Cargando…
A Biphasic Calcium Sulphate/Hydroxyapatite Carrier Containing Bone Morphogenic Protein-2 and Zoledronic Acid Generates Bone
In orthopedic surgery, large amount of diseased or injured bone routinely needs to be replaced. Autografts are mainly used but their availability is limited. Commercially available bone substitutes allow bone ingrowth but lack the capacity to induce bone formation. Thus, off-the-shelf osteoinductive...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870695/ https://www.ncbi.nlm.nih.gov/pubmed/27189411 http://dx.doi.org/10.1038/srep26033 |
_version_ | 1782432478519099392 |
---|---|
author | Raina, Deepak Bushan Isaksson, Hanna Hettwer, Werner Kumar, Ashok Lidgren, Lars Tägil, Magnus |
author_facet | Raina, Deepak Bushan Isaksson, Hanna Hettwer, Werner Kumar, Ashok Lidgren, Lars Tägil, Magnus |
author_sort | Raina, Deepak Bushan |
collection | PubMed |
description | In orthopedic surgery, large amount of diseased or injured bone routinely needs to be replaced. Autografts are mainly used but their availability is limited. Commercially available bone substitutes allow bone ingrowth but lack the capacity to induce bone formation. Thus, off-the-shelf osteoinductive bone substitutes that can replace bone grafts are required. We tested the carrier properties of a biphasic, calcium sulphate and hydroxyapatite ceramic material, containing a combination of recombinant human bone morphogenic protein-2 (rhBMP-2) to induce bone, and zoledronic acid (ZA) to delay early resorption. In-vitro, the biphasic material released 90% of rhBMP-2 and 10% of ZA in the first week. No major changes were found in the surface structure using scanning electron microscopy (SEM) or in the mechanical properties after adding rhBMP-2 or ZA. In-vivo bone formation was studied in an abdominal muscle pouch model in rats (n = 6/group). The mineralized volume was significantly higher when the biphasic material was combined with both rhBMP-2 and ZA (21.4 ± 5.5 mm(3)) as compared to rhBMP-2 alone (10.9 ± 2.1 mm(3)) when analyzed using micro computed tomography (μ-CT) (p < 0.01). In the clinical setting, the biphasic material combined with both rhBMP-2 and ZA can potentially regenerate large volumes of bone. |
format | Online Article Text |
id | pubmed-4870695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48706952016-06-01 A Biphasic Calcium Sulphate/Hydroxyapatite Carrier Containing Bone Morphogenic Protein-2 and Zoledronic Acid Generates Bone Raina, Deepak Bushan Isaksson, Hanna Hettwer, Werner Kumar, Ashok Lidgren, Lars Tägil, Magnus Sci Rep Article In orthopedic surgery, large amount of diseased or injured bone routinely needs to be replaced. Autografts are mainly used but their availability is limited. Commercially available bone substitutes allow bone ingrowth but lack the capacity to induce bone formation. Thus, off-the-shelf osteoinductive bone substitutes that can replace bone grafts are required. We tested the carrier properties of a biphasic, calcium sulphate and hydroxyapatite ceramic material, containing a combination of recombinant human bone morphogenic protein-2 (rhBMP-2) to induce bone, and zoledronic acid (ZA) to delay early resorption. In-vitro, the biphasic material released 90% of rhBMP-2 and 10% of ZA in the first week. No major changes were found in the surface structure using scanning electron microscopy (SEM) or in the mechanical properties after adding rhBMP-2 or ZA. In-vivo bone formation was studied in an abdominal muscle pouch model in rats (n = 6/group). The mineralized volume was significantly higher when the biphasic material was combined with both rhBMP-2 and ZA (21.4 ± 5.5 mm(3)) as compared to rhBMP-2 alone (10.9 ± 2.1 mm(3)) when analyzed using micro computed tomography (μ-CT) (p < 0.01). In the clinical setting, the biphasic material combined with both rhBMP-2 and ZA can potentially regenerate large volumes of bone. Nature Publishing Group 2016-05-18 /pmc/articles/PMC4870695/ /pubmed/27189411 http://dx.doi.org/10.1038/srep26033 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Raina, Deepak Bushan Isaksson, Hanna Hettwer, Werner Kumar, Ashok Lidgren, Lars Tägil, Magnus A Biphasic Calcium Sulphate/Hydroxyapatite Carrier Containing Bone Morphogenic Protein-2 and Zoledronic Acid Generates Bone |
title | A Biphasic Calcium Sulphate/Hydroxyapatite Carrier Containing Bone Morphogenic Protein-2 and Zoledronic Acid Generates Bone |
title_full | A Biphasic Calcium Sulphate/Hydroxyapatite Carrier Containing Bone Morphogenic Protein-2 and Zoledronic Acid Generates Bone |
title_fullStr | A Biphasic Calcium Sulphate/Hydroxyapatite Carrier Containing Bone Morphogenic Protein-2 and Zoledronic Acid Generates Bone |
title_full_unstemmed | A Biphasic Calcium Sulphate/Hydroxyapatite Carrier Containing Bone Morphogenic Protein-2 and Zoledronic Acid Generates Bone |
title_short | A Biphasic Calcium Sulphate/Hydroxyapatite Carrier Containing Bone Morphogenic Protein-2 and Zoledronic Acid Generates Bone |
title_sort | biphasic calcium sulphate/hydroxyapatite carrier containing bone morphogenic protein-2 and zoledronic acid generates bone |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4870695/ https://www.ncbi.nlm.nih.gov/pubmed/27189411 http://dx.doi.org/10.1038/srep26033 |
work_keys_str_mv | AT rainadeepakbushan abiphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT isakssonhanna abiphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT hettwerwerner abiphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT kumarashok abiphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT lidgrenlars abiphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT tagilmagnus abiphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT rainadeepakbushan biphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT isakssonhanna biphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT hettwerwerner biphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT kumarashok biphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT lidgrenlars biphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone AT tagilmagnus biphasiccalciumsulphatehydroxyapatitecarriercontainingbonemorphogenicprotein2andzoledronicacidgeneratesbone |