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. SO2 plays important physiological roles in living
systems and is an important antioxidant for maintaining redox homeostasis.
However, the relationship between SO2 (in water as SO32–/HSO3–) and
drug-induced AKI remains largely unknown. Herein, we report the highly
sensitive near-infrared fluorescence probe DSMN, which
for the first time reveals the relationship between SO2 and drug-induced AKI. The probe responds to SO32–/HSO3– 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 SO2 in living cells and
mice. Importantly, the probe can selectively target the kidneys, allowing
for the detection of changes in the SO2 concentration in
the kidneys. Based on this, DSMN was successfully used
to detect cisplatin-induced AKI and revealed an increase in the SO2 levels. The results indicate that SO2 is a new
biomarker for AKI and that DSMN is a powerful tool for
studying and diagnosing drug-induced AKI.