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Fully Automated GMP-Compliant Synthesis of [(18)F]FE-PE2I
In the struggle to understand and accurately diagnose Parkinson′s disease, radiopharmaceuticals and medical imaging techniques have played a major role. By being able to image and quantify the dopamine transporter density, noninvasive diagnostic imaging has become the gold standard. In the shift fro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308591/ https://www.ncbi.nlm.nih.gov/pubmed/34206688 http://dx.doi.org/10.3390/ph14070601 |
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author | Bratteby, Klas Denholt, Charlotte Lund Lehel, Szabolcs Petersen, Ida Nymann Madsen, Jacob Erlandsson, Maria Ohlsson, Tomas Herth, Matthias Manfred Gillings, Nic |
author_facet | Bratteby, Klas Denholt, Charlotte Lund Lehel, Szabolcs Petersen, Ida Nymann Madsen, Jacob Erlandsson, Maria Ohlsson, Tomas Herth, Matthias Manfred Gillings, Nic |
author_sort | Bratteby, Klas |
collection | PubMed |
description | In the struggle to understand and accurately diagnose Parkinson′s disease, radiopharmaceuticals and medical imaging techniques have played a major role. By being able to image and quantify the dopamine transporter density, noninvasive diagnostic imaging has become the gold standard. In the shift from the first generation of SPECT tracers, the fluorine-18-labeled tracer [(18)F]FE-PE2I has emerged as the agent of choice for many physicians. However, implementing suitable synthesis for the production of [(18)F]FE-PE2I has proved more challenging than expected. Through a thorough analysis of the relevant factors affecting the final radiochemical yield, we were able to implement high-yielding fully automated GMP-compliant synthesis of [(18)F]FE-PE2I on a Synthera(®)+ platform. By reaching RCYs up to 62%, it allowed us to isolate 25 GBq of the formulated product, and an optimized formulation resulted in the shelf life of 6 h, satisfying the increased demand for this radiopharmaceutical. |
format | Online Article Text |
id | pubmed-8308591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83085912021-07-25 Fully Automated GMP-Compliant Synthesis of [(18)F]FE-PE2I Bratteby, Klas Denholt, Charlotte Lund Lehel, Szabolcs Petersen, Ida Nymann Madsen, Jacob Erlandsson, Maria Ohlsson, Tomas Herth, Matthias Manfred Gillings, Nic Pharmaceuticals (Basel) Article In the struggle to understand and accurately diagnose Parkinson′s disease, radiopharmaceuticals and medical imaging techniques have played a major role. By being able to image and quantify the dopamine transporter density, noninvasive diagnostic imaging has become the gold standard. In the shift from the first generation of SPECT tracers, the fluorine-18-labeled tracer [(18)F]FE-PE2I has emerged as the agent of choice for many physicians. However, implementing suitable synthesis for the production of [(18)F]FE-PE2I has proved more challenging than expected. Through a thorough analysis of the relevant factors affecting the final radiochemical yield, we were able to implement high-yielding fully automated GMP-compliant synthesis of [(18)F]FE-PE2I on a Synthera(®)+ platform. By reaching RCYs up to 62%, it allowed us to isolate 25 GBq of the formulated product, and an optimized formulation resulted in the shelf life of 6 h, satisfying the increased demand for this radiopharmaceutical. MDPI 2021-06-22 /pmc/articles/PMC8308591/ /pubmed/34206688 http://dx.doi.org/10.3390/ph14070601 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bratteby, Klas Denholt, Charlotte Lund Lehel, Szabolcs Petersen, Ida Nymann Madsen, Jacob Erlandsson, Maria Ohlsson, Tomas Herth, Matthias Manfred Gillings, Nic Fully Automated GMP-Compliant Synthesis of [(18)F]FE-PE2I |
title | Fully Automated GMP-Compliant Synthesis of [(18)F]FE-PE2I |
title_full | Fully Automated GMP-Compliant Synthesis of [(18)F]FE-PE2I |
title_fullStr | Fully Automated GMP-Compliant Synthesis of [(18)F]FE-PE2I |
title_full_unstemmed | Fully Automated GMP-Compliant Synthesis of [(18)F]FE-PE2I |
title_short | Fully Automated GMP-Compliant Synthesis of [(18)F]FE-PE2I |
title_sort | fully automated gmp-compliant synthesis of [(18)f]fe-pe2i |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308591/ https://www.ncbi.nlm.nih.gov/pubmed/34206688 http://dx.doi.org/10.3390/ph14070601 |
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