在有限毒理学数据的情况下,局部作用物质的时间外推和种间外推。

F. Kalberlah, U. Föst, K. Schneider
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引用次数: 46

摘要

对于毒理学数据库有限的物质,通常存在以下情况:(i)缺乏合格的人体毒理学数据;(ii)缺乏足够暴露时间的研究。因此,必须进行一些外推,以得出适当的风险评估或得出职业暴露限值。本论文讨论了外推效应浓度随时间变化的可能性(时间外推,例如从亚急性暴露到慢性暴露)以及与局部作用物质(呼吸毒性物质)有关的种间外推(从动物到人类)。为了证明时间外推因素的合理性,对美国国家毒理学计划(NTP)编制的46份技术报告进行了评估,这些报告涉及亚急性、亚慢性和慢性暴露持续时间的研究。在几何平均值的基础上,发现效应浓度下降的因子为3.2(亚急性->亚慢性)、2.7(亚慢性->慢性)和6.6(亚急性->慢性)。根据动物种类(小鼠、大鼠)、性别或物质性质进行的区分没有导致平均值的任何相关变化。在许多情况下,少于终生暴露期(亚急性、亚慢性)的国家毒毒局研究与慢性研究相比,显示了不同的呼吸影响部位,因此,对长期呼吸影响(在呼吸道某些区域发生影响)进行定性预测的可能性有限。关于种间外推,气体和颗粒物质分别进行了评估。经过一些修改(例如,考虑到低溶解度颗粒的清除),1994年美国环境保护署(EPA)提出了基于动物实验数据得出人类参考浓度的可吸入颗粒物质模型。在气态物质的情况下,EPA模型的假设似乎没有充分考虑到啮齿类动物和人类上呼吸道在物质分布上的局部不均匀性以及解剖和组织学上的差异。对于气体物质的种间外推,一个默认的因素会带来相当大的不确定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time extrapolation and interspecies extrapolation for locally acting substances in case of limited toxicological data.
In the case of substances with a limited toxicological data base there is often (i) a lack of qualified human toxicological data; and (ii) a paucity of studies with adequate exposure duration. Hence, several extrapolations have to be performed to arrive at appropriate risk assessments or derive occupational exposure limits. The present paper deals with the possibilities for extrapolating the change in effect concentrations over time (time extrapolation, e.g. from subacute to chronic exposure) and for interspecies extrapolation (from animal to human) in connection with locally acting substances (respiratory toxicants). To justify the time extrapolation factors, 46 technical reports produced by the US National Toxicology Program (NTP) involving studies with subacute, subchronic and chronic exposure duration were evaluated. On the basis of geometric mean values, decreases in effect concentrations by factors of 3.2 (subacute --> subchronic), 2.7 (subchronic --> chronic) and 6.6 (subacute --> chronic) were found. Differentiation according to animal species (mouse, rat), sex or substance properties did not result in any relevant changes of the mean value. NTP studies with less than lifetime exposure periods (subacute, subchronic) in many cases showed different locations of respiratory effects compared with chronic studies, and thus offered limited possibilities for qualitative prediction of long-term respiratory effects (occurrence of effects in certain regions of the respiratory tract). With regard to interspecies extrapolation, gaseous and particulate substances were evaluated separately. With some modifications (e.g. consideration of the clearance of particles of low solubility), the 1994 US Environmental Protection Agency (EPA) model for deriving reference concentrations for humans on the basis of experimental data in animals is proposed for inhalable particulate substances. In the case of gaseous substances, the assumptions of the EPA model do not seem to consider sufficiently the local inhomogeneity in substance distribution and anatomical and histological differences between the upper respiratory tracts of rodents and humans. Considerable uncertainty would attach to a default factor for interspecies extrapolation for gaseous substances.
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