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1.
J Photochem Photobiol B ; 148: 181-187, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25956560

ABSTRACT

Fluorescent 1,4-dihydroxyanthraquinone 1 was found to demonstrate its ratiometric signaling property upon interaction with divalent zinc (Zn(2+)). While the probe itself exhibited fluorescence emission in the yellow region (λem=544 nm and 567 nm), binding with Zn(2+) induced strong emission in the orange region (λem=600 nm) which was mainly due to a combination of CHEF and ICT mechanism. The probe was found to be highly sensitive toward the detection of zinc and the limit of detection (LOD) was calculated to be 9×10(-7) M. The possibility of using this probe for real-time analysis was strongly supported by the striking stability of fluorescence signal for more than five days with similar fluorescence intensity as observed during instant signaling. The present probe works within physiological pH range and is devoid of any interference caused by the same group elements such as Cd(2+)/Hg(2+). The probe possesses excellent excitation/emission wavelength profile and can penetrate cell membrane to image low concentration of zing inside living system. The in situ formed zinc-probe ensemble was further explored as ratiometric sensing platform for detecting another bio-relevant analyte phosphate anion through a zinc-displacement approach.


Subject(s)
Anthraquinones/chemistry , Bignoniaceae/metabolism , Fluorescent Dyes/chemistry , Phosphates/chemistry , Zinc/chemistry , Anthraquinones/metabolism , Bignoniaceae/growth & development , Cadmium/chemistry , Edetic Acid/chemistry , Fluorescent Dyes/metabolism , Ions/chemistry , Mercury/chemistry , Microscopy, Fluorescence , Phosphates/analysis , Pollen/chemistry , Pollen/metabolism , Signal Transduction , Spectrometry, Fluorescence
2.
Dalton Trans ; 44(20): 9506-15, 2015 May 28.
Article in English | MEDLINE | ID: mdl-25919349

ABSTRACT

Novel molecular probes for imaging zinc in biological systems are gaining interest as they help in understanding the role of zinc in regulating various bio-events. In this regard, a new C2-symmetric molecular system has been developed and successfully applied as light-up material for signaling divalent zinc with green emission. The fluorescence enhancement was highly zinc specific and this newly developed probe bears a submicromolar detection capability. While probe and the ensemble -Zn(2+) exhibited remarkably high photostability, light-triggered fluorescence enhancement was observed in the case of -Zn(2+). The nature of the -Zn(2+) complex and the associated spectral shift are further supported by theoretical calculations. As the present probe absorbs in the visible region and emits in the green, it was preferred as a potential material for imaging zinc in biological systems including animal and plant cells such as pollen grains and fish egg cells. Such fluorescence imaging of zinc revealed the efficacy of the probe in detection and localization of zinc in various biological systems.


Subject(s)
Fluorescent Dyes/chemistry , Molecular Imaging/methods , Zinc/metabolism , Animal Shells/metabolism , Animals , Bignoniaceae/metabolism , Cyprinidae/anatomy & histology , Drug Stability , Models, Molecular , Molecular Conformation , Organometallic Compounds/chemistry , Spectrometry, Fluorescence , Zinc/chemistry
3.
Chem Commun (Camb) ; 49(91): 10739-41, 2013 Nov 25.
Article in English | MEDLINE | ID: mdl-24104701

ABSTRACT

A spirobenzopyran-quinoline (SBPQ) based sensor was synthesized which selectively detects trivalent ions viz. Al(3+), Fe(3+) and Cr(3+) through a fluorescence turn on signal in the red region (~675 nm) with the detection limit in the order of 10(-8) M. The potentiality of the probe was confirmed by employing it for fluorescence bio-imaging with Al(3+) in three different types of live-cells.


Subject(s)
Aluminum/analysis , Cations/analysis , Chromium/analysis , Ferric Compounds/analysis , Benzopyrans/chemistry , Fluorescent Dyes , Quinolines/chemistry , Spectrometry, Fluorescence , Spectrophotometry, Ultraviolet , Spiro Compounds/chemistry
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