Design of a pH-sensitive supramolecular fluorescent probe for selective cancer cell imaging

In this study, a pH-sensitive fluorescent probe was created through the host-guest assembly of an amphiphilic hydroxyphenyl benzotriazole derivative (HBT-11) and cucurbit[7]uril (CB7). The fluorescence of HBT-11 is highly dependent on the molar ratio ( r ) of CB7 to HBT-11. If r  < 1, the peak positions remain unchanged while the intensity increases with r . If r  > 1, the emission peaks shift to longer wavelengths. The complexation also results in a shift in the p K a of HBT-11. The 1:1 mixture of CB7 and HBT-11 has a p K a close to neutral pH. The supramolecular probe allows for discrimination of malignant A549 and benign HEK 293T cells owing to a pronounced 8-fold light-up effect in malignant A549 cells attributed to the pH-responsive fluorescence. Given that the selective light-up mechanism is based on the pH-sensitive fluorescence of the supramolecular probe, this approach is expected to be applicable to other cancer cells.