Fetuin-A is a predictor of mortality in organophosphate poisoning. [PDF]
Ozbay S +5 more
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Acute Toxic Injuries of Rat's Visceral Tissues Induced by Different Oximes. [PDF]
Jaćević V, Nepovimova E, Kuča K.
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Validity of different scoring systems in prediction of intensive care unit admission and mortality in acute organophosphate poisoning. [PDF]
Sobeeh FG, Eldayem YBA, Khalifa HK.
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Human CYP2C9 Metabolism of Organophosphorus Pesticides and Nerve Agent Surrogates. [PDF]
Shriwas P +6 more
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Toxic Injury to Muscle Tissue of Rats Following Acute Oximes Exposure. [PDF]
Jaćević V, Nepovimova E, Kuča K.
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Structure-activity studies of bispyridinium antinicotinics to select candidates to treat soman intoxication as part of a combined therapy. [PDF]
Turner SR +7 more
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Recent Development of Nanoparticle Platforms for Organophosphate Nerve Agent Detoxification. [PDF]
Feng K +7 more
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Obidoxime in acute organophosphate poisoning: 1 – clinical effectiveness
Clinical Toxicology, 2009The effects of obidoxime in the treatment of organophosphate poisoning were assessed by comparing the clinical course with its effects on laboratory parameters relevant to poisoning. In this article we report clinical findings and activity of cholinesterase in plasma and acetylcholinesterase (AChE) in red blood cells.
Florian, Eyer +6 more
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Interaction of obidoxime with sarin in aqueous solution
Archives of Toxicology, 1992The interaction of obidoxime (Toxogonin) with sarin was shown by different analytical methods. The UV spectrum of obidoxime at pH 7.4 yields two absorption maxima, lambda 1 = 284 nm and lambda 2 = 353 nm. The peak at lambda 2 = 353 nm is representative for the amount of zwitter-ionic obidoxime, i.e. the active form of obidoxime.
P G, Waser +5 more
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Administration of obidoxime tablets to man
Archives of Toxicology, 1976Twenty-four male volunteers were given obidoxime tablets in quantities ranging from 1.84-3.58 g in a single dose, or 7.36 g divided into 4 equal doses. With the lowest dose, average peak plasma level of the drug was 1.9 mug/ml and after the highest single dose it was 5.6 mug/ml, both attained 1.5 h after administration.
G A, Simon, M S, Tirosh, H, Edery
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