Peptide delivery to the brain via adsorptive-mediated endocytosis: advances with SynB vectors.

AAPS PharmSci Pub Date : 2002-01-01 DOI:10.1208/ps040426
Guillaume Drin, Christophe Rousselle, Jean-Michel Scherrmann, Anthony R Rees, Jamal Temsamani
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引用次数: 42

Abstract

Biological membranes normally restrict the passage of hydrophilic molecules. This impairs the use of a wide variety of drugs for biomedical applications. To overcome this problem, researchers have developed strategies that involve conjugating the molecule of interest to one of a number of peptide entities that are efficiently transported across the cell membranes. In the past decade, a number of different peptide families with the ability to cross the cell membranes have been identified. Certain of these families enter the cells by a receptor-independent mechanism, are short (10-27 amino acid residues), and can deliver successfully various cargoes across the cell membrane into the cytoplasm or nucleus. Surprisingly, some of these vectors, the SynB vectors, have also shown the ability to deliver hydrophilic molecules across the blood-brain barrier, one of the major obstacles to the development of drugs to combat diseases affecting the CNS.

通过吸附介导的内吞作用向大脑传递肽:SynB载体的进展。
生物膜通常限制亲水分子的通过。这损害了生物医学应用中各种药物的使用。为了克服这个问题,研究人员已经开发出一些策略,包括将感兴趣的分子偶联到有效地跨细胞膜运输的许多肽实体之一。在过去的十年中,许多具有穿越细胞膜能力的不同肽家族已经被确定。这些家族中的某些通过不依赖受体的机制进入细胞,它们很短(10-27个氨基酸残基),并且可以成功地将各种货物穿过细胞膜进入细胞质或细胞核。令人惊讶的是,其中一些载体,即SynB载体,也显示出了通过血脑屏障传递亲水性分子的能力,而血脑屏障是开发对抗影响中枢神经系统疾病的药物的主要障碍之一。
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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