Ligands for oral delivery of peptides across the blood-brain-barrier

Murad Al Gailani, Mengyang Liu, Jingyuan Wen
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引用次数: 8

Abstract

Peptides are short chains of amino acids linked by peptide bonds. Many peptides and proteins are limited by their poor enzymatic stability and permeability across the intestinal epithelial membranes and/or blood-brain barrier (BBB). Parenteral administration of these peptides is unfavorable because of procedural complications and low patient compliance with treatments. Instead, oral delivery is the preferred route of administration because it allows for self-administration and has a high degree of patient acceptability and compliance. Oral delivery of these peptides poses a major challenge, because the peptide drug must overcome both the physical and biochemical barriers of the gastrointestinal tract and BBB. An oral drug delivery system is beneficial because it can protect peptide drugs against degradation and deliver them to the brain, where they exert their pharmacological actions. The use of active-targeting ligands and/or cell-penetrating peptides increases penetration and uptake across the BBB. This review focuses on the diverse combinations of drug delivery systems, active-targeting ligands, and cell-penetrating peptides used to deliver peptides to the brain.
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经血脑屏障口服递送多肽的配体
肽是由肽键连接的氨基酸短链。许多肽和蛋白质由于其较差的酶稳定性和穿过肠上皮膜和/或血脑屏障(BBB)的渗透性而受到限制。这些肽的肠外给药是不利的,因为手术并发症和患者对治疗的依从性低。相反,口服给药是首选的给药途径,因为它允许自我给药,并且具有高度的患者可接受性和依从性。口服这些肽是一个重大挑战,因为肽药物必须克服胃肠道和血脑屏障的物理和生物化学屏障。口服给药系统是有益的,因为它可以保护肽类药物不被降解,并将其输送到大脑,在那里发挥药理作用。活性靶向配体和/或细胞穿透肽的使用增加了穿过血脑屏障的穿透和摄取。这篇综述的重点是药物递送系统、活性靶向配体和用于将肽递送到大脑的细胞穿透肽的不同组合。
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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