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https://apo.ansto.gov.au/dspace/handle/10238/9010
Title: | Identification of chemical byproducts in the radiofluorination of structurally complex aryliodonium salts |
Authors: | Pascali, G Del Carlo, S Rocchiccioli, S Signore, G Saccomanni, G Manera, C Macchia, M Salvadori, PA |
Keywords: | Salts Fluids Positron computed tomography Isotopes Radiochemistry Nuclear magnetic resonance Ligands High-performance liquid chromatography |
Issue Date: | 24-Aug-2014 |
Publisher: | Springer Nature |
Citation: | Pascali, G., Del Carlo, S., Rocchiccioli, S., Signore, G., Saccomanni, G., Manera, C., Macchia, M., & Salvadori, P. A. (2015). Identification of chemical byproducts in the radiofluorination of structurally complex aryliodonium salts. Journal of Radioanalytical and Nuclear Chemistry, 303(1), 1021-1027. doi:10.1007/s10967-014-3407-4 |
Abstract: | The use of direct radiofluorination of aryliodonium salts represents a promising route to new PET tracers. This study tested the use of these precursors for obtaining candidate ligands of the cannabinoid type-2 receptor. 18F-labelling was performed using microfluidic technology, which allowed obtaining good incorporation yields. A closer inspection of the chemical composition of the reaction mixture evidenced the recurrent occurrence of chemical byproducts (H-adduct) due to a reductive side reaction of these substrates. The H-adduct formation seems to be unrelated to water presence, needed for obtaining a satisfactory incorporation, and may become an important feature for assessing the real-life accessibility of new radiotracers through the use of aryliodonium precursors. © 2014 Akadémiai Kiadó, Budapest, Hungary |
Gov't Doc #: | 8842 |
URI: | https://doi.org/10.1007/s10967-014-3407-4 http://apo.ansto.gov.au/dspace/handle/10238/9010 |
ISSN: | 1588-2780 |
Appears in Collections: | Journal Articles |
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