Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/64609

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dc.contributor.authorDíaz, E.por
dc.contributor.authorValle, M. B.por
dc.contributor.authorRibeiro, Sylvie Oliveirapor
dc.contributor.authorLanceros-Méndez, S.por
dc.contributor.authorBarandiarán, J. Mpor
dc.date.accessioned2020-03-29T16:06:30Z-
dc.date.available2020-03-29T16:06:30Z-
dc.date.issued2019-
dc.identifier.citationDíaz, E.; Valle, M.B.; Ribeiro, S.; Lanceros-Mendez, S.; Barandiarán, J.M. 3D Cytocompatible Composites of PCL/Magnetite. Materials 2019, 12, 3843.por
dc.identifier.urihttps://hdl.handle.net/1822/64609-
dc.description.abstractA study of Magnetite (Fe3O4) as a suitable matrix for the improved adhesion and proliferation of MC3T3-E1 pre-osteoblast cells in bone regeneration is presented. Biodegradable and magnetic polycaprolactone (PCL)/magnetite (Fe3O4) scaffolds, which were fabricated by Thermally Induced Phase Separation, are likewise analyzed. Various techniques are used to investigate in vitro degradation at 37 °C, over 104 weeks, in a phosphate buffered saline (PBS) solution. Magnetic measurements that were performed at physiological temperature (310 K) indicated that degradation neither modified the nature nor the distribution of the magnetite nanoparticles. The coercive field strength of the porous matrices demonstrated ferromagnetic behavior and the probable presence of particle interactions. The added nanoparticles facilitated the absorption of PBS, with no considerable increase in matrix degradation rates, as shown by the Gel Permeation Chromatography (GPC) results for Mw, Mn, and I. There was no collapse of the scaffold structures that maintained their structural integrity. Their suitability for bone regeneration was also supported by the absence of matrix cytotoxicity in assays, even after additions of up to 20% magnetite.por
dc.description.sponsorshipThis work was supported by the Spanish Ministry of Economy and Competitiveness (MINECO) through the project MAT2016-76039-C4-3-R (AEI/FEDER, UE) and from the Basque Government Industry Department under the ELKARTEK, HAZITEK and PIBA programs. Supported by the Portuguese Foundation for Science and Technology (FCT) in the framework of the Strategic Funding UID/FIS/04650/2013, project POCI-01-0145-FEDER-028237 and grant SFRH/BD/111478/2015 (S.R.) is acknowledged.por
dc.description.sponsorshipTechnical and human support provided by SGIker (UPV/EHU, MICINN, GV/EJ, ERDF and ESF) is gratefully appreciated. The authors acknowledge funding by the Spanish Ministry of Economy and Competitiveness (MINECO) through the project MAT2016-76039-C4-3-R (AEI/FEDER, UE) and from the Basque Government Industry and Education Department under the ELKARTEK and HAZITEK and PIBA (PIBA-2018-06) programs. Supported by the Portuguese Foundation for Science and Technology (FCT) in the framework of the Strategic Funding UID/FIS/04650/2013, project POCI-01-0145-FEDER-028237 and grant SFRH/BD/111478/2015 (S.R.) is acknowledged.por
dc.language.isoengpor
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)por
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147414/PTpor
dc.relationSFRH/BD/111478/2015por
dc.rightsopenAccesspor
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/por
dc.subjectPCLpor
dc.subjectmagnetitepor
dc.subjectscaffoldspor
dc.subjectmagnetismpor
dc.subjectcytotoxicitypor
dc.subjectin vitro degradationpor
dc.title3D cytocompatible composites of PCL/Magnetitepor
dc.typearticlepor
dc.peerreviewedyespor
dc.relation.publisherversionhttps://www.mdpi.com/1996-1944/12/23/3843por
oaire.citationIssue23por
oaire.citationVolume12por
dc.identifier.eissn1996-1944-
dc.identifier.doi10.3390/ma12233843por
dc.subject.fosCiências Naturais::Ciências Físicaspor
dc.subject.wosScience & Technologypor
sdum.journalMaterialspor
oaire.versionVoRpor
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