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

被引:23
作者
Ungersboeck, Johanna [1 ,2 ]
Philippe, Cecile [1 ,3 ]
Mien, Leonhard-Key [1 ]
Haeusler, Daniela [1 ,3 ]
Shanab, Karem [1 ,4 ]
Lanzenberger, Rupert [5 ]
Spreitzer, Helmut [4 ]
Keppler, Bernhard K. [2 ]
Dudczak, Robert [1 ]
Kletter, Kurt [1 ]
Mitterhauser, Markus [1 ,3 ,6 ]
Wadsak, Wolfgang [1 ,2 ]
机构
[1] Med Univ Vienna, Dept Nucl Med, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Inorgan Chem, A-1090 Vienna, Austria
[3] Univ Vienna, Dept Pharmaceut Technol & Biopharmaceut, A-1090 Vienna, Austria
[4] Univ Vienna, Dept Drug & Nat Prod Synth, A-1090 Vienna, Austria
[5] Med Univ Vienna, Dept Psychiat & Psychotherapy, A-1090 Vienna, Austria
[6] Gen Hosp Vienna, Hosp Pharm, A-1090 Vienna, Austria
关键词
Microfluidic; Fluorine-18; PET; Adenosine A(3) receptor; A(3) RECEPTOR-LIGAND; CHEMICAL-SYNTHESIS; MICRO REACTORS; PET; MICROREACTORS; CHEMISTRY;
D O I
10.1016/j.nucmedbio.2010.09.009
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
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 [F-18]FE@SUPPY [5-(2-[F-18]fluoroethyl)2,4-diethyl-3-(ethylsulfanylcarbonyl)-6-phenylpyridine-5-carboxylate] and [F-18]FE@SUPPY:2 [5-ethyl-2,4-diethyl-3((2-[F-18]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 [F-18]fluoride between microfluidic and conventional methods. Methods: For the determination of optimal reaction conditions within an Advion NanoTek synthesizer, 5-50 mu l of precursor and dried [F-18] fluoride solution were simultaneously pushed through the temperature-controlled reactor (26 degrees C-180 degrees C) with defined reactant bolus flow rates (10-50 mu l/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 degrees C, 30-mu l/min pump rate per reactant (reaction overall flow rate of 60 mu l/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 [F-18]FE@SUPPY and that from 42.5% to 95.5% (P<.0001, n >= 5) for [F-18]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. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:427 / 434
页数:8
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