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1,1,2-三氯-1,2,2-三氟乙烷人体吸入药代动力学的基于生理学的数学模型。

A physiologically based mathematical model for the human inhalation pharmacokinetics of 1,1,2-trichloro-1,2,2-trifluoroethane.

作者信息

Auton T R, Woollen B H

机构信息

ICI Central Toxicology Laboratory, Macclesfield, Cheshire, UK.

出版信息

Int Arch Occup Environ Health. 1991;63(2):133-8. doi: 10.1007/BF00379077.

Abstract

A physiologically based mathematical model is described for the human inhalation pharmacokinetics of 1,1,2-trichloro-1,2,2-trifluoroethane (FC113). Physiological parameters for the model are derived from the scientific literature. Partition coefficients are determined from in vitro measurements. Predictions of the resulting model for breath and blood concentrations compare well with results of a human volunteer study described in a companion paper (Woollen et al. 1990). Using this data some alternative models are also examined with different choices of physiological parameters and partition coefficients. The mathematical model is used to examine the consequences of metabolic elimination of FC113. A value for metabolic clearance is estimated using the during-exposure breath concentration data; however, the concentrations of FC113 in breath or blood during and after exposure are shown to be insensitive to metabolic clearance. Consequently, no firm conclusion can yet be drawn as to whether FC113 is metabolised by man.

摘要

描述了一种基于生理学的数学模型,用于研究1,1,2-三氯-1,2,2-三氟乙烷(FC113)的人体吸入药代动力学。该模型的生理学参数源自科学文献。分配系数通过体外测量确定。所得模型对呼气和血液浓度的预测结果与一篇姊妹论文(Woollen等人,1990年)中描述的人体志愿者研究结果吻合良好。利用这些数据,还研究了一些采用不同生理学参数和分配系数选择的替代模型。该数学模型用于研究FC113代谢消除的后果。利用暴露期间的呼气浓度数据估算了代谢清除率;然而,暴露期间及之后呼气或血液中FC113的浓度对代谢清除率不敏感。因此,关于FC113是否会被人体代谢,目前尚无确凿结论。

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