Magnetic Particle Imaging: A Novel in Vivo Imaging Platform for Cancer Detection

被引:257
作者
Yu, Elaine Y. [1 ]
Bishop, Mindy [1 ]
Zheng, Bo [1 ]
Ferguson, R. Matthew [2 ]
Khandhar, Amit P. [2 ]
Kemp, Scott J. [2 ]
Krishnan, Kannan M. [3 ]
Goodwill, Patrick W. [4 ]
Conolly, Steven M. [1 ,5 ]
机构
[1] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[2] Lodespin Labs LLC, Seattle, WA 98103 USA
[3] Univ Washington, Dept Mat Sci, Seattle, WA 98195 USA
[4] Magnet Insight Inc, Alameda, CA 94501 USA
[5] Univ Calif Berkeley, Dept Elect Engn & Comp Sci, Berkeley, CA 94720 USA
关键词
Magnetic particle imaging; medical imaging; nanoparticles; cancer imaging; IRON-OXIDE NANOPARTICLES; MRI CONTRAST AGENTS; ENHANCED PERMEABILITY; DRUG-DELIVERY; BIODISTRIBUTION; TRACERS; FERUMOXYTOL; CLEARANCE; TOXICITY; 1ST;
D O I
10.1021/acs.nanolett.6b04865
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cancer remains one of the leading causes of death worldwide. Biomedical imaging plays a crucial role in all phases of cancer management. Physicians often need to choose the ideal diagnostic imaging modality for each clinical presentation based on complex trade-offs among spatial resolution, sensitivity, contrast, access, cost, and safety. Magnetic particle imaging (MPI) is an emerging tracer imaging modality that detects superparamagnetic iron oxide (SPIO) nanoparticle tracer with high image contrast (zero tissue background signal), high sensitivity (200 nM Fe) with linear quantitation, and zero signal depth attenuation. MPI is also safe in that it uses safe, in some cases even clinically approved, tracers and no ionizing radiation. The superb contrast, sensitivity, safety, and ability to image anywhere in the body lends MPI great promise for cancer imaging. In this study, we show for the first time the use of MPI for in vivo cancer imaging with systemic tracer administration. Here, long circulating MPI-tailored SPIOs were created and administered intravenously in tumor bearing rats. The tumor was highlighted with tumor-to background ratio of up to 50. The nanoparticle dynamics in the tumor was also well-appreciated, with initial wash-in on the tumor rim, peak uptake at 6 h, and eventual clearance beyond 48 h. Lastly, we demonstrate the quantitative nature of MPI through compartmental fitting in vivo.
引用
收藏
页码:1648 / 1654
页数:7
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