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犬类吸入卤代烃暴露的生理药代动力学(PBPK)建模

PBPK modeling of canine inhalation exposures to halogenated hydrocarbons.

作者信息

Vinegar A

机构信息

ManTech Environmental Technology, Inc., P.O. Box 31009, Dayton, Ohio 45437, USA.

出版信息

Toxicol Sci. 2001 Mar;60(1):20-7. doi: 10.1093/toxsci/60.1.20.

Abstract

Human exposure guidelines for halogenated hydrocarbons (halons) and halon replacement chemicals have been established using dose-response data obtained from canine cardiac sensitization studies. In order to provide a tool for decision makers and regulators tasked with setting guidelines for egress from exposure to halon replacement chemicals, a quantitative approach, using a physiologically based pharmacokinetic model, was established that allowed exposures to be assessed in terms of the chemical concentrations in blood during the exposure. This model, which includes a respiratory tract compartment containing a dead-space region, a pulmonary exchange area, and a breath-by-breath description of respiratory tract uptake, allows successful simulation of exhaled breath concentrations of humans during the first minute of exposure to the anesthetics halothane, isoflurane, and desflurane. In the current study, the human model was modified with canine parameters and validated with data obtained from dog studies with halothane, isoflurane, desflurane, and CFC-11. With consideration of appropriate values for ventilation and cardiac output, the model successfully simulated data collected under a variety of exposure scenarios. The canine model can be used for simulating blood concentrations associated with the potential for cardiac sensitization. These target blood concentrations can then be used with the human model for establishing safe human exposure duration. Development of the canine model stresses the need for appropriate data collection for model validation.

摘要

卤代烃(哈龙)和哈龙替代化学品的人体暴露指南是利用从犬类心脏致敏研究中获得的剂量反应数据制定的。为了为负责制定哈龙替代化学品暴露撤离指南的决策者和监管机构提供一种工具,建立了一种定量方法,即使用基于生理学的药代动力学模型,该模型能够根据暴露期间血液中的化学物质浓度来评估暴露情况。该模型包括一个呼吸道隔室,其中包含一个死腔区域、一个肺交换区域以及对呼吸道摄取的逐次呼吸描述,能够成功模拟人类在接触麻醉剂氟烷、异氟烷和地氟烷的第一分钟内呼出气体的浓度。在当前研究中,该人体模型用犬类参数进行了修正,并用从犬类氟烷、异氟烷、地氟烷和CFC - 11研究中获得的数据进行了验证。考虑到通气和心输出量的适当值,该模型成功模拟了在各种暴露场景下收集的数据。犬类模型可用于模拟与心脏致敏可能性相关的血液浓度。然后,这些目标血液浓度可与人体模型一起用于确定安全的人体暴露持续时间。犬类模型的开发强调了为模型验证进行适当数据收集的必要性。

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