Gibaldi M, McNamara P J
Eur J Clin Pharmacol. 1978 Jul 30;13(5):373-80. doi: 10.1007/BF00644611.
A pharmacokinetic model that incorporates linear binding of drug to plasma proteins and tissue indicates the same relationship between apparent volume of distribution and drug binding as that proposed by Gillette (1971) based on a simple distribution model. Apparent volume of distribution (V) is directly proportional to free fraction of drug in plasma (fp) and indirectly proportional to free fraction of drug in tissue (fT). In the case of a constant fT, a plot of V versus fp will be linear with an intercept equal to plasma volume (Vp). If fT changes with fp, an apparently linear plot may result but the intercept will exceed Vp. An approach to the calculation of fT, a composite binding parameter, is presented and illustrated by comparing the tissue binding of tolbutamide in patients during acute viral hepatitis and upon recovery.
一个包含药物与血浆蛋白和组织线性结合的药代动力学模型表明,表观分布容积与药物结合之间的关系与吉列特(1971年)基于简单分布模型提出的关系相同。表观分布容积(V)与血浆中药物的游离分数(fp)成正比,与组织中药物的游离分数(fT)成反比。在fT恒定的情况下,V对fp的作图将是线性的,截距等于血浆容积(Vp)。如果fT随fp变化,可能会得到看似线性的作图,但截距将超过Vp。本文提出并通过比较急性病毒性肝炎患者及康复后甲苯磺丁脲的组织结合情况,举例说明了一种计算fT(一个复合结合参数)的方法。