Chronic wounds remain a major clinical challenge due to their multifactorial pathology, characterised by excessive proteolytic and oxidative enzyme activity, persistent inflammation, bacterial infection, and biofilm formation. Here, we report a green, nano-enabled hydrogel fabricated through the in situ self-assembly of thiolated chitosan (TCS), driven by tannic acid/doxycycline-functionalised lignin nanoparticles (PLD NPs). Doxycycline was incorporated at a sub-inhibitory concentration (12.5 μg/mL), enabling PLD NPs (0.5 mg/mL) to inhibit matrix metalloproteinase (MMP) activity by approximately 50% without inducing antibacterial effects. Dynamic interactions between the polymer network and NPs produced injectable, self-healing hydrogels capable of stimuli-responsive NPs release under chronic wound-like conditions, including variations in pH, hydrogen peroxide, and lysozyme. Ex vivo evaluation using human chronic wound exudates demonstrated potent inhibition of MMP and myeloperoxidase activities by 73% and 80%, respectively. The hydrogels further exhibited strong antimicrobial and antibiofilm activity against Staphylococcus aureus and Pseudomonas aeruginosa , achieving 4.8- and 4.3-log reductions in bacterial viability while preventing 73% and 65% of biofilm formation, respectively. In vitro studies confirmed excellent biocompatibility with human keratinocytes and fibroblasts, together with up to 82% cellular antioxidant activity and enhanced fibroblast migration. Importantly, in an in vivo full-thickness S. aureus -infected mouse wound model, the hydrogels achieved complete wound closure within 18 days, outperforming commercial antiseptic treatments. Overall, this work demonstrates a multifunctional hydrogel platform that simultaneously modulates the chronic wound microenvironment, controls infection and biofilm formation, reduces oxidative stress, and promotes tissue regeneration, offering a promising strategy for advanced chronic wound management.
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Ahmadi et al. (2026) studied this question.
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