Chuanyu Mao, Z. Wang, Shuangjia Liu, Xiaoyu Li, Yuhan Wang, Ruxiang Luo, Min Yang, Chongzhao Ran, Yueqing Gu, Peng Wang, Jing Yang
Alzheimer’s disease (AD) has a complex pathogenesis in which superoxide anion (O 2 •– ), a key reactive oxygen species (ROS), plays a critical role. Monitoring O 2 •– is essential for understanding AD mechanisms and improving early diagnosis. Chemiluminescence imaging provides high contrast without external excitation, making it ideal for in vivo O 2 •– detection. However, few probes can specifically image O 2 •– in the AD brain. To address this, we designed a chemiluminescence probe, DIP-O, for in vivo O 2 •– imaging in AD. In vitro tests showed that DIP-O emits in the near-infrared region (708 nm) with a tissue penetration depth over 2.0 cm, high sensitivity (LOD = 27.9 nM), and excellent specificity for O 2 •– . We validated its imaging performance in peripheral inflammation models (e.g., arthritis and peritonitis), where it enabled real-time, high-contrast tracking of O 2 •– . Furthermore, DIP-O successfully crossed the blood–brain barrier and distinguished O 2 •– levels in the brains of three-month-old AD mice versus wild-type mice, indicating early diagnostic potential. Finally, we applied DIP-O to monitor age-dependent O 2 •– changes in AD mice, demonstrating its capability for sensitive imaging throughout disease progression.