Papers

Open access
Sep, 2005

In vivo effect of fluoride-substituted apatite on rat bone

Dental Materials Journal
  • Miho Inoue
  • ,
  • Hitoshi Nagatsuka
  • ,
  • Hidetsugu Tsujigiwa
  • ,
  • Masahisa Inoue
  • ,
  • Racquel Z. LeGeros
  • ,
  • Toshio Yamamoto
  • ,
  • Noriyuki Nagai

Volume
24
Number
3
First page
398
Last page
402
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.4012/dmj.24.398
Publisher
JAPANESE SOC DENTAL MATERIALS DEVICES

Different types of calcium phosphate compounds are commercially available for medical and dental applications as bone substitute materials. Biological apatites contain several kinds of minor elements such as carbonate (CO 3), magnesium (Mg), and fluoride (F) in enamel, dentin, and bone. It has been shown that F ion and F-substituted apatite promoted osteoblast proliferation and inhibited osteoclast cell activity. The purpose of this study was to investigate the in vivo rat tibia activity on F-substituted apatite (FAp). Apatites of unsintered calcium deficient apatite (CDA), and FAps, with low, medium, and high F concentrations, were implanted in rat tibia for 1 and 2 weeks. Implanted tissues were embedded in paraffin blocks, stained with hematoxylin-eosin and histomorphometrically observed. Results showed that low F concentration induced better and faster new bone formation in vivo compared to CDA. Therefore the results suggested that F as a minor element in bone rendered a suitable effect on bone formation in vivo.

Link information
DOI
https://doi.org/10.4012/dmj.24.398
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/16279730
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000233090800016&DestApp=WOS_CPL
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=28844507494&origin=inward Open access
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=28844507494&origin=inward
ID information
  • DOI : 10.4012/dmj.24.398
  • ISSN : 0287-4547
  • Pubmed ID : 16279730
  • SCOPUS ID : 28844507494
  • Web of Science ID : WOS:000233090800016

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