In vitro study of NCs/dyes complexes accumulation and dyes release kinetics in rat hepatocytes

dc.contributor.authorYefimova, S.L.
dc.contributor.authorTkacheva, T.N.
dc.contributor.authorKavok, N.S.
dc.contributor.authorKlochkov, V.K.
dc.contributor.authorSorokin, A.V.
dc.date.accessioned2017-06-06T14:34:41Z
dc.date.available2017-06-06T14:34:41Z
dc.date.issued2015
dc.description.abstractUsing fluorescence microspectoscopy and FRET-labeling of various nano-scale carriers (NCs) the efficiency and kinetics of NCs/dye molecules complexes accumulation in living cells and dye release have been studied. Organic liposome vesicles and inorganic nanoparticles (CeO₂ and GdYVO₄:Eu³⁺) were used as NCs. NCs/dyes complexes formed in aqueous solutions have been characterized. It has been shown that NCs based on GdYVO₄:Eu³⁺ nanoparticles exhibit the most effective accumulation in cells and provide very fast release of the lipophilic cargo (dyes molecules). Lipophilic compound (cholesterol) embedded into the NCs/dyes complexes decreases noticeably the rate of lipophilic dyes release and reduces the affinity of the complex interaction with hepatocytes. GdYVO₄:Eu³⁺ NPs could be used as a nano-scale platform for controlled intracellular delivering of hydrophobic agents.uk_UA
dc.identifier.citationIn vitro study of NCs/dyes complexes accumulation and dyes release kinetics in rat hepatocytes / S.L. Yefimova, T.N. Tkacheva, N.S. Kavok, V.K. Klochkov, A.V. Sorokin// Functional Materials. — 2015. — Т. 22, № 2. — С. 199-206. — Бібліогр.: 31 назв. — англ.uk_UA
dc.identifier.issn1027-5495
dc.identifier.otherDOI: http://dx.doi.org/10.15407/fm22.02.199
dc.identifier.urihttps://nasplib.isofts.kiev.ua/handle/123456789/119352
dc.language.isoenuk_UA
dc.publisherНТК «Інститут монокристалів» НАН Україниuk_UA
dc.relation.ispartofFunctional Materials
dc.statuspublished earlieruk_UA
dc.subjectCharacterization and propertiesuk_UA
dc.titleIn vitro study of NCs/dyes complexes accumulation and dyes release kinetics in rat hepatocytesuk_UA
dc.typeArticleuk_UA

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