Effect of varying the Mg with Ca content in highly porous phosphate-based glass microspheres
This paper reports on the role of phosphate-based glass (PBG) microspheres and their physicochemical properties including in vitro biological response to human mesenchymal stem cells (hMSCs). Solid and porous microspheres were prepared via a flame spheroidisation process. The Mg content in the PBG f...
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description | This paper reports on the role of phosphate-based glass (PBG) microspheres and their physicochemical properties including in vitro biological response to human mesenchymal stem cells (hMSCs). Solid and porous microspheres were prepared via a flame spheroidisation process. The Mg content in the PBG formulations explored was reduced from 24 to 2 mol% with a subsequent increase in Ca content. A small quantity of TiO2 (1 mol%) was added to the lower Mg-content glass (2 mol%) to avoid crystallisation. Morphological and physical characterisation of porous microspheres revealed interconnected porosity (up to 76 ± 5 %), average external pore sizes of 55 ± 5 μm with surface areas ranging from 0.38 to 0.43 m2 g−1. Degradation and ion release studies conducted compared the solid (non-porous) and porous microspheres and revealed 1.5 to 2.5 times higher degradation rate for porous microspheres. Also, in vitro bioactivity studies using simulated body fluid (SBF) revealed Ca/P ratios for porous microspheres of all three glass formulations were between 0.75 and 0.92 which were within the range suggested for precipitated amorphous calcium phosphate. Direct cell seeding and indirect cell culture studies (via incubation with microsphere degradation products) revealed hMSCs were able to grow and undergo osteogenic differentiation in vitro, confirming cytocompatibility of the formulations tested. However, the higher Mg content (24 mol%) porous microsphere showed the most potent osteogenic response and is therefore considered as a promising candidate for bone repair applications.
[Display omitted]
•Porous phosphate glass microspheres were produced via flame spheroidisation.•Fully interconnected porosity of the microspheres was achieved (up to 76%).•Amorphous calcium phosphate formed on the porous microspheres.•Microspheres were able to incorporate and support stem cells within the pores. |
doi_str_mv | 10.1016/j.msec.2020.111668 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2487152527</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0928493120335864</els_id><sourcerecordid>2487152527</sourcerecordid><originalsourceid>FETCH-LOGICAL-c428t-cb6b1fb1412784bc3c159ff51893392f27af7edcefa4e6b5be53c082df11b2123</originalsourceid><addsrcrecordid>eNp9kU2LFDEQhoMo7rj6BzxIwIuXHlOV_kiDFxnWD1jxojchJOnKdIb-MulZ2X9vmlk9ePBUUDz1UvUUYy9B7EFA_fa0HxO5PQrMDYC6Vo_YDlQjCwEtPGY70aIqylbCFXuW0kmIWskGn7IrKauyUlLu2I8b78mtfPb8zsT7MB352hP_cuS_wtrzg-FunlaaVh4m3odjP9zzZY7zOfGln9PSm5UKaxJ1_DiYlPgYXNz6FCk9Z0-8GRK9eKjX7PuHm2-HT8Xt14-fD-9vC1eiWgtnawveQgnYqNI66aBqva9AtVK26LExvqHOkTcl1bayVEknFHYewCKgvGZvLrlLnH-eKa16DMnRMJiJ8qYaS9VAhRU2GX39D3qaz3HK22WqbRBlW0Om8EJtt6RIXi8xjNmPBqE39_qkN_d6c68v7vPQq4fosx2p-zvyR3YG3l0Ayi7uAkWdXKDJURdi_oHu5vC__N9D05T1</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2497223961</pqid></control><display><type>article</type><title>Effect of varying the Mg with Ca content in highly porous phosphate-based glass microspheres</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Islam, Md Towhidul ; Macri-Pellizzeri, Laura ; Hossain, Kazi M. Zakir ; Sottile, Virginie ; Ahmed, Ifty</creator><creatorcontrib>Islam, Md Towhidul ; Macri-Pellizzeri, Laura ; Hossain, Kazi M. Zakir ; Sottile, Virginie ; Ahmed, Ifty</creatorcontrib><description>This paper reports on the role of phosphate-based glass (PBG) microspheres and their physicochemical properties including in vitro biological response to human mesenchymal stem cells (hMSCs). Solid and porous microspheres were prepared via a flame spheroidisation process. The Mg content in the PBG formulations explored was reduced from 24 to 2 mol% with a subsequent increase in Ca content. A small quantity of TiO2 (1 mol%) was added to the lower Mg-content glass (2 mol%) to avoid crystallisation. Morphological and physical characterisation of porous microspheres revealed interconnected porosity (up to 76 ± 5 %), average external pore sizes of 55 ± 5 μm with surface areas ranging from 0.38 to 0.43 m2 g−1. Degradation and ion release studies conducted compared the solid (non-porous) and porous microspheres and revealed 1.5 to 2.5 times higher degradation rate for porous microspheres. Also, in vitro bioactivity studies using simulated body fluid (SBF) revealed Ca/P ratios for porous microspheres of all three glass formulations were between 0.75 and 0.92 which were within the range suggested for precipitated amorphous calcium phosphate. Direct cell seeding and indirect cell culture studies (via incubation with microsphere degradation products) revealed hMSCs were able to grow and undergo osteogenic differentiation in vitro, confirming cytocompatibility of the formulations tested. However, the higher Mg content (24 mol%) porous microsphere showed the most potent osteogenic response and is therefore considered as a promising candidate for bone repair applications.
[Display omitted]
•Porous phosphate glass microspheres were produced via flame spheroidisation.•Fully interconnected porosity of the microspheres was achieved (up to 76%).•Amorphous calcium phosphate formed on the porous microspheres.•Microspheres were able to incorporate and support stem cells within the pores.</description><identifier>ISSN: 0928-4931</identifier><identifier>EISSN: 1873-0191</identifier><identifier>DOI: 10.1016/j.msec.2020.111668</identifier><identifier>PMID: 33545833</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Bioactivity ; Biocompatibility ; Biological activity ; Biological properties ; Biomedical materials ; Body fluids ; Bone healing ; Calcium ; Calcium phosphates ; Cell culture ; Crystallization ; Cytocompatibility ; Degradation ; Degradation products ; Differentiation (biology) ; Glass ; Humans ; In vitro methods and tests ; Incubation ; Ion release ; Magnesium ; Materials science ; Mesenchyme ; Microspheres ; Osteogenesis ; Osteogenic differentiation ; Phosphates ; Physicochemical properties ; Porosity ; Porous microspheres ; Spheroidizing ; Stem cells ; Thermal properties ; Titanium dioxide</subject><ispartof>Materials Science & Engineering C, 2021-01, Vol.120, p.111668-111668, Article 111668</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright © 2020 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Jan 2021</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-cb6b1fb1412784bc3c159ff51893392f27af7edcefa4e6b5be53c082df11b2123</citedby><cites>FETCH-LOGICAL-c428t-cb6b1fb1412784bc3c159ff51893392f27af7edcefa4e6b5be53c082df11b2123</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.2020.111668$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33545833$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Islam, Md Towhidul</creatorcontrib><creatorcontrib>Macri-Pellizzeri, Laura</creatorcontrib><creatorcontrib>Hossain, Kazi M. Zakir</creatorcontrib><creatorcontrib>Sottile, Virginie</creatorcontrib><creatorcontrib>Ahmed, Ifty</creatorcontrib><title>Effect of varying the Mg with Ca content in highly porous phosphate-based glass microspheres</title><title>Materials Science & Engineering C</title><addtitle>Mater Sci Eng C Mater Biol Appl</addtitle><description>This paper reports on the role of phosphate-based glass (PBG) microspheres and their physicochemical properties including in vitro biological response to human mesenchymal stem cells (hMSCs). Solid and porous microspheres were prepared via a flame spheroidisation process. The Mg content in the PBG formulations explored was reduced from 24 to 2 mol% with a subsequent increase in Ca content. A small quantity of TiO2 (1 mol%) was added to the lower Mg-content glass (2 mol%) to avoid crystallisation. Morphological and physical characterisation of porous microspheres revealed interconnected porosity (up to 76 ± 5 %), average external pore sizes of 55 ± 5 μm with surface areas ranging from 0.38 to 0.43 m2 g−1. Degradation and ion release studies conducted compared the solid (non-porous) and porous microspheres and revealed 1.5 to 2.5 times higher degradation rate for porous microspheres. Also, in vitro bioactivity studies using simulated body fluid (SBF) revealed Ca/P ratios for porous microspheres of all three glass formulations were between 0.75 and 0.92 which were within the range suggested for precipitated amorphous calcium phosphate. Direct cell seeding and indirect cell culture studies (via incubation with microsphere degradation products) revealed hMSCs were able to grow and undergo osteogenic differentiation in vitro, confirming cytocompatibility of the formulations tested. However, the higher Mg content (24 mol%) porous microsphere showed the most potent osteogenic response and is therefore considered as a promising candidate for bone repair applications.
[Display omitted]
•Porous phosphate glass microspheres were produced via flame spheroidisation.•Fully interconnected porosity of the microspheres was achieved (up to 76%).•Amorphous calcium phosphate formed on the porous microspheres.•Microspheres were able to incorporate and support stem cells within the pores.</description><subject>Bioactivity</subject><subject>Biocompatibility</subject><subject>Biological activity</subject><subject>Biological properties</subject><subject>Biomedical materials</subject><subject>Body fluids</subject><subject>Bone healing</subject><subject>Calcium</subject><subject>Calcium phosphates</subject><subject>Cell culture</subject><subject>Crystallization</subject><subject>Cytocompatibility</subject><subject>Degradation</subject><subject>Degradation products</subject><subject>Differentiation (biology)</subject><subject>Glass</subject><subject>Humans</subject><subject>In vitro methods and tests</subject><subject>Incubation</subject><subject>Ion release</subject><subject>Magnesium</subject><subject>Materials science</subject><subject>Mesenchyme</subject><subject>Microspheres</subject><subject>Osteogenesis</subject><subject>Osteogenic differentiation</subject><subject>Phosphates</subject><subject>Physicochemical properties</subject><subject>Porosity</subject><subject>Porous microspheres</subject><subject>Spheroidizing</subject><subject>Stem cells</subject><subject>Thermal properties</subject><subject>Titanium dioxide</subject><issn>0928-4931</issn><issn>1873-0191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2LFDEQhoMo7rj6BzxIwIuXHlOV_kiDFxnWD1jxojchJOnKdIb-MulZ2X9vmlk9ePBUUDz1UvUUYy9B7EFA_fa0HxO5PQrMDYC6Vo_YDlQjCwEtPGY70aIqylbCFXuW0kmIWskGn7IrKauyUlLu2I8b78mtfPb8zsT7MB352hP_cuS_wtrzg-FunlaaVh4m3odjP9zzZY7zOfGln9PSm5UKaxJ1_DiYlPgYXNz6FCk9Z0-8GRK9eKjX7PuHm2-HT8Xt14-fD-9vC1eiWgtnawveQgnYqNI66aBqva9AtVK26LExvqHOkTcl1bayVEknFHYewCKgvGZvLrlLnH-eKa16DMnRMJiJ8qYaS9VAhRU2GX39D3qaz3HK22WqbRBlW0Om8EJtt6RIXi8xjNmPBqE39_qkN_d6c68v7vPQq4fosx2p-zvyR3YG3l0Ayi7uAkWdXKDJURdi_oHu5vC__N9D05T1</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>Islam, Md Towhidul</creator><creator>Macri-Pellizzeri, Laura</creator><creator>Hossain, Kazi M. Zakir</creator><creator>Sottile, Virginie</creator><creator>Ahmed, Ifty</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>202101</creationdate><title>Effect of varying the Mg with Ca content in highly porous phosphate-based glass microspheres</title><author>Islam, Md Towhidul ; Macri-Pellizzeri, Laura ; Hossain, Kazi M. Zakir ; Sottile, Virginie ; Ahmed, Ifty</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-cb6b1fb1412784bc3c159ff51893392f27af7edcefa4e6b5be53c082df11b2123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Bioactivity</topic><topic>Biocompatibility</topic><topic>Biological activity</topic><topic>Biological properties</topic><topic>Biomedical materials</topic><topic>Body fluids</topic><topic>Bone healing</topic><topic>Calcium</topic><topic>Calcium phosphates</topic><topic>Cell culture</topic><topic>Crystallization</topic><topic>Cytocompatibility</topic><topic>Degradation</topic><topic>Degradation products</topic><topic>Differentiation (biology)</topic><topic>Glass</topic><topic>Humans</topic><topic>In vitro methods and tests</topic><topic>Incubation</topic><topic>Ion release</topic><topic>Magnesium</topic><topic>Materials science</topic><topic>Mesenchyme</topic><topic>Microspheres</topic><topic>Osteogenesis</topic><topic>Osteogenic differentiation</topic><topic>Phosphates</topic><topic>Physicochemical properties</topic><topic>Porosity</topic><topic>Porous microspheres</topic><topic>Spheroidizing</topic><topic>Stem cells</topic><topic>Thermal properties</topic><topic>Titanium dioxide</topic><toplevel>online_resources</toplevel><creatorcontrib>Islam, Md Towhidul</creatorcontrib><creatorcontrib>Macri-Pellizzeri, Laura</creatorcontrib><creatorcontrib>Hossain, Kazi M. Zakir</creatorcontrib><creatorcontrib>Sottile, Virginie</creatorcontrib><creatorcontrib>Ahmed, Ifty</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Materials Science & Engineering C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Islam, Md Towhidul</au><au>Macri-Pellizzeri, Laura</au><au>Hossain, Kazi M. Zakir</au><au>Sottile, Virginie</au><au>Ahmed, Ifty</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of varying the Mg with Ca content in highly porous phosphate-based glass microspheres</atitle><jtitle>Materials Science & Engineering C</jtitle><addtitle>Mater Sci Eng C Mater Biol Appl</addtitle><date>2021-01</date><risdate>2021</risdate><volume>120</volume><spage>111668</spage><epage>111668</epage><pages>111668-111668</pages><artnum>111668</artnum><issn>0928-4931</issn><eissn>1873-0191</eissn><abstract>This paper reports on the role of phosphate-based glass (PBG) microspheres and their physicochemical properties including in vitro biological response to human mesenchymal stem cells (hMSCs). Solid and porous microspheres were prepared via a flame spheroidisation process. The Mg content in the PBG formulations explored was reduced from 24 to 2 mol% with a subsequent increase in Ca content. A small quantity of TiO2 (1 mol%) was added to the lower Mg-content glass (2 mol%) to avoid crystallisation. Morphological and physical characterisation of porous microspheres revealed interconnected porosity (up to 76 ± 5 %), average external pore sizes of 55 ± 5 μm with surface areas ranging from 0.38 to 0.43 m2 g−1. Degradation and ion release studies conducted compared the solid (non-porous) and porous microspheres and revealed 1.5 to 2.5 times higher degradation rate for porous microspheres. Also, in vitro bioactivity studies using simulated body fluid (SBF) revealed Ca/P ratios for porous microspheres of all three glass formulations were between 0.75 and 0.92 which were within the range suggested for precipitated amorphous calcium phosphate. Direct cell seeding and indirect cell culture studies (via incubation with microsphere degradation products) revealed hMSCs were able to grow and undergo osteogenic differentiation in vitro, confirming cytocompatibility of the formulations tested. However, the higher Mg content (24 mol%) porous microsphere showed the most potent osteogenic response and is therefore considered as a promising candidate for bone repair applications.
[Display omitted]
•Porous phosphate glass microspheres were produced via flame spheroidisation.•Fully interconnected porosity of the microspheres was achieved (up to 76%).•Amorphous calcium phosphate formed on the porous microspheres.•Microspheres were able to incorporate and support stem cells within the pores.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>33545833</pmid><doi>10.1016/j.msec.2020.111668</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bioactivity Biocompatibility Biological activity Biological properties Biomedical materials Body fluids Bone healing Calcium Calcium phosphates Cell culture Crystallization Cytocompatibility Degradation Degradation products Differentiation (biology) Glass Humans In vitro methods and tests Incubation Ion release Magnesium Materials science Mesenchyme Microspheres Osteogenesis Osteogenic differentiation Phosphates Physicochemical properties Porosity Porous microspheres Spheroidizing Stem cells Thermal properties Titanium dioxide |
title | Effect of varying the Mg with Ca content in highly porous phosphate-based glass microspheres |
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