Construction of an optimal destructive sampling design for noncompartmental AUC estimation.

F Vandenhende, M Comblain, M H Delsemme, W Dewe, W P Hoffman, B Boulanger
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引用次数: 7

Abstract

Based on toxicokinetic studies of a destructive sampling design, this work was aimed at selecting the number of time points, their locations, and the number of replicates per time point in order to obtain the most accurate and precise noncompartmental estimate of the area under the concentration-time curve (AUC). From a prior population pharmacokinetic model, the design is selected to minimize the scaled mean squared error of AUC. Designs are found for various sample sizes, number of time points, and a distribution of animals across time points from being very unbalanced to balanced. Their efficiencies are compared both theoretically and based on simulations. An algorithm has been implemented for this purpose using the symbolic resolution and numerical minimization capabilities of Mathematica and an example of its use is provided. This method provides efficient tools for constructing, validating, and comparing optimal sampling designs for destructive sampled toxicokinetic studies.

非区隔AUC估计的最优破坏性抽样设计。
基于破坏性采样设计的毒性动力学研究,本工作旨在选择时间点的数量、位置和每个时间点的重复次数,以获得最准确和精确的浓度-时间曲线下面积(AUC)的非区隔估计。从先前的群体药代动力学模型中,选择设计以最小化AUC的标度均方误差。设计适用于不同的样本量、时间点数量,以及动物在时间点上的分布,从非常不平衡到平衡。在理论和仿真的基础上比较了它们的效率。为此目的,利用Mathematica的符号分辨率和数值最小化功能实现了一种算法,并提供了其使用示例。该方法为构建、验证和比较破坏性样本毒性动力学研究的最佳抽样设计提供了有效的工具。
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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