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3D printing of strontium-enriched biphasic calcium phosphate scaffolds for bone regeneration

dc.contributor.authorOliveira, Rodrigo L M S
dc.contributor.authorFerraz, Marcos C
dc.contributor.authorCardoso, Lais Medeiros [UNESP]
dc.contributor.authorLi, Zhongrui
dc.contributor.authorAlbers, Ana Paula F
dc.contributor.authorBottino, Marco C
dc.contributor.authorTrichês, Eliandra S
dc.date.accessioned2026-06-30T17:50:52Z
dc.date.issued2024-09-03
dc.description.abstractCalcium phosphate (CaP) scaffolds doping with therapeutic ions are one of the focuses of recent bone tissue engineering research. Among the therapeutic ions, strontium stands out for its role in bone remodeling. This work reports a simple method to produce Sr-doped 3D-printed CaP scaffolds, using Sr-doping to induce partial phase transformation from β-tricalcium phosphate (β-TCP) to hydroxyapatite (HA), resulting in a doped biphasic calcium phosphate (BCP) scaffold. Strontium carbonate (SrCO<sub>3</sub>) was incorporated in the formulation of the 3D-printing ink, studying β-TCP:SrO mass ratios of 100:0, 95:5, and 90:10 (named as β-TCP, β-TCP/5-Sr, and β-TCP/10-Sr, respectively). Adding SrCO<sub>3</sub> in the 3D-printing ink led to a slight increase in viscosity but did not affect its printability, resulting in scaffolds with a high printing fidelity compared to the computational design. Interestingly, Sr was incorporated into the lattice structure of the scaffolds, forming hydroxyapatite (HA). No residual SrO or SrCO<sub>3</sub> were observed in the XRD patterns of any composition, and HA was the majority phase of the β-TCP/10-Sr scaffolds. The addition of Sr increased the compression strength of the scaffolds, with both β-TCP/5-Sr and β-TCP/10-Sr performing better than the β-TCP. Overall, β-TCP/5-Sr presented higher mineralized nodules and mechanical strength, while β-TCP scaffolds presented superior cell viability. The incorporation of SrCO<sub>3</sub> in the ink formulation is a viable method to obtain Sr-BCP scaffolds. Thus, this approach could be explored with other CaP scaffolds aiming to optimize their performance and the addition of alternative therapeutic ions.
dc.description.affiliationBioceramics Laboratory, Instituto de Ciência e Tecnologia, Universidade Federal de São Paulo - UNIFESP, 12231-280, São José dos Campos, SP, Brazil.
dc.description.affiliationDepartment of Dental Materials and Prosthodontics, Araraquara School of Dentistry, Sao Paulo State University - UNESP, 14801-385, Araraquara, SP, Brazil; Department of Cariology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, 48109, USA.
dc.description.affiliationElectron Microbeam Analysis Laboratory, University of Michigan, Ann Arbor, MI, 48109, USA.
dc.description.affiliationDepartment of Cariology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, 48109, USA; Department of Biomedical Engineering, College of Engineering, University of Michigan, Ann Arbor, MI, 48109, USA. Electronic address: mbottino@umich.edu.
dc.description.affiliationBioceramics Laboratory, Instituto de Ciência e Tecnologia, Universidade Federal de São Paulo - UNIFESP, 12231-280, São José dos Campos, SP, Brazil; Department of Cariology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, 48109, USA. Electronic address: eliandra.sousa@unifesp.br.
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics, Araraquara School of Dentistry, Sao Paulo State University - UNESP, 14801-385, Araraquara, SP, Brazil; Department of Cariology, Restorative Sciences, and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, MI, 48109, USA.
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1175382721
dc.identifier.dimensionspub.1175382721
dc.identifier.doi10.1016/j.jmbbm.2024.106717
dc.identifier.issn1751-6161
dc.identifier.issn1878-0180
dc.identifier.orcid0000-0002-9886-8590
dc.identifier.orcid0000-0002-8655-6020
dc.identifier.orcid0000-0001-8740-2464
dc.identifier.orcid0000-0002-9923-8611
dc.identifier.orcid0000-0001-5371-7628
dc.identifier.pmid39243571
dc.identifier.urihttps://hdl.handle.net/11449/326928
dc.publisherElsevier
dc.relation.ispartofJournal of the Mechanical Behavior of Biomedical Materials; v. 160; p. 106717
dc.rights.accessRightsAcesso restritopt
dc.rights.sourceRightsclosed
dc.sourceDimensions
dc.title3D printing of strontium-enriched biphasic calcium phosphate scaffolds for bone regeneration
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt

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