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Quantum dot-based assay for Cu2+ quantification in bacterial cell culture

Authordc.contributor.authorDurán Toro, V. 
Authordc.contributor.authorGran Scheuch, A. es_CL
Authordc.contributor.authorÓrdenes Aenishanslins, N. es_CL
Authordc.contributor.authorMonrás, J. P. es_CL
Authordc.contributor.authorSaona, L. A. es_CL
Authordc.contributor.authorVenegas, F. A. es_CL
Authordc.contributor.authorChasteen, T. G. es_CL
Authordc.contributor.authorBravo, D. es_CL
Authordc.contributor.authorPérez Donoso, José es_CL
Admission datedc.date.accessioned2014-12-18T18:58:44Z
Available datedc.date.available2014-12-18T18:58:44Z
Publication datedc.date.issued2014
Cita de ítemdc.identifier.citationAnalytical Biochemistry 450 (2014) 30–36en_US
Identifierdc.identifier.otherdx.doi.org/10.1016/j.ab.2014.01.001
Identifierdc.identifier.urihttp://repositorio.uchile.cl/handle/2250/121920
General notedc.descriptionArtículo de publicación ISIen_US
Abstractdc.description.abstractA simple and sensitive method for quantification of nanomolar copper with a detection limit of 1.2 x 10-10 M and a linear range from 10-9 to 10-8 M is reported. For the most useful analytical concentration of quantum dots, 1160 lg/ml, a 1/Ksv value of 11 lM Cu2+ was determined. The method is based on the interaction of Cu2+ with glutathione-capped CdTe quantum dots (CdTe–GSH QDs) synthesized by a simple and economic biomimetic method. Green CdTe–GSH QDs displayed the best performance in copper quantification when QDs of different sizes/colors were tested. Cu2+ quantification is highly selective given that no significant interference of QDs with 19 ions was observed. No significant effects on Cu2+ quantification were determined when different reaction matrices such as distilled water, tap water, and different bacterial growth media were tested. The method was used to determine copper uptake kinetics on Escherichia coli cultures. QD-based quantification of copper on bacterial supernatants was compared with atomic absorption spectroscopy as a means of confirming the accuracy of the reported method. The mechanism of Cu2+-mediated QD fluorescence quenching was associated with nanoparticle decomposition.en_US
Patrocinadordc.description.sponsorshipThis work was supported by Fondecyt 11110077 (J.M.P.), 11110076 (D.B.), Anillo ACT 1107 (J.M.P. and V.D.), Anillo ACT 1111 (D.B. and J.M.P.), and INACH grant T-19_11 (J.M.P. and D.B.). T.G.C. gratefully acknowledges support from the Robert A. Welch Foundation (X-011). A doctoral fellowship from CONICYT (Comisión Nacional de Ciencia y Tecnología) to J.P.M. is also acknowledged.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherElsevieren_US
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Keywordsdc.subjectQuantum dotsen_US
Títulodc.titleQuantum dot-based assay for Cu2+ quantification in bacterial cell cultureen_US
Document typedc.typeArtículo de revistaen_US


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile