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在 1.5T 场强下使用平衡稳态自由进动成像技术对小鼠脑内铁标记细胞和乳腺癌转移灶进行单次扫描检测。

In vivo single scan detection of both iron-labeled cells and breast cancer metastases in the mouse brain using balanced steady-state free precession imaging at 1.5 T.

机构信息

Imaging Research Laboratories, Robarts Research Institute, London, ON, Canada.

出版信息

J Magn Reson Imaging. 2011 Jul;34(1):231-8. doi: 10.1002/jmri.22593.


DOI:10.1002/jmri.22593
PMID:21698713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3501681/
Abstract

PURPOSE: To simultaneously detect iron-labeled cancer cells and brain tumors in vivo in one scan, the balanced steady-state free precession (b-SSFP) imaging sequence was optimized at 1.5 T on mice developing brain metastases subsequent to the injection of micron-sized iron oxide particle-labeled human breast cancer cells. MATERIALS AND METHODS: b-SSFP sequence parameters (repetition time, flip angle, and receiver bandwidth) were varied and the signal-to-noise ratio, contrast between the brain and tumors, and the number of detected iron-labeled cells were evaluated. RESULTS: Optimal b-SSFP images were acquired with a 26 msec repetition time, 35° flip angle, and bandwidth of ±21 kHz. b-SSFP images were compared with T(2) -weighted 2D fast spin echo (FSE) and 3D spoiled gradient recalled echo (SPGR) images. The mean tumor-brain contrast-to-noise ratio and the ability to detect iron-labeled cells were the highest in the b-SSFP images. CONCLUSION: A single b-SSFP scan can be used to visualize both iron-labeled cells and brain metastases.

摘要

目的:为了在一次扫描中同时检测体内铁标记的癌细胞和脑肿瘤,我们在 1.5T 磁共振上对注射了微米级超顺磁氧化铁标记的人乳腺癌细胞的小鼠脑转移模型进行了优化。

材料与方法:我们改变了平衡稳态自由进动(b-SSFP)序列的参数(重复时间、翻转角和接收带宽),并评估了信噪比、脑与肿瘤之间的对比度和检测到的铁标记细胞的数量。

结果:优化的 b-SSFP 图像采集条件为重复时间 26msec、翻转角 35°、带宽为正负 21kHz。b-SSFP 图像与 T2 加权二维快速自旋回波(FSE)和三维扰相梯度回波(SPGR)图像进行了比较。b-SSFP 图像的肿瘤与脑的平均对比噪声比和检测铁标记细胞的能力最高。

结论:单次 b-SSFP 扫描可用于可视化铁标记细胞和脑转移瘤。

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In vivo single scan detection of both iron-labeled cells and breast cancer metastases in the mouse brain using balanced steady-state free precession imaging at 1.5 T.

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本文引用的文献

[1]
The use of cellular magnetic resonance imaging to track the fate of iron-labeled multipotent stromal cells after direct transplantation in a mouse model of spinal cord injury.

Mol Imaging Biol. 2011-8

[2]
Imaging iron-loaded mouse glioma tumors with bSSFP at 3 T.

Magn Reson Med. 2010-7

[3]
The X-space formulation of the magnetic particle imaging process: 1-D signal, resolution, bandwidth, SNR, SAR, and magnetostimulation.

IEEE Trans Med Imaging. 2010-6-7

[4]
Uptake of ANG1005, a novel paclitaxel derivative, through the blood-brain barrier into brain and experimental brain metastases of breast cancer.

Pharm Res. 2009-9-23

[5]
Magnetic resonance imaging assessment of macrophage accumulation in mouse brain after experimental traumatic brain injury.

J Neurotrauma. 2009-9

[6]
Semiquantitation of mouse dendritic cell migration in vivo using cellular MRI.

J Immunother. 2009-4

[7]
3D TrueFISP imaging of mouse brain at 4.7T and 9.4T.

J Magn Reson Imaging. 2008-8

[8]
Reactive glia are recruited by highly proliferative brain metastases of breast cancer and promote tumor cell colonization.

Clin Exp Metastasis. 2008

[9]
Ex-vivo cellular MRI with b-SSFP: quantitative benefits of 3T over 1.5 T.

MAGMA. 2008-7

[10]
In vivo tracking of stem cells in brain and spinal cord injury.

Prog Brain Res. 2007

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