Volume 28, Issue 30
Full Paper

Emancipating Target‐Functionalized Carbon Dots from Autophagy Vesicles for a Novel Visualized Tumor Therapy

Jipeng Li

Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai, 200011 China

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Siwei Yang

Center for Excellence in Superconducting Electronics (CENSE), State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology (SIMIT), Chinese Academy of Science, Shanghai, 200500 China

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Yuan Deng

Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai, 200011 China

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Peiwei Chai

Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai, 200011 China

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Yucheng Yang

Center for Excellence in Superconducting Electronics (CENSE), State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology (SIMIT), Chinese Academy of Science, Shanghai, 200500 China

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Xiaoyu He

Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai, 200011 China

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Xiaoming Xie

Center for Excellence in Superconducting Electronics (CENSE), State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology (SIMIT), Chinese Academy of Science, Shanghai, 200500 China

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Zhenhui Kang

Corresponding Author

E-mail address: zhkang@suda.edu.cn

Jiangsu Key Laboratory for Carbon‐based Functional Materials and Devices, Institute of Functional Nano and Soft Materials (FUNSOM), Soochow University, Suzhou, 215123 China

E‐mail: zhkang@suda.edu.cn, gqding@mail.sim.ac.cn, fangzzfang@163.com, fanxq@sjtu.edu.cnSearch for more papers by this author
Guqiao Ding

Corresponding Author

E-mail address: gqding@mail.sim.ac.cn

Center for Excellence in Superconducting Electronics (CENSE), State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology (SIMIT), Chinese Academy of Science, Shanghai, 200500 China

E‐mail: zhkang@suda.edu.cn, gqding@mail.sim.ac.cn, fangzzfang@163.com, fanxq@sjtu.edu.cnSearch for more papers by this author
Huifang Zhou

Corresponding Author

E-mail address: fangzzfang@163.com

Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai, 200011 China

E‐mail: zhkang@suda.edu.cn, gqding@mail.sim.ac.cn, fangzzfang@163.com, fanxq@sjtu.edu.cnSearch for more papers by this author
Xianqun Fan

Corresponding Author

E-mail address: fanxq@sjtu.edu.cn

Department of Ophthalmology, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai, 200011 China

E‐mail: zhkang@suda.edu.cn, gqding@mail.sim.ac.cn, fangzzfang@163.com, fanxq@sjtu.edu.cnSearch for more papers by this author
First published: 28 May 2018
Citations: 27

Abstract

Killing the tumor cells by a visualized targeting system is a promising strategy with which to achieve high efficiency, low side effects, and a high survival rate for tumor therapy. Here, an autophagy regulation strategy is reported by emancipating target‐functionalized carbon dots from autophagy vesicles for the efficient visualized tumor therapy. The folic acid modified N‐doped carbon dots (FN‐CDs) are selectively endocytosed (specific cellular uptake rate >93.40%) and stably existed in autophagic vacuoles in tumor cells. Next, the autophagic vacuoles are “opened” by the autophagy inhibitors. Released FN‐CDs activate both the intrinsic and extrinsic apoptotic signaling pathway and kill tumor cells efficiently. This method achieves therapeutic effects with high performance in 26 types of tumor cell lines. Animal experiments show that the 30 d survival rate of this therapeutic strategy is much higher than that with traditional drug treatment. Real‐time imaging/monitoring and its effects on the intelligent tumor therapy are also demonstrated based on the stable, strong, green emission from FN‐CDs.

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