Gangliosides are biologically important glycolipids widely distributed in vertebrate cells. An important member of the ganglioside family is the monosialylganglioside GM1, which has been suggested as a potential therapeutic for Parkinson’s disease. In the current study, a late-stage radiofluorination protocol was developed, in which fluorine-18 was introduced by substitution of a terminal tosyl group in the fatty acid backbone of GM1. The radiofluorination procedure was remarkably simple and furnished the radiofluorinated ganglioside, [18F]F-GM1, in high quantity and quality without protection of the glycosyl moiety. A PET measurement in cynomolgus monkey revealed high uptake of [18F]F-GM1 in heart, bone marrow and lungs but low (<0.4% of injected dose) distribution in the brain. Thus, choosing administration route of GM1 for the therapy of CNS disorders poses further challenges. The present study demonstrates the importance of applying PET microdosing studies in guiding early clinical drug development.
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