Daimon Takashi, Goto Masashi
Department of Drug Evaluation and Informatics, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka 422-8526, Japan.
Stat Med. 2007 Jun 30;26(14):2799-812. doi: 10.1002/sim.2736.
In pharmacokinetics, compartment models are often used to describe the time course of blood concentration after the administration of a drug. In this article, we propose an optimal design criterion for precise estimation of parameters included in the compartment model and illustrate the non-sequential design of sampling times of blood drug concentration data in individual pharmacokinetics. The proposed optimal design criterion minimizes the determinant of the mean-squared error matrix of the parameter estimator that is quadratically approximated by the curvature array. Therefore, the proposed criterion considers the intrinsic and parameter-effects nonlinearity underlying the compartment model, and so is applicable in a pharmacokinetic experiment where the sample size of the blood drug concentration data is quite small.
在药代动力学中,房室模型常用于描述药物给药后血药浓度随时间的变化过程。在本文中,我们提出了一种用于精确估计房室模型中参数的最优设计准则,并阐述了个体药代动力学中血药浓度数据采样时间的非序贯设计。所提出的最优设计准则使由曲率阵列二次近似得到的参数估计器的均方误差矩阵的行列式最小化。因此,所提出的准则考虑了房室模型潜在的内在和参数效应非线性,适用于血药浓度数据样本量相当小的药代动力学实验。