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人类变异性与非癌症风险评估——默认不确定性因素分析

Human variability and noncancer risk assessment--an analysis of the default uncertainty factor.

作者信息

Renwick A G, Lazarus N R

机构信息

Clinical Pharmacology Group, University of Southampton, United Kingdom.

出版信息

Regul Toxicol Pharmacol. 1998 Feb;27(1 Pt 1):3-20.

PMID:9629592
Abstract

A 10-fold uncertainty factor is used for noncancer risk assessments to allow for possible interindividual differences between humans in the fate of the chemical in the body (kinetics) and target organ sensitivity (dynamics). Analysis of a database on the variability in each of these aspects is consistent with an even subdivision of the 10-fold factor into 10(0.5) (3.16) for kinetics and 10(0.5) (3.16) for dynamics. Analysis of the number of subjects in a normally and log-normally distributed population which would not be covered by factors of 3.16 supports this subdivision and also the use of a 10-fold factor to allow for both aspects. Analysis of kinetic data for subgroups of the population indicates that the standard default value of 3.16 for kinetics will not be adequate for all routes of elimination and all groups of the population. A scheme is proposed which would allow the selection of appropriate default uncertainty factors based on knowledge of the biological fate and effects of the chemical under review.

摘要

在非癌症风险评估中使用10倍的不确定性系数,以考虑人体对化学物质在体内的代谢情况(动力学)和靶器官敏感性(动力学)方面可能存在的个体差异。对这些方面各自变异性的数据库分析表明,将10倍系数平均细分为动力学方面的10(0.5)(3.16)和动力学方面的10(0.5)(3.16)是合理的。对正态分布和对数正态分布人群中未被3.16系数涵盖的受试者数量进行分析,支持了这种细分以及使用10倍系数来综合考虑这两个方面。对人群亚组的动力学数据进行分析表明,动力学方面3.16的标准默认值并不适用于所有消除途径和所有人群组。本文提出了一种方案,该方案可根据对所审查化学物质的生物学命运和效应的了解来选择合适的默认不确定性系数。

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