Peroxynitrite (ONOO-), a strong oxidizing agent, has an important function in the pathogenesis of various diseases, including cardiovascular, inflammatory and neurodegenerative diseases. Specifically, mitochondrial ONOO- exacerbates liver injury by driving oxidative/nitrative stress and mitochondrial dysfunction, ultimately triggering dual apoptotic-necrotic hepatocyte death pathways. ONOO- and its functions have been widely studied by fluorescence imaging probes, owing to their strong sensitivity, non-invasiveness, and real-time ability. However, existing probes are heavily constrained by interference from other reactive species. Herein, we describe a luminescent iridium(III) complex (1) with an N-morpholinoarylimine moiety as the recognition site for ONOO- for imaging mitochondrial ONOO-. The probe shows high luminescence response to ONOO- in aqueous buffer, with a luminescence enhancement of 27-fold at 100 μM ONOO- and a limit of detection (LOD) of 0.65 μM, as well as high selectivity over other reactive species. Furthermore, the probe can sense both exogenous and endogenous mitochondrial ONOO-. Further experiments demonstrated it could visualize exogenous ONOO- in 3D multicellular tumor spheroids (MCTSs) and unmask endogenous ONOO- production through an NADPH oxidase 4 (NOX-4)-mediated pathway in drug-induced liver cells. This work demonstrates the potential of this strategy for developing imaging tools for probing the pathological roles of subcellar ONOO- and diagnosing liver injury in the clinic.
Kong et al. (Tue,) studied this question.