An Ultrasound Activated Vesicle of Janus Au-MnO Nanoparticles for Promoted Tumor Penetration and Sono-Chemodynamic Therapy of Orthotopic Liver Cancer

被引:312
作者
Lin, Xiahui [1 ]
Liu, Shuya [2 ]
Zhang, Xuan [1 ]
Zhu, Rong [1 ]
Chen, Shan [1 ]
Chen, Xiaoyuan [3 ]
Song, Jibin [1 ]
Yang, Huanghao [1 ]
机构
[1] Fuzhou Univ, Coll Chem, MOE Key Lab Analyt Sci Food Safety & Biol Inst, Fuzhou 350108, Fujian, Peoples R China
[2] Fuzhou Univ, Coll Biol Sci & Engn, Fuzhou 350108, Fujian, Peoples R China
[3] NIBIB, Lab Mol Imaging & Nanomed LOMIN, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
chemodynamic therapy; Janus nanoparticles; self-assembly; sonodynamic therapy; ultrasound; SONODYNAMIC THERAPY; ACOUSTIC CAVITATION; NANOSONOSENSITIZERS;
D O I
10.1002/anie.201912768
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Sonodynamic therapy (SDT) has the advantages of high penetration, non-invasiveness, and controllability, and it is suitable for deep-seated tumors. However, there is still a lack of effective sonosensitizers with high sensitivity, safety, and penetration. Now, ultrasound (US) and glutathione (GSH) dual responsive vesicles of Janus Au-MnO nanoparticles (JNPs) were coated with PEG and a ROS-sensitive polymer. Upon US irradiation, the vesicles were disassembled into small Janus Au-MnO nanoparticles (NPs) with promoted penetration ability. Subsequently, GSH-triggered MnO degradation simultaneously released smaller Au NPs as numerous cavitation nucleation sites and Mn2+ for chemodynamic therapy (CDT), resulting in enhanced reactive oxygen species (ROS) generation. This also allowed dual-modality photoacoustic imaging in the second near-infrared (NIR) window and T-1-MR imaging due to the released Mn2+, and inhibited orthotopic liver tumor growth via synergistic SDT/CDT.
引用
收藏
页码:1682 / 1688
页数:7
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