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[对正在研发的新物质副作用概况的理解。实验毒理学方面]

[Comprehension of the side effect profile of a new substance under development. Experimental toxicological aspects].

作者信息

Mayer D, Cojocel C

机构信息

Hoechst AG, Frankfurt, Germany.

出版信息

Infection. 1991;19 Suppl 1:S4-8. doi: 10.1007/BF01644726.

Abstract

The detection of undesirable side effects takes place at several stages in the development of a drug. For this purpose all important endpoints such as acute toxicity, local tolerance, allergenicity, genotoxicity, subchronic/chronic toxicity and reproduction toxicity (male and female fertility, teratogenicity, peri- and postnatal studies) serve to establish the major toxicological characteristics. Comparative metabolism studies are carried out in order to optimize the extrapolation of the results obtained in animal experiments to humans. Special, non-routine studies must be adopted for testing cephalosporins and quinolones. Examples of these are provided.

摘要

药物不良反应的检测在药物研发的多个阶段进行。为此,所有重要的终点指标,如急性毒性、局部耐受性、致敏性、遗传毒性、亚慢性/慢性毒性和生殖毒性(雄性和雌性生育力、致畸性、围产期和产后研究),都用于确定主要的毒理学特征。开展比较代谢研究,以便优化从动物实验获得的结果向人体的外推。对于头孢菌素和喹诺酮类药物的检测,必须采用特殊的非常规研究。文中给出了这些研究的示例。

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