AI Article Synopsis

  • Refraction-contrast computed tomography (RCT) can create 3D images of soft biological tissues with image quality close to stained 2D pathological images, but struggles with spatial resolution due to X-ray beam blurring.
  • Currently, RCT can only observe structures around 20 µm, which limits its ability to distinguish between benign and malignant tumors that require observing cell nuclei approximately 5-10 µm in size.
  • This study explored improving RCT's imaging capabilities by using X-ray dynamical diffraction theory to analyze the impact of different analyzer thicknesses and pixel sizes on the visualization of cell nuclei.

Article Abstract

Refraction-contrast computed tomography (RCT) using a refractive angle analyzer of Si perfect crystal can reconstruct the three-dimensional structure of biological soft tissue with contrast comparable to that of stained two-dimensional pathological images. However, the blurring of X-ray beam by the analyzer has prevented improvement of the spatial resolution of RCT, and the currently possible observation of tissue structure at a scale of approximately 20 µm provides only limited medical information. As in pathology, to differentiate between benign and malignant forms of cancer, it is necessary to observe the distribution of the cell nucleus, which is approximately 5-10 µm in diameter. In this study, based on the X-ray dynamical diffraction theory using the Takagi-Taupin equation, which calculates the propagation of X-ray energy in crystals, an analyzer crystal optical system depicting the distribution of cell nuclei was investigated by RCT imaging simulation experiments in terms of the thickness of the Laue-case analyzer, the camera pixel size and the difference in spatial resolution between the Bragg-case and Laue-case analyzers.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666655PMC
http://dx.doi.org/10.1038/s41598-022-24249-8DOI Listing

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