Introduction: The application of bone morphogenic proteins (BMPs) is a prominent area of research for application in bone tissue engineering. This biological protein is generally combined with a gel or a collagenous carrier to facilitate its delivery. However, this results in poorly controlling the release of the bioactive cue potentially leading to significant adverse effects. A novel strategy involves the absorption of the BMP onto a biomaterial scaffold in order to alter the release kinetic. In this study, we investigated the impact of surface modification of polycaprolactone (PCL) 3D printed scaffolds onto BMP-2 adsorption efficacy and release.
Materials and Methods: The scaffold were 3D printed using an in house Fused Deposition modelling equipment. The scaffold surface modification was achieved by immersing the construct into a solvent (acetone) of the PCL or by depositing a layer of calcium phosphate in order to increase the roughness and the surface area per volume available for the BMP adsorption. Following surface modification, BMP-2 was adsorbed to 3D printed PCL scaffolds (non modified, solvent treatments and Calcium Phosphate treatment) by immersion in a 0.1 μg/μL BMP-2 solution for 1h at room temperature.
Results and Discussion: Acetone treatments increased significantly material roughness and surface area as measured by AFM and BET. It was also demonstrated that the surface modification significantly impact on the wettability of the scaffold. After exposure scaffolds in BMP-2 solution, the highest adsorption efficiency was found for the acetone treated group which had around 20-30% of BMP adsorbed, which is consistent with previous studies.
Conclusion: We demonstrated that adsorption of BMP-2 can be achieved in treated 3D printed scaffolds and resulting in a maximum of 30% of BMP attached to the scaffold.
References:
[1] Darilis Sua´rez-Gonza´lez et. all, "Controlled Multiple Growth Factor Delivery from Bone Tissue Engineering Scaffolds via Designed Affinity", Tissue engineering: Part A Volume 20,15-16, 2014
[2] Janki J. Patel, "Bone Morphogenetic Protein-2 Adsorption onto Poly-e-caprolactone Better Preserves Bioactivity In Vitro and Produces More Bone In Vivo than Conjugation Under Clinically Relevant Loading Scenarios", Tissue engineering: Part C Volume 21,5, 2015