Silk fibroin and hydroxypropyl cellulose composite injectable hydrogel-containing extracellular vesicles for myocardial infarction repair

被引:2
|
作者
Hua, Yinjian [1 ,2 ]
He, Zhengfei [3 ]
Ni, Yunjie [3 ]
Sun, Linggang [3 ]
Wang, Rui [1 ,2 ]
Li, Yan [1 ,2 ]
Li, Xintong [4 ]
Jiang, Guohua [1 ,2 ]
机构
[1] Zhejiang Sci Tech Univ, Sch Mat Sci & Engn, Hangzhou 310018, Peoples R China
[2] Int Sci & Technol Cooperat Base Intelligent Biomat, Hangzhou 310018, Peoples R China
[3] First Peoples Hosp, Dept Cardiol, Hangzhou 311400, Peoples R China
[4] Zhejiang Zhongwei Med Res Ctr, Dept Med, Hangzhou 310018, Peoples R China
来源
关键词
myocardial infarction; injectable hydrogel; extracellular vesicles;
D O I
10.1088/2057-1976/ad40b2
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Extracellular vesicles (EVs) have been recognized as one of the promising specific drugs for myocardial infarction (MI) prognosis. Nevertheless, low intramyocardial retention of EVs remains a major impediment to their clinical application. In this study, we developed a silk fibroin/hydroxypropyl cellulose (SF/HPC) composite hydrogel combined with AC16 cell-derived EVs targeted modification by folic acid for the treatment of acute myocardial infarction repair. EVs were functionalized by distearoylphosphatidyl ethanolamine-polyethylene glycol (DSPE-PEG-FA) via noncovalent interaction for targeting and accelerating myocardial infarction repair. In vitro, cytocompatibility analyses revealed that the as-prepared hydrogels had excellent cell viability by MTT assay and the functionalized EVs had higher cell migration by scratch assay. In vivo, the composite hydrogels can promote myocardial tissue repair effects by delaying the process of myocardial fibrosis and promoting angiogenesis of infarct area in MI rat model.
引用
收藏
页数:10
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