Improving drug delivery to the brain: the prodrug approach.

Expert opinion on drug delivery Pub Date : 2024-05-01 Epub Date: 2024-05-16 DOI:10.1080/17425247.2024.2355180
Kristiina M Huttunen
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Abstract

Introduction: The prodrug approach has been thought to be a simple solution to improve brain drug delivery for decades. Nevertheless, it still comes as a surprise that there is relatively little success in the field. The best example anti-parkinsonian drug levodopa has been serendipitously discovered to be a transporter-utilizing brain-delivered prodrug rather than a rationally developed one.

Areas covered: The lack of success can mainly be explained by the insufficient understanding of the role of membrane proteins that can facilitate drug delivery at dynamic barriers, such as the blood-brain barrier (BBB), but also by the sparse knowledge of prodrug bioconverting enzymes in the brain. This review summarizes the current status of the prodrug attempts that have been developed in the past to improve brain drug delivery.

Expert opinion: With the expandingly improved analytical and computational technologies, it is anticipated that enhanced brain drug delivery will be eventually achieved for most of the central nervous system (CNS) acting drugs. However, this requires that carrier-mediated (pro)drug delivery methods are implemented in the very early phases of the drug development processes and not as a last step to survive a problematic investigational drug candidate.

改善脑部给药:原药方法。
导言:几十年来,原药方法一直被认为是改善脑部给药的简单解决方案。然而,令人惊讶的是,该领域的成功案例仍然相对较少。最好的例子是抗帕金森病药物左旋多巴被偶然发现是一种利用转运体的脑给药原药,而不是一种合理开发的原药:之所以没有取得成功,主要是因为人们对可促进药物在血脑屏障(BBB)等动态屏障上递送的膜蛋白的作用认识不足,而且对脑内原药生物转换酶的了解也很少。本综述总结了过去为改善脑部给药而开发的原药尝试的现状:专家观点:随着分析和计算技术的不断改进,预计大多数作用于中枢神经系统(CNS)的药物最终都将实现脑部给药。然而,这要求在药物开发过程的早期阶段就采用载体介导的(促)给药方法,而不是将其作为最后一步,使有问题的候选研究药物得以存活。
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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