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11CO bonds made easily for positron emission tomography radiopharmaceuticals

Research output: Contribution to journalArticle

Benjamin H. Rotstein, Steven H. Liang, Michael S. Placzek, Jacob M. Hooker, Antony D. Gee, Frédéric Dollé, Alan A. Wilson, Neil Vasdev

Original languageEnglish
Pages (from-to)4708-4726
Number of pages19
JournalCHEMICAL SOCIETY REVIEWS
Volume45
Issue number17
DOIs
Published8 Jun 2016

King's Authors

Abstract

The positron-emitting radionuclide carbon-11 (11C, t1/2 = 20.3 min) possesses the unique potential for radiolabeling of any biological, naturally occurring, or synthetic organic molecule for in vivo positron emission tomography (PET) imaging. Carbon-11 is most often incorporated into small molecules by methylation of alcohol, thiol, amine or carboxylic acid precursors using [11C]methyl iodide or [11C]methyl triflate (generated from [11C]carbon dioxide or [11C]methane). Consequently, small molecules that lack an easily substituted 11C-methyl group are often considered to have non-obvious strategies for radiolabeling and require a more customized approach. [11C]Carbon dioxide itself, [11C]carbon monoxide, [11C]cyanide, and [11C]phosgene represent alternative reactants to enable 11C-carbonylation. Methodologies developed for preparation of 11C-carbonyl groups have had a tremendous impact on the development of novel PET tracers and provided key tools for clinical research. 11C-Carbonyl radiopharmaceuticals based on labeled carboxylic acids, amides, carbamates and ureas now account for a substantial number of important imaging agents that have seen translation to higher species and clinical research of previously inaccessible targets, which is a testament to the creativity, utility and practicality of the underlying radiochemistry.

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