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Strontium enhances osseointegration of calcium phosphate cement: a histomorphometric pilot study in ovariectomized rats
BACKGROUND: Calcium phosphate cements are used frequently in orthopedic and dental surgeries. Strontium-containing drugs serve as systemic osteoblast-activating medication in various clinical settings promoting mechanical stability of the osteoporotic bone. METHODS: Strontium-containing calcium phos...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3680072/ https://www.ncbi.nlm.nih.gov/pubmed/23758869 http://dx.doi.org/10.1186/1749-799X-8-16 |
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author | Baier, Martin Staudt, Patric Klein, Roman Sommer, Ulrike Wenz, Robert Grafe, Ingo Meeder, Peter Jürgen Nawroth, Peter P Kasperk, Christian |
author_facet | Baier, Martin Staudt, Patric Klein, Roman Sommer, Ulrike Wenz, Robert Grafe, Ingo Meeder, Peter Jürgen Nawroth, Peter P Kasperk, Christian |
author_sort | Baier, Martin |
collection | PubMed |
description | BACKGROUND: Calcium phosphate cements are used frequently in orthopedic and dental surgeries. Strontium-containing drugs serve as systemic osteoblast-activating medication in various clinical settings promoting mechanical stability of the osteoporotic bone. METHODS: Strontium-containing calcium phosphate cement (SPC) and calcium phosphate cement (CPC) were compared regarding their local and systemic effects on bone tissue in a standard animal model for osteoporotic bone. A bone defect was created in the distal femoral metaphysis of 60 ovariectomized Sprague-Dawley rats. CPC and SPC were used to fill the defects in 30 rats in each group. Local effects were assessed by histomorphometry at the implant site. Systemic effects were assessed by bone mineral density (BMD) measurements at the contralateral femur and the spine. RESULTS: Faster osseointegration and more new bone formation were found for SPC as compared to CPC implant sites. SPC implants exhibited more cracks than CPC implants, allowing more bone formation within the implant. Contralateral femur BMD and spine BMD did not differ significantly between the groups. CONCLUSIONS: The addition of strontium to calcium phosphate stimulates bone formation in and around the implant. Systemic release of strontium from the SPC implants did not lead to sufficiently high serum strontium levels to induce significant systemic effects on bone mass in this rat model. |
format | Online Article Text |
id | pubmed-3680072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36800722013-06-13 Strontium enhances osseointegration of calcium phosphate cement: a histomorphometric pilot study in ovariectomized rats Baier, Martin Staudt, Patric Klein, Roman Sommer, Ulrike Wenz, Robert Grafe, Ingo Meeder, Peter Jürgen Nawroth, Peter P Kasperk, Christian J Orthop Surg Res Research Article BACKGROUND: Calcium phosphate cements are used frequently in orthopedic and dental surgeries. Strontium-containing drugs serve as systemic osteoblast-activating medication in various clinical settings promoting mechanical stability of the osteoporotic bone. METHODS: Strontium-containing calcium phosphate cement (SPC) and calcium phosphate cement (CPC) were compared regarding their local and systemic effects on bone tissue in a standard animal model for osteoporotic bone. A bone defect was created in the distal femoral metaphysis of 60 ovariectomized Sprague-Dawley rats. CPC and SPC were used to fill the defects in 30 rats in each group. Local effects were assessed by histomorphometry at the implant site. Systemic effects were assessed by bone mineral density (BMD) measurements at the contralateral femur and the spine. RESULTS: Faster osseointegration and more new bone formation were found for SPC as compared to CPC implant sites. SPC implants exhibited more cracks than CPC implants, allowing more bone formation within the implant. Contralateral femur BMD and spine BMD did not differ significantly between the groups. CONCLUSIONS: The addition of strontium to calcium phosphate stimulates bone formation in and around the implant. Systemic release of strontium from the SPC implants did not lead to sufficiently high serum strontium levels to induce significant systemic effects on bone mass in this rat model. BioMed Central 2013-06-07 /pmc/articles/PMC3680072/ /pubmed/23758869 http://dx.doi.org/10.1186/1749-799X-8-16 Text en Copyright © 2013 Baier et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Baier, Martin Staudt, Patric Klein, Roman Sommer, Ulrike Wenz, Robert Grafe, Ingo Meeder, Peter Jürgen Nawroth, Peter P Kasperk, Christian Strontium enhances osseointegration of calcium phosphate cement: a histomorphometric pilot study in ovariectomized rats |
title | Strontium enhances osseointegration of calcium phosphate cement: a histomorphometric pilot study in ovariectomized rats |
title_full | Strontium enhances osseointegration of calcium phosphate cement: a histomorphometric pilot study in ovariectomized rats |
title_fullStr | Strontium enhances osseointegration of calcium phosphate cement: a histomorphometric pilot study in ovariectomized rats |
title_full_unstemmed | Strontium enhances osseointegration of calcium phosphate cement: a histomorphometric pilot study in ovariectomized rats |
title_short | Strontium enhances osseointegration of calcium phosphate cement: a histomorphometric pilot study in ovariectomized rats |
title_sort | strontium enhances osseointegration of calcium phosphate cement: a histomorphometric pilot study in ovariectomized rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3680072/ https://www.ncbi.nlm.nih.gov/pubmed/23758869 http://dx.doi.org/10.1186/1749-799X-8-16 |
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