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评估因素——在化学品健康风险评估中的应用

Assessment factors--applications in health risk assessment of chemicals.

作者信息

Falk-Filipsson Agneta, Hanberg Annika, Victorin Katarina, Warholm Margareta, Wallén Maria

机构信息

Swedish Chemicals Agency, P.O. Box 2, Esplanaden 3A, SE-172 13, Sundbyberg, Sweden.

出版信息

Environ Res. 2007 May;104(1):108-27. doi: 10.1016/j.envres.2006.10.004. Epub 2006 Dec 12.

Abstract

We review the scientific basis for default assessment factors used in risk assessment of nongenotoxic chemicals including the use of chemical- and pathways specific assessment factors, and extrapolation approaches relevant to species differences, age and gender. One main conclusion is that the conventionally used default factor of 100 does not cover all inter-species and inter-individual differences. We suggest that a species-specific default factor based on allometric scaling should be used for inter-species extrapolation (basal metabolic rate). Regarding toxicodynamic and remaining toxicokinetic differences we suggest that a percentile from a probabilistic distribution is chosen to derive the assessment factor. Based on the scarce information concerning the human-to-human variability it is more difficult to suggest a specific assessment factor. However, extra emphasis should be put on sensitive populations such as neonates and genetically sensitive subgroups, and also fetuses and children which may be particularly vulnerable during development and maturation. Factors that also need to be allowed for are possible gender differences in sensitivity, deficiencies in the databases, nature of the effect, duration of exposure, and route-to-route extrapolation. Since assessment factors are used to compensate for lack of knowledge we feel that it is prudent to adopt a "conservative" approach, erring on the side of protectiveness.

摘要

我们回顾了非遗传毒性化学物质风险评估中默认评估因子的科学依据,包括化学物质和特定途径评估因子的使用,以及与物种差异、年龄和性别相关的外推方法。一个主要结论是,传统使用的默认因子100并不能涵盖所有种间和个体间差异。我们建议,种间外推(基础代谢率)应使用基于异速生长比例的物种特异性默认因子。关于毒效动力学和其余的毒代动力学差异,我们建议从概率分布中选择一个百分位数来得出评估因子。基于关于人与人之间变异性的稀缺信息,更难提出一个具体的评估因子。然而,应特别关注敏感人群,如新生儿和遗传敏感亚组,以及胎儿和儿童,他们在发育和成熟过程中可能特别脆弱。还需要考虑的因素包括敏感性方面可能存在的性别差异、数据库的缺陷、效应的性质、暴露持续时间以及途径间外推。由于评估因子用于弥补知识的不足,我们认为采取“保守”方法是审慎的,宁求保护过度。

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