Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10916069 | Nuclear Medicine and Biology | 2013 | 9 Pages |
Abstract
The novel PET tracer, [18F]FMePhe, is readily synthesized in good yield from a cyclic sulfamidate precursor. Biodistribution and microPET studies in the DBT model demonstrate good tumor to tissue ratios and tumor visualization, with enantiomer [18F]9a having higher tumor uptake. However, the brain availability of both enantiomers was lower than expected for system L substrates, suggesting the [18F]fluorine group in the β-position affects uptake of these compounds by system L transporters.
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Authors
Chaofeng Huang, Liya Yuan, Keith M. Rich, Jonathan McConathy,