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评估毒理学终点以确定有害物质的最低风险水平。

Evaluating toxicologic end points to derive minimal risk levels for hazardous substances.

作者信息

Chou C H Selene J, Williams Malcolm, Jones Dennis, De Rosa Christopher T

机构信息

Division of Toxicology, Agency for Toxic Substances and Disease Registry, Department of Health and Human Services, 1600 Clifton Road, NE, MS E29, Atlanta, Georgia 30333, USA.

出版信息

Int J Hyg Environ Health. 2002 Mar;205(1-2):71-5. doi: 10.1078/1438-4639-00131.

Abstract

The Agency for Toxic Substances and Disease Registry (ATSDR) uses chemical-specific minimal risk levels (MRLs) to assist in evaluating public health risks associated with exposure to hazardous substances. MRLs are estimates of daily human exposure to a chemical that are likely to be without an appreciable risk of adverse noncancer health effects over a specified duration of exposure. MRLs serve as screening levels for health assessors to identify contaminants and potential health effects that may be of concern for populations living near hazardous waste sites and chemical releases. MRLs are derived from toxicologic data complied from a comprehensive literature search and are presented in ATSDR's toxicological profile for that substance. They are based on the most sensitive substance-induced end point considered to be of relevance to humans. MRLs for each substance are derived for acute (1-14 days), intermediate (15-364 days), and chronic (365 days and longer) exposure durations, and for the oral and inhalation routes of exposure. In this paper, we present an overview of the approach used for evaluating the toxicologic end points in deriving the MRLs. Examples are given to illustrate the agency's efforts to achieve increased understanding, reduced uncertainty and improved public health guidance.

摘要

有毒物质与疾病登记署(ATSDR)使用特定化学物质的最低风险水平(MRLs)来协助评估与接触有害物质相关的公共健康风险。MRLs是对人类每日接触某种化学物质的估计值,在特定的接触时间段内,这种接触不太可能产生明显的非癌症健康不良影响风险。MRLs作为健康评估人员的筛选水平,用于识别可能受危险废物场地和化学品泄漏影响的人群所关注的污染物和潜在健康影响。MRLs源自通过全面文献检索汇编的毒理学数据,并在ATSDR针对该物质的毒理学概况中呈现。它们基于被认为与人类相关的最敏感的物质诱导终点。每种物质的MRLs是针对急性(1 - 14天)、中间(15 - 364天)和慢性(365天及更长时间)接触持续时间以及口服和吸入接触途径得出的。在本文中,我们概述了在推导MRLs时用于评估毒理学终点的方法。文中给出了示例,以说明该机构为增进理解、减少不确定性和改进公共健康指导所做的努力。

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