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dc.contributor.authorTredwin, Christopher
dc.contributor.authorYoung, AM
dc.contributor.authorAbou Neel, EA
dc.contributor.authorGeorgiou, G
dc.contributor.authorKnowles, JC
dc.date.accessioned2016-03-08T08:58:08Z
dc.date.available2016-03-08T08:58:08Z
dc.date.issued2014-01
dc.identifier.issn0957-4530
dc.identifier.issn1573-4838
dc.identifier.urihttp://hdl.handle.net/10026.1/4378
dc.description.abstract

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 PO4 (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.

dc.format.extent47-53
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoeng
dc.publisherSpringer Science and Business Media LLC
dc.subjectApatites
dc.subjectBiocompatible Materials
dc.subjectBone Substitutes
dc.subjectCell Proliferation
dc.subjectCell Survival
dc.subjectCoated Materials, Biocompatible
dc.subjectCrystallization
dc.subjectDurapatite
dc.subjectGels
dc.subjectHumans
dc.subjectHydroxyapatites
dc.subjectMaterials Testing
dc.subjectProstheses and Implants
dc.subjectTitanium
dc.subjectTumor Cells, Cultured
dc.titleHydroxyapatite, fluor-hydroxyapatite and fluorapatite produced via the sol–gel method: dissolution behaviour and biological properties after crystallisation
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000329657900005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue1
plymouth.volume25
plymouth.publication-statusPublished
plymouth.journalJournal of Materials Science: Materials in Medicine
dc.identifier.doi10.1007/s10856-013-5050-y
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Dental School
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA03 Allied Health Professions, Dentistry, Nursing and Pharmacy
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeUnited States
dcterms.dateAccepted2013-09-07
dc.identifier.eissn1573-4838
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1007/s10856-013-5050-y
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2014-01
rioxxterms.typeJournal Article/Review


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