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Low-Dose Imaging in a New Preclinical Total-Body PET/CT Scanner
Ionizing radiation constitutes a health risk to imaging scientists and study animals. Both PET and CT produce ionizing radiation. CT doses in pre-clinical in vivo imaging typically range from 50 to 1,000 mGy and biological effects in mice at this dose range have been previously described. [(18)F]FDG...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509903/ https://www.ncbi.nlm.nih.gov/pubmed/31131277 http://dx.doi.org/10.3389/fmed.2019.00088 |
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author | Molinos, Cesar Sasser, Todd Salmon, Phil Gsell, Willy Viertl, David Massey, James C. Mińczuk, Krzysztof Li, Jie Kundu, Bijoy K. Berr, Stuart Correcher, Carlos Bahadur, Ali Attarwala, Ali A. Stark, Simon Junge, Sven Himmelreich, Uwe Prior, John O. Laperre, Kjell Van Wyk, Sonica Heidenreich, Michael |
author_facet | Molinos, Cesar Sasser, Todd Salmon, Phil Gsell, Willy Viertl, David Massey, James C. Mińczuk, Krzysztof Li, Jie Kundu, Bijoy K. Berr, Stuart Correcher, Carlos Bahadur, Ali Attarwala, Ali A. Stark, Simon Junge, Sven Himmelreich, Uwe Prior, John O. Laperre, Kjell Van Wyk, Sonica Heidenreich, Michael |
author_sort | Molinos, Cesar |
collection | PubMed |
description | Ionizing radiation constitutes a health risk to imaging scientists and study animals. Both PET and CT produce ionizing radiation. CT doses in pre-clinical in vivo imaging typically range from 50 to 1,000 mGy and biological effects in mice at this dose range have been previously described. [(18)F]FDG body doses in mice have been estimated to be in the range of 100 mGy for [(18)F]FDG. Yearly, the average whole body doses due to handling of activity by PET technologists are reported to be 3–8 mSv. A preclinical PET/CT system is presented with design features which make it suitable for small animal low-dose imaging. The CT subsystem uses a X-source power that is optimized for small animal imaging. The system design incorporates a spatial beam shaper coupled with a highly sensitive flat-panel detector and very fast acquisition (<10 s) which allows for whole body scans with doses as low as 3 mGy. The mouse total-body PET subsystem uses a detector architecture based on continuous crystals, coupled to SiPM arrays and a readout based in rows and columns. The PET field of view is 150 mm axial and 80 mm transaxial. The high solid-angle coverage of the sample and the use of continuous crystals achieve a sensitivity of 9% (NEMA) that can be leveraged for use of low tracer doses and/or performing rapid scans. The low-dose imaging capabilities of the total-body PET subsystem were tested with NEMA phantoms, in tumor models, a mouse bone metabolism scan and a rat heart dynamic scan. The CT imaging capabilities were tested in mice and in a low contrast phantom. The PET low-dose phantom and animal experiments provide evidence that image quality suitable for preclinical PET studies is achieved. Furthermore, CT image contrast using low dose scan settings was suitable as a reference for PET scans. Total-body mouse PET/CT studies could be completed with total doses of <10 mGy. |
format | Online Article Text |
id | pubmed-6509903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65099032019-05-24 Low-Dose Imaging in a New Preclinical Total-Body PET/CT Scanner Molinos, Cesar Sasser, Todd Salmon, Phil Gsell, Willy Viertl, David Massey, James C. Mińczuk, Krzysztof Li, Jie Kundu, Bijoy K. Berr, Stuart Correcher, Carlos Bahadur, Ali Attarwala, Ali A. Stark, Simon Junge, Sven Himmelreich, Uwe Prior, John O. Laperre, Kjell Van Wyk, Sonica Heidenreich, Michael Front Med (Lausanne) Medicine Ionizing radiation constitutes a health risk to imaging scientists and study animals. Both PET and CT produce ionizing radiation. CT doses in pre-clinical in vivo imaging typically range from 50 to 1,000 mGy and biological effects in mice at this dose range have been previously described. [(18)F]FDG body doses in mice have been estimated to be in the range of 100 mGy for [(18)F]FDG. Yearly, the average whole body doses due to handling of activity by PET technologists are reported to be 3–8 mSv. A preclinical PET/CT system is presented with design features which make it suitable for small animal low-dose imaging. The CT subsystem uses a X-source power that is optimized for small animal imaging. The system design incorporates a spatial beam shaper coupled with a highly sensitive flat-panel detector and very fast acquisition (<10 s) which allows for whole body scans with doses as low as 3 mGy. The mouse total-body PET subsystem uses a detector architecture based on continuous crystals, coupled to SiPM arrays and a readout based in rows and columns. The PET field of view is 150 mm axial and 80 mm transaxial. The high solid-angle coverage of the sample and the use of continuous crystals achieve a sensitivity of 9% (NEMA) that can be leveraged for use of low tracer doses and/or performing rapid scans. The low-dose imaging capabilities of the total-body PET subsystem were tested with NEMA phantoms, in tumor models, a mouse bone metabolism scan and a rat heart dynamic scan. The CT imaging capabilities were tested in mice and in a low contrast phantom. The PET low-dose phantom and animal experiments provide evidence that image quality suitable for preclinical PET studies is achieved. Furthermore, CT image contrast using low dose scan settings was suitable as a reference for PET scans. Total-body mouse PET/CT studies could be completed with total doses of <10 mGy. Frontiers Media S.A. 2019-05-03 /pmc/articles/PMC6509903/ /pubmed/31131277 http://dx.doi.org/10.3389/fmed.2019.00088 Text en Copyright © 2019 Molinos, Sasser, Salmon, Gsell, Viertl, Massey, Mińczuk, Li, Kundu, Berr, Correcher, Bahadur, Attarwala, Stark, Junge, Himmelreich, Prior, Laperre, Van Wyk and Heidenreich. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Molinos, Cesar Sasser, Todd Salmon, Phil Gsell, Willy Viertl, David Massey, James C. Mińczuk, Krzysztof Li, Jie Kundu, Bijoy K. Berr, Stuart Correcher, Carlos Bahadur, Ali Attarwala, Ali A. Stark, Simon Junge, Sven Himmelreich, Uwe Prior, John O. Laperre, Kjell Van Wyk, Sonica Heidenreich, Michael Low-Dose Imaging in a New Preclinical Total-Body PET/CT Scanner |
title | Low-Dose Imaging in a New Preclinical Total-Body PET/CT Scanner |
title_full | Low-Dose Imaging in a New Preclinical Total-Body PET/CT Scanner |
title_fullStr | Low-Dose Imaging in a New Preclinical Total-Body PET/CT Scanner |
title_full_unstemmed | Low-Dose Imaging in a New Preclinical Total-Body PET/CT Scanner |
title_short | Low-Dose Imaging in a New Preclinical Total-Body PET/CT Scanner |
title_sort | low-dose imaging in a new preclinical total-body pet/ct scanner |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509903/ https://www.ncbi.nlm.nih.gov/pubmed/31131277 http://dx.doi.org/10.3389/fmed.2019.00088 |
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