McCarty L S, Borgert C J
L.S. McCarty Scientific Research & Consulting, 94 Oakhaven Drive, Markham, Ont., Canada L6C 1X8.
Regul Toxicol Pharmacol. 2006 Jul;45(2):119-43. doi: 10.1016/j.yrtph.2006.03.004. Epub 2006 May 15.
An analysis of current mixture theory, policy, and practice was conducted by examining standard reference texts, regulatory guidance documents, and journal articles. Although this literature contains useful theoretical concepts, clear definitions of most terminology, and well developed protocols for study design and statistical analysis, no general theoretical basis for the mechanisms and interactions of mixture toxicity could be discerned. There is also a poor understanding of the relationship between exposure-based and internal received dose metrics. This confounds data interpretation and limits reliable determinations of the nature and extent of additivity. The absence of any generally accepted classification scheme for either modes/mechanisms of toxic action or of mechanisms of toxicity interactions is problematic as it produces a cycle in which research and policy are interdependent and mutually limiting. Current regulatory guidance depends heavily on determination of toxicological similarity concluded from the presence of a few prominent constituents, assumed from a common toxicological effect, or presumed from an alleged similar toxic mode/mechanism. Additivity, or the lack of it, is largely based on extrapolation of existing knowledge for single chemicals in this context. Thus, regulatory risk assessment protocols lack authoritative theoretical underpinnings, creating substantial uncertainty. Development of comprehensive classification schemes for modes/mechanisms of toxic action and mechanisms of interaction is needed to ensure a sound theoretical foundation for mixture-related regulatory activity and provide a firm basis for iterative hypothesis development and experimental testing.
通过查阅标准参考文献、监管指导文件和期刊文章,对当前的混合物理论、政策和实践进行了分析。尽管这些文献包含有用的理论概念、大多数术语的明确定义以及完善的研究设计和统计分析方案,但未能识别出混合物毒性机制和相互作用的一般理论基础。对基于暴露的剂量指标与体内吸收剂量指标之间的关系也了解不足。这混淆了数据解释,并限制了对相加性的性质和程度进行可靠的判定。对于毒性作用模式/机制或毒性相互作用机制,缺乏任何普遍接受的分类方案,这是个问题,因为它产生了一个循环,在这个循环中,研究和政策相互依赖且相互限制。当前的监管指导在很大程度上依赖于根据少数突出成分的存在、共同的毒理学效应或所谓相似的毒性模式/机制推断出的毒理学相似性的判定。在这种情况下,相加性或缺乏相加性很大程度上基于对单一化学品现有知识的外推。因此,监管风险评估方案缺乏权威性的理论基础,造成了很大的不确定性。需要制定毒性作用模式/机制和相互作用机制的综合分类方案,以确保混合物相关监管活动有坚实的理论基础,并为迭代假设的形成和实验测试提供坚实依据。