Analysis of nonlinear and nonsteady state hepatic extraction with the dispersion model using the finite difference method.

A Hisaka, Y Sugiyama
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引用次数: 59

Abstract

A numerical calculation method for dispersion models was developed to analyze nonlinear and nonsteady hepatic elimination of substances. The finite difference method (FDM), a standard numerical calculation technique, was utilized to solve nonlinear partial differential equations of the dispersion model. Using this method, flexible application of the dispersion model becomes possible, because (i) nonlinear kinetics can be incorporated anywhere, (ii) the input function can be altered arbitrarily, and (iii) the number of compartments can be increased as needed. This method was implemented in a multipurpose nonlinear least-squares fitting computer program, Napp (Numeric Analysis Program for Pharmacokinetics). We simulated dilution curves for several nonlinear two-compartment hepatic models in which the saturable process is assumed in transport or metabolism, and investigated whether they could definitely be discriminated from each other. Preliminary analysis of the rat liver perfusion data of a cyclic pentapeptide, BQ-123, was performed by this method to demonstrate its applicability.

用有限差分法分析离散模型的非线性非稳态肝脏提取。
提出了一种色散模型的数值计算方法,用于分析物质的非线性非稳态肝消。利用有限差分法(FDM)这一标准数值计算技术,求解了色散模型的非线性偏微分方程。使用这种方法,分散模型的灵活应用成为可能,因为(i)非线性动力学可以在任何地方加入,(ii)输入函数可以任意改变,(iii)室的数量可以根据需要增加。该方法在多用途非线性最小二乘拟合计算机程序Napp (numerical Analysis program for Pharmacokinetics)中实现。我们模拟了几种非线性双室肝模型的稀释曲线,其中假设在运输或代谢过程中存在饱和过程,并研究了它们是否可以明确地相互区分。通过对环五肽BQ-123的大鼠肝脏灌注数据进行初步分析,验证了该方法的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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