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A red blood cell-derived bionic microrobot capable of hierarchically adapting to five critical stages in systemic drug delivery.
Zhu, Ya-Xuan; Jia, Hao-Ran; Jiang, Yao-Wen; Guo, Yuxin; Duan, Qiu-Yi; Xu, Ke-Fei; Shan, Bai-Hui; Liu, Xiaoyang; Chen, Xiaokai; Wu, Fu-Gen.
Afiliação
  • Zhu YX; State Key Laboratory of Digital Medical Engineering Jiangsu Key Laboratory for Biomaterials and Devices School of Biological Science and Medical Engineering Southeast University Nanjing Jiangsu People's Republic of China.
  • Jia HR; Shanghai Tenth People's Hospital Shanghai Frontiers Science Center of Nanocatalytic Medicine School of Medicine Tongji University Shanghai People's Republic of China.
  • Jiang YW; State Key Laboratory of Digital Medical Engineering Jiangsu Key Laboratory for Biomaterials and Devices School of Biological Science and Medical Engineering Southeast University Nanjing Jiangsu People's Republic of China.
  • Guo Y; The Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital) Hangzhou Institute of Medicine (HIM) Chinese Academy of Sciences Hangzhou Zhejiang People's Republic of China.
  • Duan QY; State Key Laboratory of Digital Medical Engineering Jiangsu Key Laboratory for Biomaterials and Devices School of Biological Science and Medical Engineering Southeast University Nanjing Jiangsu People's Republic of China.
  • Xu KF; State Key Laboratory of Digital Medical Engineering Jiangsu Key Laboratory for Biomaterials and Devices School of Biological Science and Medical Engineering Southeast University Nanjing Jiangsu People's Republic of China.
  • Shan BH; State Key Laboratory of Digital Medical Engineering Jiangsu Key Laboratory for Biomaterials and Devices School of Biological Science and Medical Engineering Southeast University Nanjing Jiangsu People's Republic of China.
  • Liu X; State Key Laboratory of Digital Medical Engineering Jiangsu Key Laboratory for Biomaterials and Devices School of Biological Science and Medical Engineering Southeast University Nanjing Jiangsu People's Republic of China.
  • Chen X; State Key Laboratory of Digital Medical Engineering Jiangsu Key Laboratory for Biomaterials and Devices School of Biological Science and Medical Engineering Southeast University Nanjing Jiangsu People's Republic of China.
  • Wu FG; State Key Laboratory of Digital Medical Engineering Jiangsu Key Laboratory for Biomaterials and Devices School of Biological Science and Medical Engineering Southeast University Nanjing Jiangsu People's Republic of China.
Exploration (Beijing) ; 4(2): 20230105, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38855612
ABSTRACT
The tumour-targeting efficiency of systemically delivered chemodrugs largely dictates the therapeutic outcome of anticancer treatment. Major challenges lie in the complexity of diverse biological barriers that drug delivery systems must hierarchically overcome to reach their cellular/subcellular targets. Herein, an "all-in-one" red blood cell (RBC)-derived microrobot that can hierarchically adapt to five critical stages during systemic drug delivery, that is, circulation, accumulation, release, extravasation, and penetration, is developed. The microrobots behave like natural RBCs in blood circulation, due to their almost identical surface properties, but can be magnetically manipulated to accumulate at regions of interest such as tumours. Next, the microrobots are "immolated" under laser irradiation to release their therapeutic cargoes and, by generating heat, to enhance drug extravasation through vascular barriers. As a coloaded agent, pirfenidone (PFD) can inhibit the formation of extracellular matrix and increase the penetration depth of chemodrugs in the solid tumour. It is demonstrated that this system effectively suppresses both primary and metastatic tumours in mouse models without evident side effects, and may represent a new class of intelligent biomimicking robots for biomedical applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Exploration (Beijing) Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Exploration (Beijing) Ano de publicação: 2024 Tipo de documento: Article
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