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使用自组装肽递送治疗剂和分子。

Delivery of therapeutics and molecules using self-assembled peptides.

作者信息

Sundar S, Chen Y, Tong Y W

机构信息

4 Engineering Drive 4, Singapore 117576.

出版信息

Curr Med Chem. 2014;21(22):2469-79. doi: 10.2174/0929867321666131212152637.

Abstract

The use of nanobiotechnology in the formulation of drug carriers has been gaining popularity in recent years. Peptide self-assembly technology is a particularly attractive option due to its simplicity and programmability. Selfassembling peptide amphiphiles are surfactant-like molecules that are capable of spontaneous organization into a variety of nanostructures. The structural and functional features of these nanostructures can be designed through alterations to the peptide sequence. With a keen understanding of the supramolecular principles governing the non-covalent interactions involved, drug loading strategies can be customised. Hydrophobic drugs can be hidden within the core via aromatic interactions while gene-based therapeutics can be complexed with a cationic region of lysine residues. This review article focuses on the application of self-assembling peptide amphiphiles to drug delivery in the area of anti-cancer therapeutics, protein- and peptide-based therapeutics and nucleic acid-based therapeutics. Specific examples are used to discuss the various systems available and emphasis is given to the encapsulation and release mechanism.

摘要

近年来,纳米生物技术在药物载体配方中的应用越来越受到欢迎。肽自组装技术因其简单性和可编程性而成为特别有吸引力的选择。自组装肽两亲分子是类似表面活性剂的分子,能够自发组织成各种纳米结构。这些纳米结构的结构和功能特征可以通过改变肽序列来设计。在深入理解控制非共价相互作用的超分子原理的基础上,可以定制药物负载策略。疏水性药物可以通过芳香相互作用隐藏在核心内,而基于基因的治疗剂可以与赖氨酸残基的阳离子区域复合。本文综述聚焦于自组装肽两亲分子在抗癌治疗、基于蛋白质和肽的治疗以及基于核酸的治疗领域的药物递送应用。通过具体实例讨论了现有的各种系统,并重点介绍了包封和释放机制。

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