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9.4 T small animal MRI using clinical components for direct translational studies
BACKGROUND: Magnetic resonance is a major preclinical and clinical imaging modality ideally suited for longitudinal studies, e.g. in pharmacological developments. The lack of a proven platform that maintains an identical imaging protocol between preclinical and clinical platforms is solved with the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745792/ https://www.ncbi.nlm.nih.gov/pubmed/29282070 http://dx.doi.org/10.1186/s12967-017-1373-7 |
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author | Felder, Jörg Celik, A. Avdo Choi, Chang-Hoon Schwan, Stefan Shah, N. Jon |
author_facet | Felder, Jörg Celik, A. Avdo Choi, Chang-Hoon Schwan, Stefan Shah, N. Jon |
author_sort | Felder, Jörg |
collection | PubMed |
description | BACKGROUND: Magnetic resonance is a major preclinical and clinical imaging modality ideally suited for longitudinal studies, e.g. in pharmacological developments. The lack of a proven platform that maintains an identical imaging protocol between preclinical and clinical platforms is solved with the construction of an animal scanner based on clinical hard- and software. METHODS: A small animal magnet and gradient system were connected to a clinical MR system. Several hardware components were either modified or built in-house to achieve compatibility. The clinical software was modified to account for the different field-of-view of a preclinical MR system. The established scanner was evaluated using clinical QA protocols, and platform compatibility for translational research was verified against clinical scanners of different field strength. RESULTS: The constructed animal scanner operates with the majority of clinical imaging sequences. Translational research is greatly facilitated as protocols can be shared between preclinical and clinical platforms. Hence, when maintaining sequences parameters, maximum similarity between pulses played out on a human or an animal system is maintained. CONCLUSION: Coupling of a small animal magnet with a clinical MR system is a flexible, easy to use way to establish and advance translational imaging capability. It provides cost and labor efficient translational capability as no tedious sequence reprogramming between moieties is required and cross-platform compatibility of sequences facilitates multi-center studies. |
format | Online Article Text |
id | pubmed-5745792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57457922018-01-03 9.4 T small animal MRI using clinical components for direct translational studies Felder, Jörg Celik, A. Avdo Choi, Chang-Hoon Schwan, Stefan Shah, N. Jon J Transl Med Methodology BACKGROUND: Magnetic resonance is a major preclinical and clinical imaging modality ideally suited for longitudinal studies, e.g. in pharmacological developments. The lack of a proven platform that maintains an identical imaging protocol between preclinical and clinical platforms is solved with the construction of an animal scanner based on clinical hard- and software. METHODS: A small animal magnet and gradient system were connected to a clinical MR system. Several hardware components were either modified or built in-house to achieve compatibility. The clinical software was modified to account for the different field-of-view of a preclinical MR system. The established scanner was evaluated using clinical QA protocols, and platform compatibility for translational research was verified against clinical scanners of different field strength. RESULTS: The constructed animal scanner operates with the majority of clinical imaging sequences. Translational research is greatly facilitated as protocols can be shared between preclinical and clinical platforms. Hence, when maintaining sequences parameters, maximum similarity between pulses played out on a human or an animal system is maintained. CONCLUSION: Coupling of a small animal magnet with a clinical MR system is a flexible, easy to use way to establish and advance translational imaging capability. It provides cost and labor efficient translational capability as no tedious sequence reprogramming between moieties is required and cross-platform compatibility of sequences facilitates multi-center studies. BioMed Central 2017-12-28 /pmc/articles/PMC5745792/ /pubmed/29282070 http://dx.doi.org/10.1186/s12967-017-1373-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Felder, Jörg Celik, A. Avdo Choi, Chang-Hoon Schwan, Stefan Shah, N. Jon 9.4 T small animal MRI using clinical components for direct translational studies |
title | 9.4 T small animal MRI using clinical components for direct translational studies |
title_full | 9.4 T small animal MRI using clinical components for direct translational studies |
title_fullStr | 9.4 T small animal MRI using clinical components for direct translational studies |
title_full_unstemmed | 9.4 T small animal MRI using clinical components for direct translational studies |
title_short | 9.4 T small animal MRI using clinical components for direct translational studies |
title_sort | 9.4 t small animal mri using clinical components for direct translational studies |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745792/ https://www.ncbi.nlm.nih.gov/pubmed/29282070 http://dx.doi.org/10.1186/s12967-017-1373-7 |
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