Designed peptide amphiphiles as scaffolds for tissue engineering

两亲性 超分子化学 自愈水凝胶 纳米纤维 化学 共轭体系 组织工程 生物相容性 组合化学 纳米技术 生物物理学 生物化学 材料科学 分子 共聚物 有机化学 生物 聚合物 遗传学
作者
Weizhen Sun,David A. Gregory,Xiaoyong Zhao
出处
期刊:Advances in Colloid and Interface Science [Elsevier]
卷期号:314: 102866-102866 被引量:5
标识
DOI:10.1016/j.cis.2023.102866
摘要

Peptide amphiphiles (PAs) are peptide-based molecules that contain a peptide sequence as a head group covalently conjugated to a hydrophobic segment, such as lipid tails. They can self-assemble into well-ordered supramolecular nanostructures such as micelles, vesicles, twisted ribbons and nanofibers. In addition, the diversity of natural amino acids gives the possibility to produce PAs with different sequences. These properties along with their biocompatibility, biodegradability and a high resemblance to native extracellular matrix (ECM) have resulted in PAs being considered as ideal scaffold materials for tissue engineering (TE) applications. This review introduces the 20 natural canonical amino acids as building blocks followed by highlighting the three categories of PAs: amphiphilic peptides, lipidated peptide amphiphiles and supramolecular peptide amphiphile conjugates, as well as their design rules that dictate the peptide self-assembly process. Furthermore, 3D bio-fabrication strategies of PAs hydrogels are discussed and the recent advances of PA-based scaffolds in TE with the emphasis on bone, cartilage and neural tissue regeneration both in vitro and in vivo are considered. Finally, future prospects and challenges are discussed.
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