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BUILDING A STRUCTURED MODEL OF A COMPLEX PHARMACOKINETIC SYSTEM WITH TIME DELAYS

机译:建立具有时间延迟的复杂药动学系统的结构模型

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This paper presents a description of the procedure for building a structured model of a complex pharmacokinetic system on using its transfer function. The example employed is that of the pharmacokinetic system based on gentamicin plasma concentrations after intravenous and intratracheal administration to guinea pigs, describing the pathway of the drug into the systemic circulation after the extravascular injection mentioned. The structured model selected consisted of a submodel of a proportional linear subsystem, two submodels of simple linear dynamic subsystems with time constants of 0.135 ± 0.065 hr (95% I.C.) and 0.052 ± 0.049 hr, and two submodels of parallel subsystems with time delays of 0.254 ± 0.046 hr and 1.135 ± 0.288 hr, connected in serial. Two estimates of the mean residence time of the total amount of gentamicin in the system, i.e. 0.347 and 0.335 hr, were obtained, based on the system frequency and structured model, respectively. From the methodological point of view, our paper demonstrates the efficiency of combination of modelling in the frequency and in the time domain, designed to facilitate studies of pharmacokinetic systems.
机译:本文介绍了使用其传递函数构建复杂药代动力学系统结构模型的过程。所用的实例是基于对豚鼠静脉内和气管内给药后庆大霉素血浆浓度的药代动力学系统,描述了所述血管外注射后药物进入体循环的途径。选择的结构化模型包括比例线性子系统的子模型,时间常数为0.135±0.065 hr(95%IC)和0.052±0.049 hr的简单线性动态子系统的两个子模型,以及时延为的并行子系统的两个子模型。串联连接的0.254±0.046小时和1.135±0.288小时基于系统频率和结构模型,分别获得了庆大霉素总量在系统中的平均停留时间的两个估计值,即0.347和0.335 hr。从方法论的角度来看,本文证明了在频域和时域中组合建模的效率,旨在促进药代动力学系统的研究。

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