Highlighting the versatility of the Tracerlab synthesis modules. Part 2: fully automated production of [11C]‐labeled radiopharmaceuticals using a Tracerlab FXC‐Pro |
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Authors: | Xia Shao Raphaël Hoareau Adam C Runkle Louis J M Tluczek Brian G Hockley Bradford D Henderson Peter J H Scott |
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Institution: | Department of Radiology, The University of Michigan School of Medicine, , Ann Arbor, MI, 48109 USA |
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Abstract: | The field of radiochemistry is moving toward exclusive use of automated synthesis modules for production of clinical radiopharmaceutical doses. Such a move not only comes with many advantages but also presents radiochemists with the challenge of re‐configuring synthesis modules for production of radiopharmaceuticals that require non‐conventional radiochemistry while maintaining full automation. Herein, we continue our series of articles showcasing the versatility of the Tracerlab FX synthesis modules by presenting straightforward, fully automated methods for preparing a range of carbon‐11 labeled radiopharmaceuticals using a Tracerlab FXC‐Pro. Strategies for production of 11C]acetate, 11C]carfentanil, 11C]choline, 11C]3‐amino‐4‐2‐(di(methyl)amino)methyl]phenyl]sulfanylbenzonitrile (11C]DASB), (+)‐a‐11C]dihydroterabenazine (11C]DTBZ), 11C]flumazenil (11C]FMZ), meta‐hydroxyephedrine (11C]HED), 11C]methionine, 11C]PBR28, 11C]Pittsburgh Compound B (11C]PiB), 1‐11C]methylpiperidin‐4‐yl propionate (11C]PMP), and 11C]raclopride are presented. Copyright © 2011 John Wiley & Sons, Ltd. |
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Keywords: | positron emission tomography automated radiopharmaceutical synthesis carbon‐11 radiochemistry |
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