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Diabetic chronic wounds are difficult to heal because persistent hyperglycemia is associated with excessive reactive oxygen species (ROS), impaired angiogenesis, and prolonged inflammation. Here, we developed an Fe3O4@PDA-containing PVA/gelatin/borate hydrogel (FP-PVG) with catalase-like activity. FP-PVG scavenged ROS and promoted H2O2-responsive oxygen generation, while the FP nanocomposite and hydrogel matrix contributed to antibacterial activity. In vitro, FP-PVG showed strong ABTS radical-scavenging activity (98.97% at 2 mg mL-1), favorable cytocompatibility, and improved cell migration under oxidative stress. It also reduced CD86 expression and increased CD163 expression in macrophages, consistent with a shift toward a reparative phenotype. In a diabetic mouse wound model, FP-PVG accelerated wound closure and was associated with reduced oxidative stress and inflammation, increased angiogenesis, and improved tissue regeneration. These findings support FP-PVG as a multifunctional hydrogel dressing for regulating the diabetic wound microenvironment.
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Xu et al. (2026) studied this question.
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