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Effect of core materials for core fabrication for dental implants on in-vitro cytocompatibility of MC3T3-E1 cells

BACKGROUND: Despite the wide use of dental materials for CAD/CAM system in prosthetic treatment, the effect of the materials, which are used as dental implants core fabricated, on cells involved in dental implant osseointegration is uncertain. This study aimed to investigate and compare the effect o...

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Autores principales: Park, Jung-Hyun, Lee, Hyun, Kang, Seen-Young, Kim, Junesun, Kim, Ji-Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918698/
https://www.ncbi.nlm.nih.gov/pubmed/31849322
http://dx.doi.org/10.1186/s12903-019-0985-0
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author Park, Jung-Hyun
Lee, Hyun
Kang, Seen-Young
Kim, Junesun
Kim, Ji-Hwan
author_facet Park, Jung-Hyun
Lee, Hyun
Kang, Seen-Young
Kim, Junesun
Kim, Ji-Hwan
author_sort Park, Jung-Hyun
collection PubMed
description BACKGROUND: Despite the wide use of dental materials for CAD/CAM system in prosthetic treatment, the effect of the materials, which are used as dental implants core fabricated, on cells involved in dental implant osseointegration is uncertain. This study aimed to investigate and compare the effect of single core materials used for dental implants fabricated by the dental prostheses fabrication process and the CAD/CAM milling method on MC3T3-E1 cells. METHODS: The materials used for prostheses restoration in this experiment were Porcelain Fused Gold (P.F.G), Lithium disilicate glass ceramic (LiSi(2)), Zirconia (ZrO(2)), Nickel-Chromium (Ni-Cr) and Cobalt-Chromium (Co-Cr). MC3T3-E1 cells were cultured and used, the cell adhesion and morphology were observed and analyzed using confocal laser scanning microscopy (CLSM). Methoxyphenyl tetrazolium salt (MTS) and alkaline phosphatase (ALP) assay were used to observe the cell proliferation and differentiation. RESULTS: CLSM revealed irregular cell adhesion and morphology and the filopodia did not spread in the Ni-Cr specimen group. Significantly high cell proliferation was observed in the ZrO(2) specimen group. The LiSi(2) specimen group presented significantly high cell differentiation. Intergroup comparison of cell proliferation and differentiation between the Ni-Cr specimen group and all other specimen groups showed significant differences (p < .05). CONCLUSION: Cell proliferation and differentiation were observed from the cores, which were fabricated with all specimen groups on cytocompatibility except the Ni-Cr specimen group.
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spelling pubmed-69186982019-12-20 Effect of core materials for core fabrication for dental implants on in-vitro cytocompatibility of MC3T3-E1 cells Park, Jung-Hyun Lee, Hyun Kang, Seen-Young Kim, Junesun Kim, Ji-Hwan BMC Oral Health Research Article BACKGROUND: Despite the wide use of dental materials for CAD/CAM system in prosthetic treatment, the effect of the materials, which are used as dental implants core fabricated, on cells involved in dental implant osseointegration is uncertain. This study aimed to investigate and compare the effect of single core materials used for dental implants fabricated by the dental prostheses fabrication process and the CAD/CAM milling method on MC3T3-E1 cells. METHODS: The materials used for prostheses restoration in this experiment were Porcelain Fused Gold (P.F.G), Lithium disilicate glass ceramic (LiSi(2)), Zirconia (ZrO(2)), Nickel-Chromium (Ni-Cr) and Cobalt-Chromium (Co-Cr). MC3T3-E1 cells were cultured and used, the cell adhesion and morphology were observed and analyzed using confocal laser scanning microscopy (CLSM). Methoxyphenyl tetrazolium salt (MTS) and alkaline phosphatase (ALP) assay were used to observe the cell proliferation and differentiation. RESULTS: CLSM revealed irregular cell adhesion and morphology and the filopodia did not spread in the Ni-Cr specimen group. Significantly high cell proliferation was observed in the ZrO(2) specimen group. The LiSi(2) specimen group presented significantly high cell differentiation. Intergroup comparison of cell proliferation and differentiation between the Ni-Cr specimen group and all other specimen groups showed significant differences (p < .05). CONCLUSION: Cell proliferation and differentiation were observed from the cores, which were fabricated with all specimen groups on cytocompatibility except the Ni-Cr specimen group. BioMed Central 2019-12-18 /pmc/articles/PMC6918698/ /pubmed/31849322 http://dx.doi.org/10.1186/s12903-019-0985-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Park, Jung-Hyun
Lee, Hyun
Kang, Seen-Young
Kim, Junesun
Kim, Ji-Hwan
Effect of core materials for core fabrication for dental implants on in-vitro cytocompatibility of MC3T3-E1 cells
title Effect of core materials for core fabrication for dental implants on in-vitro cytocompatibility of MC3T3-E1 cells
title_full Effect of core materials for core fabrication for dental implants on in-vitro cytocompatibility of MC3T3-E1 cells
title_fullStr Effect of core materials for core fabrication for dental implants on in-vitro cytocompatibility of MC3T3-E1 cells
title_full_unstemmed Effect of core materials for core fabrication for dental implants on in-vitro cytocompatibility of MC3T3-E1 cells
title_short Effect of core materials for core fabrication for dental implants on in-vitro cytocompatibility of MC3T3-E1 cells
title_sort effect of core materials for core fabrication for dental implants on in-vitro cytocompatibility of mc3t3-e1 cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918698/
https://www.ncbi.nlm.nih.gov/pubmed/31849322
http://dx.doi.org/10.1186/s12903-019-0985-0
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