Abstract
Photodynamic therapy (PDT) is a non-invasive
therapeutic strategy for cancer treatment but it always suffers from low
reactive oxygen species (ROS) efficiency generated from traditional organic dyes owing to weak
absorption in the optical transparent window of biological tissues and
fluorescence quenching at a concentrated solution or in nanoparticles. Herein, we present cationic
lipid-encapsulated aggregation-induced emission (AIE) nanoparticles (NPs) that
have a high quantum yield (23%) and a maximum two-photon absorption (TPA) cross-section
of 560 GM irradiated by near infrared light (800 nm). The AIE NPs can
serve as imaging agents for spatiotemporal
imaging of tumor tissues with a penetration depth up to 505 µm on mice melanoma model. Noteworthy, the AIE NPs can efficiently generate
singlet oxygen (1O2) and highly toxic hydroxyl
radicals (·OH) upon 800 nm-light irradiation for photodynamic tumor ablation. In addition, the AIE NPs can be
effectively cleared from the mouse body after the imaging and therapy. This
study provides a new strategy to develop theranostic agent for cancer
image-guided PDT with high brightness, superior photostability and high
biosafety