Multi-pinhole fluorescent x-ray computed tomography for molecular imaging

Abstract We propose a multi-pinhole fluorescent x-ray computed tomography (mp-FXCT) technique for preclinical molecular imaging that can provide the complete data necessary to produce 3-D tomographic images during anaesthesia. In this method, multiple projections are simultaneously acquired through...

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Main Authors: Tenta Sasaya, Naoki Sunaguchi, Kazuyuki Hyodo, Tsutomu Zeniya, Tetsuya Yuasa
Format: Article
Language:English
Published: Nature Publishing Group 2017-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-05179-2
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spelling doaj-d988c5ee89eb4340859c19f76b4cc04f2020-12-08T01:20:39ZengNature Publishing GroupScientific Reports2045-23222017-07-017111210.1038/s41598-017-05179-2Multi-pinhole fluorescent x-ray computed tomography for molecular imagingTenta Sasaya0Naoki Sunaguchi1Kazuyuki Hyodo2Tsutomu Zeniya3Tetsuya Yuasa4Graduate School of Science and Engineering, Yamagata UniversityGraduate School of Medicine, Nagoya UniversityInstitute of Materials Structure Science, High Energy Accelerator Organization (KEK)Graduate School of Science and Technology, Hirosaki UniversityGraduate School of Science and Engineering, Yamagata UniversityAbstract We propose a multi-pinhole fluorescent x-ray computed tomography (mp-FXCT) technique for preclinical molecular imaging that can provide the complete data necessary to produce 3-D tomographic images during anaesthesia. In this method, multiple projections are simultaneously acquired through a multi-pinhole collimator with a 2-D detector and full-field volumetric beam to accelerate the data acquisition process and enhance the signal-to-noise ratios of the projections. We constructed a 15-pinhole mp-FXCT imaging system at beamline ARNE-7A at KEK and performed preliminary experiments to investigate its imaging properties using physical phantoms and a non-radioactive I imaging agent. The mp-FXCT system could detect an I concentration of 0.038 mg/ml, the minimum required for in-vivo imaging, at a spatial resolution of about 0.3 mm during a data acquisition time of 90 min, which is less than the time for which anaesthesia is effective and suggests that preclinical molecular imaging is feasible with mp-FXCT.https://doi.org/10.1038/s41598-017-05179-2
collection DOAJ
language English
format Article
sources DOAJ
author Tenta Sasaya
Naoki Sunaguchi
Kazuyuki Hyodo
Tsutomu Zeniya
Tetsuya Yuasa
spellingShingle Tenta Sasaya
Naoki Sunaguchi
Kazuyuki Hyodo
Tsutomu Zeniya
Tetsuya Yuasa
Multi-pinhole fluorescent x-ray computed tomography for molecular imaging
Scientific Reports
author_facet Tenta Sasaya
Naoki Sunaguchi
Kazuyuki Hyodo
Tsutomu Zeniya
Tetsuya Yuasa
author_sort Tenta Sasaya
title Multi-pinhole fluorescent x-ray computed tomography for molecular imaging
title_short Multi-pinhole fluorescent x-ray computed tomography for molecular imaging
title_full Multi-pinhole fluorescent x-ray computed tomography for molecular imaging
title_fullStr Multi-pinhole fluorescent x-ray computed tomography for molecular imaging
title_full_unstemmed Multi-pinhole fluorescent x-ray computed tomography for molecular imaging
title_sort multi-pinhole fluorescent x-ray computed tomography for molecular imaging
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-07-01
description Abstract We propose a multi-pinhole fluorescent x-ray computed tomography (mp-FXCT) technique for preclinical molecular imaging that can provide the complete data necessary to produce 3-D tomographic images during anaesthesia. In this method, multiple projections are simultaneously acquired through a multi-pinhole collimator with a 2-D detector and full-field volumetric beam to accelerate the data acquisition process and enhance the signal-to-noise ratios of the projections. We constructed a 15-pinhole mp-FXCT imaging system at beamline ARNE-7A at KEK and performed preliminary experiments to investigate its imaging properties using physical phantoms and a non-radioactive I imaging agent. The mp-FXCT system could detect an I concentration of 0.038 mg/ml, the minimum required for in-vivo imaging, at a spatial resolution of about 0.3 mm during a data acquisition time of 90 min, which is less than the time for which anaesthesia is effective and suggests that preclinical molecular imaging is feasible with mp-FXCT.
url https://doi.org/10.1038/s41598-017-05179-2
work_keys_str_mv AT tentasasaya multipinholefluorescentxraycomputedtomographyformolecularimaging
AT naokisunaguchi multipinholefluorescentxraycomputedtomographyformolecularimaging
AT kazuyukihyodo multipinholefluorescentxraycomputedtomographyformolecularimaging
AT tsutomuzeniya multipinholefluorescentxraycomputedtomographyformolecularimaging
AT tetsuyayuasa multipinholefluorescentxraycomputedtomographyformolecularimaging
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