Biological and Morphological Effects of Apatite Kinds (Sheep/Synthetic) on MgO Reinforced Bone Tissue with Hydroxyapatite Matrix

A. Akilli Aria, H. Evlenb, N. Demirkolc aMechanical Engineering, Amasya University, 05300, Amasya, Turkey bIndustrial Design Engineering, Karabuk University, 78050, Karabuk, Turkey cDepartment of Ceramic, Kocaeli University, Kocaeli, 41140, Turkey

Full Text PDF

In this study, the biological and morphological structure of the bone tissue of hydroxyapatite produced from synthetic and natural bone was investigated. For this purpose, a three-dimensional bioprinter was designed and manufactured. For the production of bone tissue scaffolds, 10 wt% magnesium oxide added to synthetic hydroxyapatite and sheep hydroxyapatite bioink composites were prepared. The rheological analysis of the prepared bioinks was carried out. With the produced three-dimensional bioprinter, 10×10×2 mm3 bone tissue scaffolds were bioprinted. Calcium chloride was used to form connective tissue between layers. 4 weeks of in-vitro bioactivity tests were applied in order to observe the behavior of the produced bone scaffolds and the formation of apatite in the body. After the bioactivity tests, scanning electron microscope and energy dispersive spectrometry analyzes were performed. In addition, a 3-4,5-dimethyl-thiazolyl-2,5-diphenyltetrazolium bromide test was performed in the laboratory environment of the bone tissue scaffolds. In this test, cytotoxicity analyses and cell counts were performed by fibroblast and osteoblast cell loading. Viability and cell proliferation were observed using the phalloidin staining method, and comparisons were made between the mixtures. As a result of the study, the printing ability of both bioinks on the three-dimensional bioprinter was successful. Thus, the bone tissue scaffold of the printed bioink was produced in the desired porous structure. Apatite formations were observed in the scanning electron microscope images of the bone tissue scaffolds that were kept in artificial body fluid for 4 weeks. In the cell culture analysis performed at the last stage with cell viability analysis, the continuation of cell viability was promising.

DOI:10.12693/APhysPolA.142.201 topics: magnesium oxide, bioink, bone scaffold, cell culture