Department of Medical Physics and Biomedical Engineering, University College London, Gower Street, London, WC1E 6BT, UK.
Biological Services, University College London, Gower Street, London, WC1E 6BT, UK.
Mol Imaging Biol. 2020 Jun;22(3):539-548. doi: 10.1007/s11307-019-01396-5.
To enable a preliminary assessment of the suitability of edge illumination (EI) x-ray phase contrast (XPC) micro x-ray computed tomography (micro-CT) to preclinical imaging. Specifically, to understand how different acquisition schemes and their combination with dedicated data processing affect contrast-to-noise ratio (CNR) and spatial resolution, while providing control over scan time and radiation dose delivery.
Deceased mice (n = 3) were scanned with an EI XPC micro-CT setup operated under different settings, leading to scan times between 18 h and 13 min. For the shortest scan, the entrance dose was measured with a calibrated PTW 23344 ion chamber. Different data processing methods were applied, retrieving either separate attenuation and phase images, or hybrid (combined attenuation and phase) images. A quantitative comparison was performed based on CNR and spatial resolution measurements for a soft tissue interface.
All phase-based images have led to a higher CNR for the considered soft tissue interface than the attenuation image, independent of scan time. The best relative CNR (a sixfold increase) was observed in one of the hybrid images. Spatial resolution was found to be connected to scan time, with a resolution of approximately 20 μm and 60 μm achieved for the longest and shortest scans, respectively. An entrance dose of approximately 300 mGy was estimated for the scan performed within 13 min.
Despite their preliminary nature, our results suggest that EI XPC bears potential for enhancing the utility of preclinical micro-CT, and, pending further research and development, could ultimately become a valuable technique in this field.
初步评估边缘照明(EI)X 射线相衬(XPC)微 X 射线计算机断层扫描(micro-CT)在临床前成像中的适用性。具体而言,了解不同的采集方案及其与专用数据处理的结合如何影响对比噪声比(CNR)和空间分辨率,同时控制扫描时间和辐射剂量传递。
对 3 只死亡小鼠进行了 EI XPC 微 CT 扫描,采用不同的设置,扫描时间在 18 小时至 13 分钟之间。对于最短的扫描,使用经过校准的 PTW 23344 离子室测量入口剂量。应用了不同的数据处理方法,分别获取单独的衰减和相位图像,或混合(组合衰减和相位)图像。基于软组织界面的 CNR 和空间分辨率测量进行了定量比较。
所有基于相位的图像都导致了所考虑的软组织界面的 CNR 高于衰减图像,与扫描时间无关。在一种混合图像中观察到最佳相对 CNR(增加了六倍)。空间分辨率与扫描时间有关,最长和最短扫描的分辨率分别约为 20μm 和 60μm。估计最短扫描的入口剂量约为 300mGy。
尽管它们是初步的,但我们的结果表明,EI XPC 有可能增强临床前 micro-CT 的实用性,并且在进一步的研究和开发之后,最终可能成为该领域的一项有价值的技术。