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非线性血浆蛋白结合情况下游离药物浓度与总药物浓度的抛物线方程。

Parabolic equation relating free and total drug concentrations in cases of nonlinear plasma protein binding.

作者信息

Behm H L, Wagner J G

出版信息

J Pharm Sci. 1981 Jul;70(7):802-4. doi: 10.1002/jps.2600700725.

Abstract

In many cases of nonlinear drug-protein binding, investigators have fitted data to the classical Langmuir model with two classes of binding sites involving four parameters. For human serum albumin binding of tolmetin and salicylate, a simple two-parameter parabolic equation relating free to total concentrations fitted the binding data better. Thus, the free fraction corresponding to the serum or plasma drug concentration in the blood sample taken from a subject can be estimated directly from the parabolic model. This is not the case when the Langmuir model is used to describe nonlinear binding data since the positive root of a cubic equation must be obtained to estimate the free from the total concentration. The direct relationship between free and total drug concentrations would be useful in many clinical situations.

摘要

在许多非线性药物-蛋白质结合的案例中,研究人员已将数据拟合到具有两类涉及四个参数的结合位点的经典朗缪尔模型。对于托美汀和水杨酸盐与人血清白蛋白的结合,一个将游离浓度与总浓度相关联的简单双参数抛物线方程能更好地拟合结合数据。因此,可直接从抛物线模型估算取自受试者的血样中与血清或血浆药物浓度相对应的游离分数。而当使用朗缪尔模型描述非线性结合数据时情况并非如此,因为必须求解一个三次方程的正根才能从总浓度估算游离浓度。游离药物浓度与总药物浓度之间的直接关系在许多临床情形中会很有用。

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