Colorimetric fluorescence of the 1,10-phenantholineyl-imidazole sensor probe for the selective detection of Zn2+ and Cd2+ ions
[Display omitted] •The low detection limit of the probe PIN indicates its good stability.•Zn2+ and Cd2+ ions could be quickly detected using probe PIN with high selectivity and immunity to interference.•Zn2+ and Cd2+ ion sin HepG-2 live cells could be imaged by probe PIN with low toxicity to cells....
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Veröffentlicht in: | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Molecular and biomolecular spectroscopy, 2025-03, Vol.328, p.125436, Article 125436 |
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Sprache: | eng |
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•The low detection limit of the probe PIN indicates its good stability.•Zn2+ and Cd2+ ions could be quickly detected using probe PIN with high selectivity and immunity to interference.•Zn2+ and Cd2+ ion sin HepG-2 live cells could be imaged by probe PIN with low toxicity to cells.
A colorimetric fluorescent probe, 4-(1H-imidazolo[4,5-f][1,10]phenanthroline-2-yl)-N, N-diphenylaniline (PIN), was designed, synthesized and characterized for the sensitive and selective detection of Zn2+ and Cd2+. The color of the solution changed from blue to yellow visible to the naked eye with the addition of Zn2+ and Cd2+. The probe PIN showed good anti-interference to Zn2+ and Cd2+ in the presence of a variety of metal ions, and the fluorescence intensity showed a good linear relationship with the concentrations of Zn2+ and Cd2+, with detection limits of 34.84 nM and 35.76 nM, respectively. The probe PIN complexed 2:1 with Zn2+ and Cd2+, and the complexation constants were 1.03 × 104 M−1 (PIN − Zn2+, R2 = 0.9971) and 1.50 × 104 M−1 (PIN − Cd2+, R2 = 0.9981), respectively. In addition, the PIN could be recovered by EDTA and could be effectively monitored for Zn2+ and Cd2+ at pH 4–11, with good results in actual water samples. The HepG-2 cells maintained over 95 % of viability after 24 h exposure to PIN, which identified the extremely low toxic of PIN and could be used for in vivo cell imaging. |
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ISSN: | 1386-1425 |
DOI: | 10.1016/j.saa.2024.125436 |