流变学
聚合
化学
生物相容性材料
高分子化学
两亲性
超分子化学
材料科学
自组装
微观结构
化学工程
芯(光纤)
超分子聚合物
生物物理学
纳米技术
纳米结构
氨基酸
聚合物
共聚物
作者
Daniel José da Silva,Gabriella Mendes Cobe,Raphael Colonese Vlasman,Luiz Henrique Catalani
出处
期刊:ACS Polymers Au
[American Chemical Society]
日期:2025-10-22
卷期号:5 (6): 907-918
被引量:2
标识
DOI:10.1021/acspolymersau.5c00098
摘要
High Resolution Image Download MS PowerPoint Slide Polypeptides are attractive, renewable, and biocompatible materials for broad potential biomedical, pharmaceutical, and regenerative medicine applications. In this study, star-shaped 3-arm amphiphilic polypeptides with self-assembly characteristics were synthesized by ring-opening polymerization (ROP) of N -carboxyanhydride (NCA), incorporating l -leucine and l -lysine to form a core–shell structure. These polymers were thoroughly characterized through various techniques, revealing that their rheological behavior and self-assembly are influenced by factors such as the length of the star-shaped arms, the proportion of hydrophobic amino acids, and the surrounding pH. The synthesized polypeptides can self-assemble into five distinct secondary structures, mimicking natural proteins. Our findings evidence that the design of the block size of the hydrophilic l -lysine core and hydrophobic l -leucine shell shapes the ability to form a physical hydrogel, exhibiting shear-thinning rheological characteristics and a rapid mechanical response. The internal microstructure of the hydrogel is based on a supramolecular self-assembly structure consisting of highly connected nanofibrils.
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