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A new approach to produce [(18)F]MC225 via one-step synthesis, a PET radiotracer for measuring P-gp function
BACKGROUND: [(18)F]MC225 is a radiotracer for imaging P-glycoprotein (P-gp) function at the blood-brain barrier. The P-gp function can be altered due to different factors, for instance, decreased P-gp function has been described in patients with Alzheimer’s or Parkinson’s Disease. The current applie...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282851/ https://www.ncbi.nlm.nih.gov/pubmed/34264435 http://dx.doi.org/10.1186/s41181-021-00139-8 |
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author | Garcia-Varela, Lara Attia, Khaled Sembrano, John Carlo Jacquet, Olivier Antunes, Inês F. Kwizera, Chantal Visser, Ton J. Dierckx, Rudi A. J. O. Elsinga, Philip H. Luurtsema, Gert |
author_facet | Garcia-Varela, Lara Attia, Khaled Sembrano, John Carlo Jacquet, Olivier Antunes, Inês F. Kwizera, Chantal Visser, Ton J. Dierckx, Rudi A. J. O. Elsinga, Philip H. Luurtsema, Gert |
author_sort | Garcia-Varela, Lara |
collection | PubMed |
description | BACKGROUND: [(18)F]MC225 is a radiotracer for imaging P-glycoprotein (P-gp) function at the blood-brain barrier. The P-gp function can be altered due to different factors, for instance, decreased P-gp function has been described in patients with Alzheimer’s or Parkinson’s Disease. The current applied radiosynthesis of [(18)F]MC225 involves 2 steps, including the distillation of the [(18)F] fluoroethylbromide intermediate. To develop a more robust synthetic procedure, it is of interest to produce the radiotracer via a 1-step synthesis. The present study describes a new synthetic approach to produce [(18)F]MC225 via direct (18)F-fluorination. Moreover, we also provide the appropriate conditions for the automation of the synthesis. A mesylate precursor was synthesized via a multi-step synthetic route and used for the radiolabeling. The nucleophilic substitution of the mesylate group by [(18)F] Fluoride was automated in two different synthesis modules: IBA Synthera and Eckert and Ziegler PharmTracer (E&Z). RESULTS: The mesylate precursor was synthesized in 7 steps starting with 5-hydroxy-1-tetralone (commercially available) in practical yields. The stability of the precursor was improved via mesylate salt formation method. The radiolabeling was done by adding the mesylate precursor dissolved in DMF to the dried [(18)F]KF/K(2.2.2) complex and heating at 140 °C for 30 min. Quality control by UPLC confirmed the production of [(18)F]MC225 with a molar activity (A(m)) higher than 100 GBq/micromole. The synthesis time in Synthera was 106 min and the product was obtained with a radiochemical purity higher than 95% and RCY of 6.5%, while the production in E&Z lasted 120 min and the product had a lower radiochemical purity (91%) and RCY (3.8%). CONCLUSIONS: [(18)F]MC225 was successfully produced via a 1-step reaction. The procedure is suitable for automation using commercially available synthesis modules. The automation of the radiosynthesis in the Synthera module allows the production of the [(18)F]MC225 by a reliable and simple method. |
format | Online Article Text |
id | pubmed-8282851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-82828512021-07-20 A new approach to produce [(18)F]MC225 via one-step synthesis, a PET radiotracer for measuring P-gp function Garcia-Varela, Lara Attia, Khaled Sembrano, John Carlo Jacquet, Olivier Antunes, Inês F. Kwizera, Chantal Visser, Ton J. Dierckx, Rudi A. J. O. Elsinga, Philip H. Luurtsema, Gert EJNMMI Radiopharm Chem Research Article BACKGROUND: [(18)F]MC225 is a radiotracer for imaging P-glycoprotein (P-gp) function at the blood-brain barrier. The P-gp function can be altered due to different factors, for instance, decreased P-gp function has been described in patients with Alzheimer’s or Parkinson’s Disease. The current applied radiosynthesis of [(18)F]MC225 involves 2 steps, including the distillation of the [(18)F] fluoroethylbromide intermediate. To develop a more robust synthetic procedure, it is of interest to produce the radiotracer via a 1-step synthesis. The present study describes a new synthetic approach to produce [(18)F]MC225 via direct (18)F-fluorination. Moreover, we also provide the appropriate conditions for the automation of the synthesis. A mesylate precursor was synthesized via a multi-step synthetic route and used for the radiolabeling. The nucleophilic substitution of the mesylate group by [(18)F] Fluoride was automated in two different synthesis modules: IBA Synthera and Eckert and Ziegler PharmTracer (E&Z). RESULTS: The mesylate precursor was synthesized in 7 steps starting with 5-hydroxy-1-tetralone (commercially available) in practical yields. The stability of the precursor was improved via mesylate salt formation method. The radiolabeling was done by adding the mesylate precursor dissolved in DMF to the dried [(18)F]KF/K(2.2.2) complex and heating at 140 °C for 30 min. Quality control by UPLC confirmed the production of [(18)F]MC225 with a molar activity (A(m)) higher than 100 GBq/micromole. The synthesis time in Synthera was 106 min and the product was obtained with a radiochemical purity higher than 95% and RCY of 6.5%, while the production in E&Z lasted 120 min and the product had a lower radiochemical purity (91%) and RCY (3.8%). CONCLUSIONS: [(18)F]MC225 was successfully produced via a 1-step reaction. The procedure is suitable for automation using commercially available synthesis modules. The automation of the radiosynthesis in the Synthera module allows the production of the [(18)F]MC225 by a reliable and simple method. Springer International Publishing 2021-07-15 /pmc/articles/PMC8282851/ /pubmed/34264435 http://dx.doi.org/10.1186/s41181-021-00139-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Garcia-Varela, Lara Attia, Khaled Sembrano, John Carlo Jacquet, Olivier Antunes, Inês F. Kwizera, Chantal Visser, Ton J. Dierckx, Rudi A. J. O. Elsinga, Philip H. Luurtsema, Gert A new approach to produce [(18)F]MC225 via one-step synthesis, a PET radiotracer for measuring P-gp function |
title | A new approach to produce [(18)F]MC225 via one-step synthesis, a PET radiotracer for measuring P-gp function |
title_full | A new approach to produce [(18)F]MC225 via one-step synthesis, a PET radiotracer for measuring P-gp function |
title_fullStr | A new approach to produce [(18)F]MC225 via one-step synthesis, a PET radiotracer for measuring P-gp function |
title_full_unstemmed | A new approach to produce [(18)F]MC225 via one-step synthesis, a PET radiotracer for measuring P-gp function |
title_short | A new approach to produce [(18)F]MC225 via one-step synthesis, a PET radiotracer for measuring P-gp function |
title_sort | new approach to produce [(18)f]mc225 via one-step synthesis, a pet radiotracer for measuring p-gp function |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282851/ https://www.ncbi.nlm.nih.gov/pubmed/34264435 http://dx.doi.org/10.1186/s41181-021-00139-8 |
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