Detectability of fluorescent gold nanoparticles under micro-CT and optical projection tomography imaging

被引:3
作者
Kozomara, Stevo [1 ]
Ford, Nancy L. [1 ,2 ]
机构
[1] Univ British Columbia, Dept Oral Biol & Med Sci, Vancouver, BC, Canada
[2] Univ British Columbia, Dept Phys & Astron, Vancouver, BC, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
gold nanorods; nanoparticles; melanoma; micro-computed tomography; optical projection tomography; COMPUTED-TOMOGRAPHY; TUMOR-GROWTH;
D O I
10.1117/1.JMI.7.2.026002
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
Purpose: Preclinical studies often compare micro-computed tomography (micro-CT) imaging with histology using optical microscopy of fluorescently labeled slides. However, correlating the images is difficult because the tissues appear differently in the two modalities. It would be valuable to have a single contrast medium visible on both radiographic and optical imaging. Approach: We have explored the detectability of fluorescently labeled gold nanoparticles under micro-CT and optical projection tomography (OPT) in agarose phantoms and a murine melanoma tumor model. Murine melanoma cells were used to induce tumor growth in the right hind legs of 12 C57B16 mice, with the maximal tumor size of 1 cm(3). We injected Cy3 fluorescently coated gold nanorods directly into the tumors. The mice were scanned with in vivo micro-CT (for pre- and post-contrast scans). Once euthanized, the hind leg was dissected and scanned with a higher resolution specimen micro-CT and OPT. Results: The distribution of the gold nanoparticles appeared to be contained and isolated to the tumor. Alignment of micro-CT specimen scans with the OPT scans was possible, although there was also autofluorescence of the surrounding muscle tissue. Conclusions: This study highlights the potential use of fluorescently labeled gold nanoparticles for imaging murine melanoma tumors using micro-CT and OPT. (C) The Authors. Published by SPIE under a Creative Commons Attribution 4.0 Unported License.
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页数:12
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