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<p>Drug-resistant bacterial infections in diabetic wound severely impair healing and may lead to life-threatening complications. Herein, a simple glucose oxidase (GOX) biomineralization nanozyme of GOX@CeO<sub>2</sub> was prepared which was further encapsulated with polydopamine (PDA) nanolayer (GOX@CeO<sub>2</sub>@PDA termed as GCP<sub>NPs</sub>) for diabetic wounds treatment. Due to the GOX and peroxidase (POD)-like activities of GCP<sub>NPs</sub>, the excessive glucose at wound site could be consumed to conduct starvation therapy, which also activated cascade reaction to generate reactive oxygen species (ROS) to achieve chemodynamic therapy (CDT). The synergistic effect of cryogenic photothermal therapy (C-PTT) from PDA nanolayer could boost the wound healing. To further improve the therapy efficiency, biodegradable microneedles (MNs) were prepared to encapsulate the GCP<sub>NPs</sub>, facilitating intimate contact between the nanodrugs and the deeper layers of the wound. In vitro and in vivo experimental results demonstrate the remarkable antibacterial property of the GCP<sub>NPs</sub> against drug-resistant bacteria via the synergistic function of starvation therapy, CDT and C-PTT, which could promote epidermal tissue formation and collagen deposition to accelerate wound healing with negligible damage to healthy tissues. The consumption of glucose also contributes to the recovery of diabetic mice. These results highlight the potential of GCP<sub>NPs</sub> in the treatment of bacterial infected diabetic wounds.</p> Graphical abstract <p></p>

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Biomineralization nanozyme-based biodegradable microneedle for accelerating bacteria-infected diabetic wound healing

  • 期刊论文

  • 发表日期：

    2026年5月22日

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  • Hanyue Sun,
  • Hua Zhang,
  • Xiying Chen,
  • Xian Li,
  • Liyu Shi,
  • Zhanhui Tao,
  • Yaqing Liu

摘要

Drug-resistant bacterial infections in diabetic wound severely impair healing and may lead to life-threatening complications. Herein, a simple glucose oxidase (GOX) biomineralization nanozyme of GOX@CeO2 was prepared which was further encapsulated with polydopamine (PDA) nanolayer (GOX@CeO2@PDA termed as GCPNPs) for diabetic wounds treatment. Due to the GOX and peroxidase (POD)-like activities of GCPNPs, the excessive glucose at wound site could be consumed to conduct starvation therapy, which also activated cascade reaction to generate reactive oxygen species (ROS) to achieve chemodynamic therapy (CDT). The synergistic effect of cryogenic photothermal therapy (C-PTT) from PDA nanolayer could boost the wound healing. To further improve the therapy efficiency, biodegradable microneedles (MNs) were prepared to encapsulate the GCPNPs, facilitating intimate contact between the nanodrugs and the deeper layers of the wound. In vitro and in vivo experimental results demonstrate the remarkable antibacterial property of the GCPNPs against drug-resistant bacteria via the synergistic function of starvation therapy, CDT and C-PTT, which could promote epidermal tissue formation and collagen deposition to accelerate wound healing with negligible damage to healthy tissues. The consumption of glucose also contributes to the recovery of diabetic mice. These results highlight the potential of GCPNPs in the treatment of bacterial infected diabetic wounds.

Graphical abstract