自愈水凝胶
明胶
生物相容性
极限抗拉强度
肿胀 的
伤口愈合
材料科学
共价键
生物医学工程
化学工程
化学
复合材料
高分子化学
外科
生物化学
有机化学
冶金
工程类
医学
作者
Chunyan Dou,Zheng Li,Ying Luo,Jixian Gong,Qiujin Li,Jianfei Zhang,Qingsong Zhang,Changsheng Qiao
标识
DOI:10.1016/j.ijbiomac.2022.01.057
摘要
Building bio-based hydrogels with high strength and biocompatibility is still a challenge. Herein, we successfully constructed a hybrid double-network (DN) full biological hydrogel with excellent mechanical properties and biocompatibility by introducing a physically cross-linked gelatin (GEL) network in a covalently cross-linked poly (γ-glutamic acid) (γ-PGA) network. The γ-PGA-GEL DN hydrogel demonstrated ultra-high compression performance (38 MPa), which was better than all currently reported γ-PGA-based hydrogels, and its tensile performance (0.27 MPa) was also satisfactory. Due to the unique multi-crosslinked DN structure, the γ-PGA-GEL DN hydrogel had better recovery and healing properties than those of the γ-PGA single-network (SN) hydrogel. In addition, the γ-PGA-GEL DN hydrogel exhibited good transparency, swelling and degradability. In vitro cell experiments demonstrated that the γ-PGA-GEL DN hydrogel was beneficial to cell adhesion and proliferation. The evaluation of the full-thickness skin defects model in rats exhibited that the γ-PGA-GEL DN hydrogel could significantly accelerate wound healing. These results indicated that the γ-PGA-GEL DN hydrogel was an ideal candidate material for wound dressing.
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