Опубликована: Янв. 1, 2023
The combination of diagnostic and therapeutic agents in the form theranostic platforms is receiving increasing attention to enhance tumor efficacy. However, traditional systems relying on simultaneous encapsulation, embedding or conjugation various onto nanocarriers always require intricate synthetic process. Herein, a supramolecular drug-drug self-delivery nanosystem (DSDN) based newly developed aggregation-induced emission (AIE) photosensitizer (CBTM) an anti-tumor tyroservaltide (YSV) was constructed integrate near-infrared (NIR) fluorescence, photodynamic, chemotherapeutic effects. Transmission electron microscopy (TEM) dynamic light scattering (DLS) confirmed that YSV CBTM could co-assemble into YSV/CBTM nanoparticles via π-π stacking hydrogen bonding, with regular round-shape morphology homogeneous size. Inspiringly, entered CT26 cells high NIR fluorescence emission, allowing preoperative diagnosis. Meanwhile, as-prepared efficiently produce reactive oxygen species (ROS) under irradiation for effective photodynamic ablation cells. More importantly, peptide drug not only improve availability CBTM, but also serve as toxic adjuvant therapy (PDT) efficacy CBTM. Thereafter, most tumors were thoroughly ablated by combining PDT chemotherapy (CT) maximal killing colorectal tissues. Regarding advantages nanosystem, we believe this strategy significantly potentiate survival cancer mice maximizing efficacy, offer prospective insights advanced applications.
Язык: Английский