• Developed novel hyaluronic acid-modified copper-DMSA nanoparticles (Cu-DMSA-HA NPs) for targeted NSCLC therapy.
• HA surface modification enables selective targeting of CD44-overexpressing cancer cells, enhancing uptake and specificity.
• NPs deplete glutathione and sustain ROS production via Fenton-like reaction, inducing ferroptosis and suppressing tumor growth.
• In vitro and in vivo results demonstrate robust catalytic activity and tumor specificity, highlighting clinical translation potential.
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