1. Imaging of Fluoride Ion in Living Cells and Tissues with a Two-Photon Ratiometric Fluorescence Probe
- Author
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Haixia Zhang, Zhenjie Chen, Xinyue Zhu, Jianjian Zhang, Jianxi Wang, and Xiaoyu Zhang
- Subjects
Fluorophore ,Cell Survival ,Proton Magnetic Resonance Spectroscopy ,Electrons ,two-photon excited ,lcsh:Chemical technology ,Photochemistry ,Biochemistry ,Article ,Analytical Chemistry ,Ion ,chemistry.chemical_compound ,Fluorides ,Mice ,Two-photon excitation microscopy ,ratiometric fluorescence ,Microscopy ,Animals ,Humans ,lcsh:TP1-1185 ,Electrical and Electronic Engineering ,Instrumentation ,Fluorescent Dyes ,Ions ,Photons ,Microscopy, Confocal ,fluoride ,imaging ,Fluorescence ,Atomic and Molecular Physics, and Optics ,Ratiometric fluorescence ,Molecular Imaging ,Spectrometry, Fluorescence ,chemistry ,Molecular imaging ,Fluoride ,HeLa Cells - Abstract
A reaction-based two-photon (TP) ratiometric fluorescence probe Z2 has been developed and successfully applied to detect and image fluoride ion in living cells and tissues. The Z2 probe was designed designed to utilize an ICT mechanism between n-butylnaphthalimide as a fluorophore and tert-butyldiphenylsilane (TBDPS) as a response group. Upon addition of fluoride ion, the Si-O bond in the Z2 would be cleaved, and then a stronger electron-donating group was released. The fluorescent changes at 450 and 540 nm, respectively, made it possible to achieve ratiometric fluorescence detection. The results indicated that the Z2 could ratiometrically detect and image fluoride ion in living cells and tissues in a depth of 250 μm by two-photon microscopy (TPM).
- Published
- 2015