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大鼠中四氯乙烯的泌乳转移

Lactational transfer of tetrachloroethylene in rats.

作者信息

Byczkowski J Z, Fisher J W

机构信息

ManTech Environmental Technology, Inc., Dayton, Ohio 45437-0009.

出版信息

Risk Anal. 1994 Jun;14(3):339-49. doi: 10.1111/j.1539-6924.1994.tb00250.x.

Abstract

Tetrachloroethylene (PCE) is a commonly used organic solvent and a suspected human carcinogen, reportedly transferred to human breast milk following inhalation exposure. Transfer of PCE to milk may represent a threat to the nursing infant. A physiologically based pharmacokinetic (PBPK) model was developed to quantitatively assess the transfer of inhaled PCE into breast milk and the consequent exposure of the nursing infant. The model was validated in lactating rats. Lactating Sprague-Dawley female rats were exposed via inhalation to PCE at concentrations ranging from 20-1000 ppm, and then returned to their nursing, 10- to 11-day-old pups. Tetrachloroethylene concentrations in the air, blood, milk, and tissue were determined by gas chromatography and compared to model predictions. The model described the distribution of inhaled PCE in maternal blood and milk, as well as the nursed pup's gastrointestinal tract, blood, and tissue. Several computer simulations of PCE distribution kinetics in exhaled air, blood, and milk of exposed human subjects were run and compared with limited human data available from the literature. It is concluded that the PBPK model successfully described the concentration of PCE in both lactating rats and humans. Although predictions vs. observations were good, the model slightly underpredicted the peak whole pup PCE concentration and underpredicted systemic clearance of PCE from the pup.

摘要

四氯乙烯(PCE)是一种常用的有机溶剂,也是一种疑似人类致癌物,据报道,吸入接触后它会转移到人类母乳中。PCE转移到乳汁中可能会对哺乳期婴儿构成威胁。我们建立了一个基于生理学的药代动力学(PBPK)模型,以定量评估吸入的PCE向母乳中的转移以及由此导致的哺乳期婴儿的暴露情况。该模型在泌乳大鼠中得到了验证。将泌乳的斯普拉格-道利雌性大鼠通过吸入暴露于浓度范围为20 - 1000 ppm的PCE中,然后让它们回到自己10至11日龄的幼崽身边进行哺乳。通过气相色谱法测定空气、血液、乳汁和组织中的四氯乙烯浓度,并与模型预测结果进行比较。该模型描述了吸入的PCE在母体血液和乳汁以及哺乳幼崽的胃肠道、血液和组织中的分布情况。我们对暴露的人类受试者呼出的空气、血液和乳汁中PCE分布动力学进行了几次计算机模拟,并与文献中有限的人类数据进行了比较。得出的结论是,PBPK模型成功地描述了泌乳大鼠和人类体内PCE的浓度。尽管预测值与观测值吻合良好,但该模型略微低估了幼崽体内PCE的峰值浓度,并且低估了PCE从幼崽体内的全身清除率。

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