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dc.contributor.authorAri, A. Akilli
dc.contributor.authorEvlen, H.
dc.contributor.authorDemirkol, N.
dc.date.accessioned2024-03-12T19:30:03Z
dc.date.available2024-03-12T19:30:03Z
dc.date.issued2022
dc.identifier.issn0587-4246
dc.identifier.issn1898-794X
dc.identifier.urihttps://doi.org/10.12693/APhysPolA.142.201
dc.identifier.urihttps://hdl.handle.net/20.500.12450/2469
dc.description.abstractIn 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 x 10 x 2 mm(3) 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-thiazoly1-2,5-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.en_US
dc.description.sponsorshipScientific Research Project Department of Karabuk University [KBUBAP-17-DR-303]en_US
dc.description.sponsorshipThe authors thank the Scientific Research Project Department of Karabuk University for financial support as part of the KBUBAP-17-DR-303 project.en_US
dc.language.isoengen_US
dc.publisherPolish Acad Sciences Inst Physicsen_US
dc.relation.ispartofActa Physica Polonica Aen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectmagnesium oxideen_US
dc.subjectbioinken_US
dc.subjectbone scaffolden_US
dc.subjectcell cultureen_US
dc.titleBiological and Morphological Effects of Apatite Kinds (Sheep/Synthetic) on MgO Reinforced Bone Tissue with Hydroxyapatite Matrixen_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.identifier.volume142en_US
dc.identifier.issue2en_US
dc.identifier.startpage201en_US
dc.identifier.endpage210en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85139822540en_US
dc.identifier.doi10.12693/APhysPolA.142.201
dc.department-temp[Ari, A. Akilli] Amasya Univ, Mech Engn, TR-05300 Amasya, Turkey; [Evlen, H.] Karabuk Univ, Ind Design Engn, TR-78050 Karabuk, Turkey; [Demirkol, N.] Kocaeli Univ, Dept Ceram, TR-41140 Kocaeli, Turkeyen_US
dc.identifier.wosWOS:000868984600002en_US


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