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Melt Electrowritten Scaffold-Reinforced Affibody-Conjugated Hydrogels for Controlled Bone Morphogenetic Protein-2
Jonathan Dorogin1, Yan C Pacheco1, Patrick C Hall1
1Department of Bioengineering, Phil and Penny Knight Campus for Accelerating Scientific Impact, University of Oregon.
Biorxiv : the Preprint Server for Biology
|November 24, 2025
Summary
A novel hydrogel delivery system enhances bone regeneration by controlling the release of bone morphogenetic protein-2 (BMP-2) and improving mechanical stability, leading to better bone healing in rats.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Regenerative Medicine
Background:
- Bone morphogenetic protein-2 (BMP-2) is crucial for bone regeneration but faces challenges with uncontrolled release from collagen sponges, leading to adverse effects.
- Existing hydrogels offer tunable protein release but lack mechanical strength and stability for practical applications.
Purpose of the Study:
- To develop a dual-function hydrogel system for controlled BMP-2 delivery, integrating mechanical reinforcement and affinity-based release.
- To evaluate the efficacy of this system in enhancing bone regeneration and protein retention in vivo.
Main Methods:
- Fabrication of a melt electrowritten (MEW) scaffold-reinforced, affibody-conjugated polyethylene glycol maleimide (PEG-mal) hydrogel.
- Incorporation of BMP-2-specific affibodies for affinity-controlled release and MEW scaffolds for mechanical enhancement.
- Assessment of hydrogel stability, protein release kinetics, and in vivo bone regeneration in rat femoral defects.
Main Results:
- MEW scaffolds improved hydrogel handling, compressive resistance, and stability through lyophilization and rehydration.
- Affibody conjugation enabled tunable BMP-2 release, maintained after lyophilization and rehydration.
- In vivo studies showed enhanced BMP-2 retention, increased bone volume, and improved defect bridging with the reinforced hydrogel system.
Conclusions:
- The developed hydrogel system effectively combines mechanical reinforcement with tunable protein-material affinity interactions for advanced BMP-2 delivery.
- This integrated platform represents a significant advancement for hydrogel-based therapeutic strategies in musculoskeletal repair and other regenerative applications.
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