Engineering Injectable Coassembled Hydrogel by Photothermal Driven Chitosan-Stabilized MoS<sub>2</sub> Nanosheets for Infected Wound Healing.

Wang, Peilei; Wu, Jingwen; Xiao, Xiaolin; Fan, Yujiang; Han, Xianglong; Sun, Yong · ACS Nano · 2024

basic_science · Level V

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Abstract

The application of enzyme-like molybdenum disulfide (MoS<sub>2</sub>) in tissue repair was confronted with stable dispersion, solubilization, and biotoxicity. Here, the injectable self-healing hydrogel was successfully designed using a step-by-step coassembly of chitosan and MoS<sub>2</sub>. Polyphenolic chitosan as a "structural stabilizer" of MoS<sub>2</sub> nanosheets reconstructed well-dispersed MoS<sub>2</sub>@CSH nanosheets, which improved the biocompatibility of traditional MoS<sub>2</sub>, and strengthened its photothermal conversion and enzyme-like activities, guaranteeing highly efficient radical scavenging and antimicrobial properties. Furthermore, the polyphenol chitosan was employed again as a "molecular cross-linking agent" to form the injectable NIR-responsive MoS<sub>2</sub>@CSH hydrogel by accelerating hydrogen-bond interaction among chitosan and the multicross-linking reaction among polyphenols. The rapid self-healing ability was conducive to wound closure and dynamic adaptability. An experimental study on infected wound healing demonstrated that MoS<sub>2</sub>@CSH hydrogel could substantially eradicate bacteria and accelerate the angiogenesis of infected wounds. The photothermal-driven coassembly of MoS<sub>2</sub> and polycation provided an alternative strategy for infected wound healing.

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