Back to Search Start Over

3D printed β-tricalcium phosphate versus synthetic bone mineral scaffolds: A comparative in vitro study of biocompatibility.

Authors :
Slavin BV
Mirsky NA
Stauber ZM
Nayak VV
Smay JE
Rivera CF
Mijares DQ
Coelho PG
Cronstein BN
Tovar N
Witek L
Source :
Bio-medical materials and engineering [Biomed Mater Eng] 2024; Vol. 35 (4), pp. 365-375.
Publication Year :
2024

Abstract

Background: β-tricalcium phosphate (β-TCP) has been successfully utilized as a 3D printed ceramic scaffold in the repair of non-healing bone defects; however, it requires the addition of growth factors to augment its regenerative capacity. Synthetic bone mineral (SBM) is a novel and extrudable carbonate hydroxyapatite with ionic substitutions known to facilitate bone healing. However, its efficacy as a 3D printed scaffold for hard tissue defect repair has not been explored.<br />Objective: To evaluate the biocompatibility and cell viability of human osteoprecursor (hOP) cells seeded on 3D printed SBM scaffolds via in vitro analysis.<br />Methods: SBM and β-TCP scaffolds were fabricated via 3D printing and sintered at various temperatures. Scaffolds were then subject to qualitative cytotoxicity testing and cell proliferation experiments utilizing (hOP) cells.<br />Results: SBM scaffolds sintered at lower temperatures (600 °C and 700 °C) induced greater levels of acute cellular stress. At higher sintering temperatures (1100 °C), SBM scaffolds showed inferior cellular viability relative to β-TCP scaffolds sintered to the same temperature (1100 °C). However, qualitative analysis suggested that β-TCP presented no evidence of morphological change, while SBM 1100 °C showed few instances of acute cellular stress.<br />Conclusion: Results demonstrate SBM may be a promising alternative to β-TCP for potential applications in bone tissue engineering.

Details

Language :
English
ISSN :
1878-3619
Volume :
35
Issue :
4
Database :
MEDLINE
Journal :
Bio-medical materials and engineering
Publication Type :
Academic Journal
Accession number :
38578877
Full Text :
https://doi.org/10.3233/BME-230214