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利用细胞穿透肽将药物递送至中枢神经系统的能力。

Harnessing the capacity of cell-penetrating peptides for drug delivery to the central nervous system.

作者信息

Kang Ting, Gao Xiaoling, Chen Jun

机构信息

Key Laboratory of Smart Drug Delivery, Ministry of Education & PLA, School of Pharmacy, Fudan University, Lane 826, Zhangheng Road, Shanghai 201203, PR China.

出版信息

Curr Pharm Biotechnol. 2014;15(3):220-30. doi: 10.2174/1389201015666140617094952.

Abstract

The existence of blood-brain barrier (BBB) represents the most formidable challenge for drug delivery to the central nervous system (CNS). Modern breakthrough in biology offers multiple choices for overcoming this barrier but yields modest outcomes for clinical application due to various problems such as safety concerns, insufficient delivery efficiency and poor penetration. Cell penetrating peptides (CPPs) possessing powerful transmembrane capacity have been shown to be effective transport vectors for bioactive molecules and an attractive alternative to traditional active targeting approaches. However, the non-specificity of CPPs has hindered them from targeting a desired site of action. Promisingly, design of novel CPP-mediated nanoparticulate delivery systems with specific targeting property may extricate CPPs from the dilemma. In this review, both the traditional and novel applications of CPPs-based strategies for CNS drug delivery will be discussed.

摘要

血脑屏障(BBB)的存在是药物递送至中枢神经系统(CNS)面临的最严峻挑战。生物学领域的现代突破为克服这一屏障提供了多种选择,但由于安全性担忧、递送效率不足和穿透性差等各种问题,临床应用的效果并不理想。具有强大跨膜能力的细胞穿透肽(CPPs)已被证明是生物活性分子的有效转运载体,是传统主动靶向方法的一个有吸引力的替代方案。然而,CPPs的非特异性阻碍了它们靶向所需的作用部位。令人欣慰的是,设计具有特异性靶向特性的新型CPP介导的纳米颗粒递送系统可能会使CPPs摆脱困境。在这篇综述中,将讨论基于CPPs的策略在CNS药物递送中的传统和新型应用。

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