Title of article :
New approach for the synthesis of [18F]fluoroethyltyrosine for cancer imaging: Simple, fast, and high yielding automated synthesis Original Research Article
Author/Authors :
M. Zuhayra، نويسنده , , A. Alfteimi، نويسنده , , C. Von Forstner، نويسنده , , U. Lützen، نويسنده , , B. Meller، نويسنده , , E. Henze، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Abstract :
O-(2-[18F]fluoroethyl)-l-tyrosine ([18F]FET) is one of the first 18F-labeled amino acids for imaging amino acid metabolism in tumors. This tracer overcomes the disadvantages of [18F]fluorodeoxyglucose, [18F]FDG, and [11C]methionine, [11C]MET. Nevertheless, the various synthetic methods providing 18F[FET] exhibit a big disadvantage concerning the necessity of two purification steps during the synthesis including HPLC purification, which causes difficulties in the automation, moderate yields, and long synthesis times >60 min.
Keywords :
Fluoroethyltyrosine , PET , Fluoroethylation , F-18
Journal title :
Bioorganic and Medicinal Chemistry
Journal title :
Bioorganic and Medicinal Chemistry