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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...

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Autores principales: Felder, Jörg, Celik, A. Avdo, Choi, Chang-Hoon, Schwan, Stefan, Shah, N. Jon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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.
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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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