Development of a new fluorescent probe for transition metal cations based upon fluorescence resonance energy transfer Original Research Article

A novel fluorescent probe for metal cations, which has a large Stokes shift, was synthesized from the reaction of N-(3-carboxy-2-naphthyl)-ethylenediamine-N,N′,N′-triacetic acid (CNEDTA) with 4-(N,N-dimethylaminosulfonyl)-7-(2-aminoethylamino)-2,1,3-benzoxadiazole (DBD-ED). The large Stokes shift is due to the FRET phenomenon between a donor (CNEDTA) and an acceptor (DBD-ED) fluorophore. When the fluorescent probe, DBD-ED–CNEDTA, was excited at 240, 340 and 440 nm, an emission maximum was observed only at 560 nm. However, the fluorescence (FL) at 480 nm, based upon the CNEDTA moiety, was not detected with excitation at 340 nm. The FL intensity of DBD-ED–CNEDTA was dependent upon the acidity of the medium and highest at pH 4.1. DBD-ED–CNEDTA reacted with metal cations, i.e., Zn, Cd, Al, Y, and La, in aqueous medium to form chelates. The spectral change of FL excitation and emission was small before and after the addition of the metal ions. However, the FL intensity was dependent upon the concentrations of the metal ions. In the case of Zn2+, the molar ratio bound with DBD-ED–CNEDTA was calculated as 1:1. The FL intensities after chelate formation of Zn/DBD-ED–CNEDTA (1:1) were enhanced by 3.8-fold (excitation at 340 nm, emission at 560 nm), 4.2-fold (excitation at 440 nm, emission at 560 nm), and 5.9-fold (excitation at 240 nm, emission at 560 nm), respectively. The FL probe was applied to the determination of Zn in a food supplement.