With
the widespread use of drugs, drug-induced acute kidney injury
(AKI) has become an increasingly serious health concern worldwide.
Currently, early diagnosis of drug-induced AKI remains challenging
because of the lack of effective biomarkers and noninvasive imaging
tools. SO<sub>2</sub> plays important physiological roles in living
systems and is an important antioxidant for maintaining redox homeostasis.
However, the relationship between SO<sub>2</sub> (in water as SO<sub>3</sub><sup>2–</sup>/HSO<sub>3</sub><sup>–</sup>) and
drug-induced AKI remains largely unknown. Herein, we report the highly
sensitive near-infrared fluorescence probe <b>DSMN</b>, which
for the first time reveals the relationship between SO<sub>2</sub> and drug-induced AKI. The probe responds to SO<sub>3</sub><sup>2–</sup>/HSO<sub>3</sub><sup>–</sup> selectively and rapidly (within
seconds) and shows a significant turn-on fluorescence at 710 nm with
a large Stokes shift (125 nm). With these properties, the probe was
successfully applied to detect SO<sub>2</sub> in living cells and
mice. Importantly, the probe can selectively target the kidneys, allowing
for the detection of changes in the SO<sub>2</sub> concentration in
the kidneys. Based on this, <b>DSMN</b> was successfully used
to detect cisplatin-induced AKI and revealed an increase in the SO<sub>2</sub> levels. The results indicate that SO<sub>2</sub> is a new
biomarker for AKI and that <b>DSMN</b> is a powerful tool for
studying and diagnosing drug-induced AKI.