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药物发现与开发过程中的毒理学

Toxicology in the drug discovery and development process.

作者信息

Dorato Michael A, Buckley Lorrene A

机构信息

Lilly Research Laboratories, Greenfield, Indiana, USA.

出版信息

Curr Protoc Pharmacol. 2006 Apr;Chapter 10:Unit10.3. doi: 10.1002/0471141755.ph1003s32.

Abstract

The primary objective of toxicology studies in the drug development process is to evaluate the safety of potential drug candidates. This is accomplished using relevant animal models and validated procedures. The ultimate goal is to translate the animal model responses into an understanding of the risk for human subjects. To this end, the toxicologist must be aware of the international guidelines for safety evaluation, as well as traditional and nontraditional toxicology models. As described in this unit, the typical toxicology profile consists of safety pharmacology, genetic toxicology, acute and subchronic toxicology, chronic toxicology, absorption, distribution, metabolism, and excretion (ADME) studies, reproductive and developmental toxicology, and an evaluation of carcinogenic potential.

摘要

在药物研发过程中,毒理学研究的主要目标是评估潜在候选药物的安全性。这是通过使用相关动物模型和经过验证的程序来实现的。最终目标是将动物模型的反应转化为对人类受试者风险的理解。为此,毒理学家必须了解国际安全评估指南以及传统和非传统毒理学模型。如本单元所述,典型的毒理学概况包括安全药理学、遗传毒理学、急性和亚慢性毒理学、慢性毒理学、吸收、分布、代谢和排泄(ADME)研究、生殖和发育毒理学以及致癌潜力评估。

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