Near-Infrared Chemiluminescence Imaging of Chemotherapy-Induced Peripheral Neuropathy

Chemotherapy-induced peripheral neuropathy (CIPN) has a high prevalence but is poorly managed for cancer patients due to the lack of reliable and sensitive diagnostic techniques. Molecular optical imaging can provide a noninvasive way for real-time monitoring of CIPN; However, this is not reported, likely due to the absence of optical probes capable of imaging deep into the spinal canal and possessing sufficient sensitivity for minimal dosage through local injection into the dorsal root ganglia. Herein, a near-infrared (NIR) chemiluminophore (MPBD) with a chemiluminescence quantum yield higher than other reported probes is synthesized and a NIR activatable chemiluminescent probe (CalCL) is developed for in vivo imaging of CIPN. CalCL is constructed by caging MPBD with calpain-cleavable peptide moiety while conjugating polyethylene glycol chain to endow water solubility. Due to the deep-tissue penetration of chemiluminescence and specific turn-on response of CalCL toward calpain (a hallmark of CIPN), it allows for sensitive detection of paclitaxel-mediated CIPN in living mice, which is unattainable by fluorescence imaging. This study thus not only develops a highly efficient chemiluminescent probe, but also presents the first optical imaging approach toward high-throughput screening of neurotoxic drugs. A highly bright near-infrared chemiluminophore is synthesized and developed into a water-soluble activatable probe (CalCL) for in vivo imaging of drug-induced peripheral neuropathy.image

Automated summary

Chemotherapy-induced peripheral neuropathy (CIPN) is common in cancer patients but poorly managed due to the lack of reliable diagnostic techniques. In this study, a near-infrared chemiluminophore (MPBD) was synthesized and developed into a water-soluble activatable probe (CalCL) for in vivo imaging of CIPN. The probe allows for sensitive detection of paclitaxel-mediated CIPN in living mice, which is not achievable with fluorescence imaging. This research not only develops a highly efficient chemiluminescent probe, but also presents the first optical imaging approach for high-throughput screening of neurotoxic drugs.