Eadon G, Kaminsky L, Silkworth J, Aldous K, Hilker D, O'Keefe P, Smith R, Gierthy J, Hawley J, Kim N
Environ Health Perspect. 1986 Dec;70:221-7. doi: 10.1289/ehp.8670221.
Sufficient toxicological data are now available to permit use of conventional risk assessment techniques to estimate the hazards associated with human exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD). However, many real-world exposures involve complex mixtures of dibenzodioxins, dibenzofurans, and related compounds. Historical approaches to risk assessment on such mixtures have ranged from ignoring all compounds except 2,3,7,8-TCDD itself to assuming that all compounds have potencies equal to 2,3,7,8-TCDD. An alternative approach which uses existing literature data and analytical results to calculate the "2,3,7,8-TCDD equivalent" concentration of a mixture in order to "predict" its biological potency relative to 2,3,7,8-TCDD itself is advanced here. Previously reported in vivo acute and subchronic studies and some recently obtained analytical chemistry data are integrated here to clarify the utility of this important approach and to assess the uncertainties associated with its use. This predictive approach, and various conceptually similar ones, have now found wide applicability to the risk assessment process associated with exposure to complex mixtures of dioxins, dibenzofurans, and related compounds.
现在已有足够的毒理学数据,可以使用传统风险评估技术来估算人类接触2,3,7,8 - 四氯二苯并 - 对 - 二噁英(2,3,7,8 - TCDD)相关的危害。然而,许多实际接触情况涉及二苯并二噁英、二苯并呋喃及相关化合物的复杂混合物。针对此类混合物的风险评估,以往的方法从只考虑2,3,7,8 - TCDD本身而忽略所有其他化合物,到假定所有化合物的毒性与2,3,7,8 - TCDD相同。本文提出一种替代方法,该方法利用现有文献数据和分析结果来计算混合物的“2,3,7,8 - TCDD当量”浓度,以便“预测”其相对于2,3,7,8 - TCDD本身的生物活性。本文整合了先前报道的体内急性和亚慢性研究以及一些最近获得的分析化学数据,以阐明这一重要方法的实用性,并评估其使用过程中存在的不确定性。这种预测方法以及各种概念上类似的方法,现已广泛应用于与二噁英、二苯并呋喃及相关化合物复杂混合物接触相关的风险评估过程。