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Updated: Jun 10, 2026

Optimizing Extracellular Vesicle Delivery Using a Core-Sheath 3D-Bioprinted Scaffold for Chronic Wound Management
Published on: February 28, 2025
Corynoline and Extracellular Vesicles Co-Loaded Scaffold Accelerates Vascularized Bone Regeneration with Photothermal
Rou Li1, Chaochen Wang2, Yong Xie3
1China-Japan Friendship Hospital (Institute of Clinical Medical Sciences), Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
This study presents a novel near-infrared (NIR)-responsive scaffold for bone defect repair, utilizing corynoline and extracellular vesicles for enhanced regeneration and reduced inflammation.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Nanotechnology
Background:
- Autologous bone grafting faces limitations like donor site scarcity and immune issues.
- Effective bone defect repair requires strategies beyond traditional grafting.
- Developing advanced scaffolds is crucial for enhanced bone regeneration.
Purpose of the Study:
- To create a multifunctional, NIR-responsive composite scaffold for controlled delivery of corynoline (Cor) and extracellular vesicles (EVs).
- To investigate the scaffold's potential in enhancing bone regeneration by modulating the immune microenvironment and promoting vascularization.
- To address the clinical challenge of bone defect repair with a novel biomaterial solution.
Main Methods:
- Fabrication of a composite scaffold using β-tricalcium phosphate (β-TCP) coated with polydopamine (PDA).
- Immobilization of corynoline (Cor) and extracellular vesicles (EVs) onto the PDA-coated scaffold.
- Utilizing near-infrared (NIR) irradiation to trigger controlled and sustained release of bioactive factors.
- In vitro and in vivo evaluation of the scaffold's efficacy in promoting bone regeneration, vascularization, and immune modulation.
Main Results:
- The PDA coating enabled efficient immobilization and NIR-triggered, sustained release of Cor and EVs for over 14 days.
- Corynoline promoted M2 macrophage polarization, reducing inflammation, while EVs enhanced angiogenesis and osteogenesis.
- NIR stimulation of the scaffold effectively modulated the immune microenvironment and promoted vascularized bone regeneration.
- In vivo studies showed significantly enhanced new bone formation, reduced inflammation, increased cell recruitment, and accelerated vascularization.
Conclusions:
- The developed multifunctional, NIR-responsive scaffold offers a promising strategy for efficient and controlled bone defect repair.
- This approach effectively combines biomaterial design with controlled release of therapeutic agents to enhance bone regeneration.
- The scaffold's ability to modulate the immune microenvironment and promote vascularization represents a significant advancement in regenerative medicine.
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