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dc.contributor.authorMachado, Thales Rafael
dc.contributor.authorLeite, I. S.
dc.contributor.authorInada, N. M.
dc.contributor.authorLi, Maximo Siu
dc.contributor.authorDa Silva, J. S.
dc.contributor.authorAndres, Juan
dc.contributor.authorBeltrán Mir, Héctor
dc.contributor.authorCordoncillo, Eloisa
dc.contributor.authorLongo, Elson
dc.date.accessioned2020-04-03T10:10:08Z
dc.date.available2020-04-03T10:10:08Z
dc.date.issued2019
dc.identifier.citationMACHADO, T. R., et al. Designing biocompatible and multicolor fluorescent hydroxyapatite nanoparticles for cell-imaging applications. Materials Today Chemistry, 2019, vol. 14, p. 100211.ca_CA
dc.identifier.issn2468-5194
dc.identifier.urihttp://hdl.handle.net/10234/187298
dc.description.abstractIn recent years, there has been a growing effort toward the synthesis, engineering and property tuning of biocompatible nanoparticles (NPs) that can be detected by confocal microscopy and then used as fluorescent probes. Defect-related fluorescent hydroxyapatite (HA) is attracting considerable attention as a suitable material for cell-imaging owing to its excellent biocompatibility, biodegradability, easy cell internalization capability, and its stable and intense blue fluorescence. Although the self-activated fluorescence of HA is advantageous, as it avoids the use of lanthanide dopants, organic dyes, or the need to be combined with other fluorescent inorganic nanocrystals, its preparation by simple procedures with fine control of the defects which govern this property remains challenging. In this study, we propose a new, simple, and cost-effective strategy of fluorescence imaging using HA nanorods (HAnrs) obtained by chemical precipitation followed by heat treatment at relative low temperature (350°C) without using any sophisticated equipment or inorganic/organic additives. Structural, compositional, and morphological analysis, as well as a cytotoxicity assay, are described in detail. The fluorescence characterization of HAnrs shows an intense bluish-white broad-band emission (λmax = 535 nm), and the defects which cause this behavior are studied by temperature-dependent photoluminescence measurements (38–300 K). Moreover, the high density of defects in heat-treated HA leads to tunable fluorescent property (λmax = 399–650 nm) across the entire visible spectrum as a function of the excitation wavelength (λexc = 330–630 nm) with the potential for further multicolor imaging applications. Labeling results by confocal microscopy show that HAnr co-cultured with human dermal fibroblast cell line exhibit fluorescence signals in the cells even after 48 h of incubation with no evident cytotoxic effects. Therefore, heat-treated fluorescent HAnr can be utilized for tracking and monitoring cells and is a safe alternative for the traditional probes used in bioimaging procedures.ca_CA
dc.format.extent12 p.ca_CA
dc.language.isoengca_CA
dc.publisherElsevierca_CA
dc.relation.isPartOfMaterials Today Chemistry, 2019, vol. 14, p. 100211.ca_CA
dc.rights2468-5194/©2019 Elsevier Ltd. All rights reserved.Materials Today Chemistry 14 (2019) 100211ca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectHydroxyapatiteca_CA
dc.subjectBioimagingca_CA
dc.subjectDefectsca_CA
dc.subjectFluorescenceca_CA
dc.subjectChemical precipitationca_CA
dc.titleDesigning biocompatible and multicolorfluorescent hydroxyapatitenanoparticles for cell-imaging applicationsca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttps://doi.org/10.1016/j.mtchem.2019.100211
dc.relation.projectID001; 2013/11144-3; 2013/07296-2; 2013/07276-1; 2009/54035-4; 141964/2018-9; PrometeoII/2014/022; ACOMP/2015/1202; UJI-B2016-25; UJI-B2016-38; CTQ2015-65207-P; MAT2016-80410-Pca_CA
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttps://www.sciencedirect.com/science/article/pii/S246851941930223Xca_CA
dc.type.versioninfo:eu-repo/semantics/publishedVersionca_CA


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