Light triggered release of a triple action porphyrin-cisplatin conjugate evokes stronger immunogenic cell death for chemotherapy, photodynamic therapy and cancer immunotherapy

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作者
Haiqin Song
Zhenghao Cai
Juyi Li
Haihua Xiao
Ruogu Qi
Minhua Zheng
机构
[1] Ruijin Hospital,Department of General Surgery, School of Medicine
[2] Shanghai Jiaotong University,Department of Materials Science and Chemical Engineering
[3] Stony Brook University,Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Polymer Physics and Chemistry, Institute of Chemistry
[4] Chinese Academy of Sciences,School of Medicine and Holistic Integrative Medicine
[5] Nanjing University of Chinese Medicine,undefined
关键词
Porphyrin; Cisplatin; Immunogenic cell death; Cancer immunotherapy; Photodynamic therapy; Nanoparticles;
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摘要
Photodynamic therapy (PDT) has emerged as an attractive therapeutic approach which can elicit immunogenic cell death (ICD). However, current ICD inducers are still very limited as the representative ICD induces of photosensitizers can only evoke insufficient ICD to achieve unsatisfactory cancer immunotherapy. Herein, we demonstrated the use of a triple action cationic porphyrin-cisplatin conjugate (Pt-1) for drug delivery by a reactive oxygen species (ROS) sensitive polymer as nanoparticles (NP@Pt-1) for combined chemotherapy, PDT and immunotherapy. This unique triple action Pt-1 contains both chemotherapeutic Pt drugs and Porphyrin as a photosensitizer to generate ROS for PDT. Moreover, the ROS generated by Pt-1 can on the one hand degrade polymer carriers to release Pt-1 for chemotherapy and PDT. On the other hand, the ROS generated by Pt-1 subsequently triggered the ICD cascade for immunotherapy. Taken together, we demonstrated that NP@Pt-1 were the most effective and worked in a triple way. This study could provide us with new insight into the development of nanomedicine for chemotherapy, PDT as well as cancer immunotherapy.
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