Multiple-Armed Tetrahedral DNA Nanostructures for Tumor-Targeting, Dual-Modality in Vivo Imaging

被引:145
|
作者
Jiang, Dawei [1 ,2 ]
Sun, Yanhong [1 ,2 ]
Li, Jiang [1 ,2 ]
Li, Qian [1 ,2 ]
Lv, Min [1 ,2 ]
Zhu, Bing [1 ,2 ]
Tian, Tian [1 ,2 ]
Cheng, Dengfeng [3 ]
Xia, Jiaoyun [4 ]
Zhang, Lan [1 ,2 ]
Wang, Lihua [1 ,2 ]
Huang, Qing [1 ,2 ]
Shi, Jiye [5 ]
Fan, Chunhai [1 ,2 ]
机构
[1] Chinese Acad Sci, Div Phys Biol, Shanghai 201800, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, CAS Key Lab Interfacial Phys & Technol, Bioimaging Ctr, Shanghai 201800, Peoples R China
[3] Fudan Univ, Zhongshan Hosp, Dept Nucl Med, Shanghai 200032, Peoples R China
[4] Changsha Univ Sci & Technol, Sch Chem & Biol Engn, Changsha 410004, Hunan, Peoples R China
[5] UCB Pharma, Slough SL1 14EN, Berks, England
基金
美国国家科学基金会;
关键词
tetrahedral DNA nanostructures; tumor targeting; dual-modality imaging; single-photon emission computed tomography; near-infrared fluorescence; QUANTUM DOTS; MULTIFUNCTIONAL NANOPARTICLES; INORGANIC NANOPARTICLES; CARBON NANOTUBES; CANCER-THERAPY; DELIVERY; STABILITY; SPECT; PET; NANOTECHNOLOGY;
D O I
10.1021/acsami.5b10792
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this work, we have developed multiple-armed DNA tetrahedral nanostructures (TDNs) for dual-modality in vivo imaging using near-infrared (NIR) fluorescence and single-photon emission computed tomography (SPECT). We found that the presence of arm strands in TDNs remarkably enhanced their in vitro stability, allowing them to stay intact for at least 12 h in serum. By using NIR fluorescence imaging, we evaluated in mice the pharmacokinetics of TDNs, which exhibited distinctly different in vivo biodistribution patterns compared with those of double-stranded (ds)DNA. We also noticed that TDNs had twofold longer circulation time in the blood system than that of dsDNA. With the use of multiple armed TDNs, we could precisely anchor an exact number of functional groups including tumor-targeting folic acid (FA), NIR emitter Dylight 755, and radioactive isotope Tc-99m on prescribed positions of TDNs, which showed the capability of targeted imaging ability in cancer cells. Furthermore, we realized noninvasive tumor-targeting imaging in tumor-bearing mice by using both NIR and SPECT modalities.
引用
收藏
页码:4378 / 4384
页数:7
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