An injectable peptide hydrogel with excellent self-healing ability to continuously release salvianolic acid B for myocardial infarction

被引:86
作者
Chen, Rui [1 ]
Zhu, Chenqi [1 ,2 ,3 ]
Xu, Liu [1 ]
Gu, Yi [1 ]
Ren, Shujing [1 ]
Bai, Hua [4 ]
Zhou, Qin [2 ,3 ]
Liu, Xin [2 ,3 ]
Lu, Shengfeng [4 ]
Bi, Xiaolin [1 ]
Li, Weidong [1 ]
Jia, Xiaobin [5 ]
Chen, Zhipeng [1 ]
机构
[1] Nanjing Univ Chinese Med, Coll Pharm, Nanjing 210023, Peoples R China
[2] Nanjing Med Univ, Affiliated Suzhou Hosp, Dept Pharm, Suzhou 215002, Peoples R China
[3] Nanjing Med Univ, Gusu Sch, Suzhou 215002, Peoples R China
[4] Nanjing Univ Chinese Med, Key Lab Acupuncture & Med Res, Minist Educ, Nanjing 210023, Peoples R China
[5] China Pharmaceut Univ, Sch Tradit Chinese Pharm, Nanjing 211198, Peoples R China
关键词
Myocardial infarction; Elastin-mimic hydrogel; Salvianolic acid B; Transglutaminase; Polydopamine nanoparticles; CROSS-LINKING; TRANSGLUTAMINASE; MECHANISM; DELIVERY; CELLS;
D O I
10.1016/j.biomaterials.2021.120855
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Drug-loaded hydrogels can improve blood supply and inhibit extracellular matrix degradation after myocardial infarction. However, due to the continual dynamic motion of cardiac tissue, the hydrogel structure cannot be reconstructed in time, causing accelerated degradation and drug burst release. Here, a novel, superior, selfhealing elastin-mimic peptide hydrogel (EMH) was fabricated for the local delivery of salvianolic acid B (SaB). The self-healing ability of EMH is enhanced by SaB-loaded polydopamine nanoparticles (SaB-PDA). In vitro, the pre-hydrogel (SaB-PDA/pre-EMH) is endowed with excellent biocompatibility and a low viscosity, making it suitable for intramyocardial injection. Once injected into the myocardial infarction (MI) region, SaBPDA/pre-EMH can form SaB-PDA/EMH with great mechanical strength under the action of upregulated transglutaminase (TGase) in heart tissue post-MI. The superior self-healing ability of SaB-PDA/EMH allows for an increase in retention time in the beating ventricular wall. Therefore, with long-term release of SaB, SaB-PDA/ EMH can inhibit ventricular remodeling and promote angiogenesis for MI treatment.
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页数:10
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