...
首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Strategies in case of positive in vivo results in genotoxicity testing.
【24h】

Strategies in case of positive in vivo results in genotoxicity testing.

机译:体内阳性的策略会导致基因毒性测试。

获取原文
获取原文并翻译 | 示例
           

摘要

At the 2009 International Workshop on Genotoxicity Testing in Basel, an expert group gathered to provide guidance on suitable follow-up tests to describe risk when basic in vivo genotoxicity tests have yielded positive results. The working group agreed that non-linear dose-response curves occur in vivo with at least some DNA-reactive agents. Quantitative risk assessment in such cases requires the use of (1) adequate data, i.e., the use of all available data for the selection of reliable in vivo models to be used for quantitative risk assessment, (2) appropriate mathematical models and statistical analysis for characterizing the dose-response relationships and allowing the use of quantitative and dose-response information in the interpretation of results, (3) mode of action (MOA) information for the evaluation and analysis of risk, and (4) reliable assessments of the internal dose across species for deriving acceptable margins of exposure and risk levels. Hence, the elucidation of MOA and understanding of the mechanism underlying the dose-response curve are important components of risk assessment. The group agreed on the need for (i) the development of in vivo assays, especially multi-endpoint, multi-species assays, with emphasis on those applicable to humans, and (ii) consensus about the most appropriate mathematical models and statistical analyses for defining non-linear dose-responses and exposure levels associated with acceptable risk.
机译:在2009年巴塞尔国际遗传毒性测试研讨会上,一个专家组聚集在一起,就适当的后续测试提供指导,以描述基本的体内遗传毒性测试产生积极结果时的风险。该工作组同意,至少在某些DNA反应剂的体内,会出现非线性剂量反应曲线。在这种情况下,定量风险评估需要使用(1)足够的数据,即使用所有可用数据来选择用于定量风险评估的可靠体内模型,(2)适当的数学模型和统计分析表征剂量-反应关系并允许在结果解释中使用定量和剂量-反应信息;(3)用于评估和分析风险的作用方式(MOA)信息;以及(4)对内部的可靠评估跨物种的剂量,以得出可接受的接触范围和风险水平。因此,对MOA的阐明和对剂量反应曲线基础的理解是风险评估的重要组成部分。该小组一致认为有必要(i)开发体内测定法,尤其是多端点,多物种测定法,重点是适用于人类的测定法,以及(ii)就最合适的数学模型和统计学分析达成共识定义与可接受风险相关的非线性剂量反应和暴露水平。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号