H2O2-activated in situ polymerization of aniline derivative in hydrogel for real-time monitoring and inhibition of wound bacterial infection

伤口愈合 聚合 苯胺 自愈水凝胶 原位 材料科学 过氧化氢 光热治疗 组合化学 聚合物 化学 纳米技术 高分子化学 有机化学 外科 医学 复合材料
作者
Aihui Wang,Guishi Fan,Hongli Qi,Hongyan Li,Congcong Pang,Zhongkai Zhu,Shichen Ji,Hong Liang,Bang‐Ping Jiang,Xing‐Can Shen
出处
期刊:Biomaterials [Elsevier BV]
卷期号:289: 121798-121798 被引量:65
标识
DOI:10.1016/j.biomaterials.2022.121798
摘要

Wound is highly susceptible to bacterial infection, which can cause chronic wound and serial complications. However, timely treatment is hampered by the lack of real-time monitoring of wound status and effective therapeutic systems. Herein, in situ biosynthesis of functional conjugated polymer in artificial hydrogel was developed via the utilization of biological microenvironment to realize monitoring in real time of wound infection and inhibition of bacteria for the first time. Specially, an easily polymerizable aniline dimer derivative (N-(3-sulfopropyl) p-aminodiphenylamine, SPA) was artfully in situ polymerized into polySPA (PSPA) in calcium alginate hydrogel, which was initiated via the catalysis of hydrogen peroxide (H2O2) overexpressed in infected wound to produce hydroxyl radical (•OH) by preloaded horseradish peroxidase (HRP). Benefitting from outstanding near infrared (NIR) absorption of PSPA, such polymerization can be ingeniously used for real-time monitoring of H2O2 via naked-eye and photoacoustic signal, as well as NIR light-mediated photothermal inhibition of bacteria. Furthermore, combining the persistent chemodynamic activity of •OH, the in vivo experimental data proved that the wound healing rate was 99.03% on the 11th day after treatment. Therefore, the present work opens the way to manipulate in situ biosynthesis of functional conjugated polymer in artificial hydrogels for overcoming the issues on wound theranostics.
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