A rapid method for the generation of uniform acellular bone explants: a technical note

<p>Abstract</p> <p>Background</p> <p>Bone graft studies lack standardized controls. We aim to present a quick and reliable method for the intra-operative generation of acellular bone explants.</p> <p>Methods</p> <p>Therefore, ovine cancellous bon...

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Main Authors: Simpson Angharad E, Furlong Pamela I, Braunstein Volker, Jähn Katharina, Richards R Geoff, Stoddart Martin J
Format: Article
Language:English
Published: BMC 2010-05-01
Series:Journal of Orthopaedic Surgery and Research
Online Access:http://www.josr-online.com/content/5/1/32
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spelling doaj-d6954cf41b3b4a7f82590b2e3960cc752020-11-24T23:27:18ZengBMCJournal of Orthopaedic Surgery and Research1749-799X2010-05-01513210.1186/1749-799X-5-32A rapid method for the generation of uniform acellular bone explants: a technical noteSimpson Angharad EFurlong Pamela IBraunstein VolkerJähn KatharinaRichards R GeoffStoddart Martin J<p>Abstract</p> <p>Background</p> <p>Bone graft studies lack standardized controls. We aim to present a quick and reliable method for the intra-operative generation of acellular bone explants.</p> <p>Methods</p> <p>Therefore, ovine cancellous bone explants from the iliac crest were prepared and used to test several methods for the induction of cell death. Over night heat inactivation was used as positive treatment control, methods to be investigated included UV light, or X- ray exposure, incubation in a hypotonic solution (salt-free water) and a short cycle of repeated freezing and thawing.</p> <p>Results</p> <p>Viability of treated and 2 days cultured bone explants was investigated by lactate dehydrogenase assay. Non-treated cultured control explants maintained around 50% osteocyte viability, while osteocyte survival after the positive treatment control was abolished. The most dramatic loss in cell viability, together with a low standard deviation, was a repeated cycle of freezing and thawing.</p> <p>Conclusions</p> <p>To summarize, we present a freeze-thaw method for the creation of acellular bone explants, which is easy to perform, not time-consuming and provides consistent results.</p> http://www.josr-online.com/content/5/1/32
collection DOAJ
language English
format Article
sources DOAJ
author Simpson Angharad E
Furlong Pamela I
Braunstein Volker
Jähn Katharina
Richards R Geoff
Stoddart Martin J
spellingShingle Simpson Angharad E
Furlong Pamela I
Braunstein Volker
Jähn Katharina
Richards R Geoff
Stoddart Martin J
A rapid method for the generation of uniform acellular bone explants: a technical note
Journal of Orthopaedic Surgery and Research
author_facet Simpson Angharad E
Furlong Pamela I
Braunstein Volker
Jähn Katharina
Richards R Geoff
Stoddart Martin J
author_sort Simpson Angharad E
title A rapid method for the generation of uniform acellular bone explants: a technical note
title_short A rapid method for the generation of uniform acellular bone explants: a technical note
title_full A rapid method for the generation of uniform acellular bone explants: a technical note
title_fullStr A rapid method for the generation of uniform acellular bone explants: a technical note
title_full_unstemmed A rapid method for the generation of uniform acellular bone explants: a technical note
title_sort rapid method for the generation of uniform acellular bone explants: a technical note
publisher BMC
series Journal of Orthopaedic Surgery and Research
issn 1749-799X
publishDate 2010-05-01
description <p>Abstract</p> <p>Background</p> <p>Bone graft studies lack standardized controls. We aim to present a quick and reliable method for the intra-operative generation of acellular bone explants.</p> <p>Methods</p> <p>Therefore, ovine cancellous bone explants from the iliac crest were prepared and used to test several methods for the induction of cell death. Over night heat inactivation was used as positive treatment control, methods to be investigated included UV light, or X- ray exposure, incubation in a hypotonic solution (salt-free water) and a short cycle of repeated freezing and thawing.</p> <p>Results</p> <p>Viability of treated and 2 days cultured bone explants was investigated by lactate dehydrogenase assay. Non-treated cultured control explants maintained around 50% osteocyte viability, while osteocyte survival after the positive treatment control was abolished. The most dramatic loss in cell viability, together with a low standard deviation, was a repeated cycle of freezing and thawing.</p> <p>Conclusions</p> <p>To summarize, we present a freeze-thaw method for the creation of acellular bone explants, which is easy to perform, not time-consuming and provides consistent results.</p>
url http://www.josr-online.com/content/5/1/32
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