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Development of a fully automated low‐pressure [(11)C]CO carbonylation apparatus
[(11)C]carbon monoxide ([(11)C]CO) is a versatile synthon for radiolabeling of drug‐like molecules for imaging studies with positron emission tomography (PET). We here report the development of a novel, user‐friendly, fully automated, and good manufacturing practice (GMP) compliant low‐pressure synt...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590049/ https://www.ncbi.nlm.nih.gov/pubmed/32588452 http://dx.doi.org/10.1002/jlcr.3866 |
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author | Ferrat, Mélodie El Khoury, Youssef Larsen, Peter Dahl, Kenneth Halldin, Christer Schou, Magnus |
author_facet | Ferrat, Mélodie El Khoury, Youssef Larsen, Peter Dahl, Kenneth Halldin, Christer Schou, Magnus |
author_sort | Ferrat, Mélodie |
collection | PubMed |
description | [(11)C]carbon monoxide ([(11)C]CO) is a versatile synthon for radiolabeling of drug‐like molecules for imaging studies with positron emission tomography (PET). We here report the development of a novel, user‐friendly, fully automated, and good manufacturing practice (GMP) compliant low‐pressure synthesis module for (11)C‐carbonylation reactions using [(11)C]CO. In this synthesis module, [(11)C]CO was reliably prepared from cyclotron‐produced [(11)C]carbon dioxide ([(11)C]CO(2)) by reduction over heated molybdenum and delivered to the reaction vessel within 7 min after end of bombardment, with an overall radiochemical yield (RCY) of 71%. [(11)C]AZ13198083, a histamine type‐3 receptor ligand, was used as a model compound to assess the functionality of the radiochemistry module. At full batch production conditions (55 μA, 30 min), our newly developed low‐pressure (11)C‐carbonylation apparatus enabled us to prepare [(11)C]AZ13198083 in an isolated radioactivity of 8540 ± 1400 MBq (n = 3). The radiochemical purity of each of the final formulated batches exceeded 99%, and all other quality control tests results conformed with specifications typically set for carbon‐11 labeled radiopharmaceuticals. In conclusion, this novel radiochemistry system offers a convenient GMP compliant production drugs and radioligands for imaging studies in human subjects. |
format | Online Article Text |
id | pubmed-7590049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75900492020-10-30 Development of a fully automated low‐pressure [(11)C]CO carbonylation apparatus Ferrat, Mélodie El Khoury, Youssef Larsen, Peter Dahl, Kenneth Halldin, Christer Schou, Magnus J Labelled Comp Radiopharm Note [(11)C]carbon monoxide ([(11)C]CO) is a versatile synthon for radiolabeling of drug‐like molecules for imaging studies with positron emission tomography (PET). We here report the development of a novel, user‐friendly, fully automated, and good manufacturing practice (GMP) compliant low‐pressure synthesis module for (11)C‐carbonylation reactions using [(11)C]CO. In this synthesis module, [(11)C]CO was reliably prepared from cyclotron‐produced [(11)C]carbon dioxide ([(11)C]CO(2)) by reduction over heated molybdenum and delivered to the reaction vessel within 7 min after end of bombardment, with an overall radiochemical yield (RCY) of 71%. [(11)C]AZ13198083, a histamine type‐3 receptor ligand, was used as a model compound to assess the functionality of the radiochemistry module. At full batch production conditions (55 μA, 30 min), our newly developed low‐pressure (11)C‐carbonylation apparatus enabled us to prepare [(11)C]AZ13198083 in an isolated radioactivity of 8540 ± 1400 MBq (n = 3). The radiochemical purity of each of the final formulated batches exceeded 99%, and all other quality control tests results conformed with specifications typically set for carbon‐11 labeled radiopharmaceuticals. In conclusion, this novel radiochemistry system offers a convenient GMP compliant production drugs and radioligands for imaging studies in human subjects. John Wiley and Sons Inc. 2020-08-27 2020-10 /pmc/articles/PMC7590049/ /pubmed/32588452 http://dx.doi.org/10.1002/jlcr.3866 Text en © 2020 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 http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Note Ferrat, Mélodie El Khoury, Youssef Larsen, Peter Dahl, Kenneth Halldin, Christer Schou, Magnus Development of a fully automated low‐pressure [(11)C]CO carbonylation apparatus |
title | Development of a fully automated low‐pressure [(11)C]CO carbonylation apparatus |
title_full | Development of a fully automated low‐pressure [(11)C]CO carbonylation apparatus |
title_fullStr | Development of a fully automated low‐pressure [(11)C]CO carbonylation apparatus |
title_full_unstemmed | Development of a fully automated low‐pressure [(11)C]CO carbonylation apparatus |
title_short | Development of a fully automated low‐pressure [(11)C]CO carbonylation apparatus |
title_sort | development of a fully automated low‐pressure [(11)c]co carbonylation apparatus |
topic | Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590049/ https://www.ncbi.nlm.nih.gov/pubmed/32588452 http://dx.doi.org/10.1002/jlcr.3866 |
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