Literature DB >> 21492791

Microfluidic preparation of [18F]FE@SUPPY and [18F]FE@SUPPY:2--comparison with conventional radiosyntheses.

Johanna Ungersboeck1, Cécile Philippe, Leonhard-Key Mien, Daniela Haeusler, Karem Shanab, Rupert Lanzenberger, Helmut Spreitzer, Bernhard K Keppler, Robert Dudczak, Kurt Kletter, Markus Mitterhauser, Wolfgang Wadsak.   

Abstract

INTRODUCTION: Recently, first applications of microfluidic principles for radiosyntheses of positron emission tomography compounds were presented, but direct comparisons with conventional methods were still missing. Therefore, our aims were (1) the set-up of a microfluidic procedure for the preparation of the recently developed adenosine A(3)-receptor tracers [(18)F]FE@SUPPY [5-(2-[(18)F]fluoroethyl)2,4-diethyl-3-(ethylsulfanylcarbonyl)-6-phenylpyridine-5-carboxylate] and [(18)F]FE@SUPPY:2 [5-ethyl-2,4-diethyl-3-((2-[(18)F]fluoroethyl)sulfanylcarbonyl)-6-phenylpyridine-5-carboxylate] and (2) the direct comparison of reaction conditions and radiochemical yields of the no-carrier-added nucleophilic substitution with [(18)F]fluoride between microfluidic and conventional methods.
METHODS: For the determination of optimal reaction conditions within an Advion NanoTek synthesizer, 5-50 μl of precursor and dried [(18)F]fluoride solution were simultaneously pushed through the temperature-controlled reactor (26 °C-180 °C) with defined reactant bolus flow rates (10-50 μl/min). Radiochemical incorporation yields (RCIYs) and overall radiochemical yields for large-scale preparations were compared with data from conventional batch-mode syntheses.
RESULTS: Optimal reaction parameters for the microfluidic set-up were determined as follows: 170 °C, 30-μl/min pump rate per reactant (reaction overall flow rate of 60 μl/min) and 5-mg/ml precursor concentration in the reaction mixture. Applying these optimized conditions, we observed a significant increase in RCIY from 88.2% to 94.1% (P < .0001, n ≥ 11) for [(18)F]FE@SUPPY and that from 42.5% to 95.5% (P<.0001, n ≥ 5) for [(18)F]FE@SUPPY:2 using microfluidic instead of conventional heating. Precursor consumption was decreased from 7.5 and 10 mg to 1 mg per large-scale synthesis for both title compounds, respectively.
CONCLUSION: The direct comparison of radiosyntheses data applying a conventional method and a microfluidic approach revealed a significant increase of RCIY using the microfluidic approach.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21492791     DOI: 10.1016/j.nucmedbio.2010.09.009

Source DB:  PubMed          Journal:  Nucl Med Biol        ISSN: 0969-8051            Impact factor:   2.408


  6 in total

1.  Microfluidic radiolabeling of biomolecules with PET radiometals.

Authors:  Dexing Zeng; Amit V Desai; David Ranganathan; Tobias D Wheeler; Paul J A Kenis; David E Reichert
Journal:  Nucl Med Biol       Date:  2012-10-15       Impact factor: 2.408

2.  Plug-and-play modules for flexible radiosynthesis.

Authors:  Henry Herman; Graciela Flores; Kevin Quinn; Mark Eddings; Sebastian Olma; Melissa D Moore; Huijiang Ding; Krzysztof P Bobinski; Mingwei Wang; Dirk Williams; Darin Wiliams; Clifton Kwang-Fu Shen; Michael E Phelps; R Michael van Dam
Journal:  Appl Radiat Isot       Date:  2013-04-25       Impact factor: 1.513

3.  Batch-reactor microfluidic device: first human use of a microfluidically produced PET radiotracer.

Authors:  Artem Lebedev; Reza Miraghaie; Kishore Kotta; Carroll E Ball; Jianzhong Zhang; Monte S Buchsbaum; Hartmuth C Kolb; Arkadij Elizarov
Journal:  Lab Chip       Date:  2012-11-07       Impact factor: 6.799

Review 4.  The Current Role of Microfluidics in Radiofluorination Chemistry.

Authors:  Karla-Anne Knapp; Michael L Nickels; H Charles Manning
Journal:  Mol Imaging Biol       Date:  2020-06       Impact factor: 3.488

5.  Preparation and First Preclinical Evaluation of [(18)F]FE@SNAP: A Potential PET Tracer for the Melanin-Concentrating Hormone Receptor-1 (MCHR1).

Authors:  Cécile Philippe; Lukas Nics; Markus Zeilinger; Eva Schirmer; Helmut Spreitzer; Georgios Karanikas; Rupert Lanzenberger; Helmut Viernstein; Wolfgang Wadsak; Markus Mitterhauser
Journal:  Sci Pharm       Date:  2013-07-01

6.  Development and implementation of ISAR, a new synthesis platform for radiopharmaceutical production.

Authors:  Christopher Frank; Georg Winter; Fredrik Rensei; Victor Samper; Allen F Brooks; Brian G Hockley; Bradford D Henderson; Christian Rensch; Peter J H Scott
Journal:  EJNMMI Radiopharm Chem       Date:  2019-09-18
  6 in total

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