Weiss M
J Math Biol. 1982;15(3):305-18. doi: 10.1007/BF00275690.
Characterizing the tissue distribution kinetics of drugs by physiological and physico-chemical parameters and using a circulatory model the time course of blood concentration after intravenous injection is predicted for linear pharmacokinetic systems. The interrelationships between the first three (zero to second) moments of the distribution functions of organ transfer times, circulation times and residence times of drug molecules in the body are described. Utilizing literature data the model is applied to the analysis of lidocain kinetics in humans.
通过生理和物理化学参数表征药物的组织分布动力学,并使用循环模型预测线性药代动力学系统静脉注射后血药浓度的时间进程。描述了药物分子在体内器官转运时间、循环时间和停留时间分布函数的前三个(零至二阶)矩之间的相互关系。利用文献数据,将该模型应用于人体利多卡因动力学分析。