Badea C T, Stanton I N, Johnston S M, Johnson G A, Therien M J
Center for In Vivo Microscopy, Department of Radiology, French Family Science Center, 124 Science Drive, Duke University, Durham, NC 27708.
Proc SPIE Int Soc Opt Eng. 2012;8313:83130T. doi: 10.1117/12.911465. Epub 2012 Feb 23.
X-ray Luminescence CT (XLCT) is a hybrid imaging modality combining x-ray and optical imaging in which x-ray luminescent nanophosphors (NPs) are used as emissive imaging probes. NPs are easily excited using common CT energy x-ray beams, and the NP luminescence is efficiently collected using sensitive light based detection systems. XLCT can be recognized as a close analog to fluorescence diffuse optical tomography (FDOT). However, XLCT has remarkable advantages over FDOT due to the substantial excitation penetration depths provided by x-rays relative to laser light sources, long term photo-stability of NPs, and the ability to tune NP emission within the NIR spectral window. Since XCLT uses an x-ray pencil beam excitation, the emitted light can be measured and back-projected along the x-ray path during reconstruction, where the size of the X-ray pencil beam determines the resolution for XLCT. In addition, no background signal competes with NP luminescence (i.e., no auto fluorescence) in XLCT. Currently, no small animal XLCT system has been proposed or tested. This paper investigates an XLCT system built and integrated with a dual source micro-CT system. Two novel sampling paradigms that result in more efficient scanning are proposed and tested via simulations. Our preliminary experimental results in phantoms indicate that a basic CT-like reconstruction is able to recover a map of the NP locations and differences in NP concentrations. With the proposed dual source system and faster scanning approaches, XLCT has the potential to revolutionize molecular imaging in preclinical studies.
X射线发光计算机断层扫描(XLCT)是一种将X射线和光学成像相结合的混合成像模式,其中X射线发光纳米磷光体(NPs)被用作发射成像探针。使用普通CT能量的X射线束很容易激发NPs,并且使用基于灵敏光的检测系统可以有效地收集NP发光。XLCT可以被认为是荧光漫射光学断层扫描(FDOT)的紧密类似物。然而,由于相对于激光光源,X射线提供了显著的激发穿透深度、NPs的长期光稳定性以及在近红外光谱窗口内调节NP发射的能力,XLCT相对于FDOT具有显著优势。由于XCLT使用X射线笔形束激发,在重建过程中可以沿着X射线路径测量并反投影发射光,其中X射线笔形束的大小决定了XLCT的分辨率。此外,在XLCT中没有背景信号与NP发光竞争(即没有自发荧光)。目前,尚未提出或测试过小动物XLCT系统。本文研究了一种与双源微型CT系统构建并集成的XLCT系统。提出了两种能实现更高效扫描的新型采样范式,并通过模拟进行了测试。我们在模型中的初步实验结果表明,一种基本的类似CT的重建能够恢复NP位置图和NP浓度差异。借助所提出的双源系统和更快的扫描方法,XLCT有潜力在临床前研究中彻底改变分子成像。