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dc.rights.licenseopenen_US
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorMAUREL, Delphine B
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorFÉNELON, Mathilde
dc.contributor.authorAID-LAUNAIS, Rachida
dc.contributor.authorBIDAULT, Laurent
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorLE NIR, Alice
dc.contributor.authorRENARD, Martine
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorFRICAIN, Jean-Christophe
ORCID: 0000-0001-7855-6437
dc.contributor.authorLETOURNEUR, Didier
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorAMÉDÉE, Joëlle
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorCATROS, Sylvain
dc.date.accessioned2021-12-21T08:31:04Z
dc.date.available2021-12-21T08:31:04Z
dc.date.issued2021-01-01
dc.identifier.issn1552-4965en_US
dc.identifier.otherhttps://onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fjbm.a.37176&file=jbma37176-sup-0001-VideoS1.zipen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/124225
dc.description.abstractEnMicrobeads consisting of pullulan and dextran supplemented with hydroxyapatite have recently been developed for bone tissue engineering applications. Here, we evaluate the bone formation in two different preclinical models after injection of microbeads reconstituted with either saline buffer or autologous blood. Addition of saline solution or autologous blood to dried microbeads packaged into syringes allowed an easy injection. In the first rat bone defect model performed in the femoral condyle, microcomputed tomography performed after 30 and 60 days revealed an important mineralization process occurring around and within the core of the microbeads in both conditions. Bone volume/total volume measurements revealed no significant differences between the saline solution and the autologous blood groups. Histologically, osteoid tissue was evidenced around and in contact of the microbeads in both conditions. Using the sinus lift model performed in sheep, cone beam computed tomography revealed an important mineralization inside the sinus cavity for both groups after 3 months of implantation. Representative Masson trichrome staining images showed that bone formation occurs at the periphery and inside the microbeads in both conditions. Quantitative evaluation of the new bone formation displayed no significant differences between groups. In conclusion, reconstitution of microbeads with autologous blood did not enhance the regenerative capacity of these microbeads compared to the saline buffer group. This study is of particular interest for clinical applications in oral and maxillofacial surgery.
dc.language.isoENen_US
dc.subject.enbone regeneration
dc.subject.eninjectable matrix
dc.subject.ennatural polysaccharides
dc.subject.enoral surgery
dc.title.enBone regeneration in both small and large preclinical bone defect models using an injectable polymer-based substitute containing hydroxyapatite and reconstituted with saline or autologous blood.
dc.title.alternativeJ Biomed Mater Res Aen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/jbm.a.37176en_US
dc.subject.halSciences de l'ingénieur [physics]/Matériaux
dc.identifier.pubmed33797182en_US
bordeaux.journalJournal of Biomedical Materials Research Part Aen_US
bordeaux.page1840-1848en_US
bordeaux.volume109en_US
bordeaux.hal.laboratoriesBioingénierie Tissulaire (BioTis) - UMR_S 1026en_US
bordeaux.issue10en_US
bordeaux.institutionCNRSen_US
bordeaux.institutionINSERMen_US
bordeaux.institutionCHU de Bordeauxen_US
bordeaux.institutionInstitut Bergoniéen_US
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-03767019
hal.version1
hal.date.transferred2022-09-01T13:29:52Z
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Biomedical%20Materials%20Research%20Part%20A&rft.date=2021-01-01&rft.volume=109&rft.issue=10&rft.spage=1840-1848&rft.epage=1840-1848&rft.eissn=1552-4965&rft.issn=1552-4965&rft.au=MAUREL,%20Delphine%20B&F%C3%89NELON,%20Mathilde&AID-LAUNAIS,%20Rachida&BIDAULT,%20Laurent&LE%20NIR,%20Alice&rft.genre=article


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