| Literature DB >> 33975276 |
Rui Chen1, Chenqi Zhu2, Liu Xu1, Yi Gu1, Shujing Ren1, Hua Bai3, Qin Zhou4, Xin Liu4, Shengfeng Lu3, Xiaolin Bi1, Weidong Li1, Xiaobin Jia5, Zhipeng Chen6.
Abstract
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.Entities:
Keywords: Elastin-mimic hydrogel; Myocardial infarction; Polydopamine nanoparticles; Salvianolic acid B; Transglutaminase
Year: 2021 PMID: 33975276 DOI: 10.1016/j.biomaterials.2021.120855
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479