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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...

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Autores principales: Ferrat, Mélodie, El Khoury, Youssef, Larsen, Peter, Dahl, Kenneth, Halldin, Christer, Schou, Magnus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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