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蛋白质结合的药代动力学方面(作者译)

[Pharmaco-kinetic aspects of protein-binding (author's transl)].

作者信息

Kurz H

出版信息

Klin Wochenschr. 1978 Dec 15;56(24):1195-204. doi: 10.1007/BF01477075.

Abstract

Binding of drugs to plasma proteins will influence distribution and elimination especially if factors interfere altering the extent of binding. These factors are: dependence on species, age, H+-concentration, speed of i.v. injection or the interaction of another drug for instance. Considering the quantitative aspects changes in binding to the plasma proteins will turn only then relevant to drug action if the extent of alteration is very large or the drugs are bound to a very high degree. But the scene changes completely if the binding to other proteins of the organism is considered. Experimental results concerning the binding of drugs to hemoglobin and muscle tissue suggest that this kind of binding is possibly more effective in pharmacokinetics than binding to plasma proteins.

摘要

药物与血浆蛋白的结合会影响分布和消除,尤其是当有因素干扰改变结合程度时。这些因素包括:物种依赖性、年龄、氢离子浓度、静脉注射速度或另一种药物的相互作用等。从定量方面考虑,只有当改变程度非常大或药物结合程度非常高时,与血浆蛋白结合的变化才会与药物作用相关。但如果考虑药物与机体其他蛋白质的结合,情况就完全不同了。关于药物与血红蛋白和肌肉组织结合的实验结果表明,这种结合在药代动力学中可能比与血浆蛋白的结合更有效。

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