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A new technique for the radiolabelling of mixed leukocytes with zirconium‐89 for inflammation imaging with positron emission tomography
Mixed leukocyte (white blood cells [WBCs]) trafficking using positron emission tomography (PET) is receiving growing interest to diagnose and monitor inflammatory conditions. PET, a high sensitivity molecular imaging technique, allows precise quantification of the signal produced from radiolabelled...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074313/ https://www.ncbi.nlm.nih.gov/pubmed/27061114 http://dx.doi.org/10.1002/jlcr.3392 |
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author | Fairclough, M. Prenant, C. Ellis, B. Boutin, H. McMahon, A. Brown, G. Locatelli, P. Jones, A.K.P. |
author_facet | Fairclough, M. Prenant, C. Ellis, B. Boutin, H. McMahon, A. Brown, G. Locatelli, P. Jones, A.K.P. |
author_sort | Fairclough, M. |
collection | PubMed |
description | Mixed leukocyte (white blood cells [WBCs]) trafficking using positron emission tomography (PET) is receiving growing interest to diagnose and monitor inflammatory conditions. PET, a high sensitivity molecular imaging technique, allows precise quantification of the signal produced from radiolabelled moieties. We have evaluated a new method for radiolabelling WBCs with either zirconium‐89 ((89)Zr) or copper‐64 ((64)Cu) for PET imaging. Chitosan nanoparticles (CNs) were produced by a process of ionotropic gelation and used to deliver radiometals into WBCs. Experiments were carried out using mixed WBCs freshly isolated from whole human blood. WBCs radiolabelling efficiency was higher with [(89)Zr]‐loaded CN (76.8 ± 9.6% (n = 12)) than with [(64)Cu]‐loaded CN (26.3 ± 7.0 % (n = 7)). [(89)Zr]‐WBCs showed an initial loss of 28.4 ± 5.8% (n = 2) of the radioactivity after 2 h. This loss was then followed by a plateau as (89)Zr remains stable in the cells. [(64)Cu]‐WBCs showed a loss of 85 ± 6% (n = 3) of the radioactivity after 1 h, which increased to 96 ± 6% (n = 3) loss after 3 h. WBC labelling with [(89)Zr]‐loaded CN showed a fast kinetic of leukocyte association, high labelling efficiency and a relatively good retention of the radioactivity. This method using (89)Zr has a potential application for PET imaging of inflammation. |
format | Online Article Text |
id | pubmed-5074313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50743132016-11-04 A new technique for the radiolabelling of mixed leukocytes with zirconium‐89 for inflammation imaging with positron emission tomography Fairclough, M. Prenant, C. Ellis, B. Boutin, H. McMahon, A. Brown, G. Locatelli, P. Jones, A.K.P. J Labelled Comp Radiopharm Research Articles Mixed leukocyte (white blood cells [WBCs]) trafficking using positron emission tomography (PET) is receiving growing interest to diagnose and monitor inflammatory conditions. PET, a high sensitivity molecular imaging technique, allows precise quantification of the signal produced from radiolabelled moieties. We have evaluated a new method for radiolabelling WBCs with either zirconium‐89 ((89)Zr) or copper‐64 ((64)Cu) for PET imaging. Chitosan nanoparticles (CNs) were produced by a process of ionotropic gelation and used to deliver radiometals into WBCs. Experiments were carried out using mixed WBCs freshly isolated from whole human blood. WBCs radiolabelling efficiency was higher with [(89)Zr]‐loaded CN (76.8 ± 9.6% (n = 12)) than with [(64)Cu]‐loaded CN (26.3 ± 7.0 % (n = 7)). [(89)Zr]‐WBCs showed an initial loss of 28.4 ± 5.8% (n = 2) of the radioactivity after 2 h. This loss was then followed by a plateau as (89)Zr remains stable in the cells. [(64)Cu]‐WBCs showed a loss of 85 ± 6% (n = 3) of the radioactivity after 1 h, which increased to 96 ± 6% (n = 3) loss after 3 h. WBC labelling with [(89)Zr]‐loaded CN showed a fast kinetic of leukocyte association, high labelling efficiency and a relatively good retention of the radioactivity. This method using (89)Zr has a potential application for PET imaging of inflammation. John Wiley and Sons Inc. 2016-04-08 2016-06-15 /pmc/articles/PMC5074313/ /pubmed/27061114 http://dx.doi.org/10.1002/jlcr.3392 Text en Copyright © 2016 The Authors. Journal of Labelled Compounds and Radiopharmaceuticals published by John Wiley & Sons, Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Fairclough, M. Prenant, C. Ellis, B. Boutin, H. McMahon, A. Brown, G. Locatelli, P. Jones, A.K.P. A new technique for the radiolabelling of mixed leukocytes with zirconium‐89 for inflammation imaging with positron emission tomography |
title | A new technique for the radiolabelling of mixed leukocytes with zirconium‐89 for inflammation imaging with positron emission tomography |
title_full | A new technique for the radiolabelling of mixed leukocytes with zirconium‐89 for inflammation imaging with positron emission tomography |
title_fullStr | A new technique for the radiolabelling of mixed leukocytes with zirconium‐89 for inflammation imaging with positron emission tomography |
title_full_unstemmed | A new technique for the radiolabelling of mixed leukocytes with zirconium‐89 for inflammation imaging with positron emission tomography |
title_short | A new technique for the radiolabelling of mixed leukocytes with zirconium‐89 for inflammation imaging with positron emission tomography |
title_sort | new technique for the radiolabelling of mixed leukocytes with zirconium‐89 for inflammation imaging with positron emission tomography |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074313/ https://www.ncbi.nlm.nih.gov/pubmed/27061114 http://dx.doi.org/10.1002/jlcr.3392 |
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