Li Yongmei, McCabe Michelle, Podila Lalitha, Tracy Timothy S, Tweedie Donald J
Drug Metabolism and Pharmacokinetics, Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, USA.
Methods Mol Biol. 2014;1113:441-60. doi: 10.1007/978-1-62703-758-7_20.
An appreciation of the principles of enzyme kinetics can be applied in a number of drug metabolism applications. The concept for this chapter arose from a simple discussion on selecting appropriate time points to most efficiently assess metabolite profiles in a human Phase 1a clinical study (Subheading 4). By considering enzyme kinetics, a logical approach to the issue was derived. The dialog was an important learning opportunity for the participants in the discussion, and we have endeavored to capture this experience with other questions related to determination of K m and V max parameters, a consideration of the value of hepatocytes versus liver microsomes and enzyme inhibition parameters.
对酶动力学原理的理解可应用于许多药物代谢应用中。本章的概念源于一次关于在人体1a期临床研究中选择合适时间点以最有效地评估代谢物谱的简单讨论(小标题4)。通过考虑酶动力学,得出了处理该问题的合理方法。这次对话对讨论参与者来说是一次重要的学习机会,我们努力将这一经验与其他相关问题相结合,这些问题涉及Km和Vmax参数的测定、对肝细胞与肝微粒体价值的考量以及酶抑制参数。