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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2017-07-01
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Online Access: | https://doi.org/10.1038/s41598-017-05179-2 |
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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 |
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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 |
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