TY - JOUR
T1 - Enhanced hyperspectral tomography for bioimaging by spatiospectral reconstruction
AU - Warr, Ryan
AU - Ametova, Evelina
AU - Cernik, Robert
AU - Fardell, Gemma
AU - Handschuh, Stephan
AU - Jorgensen, Jakob
AU - Papoutsellis, Evangelos
AU - Pasca, Edoardo
AU - Withers, Philip
N1 - Funding Information:
We acknowledge the following EPSRC grants for funding that have enabled this project: “A Reconstruction Toolkit for Multichannel CT” (EP/P02226X/1) and “CCPi: Collaborative Computational Project in Tomographic Imaging” (EP/M022498/1 and EP/T026677/1). PJW and RW acknowledge support from the European Research Council Grant No. 695638 CORREL-CT. JSJ was partially supported by The Villum Foundation (Grant No. 25893). EA was partially funded by the Federal Ministry of Education and Research (BMBF) and the Baden-Württemberg Ministry of Science as part of the Excellence Strategy of the German Federal and State Governments. The Manchester (Henry Moseley) X-ray Imaging Facility was funded in part by the EPSRC (Grants EP/ F007906/1, EP/F001452/1 and EP/M010619/1). This work makes use of computational support by CoSeC, the Computational Science Centre for Research Communities, through CCPi.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/10/21
Y1 - 2021/10/21
N2 - Here we apply hyperspectral bright field imaging to collect computed tomographic images with excellent energy resolution (~1 keV), applying it for the first time to map the distribution of stain in a fixed biological sample through its characteristic K-edge. Conventionally, because the photons detected at each pixel are distributed across as many as 200 energy channels, energy-selective images are characterised by low count-rates and poor signal-to-noise ratio. This means high X-ray exposures, long scan times and high doses are required to image unique spectral markers. Here, we achieve high quality energy-dispersive tomograms from low dose, noisy datasets using a dedicated iterative reconstruction algorithm. This exploits the spatial smoothness and inter-channel structural correlation in the spectral domain using two carefully chosen regularisation terms. For a multi-phase phantom, a reduction in scan time of 36 times is demonstrated. Spectral analysis methods including K-edge subtraction and absorption step-size fitting are evaluated for an ex vivo, single (iodine)-stained biological sample, where low chemical concentration and inhomogeneous distribution can affect soft tissue segmentation and visualisation. The reconstruction algorithms are available through the open-source Core Imaging Library. Taken together, these tools offer new capabilities for visualisation and elemental mapping, with promising applications for multiply-stained biological specimens.
AB - Here we apply hyperspectral bright field imaging to collect computed tomographic images with excellent energy resolution (~1 keV), applying it for the first time to map the distribution of stain in a fixed biological sample through its characteristic K-edge. Conventionally, because the photons detected at each pixel are distributed across as many as 200 energy channels, energy-selective images are characterised by low count-rates and poor signal-to-noise ratio. This means high X-ray exposures, long scan times and high doses are required to image unique spectral markers. Here, we achieve high quality energy-dispersive tomograms from low dose, noisy datasets using a dedicated iterative reconstruction algorithm. This exploits the spatial smoothness and inter-channel structural correlation in the spectral domain using two carefully chosen regularisation terms. For a multi-phase phantom, a reduction in scan time of 36 times is demonstrated. Spectral analysis methods including K-edge subtraction and absorption step-size fitting are evaluated for an ex vivo, single (iodine)-stained biological sample, where low chemical concentration and inhomogeneous distribution can affect soft tissue segmentation and visualisation. The reconstruction algorithms are available through the open-source Core Imaging Library. Taken together, these tools offer new capabilities for visualisation and elemental mapping, with promising applications for multiply-stained biological specimens.
U2 - 10.1038/s41598-021-00146-4
DO - 10.1038/s41598-021-00146-4
M3 - Article
VL - 11
JO - Scientific Reports
JF - Scientific Reports
SN - 2045-2322
IS - 1
M1 - 20818
ER -