A coumarin-based fluorescent probe for sensitive monitoring H2O2 in water and living cells

By introducing boronate esters as a recognition unit, a fluorescent probe (Probe 1) was developed for the qualitative and quantitative determination of hydrogen peroxide. Absorbance spectra and fluorescence emission spectra of Probe 1 and the reaction product were studied. It was found that maximum absor-bance peak changed from 321 nm to 372 nm and an emission peak centered at 451 nm appeared. The fluorescence intensity at 451 nm enhanced with the linear increase of the H2O2 concentration (0- 180 lM) and the detection limit was calculated to be 118.2 nM. Even in the presence of various ions, the fluorescence intensity remained relatively unchanged. Moreover, Probe 1 was further used to image macrophage RAW264.7 and colon cancer cell SW480 because it worked excellently under leaning alka-linity condition, which indicated the good cell-membrane permeability of Probe 1 and its potential ability to detect the exogenous and endogenous H2O2 in living organisms.(c) 2022 Elsevier Ltd. All rights reserved.

Automated summary

By introducing boronate esters as a recognition unit, a fluorescent probe (Probe 1) was developed for the qualitative and quantitative determination of hydrogen peroxide. The probe exhibited a change in absorbance and fluorescence emission spectra upon reaction with hydrogen peroxide, and it showed high sensitivity with a detection limit of 118.2 nM. The probe also demonstrated good stability and selectivity in the presence of various ions and was successfully used for imaging macrophage and colon cancer cells.