Self-assembly of amphiphilic amino acid derivatives for biomedical applications

被引:46
作者
Wang, Tengfei [1 ]
Menard-Moyon, Cecilia [1 ]
Bianco, Alberto [1 ]
机构
[1] Univ Strasbourg, ISIS, UPR3572, Immunol Immunopathol & Therapeut Chem,CNRS, F-67000 Strasbourg, France
关键词
POLY(ETHYLENE GLYCOL); CONTROLLED-RELEASE; ROSETTE NANOTUBES; FATTY-ACIDS; L-LEUCINE; DRUG; CHITOSAN; DESIGN; NANOPARTICLES; VESICLES;
D O I
10.1039/d1cs01064f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amino acids are one of the simplest biomolecules and they play an essential role in many biological processes. They have been extensively used as building blocks for the synthesis of functional nanomaterials, thanks to their self-assembly capacity. In particular, amphiphilic amino acid derivatives can be designed to enrich the diversity of amino acid-based building blocks, endowing them with specific properties and/or promoting self-assembly through hydrophobic interactions, hydrogen bonding, and/or pi-stacking. In this review, we focus on the design of various amphiphilic amino acid derivatives able to self-assemble into different types of nanostructures that were exploited for biomedical applications, thanks to their excellent biocompatibility and biodegradability.
引用
收藏
页码:3535 / 3560
页数:26
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