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A Ferroptosis-Inducing Arsenene-Iridium Nanoplatform for Synergistic Immunotherapy in Pancreatic Cancer
Authors:Xinyang Zhao  Xingyun Wang  Wei Zhang  Tian Tian  Jingyi Zhang  Jing Wang  Prof. Wei Wei  Prof. Zijian Guo  Prof. Jing Zhao  Xiuxiu Wang
Affiliation:1. Chemistry and Biomedicine Innovation Center (ChemBIC), State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023 China;2. School of Life Sciences, Nanjing University, Nanjing, 210023 China

These authors contributed equally.;3. School of Life Sciences, Nanjing University, Nanjing, 210023 China

Abstract:Due to multidrug resistance and the high risk of recurrence, effective and less toxic alternative pancreatic cancer treatments are urgently needed. Pancreatic cancer cells are highly resistant to apoptosis but sensitive to ferroptosis. In this study, an innovative nanoplatform ( AsIr@PDA ) was developed by electrostatic adsorption of a cationic iridium complex ( IrFN ) onto two-dimensional (2D) arsenene nanosheets. This nanoplatform exhibits superior ferroptosis-inducing effects with high drug loading capacity and, importantly, excellent anti-cancer immune activation function, leading to efficient elimination of pancreatic tumors with no observable side effects. Interestingly, AsIr@PDA significantly prevents the recurrence of pancreatic cancer in vivo when compared with a cisplatin-loaded nanoplatform. This designed nanoplatform demonstrated superior therapeutic efficacy by synergistic ferroptosis-induced chemotherapy with immunotherapy via an all-in-one strategy, providing new insights for future pancreatic cancer therapy.
Keywords:arsenene  iridium  ferroptosis  immunogenic cell death  pancreatic cancer
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