Spectral encoding of spatial frequency approach for imaging and characterization of 3D structures

S. Uttam, S. Alexandrov, R. Bista, Yang Liu
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Abstract

Probing the internal 3D structure of label-free objects, such as biological cells and tissues in their natural environments, with nano-scale accuracy and sensitivity is of great importance in many biomedical applications. Using the 3D scattering potential description of an object's structure, we present the principle of spectral encoding of 3D spatial frequency (SESF) that encodes different spatial frequencies of the scattering potential into corresponding wavelengths. The SESF principle allows us to (1) perform real-time quantitative dominant-structure imaging of a label-free object. This imaging approach produces a color map in real time in which dominant axial spatial period (or frequency) at each image point is encoded as a corresponding spectral color. We demonstrate the efficacy of real-time imaging using model systems and show the potential of this technique to detect dominant structural changes in pre-cancerous cells that are not visible using conventional microscopy. (2) We extend the SESF principle to measure the entire axial spatial period distribution for each image point. Experimental results based on characterization of cell cycle phases are presented along with comparison with structural information extracted from TEM cell images. (3) Finally, we present spectral tomographic imaging (STI), a new SESF-based integrated tomographic approach that is able to simultaneously reconstruct the 3D object with sub-micron resolution, and also provide spatially-resolved characterization of its structure that has the ability to construct local axial spatial period distribution for any 3D sub-region of interest within the object. Simulation-based examples are presented. In all three cases structural characterization is achieved with nanoscale sensitivity and accuracy.
光谱编码的空间频率方法成像和表征的三维结构
以纳米级的精度和灵敏度探测自然环境中无标记物体(如生物细胞和组织)的内部三维结构,在许多生物医学应用中具有重要意义。利用物体结构的三维散射势描述,提出了三维空间频率(SESF)的频谱编码原理,将散射势的不同空间频率编码为相应波长。SESF原理使我们能够(1)对无标签物体进行实时定量优势结构成像。这种成像方法实时生成彩色地图,其中每个图像点的主要轴向空间周期(或频率)被编码为相应的光谱颜色。我们利用模型系统证明了实时成像的有效性,并展示了该技术在检测癌前细胞中主要结构变化方面的潜力,这些变化在传统显微镜下是看不见的。(2)我们将SESF原理扩展到测量每个图像点的整个轴向空间周期分布。给出了基于细胞周期期特征的实验结果,并与TEM细胞图像提取的结构信息进行了比较。(3)最后,我们提出了光谱层析成像(STI),这是一种新的基于sesf的集成层析成像方法,能够同时以亚微米分辨率重建3D物体,并提供其结构的空间分辨率表征,能够为物体内任何感兴趣的3D子区域构建局部轴向空间周期分布。给出了基于仿真的实例。在这三种情况下,结构表征都以纳米级的灵敏度和准确性实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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