Enhanced Bone Healing in Critical-Sized Rabbit Femoral Defects: Impact of Helical and Alternate Scaffold Architectures

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Anatomía, Produción Animal e Ciencias Clínicas Veterinarias
dc.contributor.authorAlonso-Fernández, Iván
dc.contributor.authorJostein Haugen, Håvard
dc.contributor.authorParreiras Nogueira, Liebert
dc.contributor.authorLópez-Álvarez, Miriam
dc.contributor.authorGonzález, Pío
dc.contributor.authorLópez Peña, Mónica
dc.contributor.authorGonzález Cantalapiedra, Antonio
dc.contributor.authorMuñoz Guzón, Fernando María
dc.date.accessioned2025-01-27T10:58:31Z
dc.date.available2025-01-27T10:58:31Z
dc.date.issued2022-04-29
dc.description.abstractThis study investigates the effect of scaffold architecture on bone regeneration, focusing on 3D-printed polylactic acid–bioceramic calcium phosphate (PLA-bioCaP) composite scaffolds in rabbit femoral condyle critical defects. We explored two distinct scaffold designs to assess their influence on bone healing and scaffold performance. Structures with alternate (0°/90°) and helical (0°/45°/90°/135°/180°) laydown patterns were manufactured with a 3D printer using a fused deposition modeling technique. The scaffolds were meticulously characterized for pore size, strut thickness, porosity, pore accessibility, and mechanical properties. The in vivo efficacy of these scaffolds was evaluated using a femoral condyle critical defect model in eight skeletally mature New Zealand White rabbits. Then, the results were analyzed micro-tomographically, histologically, and histomorphometrically. Our findings indicate that both scaffold architectures are biocompatible and support bone formation. The helical scaffolds, characterized by larger pore sizes and higher porosity, demonstrated significantly greater bone regeneration than the alternate structures. However, their lower mechanical strength presented limitations for use in load-bearing sites.
dc.description.peerreviewedSI
dc.description.sponsorshipThis study was funded by the GRC support program from Xunta de Galicia (GRC ED431C 2021/19 and ED431C 2021/49) and the UE project IBEROS+ (0072_IBEROS_MAIS_1_E) financed by the POCTEP 2021-2027 FEDER program. Institutional Review Board Statement: The animal study protocol was approved by the Ethics Committee of University of Santiago de Compostela (protocol code: 02/20/LU-002 and date of approval: 12 May 2020). Data Availability Statement: Data supporting the reported results can be requested to the authors.. I.A. acknowledges the XUNTA de Galicia for his pre-doctoral contract (Ref. ED481A 2021/137) from Galician Government Consellería de Cultura, Educación e Universidades.
dc.identifier.citationAlonso-Fernández, I.; Haugen, H.J.; Nogueira, L.P.; López-Álvarez, M.; González, P.; López-Peña, M.; González-Cantalapiedra, A.; Muñoz-Guzón, F. Enhanced Bone Healing in Critical-Sized Rabbit Femoral Defects: Impact of Helical and Alternate Scaffold Architectures. Polymers 2024, 16, 1243. https://doi.org/10.3390/polym16091243
dc.identifier.doi10.3390/polym16091243
dc.identifier.issn2073-4360
dc.identifier.urihttps://hdl.handle.net/10347/39052
dc.issue.number9
dc.journal.titlePolymers
dc.language.isoeng
dc.publisherMDPI
dc.relation.projectIDi
dc.relation.publisherversionhttps://doi.org/10.3390/polym16091243
dc.rights© 2024 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 (https://creativecommons.org/licenses/by/4.0/).
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectPolylactic acid
dc.subjectBioceramic
dc.subject3D-printing technology
dc.subjectComposite scaffolds
dc.subjectScaffold architecture
dc.subjectBone regeneration
dc.titleEnhanced Bone Healing in Critical-Sized Rabbit Femoral Defects: Impact of Helical and Alternate Scaffold Architectures
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number19
dspace.entity.typePublication
relation.isAuthorOfPublication840bdd31-d439-4626-9073-4b0703cd282f
relation.isAuthorOfPublication50937d7f-dd85-4b44-8dc3-58cf414271f5
relation.isAuthorOfPublicationa80b7053-e349-4aaa-9aa0-fe8dc7043ac2
relation.isAuthorOfPublication.latestForDiscovery840bdd31-d439-4626-9073-4b0703cd282f

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