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New MAO coatings on multiprincipal equimassic β TiNbTaZr and TiNbTaZrMo alloys

dc.contributor.authorSantos, Rafael F.M. dos
dc.contributor.authorKuroda, Pedro A.B.
dc.contributor.authorAlmeida, Gerson S. de [UNESP]
dc.contributor.authorZambuzzi, Willian Fernando [UNESP]
dc.contributor.authorGrandini, Carlos R. [UNESP]
dc.contributor.authorAfonso, Conrado R.M.
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)pt
dc.date.accessioned2026-08-04T14:14:15Z
dc.date.issued2025-06-01
dc.description.abstractβ titanium alloys are essential in biomedical applications due to their combination of high strength, low elastic modulus, and biocompatibility. Although high-entropy alloys (BioHEAs) containing Nb, Zr, Ta, and Mo offer high mechanical strength, their elevated elastic modulus can lead to stress shielding in orthopedic applications. To address these limitations, β-stable alloys with enhanced mechanical and surface properties are being developed to support osseointegration and cellular adhesion. The work focuses on innovative medium (MEA) and high entropy (HEA) equimassic β Ti alloys (quaternary Ti-25Ta-25Nb-25Zr and quinary Ti-20Zr-20Ta-20Nb-20Mo in wt.%) treated with micro-arc oxidation (MAO) to optimize their performance as biomaterials. The MAO process generated bioactive coatings enriched with Ca, P, and Mg, promoting bone cell proliferation. X-ray diffraction (XRD) identified β phase structures and revealed amorphous or partially crystalline coatings, with a ZrO₂ cubic phase noted in the MEA quaternary Ti-25Ta-25Nb-25Zr alloy. Surface morphology assessments showed porous and lamellar topographies that varied with alloy composition, resulting in increased hydrophilicity and optimal roughness. Confocal microscopy confirmed that the MAO coating thickness on MEA quaternary Ti-25Ta-25Nb-25Zr (10.4 μm) surpassed that on HEA (high entropy alloy) quinary Ti-20Zr-20Ta-20Nb-20Mo (4.2 μm). Cell viability and adhesion assays indicated significant biocompatibility, particularly for MEA (medium entropy alloy) quaternary Ti-25Ta-25Nb-25Zr, which benefits from a Mo-free composition. These results underscore the potential of these multiprincipal equimassic bcc (body centered cubic) β alloys for biomedical applications, possibly enhancing osteoblast attachment and sustain cell viability effectively.
dc.description.affiliationUFSCar – Universidade Federal de São Carlos, Materials Engineering Department (DEMa), 13565-905, São Carlos, SP, Brazil
dc.description.affiliationUNILA – Universidade Federal da Integração Latino-Americana, 85870-650, Foz do Iguaçu, PR, Brazil
dc.description.affiliationUNESP – Universidade Estadual Paulista, Laboratory of Bioassays and Cellular Dynamics, Department of Chemical Biological Sciences, Institute of Biosciences, 18618-687, Botucatu, SP, Brazil
dc.description.affiliationUNESP – Universidade Estadual Paulista, Laboratório de Anelasticidade e Biomateriais, 17033-360, Bauru, SP, Brazil
dc.description.affiliationUnespUNESP – Universidade Estadual Paulista, Laboratory of Bioassays and Cellular Dynamics, Department of Chemical Biological Sciences, Institute of Biosciences, 18618-687, Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP – Universidade Estadual Paulista, Laboratório de Anelasticidade e Biomateriais, 17033-360, Bauru, SP, Brazil
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1183407475
dc.identifier.dimensionspub.1183407475
dc.identifier.doi10.1016/j.bea.2024.100139
dc.identifier.issn2667-0992
dc.identifier.orcid0000-0003-1710-487X
dc.identifier.orcid0000-0001-9867-9186
dc.identifier.orcid0000-0002-0208-0441
dc.identifier.orcid0000-0002-4149-5965
dc.identifier.orcid0000-0002-3336-309X
dc.identifier.orcid0000-0001-7505-8467
dc.identifier.urihttps://hdl.handle.net/11449/329026
dc.publisherElsevier
dc.relation.ispartofBiomedical Engineering Advances; v. 9; p. 100139
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightsgold
dc.sourceDimensions
dc.titleNew MAO coatings on multiprincipal equimassic β TiNbTaZr and TiNbTaZrMo alloys
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationab63624f-c491-4ac7-bd2c-767f17ac838d
relation.isOrgUnitOfPublication.latestForDiscoveryab63624f-c491-4ac7-bd2c-767f17ac838d
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt

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