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肽两亲物在药物应用中的作用

Peptide Amphiphiles for Pharmaceutical Applications.

机构信息

Department of Pharmacy, Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, 80828, Barcelona, Spain.

Unit of Synthesis and Biomedical Applications of Peptides, IQAC-CSIC, 08034, Barcelona, Spain.

出版信息

Curr Med Chem. 2024;31(11):1332-1347. doi: 10.2174/0929867330666230408203820.

Abstract

During the last few decades, several efforts have been made towards developing biocompatible materials. Among them, peptide amphiphiles (PAs) constitute a novel nanotechnological strategy used in the field of biomedicine since they can provide tissue- specific binding and localization. PAs possess several regions combining hydrophobic and hydrophilic areas that are able to self-assemble in aqueous media, forming different tertiary nanostructures able to interact with cellular membranes. Moreover, these molecules can be tuned by incorporating collagen, lipids, or fluorescent markers. In addition, they can also be used as carriers in order to encapsulate active compounds for drug delivery showing promising features in this area. In this review, the self-assembled structures of PAs as well as their pharmacological applications have been summarized. Furthermore, their use as drug delivery systems has been highlighted and the latest advances in this field have been reviewed.

摘要

在过去的几十年中,人们做出了许多努力来开发生物相容性材料。其中,肽两亲物(PAs)构成了一种用于生物医学领域的新型纳米技术策略,因为它们能够提供组织特异性结合和定位。PAs 具有几个组合疏水和亲水区域的区域,能够在水介质中自组装,形成不同的三级纳米结构,能够与细胞膜相互作用。此外,通过掺入胶原蛋白、脂质或荧光标记物,可以对这些分子进行调整。此外,它们还可用作载体,以封装用于药物递送的活性化合物,在该领域显示出有希望的特性。在这篇综述中,总结了 PAs 的自组装结构及其在药理学上的应用。此外,还强调了它们作为药物传递系统的用途,并回顾了该领域的最新进展。

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