Development and Human Extrapolation of Physiologically Based Toxicokinetic Models for Chlorinated Polyfluoroalkyl Ether Sulfonates from Rats

毒物动力学 生物累积 化学 生物监测 人类健康 环境化学 乙醚 外推法 内照射剂量 毒性 基于生理学的药代动力学模型 药理学 色谱法 风险评估 肝毒性 毒理 健康风险 药代动力学
作者
Jing Zhang,Huihui Bao,Wen-Hui Zhao,Long-Sheng Fan,Hao Zhou,Ting Ruan,Yun-Ting Zhang,Lili Liu,Dan Cai,Sizhe Xie,Guang-Hui Dong,Wei-Chun Chou,Lei Zhang,Xiao-Wen Zeng
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:60 (12): 9117-9128
标识
DOI:10.1021/acs.est.5c18780
摘要

Chlorinated polyfluoroalkyl ether sulfonates (F-53B, including 6:2 Cl-PFESA and 8:2 Cl-PFESA) are typical alternatives to perfluorooctanesulfonate in China. However, they are persistent and frequently detected in the environment and humans and pose bioaccumulation and health risks. The limited understanding of F-53B's toxicokinetic data hinders its risk assessment. This study aimed to develop physiologically based toxicokinetic (PBTK) models for 6:2 Cl-PFESA and 8:2 Cl-PFESA in rats and to extrapolate the models to humans. Male rats were administered a single 100 μg/kg dose of F-53B (with a 6:2 Cl-PFESA to 8:2 Cl-PFESA ratio of about 9:1) via gavage and intravenous injection, and biosample concentrations were quantified using ultrahigh-performance liquid chromatography-mass spectrometry. Results showed that 6:2 Cl-PFESA was mainly distributed to the liver and plasma, while 8:2 Cl-PFESA was primarily distributed to the liver and lung. The developed PBTK models successfully predicted 100% of 6:2 Cl-PFESA and 92% of 8:2 Cl-PFESA concentrations within a 2-fold range of the observed values. These models were subsequently extrapolated to humans and validated with human biomonitoring data. This study establishes PBTK models for F-53B in the general adult population, enhancing quantitative risk assessments under real-world scenarios.
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