Optimal duration of PET studies with 18F-fluoroethyl- diprenorphine

Henning Boecker, Till Sprenger, Gjermund Henriksen, Thomas R. Toelle, Mary E. Spilker

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

The tracer 6-O-(2-18F-fluoroethyl)-6-O-desmethyldiprenorphine (18F-FDPN) provides enhanced flexibility to PET studies of the opioidergic system because the label has a longer half-life than the label of 11C-diprenorphine. Here we evaluated the ideal length of PET studies with 18F-FDPN. Methods: 18F-FDPN binding kinetics were quantified with protocols of different lengths by use of a 1-tissue or a 2-tissue compartment model for different volumes of interest. Furthermore, the effects of scanning duration were assessed by parametric analyses. Results: A 90-min protocol resulted in less than 10% bias in distribution volume (DV) relative to the full-length protocol. Correlation analyses of the DV estimates for the full-length protocol and the shortened protocols showed good replication of DV estimates for regions with both low and high levels of binding at schedules of up to 90 min. Conclusion: Data sampling in dynamic 18F-FDPN PET acquisitions should not be shorter than 90 min to maintain reliable estimates of DV.

Original languageEnglish
Pages (from-to)2092-2096
Number of pages5
JournalJournal of Nuclear Medicine
Volume46
Issue number12
StatePublished - 2005

Keywords

  • F-fluoroethyl-diprenorphine
  • Ligand analysis
  • PET
  • Protocol optimization

Fingerprint

Dive into the research topics of 'Optimal duration of PET studies with 18F-fluoroethyl- diprenorphine'. Together they form a unique fingerprint.

Cite this