Regulation of Charge Transfer Pathway in Ag‐ZnIn2S4 Nanowires for Visible Photodynamic Therapy on Candida Albicans Infections

Photodynamic therapy (PDT) is receiving extensive attention as an antimicrobial strategy that does not cause drug resistance by reactive oxygen species (ROS). Herein, hierarchical Ag‐ZnIn2S4 (Ag‐ZIS) core‐shell nanowires are synthesized by in situ Metal‐Organic Framework derived method for efficient PDT of Candida albicans (C. albicans). The core‐shell structure enables spatial synergy strategy to regulate the charge transfer pathway under visible light excitation, in which the Ag nanowires are like the highway for the photogenerated electrons. The enhanced charge carrier separation efficiency greatly increased the chances for the generation of ROS. As expected, the optimized Ag‐ZIS nanowires exhibit excellent performance for inactivation of C. albicans under visible light irradiation (λ ≥ 420 nm, 15 min), and the effective sterilization concentration is as high as 107CFU mL‐1. Moreover, in vivo infection experiments suggested that the PDT effect of Ag‐ZIS nanowires on the mouse wound healing is better than that of the clinical Ketoconazole drug. The PDT antifungal mechanism of Ag‐ZIS nanowires is also investigated, and superoxide anion is found to be the predominant active species to causes C. albicans damage. This work provides a new perspective for designing novel interface structures to regulate charge transfer to achieve efficient PDT antifungal therapy. Hierarchical Ag‐ZIS core–shell nanowires are synthesized by in situ MOF derived method, in which the Ag nanowires are like the highway for the photogenerated electrons. The unique Ag‐ZIS nanowires exhibited prominent efficiency for the generation of ROS to PDT on C. albicans infections.