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控制持久性有机污染物——下一步是什么?

Controlling persistent organic pollutants-what next?

机构信息

Stockholm Environment Institute at York, University of York, York, United Kingdom.

出版信息

Environ Toxicol Pharmacol. 1998 Nov 1;6(3):143-75. doi: 10.1016/s1382-6689(98)00036-2.

Abstract

Within the context of current international initiatives on the control of persistent organic pollutants (POPs), an overview is given of the scientific knowledge relating to POP sources, emissions, transport, fate and effects. At the regional scale, improvements in mass balance models for well-characterised POPs are resulting in an ability to estimate their environmental concentrations with sufficient accuracy to be of help for some regulatory purposes. The relevance of the parameters used to define POPs within these international initiatives is considered with an emphasis on mechanisms for adding new substances to the initial lists. A tiered approach is proposed for screening the large number of untested chemical substances according to their long-range transport potential, persistence and bioaccumulative potential prior to more detailed risk assessments. The importance of testing candidate POPs for chronic toxicity (i.e. for immunotoxicity, endocrine disruption and carcinogenicity) is emphasised as is a need for the further development of relevant SAR (structure activity relationship) models and in vitro and in vivo tests for these effects. Where there is a high level of uncertainty at the risk assessment stage, decision-makers may have to rely on expert judgement and weight-of-evidence, taking into account the precautionary principle and the views of relevant stake-holders. Close co-operation between the various international initiatives on POPs will be required to ensure that assessment criteria and procedures are as compatible as possible.

摘要

在当前国际持久性有机污染物(POPs)控制倡议的背景下,概述了与 POPs 源、排放、迁移、归宿和效应相关的科学知识。在区域尺度上,对特征明确的 POPs 的质量平衡模型进行了改进,从而能够以足够的精度估算其环境浓度,以便在某些监管目的方面提供帮助。考虑了这些国际倡议中用于定义 POPs 的参数的相关性,重点是为初始清单添加新物质的机制。提出了一种分层方法,根据远距离迁移潜力、持久性和生物累积潜力,对大量未经测试的化学物质进行筛选,然后再进行更详细的风险评估。强调了对候选 POPs 进行慢性毒性(即免疫毒性、内分泌干扰和致癌性)测试的重要性,还需要进一步开发相关 SAR(结构-活性关系)模型和这些效应的体外和体内测试。在风险评估阶段存在高度不确定性的情况下,决策者可能不得不依靠专家判断和证据权重,同时考虑到预防原则和相关利益相关者的观点。需要密切合作,以确保评估标准和程序尽可能兼容。

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