Cheng H, Gillespie W R
Department of Drug Metabolism, Merck Research Laboratories, West Point, Pennsylvania 19486, USA.
J Pharmacokinet Biopharm. 1996 Aug;24(4):389-402. doi: 10.1007/BF02353519.
Based on a generalized model, equations for calculating the mean residence time in the body at single dose (MRT) and at steady state (MRTss), apparent steady-state volume of distribution (Vss), and steady-state volume of distribution (Vss) are derived for a drug exhibiting nonlinear protein binding. Interrelationships between Vss and Vss as well as between MRT and MRTss are also discussed and illustrated with simulated data. In addition, a method for estimating the central volume of distribution of the bound drug and the sum of the central volume of distribution of the unbound drug and the area under the first moment curve of distribution function for drugs with nonlinear protein binding is proposed and illustrated with both simulated and published data.
基于一个通用模型,推导了用于计算单剂量给药时体内平均驻留时间(MRT)和稳态时体内平均驻留时间(MRTss)、表观稳态分布容积(Vss)以及稳态分布容积(Vss)的方程,该模型适用于表现出非线性蛋白结合的药物。还讨论了Vss与Vss之间以及MRT与MRTss之间的相互关系,并用模拟数据进行了说明。此外,提出了一种估算结合药物的中央分布容积以及未结合药物的中央分布容积与分布函数一阶矩曲线下面积之和的方法,该方法适用于具有非线性蛋白结合的药物,并用模拟数据和已发表的数据进行了说明。