Himmelstein K J, Lutz R J
Department of Chemical and Petroleum Engineering, The University of Kansas, Lawrence, Kansas 66045, USA.
J Pharmacokinet Biopharm. 1979 Apr;7(2):127-45. doi: 10.1007/BF01059734.
The physiological pharmacokinetic approach to the modeling of drug distribution is reviewed. These models allow extrapolation outside the range of data with some confidence if the dominant mechanisms of transport are sufficiently well understood. In addition, it is possible to extrapolate to other species. Compartments correspond to anatomical spaces so that biochemical interactions (including drug effect or pharmacodynamics) can be incorporated in the model. The articles summarized in this review are limited to models dealing with drug application.
本文综述了药物分布建模的生理药代动力学方法。如果对主要转运机制有足够深入的了解,这些模型能够在一定程度上自信地外推超出数据范围的情况。此外,还可以外推到其他物种。房室对应于解剖学空间,从而可以将生化相互作用(包括药物效应或药效学)纳入模型。本综述中总结的文章仅限于处理药物应用的模型。