Automated and efficient radiosynthesis of [(18)F]FLT using a low amount of precursor
Autor: | Patrice Laquerriere, Frederic Boisson, Patrice Marchand, David Brasse, Michel Pellicioli, Jacky Schuler, Ali Ouadi |
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Přispěvatelé: | Institut Pluridisciplinaire Hubert Curien (IPHC), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Département de Radiobiologie, Hadronthérapie et Imagerie Moléculaire (DRHIM-IPHC), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Centre de biophysique moléculaire (CBM), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université d'Orléans (UO), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Université d'Orléans (UO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS) |
Jazyk: | francouzština |
Rok vydání: | 2016 |
Předmět: |
Quality Control
[PHYS]Physics [physics] Cancer Research Radiochemistry Elution Radiosynthesis chemistry.chemical_element Chemistry Techniques Synthetic Combinatorial chemistry Dideoxynucleosides 030218 nuclear medicine & medical imaging methods Automation 03 medical and health sciences 0302 clinical medicine Fully automated chemistry 030220 oncology & carcinogenesis [PHYS.PHYS.PHYS-MED-PH]Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph] Fluorine Molecular Medicine Radiology Nuclear Medicine and imaging Aucun ComputingMilieux_MISCELLANEOUS |
Zdroj: | Nuclear Medicine and Biology Nuclear Medicine and Biology, Elsevier, 2016, 43 (8), pp.520-527. ⟨10.1016/j.nucmedbio.2016.05.009⟩ |
ISSN: | 0969-8051 |
DOI: | 10.1016/j.nucmedbio.2016.05.009⟩ |
Popis: | Since 1991 until now, many radiosyntheses of [(18)F]FLT have been published. Most of them suffer from side reactions and/or difficult purification related to the large amount of precursor necessary for the labeling step. A fully automated synthesis using only commercial and unmodified materials with a reduced amount of precursor would be desirable. We first explored the possibility to elute efficiently [(18)F]fluorine from commercial and unmodified cartridges with various amount of base. Based on these results, 10mg and 5mg of precursors were used for the fluorination step. The best conditions were transposed in an automated process for a one pot two steps synthesis of labeled FLT. Using commercial and non-treated carbonate form of QMA cartridges, we were able to elute quantitatively the [(18)F]fluorine with a very low amount of base (0.59mg) and, with only 5mg of precursor, to perform an efficient fluorination reaction with up to 94% incorporation of [(18)F]fluorine. The synthesis was fully automated and radiochemical yields of 54% (decay corrected) were obtained within a synthesis time of 52minutes. We demonstrate that a fully automated and efficient radiosynthesis of [(18)F]FLT is feasible with only 5mg of precursor. Compare to the present state of the art, our method provides high yields of pure [(18)F]FLT and is broadly adaptable to other synthesis automates. journal article research support, non-u.s. gov't 2016 08 2016 05 21 imported |
Databáze: | OpenAIRE |
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