Sorry, I don't understand your search. ×
Back to Search Start Over

Red-emission carbon dots as fluorescent "on–off–on" probe for highly sensitive and selective detection of Cu2+ and glutathione.

Authors :
Ning, Gan
Li, Bo
Liu, Jiajia
Xiao, Qi
Huang, Shan
Source :
Analytical & Bioanalytical Chemistry. Mar2022, Vol. 414 Issue 6, p2219-2233. 15p.
Publication Year :
2022

Abstract

A highly sensitive and selective fluorescent "on–off–on" strategy is established for the synchronous detection of Cu2+ and glutathione in aqueous solution. Red carbon dots (R-CDs) were prepared by using precursors of 4,5-difluoro-1,2-phenylenediamine and citric acid via a one-step hydrothermal strategy. R-CDs show a relatively long fluorescence lifetime of 3.47 ns under 455 nm excitation and high absolute fluorescent quantum yield of 20.1% with an excitation wavelength of 550 nm. R-CDs exhibit a marked pH-responsive fluorescence property with no significant perturbation from pH 4 to pH 13 even after five cycles. R-CDs with higher concentration of 750 μg·mL−1 exhibit no significant cytotoxicity and good biocompatibility on HeLa cells and A549 cells after incubation for 48 h. The fluorescence of R-CDs at 619 nm (excited at 550 nm) is quenched statically by Cu2+ and recovered by glutathione subsequently, resulting in a fluorescent "on–off–on" assay for the synchronous detection of Cu2+ and glutathione. Under optimal conditions, the linear response covers the Cu2+ concentration range of 1 to 50 μM and the glutathione concentration range of 1 to 70 μM. Detection limits of Cu2+ and glutathione are 0.16 and 0.41 μM, respectively. This fluorescent probe is applied to the determination of Cu2+ and glutathione in authentic samples with satisfying results. Such an assay broadens the potential application of CDs in environmental areas and clinical therapy fields. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16182642
Volume :
414
Issue :
6
Database :
Academic Search Index
Journal :
Analytical & Bioanalytical Chemistry
Publication Type :
Academic Journal
Accession number :
155105975
Full Text :
https://doi.org/10.1007/s00216-021-03859-7