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Journal of Nuclear Medicine Vol. 46 No. 12 2092-2096
© 2005 by Society of Nuclear Medicine


Basic Science Investigations

Optimal Duration of PET Studies with 18F-Fluoroethyl-Diprenorphine

Henning Boecker, MD1, Till Sprenger, MD2, Gjermund Henriksen, PhD1, Thomas R. Toelle, MD2 and Mary E. Spilker, PhD1

1 Department of Nuclear Medicine, Klinikum Rechts der Isar, Technische Universität München, Munich, Germany
2 Department of Neurology, Klinikum Rechts der Isar, Technische Universität München, Munich, Germany

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.

Key Words: 18F-fluoroethyl-diprenorphine • PET • protocol optimization • ligand analysis


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[Abstract] [Full Text] [PDF]




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