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A new stochastic approach to multi-compartment pharmacokinetic models: probability of traveling route and distribution of residence time in linear and nonlinear systems.

机译:一种多室药代动力学模型的新随机方法:线性和非线性系统中的行进路径概率和停留时间分布。

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摘要

Drug kinetics in human has been studied from both deterministic and stochastic perspectives. However, little research has been done to systematically determine the probability for a drug molecule to follow a specific traveling route. Recently a method was developed to estimate this probability and the probability density function of residence time in linear systems. In this paper, we provide a rigorous proof of the main results of the previous paper and extend the method to nonlinear multi-compartment systems. A novel concept of compartment expansion is introduced to facilitate the development of our method. This formulation resolves computational difficulties associated with nonlinear systems, allowing for direct estimation of the probability intensity coefficients, and subsequently the transition probability and probability density function of the residence time. With such expansion of the methodology, it becomes both practical and feasible to apply it in the real-world drug development where drug disposition patterns are often nonlinear. The method can be used to estimate drug exposure at any site of interest, thus may help us to gain better understanding about the impact of drug exposure on efficacy and safety.
机译:已经从确定性和随机的角度研究了人类的药物动力学。但是,很少有研究来系统地确定药物分子遵循特定行进路线的可能性。最近,开发了一种方法来估计此概率以及线性系统中停留时间的概率密度函数。在本文中,我们提供了对以前论文主要结果的严格证明,并将该方法扩展到非线性多室系统。介绍了一种新颖的隔室扩展概念,以促进我们方法的发展。该公式解决了与非线性系统相关的计算难题,允许直接估计概率强度系数,并随后估计停留时间的跃迁概率和概率密度函数。随着这种方法的扩展,将其应用于现实世界中药物配置模式通常是非线性的药物开发既实用又可行。该方法可用于估计任何感兴趣部位的药物暴露,从而可以帮助我们更好地了解药物暴露对功效和安全性的影响。

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