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Method to study sample object size limit of small-angle x-ray scattering computed tomography

机译:研究小角度X射线散射计算机断层摄影的样本对象尺寸极限的方法

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Small-angle x-ray scattering (SAXS) imaging is an emerging medical tool that can be used for in vivo detailed tissue characterization and has the potential to provide added contrast to conventional x-ray projection and CT imaging. We used a publicly available MC-GPU code to simulate x-ray trajectories in a SAXS-CT geometry for a target material embedded in a water background material with varying sample sizes (1, 3, 5, and 10 mm). Our target materials were water solution of gold nanoparticle (GNP) spheres with a radius of 6 nm and a water solution with dissolved serum albumin (BSA) proteins due to their well-characterized scatter profiles at small angles and highly scattering properties. The background material was water. Our objective is to study how the reconstructed scatter profile degrades at larger target imaging depths and increasing sample sizes. We have found that scatter profiles of the GNP in water can still be reconstructed at depths up to 5 mm embedded at the center of a 10 mm sample. Scatter profiles of BSA in water were also reconstructed at depths up to 5 mm in a 10 mm sample but with noticeable signal degradation as compared to the GNP sample. This work presents a method to study the sample size limits for future SAXS-CT imaging systems.
机译:小角X射线散射(SAXS)成像是一种新兴的医疗工具,可用于体内详细的组织表征,并且有可能为常规的X射线投影和CT成像提供更多的对比度。我们使用了公开可用的MC-GPU代码来模拟SAXS-CT几何形状中的X射线轨迹,该目标材料嵌入了具有不同样本大小(1、3、5和10 mm)的水本底材料中的目标材料。我们的目标材料是半径为6 nm的金纳米颗粒(GNP)球的水溶液和具有溶解的血清白蛋白(BSA)蛋白质的水溶液,这是因为它们在小角度和高度散射特性下具有良好的散射特性。背景材料是水。我们的目标是研究在较大的目标成像深度和增加的样本量下,重建的散射轮廓如何退化。我们发现,在10 mm样本的中心埋入的最大5 mm深度处,仍可以重建水中GNP的散射曲线。在10 mm样品中,BSA在水中的散射曲线也可以重建到5 mm的深度,但与GNP样品相比,信号衰减明显。这项工作提出了一种研究未来SAXS-CT成像系统的样本量限制的方法。

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