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 language | English |
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Pages (from-to) | 2092-2096 |
Number of pages | 5 |
Journal | Journal of Nuclear Medicine |
Volume | 46 |
Issue number | 12 |
State | Published - 2005 |
Keywords
- F-fluoroethyl-diprenorphine
- Ligand analysis
- PET
- Protocol optimization