| Literature DB >> 25300215 |
Jian Xu1, Shaobo Sun2, Qian Li3, Ying Yue3, Yingdong Li2, Shijun Shao4.
Abstract
A novel probe incorporating quaternized 4-pyridinium group into a BODIPY molecule was synthesized and studied for the selective detection of fluoride ions (F(-)) in aqueous solution. The design was based on a fluoride-specific desilylation reaction and the "Turn-On" fluorescent response of probe 1 to F(-) was ascribed to the inhibition of photoinduced electron transfer (PET) process. The probe displayed many desired properties such as high specificity, appreciable solubility, desirable response time and low toxicity to mammalian cells. There was a good linearity between the fluorescence intensity and the concentrations of F(-) in the range of 0.1-1mM with a detection limit of 0.02 mM. The sensing mechanism was confirmed by the NMR, electrospray ionization mass spectrum, optical spectroscopy and the mechanism of "Turn-On" fluorescent response was also determinated by a density functional theory (DFT) calculation using Gaussian 03 program. Moreover, the probe was successfully applied for the fluorescence imaging of F(-) in human epithelial lung cancer (A549) cells and alveolar type II (ATII) cells under physiological conditions.Entities:
Keywords: A549 and ATII cells; DFT calculation; Fluoride ions sensing; Live-cell imaging; “Turn-On” fluorescent probe
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Year: 2014 PMID: 25300215 DOI: 10.1016/j.aca.2014.08.014
Source DB: PubMed Journal: Anal Chim Acta ISSN: 0003-2670 Impact factor: 6.558