2015
DOI: 10.1039/c5ra11841g
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Highly sensitive and selective detection of biothiols by a new low dose colorimetric and fluorescent probe

Abstract: In this paper, a new low dose fluorescent probe with excellent sensing properties for detection of biothiols (GSH, Cys and Hcy) was developed. This probe shows rapid response, high selectivity and sensitivity for biothiols with dual colorimetric and fluorescent turn-on signal changes. The detection limit of this probe for biothiols was found to be <10 nM based on the fluorescent detection. More importantly, this probe can be used to image biothiols effectively in living cells even with a low dose of 0.2 μM.

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Cited by 25 publications
(4 citation statements)
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“…The cyano group is an electron acceptor, and the alkoxy group is an electron donor, making PFE-CN-2 with an electron donor–conjugated system–electron acceptor (D-π-A) structure. This structure makes the fluorescence enhancement of PFE-CN-2 and the maximal absorption/emission red-shifting about 6 nm compared to PFE-1, which is consistent with that previously reported in the literature. , Because of 2,4-dinitrobenzenesulfonyl, an electron-withdrawing group, being linked as a side chain of PFE-NP-3 (electron acceptor–conjugated system–electron acceptor, A-π-A), PFE-NP-3 fluorescence is quenched by photoinduced electron transfer (PET) effect, leading to the poorest fluorescence intensity. To further compare the photophysical properties of the four kinds of CCPs, the absolute fluorescence quantum yield (Φ F ) in aqueous solution was measured. The cationic conjugated polymers were excited with the corresponding maximal absorption wavelength.…”
Section: Resultssupporting
confidence: 90%
“…The cyano group is an electron acceptor, and the alkoxy group is an electron donor, making PFE-CN-2 with an electron donor–conjugated system–electron acceptor (D-π-A) structure. This structure makes the fluorescence enhancement of PFE-CN-2 and the maximal absorption/emission red-shifting about 6 nm compared to PFE-1, which is consistent with that previously reported in the literature. , Because of 2,4-dinitrobenzenesulfonyl, an electron-withdrawing group, being linked as a side chain of PFE-NP-3 (electron acceptor–conjugated system–electron acceptor, A-π-A), PFE-NP-3 fluorescence is quenched by photoinduced electron transfer (PET) effect, leading to the poorest fluorescence intensity. To further compare the photophysical properties of the four kinds of CCPs, the absolute fluorescence quantum yield (Φ F ) in aqueous solution was measured. The cationic conjugated polymers were excited with the corresponding maximal absorption wavelength.…”
Section: Resultssupporting
confidence: 90%
“…actively used as fluorescent probes for rapid detection of H2S [4], benzenethiols [5], biothiols [6], selenocysteine [7],…”
Section: -Benzothiazolylcoumarins Arementioning
confidence: 99%
“…Among them, fluorescence detection approaches, owing to their advantages of excellent sensitivity, low cost, high spatiotemporal resolution, ease of observation and noninvasive detection, have attracted interest in biological imaging analysis, clinical disease diagnosis, food detection, and environmental detection [17][18][19][20]. At present, a number of fluorescent Molecules 2021, 26, 2337 2 of 12 probes have been designed for biothiols imaging [21][22][23][24][25][26][27][28][29]. Despite great efforts, some defects associated with current sensors, including low selectivity, complicated syntheses, low biocompatibility or a small Stokes shift (<100 nm), still remain.…”
Section: Introductionmentioning
confidence: 99%