A highly selective colorimetric and fluorescent probe for quantitative detection of Cu/Co: The unique ON-OFF-ON fluorimetric detection strategy and applications in living cells/zebrafish.

Spectrochim Acta A Mol Biomol Spectrosc

Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics, School of Pharmacy, Tianjin Medical University, Tianjin 300070, PR China. Electronic address:

Published: March 2020

Identifying and detecting similar target cations through combining "turn on" and "turn off" fluorescence mechanism is effective and challenging. Now a new colorimetric and ON-OFF-ON fluorescent probe N'-((7-(diethylamino)-2-oxo-2H-chromen-3-yl)methylene)-3-hydroxy-2-naphthohydrazide (L) was reported, which could detect Cu and Co in phosphate buffered CHCHOH-HO solvent system. With the assistance of glutathione and pH adjustment, a unique ON-OFF-ON fluorescence detection strategy could be achieved for distinguishing Cu and Co. The emission of probe could recover from the L-Cu and L-Co system by addition of GSH or adjusting pH value to 4, respectively, which is due to the abolishment of paramagnetic Cu/Co. Based on fluorescence titration experiments, the limit of detection was determined as 3.84 × 10 M and 4.55 × 10 M for Cu and Co, respectively. Meanwhile, the detection limit reached 6.21 × 10 M for Cu and 6.96 × 10 M for Co according to absorbance signal output. Fast recognition of Cu/Co can be achieved by obvious color changes from green to colorless under UV light, as well as from yellow to orange-red in room light. The binding mode of L toward Cu and Co have been systematically studied by Job's plot analysis, ESI-MS, IR and density functional theory calculations. Most strikingly, further practical applications of the probe L in fluorescence imaging were investigated in MCF-7 cells and zebrafish due to its low cytotoxicity and good optical properties, suggesting that L could serve as a fluorescent sensor for tracking Cu and Coin vivo.

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http://dx.doi.org/10.1016/j.saa.2019.117763DOI Listing

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