Metal polyphenol CA-V nanozymes promote acute wound healing by destroying the ROS-inflammation cascade cycle

Liuqin Huang1, Xinyu Zhao2,3, Shuo Zhang2,3

  • 1Liuzhou Hospital, Guangzhou Women and Children's Medical Center, Liuzhou, 545616, China.

Materials Today. Bio
|December 16, 2025
PubMed

Insights

This study introduces caffeic acid-vanadium (CA-V) nanozymes to accelerate wound healing by targeting reactive oxygen species (ROS) and inflammation. CA-V nanozymes show promising results in promoting skin repair and reducing oxidative stress.

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Wound Healing Research

Background:

  • Skin ulceration severely impairs barrier function, delaying healing due to high reactive oxygen species (ROS) and inflammatory factors.
  • Current clinical treatments for skin ulcers have limited efficacy, necessitating novel therapeutic strategies.
  • Targeting the ROS-inflammatory cycle is crucial for accelerating early wound healing.

Purpose of the Study:

  • To construct a metal polyphenol nanozyme with multienzyme activity to address ROS-induced inflammation and promote wound healing.
  • To investigate the therapeutic potential of caffeic acid-vanadium (CA-V) nanoparticles for acute wound treatment.

Main Methods:

  • Hydrothermal synthesis of caffeic acid and ammonium metavanadate, followed by purification to obtain CA-V nanoparticles.
  • In vitro assays to evaluate antioxidant (SOD-like, CAT-like) and ROS/RNS scavenging activities, and fibroblast migration.
  • In vivo studies in mice, including oxidative stress models and RNA sequencing, to assess anti-inflammatory, pro-angiogenic, and wound healing effects.

Main Results:

  • CA-V nanoparticles demonstrated significant SOD-like and CAT-like activities, effectively eliminating ROS/RNS and promoting fibroblast migration.
  • In vitro and in vivo experiments showed CA-V possesses strong antioxidant and antiapoptotic properties, downregulating key inflammatory pathways (TNF-α, IL-17).
  • CA-V accelerated wound healing in mice by reducing inflammation, promoting angiogenesis, and improving collagen arrangement, with good biosafety.

Conclusions:

  • The developed CA-V nanozyme effectively targets the ROS-inflammatory cycle, offering a promising therapeutic strategy for accelerating early acute wound healing.
  • CA-V nanozymes exhibit potent antioxidant, anti-inflammatory, and pro-healing properties, making them a viable option for advanced wound care.
  • This approach provides a novel and effective therapeutic strategy for promoting early wound healing by mitigating oxidative stress and inflammation.

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