Spatio-Temporally Reporting Dose-Dependent Chemotherapy via Uniting Dual-Modal MRI/NIR Imaging

被引:58
|
作者
Ma, Yiyu [1 ,2 ]
Yan, Chenxu [1 ,2 ]
Guo, Zhiqian [1 ,2 ]
Tan, Guang [1 ,2 ]
Niu, Dechao [3 ]
Li, Yongsheng [3 ]
Zhu, Wei-Hong [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Frontiers Sci Ctr Mat & Dynam Chem, Key Lab Adv Mat, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Sch Chem & Mol Engn, Frontiers Sci Ctr Mat & Dynam Chem, Inst Fine Chem Joint Int Res Lab Precis Chem & Mo, Shanghai 200237, Peoples R China
[3] East China Univ Sci & Technol, Sch Mat Sci & Engn, Minist Educ, Key Lab Ultrafine Mat, Shanghai 200237, Peoples R China
基金
中国博士后科学基金;
关键词
assembly nanotheranostics; chemodynamic therapy; fluorescent probes; magnetic resonance imaging; near-infrared dual-channel; PROBE; FLUORESCENCE; TRACKING; PRODRUG; H2O2;
D O I
10.1002/anie.202009380
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Unpredictable in vivo therapeutic feedback of hydroxyl radical ((OH)-O-.) efficiency is the major bottleneck of chemodynamic therapy. Herein, we describe novel Fenton-based nanotheranostics NQ-Cy@Fe&GOD for spatio-temporally reporting intratumor(.)OH-mediated treatment, which innovatively unites dual-channel near-infrared (NIR) fluorescence and magnetic resonance imaging (MRI) signals. Specifically, MRI signal traces the dose distribution of Fenton-based iron oxide nanoparticles (IONPs) with high-spatial resolution, meanwhile timely fluorescence signal quantifies(.)OH-mediated therapeutic response with high spatio-temporal resolution. NQ-Cy@Fe&GOD can successfully monitor the intracellular release of IONPs and(.)OH-induced NQO1 enzyme in living cells and tumor-bearing mice, which makes a breakthrough in conquering the inherent unpredictable obstacles on spatio-temporally reporting chemodynamic therapy, so as to manipulate dose-dependent therapeutic process.
引用
收藏
页码:21143 / 21150
页数:8
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