Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA

Detalhes bibliográficos
Autor(a) principal: Neves, Ângela C. B.
Data de Publicação: 2021
Outros Autores: Hrynchak, Ivanna, Fonseca, Inês, Alves, Vítor H. P., Pereira, Mariette M., Falcão, Amílcar, Abrunhosa, Antero J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/103869
https://doi.org/10.1186/s41181-021-00126-z
Resumo: The neurotracer 6-[18F] FDOPA has been, for many years, a powerful tool in PET imaging of neuropsychiatric diseases, movement disorders and brain malignancies. More recently, it also demonstrated good results in the diagnosis of other malignancies such as neuroendocrine tumours, pheochromocytoma or pancreatic adenocarcinoma.The multiple clinical applications of this tracer fostered a very strong interest in the development of new and improved methods for its radiosynthesis. The no-carrier-added nucleophilic 18F-fluorination process has gained increasing attention, in recent years, due to the high molar activities obtained, when compared with the other methods although the radiochemical yield remains low (17-30%). This led to the development of several nucleophilic synthetic processes in order to obtain the product with molar activity, radiochemical yield and enantiomeric purity suitable for human PET studies.Automation of the synthetic processes is crucial for routine clinical use and compliance with GMP requirements. Nevertheless, the complexity of the synthesis makes the production challenging, increasing the chance of failure in routine production. Thus, for large-scale clinical application and wider use of this radiopharmaceutical, progress in the automation of this complex radiosynthesis is of critical importance.This review summarizes the most recent developments of 6-[18F]FDOPA radiosynthesis and discusses the key issues regarding its automation for routine clinical use.
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spelling Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA6-[18F]FDOPAAutomated synthesisNonproteinogenic amino acidPETRadiochemistryThe neurotracer 6-[18F] FDOPA has been, for many years, a powerful tool in PET imaging of neuropsychiatric diseases, movement disorders and brain malignancies. More recently, it also demonstrated good results in the diagnosis of other malignancies such as neuroendocrine tumours, pheochromocytoma or pancreatic adenocarcinoma.The multiple clinical applications of this tracer fostered a very strong interest in the development of new and improved methods for its radiosynthesis. The no-carrier-added nucleophilic 18F-fluorination process has gained increasing attention, in recent years, due to the high molar activities obtained, when compared with the other methods although the radiochemical yield remains low (17-30%). This led to the development of several nucleophilic synthetic processes in order to obtain the product with molar activity, radiochemical yield and enantiomeric purity suitable for human PET studies.Automation of the synthetic processes is crucial for routine clinical use and compliance with GMP requirements. Nevertheless, the complexity of the synthesis makes the production challenging, increasing the chance of failure in routine production. Thus, for large-scale clinical application and wider use of this radiopharmaceutical, progress in the automation of this complex radiosynthesis is of critical importance.This review summarizes the most recent developments of 6-[18F]FDOPA radiosynthesis and discusses the key issues regarding its automation for routine clinical use.Springer Nature2021-03-10info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/103869http://hdl.handle.net/10316/103869https://doi.org/10.1186/s41181-021-00126-zeng2365-421X336890562365-421XNeves, Ângela C. B.Hrynchak, IvannaFonseca, InêsAlves, Vítor H. P.Pereira, Mariette M.Falcão, AmílcarAbrunhosa, Antero J.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-12-06T21:39:26Zoai:estudogeral.uc.pt:10316/103869Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:20:38.226833Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA
title Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA
spellingShingle Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA
Neves, Ângela C. B.
6-[18F]FDOPA
Automated synthesis
Nonproteinogenic amino acid
PET
Radiochemistry
title_short Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA
title_full Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA
title_fullStr Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA
title_full_unstemmed Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA
title_sort Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA
author Neves, Ângela C. B.
author_facet Neves, Ângela C. B.
Hrynchak, Ivanna
Fonseca, Inês
Alves, Vítor H. P.
Pereira, Mariette M.
Falcão, Amílcar
Abrunhosa, Antero J.
author_role author
author2 Hrynchak, Ivanna
Fonseca, Inês
Alves, Vítor H. P.
Pereira, Mariette M.
Falcão, Amílcar
Abrunhosa, Antero J.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Neves, Ângela C. B.
Hrynchak, Ivanna
Fonseca, Inês
Alves, Vítor H. P.
Pereira, Mariette M.
Falcão, Amílcar
Abrunhosa, Antero J.
dc.subject.por.fl_str_mv 6-[18F]FDOPA
Automated synthesis
Nonproteinogenic amino acid
PET
Radiochemistry
topic 6-[18F]FDOPA
Automated synthesis
Nonproteinogenic amino acid
PET
Radiochemistry
description The neurotracer 6-[18F] FDOPA has been, for many years, a powerful tool in PET imaging of neuropsychiatric diseases, movement disorders and brain malignancies. More recently, it also demonstrated good results in the diagnosis of other malignancies such as neuroendocrine tumours, pheochromocytoma or pancreatic adenocarcinoma.The multiple clinical applications of this tracer fostered a very strong interest in the development of new and improved methods for its radiosynthesis. The no-carrier-added nucleophilic 18F-fluorination process has gained increasing attention, in recent years, due to the high molar activities obtained, when compared with the other methods although the radiochemical yield remains low (17-30%). This led to the development of several nucleophilic synthetic processes in order to obtain the product with molar activity, radiochemical yield and enantiomeric purity suitable for human PET studies.Automation of the synthetic processes is crucial for routine clinical use and compliance with GMP requirements. Nevertheless, the complexity of the synthesis makes the production challenging, increasing the chance of failure in routine production. Thus, for large-scale clinical application and wider use of this radiopharmaceutical, progress in the automation of this complex radiosynthesis is of critical importance.This review summarizes the most recent developments of 6-[18F]FDOPA radiosynthesis and discusses the key issues regarding its automation for routine clinical use.
publishDate 2021
dc.date.none.fl_str_mv 2021-03-10
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/103869
http://hdl.handle.net/10316/103869
https://doi.org/10.1186/s41181-021-00126-z
url http://hdl.handle.net/10316/103869
https://doi.org/10.1186/s41181-021-00126-z
dc.language.iso.fl_str_mv eng
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33689056
2365-421X
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dc.publisher.none.fl_str_mv Springer Nature
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dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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