Surface modification of Ti40Cu40Zr11Fe3Sn3Ag3 amorphous alloy for enhanced biocompatibility in implant applications

dc.bibliographicCitation.firstPage2333
dc.bibliographicCitation.journalTitleJournal of Materials Research and Technology
dc.bibliographicCitation.lastPage2346
dc.bibliographicCitation.volume30
dc.contributor.authorTiwari, Kirti
dc.contributor.authorBlanquer, Andreu
dc.contributor.authorPavan, Cristina
dc.contributor.authorTomatis, Maura
dc.contributor.authorNavas, Nora Fernandez
dc.contributor.authorScaglione, Federico
dc.contributor.authorFiore, Gianluca
dc.contributor.authorTurci, Francesco
dc.contributor.authorNogués, Carme
dc.contributor.authorRizzi, Paola
dc.date.accessioned2024-10-15T08:49:06Z
dc.date.available2024-10-15T08:49:06Z
dc.date.issued2024
dc.description.abstractThis study focuses on the design of a new Ti based multicomponent amorphous alloy for the development of biocompatible implant materials with enhanced hemocompatibility and cytocompatibility. While this class of amorphous alloys has shown its potential for biomedical implant applications, there are major concerns due to the presence of elements such as copper which can lead to cytotoxicity in the human body during long term implantation. Nevertheless, copper is indispensable in the development of an amorphous alloy. Thus, the objective of this work is to selectively remove copper from the surface of the Ti40Cu40Zr11Fe3Sn3Ag3 (at%) amorphous alloy using the dealloying technique and produce a patterned protective passivated surface rich in Ti and Zr oxides. Nitric acid (HNO3) has been found to be effective in depleting copper from the sample surface. Optimization of treatment parameters such as temperature (70 °C and room temperature) yielded drastic differences in the morphology of the samples studied using Field-Emission Scanning Electron Microscopy. The treated sample surface demonstrated good hemocompatibility and cytocompatibility with primary human osteoblast cells (HOb) and human osteosarcoma cell line (Saos-2). Additionally, the treated samples showed higher ability to produce reactive oxygen species with respect to pristine samples, which could be convenient for preserving the implant from bacterial contamination. These findings contribute to the advancement of producing copper-depleted nanostructured Ti based amorphous alloys for biomedical implant applications.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/16776
dc.identifier.urihttps://doi.org/10.34657/15798
dc.language.isoeng
dc.publisherRio de Janeiro : Elsevier
dc.relation.doihttps://doi.org/10.1016/j.jmrt.2024.03.225
dc.relation.essn2214-0697
dc.relation.issn2238-7854
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subject.ddc670
dc.subject.otherAmorphous alloyeng
dc.subject.otherBiocompatibilityeng
dc.subject.otherBiomedical implanteng
dc.subject.otherDealloyingeng
dc.subject.otherHemocompatibilityeng
dc.subject.otherSurface treatmenteng
dc.subject.otherTi based alloyeng
dc.titleSurface modification of Ti40Cu40Zr11Fe3Sn3Ag3 amorphous alloy for enhanced biocompatibility in implant applicationseng
dc.typeArticle
dc.typeText
tib.accessRightsopenAccess
wgl.contributorIFWD
wgl.subjectChemieger
wgl.subjectPhysikger
wgl.typeZeitschriftenartikelger
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