Brée F, Houin G, Barré J, Moretti J L, Wirquin V, Tillement J P
Clin Pharmacokinet. 1986 Jul-Aug;11(4):336-42. doi: 10.2165/00003088-198611040-00006.
The volumes of distribution of many acidic drugs have been shown to be close to that of their binding protein, i.e. serum albumin. The distribution of basic drugs mainly bound to alpha 1-acid glycoprotein (AAG) can be questioned with respect to its dependency upon the distribution of this plasma protein. So, a pharmacokinetic study was performed in 7 subjects with human 125I-labelled alpha 1-acid glycoprotein. The steady-state volume of distribution was found to be 5.37 +/- 0.82L. The central volume was 3.23 +/- 0.33L, close to that of plasma volume and the peripheral volume was 2.14 +/- 0.63L. These data allowed the establishment of an equation giving access to the volume of distribution of a basic drug by relating its unbound fraction to physiological distribution of alpha 1-acid glycoprotein. The values yielded by this equation show that the actual and calculated volumes of distribution of basic drugs mainly bound to AAG are discrepant. This protein is thus not the main factor controlling the distribution of basic drugs within the body.
许多酸性药物的分布容积已被证明与其结合蛋白(即血清白蛋白)的分布容积相近。主要与α1-酸性糖蛋白(AAG)结合的碱性药物的分布,就其对这种血浆蛋白分布的依赖性而言,是值得质疑的。因此,对7名受试者进行了一项使用人125I标记的α1-酸性糖蛋白的药代动力学研究。发现稳态分布容积为5.37±0.82L。中心容积为3.23±0.33L,接近血浆容积,外周容积为2.14±0.63L。这些数据使得能够建立一个方程,通过将碱性药物的游离分数与其α1-酸性糖蛋白的生理分布相关联,来获得其分布容积。该方程得出的值表明,主要与AAG结合的碱性药物的实际分布容积和计算分布容积存在差异。因此,这种蛋白不是控制碱性药物在体内分布的主要因素。