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Updated: Jan 8, 2026

In Vivo Imaging of Reactive Oxygen Species in a Murine Wound Model
Published on: November 17, 2018
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.
Abstract:
Skin ulceration impairs barrier function, and high concentrations of reactive oxygen species (ROS) and inflammatory factors in the wound microenvironment significantly delay the healing process. The effects of current clinical treatment schemes are limited, and a new strategy with both economic benefits and remarkable curative effects is urgently needed. Therefore, we constructed a metal polyphenol nanozyme with multienzyme activity aimed at targeting the key vicious cycle of ROS-induced inflammation and accelerating the early healing of wounds. First, caffeic acid and NH4VO3 were synthesized via a simple hydrothermal method, and then, purified CA-V nanoparticles were obtained via dialysis and freeze-drying. In vitro experiments revealed that it has good SOD-like enzyme and CAT-like activities, can eliminate ROS/RNS, and can promote the migration of fibroblasts to complete epithelization. The results of the oxidative stress model and RNA sequencing revealed that it has excellent antioxidant and antiapoptotic abilities and obviously downregulates TNF-α and IL-17, which are typical inflammatory pathways. In vivo experiments and RNA sequencing in mice also verified that CA-V can slow inflammation, promote angiogenesis and collagen arrangement, and accelerate wound healing. Notably, CA-V has good biosafety in vitro and in vivo. The use of the ROS-inflammatory circulation system as a therapeutic target provides a promising therapeutic strategy for promoting early healing of acute wounds.
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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