Biofunctional quantum dots as fluorescence probe for cell-specific targeting

Zur Kurzanzeige

dc.identifier.uri http://dx.doi.org/10.15488/961
dc.identifier.uri http://www.repo.uni-hannover.de/handle/123456789/985
dc.contributor.author Ag, Didem
dc.contributor.author Bongartz, Rebecca
dc.contributor.author Dogan, Leyla Eral
dc.contributor.author Seleci, Muharrem
dc.contributor.author Walter, Johanna-Gabriela
dc.contributor.author Demirkol, Dilek Odaci
dc.contributor.author Stahl, Frank
dc.contributor.author Ozcelik, Serdar
dc.contributor.author Timur, Suna
dc.contributor.author Scheper, Thomas
dc.date.accessioned 2016-12-22T07:48:54Z
dc.date.available 2016-12-22T07:48:54Z
dc.date.issued 2014
dc.identifier.citation Ag, D.; Bongartz, R.; Dogan, L.E.; Seleci, M.; Walter, J.-G.; et al.: Biofunctional quantum dots as fluorescence probe for cell-specific targeting. In: Colloids and Surfaces B: Biointerfaces 114 (2014), S. 96-103. DOI: https://doi.org/10.1016/j.colsurfb.2013.09.033
dc.description.abstract We describe here the synthesis, characterization, bioconjugation, and application of water-soluble thioglycolic acid TGA-capped CdTe/CdS quantum dots (TGA-QDs) for targeted cellular imaging. Anti-human epidermal growth factor receptor 2 (HER2) antibodies were conjugated to TGA-QDs to target HER2-overexpressing cancer cells. TGA-QDs and TGA-QDs/anti-HER2 bioconjugates were characterized by fluorescence and UV-Vis spectroscopy, X-ray diffraction (XRD), hydrodynamic sizing, electron microscopy, and gel electrophoresis. TGA-QDs and TGA-QDs/anti-HER2 were incubated with cells to examine cytotoxicity, targeting efficiency, and cellular localization. The cytotoxicity of particles was measured using an MTT assay and the no observable adverse effect concentration (NOAEC), 50% inhibitory concentration (IC50), and total lethal concentration (TLC) were calculated. To evaluate localization and targeting efficiency of TGA-QDs with or without antibodies, fluorescence microscopy and flow cytometry were performed. Our results indicate that antibody-conjugated TGA-QDs are well-suited for targeted cellular imaging studies. eng
dc.description.sponsorship TUBITAK/109T573
dc.description.sponsorship BMBF/01DL12013
dc.description.sponsorship Ege University Scientific Research/2012/FEN/0071
dc.language.iso eng
dc.publisher Amsterdam : Elsevier
dc.relation.ispartofseries Colloids and Surfaces B: Biointerfaces 114 (2014)
dc.rights CC BY-NC-ND 3.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/3.0/
dc.subject Anti-HER2 eng
dc.subject Bioconjugation eng
dc.subject Cell specific targeting eng
dc.subject Imaging eng
dc.subject Quantum dots eng
dc.subject Electrophoresis eng
dc.subject Fluorescence eng
dc.subject Fluorescence microscopy eng
dc.subject Imaging techniques eng
dc.subject Semiconductor quantum dots eng
dc.subject Ultraviolet visible spectroscopy eng
dc.subject X ray diffraction eng
dc.subject Anti-HER2 eng
dc.subject Bio-conjugation eng
dc.subject Cellular localization eng
dc.subject Epidermal growth factor receptor 2 eng
dc.subject Fluorescence probes eng
dc.subject Gel electrophoresis eng
dc.subject Inhibitory concentration eng
dc.subject Lethal concentration eng
dc.subject Antibodies eng
dc.subject 3 (4,5 dimethyl 2 thiazolyl) 2,5 diphenyltetrazolium bromide eng
dc.subject cadmium eng
dc.subject epidermal growth factor receptor 2 eng
dc.subject epidermal growth factor receptor 2 antibody eng
dc.subject quantum dot eng
dc.subject receptor antibody eng
dc.subject sulfur eng
dc.subject tellurium eng
dc.subject thioglycolic acid eng
dc.subject unclassified drug eng
dc.subject animal cell eng
dc.subject cancer cell eng
dc.subject cancer diagnosis eng
dc.subject cell assay eng
dc.subject cell labeling eng
dc.subject cell specificity eng
dc.subject cell surface eng
dc.subject cellular distribution eng
dc.subject controlled study eng
dc.subject drug concentration eng
dc.subject drug conjugation eng
dc.subject drug cytotoxicity eng
dc.subject drug design eng
dc.subject drug solubility eng
dc.subject drug synthesis eng
dc.subject electron microscopy eng
dc.subject flow cytometry eng
dc.subject fluorescence imaging eng
dc.subject fluorescence microscopy eng
dc.subject human cell eng
dc.subject hydrodynamics eng
dc.subject internalization eng
dc.subject lung cancer eng
dc.subject mouse eng
dc.subject no observable adverse effect concentration eng
dc.subject nonhuman eng
dc.subject priority journal eng
dc.subject protein expression eng
dc.subject target cell eng
dc.subject total lethal concentration eng
dc.subject ultraviolet spectroscopy eng
dc.subject X ray diffraction eng
dc.subject Anti-HER2 eng
dc.subject Cell specific targeting eng
dc.subject Cadmium Compounds eng
dc.subject Cell Death eng
dc.subject Cell Membrane eng
dc.subject Cell Survival eng
dc.subject Cells eng
dc.subject Fluorescent Dyes eng
dc.subject Light eng
dc.subject Mice eng
dc.subject Microscopy, Fluorescence eng
dc.subject NIH 3T3 Cells eng
dc.subject Receptor, erbB-2 eng
dc.subject Reproducibility of Results eng
dc.subject Tellurium eng
dc.subject Thioglycolates eng
dc.subject X-Ray Diffraction eng
dc.subject.ddc 570 | Biowissenschaften, Biologie ger
dc.title Biofunctional quantum dots as fluorescence probe for cell-specific targeting eng
dc.type Article
dc.type Text
dc.relation.issn 09277765
dc.relation.doi https://doi.org/10.1016/j.colsurfb.2013.09.033
dc.bibliographicCitation.volume 114
dc.bibliographicCitation.firstPage 96
dc.bibliographicCitation.lastPage 103
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


Die Publikation erscheint in Sammlung(en):

Zur Kurzanzeige

 

Suche im Repositorium


Durchblättern

Mein Nutzer/innenkonto

Nutzungsstatistiken