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In Vivo Fluorine Imaging Using 1.5 Tesla MRI for Depiction of Experimental Myocarditis in a Rodent Animal Model

The usefulness of perfluorocarbon nanoemulsions for the imaging of experimental myocarditis has been demonstrated in a high-field 9.4 Tesla MRI scanner. Our proof-of-concept study investigated the imaging capacity of PFC-based (19)F/(1)H MRI in an animal myocarditis model using a clinical field stre...

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Autores principales: Dietrich, Thore, Bujak, Stephan Theodor, Keller, Thorsten, Schnackenburg, Bernhard, Bourayou, Riad, Gebker, Rolf, Graf, Kristof, Fleck, Eckart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361831/
https://www.ncbi.nlm.nih.gov/pubmed/37484527
http://dx.doi.org/10.1155/2023/4659041
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author Dietrich, Thore
Bujak, Stephan Theodor
Keller, Thorsten
Schnackenburg, Bernhard
Bourayou, Riad
Gebker, Rolf
Graf, Kristof
Fleck, Eckart
author_facet Dietrich, Thore
Bujak, Stephan Theodor
Keller, Thorsten
Schnackenburg, Bernhard
Bourayou, Riad
Gebker, Rolf
Graf, Kristof
Fleck, Eckart
author_sort Dietrich, Thore
collection PubMed
description The usefulness of perfluorocarbon nanoemulsions for the imaging of experimental myocarditis has been demonstrated in a high-field 9.4 Tesla MRI scanner. Our proof-of-concept study investigated the imaging capacity of PFC-based (19)F/(1)H MRI in an animal myocarditis model using a clinical field strength of 1.5 Tesla. To induce experimental myocarditis, five male rats (weight ~300 g, age ~50 days) were treated with one application per week of doxorubicin (2 mg/kg BW) over a period of six weeks. Three control animals received the identical volume of sodium chloride 0.9% instead. Following week six, all animals received a single 4 ml injection of an 20% oil-in-water perfluorooctylbromide nanoemulsion 24 hours prior to in vivo(1)H/(19)F imaging on a 1.5 Tesla MRI. After euthanasia, cardiac histology and immunohistochemistry using CD68/ED1 macrophage antibodies were performed, measuring the inflamed myocardium in μm(2) for further statistical analysis to compare the extent of the inflammation with the (19)F-MRI signal intensity. All animals treated with doxorubicin showed a specific signal in the myocardium, while no myocardial signal could be detected in the control group. Additionally, the doxorubicin group showed a significantly higher SNR for (19)F and a stronger CD68/ED1 immunhistoreactivity compared to the control group. This proof-of-concept study demonstrates that perfluorocarbon nanoemulsions could be detected in an in vivo experimental myocarditis model at a currently clinically relevant field strength.
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spelling pubmed-103618312023-07-22 In Vivo Fluorine Imaging Using 1.5 Tesla MRI for Depiction of Experimental Myocarditis in a Rodent Animal Model Dietrich, Thore Bujak, Stephan Theodor Keller, Thorsten Schnackenburg, Bernhard Bourayou, Riad Gebker, Rolf Graf, Kristof Fleck, Eckart Int J Biomed Imaging Research Article The usefulness of perfluorocarbon nanoemulsions for the imaging of experimental myocarditis has been demonstrated in a high-field 9.4 Tesla MRI scanner. Our proof-of-concept study investigated the imaging capacity of PFC-based (19)F/(1)H MRI in an animal myocarditis model using a clinical field strength of 1.5 Tesla. To induce experimental myocarditis, five male rats (weight ~300 g, age ~50 days) were treated with one application per week of doxorubicin (2 mg/kg BW) over a period of six weeks. Three control animals received the identical volume of sodium chloride 0.9% instead. Following week six, all animals received a single 4 ml injection of an 20% oil-in-water perfluorooctylbromide nanoemulsion 24 hours prior to in vivo(1)H/(19)F imaging on a 1.5 Tesla MRI. After euthanasia, cardiac histology and immunohistochemistry using CD68/ED1 macrophage antibodies were performed, measuring the inflamed myocardium in μm(2) for further statistical analysis to compare the extent of the inflammation with the (19)F-MRI signal intensity. All animals treated with doxorubicin showed a specific signal in the myocardium, while no myocardial signal could be detected in the control group. Additionally, the doxorubicin group showed a significantly higher SNR for (19)F and a stronger CD68/ED1 immunhistoreactivity compared to the control group. This proof-of-concept study demonstrates that perfluorocarbon nanoemulsions could be detected in an in vivo experimental myocarditis model at a currently clinically relevant field strength. Hindawi 2023-07-14 /pmc/articles/PMC10361831/ /pubmed/37484527 http://dx.doi.org/10.1155/2023/4659041 Text en Copyright © 2023 Thore Dietrich et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dietrich, Thore
Bujak, Stephan Theodor
Keller, Thorsten
Schnackenburg, Bernhard
Bourayou, Riad
Gebker, Rolf
Graf, Kristof
Fleck, Eckart
In Vivo Fluorine Imaging Using 1.5 Tesla MRI for Depiction of Experimental Myocarditis in a Rodent Animal Model
title In Vivo Fluorine Imaging Using 1.5 Tesla MRI for Depiction of Experimental Myocarditis in a Rodent Animal Model
title_full In Vivo Fluorine Imaging Using 1.5 Tesla MRI for Depiction of Experimental Myocarditis in a Rodent Animal Model
title_fullStr In Vivo Fluorine Imaging Using 1.5 Tesla MRI for Depiction of Experimental Myocarditis in a Rodent Animal Model
title_full_unstemmed In Vivo Fluorine Imaging Using 1.5 Tesla MRI for Depiction of Experimental Myocarditis in a Rodent Animal Model
title_short In Vivo Fluorine Imaging Using 1.5 Tesla MRI for Depiction of Experimental Myocarditis in a Rodent Animal Model
title_sort in vivo fluorine imaging using 1.5 tesla mri for depiction of experimental myocarditis in a rodent animal model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361831/
https://www.ncbi.nlm.nih.gov/pubmed/37484527
http://dx.doi.org/10.1155/2023/4659041
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