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Comparing the signal enhancement of a gadolinium based and an iron-oxide based contrast agent in low-field MRI
Recently, there has been a renewed interest in low-field MRI. Contrast agents (CA) in MRI have magnetic behavior dependent on magnetic field strength. Therefore, the optimal contrast agent for low-field MRI might be different from what is used at higher fields. Ultra-small superparamagnetic iron-oxi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370648/ https://www.ncbi.nlm.nih.gov/pubmed/34403442 http://dx.doi.org/10.1371/journal.pone.0256252 |
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author | van Zandwijk, Jordy K. Simonis, Frank F. J. Heslinga, Friso G. Hofmeijer, Elfi I. S. Geelkerken, Robert H. ten Haken, Bennie |
author_facet | van Zandwijk, Jordy K. Simonis, Frank F. J. Heslinga, Friso G. Hofmeijer, Elfi I. S. Geelkerken, Robert H. ten Haken, Bennie |
author_sort | van Zandwijk, Jordy K. |
collection | PubMed |
description | Recently, there has been a renewed interest in low-field MRI. Contrast agents (CA) in MRI have magnetic behavior dependent on magnetic field strength. Therefore, the optimal contrast agent for low-field MRI might be different from what is used at higher fields. Ultra-small superparamagnetic iron-oxides (USPIOs), commonly used as negative CA, might also be used for generating positive contrast in low-field MRI. The purpose of this study was to determine whether an USPIO or a gadolinium based contrast agent is more appropriate at low field strengths. Relaxivity values of ferumoxytol (USPIO) and gadoterate (gadolinium based) were used in this research to simulate normalized signal intensity (SI) curves within a concentration range of 0–15 mM. Simulations were experimentally validated on a 0.25T MRI scanner. Simulations and experiments were performed using spin echo (SE), spoiled gradient echo (SGE), and balanced steady-state free precession (bSSFP) sequences. Maximum achievable SIs were assessed for both CAs in a range of concentrations on all sequences. Simulations at 0.25T showed a peak in SIs at low concentrations ferumoxytol versus a wide top at higher concentrations for gadoterate in SE and SGE. Experiments agreed well with the simulations in SE and SGE, but less in the bSSFP sequence due to overestimated relaxivities in simulations. At low magnetic field strengths, ferumoxytol generates similar signal enhancement at lower concentrations than gadoterate. |
format | Online Article Text |
id | pubmed-8370648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-83706482021-08-18 Comparing the signal enhancement of a gadolinium based and an iron-oxide based contrast agent in low-field MRI van Zandwijk, Jordy K. Simonis, Frank F. J. Heslinga, Friso G. Hofmeijer, Elfi I. S. Geelkerken, Robert H. ten Haken, Bennie PLoS One Research Article Recently, there has been a renewed interest in low-field MRI. Contrast agents (CA) in MRI have magnetic behavior dependent on magnetic field strength. Therefore, the optimal contrast agent for low-field MRI might be different from what is used at higher fields. Ultra-small superparamagnetic iron-oxides (USPIOs), commonly used as negative CA, might also be used for generating positive contrast in low-field MRI. The purpose of this study was to determine whether an USPIO or a gadolinium based contrast agent is more appropriate at low field strengths. Relaxivity values of ferumoxytol (USPIO) and gadoterate (gadolinium based) were used in this research to simulate normalized signal intensity (SI) curves within a concentration range of 0–15 mM. Simulations were experimentally validated on a 0.25T MRI scanner. Simulations and experiments were performed using spin echo (SE), spoiled gradient echo (SGE), and balanced steady-state free precession (bSSFP) sequences. Maximum achievable SIs were assessed for both CAs in a range of concentrations on all sequences. Simulations at 0.25T showed a peak in SIs at low concentrations ferumoxytol versus a wide top at higher concentrations for gadoterate in SE and SGE. Experiments agreed well with the simulations in SE and SGE, but less in the bSSFP sequence due to overestimated relaxivities in simulations. At low magnetic field strengths, ferumoxytol generates similar signal enhancement at lower concentrations than gadoterate. Public Library of Science 2021-08-17 /pmc/articles/PMC8370648/ /pubmed/34403442 http://dx.doi.org/10.1371/journal.pone.0256252 Text en © 2021 van Zandwijk et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article van Zandwijk, Jordy K. Simonis, Frank F. J. Heslinga, Friso G. Hofmeijer, Elfi I. S. Geelkerken, Robert H. ten Haken, Bennie Comparing the signal enhancement of a gadolinium based and an iron-oxide based contrast agent in low-field MRI |
title | Comparing the signal enhancement of a gadolinium based and an iron-oxide based contrast agent in low-field MRI |
title_full | Comparing the signal enhancement of a gadolinium based and an iron-oxide based contrast agent in low-field MRI |
title_fullStr | Comparing the signal enhancement of a gadolinium based and an iron-oxide based contrast agent in low-field MRI |
title_full_unstemmed | Comparing the signal enhancement of a gadolinium based and an iron-oxide based contrast agent in low-field MRI |
title_short | Comparing the signal enhancement of a gadolinium based and an iron-oxide based contrast agent in low-field MRI |
title_sort | comparing the signal enhancement of a gadolinium based and an iron-oxide based contrast agent in low-field mri |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370648/ https://www.ncbi.nlm.nih.gov/pubmed/34403442 http://dx.doi.org/10.1371/journal.pone.0256252 |
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