Preclinical 19F MRI cell tracking at 3 Tesla

被引:17
作者
Makela, Ashley V. [1 ,2 ]
Foster, Paula J. [1 ,2 ]
机构
[1] Robarts Res Inst, London, ON, Canada
[2] Western Univ, Dept Med Biophys, 1151 Richmond St North, London, ON N6A 5B7, Canada
关键词
19-Fluorine (F-19); Magnetic resonance imaging (MRI); Cancer; Cell tracking; Tumor-associated macrophage (TAM); TUMOR-ASSOCIATED MACROPHAGES; BREAST-CANCER; IRON; VISUALIZATION; INFLAMMATION; QUANTIFICATION; REJECTION; EMULSION;
D O I
10.1007/s10334-018-0715-7
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
PurposeTo develop methods for fluorine-19 (F-19) MRI cell tracking in mice on a 3Tesla clinical scanner. Compared to iron-based cell tracking, F-19 MRI has lower sensitivity and, consequently, preclinical F-19 cell tracking has only been performed at relatively high magnetic field strengths (>3T). Here, we focus on using F-19 MRI to detect macrophages in tumors; macrophage density is an indication of tumor aggressiveness and, therefore, F-19 MRI could be used as an imaging biomarker.MethodsPerfluorocarbon (PFC)-labeled macrophages were imaged at 3T and NMR spectroscopy was performed to validate F-19 spin quantification. In vivo F-19 MRI was performed on tumor-bearing mice, post-PFC at both 9.4T and 3T. 3T MRI utilized varying NEX and F-19 images were analyzed two different ways for F-19 quantification.ResultsAs few as 25,000 cells could be detected as cell pellets at 3T. F-19 quantification in cell pellets by 3T MRI agreed with NMR spectroscopy. F-19 signal was observed in the liver, spleen and tumor in all mice at 9.4T and 3T and there was no significant difference in F-19 spin quantification.ConclusionThis study demonstrates the ability to detect and quantify F-19 signal in murine tumors using F-19 MRI at 3T.
引用
收藏
页码:123 / 132
页数:10
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