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

被引:70
作者
Hisaka, A
Sugiyama, Y
机构
[1] Banyu Pharmaceut Co Ltd, Dev Res Lab, Menuma 3600214, Japan
[2] Univ Tokyo, Fac Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
来源
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS | 1998年 / 26卷 / 05期
关键词
nonlinear pharmacokinetics; dispersion model; multiple indicator dilution; hepatic clearance; transit time distribution; finite difference method; nonlinear partial differential equation; computer simulation; BQ-123;
D O I
10.1023/A:1023294632129
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:495 / 519
页数:25
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