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Tracerlab fxf n reaction module

Manufactured by GE Healthcare

The TRACERlab FXF-N reaction module is a compact and automated synthesis platform for the production of radiopharmaceuticals. It is designed to facilitate the efficient and reproducible synthesis of a variety of radiolabeled compounds, including positron emission tomography (PET) tracers. The module provides a controlled environment for the synthesis process and includes features to ensure consistent and reliable results.

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2 protocols using tracerlab fxf n reaction module

1

Radiosynthesis of [18F]FDG Precursor

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3-N-Boc-5′-O-dimethoxytrityl-3′-O-nosyl-thymidine, 2,3′-anhydro-5′-O-benzoyl-2′-deoxythymidine, 3′-deoxy-3′-fluorothymidine, and tetrabutylammonium hydrogen carbonate (TBAHCO3, 75 mM in ethanol) were purchased from ABX (Advanced Biochemical Compounds, Radeberg, Germany). All trapping and purification cartridges were purchased from Waters (Milford, MA) or Grace Davison Discovery Sciences (Deerfield, OR). Anhydrous acetonitrile, potassium carbonate (K2CO3), dimethyl sulfoxide (DMSO), sodium hydroxide (NaOH), hydrochloric acid (HCl), and Kryptofix-222 were purchased from Sigma-Aldrich (St. Louis, MO), and absolute ethanol (200 proof) from Pharmaco Aaper (Brookfield, CT). Membrane filters (0.2-μm) were purchased from Pall (Port Washington, NY). Manifold kits for FDG were purchased from Rotem Industries, Inc. (Arava, Israel). All radiosyntheses were performed using either a Bioscan Coincidence GE FDG reaction module (Fairfield, CT) or a GE TRACERlab FXF-N reaction module. Analytical HPLC was performed using a Hitachi HPLC system (LaChrom Elite) equipped with in-line Hitachi UV (LaChrom Elite model L-2400) and radiometric (Carroll-Ramsey Associates, Berkeley, CA) detectors and a Hitachi LaChrom reversed-phase analytical column (150 mm × 4.6 mm). MicroPET scanning was accomplished using a Concorde Microsystems Focus 220 (Siemens, Berlin, Germany).
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2

Radiolabeled Dopamine Transporter Tracer Protocol

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[18F]-FE-PE2I was produced by the Vanderbilt Radiochemistry Core laboratory under cGMP protocols. The synthetic preparation was carried out utilizing a Tracerlab FXFN reaction module (GE Healthcare) and was synonymous to a previously published preparation50 (link). Serial scan acquisition was started simultaneously with a slow bolus injection (mean = 4.63 ± 0.34 mCi; 171.31 ± 12.58 MBq) of the DAT tracer [18F]-FE-PE2I (specific activity = 2302 ± 1445 Ci/mmol). CT scans were collected for attenuation correction prior to the emission scan. FE-PE2I data were collected during one 61-min dynamic scan with acquisition times listed in Table S1. While previous human PET studies using FE-PE2I used 90 min dynamic scan acquisitions46 (link),48 (link), we chose the 61 min acquisition time to improve participant comfort given that the correlation between putamen FE-PE2I BPND collected after 61 and 90 min in 4 pilot subjects was extremely high (r = 0.997, mean percentage of BPND difference = 2.06 ± 1.72). All PET data were collected on a GE Discovery STE PET scanner (GE Healthcare, Milwaukee, USA).
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