Investigation on the impact of three different quaternary methyl ammonium cartridges on the radiosynthetic yields of [18 F]fluoromethyl tosylate
- PMID: 31236995
- DOI: 10.1002/jlcr.3781
Investigation on the impact of three different quaternary methyl ammonium cartridges on the radiosynthetic yields of [18 F]fluoromethyl tosylate
Abstract
Our recent investigations for the radiosynthesis of [18 F]fluoromethyl tosylate have highlighted that choice of quaternary methyl ammonium (QMA) cartridge used during the radiosynthesis can significantly impact the radiochemical yields. Often the details of the QMA cartridge used in fluourine-18 syntheses are not fully described. However, our studies demonstrate that the type, the size, and nature (method by which it has been conditioned) of the QMA cartridge used during the radiosynthesis can make a significant impact in the labelling efficiency. This paper investigates the use of three QMA cartridges and demonstrates that radiochemical yield (decay corrected) of [18 F]fluoromethyl tosylate can increase from 46% to 60% by simply changing the QMA cartridge (and leaving all other reagents and labelling conditions exactly the same). These learnings may be applied to improve the radiochemical yields of a number of [18 F]-fluorinated tracers (and synthons), where the labelling step is base-sensitive to increase the radiochemical yield, thereby significantly benefiting the radiochemistry and nuclear medicine community. This paper also highlights the necessity of the radiochemistry community to ensure the details of QMA cartridges used in fluorine-18 chemistry are fully and accurately described, since this will improve the translation of radiochemical methods from one laboratory to another.
Keywords: PET; QMA; [18F]Fluoromethyl tosylate; [18F]Fluoromethylation; synthon.
© 2019 John Wiley & Sons, Ltd.
Similar articles
-
Automated synthesis and purification of [18F]fluoro-[di-deutero]methyl tosylate.J Labelled Comp Radiopharm. 2013 Jun 15;56(7):360-3. doi: 10.1002/jlcr.3043. Epub 2013 Apr 17. J Labelled Comp Radiopharm. 2013. PMID: 24285440
-
One-step high-radiochemical-yield synthesis of [18F]FP-CIT using a protic solvent system.Nucl Med Biol. 2007 May;34(4):345-51. doi: 10.1016/j.nucmedbio.2007.02.007. Nucl Med Biol. 2007. PMID: 17499723
-
A fully automated radiosynthesis of [18F]fluoroethyl-diprenorphine on a single module by use of SPE cartridges for preparation of high quality 2-[18F]fluoroethyl tosylate.Molecules. 2013 Jun 20;18(6):7271-8. doi: 10.3390/molecules18067271. Molecules. 2013. PMID: 23787515 Free PMC article.
-
Fluorine-18 radiochemistry, labeling strategies and synthetic routes.Bioconjug Chem. 2015 Jan 21;26(1):1-18. doi: 10.1021/bc500475e. Epub 2014 Dec 12. Bioconjug Chem. 2015. PMID: 25473848 Free PMC article. Review.
-
Radiosynthesis of [18)F]trifluoroalkyl groups: scope and limitations.Biomed Res Int. 2014;2014:380124. doi: 10.1155/2014/380124. Epub 2014 Jul 10. Biomed Res Int. 2014. PMID: 25110676 Free PMC article. Review.
Cited by
-
[18F]Tosyl fluoride as a versatile [18F]fluoride source for the preparation of 18F-labeled radiopharmaceuticals.Sci Rep. 2023 Feb 23;13(1):3182. doi: 10.1038/s41598-023-30200-2. Sci Rep. 2023. PMID: 36823435 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources