Schoeny R S, Margosches E
Environmental Criteria and Assessment Office, U.S. Environmental Protection Agency, Cincinnati, Ohio.
Toxicol Ind Health. 1989 Oct;5(5):825-37. doi: 10.1177/074823378900500518.
The U.S. EPA must provide guidance as to health risk assessment of mixtures from a variety of sources such as wastewaters, hazardous waste sites and air particulates. One approach to risk assessment of mixtures is to add up risk assessments for individual components identified as part of the mixture, after considering the potential for interaction among those components. This provides an index of hazard potential but not a quantitative estimate. When data on mixture components are incomplete, but these components are isomers or congeners of a well-studied chemical, another technique--use of toxic equivalency factors--can be applied. This approach has been proposed for estimating risk associated with chlorinated dioxins and dibenzofurans. A third approach, that of relative or comparative potency, is based on the assumption that for similar but not necessarily definable complex mixtures, a measure of relative potency based on data from in vitro tests can be correlated in a constant fashion with relative potency from an in vivo bioassay. The degree of confidence in the appropriateness of a relative potency method rests upon the way potency is measured and the validity of underlying assumptions (the degree to which these assumptions can be tested). One class of assumptions involves choice of the model or procedure for deriving the quantitative risk estimates. A second set of assumptions deals with mechanism of action, and whether such considerations add bias or, in fact, refine the relative potency judgment. The choice of short-term tests appropriate for use in establishing the potency relationships is also a factor to be considered. This paper presents examples of proposed uses of relative potency in risk assessment and outlines some areas for further study.
美国环境保护局必须就来自各种来源(如废水、危险废物场地和空气颗粒物)的混合物的健康风险评估提供指导。混合物风险评估的一种方法是在考虑混合物中各成分之间相互作用的可能性之后,将确定为混合物一部分的各个成分的风险评估相加。这提供了一个潜在危害指数,但不是定量估计。当混合物成分的数据不完整,但这些成分是一种经过充分研究的化学物质的异构体或同系物时,可以应用另一种技术——使用毒性当量因子。这种方法已被提议用于估计与氯代二噁英和二苯并呋喃相关的风险。第三种方法,即相对或比较效力法,基于这样的假设:对于相似但不一定可定义的复杂混合物,基于体外试验数据的相对效力测量可以以恒定方式与体内生物测定的相对效力相关联。对相对效力方法适当性的置信度取决于效力的测量方式和基本假设的有效性(这些假设可被检验的程度)。一类假设涉及用于得出定量风险估计的模型或程序的选择。第二组假设涉及作用机制,以及这些考虑是否会增加偏差,或者实际上是否会完善相对效力判断。选择适合用于建立效力关系的短期试验也是一个需要考虑的因素。本文给出了在风险评估中使用相对效力的提议示例,并概述了一些需要进一步研究的领域。