EXIRAD-HE

Multi-pinhole high-resolution ex vivo imaging of high-energy isotopes

Journal Article (2020)
Author(s)

Minh Phuong Nguyen (TU Delft - RST/Biomedical Imaging)

M.C. Goorden (TU Delft - RST/Biomedical Imaging)

F. J. Beekman (University Medical Center Utrecht, MILabs B.V., TU Delft - RST/Biomedical Imaging)

Research Group
RST/Biomedical Imaging
Copyright
© 2020 M.P. Nguyen, M.C. Goorden, F.J. Beekman
DOI related publication
https://doi.org/10.1088/1361-6560/abbb77
More Info
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Publication Year
2020
Language
English
Copyright
© 2020 M.P. Nguyen, M.C. Goorden, F.J. Beekman
Research Group
RST/Biomedical Imaging
Issue number
22
Volume number
65
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Abstract

We recently developed a dedicated focusing multi-pinhole collimator for a stationary SPECT system that offers down to 120 m (or 1.7 nL) spatial resolution SPECT images of cryo-cooled tissue samples (EXIRAD-3D). This collimator is suitable for imaging isotopes that are often used in small animal and diagnostic SPECT such as 125I (27 keV), 201Tl (71 keV), 99mTc (140 keV), and 111In (171 and 245 keV). The goal of the present work is to develop high-resolution pinhole imaging of tissue samples containing isotopes with high-energy photon emissions, for example, therapeutic alpha and beta emitters that co-emit high energy gammas (e.g. 213Bi (440 keV) and 131I (364 keV)) or 511 keV annihilation photons from PET isotopes. To this end, we optimise and evaluate a new high energy small-bore multi-pinhole collimator through simulations. The collimator-geometry was first optimised by simulating a Derenzo phantom scan with a biologically realistic activity concentration of 18F at two system sensitivities (0.30% and 0.60%) by varying pinhole placements. Subsequently, the wall thickness was selected based on reconstructions of a Derenzo phantom and a uniform phantom. The obtained collimators were then evaluated for 131I (364 keV), 213Bi (440 keV), 64Cu (511 keV), and 124I (511 + 603 keV) with biologically realistic activity concentrations, and also for some high activity concentrations of 18F, using digital resolution, mouse knee joint, and xenograft phantoms. Our results show that placing pinhole centres at a distance of 8 mm from the collimator inner wall yields good image quality, while a wall thickness of 43 mm resulted in sufficient shielding. The collimators offer resolutions down to 0.35 mm, 0.6 mm, 0.5 mm, 0.6 mm, and 0.5 mm when imaging 131I, 213Bi, 18F, 64Cu, and 124I, respectively, contained in tissue samples at biologically achievable activity concentrations.