10 results on '"B. Vyas"'
Search Results
2. Potentiometric Studies on Transition Metal Complexes of Substituted Derivative of Coumarin-Part 1
- Author
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K. B. Vyas, G. R. Jani, and M. V. Hathi
- Subjects
Chemistry ,QD1-999 - Abstract
The formation constants of binary complexes of d10 metal ions Cu(II), Ni(II), Co(II) and Mn(II) with 3-[{3-(3’-chloro phenyl}-prop-2-enoyl]-4-hydroxy-6-methyl-2H-chromen-2-one have been studied by using Irving-Rossoti method at constant temperature 30±1 °C and ionic strength μ=0.1 M dM-3 was held constant using sodium nitrate as an electrolyte. The factors influencing formation and stabilities of binary complexes have been discussed.
- Published
- 2009
- Full Text
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3. Carbofuran detected on weathered raptor carcass feet
- Author
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Wayne Bauer, James W. Spann, Craig S. Hulse, Sabra Olson, and Nimish B. Vyas
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Veterinary medicine ,chemistry.chemical_compound ,chemistry ,Ecology ,parasitic diseases ,food and beverages ,Biology ,Carbofuran ,Predator ,Nature and Landscape Conservation - Abstract
The cause of death for raptors poisoned at illegal carbofuran-laced predator baits is often not confirmed because the carcass matrices that are conventionally analyzed are not available due to decomposition and scavenging. However, many such carcasses retain intact feet that may have come into contact with carbofuran. Eastern screech owls (Otus asio) were exposed to carbofuran via simulated predator baits. Detection of carbofuran from owl feet weathered for 28 days demonstrated the temporal reliability of using feet during a forensic investigation. Raptor carcasses previously not submitted for residue analysis because of a lack of the conventional matrices may now be salvaged for their feet.
- Published
- 2005
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4. ChemInform Abstract: A New Route to Metal Hydrides
- Author
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W. C. Fang, M. E. Badding, Donald W. Murphy, B. Vyas, M. Thomas, and S. M. Zahurak
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Aqueous solution ,Chemistry ,Hydride ,Inorganic chemistry ,Intermetallic ,General Medicine ,Borohydride ,Decrepitation ,Metal ,chemistry.chemical_compound ,Transition metal ,visual_art ,Reagent ,visual_art.visual_art_medium - Abstract
Aqueous borohydride is shown to be an effective reagent for hydriding metals and intermetallics. It is the hydriding equivalent of 20-30 atm of H[sub 2]. The reaction is a convenient way to screen materials for hydride formation and possible utility in applications such as nickel-metal hydride batteries. The reaction is also a convenient alternative to decrepitation for the production of free flowing powders. 16 refs., 1 fig., 1 tab.
- Published
- 2010
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5. ChemInform Abstract: A Novel Plating Process for Microencapsulating Metal Hydrides
- Author
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H. H. Law, B. Vyas, G. W. Kammlott, and S. M. Zahurak
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Hydrogen ,Hydride ,Chemistry ,Metallurgy ,chemistry.chemical_element ,General Medicine ,engineering.material ,Copper ,Metal ,Nickel ,Coating ,visual_art ,Plating ,Electrode ,engineering ,visual_art.visual_art_medium - Abstract
One approach to increasing the lifetime of the metal hydride electrode has been the use of conventional electroless plating to produce a coating of copper or nickel on the surface of the metal hydride powders. In this paper, a novel method for microencapsulating the active electrode powders is presented. This new plating technique takes advantage of the reducing power of hydrogen already stored inside the metal hydride to plate a variety of metals onto metal hydride materials. This method greatly simplifies electroless plating for these powders, eliminating the need for stabilizers and additives typically required for conventional electroless plating solutions. Metals that can be electrolessly plated with stored hydrogen have been identified based on thermodynamic considerations. Experimentally, micrometers thick coatings of copper, silver, and nickel have been plated on several metal hydrides.
- Published
- 2010
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6. An Unusual Case of Poststroke Hallucinations
- Author
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Connie E. Poetter, Bavna B. Vyas, James A. Haley, and Jonathan T. Stewart
- Subjects
medicine.medical_specialty ,Text mining ,Unusual case ,business.industry ,medicine ,Geriatrics and Gerontology ,Psychiatry ,business - Published
- 2012
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7. FIELD EVALUATION OF AN AVIAN RISK ASSESSMENT MODEL
- Author
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Craig S. Hulse, Nimish B. Vyas, James W. Spann, Robert Leffel, Martin Torrez, Shannon L. Borges, Richard S. Bennett, and Bruce I. Williams
- Subjects
Risk analysis ,Diazinon ,Health, Toxicology and Mutagenesis ,Population Dynamics ,Models, Biological ,Risk Assessment ,Branta ,Birds ,Toxicology ,chemistry.chemical_compound ,Toxicity Tests ,Animals ,Environmental Chemistry ,Ecotoxicology ,United States Environmental Protection Agency ,biology ,Wettable powder ,Brain ,biology.organism_classification ,United States ,chemistry ,Feather ,visual_art ,Toxicity ,visual_art.visual_art_medium ,Acetylesterase ,Risk assessment - Abstract
We conducted two laboratory subacute dietary toxicity tests and one outdoor subacute dietary toxicity test to determine the effectiveness of the U.S. Environmental Protection Agency's deterministic risk assessment model for evaluating the potential of adverse effects to birds in the field. We tested technical-grade diazinon and its D.Z.N 50W (50% diazinon active ingredient wettable powder) formulation on Canada goose (Branta canadensis) goslings. Brain acetylcholinesterase activity was measured, and the feathers and skin, feet, and gastrointestinal contents were analyzed for diazinon residues. The dose-response curves showed that diazinon was significantly more toxic to goslings in the outdoor test than in the laboratory tests. The deterministic risk assessment method identified the potential for risk to birds in general, but the factors associated with extrapolating from the laboratory to the field, and from the laboratory test species to other species, resulted in the underestimation of risk to the goslings. The present study indicates that laboratory-based risk quotients should be interpreted with caution.
- Published
- 2006
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8. ACEPHATE AFFECTS MIGRATORY ORIENTATION OF THE WHITE-THROATED SPARROW (ZONOTRICHIA ALBICOLLIS)
- Author
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Elwood F. Hill, John R. Sauer, Wayne J. Kuenzel, and Nimish B. Vyas
- Subjects
biology ,Ecology ,Health, Toxicology and Mutagenesis ,Zonotrichia ,Emberizidae ,Pesticide ,biology.organism_classification ,Passerine ,chemistry.chemical_compound ,White-throated sparrow ,chemistry ,biology.animal ,Juvenile ,Environmental Chemistry ,Organophosphorus pesticides ,Acephate - Abstract
Migratory white-throated sparrows (Zonotrichia albicollis) were exposed to acephate (acetylphosphoramidothioic acid O, S-dimethyl ester), an organophosphorus pesticide, to determine its effects on migratory orientation and behavior. Birds were also exposed to polarizer sheets to determine the mechanism by which acephate may affect migratory orientation. Adult birds exposed to 256 ppm acephate a.i. were not able to establish a preferred migratory orientation and exhibited random activity. All juvenile treatment groups displayed a seasonally correct southward migratory orientation. We hypothesize that acephate may have produced aberrant migratory behavior by affecting the memory of the migratory route and wintering ground. This experiment reveals that an environmentally relevant concentration of a common organophosphorus pesticide can alter migratory orientation, but its effect is markedly different between adult and juvenile sparrows. Results suggest that the survival of free-flying adult passerine migrants may be compromised following organophosphorus pesticide exposure.
- Published
- 1995
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9. Continuous intravenous anaesthesia with Althesin for resection of tracheal stenosis
- Author
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S. M. Lyons, John W. Dundee, and A. B. Vyas
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Adult ,medicine.medical_specialty ,Adolescent ,medicine.medical_treatment ,Intravenous anaesthesia ,Tracheal resection ,Resection ,medicine ,Humans ,Intubation ,Infusions, Parenteral ,Respiratory system ,Anaesthetic management ,business.industry ,Carbon Dioxide ,respiratory system ,Tracheal Stenosis ,Surgery ,Oxygen ,Anesthesiology and Pain Medicine ,Alfaxalone Alfadolone Mixture ,Anesthesia ,Anesthesia, Intravenous ,Female ,business ,Tracheal segment - Abstract
Summary The anaesthetic management of patients undergoing tracheal resection for tracheal stenosis and the advantage of the maintenance of spontaneous respiration without intubation of the distal tracheal segment is discussed. The case reports of two such patients using a continuous intravenous infusion of Althesin with maintenance of spontaneous respiration are presented. The technique expedited the surgical re-anastomosis due to lack of instrumentation in the surgical field. While some mild respiratory depression as evidenced by carbon dioxide retention did occur, the technique is worthy of consideration for the procedure.
- Published
- 1983
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10. Inhibitors of microsomal prostaglandin E2 synthase-1 enzyme as emerging anti-inflammatory candidates.
- Author
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Bahia MS, Katare YK, Silakari O, Vyas B, and Silakari P
- Subjects
- Animals, Enzyme Inhibitors chemistry, Humans, Intramolecular Oxidoreductases chemistry, Microsomes drug effects, Prostaglandin-E Synthases, Anti-Inflammatory Agents pharmacology, Enzyme Inhibitors pharmacology, Intramolecular Oxidoreductases antagonists & inhibitors, Microsomes enzymology
- Abstract
Cyclooxygenases (COX-1 and COX-2) catalyze the conversion of arachidonic acid (AA) into PGH2 that is further metabolized by terminal prostaglandin (PG) synthases into biologically active PGs, for example, prostaglandin E2 (PGE2), prostacyclin I2 (PGI2), thromboxane A2 (TXA2), prostaglandin D2 (PGD2), and prostaglandin F2 alpha (PGF2α). Among them, PGE2 is a widely distributed PG in the human body, and an important mediator of inflammatory processes. The successful modulation of this PG provides a beneficial strategy for the potential anti-inflammatory therapy. For instance, nonsteroidal anti-inflammatory agents (NSAIDs), both classical nonselective (cNSAIDs) and the selective COX-2 inhibitors (coxibs) attenuate the generation of PGH2 from AA that in turn reduces the synthesis of PGE2 and modifies the inflammatory conditions. However, the long-term use of these agents causes severe side effects due to the nonselective inhibition of other PGs, such as PGI2 and TXA2, etc. Microsomal prostaglandin E2 synthase-1 (mPGES-1), a downstream PG synthase, specifically catalyzes the biosynthesis of COX-2-derived PGE2 from PGH2, and describes itself as a valuable therapeutic target for the treatment of acute and chronic inflammatory disease conditions. Therefore, the small molecule inhibitors of mPGES-1 would serve as a beneficial anti-inflammatory therapy, with reduced side effects that are usually associated with the nonselective inhibition of PG biosynthesis.
- Published
- 2014
- Full Text
- View/download PDF
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