4.7 Article

Facile synthesis of N-doped carbon dots for direct/indirect detection of heavy metal ions and cell imaging

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 28, Issue 16, Pages 19878-19889

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-020-11880-z

Keywords

Carbon dots; Fe3+; Cr(VI); Cellular imaging; Cellular toxicity; Facile synthesis

Funding

  1. Key Technologies Research and Development Program [2016YFC0501205, 2016YFC0501208, 2017YFD0200706]
  2. National Natural Science Foundation of China [21775163]

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In this study, a method for the determination of Fe3+ and Cr(VI) was developed using L-arginine/D-glucose carbon quantum dots (Arg/Glu-CQDs) synthesized through a facile hydrothermal process. Arg/Glu-CQDs showed sensitive and selective response to Fe3+ and could be used as a fluorescence sensor system for detecting Fe3+ and Cr(VI) in river water samples. Additionally, Arg/Glu-CQDs were found to be non-cytotoxic and could potentially be applied in bioimaging.
In this study, an approach for the facile, rapid, energy-saving, and sensitive determination of Fe3+ and Cr(VI) was developed. L-arginine/D-glucose carbon quantum dots (Arg/Glu-CQDs), with a photoluminescence quantum yield of 21%, were synthesized from L-arginine and D-glucose through a facile, hydrothermal process. The maximum emission wavelength of Arg/Glu-CQDs was observed at 450 nm, under an excitation wavelength of 365 nm. In addition, Arg/Glu-CQDs exhibited a sensitive and selective response to Fe3+ compared to Fe2+ and other metal ions. The Arg/Glu-CQDs' fluorescence was noticeably quenched through the inner filter effect (IFE) when Arg/Glu-CQDs were mixed with Fe3+. Accordingly, the Arg/Glu-CQDs/Fe2+ system could selectively detect Cr(VI); Cr(VI) could oxidize Fe2+ to Fe3+ and quench the fluorescence. The fluorescence sensor system (i.e., the Arg/Glu-CQDs/Fe2+ system) showed high sensitivity and excellent selectivity for the detection of Fe3+ and Cr(VI) in river water samples. Satisfactory detection efficiencies ranging from 97.07 to 103.46% were obtained. The cytotoxicity of Arg/Glu-CQDs was evaluated through an MTT assay using A549 cells as the target, to extend the application of Arg/Glu-CQDs to biological systems; the MTT assay indicated that the Arg/Glu-CQDs is non-cytotoxicity. Arg/Glu-CQDs were also successfully imaged in A549 cells indicating further application possibilities in bioimaging.

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