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Article: Effects of fluoridation of porcine hydroxyapatite on osteoblastic activity of human MG63 cells

TitleEffects of fluoridation of porcine hydroxyapatite on osteoblastic activity of human MG63 cells
Authors
Keywordsbiological hydroxyapatite
fluoridation
materialcell interactions
osteoblasts
porcine hydroxyapatite
Issue Date2015
Citation
Science and Technology of Advanced Materials, 2015, v. 16, n. 3, article no. 035006 How to Cite?
AbstractBiological hydroxyapatite, derived from animal bones, is the most widely used bone substitute in orthopedic and dental treatments. Fluorine is the trace element involved in bone remodeling and has been confirmed to promote osteogenesis when administered at the appropriate dose. To take advantage of this knowledge, fluorinated porcine hydroxyapatite (FPHA) incorporating increasing levels of fluoride was derived from cancellous porcine bone through straightforward chemical and thermal treatments. Physiochemical characteristics, including crystalline phases, functional groups and dissolution behavior, were investigated on this novel FPHA. Human osteoblast-like MG63 cells were cultured on the FPHA to examine cell attachment, cytoskeleton, proliferation and osteoblastic differentiation for in vitro cellular evaluation. Results suggest that fluoride ions released from the FPHA play a significant role in stimulating osteoblastic activity in vitro, and appropriate level of fluoridation (1.5 to 3.1 atomic percents of fluorine) for the FPHA could be selected with high potential for use as a bone substitute.
Persistent Identifierhttp://hdl.handle.net/10722/311398
ISSN
2021 Impact Factor: 7.821
2020 SCImago Journal Rankings: 1.693
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLi, Zhipeng-
dc.contributor.authorHuang, Baoxin-
dc.contributor.authorMai, Sui-
dc.contributor.authorWu, Xiayi-
dc.contributor.authorZhang, Hanqing-
dc.contributor.authorQiao, Wei-
dc.contributor.authorLuo, Xin-
dc.contributor.authorChen, Zhuofan-
dc.date.accessioned2022-03-22T11:53:50Z-
dc.date.available2022-03-22T11:53:50Z-
dc.date.issued2015-
dc.identifier.citationScience and Technology of Advanced Materials, 2015, v. 16, n. 3, article no. 035006-
dc.identifier.issn1468-6996-
dc.identifier.urihttp://hdl.handle.net/10722/311398-
dc.description.abstractBiological hydroxyapatite, derived from animal bones, is the most widely used bone substitute in orthopedic and dental treatments. Fluorine is the trace element involved in bone remodeling and has been confirmed to promote osteogenesis when administered at the appropriate dose. To take advantage of this knowledge, fluorinated porcine hydroxyapatite (FPHA) incorporating increasing levels of fluoride was derived from cancellous porcine bone through straightforward chemical and thermal treatments. Physiochemical characteristics, including crystalline phases, functional groups and dissolution behavior, were investigated on this novel FPHA. Human osteoblast-like MG63 cells were cultured on the FPHA to examine cell attachment, cytoskeleton, proliferation and osteoblastic differentiation for in vitro cellular evaluation. Results suggest that fluoride ions released from the FPHA play a significant role in stimulating osteoblastic activity in vitro, and appropriate level of fluoridation (1.5 to 3.1 atomic percents of fluorine) for the FPHA could be selected with high potential for use as a bone substitute.-
dc.languageeng-
dc.relation.ispartofScience and Technology of Advanced Materials-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectbiological hydroxyapatite-
dc.subjectfluoridation-
dc.subjectmaterialcell interactions-
dc.subjectosteoblasts-
dc.subjectporcine hydroxyapatite-
dc.titleEffects of fluoridation of porcine hydroxyapatite on osteoblastic activity of human MG63 cells-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1088/1468-6996/16/3/035006-
dc.identifier.pmid27877807-
dc.identifier.pmcidPMC5099844-
dc.identifier.scopuseid_2-s2.0-84937945912-
dc.identifier.volume16-
dc.identifier.issue3-
dc.identifier.spagearticle no. 035006-
dc.identifier.epagearticle no. 035006-
dc.identifier.isiWOS:000357424000027-

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