生物膜
光热治疗
材料科学
生物污染
伤口愈合
单宁酸
粘附
自愈水凝胶
壳聚糖
核化学
微生物学
高分子化学
化学
膜
纳米技术
细菌
有机化学
生物化学
复合材料
生物
免疫学
遗传学
作者
Lixia Li,Zhiqin Zhao,Yuhang Gao,Xiaohe Jiang,Haimeng Liu,Xiaolu Guo,Xiaohua Huang,Li Zhou,Chanjuan Liu,Xing‐Can Shen
标识
DOI:10.1021/acsami.5c17481
摘要
The development of multifunctional hydrogel dressings integrating injectability, self-healing capability, tissue adhesion, multimodal antibacterial mechanisms, and real-time wound status monitoring remains a critical challenge for combating bacterial biofilms and accelerating wound healing. Herein, we present a dynamically cross-linked nanocomposite hydrogel (QCS-TA/LDH-panis) via Fe3+/Mn2+-mediated coordination between tannic acid (TA)-modified quaternized chitosan (QCS-TA) and polysulfonatoaniline-intercalated FeMn-layered double hydroxide (LDH-panis). The LDH-panis nanohybrids, synthesized through in situ polymerization of 3-sulfonatoaniline within FeMn-LDH interlayers, exhibit a near-infrared (NIR)-responsive photothermal effect (η = 64.3%) and pH/H2O2-activated peroxidase-like activity for biofilm-disrupting hydroxyl radical (•OH) generation. Concurrently, the QCS-TA matrix enables a "capture-and-kill" mechanism via electrostatic interactions (quaternary ammonium groups) and bacterial affinity adhesion (catechol/pyrogallol moieties). Under near-infrared (NIR) irradiation, synergistic mild photothermal/chemodynamic therapy (mPTT/CDT) combined with contact-killing achieved >95% eradication of Staphylococcus aureus and Escherichia coli biofilms. Notably, the hydrogel's conductivity enabled real-time monitoring of wound exudate and temperature fluctuation during the healing progression. In vivo evaluations confirmed accelerated infected wound regeneration (98.2% closure in 12 days) through biofilm elimination, inflammatory suppression, reepithelialization, and collagen deposition. This multifunctional hydrogel unifies dynamic adaptability, multimodal antibacterial therapy, and sensing intelligence, offering a promising strategy for the clinical management of biofilm-associated infection.
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