Computer-based Evolutionary Search for a Nonlinear Conversion Function for Establishing In Vitro-In Vivo Correlation (IVIVC) of Oral Drug Formulations

被引:12
|
作者
Yamashita, Fumiyoshi [1 ]
Fujita, Atsuto
Zhang, Xingyi
Sasa, Yukako
Mihara, Kiyoshi [3 ]
Hashida, Mitsuru [2 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Inst Integrated Cell Mat Sci, Kyoto 6068501, Japan
[3] Musashino Univ, Res Ctr Clin Pharm, Fac Pharm, Nishitokyo, Japan
基金
日本学术振兴会;
关键词
in vitro-in vivo correlation; genetic expression programming; genetic algorithm; nonlinear optimization; diltiazem; sustained release; EXTENDED-RELEASE FORMULATION; DOSAGE FORM; DILTIAZEM; PHARMACOKINETICS; ABSORPTION;
D O I
10.2133/dmpk.DMPK-11-RG-075
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Establishment of in vitro in vivo correlation (IVIVC) accelerates optimization of desirable drug formulations and/or modification of the manufacturing processes in the scale-up and post-approval periods. This article presents a method of finding the optimal conversion function for establishing Level A point-to-point IVIVC, based on a computer-based evolutionary search technique. Gene expression programming (GEP) is a technique for optimizing a mathematical expression tree with the help of a genetic algorithm. A parameter optimization routine, which minimizes the number of parameters in the mathematical expression trees and estimates the best-fit parameter values, was implemented in the GEP algorithm. Feasibility of the computer program was investigated using the in vitro and in vivo data for sustained release diltiazem formulations. It provided a mathematical equation that, from their in vitro dissolution profiles, successfully predicts the plasma concentration profiles of three different formulations of diltiazem following oral administration. Because the present approach does not use intravenous injection data like conventional IVIVC analyses, it is widely applicable to the evaluation of various oral formulations.
引用
收藏
页码:280 / 285
页数:6
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