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The Influence of 1α.25-Dihydroxyvitamin D3 Coating on Implant Osseointegration in the Rabbit Tibia

OBJECTIVES: This study aims to evaluate bone response to an implant surface modified by 1α,25-dihydroxyvitamin D3 [1.25-(OH)(2)D(3)] in vivo and the potential link between 1.25-(OH) 2D3 surface concentration and bone response. MATERIAL AND METHODS: Twenty-eight implants were divided into 4 groups (1...

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Autores principales: Naito, Yoshihito, Jimbo, Ryo, Bryington, Matthew S., Vandeweghe, Stefan, Chrcanovic, Bruno R., Tovar, Nick, Ichikawa, Tetsuo, Coelho, Paulo G., Wennerberg, Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Stilus Optimus 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219862/
https://www.ncbi.nlm.nih.gov/pubmed/25386230
http://dx.doi.org/10.5037/jomr.2014.5303
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author Naito, Yoshihito
Jimbo, Ryo
Bryington, Matthew S.
Vandeweghe, Stefan
Chrcanovic, Bruno R.
Tovar, Nick
Ichikawa, Tetsuo
Coelho, Paulo G.
Wennerberg, Ann
author_facet Naito, Yoshihito
Jimbo, Ryo
Bryington, Matthew S.
Vandeweghe, Stefan
Chrcanovic, Bruno R.
Tovar, Nick
Ichikawa, Tetsuo
Coelho, Paulo G.
Wennerberg, Ann
author_sort Naito, Yoshihito
collection PubMed
description OBJECTIVES: This study aims to evaluate bone response to an implant surface modified by 1α,25-dihydroxyvitamin D3 [1.25-(OH)(2)D(3)] in vivo and the potential link between 1.25-(OH) 2D3 surface concentration and bone response. MATERIAL AND METHODS: Twenty-eight implants were divided into 4 groups (1 uncoated control, 3 groups coated with 1.25-(OH)(2)D(3) in concentrations of 10(-8), 10(-7) and 10(-6) M respectively), placed in the rabbit tibia for 6 weeks. Topographical analyses were carried out on coated and uncoated discs using interferometer and atomic-force-microscope (AFM). Twenty-eight implants were histologically observed (bone-to-implant-contact [BIC] and new-bone-area [NBA]). RESULTS: The results showed that the 1.25-(OH)(2)D(3) coated implants presented a tendency to osseointegrate better than the non-coated surfaces, the differences were not significant (P > 0.05). CONCLUSIONS: The effect of 1.25-(OH)(2)D(3) coating to implants suggested possible dose dependent effects, however no statistical differences could be found. It is thought that the base substrate topography (turned) could not sustain sufficient amount of 1.25-(OH)(2)D(3) enough to present significant biologic responses. Thus, development a base substrate that can sustain 1.25-(OH)(2)D(3) for a long period is necessary in future studies.
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spelling pubmed-42198622014-11-10 The Influence of 1α.25-Dihydroxyvitamin D3 Coating on Implant Osseointegration in the Rabbit Tibia Naito, Yoshihito Jimbo, Ryo Bryington, Matthew S. Vandeweghe, Stefan Chrcanovic, Bruno R. Tovar, Nick Ichikawa, Tetsuo Coelho, Paulo G. Wennerberg, Ann J Oral Maxillofac Res Original Paper OBJECTIVES: This study aims to evaluate bone response to an implant surface modified by 1α,25-dihydroxyvitamin D3 [1.25-(OH)(2)D(3)] in vivo and the potential link between 1.25-(OH) 2D3 surface concentration and bone response. MATERIAL AND METHODS: Twenty-eight implants were divided into 4 groups (1 uncoated control, 3 groups coated with 1.25-(OH)(2)D(3) in concentrations of 10(-8), 10(-7) and 10(-6) M respectively), placed in the rabbit tibia for 6 weeks. Topographical analyses were carried out on coated and uncoated discs using interferometer and atomic-force-microscope (AFM). Twenty-eight implants were histologically observed (bone-to-implant-contact [BIC] and new-bone-area [NBA]). RESULTS: The results showed that the 1.25-(OH)(2)D(3) coated implants presented a tendency to osseointegrate better than the non-coated surfaces, the differences were not significant (P > 0.05). CONCLUSIONS: The effect of 1.25-(OH)(2)D(3) coating to implants suggested possible dose dependent effects, however no statistical differences could be found. It is thought that the base substrate topography (turned) could not sustain sufficient amount of 1.25-(OH)(2)D(3) enough to present significant biologic responses. Thus, development a base substrate that can sustain 1.25-(OH)(2)D(3) for a long period is necessary in future studies. Stilus Optimus 2014-10-01 /pmc/articles/PMC4219862/ /pubmed/25386230 http://dx.doi.org/10.5037/jomr.2014.5303 Text en Copyright © Naito Y, Jimbo R, Bryington MS, Vandeweghe S, Chrcanovic BR, Tovar N, Ichikawa T, Coelho PG, Wennerberg A. Published in the JOURNAL OF ORAL & MAXILLOFACIAL RESEARCH (http://www.ejomr.org), 1 October 2014. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article, first published in the JOURNAL OF ORAL & MAXILLOFACIAL RESEARCH, distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 UnportedLicense (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work and is properly cited. The copyright, license information and link to the original publication on (http://www.ejomr.org) must be included.
spellingShingle Original Paper
Naito, Yoshihito
Jimbo, Ryo
Bryington, Matthew S.
Vandeweghe, Stefan
Chrcanovic, Bruno R.
Tovar, Nick
Ichikawa, Tetsuo
Coelho, Paulo G.
Wennerberg, Ann
The Influence of 1α.25-Dihydroxyvitamin D3 Coating on Implant Osseointegration in the Rabbit Tibia
title The Influence of 1α.25-Dihydroxyvitamin D3 Coating on Implant Osseointegration in the Rabbit Tibia
title_full The Influence of 1α.25-Dihydroxyvitamin D3 Coating on Implant Osseointegration in the Rabbit Tibia
title_fullStr The Influence of 1α.25-Dihydroxyvitamin D3 Coating on Implant Osseointegration in the Rabbit Tibia
title_full_unstemmed The Influence of 1α.25-Dihydroxyvitamin D3 Coating on Implant Osseointegration in the Rabbit Tibia
title_short The Influence of 1α.25-Dihydroxyvitamin D3 Coating on Implant Osseointegration in the Rabbit Tibia
title_sort influence of 1α.25-dihydroxyvitamin d3 coating on implant osseointegration in the rabbit tibia
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219862/
https://www.ncbi.nlm.nih.gov/pubmed/25386230
http://dx.doi.org/10.5037/jomr.2014.5303
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