Effect of pre-treatment of crystallized bioactive glass with cell culture media on structure, degradability, and biocompatibility

The silicate glass 45S5 Bioglass® (BG) is a potential scaffold material for bone regeneration because of its excellent bioactivity, biocompatibility and ability to form a strong bond with bone tissues, via the formation of an apatite layer on its surface. The evaluation of in vitro bioactivity in ph...

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Veröffentlicht in:Materials Science & Engineering C 2019-04, Vol.97, p.188-197
Hauptverfasser: Thavornyutikarn, Boonlom, Feltis, Bryce, Wright, Paul F.A., Turney, Terence W.
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Turney, Terence W.
description The silicate glass 45S5 Bioglass® (BG) is a potential scaffold material for bone regeneration because of its excellent bioactivity, biocompatibility and ability to form a strong bond with bone tissues, via the formation of an apatite layer on its surface. The evaluation of in vitro bioactivity in physiological body fluids, whilst challenging, can offer some insights for developing the bone-bonding ability of these glasses in vivo. In this study, we investigated the influence of three different cell culture and tissue fluid-like solutions on the dissolution and calcium-phosphate (CaP) based re-precipitation behaviour at the glass-liquid interface. We also examined pre-treatment of BG with these biological solutions, and how its influence on bone-forming MG-63 osteoblastic cell proliferation, viability and adhesion. The biological solutions used in this comparative study were: commercial cell culture medium (DMEM), a DMEM solution without organic components (DML) and a simulated body fluid (SBF), incorporating TRIS-buffer. Incubation of BG in these solutions over 28 days resulted in differences in weight loss, solution pH and ion release, and the development of CaP-based surface layers. XRD and FT-IR analyses showed clear differences in the characteristics of the CaP-based coating layers formed by the different solutions. The interfacial reactivity between the glass and the solutions depended on the composition and properties of the solutions. The formation of the CaP layer occurred more rapidly in SBF due to the presence of TRIS-buffer, which also significantly accelerated glass dissolution, further reducing the BG mass in SBF. MG-63 osteoblasts proliferated and spread more rapidly across the surfaces of all pre-conditioned BG, compared to fresh BG. The experimental results of this work help clarify differences between in vitro bioactivity of BG observed in cell culture solutions and in vivo BG bioactivity. Pre-treatment of Bioglass with different cell culture solutions induces development of various calcium phosphate-based coating layers on the glass surface and enhances biocompatibility. [Display omitted] •Pre-treatment with different cell culture solutions controls the surface chemistry of crystallized 45S5 Bioglass®.•XRD and FT-IR show a range of surface calcium phosphate phases are formed.•Pre-treatment conditions also determine bone-forming MG-63 osteoblastic cell proliferation, viability and adhesion.•The results clarify differences between in vitro
doi_str_mv 10.1016/j.msec.2018.12.034
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The evaluation of in vitro bioactivity in physiological body fluids, whilst challenging, can offer some insights for developing the bone-bonding ability of these glasses in vivo. In this study, we investigated the influence of three different cell culture and tissue fluid-like solutions on the dissolution and calcium-phosphate (CaP) based re-precipitation behaviour at the glass-liquid interface. We also examined pre-treatment of BG with these biological solutions, and how its influence on bone-forming MG-63 osteoblastic cell proliferation, viability and adhesion. The biological solutions used in this comparative study were: commercial cell culture medium (DMEM), a DMEM solution without organic components (DML) and a simulated body fluid (SBF), incorporating TRIS-buffer. Incubation of BG in these solutions over 28 days resulted in differences in weight loss, solution pH and ion release, and the development of CaP-based surface layers. XRD and FT-IR analyses showed clear differences in the characteristics of the CaP-based coating layers formed by the different solutions. The interfacial reactivity between the glass and the solutions depended on the composition and properties of the solutions. The formation of the CaP layer occurred more rapidly in SBF due to the presence of TRIS-buffer, which also significantly accelerated glass dissolution, further reducing the BG mass in SBF. MG-63 osteoblasts proliferated and spread more rapidly across the surfaces of all pre-conditioned BG, compared to fresh BG. The experimental results of this work help clarify differences between in vitro bioactivity of BG observed in cell culture solutions and in vivo BG bioactivity. Pre-treatment of Bioglass with different cell culture solutions induces development of various calcium phosphate-based coating layers on the glass surface and enhances biocompatibility. [Display omitted] •Pre-treatment with different cell culture solutions controls the surface chemistry of crystallized 45S5 Bioglass®.•XRD and FT-IR show a range of surface calcium phosphate phases are formed.•Pre-treatment conditions also determine bone-forming MG-63 osteoblastic cell proliferation, viability and adhesion.•The results clarify differences between in vitro bioactivity of sintered Bioglass in cell culture solutions.</description><identifier>ISSN: 0928-4931</identifier><identifier>EISSN: 1873-0191</identifier><identifier>DOI: 10.1016/j.msec.2018.12.034</identifier><identifier>PMID: 30678903</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Apatite ; Bioactive glass ; Biocompatibility ; Biocompatible Materials - chemistry ; Bioglass ; Biological activity ; Biomedical materials ; Biotechnology ; Body fluids ; Body weight loss ; Bone growth ; Buffers ; Calcium ; Calcium phosphates ; Calcium Phosphates - chemistry ; Cell Adhesion ; Cell culture ; Cell Line ; Cell Proliferation ; Ceramics - chemistry ; Chemical precipitation ; Comparative studies ; Conditioning ; Crystallization ; Culture media ; Culture Media - chemistry ; Degradability ; Dissolution ; Humans ; Hydrogen-Ion Concentration ; In vitro methods and tests ; In vivo methods and tests ; Incubation ; Materials science ; Materials Testing ; Microscopy, Electron, Scanning ; Osteoblasts ; Osteoblasts - cytology ; Osteogenesis ; Pretreatment ; Regeneration ; Regeneration (physiology) ; Spectroscopy, Fourier Transform Infrared ; Surface layers ; Surface reactivity ; Surgical implants ; Tissue culture ; Tissues ; Viability ; Weight loss ; X-Ray Diffraction</subject><ispartof>Materials Science &amp; Engineering C, 2019-04, Vol.97, p.188-197</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. 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The evaluation of in vitro bioactivity in physiological body fluids, whilst challenging, can offer some insights for developing the bone-bonding ability of these glasses in vivo. In this study, we investigated the influence of three different cell culture and tissue fluid-like solutions on the dissolution and calcium-phosphate (CaP) based re-precipitation behaviour at the glass-liquid interface. We also examined pre-treatment of BG with these biological solutions, and how its influence on bone-forming MG-63 osteoblastic cell proliferation, viability and adhesion. The biological solutions used in this comparative study were: commercial cell culture medium (DMEM), a DMEM solution without organic components (DML) and a simulated body fluid (SBF), incorporating TRIS-buffer. Incubation of BG in these solutions over 28 days resulted in differences in weight loss, solution pH and ion release, and the development of CaP-based surface layers. XRD and FT-IR analyses showed clear differences in the characteristics of the CaP-based coating layers formed by the different solutions. The interfacial reactivity between the glass and the solutions depended on the composition and properties of the solutions. The formation of the CaP layer occurred more rapidly in SBF due to the presence of TRIS-buffer, which also significantly accelerated glass dissolution, further reducing the BG mass in SBF. MG-63 osteoblasts proliferated and spread more rapidly across the surfaces of all pre-conditioned BG, compared to fresh BG. The experimental results of this work help clarify differences between in vitro bioactivity of BG observed in cell culture solutions and in vivo BG bioactivity. Pre-treatment of Bioglass with different cell culture solutions induces development of various calcium phosphate-based coating layers on the glass surface and enhances biocompatibility. [Display omitted] •Pre-treatment with different cell culture solutions controls the surface chemistry of crystallized 45S5 Bioglass®.•XRD and FT-IR show a range of surface calcium phosphate phases are formed.•Pre-treatment conditions also determine bone-forming MG-63 osteoblastic cell proliferation, viability and adhesion.•The results clarify differences between in vitro bioactivity of sintered Bioglass in cell culture solutions.</description><subject>Apatite</subject><subject>Bioactive glass</subject><subject>Biocompatibility</subject><subject>Biocompatible Materials - chemistry</subject><subject>Bioglass</subject><subject>Biological activity</subject><subject>Biomedical materials</subject><subject>Biotechnology</subject><subject>Body fluids</subject><subject>Body weight loss</subject><subject>Bone growth</subject><subject>Buffers</subject><subject>Calcium</subject><subject>Calcium phosphates</subject><subject>Calcium Phosphates - chemistry</subject><subject>Cell Adhesion</subject><subject>Cell culture</subject><subject>Cell Line</subject><subject>Cell Proliferation</subject><subject>Ceramics - chemistry</subject><subject>Chemical precipitation</subject><subject>Comparative studies</subject><subject>Conditioning</subject><subject>Crystallization</subject><subject>Culture media</subject><subject>Culture Media - chemistry</subject><subject>Degradability</subject><subject>Dissolution</subject><subject>Humans</subject><subject>Hydrogen-Ion Concentration</subject><subject>In vitro methods and tests</subject><subject>In vivo methods and tests</subject><subject>Incubation</subject><subject>Materials science</subject><subject>Materials Testing</subject><subject>Microscopy, Electron, Scanning</subject><subject>Osteoblasts</subject><subject>Osteoblasts - cytology</subject><subject>Osteogenesis</subject><subject>Pretreatment</subject><subject>Regeneration</subject><subject>Regeneration (physiology)</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><subject>Surface layers</subject><subject>Surface reactivity</subject><subject>Surgical implants</subject><subject>Tissue culture</subject><subject>Tissues</subject><subject>Viability</subject><subject>Weight loss</subject><subject>X-Ray Diffraction</subject><issn>0928-4931</issn><issn>1873-0191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kTtvFDEUhS0EIkvgD1AgSzQUmcHvsSUaFIWHFIkGastj3wlezWOxPYmWjn-OJxsoKKgsHX33XN9zEHpJSUsJVW_37ZTBt4xQ3VLWEi4eoR3VHW8INfQx2hHDdCMMp2foWc57QpTmHXuKzjhRnTaE79Cvq2EAX_Ay4EOCpiRwZYL5XvDpmIsbx_gTAu7j4nyJt4BvRpczvovlO_YwjtivY1kT4AlCdHiZcS5p9Zt0gQPcJBdcH8dYjhfYzfdGfpkOrsST-hw9GdyY4cXDe46-fbj6evmpuf7y8fPl--vGC0ZLw-QQnNMEZKec5kLWs2hfT1eCMtlrZpQb-qCFUMo4Z2SAIDkVipsghAF-jt6cfA9p-bFCLnaKeTvAzbCs2TLaGaGkNLqir_9B98ua5vq7StW9kmi5UexE-bTknGCwhxQnl46WErsVZPd2K8huBVnKbC2oDr16sF77GtjfkT-NVODdCYCaxW2EZLOPMPsabqpF2bDE__n_Bnt0opY</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Thavornyutikarn, Boonlom</creator><creator>Feltis, Bryce</creator><creator>Wright, Paul F.A.</creator><creator>Turney, Terence W.</creator><general>Elsevier B.V</general><general>Elsevier BV</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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20190401</creationdate><title>Effect of pre-treatment of crystallized bioactive glass with cell culture media on structure, degradability, and biocompatibility</title><author>Thavornyutikarn, Boonlom ; 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The evaluation of in vitro bioactivity in physiological body fluids, whilst challenging, can offer some insights for developing the bone-bonding ability of these glasses in vivo. In this study, we investigated the influence of three different cell culture and tissue fluid-like solutions on the dissolution and calcium-phosphate (CaP) based re-precipitation behaviour at the glass-liquid interface. We also examined pre-treatment of BG with these biological solutions, and how its influence on bone-forming MG-63 osteoblastic cell proliferation, viability and adhesion. The biological solutions used in this comparative study were: commercial cell culture medium (DMEM), a DMEM solution without organic components (DML) and a simulated body fluid (SBF), incorporating TRIS-buffer. Incubation of BG in these solutions over 28 days resulted in differences in weight loss, solution pH and ion release, and the development of CaP-based surface layers. XRD and FT-IR analyses showed clear differences in the characteristics of the CaP-based coating layers formed by the different solutions. The interfacial reactivity between the glass and the solutions depended on the composition and properties of the solutions. The formation of the CaP layer occurred more rapidly in SBF due to the presence of TRIS-buffer, which also significantly accelerated glass dissolution, further reducing the BG mass in SBF. MG-63 osteoblasts proliferated and spread more rapidly across the surfaces of all pre-conditioned BG, compared to fresh BG. The experimental results of this work help clarify differences between in vitro bioactivity of BG observed in cell culture solutions and in vivo BG bioactivity. Pre-treatment of Bioglass with different cell culture solutions induces development of various calcium phosphate-based coating layers on the glass surface and enhances biocompatibility. [Display omitted] •Pre-treatment with different cell culture solutions controls the surface chemistry of crystallized 45S5 Bioglass®.•XRD and FT-IR show a range of surface calcium phosphate phases are formed.•Pre-treatment conditions also determine bone-forming MG-63 osteoblastic cell proliferation, viability and adhesion.•The results clarify differences between in vitro bioactivity of sintered Bioglass in cell culture solutions.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30678903</pmid><doi>10.1016/j.msec.2018.12.034</doi><tpages>10</tpages></addata></record>
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subjects Apatite
Bioactive glass
Biocompatibility
Biocompatible Materials - chemistry
Bioglass
Biological activity
Biomedical materials
Biotechnology
Body fluids
Body weight loss
Bone growth
Buffers
Calcium
Calcium phosphates
Calcium Phosphates - chemistry
Cell Adhesion
Cell culture
Cell Line
Cell Proliferation
Ceramics - chemistry
Chemical precipitation
Comparative studies
Conditioning
Crystallization
Culture media
Culture Media - chemistry
Degradability
Dissolution
Humans
Hydrogen-Ion Concentration
In vitro methods and tests
In vivo methods and tests
Incubation
Materials science
Materials Testing
Microscopy, Electron, Scanning
Osteoblasts
Osteoblasts - cytology
Osteogenesis
Pretreatment
Regeneration
Regeneration (physiology)
Spectroscopy, Fourier Transform Infrared
Surface layers
Surface reactivity
Surgical implants
Tissue culture
Tissues
Viability
Weight loss
X-Ray Diffraction
title Effect of pre-treatment of crystallized bioactive glass with cell culture media on structure, degradability, and biocompatibility
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