体内
药物发现
药品
血浆蛋白结合
药理学
化学
药物作用
等离子体化学
效力
等离子体
计算生物学
体外
生物化学
医学
生物
生物技术
物理
量子力学
标识
DOI:10.1517/17460441.2.1.51
摘要
Plasma protein binding of drugs is a well-recognised phenomena, but it is only recently that the implications for drug action in vivo have been fully appreciated. Plasma proteins, by virtue of their high concentration, control the free drug concentration in plasma and in compartments in equilibrium with plasma, thereby, effectively attenuating drug potency in vivo. The historical background and thermodynamic basis for the 'Free Drug Principle' is presented, along with special considerations for intracellular targets, deep compartments and α1-acid glycoprotein binding. Real and apparent exceptions to the principle are discussed along with a survey of citations from the recent medicinal chemistry literature.
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