A Natural product-based composite nanozyme synergistically induces ferroptosis for lung cancer therapy

  • RSC Adv. 2026 May 26;16(31):28583-28591. doi: 10.1039/d6ra00383d.
Yishun Jin  1 Chen Huang  2 Zhenbo Geng  1 Huang Li  3 Huiqing Ge  2 Pengfei Wang  1 Chaojun Dai  1 Jun Li  4  5 Xiaohua Yan  1 Chen Li  6 Yan Zheng  7
Affiliations
  • 1. Department of Traditional Chinese Medicine, Fuzhou University Affiliated Provincial Hospital Fuzhou 350001 China [email protected].
  • 2. Department of Thoracic Surgery, Fuzhou University Affiliated Provincial Hospital Fuzhou China.
  • 3. School of Pharmacy, Fujian University of Traditional Chinese Medicine Fuzhou 350122 China.
  • 4. Department of Critical Care Medicine, Fuzhou University Affiliated Provincial Hospital, Fujian Provincial Hospital Fuzhou 350001 China.
  • 5. Fujian Provincial Center for Critical Care Medicine, Fujian Provincial Key Laboratory of Critical Care Medicine Fuzhou 350001 China.
  • 6. College of Pharmacy, Hainan Academy of Medical Sciences, Hainan Medical University Haikou Hainan 571199 China [email protected].
  • 7. Department of Oncology, Fuzhou University Affiliated Provincial Hospital China [email protected].
Abstract

The treatment of lung Cancer remains a significant clinical challenge. Inducing Ferroptosis is a promising therapeutic strategy to overcome treatment resistance in lung Cancer. Herein, we report a composite nanozyme, Fe@Arc, engineered by coordinating arctigenin with iron ions followed by a high-temperature carbonization. This fabrication method yielded a nanozyme with a high drug-loading capacity and controlled release kinetics. Following intravenous administration, Fe@Arc efficiently accumulated at the tumor site owing to its enhanced permeability and retention effect. In the tumor site, it exerted a potent anti-tumor effect by catalyzing the Fenton reaction and releasing arctigenin, which synergistically triggered Ferroptosis in Cancer cells. This work presents a multifaceted platform that not only overcomes the pharmacological limitations of herbal extracts but also establishes a robust framework for developing novel Ferroptosis inducers, demonstrating significant potential for clinical translation.

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