Journal
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
Volume 348, Issue -, Pages 246-254Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotochem.2017.08.055
Keywords
Aminothiazole; Fluorescent probe; H-1 NMR titration; Binding constant; Detection limit; Live cell imaging
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Funding
- UGC, New Delhi [43-204/2014 (SR)]
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An efficient, aminothiazole based, fluorescent probe (E)-2-(2-aminothiazol-5-y1)-N'-((2-hydroxynaphthalen-1-yl)methylene)acetohydrazide (NTH) for the detection of Ala' ions was synthesized and characterized by different physico-chemical and spectroscopic tools. An attractive glowing blue color was observed in the presence of Al3+ with single channel emissions for NTH (lambda(em) 451 & lambda(ex) 391 nm). NTH, selectively detected Al3+ ions among various other ions without any significant interference in Tris-HC1 buffer solution (10 mM, pH similar to 7.4). The >C=N- isomerization was responsible for the turn 'on' fluorescence response after Al3+ binding. The stoichiometry of NTH with AO+ was determined to be 1:1 by Job's plot. The binding constant and limit of detection (LOD) were observed as 3.65 x 10(9)M(-1) and 1.09 x 10(-9)M, respectively. The H-1 NMR titration and DFT studies were also performed in support of binding details of NTH-Al3+ complex. MIT assay on live A549 cells suggested viability of the probe to A549 cells even at higher concentration (100 M) with no serious cytotoxicity in cells. Live cell imaging study clearly indicated that the accumulation of Al3+ in the cytoplasm of cells could be detected by NTH. (C) 2017 Elsevier B.V. All rights reserved.
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