Cyclic molecules exhibit distinct advantages in drug
discovery
and delivery. Herein, we synthesized a cyclic BODIPY photosensitizer
(BR) and constructed a versatile platform for inducing pyroptosis
and enhancing tumor photoimmunotherapy. Benefiting from the cyclic
structure, BR could assemble into nanoparticles (BRNs) with robust
long-term colloidal stability. The single-crystal X-ray diffraction
result indicates that the intermolecular forces of BR are mainly π–π
stacking interactions and H-bonds. Furthermore, the dimers of indoleamine
2,3-dioxygenase inhibitor were loaded to form BRGNs for alleviating
immunosuppression tumor microenvironment. BRGNs generate reactive
oxygen species and disrupt intracellular redox homeostasis upon irradiation,
leading to mitochondrial damage and innate immunogenic pyroptosis.
Subsequently, intracellularly abundant cytokines and contents are
released to elicit robust immune responses for inhibiting the tumor
growth. In brief, this work brings an approach to build cyclic carriers
integrating phototherapy and immunotherapy.