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药品中遗传毒性杂质的鉴定、控制和测定策略:制药行业视角。

Strategies for the identification, control and determination of genotoxic impurities in drug substances: a pharmaceutical industry perspective.

机构信息

Hetero Drugs Ltd. (R&D), Plot No. B. 80 & 81, APIE, Balanagar, Hyderabad 500018, Andhra Pradesh, India.

出版信息

J Pharm Biomed Anal. 2011 Jun 25;55(4):662-7. doi: 10.1016/j.jpba.2010.11.039. Epub 2010 Dec 3.

Abstract

Regulations alarmed the control of genotoxic impurities in drug substances at lower level based on the threshold of toxicological concern and daily dose. This review explores the details of various regulations and guidances, toxicology assessment, identification of structural alerts, synthetic origins, different synthetic approaches for elimination or control, various analytical determination strategies and pharmaceutical industry concern towards genotoxic impurities.

摘要

基于毒理学关注阈值和日剂量,法规对药品中遗传毒性杂质的控制提出了更低水平的要求。本综述探讨了各种法规和指南的细节、毒理学评估、结构警示的识别、来源的合成、消除或控制的不同合成方法、各种分析测定策略以及制药行业对遗传毒性杂质的关注。

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