| Literature DB >> 30592403 |
Wei Wang1, Jingrui Chen2,3, Min Li2,3, Huizhen Jia1, Xiaoxu Han1, Jingxuan Zhang1, Yang Zou1, Baoyu Tan1, Wei Liang1, Yingying Shang1, Qian Xu4, Sigen A4, Wenxin Wang4, Jingyuan Mao2, Xiumei Gao3, Guanwei Fan2,3, Wenguang Liu1.
Abstract
Drug-loaded injectable hydrogels have been proven to possess huge potential for applications in tissue engineering. However, increasing the drug loading capacity and regulating the release system to adapt to the microenvironment after myocardial infarction face a huge challenge. In this research, an ROS-sensitive injectable hydrogel strengthened by self-nanodrugs was constructed. A hyperbranched ROS-sensitive macromer (HB-PBAE) with multiacrylate end groups was synthesized through dynamic controlled Michael addition. Meanwhile, a simple protocol based on dopamine polymerization was employed to generate a polydopamine (PDA) layer deposited on the tanshinone IIA (TIIA) nanoparticles (NPs) formed from spontaneous hydrophobic self-assembly. The HB-PBAE reacted with thiolate-modified hyaluronic acid (HA-SH) to form an in situ hydrogel, where TIIA@PDA NPs can be conveniently entrapped through the chemical cross-link between thiolate and quinone groups on PDA, which doubles the modulus of hydrogels. The in vivo degradation behavior of the hydrogels was characterized by MRI, exhibiting a much slower degradation behavior that is markedly different from that of in vitro. Importantly, a significant improvement of cardiac functions was achieved after hydrogel injection in terms of increased ejection fraction and decreased infarction size, accompanied by inhibition of the expression of inflammation factors, such as IL-1β, IL-6, and TNF-α.Entities:
Keywords: Hyperbranched polymer; Injectable hydrogel; Myocardial infarction; ROS; Tanshinone IIA
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Year: 2019 PMID: 30592403 DOI: 10.1021/acsami.8b20158
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229