Publication | Open Access
Highlighting the versatility of the Tracerlab synthesis modules. Part 2: fully automated production of [<sup>11</sup>C]‐labeled radiopharmaceuticals using a Tracerlab FX<sub>C‐Pro</sub>
60
Citations
97
References
2011
Year
Combinatorial ChemistryTracerlab Synthesis ModulesDiversity Oriented SynthesisBiochemistryNatural SciencesMedicineDiversity-oriented SynthesisRadiopharmaceuticalsSynthesis ModulesAutomated Synthesis ModulesTracerlab Fx C‐proRadiopharmaceutical TherapyRadioanalytical ChemistryPharmacologySmall MoleculesBiomolecular EngineeringNatural Product Synthesis
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 FX C‐Pro . Strategies for production of [ 11 C]acetate, [ 11 C]carfentanil, [ 11 C]choline, [ 11 C]3‐amino‐4‐[2‐[(di(methyl)amino)methyl]phenyl]sulfanylbenzonitrile ([ 11 C]DASB), (+)‐a‐[ 11 C]dihydroterabenazine ([ 11 C]DTBZ), [ 11 C]flumazenil ([ 11 C]FMZ), meta‐hydroxyephedrine ([ 11 C]HED), [ 11 C]methionine, [ 11 C]PBR28, [ 11 C]Pittsburgh Compound B ([ 11 C]PiB), 1‐[ 11 C]methylpiperidin‐4‐yl propionate ([ 11 C]PMP), and [ 11 C]raclopride are presented. Copyright © 2011 John Wiley & Sons, Ltd.
| Year | Citations | |
|---|---|---|
Page 1
Page 1