A Ratiometric Fluorescent Probe for Imaging Hydrogen Peroxide in Living Cells
- Corresponding author: Ji Min, 101010516@seu.edu.cn Wang Peng, wangpeng@cpu.edu.cn
Citation:
Yang Min, Xia Lili, Zhou Xiaoqin, Jia Chengli, Ji Min, Wang Peng. A Ratiometric Fluorescent Probe for Imaging Hydrogen Peroxide in Living Cells[J]. Chinese Journal of Organic Chemistry,
;2020, 40(9): 2888-2894.
doi:
10.6023/cjoc202002030
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Insert: the color changes of the systems after adding H2O2 (500 μmol/L) to the probe HDP-1 (10 μmol/L) under visible light. "—" represents HDP-1 (10 μmol/L) without H2O2; "+" represents HDP-1 (10 μmol/L) with H2O2 (500 μmol/L)
(1) Blank, (2) H2O2 (200 μmol/L), (3) Cu2+ (1 mmol/L), (4) Na+(1 mmol/L), (5) Zn2+ (1 mmol/L), (6) ClO- (500 μmol/L), (7) •OH (500 μmol/L), (8) •O2- (500 μmol/L), (9) •OtBu (500 μmol/L), (10) TBHP (500 μmol/L), (11) CN- (500 μmol/L), (12) HSO3- (500 μmol/L), (13) Cys (1 mmol/L), (14) Hcy (1 mmol/L), (15) GSH (1 mmol/L). λex=420 nm
(a~d) Cells were co-cultured with probe HDP-1 (10 μmol/L), (e~h) cells were co-cultured with probe HDP-1 (10 μmol/L) for 30 min after pre-treatment with LPS (10 μg/mL), and (i~l) cells co-cultured with probe HDP-1 (10 μmol/L) for 30 min after pre-treatment with H2O2 (100 μmol/L). Green channel: λem=497~557 nm. Red channel: λem=570~625 nm.λex=420 nm. Scale bar: 10 μm