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一室模型一级速率和米氏消除同时存在的持续输注情况:解析解和药物暴露公式。

Constant infusion case of one compartment pharmacokinetic model with simultaneous first-order and Michaelis-Menten elimination: analytical solution and drug exposure formula.

机构信息

Department of Mathematics, Shanghai Maritime University, Shanghai, 201306, People's Republic of China.

Faculté de pharmacie, Université de Montréal, Montreal, QC, H3C 3J7, Canada.

出版信息

J Pharmacokinet Pharmacodyn. 2021 Aug;48(4):495-508. doi: 10.1007/s10928-021-09740-5. Epub 2021 Feb 24.

Abstract

The main objective of this article is to propose the closed-form solution of one-compartment pharmacokinetic model with simultaneous first-order and Michaelis-Menten elimination for the case of constant infusion. For the case of bolus administration, we have previously established a closed-form solution of the model through introducing a transcendent X function. In the same vein, we found here a closed-form solution of constant infusion could be realized through introducing another transcendent Y function. For the general case of constant infusion of limited duration, the closed-form solution is then fully expressed using both X and Y functions. As direct results, several important pharmacokinetic surrogates, such as peak concentration [Formula: see text] and total drug exposure AUC[Formula: see text], are found the closed-form expressions and ready to be analyzed. The new pharmacokinetic knowledge we have gained on these parameters, which largely exhibits in a nonlinear feature, is in clear contrast to that of the linear case. Finally, with a pharmacokinetic model adapted from that formerly reported on phenytoin, we numerically analyzed and illustrated the roles of different model parameters and discussed their influence on drug exposure. To conclude, the present findings elucidate the intrinsic quantitative structural properties of such pharmacokinetic model and provide a new avenue for future modelling and rational drug designs.

摘要

本文的主要目的是提出在恒速输注情况下,同时具有一级和米氏消除的单室药代动力学模型的闭式解。对于推注给药的情况,我们之前通过引入超越函数 X 建立了模型的闭式解。同样,我们在这里发现,可以通过引入另一个超越函数 Y 来实现恒速输注的闭式解。对于有限持续时间的一般恒速输注情况,使用 X 和 Y 函数可以完全表示闭式解。作为直接结果,找到了几个重要的药代动力学替代物,如峰浓度 [Formula: see text] 和总药物暴露 AUC[Formula: see text],找到了闭式解表达式并可以进行分析。与线性情况相比,我们在这些参数上获得了新的药代动力学知识,这些知识主要表现为非线性特征。最后,我们使用从前瞻性苯妥英报告的药代动力学模型进行数值分析和说明了不同模型参数的作用,并讨论了它们对药物暴露的影响。总之,本研究阐明了这种药代动力学模型的内在定量结构特性,并为未来的建模和合理药物设计提供了新的途径。

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