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dc.creatorDojčilović, Radovan
dc.creatorPajović, Jelena D.
dc.creatorBožanić, Dušan K.
dc.creatorJović, Nataša
dc.creatorPavlović, Vera P.
dc.creatorPavlović, Vladimir B.
dc.creatorAcković, Lea Lenhardt
dc.creatorZeković, Ivana
dc.creatorDramićanin, Miroslav
dc.creatorKaščakova, Slavka
dc.creatorRefregiers, Matthieu
dc.creatorRašić, Goran
dc.creatorVlahović, Branislav
dc.creatorDjoković, Vladimir
dc.date.accessioned2022-09-19T18:30:40Z
dc.date.available2022-09-19T18:30:40Z
dc.date.issued2018
dc.identifier.issn2053-1583
dc.identifier.urihttps://machinery.mas.bg.ac.rs/handle/123456789/2868
dc.description.abstractThe interaction of partially reduced graphene oxide (prGO) and Huh7.5.1 liver cancer cells was investigated by means of DUV fluorescence bioimaging. The prGO sample was obtained by the reduction (to a certain extent) of the initially prepared graphene oxide (GO) nanosheets with hydrazine. The fluorescence of the GO nanosheets increases with time of the reduction due to a change in ratio of the sp(2) and sp(3) carbon sites and the prGO sample was extracted from the dispersion after 6 min, when the intensity of the fluorescence reached its maximum. The reduction process was left to proceed further to saturation until highly reduced graphene oxide (denoted here as rGO) was obtained. GO, prGO and rGO samples were investigated by structural (scanning electron microscopy (SEM), scanning transmission electron microscopy coupled with energy dispersive spectrometry (STEM-EDS)) and spectroscopic (UV-vis, photoluminescence (PL), Raman) methods. After that, Huh7.5.1 cells were incubated with GO, prGO and rGO nanosheets and used in bioimaging studies, which were performed on DISCO beamline of synchrotron SOLEIL. It was found that the prGO significantly enhanced the fluorescence of the cells and increased the intensity of the signal by similar to 2.5 times. Time-lapse fluorescence microscopy experiments showed that fluorescence dynamics strongly depends on the type of nanosheets used. The obtained prGO nanostructure can be easily conjugated with aromatic ring containing drugs, which opens a possibility for its applications in fluorescence microscopy monitored drug delivery.en
dc.publisherIOP Publishing Ltd, Bristol
dc.relationNSF CREST [HRD-0833184]
dc.relationNASA [NNX09AV07A]
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172056/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/45020/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/171029/RS//
dc.relation.isversionofhttps://machinery.mas.bg.ac.rs/handle/123456789/4042
dc.rightsrestrictedAccess
dc.source2D Materials
dc.subjectgraphene oxideen
dc.subjectfluorescenceen
dc.subjectcellsen
dc.subjectcanceren
dc.subjectbioimagingen
dc.titleDUV fluorescence bioimaging study of the interaction of partially reduced graphene oxide and liver cancer cellsen
dc.typearticle
dc.rights.licenseARR
dc.citation.issue4
dc.citation.other5(4): -
dc.citation.rankaM21
dc.citation.spage045019
dc.citation.volume5
dc.description.otherPeer reviewed version of the paper: [https://machinery.mas.bg.ac.rs/handle/123456789/4042]
dc.identifier.doi10.1088/2053-1583/aad72b
dc.identifier.scopus2-s2.0-85054724220
dc.identifier.wos000441754800003
dc.type.versionpublishedVersion


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