Imaging and detection of sulfite in acute liver injury with a novel quinoxaline-based fluorescent probe

Herein, a novel fluorescent probe HZY was developed for monitoring the sulfite (SO32 � ) dynamics. For the first time, the SO32 � triggered implement was applied in the acute liver injury (ALI) model. The levulinate was selected to achieve the specific and relatively steady recognition reaction. With the addition of SO32 , the fluorescence response of HZY exhibited a large Stokes shift of 110 nm under the 380 nm excitation. The merits included high selectivity under various pH conditions. Compared with the reported fluorescent probes for sulfite, HZY indicated above-moderate performances including remarkable and rapid response (40 folds, within 15 min), and high sensitivity (limit of detection = 0.21 & mu;M). Further, HZY could visualize the exogenous and endogenous SO32 � level in living cells. Moreover, HZY could gauge the changing levels of SO32 � in three types (induced by CCl4, APAP, and alcohol) of ALI models. Both in vivo imaging and depth-of-penetration fluorescence imaging demonstrated that HZY could characterize the developmental and therapeutic status during the liver injury process by measuring the dynamic of SO32- . The successful implementation of this project would promote the accurate in-situ detection of SO32 � in liver injury, which was expected to guide the pre-clinical diagnosis and clinical practice.

Automated summary

A new fluorescent probe HZY was developed for monitoring the dynamics of sulfite (SO32-). The probe was successfully applied in an acute liver injury (ALI) model, showing high selectivity and sensitivity. HZY could visualize the levels of SO32- in living cells and gauge the changing levels of SO32- in different ALI models. The implementation of this project has important implications for the accurate detection of SO32- in liver injury and can guide pre-clinical diagnosis and clinical practice.