de Campos Michel Leandro, Padilha Elias Carvalho, Peccinini Rosângela Gonçalves
Sao Paulo State University - UNESP School of Pharmaceutical Sciences Rodovia Araraquara-Jau Km. 01 s/n, City: Araraquara, State: Sao Paulo, Zip code: 14801-902; Brazil.
Drug Metab Lett. 2014 Jul;7(2):105-16. doi: 10.2174/1872312808666140317155008.
In drug discovery and development, the kinetic study of active metabolites plays an important role, helping to define the time course of the drug in the body and its activity or toxicity. After a pharmacokinetics assessment of a drug and its metabolite or a prodrug and its parent-drug, several parameters can be calculated. In some cases, achieving the objective of the study does not require all possible parameters to be calculated. When parameters are calculated, it is essential that their denotations are widely accepted and used. However, some parameters undergo a certain variability of denotation, which may confuse some readers. Thus, this review summarizes the current published data for experimental pharmacokinetic parameters of metabolites and the calculations involved in simple metabolite pharmacokinetic studies. It also evaluates the most common pharmacokinetic parameters in the literature and suggests metabolite parameters that could be determined to help advance metabolite kinetic models.
在药物发现与开发过程中,活性代谢物的动力学研究起着重要作用,有助于确定药物在体内的时间进程及其活性或毒性。在对一种药物及其代谢物或前药及其母药进行药代动力学评估后,可以计算出几个参数。在某些情况下,实现研究目标并不需要计算所有可能的参数。当计算参数时,其表示方式必须被广泛接受和使用。然而,一些参数的表示方式存在一定的变异性,这可能会使一些读者感到困惑。因此,本综述总结了目前已发表的关于代谢物实验药代动力学参数的数据以及简单代谢物药代动力学研究中所涉及的计算。它还评估了文献中最常见的药代动力学参数,并提出了可以确定的代谢物参数,以帮助推进代谢物动力学模型。