Results suggest that integrating IR780SS into a hydrogen-bonded hydrogel not only enables effective antibacterial phototherapy but also facilitates functional wound reconstruction, providing valuable insight into the clinical development of regenerative dressings for MRSA-infected wounds.
Abstract
Methicillin-resistant Staphylococcus aureus (MRSA)-infected wounds present a significant clinical challenge due to persistent inflammation and impaired tissue regeneration. Here, we developed an IR780SS-engineered hydrogel with a hydrogen-bond-regulated network for infected wound treatment. In this system, IR780SS serves not only as a NIR photosensitizer, but also as an active component that interacts with the hydrogel matrix through hydrogen bonding, hydrophobic interactions, and π-π stacking. These interactions improve the stability and dispersion of IR780SS within the hydrogel and help preserve its photoactivity. Under 808 nm NIR irradiation, the hydrogel generates mild local hyperthermia and abundant ROS, producing antibacterial effects through combined action of PTT and PDT mechanisms. This treatment disrupts bacterial membranes and induces severe oxidative damage inside bacterial cells, leading to the near-complete elimination of drug-resistant bacteria. In a MRSA-infected wound model, rapid bacterial clearance promoted the transition from the inflammatory phase to the proliferative phase and resulted in a wound closure rate of 85.6% on day 11. Histological and immunofluorescence analyses further confirmed improved tissue repair, including enhanced re-epithelialization, angiogenic responses, and collagen remodeling, as evidenced by increased cytokeratin 14 (CK14) and smooth muscle actin (α-SMA) expression, together with more organized collagen deposition. These results suggest that integrating IR780SS into a hydrogen-bonded hydrogel not only enables effective antibacterial phototherapy but also facilitates functional wound reconstruction, providing valuable insight into the clinical development of regenerative dressings for MRSA-infected wounds.
Infected skin wounds demand integrated strategies for rapid bacterial clearance and tissue repair. We developed a β-glucan–gelatin–tannic acid–Cu9S8 (CSGGT) composite hydrogel combining NIR-II photothermal therapy (1064 nm) with a bioactive physical network. The hydrogel exhibited self-healing, injectability, rapid swelling, and excellent biocompatibility. Cu9S8 nanoparticles (photothermal conversion efficiency: 43.87%) enabled efficient bacterial killing (≥2.5-log reduction for S. aureus and E. coli) under laser irradiation. In an S. aureus-infected murine full-thickness wound model, CSGGT + NIR achieved near-complete closure by day 12, with robust re-epithelialization, regenerated skin appendages, dense collagen deposition, and reduced inflammatory infiltration, significantly outperforming all controls. No systemic toxicity was observed. This work presents a combined therapeutic platform that merges immediate photothermal antibacterial action with sustained pro-healing microenvironment support, offering a promising non-antibiotic solution for infected wound management.
The in vivo experiments and transcriptome analysis demonstrated that the combination of CTA hydrogel and NIR treatment significantly accelerated the healing process of MRSA-infected wounds by eliminating antibiotic-resistant bacterial infections, regulating inflammatory responses, promoting collagen deposition and angiogenesis.
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