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Strategy of the scientific committee on occupational exposure limits (SCOEL) in the derivation of occupational exposure limits for carcinogens and mutagens

机译:致癌物和诱变剂的职业接触限值推导中的职业接触限值科学委员会(SCOEL)的策略

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摘要

Setting standards, such as occupational exposure limits (OELs) for carcinogenic substances must consider modes of action. At the European Union level, the scientific committee on occupational exposure limits (SCOEL) has discussed a number of chemical carcinogens and has issued recommendations. For some carcinogens, health-based OELs were recommended, while quantitative assessments of carcinogenic risks were performed for others. For purposes of setting limits this led to the consideration of the following groups of carcinogens. (A) Non-threshold genotoxic carcinogens; for low-dose assessment of risk, the linear non-threshold (LNT) model appears appropriate. For these chemicals, regulations (risk management) may be based on the ALARA principle (“as low as reasonably achievable”), technical feasibility, and other socio-political considerations. (B) Genotoxic carcinogens, for which the existence of a threshold cannot be sufficiently supported at present. In these cases, the LNT model may be used as a default assumption, based on the scientific uncertainty. (C) Genotoxic carcinogens with a practical threshold, as supported by studies on mechanisms and/or toxicokinetics; health-based exposure limits may be based on an established NOAEL (no observed adverse effect level). (D) Non-genotoxic carcinogens and non-DNA-reactive carcinogens; for these compounds a true (“perfect”) threshold is associated with a clearly founded NOAEL. The mechanisms shown by tumour promoters, spindle poisons, topoisomerase II poisons and hormones are typical examples of this category. Health-based OELs are derived for carcinogens of groups C and D, while a risk assessment is carried out for carcinogens of groups A and B. Substantial progress is currently being made in the incorporation of new types of mechanistic data into these regulatory procedures.
机译:制定标准,例如致癌物质的职业接触限值(OEL),必须考虑作用方式。在欧盟一级,职业暴露极限科学委员会(SCOEL)讨论了许多化学致癌物并发布了建议。对于某些致癌物,建议使用基于健康的OEL,而对其他致癌物进行定量评估。为了设定限制,这导致考虑以下几类致癌物。 (A)非阈值遗传毒性致癌物;对于低剂量风险评估,线性非阈值(LNT)模型似乎很合适。对于这些化学品,法规(风险管理)可以基于ALARA原则(“尽可能合理地降低”),技术可行性和其他社会政治因素。 (B)目前尚不能充分支持阈值存在的遗传毒性致癌物。在这些情况下,基于科学的不确定性,可以将LNT模型用作默认假设。 (C)具有实用阈值的遗传毒性致癌物,并得到了有关机理和/或毒代动力学的研究的支持;基于健康的暴露极限可能基于已建立的NOAEL(未观察到不利影响水平)。 (D)非遗传毒性致癌物和非DNA反应性致癌物;对于这些化合物,真正的(“完美”)阈值与明确建立的NOAEL有关。肿瘤启动子,纺锤体毒物,拓扑异构酶II毒物和激素所显示的机制是此类的典型例子。基于健康的OELs源自C和D组的致癌物,同时针对A和B组的致癌物进行了风险评估。目前正在将新型机械数据纳入这些监管程序中取得了实质性进展。

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