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Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium

机译:不透射线聚合物注入介质对临床前标本脉管的MicroCT成像和血管直径定量的优化

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摘要

Vascular networks within a living organism are complex, multi-dimensional, and challenging to image capture. Radio-angiographic studies in live animals require a high level of infrastructure and technical investment in order to administer costly perfusion mediums whose signals metabolize and degrade relatively rapidly, diminishing within a few hours or days. Additionally, live animal specimens must not be subject to long duration scans, which can cause high levels of radiation exposure to the specimen, limiting the quality of images that can be captured. Lastly, despite technological advances in live-animal specimen imaging, it is quite difficult to minimize or prevent movement of a live animal, which can cause motion artifacts in the final data output. It is demonstrated here that through the use of postmortem perfusion protocols of radiopaque silicone polymer mediums and ex-vivo organ harvest, it is possible to acquire a high level of vascular signal in preclinical specimens through the use of micro-computed tomographic (microCT) imaging. Additionally, utilizing high-order rendering algorithms, it is possible to further derive vessel morphometrics for qualitative and quantitative analysis.
机译:活生物体内的血管网络是复杂的,多维的,并且难以捕获图像。活体动物的放射血管造影研究需要高水平的基础设施和技术投入,以管理昂贵的灌注介质,这些介质的信号代谢和降解相对较快,并在数小时或数天内消失。此外,活体动物标本不得进行长时间扫描,否则可能导致标本暴露于高水平的辐射下,从而限制了可捕获图像的质量。最后,尽管在活体动物标本成像技术方面取得了进步,但是要最大限度地减少或阻止活体动物的运动还是非常困难的,这可能会导致最终数据输出中出现运动伪影。在此证明,通过使用不透射线的有机硅聚合物介质的事后灌注方案和离体器官收获,可以通过使用微计算机断层扫描(microCT)成像在临床前样本中获取高水平的血管信号。此外,利用高阶渲染算法,可以进一步导出容器的形态计量学,以进行定性和定量分析。

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