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Bone response to physical‐vapour‐deposited titanium dioxide coatings on titanium implants

Identifieur interne : 001921 ( Istex/Corpus ); précédent : 001920; suivant : 001922

Bone response to physical‐vapour‐deposited titanium dioxide coatings on titanium implants

Auteurs : Ahmed M. Ballo ; Dorota Bjöörn ; Maria Strand ; Anders Palmquist ; Jukka Lausmaa ; Peter Thomsen

Source :

RBID : ISTEX:338523DF86EF8A7A89D93A5D194DF435C2EF5DCF

English descriptors

Abstract

The aim of this study was to investigate the correlation between coating thickness and the crystal structure of physical‐vapour‐deposited (PVD) titanium dioxide coatings, and to evaluate their in vivo biocompatibility.

Url:
DOI: 10.1111/j.1600-0501.2012.02509.x

Links to Exploration step

ISTEX:338523DF86EF8A7A89D93A5D194DF435C2EF5DCF

Le document en format XML

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<div type="abstract">The aim of this study was to investigate the correlation between coating thickness and the crystal structure of physical‐vapour‐deposited (PVD) titanium dioxide coatings, and to evaluate their in vivo biocompatibility.</div>
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<abstract>The aim of this study was to investigate the correlation between coating thickness and the crystal structure of physical‐vapour‐deposited (PVD) titanium dioxide coatings, and to evaluate their in vivo biocompatibility.</abstract>
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Objectives
<p>The aim of this study was to investigate the correlation between coating thickness and the crystal structure of physical‐vapour‐deposited (
<hi rend="fc">PVD</hi>
) titanium dioxide coatings, and to evaluate their
<hi rend="italic">in vivo</hi>
biocompatibility.</p>
Materials and methods
<p>The
<hi rend="fc">PVD
<hi rend="fr">TiO</hi>
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<hi rend="subscript">2</hi>
coatings of different thickness were deposited on machined titanium grade 2 screw‐shaped implants. Non‐coated titanium implants were used as controls. Coating properties such as thickness, crystal structure, coating morphology and roughness were characterized.</p>
<p>Forty‐eight implants were placed randomly into both tibias of 16 rats. The animals were euthanized 7 and 28 days postsurgery and block biopsies were prepared for histology, histomorphometry and
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analysis.</p>
Results
<p>The thicknesses of the
<hi rend="fc">PVD
<hi rend="fr">TiO</hi>
</hi>
<hi rend="subscript">2</hi>
coatings were 120 and 1430 nm respectively. Histologically, new bone formed on all implant surfaces. The mean percentage of newly formed bone in contact with the implant (
<hi rend="fc">BIC</hi>
) was significantly higher at early healing time (7 days) for the 120 nm thick
<hi rend="fc">PVD</hi>
coating (39 ± 14%) than for both the 1430 nm thick
<hi rend="fc">PVD</hi>
coating (22 ± 10%) (
<hi rend="italic">P</hi>
 = 0.043) and the machined surface (22 ± 9%) (
<hi rend="italic">P</hi>
 = 0.028). This difference was no longer evident after 28 days (
<hi rend="italic">P</hi>
 = 0.867).</p>
Conclusion
<p>Bone formation and bone‐to‐implant contact are achieved to the same degree for
<hi rend="fc">
<hi rend="fr">TiO</hi>
</hi>
<hi rend="subscript">2</hi>
surface modifications prepared by a
<hi rend="fc">PVD</hi>
process as clinically used, machined titanium. Furthermore, a relatively thinner
<hi rend="fc">PVD</hi>
coating promotes a higher degree of bone apposition shortly after implantation, thereby providing rationales for exploring the potential clinical use of these modifications.</p>
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<fundingAgency>Swedish Research Council</fundingAgency>
<fundingNumber>K2012‐52X‐09495‐25‐3</fundingNumber>
</fundingInfo>
<abstractGroup>
<abstract type="main" xml:id="clr2509-abs-0001">
<title type="main">Abstract</title>
<section xml:id="clr2509-sec-0001">
<title type="main">Objectives</title>
<p>The aim of this study was to investigate the correlation between coating thickness and the crystal structure of physical‐vapour‐deposited (
<fc>PVD</fc>
) titanium dioxide coatings, and to evaluate their
<i>in vivo</i>
biocompatibility.</p>
</section>
<section xml:id="clr2509-sec-0002">
<title type="main">Materials and methods</title>
<p>The
<fc>PVD
<fr>TiO</fr>
</fc>
<sub>2</sub>
coatings of different thickness were deposited on machined titanium grade 2 screw‐shaped implants. Non‐coated titanium implants were used as controls. Coating properties such as thickness, crystal structure, coating morphology and roughness were characterized.</p>
<p>Forty‐eight implants were placed randomly into both tibias of 16 rats. The animals were euthanized 7 and 28 days postsurgery and block biopsies were prepared for histology, histomorphometry and
<fc>SEM</fc>
analysis.</p>
</section>
<section xml:id="clr2509-sec-0003">
<title type="main">Results</title>
<p>The thicknesses of the
<fc>PVD
<fr>TiO</fr>
</fc>
<sub>2</sub>
coatings were 120 and 1430 nm respectively. Histologically, new bone formed on all implant surfaces. The mean percentage of newly formed bone in contact with the implant (
<fc>BIC</fc>
) was significantly higher at early healing time (7 days) for the 120 nm thick
<fc>PVD</fc>
coating (39 ± 14%) than for both the 1430 nm thick
<fc>PVD</fc>
coating (22 ± 10%) (
<i>P</i>
 = 0.043) and the machined surface (22 ± 9%) (
<i>P</i>
 = 0.028). This difference was no longer evident after 28 days (
<i>P</i>
 = 0.867).</p>
</section>
<section xml:id="clr2509-sec-0004">
<title type="main">Conclusion</title>
<p>Bone formation and bone‐to‐implant contact are achieved to the same degree for
<fc>
<fr>TiO</fr>
</fc>
<sub>2</sub>
surface modifications prepared by a
<fc>PVD</fc>
process as clinically used, machined titanium. Furthermore, a relatively thinner
<fc>PVD</fc>
coating promotes a higher degree of bone apposition shortly after implantation, thereby providing rationales for exploring the potential clinical use of these modifications.</p>
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<title>Bone response to physical‐vapour‐deposited titanium dioxide coatings on titanium implants</title>
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<name type="personal">
<namePart type="given">Ahmed M.</namePart>
<namePart type="family">Ballo</namePart>
<affiliation>Department of Biomaterials, Institute for Clinical Sciences, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden</affiliation>
<affiliation>BIOMATCELL, VINN Excellence Center of Biomaterials and Cell Therapy, Gothenburg, Sweden</affiliation>
<affiliation>Department of Biomaterials, Institute for Clinical SciencesThe Sahlgrenska Academy at the University of GothenburgGothenburg, SwedenTel.: +46 31 786 2898Fax: +46 78 629 41e‐mail:</affiliation>
<affiliation>E-mail: ahmed.ballo@gu.se</affiliation>
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<name type="personal">
<namePart type="given">Dorota</namePart>
<namePart type="family">Bjöörn</namePart>
<affiliation>Sandvik Tooling R&D Materials and Processes, Stockholm, Sweden</affiliation>
<affiliation>BIOMATCELL, VINN Excellence Center of Biomaterials and Cell Therapy, Gothenburg, Sweden</affiliation>
<role>
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<affiliation>Sandvik Tooling R&D Materials and Processes, Stockholm, Sweden</affiliation>
<affiliation>BIOMATCELL, VINN Excellence Center of Biomaterials and Cell Therapy, Gothenburg, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<namePart type="given">Anders</namePart>
<namePart type="family">Palmquist</namePart>
<affiliation>Department of Biomaterials, Institute for Clinical Sciences, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden</affiliation>
<affiliation>BIOMATCELL, VINN Excellence Center of Biomaterials and Cell Therapy, Gothenburg, Sweden</affiliation>
<role>
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</role>
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<name type="personal">
<namePart type="given">Jukka</namePart>
<namePart type="family">Lausmaa</namePart>
<affiliation>Department of Chemistry and Materials Technology, SP Technical Research Institute of Sweden, Borås, Sweden</affiliation>
<affiliation>BIOMATCELL, VINN Excellence Center of Biomaterials and Cell Therapy, Gothenburg, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<namePart type="given">Peter</namePart>
<namePart type="family">Thomsen</namePart>
<affiliation>Department of Biomaterials, Institute for Clinical Sciences, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden</affiliation>
<affiliation>BIOMATCELL, VINN Excellence Center of Biomaterials and Cell Therapy, Gothenburg, Sweden</affiliation>
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<abstract>The aim of this study was to investigate the correlation between coating thickness and the crystal structure of physical‐vapour‐deposited (PVD) titanium dioxide coatings, and to evaluate their in vivo biocompatibility.</abstract>
<abstract>The PVD TiO 2 coatings of different thickness were deposited on machined titanium grade 2 screw‐shaped implants. Non‐coated titanium implants were used as controls. Coating properties such as thickness, crystal structure, coating morphology and roughness were characterized. Forty‐eight implants were placed randomly into both tibias of 16 rats. The animals were euthanized 7 and 28 days postsurgery and block biopsies were prepared for histology, histomorphometry and SEM analysis.</abstract>
<abstract>The thicknesses of the PVDTiO 2 coatings were 120 and 1430 nm respectively. Histologically, new bone formed on all implant surfaces. The mean percentage of newly formed bone in contact with the implant (BIC) was significantly higher at early healing time (7 days) for the 120 nm thick PVD coating (39 ± 14%) than for both the 1430 nm thick PVD coating (22 ± 10%) (P = 0.043) and the machined surface (22 ± 9%) (P = 0.028). This difference was no longer evident after 28 days (P = 0.867).</abstract>
<abstract>Bone formation and bone‐to‐implant contact are achieved to the same degree for TiO 2 surface modifications prepared by a PVD process as clinically used, machined titanium. Furthermore, a relatively thinner PVD coating promotes a higher degree of bone apposition shortly after implantation, thereby providing rationales for exploring the potential clinical use of these modifications.</abstract>
<note type="funding">BIOMATCELL, VINN Excellence Center of Biomaterials and Cell Therapy</note>
<note type="funding">Swedish Research Council - No. K2012‐52X‐09495‐25‐3; </note>
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<topic>implant</topic>
<topic>in vivo</topic>
<topic>osseointegration</topic>
<topic>surface coating</topic>
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<date>2013</date>
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