Related Experiment Video
Updated: Aug 17, 2025

07:34
Excitation-Scanning Hyperspectral Imaging Microscopy to Efficiently Discriminate Fluorescence Signals
Published on: August 22, 2019
8.1K
Multi-material spectral photon-counting micro-CT with minimum residual decomposition and self-supervised deep
Optics Express
|December 16, 2022
Summary
This study introduces a novel spectral micro-CT system that overcomes limitations in energy resolution and noise. The enhanced system accurately differentiates materials with closely spaced K-edges, improving spectral imaging capabilities.
Area of Science:
- Medical Imaging
- Materials Science
- Physics
Background:
- Spectral micro-CT imaging faces challenges with energy resolution and noise amplification.
- Small pixel size detectors (< 100x100 µm²) exacerbate charge sharing and noise issues.
Purpose of the Study:
- To develop a cone-beam micro-CT setup addressing spectral imaging limitations.
- To enhance material discrimination and image quality in spectral micro-CT.
Main Methods:
- Utilized a CdTe photon counting detector with hardware charge summing.
- Implemented an image processing pipeline with spectral response modeling and minimum-residual basis material decomposition (MR-BMD).
- Applied self-supervised deep convolutional denoising to acquired projections (45x45 µm² pixel size).
Main Results:
- Successfully discriminated between materials with K-edges separated by only a few keV (e.g., Iodine and Barium).
- Demonstrated sharp discrimination capabilities using combined hardware and software solutions.
- Evaluated quantitative performance of reconstructed decomposed images (water, bone, I, Ba, Gd).
Conclusions:
- The developed spectral micro-CT system effectively overcomes hardware and software limitations.
- The innovative approach significantly improves material differentiation and image quality in spectral micro-CT.
- This work provides a robust platform for quantitative spectral micro-CT analysis.
Related Concept Videos
Electron Microscope Tomography and Single-particle Reconstruction
2.5K
Transmission electron microscopy (TEM) can be used to determine the 3D structure of biological samples with the help of techniques such as electron microscope tomography and single-particle reconstruction. While single-particle reconstruction can examine macromolecules and macromolecular complexes in vitro conditions only, tomography permits the study of cell components or small cells in vivo.
Electron Tomography
Electron tomography can be performed either in TEM or STEM (scanning transmission...
Electron Tomography
Electron tomography can be performed either in TEM or STEM (scanning transmission...
2.5K
Super-resolution Fluorescence Microscopy
7.1K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
7.1K
Deconvolution
221
Deconvolution, also known as inverse filtering, is the process of extracting the impulse response from known input and output signals. This technique is vital in scenarios where the system's characteristics are unknown, and they must be inferred from the observable signals.
Deconvolution involves several mathematical techniques to derive the impulse response. One common approach is polynomial division. In this method, the input and output sequences are treated as coefficients of...
Deconvolution involves several mathematical techniques to derive the impulse response. One common approach is polynomial division. In this method, the input and output sequences are treated as coefficients of...
221
Difference from Background: Limit of Detection
6.7K
The limit of detection (LOD) is the smallest amount of analyte that can be distinguished from the background noise. The LOD value corresponds to the concentration at which the analyte signal is three times larger than the standard deviation of the blank signal. Below this value, the analyte signal cannot be differentiated from the background noise. It is calculated by dividing the calibration slope by 3 times the standard deviation of the blank signals.
The LOD indicates the presence or absence...
The LOD indicates the presence or absence...
6.7K
Phase Contrast and Differential Interference Contrast Microscopy
8.3K
Phase-Contrast Microscopes
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...
8.3K

