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Optimization of the preparation of fluorine‐18‐labeled steroid receptor ligands 16alpha‐[ 18 F]fluoroestradiol (FES), [ 18 F]fluoro furanyl norprogesterone (FFNP), and 16beta‐[ 18 F]fluoro‐5alpha‐dihydrotestosterone (FDHT) as radiopharmaceuticals
Author(s) -
Zhou Dong,
Lin Mai,
Yasui Norio,
AlQahtani Mohammed H.,
Dence Carmen S.,
Schwarz Sally,
Katzenellenbogen John A.
Publication year - 2014
Publication title -
journal of labelled compounds and radiopharmaceuticals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 47
eISSN - 1099-1344
pISSN - 0362-4803
DOI - 10.1002/jlcr.3191
Subject(s) - chemistry , yield (engineering) , radiochemistry , trifluoromethanesulfonate , mesylate , nuclear chemistry , stereochemistry , organic chemistry , materials science , metallurgy , catalysis
Fluorine‐18‐labeled steroid receptor tracers, 16 α ‐[ 18 F]fluoroestradiol (FES), [ 18 F]fluoro furanyl norprogesterone (FFNP), and 16 β ‐[ 18 F]fluoro‐5 α ‐dihydrotestosterone (FDHT), are important imaging tools for studies of breast and prostate cancers using positron emission tomography (PET). The automated production of these ligands with high specific activity (SA) as radiopharmaceuticals requires modification and optimization of the currently reported methods. [ 18 F]FES with high SA was synthesized in over 60% radiochemical yield (RCY) at the end of synthesis (EOS) using a small amount of precursor (1) (as low as 0.3 mg) and 1 M H 2 SO 4 for deprotection of the intermediate (2). [ 18 F]FFNP was synthesized in up to 77% RCY at EOS using the triflate precursor (4) at room temperature or in 25% RCY using the mesylate precursor (6) at 65°C. Both methods are highly reproducible and afford high SA. [ 18 F]FDHT was synthesized by radiofluoride incorporation at room temperature, reduction with NaBH 4 , and deprotection with HCl/acetone, giving [ 18 F]FDHT in up to 75% yield (RCY). All of these methods can be easily translated to automated production. The information provided here will aid in the development of automated production of these steroid receptor tracers with high or improved yields, optimal SA, and ease of processing for research and clinical use. Copyright © 2014 John Wiley & Sons, Ltd.