Prodrugs and their activation mechanisms for brain drug delivery.

IF 4.1 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ida Aaberg Lillethorup, Andreas Victor Hemmingsen, Katrine Qvortrup
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引用次数: 0

Abstract

Prodrugs are masked drugs that first become pharmacologically active after undergoing a structural change in vivo. They are designed to improve physicochemical/biopharmaceutical drug properties and increase site specificity. The prodrug approach is important when developing brain-targeting drugs due to the presence of the brain barriers that seriously limit the brain entry of highly polar, multifunctional drug entities. While several excellent reviews summarize the structural modifications facilitating transport across the brain barriers, a summary of mechanisms used for the activation of the prodrug in the brain is missing. Given the high need for innovative discoveries in brain drug development, we here review the most important tools being developed since 2000 for CNS prodrug activation.

前药及其脑给药激活机制。
前药是被掩盖的药物,在体内发生结构变化后首先具有药理活性。它们旨在改善物理化学/生物制药药物特性并增加位点特异性。由于脑屏障的存在严重限制了高极性、多功能药物实体进入大脑,因此在开发脑靶向药物时,前药方法非常重要。虽然有几篇优秀的综述总结了促进脑屏障运输的结构修饰,但对大脑中前药激活的机制的总结却缺失。鉴于大脑药物开发对创新发现的高度需求,我们在这里回顾了自2000年以来开发的用于中枢神经系统前药激活的最重要工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
自引率
2.40%
发文量
129
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