药物中基因毒性杂质的研究进展

A. Patel, Ashish H. Asnani, A. Vyas, Nilesh Patel, Ajay I. Patel, Arvind N. Lumbhani
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引用次数: 12

摘要

药物中的基因毒性杂质(GTIs)由于其潜在的人类致癌性而越来越受到制药行业的关注。文献目前缺乏对不同种类gti的分析测定指南。本文简要介绍了基因毒性杂质(GTI)的来源、分类和现有的控制药物中基因毒性杂质的监管方法,以及不同类型的基因毒性杂质的信息和每一类的例子。研究人员很难检测到微量水平的GTI所以检测方法也在图表中给出,几乎所有的GTI都是致突变性的但正如亚硝胺所示,它是致突变性的它的致癌性也被证明了但没有这样强有力的证据和文献表明遗传毒性。因此,它被列入致突变和致癌物。并讨论了控制遗传毒性的不同控制策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Brief Review on Genotoxic impurities in Pharmaceuticals
Genotoxic impurities (GTIs) in pharmaceuticals are increasing concern to pharmaceutical industries due to their potential for human carcinogenicity. The literature currently lacks the Guidance for the analytical determination of diverse classes of GTIs. This review article provides brief information regarding Genotoxic impurity (GTI), its sources, their classification, and existing regulatory approaches to control Genotoxic impurities in Pharmaceuticals, also information regarding different types of GTI and examples of each class. It is very difficult for researchers to detect GTI at Trace level so the detection method is also given in the chart, almost all the GTI are Mutagenic but as shown in Nitrosamines it is Mutagenic and its carcinogenicity is also proved but there are no such strong evidence and literature which shows genotoxicity. So, it is included as Mutagenic & carcinogenic. Different Control strategies to control Genotoxicity are also discussed.
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