Introduction
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Toxicokinetics differs from pharmacokinetics. In clinical toxicology cases one deals with:
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Whether the problem relates to poisoning or residues, toxicokinetic data may be used either:
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to predict 'normal' rates of metabolic change (activation or detoxification) and/or elimination, or
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to choose methods to help decrease the toxicant concentration at the receptor (e.g., to limit absorption, or increase detoxification or excretion)
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As compared to typical uses of therapeutic drugs, in toxicoses, kinetics are more likely to be altered by:
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Saturation of enzymes involved in metabolism (detoxification or toxification) or of enzymes employed in carrier systems necessary for elimination
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Organ system dysfunction or failure : For toxicant-induced liver or kidney damage that alters metabolism and/or elimination of the toxicant e.g. circulatory problems resulting in hypotension secondary to shock, acidosis due to exertion and seizures.
- Before toxicity can develop, a substance must come into contact with a body surface such as skin, eye or mucosa of the alimentary or respiratory tract.
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Last modified: Tuesday, 27 December 2011, 12:52 AM