兽药人类食品安全评价中的种间考虑。

AAPS PharmSci Pub Date : 2002-01-01 DOI:10.1208/ps040434
Arthur L Craigmill, Kristy A Cortright
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引用次数: 16

摘要

残留物由母体药物和代谢物组成,因此种间比较必须考虑比较异种代谢。本文的重点将是建立人类食品安全所需的残留研究,以及影响动物源性食品中药物残留的种间药代动力学差异和相似性。为了说明可能使这些比较复杂化和有助于这些比较的因素,将详细检查两种药物:伊维菌素和芬苯达唑。此外,还将介绍两个美国项目的活动,即食品动物残留避免数据库(FARAD)和NRSP-7(国家研究支持项目7号)小用动物药物项目,以及可能用于物种差异研究的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interspecies considerations in the evaluation of human food safety for veterinary drugs.

Residues are composed of the parent drug and metabolites, and therefore interspecies comparisons must involve a consideration of comparative xenobiotic metabolism. The focus of this article will be the residue studies that are required to establish human food safety, and the interspecies pharmacokinetic differences and similarities that impact drug residues in animal- derived foods. To illustrate the factors that can complicate and assist these comparisons, 2 drugs will be examined in detail: ivermectin and fenbendazole. In addition, the activities of 2 US programs, the Food Animal Residue Avoidance Databank (FARAD) and the NRSP-7 (National Research Support Project Number 7) Minor Use Animal Drug Program will be presented, along with strategies that may be employed in the study of species differences.

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