用扩展的对流-分散模型建立肝脏消除和器官分布动力学模型。

M S Roberts, Y G Anissimov
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引用次数: 28

摘要

传统的对流-弥散(也称为轴向弥散)模型被广泛用于将肝脏可利用性(F)和清除率(Cl)与肝脏形态和生理联系起来,并预测肝血流变化等对F和Cl的影响。已经开发了一种扩展形式的对流-弥散模型,以充分描述血管标志物在灌注肝脏后短时间和长时间的流出浓度-时间分布。该模型基于通量浓度和导管和大血管的卷积,假设肝细胞内溶质的消除遵循快速分布或径向扩散。该模型包括一个二级血管室,假定为相互连接的正弦。对提取溶质的平均肝脏传递时间(MTT)和归一化方差(CV2)的分析表明,随着肝脏提取量的增加,扩展和未加权的传统对流-弥散模型的MTT和CV2预测之间的差异减小。在所有的溶质萃取中,F和Cl的对应度都在95%以上。此外,分析表明,只要存在显著的肝脏提取,无论代表渗透率、体积和清除参数的速率常数的大小如何,扩展模型和常规模型的流出浓度-时间曲线基本上是相同的。总之,新开发的扩展对流-分散模型的应用表明,未加权的传统对流-分散模型可以用来描述提取的溶质的配置,特别是在实验和临床情况下估计肝脏的可利用性和清除率。
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Modeling of hepatic elimination and organ distribution kinetics with the extended convection-dispersion model.

The conventional convection-dispersion (also called axial dispersion) model is widely used to interrelate hepatic availability (F) and clearance (Cl) with the morphology and physiology of the liver and to predict effects such as changes in liver blood flow on F and Cl. An extended form of the convection-dispersion model has been developed to adequately describe the outflow concentration-time profiles for vascular markers at both short and long times after bolus injections into perfused livers. The model, based on flux concentration and a convolution of catheters and large vessels, assumes that solute elimination in hepatocytes follows either fast distribution into or radial diffusion in hepatocytes. The model includes a secondary vascular compartment, postulated to be interconnecting sinusoids. Analysis of the mean hepatic transit time (MTT) and normalized variance (CV2) of solutes with extraction showed that the discrepancy between the predictions of MTT and CV2 for the extended and unweighted conventional convection-dispersion models decreases as hepatic extraction increases. A correspondence of more than 95% in F and Cl exists for all solute extractions. In addition, the analysis showed that the outflow concentration-time profiles for both the extended and conventional models are essentially identical irrespective of the magnitude of rate constants representing permeability, volume, and clearance parameters, providing that there is significant hepatic extraction. In conclusion, the application of a newly developed extended convection-dispersion model has shown that the unweighted conventional convection-dispersion model can be used to describe the disposition of extracted solutes and, in particular, to estimate hepatic availability and clearance in both experimental and clinical situations.

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Edward R. Garrett 1920–1993 Edward R. Garrett: A biographical sketch Erratum to: Simple approximate formulas for calculating the time to clear drug and the time to accumulate drug when the plasma disposition curve of the drug is multiexponential Erratum to: Simplified methods for the evaluation of the parameters of the time course of plasma concentration in the one-compartment body model with first-order invasion and first-order drug elimination including methods for ascertaining when such rate constants are equal Erratum to: Comparative physiological pharmacokinetics of fenatyl and alfenatil in rats and humans based on parametric single-tissue models
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