Three-dimensional imaging of whole rodent organs using optical computed and emission tomography

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作者
Duke University Medical Center, Department of Radiation Oncology and Biomedical Engineering, Durham, NC 27710, United States [1 ]
不详 [2 ]
不详 [3 ]
不详 [4 ]
机构
来源
J Biomed Opt | 2007年 / 1卷
基金
美国国家卫生研究院;
关键词
Biological organs - Fluorescence microscopy - Optical tomography - Three dimensional - Tissue;
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摘要
We explore the potential of optical computed tomography (optical-CT) and optical emission computed tomography (optical-ECT) in a new area - whole organ imaging. The techniques are implemented on an in-house prototype benchtop system with improved image quality and the capacity to image larger samples (up to 3 cm) than previous systems based on stereo microscopes. Imaging performance tests confirm high geometrical accuracy, accurate relative measurement of linear attenuation coefficients, and the ability to image features at the 50-μm level. Optical labeling of organ microvasculature was achieved using two stains deposited via natural in vivo circulatory processes: a passive absorbing ink-based stain and an active fluorescin FITC-lectin conjugate. The lectin protein binds to the enclothelial lining, and FITC fluorescense enables optical-ECT imaging. Three-dimensional (3-D) optical-CT images have been acquired of a normal rat heart and left lung and a mouse right lung showing exquisite detail of the functional vasculature and relative perfusion distribution. Coregistered optical-ECT images were also acquired of the mouse lung and kidney. Histological sections confirmed effective labeling of microvasculature throughout the organs. The advantages of optical-CT and optical-ECT include the potential for a unique combination of high resolution and high contrast and compatibility with a wide variety of optical probes, including gene expression labeling fluorescent reporter proteins. © 2007 Society of Photo-Optical Instrumentation Engineers.
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