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PEG-modified gadolinium nanoparticles as contrast agents for in vivo micro-CT
Vascular research is largely performed in rodents with the goal of developing treatments for human disease. Micro-computed tomography (micro-CT) provides non-destructive three-dimensional imaging that can be used to study the vasculature of rodents. However, to distinguish vasculature from other sof...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367985/ https://www.ncbi.nlm.nih.gov/pubmed/34400681 http://dx.doi.org/10.1038/s41598-021-95716-x |
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author | Cruje, Charmainne Dunmore-Buyze, P. Joy Grolman, Eric Holdsworth, David W. Gillies, Elizabeth R. Drangova, Maria |
author_facet | Cruje, Charmainne Dunmore-Buyze, P. Joy Grolman, Eric Holdsworth, David W. Gillies, Elizabeth R. Drangova, Maria |
author_sort | Cruje, Charmainne |
collection | PubMed |
description | Vascular research is largely performed in rodents with the goal of developing treatments for human disease. Micro-computed tomography (micro-CT) provides non-destructive three-dimensional imaging that can be used to study the vasculature of rodents. However, to distinguish vasculature from other soft tissues, long-circulating contrast agents are required. In this study, we demonstrated that poly(ethylene glycol) (PEG)-coated gadolinium nanoparticles can be used as a vascular contrast agent in micro-CT. The coated particles could be lyophilized and then redispersed in an aqueous solution to achieve 100 mg/mL of gadolinium. After an intravenous injection of the contrast agent into mice, micro-CT scans showed blood pool contrast enhancements of at least 200 HU for 30 min. Imaging and quantitative analysis of gadolinium in tissues showed the presence of contrast agent in clearance organs including the liver and spleen and very low amounts in other organs. In vitro cell culture experiments, subcutaneous injections, and analysis of mouse body weight suggested that the agents exhibited low toxicity. Histological analysis of tissues 5 days after injection of the contrast agent showed cytotoxicity in the spleen, but no abnormalities were observed in the liver, lungs, kidneys, and bladder. |
format | Online Article Text |
id | pubmed-8367985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83679852021-08-17 PEG-modified gadolinium nanoparticles as contrast agents for in vivo micro-CT Cruje, Charmainne Dunmore-Buyze, P. Joy Grolman, Eric Holdsworth, David W. Gillies, Elizabeth R. Drangova, Maria Sci Rep Article Vascular research is largely performed in rodents with the goal of developing treatments for human disease. Micro-computed tomography (micro-CT) provides non-destructive three-dimensional imaging that can be used to study the vasculature of rodents. However, to distinguish vasculature from other soft tissues, long-circulating contrast agents are required. In this study, we demonstrated that poly(ethylene glycol) (PEG)-coated gadolinium nanoparticles can be used as a vascular contrast agent in micro-CT. The coated particles could be lyophilized and then redispersed in an aqueous solution to achieve 100 mg/mL of gadolinium. After an intravenous injection of the contrast agent into mice, micro-CT scans showed blood pool contrast enhancements of at least 200 HU for 30 min. Imaging and quantitative analysis of gadolinium in tissues showed the presence of contrast agent in clearance organs including the liver and spleen and very low amounts in other organs. In vitro cell culture experiments, subcutaneous injections, and analysis of mouse body weight suggested that the agents exhibited low toxicity. Histological analysis of tissues 5 days after injection of the contrast agent showed cytotoxicity in the spleen, but no abnormalities were observed in the liver, lungs, kidneys, and bladder. Nature Publishing Group UK 2021-08-16 /pmc/articles/PMC8367985/ /pubmed/34400681 http://dx.doi.org/10.1038/s41598-021-95716-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Cruje, Charmainne Dunmore-Buyze, P. Joy Grolman, Eric Holdsworth, David W. Gillies, Elizabeth R. Drangova, Maria PEG-modified gadolinium nanoparticles as contrast agents for in vivo micro-CT |
title | PEG-modified gadolinium nanoparticles as contrast agents for in vivo micro-CT |
title_full | PEG-modified gadolinium nanoparticles as contrast agents for in vivo micro-CT |
title_fullStr | PEG-modified gadolinium nanoparticles as contrast agents for in vivo micro-CT |
title_full_unstemmed | PEG-modified gadolinium nanoparticles as contrast agents for in vivo micro-CT |
title_short | PEG-modified gadolinium nanoparticles as contrast agents for in vivo micro-CT |
title_sort | peg-modified gadolinium nanoparticles as contrast agents for in vivo micro-ct |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367985/ https://www.ncbi.nlm.nih.gov/pubmed/34400681 http://dx.doi.org/10.1038/s41598-021-95716-x |
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