Hydrogel coating based on dopamine-modified hyaluronic acid and gelatin with spatiotemporal drug release capacity for quick endothelialization and long-term anticoagulation

被引:7
作者
Jiang, Yongchao [1 ]
Guo, Yingying [1 ]
Wang, Haonan [2 ]
Wang, Xiaofeng [2 ]
Li, Qian [2 ]
机构
[1] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Natl Ctr Int Res Micronano Molding Technol, Zhengzhou 450001, Peoples R China
基金
对外科技合作项目(国际科技项目);
关键词
Hyaluronic acid; Drug release; Endothelialization; VASCULAR GRAFTS; HEPARIN; SURFACE; ANTITHROMBOGENICITY; HEMOCOMPATIBILITY; ANGIOGENESIS; PERFORMANCE; STRATEGIES; IMPROVES; PATENCY;
D O I
10.1016/j.ijbiomac.2022.123113
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Due to the vital roles of vascular intima in preventing thrombus generation and maintaining vascular patency, methods to promote quick endothelialization on vascular grafts have drawn much attention. In this study, we novelly applied a double-layered hydrogel coating with spatiotemporal drug release capacity on a poly-caprolactone (PCL) fibrous scaffold. The composite coating consisted of an inner dopamine-modified hyaluronic acid (HA) hydrogel and an outer gelatin hydrogel, which were generated via different crosslinking methods. Especially, heparin and chondroitin sulfate were introduced to the HA and gelatin hydrogels during the pro-cessing, thus endowing the vascular scaffold spatiotemporal drug release behavior. The composite coating developed surface hydrophilicity and mechanical properties of the PCL scaffold meanwhile stimulating the proliferation and angiogenesis behaviors of endothelial cells. Long-term anticoagulation property of the modified scaffold was also demonstrated in vitro. This investigation provides a universal strategy for quick endotheliali-zation and long-term anticoagulation promotion of vascular grafts, which may be potentially used in treating cardiovascular diseases.
引用
收藏
页数:8
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