A "turn-on" inverse opal photonic crystal fluorescent sensing film for detection of cysteine and its bioimaging of living cells.

Abstract

A "turn-on" inverse opal photonic crystal fluorescent sensing film infiltrated with a coumarin derivative is reported for the reliable and accurate detection of cysteine in human serum and fluorescence imaging of living cells. The coumarin derivative containing allyl ester specifically reacts with cysteine by ammonolysis to generate a fluorescent product whose emission wavelength is at ~ 535nm, providing a selective fluorescence detection for cysteine. The emitted fluorescence is significantly enhanced due to the slow photon effect derived from the photonic crystal film. This is because the emission wavelength is overlapped with the blue-band edge of the photonic stopband of the selected inverse opal film. The fluorescence enhancement effect endows the prepared inverse opal film with highly sensitive detection with a limit of detection of 3.23 × 10-9mol/L and a wide linear detection range of 1 × 10-7 - 1 × 10-3mol/L. A fast response within 30s toward cysteine is also achieved due to the three-dimensional interconnected macroporous structure with a high-specific surface area of the inverse opal film. The prepared inverse opal fluorescent sensing film has been successfully applied to the detection of cysteine in human serum and bioimaging of living cells. In the diluted human serum, the recoveries for the detection of cysteine were 97.92 - 107.20%, and the relative standard deviations were 2.61-9.04%, demonstrating the potential applicability of the inverse opal fluorescent sensing film to real sample analysis. The method may provide a universal strategy for constructing various photonic crystal fluorescent sensing films by using different fluorescent probes.