Sono-enzymatically engineered tannic acid/doxycycline-lignin nanoparticles enable self-assembled bioactive chitosan hydrogels for chronic wound healing
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Updated: Nov 6, 2026

Doxycycline Loaded Collagen-Chitosan Composite Scaffold for the Accelerated Healing of Diabetic Wounds
Published on: August 21, 2021
Reza Ahmadi1, Eva Ramon1, Katerina Todorova2
1Group of Molecular and Industrial Biotechnology, Department of Chemical Engineering, Universitat Politècnica de Catalunya, Rambla Sant Nebridi, 22, Terrassa, 08222, Spain.
Abstract:
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.
