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Hydroxyapatite, fluor-hydroxyapatite and fluorapatite produced via the sol–gel method: dissolution behaviour and biological properties after crystallisation

Hydroxyapatite (HA), fluor-hydroxyapatite (FHA) with varying levels of fluoride ion substitution and fluorapatite (FA) were synthesised by the sol–gel method as possible implant coating or bone-grafting materials. Calcium nitrate and triethyl phosphite were used as precursors under an ethanol–water...

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Autores principales: Tredwin, Christopher J., Young, Anne M., Abou Neel, Ensanya A., Georgiou, George, Knowles, Jonathan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890558/
https://www.ncbi.nlm.nih.gov/pubmed/24052344
http://dx.doi.org/10.1007/s10856-013-5050-y
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author Tredwin, Christopher J.
Young, Anne M.
Abou Neel, Ensanya A.
Georgiou, George
Knowles, Jonathan C.
author_facet Tredwin, Christopher J.
Young, Anne M.
Abou Neel, Ensanya A.
Georgiou, George
Knowles, Jonathan C.
author_sort Tredwin, Christopher J.
collection PubMed
description Hydroxyapatite (HA), fluor-hydroxyapatite (FHA) with varying levels of fluoride ion substitution and fluorapatite (FA) were synthesised by the sol–gel method as possible implant coating or bone-grafting materials. Calcium nitrate and triethyl phosphite were used as precursors under an ethanol–water based solution. Different amounts of ammonium fluoride were incorporated for the preparation of the FHA and FA sol–gels. After heating and powdering the sol–gels, dissolution behaviour was assessed using ion chromatography to measure Ca(2+) and PO(4) (3−) ion release. Biological behaviour was assessed using cellular proliferation with human osteosarcoma cells and alamarBlue™ assay. Statistical analysis was performed with a two way analysis of variance and post hoc testing with a Bonferroni correction. Increasing fluoride substitution into an apatite structure decreased the dissolution rate. Increasing the firing temperature of the HA, FHA and FA sol–gels up to 1,000 °C decreased the dissolution rate. There was significantly higher cellular proliferation on highly substituted FHA and FA than on HA or Titanium. The properties of an implant coating or bone grafting material can be tailored to meet specific requirements by altering the amount of fluoride that is incorporated into the original apatite structure. The dissolution behaviour can further be altered by the temperature at which the sol–gel is fired.
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spelling pubmed-38905582014-01-28 Hydroxyapatite, fluor-hydroxyapatite and fluorapatite produced via the sol–gel method: dissolution behaviour and biological properties after crystallisation Tredwin, Christopher J. Young, Anne M. Abou Neel, Ensanya A. Georgiou, George Knowles, Jonathan C. J Mater Sci Mater Med Article Hydroxyapatite (HA), fluor-hydroxyapatite (FHA) with varying levels of fluoride ion substitution and fluorapatite (FA) were synthesised by the sol–gel method as possible implant coating or bone-grafting materials. Calcium nitrate and triethyl phosphite were used as precursors under an ethanol–water based solution. Different amounts of ammonium fluoride were incorporated for the preparation of the FHA and FA sol–gels. After heating and powdering the sol–gels, dissolution behaviour was assessed using ion chromatography to measure Ca(2+) and PO(4) (3−) ion release. Biological behaviour was assessed using cellular proliferation with human osteosarcoma cells and alamarBlue™ assay. Statistical analysis was performed with a two way analysis of variance and post hoc testing with a Bonferroni correction. Increasing fluoride substitution into an apatite structure decreased the dissolution rate. Increasing the firing temperature of the HA, FHA and FA sol–gels up to 1,000 °C decreased the dissolution rate. There was significantly higher cellular proliferation on highly substituted FHA and FA than on HA or Titanium. The properties of an implant coating or bone grafting material can be tailored to meet specific requirements by altering the amount of fluoride that is incorporated into the original apatite structure. The dissolution behaviour can further be altered by the temperature at which the sol–gel is fired. Springer US 2013-09-20 2014 /pmc/articles/PMC3890558/ /pubmed/24052344 http://dx.doi.org/10.1007/s10856-013-5050-y Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Tredwin, Christopher J.
Young, Anne M.
Abou Neel, Ensanya A.
Georgiou, George
Knowles, Jonathan C.
Hydroxyapatite, fluor-hydroxyapatite and fluorapatite produced via the sol–gel method: dissolution behaviour and biological properties after crystallisation
title Hydroxyapatite, fluor-hydroxyapatite and fluorapatite produced via the sol–gel method: dissolution behaviour and biological properties after crystallisation
title_full Hydroxyapatite, fluor-hydroxyapatite and fluorapatite produced via the sol–gel method: dissolution behaviour and biological properties after crystallisation
title_fullStr Hydroxyapatite, fluor-hydroxyapatite and fluorapatite produced via the sol–gel method: dissolution behaviour and biological properties after crystallisation
title_full_unstemmed Hydroxyapatite, fluor-hydroxyapatite and fluorapatite produced via the sol–gel method: dissolution behaviour and biological properties after crystallisation
title_short Hydroxyapatite, fluor-hydroxyapatite and fluorapatite produced via the sol–gel method: dissolution behaviour and biological properties after crystallisation
title_sort hydroxyapatite, fluor-hydroxyapatite and fluorapatite produced via the sol–gel method: dissolution behaviour and biological properties after crystallisation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890558/
https://www.ncbi.nlm.nih.gov/pubmed/24052344
http://dx.doi.org/10.1007/s10856-013-5050-y
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