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dc.contributor.authorSánchez Bodón, Julia
dc.contributor.authorAndrade del Olmo, Jon
dc.contributor.authorAlonso, Jose María
dc.contributor.authorMoreno Benítez, María Isabel ORCID
dc.contributor.authorVilas Vilela, José Luis ORCID
dc.contributor.authorPérez Álvarez, Leyre
dc.date.accessioned2022-01-14T10:51:49Z
dc.date.available2022-01-14T10:51:49Z
dc.date.issued2021-12-31
dc.identifierdoi: 10.3390/polym14010165
dc.identifier.issn2073-4360,
dc.identifier.urihttp://hdl.handle.net/10810/54992
dc.description.abstractTitanium (Ti) and its alloys have been demonstrated over the last decades to play an important role as inert materials in the field of orthopedic and dental implants. Nevertheless, with the widespread use of Ti, implant-associated rejection issues have arisen. To overcome these problems, antibacterial properties, fast and adequate osseointegration and long-term stability are essential features. Indeed, surface modification is currently presented as a versatile strategy for developing Ti coatings with all these challenging requirements and achieve a successful performance of the implant. Numerous approaches have been investigated to obtain stable and well-organized Ti coatings that promote the tailoring of surface chemical functionalization regardless of the geometry and shape of the implant. However, among all the approaches available in the literature to functionalize the Ti surface, a promising strategy is the combination of surface pre-activation treatments typically followed by the development of intermediate anchoring layers (self-assembled monolayers, SAMs) that serve as the supporting linkage of a final active layer. Therefore, this paper aims to review the latest approaches in the biomedical area to obtain bioactive coatings onto Ti surfaces with a special focus on (i) the most employed methods for Ti surface hydroxylation, (ii) SAMs-mediated active coatings development, and (iii) the latest advances in active agent immobilization and polymeric coatings for controlled release on Ti surfaces.es_ES
dc.description.sponsorshipThis research was funding by Basque Government (ELKARTEK program, HAZITEK program–IMABI exp number ZE-2019/00012), Department of Development and Infrastructures of the Basque Country, University of the Basque Country UPV/EHU (GIU 207075), Ministry of Economy, Industry and Competitiveness (grant MAT2017-89553-P) and i+Med S. Coop.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/MAT2017-89553-Pes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjecttitaniumes_ES
dc.subjectsurface modificationes_ES
dc.subjectbioactive coatingses_ES
dc.subjectpre-activation treatmentses_ES
dc.subjectself-assembled monolayer (SAM)es_ES
dc.subjectactive layeres_ES
dc.subjectimmobilizationes_ES
dc.subjectcontrolled releasees_ES
dc.titleBioactive Coatings on Titanium: A Review on Hydroxylation, Self-Assembled Monolayers (SAMs) and Surface Modification Strategieses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2022-01-10T14:38:16Z
dc.rights.holder2021 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/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/2073-4360/14/1/165/htmes_ES
dc.identifier.doi10.3390/polym14010165
dc.departamentoesQuímica física
dc.departamentoeuKimika fisikoa


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2021 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/).
Except where otherwise noted, this item's license is described as 2021 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/).