Engineering Injectable Coassembled Hydrogel by Photothermal Driven Chitosan-Stabilized MoS<sub>2</sub> Nanosheets for Infected Wound Healing.
basic_science · Level V
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- Record sourced from PubMed, PMID 39305262.
- Also identified by DOI 10.1021/acsnano.4c08883.
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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.
Medical subject headings
- Molybdenum
- Chitosan
- Disulfides
- Wound Healing
- Hydrogels