Ultra-small iron-gallic acid coordination polymer nanoparticles for chelator-free labeling of 64Cu and multimodal imaging-guided photothermal therapy

被引:87
作者
Jin, Qiutong [1 ]
Zhu, Wenjun [1 ]
Jiang, Dawei [2 ,3 ,4 ]
Zhang, Rui [1 ]
Kutyreff, Christopher J. [2 ,3 ]
Engle, Jonathan W. [2 ,3 ]
Huang, Peng [4 ]
Cai, Weibo [2 ,3 ]
Liu, Zhuang [1 ]
Cheng, Liang [1 ]
机构
[1] Soochow Univ, CNST, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Inst Funct Nano & Soft Mat FUNSOM, Suzhou 215123, Jiangsu, Peoples R China
[2] Univ Wisconsin, Dept Radiol, Madison, WI 53705 USA
[3] Univ Wisconsin, Dept Med Phys, Madison, WI 53705 USA
[4] Shenzhen Univ, Hlth Sci Ctr, Sch Biomed Engn, Guangdong Key Lab Biomed Measurements & Ultrasoun, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
METAL-ORGANIC FRAMEWORKS; CANCER-THERAPY; DRUG-DELIVERY; NANOSHEETS; ABLATION; TUMOR; CLEARANCE; NANORODS;
D O I
10.1039/c7nr03086j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cancer nanotechnology has become the hot topic nowadays. While various kinds of nanomaterials have been widely explored for innovative cancer imaging and therapy applications, safe multifunctional nanoagents without long-term retention and toxicity are still demanded. Herein, iron-gallic acid coordination nanoparticles (Fe-GA CPNs) with ultra-small sizes are successfully synthesized by a simple method for multimodal imaging-guided cancer therapy. After surface modification with polyethylene glycol (PEG), the synthesized Fe-GA-PEG CPNs show high stability in various physiological solutions. Taking advantage of high near-infrared (NIR) absorbance as well as the T1-MR contrasting ability of Fe-GA-PEG CPNs, in vivo photoacoustic tomography (PAT) and magnetic resonance (MR) bimodal imaging are carried out, revealing the efficient passive tumor targeting of these ultra-small CPNs after intravenous (i.v.) injection. Interestingly, such Fe-GA-PEG CPNs could be labeled with the Cu-64 isotope via a chelator-free method for in vivo PET imaging, which also illustrates the high tumor uptake of Fe-GA CPNs. We further utilize Fe-GA-PEG CPNs for in vivo photothermal therapy and achieve highly effective tumor destruction after i.v. injection of Fe-GA-PEG CPNs and the following NIR laser irradiation of the tumors, without observing any apparent toxicity of such CPNs to the treated animals. Our work highlights the promise of ultra-small iron coordination nanoparticles for imaging-guided cancer therapy.
引用
收藏
页码:12609 / 12617
页数:9
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