Advances in the automated synthesis of 6-[18F]Fluoro-L-DOPA
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , |
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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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 |
format |
article |
status_str |
publishedVersion |
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 |
language |
eng |
dc.relation.none.fl_str_mv |
2365-421X 33689056 2365-421X |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Springer Nature |
publisher.none.fl_str_mv |
Springer Nature |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799134098445303808 |