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Spectrochim Acta A Mol Biomol Spectrosc ; 314: 124162, 2024 Jun 05.
Article in English | MEDLINE | ID: mdl-38522377

ABSTRACT

In recent years, hemi-cyanine dyes have been widely used as biological probes due to their red-light emission characteristics and high fluorescence quantum yield. In this study, we synthesized a novel hemi-cyanine dye containing a tetrahydropyridine ring. A lysosomal target was introduced into its structure to create a new pH-sensitive near-infrared fluorescent probe that successfully targeted lysosomes. The results showed that when the probe solution was excited at the absorption wavelength of 650 nm, its fluorescence emission wavelength was about 700 nm, and the peak intensity changed with different pH values in a wide range. Therefore, this probe enabled non-invasive detection of changes in the acidic environment of lysosomes in living organisms and showed good imaging capabilities. Moreover, the probe displays high sensitivity and good stability. The theoretical calculation of a probe structure has also been completed to discuss the relationship between structure and property.


Subject(s)
Fluorescent Dyes , Quinolines , Humans , Fluorescence , Fluorescent Dyes/chemistry , Hydrogen-Ion Concentration , Lysosomes/chemistry , Quinolines/analysis , HeLa Cells
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