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植物保护产品活性成分、杂质及代谢物遗传毒性评估的监管要求。

Regulatory requirements for genotoxicity assessment of plant protection product active ingredients, impurities, and metabolites.

作者信息

Booth Ewan D, Rawlinson Paul J, Maria Fagundes Priscila, Leiner Kevin A

机构信息

Department of Toxicology and Health Sciences, Syngenta Ltd, Jealott's Hill International Research Centre, Bracknell, Berkshire, United Kingdom.

Department of Product Safety, Syngenta Protecao de Cultivos Ltda, Sao Paulo, SP, 04795-900, Brazil.

出版信息

Environ Mol Mutagen. 2017 Jun;58(5):325-344. doi: 10.1002/em.22084. Epub 2017 Mar 22.

Abstract

Active ingredients in plant protection products are subject to rigorous safety assessment during their development, including assessment of genotoxicity. Plant protection products are used for agriculture in multiple regions and for the registration of active ingredients it is necessary to satisfy the data requirements of these different regions. There are no overarching global agreements on which genotoxicity studies need to be conducted to satisfy the majority of regulatory authorities. The implementation of new OECD guidelines for the in vitro micronucleus, transgenic rodent somatic and germ cell gene mutation and in vivo comet assays, as well as the revision of a number of other OECD test guidelines has resulted in some changes to data requirements. This review describes the genotoxicity data requirements for chemical active ingredients as well as biologicals, microbials, ground water metabolites, metabolites, and impurities in a number of regions. Similarities and differences are highlighted. Environ. Mol. Mutagen. 58:325-344, 2017. © 2017 Wiley Periodicals, Inc.

摘要

植物保护产品中的活性成分在其研发过程中要接受严格的安全性评估,包括遗传毒性评估。植物保护产品在多个地区用于农业,对于活性成分的注册,有必要满足这些不同地区的数据要求。对于需要开展哪些遗传毒性研究以满足大多数监管当局的要求,目前尚无全面的全球协议。经合组织(OECD)关于体外微核试验、转基因啮齿动物体细胞和生殖细胞基因突变试验以及体内彗星试验的新指南的实施,以及对其他一些经合组织试验指南的修订,导致数据要求发生了一些变化。本综述描述了多个地区对化学活性成分以及生物制品、微生物、地下水代谢物、代谢物和杂质的遗传毒性数据要求。突出了异同点。《环境与分子突变》58:325 - 344,2017年。©2017威利期刊公司

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