ABSTRACT Parkinson's disease (PD) pathogenesis has been linked to the aberrant accumulation of lipid droplets (LDs). Understanding the situation of LD accumulation and its dynamic variations in the neural tissues of PD patients is therefore crucial for deciphering the underlying pathophysiological mechanisms of this neurodegenerative disorder. Developing a specific fluorescent probe for LDs that can also function within the brain presents a significant challenge. This study introduces a NIR (near‐infrared) emitting fluorescent probe, QCN‐TP, through step‐by‐step molecular design strategy, based on a novel framework of dye, characterized by multiple advantageous properties, including polarity sensitivity, a substantial Stokes shift (150–280 nm), and aggregation‐induced emission (AIE). The probe, QCN‐TP, demonstrates remarkable sensitivity and selectivity in the recognition of LD accumulation, with enhanced deep tissue penetration capabilities. Notably, QCN‐TP effectively monitors both the presence of intracellular LDs and their dynamic content variations in MPP + ‐induced PD cell models. Furthermore, the probe enables in vivo imaging of abnormal LD accumulation in the brain tissue of PD model mice. This probe offers a useful tool for real‐time monitoring of lipid dynamics, with potential applications in PD research and drug discovery.
Li et al. (Wed,) studied this question.