自愈水凝胶
生物相容性
生物医学工程
弹性蛋白
心肌梗塞
血管生成
细胞外基质
材料科学
下调和上调
药理学
体内
医学
化学
心脏病学
内科学
生物化学
生物
病理
生物技术
高分子化学
冶金
基因
作者
Rui Chen,Chenqi Zhu,Xu Liu,Yi Gu,Shujing Ren,Hua Bai,Qin Zhou,Xin Liu,Sheng-Feng Lu,Xiaolin Bi,Weidong Li,Xiaobin Jia,Zhipeng Chen
出处
期刊:Biomaterials
[Elsevier]
日期:2021-04-29
卷期号:274: 120855-120855
被引量:67
标识
DOI:10.1016/j.biomaterials.2021.120855
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, self-healing 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, SaB-PDA/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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