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First published online January 21, 2009, 10.2967/jnumed.108.055756
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Journal of Nuclear Medicine Vol. 50 No. 2 309-315
© 2009 by Society of Nuclear Medicine

doi: 10.2967/jnumed.108.055756

Basic Science Investigation

Radiation Dosimetry of β-Amyloid Tracers 11C-PiB and 18F-BAY94-9172

Graeme J. O'Keefe1, Timothy H. Saunder1, Steven Ng1, Uwe Ackerman1, Henri J. Tochon-Danguy1, J. Gordon Chan1, Sylvia Gong1, Thomas Dyrks2, Stefanie Lindemann2, Gerhard Holl2, Ludger Dinkelborg2, Victor Villemagne1 and Christopher C. Rowe1

1 Centre for Positron Emission Tomography, Austin Hospital, Heidelberg, Victoria, Australia; and 2 Bayer Schering Pharma, Berlin, Germany

Correspondence: For correspondence or reprints contact: Graeme J. O'Keefe, Centre for Positron Emission Tomography, Austin Hospital, Studley Rd., Heidelberg, Victoria 3084, Australia. E-mail: graeme.okeefe{at}petnm.unimelb.edu.au

β-Amyloid (Aβ) imaging has great potential to aid in the diagnosis of Alzheimer disease and the development of therapeutics. The radiation dosimetry of Aβ radioligands may influence their application; therefore, we calculated and compared the effective doses (EDs) of 11C-PiB and a new 18F-labeled ligand, 18F-BAY94-9172. Methods: Attenuation-corrected whole-body scans were performed at 0, 15, 30, 45, and 60 min after injection of 350 ± 28 MBq (mean ± SD) of 11C-PiB in 6 subjects and at 0, 20, 60, 120, and 180 min after injection of 319 ± 27 MBq of 18F-BAY94-9172 in 3 subjects. Coregistered CT was used to define volumes of interest (VOIs) on the PET images. The source organs were the brain, lungs, liver, kidneys, spleen, and vertebrae. The VOIs for the contents of the gallbladder, urinary bladder, lower large intestine, upper large intestine, and small intestine were also defined. Total activity in each organ at each time point was calculated by use of reference organ volumes. The resultant time–activity curves were fitted with constrained exponential fits, and cumulated activities were determined. A dynamic bladder voiding model was used. The OLINDA/EXM program was used to calculate the whole-body EDs from the acquired data. Results: For 11C-PiB, the highest absorbed doses were in the gallbladder wall (44.80 ± 29.30 µGy/MBq), urinary bladder wall (26.30 ± 8.50 µGy/MBq), liver (19.88 ± 3.58 µGy/MBq), and kidneys (12.92 ± 3.37 µGy/MBq). The ED was 5.29 ± 0.66 µSv/MBq. For 18F-BAY94-9172, the highest doses were also in the gallbladder wall (132.40 ± 43.40 µGy/MBq), urinary bladder wall (24.77 ± 7.36 µGy/MBq), and liver (39.07 ± 8.31 µGy/MBq). The ED was 14.67 ± 1.39 µSv/MBq. Conclusion: The estimated organ doses for 11C-PiB were comparable to those reported in earlier research. With the doses used in published studies (300–700 MBq), the EDs would range from 1.6 to 3.7 mSv. The ED of 18F-BAY94-9172 was 30% lower than that of 18F-FDG and, at the published dose of 300 MBq, would yield an ED of 4.4 mSv. The dosimetry of both Aβ radioligands is suitable for clinical and research applications.

Key Words: PET • radiation dosimetry • 11C-PiB • 18F-BAY94-9172

COPYRIGHT © 2009 by the Society of Nuclear Medicine, Inc.


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M. Koole, D. M. Lewis, C. Buckley, N. Nelissen, M. Vandenbulcke, D. J. Brooks, R. Vandenberghe, and K. Van Laere
Whole-Body Biodistribution and Radiation Dosimetry of 18F-GE067: A Radioligand for In Vivo Brain Amyloid Imaging
J. Nucl. Med., May 1, 2009; 50(5): 818 - 822.
[Abstract] [Full Text] [PDF]




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