自愈水凝胶
材料科学
自愈
伤口愈合
胶粘剂
皮肤修复
透明质酸
聚合物
泊洛沙姆
粘附
生物医学工程
高分子化学
纳米技术
复合材料
图层(电子)
外科
共聚物
病理
替代医学
生物
医学
遗传学
作者
Bo Yang,Jiliang Song,Yuhang Jiang,Ming Li,Jingjing Wei,Jiajun Qin,Wanjia Peng,Fernando López Lasaosa,Yiyan He,Hongli Mao,Jun Yang,Zhongwei Gu
标识
DOI:10.1021/acsami.0c18948
摘要
The development of natural polymer-based hydrogels, combining outstanding injectability, self-healing, and tissue adhesion, with mechanical performance, able to facilitate full-thickness skin wound healing, remains challenging. We have developed an injectable micellar hydrogel (AF127/HA-ADH/OHA-Dop) with outstanding adhesive and self-healing properties able to accelerate full-thickness skin wound healing. Dopamine-functionalized oxidized hyaluronic acid (OHA-Dop), adipic acid dihydrazide-modified HA (HA-ADH), and aldehyde-terminated Pluronic F127 (AF127) were employed as polymer backbones. They were cross-linked in situ using Schiff base dynamic covalent bonds (AF127 micelle/HA-ADH network and HA-ADH/OHA-Dop network), hydrogen bonding, and π–π stacking interactions. The resulting multicross-linked double-network design forms a micellar hydrogel. The unique multicross-linked double-network structure endows the hydrogel with both improved injection abilities and mechanical performance while self-healing faster than single-network hydrogels. Inspired by mussel foot adhesive protein, OHA-Dop mimics the catechol groups seen in mussel proteins, endowing hydrogels with robust adhesion properties. We also demonstrate the potential of our hydrogels to accelerate full-thickness cutaneous wound closure and improve skin regeneration with reduced scarring. We anticipate that our hydrogel platform based on a novel multicross-linked double-network design will transform the future development of multifunctional wound dressings.
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