Láznícek M, Kvĕtina J, Mazák J, Krch V
J Pharm Pharmacol. 1987 Feb;39(2):79-83. doi: 10.1111/j.2042-7158.1987.tb06949.x.
Relationships between plasma protein binding of 11 organic acids (benzoic and phenylacetic acid derivatives) and their lipophilicity were studied in man, rabbits, rats and mice. For description, the relationship fu = 1/(1 + aDb) was developed, where fu is the fraction of the unbound drug in plasma, D is the partition coefficient octanol/water and a and b are parameters. While the value of the parameter a is widely different in interspecies comparison, the value of the parameter b is very close in all species studied and is approximately equal to 1. The model used allows the simple calculation of the extent of plasma binding of structurally similar drugs from their lipophilicity, or conversion of the extent of plasma binding from one species to another.
在人、兔、大鼠和小鼠中研究了11种有机酸(苯甲酸和苯乙酸衍生物)的血浆蛋白结合与其亲脂性之间的关系。为了进行描述,建立了关系式fu = 1/(1 + aDb),其中fu是血浆中未结合药物的分数,D是辛醇/水分配系数,a和b是参数。虽然在种间比较中参数a的值差异很大,但在所研究的所有物种中参数b的值非常接近,约等于1。所使用的模型允许根据结构相似药物的亲脂性简单计算其血浆结合程度,或将一种物种的血浆结合程度转换为另一种物种的。