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The Use of Magnetic Resonance Imaging for Non-Invasive Assessment of Venofer® Biodistribution in Rats
PURPOSE: The aim of this study was to determine the potential of magnetic resonance imaging to evaluate the biodistribution of exogenous iron within 24 h after one single injection of Venofer® (iron sucrose). METHODS: Venofer® was evaluated in vitro for its ability to generate contrast in MR images....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843693/ https://www.ncbi.nlm.nih.gov/pubmed/29520577 http://dx.doi.org/10.1007/s11095-018-2348-y |
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author | Span, Kimberley Pieters, Ebel H. E. Hennink, Wim E. van der Toorn, Annette Brinks, Vera Dijkhuizen, Rick M. van Tilborg, Geralda A. F. |
author_facet | Span, Kimberley Pieters, Ebel H. E. Hennink, Wim E. van der Toorn, Annette Brinks, Vera Dijkhuizen, Rick M. van Tilborg, Geralda A. F. |
author_sort | Span, Kimberley |
collection | PubMed |
description | PURPOSE: The aim of this study was to determine the potential of magnetic resonance imaging to evaluate the biodistribution of exogenous iron within 24 h after one single injection of Venofer® (iron sucrose). METHODS: Venofer® was evaluated in vitro for its ability to generate contrast in MR images. Subsequently, iron disposition was assessed in rats with MRI, in vivo up to 3 h and post mortem at 24 h after injection of Venofer®, at doses of 10- and 40 mg/kg body weight (n = 2 × 4), or saline (n = 4). RESULTS: Within 10–20 min after injection of Venofer®, transverse relaxation rates (R(2)) clearly increased, representative of a local increase in iron concentration, in liver, spleen and kidney, including the kidney medulla and cortex. In liver and spleen R(2) values remained elevated up to 3 h post injection, while the initial R(2) increase in the kidney was followed by gradual decrease towards baseline levels. Bone marrow and muscle tissue did not show significant increases in R(2) values. Whole-body post mortem MRI showed most prominent iron accumulation in the liver and spleen at 24 h post injection, which corroborated the in vivo results. CONCLUSIONS: MR imaging is a powerful imaging modality for non-invasive assessment of iron distribution in organs. It is recommended to use this whole-body imaging approach complementary to other techniques that allow quantification of iron disposition at a (sub)cellular level. |
format | Online Article Text |
id | pubmed-5843693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-58436932018-03-19 The Use of Magnetic Resonance Imaging for Non-Invasive Assessment of Venofer® Biodistribution in Rats Span, Kimberley Pieters, Ebel H. E. Hennink, Wim E. van der Toorn, Annette Brinks, Vera Dijkhuizen, Rick M. van Tilborg, Geralda A. F. Pharm Res Research Paper PURPOSE: The aim of this study was to determine the potential of magnetic resonance imaging to evaluate the biodistribution of exogenous iron within 24 h after one single injection of Venofer® (iron sucrose). METHODS: Venofer® was evaluated in vitro for its ability to generate contrast in MR images. Subsequently, iron disposition was assessed in rats with MRI, in vivo up to 3 h and post mortem at 24 h after injection of Venofer®, at doses of 10- and 40 mg/kg body weight (n = 2 × 4), or saline (n = 4). RESULTS: Within 10–20 min after injection of Venofer®, transverse relaxation rates (R(2)) clearly increased, representative of a local increase in iron concentration, in liver, spleen and kidney, including the kidney medulla and cortex. In liver and spleen R(2) values remained elevated up to 3 h post injection, while the initial R(2) increase in the kidney was followed by gradual decrease towards baseline levels. Bone marrow and muscle tissue did not show significant increases in R(2) values. Whole-body post mortem MRI showed most prominent iron accumulation in the liver and spleen at 24 h post injection, which corroborated the in vivo results. CONCLUSIONS: MR imaging is a powerful imaging modality for non-invasive assessment of iron distribution in organs. It is recommended to use this whole-body imaging approach complementary to other techniques that allow quantification of iron disposition at a (sub)cellular level. Springer US 2018-03-08 2018 /pmc/articles/PMC5843693/ /pubmed/29520577 http://dx.doi.org/10.1007/s11095-018-2348-y Text en © The Author(s) 2018 Open Access This 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. |
spellingShingle | Research Paper Span, Kimberley Pieters, Ebel H. E. Hennink, Wim E. van der Toorn, Annette Brinks, Vera Dijkhuizen, Rick M. van Tilborg, Geralda A. F. The Use of Magnetic Resonance Imaging for Non-Invasive Assessment of Venofer® Biodistribution in Rats |
title | The Use of Magnetic Resonance Imaging for Non-Invasive Assessment of Venofer® Biodistribution in Rats |
title_full | The Use of Magnetic Resonance Imaging for Non-Invasive Assessment of Venofer® Biodistribution in Rats |
title_fullStr | The Use of Magnetic Resonance Imaging for Non-Invasive Assessment of Venofer® Biodistribution in Rats |
title_full_unstemmed | The Use of Magnetic Resonance Imaging for Non-Invasive Assessment of Venofer® Biodistribution in Rats |
title_short | The Use of Magnetic Resonance Imaging for Non-Invasive Assessment of Venofer® Biodistribution in Rats |
title_sort | use of magnetic resonance imaging for non-invasive assessment of venofer® biodistribution in rats |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843693/ https://www.ncbi.nlm.nih.gov/pubmed/29520577 http://dx.doi.org/10.1007/s11095-018-2348-y |
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