Suppr超能文献

设计既能优化血脑屏障通透性又能优化脑内分布的药物。

Designing drugs optimized for both blood-brain barrier permeation and intra-cerebral partition.

机构信息

Dipartimento di Scienze del Farmaco e della Salute, Università degli Studi di Catania, Catania, Italy.

出版信息

Expert Opin Drug Discov. 2024 Mar;19(3):317-329. doi: 10.1080/17460441.2023.2294118. Epub 2023 Dec 25.

Abstract

INTRODUCTION

With the increasing incidence and prevalence of neurological disorders globally, there is a paramount need for new pharmacotherapies. BBB effectively protects the brain but raises a profound challenge to drug permeation, with less than 2% of most drugs reaching the CNS.

AREAS COVERED

This article reviews aspects of the most recent design strategies, providing insights into ideas and concepts in CNS drug discovery. An overview of the products available on the market is given and why clinical trials are continuously failing is discussed.

EXPERT OPINION

Among the available CNS drugs, small molecules account for most successful CNS therapeutics due to their ability to penetrate the BBB through passive or carrier-mediated mechanisms. The development of new CNS drugs is very difficult. To date, there is a lack of effective drugs for alleviating or even reversing the progression of brain diseases. Particularly, the use of artificial intelligence strategies, together with more appropriate animal models, may enable the design of molecules with appropriate permeation, to elicit a biological response from the neurotherapeutic target.

摘要

简介

随着全球神经疾病的发病率和流行率不断上升,对新的药物疗法的需求迫在眉睫。血脑屏障(BBB)有效地保护了大脑,但却对药物渗透造成了极大的挑战,大多数药物只有不到 2%能够到达中枢神经系统(CNS)。

涵盖领域

本文综述了最近设计策略的各个方面,为 CNS 药物发现的思路和概念提供了深入的见解。概述了市场上现有的产品,并讨论了为什么临床试验持续失败。

专家意见

在现有的 CNS 药物中,小分子由于能够通过被动或载体介导的机制穿透血脑屏障,成为大多数成功的 CNS 治疗药物。新的 CNS 药物的开发非常困难。迄今为止,缺乏有效的药物来缓解甚至逆转脑部疾病的进展。特别是,人工智能策略的使用,以及更合适的动物模型,可能使设计具有适当渗透性的分子成为可能,从而从神经治疗靶点引发生物学反应。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验