Journal
ANALYST
Volume 140, Issue 2, Pages 574-581Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4an01934b
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Funding
- National Natural Science Foundation of China [20972170, 21275150]
- Funds for Distinguished Young Scientists of Gansu [1210RJDA013]
- Natural Science Foundation of Gansu province [1107RJYA069]
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A novel Turn-On fluorescent probe, quaternarized 4-pyridinyl-substituted BODIPY dye by incorporating a 5-nitrofuran moiety, was developed and applied for imaging the hypoxic status of tumor cells by the indirect detection of nitroreductase. The design was based on a nitroreductase-catalyzed reduction of the nitrofuran moiety in the presence of reduced nicotinamide adenine dinucleotide (NADH) as an electron donor and followed by the 1,6-rearrangement-elimination and the release of free 4-pyridinyl-substituted BODIPY dye 2. This probe displayed desired properties such as high specificity, Turn-On fluorescence response with suitable sensitivity, appreciable water solubility and rapid response time (within 5 min). Moreover, as a biocompatible molecule, the probe has been successfully applied for imaging the hypoxic status of tumor cells (e. g. A549 cells) and especially used for real-time determination of nitroreductase produced by Escherichia coli. Therefore, we hope to apply this novel method in the biomedical research fields for the imaging of disease-relevant hypoxia and detection of pathogenic microorganisms.
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