Abstract
Cadmium sulfide quantum dots (CdS QDs) were synthesized with 3-mercaptopropionic acid (MPA) as protective agent, which were characterized by TEM, UV–vis, fluorescence, XRD and TGA. Based on the fluorescence quenching of 3-MPA-CdS QDs, the indirect methods for the determination of furazolidone (FZD) and nitrofurantoin (NFT) were established. The interaction between FZD/NFT and CdS QDs was investigated by using fluorescence, resonance light scattering, UV–vis and FT-IR. The analyses of Stern-Volmer and fluorescence lifetime indicated that the two quenching systems were all static. The binding constant (Ka) of FZD/NFT-CdS QDs was 1.20 × 104/1.81 × 104 L/mol at 293 K, respectively. Hydrogen bond or van der Waals force was the main binding force between CdS QDs and drugs. Under optimum experimental conditions, the concentration of FZD/NFT was respectively highly correlated with the fluorescence intensity ratio in the range of 0.27 – 36.03/0.57 – 28.58 μg mL−1. The interference experiments showed that the methods had good selectivity. The limit of detection (LOD) for FZD/NFT was 0.02/0.01 μg mL−1. The contents of FZD and NFT in fish samples were determined, and the recoveries were 97.41–99.52 % and 96.64–100.49 %, respectively.
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