Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/34310
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dc.contributor.authorCicuéndez, Mónicapt_PT
dc.contributor.authorCasarrubios, Laurapt_PT
dc.contributor.authorBarroca, Natáliapt_PT
dc.contributor.authorSilva, Danielapt_PT
dc.contributor.authorFeito, María Josépt_PT
dc.contributor.authorDiez-Orejas, Rosalíapt_PT
dc.contributor.authorMarques, Paula A. A. P.pt_PT
dc.contributor.authorPortolés, María Teresapt_PT
dc.date.accessioned2022-07-26T16:21:58Z-
dc.date.available2022-07-26T16:21:58Z-
dc.date.issued2021-07-01-
dc.identifier.issn1661-6596pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/34310-
dc.description.abstractGraphene and its derivatives are very promising nanomaterials for biomedical applications and are proving to be very useful for the preparation of scaffolds for tissue repair. The response of immune cells to these graphene-based materials (GBM) appears to be critical in promoting regeneration, thus, the study of this response is essential before they are used to prepare any type of scaffold. Another relevant factor is the variability of the GBM surface chemistry, namely the type and quantity of oxygen functional groups, which may have an important effect on cell behavior. The response of RAW-264.7 macrophages to graphene oxide (GO) and two types of reduced GO, rGO15 and rGO30, obtained after vacuum-assisted thermal treatment of 15 and 30 min, respectively, was evaluated by analyzing the uptake of these nanostructures, the intracellular content of reactive oxygen species, and specific markers of the proinflammatory M1 phenotype, such as CD80 expression and secretion of inflammatory cytokines TNF-α and IL-6. Our results demonstrate that GO reduction resulted in a decrease of both oxidative stress and proinflammatory cytokine secretion, significantly improving its biocompatibility and potential for the preparation of 3D scaffolds able of triggering the appropriate immune response for tissue regeneration.pt_PT
dc.language.isoengpt_PT
dc.publisherMDPIpt_PT
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/829060/EUpt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectCytokinept_PT
dc.subjectGraphene oxidept_PT
dc.subjectImmune responsept_PT
dc.subjectMacrophagept_PT
dc.subjectReduced graphene oxidept_PT
dc.titleBenefits in the macrophage response due to graphene oxide reduction by thermal treatmentpt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.issue13pt_PT
degois.publication.titleInternational Journal of Molecular Sciencespt_PT
degois.publication.volume22pt_PT
dc.identifier.doi10.3390/ijms22136701pt_PT
dc.identifier.essn1422-0067pt_PT
dc.identifier.articlenumber6701pt_PT
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DEM - Artigos

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