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基于生理学的药代动力学建模:一种组织分布的亚室模型。

Physiologically based pharmacokinetic modelling: a sub-compartmentalized model of tissue distribution.

作者信息

von Kleist Max, Huisinga Wilhelm

机构信息

Department of Mathematics and Computer Science, and DFG Research Center Matheon, Freie Universität Berlin, Berlin, Germany.

出版信息

J Pharmacokinet Pharmacodyn. 2007 Dec;34(6):789-806. doi: 10.1007/s10928-007-9071-3. Epub 2007 Sep 25.

Abstract

We present a sub-compartmentalized model of drug distribution in tissue that extends existing approaches based on the well-stirred tissue model. It is specified in terms of differential equations that explicitly account for the drug concentration in erythrocytes, plasma, interstitial and cellular space. Assuming, in addition, steady state drug distribution and by lumping the different sub-compartments, established models to predict tissue-plasma partition coefficients can be derived in an intriguingly simple way. This direct link is exploited to explicitly construct and parameterize the sub-compartmentalized model for moderate to strong bases, acids, neutrals and zwitterions. The derivation highlights the contributions of the different tissue constituents and provides a simple and transparent framework for the construction of novel tissue distribution models.

摘要

我们提出了一种组织中药物分布的亚区室化模型,该模型扩展了基于充分搅拌组织模型的现有方法。它是根据微分方程指定的,这些方程明确考虑了红细胞、血浆、间质和细胞空间中的药物浓度。此外,假设药物分布处于稳态并通过将不同的亚区室归并在一起,可以以一种非常简单的方式推导出用于预测组织-血浆分配系数的既定模型。利用这种直接联系,为中强碱、酸、中性物质和两性离子明确构建并参数化了亚区室化模型。该推导突出了不同组织成分的贡献,并为构建新型组织分布模型提供了一个简单且透明的框架。

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