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Spectrally resolving and scattering-compensated x-ray luminescence/fluorescence computed tomography

机译:光谱分辨和散射补偿X射线荧光/荧光计算机断层扫描

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摘要

The nanophosphors, or other similar materials, emit near-infrared (NIR) light upon x-ray excitation. They were designed as optical probes for in vivo visualization and analysis of molecular and cellular targets, pathways, and responses. Based on the previous work on x-ray fluorescence computed tomography (XFCT) and x-ray luminescence computed tomography (XLCT), here we propose a spectrally-resolving and scattering-compensated x-ray luminescence/fluorescence computed tomography (SXLCT or SXFCT) approach to quantify a spatial distribution of nanophosphors (other similar materials or chemical elements) within a biological object. In this paper, the x-ray scattering is taken into account in the reconstruction algorithm. The NIR scattering is described in the diffusion approximation model. Then, x-ray excitations are applied with different spectra, and NIR signals are measured in a spectrally resolving fashion. Finally, a linear relationship is established between the nanophosphor distribution and measured NIR data using the finite element method and inverted using the compressive sensing technique. The numerical simulation results demonstrate the feasibility and merits of the proposed approach.
机译:纳米磷光体或其他类似材料在x射线激发后发出近红外(NIR)光。它们被设计为光学探针,用于体内可视化和分析分子和细胞靶标,途径和反应。基于以前的X射线荧光计算机断层扫描(XFCT)和X射线荧光计算机断层扫描(XLCT)的工作,在这里,我们提出了一种光谱分辨和散射补偿的X射线荧光/荧光计算机断层扫描(SXLCT或SXFCT)一种量化生物对象内纳米磷光体(其他类似材料或化学元素)的空间分布的方法。本文在重建算法中考虑了X射线散射。 NIR散射在扩散近似模型中描述。然后,以不同的光谱施加X射线激发,并以光谱分辨的方式测量NIR信号。最后,使用有限元方法在纳米磷光体分布和测得的NIR数据之间建立线性关系,并使用压缩感测技术将其反转。数值仿真结果证明了该方法的可行性和优点。

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