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Biocompatible Customized 3D Bone Scaffolds Treated with CRFP, an Osteogenic Peptide
Currently used synthetic bone graft substitutes (BGS) are either too weak to bear the principal load or if metallic, they can support loading, but can lead to stress shielding and are unable to integrate fully. In this study, we developed biocompatible, 3D printed scaffolds derived from µCT images o...
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Published in: | Bioengineering (Basel) 2021-11, Vol.8 (12), p.199 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Currently used synthetic bone graft substitutes (BGS) are either too weak to bear the principal load or if metallic, they can support loading, but can lead to stress shielding and are unable to integrate fully. In this study, we developed biocompatible, 3D printed scaffolds derived from µCT images of the bone that can overcome these issues and support the growth of osteoblasts.
Cylindrical scaffolds were fabricated with acrylonitrile butadiene styrene (ABS) and Stratasys
MED 610 (MED610) materials. The 3D-printed scaffolds were seeded with
calvaria cells (MC3T3). After the cells attained confluence, osteogenesis was induced with and without the addition of calcitonin receptor fragment peptide (CRFP) and the bone matrix production was analyzed. Mechanical compression testing was carried out to measure compressive strength, stiffness, and elastic modulus.
For the ABS scaffolds, there was a 9.8% increase in compressive strength (
< 0.05) in the scaffolds with no pre-coating and the treatment with CRFP, compared to non-treated scaffolds. Similarly, MED610 scaffolds treated with CRFP showed an 11.9% (polylysine pre-coating) and a 20% (no pre-coating) increase (
< 0.01) in compressive strength compared to non-treated scaffolds.
MED610 scaffolds are excellent BGS as they support osteoblast growth and show enhanced bone growth with enhanced compressive strength when augmented with CRFP. |
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ISSN: | 2306-5354 2306-5354 |
DOI: | 10.3390/bioengineering8120199 |