Zirconia coated titanium for implants and their interactions with osteoblast cells
The anodic plasma-electrochemical oxidation in aqueous electrolytes of Zr(SO4)2 was used to prepare new zirconia/titania-based surfaces M1 (Ti, Zr and O: 7–10, 22–27 and 65–69at.%) and M2 (Ti, Zr and O: 11–13, 20–23 and 64–69at.%). The chemical composition and the microstructure of these coatings we...
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Veröffentlicht in: | Materials Science & Engineering C 2014-11, Vol.44, p.254-261 |
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creator | Kaluđerović, Milena R. Schreckenbach, Joachim P. Graf, Hans-Ludwig |
description | The anodic plasma-electrochemical oxidation in aqueous electrolytes of Zr(SO4)2 was used to prepare new zirconia/titania-based surfaces M1 (Ti, Zr and O: 7–10, 22–27 and 65–69at.%) and M2 (Ti, Zr and O: 11–13, 20–23 and 64–69at.%). The chemical composition and the microstructure of these coatings were characterized by surface and solid state techniques such as scanning electron microscopy, electron probe microanalysis, Raman spectroscopy and X-ray diffraction. These mixed oxides of ZrO2/TiO2 surfaces consist up to 84% (m/m) of ZrO2 and 16% (m/m) of TiO2. Monoclinic zirconia was detected as the dominant microcrystalline phase. In vitro studies were conducted on primary human osteoblast cells. MTT and DAPI assays were used for assessment on cell proliferation. Immunohistochemical analyses of morphology, cell cluster formation and expression of bone sialoprotein (BSP) and osteocalcin (OC) were performed. Novel surfaces M1 and M2 induced proliferation and expression of OC and BSP similarly to Ticer, used in clinical practice. Furthermore, the presence of zirconia on titanium surface has a higher beneficial effect on the osteoblast morphological changes and cell cluster formation.
[Display omitted]
•Surfaces M1 and M2 (up to 84% (m/m) ZrO2 and 16% (m/m) TiO2) were prepared.•Novel materials promote proliferation of human osteoblasts similarly to Ticer.•Morphological changes and cell cluster formation are induced faster on M1 and M2.•Higher expression of OC and BSP is caused by M1 and M2.•M1 and M2 may influence the rate of bone formation. |
doi_str_mv | 10.1016/j.msec.2014.08.032 |
format | Article |
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[Display omitted]
•Surfaces M1 and M2 (up to 84% (m/m) ZrO2 and 16% (m/m) TiO2) were prepared.•Novel materials promote proliferation of human osteoblasts similarly to Ticer.•Morphological changes and cell cluster formation are induced faster on M1 and M2.•Higher expression of OC and BSP is caused by M1 and M2.•M1 and M2 may influence the rate of bone formation.</description><identifier>ISSN: 0928-4931</identifier><identifier>EISSN: 1873-0191</identifier><identifier>DOI: 10.1016/j.msec.2014.08.032</identifier><identifier>PMID: 25280704</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Anodic plasma-electrochemical oxidation ; Bone sialoprotein ; Cell Proliferation - drug effects ; Cells, Cultured ; Coated Materials, Biocompatible - chemistry ; Coated Materials, Biocompatible - pharmacology ; Humans ; Implants ; Integrin-Binding Sialoprotein - genetics ; Integrin-Binding Sialoprotein - metabolism ; Microscopy, Electron, Scanning ; Osteoblasts ; Osteoblasts - cytology ; Osteoblasts - drug effects ; Osteocalcin ; Osteocalcin - genetics ; Osteocalcin - metabolism ; Prostheses and Implants ; Spectrum Analysis, Raman ; Surface Properties ; Titanium - chemistry ; Titanium - pharmacology ; X-Ray Diffraction ; Zirconia ; Zirconium - chemistry ; Zirconium - pharmacology</subject><ispartof>Materials Science & Engineering C, 2014-11, Vol.44, p.254-261</ispartof><rights>2014 Elsevier B.V.</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-47fbcd00a3fc7d64be371a6f944908a4e630be32c017b0316a9547ce528a5d533</citedby><cites>FETCH-LOGICAL-c426t-47fbcd00a3fc7d64be371a6f944908a4e630be32c017b0316a9547ce528a5d533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.msec.2014.08.032$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25280704$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaluđerović, Milena R.</creatorcontrib><creatorcontrib>Schreckenbach, Joachim P.</creatorcontrib><creatorcontrib>Graf, Hans-Ludwig</creatorcontrib><title>Zirconia coated titanium for implants and their interactions with osteoblast cells</title><title>Materials Science & Engineering C</title><addtitle>Mater Sci Eng C Mater Biol Appl</addtitle><description>The anodic plasma-electrochemical oxidation in aqueous electrolytes of Zr(SO4)2 was used to prepare new zirconia/titania-based surfaces M1 (Ti, Zr and O: 7–10, 22–27 and 65–69at.%) and M2 (Ti, Zr and O: 11–13, 20–23 and 64–69at.%). The chemical composition and the microstructure of these coatings were characterized by surface and solid state techniques such as scanning electron microscopy, electron probe microanalysis, Raman spectroscopy and X-ray diffraction. These mixed oxides of ZrO2/TiO2 surfaces consist up to 84% (m/m) of ZrO2 and 16% (m/m) of TiO2. Monoclinic zirconia was detected as the dominant microcrystalline phase. In vitro studies were conducted on primary human osteoblast cells. MTT and DAPI assays were used for assessment on cell proliferation. Immunohistochemical analyses of morphology, cell cluster formation and expression of bone sialoprotein (BSP) and osteocalcin (OC) were performed. Novel surfaces M1 and M2 induced proliferation and expression of OC and BSP similarly to Ticer, used in clinical practice. Furthermore, the presence of zirconia on titanium surface has a higher beneficial effect on the osteoblast morphological changes and cell cluster formation.
[Display omitted]
•Surfaces M1 and M2 (up to 84% (m/m) ZrO2 and 16% (m/m) TiO2) were prepared.•Novel materials promote proliferation of human osteoblasts similarly to Ticer.•Morphological changes and cell cluster formation are induced faster on M1 and M2.•Higher expression of OC and BSP is caused by M1 and M2.•M1 and M2 may influence the rate of bone formation.</description><subject>Anodic plasma-electrochemical oxidation</subject><subject>Bone sialoprotein</subject><subject>Cell Proliferation - drug effects</subject><subject>Cells, Cultured</subject><subject>Coated Materials, Biocompatible - chemistry</subject><subject>Coated Materials, Biocompatible - pharmacology</subject><subject>Humans</subject><subject>Implants</subject><subject>Integrin-Binding Sialoprotein - genetics</subject><subject>Integrin-Binding Sialoprotein - metabolism</subject><subject>Microscopy, Electron, Scanning</subject><subject>Osteoblasts</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - drug effects</subject><subject>Osteocalcin</subject><subject>Osteocalcin - genetics</subject><subject>Osteocalcin - metabolism</subject><subject>Prostheses and Implants</subject><subject>Spectrum Analysis, Raman</subject><subject>Surface Properties</subject><subject>Titanium - chemistry</subject><subject>Titanium - pharmacology</subject><subject>X-Ray Diffraction</subject><subject>Zirconia</subject><subject>Zirconium - chemistry</subject><subject>Zirconium - pharmacology</subject><issn>0928-4931</issn><issn>1873-0191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLxDAUhYMozjj6B1xIl25abx7TB7gR8QUDgujGTUjTWyZD24xJqvjvTZnRpasL555zuPcj5JxCRoHmV5us96gzBlRkUGbA2QGZ07LgKdCKHpI5VKxMRcXpjJx4vwHIS16wYzJjS1ZCAWJOXt6N03YwKtFWBWySYIIazNgnrXWJ6bedGoJP1BA3azRRGgI6pYOxg0--TFgn1ge0dad8SDR2nT8lR63qPJ7t54K83d-93j6mq-eHp9ubVaoFy0MqirbWDYDirS6aXNTIC6rythKiglIJzDlEjWmgRQ2c5qpaikJjPF0tmyXnC3K56906-zGiD7I3frpADWhHL2kOFQXgUEYr21m1s947bOXWmV65b0lBTizlRk4s5cRSQikjyxi62PePdY_NX-QXXjRc7wwYv_w06KTXBgeNjXGog2ys-a__B4vshdw</recordid><startdate>20141101</startdate><enddate>20141101</enddate><creator>Kaluđerović, Milena R.</creator><creator>Schreckenbach, Joachim P.</creator><creator>Graf, Hans-Ludwig</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20141101</creationdate><title>Zirconia coated titanium for implants and their interactions with osteoblast cells</title><author>Kaluđerović, Milena R. ; Schreckenbach, Joachim P. ; Graf, Hans-Ludwig</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-47fbcd00a3fc7d64be371a6f944908a4e630be32c017b0316a9547ce528a5d533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Anodic plasma-electrochemical oxidation</topic><topic>Bone sialoprotein</topic><topic>Cell Proliferation - drug effects</topic><topic>Cells, Cultured</topic><topic>Coated Materials, Biocompatible - chemistry</topic><topic>Coated Materials, Biocompatible - pharmacology</topic><topic>Humans</topic><topic>Implants</topic><topic>Integrin-Binding Sialoprotein - genetics</topic><topic>Integrin-Binding Sialoprotein - metabolism</topic><topic>Microscopy, Electron, Scanning</topic><topic>Osteoblasts</topic><topic>Osteoblasts - cytology</topic><topic>Osteoblasts - drug effects</topic><topic>Osteocalcin</topic><topic>Osteocalcin - genetics</topic><topic>Osteocalcin - metabolism</topic><topic>Prostheses and Implants</topic><topic>Spectrum Analysis, Raman</topic><topic>Surface Properties</topic><topic>Titanium - chemistry</topic><topic>Titanium - pharmacology</topic><topic>X-Ray Diffraction</topic><topic>Zirconia</topic><topic>Zirconium - chemistry</topic><topic>Zirconium - pharmacology</topic><toplevel>online_resources</toplevel><creatorcontrib>Kaluđerović, Milena R.</creatorcontrib><creatorcontrib>Schreckenbach, Joachim P.</creatorcontrib><creatorcontrib>Graf, Hans-Ludwig</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Materials Science & Engineering C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaluđerović, Milena R.</au><au>Schreckenbach, Joachim P.</au><au>Graf, Hans-Ludwig</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Zirconia coated titanium for implants and their interactions with osteoblast cells</atitle><jtitle>Materials Science & Engineering C</jtitle><addtitle>Mater Sci Eng C Mater Biol Appl</addtitle><date>2014-11-01</date><risdate>2014</risdate><volume>44</volume><spage>254</spage><epage>261</epage><pages>254-261</pages><issn>0928-4931</issn><eissn>1873-0191</eissn><abstract>The anodic plasma-electrochemical oxidation in aqueous electrolytes of Zr(SO4)2 was used to prepare new zirconia/titania-based surfaces M1 (Ti, Zr and O: 7–10, 22–27 and 65–69at.%) and M2 (Ti, Zr and O: 11–13, 20–23 and 64–69at.%). The chemical composition and the microstructure of these coatings were characterized by surface and solid state techniques such as scanning electron microscopy, electron probe microanalysis, Raman spectroscopy and X-ray diffraction. These mixed oxides of ZrO2/TiO2 surfaces consist up to 84% (m/m) of ZrO2 and 16% (m/m) of TiO2. Monoclinic zirconia was detected as the dominant microcrystalline phase. In vitro studies were conducted on primary human osteoblast cells. MTT and DAPI assays were used for assessment on cell proliferation. Immunohistochemical analyses of morphology, cell cluster formation and expression of bone sialoprotein (BSP) and osteocalcin (OC) were performed. Novel surfaces M1 and M2 induced proliferation and expression of OC and BSP similarly to Ticer, used in clinical practice. Furthermore, the presence of zirconia on titanium surface has a higher beneficial effect on the osteoblast morphological changes and cell cluster formation.
[Display omitted]
•Surfaces M1 and M2 (up to 84% (m/m) ZrO2 and 16% (m/m) TiO2) were prepared.•Novel materials promote proliferation of human osteoblasts similarly to Ticer.•Morphological changes and cell cluster formation are induced faster on M1 and M2.•Higher expression of OC and BSP is caused by M1 and M2.•M1 and M2 may influence the rate of bone formation.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25280704</pmid><doi>10.1016/j.msec.2014.08.032</doi><tpages>8</tpages></addata></record> |
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subjects | Anodic plasma-electrochemical oxidation Bone sialoprotein Cell Proliferation - drug effects Cells, Cultured Coated Materials, Biocompatible - chemistry Coated Materials, Biocompatible - pharmacology Humans Implants Integrin-Binding Sialoprotein - genetics Integrin-Binding Sialoprotein - metabolism Microscopy, Electron, Scanning Osteoblasts Osteoblasts - cytology Osteoblasts - drug effects Osteocalcin Osteocalcin - genetics Osteocalcin - metabolism Prostheses and Implants Spectrum Analysis, Raman Surface Properties Titanium - chemistry Titanium - pharmacology X-Ray Diffraction Zirconia Zirconium - chemistry Zirconium - pharmacology |
title | Zirconia coated titanium for implants and their interactions with osteoblast cells |
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