Multi-Crosslinked Hydrogels with Instant Self-Healing and Tissue Adhesive Properties for Biomedical Applications

被引:18
|
作者
Jiang, Yongchao [1 ,2 ]
Li, Gaiying [1 ]
Wang, Haonan [2 ]
Li, Qian [2 ]
Tang, Keyong [1 ]
机构
[1] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Natl Ctr Int Res Micronano Molding Technol, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
hydrogel; polysaccharide; self-healing; tissue adhesive; COMPOSITE HYDROGELS; KONJAC GLUCOMANNAN; HEMOSTASIS; RELEASE;
D O I
10.1002/mabi.202100443
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Due to the defects like long gelling time, inferior mechanical properties and weak adhesion, in situ forming hydrogels are still restricted in biomedical applications like viscera rupture and targeted therapy. To address these problems, a new kind of multi-crosslinked hydrogel (G-OKG-DA) consisting of gelatin, oxidized konjac glucomannan (OKG), and dopamine (DA) is proposed in this study. The resulting hybrid hydrogel is endowed with a short gelling time (approximate to 3 min) and injectable capacity. According to the mechanical and adhesive tests, G-OKG-DA hydrogel shows a robust tensile strength of 23.94 kPa, as well as a higher adhesive strength (approximate to 150 kPa) than commercial fibrin glue. In addition, an instant self-healing behavior of G-OKG-DA hydrogel can be found, which is attributed to multi-cross-linking reactions including Schiff-based dynamic covalent bonds between OKG and gelatin, oxidative polymerization of DA, and catechol-mediated chemistry like Michael addition and DA-quinone coupling. Importantly, the multi-crosslinked hydrogel will not compromise its hemocompatibility and cytocompatibility in vitro, suggesting potential applications in biomedical fields as tissue adhesive and implants.
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页数:9
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