Intrinsically Zirconium-89-Labeled Manganese Oxide Nanoparticles for In Vivo Dual-Modality Positron Emission Tomography and Magnetic Resonance Imaging

被引:31
作者
Zhan, Yonghua [1 ]
Ehlerding, Emily B. [2 ]
Shi, Sixiang [3 ]
Graves, Stephen A. [2 ]
Goel, Shreya [3 ]
Engle, Jonathan W. [2 ]
Liang, Jimin [1 ]
Cai, Weibo [2 ,3 ]
机构
[1] Xidian Univ, Sch Life Sci & Technol, Minist Educ, Engn Res Ctr Mol & Neuro Imaging, Xian 710071, Shaanxi, Peoples R China
[2] Univ Wisconsin, Dept Med Phys, Madison, WI 53705 USA
[3] Univ Wisconsin, Dept Radiol, Madison, WI 53705 USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
Manganese Oxide Nanoparticles; Positron Emission Tomography; Magnetic Resonance Imaging; Zirconium-89; Chelator-Free; MNO NANOPARTICLES; CELLULAR MRI; CANCER; CONTRAST; AGENT; PLATFORM; PET/MRI; NANOCRYSTALS; ANGIOGENESIS; NANOPROBES;
D O I
10.1166/jbn.2018.2498
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Manganese-based nanoparticles (NPs) have recently attracted much attention in the field of biomedical imaging due to their impressive enhanced T-1 contrast ability. Although the reported manganese-based NPs have exhibited good imaging capabilities as contrast agents, it is still urgent to develop novel multifunctional manganese-based imaging probes for future biomedical imaging, especially PET/MRI probes. Herein, we present chelator-free zirconium-89 (Zr-89, t(1/2): 78.4 h) labeling of manganese oxide NPs (Mn3O4@PEG) with similar to 78% labeling yield and good stability. Serial positron emission tomography (PET) and magnetic resonance imaging (MRI) studies non-invasively assessed the biodistribution patterns of the NPs and the feasibility of in vivo dual-modality imaging and lymph-node mapping. Since Mn3O4 NPs exhibited desirable properties for enhanced T-1 imaging and the simplicity of chelator-free radiolabeling, [Zr-89]Mn3O4@PEG NPs offer a novel, simple, safe and accurate nanoplatforms for future precise cancer imaging and diagnosis.
引用
收藏
页码:900 / 909
页数:10
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