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Calcium Sulphate/Hydroxyapatite Carrier for Bone Formation in the Femoral Neck of Osteoporotic Rats

This study investigated bone regeneration in the femoral neck canal of osteoporotic rats using a novel animal model. A calcium sulphate (CS)/hydroxyapatite (HA) carrier was used to deliver a bisphosphonate, zoledronic acid (ZA), locally, with or without added recombinant human bone morphogenic prote...

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Autores principales: Širka, Aurimas, Raina, Deepak Bushan, Isaksson, Hanna, Tanner, K. Elizabeth, Smailys, Alfredas, Kumar, Ashok, Tarasevičius, Šarūnas, Tägil, Magnus, Lidgren, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302674/
https://www.ncbi.nlm.nih.gov/pubmed/29855219
http://dx.doi.org/10.1089/ten.tea.2018.0075
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author Širka, Aurimas
Raina, Deepak Bushan
Isaksson, Hanna
Tanner, K. Elizabeth
Smailys, Alfredas
Kumar, Ashok
Tarasevičius, Šarūnas
Tägil, Magnus
Lidgren, Lars
author_facet Širka, Aurimas
Raina, Deepak Bushan
Isaksson, Hanna
Tanner, K. Elizabeth
Smailys, Alfredas
Kumar, Ashok
Tarasevičius, Šarūnas
Tägil, Magnus
Lidgren, Lars
author_sort Širka, Aurimas
collection PubMed
description This study investigated bone regeneration in the femoral neck canal of osteoporotic rats using a novel animal model. A calcium sulphate (CS)/hydroxyapatite (HA) carrier was used to deliver a bisphosphonate, zoledronic acid (ZA), locally, with or without added recombinant human bone morphogenic protein-2 (rhBMP-2). Twenty-eight-week-old ovariectomized Sprague–Dawley rats were used. A 1 mm diameter and 8 mm long defect was created in the femoral neck by drilling from the lateral cortex in the axis of the femoral neck, leaving the surrounding cortex intact. Three treatment groups and one control group were used: (1) CS/HA alone, (2) CS/HA + ZA (10 μg) (3) CS/HA + ZA (10 μg) + rhBMP-2 (4 μg), and (4) empty defect (control). The bone formation was assessed at 4 weeks post surgery using in vivo micro computed tomography (micro-CT). At 8 weeks post surgery, the animals were sacrificed, and both defect and contralateral femurs were subjected to micro-CT, mechanical testing, and histology. Micro-CT results showed that the combination of CS/HA with ZA or ZA + rhBMP-2 increased the bone formation in the defect when compared to the other groups and to the contralateral hips. Evidence of new dense bone formation in CS/HA + ZA and CS/HA + ZA + rhBMP-2 groups was seen histologically. Mechanical testing results showed no differences in the load to fracture between the treatments in either of the treated or contralateral legs. The CS/HA biomaterial can be used as a carrier for ZA and rhBMP-2 to regenerate bone in the femoral neck canal of osteoporotic rats.
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spelling pubmed-63026742018-12-26 Calcium Sulphate/Hydroxyapatite Carrier for Bone Formation in the Femoral Neck of Osteoporotic Rats Širka, Aurimas Raina, Deepak Bushan Isaksson, Hanna Tanner, K. Elizabeth Smailys, Alfredas Kumar, Ashok Tarasevičius, Šarūnas Tägil, Magnus Lidgren, Lars Tissue Eng Part A Original Articles This study investigated bone regeneration in the femoral neck canal of osteoporotic rats using a novel animal model. A calcium sulphate (CS)/hydroxyapatite (HA) carrier was used to deliver a bisphosphonate, zoledronic acid (ZA), locally, with or without added recombinant human bone morphogenic protein-2 (rhBMP-2). Twenty-eight-week-old ovariectomized Sprague–Dawley rats were used. A 1 mm diameter and 8 mm long defect was created in the femoral neck by drilling from the lateral cortex in the axis of the femoral neck, leaving the surrounding cortex intact. Three treatment groups and one control group were used: (1) CS/HA alone, (2) CS/HA + ZA (10 μg) (3) CS/HA + ZA (10 μg) + rhBMP-2 (4 μg), and (4) empty defect (control). The bone formation was assessed at 4 weeks post surgery using in vivo micro computed tomography (micro-CT). At 8 weeks post surgery, the animals were sacrificed, and both defect and contralateral femurs were subjected to micro-CT, mechanical testing, and histology. Micro-CT results showed that the combination of CS/HA with ZA or ZA + rhBMP-2 increased the bone formation in the defect when compared to the other groups and to the contralateral hips. Evidence of new dense bone formation in CS/HA + ZA and CS/HA + ZA + rhBMP-2 groups was seen histologically. Mechanical testing results showed no differences in the load to fracture between the treatments in either of the treated or contralateral legs. The CS/HA biomaterial can be used as a carrier for ZA and rhBMP-2 to regenerate bone in the femoral neck canal of osteoporotic rats. Mary Ann Liebert, Inc., publishers 2018-12-01 2018-12-03 /pmc/articles/PMC6302674/ /pubmed/29855219 http://dx.doi.org/10.1089/ten.tea.2018.0075 Text en © Aurimas Širka et al. 2018; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Širka, Aurimas
Raina, Deepak Bushan
Isaksson, Hanna
Tanner, K. Elizabeth
Smailys, Alfredas
Kumar, Ashok
Tarasevičius, Šarūnas
Tägil, Magnus
Lidgren, Lars
Calcium Sulphate/Hydroxyapatite Carrier for Bone Formation in the Femoral Neck of Osteoporotic Rats
title Calcium Sulphate/Hydroxyapatite Carrier for Bone Formation in the Femoral Neck of Osteoporotic Rats
title_full Calcium Sulphate/Hydroxyapatite Carrier for Bone Formation in the Femoral Neck of Osteoporotic Rats
title_fullStr Calcium Sulphate/Hydroxyapatite Carrier for Bone Formation in the Femoral Neck of Osteoporotic Rats
title_full_unstemmed Calcium Sulphate/Hydroxyapatite Carrier for Bone Formation in the Femoral Neck of Osteoporotic Rats
title_short Calcium Sulphate/Hydroxyapatite Carrier for Bone Formation in the Femoral Neck of Osteoporotic Rats
title_sort calcium sulphate/hydroxyapatite carrier for bone formation in the femoral neck of osteoporotic rats
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302674/
https://www.ncbi.nlm.nih.gov/pubmed/29855219
http://dx.doi.org/10.1089/ten.tea.2018.0075
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