PT  - JOURNAL ARTICLE
AU  - Schacht, Anna Christina
AU  - Sørensen, Michael
AU  - Munk, Ole Lajord
AU  - Frisch, Kim
TI  - Radiosynthesis of <em>N</em>-<sup>11</sup>C-Methyl-Taurine–Conjugated Bile Acids and Biodistribution Studies in Pigs by PET/CT
AID  - 10.2967/jnumed.115.161711
DP  - 2016 Apr 01
TA  - Journal of Nuclear Medicine
PG  - 628--633
VI  - 57
IP  - 4
4099  - http://jnm.snmjournals.org/content/57/4/628.short
4100  - http://jnm.snmjournals.org/content/57/4/628.full
SO  - J Nucl Med2016 Apr 01; 57
AB  - During cholestasis, accumulation of conjugated bile acids may occur in the liver and lead to hepatocellular damage. Inspired by our recent development of N-11C-methyl-glycocholic acid—that is, 11C-cholylsarcosine—a tracer for PET of the endogenous glycine conjugate of cholic acid, we report here a radiosynthesis of N-11C-methyl-taurine–conjugated bile acids and biodistribution studies in pigs by PET/CT. Methods: A radiosynthesis of N-11C-methyl-taurine–conjugated bile acids was developed and used to prepare N-11C-methyl-taurine conjugates derived from cholic, chenodeoxycholic, deoxycholic, ursodeoxycholic, and lithocholic acid. The lipophilicity of these new tracers was determined by reversed-phase thin-layer chromatography. The effect of lipophilicity and structure on the biodistribution was investigated in pigs by PET/CT using the tracers derived from cholic acid (3α-OH, 7α-OH, 12α-OH), ursodeoxycholic acid (3α-OH, 7β-OH), and lithocholic acid (3α-OH). Results: The radiosyntheses of the N-11C-methyl-taurine–conjugated bile acids proceeded with radiochemical yields of 61% (decay-corrected) or greater and radiochemical purities greater than 99%. PET/CT in pigs revealed that the tracers were rapidly taken up by the liver and secreted into bile. There was no detectable radioactivity in urine. Significant reflux of N-11C-methyl-taurolithocholic acid into the stomach was observed. Conclusion: We have successfully developed a radiosynthesis of N-11C-methyl-taurine–conjugated bile acids. These tracers behave in a manner similar to endogenous taurine–conjugated bile acids in vivo and are thus promising for functional PET of patients with cholestatic diseases.