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Biodistribution, kinetics, and biological fate of SPION microbubbles in the rat

BACKGROUND: In the present investigation, we studied the kinetics and biodistribution of a contrast agent consisting of poly(vinyl alcohol) (PVA) microbubbles containing superparamagnetic iron oxide (SPION) trapped between the PVA layers (SPION microbubbles). METHODS: The biological fate of SPION mi...

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Autores principales: Barrefelt, Åsa, Saghafian, Maryam, Kuiper, Raoul, Ye, Fei, Egri, Gabriella, Klickermann, Moritz, Brismar, Torkel B, Aspelin, Peter, Muhammed, Mamoun, Dähne, Lars, Hassan, Moustapha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767493/
https://www.ncbi.nlm.nih.gov/pubmed/24023513
http://dx.doi.org/10.2147/IJN.S49948
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author Barrefelt, Åsa
Saghafian, Maryam
Kuiper, Raoul
Ye, Fei
Egri, Gabriella
Klickermann, Moritz
Brismar, Torkel B
Aspelin, Peter
Muhammed, Mamoun
Dähne, Lars
Hassan, Moustapha
author_facet Barrefelt, Åsa
Saghafian, Maryam
Kuiper, Raoul
Ye, Fei
Egri, Gabriella
Klickermann, Moritz
Brismar, Torkel B
Aspelin, Peter
Muhammed, Mamoun
Dähne, Lars
Hassan, Moustapha
author_sort Barrefelt, Åsa
collection PubMed
description BACKGROUND: In the present investigation, we studied the kinetics and biodistribution of a contrast agent consisting of poly(vinyl alcohol) (PVA) microbubbles containing superparamagnetic iron oxide (SPION) trapped between the PVA layers (SPION microbubbles). METHODS: The biological fate of SPION microbubbles was determined in Sprague-Dawley rats after intravenous administration. Biodistribution and elimination of the microbubbles were studied in rats using magnetic resonance imaging for a period of 6 weeks. The rats were sacrificed and perfusion-fixated at different time points. The magnetic resonance imaging results obtained were compared with histopathologic findings in different organs. RESULTS: SPION microbubbles could be detected in the liver using magnetic resonance imaging as early as 10 minutes post injection. The maximum signal was detected between 24 hours and one week post injection. Histopathology showed the presence of clustered SPION microbubbles predominantly in the lungs from the first time point investigated (10 minutes). The frequency of microbubbles declined in the pulmonary vasculature and increased in pulmonary, hepatic, and splenic macrophages over time, resulting in a relative shift from the lungs to the spleen and liver. Meanwhile, macrophages showed increasing signs of cytoplasmic iron accumulation, initially in the lungs, then followed by other organs. CONCLUSION: The present investigation highlights the biological behavior of SPION microbubbles, including organ distribution over time and indications for biodegradation. The present results are essential for developing SPION microbubbles as a potential contrast agent and/or a drug delivery vehicle for specific organs. Such a vehicle will facilitate the use of multimodality imaging techniques, including ultrasound, magnetic resonance imaging, and single positron emission computed tomography, and hence improve diagnostics, therapy, and the ability to monitor the efficacy of treatment.
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spelling pubmed-37674932013-09-10 Biodistribution, kinetics, and biological fate of SPION microbubbles in the rat Barrefelt, Åsa Saghafian, Maryam Kuiper, Raoul Ye, Fei Egri, Gabriella Klickermann, Moritz Brismar, Torkel B Aspelin, Peter Muhammed, Mamoun Dähne, Lars Hassan, Moustapha Int J Nanomedicine Original Research BACKGROUND: In the present investigation, we studied the kinetics and biodistribution of a contrast agent consisting of poly(vinyl alcohol) (PVA) microbubbles containing superparamagnetic iron oxide (SPION) trapped between the PVA layers (SPION microbubbles). METHODS: The biological fate of SPION microbubbles was determined in Sprague-Dawley rats after intravenous administration. Biodistribution and elimination of the microbubbles were studied in rats using magnetic resonance imaging for a period of 6 weeks. The rats were sacrificed and perfusion-fixated at different time points. The magnetic resonance imaging results obtained were compared with histopathologic findings in different organs. RESULTS: SPION microbubbles could be detected in the liver using magnetic resonance imaging as early as 10 minutes post injection. The maximum signal was detected between 24 hours and one week post injection. Histopathology showed the presence of clustered SPION microbubbles predominantly in the lungs from the first time point investigated (10 minutes). The frequency of microbubbles declined in the pulmonary vasculature and increased in pulmonary, hepatic, and splenic macrophages over time, resulting in a relative shift from the lungs to the spleen and liver. Meanwhile, macrophages showed increasing signs of cytoplasmic iron accumulation, initially in the lungs, then followed by other organs. CONCLUSION: The present investigation highlights the biological behavior of SPION microbubbles, including organ distribution over time and indications for biodegradation. The present results are essential for developing SPION microbubbles as a potential contrast agent and/or a drug delivery vehicle for specific organs. Such a vehicle will facilitate the use of multimodality imaging techniques, including ultrasound, magnetic resonance imaging, and single positron emission computed tomography, and hence improve diagnostics, therapy, and the ability to monitor the efficacy of treatment. Dove Medical Press 2013 2013-08-26 /pmc/articles/PMC3767493/ /pubmed/24023513 http://dx.doi.org/10.2147/IJN.S49948 Text en © 2013 Barrefelt et al. This work is published by Dove Medical Press Ltd, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Ltd, provided the work is properly attributed
spellingShingle Original Research
Barrefelt, Åsa
Saghafian, Maryam
Kuiper, Raoul
Ye, Fei
Egri, Gabriella
Klickermann, Moritz
Brismar, Torkel B
Aspelin, Peter
Muhammed, Mamoun
Dähne, Lars
Hassan, Moustapha
Biodistribution, kinetics, and biological fate of SPION microbubbles in the rat
title Biodistribution, kinetics, and biological fate of SPION microbubbles in the rat
title_full Biodistribution, kinetics, and biological fate of SPION microbubbles in the rat
title_fullStr Biodistribution, kinetics, and biological fate of SPION microbubbles in the rat
title_full_unstemmed Biodistribution, kinetics, and biological fate of SPION microbubbles in the rat
title_short Biodistribution, kinetics, and biological fate of SPION microbubbles in the rat
title_sort biodistribution, kinetics, and biological fate of spion microbubbles in the rat
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767493/
https://www.ncbi.nlm.nih.gov/pubmed/24023513
http://dx.doi.org/10.2147/IJN.S49948
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