that of protamine while possessing lower immunogenicity. Cationic polysaccharides of various structures neutralize UFH. Dex40-GTMAC3 is a promising and potentially better UFH antidote than protamine.

  2. Antidotes, antibody-mediated immunity and the future of pharmaceutical product development.

    Science.gov (United States)

    Caoili, Salvador Eugenio C

    2013-02-01

    If new scientific knowledge is to be more efficiently generated and applied toward the advancement of health, human safety must be more effectively addressed in the conduct of research. Given the present difficulties of accurately predicting biological outcomes of novel interventions in vivo, the imperative of human safety suggests the development of novel pharmaceutical products in tandem with their prospective antidotes in anticipation of possible adverse events, to render the risks of initial clinical trials more acceptable from a regulatory standpoint. Antibody-mediated immunity provides a generally applicable mechanistic basis for developing antidotes to both biologicals and small-molecule drugs (such that antibodies may serve as antidotes to pharmaceutical agents as a class including other antibodies) and also for the control and prevention of both infectious and noninfectious diseases via passive or active immunization. Accordingly, the development of prophylactic or therapeutic passive-immunization strategies using antipeptide antibodies is a plausible prelude to the development of corresponding active-immunization strategies using peptide-based vaccines. In line with this scheme, global proliferation of antibody- and vaccine-production technologies, especially those that obviate dependence on the cold chain for storage and transport of finished products, could provide geographically distributed breakout capability against emerging and future health challenges.

  3. Identification, solubility enhancement and in vivo testing of a cyanide antidote candidate.

    Science.gov (United States)

    Kovacs, Kristof; Ancha, Madhuri; Jane, Mario; Lee, Stephen; Angalakurthi, Siva; Negrito, Maelani; Rasheed, Senan; Nwaneri, Assumpta; Petrikovics, Ilona

    2013-06-14

    Present studies focused on the in vitro testing, the solubility enhancement and the in vivo testing of methyl propyl trisulfide (MPTS), a newly identified sulfur donor to treat cyanide (CN) intoxication. To enhance the solubility of the lipophilic MPTS, various FDA approved co-solvents, surfactants and their combinations were applied. The order of MPTS solubility in the given co-solvents was found to be the following: ethanol > PEG 200 ≈ PEG400 ≈ PEG300 > PG. The maximum solubility of MPTS was found at 90% ethanol of 177.11 ± 12.17 mg/ml. The order of MPTS solubility in different surfactants is Cremophor EL>Cremophor RH40>polysorbate 80>sodium deoxycholate>sodium cholate. The maximum solubility of 40.99 mg/ml was achieved with 20% Cremophor EL. A synergistic solubilizing effect encountered with the combination of 20% Cremophor EL+75% ethanol lead to a 2900-fold increase (compared to water solubility) in solubility. The in vivo efficacy using intramuscular administration was determined on a therapeutic mice model and expressed as a ratio of CN LD50 with and without the test antidote(s) (APR). Intramuscular administration was shown to be effective and the therapeutic antidotal protection by MPTS alone and MPTS+thiosulfate (TS) was significantly higher than the present therapy of TS.

  4. An effective method to probe local magnetostatic properties in a nanometric FePd antidot array

    Energy Technology Data Exchange (ETDEWEB)

    Beron, F; Pirota, K R; Knobel, M [Instituto de Fisica Gleb Wataghin, Universidade Estadual de Campinas, Rua Sergio Buarque de Holanda, 777, Cidade Universitaria ' Zeferino Vaz' , Campinas 13083-859, SP (Brazil); Vega, V; Prida, V M; Fernandez, A; Hernando, B, E-mail: fberon@ifi.unicamp.br [Depto. Fisica, Universidad de Oviedo, Calvo Sotelo s/n, 33007 Oviedo, Asturias (Spain)

    2011-01-15

    A simple method to quantitatively characterize the local magnetic behaviour of a patterned nanostructure, like a ferromagnetic thin film of antidot arrays, is proposed. The first-order reversal curve (FORC) analysis, coupled with simulations using physically meaningful hysterons, allows us to obtain a quantitative and physically related description of the interaction field and each magnetization reversal process. The hysterons system is built from previously known hypotheses on the magnetic behaviour of the sample. This method was successfully applied to a highly hexagonal ordered FePd antidot array with nanometric dimensions. We achieved a complete characterization of the two different magnetization reversal mechanisms in function of the in-plane applied field angle. For a narrow range of high fields, the magnetization initiates rotating reversibly around the pores, while at lower fields, domain walls are nucleated and propagated. This in-plane magnetization reversal mechanism, partly reversible and partly irreversible, is the only angularly dependent one. While going away from the easy axis, its reversible proportion increases, as well as its switching field distribution. Finally, the results indicate that the high surface roughness between adjacent holes of the antidot thin film induces a parallel interaction field. The proposed method demonstrates its ability also to be applied to characterizing patterned nanostructures with rather complex magnetization reversal processes.

  5. Use of cyanide antidotes in burn patients with suspected inhalation injuries in North America: a cross-sectional survey.

    Science.gov (United States)

    Dumestre, Danielle; Nickerson, Duncan

    2014-01-01

    This study aimed to assess the use of cyanide antidotes and the determine the opinion on empiric administration of hydroxocobalamin in North American burn patients with suspected smoke inhalation injuries. An online cross-sectional survey was sent to directors of 90 major burn centers in North America, which were listed on the American Burn Association Web site. A multiple-choice format was used to determine the percentage of patients tested for cyanide poisoning on admission, the current administration of a cyanide antidote based solely on clinical suspicion of poisoning, and the antidote used. To ascertain views on immediate administration of hydroxocobalamin before confirmation of cyanide poisoning an option was included to expand the response in written format. Twenty-nine of 90 burn directors (32%) completed the survey. For the population of interest, the majority of burn centers (59%) do not test for cyanide poisoning on admission and do not administer an antidote based solely on clinical suspicion of cyanide poisoning (58%). The most commonly available antidote is hydroxocobalamin (50%), followed by the cyanide antidote kit (29%). The opinion regarding instant administration of hydroxocobalamin when inhalation injury is suspected is mixed: 31% support its empiric use, 17% do not, and the remaining 52% have varying degrees of confidence in its utility. In North America, most patients burnt in closed-space fires with inhalation injuries are neither tested for cyanide poisoning in a timely manner nor empirically treated with a cyanide antidote. Although studies have shown the safety and efficacy of empiric and immediate administration of hydroxocobalamin, most centers are not willing to do so.

  6. Large negative magnetoresistance induced by interplay between smooth disorder and antidots in AlGaN/GaN HEMT structures

    Science.gov (United States)

    Mishra, M. K.; Sharma, R. K.; Tyagi, R.; Manchanda, R.; Pandey, A. K.; Thakur, O. P.; Muralidharan, R.

    2016-04-01

    Large low temperature negative magnetoresistance (NMR) experimentally observed in AlGaN/GaN high electron mobility transistors (HEMT) structures grown by metalorganic chemical vapour deposition on sapphire substrate has been reported. A linear B -1 ln B dependence of magnetoresistance observed in our samples indicates the presence of random antidot array together with smooth disorder. It is proposed that the antidots are linked with high bandgap AlN rich regions formed due to possible Al-Ga segregation at the interface during growth and the smooth random disorder is due to interface roughness. The antidot density is estimated to be of ˜7 to 8 × 1010 cm-2 in our samples. The magnitude of NMR is also correlated with the extent of interface roughness indicated by x-ray reflectivity. It is also proposed that the formation of antidots is related with the lattice mismatch between substrate and epitaxial heterostructures. The NMR in AlGaN/GaN HEMT structures grown on SiC substrates having relatively lower lattice mismatch has been shown to have a usual B 2 and ln T dependences indicating only electron-electron interaction and absence of antidot-like scatterers.

  7. Magnetic transition from dot to antidot regime in large area Co/Pd nanopatterned arrays with perpendicular magnetization

    Science.gov (United States)

    Krupinski, M.; Mitin, D.; Zarzycki, A.; Szkudlarek, A.; Giersig, M.; Albrecht, M.; Marszałek, M.

    2017-02-01

    We have studied the transition between two different magnetization reversal mechanisms for thin Co/Pd multilayers with perpendicular magnetic anisotropy, appearing in magnetic dot and antidot arrays, which were prepared by nanosphere lithography. Various ordered arrays of nanostuctures, both magnetic dots and antidots, were created by varying size and distance between the nanospheres employing RF-plasma etching. We have shown that the coercivity values reach a maximum for the array of antidots with a separation length close to the domain wall width. In this case, each area between three adjacent holes corresponds to a single domain configuration, which can be switched individually. On the contrary, small hole sizes and large volume of material between them results in domain wall propagation throughout the system accompanied by strong domain wall pinning at the holes. We have also shown the impact of edge effects on the magnetic anisotropy energy.

  8. STABILITY ANALYSIS OF A COMPUTER VIRUS PROPAGATION MODEL WITH ANTIDOTE IN VULNERABLE SYSTEM

    Institute of Scientific and Technical Information of China (English)

    Nguyen Huu KHANH; Nguyen Bich HUY

    2016-01-01

    We study a proposed model describing the propagation of computer virus in the network with antidote in vulnerable system. Mathematical analysis shows that dynamics of the spread of computer viruses is determined by the threshold R0. If R0 ≤ 1, the virus-free equilibrium is globally asymptotically stable, and if R0 >1, the endemic equilibrium is globally asymptotically stable. Lyapunov functional method as well as geometric approach are used for proving the global stability of equilibria. A numerical investigation is carried out to confirm the analytical results. Through parameter analysis, some effective strategies for eliminating viruses are suggested.

  9. On the tunneling effect for magnetic Schrodinger operators in antidot lattices

    CERN Document Server

    Frank, R L

    2004-01-01

    We study the Schr\\"odinger operator $(h\\mathbf{D}-\\mathbf{A})^2$ with periodic magnetic field $B= \\text{curl}\\,\\mathbf{A}$ in an antidot lattice $\\Omega_\\infty=\\R^2\\setminus\\bigcup_{\\alpha\\in\\Gamma}(U+\\alpha)$. Neumann boundary conditions lead to spectrum below $h\\inf B$. Under suitable assumptions on a "one-well problem" we prove that this spectrum is localized inside an exponentially small interval in the semi-classical limit $h\\rightarrow 0$. For this purpose we construct a basis of the corresponding spectral subspace with natural localization and symmetry properties.

  10. Abnormal magnetoresistance behavior in Nb thin films with rectangular arrays of antidots

    Institute of Scientific and Technical Information of China (English)

    Zhang Wei-Jun; Zhao Shi-Ping; Qiu Xiang-Gang; He Shi-Kun; Li Bo-Hong; Cheng Fei; Xu Bing; Wen Zhen-Chao; Cao Wen-Hui; Xiao Hong; Han Xiu-Feng

    2012-01-01

    Magnetoresistance in superconducting Nb films perforated with rectangular arrays of antidots (holes) is investigated at various temperatures and currents.Normally,the magnetoresistance increases with the increasing magnetic field.In this paper,we report a reverse behavior in a certain range of high fields after vortex reconfiguration transition,where the resistances at non-matching fields are smaller than those in the low field regime.This phenomenon is due to a strong caging effect,in which the interstitial vortices are trapped among the pinned multiquanta vortices.This effect is temperature and current dependent.

  11. Cyclotron resonance in two-dimensional electron system with self-organized antidots

    CERN Document Server

    Suchalkin, S D; Zundel, M; Nachtwei, G; Klitzing, K V; Eberl, K

    2001-01-01

    The data on the experimental study on the cyclotron resonance in the two-dimensional electron system with the random scattering potential, conditioned by the massif of the AlInAs self-organized quantum islands, formed in the AlGaAs/GaAs heterotransition plane, are presented. The sharp narrowing of the cyclotron resonance with increase in the magnetic field, explained by the charge scattering peculiarities in the given potential is established. The obtained results suggest the strongly correlated electron state in the strong magnetic fields by the carriers concentrations lesser than the antidots concentrations

  12. Inhibition by ice cream of the antidotal efficacy of activated charcoal.

    Science.gov (United States)

    Levy, G; Soda, D M; Lampman, T A

    1975-03-01

    A study was conducted to determine if ice cream and sherbet interfered with the adsorption of aspirin onto activated charcoal both in vivo and in vitro. An aqueous suspension of 20 g activated charcoal decreased the absorption of 1 g aspirin by 65%; the same dose of activated charcoal with 50 g of ice cream reduced aspirin absorption by only 42% under otherwise identical conditions. In vitro tests showed that different ice creams and sherbet decrease the adsoprtion of aspirin onto activated charcoal. Thus, although ice cream is useful for preparing palatable suspensions of activated charcoal, it decreases appreciably the antidotal efficacy of the adsorbent.

  13. Cyanide Antidotes for Mass Casualties: Comparison of Intramuscular Injector by Autoinjector, Intraosseous Injection, and Inhalational Delivery

    Science.gov (United States)

    2015-12-01

    liquid feed system. It can deliver flow rates of up to 0.2 ml/min, allowing a cyanide antidote to be given in about five minutes. We have shown...state of mitochondrial cytochrome c from the neocortex of the mammalian brain,” Biomed. Opt. Express 3(8), 1933–1946 (2012). 20. B. Chance and W. Bank ...growth rate of the MHz Faraday waves excited on a medicinal liquid layer together facilitate ejection of monodisperse droplets of desirable size range

  14. The role of the hospital pharmacy in the storage and supply of antidotes

    Directory of Open Access Journals (Sweden)

    Luisa Lombardo

    2013-12-01

    Full Text Available Cases of poisoning have been analyzed with the aim of estimating both the incidence and the seriousness of such xenobiotic effects, the major determinant agents, and the related antidotes used in hospital departments. From 2009 to November 2012, a survey of the availability of antidotes in the emergency room services was carried out in all hospital pharmacies under the Palermo Health Authority: Policlinico Paolo Giaccone, ARNAS Civico di Cristina Benefratelli, Azienda Ospedaliera Ospedali Riuniti Villa Sofia-Cervello. Figures show that the majority of poisoning events were caused by the use/abuse of drugs, especially psychopharmaceuticals, alcohol and narcotic substances. This overdose of medical drugs and its various causes is a cause for concern and highlights the fact that this tendency has not regressed over the years. Doctors and pharmacists should raise patients’ awareness about how to use drugs correctly, and make adequate information available to all patients in order to, first, reduce the risks, and second, reduce the cost of treatment for intoxication.

  15. Optimal choice of acetylcholinesterase reactivators for antidotal treatment of nerve agent intoxication.

    Science.gov (United States)

    Bajgar, Jirí

    2010-01-01

    The studies dealing with mechanism of organophosphates (OP)/nerve agent action, prophylaxis and treatment of intoxications is a very hot topic at present. Though the research is very intensive, unfortunately, up to now, there is not universal or significantly better reactivator sufficiently effective against all nerve agents/OP when compared with presently available oximes (pralidoxime, methoxime, obidoxime, trimedoxime, HI-6). The use of the most effective reactivator (HI-6) using simple type of autoinjector (e.g. ComboPen) is strictly limited because of decomposition of HI-6 in solution. Thanks to better solubility it is clear that another salt of HI-6 (dimethanesulfonate, HI-6 DMS) is more convenient for the use as antidote against nerve agents in the autoinjector than HI-6 chloride (Cl). It was clearly demonstrated that reactivation potency of HI-6 DMS in comparison with HI-6 Cl in vivo was the same and bioavailability of HI-6 DMS is better than that of HI-6 Cl. Three chambered autoinjector allows administration of all three antidotes (atropine, reactivator, diazepam) simultaneously. Moreover, the content of chambers can be changed according to proposed requirements. Possible way to solve the problem of universal reactivator could be the use of two reactivators. Three chambered autoinjector is an ideal device for this purpose.

  16. Saffron as an antidote or a protective agent against natural or chemical toxicities.

    Science.gov (United States)

    Razavi, Bibi Marjan; Hosseinzadeh, Hossein

    2015-05-01

    Saffron (Crocus sativus) is an extensively used food additive for its color and taste. Since ancient times this plant has been introduced as a marvelous medicine throughout the world. The wide spectrum of saffron pharmacological activities is related to its major constituents including crocin, crocetin and safranal. Based on several studies, saffron and its active ingredients have been used as an antioxidant, antiinflammatory and antinociceptive, antidepressant, antitussive, anticonvulsant, memory enhancer, hypotensive and anticancer. According to the literatures, saffron has remarkable therapeutic effects. The protective effects of saffron and its main constituents in different tissues including brain, heart, liver, kidney and lung have been reported against some toxic materials either natural or chemical toxins in animal studies.In this review article, we have summarized different in vitro and animal studies in scientific databases which investigate the antidotal and protective effects of saffron and its major components against natural toxins and chemical-induced toxicities. Due to the lake of human studies, further investigations are required to ascertain the efficacy of saffron as an antidote or a protective agent in human intoxication.

  17. In vitro Evaluation of New Acetylcholinesterase Reactivators as Casual Antidotes against Tabun and Cyclosarin

    Energy Technology Data Exchange (ETDEWEB)

    Kuca, Kamil; Jun, Daniel; Jung, Young Sik [Faculty of Military Health Sciences, Trebesska (Cyprus); Kim, Tae Hyuk; Cabal, Jiri [Korea Research Institute of Chemical Technology, Daejeon (Korea, Republic of)

    2006-03-15

    Nerve agents (sarin, tabun, soman and VX) are class of military important substances able to cause many severe intoxications during few minutes. Currently, the threat of misuse of these agents is daily discussed. Unfortunately, there is no single antidote able to treat intoxication caused by all of these agents. Owing to this fact, new generation of antidotes, especially acetylcholinesterase (AChE: EC 3.1.1.7) reactivators, is still developed. In this study, we have tested four newly developed AChE reactivators: 1-(4-hydroxyiminomethylpyridinium)- 5-(4-carbamoylpyridinium)-3-oxa-pentane dibromide (1), 1-(3-hydroxyiminomethylpyridinium)- 5-(4-carbamoylpyridinium)-3-oxa-pentane dibromide (2), 1,5-bis(2-hydroxyiminomethylpyridinium)- 3-oxa-pentane dichloride (3) and 1,5-bis(4-hydroxyiminomethylpyridinium)-3-oxa-pentane dibromide (4) for their potency to reactivate in vitro tabun and cyclosarin-inhibited AChE. Their reactivation efficacy was compared with currently the most promising oxime HI-6 (1-(2-hydroxyiminomethylpyridinium)-3-(4- carbamoylpyridinium)-2-oxa-propane dichloride). According to obtained results, two AChE reactivators 1 and 4 were able to reactivate tabun-inhibited AChE. On the contrary, there was no better AChE reactivator than HI- 6 able to reactivate cyclosarin-inhibited AChE.

  18. Magneto-optical properties for antiferromagnetically coupled CoPt stacked films with hexagonal anti-dot lattices

    Science.gov (United States)

    Yamane, Haruki; Kobayashi, Masanobu

    2014-01-01

    The influence of two-dimensional array structures (hexagonal anti-dot lattices) on magneto-optical (MO) properties was investigated in perpendicular antiferromagnetically coupled Co80Pt20 stacked films containing ZnO optical interference layers. Antiferromagnetic exchange coupling was generated in a [CoPt/Ru/CoPt] tri-layered structure, and anti-dot lattices were formed on both CoPt layers. The exchange coupling between the CoPt layers across a very thin 0.46-nm Ru interlayer was maintained even after nanofabrication. Characteristic MO hysteresis loops were measured by a 405-nm wavelength incident light on samples containing a 50-nm ZnO optical interference layer. The anti-dot lattice with a 200-nm diameter hole exhibited an increase in the residual Kerr rotation angle owing to the antiparallel magnetization alignment of the CoPt layers. Furthermore, compared with samples without the interference layer, the figure of merit for the anti-dot lattice with a 200-nm diameter hole was enhanced by inserting a 100-nm ZnO interference layer. These improvements are attributed to MO interference effects inside the stacked films.

  19. Stability study of a new antidote drug combination (Atropine-HI-6-Prodiazepam) for treatment of organophosphate poisoning.

    Science.gov (United States)

    Clair, P; Wiberg, K; Granelli, I; Carlsson Bratt, I; Blanchet, G

    2000-01-01

    The main purpose of this study was to investigate the chemical stability of a new antidote combination for the treatment of organophosphate poisoning. The antidote combination was packed (enclosed) in two plastic compartments separated by a barrier film. One of them contained a powder oxime cholinesterase reactivator (HI-6-monohydrate 1-[[[4-(aminocarbonyl)pyridinio]methoxy]methyl]-2-[(hydro xyimino)meth yl]-pyridinium dichloride). The other contained an anticholinergic (Atropine) and an anticonvulsant (Prodiazepam or Avizafone (L-lysyl-N-(2-benzoyl-4-chlorophenyl)-N-methyl-glycinamide dihydrochloride) drug in a liquid mixture. The plastic compartments were mounted in an autoinjector device to study the dissolution of HI-6 by ejection of the solution. Drug analysis was performed by high-performance liquid chromatography. The results obtained after 6 months show that this new antidote combination is stable. The amount of each antidote is unchanged during the study. Some known degradation products can be detected in small amounts. The autoinjector mechanism used, gives a complete dissolution of HI-6 powder in the liquid mixture throughout the study.

  20. Molecular Mechanism Underlying Pathogenesis of Lewisite-Induced Cutaneous Blistering and Inflammation: Chemical Chaperones as Potential Novel Antidotes.

    Science.gov (United States)

    Li, Changzhao; Srivastava, Ritesh K; Weng, Zhiping; Croutch, Claire R; Agarwal, Anupam; Elmets, Craig A; Afaq, Farrukh; Athar, Mohammad

    2016-10-01

    Lewisite is a potent arsenic-based chemical warfare agent known to induce painful cutaneous inflammation and blistering. Only a few modestly effective antidotes have so far been described in the literature. However, the discovery of effective antidotes for lewisite was hampered by the paucity of the exact molecular mechanism underlying its cutaneous pathogenesis. We investigated the molecular mechanism underlying lewisite-induced cutaneous blistering and inflammation and describe its novel antidotes. On the basis of our initial screening, we used a highly sensitive murine model that recapitulates the known human pathogenesis of arsenicals-induced cutaneous inflammation and blistering. Topically administered lewisite induced potent acute inflammation and microvesication in the skin of Ptch1(+/-)/SKH-1 mice. Even at a very low dose, lewisite up-regulates unfolded protein response signaling, inflammatory response, and apoptosis. These cutaneous lesions were associated with production of reactive oxygen species and extensive apoptosis of the epidermal keratinocytes. We confirmed that activation of reactive oxygen species-dependent unfolded protein response signaling is the underlying molecular mechanism of skin damage. Similar alterations were noticed in lewisite-treated cultured human skin keratinocytes. We discovered that chemical chaperone 4-phenyl butyric acid and antioxidant N-acetylcysteine, which significantly attenuate lewisite-mediated skin injury, can serve as potent antidotes. These data reveal a novel molecular mechanism underlying the cutaneous pathogenesis of lewisite-induced lesions. We also identified novel potential therapeutic targets for lewisite-mediated cutaneous injury.

  1. The antidotal efficacy of the bispyridinium oximes K027 and TMB-4 against tabun poisoning in mice.

    Science.gov (United States)

    Berend, Suzana; Radić, Bozica; Kuca, Kamil; Lucić Vrdoljak, Ana

    2010-09-06

    A toxic effect of highly toxic nervous agents is irreversible inhibition of vitally important enzyme acethylcholinesterase (AChE). Inhibition of AChE results in accumulation of acetylcholine (ACh) at the synaptic cleft of the cholinergic neurons, leading to overstimulation of cholinergic receptors. The highly toxic nature of tabun has been known for many years, but there are still serious limitations to the antidotal therapy. In this paper a bispyridinium compound K027 [1-(4-hydroxyiminomethylpyridinium)-3-(-4-carbamoylpyridinium) propane dibromide] was tested as potential antidote in tabun poisoned mice. Oxime TMB-4 was included for comparison. The therapeutic efficacy of applied antidotal regimens was tested as pretreatment given 15 min before tabun poisoning and/or as therapy given 1 min after tabun poisoning. Using oxime K027 (25% of its LD(50)) plus atropine as both, pretreatment and therapy, we showed that this combination can protect mice 8 times better than the therapy alone. Under these experimental conditions we confirmed good antidotal efficacy of K027. Moreover, its low acute toxicity is as much as beneficial effect in contrast to high toxicity of currently used TMB-4.

  2. Two new species of Curcuma (Zingiberaceae) used as cobra-bite antidotes

    Institute of Scientific and Technical Information of China (English)

    Arunrat CHAVEERACH; Runglawan SUDMOON; Tawatchai TANEE; Piya MOKKAMUL; Nison SATTAYASAI; Jintana SATTAYASAI

    2008-01-01

    Two new species of Curcuma, C. sattayasaii A. Chaveerach & R. Sudmoon and C. zedoaroides A. Chaveerach & T. Tanee with rhizomes traditionally used for many decades as cobra-bite antidotes are described and illustrated. Curcuma sattayasaii is similar to C. longa L., but differs in rhizome horizontally branching on ground;coma bracts pinkish-white or pinkish-pale green;corolla pale yellow with orange tip;labellum pale orange with an orange central band;anther crest very short, broadly ovate, wider than long. Curcuma zedoaroides is similar to C. zedoaria (Christm.) Roscoe, but differs in rhizome branching pattern;the protruding secondary rhizomes curved down;blades oblong to oblong-lanceolate;peduncle glabrous;fertile and coma bracts glabrous;corolla lobes pale yellow to white, lateral lobe ovate, dorsal lobe broadly ovate. The new taxa have been found in a village of Khon Kaen Province, Northeastern Thailand.

  3. Biomimetic enzyme nanocomplexes and their use as antidotes and preventive measures for alcohol intoxication

    Science.gov (United States)

    Liu, Yang; Du, Juanjuan; Yan, Ming; Lau, Mo Yin; Hu, Jay; Han, Hui; Yang, Otto O.; Liang, Sheng; Wei, Wei; Wang, Hui; Li, Jianmin; Zhu, Xinyuan; Shi, Linqi; Chen, Wei; Ji, Cheng; Lu, Yunfeng

    2013-03-01

    Organisms have sophisticated subcellular compartments containing enzymes that function in tandem. These confined compartments ensure effective chemical transformation and transport of molecules, and the elimination of toxic metabolic wastes. Creating functional enzyme complexes that are confined in a similar way remains challenging. Here we show that two or more enzymes with complementary functions can be assembled and encapsulated within a thin polymer shell to form enzyme nanocomplexes. These nanocomplexes exhibit improved catalytic efficiency and enhanced stability when compared with free enzymes. Furthermore, the co-localized enzymes display complementary functions, whereby toxic intermediates generated by one enzyme can be promptly eliminated by another enzyme. We show that nanocomplexes containing alcohol oxidase and catalase could reduce blood alcohol levels in intoxicated mice, offering an alternative antidote and prophylactic for alcohol intoxication.

  4. Piecewise parabolic negative magnetoresistance of two-dimensional electron gas with triangular antidot lattice

    Energy Technology Data Exchange (ETDEWEB)

    Budantsev, M. V., E-mail: budants@isp.nsc.ru; Lavrov, R. A.; Pogosov, A. G.; Zhdanov, E. Yu.; Pokhabov, D. A. [Russian Academy of Sciences, Rzhanov Institute of Semiconductor Physics, Siberian Branch (Russian Federation)

    2011-02-15

    Extraordinary piecewise parabolic behavior of the magnetoresistance has been experimentally detected in the two-dimensional electron gas with a dense triangular lattice of antidots, where commensurability magnetoresistance oscillations are suppressed. The magnetic field range of 0-0.6 T can be divided into three wide regions, in each of which the magnetoresistance is described by parabolic dependences with high accuracy (comparable to the experimental accuracy) and the transition regions between adjacent regions are much narrower than the regions themselves. In the region corresponding to the weakest magnetic fields, the parabolic behavior becomes almost linear. The observed behavior is reproducible as the electron gas density changes, which results in a change in the resistance by more than an order of magnitude. Possible physical mechanisms responsible for the observed behavior, including so-called 'memory effects,' are discussed.

  5. Theoretical study on electronic properties of MoS{sub 2} antidot lattices

    Energy Technology Data Exchange (ETDEWEB)

    Shao, Li; Chen, Guangde; Ye, Honggang, E-mail: hgye@mail.xjtu.edu.cn; Wu, Yelong; Niu, Haibo; Zhu, Youzhang [Department of Applied Physics and the MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, Xi' an Jiaotong University, Xi' an, Shaanxi 710049 (China)

    2014-09-21

    Motivated by the state of the art method for etching hexagonal array holes in molybdenum disulfide (MoS{sub 2}), the electronic properties of MoS{sub 2} antidot lattices (MoS{sub 2}ALs) with zigzag edge were studied with first-principles calculations. Monolayer MoS{sub 2}ALs are semiconducting and the band gaps converge to constant values as the supercell area increases, which can be attributed to the edge effect. Multilayer MoS{sub 2}ALs and chemical adsorbed MoS{sub 2}ALs by F atoms show metallic behavior, while the structure adsorbed with H atoms remains to be semiconducting with a tiny bandgap. Our results show that forming periodically repeating structures in MoS{sub 2} can develop a promising technique for engineering nano materials and offer new opportunities for designing MoS{sub 2}-based nanoscale electronic devices and chemical sensors.

  6. Isoniazid overdose : a case series, literature review and survey of antidote availability.

    Science.gov (United States)

    Maw, Graeme; Aitken, Peter

    2003-01-01

    Tuberculosis has re-emerged as a significant public health threat over the last decade both globally and within Australia. This is thought to be largely due to the HIV epidemic, a growing itinerant population, and immigration. The antibiotic isoniazid remains an integral part of drug therapy. With the numbers of patients receiving isoniazid remaining high, the number of cases of acute poisoning is expected to be significant. This paper presents a series of two cases of isoniazid poisoning presenting to a tertiary referral centre in North Queensland. Isoniazid toxicity produces a triad of coma, metabolic acidosis and seizures. The seizures are often refractory to traditional antiepileptics. A specific antidote is available (pyridoxine [vitamin B6]) and both patients were administered this as part of their treatment. We also surveyed all hospitals in Australia with an accredited adult Emergency Department to assess the availability of pyridoxine.

  7. A breakthrough on Amanita phalloides poisoning: an effective antidotal effect by polymyxin B.

    Science.gov (United States)

    Garcia, Juliana; Costa, Vera Marisa; Carvalho, Alexandra T P; Silvestre, Ricardo; Duarte, José Alberto; Dourado, Daniel F A R; Arbo, Marcelo D; Baltazar, Teresa; Dinis-Oliveira, Ricardo Jorge; Baptista, Paula; de Lourdes Bastos, Maria; Carvalho, Félix

    2015-12-01

    Amanita phalloides is responsible for more than 90 % of mushroom-related fatalities, and no effective antidote is available. α-Amanitin, the main toxin of A. phalloides, inhibits RNA polymerase II (RNAP II), causing hepatic and kidney failure. In silico studies included docking and molecular dynamics simulation coupled to molecular mechanics with generalized Born and surface area method energy decomposition on RNAP II. They were performed with a clinical drug that shares chemical similarities to α-amanitin, polymyxin B. The results show that polymyxin B potentially binds to RNAP II in the same interface of α-amanitin, preventing the toxin from binding to RNAP II. In vivo, the inhibition of the mRNA transcripts elicited by α-amanitin was efficiently reverted by polymyxin B in the kidneys. Moreover, polymyxin B significantly decreased the hepatic and renal α-amanitin-induced injury as seen by the histology and hepatic aminotransferases plasma data. In the survival assay, all animals exposed to α-amanitin died within 5 days, whereas 50 % survived up to 30 days when polymyxin B was administered 4, 8, and 12 h post-α-amanitin. Moreover, a single dose of polymyxin B administered concomitantly with α-amanitin was able to guarantee 100 % survival. Polymyxin B protects RNAP II from inactivation leading to an effective prevention of organ damage and increasing survival in α-amanitin-treated animals. The present use of clinically relevant concentrations of an already human-use-approved drug prompts the use of polymyxin B as an antidote for A. phalloides poisoning in humans.

  8. The toxicokinetics and toxicodynamics of organophosphonates versus the pharmacokinetics and pharmacodynamics of oxime antidotes: biological consequences.

    Science.gov (United States)

    Voicu, Victor A; Thiermann, Horst; Rădulescu, Flavian Stefan; Mircioiu, Constantin; Miron, Dalia Simona

    2010-02-01

    This paper presents basic data on organophosphonate (OP) mechanisms of action, especially by toxicokinetic/toxicodynamic (TK/TD) process correlations. It is generally accepted that at least during onset of OP biological systems interaction, blood and tissue cholinesterase's inhibition represents OP exposure marker and initiating mechanisms for toxicodynamic effects, characteristic for cholinergic crisis. OP penetrability of various biological barriers conditioning TK characteristics are determined by a series of physico-chemical properties. Non-cholinergic effects, direct interactions with cellular structures and subsequent effects (excitotoxicity) triggered by cholinergic crisis are also briefly presented. Opposed to these OP TK/TD characteristics, the authors analysed the pharmacokinetic/pharmacodynamic (PK/PD) characteristics and their correlations for oximes, as basic OP antidotes, besides atropine and anticonvulsants. Phosphorilated cholinesterasis reactivators are mono or bispyridinium derivatives with quaternary ammonium atoms, high water solubility, ionized at physiological pH, distribution in extra-cellular space, very low digestive absorption and blood-brain barrier (BBB) penetrability. OP nerve gas acute toxicity is correlated with anti-acetylcholinesterase (AChE) activity and partition coefficient. The toxicity rank seems to be determined by lipophilicity, besides their specific AChE inhibitory property. It has the effect that acute toxicity is the resultant of a TD process closely linked and dependent in vivo upon molecular descriptors determinant for the TK process. For cholinesterasis reactivators, molecular and PK characteristics limit their effects, especially to the peripheral level. The absent or much reduced BBB penetrability allowed some researchers to suggest that reactivators' penetration and presence at central level are not necessary. The study of PK/PD correlations, molecular descriptors and biological membrane permeability of oximes can

  9. Availability of antidotes and key emergency drugs in tertiary care hospitals of Punjab and assessment of the knowledge of health care professionals in the management of poisoning cases.

    Science.gov (United States)

    Arslan, Naheed; Khiljee, Sonia; Bakhsh, Allah; Ashraf, Muhammad; Maqsood, Iram

    2016-03-01

    This study was conducted to evaluate the availability of antidotes/key emergency drugs in tertiary care hospitals of the Punjab province, and to assess the knowledge of health care professionals in the stocking and administration of antidotes in the proper management of poisoning cases. Seventeen (n=17) tertiary care hospitals of Punjab Pakistan were selected. Two performas (A and B) were designed for 26 antidotes/key emergency drugs and given to the hospital pharmacists and physicians respectively. It was observed that Activated Charcoal, being the universal antidote was found only in 6 hospitals (41%). Digoxin Immune Fab, Edentate Calcium disodium and Glucagon were not available in emergency department of any hospital and even not included in the formulary of any hospital. About 80% pharmacists were aware of the method of preparation of Activated Charcoal and 85% physicians were familiar with its route of administration. Data showed that tertiary care hospitals of Punjab do not stock antidotes according to national drug policy. Moreover the study strongly suggests the development of health care centers and professional by organizing antidote awareness programs, continuous education and record keeping of poisonous cases and availability of emergency drugs around the clock.

  10. All-electrical detection of spin dynamics in magnetic antidot lattices by the inverse spin Hall effect

    Energy Technology Data Exchange (ETDEWEB)

    Jungfleisch, Matthias B. [Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439, USA; Zhang, Wei [Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439, USA; Ding, Junjia [Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439, USA; Jiang, Wanjun [Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439, USA; Sklenar, Joseph [Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439, USA; Department of Physics and Astronomy, Northwestern University, Evanston, Illinois 60208, USA; Pearson, John E. [Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439, USA; Ketterson, John B. [Department of Physics and Astronomy, Northwestern University, Evanston, Illinois 60208, USA; Hoffmann, Axel [Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439, USA

    2016-02-01

    The understanding of spin dynamics in laterally confined structures on sub-micron length scales has become a significant aspect of the development of novel magnetic storage technologies. Numerous ferromagnetic resonance measurements, optical characterization by Kerr microscopy and Brillouin light scattering spectroscopy and x-ray studies were carried out to detect the dynamics in patterned magnetic antidot lattices. Here, we investigate Oersted-field driven spin dynamics in rectangular Ni80Fe20/Pt antidot lattices with different lattice parameters by electrical means. When the system is driven to resonance, a dc voltage across the length of the sample is detected that changes its sign upon field reversal, which is in agreement with a rectification mechanism based on the inverse spin Hall effect. Furthermore, we show that the voltage output scales linearly with the applied microwave drive in the investigated range of powers. Our findings have direct implications on the development of engineered magnonics applications and devices.

  11. Optically induced spin wave dynamics in [Co/Pd]{sub 8} antidot lattices with perpendicular magnetic anisotropy

    Energy Technology Data Exchange (ETDEWEB)

    Pal, S.; Das, K.; Barman, A., E-mail: abarman@ybose.res.in [Thematic Unit of Excellence on Nanodevice Technology and Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700 098 (India); Klos, J. W.; Gruszecki, P.; Krawczyk, M., E-mail: krawczyk@amu.edu.pl [Faculty of Physics, A. Mickiewicz University in Poznan, Umultowska 85, 61-614 Poznań (Poland); Hellwig, O. [San Jose Research Center, HGST, a Western Digital Company, 3403 Yerba Buena Rd., San Jose, California 95135 (United States)

    2014-10-20

    We present an all-optical time-resolved measurement of spin wave (SW) dynamics in a series of antidot lattices based on [Co(0.75 nm)/Pd(0.9 nm)]{sub 8} multilayer (ML) systems with perpendicular magnetic anisotropy. The spectra depend significantly on the areal density of the antidots. The observed SW modes are qualitatively reproduced by the plane wave method. The interesting results found in our measurements and calculations at small lattice constants can be attributed to the increase of areal density of the shells with modified magnetic properties probably due to distortion of the regular ML structure by the Ga ion bombardment and to increased coupling between localized modes. We propose and discuss the possible mechanisms for this coupling including exchange interaction, tunnelling, and dipolar interactions.

  12. Structure of a prereaction complex between the nerve agent sarin, its biological target acetylcholinesterase, and the antidote HI-6.

    Science.gov (United States)

    Allgardsson, Anders; Berg, Lotta; Akfur, Christine; Hörnberg, Andreas; Worek, Franz; Linusson, Anna; Ekström, Fredrik J

    2016-05-17

    Organophosphorus nerve agents interfere with cholinergic signaling by covalently binding to the active site of the enzyme acetylcholinesterase (AChE). This inhibition causes an accumulation of the neurotransmitter acetylcholine, potentially leading to overstimulation of the nervous system and death. Current treatments include the use of antidotes that promote the release of functional AChE by an unknown reactivation mechanism. We have used diffusion trap cryocrystallography and density functional theory (DFT) calculations to determine and analyze prereaction conformers of the nerve agent antidote HI-6 in complex with Mus musculus AChE covalently inhibited by the nerve agent sarin. These analyses reveal previously unknown conformations of the system and suggest that the cleavage of the covalent enzyme-sarin bond is preceded by a conformational change in the sarin adduct itself. Together with data from the reactivation kinetics, this alternate conformation suggests a key interaction between Glu202 and the O-isopropyl moiety of sarin. Moreover, solvent kinetic isotope effect experiments using deuterium oxide reveal that the reactivation mechanism features an isotope-sensitive step. These findings provide insights into the reactivation mechanism and provide a starting point for the development of improved antidotes. The work also illustrates how DFT calculations can guide the interpretation, analysis, and validation of crystallographic data for challenging reactive systems with complex conformational dynamics.

  13. Evaluation of the benefit of the bispyridinium compound MB327 for the antidotal treatment of nerve agent-poisoned mice.

    Science.gov (United States)

    Kassa, Jiri; Pohanka, Miroslav; Timperley, Christopher M; Bird, Mike; Green, A Christopher; Tattersall, John E H

    2016-06-01

    The potency of the bispyridinium non-oxime compound MB327 [1,1'-(propane-1,3-diyl)bis(4-tert-butylpyridinium) diiodide] to increase the therapeutic efficacy of the standard antidotal treatment (atropine in combination with an oxime) of acute poisoning with organophosphorus nerve agents was studied in vivo. The therapeutic efficacy of atropine alone - or atropine in combination with an oxime, MB327, or both an oxime and MB237 - was evaluated by the determination of LD50 values of several nerve agents (tabun, sarin and soman) in mice with and without treatment. The addition of MB327 increased the therapeutic efficacy of atropine alone, and atropine in combination with an oxime, against all three nerve agents, although differences in the LD50 values only reached statistical significance for sarin. In conclusion, the addition of the compound MB327 to the standard antidotal treatment of acute poisonings with nerve agents was beneficial regardless of the chemical structure of the nerve agent, although at the dose employed, MB327 in combination with atropine, or atropine and an oxime, provided only a modest increase in protection ratio. These results from mice, and previous ones from guinea-pigs, provide consistent evidence for additional, albeit modest, efficacy resulting from the inclusion of the antinicotinic compound MB327 in standard antidotal therapy. Given the typically steep probit slope for the dose-lethality relationship for nerve agents, such modest increases in protection ratio could provide significant survival benefit.

  14. The influence of combinations of oximes on the reactivating and therapeutic efficacy of antidotal treatment of tabun poisoning in rats and mice.

    Science.gov (United States)

    Kassa, Jiri; Karasova, Jana Zdarova; Pavlikova, Ruzena; Misik, Jan; Caisberger, Filip; Bajgar, Jiri

    2010-03-01

    The influence of the combination of oximes on the reactivating and therapeutic efficacy of antidotal treament of acute tabun poisoning was evaluated. The ability of two combinations of oximes (HI-6 + obidoxime and HI-6 + K203) to reactivate tabun-inhibited acetylcholinesterase and reduce acute toxicity of tabun was compared with the reactivating and therapeutic efficacy of antidotal treatment involving single oxime (HI-6, obidoxime, K203) using in vivo methods. Studies determining percentage of reactivation of tabun-inhibited blood and tissue acetylcholinesterase in poisoned rats showed that the reactivating efficacy of both combinations of oximes is higher than the reactivating efficacy of the most effective individual oxime in blood and diaphragm and comparable with the reactivating effects of the most effective individual oxime in brain. Moreover, both combinations of oximes were found to be slightly more efficacious in the reduction of acute lethal toxic effects in tabun-poisoned mice than the antidotal treatment involving individual oxime. A comparison of reactivating and therapeutic efficacy of individual oximes showed that the newly developed oxime K203 is slightly more effective than commonly used obidoxime and both of them are markedly more effective than the oxime HI-6. Based on the obtained data, we can conclude that the antidotal treatment involving chosen combinations of oximes brings beneficial effects for the potency of antidotal treatment to reactivate tabun-inhibited acetylcholinesterase in rats and to reduce acute toxicity of tabun in mice.

  15. Proposing an Antidote for Poisonous Phosphine in View of Mitochondrial Eectrochemistry Facts

    Directory of Open Access Journals (Sweden)

    Mohammad Abdollahi

    2012-01-01

    Full Text Available Metal phosphides in general are potent pesticides that are a common cause of human poisoning. Various salts of phosphides produce highly toxic phosphine in exposure to gastric acid that results in multi-organ damage and death. There is no antidote for phosphine poisoning and most of human poisoned cases do not survive. All we know so far is that phosphine is a mitochondrial toxin that inhibits cellular respiration and induces oxidative stress. Mechanistically, phosphine as a reducing agent interacts with metal ion cofactors at the active site of enzymes and inhibits key enzymes such as cytochrome C oxidase that lead to inhibition of mitochondrial respiration. Phosphine (E0 = −1.18 V as a reducing agent gives electrons to cytochrome C oxidase (E0 = +0.29 V. Metal phosphides with lower reduction potential are stronger electron donors and thus stronger poisons. Our hypothesis is that if an electron receiver stronger than cytochrome C oxidase is used then it would compete with cytochrome C oxidase in interaction with phosphine. This competition might prevent or reduce the inhibition of cellular respiration. This idea can be tested in an animal model of phosphine toxicity by monitoring cardiovascular state and measuring the cardiac mitochondrial function.

  16. Hydroxypyri(mi)dine-based chelators as antidotes of toxicity due to aluminum and actinides.

    Science.gov (United States)

    Santos, M A; Esteves, M A; Chaves, S

    2012-01-01

    This review is focused on recent developments on hydroxypyri(mi)dines, as aluminum and actinide chelating agents to combat the toxicity due to accumulations of these metal ions in human body resulting from excessive metal exposure. After a brief update revision of the most common processes of aluminum (Al) exposure, as well as the associated toxicities and pathologies, we will focus on the current available Al chelators and future perspective as potential antidotes of Al toxicity. Due to the similarity between Al and Fe, a major emphasis is given to the hydroxypyridinone and hydroxypyrimidinone chelators, since they are analogues of the current iron chelators in clinical use (DFP and DFO). This review includes issues such as molecular design strategies and corresponding effects on the associated physico-chemical properties, lipo-hydrophilic balance, toxicity, in vivo bioassays and current clinical applications. The hydroxypyri(mi)dine chelators are also suitable for other hard metal ions, such as the radiotoxic actinides, and so a brief review is included on the applications of these chelators in actinides scavenging.

  17. An antidote approach to reduce risk and broaden utility of antibody based therapeutics.

    Science.gov (United States)

    Portnoff, Alyse D; Gao, Cuihua; Borrok, M Jack; Gao, Xizhe; Gao, Changshou; Rainey, G Jonah

    2017-03-03

    Antibody therapeutics offer safe and effective treatment options for a broad range of diseases. One of the greatest benefits of antibody therapeutics is their extraordinarily long serum half-life, allowing infrequent dosing with long-lasting effects. One characteristic of antibodies that drives long half-life is the ability to interact with the recycling receptor, FcRn, in a pH-dependent manner. The benefit of long half-life, however, carries with it liabilities. While the positive effects of antibody therapeutics are long-lasting, any acute adverse events or chronic negative impacts, such as immunosuppression in the face of an infection, are also long-lasting. Therefore, we sought to develop antibodies with a chemical handle that alone would enjoy the long half-life of normal antibodies, but upon addition of a small-molecule antidote, would interact with the chemical handle and inhibit the antibody recycling mechanism thus leading to rapid degradation and shortened half-life in vivo. Here we present a proof of concept study where we identify sites to incorporate a nnAA that can be chemically modified to modulate FcRn interaction in vitro and antibody half-life in vivo. This is an important first step in developing safer therapeutics, and the next step will be development of technology that can perform the modifying chemistry in vivo.

  18. Fresh frozen plasma as a successful antidotal supplement in acute organophosphate poisoning.

    Science.gov (United States)

    Vučinić, Slavica; Zlatković, Milica; Antonijević, Biljana; Ćurčić, Marijana; Bošković, Bogdan

    2013-06-01

    Despite improvements to intensive care management and specific pharmacological treatments (atropine, oxime, diazepam), the mortality associated with organophosphate (OP) poisoning has not substantially decreased. The objective of this examination was to describe the role of fresh frozen plasma (FFP) in acute OP poisoning. After a deliberate ingestion of malathion, a 55-year-old male suffering from miosis, somnolence, bradycardia, muscular fasciculations, rales on auscultation, respiratory insufficiency, as well as from an inhibition of red blood cell acetylcholinesterase (AChE) and plasma butyrylcholinesterase (BuChE), was admitted to hospital. Malathion was confirmed in a concentration of 18.01 mg L(-1). Apart from supportive measures (including mechanical ventilation for four days), antidotal treatment with atropine, oxime-pralidoxime methylsulphate (Contrathion(R)), and diazepam was administered, along with FFP. The potentially beneficial effects of FFP therapy included a prompt increase of BuChE activity (from 926 IU L(-1) to 3277 IU L(-1); reference range from 7000 IU L(-1) to 19000 IU L(-1)) and a reduction in the malathion concentration, followed by clinical recovery. Due to BuChE replacement, albumin content, and volume restitution, FFP treatment may be used as an alternative approach in patients with acute OP poisoning, especially when oximes are not available.

  19. Oximes: Reactivators of phosphorylated acetylcholinesterase and antidotes in therapy against tabun poisoning.

    Science.gov (United States)

    Kovarik, Zrinka; Calić, Maja; Sinko, Goran; Bosak, Anita; Berend, Suzana; Vrdoljak, Ana Lucić; Radić, Bozica

    2008-09-25

    One of the therapeutic approaches to organophosphate poisoning is to reactivate AChE with site-directed nucleophiles such as oximes. However, pyridinium oximes 2-PAM, HI-6, TMB-4 and obidoxime, found as the most effective reactivators, have limiting reactivating potency in tabun poisoning. We tested oximes varying in the type of ring (pyridinium and/or imidazolium), the length and type of the linker between rings, and in the position of the oxime group on the ring to find more effective oximes to reactivate tabun-inhibited human erythrocyte AChE. Three of our tested pyridinium oximes K027, K048, K074, along with TMB-4, were the most promising for AChE reactivation. Promising oximes were further tested in vivo on tabun poisoned mice not only as antidotes in combination with atropine but also as pretreatment drug. Herein, we showed that a promising treatment in tabun poisoning by selected oximes and atropine could be improved if oximes are also used in pretreatment. Since the reactivating efficacy of the oximes in vitro corresponded to their therapeutic efficacy in vivo, it seems that pharmacological effect of these oximes is indeed primarily related to the reactivation of tabun-phosphorylated AChE.

  20. The influence of the time of antidotal treatment administration on the potency of newly developed oximes to counteract acute toxic effects of tabun in mice.

    Science.gov (United States)

    Kassa, Jirí

    2005-01-01

    (1) The influence of the time of administration of antidotal treatment consisting of anticholinergic drug (atropine) and newly developed oxime (K027 or K048) on its effectiveness to eliminate tabun-induced lethal toxic effects was studied in mice. (2) The therapeutic efficacy of antidotal treatment of tabun-induced acute poisoning depends on the time of its administration regardless of the choice of the oxime. (3) Our results show that both oximes studied (K027, K048) are able to sufficiently eliminate lethal effects of tabun. Nevertheless, their efficacy significantly decreases when they were administered 5 min after tabun poisoning. (4) The findings support the hypothesis that both newly developed oximes appear to be suitable oximes to counteract acute toxicity of tabun although their ability to eliminate lethal toxic effects of tabun significantly decreases with prolonged time interval between tabun challenge and antidotal treatment administration.

  1. Intravenous Lipid Emulsion as an Antidote for the Treatment of Acute Poisoning: A Bibliometric Analysis of Human and Animal Studies.

    Science.gov (United States)

    Zyoud, Sa'ed H; Waring, W Stephen; Al-Jabi, Samah W; Sweileh, Waleed M; Rahhal, Belal; Awang, Rahmat

    2016-11-01

    In recent years, there has been increasing interest in the role of intravenous lipid formulations as potential antidotes in patients with severe cardiotoxicity caused by drug toxicity. The aim of this study was to conduct a comprehensive bibliometric analysis of all human and animal studies featuring lipid emulsion as an antidote for the treatment of acute poisoning. The Scopus database search was performed on 5 February 2016 to analyse the research output related to intravenous lipid emulsion as an antidote for the treatment of acute poisoning. Research indicators used for analysis included total number of articles, date (year) of publication, total citations, value of the h-index, document types, countries of publication, journal names, collaboration patterns and institutions. A total of 594 articles were retrieved from Scopus database for the period of 1955-2015. The percentage share of global intravenous lipid emulsion research output showed that research output was 85.86% in 2006-2015 with yearly average growth in this field of 51 articles per year. The USA, United Kingdom (UK), France, Canada, New Zealand, Germany, Australia, China, Turkey and Japan accounted for 449 (75.6%) of all the publications. The total number of citations for all documents was 9,333, with an average of 15.7 citations per document. The h-index of the retrieved documents for lipid emulsion research as antidote for the treatment of acute poisoning was 49. The USA and the UK achieved the highest h-indices, 34 and 14, respectively. New Zealand produced the greatest number of documents with international collaboration (51.9%) followed by Australia (50%) and Canada (41.4%) out of the total number of publications for each country. In summary, we found an increase in the number of publications in the field of lipid emulsion after 2006. The results of this study demonstrate that the majority of publications in the field of lipid emulsion were published by high-income countries. Researchers from

  2. Plasmon–Phonon Coupling in Large-Area Graphene Dot and Antidot Arrays Fabricated by Nanosphere Lithography

    DEFF Research Database (Denmark)

    Zhu, Xiaolong; Wang, Weihua; Yan, Wei

    2014-01-01

    Nanostructured graphene on SiO2 substrates paves the way for enhanced light–matter interactions and explorations of strong plasmon–phonon hybridization in the mid-infrared regime. Unprecedented large-area graphene nanodot and antidot optical arrays are fabricated by nanosphere lithography......, with structural control down to the sub-100 nm regime. The interaction between graphene plasmon modes and the substrate phonons is experimentally demonstrated, and structural control is used to map out the hybridization of plasmons and phonons, showing coupling energies of the order 20 meV. Our findings...

  3. An effective antidote for paraquat poisonings: the treatment with lysine acetylsalicylate.

    Science.gov (United States)

    Dinis-Oliveira, R J; Pontes, H; Bastos, M L; Remião, F; Duarte, J A; Carvalho, F

    2009-01-31

    Sodium salicylate (NaSAL) has been shown to have a multifactorial protection mechanism against paraquat (PQ)-induced toxicity, due to its ability to modulate inflammatory signalling systems, to prevent oxidative stress and to its capacity to chelate PQ. Considering that currently there is no pharmaceutical formulation available for parenteral administration of NaSAL, the aim of the present study was to evaluate the antidotal feasibility of a salicylate prodrug, lysine acetylsalicylate (LAS), accessible for parenteral administrations. PQ was administered to Wistar rats by gavage (125mg/kg of PQ ion) and the treatment was performed intraperitoneally with different doses (100, 200 and 400mg/kg of body weight) of LAS. Survival rate was followed during 30 days and living animals at this endpoint were sacrificed for lung, kidney, liver, jejune and heart histological analysis. It was shown, that the salicylate prodrug, LAS, available in a large number of hospitals, is also effective in the treatment of PQ intoxications. From all tested LAS doses, 200mg/kg assured animal's full survival. Comparatively to 60% of mortality observed in PQ only exposed animals, the lethality was higher (80%) in the group that received 400mg/kg of LAS 2h after PQ administration. The dose of 100mg/kg of LAS showed only a modest protection (60% of survival). Collagen deposition was observed by histological analysis in survived animals of all experimental groups, being less pronounced in animals receiving 200mg/kg of LAS, reinforcing the importance of this dose against tissue damage induced by PQ. The results allow us to suggest that LAS should be considered in the hospital treatment of PQ poisonings.

  4. Good manufacturing practice: manufacturing of a nerve agent antidote nanoparticle suspension.

    Science.gov (United States)

    Clark, Andrew P-Z; Dixon, Hong; Cantu, Norma L; Cabell, Larry A; McDonough, Joe A

    2013-01-01

    We have established a current good manufacturing practice (GMP) manufacturing process to produce a nanoparticle suspension of 1,1'-methylenebis-4-[(hydroxyimino)methyl]pyridinium dimethanesulfonate (MMB4 DMS) in cottonseed oil (CSO) as a nerve agent antidote for a Phase 1 clinical trial. Bis-pyridinium oximes such as MMB4 were previously developed for emergency treatment of organophosphate nerve agent intoxication. Many of these compounds offer efficacy superior to monopyridinium oximes, but they have poor thermal stability due to hydrolytic cleavage in aqueous solution. We previously developed a nonaqueous nanoparticle suspension to improve the hydrothermal stability, termed Enhanced Formulation (EF). An example of this formulation technology is a suspension of MMB4 DMS nanoparticles in CSO. Due to the profound effect of particle size distribution on product quality and performance, particle size must be controlled during the manufacturing process. Therefore, a particle size analysis method for MMB4 DMS in CSO was developed and validated to use in support of good laboratory practice/GMP development and production activities. Manufacturing of EF was accomplished by milling MMB4 DMS with CSO and zirconia beads in an agitator bead mill. The resulting bulk material was filled into 5-mL glass vials at a sterile fill facility and terminally sterilized by gamma irradiation. The clinical lot was tested and released, a Certificate of Analysis was issued, and a 3-year International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) stability study started. The drug product was placed in storage for Phase 1 clinical trial distribution. A dose delivery uniformity study was undertaken to ensure that the correct doses were delivered to the patients in the clinic.

  5. Review of UV spectroscopic, chromatographic, and electrophoretic methods for the cholinesterase reactivating antidote pralidoxime (2-PAM).

    Science.gov (United States)

    John, Harald; Blum, Marc-Michael

    2012-01-01

    Pralidoxime (2-PAM) belongs to the class of monopyridinium oximes with reactivating potency on cholinesterases inhibited by phosphylating organophosphorus compounds (OPC), for example, pesticides and nerve agents. 2-PAM represents an established antidote for the therapy of anticholinesterase poisoning since the late 1950s. Quite high therapeutic concentrations in human plasma (about 13 µg/ml) lead to concentrations in urine being about 100 times higher allowing the use of less sensitive analytical techniques that were used especially in the early years after 2-PAM was introduced. In this time (mid-1950s until the end of the 1970s) 2-PAM was most often analyzed by either paper chromatography or simple UV spectroscopic techniques omitting any sample separation step. These methods were displaced completely after the establishment of column liquid chromatography in the early 1980s. Since then, diverse techniques including cation exchange, size-exclusion, reversed-phase, and ligand-exchange chromatography have been introduced. Today, the most popular method for 2-PAM quantification is ion pair chromatography often combined with UV detection representing more than 50% of all column chromatographic procedures published. Furthermore, electrophoretic approaches by paper and capillary zone electrophoresis have been successfully used but are seldom applied. This review provides a commentary and exhaustive summary of analytical techniques applied to detect 2-PAM in pharmaceutical formulations and biological samples to characterize stability and pharmacokinetics as well as decomposition and biotransformation products. Separation techniques as well as diverse detectors are discussed in appropriate detail allowing comparison of individual preferences and limitations. In addition, novel data on mass spectrometric fragmentation of 2-PAM are provided.

  6. All-electrical detection of spin dynamics in magnetic antidot lattices by the inverse spin Hall effect

    Energy Technology Data Exchange (ETDEWEB)

    Jungfleisch, Matthias B., E-mail: jungfleisch@anl.gov; Zhang, Wei; Ding, Junjia; Jiang, Wanjun; Pearson, John E.; Hoffmann, Axel [Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439 (United States); Sklenar, Joseph [Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439 (United States); Department of Physics and Astronomy, Northwestern University, Evanston, Illinois 60208 (United States); Ketterson, John B. [Department of Physics and Astronomy, Northwestern University, Evanston, Illinois 60208 (United States)

    2016-02-01

    The understanding of spin dynamics in laterally confined structures on sub-micron length scales has become a significant aspect of the development of novel magnetic storage technologies. Numerous ferromagnetic resonance measurements, optical characterization by Kerr microscopy and Brillouin light scattering spectroscopy, and x-ray studies were carried out to detect the dynamics in patterned magnetic antidot lattices. Here, we investigate Oersted-field driven spin dynamics in rectangular Ni{sub 80}Fe{sub 20}/Pt antidot lattices with different lattice parameters by electrical means and compare them to micromagnetic simulations. When the system is driven to resonance, a dc voltage across the length of the sample is detected that changes its sign upon field reversal, which is in agreement with a rectification mechanism based on the inverse spin Hall effect. Furthermore, we show that the voltage output scales linearly with the applied microwave drive in the investigated range of powers. Our findings have direct implications on the development of engineered magnonics applications and devices.

  7. Chemical Reaction between Boric Acid and Phosphine Indicates Boric Acid as an Antidote for Aluminium Phosphide Poisoning

    Directory of Open Access Journals (Sweden)

    Motahareh Soltani

    2016-08-01

    Full Text Available Objectives: Aluminium phosphide (AlP is a fumigant pesticide which protects stored grains from insects and rodents. When it comes into contact with moisture, AlP releases phosphine (PH3, a highly toxic gas. No efficient antidote has been found for AlP poisoning so far and most people who are poisoned do not survive. Boric acid is a Lewis acid with an empty p orbital which accepts electrons. This study aimed to investigate the neutralisation of PH3 gas with boric acid. Methods: This study was carried out at the Baharlou Hospital, Tehran University of Medical Sciences, Tehran, Iran, between December 2013 and February 2014. The volume of released gas, rate of gas evolution and changes in pH were measured during reactions of AlP tablets with water, acidified water, saturated boric acid solution, acidified saturated boric acid solution, activated charcoal and acidified activated charcoal. Infrared spectroscopy was used to study the resulting probable adduct between PH3 and boric acid. Results: Activated charcoal significantly reduced the volume of released gas (P <0.01. Although boric acid did not significantly reduce the volume of released gas, it significantly reduced the rate of gas evolution (P <0.01. A gaseous adduct was formed in the reaction between pure AlP and boric acid. Conclusion: These findings indicate that boric acid may be an efficient and non-toxic antidote for PH3 poisoning.

  8. Anisotropic magneto-resistance in Ni{sub 80}Fe{sub 20} antidot arrays with different lattice configurations

    Energy Technology Data Exchange (ETDEWEB)

    Coïsson, Marco, E-mail: m.coisson@inrim.it [INRIM, Electromagnetics Division, Strada delle Cacce 91, 10135 Torino (Italy); Manzin, Alessandra [INRIM, Electromagnetics Division, Strada delle Cacce 91, 10135 Torino (Italy); Barrera, Gabriele [INRIM, Electromagnetics Division, Strada delle Cacce 91, 10135 Torino (Italy); Università degli Studi di Torino, Dipartimento di Chimica, via P. Giuria 7, 10125 Torino (Italy); Celegato, Federica; Enrico, Emanuele; Tiberto, Paola; Vinai, Franco [INRIM, Electromagnetics Division, Strada delle Cacce 91, 10135 Torino (Italy)

    2014-10-15

    Highlights: • Detailed study of the magnetisation processes in antidot lattices. • Combined magnetic (MFM), magneto-transport (AMR) and numerical investigations. • Accounting for the experimentally observed differences in AMR signal amplitude in longitudinal and transverse configurations through numerical simulations. - Abstract: Ni{sub 80}Fe{sub 20} antidot arrays having different lattice geometrical properties and irregularities were prepared via electron beam lithography and self-assembling of polystyrene nanospheres. All the samples were experimentally characterised by magnetic force microscopy and room-temperature magneto-resistance measurements in different configurations. The analysis, supported by micromagnetic simulations, has been focused on the effect of lattice geometry on the magneto-resistance behaviour of these systems. The detailed investigation through micromagnetic simulations of the magnetic domain configuration as a function of the applied field allows a complete understanding of the qualitative and quantitative difference of anisotropic magneto-resistance properties that have been measured in samples with different lattice geometries and in different measurement configurations.

  9. Chemical Reaction between Boric Acid and Phosphine Indicates Boric Acid as an Antidote for Aluminium Phosphide Poisoning

    Science.gov (United States)

    Soltani, Motahareh; Shetab-Boushehri, Seyed F.; Shetab-Boushehri, Seyed V.

    2016-01-01

    Objectives: Aluminium phosphide (AlP) is a fumigant pesticide which protects stored grains from insects and rodents. When it comes into contact with moisture, AlP releases phosphine (PH3), a highly toxic gas. No efficient antidote has been found for AlP poisoning so far and most people who are poisoned do not survive. Boric acid is a Lewis acid with an empty p orbital which accepts electrons. This study aimed to investigate the neutralisation of PH3 gas with boric acid. Methods: This study was carried out at the Baharlou Hospital, Tehran University of Medical Sciences, Tehran, Iran, between December 2013 and February 2014. The volume of released gas, rate of gas evolution and changes in pH were measured during reactions of AlP tablets with water, acidified water, saturated boric acid solution, acidified saturated boric acid solution, activated charcoal and acidified activated charcoal. Infrared spectroscopy was used to study the resulting probable adduct between PH3 and boric acid. Results: Activated charcoal significantly reduced the volume of released gas (P <0.01). Although boric acid did not significantly reduce the volume of released gas, it significantly reduced the rate of gas evolution (P <0.01). A gaseous adduct was formed in the reaction between pure AlP and boric acid. Conclusion: These findings indicate that boric acid may be an efficient and non-toxic antidote for PH3 poisoning. PMID:27606109

  10. Development of an in vitro model using calcium imaging to investigate antidotal efficacy against saxitoxin. Report September 1994-September 1996

    Energy Technology Data Exchange (ETDEWEB)

    Doebler, J.A.; Dant, B.C.; Chang, F.C.T.

    1997-05-01

    Studies were conducted to investigate the utility of a novel in vitro system to monitor the efficacy of potential antidotes against sodium channel neurotoxins. Intracellular free calcium levels were measured in PC-12 (rat adrenal pheochromocytoma) cells utilizing a calcium imaging system with Fura-2 as the ratiometric calcium-sensitive indicator. Elevations in Ca(++) induced by high extracellular potassium (K(+)) and 4-aminopyridine (4-AP) were demonstrated, thus confirming the responsiveness of the system. Saxitoxin (STX), however, did not produce any alteration in Ca(++), perhaps due to a relatively low level of neuronal activity, i.e., impulse generation, in the in vitro state. Therefore, we attempted to activate PC-12 cells using the sodium channel agonist veratridine (VER) to determine whether STX could reduce enhanced Ca(++) levels. Although VER generally increased Ca(++), this response was somewhat variable and thus could not be used to demonstrate STX-induced toxic effects. Such variability may be inherent to cell lines; thus, the use of primary cultures is recommended to develop an in vitro system using Ca(++) levels as an endpoint to evaluate the efficacy of antidotes against sodium channel toxins.

  11. The influence of the time of antidotal treatment administration on its effectiveness against tabun-induced poisoning in mice.

    Science.gov (United States)

    Kassa, Jirí

    2004-01-01

    1. The influence of the time of administration of antidotal treatment consisting of anticholinergic drug (atropine) and oxime (pralidoxime, obidoxime, HI-6 or trimedoxime) on its effectiveness to eliminate tabun-induced lethal effects was studied in mice. 2. The therapeutic efficacy of antidotal treatment of tabun-induced acute poisoning depends on the time of its administration when obidoxime or the oxime HI-6 was used as an acetylcholinesterase reactivator. 3. Pralidoxime is practically ineffective to eliminate acute toxic effects of tabun regardless of the time of its administration. 4. Our results show that trimedoxime seems to be the most effective to eliminate lethal effects of tabun. In addition, its efficacy does not decrease when it is administered 5 min after tabun poisoning. 5. The findings support the hypothesis that trimedoxime appears to be the most suitable oxime to counteract acute toxicity of tabun because of its ability to eliminate lethal effects of tabun when it is injected 5 min after tabun challenge on the contrary to other oximes tested.

  12. The influence of antidotal treatment of low-level tabun exposure on cognitive functions in rats using a water maze.

    Science.gov (United States)

    Kassa, J; Kunesova, G

    2006-01-01

    In this study, the influence of antidotal treatment of tabun poisoning on cognitive function, in the case of low-level tabun exposure, was studied. The impairment of cognitive function was evaluated by the measurement of spatial learning and memory in rats poisoned with a sublethal dose of tabun and treated with atropine alone or in combination with newly developed oximes {K027 [1-(4-hydroxyiminomethyl- pyridinium)-3-(4-carbamoylpyridinium) propane dibromide] and K048 [1-(4-hydroxyimino- methylpyridinium)-3-(4-carbamoylpyridinium) butane dibromide]} or currently available oxime (trimedoxime), using the Morris water maze. While atropine alone caused an impairment of studied cognitive functions, the addition of an oxime to atropine contributes to the improvement of cognitive performance of treated tabun-poisoned rats regardless of the type of oxime. The differences in the ameliorative effects of oximes on atropine-induced mnemonic deficits were not significant. Therefore, each low-level nerve agent exposure should be treated by complex antidotal treatment consisting of anticholinergic drug and oxime.

  13. In vitro and in vivo comparison of sulfur donors as antidotes to acute cyanide intoxication.

    Science.gov (United States)

    Baskin, S I; Porter, D W; Rockwood, G A; Romano, J A; Patel, H C; Kiser, R C; Cook, C M; Ternay, A L

    1999-01-01

    Antidotes for cyanide (CN) intoxication include the use of sulfane sulfur donors (SSDs), such as thiosulfate, which increase the conversion of CN to thiocyanate by the enzyme rhodanese. To develop pretreatments that might be useful against CN, SSDs with greater lipophilicity than thiosulfate were synthesized and assessed. The ability of SSDs to protect mice against 2LD50 of sodium cyanide (NaCN) administered either 15 or 60 min following administration of an SSD was assessed. To study the mechanism of action of the SSD, the candidate compounds were examined in vitro for their effect on rhodanese and 3-mercaptopyruvate sulfurtransferase (MST) activity under increasing SSD concentrations. Tests were conducted on nine candidate SSDs: ICD1021 (3-hydroxypyridin-2-yl N-[(N-methyl-3-aminopropyl)]-2-aminoethyl disulfide dihydrochloride), ICD1022, (3-hydroxypyridin-2-yl N-[(N-methyl-3-aminopropyl)]-2-aminoethyl disulfide trihydrochloride), ICD1584 (diethyl tetrasulfide), ICD1585 (diallyl tetrasulfide), ICD1587 (diisopropyl tetrasulfide); ICD1738 (N-(3-aminopropyl)-2-aminoethyl 2-oxopropyl disulfide dihydrochloride), ICD1816 (3,3'-tetrathiobis-N-acctyl-L-alanine), ICD2214 (2-aminoethyl 4-methoxyphenyl disulfide hydrochloride) and ICD2467 (bis(4-methoxyphenyl) disulfide). These tests demonstrated that altering the chemical substituent of the longer chain sulfide modified the ability of the candidate SSD to protect against CN toxicity. At least two of the SSDs at selected doses provided 100% protection against 2LD50 of NaCN, normally an LD99. All compounds were evaluated using locomotor activity as a measure of potential adverse behavioral effects. Positive hypoactivity relationships were found with several disulfides but none was found with ICD1584, a tetrasulfide. Separate studies suggest that the chemical reaction of potassium cyanide (KCN) and cystine forms the toxic metabolite 2-iminothiazolidine-4-carboxylic acid. An alternative detoxification pathway, one not primarily

  14. Observation of a hole-size-dependent energy shift of the surface-plasmon resonance in Ni antidot thin films

    Energy Technology Data Exchange (ETDEWEB)

    Fang, H.; Akinoglu, E. M.; Fumagalli, P., E-mail: paul.fumagalli@fu-berlin.de [Institut für Experimentalphysik, Freie Universität Berlin, 14195 Berlin (Germany); Caballero, B.; García-Martín, A. [IMM-Instituto de Microelectrónica de Madrid (CNM-CSIC), Isaac Newton 8, PTM, Tres Cantos, E-28760 Madrid (Spain); Papaioannou, E. Th. [Fachbereich Physik and Landesforschungszentrum OPTIMAS, Technische Universität Kaiserslautern, 67663 Kaiserslautern (Germany); Cuevas, J. C. [Departamento de Física Teórica de la Materia Condensada and Condensed Matter Physics Center (IFIMAC), Universidad Autónoma de Madrid, E-28049 Madrid (Spain); Giersig, M. [Institut für Experimentalphysik, Freie Universität Berlin, 14195 Berlin (Germany); Helmholtz Zentrum Berlin, Institute of Nanoarchitectures for Energy Conversion, 14195 Berlin (Germany)

    2015-04-13

    A combined experimental and theoretical study of the magneto-optic properties of a series of nickel antidot thin films is presented. The hole diameter varies from 869 down to 636 nm, while the lattice periodicity is fixed at 920 nm. This results in an overall increase of the polar Kerr rotation with decreasing hole diameter due to the increasing surface coverage with nickel. In addition, at photon energies of 2.7 and 3.3 eV, where surface-plasmon excitations are expected, we observe distinct features in the polar Kerr rotation not present in continuous nickel films. The spectral position of the peaks exhibits a red shift with decreasing hole size. This is explained within the context of an effective medium theory by a change in the effective dielectric function of the Ni thin films.

  15. Melatonin as a possible antidote to UV radiation induced cutaneous damages and immune-suppression: An overview.

    Science.gov (United States)

    Goswami, Soumik; Haldar, Chandana

    2015-12-01

    The sun rays brings along the ultraviolet radiations (UVRs) which prove deleterious for living organisms. The UVR is a known mutagen and is the prime cause of skin carcinomas. UVR causes acute oxidative stress and this in turn deteriorates other physiological functions. Inflammatory conditions and elevation of pro-inflammatory molecules are also associated with UVR mediated cellular damages. The inflammatory conditions can secondarily trigger the generation of free radicals and this act cumulatively in further deterioration of tissue homeostasis. Photoimmunologists have also related UVR to the suppression of not only cutaneous but also systemic immunity by different mechanisms. Some researchers have proposed the use of various plant products as antioxidants against UVR induced oxidative imbalances but Melatonin is gaining rapid interest as a product that can be utilized to delineate the pathological effects of UVR since it is an established antioxidant. Besides the antioxidative nature, the capacity of melatonin to attenuate apoptosis and more importantly the efficacy of its metabolites to further aid in the detoxification of free radicals have made it a key player to be utilized against UVR mediated aggravated conditions. However, there is need for further extensive investigation to speculate melatonin as an antidote to UVR. Although too early to prescribe melatonin as a clinical remedy, the hormone can be integrated into dermal formulations or oral supplements to prevent the ever increasing incidences of skin cancers due to the prevalence of the UVR on the surface of the earth. The present review focuses and substantiates the work by different photo-biologists demonstrating the protective effects of melatonin and its metabolites against solar UVR - Melatonin as a possible antidote to UV radiation induced cutaneous damages and immune-suppression: an overview. J Photochem Photobiol B.

  16. Introduction to the US Expert Guidelines for Stocking of Antidotes in Hospitals%《美国提供急诊服务医院解毒剂存储专家建议》介绍

    Institute of Scientific and Technical Information of China (English)

    孙树森; 司延斌; 赵志刚

    2014-01-01

    Antidotes are a critical component in the care of poisoned patients. Insufficient stocking of a diverse group of antidotes has been documented repeatedly in many countries, including the United States and Canada. Expert consensus guidelines for stocking of antidotes in hospitals that provide emergency care have been published in 2009 in the United States. This article briefly introduced expert consensus guideline and the concept of antidote hazard vulnerability assessment that could be utilized to guide hospitals in developing antidote stock list. The above description about the utility and management of the guideline for appropriate antidote stocking can provide reference for China.%解毒剂是治疗和挽救中毒患者的关键措施,但包括美国和加拿大等诸多国家的报道一再证明临床普遍存在解毒剂存储品种及数量不足的情况。2009年美国发布了提供急诊服务的医院解毒剂存储专家建议。本文简介了用于指导医院合理存储解毒剂的美国专家建议和“解毒剂灾害脆弱性评估”概念,以期对中国解毒剂使用管理提供借鉴。

  17. Intravenous Cobinamide, a Novel Cyanide Antidote, versus Hydroxocobalamin in the Treatment of Acute Cyanide Toxicity and Apnea in a Swine (Sus scrofa) Model

    Science.gov (United States)

    2013-02-12

    treatment of acute, severe cyanide induced cardiotoxicity of severe hypotension and of cardiac arrest in a swine (Sus Scrofa ) model Intravenous...cobinamide, a novel cyanide antidote, versus hydroxocobalamin in the treatment of acute cyanide toxicity and apnea in a swine (Sus Scrofa ) model...hydroxocobalamin in the treatment of acute cyanide toxicity and apnea in a swine (Sus Scrofa ) model Background: Hydroxocobalamin (HOC) is an FDA approved

  18. The I{sub c}(H)-T{sub c}(H) phase boundary of superconducting Nb thin films with periodic and quasiperiodic antidot arrays

    Energy Technology Data Exchange (ETDEWEB)

    Bothner, D.; Kemmler, M.; Cozma, R.; Kleiner, R.; Koelle, D. [Physikalisches Institut and Center for Collective Quantum Phenomena, Universitaet Tuebingen (Germany); Misko, V.; Peeters, F. [Departement Fysica, Universiteit Antwerpen (Belgium); Nori, F. [Advanced Science Institute, RIKEN (Japan)

    2011-07-01

    The magnetic field dependent critical current I{sub c}(H) of superconducting thin films with artificial defects strongly depends on the symmetry of the defect arrangement. Likewise the critical temperature T{sub c}(H) of superconducting wire networks is heavily influenced by the symmetry of the system. Here we present experimental data on the I{sub c}(H)-T{sub c}(H) phase boundary of Nb thin films with artificial defect lattices of different symmetries. For this purpose we fabricated 60 nm thick Nb films with antidots in periodic (triangular) and five different quasiperiodic arrangements. The parameters of the antidot arrays were varied to investigate the influence of antidot diameter and array density. Experiments were performed with high temperature stability ({delta}T<1 mK) at 0.5{<=}T/T{sub c}{<=}1. From the I-V-characteristics at variable H and T we extract I{sub c}(H) and T{sub c}(H) for different voltage and resistance criteria. The experimental data for the critical current density are compared with results from numerical molecular dynamics simulations.

  19. The utility of chelating agents as antidotes for nephrotoxicity of gold sodium thiomalate in adjuvant-arthritic rats.

    Science.gov (United States)

    Takahashi, Y; Funakoshi, T; Shimada, H; Kojima, S

    1995-03-31

    The effects of 2,3-dimercaptopropane sulphonate (DMPS) and N-(2-mercapto-2-methylpropanoyl)-L-cysteine (bucillamine) against the renal damage induced by gold sodium thiomalate (AuTM) in adjuvant-arthritic rats were studied. Arthritic rats induced by adjuvant using Mycobacterium butyricum were injected intraperitoneally with a chelating agent (0.6 mmol/kg) immediately after intramuscular injection of AuTM (0.066 mmol/kg) every other day for 21 days. Treatment with DMPS and bucillamine prevented increases in the urinary excretion of protein, aspartate aminotransferase, and glucose and blood urea nitrogen level after AuTM injection. AuTM prevented the increase in both adjuvant-injected and uninjected hind-feet volumes. The prevention of these inflamed lesions by AuTM was not affected by DMPS and bucillamine. These chelating agents decreased the gold concentration in the kidney and liver after AuTM administration, but did not affect the hepatic and renal concentrations of copper, zinc, iron, and calcium except the renal copper level after AuTM. These findings suggest that DMPS and bucillamine are very useful antidotes for gold toxicity.

  20. dc and ac magnetic properties of thin-walled Nb cylinders with and without a row of antidots.

    Science.gov (United States)

    Tsindlekht, M I; Genkin, V M; Felner, I; Zeides, F; Katz, N; Gazi, Š; Chromik, Š; Dobrovolskiy, O V; Sachser, R; Huth, M

    2016-06-01

    dc and ac magnetic properties of two thin-walled superconducting Nb cylinders with a rectangular cross-section are reported. Magnetization curves and the ac response were studied on as-prepared and patterned samples in magnetic fields parallel to the cylinder axis. A row of micron-sized antidots (holes) was made in the film along the cylinder axis. Avalanche-like jumps of the magnetization are observed for both samples at low temperatures for magnetic fields not only above H c1, but in fields lower than H c1 in the vortex-free region. The positions of the jumps are not reproducible and they change from one experiment to another, resembling vortex lattice instabilities usually observed for magnetic fields larger than H c1. At temperatures above [Formula: see text] and [Formula: see text] the magnetization curves become smooth for the patterned and the as-prepared samples, respectively. The magnetization curve of a reference planar Nb film in the parallel field geometry does not exhibit jumps in the entire range of accessible temperatures. The ac response was measured in constant and swept dc magnetic field modes. Experiment shows that ac losses at low magnetic fields in a swept field mode are smaller for the patterned sample. For both samples the shapes of the field dependences of losses and the amplitude of the third harmonic are the same in constant and swept field near H c3. This similarity does not exist at low fields in a swept mode.

  1. Influence of commonly used clinical antidotes on antioxidant systems in human hepatocyte culture intoxicated with alpha-amanitin.

    Science.gov (United States)

    Magdalan, Jan; Piotrowska, Aleksandra; Gomułkiewicz, Agnieszka; Sozański, Tomasz; Szeląg, Adam; Dziegięl, Piotr

    2011-01-01

    α-Amanitin (α-AMA) is the main toxin of Amanita phalloides and its subspecies (A. virosa and A. verna). The primary mechanism of α-AMA toxicity is associated with protein synthesis blocking in hepatocytes. Additionally, α-AMA exhibits prooxidant properties that may contribute to its severe hepatotoxicity. The aim of the present study was to assess the effect of α-AMA on lipid peroxidation and the activities of superoxide dismutase (SOD) and catalase (CAT) in human hepatocyte culture. The effects of benzylpenicillin (BPCN), N-acetyl-L-cysteine (ACC), and silibinin (SIL) on SOD and CAT activities and on lipid peroxidation in human hepatocyte culture intoxicated with α-AMA were also examined. In human hepatocyte culture, 48-hour exposure to α-AMA at a 2-μM concentration caused an increase in SOD activity, a reduction of CAT activity, and a significant increase in lipid peroxidation. Changes in SOD and CAT activity caused by α-AMA could probably enhance lipid peroxidation by increased generation of hydrogen peroxide combined with reduced detoxification of that oxygen radical. The addition of antidotes (ACC or SIL) to the culture medium provided more effective protection against lipid peroxidation in human hepatocytes intoxicated with α-AMA than the addition of BPCN, possessing no antioxidant properties.

  2. Targeting Two Coagulation Cascade Proteases with a Bivalent Aptamer Yields a Potent and Antidote-Controllable Anticoagulant.

    Science.gov (United States)

    Soule, Erin E; Bompiani, Kristin M; Woodruff, Rebecca S; Sullenger, Bruce A

    2016-02-01

    Potent and rapid-onset anticoagulation is required for several clinical settings, including cardiopulmonary bypass surgery. In addition, because anticoagulation is associated with increased bleeding following surgery, the ability to rapidly reverse such robust anticoagulation is also important. Previously, we observed that no single aptamer was as potent as heparin for anticoagulating blood. However, we discovered that combinations of two aptamers were as potent as heparin. Herein, we sought to combine two individual anticoagulant aptamers into a single bivalent RNA molecule in an effort to generate a single molecule that retained the potent anticoagulant activity of the combination of individual aptamers. We created four bivalent aptamers that can inhibit Factor X/Xa and prothrombin/thrombin and anticoagulate plasma, as well as the combination of individual aptamers. Detailed characterization of the shortest bivalent aptamer indicates that each aptamer retains full binding and functional activity when presented in the bivalent context. Finally, reversal of this bivalent aptamer with a single antidote was explored, and anticoagulant activity could be rapidly turned off in a dose-dependent manner. These studies demonstrate that bivalent anticoagulant aptamers represent a novel and potent approach to actively and reversibly control coagulation.

  3. Relationship-centred care: antidote, guidepost or blind alley? The epistemology of 21st century health care.

    Science.gov (United States)

    Wyer, Peter C; Alves Silva, Suzana; Post, Stephen G; Quinlan, Patricia

    2014-12-01

    Contemporary health care is increasing in complexity and lacks a unifying understanding of epistemology, methodology and goals. Lack of conceptual consistency in concepts such as 'patient-centred care' (PCC) typifies system-wide discordance. We contrast the fragmented descriptions of PCC and related tools to its own origins in the writings of Balint and to a subsequent construct, relationship-centred care (RCC). We identify the explicit and elaborated connection between RCC and a defined epistemological foundation as a distinguishing feature of the construct and we demonstrate that this makes possible the recognition of alignments between RCC and independently developed constructs. Among these, we emphasize Schon's reflective practice, Nonaka's theory of organizational knowledge creation and the research methodology of realist synthesis. We highlight the relational principles common to these domains and to their common epistemologies and illustrate unsatisfying consequences of adherence to less adequate epistemological frameworks such as positivism. We offer RCC not as an 'antidote' to the dilemmas identified at the outset but as an example that illuminates the value and importance of explicit identification of the premises and assumptions underlying approaches to improvement of the health care system. We stress the potential value of identifying epistemological affinities across otherwise disparate fields and disciplines.

  4. "Too good to be true": the controversy over the use of permanganate of potash as an antidote to snake poison and the circulation of Brazilian physiology in the nineteenth century.

    Science.gov (United States)

    Vimieiro Gomes, Ana Carolina

    2012-01-01

    This article examines an international controversy over the most visible scientific event of Brazilian physiology in the nineteenth century. In 1881, Brazilian scientist João Baptista Lacerda stated that he had found an efficient antidote to the poison of Brazilian snakes: permanganate of potash (nowadays, potassium permanganate). His findings were given great publicity in Brazil and traveled rapidly around the world. Scientists, especially in France, contradicted Lacerda's claims. They argued that permanganate of potash could not be a genuine antidote to snake bites since it could not neutralize snake venom when diffused in the body. Lacerda turned down such criticism, claiming that clinical observation provided solid evidence for the drug's local action, on the spot surrounding the bite. The controversy over the use of permanganate of potash as an antidote to snake bite illustrates different regimes of proof that could be mobilized in favor of a physiological discovery.

  5. Arrays of nanostructured antidot in Ni{sub 80}Fe{sub 20} magnetic thin films by photolithography of polystyrene nanospheres

    Energy Technology Data Exchange (ETDEWEB)

    Tiberto, Paola, E-mail: tiberto@inrim.it [INRIM, Electromagnetism Dept., Torino (Italy); Boarino, Luca; Celegato, Federica; Barrera, Gabriele; De Leo, Natascia; Coisson, Marco; Vinai, Franco [INRIM, Electromagnetism Dept., Torino (Italy); Allia, Paolo [INRIM, Electromagnetism Dept., Torino (Italy); DISMIC, Politecnico di Torino (Italy)

    2012-10-15

    Highlights: Black-Right-Pointing-Pointer Arrays of antidot in Ni{sub 80}Fe{sub 20} thin films by photolithography of polystyrene nanospheres. Black-Right-Pointing-Pointer Well-ordered Antidot arrays on a large scale. Black-Right-Pointing-Pointer Novel method exploiting optical lithography with enhanced spatial resolution. Black-Right-Pointing-Pointer We report on the presence of an anisotropic magnetoresistance signal. - Abstract: Ordered nanostructures consisting in arrays of nanopores and nanoholes in magnetic thin films have been the subject of intensive research. In this work, a novel multi-step lithography process based on self-assembling of polystyrene nanospheres is proposed to pattern arrays of nanoholes on a Ni{sub 80}Fe{sub 20} thin film. Such a method allows antidot patterns to be fabricated on a wider area with respect to the standard sequential lithography. A polymeric mask is created by depositing a layer of polystyrene nanospheres on a photoresist subsequently exposed to a mercury lamp. The novelty in the procedure lies in exploiting low-cost and fast, non-sequential optical lithography with enhanced spatial resolution. Arrays of holes having mean size ranging in the interval of 250-280 nm depending on the experimental conditions have been prepared in Ni{sub 80}Fe{sub 20} films of different thickness (between 20 and 60 nm). Sample morphology has been checked by scanning electron microscopy. Magnetic and magnetotransport properties have been measured as a function of temperature on films of different thickness. An anisotropic magnetoresistance effect has been observed in all patterned films independent on the film thickness. This result, similar to the ones reported for patterned nanostructure obtained with conventional lithography techniques, confirms the potential of the proposed technique.

  6. New in silico insights into the inhibition of RNAP II by α-amanitin and the protective effect mediated by effective antidotes.

    Science.gov (United States)

    Garcia, Juliana; Carvalho, Alexandra T P; Dourado, Daniel F A R; Baptista, Paula; de Lourdes Bastos, Maria; Carvalho, Félix

    2014-06-01

    Poisonous α-amanitin-containing mushrooms are responsible for the major cases of fatalities after mushroom ingestion. α-Amanitin is known to inhibit the RNA polymerase II (RNAP II), although the underlying mechanisms are not fully understood. Benzylpenicillin, ceftazidime and silybin have been the most frequently used drugs in the management of α-amanitin poisoning, mostly based on empirical rationale. The present study provides an in silico insight into the inhibition of RNAP II by α-amanitin and also on the interaction of the antidotes on the active site of this enzyme. Docking and molecular dynamics (MD) simulations combined with molecular mechanics-generalized Born surface area method (MM-GBSA) were carried out to investigate the binding of α-amanitin and three antidotes benzylpenicillin, ceftazidime and silybin to RNAP II. Our results reveal that α-amanitin should affects RNAP II transcription by compromising trigger loop (TL) function. The observed direct interactions between α-amanitin and TL residues Leu1081, Asn1082, Thr1083, His1085 and Gly1088 alters the elongation process and thus contribute to the inhibition of RNAP II. We also present evidences that α-amanitin can interact directly with the bridge helix residues Gly819, Gly820 and Glu822, and indirectly with His816 and Phe815. This destabilizes the bridge helix, possibly causing RNAP II activity loss. We demonstrate that benzylpenicillin, ceftazidime and silybin are able to bind to the same site as α-amanitin, although not replicating the unique α-amanitin binding mode. They establish considerably less intermolecular interactions and the ones existing are essential confine to the bridge helix and adjacent residues. Therefore, the therapeutic effect of these antidotes does not seem to be directly related with binding to RNAP II. RNAP II α-amanitin binding site can be divided into specific zones with different properties providing a reliable platform for the structure-based drug design of

  7. 口服抗凝药解毒剂的研究进展%Research progress on antidotes for oral anticoagulants

    Institute of Scientific and Technical Information of China (English)

    孙双勇; 郝春华; 张蕊; 石冰卓; 赵专友; 王维亭

    2016-01-01

    In recent years, new oral anticoagulants (NOACs) had made great development, and they gradually replaced the traditional anticoagulants to become the first-line drug of choice for clinic. Compared with conventional anticoagulants, their bleeding side effects were close to or less, but they still had a certain risk of bleeding. Traditional anticoagulant antidotes had poor detoxifying effect of NOACs, which led to a great deal of inconvenience and risk for the use of these drugs. Specific antidotes for NOACs were under development, and preliminary tests had achieved good results. Most representative drugs of these antidotes included andexanet alfa of Portola Pharmaceuticals, idarucizumab of Boehringer Ingelheim, and aripazine of Perosphere. This article reviewed research progress and problems of these three NOACs antidotes.%近年来新型口服抗凝药(NOACs)取得很大的发展,逐渐取代传统抗凝药而成为临床一线的首选药物。尽管与传统抗凝药物相比,NOACs 的出血副作用相当或更小,但依然存在着一定的出血风险。传统抗凝药物的解毒剂对 NOACs 的解毒效果不佳,为该类药物的使用带来很大的风险和不便。针对NOACs的特殊解毒剂正在开发当中,前期试验已取得不错的结果。这些解毒剂最具有代表性的药物包括Portola制药公司的andexanet alfa、勃林格殷格翰公司的idarucizumab以及Perosphere公司的aripazine,主要针对这3种NOACs解毒剂的研究进展以及存在的问题进行综述。

  8. Lipid profile and atherogenic predictor indices of albino rabbits administered coconut water as antidote to paracetamol overdose

    Directory of Open Access Journals (Sweden)

    Chidi Uzoma Igwe

    2016-11-01

    Full Text Available Objective: To investigate the effects of coconut water intake on lipid profile and atherogenic predictor indices of albino rabbits overdosed with paracetamol using standard methods. Methods: Thirty-five albino rabbits weighing between 800–1200 g and aged between 2 and 3 months, were divided into 7 groups (I–VII of 5 animals each. Groups I, II and III were orally administered distilled water (20 mL/kg body weight, coconut water (20 mL/kg body weight and paracetamol (1000 mg/kg body weight respectively, for 7 days. Groups IV and V were administered coconut water (20 mL/kg body weight and silymarin (35 mg/kg body weight, respectively, for 6 days, then paracetamol (1000 mg/kg body weight on the 7th day. Groups VI and VII were administered distilled water for 6 days, paracetamol on the 7th day, then coconut water and silymarin, respectively, after 3 h. Results: The results showed that paracetamol overdose significantly reduced (P < 0.05 the mean body weight of the animals, increased the concentrations of serum total cholesterol, triacylglycerol, very low density lipoprotein cholesterol, low density lipoprotein cholesterol and the atherogenic predictor indices but reduced the serum high density lipoprotein cholesterol concentration of the animals relative to the control. The observed changes in the lipid profile and atherogenic predictor indices were countered more by post- than pre-treatment with coconut water and silymarin. Conclusions: The results indicated that coconut water acted as an effective antidote to paracetamol overdose-induced lipid abnormality in animals.

  9. IN-VITRO KINETICS, ADSORPTION ISOTHERM, AND EFFECT OF PH ON ANTIDOTAL EFFECT OF ACTIVATED CHARCOAL IN TRAMADOL HYDROCHLORIDE INTOXICATION

    Directory of Open Access Journals (Sweden)

    Pandeya S

    2016-02-01

    Full Text Available Tramadol overdose has been one of the most frequent causes of drug poisoning in the recent years, especially in young adult males. In the current work, the in-vitro study on adsorption kinetics and the effect of pH on antidotal effect of activated charcoal (AC in tramadol hydrochloride intoxication were carried out. For adsorption study tramadol hydrochloride solutions of various concentrations were prepared in both simulated gastric fluid (SGF and simulated intestinal fluid (SIF and analyzed by UV spectrophotometer. For kinetics study tramadol hydrochloride and charcoal in ratio 1:5 was kept in 6 different flasks and sonicated for 5, 10, 15, 20, 25 and 30 minutes and analyzed spectrophotometrically. The data were plotted among two most commonly used adsorption isotherm, Langmuir isotherm and Freundlich isotherm and their coefficient of determination (R2 was compared to get the best adsorption isotherm equation. The kinetics study was done in both SGF and SIF. The result showed that AC 50 gm can adsorb 4802.692 mg tramadol hydrochloride at gastric environment and 8064.516 mg tramadol hydrochloride at intestinal environment. The R2 value in the current study is found to be more in SIF (0.986 than in SGF (0.985. In accordance to the value of R2, the pseudo second order kinetics model fit best for this study with R2 value of 0.9997 in SGF and 0.9994 in SIF. From the current study it can be concluded that 50g AC has the capacity to adsorb sufficient amount of tramadol hydrochloride and the kinetics followed during the adsorption was pseudo-second order.

  10. Risk factors related to poor outcome after methanol poisoning and the relation between outcome and antidotes--a multicenter study.

    Science.gov (United States)

    Paasma, Raido; Hovda, Knut Erik; Hassanian-Moghaddam, Hossein; Brahmi, Nozha; Afshari, Reza; Sandvik, Leiv; Jacobsen, Dag

    2012-11-01

    INTRODUCTION. Thorough prognostic and metabolic studies of methanol poisonings are scarce. Our aims were to evaluate the factors associated with sequelae and death from methanol poisoning, to develop a simple risk-assessment chart to evaluate factors associated with sequelae and death from methanol poisoning, and to compare the antidotes ethanol and fomepizole. PATIENTS AND METHODS. We present a retrospective observational case series of methanol-poisoned patients from Norway (1979 and 2002-2005), Estonia (2001) and Tunisia (2003/2004), and patients from two different centers in Iran (Teheran 2004-2009 and Mashhad 2009-2010) who were identified by a positive serum methanol and had a blood acid-base status drawn on admission. The patients were divided into different groups according to their outcome: Survived, survived with sequelae, and died. RESULTS. A total of 320 patients were identified and 117 were excluded. Of the remaining 203 patients, 48 died, and 34 were discharged with neurological sequelae. A pH < 7.00 was found to be the strongest risk factor for poor outcome, along with coma (Glasgow Coma Scale (GCS) < 8) and a pCO(2) ≥ 3.1 kPa in spite of a pH < 7.00. More patients died despite hyperventilation (low pCO(2)) in the ethanol group. CONCLUSIONS. Low pH (pH < 7.00), coma (GCS < 8), and inadequate hyperventilation (pCO(2) ≥ 3.1 kPa in spite of a pH < 7.00) on admission were the strongest predictors of poor outcome after methanol poisoning. A simple flow-chart may help identify the patients associated with a poor outcome.

  11. The role of multifunctional drug therapy as an antidote to combat experimental subacute neurotoxicity induced by organophosphate pesticides.

    Science.gov (United States)

    Singh, Satinderpal; Prakash, Atish; Kaur, Shamsherjit; Ming, Long Chiau; Mani, Vasudevan; Majeed, Abu Bakar Abdul

    2016-08-01

    Organophosphate pesticides are used in agriculture where they are associated with numerous cases of intentional and accidental misuse. These toxicants are potent inhibitors of cholinesterases leading to a massive build-up of acetylcholine which induces an array of deleterious effects, including convulsions, oxidative damage and neurobehavioral deficits. Antidotal therapies with atropine and oxime yield a remarkable survival rate, but fail to prevent neuronal damage and behavioral problems. It has been indicated that multifunction drug therapy with potassium channel openers, calcium channel antagonists and antioxidants (either single-agent therapy or combination therapy) may have the potential to prevent cell death and/or slow down the processes of secondary neuronal damage. The aim of the present study, therefore, was to make a relative assessment of the potential effects of nicorandil (2 mg/kg), clinidipine (10 mg/kg), and grape seed proanthocyanidin (GSPE) extract (200 mg/kg) individually against subacute chlorpyrifos induced toxicity. The test drugs were administered to Wistar rats 2 h after exposure to Chlorpyrifos (CPF). Different behavioral studies and biochemical estimation has been carried in the study. The results showed that chronic administration of CPF significantly impaired learning and memory, along with motor coordination, and produced a marked increase in oxidative stress along with significantly reduced acetylcholine esterase (AChE) activity. Treatment with nicorandil, clinidipine and GSPE was shown to significantly improve memory performance, attenuate oxidative damage and enhance AChE activity in rats. The present study also suggests that a combination of nicorandil, clinidipine, and GSPE has a better neuroprotective effect against subacute CPF induced neurotoxicity than if applied individually. © 2015 Wiley Periodicals, Inc. Environ Toxicol 31: 1017-1026, 2016.

  12. Antidotal effect of combinations obidoxime/HI-6 and memantine in mice poisoned with soman, dichlorvos or heptenophos

    Directory of Open Access Journals (Sweden)

    Antonijević Biljana

    2011-01-01

    Full Text Available Introduction/Aim. In acute organophosphate poisoning the issue of special concern is the appearance of muscle fasciculations and convulsions that cannot be adequately antagonised by the use of atropine and oxime therapy. The aim of this study was to examine atidotal effect of obidoxime or HI-6 combinations with memantine in mice poisoned with soman, dichlorvos or heptenophos. Methods. Male Albino mice were pretreated intravenously (iv with increasing doses of oximes and/or memantine (10 mg/kg at various times before poisoning with 1.3 LD-50 of soman, dichlorvos or heptenophos, in order to determine the median effective dose and the efficacy half-time. In a separate experiment, cerebral extravasation of Evans blue dye (40 mg/kg iv was examined after application of memantine (10 mg/kg iv, midazolam (2.5 mg/kg intraperitonealy - ip and ketamine (20 mg/kg ip 5 minutes before soman (1 LD-50 subcutaneously - sc. Results. Coadministration of memantine induced a significant decrease in median effective dose in null time of both HI-6 (7.96 vs 1.79 mmoL/kg in soman poisoning and obidoxime (16.80 vs 2.75 mmoL/kg in dichlorvos poisoning; 21.56 vs 6.63 mmoL/kg in heptenophos poisoning. Memantine and midazolam succeded to counteract the soman-induced proconvulsive activity. Conclusion. Memantine potentiated the antidotal effect of HI-6 against a lethal dose of soman, as well as the ability of obidoxime to antagonize the toxic effects of dichlorvos and heptenophos probably partly due to its anticonvulsive properties.

  13. Lipid proifle and atherogenic predictor indices of albino rabbits administered coconut water as antidote to paracetamol overdose

    Institute of Scientific and Technical Information of China (English)

    Chidi Uzoma Igwe; Callistus Izunna Iheme; Chinwe Slyvanus Alisi; Linus Ahuwaraeze Nwaogu; Chiedozie Onyejiaka Ibegbulem; Aloysius Chinedu Ene

    2016-01-01

    ABSTRACT Objective:To investigate the effects of coconut water intake on lipid profile and atherogenic predictor indices of albino rabbits overdosed with paracetamol using standard methods. Methods:Thirty-five albino rabbits weighing between 800–1 200 g and aged between 2 and 3 months, were divided into 7 groups (I–VII) of 5 animals each. Groups I, II andIII were orally administered distilled water (20 mL/kg body weight), coconut water (20 mL/kg body weight) and paracetamol (1 000 mg/kg body weight) respectively, for 7 days. Groups IV and V were administered coconut water (20 mL/kg body weight) and silymarin (35 mg/kg body weight), respectively, for 6 days, then paracetamol (1 000 mg/kg body weight) on the 7th day. GroupsVI andVII were administered distilled water for 6 days, paracetamol on the 7th day, then coconut water and silymarin, respectively, after 3 h. Results: The results showed that paracetamol overdose significantly reduced (P < 0.05) the mean body weight of the animals, increased the concentrations of serum total cholesterol, triacylglycerol, very low density lipoprotein cholesterol, low density lipoprotein cholesterol and the atherogenic predictor indices but reduced the serum high density lipoprotein cholesterol concentration of the animals relative to the control. The observed changes in the lipid profile and atherogenic predictor indices were countered more by post- than pre-treatment with coconut water and silymarin. Conclusions: The results indicated that coconut water acted as an effective antidote to paracetamol overdose-induced lipid abnormality in animals.

  14. The Antidotal Effects of High-dosage γ-Aminobutyric Acid on Acute Tetramine Poisoning as Compared with Sodium Dimercaptopropane Sulfonate

    Institute of Scientific and Technical Information of China (English)

    SUN Peng; HAN Jiyuan; WENG Yuying

    2007-01-01

    To investigate the therapeutic effect of high-dosage γ-aminobutyric acid (GABA) on acute tetramine (TET) poisoning, 50 Kunming mice were divided into 5 groups at random and the antidotal effects of GABA or sodium dimercaptopropane sulfonate (Na-DMPS) on poisoned mice in different groups were observed in order to compare the therapeutic effects of high-dosage GABA with those of Na-DMPS. Slices of brain tissue of the poisoned mice were made to examine pathological changes of cells. The survival analysis was employed. Our results showed that both high-dosage GABA and Na-DMPS could obviously prolong the survival time, delay onset of convulsion and muscular twitch, and ameliorate the symptoms after acute tetramine poisoning in the mice.Better effects could be achieved with earlier use of high dosage GABA or Na-DMPS. There was no significant difference in prolonging the survival time between high-dose GABA and Na-DMPS used immediately after poisioning. It is concluded that high-dosage GABA can effectively antagonize acute toxicity of teramine in mice. And it is suggested that high-dosage GABA may be used as an excellent antidote for acute TET poisoning in clinical practice. The indications and correct dosage for clinical use awaits to be further studied.

  15. Widening the path and window of opportunity for FDA approval of non-vitamin K oral anticoagulant specific antidotes and reversal agents.

    Science.gov (United States)

    Patel, Sunny; Steen, Dylan

    2016-02-01

    There remains a need for safe, immediately effective, and easy to administer antidotes for patients taking novel oral anticoagulants (NOACs) in the settings of major bleeding, need for emergency surgery, and accidental overdose. We review considerations for the successful safety and effectiveness evaluation of potential antidotes currently under development. These compounds are in expedited regulatory approval programs aimed at accelerating the preclinical and clinical evaluation and approval processes for treatments of serious conditions. We review the features of these expedited programs as well as the FDA's efforts to broadly advance the efficiency of drug development and increase the number of new compounds brought to market. The critical path initiative and regulatory science initiative have resulted in numerous successful programs to address current challenges such as a paucity of validated biomarkers and surrogate endpoints as well as unreliable animal models of toxicity. The FDA has also advocated for increased use of pharmacokinetic/pharmacodynamic modeling and adaptive trial design. These efforts foster collaboration between academia, industry and the public sector across interdisciplinary sciences and may continue to widen the pathway for NOAC-specific reversal agents and other novel compounds.

  16. Sulfidation as a natural antidote to metallic nanoparticles is overestimated: CuO sulfidation yields CuS nanoparticles with increased toxicity in medaka (Oryzias latipes) embryos.

    Science.gov (United States)

    Li, Lingxiangyu; Hu, Ligang; Zhou, Qunfang; Huang, Chunhua; Wang, Yawei; Sun, Cheng; Jiang, Guibin

    2015-02-17

    Sulfidation is considered as a natural antidote to toxicity of metallic nanoparticles (NPs). The detoxification contribution from sulfidation, however, may vary depending on sulfidation mechanisms. Here we present the dissolution-precipitation instead of direct solid-state-shell mechanism to illustrate the process of CuO-NPs conversion to CuS-NPs in aqueous solutions. Accordingly, the CuS-NPs at environmentally relevant concentrations showed much stronger interference on Japanese medaka (Oryzias latipes) embryo hatching than CuO-NPs, which was probably due to elevated free copper ions released from CuS-NPs, leading to significant increase in oxidative stress and causing toxicity in embryos. The larval length was significantly reduced by CuS-NPs, however, no other obviously abnormal morphological features were identified in the hatched larvae. Co-introduction of a metal ion chelator [ethylene diamine tetraacetic acid (EDTA)] could abolish the hatching inhibition induced by CuS-NPs, indicating free copper ions released from CuS-NPs play an important role in hatching interference. This work documents for the first time that sulfidation as a natural antidote to metallic NPs is being overestimated, which has far reaching implications for risk assessment of metallic NPs in aquatic environment.

  17. Proposing Boric Acid as an Antidote for Aluminium Phosphide Poisoning by Investigation of the Chemical Reaction Between Boric Acid and Phosphine

    Directory of Open Access Journals (Sweden)

    Motahareh Soltani

    2013-01-01

    Full Text Available Aluminium phosphide (AlP is a storage fumigant pesticide, which is used to protect stored grains especially from insects and rodents. It releases phosphine (PH3 gas, a highly toxic mitochondrial poison, in contact with moisture, particularly if acidic. Although the exact mechanism of action is unknown so far, the major mechanism of PH3 toxicity seems to be the inhibition of cytochrome-c oxidase and oxidative phosphorylation which eventually results in adenosine triphosphate (ATP depletion and cell death. Death due to AlP poisoning seems to be as a result of myocardial damage. No efficient antidote has been found for AlP poisoning so far, and unfortunately, most of the poisoned human cases die. PH3, like ammonia (NH3, is a Lewis base with a lone-pair electron. However, boric acid (B(OH3 is a Lewis acid with an empty p orbital. It is predicted that lone-pair electron from PH3 is shared with the empty p orbital from B(OH3 and a compound forms in which boron attains its octet. In other words, PH3 is trapped and neutralised by B(OH3. The resulting polar reaction product seems to be excretable by the body due to hydrogen bonding with water molecules. The present article proposes boric acid as a non-toxic and efficient trapping agent and an antidote for PH3 poisoning by investigating the chemical reaction between them.

  18. The ratio between CcdA and CcdB modulates the transcriptional repression of the ccd poison-antidote system.

    Science.gov (United States)

    Afif, H; Allali, N; Couturier, M; Van Melderen, L

    2001-07-01

    The ccd operon of the F plasmid encodes CcdB, a toxin targeting the essential gyrase of Escherichia coli, and CcdA, the unstable antidote that interacts with CcdB to neutralize its toxicity. Although work from our group and others has established that CcdA and CcdB are required for transcriptional repression of the operon, the underlying mechanism remains unclear. The results presented here indicate that, although CcdA is the DNA-binding element of the CcdA-CcdB complex, the stoichiometry of the two proteins determines whether or not the complex binds to the ccd operator-promoter region. Using electrophoretic mobility shift assays, we show that a (CcdA)2-(CcdB)2 complex binds DNA. The addition of extra CcdB to that protein-DNA complex completely abolishes DNA retardation. Based on these results, we propose a model in which the ratio between CcdA and CcdB regulates the repression state of the ccd operon. When the level of CcdA is superior or equal to that of CcdB, repression results. In contrast, derepression occurs when CcdB is in excess of CcdA. By ensuring an antidote-toxin ratio greater than one, this mechanism could prevent the harmful effect of CcdB in plasmid-containing bacteria.

  19. Tunable spin wave spectra in two-dimensional Ni{sub 80}Fe{sub 20} antidot lattices with varying lattice symmetry

    Energy Technology Data Exchange (ETDEWEB)

    Mandal, R.; Barman, S.; Saha, S.; Barman, A., E-mail: abarman@bose.res.in [Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700 098 (India); Otani, Y. [CEMS-RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198 (Japan); Institute for Solid State Physics, University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa, Chiba 277-8581 (Japan)

    2015-08-07

    Ferromagnetic antidot lattices are important systems for magnetic data storage and magnonic devices, and understanding their magnetization dynamics by varying their structural parameters is an important problems in magnetism. Here, we investigate the variation in spin wave spectrum in two-dimensional nanoscale Ni{sub 80}Fe{sub 20} antidot lattices with lattice symmetry. By varying the bias magnetic field values in a broadband ferromagnetic resonance spectrometer, we observed a stark variation in the spin wave spectrum with the variation of lattice symmetry. The simulated mode profiles showed further difference in the spatial nature of the modes between different lattices. While for square and rectangular lattices extended modes are observed in addition to standing spin wave modes, all modes in the hexagonal, honeycomb, and octagonal lattices are either localized or standing waves. In addition, the honeycomb and octagonal lattices showed two different types of modes confined within the honeycomb (octagonal) units and between two such consecutive units. Simulated internal magnetic fields confirm the origin of such a wide variation in the frequency and spatial nature of the spin wave modes. The tunability of spin waves with the variation of lattice symmetry is important for the design of future magnetic data storage and magnonic devices.

  20. Low molecular weight protamine (LMWP) as nontoxic heparin/low molecular weight heparin antidote (I): preparation and characterization.

    Science.gov (United States)

    Chang, L C; Lee, H F; Yang, Z; Yang, V C

    2001-01-01

    LMWP analogue-CRRRRRRR-and it was found that its heparin-neutralizing ability was increased by changing from a monomeric to a dimeric structure of this analogue peptide. Based on these results, the structural requirement for a compound to function as an effective heparin antidote and the possible mechanism involved in heparin neutralization were established.

  1. Utilisation de l'assistant grammatical Antidote dans le cadre d'activités de révision - Analyse exploratoire de protocoles d'observation Using Antidote in Revision Tasks: An Exploratory Study of Grammar Checker Usage Through Verbal Protocol Analysis

    Directory of Open Access Journals (Sweden)

    Patrick Durel

    2006-06-01

    Full Text Available Cette étude examine les opérations mentales d'apprenants utilisant l'assistant grammatical Antidote en phase de révision de leurs productions écrites. Analysant des données obtenues à partir de la méthode des protocoles verbaux, ce travail montre comment ce type d'activité de révision assistée par ordinateur conduit l'apprenant à manipuler, construire, renforcer ou élargir le champ d'application de ses connaissances, qu'elles soient déclaratives ou procédurales. Les éléments dégagés indiquent que l'utilisation d'Antidote peut être vecteur d'apprentissage et offrent quelques pistes permettant de concevoir des activités de révision assistée par ordinateur qui s'inscrivent dans le cadre d'une didactique de la production scripturale.This study explores learners' cognitive processes when using the grammar assistant software Antidote during the revision phase of their composition. Analysing data obtained using a hybrid form of verbal protocols, it shows how computer-assisted revision activity can lead learners to manipulate, build or reinforce declarative and procedural knowledge. We argue that using grammar assistant software can be conducive to learning. The results of the analysis provide an insight into how such a tool can be integrated into classroom activities, contributing to writing quality and the acquisition of revision strategies.

  2. [Inhalation therapy: inhaled generics, inhaled antidotes, the future of anti-infectives and the indications of inhaled pentamidine. GAT aerosolstorming, Paris 2012].

    Science.gov (United States)

    Peron, N; Le Guen, P; Andrieu, V; Bardot, S; Ravilly, S; Oudyi, M; Dubus, J-C

    2013-12-01

    The working group on aerosol therapy (GAT) of the Société de pneumologie de langue française (SPLF) organized its third "Aerosolstorming" in 2012. During the course of one day, different aspects of inhaled therapy were discussed, and these will be treated separately in two articles, this one being the first. Inhaled products represent a large volume of prescriptions both in the community and in hospital settings and they involve various specialties particularly ENT and respiratory care. Technical aspects of the development of these products, their mode of administration and compliance with their indications are key elements for the effective therapeutic use of inhaled treatments. In this first article, we will review issues concerning generic inhaled products, the existence of inhaled antidotes, new anti-infective agents and indications for inhaled pentamidine.

  3. Use of Molecular Dynamics for the Refinement of an Electrostatic Model for the In Silico Design of a Polymer Antidote for the Anticoagulant Fondaparinux

    Directory of Open Access Journals (Sweden)

    Adriana Cajiao

    2013-01-01

    Full Text Available Molecular dynamics (MD simulations results are herein incorporated into an electrostatic model used to determine the structure of an effective polymer-based antidote to the anticoagulant fondaparinux. In silico data for the polymer or its cationic binding groups has not, up to now, been available, and experimental data on the structure of the polymer-fondaparinux complex is extremely limited. Consequently, the task of optimizing the polymer structure is a daunting challenge. MD simulations provided a means to gain microscopic information on the interactions of the binding groups and fondaparinux that would have otherwise been inaccessible. This was used to refine the electrostatic model and improve the quantitative model predictions of binding affinity. Once refined, the model provided guidelines to improve electrostatic forces between candidate polymers and fondaparinux in order to increase association rate constants.

  4. [No support for lipid therapy as an effective antidote in acute intoxication. A systematic literature review and analysis of 114 case reports].

    Science.gov (United States)

    Forsberg, Matilda; Forsberg, Sune; Höjer, Jonas

    2015-09-29

    Lipid rescue is increasingly used as treatment of various types of poisoning despite weak scientific evidence. Some experimental studies have confirmed a positive effect, but others have failed. Clinical studies are lacking, wherefore we decided to do a systematic review of all published human cases. Case reports were searched for in PubMed and Web of Science and thereafter examined by two experts according to an assessment form grading the probability for a causal connection between lipid rescue and improved symptoms. A total of 114 case reports were identified. No correlation was found between the ratings of the cases and the fat solubility of the respective toxins. The findings do not support the predication that lipid rescue is an effective antidote, not even in cases involving local anaesthetics. In view of the potentially negative effects of lipid rescue, it seems reasonable to strictly limit its indication to life-threatening situations where conventional therapies have failed.

  5. Effect of various antidotes on biliary excretion of arsenic in isolated perfused livers of guinea pigs after acute experimental poisoning with As2O3.

    Science.gov (United States)

    Reichl, F X; Mückter, H; Kreppel, H; Forth, W

    1992-05-01

    The effect of the dithiols British Anti-Kewisite (BAL), dimercaptopropanesulfonic acid (DMPS), dimercaptosuccinic acid (DMSA) and a new metal binding agent 2,3-bis-(acetylthio)- propanesulfonamide (BAPSA) on the biliary excretion of arsenic in perfused livers of guinea pigs after acute experimental poisoning with As2O3 was investigated. Guinea pigs received As2O3, 10.0 mg/kg subcutaneously at 9 a.m. as a single injection. One hour after the injection the livers were perfused (2.5 ml x min.-1 x g-1 liver) with Krebs-Henseleit buffer and glucose for 80 min. After 40 min. of saline perfusion (control) 0.1 or 0.7 mmol/l BAL, DMSA, DMPS, or BAPSA were added to the perfusate and arsenic elimination in the bile and effluent perfusate was measured. The biliary excretion of arsenic in control livers between 40 and 80 min. was 0.7% of the total arsenic liver content before perfusion (= arsenic liver content after perfusion + portion excreted in the bile+perfusate). After antidote addition (0.1 mmol/l) the excretion was 0.2% for livers perfused with BAL, 6.8% for DMSA, 10.6% for DMPS, and 11.1% for BAPSA, respectively. After 0.7 mmol/l antidote the excretion of arsenic was 0.1% in livers perfused with BAL, 9.6% for DMSA, 12.3% for DMPS, and 13.3% for BAPSA, respectively. Except BAL, all compounds and most effectively BAPSA increased biliary excretion of arsenic. This indicates that excretion of arsenic which normally is mainly renal is shifted towards faecal excretion by the dithiols.

  6. 升麻解毒药对在方剂中的作用%Formula effect of drug combinations paired by herbs Cimicifuga as antidote

    Institute of Scientific and Technical Information of China (English)

    张均克

    2011-01-01

    文章就升麻的解毒功效及其药对组合在方剂配伍中的作用,结合本草文献、实验研究和临床经验进行了论述.总结出升麻的解毒作用主要有解时疫疠毒、解疮疡斑疹肿毒、解虫毒和解药毒4个方面.并分别阐述了升麻配玄参、配生地黄、配大青、配黄连、配石膏、配虎杖、配鳖甲、配金银花和连翘、配甘草、配牛蒡子、配马蔺子、配射干、配牛蒡子和桔梗、配葛根、配黄芩、配黄柏、配芍药的意义.%This paper discussed the detoxification efficacy of Cimicifuga and its drug combinations in the prescription compatibility by herbal literature research, experimental research and clinical experience and other methods.Summarized that detoxification efficacy of Cimicifuga including four aspects: detoxication of the epidemic pestilence, the sore rash swollen poison, the insect poison and the antidote to poison. Expounded that formula effect of Paired Herbs or drug combinations paired by Cimicifuga as antidote respectively with Scrophularia , with Rehmannia glutinosa (Gaertn.)Libosch, with Cleredendrum cwtophyllum Turcz, with Coptidis Chinensis, with Gypsum Fibrosum, with Polygonum cuspidatum Sieb.Et Zucc, with Carapax Trionycis, with Lonicerae and Forsythiae, with Glycyrrhiza, with Arctium, with Semen Iridis(Seed of Chinese Small Iris), with Rhizoma Belamcandae, with Arctium and Radix Platycodonis , with Pueraria lobata(Willd.)Ohwi, with Radix Scutellariae, with Phellodendron Chinense Schnei, with Paeonia lactiflora Pall, with peony,etc.

  7. Trends in toxic alcohol exposures in the United States from 2000 to 2013: a focus on the use of antidotes and extracorporeal treatments.

    Science.gov (United States)

    Ghannoum, Marc; Hoffman, Robert S; Mowry, James B; Lavergne, Valery

    2014-01-01

    Morbidity and mortality from toxic alcohols like ethylene glycol and methanol remain prevalent worldwide. The introduction of fomepizole, a potent blocker of alcohol dehydrogenase, has modified current practice over the last 15 years. The aim of the study was to describe the characteristics of toxic alcohol poisoning reported to US poison centers, the trends in the incidence of antidote use and hemodialysis treatment, as well as the related mortality. A retrospective study of all electronic entries from the AAPCC National Poison Data System database, from the years 2000 to 2013 was reviewed. When considering all exposures, the great majority of patients had a benign outcome. Major effects (e.g., life threatening) occurred in 2.1% and 4.9% of methanol and ethylene glycol cases, respectively. Mortality rates were similar for both toxic alcohols, approximately 0.6%. When only considering ingestions reported to healthcare facilities, a major effect was reported in 9.5% and 20.5%, and the mortality rate was 2.9% and 2.4% for methanol and ethylene glycol exposures, respectively, and remained constant over time. The use of fomepizole increased statistically over the study period while that of ethanol decreased, until it became proportionally negligible by 2012-2013. The use of hemodialysis significantly decreased in "Early" ethylene glycol exposures during the study period. Similar to other reports, it appears that the use of fomepizole has largely supplanted ethanol as the antidote of choice in toxic alcohol exposures and may decrease the requirements for hemodialysis in patients poisoned with ethylene glycol who have no acidosis and normal kidney function.

  8. Status investigation on the reserve of antidotes in chemical poisoning emergency institutions in Guangdong%广东化学中毒应急机构解毒药物储备状况调查

    Institute of Scientific and Technical Information of China (English)

    李伟均; 丘创逸; 陈嘉斌; 李荣宗; 黄永顺

    2010-01-01

    目的 了解广东化学中毒应急机构解毒药物储备状况,为做好应急救援药品储备提供依据.方法 采用问卷调查与实地考察相结合的方式,调查广东化学中毒应急机构12种应急解毒药物储备状况.结果 调查76家市、县(区)化学中毒应急机构,目前没有一家机构能全部储备12种应急解毒药物,仅有14家(18.4%)储备了2~10种解毒药物;有61家机构(80.3%)建立了紧急药物购置渠道;14家(18.4%)机构既无应急药品储备又无建立紧急购置渠道.结论 广东化学中毒应急机构解毒药物储备状况不佳.储备率低、品种少,急需补充储备,尤其应优先补充氰化物、硫化氢、有机磷农药等急性化学中毒的特效解毒药物.%Objective To understand the status of the reserve of antidotes in chemical poisoning emergency institutions in Guangdong and to provide the basis to improve the storage.Method With the questionnaire and on-the-spot survey, the reserve of 12 kinds of antidotes in chemical poisoning emergency institutions in Guangdong were investigated.Results Within 76 institutions responsible for chemical poi-soning emergency at city, country or district levels, no one could reserve all 12 kinds of antidotes. Only 14 institutions (18.4%) had 2 to 10 kinds of the antidotes. 61 institutions (80.3%) established the links to purchase the necessary antidotes but 14 (18.4%) had neither the reserve nor the links.Conclusion The status is dissatisfied for both of the amounts and categories of the reserved antidotes are in chemical poisoning emergency institutions in Guangdong. The reserve should be supplemented immediately, especially those against the acute chemical poisonings of cyanide, sulfureted hydrogen and organophosphorous insecticide.

  9. Antidotes for Cyanide Poisoning

    Science.gov (United States)

    2013-01-01

    the treatment of acute cyanide toxicity in a swine (Sus scrofa ) model. Ann Emerg Med Jun 2012; 59:532 539. 3 Bebarta VS, Tanen DA, Lairet J, Dixon PS...a swine (Sus scrofa ) model. Ann Emerg Med 2010; 55:345 351. 4 Bebarta VS, Pitotti RL, Dixon PS, Valtier S, Esquivel L, Bush A, Little CM

  10. A Universal Antidote

    Science.gov (United States)

    1988-01-01

    Last fall two of the Big Three U.S. automakers concluded arrangements with Alcide Corporation for distribution of Alcide's patented Ren New Air Conditioning Disinfectant. Special properties of Alcide formulation enable it to destroy mold and fungus as well as bacteria and viruses with minimal harm to humans, animals and/or plants. This allows use of the product to disinfect and deodorize auto air conditioners without removing them and without any lingering toxicity. Disinfectant/deodorizer is one of a wide range of Alcide formulations engineered for a variety of purposes, spanning automotive, medical, agricultural, pharmaceutical and consumer markets. Alcide is not strictly speaking a spinoff from aerospace technology, but the products and company that makes them are beneficiaries of assistance provided by NERAC, Inc.

  11. 常用特殊解毒药应用中的剂量问题和药动学研究进展%Study progress on dose problem and pharmacokinetics of commonly used special antidote

    Institute of Scientific and Technical Information of China (English)

    宋亚娟; 刘扬; 丁国华

    2009-01-01

    探讨特殊解毒药应用中的剂量问题,了解其药动学研究概况.收集近30年有关的代表性文献,对特殊解毒药的临床应用、与剂量有关的不良反应、药动学以及常用的检测方法进行了归纳和分析.特殊解毒药在临床上救治中毒疗效显著,但由于剂量不足或过量所引起的不良反应和二次伤害也较为突出.特殊解毒药在临床应用中剂量问题仍是解毒成功的关键,对其体内正常参考值的了解和对其药动学的研究及深入探讨,是临床上准确掌握特殊解毒药应用剂量的一个必要前提.%To investigate the problems about dosage and pharmacokinetics of special antidotes in applications. Collected and analyzed the references about clinical applications, dosage correlative adverse reactions, pharmacokinetics and assaying methods of special antidotes in the last 30 years. Though special antidotes have significant effects in the clinical treatment of poisoning, theirs secondary damages and adverse reactions caused by inadequacy dose or overdose are also more prominent. The problems about the dosage of special antidotes in the clinical application are still the key to successful deintoxication. To handle the dosage accurately in clinical use, and to study their pharmacokinetics is necessary.

  12. Identification of a mechanism by which the methylmercury antidotes N-acetylcysteine and dimercaptopropanesulfonate enhance urinary metal excretion: transport by the renal organic anion transporter-1.

    Science.gov (United States)

    Koh, Albert S; Simmons-Willis, Tracey A; Pritchard, John B; Grassl, Steven M; Ballatori, Nazzareno

    2002-10-01

    N-Acetylcysteine (NAC) and dimercaptopropanesulfonate (DMPS) are sulfhydryl-containing compounds that produce a dramatic acceleration of urinary methylmercury (MeHg) excretion in poisoned animals, but the molecular mechanism for this effect is unknown. NAC and DMPS are themselves excreted in urine in high concentrations. The present study tested the hypothesis that the complexes formed between MeHg and these anionic chelating agents are transported from blood into proximal tubule cells by the basolateral membrane organic anion transporters (Oat) 1 and Oat3. Xenopus laevis oocytes expressing rat Oat1 showed increased uptake of [(14)C]MeHg when complexed with either NAC or DMPS but not when complexed with L-cysteine, glutathione, dimercaptosuccinate, penicillamine, or gamma-glutamylcysteine. In contrast, none of these MeHg complexes were transported by Oat3-expressing oocytes. The apparent K(m) values for Oat1-mediated transport were 31 +/- 2 microM for MeHg-NAC and 9 +/- 2 microM for MeHg-DMPS, indicating that these are relatively high-affinity substrates. Oat1-mediated uptake of [(14)C]MeHg-NAC and [(14)C]MeHg-DMPS was inhibited by prototypical substrates for Oat1, including p-aminohippurate (PAH), and was trans-stimulated when oocytes were preloaded with 2 mM glutarate but not glutamate. Conversely, efflux of [(3)H]PAH from Oat1-expressing oocytes was trans-stimulated by glutarate, PAH, NAC, DMPS, MeHg-NAC, MeHg-DMPS, and a mercapturic acid, indicating that these are transported solutes. [(3)H]PAH uptake was competitively inhibited by NAC (K(i) of 2.0 +/- 0.3 mM) and DMPS (K(i) of 0.10 +/- 0.02 mM), providing further evidence that these chelating agents are substrates for Oat1. These results indicate that the MeHg antidotes NAC and DMPS and their mercaptide complexes are transported by Oat1 but are comparatively poor substrates for Oat3. This is the first molecular identification of a transport mechanism by which these antidotes may enhance urinary excretion of

  13. Ag antidot array modified TiO2 film and its photocatalysis performance%Ag反点阵列修饰TiO2薄膜的制备及光催化性能研究

    Institute of Scientific and Technical Information of China (English)

    祁洪飞; 刘大博; 成波; 郝维昌; 王天民

    2012-01-01

    采用胶体晶体模板技术和磁控溅射工艺,通过调制溅射功率,制备了一系列不同形貌的Ag反点阵列修饰TiO2复合薄膜.通过扫描电子显微镜(SEM),X射线衍射(XRD),紫外一可见分光光度计(UV-Vis)和四探针测试仪等手段对样品的结构和光催化性能进行了表征.实验结果表明:Ag反点阵列的形貌对样品光催化性能有显著影响.随着反点孔径的减小,其导电性能迅速提升,样品的光催化性能逐渐增强.孔径为710nm时,复合薄膜的光催化性能达到最高.随后,继续减小孔径,样品的光催化性能出现了一定程度的下降,这是载流子损耗增多和遮光面积增大引起的.经Ag反点阵列修饰的样品的光催化性能均明显优于TiO2薄膜,主要是由于反点阵列可有效分离光生载流子,因此使其光催化活性得到显著提高.%Ag antidot arrays modified TiO2 films are obtained by PS colloidal crystal template technique and magnetron sputtering method, and the microstructure of Ag antidot array is modulated through controlling the sputtering power. And then, the structural and the photocatalysis performances of all samples are characterized by using scanning electron microscopy, X-ray diffraction, UV-Vis spec- trophotometer, and four-point probe. The experimental results show that the microstructure of Ag antidot array significantly influences the photocatalysis performance of the sample. With the diameter of the antidot array decreasing, the photocatalysis performance of the sample is enhanced due to the increase of conducting ability. The photocatalysis performance is highest, when the diameter of the anti- dot array is 710 nm. Subsequently, with the diameter of the antidot array further decreasing, the photocatalysis performance decreases to a certain extent, which results from the increases of the carder ioss and the light shading area. The photocatalysis performance of Ag

  14. Intravascular Residence Time Determination for the Cyanide Antidote Dimethyl Trisulfide in Rat by Using Liquid-Liquid Extraction Coupled with High Performance Liquid Chromatography

    Science.gov (United States)

    De Silva, Deepthika; Lee, Steven; Duke, Anna; Angalakurthi, Siva; Chou, Ching-En; Ebrahimpour, Afshin; Thompson, David E.

    2016-01-01

    These studies represent the first report on the intravascular residence time determinations for the cyanide antidote dimethyl trisulfide (DMTS) in a rat model by using high performance liquid chromatography coupled with ultraviolet absorption spectroscopy (HPLC-UV). The newly developed sample preparation included liquid-liquid extraction by cyclohexanone. The calibration curves showed a linear response for DMTS concentrations between 0.010 and 0.30 mg/mL with R2 = 0.9994. The limit of detection for DMTS via this extraction method was 0.010 mg/mL, and the limit of quantitation was 0.034 mg/mL. Thus this calibration curve provided a tool for determining DMTS in the range between 0.04 and 0.30 mg/mL. Rats were given 20 mg/kg DMTS dose (in 15% Polysorbate 80) intravenously, and blood samples were taken 15, 60, 90, 120, and 240 min after DMTS injections. The data points were plotted as DMTS concentration in RBCs versus time, and the intravascular residence time was determined graphically. The results indicated a half-life of 36 min in a rat model, suggesting that the circulation time is long enough to provide a reasonable time interval for cyanide antagonism. PMID:28053802

  15. Intravascular Residence Time Determination for the Cyanide Antidote Dimethyl Trisulfide in Rat by Using Liquid-Liquid Extraction Coupled with High Performance Liquid Chromatography

    Directory of Open Access Journals (Sweden)

    Deepthika De Silva

    2016-01-01

    Full Text Available These studies represent the first report on the intravascular residence time determinations for the cyanide antidote dimethyl trisulfide (DMTS in a rat model by using high performance liquid chromatography coupled with ultraviolet absorption spectroscopy (HPLC-UV. The newly developed sample preparation included liquid-liquid extraction by cyclohexanone. The calibration curves showed a linear response for DMTS concentrations between 0.010 and 0.30 mg/mL with R2 = 0.9994. The limit of detection for DMTS via this extraction method was 0.010 mg/mL, and the limit of quantitation was 0.034 mg/mL. Thus this calibration curve provided a tool for determining DMTS in the range between 0.04 and 0.30 mg/mL. Rats were given 20 mg/kg DMTS dose (in 15% Polysorbate 80 intravenously, and blood samples were taken 15, 60, 90, 120, and 240 min after DMTS injections. The data points were plotted as DMTS concentration in RBCs versus time, and the intravascular residence time was determined graphically. The results indicated a half-life of 36 min in a rat model, suggesting that the circulation time is long enough to provide a reasonable time interval for cyanide antagonism.

  16. Coordination Chemistry of One Antidotal Traditional Chinese Medicine with Cd2+%03A解毒健脾中药驱除镉的分子机理

    Institute of Scientific and Technical Information of China (English)

    朱志良; 乔俊莲; 陈与德; 孙爱贞

    2000-01-01

    在(38.5±0.1)℃,硝酸钾维持离子强度为0.1的条件下,利用pH电位滴定法,通过03A中药与Cd2+的配位化学研究,发现03A中药作为一种以氨基酸为主体化学成分的复合方剂能与Cd2+等有毒重金属形成稳定的配合物,其排除体内有毒重金属的效果远好于传统的EDTA-Zn盐,并且对体内必需微量元素Zn的存在不会产生明显的影响,从配位化学角度对该中药在临床上的有效促排有毒重金属现象从分子水平作出了解释.%A pH- potentiometric titration method has been used to determine the acid dissociation constants of one antidotal traditional Chinese medicine. The stability constants of the complexes of this medicine with Cd2 + at 38.5 ℃ and ionic strength I = 0.1 has also been determined. The mechanism of Cd2 + excretion and detoxification with this medicine are discussed.

  17. Research progress in antidotes of nerve agents in the USA%美国神经性毒剂救治研究进展

    Institute of Scientific and Technical Information of China (English)

    程晋; 但国蓉; 赵远鹏; 王健; 叶枫; 赵吉清; 邹仲敏

    2015-01-01

    Nerve agent not only inhibit acetylcholinesterase ( AChE) at an early stage, but also induce prolonged and progressive neuroinflammation and delayed neurodegeneration.Recently, the US National Institute of Health ( NIH) has sponsored some major programs of toxic mechanisms and treatment of nerve agents, which aims at the development of quick and effective treatment to acute intoxication and delayed effect.The experimentally effective new antidotes mainly include AChE-targeting drugs, broad-spectrum reactivators and scavengers, antiinflamatory and nerve protection drugs.%神经性毒剂除了在早期抑制乙酰胆碱酯酶( AChE)外,也导致长期的进行性神经炎和迟发神经退行性病变。近年来,美国国立卫生研究院资助了多项神经性毒剂中毒机制和治疗药物的研究,旨在快速高效对抗神经性毒剂急性中毒及远后效应。正在研制的治疗药物主要包括AChE靶向药物、广谱重活化剂和生物清除剂、抗炎及神经保护药。

  18. Crystallization of the C-terminal domain of the addiction antidote CcdA in complex with its toxin CcdB

    Energy Technology Data Exchange (ETDEWEB)

    Buts, Lieven; De Jonge, Natalie; Loris, Remy, E-mail: reloris@vub.ac.be; Wyns, Lode; Dao-Thi, Minh-Hoa [Department of Molecular and Cellular Interactions, Vlaams Interinuversitair Instituut voor Biotechnologie and Laboratorium voor Ultrastructuur, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussel (Belgium)

    2005-10-01

    The CcdA C-terminal domain was crystallized in complex with CcdB in two crystal forms that diffract to beyond 2.0 Å resolution. CcdA and CcdB are the antidote and toxin of the ccd addiction module of Escherichia coli plasmid F. The CcdA C-terminal domain (CcdA{sub C36}; 36 amino acids) was crystallized in complex with CcdB (dimer of 2 × 101 amino acids) in three different crystal forms, two of which diffract to high resolution. Form II belongs to space group P2{sub 1}2{sub 1}2{sub 1}, with unit-cell parameters a = 37.6, b = 60.5, c = 83.8 Å and diffracts to 1.8 Å resolution. Form III belongs to space group P2{sub 1}, with unit-cell parameters a = 41.0, b = 37.9, c = 69.6 Å, β = 96.9°, and diffracts to 1.9 Å resolution.

  19. [Antidotal effects of sulfhydryl compounds on acute poisonings by sodium ammonium dimethyl-2-(propane-1,3-dithiosulfate) monohydrate, nereistoxin and cartap].

    Science.gov (United States)

    Cao, B J; Chen, Z K; Chi, Z Q

    1990-03-01

    Sodium dimercaptopropanesulphonate (DMPS) and sodium dimercaptosuccinate (DMS) were discovered to be effective antidotes for acute poisoning of insecticides SCD [sodium ammonium dimethyl-2-(propane-1,3-dithiosulfate) monohydrate], nereistoxin (4-N,N-dimethylamino-1,2-dithiolane) and cartap (dihydronereistoxin dicarbamate). In mice, DMPS (250 mg/kg) or DMS (1000 mg/kg) ip 20 min before SCD increased LD50 of ig SCD from 97 to 374 or 251 mg/kg, respectively. The prophylactic effect of DMPS was better than that of DMS. Administration of DMPS prior to cartap increased LD50 of ig cartap from 130 to 375 mg/kg. The therapeutic effect of DMPS was also demonstrated in SCD-poisoned conscious rabbits. DMPS 62.5 mg/kg or DMS 500 mg/kg iv completely antagonized the neuromuscular blockade and respiratory depression caused by SCD, nereistoxin and cartap in anesthetized rabbits. The antagonism of SCD-induced neuromuscular blockade by cysteine (400 mg/kg, iv) was less effective and of shorter duration than that by DMPS and DMS. Dimercaprol 50 mg/kg im showed little effect on SCD-induced paralysis. The antagonistic actions of sulfhydryl compounds on neuromuscular blockade induced by these insecticides probably belong to chemical antagonism.

  20. The ClpXP protease is responsible for the degradation of the Epsilon antidote to the Zeta toxin of the streptococcal pSM19035 plasmid.

    Science.gov (United States)

    Brzozowska, Iwona; Zielenkiewicz, Urszula

    2014-03-14

    Most bacterial genomes contain different types of toxin-antitoxin (TA) systems. The ω-ε-ζ proteinaceous type II TA cassette from the streptococcal pSM19035 plasmid is a member of the ε/ζ family, which is commonly found in multiresistance plasmids and chromosomes of various human pathogens. Regulation of type II TA systems relies on the proteolysis of antitoxin proteins. Under normal conditions, the Epsilon antidote neutralizes the Zeta toxin through the formation of a tight complex. In this study, we show, using both in vivo and in vitro analyses, that the ClpXP protease is responsible for Epsilon antitoxin degradation. Using in vivo studies, we examined the stability of the plasmids with active or inactive ω-ε-ζ TA cassettes in B. subtilis mutants that were defective for different proteases. Using in vitro assays, the degradation of purified His6-Epsilon by the His6-LonBs, ClpPBs, and ClpXBs proteases from B. subtilis was analyzed. Additionally, we showed that purified Zeta toxin protects the Epsilon protein from rapid ClpXP-catalyzed degradation.

  1. 广西融水县常见清热解毒蕨类植物的初步研究%Study of Antipyretic and Antidotal Medicinal Pteridophytes in Rongshui Guangxi

    Institute of Scientific and Technical Information of China (English)

    陶玉华; 隆卫革; 曹书阁

    2015-01-01

    民间对清热解毒药用蕨类植物需求量大,应用较普遍,本研究通过野外调查、标本鉴定和查阅文献资料,对广西融水县清热解毒药用蕨类植物的种类、生态环境和药用状况等进行了初步的调查研究,记录常用的清热解毒的药用蕨类植物共41种,隶属于20科27属,广西融水县清热解毒药用蕨类植物资源丰富,药用的生物活性成分含量较高,具有重要的药用价值,目前已被开发利用的种类不多,很多种类有待于进一步研究和开发。%The antipyretic and antidotal medicinal pteridophytes have been in great demand and widely used in folk.The main species, ecological environment and medicinal status of Rongshui antipyretic and antidotal medic -inal pteridophytes are preliminarily studied through field investigation , specimen identification and information ac-cess in this study .The results show that there are 41 main species of antipyretic and antidotal medicinal pterido-phytes, belonging to 20 families and 27 genera in Guangxi , which are of rich bioactive components and important medicinal value .Many species are to be further studied and developed .

  2. Apoptosis-like cell death induced by nematocyst venom from Chrysaora helvola Brandt jellyfish and an in vitro evaluation of commonly used antidotes.

    Science.gov (United States)

    Qu, Xiaosheng; Xia, Xianghua; Lai, Zefeng; Zhong, Taozheng; Li, Gang; Fan, Lanlan; Shu, Wei

    2016-02-01

    The present work investigated the in vitro cytotoxicity of nematocyst venom (NV) from Chrysaora helvola Brandt (C. helvola) jellyfish against human MCF-7 and CNE-2 tumor cell lines. Potent cytotoxicity was quantified using the MTT assay (LC50=12.07±3.13 and 1.6±0.22μg/mL (n=4), respectively). Apoptosis-like cell death was further confirmed using the LDH release assay and Annexin V/PI double staining-based flow cytometry analysis. However, only activation of caspase-4 was observed. It is possible that some caspase-independent pathways were activated by the NV treatment. Since no reference or antivenom is available, the effects of several commonly used antidotes on the cytotoxicity of NV were examined on more sensitive CNE-2 cells to determine the appropriate emergency measures for envenomation by C. helvola. The phospholipase A2 (PLA2) inhibitor para-bromophenacyl bromide (pBPB) showed no protective effect, while Mg(2+) potentiated cytotoxicity. Voltage-gated L-type Ca(2+) channel blockers (verapamil, nifedipine and felodipine) and Na-Ca(2+) exchanger inhibitor KB-R7943 also showed no effect. Assays using Ca(2+)-free culture media or the intracellular Ca(2+) chelator BAPTA also could not inhibit the cytotoxicity. Taken together, these results suggest that PLA2 and Ca(2+) are not directly involved in the cytotoxicity of NV from C. helvola. Our work also suggests caution regarding the choice for first aid for envenomation by C. helvola jellyfish.

  3. Neutralizing activities of ethanolic extracts of six plants traditionally used in Guatemala as antidotes for the envenomation caused by the snake Bothrops asper

    Directory of Open Access Journals (Sweden)

    Patricia Saravia-Otten

    2015-07-01

    Full Text Available Many plants are reported to be used in Guatemalan traditional medicine as antidotes against various effects of the snakebite; however, very few attempts have been made to evaluate their neutralizing capacity in controlled experiments. Six plants (Acacia hindsii, Cissampelos pareira; Hamelia patens, Piper peltatum, Sansevieria hyacinthoides and Aristolochia maxima were evaluated in vitro for their ability to neutralize phospholipase A2(PLA2 and proteolytic effects of the venom of Bothrops asper, the snake responsible for approximately half of the snakebite envenomations in Central America. These effects are indicatives of the ability of B. asper venom to produce myotoxicity, hemorrhage and inflammation. Plants were collected, dried and extracted by maceration with ethanol. After pre-incubation of several amounts of each extract with a challenge dose of venom, S. hyacinthoides demonstrated a low neutralizing capacity (< DE 50 of the PLA2 effect (13.90 ± 6.41%; C. pareira (32.98 ± 5.51% and P. peltatum (24.52 ± 7.45% neutralized less than 50% of the proteolytic effect. The results suggest that neither of the tested plants should be used individually to treat the main effects of B. asper envenomation. However, the three low-active extracts might be potentiated when used in mixtures composed of several plants, as prepared by traditional healers. Given the complexity of the venom components and the multiple pathologic effects produced by B. asper envenomation, more tests are required to fully investigate the ability of this plants to neutralize the coagulant, fibrin(ogenolytic, edematizing and myotoxic effects of the venom.

  4. Catalytic-site conformational equilibrium in nerve-agent adducts of acetylcholinesterase: possible implications for the HI-6 antidote substrate specificity.

    Science.gov (United States)

    Artursson, Elisabet; Andersson, Per Ola; Akfur, Christine; Linusson, Anna; Börjegren, Susanne; Ekström, Fredrik

    2013-05-01

    Nerve agents such as tabun, cyclosarin and Russian VX inhibit the essential enzyme acetylcholinesterase (AChE) by organophosphorylating the catalytic serine residue. Nucleophiles, such as oximes, are used as antidotes as they can reactivate and restore the function of the inhibited enzyme. The oxime HI-6 shows a notably low activity on tabun adducts but can effectively reactivate adducts of cyclosarin and Russian VX. To examine the structural basis for the pronounced substrate specificity of HI-6, we determined the binary crystal structures of Mus musculus AChE (mAChE) conjugated by cyclosarin and Russian VX and found a conformational mobility of the side chains of Phe338 and His447. The interaction between HI-6 and tabun-adducts of AChE were subsequently investigated using a combination of time resolved fluorescence spectroscopy and X-ray crystallography. Our findings show that HI-6 binds to tabun inhibited Homo sapiens AChE (hAChE) with an IC50 value of 300μM and suggest that the reactive nucleophilic moiety of HI-6 is excluded from the phosphorus atom of tabun. We propose that a conformational mobility of the side-chains of Phe338 and His447 is a common feature in nerve-agent adducts of AChE. We also suggest that the conformational mobility allow HI-6 to reactivate conjugates of cyclosarin and Russian VX while a reduced mobility in tabun conjugated AChE results in steric hindrance that prevents efficient reactivation.

  5. 蓖麻粗毒蛋白中草药解毒剂的筛选%Screening on Chinese herbal medicines antidotes to raw ricin

    Institute of Scientific and Technical Information of China (English)

    孙媚华; 陈迁; 宋光泉

    2014-01-01

    为了从31种中草药中筛选出对蓖麻粗毒蛋白具有较好解毒效果的中草药提取物,采用5种不同提取方法提取中草药有效成分,以小白鼠为试验对象,就31种中草药乙醇提取物对蓖麻毒蛋白中毒小鼠的解毒效果进行了粗筛,并就5种不同提取方法提取中草药提取液对蓖麻毒蛋白中毒小鼠的解毒效果进行了比较。结果表明,31种中草药乙醇提取物中,筛选出解毒效果较好的大黄、连翘、板蓝根、防风、白芍、附子、龙血竭、升麻(广东)和升麻(西安)等9种中草药;又从这9种中草药乙醇提取物中进一步筛选出解毒效果好且效果稳定的板蓝根、白芍、龙血竭和升麻(西安)等4种中草药;在5种提取方法中,以超声波丙酮提取法提取的中草药的解毒效果最好,超声波乙醇提取法次之,超声波水提取法效果最差;而在板蓝根、白芍、龙血竭和升麻(西安)等4种中草药提取液中,则以白芍提取液的解毒效果最佳,升麻(西安)的解毒效果最差。由此可以证明,白芍,龙血竭,板蓝根和升麻(西安)为极具潜力的蓖麻粗毒蛋白中草药解毒剂。%In order to screen out Chinese herb extracts from 31 kinds of Chinese medicinal herbs herbal which have good antidotal effect on raw ricin , five different extraction methods were investigated .Mice were used as experimental subjects , 31 kinds of herbal ethanol extracts were used to sieve coarsely by the detoxifying effect of ricin poisoning on mice .The detoxifying effects of the Chinese herb extracts extracted by five different methods were compared on ricin poisoned mice .The results showed that nine kinds of Chinese medicinal herbs were found to have good detoxification from 31 kinds of herbal ethanol extracts , for example Rhubarb , Forsythia , Radix , Divaricate saposhnikovia root , White paeony root , Radix aconiti lateralis preparata , Resina

  6. Preparation and Photocatalysis Performance of Ag antidot Array/TiO2 Films%银反点阵列/TiO2材料的制备及光催化性能研究

    Institute of Scientific and Technical Information of China (English)

    戴松喦; 祁洪飞; 刘大博; 罗飞; 田野; 陈冬生

    2016-01-01

    Ag antidot arrays modified TiO2 films are obtained by PS colloidal crystal templates technique and magnetron sputtering method. And then, the microstructure and the photocatalysis performance of the samples are characterized by using scanning electron microscopy (SEM), x-ray diffraction (XRD), UV-Vis spectrophotometer, and four-point probe. The experimental results showed that Ag antidot arrays possess excellent electrical conductivity and could effectively promote the separation of surface photoinduced charge carrier of TiO2 nanoparticles, which is responsible for the remarkable increase in photocatalytic activity.%采用胶体晶体模板技术和磁控溅射工艺,制备了银反点阵列怱饰TiO2薄膜。用扫描电子显微镜、X射线衍射、紫外-可见分光光度计和四探针测试仪等手段对复合薄膜的结构和光催化性能进行了表征。结果表明,银反点阵列具有优良的导电性能,可有效抑制光生载流子的复合,增强载流子输运的效率,使TiO2的光催化性大幅提升。

  7. Preventing deaths from rising opioid overdose in the US – the promise of naloxone antidote in community-based naloxone take-home programs

    Directory of Open Access Journals (Sweden)

    Straus MM

    2013-09-01

    , it is important for federal government research agencies to initiate and support independent and rigorous evaluation of these programs to inform policymakers how effective these programs can be to save lives and curb the opioid overdose public health crisis. Keywords: prescription drug abuse, fatal opioid overdose, naloxone antidote, Good Samaritan laws, naloxone take-home program

  8. Preclinical study comparing the antidotal effect of clonidine with atropine for the treatment of acute malathion poisoning in the albino rats

    Directory of Open Access Journals (Sweden)

    Suresha K. R.

    2016-12-01

    Full Text Available Background: In developing countries 2–3 million people are acutely poisoned by organophosphorus (OP pesticides every year. There is a pressing need for new affordable antidotes and in this context clonidine which has central effect (α2 agonist has been evaluated in the albino rats presenting with signs or symptoms of acute malathion poisoning. And compared with atropine for the acte malathion poisoning in albino rats. Methods: This was a preclinical study conducted on albino rats of either sex weighing 100-150 grams were randomly divided into 4 groups (6/group. Malathion was given at the lethal dose of 54 mg/kg body weight (BW by gavage to each group. Group 1: normal saline intraperioneal (i.p. Group 2: Post treated with atropine 1.5 mg/kg BW (i.p. Group 3: Pre treated with clonidine 1mg/ kg BW (i.p, 10 minutes priore malathion. Group 4: Pre treated with clonidine and post treated with atropine. The above groups were observed for straub tail, muscle fasciculation, piloerection, lacrimation, defecation/ urination; salivation, tremors, gasping and convulsion and were recorded at time 0, 15, 30, 45 and 60 minutes after poisoning. The latency of onset of tremors, loss of righting reflex and tremors were recorded. Results were presented as percentage occurrence and Mean ± SEM. Repeated measure one way ANOVA and Fisher’s Least Significant Difference post hoc test for comparison between groups. P-value of 0.05 or less was considered for statistical significance. Results: The central effects namely straubs tail and whole body tremors are significantly improved compared to control and atropine with clonidine group (p<0.05. However convulsion shows improve in atropine alone and atropine with clonidine groups. The overall survival time has significantly increased compared to control and atropine and atropine with clonidine (P<0.05.Clonidine has not shown any effect on survival time. Conclusions: Clonidine has some central protective effect in

  9. The Antidotes to the Double Standard: Protecting the Healthcare Rights of Mentally Ill Inmates by Blurring the Line Between Estelle and Youngberg.

    Science.gov (United States)

    Goldberg, Rose Carmen

    2016-01-01

    This Note is an examination of mentally ill inmates' constitutional right to treatment. It has significant doctrinal and practical implications. In terms of doctrine, the Supreme Court has created distinct standards for the minimum levels of care for inmates (Estelle) and the civilly committed mentally ill (Youngberg). Under this framework mentally ill inmates are constitutionally equivalent to inmates generally, but are entitled to less care than the civilly committed even if they suffer the same illness. This Note explores this gap through the lens of equal protection and argues that mentally ill inmates are similarly situated to the civilly committed. It further contends that inmates constitute a "discrete and insular minority" and thus the standard establishing their right to care should be subject to strict scrutiny. This Note finds that Estelle fails this test. Practically, this Note brings visibility to a consequential area of the law neglected by scholarship. Over half of inmates are mentally ill and yet treatment in prisons is inadequate. The literature at the intersection of health, criminal justice, and constitutional rights has not constructively considered how doctrine should be changed to protect the wellbeing of this vulnerable population. Scholars have also provided little oversight of the judicial administration of justice in this field; there are few reviews of how judges actually apply treatment rights standards. This Note lessens this blind spot by exposing how courts fail to properly distinguish between different standards. This Note proposes that the most promising antidote to the Estelle-Youngberg double standard, counterintuitively, is not the creation of a uniform standard. A standard that puts mentally ill inmates on equal footing with the civilly committed would solve the doctrinal puzzle, but would be subject to Youngberg's inherent flaws and the judicial malpractice in this area. Recognizing the deficiencies of a purely judicial remedy

  10. 除草剂解毒剂解除乙草胺对水稻残留药害的活性研究%The Study on The bioactivity of Acetochlor Herbicide Antidote to Reduce the Rice's Residue Injury

    Institute of Scientific and Technical Information of China (English)

    张金艳; 曹先良

    2009-01-01

    Taking the method of the indoor bioassay to study the herbicide antidote dichloroi-N-acetyl-2-methyl-1-oxa-4-aza-Lo [4.4] nonane to reduce acetochlor on succession crop-rice's residues injury. Studing the effects of the antidote to herbicide acetochlor's detoxification by measuring rice's plant height and plant fresh weight etc.physiologlcal index. The results show that: by using different acetochlor concentration in the soil, the concentration of 8mg/kg antidote soaking that make the rice plant height and plant fresh weight etc. physical index achieve the best which make rice plant height restored to the comparion of 95.89 percent、 84.07 percent,66.32 percent and the plant fresh weight restored to the comparion of 107.56 percent,84.18 percent,67.92 percent.%采用室内生物活性测定的方法,研究了除草剂解毒剂N-二氯乙酰基-2-甲基-1-氧杂-4-氮杂-螺[4.4]壬烷减轻除草剂乙草胺对后茬作物水稻的残留药害.通过对水稻株高和株鲜重等生理指标的测定,研究了该解毒剂对除草剂乙草胺的解毒效果.试验结果表明:在施用不用浓度的乙草胺的土壤中,用浓度为8 mg·kg-1的解毒剂浸种时,对水稻株高、株鲜重等生理指标均达到最佳的解毒效果,可使龙粳14水稻的株高恢复到对照的95.89%、84.07%、66.32%;株鲜重恢复到对照的107.56%、84.18%、67.92%.

  11. Validation method in microbial limit test for antipyretic and antidotal Chinese patent medicines%清热解毒类中成药微生物限度检查方法验证

    Institute of Scientific and Technical Information of China (English)

    许威; 吴虹

    2012-01-01

    目的 研究清热解毒类中成药的抑菌作用,建立其微生物限度检查方法 .方法 按照<中国药典)2010年版一部的微生物限度检查法进行验证实验.结果 8种清热解毒类中成药均对金黄色葡萄球菌、枯草芽孢杆菌有一定的抑菌作用,可以分别通过培养基稀释法和薄膜过滤法得以消除.结论 分别建立了8种清热解毒类中成药的微生物限度检查方法 ,为该类药品的微生物检查提供参考.%Objective To study the antimicrobial effect of antipyretic and antidotal Chinese patent medicines and to establish microbial limit test method for them. Methods According to Chinese Pharmacopoeia 2010 Edition,validation method in microbial limit test for the medicines was validated. Results Eight kinds of antipyretic and antidotal Chinese patent medicines all showed inhibition effect on Staphylococcus aureus and Bacillus subtilis. The effect could be eliminated by culture medium dilution method and filtration membrane method. Conclusion Microbial limit test methods were established for the Chinese patent medicines respectivesly. The results could give experimental evidence for the kind of Chinese patent medicines.

  12. Research programs on antidotes and detection of cyanide and progress in the USA%美国氰化物中毒救治药物研发项目及其进展

    Institute of Scientific and Technical Information of China (English)

    邹仲敏; 程晋; 叶枫; 但国蓉; 蔡颖; 王健; 董兆君

    2012-01-01

    The U. S. government and the US Armed Forces have recently sponsored some major programs of cyanide research with a big budget, which aims at the development of sensitive and quick detecting techniques and effective anti -dotes in case of chemical accidents and terrorist attacks . The diffuse optical spectroscopy (DOS) technique is a non-inva-sive, quantitative measurement of physiological parameters and treatment responses . A cyanide detector that is suitable for field application to quick detection of blood cyanide is under development . The experimentally effective new antidotes for cy -anide exposure are cobinamide , 3 -mercaptopyruvate prodrug and their combined regimen . Compared with classic cyanide antidotes, these new drugs are highly effective , simply via oral or intramuscular administration.%美国政府和军队近年设立了多项氰化物相关的项目,旨在发生突发性化学事件和恐怖袭击时提供灵敏、快速的检测手段和及时、有效的救治措施.漫射分光技术无创,可定量测定有关生理终点指标和治疗反应,一种可野外使用的快速检测血氰化物水平的检测仪正处于立项研究阶段.正在研制的氰化物中毒救治药物主要有钴啉醇酰胺、3-巯基丙酮酸前体及两者的联合用药,较传统抗氰药高效,且可方便地经口服、肌注而达到治疗效果.

  13. Student Authority: Antidote to Alienation

    Science.gov (United States)

    Goodman, Joan

    2010-01-01

    The widespread disaffection of students from school is manifested in academic failure, indifference, and defiance. These problems can be alleviated, I argue, when an authority structure is developed that combines three components--freedom, power, and legitimacy. Authority understood as either power or freedom is apt to subvert students' school…

  14. 新型解毒剂T对异噁草松造成玉米药害的缓解作用%Study on the Action of Antidote T to the Injury of Clomazone on Maize Plant by Fluorescence Spectrophotometric Analysis

    Institute of Scientific and Technical Information of China (English)

    李晓薇; 李重九; 万春侯; 赵亚波; 宋淑玲; 张伟国

    2001-01-01

    After treating with clomazone and antidote T, the physiological changes of maize plants were studied by examining the dynamic characteristics of chlorophyll and fluorescence spectrum. The concentration of chlorophyll came down and the ratio of fluorescence strength to concentration of chlorophyll raised up as the concentration of clomazone increased. The injury from clomazone could be alleviated by antidote T.%通过测定植株叶绿素含量与荧光光谱特征动态变化,分析除草剂异噁草松和解毒剂T对玉米植株的生理作用。随着除草剂浓度升高,叶绿素浓度下降,单位叶绿素荧光强度比不断上升,而解毒剂T可缓解上述伤害。

  15. Illustrations from the Wellcome Library William Winstanley's pestilential poesies in "The Christians refuge: or heavenly antidotes against the plague in this time of generall contagion to which is added the charitable physician (1665)".

    Science.gov (United States)

    Miller, Kathleen

    2011-04-01

    During the Great Plague of London (1665), William Winstanley veered from his better known roles as arbiter of success and failure in his works of biography or as a comic author under the pseudonym Poor Robin, and instead engaged with his reading audience as a plague writer in the rare book The Christians Refuge: Or Heavenly Antidotes Against the Plague in this Time of Generall Contagion to Which is Added the Charitable Physician (1665). From its extensive paratexts, including a table of mortality statistics and woodcut of king death, to its temporal and providential interpretation of the disease between the covers of a single text, The Christians Refuge is a compendium of contemporary understanding of plague. This article addresses The Christians Refuge as an expression of London's print marketplace in a moment of transformation precipitated by the epidemic. The author considers the paratextual elements in The Christians Refuge that engage with the presiding norms in plague writing and publishing in 1665 and also explores how Winstanley's authorship is expressed in the work. Winstanley has long been seen as a biographer or as a humour writer; attributing The Christians Refuge extends and challenges previous perceptions of his work.

  16. Illustrations from the Wellcome Library William Winstanley’s Pestilential Poesies in The Christians Refuge: Or Heavenly Antidotes Against the Plague in this Time of Generall Contagion to Which is Added the Charitable Physician (1665)

    Science.gov (United States)

    MILLER, KATHLEEN

    2011-01-01

    During the Great Plague of London (1665), William Winstanley veered from his better known roles as arbiter of success and failure in his works of biography or as a comic author under the pseudonym Poor Robin, and instead engaged with his reading audience as a plague writer in the rare book The Christians Refuge: Or Heavenly Antidotes Against the Plague in this Time of Generall Contagion to Which is Added the Charitable Physician (1665). From its extensive paratexts, including a table of mortality statistics and woodcut of king death, to its temporal and providential interpretation of the disease between the covers of a single text, The Christians Refuge is a compendium of contemporary understanding of plague. This article addresses The Christians Refuge as an expression of London’s print marketplace in a moment of transformation precipitated by the epidemic. The author considers the paratextual elements in The Christians Refuge that engage with the presiding norms in plague writing and publishing in 1665 and also explores how Winstanley’s authorship is expressed in the work. Winstanley has long been seen as a biographer or as a humour writer; attributing The Christians Refuge extends and challenges previous perceptions of his work. PMID:21461312

  17. Estabilidad de la hidroxocobalamina en agua para inyección como antídoto contra cianuros: Elaborado de Farmacia Militar Stability of hydroxocobalamin in water for injection as cyanide antidote

    Directory of Open Access Journals (Sweden)

    J.J. Sánchez Ramos

    2012-06-01

    = 92,87% ± 6,08%; p = 0,95; n = 4; t = 472 días. La solución envasada en bolsas de polipropileno sufrió un efecto de concentración por pérdida de agua a través del envase. En los dos tipos de viales estudiados el contenido en hidroxocobalamina de la solución se mantuvo en el rango de aceptación especificado en la farmacopea: 102,09% ± 0,47% a 4º C y 102,35% ± 0,60% a 37º C para los viales COC; 101,64% ± 2,16% a 4ºC y 101,19 ± 1,75% a 37º C, para los viales de polipropileno (p = 0,95. El autoclavado de la solución a 115ºC durante 30 minutos redujo el porcentaje de hidroxocobalamina a valores fuera del rango de conformidad (95-115%. Conclusiones: La solución inyectable de cloruro de hidroxocobalamina en agua para inyección a la concentración indicada como antídoto N.B.Q. contra cianuros, lista para administrar, es estable a temperaturas inferiores a 25º C, al menos durante un periodo de 15 meses. Por su inercia química y propiedades físicas, los viales de polipropileno constituyen el envase más adecuado para esta solución, que no puede ser autoclavada, y debe ser preparada por vía aséptica sin esterilización terminal.Background: Cyanide has been used as an agent for chemical warfare, and today it is also a credible terrorism threat agent. Cyanide poisoning is the first cause of death in victims of smoke inhalation from enclosed space fires. Successful treatment for acute cyanide poisoning depends upon rapid antidotes administration, and fixation of the cyanide ion by antidotes. Hydroxocobalamin seems to be a more appropriate antidote than sodium nitrite for empiric treatment of smoke inhalation and other suspected cyanide intoxication victims in the out-of-hospital setting. Stability of hydroxocobalamin in water for injection at cyanide antidote dose has been studied throughout the time and in four types of containers. Methods: The parenteral solution was prepared by aseptic procedures without terminal sterilization, and according to the

  18. Effect and Mechanism of New Antidote in Protecting Maize from the Residual Injury of Chlorimuron%新型除草剂解毒剂减轻氯嘧磺隆残留对玉米的药害作用及机理

    Institute of Scientific and Technical Information of China (English)

    毕洪梅; 张金艳

    2012-01-01

    Maize Kenyu 6 was used as indicator plant to study the herbicide antidote N-dichloroacetyl-2-methyl-l-oxa-4-aza-spiro-4.4-nonane on protecting maize residual injury from chlorimuron by bioassay method. And discuss the mechanism of affection preliminarily. The results of experiment showed that, with the increase of chlorimuron concentration in soils, the growths of maize were inhibited. The harm of chlorimuron to maize, to some extent, reduced after soaking seeds in different concentration antidotes. The protection was the best when the residue of chlorimuron in soils was 2 μg/kg and the concentration of antidote was 5 mg/kg. The recovery rates of maize height and root length could reach 109.71% and 90.99%, the content of GSH and the activity of ALS also increased to 106.8% and 116.7%, respectively.%以垦玉6号玉米为试验材料,采用土培法研究新型除草剂解毒剂N-二氯乙酰基-2-甲基-1-氧杂-4-氮杂-螺[4.4]壬烷减轻除草剂氯嘧磺隆残留对玉米产生的药害,初步探讨其机理.研究结果表明,随土壤中氯嘧磺隆残留浓度增加,玉米生长受到抑制.采用不同浓度解毒剂浸种处理后,均可在一定程度上减轻氯嘧磺隆残留对玉米产生的药害.当土壤中氯嘧磺隆的残留浓度为2μg/kg,解毒剂的浸种浓度为5mg/kg时解毒效果最好,玉米株高和主根长的恢复率可达对照的109.71%和90.99%,幼苗中的谷胱甘肽(GSH)含量和乙酰乳酸合成酶活性(ALS)分别达到对照的106.8%和116.7%.

  19. 中医“治未病”理论与傣医“雅解”学说的初步比较研究%Preliminary comparative study of ‘treatment pre-disease' theory of traditional Chinese medicine and ‘antidote' theory of Dai medicine

    Institute of Scientific and Technical Information of China (English)

    唐琭璐; 周红黎; 郑进

    2012-01-01

    With the increasing health needs of people, modern medicine mode coordinating the relationship among person, nature and society is becoming popular. Dai medicine which is an important part of Chinese traditional medicine and traditional Chinese medicine are the treasure of Chinese culture. Both of them play an essential role on people's health. As the core theories, 'antidote' theory and the theory of 'treatment pre-disease' are also the highly generalization of prevention thought of traditional Chinese medicine and Dai medicine. The authors analyze and discuss the origins, theoretical basis, content and the use of 'treatment pre-disease' theory and 'antidote' theory in order to make them learn from each and promote their own development%随着人们对健康需求的日益提高,生理、心理和社会的现代医学模式更强调人、自然、社会的关系要协调一致,顺应自然、保健摄生,以减少疾病的发生.傣医学是我国传统医学的重要组成部分,与中医学同是中华民族传承的瑰宝,对各族人民的健康起到了至关重要的作用,而“治未病”理论与“雅解”学说分别是这两个医学的核心理论,也是中医学和傣医学预防思想的高度概括.笔者通过对“治未病”理论与“雅解”学说的起源、理论基础、内容及其运用进行分析和探讨,将两者相互借鉴学习,促进各自发展.

  20. Moral Relativism: A Philosopher's Antidote for Teachers

    Science.gov (United States)

    Jack, Henry

    1977-01-01

    The author identifies four main sources of moral relativism; defines cultural and ethical relativism, and social and personal moral relativism; and presents three arguments to refute moral relativism. (AV)

  1. Is There an Antidote to Perfectionism?

    Science.gov (United States)

    Greenspon, Thomas S.

    2014-01-01

    Within our competitive culture, some perfectionistic students do well, whereas others are overwhelmed. The personal characteristics of these perfectionistic students should not be construed as positive or adaptive perfectionism. A distinction is made between perfectionism and the pursuit of excellence. The intensity of the anxiety at the core of…

  2. Creative Reading: The Antidote to Readicide

    Science.gov (United States)

    Small, Ruth V.; Arnone, Marilyn P.

    2011-01-01

    Reading is often thought of as a skill, something to be learned and practiced. But reading can also be considered a creative art, capturing the imagination of the reader in ways that result in creative thought and expression. School librarians have a unique opportunity not only to support classroom-based reading skill building but also to serve as…

  3. Tough Talk as an Antidote to Bullying

    Science.gov (United States)

    Miller, Donna L.

    2012-01-01

    Locker rooms, hallways, and other school locales not populated by teachers are often places where bullies emerge, places where the pecking order is established by targeting any difference or idiosyncrasy. Given that bullying happens mostly in the presence of other youth and often stops when objections are raised, there is growing evidence that…

  4. Optical properties of graphene antidot lattices

    DEFF Research Database (Denmark)

    Pedersen, Thomas Garm; Flindt, Christian; Pedersen, Jesper Goor

    2008-01-01

    demonstrate that this artificial nanomaterial is a dipole-allowed direct-gap semiconductor with a very pronounced optical-absorption edge. Hence, optical infrared spectroscopy should be an ideal probe of the electronic structure. To address realistic experimental situations, we include effects due to disorder...

  5. The Liberal Arts, Antidote for Atheism

    Directory of Open Access Journals (Sweden)

    Heck Joel D.

    2014-12-01

    Full Text Available C. S. Lewis once stated that the decline of classical learning was a contributory cause of atheism. This article explores why he made this very unusual statement, describing how Lewis saw the Classics as a literature full of gods and goddesses, providing hints of truth, giving us things to write about, and preparing for the Christian faith. Using some remarkable quotations from Virgil and Plato, Lewis demonstrated how those writers anticipated both the birth and the death of Christ. Lewis’s concept of myth, powerfully present in the Classics, shows how the Gospel story itself is a “true myth,” one with a pattern that is similar to many of the pagan myths. The personal story of Lewis himself demonstrates how the Classics, and, more broadly, the liberal arts were a testimony to the truth of God and how the Greek plays of Euripides, the philosophy of Samuel Alexander, the imagination of writer William Morris, the poetry of George Herbert, and the historical sensibility of G. K. Chesterton combined (with many other similar influences to convince Lewis that the death and resurrection of Jesus Christ were especially a “true myth,” one that happened in history, demonstrating him to be the Son of God.

  6. Synthesis of Key Intermediate of Antidote HPPPD

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>Nerve agents are organophosphorus compounds (OPs) which are misused as chemical warfare agents for military and terrorism. Exposure to even small amounts of nerve agents such as tabun, soman, sarin,

  7. Clar sextets in square graphene antidot lattices

    DEFF Research Database (Denmark)

    Petersen, Rene; Pedersen, Thomas Garm; Jauho, Antti-Pekka

    2011-01-01

    A periodic array of holes transforms graphene from a semimetal into a semiconductor with a band gap tuneable by varying the parameters of the lattice. In earlier work only hexagonal lattices have been treated. Using atomistic models we here investigate the size of the band gap of a square lattice...

  8. Competitive intelligence: An antidote to downsizing

    Energy Technology Data Exchange (ETDEWEB)

    Montgomery, G.E.; Spiers, J.P.

    1996-03-15

    This article is a review of the efforts of a number of utilities to use state-of-the-art information systems to improve their operations. Of note is: (1) BellSouth Telecommunications` plans to automate its manual outside-plant engineering and design process, (2) West Ohio Gas Company`s plans to develope software packages for DOT reporting and analysis, pressure control and analysis, customer complaint tracking, and emergency response, and (3) Kentucky Utilities Company`s use of information technology to improve its trouble-outage management capability, contain the operational costs of growth by increasing labor efficiency, and provide more accurate and timely information to enhance customer service.

  9. Prosperity: The Antidote to Radical Islam

    Science.gov (United States)

    2009-04-01

    India, the Kurdistan Workers Party (PKK) versus Turkey, Chechen Separatists against Russia, and the Kashmir Separatists against India. Their...has yet appeared…” 61 Others masterfully illustrate the devastating waste of not only human lives, but of industry, art , ingenuity, wealth, and...Muslim women is disturbing. Additionally, inquisitive youths playing rock -n-roll like music or surfing the internet are often arrested in Iran

  10. Coffee as an Antidote to Knowledge Stickiness

    Science.gov (United States)

    Blackman, Deborah; Phillips, Diane

    2011-01-01

    This paper considers the concept of space and its role in both knowledge creation and overcoming knowledge stickiness. Aristotelian concepts of "freedom to" and "freedom from" are used to reconceptualise space. Informal and formal spaces, concepts and places are discussed as both specific locations and as gaps providing space for knowledge…

  11. Regular Exercise: Antidote for Deadly Diseases?

    Science.gov (United States)

    ... aging, and an increasing number of cardiovascular and diabetes deaths since 1990, greater attention and investments in interventions to promote physical activity in the general public is required," lead author ...

  12. 2015年下半年美国FDA批准的新分子实体与评价:呼吸、血液和代谢系统疾病治疗用药以及解毒剂%Updates of New Molecular Entities Approved by the FDA in the Second-Half of 2015:Respiratory, Hematology, Metabolic Diseases and Antidotes

    Institute of Scientific and Technical Information of China (English)

    孙树森; 赵志刚

    2016-01-01

    2015年下半年,FDA批准了31个新分子实体和新生物制品。本文将介绍和评价呼吸、血液和代谢系统疾病治疗用药以及解毒剂。%The US FDA approved 31 new molecular entities and new therapeutic biological products in the second-half of 2015. This article provides an update and evaluation of the new drugs approved for the treatment of respiratory, hematology and metabolic diseases,and antidotes.

  13. Effect of Antidote Tongyu Fushen Decoction on the level of urine CTGF of the phase Ⅰ-Ⅲ chronic nephritis patients%解毒通瘀复肾汤对慢性肾脏病1-3期患者尿CTGF水平的影响

    Institute of Scientific and Technical Information of China (English)

    蓝健姿; 严晓华; 阮诗玮; 金一顺; 张雪梅

    2012-01-01

    Objective: To observe the curative effect of Antidote Tongyu Fushen Decoction and Western medicine on chronic nephritis phase Ⅰ-Ⅲ patients, then explore the effective method to postpone chronic nephritis fibrosis. Methods: Patients were randomly divided into two group, the treatment group were taken Antidote Tongyu Fushen Decoction and Western medicinon(exclude Lotensin or Valsartan capsule), and the control group received Lotensin or Valsartan capsule. Results: There is not much difference between the two groups' curative effect, but the improvement of the treatment group's TCM symptoms is much better than the control group' s(P<0.05). Conclusion: The curative effect of combination of TCM and Western medicine is the same as that of pure Western medicine on the effectively reduction of the levels of urine protein and urine CTGF. But on the fact of the improvement of the TCM symptoms, the curative effect of combination of TCM and Western medicine is superior to that of pure Western medicine.%目的:观察解毒通瘀复肾汤配合西药治疗慢性肾脏病1-3期患者的疗效,探讨延缓慢性肾炎纤维化的有效方法.方法:90例患者随机分为两组,治疗组用解毒通瘀复肾汤加减配合西药,对照组用洛汀新或代文.结果:两组在总体疗效上无显著性差异,但治疗组在中医证候积分改善上明显优于西药对照组(P<0.05).结论:中西医结合治疗和单纯西药治疗均能够有效减低尿蛋白和尿结缔组织生长因子(CTGF)的水平,缓解慢性肾炎纤维化的进程,但是中西医结合治疗在改善中医症候上相对西药治疗更加有优势.

  14. The "Poison" and "Antidote" of Historical Heritage be-hind the Reality:Comment on "Statement of Confession"by Qiao Ye%现实背后历史传承的“毒”与“解”--评乔叶的《认罪书》

    Institute of Scientific and Technical Information of China (English)

    高雅

    2015-01-01

    《认罪书》无论从故事背景还是“因果报应”的逻辑而言,都是一个典型的中国传统故事,但乔叶思想的核心却围绕着“原罪”和“忏悔”“赎罪”这几个来自基督文化的词汇。“原罪”是毒,“忏悔”和“赎罪”是解,这不仅是乔叶对主人公金金及梁家人经历的提炼,也是她对于“文革”的历史和病相丛生的当下所作的见解。乔叶的观点中“忏悔”需要“认知、认证、认定、认领、认罚这些罪”,较之当代女性作家的同类主题作品,乔叶对“忏悔”和“赎罪”有更为深刻广阔的认识,但也存在着“忏悔”意识能否本土化的问题。%Viewing from not only the background of its story, but also the logic of"punitive justice","Statement of Confession"is a typical traditional Chinese story, but the core of Qiao Ye's thought revolves around such Christian words as "original sin", "repen-tance" and "atonement". "Original sin" is a poison, while "re-pentance" and "atonement" are the antidote, which is not only Qiao Ye's abstraction of the experiences of the hero Jin Jin and the Liang family, but also her view on"The Cultural Revolution"and the pathological situation at that time. In Qiao Ye's opinion,"repentance"needs"knowing, attesting, affirming, claiming these sins and taking punishment". Compared with contemporary fe-male writers' works of the same topic, Qiao Ye has a more pro-found recognition of"repentance"and"atonement", but whether the consciousness of"repentance"can be localized is a problem.

  15. 二巯基丙磺酸钠对杀虫单中毒小鼠琥珀酸脱氢酶的保护作用%Protective antidotal effects of 2.3-D imercaptopr opane-1-sulfonate sodium on the Succinate dehydrogenase activities in acute So d ium ammonium dimethyl-2-propano-1.3-dithiosulfate monohydrate intoxication mice

    Institute of Scientific and Technical Information of China (English)

    陈秀芳; 王佳珍; 胡国新; 林丹; 陈醒言

    2001-01-01

    Objective:To investigate the mechanism of acute Sodium ammonium dimethyl-2-propano-1.3-dithiosulfate monohydrate(SC D) p oison and the protective antidotal effects of 2.3-Dimercaptopropane-1-sulfona te sodium(Na-DMPS) on Succinate dehydrogenase(SDH) activities in mice.Methods:The mice were randomly divided into three groups: Contr ol group, SCD group, (Na-DMPS) group. The activities of Succinate dehydrogenas e (SDH) in mitochondria of liver and myocardium and Lactic dehydrogenase(LDH) acti vities in plasma of three groups were determined.Results:SDH decreased significantly (P<0.05) an d LDH increased remarkably (P<0.001) in SCD group compared with those of control group. SDH enha nced obviously (P<0.05) and LDH reduced notably (P<0.001) in (Na-DMPS + SCD) group than those of SCD group.Conclusion:SCD could inhibit the activities of SDH of mitochond ria consequently suppressing cell respiration in mice. Na-DMPS could antagonize significantly the inhibiting effects of SCD on the activities of SDH. This ant agonistic actions play an important role in preventing and curing SCD pois on.%目的:研究杀虫单(SCD)的中毒机理及二巯基 丙磺酸钠(Na-DMPS)对琥珀酸脱氢酶(SDH)的保护作用。方法:小鼠随机分为三组:对照组、SCD 组、(Na-DMPS + SCD)组。观察三 组小鼠肝及心肌线粒体琥珀酸脱氢酶(SDH)、血浆乳酸脱氢酶(LDH)活力的变化。结果:与对照组相比,SCD 组SDH活力显著下降(P<0.05), LDH 明显升高(P<0 .001);( Na-DMPS + SCD )组SDH活力较SCD组明显升高(P<0.05),LDH显 著降低(P<0.001) 。结论:SCD可抑制线粒体 SDH活力,抑制细胞呼吸。Na-DMPS 可拮抗其抑制 作用,这种拮抗作用在防治SCD中毒方面具有重要意义。

  16. 黄连解毒汤抑制NF-κB激活减轻心肌缺血再灌注损伤%Antidotal Decoction of Coptis reduces myocardial ischemia/reperfusion injury by inhibiting activation of NF-κB

    Institute of Scientific and Technical Information of China (English)

    付晓春; 陈建军; 王舰平

    2012-01-01

    Objective To study the protective effect of Antidotal Decoction of Coptis(ADC) on myocardial ischemia/reperfusion(I/R) injury and its mechanism. Methods A SD rat myocardial I/R injury model was established. Fifty-six SD male rats were randomly divided into sham operation group, myocardial I/R group, 1% CMC-Na control group, and low dose ADC group, medium dose ADC group, high dose ADC group, and composite red sage root group. The rats were given drugs for successive 7 days. The myocardial I/R injury model was replicated 24h after the last drug administration. SOD activity, MDA level, and myocardial infarct area were measured 40min after reperfusion to judge the protective effect of ADC on myocardium. Myocardial tissue sample was taken to measure the nuclear transcription activity of NF- k B. Results Forty minutes after reperfusion, the SOD activity, MDA level and myocardial infarct area were obviously improved in experimental groups, the nuclear transcription activity of NF- k B was significantly lower in experimental groups than in control group. Conclusion ADC protects rats against myocardial I/R injury by inhibiting the activation of NF- k B.%目的 观察黄连解毒汤(huanglian jiedu decoction,HLJDT)对大鼠心肌缺血再灌注的保护作用,进一步探讨黄连解毒汤心肌保护作用的机制.方法 采用SD大鼠心肌缺血再灌注模型(I/R),将56只SD大鼠随机等分为7组:假手术组、心肌缺血再灌注组、溶剂(1% CMC-Na)对照组、黄连解毒汤低剂量组、HLJDT中剂量组、HLJDT高剂量组,复方丹参阳性对照组,连续给药7d,末次给药24h后,复制大鼠心肌I/R损伤模型.再灌注40min后测定心肌组织超氧化物歧化酶(SOD)活性及MDA含量和心肌梗死面积,以判定黄连解毒汤对心肌的保护作用;取心肌组织测定NF-κB核转录活性.结果 再灌注40min后,实验组较缺血再灌注对照组心肌SOD活性、丙二醛(MDA)含量和梗死面积有明显改善;实验组较缺血再

  17. Investigation of the effect of regulating blood antidotal decoction on psoriatic peripheral blood vascular endothelial growth factor level%理血解毒类方对银屑病患者外周血血管内皮生长因子水平的影响

    Institute of Scientific and Technical Information of China (English)

    郝远荣

    2015-01-01

    目的:探讨理血解毒类方对银屑病患者外周血血管内皮生长因子水平的影响。方法:2012年3月-2013年3月收治寻常型银屑病患者100例,根据证候将患者分为血瘀型组、血燥型组和血热型组,其中血瘀型26例,血燥型30例,血热型44例。对照组无银屑病,共35例。使用酶联免疫吸附法检测口服活血解毒汤、养血解毒汤及凉血解毒汤前后患者的血清 VEGF 水平。结果:银屑病患者血清 VEGF 水平在治疗前较对照组明显升高,差异具有统计学意义(P<0.05),血燥型银屑病组治疗前血清VEGF显著低于血热型组,差异具有统计学意义(P<0.05);血热型组与血瘀型组比较差异无统计学意义(P>0.05);血燥型组与血瘀型组比较血清VEGF差异无统计学意义(P>0.05)。中药治疗后血燥型和血热组血清VEGF明显降低(P<0.05),经中药治疗后血瘀型组血清VEGF与治疗前比较差异无统计学意义(P>0.05)。结论:银屑病与VEGF变化具有特异性。养血解毒方、凉血解毒方治疗血燥型和血热型银屑病的机制可能为抑制血管生成。%Objective:To explore the influence of regulating blood antidotal Decoction on psoriatic peripheral blood vascular endothelial growth factor level.Methods:100 patients with psoriasis vulgaris were selected from March 2012 to March 2013.They were divided into the blood dry group with 30 cases, blood heat type with 26 cases and blood stasis type group with 44 cases.35 cases without psoriasis were as the control group.We used enzyme linked immunosorbent assay detected the serum VEGF level of the patients before and after oral Huo Xue Jie Du decoction,detoxification decoction and Liang Xue Jie Du decoction.Results:The serum VEGF level in patients with psoriasis vulgaris before treatment was significantly higher than the control group,with significant difference(P0.05).The level of serum VEGF of blood dryness type group and

  18. Effects of Glucose Oxidase on Growth Performance, Serum Parameters and Slaughter Performance of Meat Ducks and Its Antidotal Effect on Aflatoxin B1%葡萄糖氧化酶对肉鸭生长性能、血清指标和屠宰性能的影响及其解除黄曲霉毒素 B1效果

    Institute of Scientific and Technical Information of China (English)

    汤海鸥; 高秀华; 姚斌; 张广民; 王振兴; 李晓存

    2015-01-01

    This experiment was conducted to investigate the effects of diets supplemented with glucose oxidase ( GOD) on growth performance, serum parameters and slaughter performance of meat ducks and its antidotal effect on aflatoxin B1. A total of 100 Cherry Valley ducks (1-day-old) were randomly assigned to five groups with four replicates of fifty ducks in each replicate. The control group ( groupⅠ) was fed on a basic diet. The two test groups ( groupsⅡandⅢ) were fed on basic diet supplelemted with 100 and 200 g/t GOD. Aflatoxin B1 control group ( groupⅣ) was fed on basic diet with moldy corn. The groupⅤwas fed on the contaminated diet with 200 g/t GOD. The experiment lasted for 46 days. The results showed as follows:1) the average dai-ly gain and ratio of feed to gain of ducks in groupsⅡ andⅢ were significantly better than those in the control group ( P0.05) . The experiment indicated that the growth performance of ducks fed on basic diet can be significantly im-proved by supplementing GOD. The growth performance, serum parameters, slaughter performance and mor-tality rate of ducks fed diet with aflatoxin B1 can be improved by supplementing GOD.%本试验旨在研究饲粮中添加葡萄糖氧化酶( GOD)对肉鸭生长性能、血清指标和屠宰性能的影响及其解除黄曲霉毒素B1(AFB1)的效果。选用1000只健康的1日龄樱桃谷鸭,随机分为5个组,每组4个重复,每个重复50只鸭。Ⅰ组为对照组,饲喂基础饲粮;Ⅱ、Ⅲ组分别在基础饲粮中添加100和200 g/t GOD;Ⅳ组为混有AFB1超标玉米的攻毒组;Ⅴ组在Ⅳ组饲粮中添加200 g/t GOD。试验期46 d。结果表明:1)与对照组相比,Ⅱ、Ⅲ组显著提高了平均日增重( P0.05),显著低于其他各组(P<0.05)。由此可见,常规饲粮中添加GOD能显著改善肉鸭生长性能,添加GOD可改善AFB1攻毒肉鸭的生长性能、屠宰性能和血清指标,降低死亡率。

  19. Thallium Toxicity: The Problem; An Analytical Approach; An Antidotal Study

    Science.gov (United States)

    1993-05-15

    Possible toxic mechanisms of T1 include ligand formation with protein sulfhydryl groups, inhibition of cellular respiration, interaction with riboflavin ...and riboflavin -based cofactors, and disruption of calcium homeostasis. The principal clinical features of thallotoxicosis are gastroenteritis...anticorrosive), optical lenses (increases refractive index), low-temperature thermometers, dye and pigments (artist paints), semiconduc- tors, superconducting

  20. Tissue Protecting Antidotes From Anti-Apoptotic Factors of Mycoplasma

    Science.gov (United States)

    2005-12-12

    yeast, spirochetes and fungi . It was previously demonstrated that the diacyl-Lpp MALP2 from M. fermentas (as well from another Mycoplasma ssp...effects of anticancer therapy. Iin 1999 he defined p53 as a major determinant of cancer treatment side effects and suggested this protein as a target for

  1. Animal Models for Testing Antidotes Against an Oral Cyanide Challenge

    Science.gov (United States)

    2016-08-01

    transit time of the GI tract is 12 to 24 hours in an adult rat. The liver has four lobes: median, right lateral, left, and caudate. A deep fissure for...Department of Health and Human Services, Public Health Service, Agency for Toxic Substances and Disease Registry. Toxic Substance Portal web site...Toxic profile web site for cyanide; available at: http://www.atsdr.cdc.gov/substances/toxsubstance.asp?toxoid=19; http://www.atsdr.cdc.gov/ToxProfiles

  2. An Antidote for the Faculty-IT Divide

    Science.gov (United States)

    Fernandez, Luke

    2008-01-01

    Do campus IT departments harm higher education? Wall Street Journal personal-technology columnist Walt Mossberg suggested as much during a speech he gave to high-level administrators at last June's Chronicle of Higher Education presidents' forum. Mossberg caught the attention of campus CIOs when, according to the Chronicle, he described large IT…

  3. A Ghetto Land Pedagogy: An Antidote for Settler Environmentalism

    Science.gov (United States)

    Paperson, La

    2014-01-01

    A ghetto land pedagogy begins with two axioms that align it with land education more broadly, and that distinguish it from the general umbrella of environmental education. First, ghetto colonialism is a specialization of settler colonialism. Second, land justice requires decolonization, not just environmental justice. A ghetto land pedagogy thus…

  4. Recent Developments in Anti-dotes Against Anthrax.

    Science.gov (United States)

    Dhasmana, Neha; Singh, Lalit K; Bhaduri, Asani; Misra, Richa; Singh, Yogendra

    2014-01-01

    The etiologic agent of disease anthrax, Bacillus anthracis, causes recurrent outbreaks among the livestock and intermittent infections in humans across the world. Controlling animal infections by vaccination can minimize the incidence of disease in humans. Prevention of anthrax in occupationally exposed personnel is achieved through vaccination with either live spores or precipitates of culture supernatants from attenuated strains of B. anthracis. However, anthrax vaccination of the large human population is impractical as well as inappropriate. Broad-range antibiotics like amoxicillin, ciprofloxacin, clindamycin, streptomycin, and penicillin G are recommended for the treatment of human anthrax infections, but the threat of antibiotic resistant strains always remains. Moreover, in the absence of any specific symptom (s) during early infection, the diagnosis of anthrax is delayed causing elevated levels of anthrax toxin component which could be fatal. For these reasons, there is a need to develop new antimicrobial agents against virulent B. anthracis to effectively combat this fatal pathogen. Over the last two decades, extensive studies have been carried out to develop specific inhibitors against virulence factors of B. anthracis such as capsule, protective antigen, lethal factor and edema factor. Research has also been focused in developing inhibitors of anthrax toxin receptors (including the use of receptor decoys) and host furin endoproteases which are required for activation of toxin. This review highlights the recent progress made in developing the diverse countermeasures for anthrax infections targeting B. anthracis virulence factors and their counterparts in host.

  5. Secondary Physical Education Avoidance and Gender: Problems and Antidotes

    Science.gov (United States)

    Ryan, Thomas; Poirier, Yves

    2012-01-01

    Our goal was to locate and evaluate the barriers that impact and cause females to avoid secondary elective physical education courses. We sought to find answers to stop the further decline of female enrolment in secondary physical education by looking into curricula, program and instructional variables. Anecdotal evidence informed this study which…

  6. Antidotes for novel oral anticoagulants: current status and future potential.

    Science.gov (United States)

    Crowther, Mark; Crowther, Mark A

    2015-08-01

    The direct thrombin inhibitor dabigatran and the anti-Xa agents rivaroxaban, edoxaban, and apixaban are a new generation of oral anticoagulants. Their advantage over the vitamin K antagonists is the lack of the need for monitoring and dose adjustment. Their main disadvantage is currently the absence of a specific reversal agent. Dabigatran's, unlike the anti-Xa agents, absorption can be reduced by activated charcoal if administered shortly after ingestion and it can be removed from the blood with hemodialysis. Prothrombin complex concentrate, activated prothrombin complex concentrate, and recombinant factor VIIa all show some activity in reversing the anticoagulant effect of these drugs but this is based on ex vivo, animal, and volunteer studies. It is unclear, which, if any, of these drugs is the most suitable for emergency reversal. Three novel molecules (idarucizumab, andexanet, and PER977) may provide the most effective and safest way of reversal. These agents are currently in premarketing studies.

  7. SECONDARY PHYSICAL EDUCATION AVOIDANCE AND GENDER: PROBLEMS AND ANTIDOTES

    Directory of Open Access Journals (Sweden)

    Thomas Ryan

    2012-07-01

    Full Text Available Our goal was to locate and evaluate the barriers that impact and cause females to avoid secondary elective physical education courses. We sought to find answers to stop the further decline of female enrolment in secondary physical education by looking into curricula, program and instructional variables. Anecdotal evidence informed this study which was very much exploratory, building upon several key facts. First, Ontario (Canada secondary students are only required to take one credit (course in physical education in order to graduate and second, most students take the required physical education course in grade nine which is their first year of high school. Following this there is an average of 10% fewer females in every physical education class in the province of Ontario and only an average of 12% are enrolled in physical education each year. Several issues were identified and explored including self-confidence; motivation; perceived value of physical activity; opportunities for physical activity; marking scheme; competition; co-ed classes; teaching approach; and peers as possible problems and solutions.

  8. Co-Operation: The Antidote to Isolated Misery

    Science.gov (United States)

    Jones, Sarah

    2013-01-01

    This is a case study demonstrating the impact the co-operative movement has had on one co-operative school in south-west England. Lipson Co-operative Academy in Plymouth was one of the first schools to convert to become a co-operative school in 2009. The article has been co-written by members of the Academy and focuses on three transformational…

  9. Poisson distributions for sharp-time fields antidote for triviality

    CERN Document Server

    Klauder, J R

    1995-01-01

    Standard lattice-space formulations of quartic self-coupled Euclidean scalar quantum fields become trivial in the continuum limit for sufficiently high space-time dimensions, and in particular the moment generating functional for space-time smeared fields becomes a Gaussian appropriate to that of a (possibly generalized) free field. For sharp-time fields this fact implies that the ground-state expectation functional also becomes Gaussian in the continuum limit. To overcome these consequences of the central limit theorem, an auxiliary, nonclassical potential is appended to the original lattice form of the model and parameters are tuned so that a generalized Poisson field distribution emerges in the continuum limit for the ground-state probability distribution. As a consequence, the sharp-time expectation functional is infinitely divisible, but the Hamiltonian operator is such, in the general case, that the generating functional for the space-time smeared field is not infinitely divisible in Minkowski space. Th...

  10. Resilience, Flexibility and Adaptive Management - - Antidotes for Spurious Certitude?

    Directory of Open Access Journals (Sweden)

    Lance Gunderson

    1999-06-01

    Full Text Available In many cases, a predicate of adaptive environmental assessment and management (AEAM has been a search for flexibility in management institutions, or for resilience in the ecological system prior to structuring actions that are designed for learning. Many of the observed impediments to AEAM occur when there is little or no resilience in the ecological components (e.g., when there is fear of an ecosystem shift to an unwanted stability domain, or when there is a lack of flexibility in the extant power relationships among stakeholders. In these cases, a pragmatic solution is to seek to restore resilience or flexibility rather than to pursue a course of broad-scale, active adaptive management. Restoration of resilience and flexibility may occur through novel assessments or small-scale experiments, or it may occur when an unforeseen policy crisis allows for reformation or restructuring of power relationships among stakeholders.

  11. Moral Intelligence: An Antidote to Examination Malpractices in Nigerian Schools

    Science.gov (United States)

    Olusola, Olayiwola Idowu; Ajayi, Oluwagbemiga Samson

    2015-01-01

    Moral intelligence is the capacity to apply moral principles to one's own values, goals and actions (or the ability to see what is right and integrate it into one's life and actions) It is considered as the individual capacity to understand right from wrong, to have strong ethical convictions and to act on them to behave in the right and…

  12. Global Financial Regulations:An Antidote to Economic Predicament

    Institute of Scientific and Technical Information of China (English)

    BIN; ZHANG

    2014-01-01

    Due to the lack of public order in the international financial arena, asset bubbles and resource misallocations persisted over a long period of time and resulted in global financial crisis in 2008. Global financial rules, which can take on a role like that of WTO in the international trade, are urgently needed for global economic recovery. They will balance the pressure of economic restructuring between large and small countries, and push forward some countries’ domestic reforms which may hardly be implemented due to domestic politics.

  13. Migration as an antidote to rent-seeking?

    OpenAIRE

    Mariani, Fabio

    2007-01-01

    International audience; We develop a new mechanism through which skilled migration may influence economicperformance in the sending country. If agents can choose between acting asrent-seekers and engaging in productive activities, and only productive skills are exportable,a positive probability of migration (to a more secure economy) reduces therelative expected returns from rent-seeking, thus decreasing the proportion of skilledworkers who opt for ”parasitic” activities. Such an improvement ...

  14. Selenium as an antidote in the treatment of mercury intoxication.

    Science.gov (United States)

    Bjørklund, Geir

    2015-08-01

    Selenium (Se) is an essential trace element for humans. It is found in the enzyme glutathione peroxidase. This enzyme protects the organism against certain types of damage. Some data suggest that Se plays a role in the body's metabolism of mercury (Hg). Selenium has in some studies been found to reduce the toxicity of Hg salts. Selenium and Hg bind in the body to each other. It is not totally clear what impact the amount of Se has in the human body on the metabolism and toxicity of prolonged Hg exposure.

  15. And another thing .... an antidote to anti-oil

    Energy Technology Data Exchange (ETDEWEB)

    Flatern, R. von

    2002-02-26

    It has long been clear to the most casual observer that the offshore oil industry is not well loved in the US. A steady diet of uninformed news reportage, Hollywood distortions and political rhetoric, has understandably left many Americans with the impression the industry is a monument to greed run by a small but powerful cabal anxious to sacrifice the environment to their god: profit. (author)

  16. Knowledge as an antidote to environmental degradation; Kunnskap som motgift

    Energy Technology Data Exchange (ETDEWEB)

    Aakervik, Anne-Lise

    2001-07-01

    In many developing countries, hundreds of thousands of tonnes of old pesticides and toxic waste are out of control. Pollution of air, water and food is a common cause of early death in many developing countries. According to The Food and Agriculture Organisation of the United Nations (FAO), 500 000 tonnes of obsolete, useless and prohibited pesticides exists on a global scale. Putting this matter straight is an international priority. The present article briefly reviews some Norwegian engagement in training Vietnamese professionals in mapping, handling and destruction of pesticides. Such efforts are especially important in an essentially agricultural society in which half of the population is living below the poverty level.

  17. Adaptable educational courseware : an antidote to several portability problems

    NARCIS (Netherlands)

    De Diana, I.P.F.; Vries, de S.A.

    1990-01-01

    The concepts of adaptability and portability of educational software and courseware seem to be interwoven in several respects. This article explores these interrelationships in some detail, based upon the presumption that adaptable educational products are also more portable. A conceptual framework

  18. Skewed gas flow technology offers antidote to opacity derates

    Energy Technology Data Exchange (ETDEWEB)

    Boyd, M. [ATCO Power AB (Canada). Battle River Generating Station

    2001-06-01

    Deratings due to opacity problems at the Battle River Generating Station in Alberta, Canada led ATCO Power to evaluate and install skewed gas flow technology (SGFT) in one-half of the Unit 5 twin-casing electrostatic precipitator during the August 2000 outage. Preliminary operating results show that the modified casing produces opacity readings at the outlet 40% lower than those seen at the outlet of the unmodified casing. The dust loading tests indicate a 27.5% improvement in collector efficiency. This article includes a technical review and evaluation of Battle River's SGFT installation, as well as the rationale used to provide the initial economic justification. 3 figs., 1 tab., 1 photo.

  19. Continuous renal replacement therapy circuit failure after antidote administration.

    Science.gov (United States)

    Jeong, Jinwoo

    2014-12-01

    A 73-year-old man was transferred to the emergency department (ED). He was found unconscious in his house along with an empty 200-mL bottle of Basta(™), a herbicide containing 18% glufosinate. He was comatose with a Glasgow Coma Scale score of 3. As his blood pressure dropped to 60/30 mmHg despite fluids and norepinephrine, 20% intravenous fat emulsion product was injected. He experienced repeated cardiopulmonary arrests during his first 4 h in the ED. When the arrests occurred, standard cardiopulmonary resuscitation was performed, and boluses of fat emulsion were given. He was given a total of 1500 mL of 20% fat emulsion. In an attempt to correct the acidosis, continuous renal replacement therapy (CRRT) was started. Within 5 min of starting CRRT, the transmembrane pressure increased sharply and the machine stopped.

  20. Development and Efficacy Testing of Next Generation Cyanide Antidotes

    Science.gov (United States)

    2013-10-01

    13 II.1.1.2. Formulations based on Cyclodextrines , Co-Solvents and Surfactants: First attempt focused on a micellar encapsulation of DMTS. For...molar ratio 1:1) Figure 2. Solubility of DMTS in cyclodextrin solutions Figure 3. Solubility of DMTS in various co-solvents at increasing...paclitaxel. Therefore, the aim of the present study was to prepare and characterize micelles encapsulating DMTS (mDMTS) which would simultaneously

  1. Caramiphen edisylate: an optimal antidote against organophosphate poisoning.

    Science.gov (United States)

    Raveh, Lily; Eisenkraft, Arik; Weissman, Ben Avi

    2014-11-05

    Potent cholinesterase inhibitors such as sarin, induce an array of harmful effects including hypersecretion, convulsions and ultimately death. Surviving subjects demonstrate damage in specific brain regions that lead to cognitive and neurological dysfunctions. An early accumulation of acetylcholine in the synaptic clefts was suggested as the trigger of a sequence of neurochemical events such as an excessive outpour of glutamate and activation of its receptors. Indeed, alterations in NMDA and AMPA central receptors' densities were detected in brains of poisoned animals. Attempts to improve the current cholinergic-based treatment by adding potent anticonvulsants or antiglutamatergic drugs produced unsatisfactory results. In light of recent events in Syria and the probability of various scenarios of military or terrorist attacks involving organophosphate (OP) nerve agent, research should focus on finding markedly improved countermeasures. Caramiphen, an antimuscarinic drug with antiglutamatergic and GABAergic facilitating properties, was evaluated in a wide range of animals and experimental protocols against OP poisoning. Its remarkable efficacy against OP exposure was established both in prophylactic and post-exposure therapies in both small and large animals. The present review will highlight the outstanding neuroprotective effect of caramiphen as the optimal candidate for the treatment of OP-exposed subjects.

  2. Exercise: an Antidote for Behavioral Issues in Students?

    Science.gov (United States)

    ... recess, new exercise programs could be a tough sell, both Verduin and Bowling said. But, Bowling said, " ... Center, New York City; Jan. 9, 2017, Pediatrics , online HealthDay Copyright (c) 2017 HealthDay . All rights reserved. ...

  3. Pretreatment with pyridinium oximes improves antidotal therapy against tabun poisoning.

    Science.gov (United States)

    Lucić Vrdoljak, Ana; Calić, Maja; Radić, Bozica; Berend, Suzana; Jun, Daniel; Kuca, Kamil; Kovarik, Zrinka

    2006-11-10

    Oximes K033 [1,4-bis(2-hydroxyiminomethylpyridinium) butane dibromide] and K048 [1-(4-hydroxyiminomethylpyridinium)-4-(4-carbamoylpyridinium) butane dibromide] were tested as pretreatment drugs in tabun-poisoned mice followed by treatment with atropine plus K033, K048, K027 [1-(4-hydroxyiminomethylpyridinium)-3-(4-carbamoylpyridinium) propane dibromide], TMB-4 [1,3-bis(4-hydroxyiminomethylpyridinium) propane dibromide] and HI-6 [(1-(2-hydroxyiminomethylpyridinium)-3-(4-carbamoylpyridinium)-2-oxapropane dichloride)]. Oxime doses of 25% or 5% of its LD(50) were used for pretreatment 15 min before tabun-poisoning and for treatment 1 min after tabun administration to mice. The best therapeutic effect was obtained when oxime K048 (25% of its LD(50)) was used in both pretreatment and treatment with atropine. This regiment insured survival of all tested animals after the application of 10 LD(50) of tabun. In addition, since butyrylcholinesterase (BChE; EC 3.1.1.8) is considered an endogenous bioscavenger of anticholinesterase compounds and its interactions with oximes could be masked by AChE interactions, we evaluated kinetic parameters for interactions of tested oximes with native and tabun-inhibited human plasma BChE and compared them with results obtained previously for human erythrocyte acetylcholinesterase (AChE; EC 3.1.1.7). Progressive inhibition of BChE by tabun was slightly faster than that of AChE. The reactivation of tabun-inhibited BChE by oximes was very slow, and BChE binding affinity for oximes was lower than AChE's. Therefore, BChE could scavenge tabun prior to AChE inhibition, but fast oxime-assisted reactivation of tabun-inhibited AChE or protection of AChE by oxime against inhibition with tabun would not be obstructed by interaction between BChE and oximes.

  4. Reality Therapy as an Antidote to Burn-Out.

    Science.gov (United States)

    Wubbolding, Robert E.; Kessler-Bolotin, Else

    1979-01-01

    Counselor burn-out is characterized by feelings of frustration, rigidity, omnipotence, and the like. Reality therapy uses systematic plans to increase love, worth, fun, and self-discipline to deal effectively with burn-out. (Author)

  5. Antidote for Zero Tolerance: Revisiting a "Reclaiming" School.

    Science.gov (United States)

    Farner, Conrad D.

    2002-01-01

    Reports on a revisit to the Frank Lloyd Wright Middle School, which implemented strategies to deal with disciplinary problems. The school continues to progress towards creating the type of reclaiming environment necessary to ensure the needs of all students. Strategies used include alternatives to zero tolerance policy; smaller teams of students;…

  6. Host Response to Botulinum Neurotoxins for Developing Diagnostics and Antidotes

    Science.gov (United States)

    2009-09-18

    difficile 630, Clostridium perfringens ATCC13124, Clostridium perfringens str. 13, Clostridium tetani E88, Clostridium thermocellum ATCC27405. The...proteins produced by Clostridium botulinum in seven immunologically distinct serotypes named A to G. BoNTs being the causative agents of the most...8 Sequence Analysis of P-250 protein Based on the N-terminal sequence of P-250, we used the codon usage table of Clostridium botulinum Hall-A

  7. George Herbert Mead on consciousness: antidote to Cartesian absurdities?

    DEFF Research Database (Denmark)

    Willert, Søren

    experience; it is shared by humans and subhuman animals alike; (2) consciousness of environmental experience; Mead names this consciousness aspect awareness; it is exclusively human; (3) the peculiar sensed qualities attaching to consciousness, equalling what is today named qualia. Descartes...

  8. A microarray study on the molecular mechanism for the therapeutic effect of Antidotal and Myogenic Ointmen(解毒生肌膏)on the foot ulcer in diabetic rats%利用基因芯片技术阐述中药解毒生肌膏对大鼠糖尿病足溃疡作用的分子机制

    Institute of Scientific and Technical Information of China (English)

    韩会民; 于萍; 李强; 郭琳; 姜丽娟; 蒋晓宇; 吕雅丽; 庞金奎; 白忠民; 车蔚娟; 徐荣慧

    2011-01-01

    Objective To investigate the underlying mechanism for the therapeutic effect of a traditional Chinese medicinal recipe,Antidotal and Myogenic Ointment(解毒生肌膏,AMO),on the foot ulcer in diabetic rat using cDNA microarray technology.Methods 45 rats were made diabetic by i.p.injection of streptozocin.The treated animals were then fed for 6 months,and subjected to the dissection of distal popliteal artery after ligation of the vessels.Another month later,grade Ⅱ burn injury was produced on the bottom of their foot as a model of diabetic foot ulcer.The rats were then randomly divided into three groups (15 each) to receive AMO,epidermal growth factor (EGF) and saline for 30 days,with dressing change in every 2 days.The area of ulcer wound and their healing rate were recorded before and after the treatment.Total RNA was extracted from the tissue samples collected near the wound,and the expression profile of cytokine genes demonstrated using the microarry for rats.Results In comparison with the saline group difference in the level of expression was found in 25 genes (23 0f them were up-regulated and 2 down-regulated) in EGF group,and 30 genes in AMO groups (29 0f them up-regulated and l down-regulated).In comparison with EGF group,difference in level of expression was found in 16 genes in AMO group,with 11 up-regulated and 5 down-regulated.Neurotrophic factors and chemotactic factors,etc were among the genes involved.Conclusion In comparison with EGF,AMO is more effective in the treatment of foot ulcer in diabetic rats.It is possible that AMO produces such effects through the regulation of balance in cytokine expression.%目的 采用基因芯片技术探讨中药解毒生肌膏对大鼠糖尿病足溃疡的作用机制.方法 腹腔注射链脲佐菌素复制糖尿病大鼠模型,喂养到6个月时结扎腘动脉下端并切断,7个月时造成足底部皮肤深Ⅱ度烫伤复制大鼠糖尿病足溃疡模型.将模型大鼠按随机数字表法分

  9. The Mustard Consortium’s Elucidation of the Pathophysiology of Sulfur Mustard and Antidote Development

    Science.gov (United States)

    2006-09-01

    pulmonitis with varying degrees of interstitial fibrosis, neutrophilic alveolities and increased amount of visualized collagen. CEES exposure caused...2x above the levels of the control lungs. CEES exposure causes interstitial pulmonitis with varying degrees of interstitial fibrosis, neutrophilic...regulated within 1 hr. in the mustard gas exposed lungs, 1.5-fold above the control vehicle treated lungs. CEES exposure causes interstitial pulmonitis

  10. Cyanide Antidotes for Mass Casualties: Comparison of Intramuscular Injector by Autoinjector, Intraosseous Injection, and Inhalational Delivery

    Science.gov (United States)

    2014-10-01

    cyanide poisoning in a swine ( Sus Scrofa ) model. Annals of Emergency Medicine, in press, 2014 2. Mao, R.W., Lin, S.K., Tsai, S.C., Brenner, M...versus intravenous cobinamide in treating acute cyanide toxicity and apnea in a swine ( Sus Scrofa ) model. Manuscript submitted. CONCLUSION We...in a Swine ( Sus scrofa ) Model Lt Col Vikhyat S. Bebarta, MC, USAF*; David A. Tanen, MD; Susan Boudreau, RN, BSN; Maria Castaneda, MS; Lee A. Zarzabal

  11. Managing Workplace Incivility: The Role of Conflict Management Styles--Antecedent or Antidote?

    Science.gov (United States)

    Trudel, Jeannie; Reio, Thomas G., Jr.

    2011-01-01

    The workforce of the 21st century is dealing with rapid changes and increased competition across industries. Such changes place stress on management and workers alike, increasing the potential for workplace conflict and deviant workplace behaviors, including incivility. The importance of effective conflict management in the workplace has been…

  12. Study of Potential Prophylactic and Antidotal Use of Scavenging Agents in Treatment of Cyanide Poisoning

    Science.gov (United States)

    1984-11-15

    oxaloacetic cyanohydrins. Biochem. J. 31, 617-618, 1937. 9 13. Cittadini, A., Caprino , L. and Terronova, T. Effect of pyruvate on the acute cyanide...Boston, Mass. p. 173, 1973. 3. Cittadini, A., Caprino , L. and Ternanova, T. Effect of pyruvate on the acute cyanide poisoning in mice. Experientia

  13. Can N-acetyl-L-cysteine affect zinc metabolism when used as a paracetamol antidote?

    Science.gov (United States)

    Brumas, V; Hacht, B; Filella, M; Berthon, G

    1992-07-01

    N-Acetyl-L-cysteine (NAC) has long been used in the treatment of chronic lung diseases. Inhalation and oral administration of the drug are both effective in reducing mucus viscosity. In addition, NAC oral therapy allows to restore normal mucoprotein secretion in the long term. Although displaying heavy metal-complexing potential, NAC exerts no detectable influence on the metabolism of essential trace metals when used in the above context (i.e. at doses near 600 mg day-1). However, this may no longer be the case when NAC is used as an oxygen radical scavenger, like in the treatment of paracetamol poisoning. In the latter case, intravenous doses as high as 20 g day-1 are administered, which may induce excessive zinc urinary excretion. In order to allow a better appreciation of the risk of zinc depletion during NAC therapy, the present work addresses the role of this drug towards zinc metabolism at the molecular level. First, formation constants for zinc-NAC complexes have been determined under physiological conditions. Then, computer simulations for blood plasma and gastrointestinal fluid have been run to assess the influence of NAC and its metabolites (e.g. cysteine and glutathione) on zinc excretion and absorption. Blood plasma simulations reveal that NAC can effectively mobilise an important fraction of zinc into urinary excretable complexes as from concentrations of 10(-3) mol dm-3 (which corresponds to a dose of about 800 mg). This effect can still be enhanced by the action of NAC metabolites, among which cysteine is the most powerful zinc sequestering agent. In contrast, simulations relative to gastrointestinal conditions suggest that NAC should tend to increase zinc absorption, regardless of its dose.

  14. Real GPA and Real SET: Two Antidotes to Greed, Sloth and Cowardice in the College Classroom

    Science.gov (United States)

    Koper, Peter T.; Felton, James; Sanney, Kenneth J.; Mitchell, John B.

    2015-01-01

    Recently published evidence of limited learning among American college students confirms the damage done when students, faculty and institutions pursue interests that conflict with the educational process. The "disengagement compact" in which faculty tacitly trade lenient workloads and grading for higher student evaluation of teaching…

  15. Antidotal efficacy of newly synthesized dimercaptosuccinic acid (DMSA) monoesters in experimental arsenic poisoning in mice.

    Science.gov (United States)

    Kreppel, H; Reichl, F X; Kleine, A; Szinicz, L; Singh, P K; Jones, M M

    1995-07-01

    The efficacy of four newly synthesized monoesters of meso-2,3-dimercaptosuccinic acid (DMSA), mono-i-amyl- (Mi-ADMS), mono-n-amyl- (Mn-ADMS), mono-i-butyl- (Mi-BDMS), and mono-n-butyl-meso-2,3-dimercaptosuccinate (Mn-BDMS) in increasing survival and arsenic elimination in experimental arsenic poisoning was investigated. Male mice (strain NMRI) received arsenite sc (survival study: 130 mumol/kg, 7 mice/group; elimination study: 85 mumol/kg (LD5) together with a tracer dose of 73As(III), 6 mice/group). After 30 min mice were treated with 0.7 mmol/kg of DMSA or a monoester ip or via gastric tube (ig). Control animals received saline ip. In the survival study mice were observed for 30 days. In the elimination study, the 73-arsenic content of several organs (blood, liver, heart, lung, kidneys, spleen, testes, brain, small intestine, large intestine, muscle, and skin) was measured 0.5, 2, 4, 6, and 8 hr after the arsenic injection using a gamma counter. Survival increased correspondingly well with the increase of arsenic elimination. DMSA, Mi-ADMS, Mn-ADMS, Mi-BDMS, and Mn-BDMS markedly decreased arsenic content in most organs as soon as 1.5 hr after treatment. Only in small and large intestine were higher arsenic amounts found, indicating a shift in arsenic elimination from the renal to the fecal route, and thereby suggesting a protective effect for the kidneys. Given ip, the monoesters turned out to be similarly as effective as the parent drug DMSA. Following ig treatment, the DMSA monoesters Mi-ADMS and Mn-ADMS seemed to be superior to DMSA with regard to survival.(ABSTRACT TRUNCATED AT 250 WORDS)

  16. Boxes of Poison: Baroque Technique as Antidote to Simple Views of Literacy

    Science.gov (United States)

    Burnett, Cathy; Merchant, Guy

    2016-01-01

    Rich and complex meaning making experiences, such as those associated with virtual play, sit uneasily with the view of literacy reflected in and sustained by current systems of accountability in education. This article develops a baroque perspective as a way of destabilizing the "regime of truth" associated with simple models of…

  17. Arsenic and Old Language: A Habermasian Antidote for the Lethal Tobacco Ideology.

    Science.gov (United States)

    Lagergren, Paul

    The recent success of the United States antismoking movement has produced a marked decline in the U.S. smoking population. A study employed Jurgen Habermas' communicative competency theory to examine United States smoking controversy discourse and identify the most successful appeals of the antismoking movement. Analysis revealed that primary…

  18. Ethylene glycol or methanol intoxication : Which antidote should be used, fomepizole or ethanol?

    NARCIS (Netherlands)

    Rietjens, S. J.; de Lange, D. W.; Meulenbelt, J.

    2014-01-01

    Ethylene glycol (EG) and methanol poisoning can cause life-threatening complications. Toxicity of EG and methanol is related to the production of toxic metabolites by the enzyme alcohol dehydrogenase (ADH), which can lead to metabolic acidosis, renal failure (in EG poisoning), blindness (in methanol

  19. Clar Sextet Analysis of Triangular, Rectangular, and Honeycomb Graphene Antidot Lattices

    DEFF Research Database (Denmark)

    Petersen, Rene; Pedersen, Thomas Garm; Jauho, Antti-Pekka

    2011-01-01

    Pristine graphene is a semimetal and thus does not have a band gap. By making a nanometer. scale periodic array of holes In the graphene sheet a band gap may form; the size of the gap is controllable by adjusting the parameters Of the lattice. The,hole diameter, hole geometry, lattice geometry, a...

  20. Antidotes to anthrax lethal factor intoxication. Part 2: structural modifications leading to improved in vivo efficacy.

    Science.gov (United States)

    Kim, Seongjin; Jiao, Guan-Sheng; Moayeri, Mahtab; Crown, Devorah; Cregar-Hernandez, Lynne; McKasson, Linda; Margosiak, Stephen A; Leppla, Stephen H; Johnson, Alan T

    2011-04-01

    New anthrax lethal factor inhibitors (LFIs) were designed based upon previously identified potent inhibitors 1a and 2. Combining the new core structures with modifications to the C2-side chain yielded analogs with improved efficacy in the rat lethal toxin model.

  1. Why develop antidotes and reversal agents for non-vitamin K oral anticoagulants?

    Science.gov (United States)

    Washam, Jeffrey B; Piccini, Jonathan P

    2016-02-01

    Over the past several years, non-vitamin K oral anticoagulants (NOACs) have been introduced into clinical practice for the treatment of venous thromboembolism and prevention of stroke in patients with nonvalvular atrial fibrillation. Clinical trials have shown these agents to have similar or less risk of major bleeding as compared to warfarin therapy. Moreover, when patients do experience a major bleeding event administration of advanced factor products is rare, and post-bleed outcomes are similar in those receiving a NOAC compared to those receiving warfarin. However, there are situations where urgent reversal of NOAC anticoagulation would be desirable. The following review focuses on the outcomes and management strategies for patients experiencing a major bleed with warfarin or NOAC agents and describes the rationale for the development of therapies capable of targeted NOAC-reversal.

  2. Calcium channel antagonist and beta-blocker overdose: antidotes and adjunct therapies.

    Science.gov (United States)

    Graudins, Andis; Lee, Hwee Min; Druda, Dino

    2016-03-01

    Management of cardiovascular instability resulting from calcium channel antagonist (CCB) or beta-adrenergic receptor antagonist (BB) poisoning follows similar principles. Significant myocardial depression, bradycardia and hypotension result in both cases. CCBs can also produce vasodilatory shock. Additionally, CCBs, such as verapamil and diltiazem, are commonly ingested in sustained-release formulations. This can also be the case for some BBs. Peak toxicity can be delayed by several hours. Provision of early gastrointestinal decontamination with activated charcoal and whole-bowel irrigation might mitigate this. Treatment of shock requires a multimodal approach to inotropic therapy that can be guided by echocardiographic or invasive haemodynamic assessment of myocardial function. High-dose insulin euglycaemia is commonly recommended as a first-line treatment in these poisonings, to improve myocardial contractility, and should be instituted early when myocardial dysfunction is suspected. Catecholamine infusions are complementary to this therapy for both inotropic and chronotropic support. Catecholamine vasopressors and vasopressin are used in the treatment of vasodilatory shock. Optimizing serum calcium concentration can confer some benefit to improving myocardial function and vascular tone after CCB poisoning. High-dose glucagon infusions have provided moderate chronotropic and inotropic benefits in BB poisoning. Phosphodiesterase inhibitors and levosimendan have positive inotropic effects but also produce peripheral vasodilation, which can limit blood pressure improvement. In cases of severe cardiogenic shock and/or cardiac arrest post-poisoning, extracorporeal cardiac assist devices have resulted in successful recovery. Other treatments used in refractory hypotension include intravenous lipid emulsion for lipophilic CCB and BB poisoning and methylene blue for refractory vasodilatory shock.

  3. 以史为镜,避免愚行%Folly's Antidote

    Institute of Scientific and Technical Information of China (English)

    叶子南

    2008-01-01

    许多迹象显示,美国人正越来越有历史感。我希望确实如此。历史之于国家恰如记忆之于个人,记住这点是有益的。一个被剥夺了记忆的人会失去方向,不知道曾到过哪里,也不知道应走向哪里。同理,一个被剥夺了历史感的国家也将不能面对现在和未来。“向后回顾得越远,向前展望得也越远”,丘吉尔曾这么说过。

  4. There is Antidote to Bad Food%不良食物有"解药"

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    @@ 状态1:油条油条是不少人早餐的选择,可油条中大多加明矾.这种含铝的无机物,被人体吸收后会对大脑神经细胞产生损害,并且很难被人体排出而逐渐蓄积.长久对身体造成的危害是记忆力减退、抑郁和烦躁,严重的可导致"老年性痴呆"等疾病.

  5. Hydrogen Sulfide—Mechanisms of Toxicity and Development of an Antidote

    OpenAIRE

    Jingjing Jiang; Adriano Chan; Sameh Ali; Arindam Saha; Haushalter, Kristofer J.; Wai-Ling Macrina Lam; Megan Glasheen; James Parker; Matthew Brenner; Mahon, Sari B.; Patel, Hemal H.; Rajesh Ambasudhan; Stuart A. Lipton; Pilz, Renate B.; Boss, Gerry R.

    2016-01-01

    Hydrogen sulfide is a highly toxic gas—second only to carbon monoxide as a cause of inhalational deaths. Its mechanism of toxicity is only partially known, and no specific therapy exists for sulfide poisoning. We show in several cell types, including human inducible pluripotent stem cell (hiPSC)-derived neurons, that sulfide inhibited complex IV of the mitochondrial respiratory chain and induced apoptosis. Sulfide increased hydroxyl radical production in isolated mouse heart mitochondria and ...

  6. Reversible block of the calcium release channel/ryanodine receptor by protamine, a heparin antidote.

    Science.gov (United States)

    Koulen, P; Ehrlich, B E

    2000-07-01

    Channel activity of the calcium release channel from skeletal muscle, ryanodine receptor type 1, was measured in the presence and absence of protamine sulfate on the cytoplasmic side of the channel. Single-channel activity was measured after incorporating channels into planar lipid bilayers. Optimally and suboptimally calcium-activated calcium release channels were inactivated by the application of protamine to the cytoplasmic side of the channel. Recovery of channel activity was not observed while protamine was present. The addition of protamine bound to agarose beads did not change channel activity, implying that the mechanism of action involves an interaction with the ryanodine receptor rather than changes in the bulk calcium concentration of the medium. The block of channel activity by protamine could be reversed either by removal by perfusion with buffer or by the addition of heparin to the cytoplasmic side of the channel. Microinjection of protamine into differentiated C(2)C(12) mouse muscle cells prevented caffeine-induced intracellular calcium release. The results suggest that protamine acts on the ryanodine receptor in a similar but opposite manner from heparin and that protamine can be used as a potent, reversible inhibitor of ryanodine receptor activity.

  7. Ephedrine QoS: An Antidote to Slow, Congested, Bufferless NoCs

    OpenAIRE

    Juan Fang; Zhicheng Yao; Xiufeng Sui; Yungang Bao

    2014-01-01

    Datacenters consolidate diverse applications to improve utilization. However when multiple applications are colocated on such platforms, contention for shared resources like networks-on-chip (NoCs) can degrade the performance of latency-critical online services (high-priority applications). Recently proposed bufferless NoCs (Nychis et al.) have the advantages of requiring less area and power, but they pose challenges in quality-of-service (QoS) support, which usually relies on buffer-based vi...

  8. Ephedrine QoS: An Antidote to Slow, Congested, Bufferless NoCs

    Directory of Open Access Journals (Sweden)

    Juan Fang

    2014-01-01

    Full Text Available Datacenters consolidate diverse applications to improve utilization. However when multiple applications are colocated on such platforms, contention for shared resources like networks-on-chip (NoCs can degrade the performance of latency-critical online services (high-priority applications. Recently proposed bufferless NoCs (Nychis et al. have the advantages of requiring less area and power, but they pose challenges in quality-of-service (QoS support, which usually relies on buffer-based virtual channels (VCs. We propose QBLESS, a QoS-aware bufferless NoC scheme for datacenters. QBLESS consists of two components: a routing mechanism (QBLESS-R that can substantially reduce flit deflection for high-priority applications and a congestion-control mechanism (QBLESS-CC that guarantees performance for high-priority applications and improves overall system throughput. We use trace-driven simulation to model a 64-core system, finding that, when compared to BLESS, a previous state-of-the-art bufferless NoC design, QBLESS, improves performance of high-priority applications by an average of 33.2% and reduces network-hops by an average of 42.8%.

  9. An alternative antidote therapy in amitriptyline-induced rat toxicity model: theophylline.

    Science.gov (United States)

    Oransay, Kubilay; Kalkan, Sule; Hocaoglu, Nil; Arici, Aylin; Tuncok, Yesim

    2011-01-01

    We planned this study in order to investigate the effects of theophylline on cardiovascular parameters in an anaesthetized rat model of amitriptyline toxicity. In the preliminary study, we tested theophylline as 1 mg/kg of bolus, followed by a 0.5-mg/kg infusion. Toxicity was induced by the infusion of 0.94 mg/kg/min of amitriptyline up to the point of a 40-45% inhibition of mean arterial pressure (MAP). The rats were randomized to two groups: a group of 5% dextrose bolus followed by 5% dextrose infusion, and another group with theophylline bolus followed by infusion. Amitriptyline caused a significant decrease in MAP and prolongation in QRS; however, it did not alter heart rate (HR). When compared to the dextrose group, theophylline administration increased MAP, shortened prolonged QRS duration, and increased HR (P  0.05). Bolus doses followed by a continuous infusion of theophylline were found to be effective in reversing the hypotension and QRS prolongation seen in amitriptyline toxicity. One of the possible explanations of this beneficial effect is nonselective adenosine antagonism of theophylline. Further studies are needed to reveal the exact mechanism of the observed effect.

  10. Ephedrine QoS: an antidote to slow, congested, bufferless NoCs.

    Science.gov (United States)

    Fang, Juan; Yao, Zhicheng; Sui, Xiufeng; Bao, Yungang

    2014-01-01

    Datacenters consolidate diverse applications to improve utilization. However when multiple applications are colocated on such platforms, contention for shared resources like networks-on-chip (NoCs) can degrade the performance of latency-critical online services (high-priority applications). Recently proposed bufferless NoCs (Nychis et al.) have the advantages of requiring less area and power, but they pose challenges in quality-of-service (QoS) support, which usually relies on buffer-based virtual channels (VCs). We propose QBLESS, a QoS-aware bufferless NoC scheme for datacenters. QBLESS consists of two components: a routing mechanism (QBLESS-R) that can substantially reduce flit deflection for high-priority applications and a congestion-control mechanism (QBLESS-CC) that guarantees performance for high-priority applications and improves overall system throughput. We use trace-driven simulation to model a 64-core system, finding that, when compared to BLESS, a previous state-of-the-art bufferless NoC design, QBLESS, improves performance of high-priority applications by an average of 33.2% and reduces network-hops by an average of 42.8%.

  11. Mechanism of organophosphates (nerve gases and pesticides) and antidotes: electron transfer and oxidative stress.

    Science.gov (United States)

    Kovacic, Peter

    2003-12-01

    Evidence indicates that nerve gas toxins operate in ways in addition to inhibition of acetylcholine esterase. Alternative bioactivities are discussed with focus on electron transfer. The main class, including pralidoxime (2-PAM), incorporates conjugated iminium and oxime moieties that are electron affinic. Various physiological properties of iminium and oxime species are reviewed. The organophosphates encompass both nerve gases and insecticides, possessing similar properties, but different activities. Toxic manifestations are apparently due, in part, to oxidative stress. Alkylation of DNA takes place which may lead to generation of reactive oxygen species. Structure-activity relationships are examined, including reduction potentials and the captodative effect.

  12. The thrill of being violent as an antidote to posttraumatic stress disorder in Rwandese genocide perpetrators

    Directory of Open Access Journals (Sweden)

    Roland Weierstall

    2011-11-01

    Full Text Available The cumulative exposure to life-threatening events increases the risk for posttraumatic stress disorder (PTSD. However, over the course of evolutionary adaptation, intra-species killing may have also evolved as an inborn strategy leading to greater reproductive success. Assuming that homicide has evolved as a profitable strategy in humans, a protective mechanism must prevent the perpetrator from getting traumatised by self-initiated violent acts. We thus postulate an inverse relation between a person's propensity toward violence and PTSD. We surveyed a sample of 269 Rwandan prisoners who were accused or convicted for crimes related to the 1994 genocide. In structured interviews we assessed traumatic event types, types of crimes committed, the person's appetitive violence experience with the Appetitive Aggression Scale (AAS and PTSD symptom severity with the PSS-I. Using path-analysis, we found a dose-response effect between the exposure to traumatic events and the PTSD symptom severity (PSS-I. Moreover, participants who had reported that they committed more types of crimes demonstrated a higher AAS score. In turn, higher AAS scores predicted lower PTSD symptom severity scores. This study provides first empirical support that the victim's struggling can be an essential rewarding cue for perpetrators. The results also suggest that an appetitive aggression can inhibit PTSD and trauma-related symptoms in perpetrators and prevent perpetrators from getting traumatised by their own atrocities.

  13. The thrill of being violent as an antidote to posttraumatic stress disorder in Rwandese genocide perpetrators

    OpenAIRE

    Weierstall, Roland; Schaal, Susanne; Schalinski, Inga; Dusingizemungu, Jean-Pierre; Elbert, Thomas

    2011-01-01

    Background: The cumulative exposure to life-threatening events increases the risk for posttraumatic stress disorder (PTSD). However, over the course of evolutionary adaptation, intra-species killing may have also evolved as an inborn strategy leading to greater reproductive success. Assuming that homicide has evolved as a profitable strategy in humans, a protective mechanism must prevent the perpetrator from getting traumatised by self-initiated violent acts. Objective: We thus postulate an i...

  14. Intravenous lipid emulsion as antidote: a summary of published human experience.

    Science.gov (United States)

    Cave, Grant; Harvey, Martyn; Graudins, Andis

    2011-04-01

    Intravenous lipid emulsion (ILE) has been demonstrated to be effective in amelioration of cardiovascular and central nervous system sequelae of local-anaesthetic and non-local-anaesthetic drug toxicity in animal models. Sequestration of lipophilic toxins to an expanded plasma lipid phase is credited as the predominant beneficial mechanism of action of ILE. Systematic review of published human experience is however lacking. We determined to report a comprehensive literature search of all human reports of ILE application in drug poisoning. Forty-two cases of ILE use (19 local-anaesthetic, 23 non-local-anaesthetic) were identified, with anecdotal reports of successful resuscitation from cardiovascular collapse and central nervous system depression associated with ILE administration in lipophilic toxin overdose. Although significant heterogeneity was observed in both agents of intoxication, and reported outcomes; case report data suggest a possible benefit of ILE in potentially life-threatening cardio-toxicity from bupivacaine, mepivacaine, ropivacaine, haloperidol, tricyclic antidepressants, lipophilic beta blockers and calcium channel blockers. Further controlled study and systematic evaluation of human cases is required to define the clinical role of ILE in acute poisonings.

  15. Fish oil may be an antidote for the cardiovascular risk of smoking.

    Science.gov (United States)

    McCarty, M F

    1996-04-01

    The fact that the cardiovascular risk of ex-smokers approximates that of non-smokers after two years of abstinence, implies that accelerated atherogenesis is not the chief mechanism of smoking-related heart disease. Indeed, smoking or nicotine have adverse effects on blood rheology, thrombotic risk, coronary blood flow, and risk for arrhythmias. Omega-3-rich fish oils can be expected to correct or compensate for a remarkable number of the adverse impacts of smoking/nicotine: increased plasma fibrinogen, decreased erythrocyte distensibility, increased plasma and blood viscosity, increased platelet aggregability, increased plasminogen activator inhibitor levels, vasoconstriction of the coronary bed, reduced fibrillation threshold, increased triglycerides, reduced high-density lipoprotein cholesterol, and increased production of superoxide by phagocytes. Smokers who cannot overcome their addiction should be encouraged to substitute nicotine aerosols/gum for tobacco and advised to use supplementary fish oil and other cardioprotective nutrients.

  16. [Expression Of DNA-Encoded Antidote to Organophosphorus Toxins in the Methylotrophic Yeast Pichia Pastoris].

    Science.gov (United States)

    Terekhov, S S; Bobik, T V; Mokrushina, Yu A; Stepanova, A V; Aleksandrova, N M; Smirnov, I V; Belogurov, A A; Ponomarenko, N A; Gabibov, A G

    2016-01-01

    A platform for the cloning and expression of active human butyrylcholinesterase (BuChE) in the yeast Pichia pastoris is first presented. Genetic constructs for BuChE gene expression, separately and in conjunction with a proline-rich peptide called proline-rich attachment domain (PRAD), are based on the vector pPICZαA. It is shown that the highest level of production is achieved in the expression of a BuChE gene without PRAD pPICZαA. It is found that one can obtain up to 125 mg of active enzyme from 1 L of culture medium at an optimal pH environment (pH 7.6), an optical seed culture density of 3 o.u., and an optimum methanol addition mode of (0.5% methanol in the first day and 0.2% thereafter from the second day).

  17. An antidote to the imager's fallacy, or how to identify brain areas that are in limbo

    NARCIS (Netherlands)

    de Hollander, G.; Wagenmakers, E.-J.; Waldorp, L.; Forstmann, B.

    2014-01-01

    Traditionally, fMRI data are analyzed using statistical parametric mapping approaches. Regardless of the precise thresholding procedure, these approaches ultimately divide the brain in regions that do or do not differ significantly across experimental conditions. This binary classification scheme fo

  18. Prussian blue as an antidote for radioactive thallium and cesium poisoning

    Directory of Open Access Journals (Sweden)

    Altagracia-Martinez M

    2012-06-01

    Full Text Available Marina Altagracia-Martínez, Jaime Kravzov-Jinich, Juan Manuel Martínez-Núñez, Camilo Ríos-Castañeda, Francisco López-NaranjoDepartments of Biological Systems and Health Care, Biological and Health Sciences Division, Universidad Autónoma Metropolitana-Xochimilco, Mexico DF, MexicoBackground: Following the attacks on the US on September 11, 2001, potentially millions of people might experience contamination from radioactive metals. However, before the specter of such accidents arose, Prussian blue was known only as an investigational agent for accidental thallium and cesium poisoning. The purpose of this review is to update the state of the art concerning use of Prussian blue as an effective and safe drug against possible bioterrorism attacks and to disseminate medical information in order to contribute to the production of Prussian blue as a biodefense drug.Methods: We compiled articles from a systematic review conducted from January 1, 1960 to March 30, 2011. The electronic databases consulted were Medline, PubMed, the Cochrane Library, and Scopus.Results: Prussian blue is effective and safe for use against radioactive intoxications involving cesium-137 and thallium. The US Food and Drug Administration has approved Prussian blue as a drug, but there is only one manufacturer providing Prussian blue to the US. Based on the evidence, Prussian blue is effective for use against radioactive intoxications involving cesium-137 and thallium, but additional clinical research on and production of Prussian blue are needed.Keywords: Prussian blue, radioactive cesium, thallium, intoxication, biodefense drug

  19. Counting on Creativity : The Creative Class as Antidote for Neighbourhood Decline: the Case of Rotterdam

    NARCIS (Netherlands)

    J.E. Nijkamp (Jeanette)

    2016-01-01

    markdownabstractAn important assumption often underlying initiatives that stimulate the creative industries in deprived neighbourhoods is that the presence of creative entrepreneurs contributes to the regeneration of these neighbourhoods. Besides contributing to economic development, creative entrep

  20. Legalon® SIL: the antidote of choice in patients with acute hepatotoxicity from amatoxin poisoning.

    Science.gov (United States)

    Mengs, Ulrich; Pohl, Ralf-Torsten; Mitchell, Todd

    2012-08-01

    More than 90% of all fatal mushroom poisonings worldwide are due to amatoxin containing species that grow abundantly in Europe, South Asia, and the Indian subcontinent. Many cases have also been reported in North America. Initial symptoms of abdominal cramps, vomiting, and a severe cholera-like diarrhea generally do not manifest until at least six to eight hours following ingestion and can be followed by renal and hepatic failure. Outcomes range from complete recovery to fulminant organ failure and death which can sometimes be averted by liver transplant. There are no controlled clinical studies available due to ethical reasons, but uncontrolled trials and case reports describe successful treatment with intravenous silibinin (Legalon® SIL). In nearly 1,500 documented cases, the overall mortality in patients treated with Legalon® SIL is less than 10% in comparison to more than 20% when using penicillin or a combination of silibinin and penicillin. Silibinin, a proven antioxidative and anti-inflammatory acting flavonolignan isolated from milk thistle extracts, has been shown to interact with specific hepatic transport proteins blocking cellular amatoxin re-uptake and thus interrupting enterohepatic circulation of the toxin. The addition of intravenous silibinin to aggressive intravenous fluid management serves to arrest and allow reversal of the manifestation of fulminant hepatic failure, even in severely poisoned patients. These findings together with the available clinical experience justify the use of silibinin as Legalon® SIL in Amanita poisoning cases.

  1. [Combination of a universal antidote and temporary skin substitute for chemical burns: Extended case report].

    Science.gov (United States)

    Liodaki, E; Schopp, B E; Lindert, J; Krämer, R; Kisch, T; Mailänder, P; Stang, F

    2015-09-01

    In this article we describe our experiences in the treatment of chemical burns with Diphoterine(®) solution and Suprathel(®) as a temporary skin substitute material, a treatment which in the past was not commonly used for this pattern of injuries. In the study period from October 2012 to December 2013 we treated five patients (four male and one female including two children and three adults) with chemical burns by decontamination with Diphoterine(®) and wound covering with Suprathel(®). The control group included five patients with similar injury patterns who were treated with Diphoterine(®) and occlusive wound dressings. No wound infections occurred in any of the five cases and no interactions were observed between Suprathel(®) and the chemical substance involved. In four cases the skin areas with IIa-IIb degree damage showed good wound healing and only slight scarring in the follow-up after 3 months and one of the five patients had to be treated surgically. Suprathel(®) can be used as a temporary skin substitute for the treatment of skin burns and is also available for the treatment of chemical burns.

  2. Stability Characterization of a Polysorbate 80-Dimethyl Trisulfide Formulation, a Cyanide Antidote Candidate.

    Science.gov (United States)

    Bartling, Craig M; Andre, Jon C; Howland, Carrie A; Hester, Mark E; Cafmeyer, Jeffrey T; Kerr, Andrew; Petrel, Trevor; Petrikovics, Ilona; Rockwood, Gary A

    2016-03-01

    Novel cyanide countermeasures are needed for cases of a mass-exposure cyanide emergency. A lead candidate compound is dimethyl trisulfide (DMTS), which acts as a sulfur donor for rhodanese, thereby assisting the conversion of cyanide into thiocyanate. DMTS is a safe compound for consumption and, in a 15% polysorbate 80 (DMTS-PS80) formulation, has demonstrated good efficacy against cyanide poisoning in several animal models. We performed a stability study that investigated the effect of temperature, location of formulation preparation, and pH under buffered conditions. We found that while the stability of the DMTS component was fairly independent of which laboratory prepared the formulation, the concentration of DMTS in the formulation was reduced 36-58% over the course of 29 weeks when stored at room temperature. This loss typically increased with increasing temperatures, although we did not find statistical differences between the stability at different storage temperatures in all formulations. Further, we found that addition of a light buffer negatively impacted the stability, whereas the pH of that buffer did not impact stability. We investigated the factors behind the reduction of DMTS over time using various techniques, and we suggest that the instability of the formulation is governed at least partially by precipitation and evaporation, although a combination of factors is likely involved.

  3. Forces of Nature: A Scientific Antidote to The Day After Tomorrow

    Science.gov (United States)

    Folger, Peter

    2004-07-01

    Do you cringe when watching the latest disaster movie? Not because of the drama, but because the science and the scientists bear little resemblance to the real thing? Would you rather watch a movie that translates the wonder and excitement of Earth's natural forces onto the silver screen, so that people other than ourselves could see those raw forces for what they are? And perhaps learn a little about why they occur?

  4. Building a Consonance Between Religion and Science: an Antidote for the Seeming Conflict

    Directory of Open Access Journals (Sweden)

    Omomia O. Austin

    2014-05-01

    Full Text Available It is commonly argued by a school of thought that there is no relationship between religion and science. This extreme position has led to a lasting conflict, which has pitched religion against science and science against religion. The attempt in this paper is to articulate the fact that there can be an enduring consonance between religion and science. No doubt, the conflict and debate on the subject of religion and science has taken the front burner in both religious and philosophical discusses. Some scholars have argued that science has no role in religious or theological domain, while others contest that all religious concerns and considerations must be exposed to empirical investigations, and, proven by the dynamics of our intellect or reason. This paper, therefore, attempts to examine how religion and science complement each other. The author applied philosophical, sociological and historical methodology in his research. It is recommended that there is the need for dialogue between religion and science.

  5. Evidence-Informed Practice: Antidote to Propaganda in the Helping Professions?

    Science.gov (United States)

    Gambrill, Eileen

    2010-01-01

    The most concerning issue affecting the quality of practices and policies in the helping professions is the play of propaganda, which misleads us regarding what is a problem, how (or if) it can be detected, its causes, and how (or if) it can be remedied. Propaganda is defined as encouraging beliefs and actions with the least thought possible.…

  6. Girls Can Succeed in Science! Antidotes for Science Phobia in Boys and Girls.

    Science.gov (United States)

    Samuels, Linda S.

    This book provides teachers with effective strategies to help encourage all students but particularly young women who are apprehensive about science. Sections include: (1) Identifying and Overcoming Barriers to Success; (2) Specific Tactics for Classroom Success; and (3) Classroom Activities. This monograph features creative activities in life…

  7. Antidotes for Ricin Intoxication. Effects of Ricin on the Vascular Neuroeffector System

    Science.gov (United States)

    1992-10-25

    syndrome and the development of anticonjugate antibodies limited the likelihood of reaching therapeutically useful dosages with this immunoconjugate. A...Blood pressure and ECG were determined every hour 31 throughout the time period. a. Blood Pressure Hair was removed from the rabbit tail with clippers ...intervals. These were averaged to obtain the blood pressure. b. ECG Hair was removed with clippers from an area approximately 4 cm by 4 cm on either

  8. AN ANTIDOTE TO THE RESOURCE CURSE: THE BLESSING OF RENEWABLE ENERGY

    Directory of Open Access Journals (Sweden)

    Angeliki N. Menegaki

    2013-10-01

    Full Text Available This paper empirically examines the validity of the resource curse in Europe and it is the first time renewable energy is inserted in this research context. The study uses panel data with a variety of explanatory variable proxies for investment, openness, rule of law, resource endowments and human capital. It employs a single equation fixed effects model with heteroskedasticity robust covariance and a simultaneous two equation model where renewable energy enters the structural equation as an endogenous variable. The resource curse is confirmed only for crude oil and resource productivity in the single equation model while renewable energy has a positive relationship to growth. In the simultaneous two equation model, countries with high oil production and emissions also have a higher production of renewable energies.

  9. Hydrogen Sulfide--Mechanisms of Toxicity and Development of an Antidote.

    Science.gov (United States)

    Jiang, Jingjing; Chan, Adriano; Ali, Sameh; Saha, Arindam; Haushalter, Kristofer J; Lam, Wai-Ling Macrina; Glasheen, Megan; Parker, James; Brenner, Matthew; Mahon, Sari B; Patel, Hemal H; Ambasudhan, Rajesh; Lipton, Stuart A; Pilz, Renate B; Boss, Gerry R

    2016-02-15

    Hydrogen sulfide is a highly toxic gas-second only to carbon monoxide as a cause of inhalational deaths. Its mechanism of toxicity is only partially known, and no specific therapy exists for sulfide poisoning. We show in several cell types, including human inducible pluripotent stem cell (hiPSC)-derived neurons, that sulfide inhibited complex IV of the mitochondrial respiratory chain and induced apoptosis. Sulfide increased hydroxyl radical production in isolated mouse heart mitochondria and F2-isoprostanes in brains and hearts of mice. The vitamin B12 analog cobinamide reversed the cellular toxicity of sulfide, and rescued Drosophila melanogaster and mice from lethal exposures of hydrogen sulfide gas. Cobinamide worked through two distinct mechanisms: direct reversal of complex IV inhibition and neutralization of sulfide-generated reactive oxygen species. We conclude that sulfide produces a high degree of oxidative stress in cells and tissues, and that cobinamide has promise as a first specific treatment for sulfide poisoning.

  10. Hydrogen Sulfide—Mechanisms of Toxicity and Development of an Antidote

    Science.gov (United States)

    Jiang, Jingjing; Chan, Adriano; Ali, Sameh; Saha, Arindam; Haushalter, Kristofer J.; Lam, Wai-Ling Macrina; Glasheen, Megan; Parker, James; Brenner, Matthew; Mahon, Sari B.; Patel, Hemal H.; Ambasudhan, Rajesh; Lipton, Stuart A.; Pilz, Renate B.; Boss, Gerry R.

    2016-01-01

    Hydrogen sulfide is a highly toxic gas—second only to carbon monoxide as a cause of inhalational deaths. Its mechanism of toxicity is only partially known, and no specific therapy exists for sulfide poisoning. We show in several cell types, including human inducible pluripotent stem cell (hiPSC)-derived neurons, that sulfide inhibited complex IV of the mitochondrial respiratory chain and induced apoptosis. Sulfide increased hydroxyl radical production in isolated mouse heart mitochondria and F2-isoprostanes in brains and hearts of mice. The vitamin B12 analog cobinamide reversed the cellular toxicity of sulfide, and rescued Drosophila melanogaster and mice from lethal exposures of hydrogen sulfide gas. Cobinamide worked through two distinct mechanisms: direct reversal of complex IV inhibition and neutralization of sulfide-generated reactive oxygen species. We conclude that sulfide produces a high degree of oxidative stress in cells and tissues, and that cobinamide has promise as a first specific treatment for sulfide poisoning. PMID:26877209

  11. Inoculation against Wonder: Finding an Antidote in Camus, Pragmatism and the Community of Inquiry

    Science.gov (United States)

    Burgh, Gilbert; Thornton, Simone

    2016-01-01

    In this paper, we will explore how Albert Camus has much to offer philosophers of education. Although a number of educationalists have attempted to explicate the educational implications of Camus' literary works, these analyses have not attempted to extrapolate pedagogical guidelines towards developing an educational framework for children's…

  12. Methylene blue for distributive shock: a potential new use of an old antidote.

    Science.gov (United States)

    Jang, David H; Nelson, Lewis S; Hoffman, Robert S

    2013-09-01

    Methylene blue is used primarily in the treatment of patients with methemoglobinemia. Most recently, methylene blue has been used as a treatment for refractory distributive shock from a variety of causes such as sepsis and anaphylaxis. Many studies suggest that the nitric oxide-cyclic guanosine monophosphate (NO-cGMP) pathway plays a significant role in the pathophysiology of distributive shock. There are some experimental and clinical experiences with the use of methylene blue as a selective inhibitor of the NO-cGMP pathway. Methylene blue may play a role in the treatment of distributive shock when standard treatment fails.

  13. Disulfides as Cyanide Antidotes: Evidence for a New In Vivo Oxidative Pathway for Cyanide Detoxification

    Science.gov (United States)

    2009-01-01

    garlic ] have been found to be effective as in vivo therapeutic agents for cyanide intoxication (10, 11). It is believed that the efficacy of these...of sulfur-sulfur bond cleavage. J. Biol. Chem. 241, 3381–3385. (10) Iciek, M., and Wlodek, L. (2001) Biosynthesis and biological properties of

  14. Exogenous superoxide dismutase may lose its antidotal ability on rice leaves

    Science.gov (United States)

    Leaf diffusates of the resistant rice cultivars suppressed spore germination of blast fungus (Magnaporthe grisea). Bovine Cu-Zn superoxide dismutase (SOD) added to the diffusate abolished its toxicity. However, the enzyme added to the inoculum did not affect the toxicity of the diffusate. Even the s...

  15. L’analyse du travail comme antidote aux configurations douloureuses des cadres

    OpenAIRE

    Merlier, Philippe

    2009-01-01

    Le cadre a mal à son travail. Un malaise sournois envahit les organisations. Trop de configurations douloureuses, non traitées, renforcent négativement les indicateurs sociaux (stress, absentéisme, démotivation, burn-out-in, etc.). La formation intégrant un dispositif d’analyse du travail à deux étages, celui de l’individu et celui du collectif, permet-elle de lutter contre ces constats ? C’est ce que nous tentons de prouver ici. Le cadre est redevenu depuis une dizaine d’années un sujet de c...

  16. Effects of the Chemical Defense Antidote Atropine Sulfate on Helicopter Pilot Performance: An In-Flight Study

    Science.gov (United States)

    1991-06-01

    introduction of other drugs (such as alcoholic beverages or cold remedies, for example) during the study period. Subjects were free to smoke cigarettes and... lectronic AscteInc. 13 est Monrouth Parkway ,West Long4 Branch, NJ 0� lI, LillIy & Co. 1CY’T F~ist McCarty Street I ndlIa napolIis5, I N 4 f)28 5 Gou.10

  17. Medical anthropology as an antidote for ethnocentrism in Jesus research? Putting the illness–disease distinction into perspective

    Directory of Open Access Journals (Sweden)

    Pieter F. Craffert

    2011-06-01

    Full Text Available Medicine often has side-effects or unintended consequences that are more harmful than the original disease. Medical anthropology in general and the illness–disease distinction in particular has been introduced into historical Jesus research with the intent to protect it from medicocentrism and thus to offer ways of comprehending sickness and healing in the world of Jesus and his first followers without distorting these phenomena by imposing the biomedical framework onto the texts. In particular the illness–disease distinction is used for making sense of healing accounts whilst claiming to cross the cultural gap. Based on an analysis of the illness–disease distinction in medical anthropology and its use in historical Jesus research this article suggests that instead of protecting from ethnocentrism this distinction actually increases the risk of ethnocentrism and consequently distorts in many instances the healing accounts of the New Testament.

  18. RAPID MULTICOMPONENT ANALYSIS OF HEMOGLOBIN DERIVATIVES FOR CONTROLLED ANTIDOTAL USE OF METHEMOGLOBIN-FORMING AGENTS IN CYANIDE POISONING

    NARCIS (Netherlands)

    ZIJLSTRA, WG

    1993-01-01

    When cyanide poisoning is treated with a methemoglobin-forming agent, oxidative metabolism is protected at the expense of the oxygen capacity of the blood.The affinity of methemoglobin for CN- is high enough to compete with cytochrome oxidase, which protects the latter from becoming blocked, but all

  19. RISK MANAGEMENT ANTIDOTE THEORY FOR GEOLOGICAL DISASTERS%地质灾害风险管理对策论

    Institute of Scientific and Technical Information of China (English)

    卓万生

    2006-01-01

    每年一到汛期,突发性地质灾害防治工作就紧锣密鼓地进行,这反映了各级党委、政府对这项工作的重视.但是,在防灾工作的热潮背后,又反映出我们的技术支撑工作所达到的程度.本文从风险管理角度,进一步阐述预见、预防地质灾害的看法与对策.

  20. 灾难频发,有何解药?%What is the Antidote of the Frequent Disasters?

    Institute of Scientific and Technical Information of China (English)

    周宇

    2007-01-01

    @@ 最近,国家安全生产管理监督总局李毅中局长是各大媒体出镜率最高的官员了.原因很简单,7月底、8月份以来,全国发生的重大安全生产事故一桩接一桩.月初,河南陕县成功地对69名遇险矿工进行了营救,李毅中的心情无疑是欣慰的.但是不久后发生的湖南凤凰溪沱江大桥坍塌事件,再次将他的心悬了起来.

  1. Ten Common Misunderstandings, Misconceptions, Persistent Myths and Urban Legends about Likert Scales and Likert Response Formats and their Antidotes

    Directory of Open Access Journals (Sweden)

    James Carifio

    2007-01-01

    Full Text Available A recent article by Jamieson in Medical Education outlined some of the (alleged abuses of “Likert scales” with suggestions about how researchers can overcome some of the (alleged methodological pitfalls and limitations[1]. However, many of the ideas advanced in the Jamison article, as well as a great many of articles it cited, and similar recent articles in medical, health, psychology, and educational journals and books, are themselves common misunderstandings, misconceptions, conceptual errors, persistent myths and “urban legends” about “Likert scales” and their characteristics and qualities that have been propagated and perpetuated across six decades, for a variety of different reasons. This article identifies, analyses and traces many of these aforementioned problems and presents the arguments, counter arguments and empirical evidence that show these many persistent claims and myths about “Likert scales” to be factually incorrect and untrue. Many studies have shown that Likert Scales (as opposed to single Likert response format items produce interval data and that the F-test is very robust to violations of the interval data assumption and moderate skewing and may be used to analyze “Likert data” (even if it is ordinal, but not on an item-by-item “shotgun” basis, which is simply a current research and analysis practice that must stop. After sixty years, it is more than time to dispel these particular research myths and urban legends as well as the various damage and problems they cause, and put them to bed and out of their misery once and for

  2. Antidote strategies to reverse anticoagulation with TB-402, a long-acting partial inhibitor of factor VIII

    NARCIS (Netherlands)

    Tangelder, M.; Long, C.; Emmerechts, J.; Jacquemin, M.; Peerlinck, K.; Vanassche, T.; Glazer, S.; Giesen, P.; Hoylaerts, M.; Verhamme, P.

    2012-01-01

    . Background: TB-402 is a partially inhibiting antibody of factor VIII that is under development as a long-acting anticoagulant. Patients and Methods: The reversibility of FVIII inhibition by TB-402 was evaluated in vitro after spiking with recombinant human FVIII (rhFVIII), human plasma-derived FVI

  3. Amino acid profile of raw and locally processed seeds of Prosopis africana and Ricinus communis: potential antidotes to protein malnutrition

    Directory of Open Access Journals (Sweden)

    Chidi U. Igwe

    2012-04-01

    Full Text Available Background: Increasing incidence of malnutrition occasioned by high incidence of hunger,worsening food situation in the world, insufficient availability and high cost of animal protein sources, has necessitated extensive research into and use of alternative plant protein sources especially underexploited leguminous seeds.Methods: Flours from raw, boiled and fermented seeds of Prosopis africana and Ricinus communis were evaluated for crude protein and amino acid (AA profiles, and their protein qualities determined. Results: Fermentation improved the protein contents of raw seeds of P. africana and R. communis by 18.70% and 3.95% respectively. In the raw and fermented P. africana seeds, glutamate at 132.60 ± 1.30 and 182.70 ± 3.02 mg/g crude protein (mg/gcp was the most abundant amino acid (AA, while leucine (62.80 ± 0.60 and 79.50 ± 2.01 mg/gcp was the most concentrated essential amino acid (EAA. Aspartate (151.90 ± 2.01 and 170.10 ± 2.00 mg/gcp and arginine (72.80 ± 2.01 and 78.60 ± 2.00 mg/gcp were the most concentrated and abundant non-essential amino acid (NEAA and EAA in the raw and fermented samples of R. communisrespectively. The total AA concentrations (mg/gcp of raw and fermented P. africana were 733.00 and 962.60 respectively, while those of R. communis were 823.50 and 894.10 respectively. The total EAA contents (mg/gcp for P. africana were 311.00 (raw and 404.50 (fermented, and for R. communis; 401.10 (raw and 430.30 (fermented. Threonine was the limiting EAA in raw and fermented P. africana, whereas lysine was the limiting EAA in R. communis raw sample. Fermentation significantly (p<0.05 increased the individual AA compositions of P. africana and R. communis by 94% and 53% respectively, while boiling reduced these parameters significantly (p<0.05 by 47% and 82% respectively. Conclusion: P. africana and R. communis seeds are potentially important plant sources of protein and essential amino acids, and so could be of great importance in combating malnutrition and food security problems generally

  4. Antidotes to anthrax lethal factor intoxication. Part 1: Discovery of potent lethal factor inhibitors with in vivo efficacy.

    Science.gov (United States)

    Jiao, Guan-Sheng; Kim, Seongjin; Moayeri, Mahtab; Cregar-Hernandez, Lynne; McKasson, Linda; Margosiak, Stephen A; Leppla, Stephen H; Johnson, Alan T

    2010-11-15

    Sub-nanomolar small molecule inhibitors of anthrax lethal factor have been identified using SAR and Merck L915 (4) as a model compound. One of these compounds (16) provided 100% protection in a rat lethal toxin model of anthrax disease.

  5. Commitment to a purpose in life: an antidote to the suffering by individuals with social anxiety disorder.

    Science.gov (United States)

    Kashdan, Todd B; McKnight, Patrick E

    2013-12-01

    Recent acceptance- and mindfulness-based cognitive-behavioral interventions explicitly target the clarification and commitment to a purpose in life. Yet, scant empirical evidence exists on the value of purpose as a mechanism relevant to psychopathology or well-being. The present research explored daily (within-person) fluctuations in purposeful pursuits and well-being in a community sample of 84 adults with (n = 41) and without (n = 43) the generalized subtype of social anxiety disorder (SAD). After completing an idiographic measure of purpose in life, participants monitored their effort and progress toward this purpose, along with their well-being each day. Across 2 weeks of daily reports, we found that healthy controls reported increased self-esteem, meaning in life, positive emotions, and decreased negative emotions. People with SAD experienced substantial boosts in well-being indicators on days characterized by significant effort or progress toward their life purpose. We found no evidence for the reverse direction (with well-being boosting the amount of effort or progress that people with SAD devote to their purpose), and effects could not be attributed to comorbid mood or anxiety disorders. Results provide evidence for how commitment to a purpose in life enriches the daily existence of people with SAD. The current study supports principles that underlie what many clinicians are already doing with clients for SAD.

  6. From topical antidote against skin irritants to a novel counter-irritating and anti-inflammatory peptide.

    Science.gov (United States)

    Brodsky, Berta; Erlanger-Rosengarten, Avigail; Proscura, Elena; Shapira, Elena; Wormser, Uri

    2008-06-15

    The primary purpose of the present study was to investigate the mechanism of the counter-irritating activity of topical iodine against skin lesions induced by chemical and thermal stimuli. The hypothesis that iodine exerts its activity by inducing an endogenous anti-inflammatory factor was confirmed by exposing guinea pig skin to heat stimulus followed by topical iodine treatment and skin extraction. Injection of the extract into naïve guinea pigs reduced heat-induced irritation by 69%. The protective factor, identified as a new nonapeptide (histone H2A 36-44, H-Lys-Gly-Asn-Tyr-Ala-Glu-Arg-Ileu-Ala-OH), caused reduction of 40% in irritation score in heat-exposed guinea pigs. The murine analog (H-Lys-Gly-His-Tyr-Ala-Glu-Arg-Val-Gly-OH, termed IIIM1) reduced sulfur mustard (SM)-induced ear swelling at a dose-dependent bell-shape manner reaching peak activity of 1 mg/kg. Cultured keratinocytes transfected with the peptide were more resistant towards SM than the control cells. The peptide suppressed oxidative burst in activated neutrophils in a concentration-dependent manner. In addition, the peptide reduced glucose oxidase-induced skin edema in mice at a dose-dependent bell-shape manner. Apart from thermal and chemical-induced skin irritation this novel peptide might be of potential use in chronic dermal disorders such as psoriasis and pemphigus as well as non-dermal inflammatory diseases like multiple sclerosis, arthritis and colitis.

  7. Are Nontimber Forest Products the Antidote to Rainforest Degradation? Brazil Nut Extraction in Madre De Dios, Peru

    NARCIS (Netherlands)

    Escobal, J.A.; Aldana, U.

    2003-01-01

    This study explores the relationship between poverty and Amazonian forest management by Brazil nut harvesters in southeastern Peru. Although the poor rely more upon natural resource-based income than the rich, wealthier households use more forest wood and land than poorer ones. Contrary to the belie

  8. Is the Rule of Law an Antidote for Religious Tension? The Promise and Peril of Judicializing Religious Freedom (SWP 40)

    OpenAIRE

    Moustafa, Tamir; Nelson, Matthew; Schonthal, Ben; Shankar, Shylashri

    2015-01-01

    Does the ‘rule of law’ act as a force of moderation and, in matters of religion, serve as a key tool for mollifying or resolving disputes? Drawing on experiences from Sri Lanka, India, Malaysia, and Pakistan, we provide an alternative account of the link between legal processes and religious tensions, one that considers closely the roles played by constitutional law and legal procedure in perpetuating, deepening, or sustaining conflict. These case studies highlight four mechanisms that facili...

  9. An antidote to the emerging two tier organ donation policy in Canada: the Public Cadaveric Organ Donation Program.

    Science.gov (United States)

    Giles, S

    2005-04-01

    In Canada, as in many other countries, there exists an organ procurement/donation crisis. This paper reviews some of the most common kidney procurement and allocation programmes, analyses them in terms of public and private administration, and argues that privately administered living donor models are an inequitable stopgap measure, the good intentions of which are misplaced and opportunistic. Focusing on how to improve the publicly administered equitable cadaveric donation programme, and at the same time offering one possible explanation for its current failure, it is suggested that the simple moral principle of "give and you shall receive", already considered by some, be extended further. This would allow for those who are willing to sign up to be a public cadaveric donor be given a priority for receiving an organ donation should they ever require it. It is argued that this priority may provide the motivation to give that is so far lacking in Canada. This model is called the Public Cadaveric Organ Donation Program.

  10. Onion and garlic extracts as potential antidotes for cadmium-induced biochemical alterations in prostate glands of rats.

    Science.gov (United States)

    Ola-Mudathir, F K; Suru, S M

    2015-11-01

    Cadmium (Cd) has been implicated in increased prostate gland malignancy risk in both wildlife and humans. This study examines the chemoprotective roles of onion and garlic extracts on Cd-induced biochemical alterations in the prostate glands of rats. Adult male Wistar rats were randomly divided into nine groups: control group received double distilled water; Cd group received Cd alone (1.5 mg/100 g bwt per day); extract-treated groups were pre-treated with varied doses of onion and/or garlic extract (0.5 ml and 1.0 ml/100 g bwt per day) for 1 week and then co-treated with Cd (1.5 mg/100 g bwt per day) for additional 3 weeks. Oxidant/antioxidant status and acid phosphatase (ACPtotal and ACPprostatic ) activity were examined in prostate glands. Cd intoxication caused a marked (P garlic extract significantly minimised these alterations. The onion extract offered a dose-dependent protection. Our findings suggest a chemoprotective capability for onion and garlic extracts against Cd-induced biochemical alteration in the prostate glands.

  11. Effect of boron as an antidote on dry matter intake, nutrient utilization and fluorine balance in buffalo (Bubalus bubalis) exposed to high fluoride ration.

    Science.gov (United States)

    Bharti, Vijay K; Gupta, Meenakshi; Lall, D

    2008-12-01

    It is well known that excessive accumulation of fluorides can exert toxic effects on various tissues and organs so as to severely damage the health and production of animals. The aim of this study was to determine beneficial effect of boron on nutrient utilization in buffalo calves exposed to high fluoride (F) ration. For this purpose, we used three groups of four male Murrah buffalo calves (body weight 98-100 kg, aged 6-8 month) each. Control animal was given only basal diet and concentrate mixture. However, treatment I animals were fed basal diet, concentrate mixture, and F [as NaF, 60 ppm of dry matter (DM)]. The treatment II animals were fed basal diet, concentrate mixture, F (as NaF, 60 ppm of DM), and B (as sodium tetraborate, 140 ppm of DM). After 90 days of experimental feeding, a metabolism trial of 7 days duration was conducted to study the treatment effect on nutrient utilization of proximate nutrients, absorption, excretion, and retention of N, Ca, P, Fe, Zn, Cu, and F. Dietary F significantly (p matter intake and increased the apparent digestibility, absorption, and retention of F. However, boron supplementation significantly (p matter intake, fecal excretion, and percent of absorbed F excreted via urine. Apparent digestibility of proximate nutrients (viz. DM, crude protein, crude fiber, ether extract, and nitrogen free extract) was unaffected on either F or F+B treatment. However, absorption and excretion of N, Ca, P, Fe, Zn, and Cu were affected significantly (p < 0.05) on F or F+B treatment. These findings suggest that fluoride-containing diet for short duration has effect on nutrient utilization, and boron at 140-ppm dose level, in general, antagonized the absorption and retention of F and also improved the feed intake in buffalo calves.

  12. Functional Cardiorespiratory Toxicity Screening of Candidate Antiparasitic Drugs and Antidotes for Chemical Poisons. Study of the Effects of Drugs Upon the Cardiovascular and Respiratory Systems

    Science.gov (United States)

    1988-06-01

    and ZIP Code) 10. SOURCE OF FUNDING NUMBERS PROGRAM I PROJECT TASK WORK UNIT Fort Detrick ELEMENT NO. NO3M6- NO. ’ ACESSION O. Frederick, MD 21701...System In the Science and Prac- tice of Clinical Medicine , Vol. 2. Crune and Stratton, Inc., New York, 1976. Slakotos, A.N., Fiibert, M. and Hester...1 copy Dean School of Medicine Uniformed Services University of the Health Sciences 4301 Jones Bridge Road Bethesda, MD 20814-4799 I copy Commandant

  13. Adverse reactions of common antidotes and their prevention and management%常用解毒药物的不良反应及其防治

    Institute of Scientific and Technical Information of China (English)

    蒋绍锋; 孙承业

    2007-01-01

    解毒药物在急性中毒的救治中发挥重要作用,但其在救治过程中引起的不良反应容易被忽视.本文对常用解毒药物的不良反应分别进行概述,以助于临床安全应用.

  14. 刑事拘留存在的多发性问题与对策%The Usual Questions and Antidote in Criminal Detention

    Institute of Scientific and Technical Information of China (English)

    李维驹

    2002-01-01

    刑事拘留措施在刑事强制措施中占有重要地位,但是目前在公安工作实践中,对于该措施的运用存在拘留与留置混用,例外当原则,以拘代侦等问题.这些问题的解决主要有待于立法的完善,同时也需在实践中进一步加强侦查模式的转换.

  15. The modern preschool teacher's mental pressure and antidote%现代幼儿教师的心理压力与应对

    Institute of Scientific and Technical Information of China (English)

    郑晓边

    2001-01-01

    @@ 近年来,笔者受邀奔赴部分省市一些基层幼儿园,与许多幼儿教师和保育员进行过促膝交谈.在"教师的心理压力与应对"专题讨论中,大家反映的问题是发人深省的.

  16. Antidotes to anthrax lethal factor intoxication. Part 3: Evaluation of core structures and further modifications to the C2-side chain.

    Science.gov (United States)

    Jiao, Guan-Sheng; Kim, Seongjin; Moayeri, Mahtab; Crown, Devorah; Thai, April; Cregar-Hernandez, Lynne; McKasson, Linda; Sankaran, Banumathi; Lehrer, Axel; Wong, Teri; Johns, Lisa; Margosiak, Stephen A; Leppla, Stephen H; Johnson, Alan T

    2012-03-15

    Four core structures capable of providing sub-nanomolar inhibitors of anthrax lethal factor (LF) were evaluated by comparing the potential for toxicity, physicochemical properties, in vitro ADME profiles, and relative efficacy in a rat lethal toxin (LT) model of LF intoxication. Poor efficacy in the rat LT model exhibited by the phenoxyacetic acid series (3) correlated with low rat microsome and plasma stability. Specific molecular interactions contributing to the high affinity of inhibitors with a secondary amine in the C2-side chain were revealed by X-ray crystallography.

  17. 改头换面 快乐每一天 Antidotes 09/10巴黎家居流行趋势发布

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    面对一个危机不断加剧的世界,我们比任何时刻都需要家的温暖,是我们的避风港。在法国人眼中,家居装饰是仅次于亲情的人生重要的一部分,即使没有灵丹妙药,可所有的创意、诀窍、技术、颜色、幻想、优雅和生活质量汇聚成一股新的积极的能量,却能抚慰受伤的心灵。不要总盯着你的衣橱,家居同样需要跟随潮流变换风格,相信我,快乐远比你想的简单。一年两次相约,全世界家居装饰领域的专业人士和爱好者此时又齐聚MAISON&OBJET和MEUBLE PARIS的现场,感受获取最新创意潮流和更高端的产品信息。

  18. Proposing Boric Acid as an Antidote for Aluminium Phosphide Poisoning by Investigation of the Chemical Reaction Between Boric Acid and Phosphine

    OpenAIRE

    Motahareh Soltani; Seyed Farid Shetab-Boushehri; Hamidreza Mohammadi; Seyed Vahid Shetab-Boushehri

    2013-01-01

    Aluminium phosphide (AlP) is a storage fumigant pesticide, which is used to protect stored grains especially from insects and rodents. It releases phosphine (PH3) gas, a highly toxic mitochondrial poison, in contact with moisture, particularly if acidic. Although the exact mechanism of action is unknown so far, the major mechanism of PH3 toxicity seems to be the inhibition of cytochrome-c oxidase and oxidative phosphorylation which eventually results in adenosine triphosphate (ATP) depletion ...

  19. Accelerated urinary excretion of methylmercury following administration of its antidote N-acetylcysteine requires Mrp2/Abcc2, the apical multidrug resistance-associated protein.

    Science.gov (United States)

    Madejczyk, Michael S; Aremu, David A; Simmons-Willis, Tracey A; Clarkson, Thomas W; Ballatori, Nazzareno

    2007-07-01

    N-Acetylcysteine (NAC) is a sulfhydryl-containing compound that produces a dramatic acceleration of urinary methylmercury (MeHg) excretion in poisoned mice, but the molecular mechanism for this effect is poorly defined. MeHg readily binds to NAC to form the MeHg-NAC complex, and recent studies indicate that this complex is an excellent substrate for the basolateral organic anion transporter (Oat)-1, Oat1/Slc22a6, thus potentially explaining the uptake from blood into the renal tubular cells. The present study tested the hypothesis that intracellular MeHg is subsequently transported across the apical membrane of the cells into the tubular fluid as a MeHg-NAC complex using the multidrug resistance-associated protein-2 (Mrp2/Abcc2). NAC markedly stimulated urinary [(14)C]MeHg excretion in wild-type Wistar rats, and a second dose of NAC was as effective as the first dose in stimulating MeHg excretion. In contrast with the normal Wistar rats, NAC was much less effective at stimulating urinary MeHg excretion in the Mrp2-deficient (TR-) Wistar rats. The TR- rats excreted only approximately 30% of the MeHg excreted by the wild-type animals. To directly test whether MeHg-NAC is a substrate for Mrp2, studies were carried out in plasma membrane vesicles isolated from livers of TR- and control Wistar rats. Transport of MeHg-NAC was lower in vesicles prepared from TR- rats, whereas transport of MeHg-cysteine was similar in control and TR- rats. These results indicate that Mrp2 is involved in urinary MeHg excretion after NAC administration and suggest that the transported molecule is most likely the MeHg-NAC complex.

  20. [Treatment with inhibitors of new oral direct anticoagulants in patients with severe bleedings or urgent surgical procedures. The new dabigatran antidote: the place of idarucizumab in clinical practice].

    Science.gov (United States)

    Boda, Zoltán

    2016-03-20

    Only vitamin K antagonists could be applied as oral anticoagulants over the past six decades. Coumarols have narrow therapeutic range, and unpredictable anticoagulant effects are resulted by multiple drug interactions. Therefore, regular routine monitoring of the international normalized ratio is necessary. There are two groups of factor-specific anticoagulants: molecules with anti-FIIa (dabigatran) and anti-FXa (rivaroxaban, apixaban and edoxaban) effect. Author summarizes the most important clinical features of the new oral anticoagulants, their indications and the possibilities of laboratory controls. Bleedings are the most important side effects of anticoagulants. This review summarizes the current published evidences for new oral anticoagulants reversal (non-specific and specific) agents, especially in cases with severe acute bleedings or urgent surgery procedures. It reports on how to use inhibitors, the recommended doses and the most important clinical results. The review focuses on idarucizumab - already approved by the U.S. Food and Drug Administration and the European Medicines Agency - which has a key role as the first specific inhibitor of dabigatran.

  1. ECOLOGY-ECONOMICAL ASSESSMENT OF THE APPROPRIATENESS OF USING GROWTH REGULATORS, IMMUNIZERS AND ANTIDOTE OF HERBICIDES DURING GROWTH OF THE WINTER WHEAT IN THE KRASNODAR REGION

    Directory of Open Access Journals (Sweden)

    Yablonskaya Y. K.

    2015-06-01

    Full Text Available The article provides an overview of the phytosanitary condition of crops for 2011-2014 g in the Krasnodar region. In recent years, we can observe increasing of the crop losses from pests and diseases of plants. The using of different pesticides in intensive cultivation technologies of winter wheat can’t resist this. Pathogenic microorganisms acquire resistance to drugs used and become more aggressive. This creates a lot of environmental problems. Plants are almost always under environmental stress. However, it is impossible to refuse of pesticides. And they are not able to observe the immune system of the plant, and in some cases inhibit it. The present level of development of science has led to the emergence of new methods of plant protection, which is based on increasing of the capacity of the immune plants, rather than the destruction of pathogens, as in the case of the use of pesticides. We propose to apply so called "agrochemical cocktails"

  2. A Structural Biology and Protein Engineering Approach to the Development of Antidotes Against the Inhibition of Human Acetylcholinesterase by OP-based Nerve Agents

    Science.gov (United States)

    2015-05-01

    the Mosquito crystallization robot, identified conditions for formation of diffraction-quality crystals in 0.025% dichloromethane/12% PEG 20,000/0.1M...physiological AE dimer) involve residues situated at the peripheral anionic site (PAS) that might, therefore, block accessibility to the active...positive potential, which forms a non-physiological contact with monomer E, with a pink arrow pointing towards the peripheral anionic site on monomer E; (d

  3. In vivo evaluation of cholinesterase activity, oxidative stress markers, cyto- and genotoxicity of K048 oxime–a promising antidote against organophosphate poisoning.

    Science.gov (United States)

    Zunec, Suzana; Kopjar, Nevenka; Zeljezić, Davor; Kuca, Kamil; Musilek, Kamil; Lucić Vrdoljak, Ana

    2014-04-01

    K048 is a member of K-oximes, a new oxime class that has recently been confirmed effective against poisoning by the nerve agent tabun and several pesticides. The toxicity profile of the K048 oxime has not been fully characterized and its optimal therapeutic dose has not yet been established. Earlier studies report excellent results with K048 in reactivating tabun-phosphorylated AChE and in the therapy of tabun-poisoned mice. It possesses a low acute toxicity and exerts an acceptable toxicity profile on isolated human peripheral blood lymphocytes in vitro. Intraperitoneal administration of K048 in rats resulted in an LD50 of 238.3 mg/kg. In this in vivo study, we investigated cholinesterase (ChE) activity and oxidative stress marker levels (lipid peroxidation and superoxide dismutase activity) in the plasma of exposed rats after administering the compound at 25% of its LD50. Lymphocyte viability was evaluated using an acridine orange/ethidium bromide in situ fluorescent assay. The levels of primary DNA damage in rat white blood cells were measured using the alkaline comet assay. The compound applied at 25% of its LD50 did not significantly affect ChE activity and lipid peroxidation and did not cause significant changes in the SOD activity in plasma. The cytotoxicity profile of K048 in the tested dose was also acceptable, and it did not possess significant DNA-damaging potential. The obtained results are promising for further evaluations of the K048 oxime, which should include tests on a broader concentration range and longer incubation times.

  4. Research of Antidotal Effect of Herbicide Safener on Butachlor%除草剂安全剂对丁草胺解毒效果研究

    Institute of Scientific and Technical Information of China (English)

    张金艳

    2005-01-01

    采用室内生物测定的方法,通过对小麦生理指标-株高的测定,研究了除草剂安全剂3-二氯乙酰基-2-甲基-2-乙基-1,3-噁唑烷保护小麦免受除草剂丁草胺在不同浓度时的伤害.结果表明:当安全剂与丁草胺按一定浓度配比混合,对小麦有较好的保护效果,保护率可达60%~170%.

  5. A Structural Biology and Protein Engineering Approach to the Development of Antidotes against the Inhibition of Human Acetylcholinesterase by OP-based Nerve Agents

    Science.gov (United States)

    2014-03-01

    mPTA) was coupled to CNBr-activated Sepharose 4B. Purification of PNGase F: PNGase F removes N-linked polysaccharide chains from the asparagine...Centrifugal Filter Unit equipped with an Ultracel-30 membrane. Characterization of rhAChET: The purity and homogeneity of the affinity-purified...hAChE monomer is characterized by an α/β- hydrolase fold that consists of a 12-stranded central mixed β -sheet surrounded by 14 α -helices. Three

  6. INNOVATION TECHNOLOGY OF THE INTEGRATED USING OF GROWTH REGULATORS, IMMUNIZERS AND ANTIDOTE HERBICIDES IN CULTIVATION OF WINTER WHEAT IN THE KRASNODAR REGION

    Directory of Open Access Journals (Sweden)

    Yablonskaya Y. K.

    2015-06-01

    Full Text Available At present, the cultivation of agricultural products is on a level where the growth of productivity and quality is only possible by using the latest achievements of science. Scientists have been developing elements of agro-technologies of complex applications of growth regulators, fungicides and fertilizers in growing winter wheat, providing a significant increase in productivity and quality of agricultural products, reduction of labor costs, energy and all kinds of resources, sustainable harvesting, even in the zone of risky agriculture. Plant growth regulators have multifunctional properties, which are expressed in the regulation of plant growth and development, and in increasing their resilience to adverse weather conditions and many diseases. However, despite the fact that there are many examples of extremely high economic efficiency of plant growth regulators, in terms of production and use of pesticides are much inferior. Retardants and defoliants are used more widely. However, low rates of regulators and elicitors, the ability to manage with their help the growth and development of plants; change the resistance of plants to various external factors determines their prospects. We propose to apply the "agrochemical cocktails." It will induce the systemic plant resistance to the whole growing season, which is not possible in the case of using only one of the fungicides and bactericides. It is necessary to take into account the features of the functioning of the immune system of plants and to develop technological methods of influence on the key stages of the immune response of plants

  7. Bioanalytical Method to Determine the Effects of Cyanide, Cyanide Metabolites and Cyanide Antidotes on the Activity of Cytochrome C Oxidase Immobilized in an Electrode Supported Lipid Bilayer Membrane

    Science.gov (United States)

    2006-06-01

    7. Rhoten, M. C.; Hawkridge, F. M.; Wilczek, J., The reaction of cytochrome c with bovine and Bacillus stearothermophilus Cytochrome c Oxidase...transferases. Fund. and Appl. Toxicol. 1983, 3, 377-382. 27 35. Isom, G. E.; Burrows, G. E.; Way, J. L., Effect of oxygen on the antagonism of...mechanism of antagonism . Annu. Rev. Pharmacol. Toxicol. 1984, 24, 451-481. 50. Bryant, M. A.; Pemberton, E., Surface Raman scattering of self

  8. Drug: D01091 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available bolism 39 Other agents affecting metabolism 392 Antidotes 3925 Sodium thiosulfate...lassification [BR:br08303] V VARIOUS V03 ALL OTHER THERAPEUTIC PRODUCTS V03A ALL OTHER THERAPEUTIC PRODUCTS V03AB Antidotes

  9. Drug: D00517 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available ism 39 Other agents affecting metabolism 392 Antidotes 3929 Others D00517 Amyl nitrite (JP16/USP) Anatomical...L OTHER THERAPEUTIC PRODUCTS V03AB Antidotes V03AB22 Amyl nitrite D00517 Amyl nit

  10. Drug: D01572 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available sm 39 Other agents affecting metabolism 392 Antidotes 3929 Others D01572 Pralidoxime iodide (JAN/USAN) Anato...3A ALL OTHER THERAPEUTIC PRODUCTS V03AB Antidotes V03AB04 Pralidoxime D01572 Pral

  11. Drug: D00221 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available s affecting metabolism 39 Other agents affecting metabolism 392 Antidotes 3929 Others D00221 Acetylcysteine ...THER THERAPEUTIC PRODUCTS V03AB Antidotes V03AB23 Acetylcysteine D00221 Acetylcysteine (JP16/USP/INN) USP dr

  12. Drug: D00014 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available 3 Agents affecting metabolism 39 Other agents affecting metabolism 392 Antidotes 3922 Glutathiones D00014 Gl...HERAPEUTIC PRODUCTS V03A ALL OTHER THERAPEUTIC PRODUCTS V03AB Antidotes V03AB32 G

  13. Merbromin poisoning

    Science.gov (United States)

    ... a vein (by IV) Laxatives Medicine called an antidote to reverse the effect of the poison Tube ... chance for recovery. If the person takes an antidote to reverse the poison within 1 week, recovery ...

  14. Heroin overdose

    Science.gov (United States)

    ... overdose. This type of medicine is called an antidote. Naloxone is injected under the skin or into ... If an antidote can be given, recovery from an acute overdose occurs within 24 to 48 hours. Heroin is often mixed ...

  15. Methadone overdose

    Science.gov (United States)

    ... to reverse the effects of the methadone (an antidote) and to treat other symptoms Tube from the ... the better the chance for recovery. If an antidote can be given, recovery from an overdose begins ...

  16. Morphine overdose

    Science.gov (United States)

    ... through a vein (IV) Laxative Naloxone, a medicine (antidote) to reverse the effect of the poison, many ... breathing and die if medical attention or an antidote is not given right away. The person may ...

  17. Meperidine hydrochloride overdose

    Science.gov (United States)

    ... the better the chance for recovery. If an antidote can be given, recovery begins right away. People ... stay may be needed for doses of the antidote. Complications, such as pneumonia, muscle damage from lying ...

  18. Acetaminophen and codeine overdose

    Science.gov (United States)

    ... N-acetyl cysteine. This drug is called an antidote. It counteracts the effects of the acetaminophen. Without ... before treatment, brain injury may occur. If an antidote can be given, recovery from an acute overdose ...

  19. Optimization as side-effect of evolving allelopathic diversity

    NARCIS (Netherlands)

    Pagie, L.; Hogeweg, P.

    2002-01-01

    Many bacteria carry gene complexes that code for a toxin-antidote pair, e.g. colicin systems. Such gene complexes can be advantageous for its host by killing competitor bacteria while the antidote protects the host. However, in order to evolve a novel and useful toxin first a proper antidote must be

  20. Preliminary Report on the Effect of the Antidote of the Herbicide Antidote for Reducing Residual Injury of Chlorsulfuron on Corn%除草剂解毒剂对玉米绿磺隆残留药害的解毒效果初报

    Institute of Scientific and Technical Information of China (English)

    张金艳; 毕洪梅; 叶非

    2007-01-01

    采用室内盆栽和小区试验等生物测定方法,通过对玉米株高、株鲜重、单株产量、果实中支链氨基酸等指标的测定,研究了除草剂解毒剂3-二氯乙酰基-2,5-二甲基-2-乙基-1,3-噁唑烷减轻除草剂绿磺隆对玉米等后茬敏感作物伤害的生物活性.实验结果表明:上一年使用过绿磺隆的地块,下一年播种玉米时,可以通过3-二氯乙酰基-2,5-二甲基-2-乙基-1,3-噁唑烷的浸种、拌种、混喷、叶喷来减轻药害,其中混喷方法效果最好,为对照的99.41%,浸种方法仅次于混喷,为对照的95.65%.应用除草剂解毒剂使绿磺隆的残留量小于5μg/kg时,后茬可以种植玉米.

  1. Thermodynamic evaluation of activated charcoal as a poison antidote by high-performance liquid chromatography. I: Derivation and validation of an equation for Gibbs free energy of liquid-solid adsorption.

    Science.gov (United States)

    Kleeman, W P; Bailey, L C

    1988-06-01

    An in vitro method utilizing high-performance liquid chromatography (HPLC) was developed in order to investigate the adsorptive process between activated charcoal and various drugs and toxic chemicals by measuring their Gibbs free energy of adsorption from various acetonitrile:water mobile phases. This report details the derivation and validation of the equation for calculating the Gibbs free energy of liquid-solid adsorption via HPLC. The derived equation incorporates the following experimental parameters: specific surface area of the adsorbent, specific retention volume of the solute, molar volume of the mobile phase, and surface concentration of the solute in a predefined standard state. This equation was validated by means of a closed thermodynamic cycle composed of three segments. Each segment represents a different physical process: gas-solid adsorption of methyl iodide on activated charcoal, gas-liquid solution of methyl iodide in n-hexadecane, and liquid-solid adsorption of methyl iodide on activated charcoal from n-hexadecane. The Gibbs free energy for each of these thermodynamic processes was determined by the appropriate chromatographic technique. Since the cycle did not balance because it did not account for the interaction of n-hexadecane and activated charcoal, it was altered to include a gas-liquid-solid chromatographic technique. When the Gibbs free energies of solution and gas-solid adsorption determined by this chromatographic technique were incorporated into the cycle, the resulting imbalance was only 0.213 kJ/mol (1.1%), thereby validating the derived equation.

  2. 高校篮球运动员伤后不良心理的成因及矫正方法%Reason and Antidote of Basketball Athletes' Unhealthy Mental after Spotrs Injury

    Institute of Scientific and Technical Information of China (English)

    王大鹏

    2007-01-01

    分析了高校篮球运动员伤后在训练中产生的各种不良情绪,阐述了心理障碍产生的原因,提出了有效的心理调节和抑制方法.实践结果表明,通过心理训练,运动员心理素质有了一定的提高.

  3. On the Effect and Antidote of Commerce to Juvenile Culture and Spirit%论商业对青年文化和青年精神的影响及对策

    Institute of Scientific and Technical Information of China (English)

    张卓

    2003-01-01

    商业对青年文化的利用和影响,导致青年文化的沉沦;而青年精神作为青年文化的核心,势必也会受到商业的冲击和影响,甚至引起青年精神的溃败.振兴青年文化和青年精神,必须使青年摆脱享乐主义的生活方式.

  4. 网络对图书馆的冲击与图书馆的对策%The pounding of network to the library and antidoting of the library

    Institute of Scientific and Technical Information of China (English)

    李益群

    2001-01-01

    论述了网络时代对图书馆的冲击,面对各种各样对今后图书馆能否存在的消极论调,从对图书馆产生和发展的悠久历史考证,以无可争辩的事实表明,图书馆在网络环境下仍然是一个重要环节,有其无以替代的优势、图书馆的前景依然是光明的.

  5. 青海矿产资源勘探开发对策与建议%The Antidote and Advice to the Exploration and Exploitation of Qinghai's Mineral Resources

    Institute of Scientific and Technical Information of China (English)

    刘同德

    2002-01-01

    本文客观分析了中国加入WTO后,青海矿业所面临的三大挑战及存在的突出问题,并有针对性地提出发挥矿业优势,将青海的矿产资源优势转化为产品优势和经济优势,实现青海矿业可持续发展的对策与措施.

  6. The shortage and antidote about the moment way of foreign debt management in difference between investment and registered investment%当前外债"投注差"管理方法的缺陷及对策

    Institute of Scientific and Technical Information of China (English)

    陶坤

    2007-01-01

    现行外商投资企业外债"投注差"管理方法存在明显的缺陷,在一定程度上影响了外债规模控制的有效性,因此需结合外汇收支形势的发展,予以适当的调整和完善.

  7. 依托咪酯抗实验性惊厥作用及其机制%The antidotal effect and mechanism of etomidate on experimental convulsion in mice

    Institute of Scientific and Technical Information of China (English)

    孟晶; 戴体俊; 段世明; 许爱军; 郭忠民

    2006-01-01

    目的观察静脉麻醉药依托咪酯对小鼠电惊厥、药物性惊厥的作用,为临床应用提供依据,同时探讨依托咪酯的作用机制.方法以电刺激或致惊剂[士的宁、N-甲基-D-天冬氨酸(NMDA)、利多卡因]建立不同类型的小鼠惊厥模型,观察腹腔注射3种剂量的依托咪酯对小鼠强直性惊厥潜伏期、持续期、惊厥发生率、小鼠死亡率以及小鼠存活时间的影响.结果依托咪酯剂量依赖性地缩短电惊厥小鼠强直性惊厥的持续时间,延长士的宁惊厥小鼠的存活时间(P<0.01),较大剂量可完全拮抗NMDA和利多卡因引起的强直性惊厥(P<0.01).结论依托咪酯对小鼠电惊厥、士的宁、NMDA及利多卡因惊厥均有拮抗作用.依托咪酯的作用机制复杂,可能与NMDA受体、甘氨酸受体、γ-氨基丁酸A(GABAA)受体等有关.

  8. Reversed-phase ion-pair chromatography-diode array detection of the bispyridinium compound MB327: plasma analysis of a potential novel antidote for the treatment of organophosphorus poisoning.

    Science.gov (United States)

    John, Harald; Mikler, John; Worek, Franz; Thiermann, Horst

    2016-02-01

    In the case of poisoning by organophosphorus nerve agents or pesticides, there is still a lack of pharmacological treatment of the cholinergic crisis selectively targeting the nicotinic acetylcholine receptor. Recently, the compound MB327 was identified as a potential novel lead structure to close this gap, thus demanding a quantitative assay for initial pharmacokinetic (PK) studies. MB327 is a salt consisting of the dicationic bispyridinium compound (BPC) 1,1´-(propane-1,3-diyl)bis(4-tert-butylpyridinium) and two iodide counter ions. Due to the permanent positive charge of the BPC, an isocratic reversed-phase ion-pair chromatographic separation (RPIPC) was developed using heptanesulfonic acid as ion-pairing reagent and 45% v/v methanol as organic modifier (1 mL/min). Selective UV-detection (230 nm) was done by a diode array detector (DAD) for reliable, rugged, precise (RSD < 7%) and accurate (96-104%) quantitative analysis of 50 μL swine plasma (linear range 1-1000 µg BPC/mL plasma, lower limit of quantification 2 µg/mL). During method validation, diverse parameters essential for the chromatographic process were investigated to generate van´t Hoff, van Deemter and width plots allowing calculation of thermodynamic data like the distribution constant K (5.7 ± 0.3), change in enthalpy, ΔH(0) : -23.66 kJ/mol, and entropy, ΔS(0) : -65 J/(mol*K). In addition, RPIPC-DAD analysis enabled calculation of molar absorptivities of the BPC, ε230 : 17 400 ± 1100 L/(mol*cm), and iodide, ε230 : 9900 ± 400 L/(mol*cm), which determination was hampered by interference with each other in conventional cuvette UV-spectrophotometric measurements. Finally, the RPIPC-DAD procedure was applied to samples from an in vivo study of swine.

  9. Estabilidad de la hidroxocobalamina en agua para inyección como antídoto contra cianuros: Elaborado de Farmacia Militar Stability of hydroxocobalamin in water for injection as cyanide antidote

    OpenAIRE

    2012-01-01

    Introducción: Los cianuros han sido utilizados como agentes de guerra química, y hoy se consideran una amenaza terrorista real. Son también la principal causa de muerte en la intoxicación por inhalación de humo de incendios en espacios cerrados. El éxito en el tratamiento de la intoxicación depende de la rapidez con la que se administren los antídotos, y con la que estos fijen el ión cianuro. La hidroxocobalamina parece ser un antídoto más apropiado que el nitrito sódico para el tratamiento e...

  10. Toxicokinetic Profiles of Alpha-ketoglutarate Cyanohydrin, a Cyanide Detoxification Product, following Exposure to Potassium Cyanide

    Science.gov (United States)

    2013-07-15

    al., 2012). Furthermore, -Kg has been suggested as a cyanide antidote (Bhattacharya et al., 2002; Bhattacharya and Vijayaraghavan, 1991, 2002; Hume et...cyanide antidote (Bhattacharya et al., 2002; Bhattacharya and Vijayaraghavan, 1991, 2002; Hume et al., 1995; Mathangi et al., 2011; Tulsawani et al...potential exposure surro- gate. Chemical Research in Toxicology 20, 677–684. Hume , A.S., Mozingo, J.R., McIntyre, B., Ho, I.K., 1995. Antidotal

  11. Alternate Care Sites for the Management of Medical Surge in Disasters

    Science.gov (United States)

    2013-12-01

    FMS contains beds and medical and pharmaceutical resources. Outside of the main mission, to mass vaccinate or supply antidotes from the Strategic... antidotes and the more metropolitan areas of Florida have MMRS, response teams, trauma centers and caches of medical supplies and equipment. Florida...on their individual facility. Hospitals have also become a partner with the CDC to store caches of antidotes to manage the effects on patients from

  12. NATO Allied Joint Medical Publication 7: Allied Joint Medical Doctrine for Support to Chemical, Biological, Radiological, and Nuclear (CBRN) Defensive Operations, Final Draft

    Science.gov (United States)

    2014-07-31

    electronic, mechanical , photo-copying, recording or otherwise, without the prior permission of the publisher. With the exception of commercial sales, this...would potentially require a large and readily accessible antidote supply. Procedures for obtaining these antidotes must be well established. For...prophylaxis/pre-treatment medications as needed, emergency antidotes , an individual decontamination kit, and a first aid kit. 2. IPE commonly used by

  13. Submicrometric 2D ratchet effect in magnetic domain wall motion

    Energy Technology Data Exchange (ETDEWEB)

    Castán-Guerrero, C., E-mail: ccastan@unizar.es [Instituto de Ciencia de Materiales de Aragón (ICMA), CSIC – Universidad de Zaragoza, E-50009 Zaragoza (Spain); Dpto. de Física de la Materia Condensada, Universidad de Zaragoza, E-50009 Zaragoza (Spain); Herrero-Albillos, J. [Fundación ARAID, E-50004 Zaragoza (Spain); Centro Universitario de la Defensa, E-50090 Zaragoza (Spain); Instituto de Ciencia de Materiales de Aragón (ICMA), CSIC – Universidad de Zaragoza, E-50009 Zaragoza (Spain); Sesé, J. [Instituto de Nanociencia de Aragón, Laboratorio de Microscopías Avanzadas, Universidad de Zaragoza, E-50018 Zaragoza (Spain); Dpto. de Física de la Materia Condensada, Universidad de Zaragoza, E-50009 Zaragoza (Spain); Bartolomé, J.; Bartolomé, F. [Instituto de Ciencia de Materiales de Aragón (ICMA), CSIC – Universidad de Zaragoza, E-50009 Zaragoza (Spain); Dpto. de Física de la Materia Condensada, Universidad de Zaragoza, E-50009 Zaragoza (Spain); Hierro-Rodriguez, A.; Valdés-Bango, F.; Martín, J.I.; Alameda, J.M. [Dpto. Física, Universidad de Oviedo, Asturias (Spain); CINN (CSIC – Universidad de Oviedo – Principado de Asturias), Asturias (Spain); García, L.M. [Instituto de Ciencia de Materiales de Aragón (ICMA), CSIC – Universidad de Zaragoza, E-50009 Zaragoza (Spain); Dpto. de Física de la Materia Condensada, Universidad de Zaragoza, E-50009 Zaragoza (Spain)

    2014-12-15

    Strips containing arrays of submicrometric triangular antidots with a 2D square periodicity have been fabricated by electron beam lithography. A clear ratchet effect of 180° domain wall motion under a varying applied field parallel to the walls has been observed. The direction is determined by the direction of the triangle vertices. In contrast, no ratchet effect is observed when the antidot array is constituted by symmetric rhomb-shaped antidots.

  14. Plaadid / Margit Tõnson

    Index Scriptorium Estoniae

    Tõnson, Margit, 1978-

    2005-01-01

    Uutest heliplaatidest Saint Etienne "Tales From Turnpike House", "Team Sleep", Jamiroquai "Dynamite", Life Of Agony "Broken Valley", The Wallflowers "Rebel, Sweetheart", morcheeba "The Antidote", Amerie "Touch"

  15. Interventions for paracetamol (acetaminophen) overdoses. Protocol for a Cochrane Review

    DEFF Research Database (Denmark)

    Brok, J; Buckley, N; Gluud, C

    2001-01-01

    Poisoning with paracetamol (acetaminophen) is a common cause of hepatotoxicity in the Western World. Inhibition of absorption, removal from the vascular system, antidotes, and liver transplantation are interventions for paracetamol poisoning.......Poisoning with paracetamol (acetaminophen) is a common cause of hepatotoxicity in the Western World. Inhibition of absorption, removal from the vascular system, antidotes, and liver transplantation are interventions for paracetamol poisoning....

  16. Drug: D00167 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available C PRODUCTS V03A ALL OTHER THERAPEUTIC PRODUCTS V03AB Antidotes V03AB09 Dimercaprol D00167 Dimercaprol (JP16/...fecting metabolism 392 Antidotes 3923 Mercaptoacetates D00167 Dimercaprol (JP16/U...V03AB09 Therapeutic category of drugs in Japan [BR:br08301] 3 Agents affecting metabolism 39 Other agents af

  17. Anti-histamine effect of Rubia tibetica, used to treat anaphylaxis caused by tick bites in the Pamir Mountains, Afghanistan

    DEFF Research Database (Denmark)

    Jeppesen, Anne S.; Kristiansen, Uffe; Soelberg, Jens;

    2012-01-01

    The roots of Rubia tibetica are chewed as an antidote to anaphylaxis caused by bites of the tick Ornithodoros lahorensis by the Wakhi people in Afghanistan.......The roots of Rubia tibetica are chewed as an antidote to anaphylaxis caused by bites of the tick Ornithodoros lahorensis by the Wakhi people in Afghanistan....

  18. Drug: D05940 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available utic category of drugs in Japan [BR:br08301] 3 Agents affecting metabolism 39 Other agents affecting metabolism 392 Antidotes...ER THERAPEUTIC PRODUCTS V03AB Antidotes V03AB35 Sugammadex D05940 Sugammadex sodium (JAN/USAN) CAS: 343306-7

  19. Drug: D03943 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available V VARIOUS V03 ALL OTHER THERAPEUTIC PRODUCTS V03A ALL OTHER THERAPEUTIC PRODUCTS V03AB Antidotes...of drugs in Japan [BR:br08301] 3 Agents affecting metabolism 39 Other agents affecting metabolism 392 Anti...dotes 3921 EDTAs D03943 Calcium disodium edetate hydrate (JAN); Edetate calcium dis

  20. Drug: D00019 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available c category of drugs in Japan [BR:br08301] 3 Agents affecting metabolism 39 Other agents affecting metabolism 392 Antidotes...LL OTHER THERAPEUTIC PRODUCTS V03AB Antidotes V03AB26 Methionine D00019 L-Methionine (JP16); Methionine (USP

  1. Robust band gap and half-metallicity in graphene with triangular perforations

    Science.gov (United States)

    Gregersen, Søren Schou; Power, Stephen R.; Jauho, Antti-Pekka

    2016-06-01

    Ideal graphene antidot lattices are predicted to show promising band gap behavior (i.e., EG≃500 meV) under carefully specified conditions. However, for the structures studied so far this behavior is critically dependent on superlattice geometry and is not robust against experimentally realistic disorders. Here we study a rectangular array of triangular antidots with zigzag edge geometries and show that their band gap behavior qualitatively differs from the standard behavior which is exhibited, e.g., by rectangular arrays of armchair-edged triangles. In the spin unpolarized case, zigzag-edged antidots give rise to large band gaps compared to armchair-edged antidots, irrespective of the rules which govern the existence of gaps in armchair-edged antidot lattices. In addition the zigzag-edged antidots appear more robust than armchair-edged antidots in the presence of geometrical disorder. The inclusion of spin polarization within a mean-field Hubbard approach gives rise to a large overall magnetic moment at each antidot due to the sublattice imbalance imposed by the triangular geometry. Half-metallic behavior arises from the formation of spin-split dispersive states near the Fermi energy, reducing the band gaps compared to the unpolarized case. This behavior is also found to be robust in the presence of disorder. Our results highlight the possibilities of using triangular perforations in graphene to open electronic band gaps in systems with experimentally realistic levels of disorder, and furthermore, of exploiting the strong spin dependence of the system for spintronic applications.

  2. Hyperbaric oxygen therapy or hydroxycobalamin attenuates surges in brain interstitial lactate and glucose; and hyperbaric oxygen improves respiratory status in cyanide-intoxicated rats

    DEFF Research Database (Denmark)

    Lawson-Smith, P; Olsen, Niels Vidiendal; Hyldegaard, Ole

    2011-01-01

    Cyanide (CN) intoxication inhibits cellular oxidative metabolism and may result in brain damage. Hydroxycobalamin (OHCob) is one among other antidotes that may be used following intoxication with CN. Hyperbaric oxygen (HBO2) is recommended when supportive measures or antidotes fail. However...

  3. Acute experimental tabun-induced intoxication and its therapy in rats.

    Science.gov (United States)

    Krejcová, G; Kassa, J

    2004-03-01

    Pharmacological pretreatment and antidotal treatment on tabun-induced neurotoxicity were studied in male albino rats that were poisoned with a lethal dose of tabun (280 microg/kg i.m.; 100% of LD50 value) and observed at 24 hours and 7 days following tabun challenge. The neurotoxicity of tabun was evaluated using a Functional observational battery and an automatic measurement of motor activity. Pharmacological pretreatment as well as antidotal treatment were able to reverse most of tabun-induced neurotoxic signs observed at 24 hours following tabun poisoning. However, there was not significant difference between the efficacy of profylaxis and antidotal treatment to eliminate tabun-induced neurotoxicity. The combination of profylactic pretreatment and antidotal treatment seems to be slightly more effective in the elimination of tabun-induced neurotoxicity in rats at 24 hours following tabun challenge in comparison with the administration of profylactic pretreatment or antidotal treatment alone. At 7 days following tabun poisoning, very few neurotoxic signs in tabun-poisoned rats were observed regardless of administration of pharmacological pretreatment or antidotal treatment. Thus, our findings confirm that the combination of pharmacological pretreatment and antidotal treatment is not only able to protect the experimental animals from the lethal effects of tabun but also to eliminate most of tabun-induced signs of neurotoxicity in tabun-poisoned rats.

  4. Acute Cyanide Poisoning: Hydroxocobalamin and Sodium Thiosulfate Treatments with Two Outcomes following One Exposure Event

    Directory of Open Access Journals (Sweden)

    Andrew Meillier

    2015-01-01

    Full Text Available Cyanide is rapidly reacting and causes arrest of aerobic metabolism. The symptoms are diffuse and lethal and require high clinical suspicion. Remediation of symptoms and mortality is highly dependent on quick treatment with a cyanide antidote. Presently, there are two widely accepted antidotes: sodium thiosulfate and hydroxocobalamin. These treatments act on different components of cyanide’s metabolism. Here, we present two cases resulting from the same source of cyanide poisoning and the use of both antidotes separately used with differing outcomes.

  5. Drug: D08249 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available UCTS V03AB Antidotes V03AB15 Naloxone D08249 Naloxone (INN) USP drug classification [BR:br08302] Anti-Addi...ction/Substance Abuse Treatment Agents Opioid Reversal Agents Naloxone D08249 Nalox

  6. Drug: D05647 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available D05647 Drug Prussian blue insoluble (USAN); Ferric hexacyanoferrate (II); Radiogard...PRODUCTS V03AB Antidotes V03AB31 Prussian blue D05647 Prussian blue insoluble (USAN) CAS: 14038-43-8 PubChem

  7. A mouse model for studying the interaction of bisdioxopiperazines with topoisomerase IIα in vivo

    DEFF Research Database (Denmark)

    Grauslund, Morten; Vinding, Annemette; Füchtbauer, Annette C.;

    2007-01-01

    as an antidote for alleviating tissue damage and necrosis after accidental anthracycline extravasation. This dual modality of bisdioxopiperazines, including ICRF-187, raises the question of whether their pharmacological in vivo effects are mediated through interaction with topoisomerase II or via...

  8. A murine experimental anthracycline extravasation model: pathology and study of the involvement of topoisomerase II alpha and iron in the mechanism of tissue damage

    DEFF Research Database (Denmark)

    Thougaard, Annemette V; Langer, Seppo W; Hainau, Bo;

    2010-01-01

    The bisdioxopiperazine topoisomerase II catalytic inhibitor dexrazoxane has successfully been introduced into the clinic as an antidote to accidental anthracycline extravasation based on our preclinical mouse studies. The histology of this mouse extravasation model was investigated and found...

  9. Ciguatera Fish Poisoning

    Science.gov (United States)

    ... debilitating (Miller, 1991). To date there is no antidote or effectivc treatment, so supportive care and medications ... Diagnosis, Management and Treatment, Chemical Structure, and Molecular Mechanism of Action. Additional Resources Ciguatera Fish Poisoning: Treatment, ...

  10. Flumazenil, naloxone and the 'coma cocktail'.

    Science.gov (United States)

    Sivilotti, Marco L A

    2016-03-01

    Flumazenil and naloxone are considered to be pharmacologically ideal antidotes. By competitive binding at the molecular target receptors, they are highly specific antagonists of two important drug classes, the benzodiazepines and opioids, respectively. Both antidotes enjoy rapid onset and short duration after parenteral administration, are easily titrated and are essentially devoid of agonist effects. Yet only naloxone is widely used as a component of the 'coma cocktail', a sequence of empirical treatments to correct altered mental status, while experts discourage the use of flumazenil for such patients. This review contrasts the history, indications, published evidence and novel applications for each antidote in order to explain this disparity in the clinical use of these 'ideal' antidotes.

  11. Drug: D08749 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available D08749 Mixture, Drug Hydroxocobalamin - isotonic sodium chloride solution mixt Hydr...m 392 Antidotes 3929 Others D08749 Hydroxocobalamin - isotonic sodium chloride solution mixt PubChem: 96025432 ...

  12. Hyperbaric oxygen therapy or hydroxycobalamin attenuates surges in brain interstitial lactate and glucose; and hyperbaric oxygen improves respiratory status in cyanide-intoxicated rats

    DEFF Research Database (Denmark)

    Lawson-Smith, P; Olsen, Niels Vidiendal; Hyldegaard, O

    2011-01-01

    Cyanide (CN) intoxication inhibits cellular oxidative metabolism and may result in brain damage. Hydroxycobalamin (OHCob) is one among other antidotes that may be used following intoxication with CN. Hyperbaric oxygen (HBO2) is recommended when supportive measures or antidotes fail. However, the ...... this beneficial effect. In conclusion, CN intoxication in anesthetized rats produces specific uncoupling of cerebral oxidative metabolism resulting in interstitial lactate and glucose surges that may be ameliorated by treatment with either hydroxycobalamin or HBO2....

  13. Quantum information processing using designed defect states in

    DEFF Research Database (Denmark)

    Pedersen, Jesper; Flindt, Christian; Mortensen, Niels Asger

    2007-01-01

    We propose a new physical implementation of spin qubits for quantum information processing, namely defect states in antidot lattices de¯ned in the two-dimensional electron gas at a semiconductor heterostructure. Calculations of the band structure of the periodic antidot lattice are presented......-coupled defect states is calculated numerically.We ¯nd results reminiscent of double quantum dot structures, indicating that the suggested structure is a feasible physical implementation of spin qubits....

  14. Interventions for paracetamol (acetaminophen) overdoses

    DEFF Research Database (Denmark)

    Brok, J; Buckley, N; Gluud, C

    2002-01-01

    Self-poisoning with paracetamol (acetaminophen) is a common cause of hepatotoxicity in the Western World. Interventions for paracetamol poisoning encompass inhibition of absorption, removal from the vascular system, antidotes, and liver transplantation.......Self-poisoning with paracetamol (acetaminophen) is a common cause of hepatotoxicity in the Western World. Interventions for paracetamol poisoning encompass inhibition of absorption, removal from the vascular system, antidotes, and liver transplantation....

  15. Dabigatran and its reversal with recombinant factor VIIa and prothrombin complex concentrate

    DEFF Research Database (Denmark)

    Sølbeck, Sacha; Nilsson, Caroline U; Engström, Martin;

    2014-01-01

    OBJECTIVE: Dabigatran is a new oral direct thrombin inhibitor. No specific antidote exists in the event of hemorrhage, but prothrombin complex concentrate (PCC) and recombinant activated factor VII (rFVIIa) are suggested therapies. Sonoclot is a bedside viscoelastic instrument for monitoring...... of the PCC and rFVIIa in our study. Clinical studies of dabigatran-treated patients with severe bleeding are called for, as well as the continued development of specific antidotes and monitoring techniques....

  16. Magnetic Nanostructures Patterned by Self-Organized Materials

    Science.gov (United States)

    2016-01-05

    the effects of geometry and roughness on the reflection and transmission of spin waves on waveguides; mechanisms for controlling the anisotropy of...Self organized arrays of antidots . We have investigated the magnetic properties of permalloy [Journal of Magnetism and Magnetic Materials 350, 88...93 (2014)] and cobalt [Journal of Physics D: Applied Physics 47, 335001 (2014)] magnetic antidot arrays with different hole sizes. Importantly, these

  17. Due Process Mechanism and Fraudulent Practices in Nigerian Public Sector

    OpenAIRE

    Emmanuel ATAGBORO

    2015-01-01

    This study empirically examined whether due process mechanism serve as an antidote for fraudulent practices in the Nigerian public sector. Using 875 subjects in the public sector, the Pearson Product-Moment Correlation statistical tool was employed in order to establish whether due process mechanism is an antidote for fraudulent practices and also to see if due process ensures transparency in the public sector. The study found that due process ensures transparency and is an antido...

  18. Molecular dynamics of the interaction of pralidoxime and deazapralidoxime with acetylcholinesterase inhibited by the neurotoxic agent tabun

    OpenAIRE

    Gonçalves,Arlan da S.; França,Tanos C. C.; Wilter,Alan; Figueroa-Villar,José D.

    2006-01-01

    Efficient acetylcholinesterase reactivators are fundamental for the development of antidotes against poisoning by neurotoxic pesticides and chemical warfare agents. However, the mechanism of the reactivation reaction and the structural characteristics of the known reactivators are poorly understood. In order to study the dynamic behavior and the effect of the antidote net charge in the reactivation of this enzyme, we carried out a molecular dynamics study of human acetylcholinesterase inhibit...

  19. Advances in clinical toxicology.

    Science.gov (United States)

    Boehnert, M T; Lewander, W J; Gaudreault, P; Lovejoy, F H

    1985-02-01

    New data are reviewed in two areas in the management of the acute overdose: gastrointestinal decontamination and systemic antidotes. The mechanism and effectiveness of Ipecac syrup, gastric aspiration and lavage, activated charcoal, gastrointestinal dialysis, and saline cathartics are discussed. Special problems posed by disc batteries and packet ingestion of cocaine (in transporting contraband) are highlighted. The pharmacology and uses of pyridoxine and naloxone as antidotes are detailed.

  20. ŞİFÂ’İYYE ADLI ESERE GÖRE DAĞ KEÇİSİ VE YILANDA PANZEHİR ÖZELLİKLİ TAŞLAR

    Directory of Open Access Journals (Sweden)

    Muhittin Eliaçık

    2012-12-01

    Full Text Available Being a remedy for protecting the body and soul from poisons in the ancient medicine, antidote is also a term that is used for stone-based remedies. This word, which was made by adding the prefix pâd, which means something that removes harm and mischief, to the word zehr, expresses the medicine or remedies that protect the body and soul from the demolishing effects of sorrow and desolation, as well. The book, which is called Şifâ’iyye and was written by Şifâî Şaban Efendi during the period of Sultan II.Mustafa, discusses about the types of antidote and stones with features of antidote. This book of three chapters respectively discusses about mineral, animal and hatchery antidotes. The epilogue section of the book, on the other hand, explains many other stones with features of antidote. This small-volume book was prepared by Şifâî Şaban Efendi, who was a palace physician during the period of Sultan II.Mustafa, through researching many important medical books. Third chapter of this epistle mentions about animal antidotes and indicates that this stone is available in mountain goats and snakes and various explanations are made. This article introduces this section of the epistle, which involves important information in terms of pharmacology, zoology and lithology.

  1. Numerical simulation on the flux avalanche behaviors of microstructured superconducting thin films

    Science.gov (United States)

    Jing, Ze; Yong, Huadong; Zhou, Youhe

    2017-01-01

    Controlling and suppressing the propagation of magnetic flux avalanches is an important issue for the application of type-II superconductors. The effects of engineered pinning centers (antidots) on the guidance of flux avalanche propagation paths in type-II superconducting thin films are numerically investigated by solving the coupled nonlinear Maxwell's equations and the thermal diffusion equations. The field dependence of critical current density is considered in the simulation in this paper. Dynamic propagations of the thermomagnetic avalanches within the superconducting films patterned with different arrangements of antidots (like random, periodic square, and conformal mapping arrays) are presented. We reveal that presence of the antidots significantly modifies the propagation paths of the avalanches. The flux avalanche patterns of the superconducting films change with the variation of the arrangements of antidots. The patterned antidots in the form of conformal mapping arrays within the superconducting film exhibit strong guidance to the thermomagnetic avalanches. In addition, introducing the antidots in the form of conformal mapping arrays into the superconducting film can effectively lower the magnetic flux jump sizes.

  2. Curing Effect of Antidote Yiwei on Rape Injury Caused by Acetochlor and Its Functional Mechanism%益微微生物菌剂对乙草胺油菜药害的缓解效果及作用机制初步研究

    Institute of Scientific and Technical Information of China (English)

    陈然; 江慧; 李黎; 李俊凯

    2016-01-01

    为了探索益微微生物菌剂拌种缓解乙草胺油菜药害的效果及其作用机制,采用盆栽法测定了益微拌种对乙草胺油菜药害的缓解效果,采用分光光度法分别测定益微拌种对油菜叶片中还原型谷胱甘肽(GSH)、氧化型谷胱甘肽(GSSG)含量和谷胱甘肽转移酶(GST)活性的影响,并采用GC-MS法检测油菜植株中乙草胺的残留量.结果表明:乙草胺的施用量为840~1 680 g/hm2时,对油菜生长均有一定的抑制作用;用益微拌种处理后,均能显著缓解乙草胺对油菜的药害,当乙草胺用量为1 680 g/hm2、拌种量为25 g益微拌1 kg油菜种子时,油菜的株高、鲜质量恢复率分别为79.31%和178.57%.与单用乙草胺处理相比,先用益微拌种后喷施乙草胺,油菜植株中GSH含量增加,GST活性提高,同时乙草胺残留量极显著降低.说明益微微生物菌剂能提高植株中相关抗逆酶的活性,促进乙草胺的降解,从而显著缓解乙草胺对油菜的药害.

  3. A comparison of the efficacy of pyridostigmine alone and the combination of pyridostigmine with anticholinergic drugs as pharmacological pretreatment of tabun-poisoned rats and mice.

    Science.gov (United States)

    Kassa, Jirí; Vachek, J

    2002-08-15

    The ability of two types of pharmacological pretreatment (pyridostigmine alone or pyridostigmine in combination with two anticholinergic drugs) to increase the resistance of rats and mice against tabun and to increase the therapeutic efficacy of common antidotal treatment of tabun-poisoned rats and mice was compared. A significant decrease in the LD50 values of tabun was observed when mice as well as rats were pretreated with the prophylactic antidotal mixture consisting of pyridostigmine, benactyzine and trihexyphenidyle, designated PANPAL. Pyridostigmine-pretreated rats were also more resistant against acute lethal effects of tabun but pyridostigmine-induced resistance of rats was not so high as PANPAL-induced resistance. In addition, the pharmacological pretreatment with pyridostigmine alone was not able to protect mice against tabun-induced acute toxicity. The pharmacological pretreatment with pyridostigmine alone was able to increase the efficacy of currently used antidotal treatment (obidoxime in combination with atropine and diazepam) of tabun-induced poisoning, but PANPAL-induced increase in the efficacy of the same antidotal treatment was significantly higher than an increase induced by pyridostigmine alone. PANPAL-induced increase in the efficacy of antidotal treatment of tabun poisoning was also observed in mice. These findings confirm that PANPAL pretreatment of tabun-poisoned rats and mice seems to be much more suitable than currently used pyridostigmine alone.

  4. A Literature Review of the Use of Sodium Bicarbonate for the Treatment of QRS Widening.

    Science.gov (United States)

    Bruccoleri, Rebecca E; Burns, Michele M

    2016-03-01

    Sodium bicarbonate is a well-known antidote for tricyclic antidepressant (TCA) poisoning. It has been used for over half a century to treat toxin-induced sodium channel blockade as evidenced by QRS widening on the electrocardiogram (ECG). The purpose of this review is to describe the literature regarding electrophysiological mechanisms and clinical use of this antidote after poisoning by tricyclic antidepressants and other agents. This article will also address the literature supporting an increased serum sodium concentration, alkalemia, or the combination of both as the responsible mechanism(s) for sodium bicarbonate's antidotal properties. While sodium bicarbonate has been used as a treatment for cardiac sodium channel blockade for multiple other agents including citalopram, cocaine, flecainide, diphenhydramine, propoxyphene, and lamotrigine, it has uncertain efficacy with bupropion, propranolol, and taxine-containing plants.

  5. Management of cyanide toxicity in patients with burns.

    Science.gov (United States)

    MacLennan, Louise; Moiemen, Naiem

    2015-02-01

    The importance of cyanide toxicity as a component of inhalational injury in patients with burns is increasingly being recognised, and its prompt recognition and management is vital for optimising burns survival. The evidence base for the use of cyanide antidotes is limited by a lack of randomised controlled trials in humans, and in addition consideration must be given to the concomitant pathophysiological processes in patients with burns when interpreting the literature. We present a literature review of the evidence base for cyanide antidotes with interpretation in the context of patients with burns. We conclude that hydroxycobalamin should be utilised as the first-line antidote of choice in patients with burns with inhalational injury where features consistent with cyanide toxicity are present.

  6. Preparation of Ag/TiO2/ITO UV Detector and Its Photoelectronic Properties

    Directory of Open Access Journals (Sweden)

    DAI Songyan

    2016-12-01

    Full Text Available TiO2-based UV detectors with Ag antidot/TiO2/ITO sandwich structure were prepared by RF magnetron sputtering and colloidal crystal template technology. The microstructure and photoelectronic properties of the UV detectors were investigated by SEM, XRD, four point probe and semiconductor parameter instrument. The experimental results show that pore size of Ag antidot has an obvious effect on the photoelectronic properties of the detectors. With the increase of pore size, the dark current increases and the response time is prolonged, while the photocurrent is increased at first, then is decreased. Meanwhile, it is found that photoelectronic properties are optimum when the pore size is 4.2 μm. Antidot array electrodes with large pore size possess higher electrical conductivity, lower ultraviolet transmittance and higher recombination probability of electron-hole pair. Therefore, the pore size variation exhibits significant effluence on the photoelectronic properties of the UV detector.

  7. The Research of Antidotal Effect of Herbicide Safener 3-dichloroacetyl-2,5-dimethyl-2-ethyl-1,3-oxazolidine on Butachlor%除草剂安全剂3-二氯乙酰基-2,5-二甲基-2-乙基-1,3-噁唑烷对丁草胺解毒效果研究

    Institute of Scientific and Technical Information of China (English)

    张金艳

    2004-01-01

    本文主要采用室内生物测定的方法,通过对小麦生理指标--株高的测定,研究了除草剂安全剂3-二氯乙酰基-2,5-二甲基-2-乙基-1,3-噁唑烷保护小麦免受除草剂丁草胺在不同浓度时的伤害.结果表明:当安全剂与丁草胺按一定浓度配比混合,对小麦有较好的保护效果,保护率可达60%~170%.

  8. Enhanced pinning in superconducting thin films with graded pinning landscapes

    Science.gov (United States)

    Motta, M.; Colauto, F.; Ortiz, W. A.; Fritzsche, J.; Cuppens, J.; Gillijns, W.; Moshchalkov, V. V.; Johansen, T. H.; Sanchez, A.; Silhanek, A. V.

    2013-05-01

    A graded distribution of antidots in superconducting a-Mo79Ge21 thin films has been investigated by magnetization and magneto-optical imaging measurements. The pinning landscape has maximum density at the sample border, decreasing linearly towards the center. Its overall performance is noticeably superior than that for a sample with uniformly distributed antidots: For high temperatures and low fields, the critical current is enhanced, whereas the region of thermomagnetic instabilities in the field-temperature diagram is significantly suppressed. These findings confirm the relevance of graded landscapes on the enhancement of pinning efficiency, as recently predicted by Misko and Nori [Phys. Rev. B 85, 184506 (2012)].

  9. Overview, prevention and management of chemotherapy extravasation.

    Science.gov (United States)

    Kreidieh, Firas Y; Moukadem, Hiba A; El Saghir, Nagi S

    2016-02-10

    Chemotherapy extravasation remains an accidental complication of chemotherapy administration and may result in serious damage to patients. We review in this article the clinical aspects of chemotherapy extravasation and latest advances in definitions, classification, prevention, management and guidelines. We review the grading of extravasation and tissue damage according to various chemotherapeutic drugs and present an update on treatment and new antidotes including dexrazoxane for anthracyclines extravasation. We highlight the importance of education and training of the oncology team for prevention and prompt pharmacological and non-pharmacological management and stress the availability of new antidotes like dexrazoxane wherever anthracyclines are being infused.

  10. Cyanide intoxication as part of smoke inhalation - a review on diagnosis and treatment from the emergency perspective

    Directory of Open Access Journals (Sweden)

    Hyldegaard Ole

    2011-03-01

    Full Text Available Abstract This paper reviews the current literature on smoke inhalation injuries with special attention to the effects of hydrogen cyanide. It is assumed that cyanide poisoning is still an overlooked diagnosis in fire victims. Treatment against cyanide poisoning in the emergency setting should be given based on the clinical diagnosis only. Oxygen in combination with a recommended antidote should be given immediately, the first to reduce cellular hypoxia and the second to eliminate cyanide. A specific antidote is hydroxycobalamin, which can be given iv. and has few side effects.

  11. Chelation in metal intoxication—Principles and paradigms

    DEFF Research Database (Denmark)

    Aaseth, Jan; Skaug, Marit Aralt; Cao, Yang;

    2015-01-01

    of heavy metal poisoning, and available as capsules for oral use. In copper overload, DMSA appears to be a potent antidote, although d-penicillamine is still widely used. In the chelation of iron, the thiols are inefficient, since iron has higher affinity for ligands with nitrogen and oxygen, but the new...... oral iron antidotes deferiprone and desferasirox have entered into the clinical arena. Comparisons of these agents and deferoxamine infusions are in progress. General principles for research and development of new chelators are briefly outlined in this review...

  12. Enhanced Spin Hall Effect in Semiconductor Heterostructures with Artificial Potential

    Science.gov (United States)

    Eto, Mikio; Yokoyama, Tomohiro

    2009-07-01

    We theoretically investigate the extrinsic spin Hall effect (SHE) in semiconductor heterostructures, caused by scattering at an artificial potential created by an antidot, STM tip, etc. The potential is electrically tunable. First, we formulate the SHE in terms of phase shifts in the partial wave expansion for a two-dimensional electron gas. The effect is significantly enhanced by resonant scattering when the attractive potential is properly tuned. Second, we examine a three-terminal device including an antidot, which possibly produces a spin current with a polarization of more than 50%.

  13. Ethnobotanical survey of toxic plants and plant parts in Ogun State, Nigeria

    Directory of Open Access Journals (Sweden)

    Adediwura A Fred-Jaiyesimi

    2012-01-01

    Full Text Available Background: Several plants considered toxic are sometimes identified in traditional medicinal recipes. This study identified and inventoried the plants and plant parts identified as toxic in targeted local government areas of Ogun State, Nigeria. Materials and Methods: By administering tested questionnaires, information on the poisonous or toxic plants, poisonous parts, poisonous effects, modes of poisoning, and antidotes was obtained. Results and Conclusion: Ninety-two species belonging to 43 families were identified as toxic plants and these were mainly members of the Euphorbiaceae and Fabaceae families. The botanical names, poisonous parts, common names, vernacular names, modes of poisoning, antidotes, and poisonous effects are presented in a table.

  14. Robust band gap and half-metallicity in graphene with triangular perforations

    DEFF Research Database (Denmark)

    Gregersen, Søren Schou; Power, Stephen; Jauho, Antti-Pekka

    2016-01-01

    . The inclusion of spin polarization within a mean-field Hubbard approach gives rise to a large overall magnetic moment at each antidot due to the sublattice imbalance imposed by the triangular geometry. Half-metallic behavior arises from the formation of spin-split dispersive states near the Fermi energy...... disorders. Here we study a rectangular array of triangular antidots with zigzag edge geometries and show that their band gap behavior qualitatively differs from the standard behavior which is exhibited, e.g., by rectangular arrays of armchair-edged triangles. In the spin unpolarized case, zigzag......, and furthermore, of exploiting the strong spin dependence of the system for spintronic applications....

  15. AN ADDRESS DELIVERED BEFORE SCOPE'S CONFERENCE FOR EDUCATORS ON NARCOTICS AND SMOKING. (TITLE SUPPLIED).

    Science.gov (United States)

    RICE, JULIUS T.

    A SHORT HISTORY OF NARCOTICS USAGE IS PRESENTED. THE TERM DRUG DEPENDENCE IS BEING SUBSTITUTED FOR DRUG ADDICTION AND DRUG HABITUATION. THE ADVANTAGES AND DISADVANTAGES OF VARIOUS ANTIDOTES FOR OPIATES ARE DESCRIBED. THE EFFECTS OF LSD AND MARIJUANA ON PHYSICAL AND MENTAL PROCESSES ARE DESCRIBED. THE USE OF LSD FOR MEDICAL PURPOSES IS DISCUSSED.…

  16. Strategier for reversering af non-vitamin K orale antikoagulantia

    DEFF Research Database (Denmark)

    Larsen, Frederik Uttenthal; Hvas, Anne-Mette; Grove, Erik Lerkevang

    2016-01-01

    available for reversal of NOACs. Idarucizumab binds dabi­gatran for rapid reversal of its activity without procoagulant effects. Andexanet alpha (expected release in 2016) and PER977 are antidotes under clinical development. This article summarizes current and potential future options to anta­gonize NOACs....

  17. Intraosseous Hydroxocobalamin in the Treatment of Acute, Severe Cyanide Induced Cardiotoxicity in a Swine (Sus Scrofa) Model - An Alternate Administration Route for Chemical Mass Casualties

    Science.gov (United States)

    2012-04-05

    methods – LICOX (PbO2), near infrared spectrophotometry (NIRS), and microdialysis. We will use three devices to assess neurologic function after...antidotal treatment. These measures are near infrared spectroscopy, brain oxygen tension, and brain microdialysis. Hypothesis We hypothesize...cerebral near infrared spectrometry (NIRS) oxygenation, and inflammatory markers. Methods 24 swine (48-52 kg) were intubated, anesthetized, and

  18. Student Evaluation and an Introduction to Academic Discourse: "I Didn't Like it, and I Don't Know How to Improve it, Because it Works"

    Science.gov (United States)

    Kuhne, Michael; Creel, Gill

    2006-01-01

    Drawing from the theories of Paulo Freire, Patricia Bizzell, and Ira Shor, this article describes a five-year ongoing classroom research project that examines the use of peer evaluation as a process for teaching academic discourse. The findings of the project suggest a critical and democratic pedagogical antidote to the national "standards"…

  19. Pilot Decision-Making Training

    Science.gov (United States)

    1990-05-01

    Government Incu no reoponsbiy or any obligation wtsnoever. The fa tha the Governmert may have formuated or in any way supplied the said drawings seciicatons...Antidote: Good Judgment: 57 Situation 11 On final approach at night, you fly into patches of ground fog which severely limits visibility. Your altitude

  20. The Human Story at the Intersection of Ethics, Aesthetics and Social Justice

    Science.gov (United States)

    Baca, Judith F.

    2005-01-01

    Murals tell specific stories, but, because they are created from many specific stories, they also tell a common story, a story of the things that connect people to each other. In this way, muralism is an antidote for the hatred and disconnectedness in society. Moral education is participatory. It is a creative, critical and analytical process.…

  1. Drug: D07416 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available D07416 Drug Deferiprone (USAN/INN); Ferriprox (TN) C7H9NO2 139.0633 139.1519 D07416.gif Antidote, chelating...08303] V VARIOUS V03 ALL OTHER THERAPEUTIC PRODUCTS V03A ALL OTHER THERAPEUTIC PRODUCTS V03AC Iron chelating

  2. Drug: D08330 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available 23 D08330.gif Antidote, chelating ATC code: M01CC01 map07050 Antirheumatics - DMARDs and biological agents A...D08330 Drug Penicillamine hydrochloride; Pemine (TN) C5H11NO2S. HCl 185.0277 185.67

  3. Confronting the Pedagogical Challenge of Cyber Safety

    Science.gov (United States)

    Hanewald, Ria

    2008-01-01

    Cyber violence and the antidote of cyber safety are fast becoming a global concern for governments, educational authorities, teachers, parents and children alike. Despite substantial funding for information dissemination on preventative strategies and the development of electronic responses to hinder perpetrators, the phenomenon of cyber violence…

  4. WORKSHOPS-W4: Clinical Toxicology, Poisoning and Treatment%专题演讲-W4临床毒理学,中毒与治疗

    Institute of Scientific and Technical Information of China (English)

    Andrew DAWSON; Jiri BAJAR; HE Yue-Zhong

    2006-01-01

    @@ Self-poisoning with pesticides is a major problem across the Asia Pacific region. Despite this there is little coordinated effort being applied to improve the medical response to this problem. Good clinical and supportive care is the cornerstone of management of the poisoned patient and in some situations will suffice even in the absence of a specific antidote.

  5. [A patient who refused treatment after self-poisoning with paracetamol

    NARCIS (Netherlands)

    Kramers, C.; Jansman, F.G.A.; Droogleever Fortuyn, H.A.

    2006-01-01

    Two patients, a 20-year-old man and a 33-year-old woman, were admitted with paracetamol poisoning. Both patients refused treatment initially but eventually complied. The man had a paracetamol concentration of 47.5 mg/l 2.5-5.0 h after ingestion, so antidote treatment was not considered necessary. Th

  6. Current recommendations for prevention and therapy of extravasation reactions in dermato-oncology.

    Science.gov (United States)

    Kähler, Katharina C; Mustroph, Dieter; Hauschild, Axel

    2009-01-01

    Despite the introduction of many targeted therapies, a wide variety of cytostatic agents are still frequently used in dermato-oncology. In order to avoid further morbidity in tumor patients, prevention of extravasation reactions is of highest importance. The optimal management of extravasation requires an early diagnosis, the application of specific antidotes and a well-trained oncology team.

  7. Information Literacy: A Positivist Epistemology and a Politics of Outformation.

    Science.gov (United States)

    Kapitzke, Cushla

    2003-01-01

    Asserts that a positivist philosophical orientation makes the information literacy framework for school library research incompatible with emergent concepts of knowledge and epistemology for digital and online environments, reviewing government policy documents and research promoting information literacy as an antidote to information overload and…

  8. Enhanced extracorporeal elimination of valproic acid in overdose - Editorial.

    NARCIS (Netherlands)

    Engbersen, R.H.G.; Kramers, C.

    2004-01-01

    The treatment of the poisoned patient has been based on three main approaches: use of supportive nonspecific therapy, if available administration of antidotes and removal of the offending drug from the body. Gastric lavage and binding of nonabsorbed drug by activated charcoal are often used in an at

  9. Strategic Models and the Response of Government Agencies to Extreme Emergencies

    DEFF Research Database (Denmark)

    Casler, Catherine; Pierides, Dean

    to emergency management in the Australian State of Victoria after the catastrophic 2009 ‘Black Saturday’ bushfires. In the public inquiry into the disaster, centralization became an important antidote for previous shortcomings in ‘command, control and coordination’, eventually leading to the creation...

  10. Transcription of Gail Jefferson, Boston University Conference on Ethnomethodology and Conversation Analysis, 9 June 1977

    DEFF Research Database (Denmark)

    Nevile, Maurice Richard

    2015-01-01

    , a year and half after Harvey Sacks’ death, conversation analysis (CA) was becoming identified very closely with the 1974 Sacks, Schegloff & Jefferson paper ‘A simplest systematics...’. Her talk was therefore developed as “an antidote to that drastically constricted version of the field” (p.1), and as “an...

  11. Strong light-matter interaction in graphene - Invited talk

    DEFF Research Database (Denmark)

    Xiao, Sanshui

    explored for sensing of Rhodamine 6G molecules with respect to the strong surface-enhanced Raman scattering. The interaction between graphene plasmon (supported by nanodot and antidot arrays) and the substrate phonons [2] is also experimentally demonstrated and structural control is used to map out...

  12. Effects of diethyldithiocarbamate on the toxicokinetics of cadmium chloride in mice

    DEFF Research Database (Denmark)

    Andersen, O; Nielsen, J B

    1989-01-01

    in the toxicokinetics of cadmium induced by DDC are mainly due to the high cadmium doses employed and the intraperitoneal administration of DDC. At lower doses and more realistic administration routes for cadmium and DDC, the effect of DDC is less. However, still DDC does not seem to have any potential as an antidote...

  13. Effect of N-acetylcysteine on the accuracy of the prothrombin time assay of plasma coagulation factor II plus VII plus X activity in subjects infused with the drug. Influence of time and temperature

    DEFF Research Database (Denmark)

    Thorsen, S.; Teisner, A.; Jensen, S.A.;

    2009-01-01

    Objectives: The prothrombin time (PT) assay of factor II+VII+X activity is an important predictor of liver damage in paracetamol poisoned patients. It complicates interpretation of results that the antidote, acetylcysteine (NAC) depresses this activity. The aim was to investigate if NAC influences...

  14. Effect of N-acetylcysteine on the accuracy of the prothrombin time assay of plasma coagulation factor II+VII+X activity in subjects infused with the drug. Influence of time and temperature

    DEFF Research Database (Denmark)

    Thorsen, Sixtus; Teisner, Ane; Jensen, Søren Astrup;

    2009-01-01

    OBJECTIVES: The prothrombin time (PT) assay of factor II+VII+X activity is an important predictor of liver damage in paracetamol poisoned patients. It complicates interpretation of results that the antidote, acetylcysteine (NAC) depresses this activity. The aim was to investigate if NAC influences...

  15. Acute cyanide Intoxication: A rare case of survival

    Directory of Open Access Journals (Sweden)

    Durga Jethava

    2014-01-01

    Full Text Available A 30-year-old male jewellery factory worker accidentally ingested silver potassium cyanide and was brought to the emergency department in a state of shock and profound metabolic acidosis. This patient was managed hypothetically with use of injection thiopentone sodium intravenously until the antidote was received. Cyanide is a highly cytotoxic poison and it rapidly reacts with the trivalent iron of cytochrome oxidase thus paralysing the aerobic respiration. The result is severe lactic acidosis, profound shock, and its fatal outcome. The patient dies of cardio-respiratory arrest secondary to dysfunction of the medullary centres. It is rapidly absorbed, symptoms begin few seconds after exposure and death usually occurs in <30 min. The average lethal dose for potassium cyanide is about 250 mg. We used repeated doses of thiopentone sodium till the antidote kit was finally in our hands, hypothesising that it contains thiol group similar to the antidote thiosulphate. Moreover, it is an anticonvulsant. We were successful in our attempts and the patient survived though the specific antidotes could be administered after about an hour.

  16. Monitoring of dabigatran anticoagulation and its reversal in vitro by thrombelastography

    DEFF Research Database (Denmark)

    Solbeck, Sacha; Meyer, Martin A S; Johansson, Pär I;

    2014-01-01

    may not sufficiently display the effect. Furthermore, no antidote exists and reversal of the anticoagulant effect is impossible or difficult. The present study investigated the in vitro effect of dabigatran on whole blood thromboelastography (TEG) and its reversal by recombinant activated factor VII...

  17. Ideal Theory, Real Rationality

    DEFF Research Database (Denmark)

    Flyvbjerg, Bent

    as an example of a political philosopher who fails to recognize that actual political and administrative rationality lagely disrupts the relevance of his ideal prescriptopns. Michel Foucault proposed as an antidote to Habermas in a comparativestudy of the two. Machiavellian "verita effettuale" (effective truth...

  18. Drug: D00052 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available hemical (ATC) classification [BR:br08303] V VARIOUS V03 ALL OTHER THERAPEUTIC PRODUCTS V03A ALL OTHER THERAPEUTIC PRODUCTS V03AB Anti...dotes V03AB03 Edetates D00052 Edetic acid (NF/INN) CAS:

  19. Where does the lactate come from? A rare cause of reversible inhibition of mitochondrial respiration

    OpenAIRE

    Levy, Bruno; Perez, Pierre; Perny, Jessica

    2010-01-01

    Biguanide poisoning is associated with lactic acidosis. The exact mechanism of biguanide-induced lactic acidosis is not well understood. In the previous issue of Critical Care, Protti and colleagues demonstrated that biguanide-induced lactic acidosis may be due in part to a reversible inhibition of mitochondrial respiration. Thus, in the absence of an antidote, increased drug elimination through dialysis is logical.

  20. Brainwashing

    Directory of Open Access Journals (Sweden)

    K. B. Lall

    1963-07-01

    Full Text Available In this article an attempt has been made to present a brief analysis of the process brainwashing. The mechanism, the techniques employed and a brief history of brainwashing has been traced. It has been suggested that in order to resist this powerful weapon, we must understand the poison and find its antidote.