Chronic wound healing remains challenging due to the oxidative microenvironment. Prussian blue (PB) nanoparticles possessing multiple antioxidant enzyme-like activities have attracted wide attention, while their antioxidant efficacy remains unsatisfied. Herein, ultrasmall calcium-enriched Prussian blue nanoparticles (CaPB NPs) were simply constructed with high yield for the wound repair application. Owing to the ultrasmall size and synergistic effect of the generated dual active sites, the CaPB NPs were featured with prominent antioxidase-like activities, protecting cell from oxidative stress-induced damage. In addition to the effect of Ca on regulating keratinocyte and fibroblast growth, it has been demonstrated that the administration of CaPB NPs obviously promoted the wound closure as well as collagen deposition and neovascularization in the full-thickness wound defect model in mice. Importantly, the CaPB NPs treatment can effectively up-regulate the expression levels of anti-inflammatory cytokines and vascular endothelial growth factor to remodel the wound microenvironment, thereby accelerating wound healing process. Overall, this work reveals that metal atom substitution is an effective strategy to construct ultrasmall and high-catalytic-performance PB-based nanozymes and further potentiate their effectiveness for chronic wound management.
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