In Vivo Tumor-Targeted Dual-Modality PET/Optical Imaging with a Yolk/Shell-Structured Silica Nanosystem

被引:33
|
作者
Shi, Sixiang [1 ]
Chen, Feng [2 ]
Goel, Shreya [1 ]
Graves, Stephen A. [3 ]
Luo, Haiming [2 ]
Theuer, Charles P. [4 ]
Engle, Jonathan W. [3 ]
Cai, Weibo [1 ,2 ,3 ,5 ]
机构
[1] Univ Wisconsin Madison, Dept Mat Sci & Engn, 1509 Univ Ave, Madison, WI 53706 USA
[2] Univ Wisconsin Madison, Dept Radiol, Madison, WI 53705 USA
[3] Univ Wisconsin Madison, Dept Med Phys, 1530 Med Sci Ctr, Madison, WI 53706 USA
[4] TRACON Pharmaceut Inc, San Diego, CA USA
[5] Univ Wisconsin, Carbone Canc Ctr, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
Hollow mesoporous silica nanoparticle (HMSN); Quantum dot (QD); Molecular imaging; Positron emission tomography (PET); Optical imaging; CD105/endoglin; HOLLOW MESOPOROUS SILICA; GUIDED DRUG-DELIVERY; LIVING SUBJECTS; CANCER-THERAPY; NANOPARTICLES; VASCULATURE; ONCOLOGY; ENDOGLIN; AGENTS;
D O I
10.1007/s40820-018-0216-2
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Silica nanoparticles have been one of the most promising nanosystems for biomedical applications due to their facile surface chemistry and non-toxic nature. However, it is still challenging to effectively deliver them into tumor sites and noninvasively visualize their in vivo biodistribution with excellent sensitivity and accuracy for effective cancer diagnosis. In this study, we design a yolk/shell-structured silica nanosystem Cu-64-NOTA-QD@HMSN-PEG-TRC105, which can be employed for tumor vasculature targeting and dual-modality PET/optical imaging, leading to superior targeting specificity, excellent imaging capability and more reliable diagnostic outcomes. By combining vasculature targeting, pH-sensitive drug delivery, and dual-modality imaging into a single platform, as-designed yolk/shell-structured silica nanosystems may be employed for the future image-guided tumor-targeted drug delivery, to further enable cancer theranostics.
引用
收藏
页数:11
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