摘要
Photocatalytic immunotherapy has attracted significant attention due to high selectivity and low side effects. However, the poor tissue penetration of ultraviolet-visible light and the low energy of near-infrared (NIR) photons, combined with the immunosuppressive tumor microenvironment (TME), severely limit catalytic efficiency and immune activation. In this study, we designed a gradient Zn 2 + -doping polymeric carbon nitride (PCN) nanocatalyst (gZn-PCN@M), in which the Zn 2 + concentration gradually decreases from the interior to the surface of the PCN nanosheets. Under 808 nm laser irradiation, gZn-PCN@M catalyzes the decomposition of H 2 O in tumor interstitial fluid to produce hydrogen gas, which reduces the intratumoral delivery resistance, markedly enhancing the penetration depth of gZn-PCN into tumors. Meanwhile, the acidic TME and laser irradiation further promote Zn 2 + release from gZn-PCN, resulting in abnormally elevated intracellular Zn 2 + levels that triggers ROS bursts and disrupts tumor energy metabolism, thereby downregulating PD-L1 expression in tumor cells and activating antitumor immune responses. The results indicated that the inhibition rates of gZn-PCN on primary tumors and distant tumors were 96.51% and 83.69%, respectively. This study proposes a gradient ion-doping strategy for the first time to enhance the NIR responsiveness of photocatalytic nanomedicines, combined with metabolic interference to achieve efficient tumor photocatalytic immunotherapy.
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