巨噬细胞极化
单宁酸
材料科学
免疫系统
血管生成
共价键
胍
纳米技术
口腔
组织修复
变形链球菌
细胞生物学
多酚
组织工程
伤口愈合
粘附
天然组织
细胞粘附
抗氧化剂
抗菌剂
自愈
生物相容性材料
抗菌肽
蛋白酵素
生物化学
作者
Xuanzhi Liu,Meizhou Sun,Chi Xu,Shuai Lv,Guang Yang,Wei Geng,Shun Duan,Fu‐Jian Xu,Yujie Sun
标识
DOI:10.1002/adfm.202528538
摘要
ABSTRACT The dynamic and microbially rich environment of the oral cavity poses unique challenges for mucosal repair, where conventional dressings fail to achieve long‐term stability, antimicrobial protection, and immune balance simultaneously. Here, we propose a structure‐function co‐assembled polyphenol‐diamine network that integrates structural robustness and biological functionality into a single interfacial system. Through the covalent co‐assembly of tannic acid and polyhexamethylene guanidine (PHMG), the network forms a release‐free antibacterial interface in which guanidinium groups remain covalently anchored yet maintain contact‐active bactericidal capability, achieving a long‐term of killing efficacy (over 96%) against S. aureus and E. coli without side effects. Concurrently, the polymerized polyphenol framework provides strong tissue adhesion via covalent anchoring and hydrogen bonding, while exerting antioxidant and immunoregulatory effects that guide macrophage polarization toward a pro‐healing M2 phenotype and promote angiogenesis through the PI3K/Akt/HO‐1 and PI3K/Akt/HIF‐1α/VEGF signaling axes. These co‐assembled biointerfaces achieve long‐term antibacterial stability, immune microenvironment reconstruction, and accelerated tissue repair under dynamic physiological conditions. The presented polyphenol‐diamine co‐assembly strategy provides a versatile and translatable strategy for engineering multifunctional, release‐free, and immunomodulatory biointerfaces across diverse tissue repair scenarios.
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