TY - JOUR
T1 - Design optimization using GATE Monte Carlo simulations for a sub-0.5 mm resolution PET scanner with 3-layer DOI detectors
AU - Kang, Han Gyu
AU - Tashima, Hideaki
AU - Higuchi, Makoto
AU - Yamaya, Taiga
N1 - Publisher Copyright:
© 2026 Institute of Physics and Engineering in Medicine. All rights, including for text and data mining, AI training, and similar technologies, are reserved. This article is available under the terms of the https://publishingsupport.iopscience.iop.org/iop-standard/v1.
PY - 2026/2/14
Y1 - 2026/2/14
N2 - Objective. For rodent brain PET imaging, spatial resolution is the most important factor for identifying small brain structures. Previously, we developed a submillimeter resolution PET scanner with 1 mm crystal pitch using 3-layer depth-of-interaction (DOI) detectors. However, the spatial resolution was over 0.5 mm due to a relatively large crystal pitch and an unoptimized crystal layer design. Here we use Geant4 Application Tomographic Emission (GATE) Monte Carlo simulations to design and optimize a sub-0.5 mm resolution PET scanner with 3-layer DOI detectors. Methods. The proposed PET scanner has 2 rings, each of which has 16 DOI detectors, resulting in a 23.4 mm axial coverage. Each DOI detector has 3-layer lutetium yttrium orthosilicate crystal arrays with a 0.8 mm crystal pitch. We employed GATE Monte Carlo simulations to optimize three crystal layer designs, A (4 + 4 + 7 mm), B (3 + 4 + 4 mm), and C (3 + 3 + 5 mm). Spatial resolution and imaging performance were evaluated with a point source and resolution phantom using analytical and iterative algorithms. Main results. Among the three designs, design C provided the most uniform spatial resolution up to the radial offset of 15 mm. The 0.45 mm diameter rod structures were resolved clearly with design C using the iterative algorithm. The GATE simulation results agreed with the experimental data in terms of radial resolution except at the radial offset of 15 mm. Significance. We optimized the crystal layer design of the mouse brain PET scanner with GATE simulations, thereby achieving sub-0.5 mm resolution in the resolution phantom study.
AB - Objective. For rodent brain PET imaging, spatial resolution is the most important factor for identifying small brain structures. Previously, we developed a submillimeter resolution PET scanner with 1 mm crystal pitch using 3-layer depth-of-interaction (DOI) detectors. However, the spatial resolution was over 0.5 mm due to a relatively large crystal pitch and an unoptimized crystal layer design. Here we use Geant4 Application Tomographic Emission (GATE) Monte Carlo simulations to design and optimize a sub-0.5 mm resolution PET scanner with 3-layer DOI detectors. Methods. The proposed PET scanner has 2 rings, each of which has 16 DOI detectors, resulting in a 23.4 mm axial coverage. Each DOI detector has 3-layer lutetium yttrium orthosilicate crystal arrays with a 0.8 mm crystal pitch. We employed GATE Monte Carlo simulations to optimize three crystal layer designs, A (4 + 4 + 7 mm), B (3 + 4 + 4 mm), and C (3 + 3 + 5 mm). Spatial resolution and imaging performance were evaluated with a point source and resolution phantom using analytical and iterative algorithms. Main results. Among the three designs, design C provided the most uniform spatial resolution up to the radial offset of 15 mm. The 0.45 mm diameter rod structures were resolved clearly with design C using the iterative algorithm. The GATE simulation results agreed with the experimental data in terms of radial resolution except at the radial offset of 15 mm. Significance. We optimized the crystal layer design of the mouse brain PET scanner with GATE simulations, thereby achieving sub-0.5 mm resolution in the resolution phantom study.
KW - GATE simulations
KW - depth-of-interaction
KW - preclinical PET
UR - https://www.scopus.com/pages/publications/105029262943
UR - https://www.scopus.com/pages/publications/105029262943#tab=citedBy
U2 - 10.1088/1361-6560/ae3b02
DO - 10.1088/1361-6560/ae3b02
M3 - Article
C2 - 41558166
AN - SCOPUS:105029262943
SN - 0031-9155
VL - 71
JO - Physics in Medicine and Biology
JF - Physics in Medicine and Biology
IS - 3
ER -