4.5 Article

Osteogenic Differentiation Capacity of Dental Pulp Stem Cells on 3D Printed Polyurethane/Boric Acid Scaffold

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DOI: 10.1007/s12011-023-03781-2

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Dental pulp stem cells; Polyurethane; Boric acid; 3D printing; Osteogenic differentiation

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Additive manufacturing is being increasingly used in dentistry and orthopedics for creating customized implants. In this study, fused deposition modeling was used to produce 3D scaffolds made of polyurethane filament. These scaffolds were coated with boric acid using the thermionic vacuum arc technique. The coated scaffolds showed macro-pores with dimensions of approximately 0.16 mm2. The boric acid coating increased roughness and decreased wettability. Cell culture analysis confirmed the presence of boric acid on the scaffolds. The 3D printed PU scaffolds with boric acid coating showed enhanced cell viability and osteogenic differentiation of dental pulp stem cells. The expression of osteogenic markers was increased in the coated scaffold group compared to the control group.
Additive manufacturing is growing in the area of dentistry and orthopedics due to the potential for the fabrication of individual implants. In this study, fused deposition modeling which is the most popular method was used to produce 3D scaffolds having a grid pattern from the polyurethane (PU) filament. Then, this scaffold was coated with boric acid (BA) with the thermionic vacuum arc technique. The microstructure analysis showed the macro-pores having a dimension of similar to 0.16 mm(2). The BA coating increased the roughness in adverse decreased the wettability. The presence of BA on the scaffold before and after cell culture was confirmed by FESEM-EDS and ATR-FTIR. The Cell proliferation and osteogenic differentiation capacity of dental pulp stem cells (DPSCs) on uncoated and coated printed 3D PU scaffolds were also investigated. On the third day, cell viability was found to be higher (1.3-fold) in the groups containing BA. However, on the seventh day, the increase in cell proliferation in the PU+BA group was found to be less than in the other groups. According to Ca deposition analysis and Alizarin Red staining, PU+BA increased the calcium accumulation in the cells in both osteogenic induced and non-induced conditions at day 14. According to gene expression analysis, the Runx2 expression was not detected in PU+BA groups with and without differentiation medium (p <= 0.05). The expression of OCN was persistently increased up to 21-fold and 48-fold in cells on PU and PU+BA in osteogenic differentiation medium group after 14 days compared to control group (p <= 0.05). DSPP expression was observed only in PU+BA in osteogenic differentiation medium group. In line with the results that we have obtained, our 3D printed scaffolds have properties to trigger the differentiation of DPSCs cells in terms of osteogenicity.

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