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Adaptive ROS-Responsive Dual-Layered Hydrogel with Ginkgo Biloba-Derived Exosome-Like Nanovesicles for Diabetic Wound
1Department of Plastic and Aesthetic (Burn) Surgery, The Second Xiangya Hospital, Central South University, Changsha, 410011, China.
Advanced Healthcare Materials
|March 12, 2026
Summary
This study presents a novel Dual-Gel system for diabetic wound healing. It precisely controls reactive oxygen species (ROS) to manage infection and promote tissue repair.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Wound Healing Research
Background:
- Diabetic wound healing is hindered by infection and imbalanced reactive oxygen species (ROS).
- Existing hydrogel dressings struggle to address the distinct needs of different wound healing stages.
- A dynamic approach to ROS regulation is crucial for effective diabetic wound management.
Purpose of the Study:
- To develop a multifunctional bilayer hydrogel (Dual-Gel) for diabetic wound healing.
- To engineer a system that precisely regulates dynamic ROS levels in the wound microenvironment.
- To create a smart dressing that responds to wound conditions for improved healing outcomes.
Main Methods:
- Synthesized a bilayer hydrogel: Gel 1 (EPLGMA/copper ions) and Gel 2 (gelatin/ROS-cleavable linker).
- Gel 1 provides antibacterial activity and generates ROS via copper ion catalysis.
- Gel 2 degrades upon excessive ROS, releasing exosomes to promote healing.
Main Results:
- The Dual-Gel system effectively managed infection and regulated ROS levels.
- Gel 1 released ε-polylysine for antibacterial action and copper ions for ROS generation.
- Gel 2 degradation released exosomes, stimulating cell proliferation, angiogenesis, and anti-apoptosis.
Conclusions:
- The Dual-Gel system offers a novel strategy for diabetic wound management by dynamically controlling ROS.
- This smart hydrogel dressing orchestrates the release of bioactive components in response to wound microenvironment changes.
- The Dual-Gel system shows potential for improving clinical outcomes in complex diabetic wounds.
Keywords:
diabetic woundhydrogeloxidative regulationplant‐derived exosome‐like nanovesiclesreactive oxygen species‐responsive
