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化合物与血浆蛋白结合的测定。

Determination of compound binding to plasma proteins.

作者信息

Dow Natasha

机构信息

Covance Laboratories, Inc., Madison, Wisconsin, USA.

出版信息

Curr Protoc Pharmacol. 2006 Oct;Chapter 7:Unit7.5. doi: 10.1002/0471141755.ph0705s34.

Abstract

The pharmacokinetic and pharmacodynamic properties of a compound are profoundly affected by the extent of its binding to plasma proteins. Consequently, the determination of the plasma protein binding properties of a compound is essential during drug development and is increasingly required during lead prioritization. The protocols described in this unit detail the techniques of ultrafiltration and equilibrium dialysis for determination of plasma protein binding. Equilibrium dialysis is the more robust of the two techniques, whereas ultrafiltration is the more rapid. Two versions of the equilibrium dialysis technique are provided: the traditional approach and a higher-throughput 96-well plate version.

摘要

一种化合物的药代动力学和药效学特性会受到其与血浆蛋白结合程度的深刻影响。因此,在药物研发过程中,测定化合物的血浆蛋白结合特性至关重要,并且在先导化合物优先级排序过程中的需求也日益增加。本单元所描述的方案详细介绍了用于测定血浆蛋白结合的超滤和平衡透析技术。平衡透析是这两种技术中更为稳健的一种,而超滤则更为快速。文中提供了平衡透析技术的两个版本:传统方法和高通量96孔板版本。

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