Evaluating Hepatobiliary Transport with 18 F-Labeled Bile Acids: The Effect of Radiolabel Position and Bile Acid Structure on Radiosynthesis and In Vitro and In Vivo Performance.

Introduction: An in vivo determination of bile acid hepatobiliary transport efficiency can be of use in liver disease and preclinical drug development. Given the increased interest in bile acid Positron Emission Tomography- (PET-) imaging, a further understanding of the impact of 18-fluorine substitution on bile acid handling in vitro and in vivo can be of significance.

Methods: A number of bile acid analogues were conceived for nucleophilic substitution with [18 F]fluoride: cholic acid analogues of which the 3-, 7-, or 12-OH function is substituted with a fluorine atom (3 α -[18 F]FCA; 7 β -[18 F]FCA; 12 β -[18 F]FCA); a glycocholic and chenodeoxycholic acid analogue, substituted on the 3-position (3 β -[18 F]FGCA and 3 β -[18 F]FCDCA, resp.). Uptake by the bile acid transporters NTCP and OATP1B1 was evaluated with competition assays in transfected CHO and HEK cell lines and efflux by BSEP in membrane vesicles. PET-scans with the tracers were performed in wild-type mice ( n = 3 per group): hepatobiliary transport was monitored and compared to a reference tracer, namely, 3 β -[18 F]FCA.

Results: Compounds 3 α -[18 F]FCA, 3 β -[18 F]FGCA, and 3 β -[18 F]FCDCA were synthesized in moderate radiochemical yields (4-10% n.d.c.) and high radiochemical purity (>99%); 7 β -[18 F]FCA and 12 β -[18 F]FCA could not be synthesized and included further in this study. In vitro evaluation showed that 3 α -FCA, 3 β -FGCA, and 3 β -FCDCA all had a low micromolar Ki -value for NTCP, OATP1B1, and BSEP. In vivo, 3 α -[18 F]FCA, 3 β -[18 F]FGCA, and 3 β -[18 F]FCDCA displayed hepatobiliary transport with varying efficiency. A slight yet significant difference in uptake and efflux rate was noticed between the 3 α -[18 F]FCA and 3 β -[18 F]FCA epimers. Conjugation of 3 β -[18 F]FCA with glycine had no significant effect in vivo . Compound 3 β -[18 F]FCDCA showed a significantly slower hepatic uptake and efflux towards gallbladder and intestines.

Conclusion: A set of 18 F labeled bile acids was synthesized that are substrates of the bile acid transporters in vitro and in vivo and can serve as PET-biomarkers for hepatobiliary transport of bile acids.