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
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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