材料科学
生物相容性
涂层
再狭窄
透明质酸
聚电解质
生物医学工程
壳聚糖
聚合物
支架
纳米技术
化学
复合材料
生物化学
医学
外科
冶金
解剖
作者
Huining Wan,Yanyan Li,Yumei Qin,Yongqi An,Hui Yan,Xiyu Liu,Hao Zhang,Cheng Hu,Linhua Li,Daihua Fu,Yuan Yang,Yan Dai,Rifang Luo,Li Yang,Bo Zhang,Yunbing Wang
出处
期刊:Biomaterials
[Elsevier]
日期:2023-10-04
卷期号:302: 122346-122346
被引量:2
标识
DOI:10.1016/j.biomaterials.2023.122346
摘要
Drug-eluting stents have become one of the most effective methods to treat cardiovascular diseases. However, this therapeutic strategy may lead to thrombosis, stent restenosis, and intimal hyperplasia and prevent re-endothelialization. In this study, we selected 3-aminophenylboronic acid-modified hyaluronic acid and carboxylate chitosan as polyelectrolyte layers and embedded an epigallocatechin-3-gallate-tanshinone IIA sulfonic sodium (EGCG-TSS) complex to develop a sandwich-like layer-by-layer coating. The introduction of a functional molecular EGCG-TSS complex improved not only the biocompatibility of the coating but also its stability by enriching the interaction between the polyelectrolyte coatings through electrostatic interactions, hydrogen bonding, π-π stacking, and covalent bonding. We further elucidated the effectiveness of sandwich-like coatings in regulating the inflammatory response, smooth muscle cell growth behavior, stent thrombosis and restenosis suppression, and vessel re-endothelialization acceleration via in vivo and in vitro. Conclusively, we demonstrated that sandwich-like coating assisted by an EGCG-TSS complex may be an effective surface modification strategy for cardiovascular therapeutic applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI