Graphene oxide functional nanohybrids with magnetic nanoparticles for improved vectorization of doxorubicin to neuroblastoma cells

dc.bibliographicCitation.firstPage3eng
dc.bibliographicCitation.issue1eng
dc.bibliographicCitation.journalTitlePharmaceuticseng
dc.bibliographicCitation.lastPage182eng
dc.bibliographicCitation.volume11eng
dc.contributor.authorLerra, L.
dc.contributor.authorFarfalla, A.
dc.contributor.authorSanz, B.
dc.contributor.authorCirillo, G.
dc.contributor.authorVittorio, O.
dc.contributor.authorVoli, F.
dc.contributor.authorGrand, M.L.
dc.contributor.authorCurcio, M.
dc.contributor.authorNicoletta, F.P.
dc.contributor.authorDubrovska, A.
dc.contributor.authorHampel, S.
dc.contributor.authorIemma, F.
dc.contributor.authorGoya, G.F.
dc.date.accessioned2020-07-18T06:12:40Z
dc.date.available2020-07-18T06:12:40Z
dc.date.issued2019
dc.description.abstractWith the aim to obtain a site-specific doxorubicin (DOX) delivery in neuroblastoma SH-SY5Y cells, we designed an hybrid nanocarrier combining graphene oxide (GO) and magnetic iron oxide nanoparticles (MNPs), acting as core elements, and a curcumin–human serum albumin conjugate as functional coating. The nanohybrid, synthesized by redox reaction between the MNPs@GO system and albumin bioconjugate, consisted of MNPs@GO nanosheets homogeneously coated by the bioconjugate as verified by SEM investigations. Drug release experiments showed a pH-responsive behavior with higher release amounts in acidic (45% at pH 5.0) vs. neutral (28% at pH 7.4) environments. Cell internalization studies proved the presence of nanohybrid inside SH-SY5Y cytoplasm. The improved efficacy obtained in viability assays is given by the synergy of functional coating and MNPs constituting the nanohybrids: while curcumin moieties were able to keep low DOX cytotoxicity levels (at concentrations of 0.44–0.88 µM), the presence of MNPs allowed remote actuation on the nanohybrid by a magnetic field, increasing the dose delivered at the target site.eng
dc.description.fondsLeibniz_Fonds
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://doi.org/10.34657/3632
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/5003
dc.language.isoengeng
dc.publisherBasel : MDPI AGeng
dc.relation.doihttps://doi.org/10.3390/pharmaceutics11010003
dc.relation.issn1999-4923
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc610eng
dc.subject.otherGraphene oxideeng
dc.subject.otherIron oxide nanoparticleseng
dc.subject.otherMagnetic targetingeng
dc.subject.otherNanohybridseng
dc.subject.otherSynergismeng
dc.subject.otheralbumineng
dc.subject.othercurcumineng
dc.subject.otherdoxorubicineng
dc.subject.othergraphene oxideeng
dc.subject.othermagnetic iron oxide nanoparticleeng
dc.subject.othermagnetic nanoparticleeng
dc.subject.othernanoparticleeng
dc.subject.otherunclassified drugeng
dc.subject.otheracidityeng
dc.subject.otherArticleeng
dc.subject.othercell viabilityeng
dc.subject.otherconcentration (parameters)eng
dc.subject.otherconjugationeng
dc.subject.othercontrolled studyeng
dc.subject.othercytoplasmeng
dc.subject.otherdrug coatingeng
dc.subject.otherdrug cytotoxicityeng
dc.subject.otherdrug delivery systemeng
dc.subject.otherhumaneng
dc.subject.otherhuman celleng
dc.subject.otherintracellular transporteng
dc.subject.otherneuroblastoma celleng
dc.subject.otherreaction analysiseng
dc.subject.otherscanning electron microscopyeng
dc.subject.otherSH-SY5Y cell lineeng
dc.subject.othersynthesiseng
dc.titleGraphene oxide functional nanohybrids with magnetic nanoparticles for improved vectorization of doxorubicin to neuroblastoma cellseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIFWDeng
wgl.subjectMedizin, Gesundheiteng
wgl.typeZeitschriftenartikeleng
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