Multistage tumor microenvironment-responsive theranostic nanopeanuts: Toward multimode imaging guided chemo-photodynamic therapy

被引:52
|
作者
Jing, Xunan [1 ]
Zhi, Zhe [2 ]
Zhang, Ning [1 ]
Song, Huanhuan [1 ]
Xu, Yanzi [1 ]
Zhou, Guoqing [3 ]
Wang, Daquan [1 ]
Shao, Yongping [2 ]
Meng, Lingjie [1 ,3 ]
机构
[1] Xi An Jiao Tong Univ, Sch Sci, MOE Key Lab Nonequilibrium Synth & Modulat Conden, Xian Key Lab Sustainable Energy Mat Chem, Xian 710049, Peoples R China
[2] Xi An Jiao Tong Univ, Ctr Translat Med, Frontier Inst Sci & Technol, Xian 710049, Peoples R China
[3] Xi An Jiao Tong Univ, Instrumental Anal Ctr, Xian 710049, Peoples R China
基金
中国国家自然科学基金;
关键词
Tumor microenvironment; Polyphosphazene; Biodegradability; Multimodal imaging; Chemo-photodynamic therapy; IN-VIVO; NANOPARTICLES; GENERATION; NANOTUBES; NANORODS; SYNERGY; HYPOXIA; PEPTIDE;
D O I
10.1016/j.cej.2019.123893
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
It is of great importance to develop tumor microenvironment (TME) responsive and adjustable theranostic nanosystems for specific and efficient cancer treatment. However, carrier-based nanomedicines are often inefficacious in vivo due to low drug-loading efficiency, lack of synergistic effects, poor targeting specificity and limited drug accumulation in tumor tissues. Herein, we report a new multimodal theranostic nanoplatform which is assembled from Fe3O4 nanoclusters, MnO2 nanosheets with multifunctional and cross-linked polyphosphazene. This peanut-like nanoplatform exhibited enhanced chemo/photodynamic therapy (CT/PDT) effect as well as significant tumor-targeting capacity. In addition, Fe3O4 cores and MnO2 nanoshells enables T-1/T-2 magnetic resonance imaging (MRI) of tumor tissues, while photosensitizer methylene blue (MB) allows for fluorescence imaging and PDT simultaneously. Importantly, nanopeanut agents could dual-regulate intracellular oxygen and glutathione (GSH) levels in TME by MnO2 shells, to relieve hypoxic condition and produce enough ROS to induce cell apoptosis. Our research demonstrated that the multistage TME-responsive nanoplatform is ideally suitable for tumor specific drug delivery and real-time disease tracking with enhanced theranostic properties.
引用
收藏
页数:12
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