Preclinical Evaluation of an Innovative Bone Graft of Marine Origin for the Treatment of Critical-Sized Bone Defects in an Animal Model

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Anatomía, Produción Animal e Ciencias Clínicas Veterinariasgl
dc.contributor.authorOtero Pérez, Rafael
dc.contributor.authorPermuy Mendaña, María
dc.contributor.authorLópez Senra, Estefanía
dc.contributor.authorLópez Álvarez, Miriam
dc.contributor.authorLópez Peña, Mónica
dc.contributor.authorSerra, Julia
dc.contributor.authorGonzález Cantalapiedra, Antonio
dc.contributor.authorMuñoz Guzón, Fernando María
dc.contributor.authorGonzález, Pío
dc.date.accessioned2021-03-12T13:50:29Z
dc.date.available2021-03-12T13:50:29Z
dc.date.issued2021
dc.description.abstractAutogenous cancellous bone graft is the current gold standard of treatment for the management of bone defects since it possesses the properties of osteoinduction, osteoconduction, and osteogenesis. Xenografts and synthetic grafts have been widely reported as available and low-cost alternatives, which retain good osteoconductive and mechanical properties. Given the rich biodiversity of ocean organisms, marine sources are of particular interest in the search for alternative bone grafts with enhanced functionalities. The purpose of this paper is to assess the biocompatibility of a marine-derived bone graft obtained from shark tooth, which is an environmentally sustainable and abundant raw material from fishing. This research presents the findings of a preclinical trial—following UNE-EN ISO 10993—that induced a critical-sized bone defect in a rabbit model and compared the results with a commercial bovine-derived bone graft. Evaluation by micro-computed tomography and histomorphometric analysis 12 weeks after implantation revealed good osseointegration, with no signs of inflammatory foreign body reactions, fibrosis, or necrosis in any of the cases. The shark tooth-derived bone graft yielded significantly higher new bone mineral density values (54 ± 6%) than the control (27 ± 8%). Moreover, the percentage of intersection values were much higher (86 ± 8%) than the bovine-derived bone graft (30 ± 1%) used as control. The area of occupancy by bone tissue in the test material (38 ± 5%) also gave higher values than the control (30 ± 6%). The role of physicochemical properties, biphasic structure, and composition on the stimulation of bone regeneration is also discussedgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThis research was funded by Xunta de Galicia, grants IN855A 2016/06 (Programa Ignicia–GAIN), ED431C 2017/51 (Competitive Reference Groups) and ED431D 2017/13 (Research networks); and by European Union Interreg Programs, projects IBEROS (0245_IBEROS_1_E, POCTEP 2015), CVMar+i (0302_CVMAR_I_1_P, POCTEP 2015) and BLUEHUMAN (EAPA_151/2016, Atlantic Area 2016)gl
dc.identifier.citationAppl. Sci. 2021, 11(5), 2116; https://doi.org/10.3390/app11052116gl
dc.identifier.doi10.3390/app11052116
dc.identifier.essn2076-3417
dc.identifier.urihttp://hdl.handle.net/10347/24733
dc.language.isoenggl
dc.publisherMDPIgl
dc.relation.publisherversionhttps://doi.org/10.3390/app11052116gl
dc.rights© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)gl
dc.rightsAtribución 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectMarine bone graftgl
dc.subjectPreclinical trialgl
dc.subjectCalcium phosphategl
dc.subjectOsseointegrationgl
dc.subjectBiomaterialgl
dc.titlePreclinical Evaluation of an Innovative Bone Graft of Marine Origin for the Treatment of Critical-Sized Bone Defects in an Animal Modelgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
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relation.isAuthorOfPublication840bdd31-d439-4626-9073-4b0703cd282f
relation.isAuthorOfPublication50937d7f-dd85-4b44-8dc3-58cf414271f5
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relation.isAuthorOfPublication.latestForDiscovery0af5ddde-272e-4d11-9ed7-0a8bf2f81d18

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