Promotes MRSA infected wound healing by using photothermal responsive and ROS generating black phosphorus nano

Jingyi Qu1, Xinyue Yang1, Zelin Sang2

  • 1Department of Orthopaedic Surgery, Shengjing Hospital of China Medical University, Shenyang, Liaoning 110055, China.

Insights

This study introduces a novel black phosphorus nano-snowflake enhanced hydrogel for treating diabetic infected wounds. The material effectively combats drug-resistant bacteria and promotes significant wound healing through photothermal therapy and ROS generation.

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Wound Healing

Background:

  • Hyperglycemia-induced microvascular damage impairs chronic wound healing and increases susceptibility to bacterial infections.
  • The rise of antibiotic-resistant bacteria complicates the treatment of infected diabetic wounds.
  • Novel therapeutic strategies are urgently needed for diabetic wounds infected with drug-resistant pathogens.

Purpose of the Study:

  • To develop a black phosphorus nano-snowflake enhanced hydrogel (BPSFs@H) for treating diabetic infected wounds.
  • To leverage BPSFs as photothermal-responsive nanozymes for antibacterial activity and wound repair.
  • To investigate the efficacy of BPSFs@H against methicillin-resistant Staphylococcus aureus (MRSA) and its impact on wound healing.

Main Methods:

  • Synthesis of black phosphorus nano-snowflakes (BPSFs) and their incorporation into a hydrogel matrix to form BPSFs@H.
  • Evaluation of BPSFs@H's photothermal responsiveness and antibacterial activity against MRSA, including reactive oxygen species (ROS) generation.
  • In vitro assessment of BPSFs@H's effects on cell migration, neovascularization, and macrophage phenotype modulation.
  • In vivo studies using animal models to evaluate the hydrogel's efficacy in promoting diabetic wound regeneration and healing.

Main Results:

  • BPSFs@H demonstrated near-infrared (NIR) triggered photothermal responsiveness and effective inhibition of MRSA via ROS generation.
  • The hydrogel significantly promoted cell migration, neovascularization, and modulated macrophages towards an anti-inflammatory phenotype.
  • Animal studies showed that BPSFs@H substantially accelerated epithelial tissue regeneration and enhanced infected wound healing.
  • Mechanisms included augmented collagen deposition, improved inflammatory response, and accelerated angiogenesis, leading to enhanced re-epithelialization.

Conclusions:

  • BPSFs@H hydrogel presents a promising therapeutic strategy for infected diabetic wounds, particularly those caused by drug-resistant bacteria.
  • The combination of photothermal therapy, ROS generation, and biomodulation offers a multi-faceted approach to accelerate wound repair.
  • This novel biomaterial effectively addresses key challenges in diabetic wound management, including infection and impaired healing.

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