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了解前药和代谢物的药代动力学。

Understanding the pharmacokinetics of prodrug and metabolite.

作者信息

Cho Seungil, Yoon Young-Ran

机构信息

Molecular Diagnostics and Imaging Center, School of Medicine, Kyungpook National University; Clinical Trial Center, Kyungpook National University Hospital, Daegu 41944, Korea.

出版信息

Transl Clin Pharmacol. 2018 Mar;26(1):1-5. doi: 10.12793/tcp.2018.26.1.1. Epub 2018 Mar 16.

Abstract

This tutorial explains the pharmacokinetics of a prodrug and its active metabolite (or parent drug) using a two-step, consecutive, first-order irreversible reaction as a basic model for prodrug metabolism. In this model, the prodrug is metabolized and produces the parent drug, which is subsequently eliminated. The mathematical expressions for pharmacokinetic parameters were derived step by step. In addition, we visualized these expressions to help understand the relationship between pharmacokinetic parameters easily. For the elimination rate-limited and formation rate-limited metabolism, we analyzed the plasma drug concentration versus time curve of a prodrug administered intravenously.

摘要

本教程以两步连续的一级不可逆反应作为前药代谢的基本模型,解释了前药及其活性代谢物(或母体药物)的药代动力学。在此模型中,前药被代谢并产生母体药物,随后母体药物被消除。药代动力学参数的数学表达式是逐步推导出来的。此外,我们将这些表达式可视化,以帮助轻松理解药代动力学参数之间的关系。对于消除速率限制型和生成速率限制型代谢,我们分析了静脉注射前药后的血浆药物浓度-时间曲线。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7376/6989223/50d1fc5c5e8f/tcp-26-1-g001.jpg

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