New PBPK model applied to old occupational exposure to benzene.

R J Sherwood, G C Sinclair
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引用次数: 7

Abstract

An intensive program of benzene monitoring using new techniques was undertaken in Western Europe in the late 1960s and early 1970s. Significant exposure was found in the transport of benzene and gasoline, particularly during the loading of barges, and during the loading and operation of sea-going vessels. The ceiling threshold limit value of 25 ppm recommended at that time generated problems in assessing exposure, so alternative criteria were proposed. During that period some shore-based exposures were reported, and their significance was discussed in several articles. The information gained at that time is reexamined by physiologically based pharmacokinetic (PBPK) modeling and is used to help validate an improved PBPK model, which is described and tested on results from experimental exposure in a companion article. The old field data, comprising five specific studies, confirm the relevance of modeling to assessment of occupational exposure, and demonstrate its value for interpretation of field data, which is seldom as complete, systematic, or accurate as that obtained in experimental work. The model suggests that metabolism of benzene in humans may not be restricted to the liver. Sites and processes of metabolism merit further investigation.

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新PBPK模型应用于老职业苯暴露。
60年代末和70年代初在西欧开展了一项利用新技术监测苯的密集方案。在苯和汽油的运输中,特别是在驳船装载期间,以及在海船装载和操作期间,发现了大量的接触。当时建议的25 ppm的上限阈值在评估暴露时产生了问题,因此提出了替代标准。在此期间,报告了一些岸基暴露,并在几篇文章中讨论了其重要性。此时获得的信息通过基于生理的药代动力学(PBPK)模型进行重新检查,并用于帮助验证改进的PBPK模型,该模型将在同伴文章中根据实验暴露的结果进行描述和测试。由五项具体研究组成的旧现场数据证实了建模与职业暴露评估的相关性,并证明了其对现场数据解释的价值,这些数据很少像实验工作中获得的那样完整、系统或准确。该模型表明,人体对苯的代谢可能并不局限于肝脏。代谢的部位和过程值得进一步研究。
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