SNM Annual Meeting Abstracts
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     




J Nucl Med. 2008; 49 (Supplement 1):50P
This Article
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by Bergmann, R.
Right arrow Articles by Wuest, F.
PubMed
Right arrow Articles by Bergmann, R.
Right arrow Articles by Wuest, F.

Oncology-Basic Science: Basic Science

Imaging - Peptides and Small Molecules

A comparative study of n.c.a. sodium [18F]fluoroacetate and sodium [11C]acetate in xenotransplanted tumor bearing mice

Ralf Bergmann1, Susan Richter1, Jens Pietzsch1, Bettina Beuthien-Baumann2 and Frank Wuest1

1 Radiopharmaceutical Biology, Forschungszentrum Dresden, Dresden, Germany; 2 Department of Nuclear Medicine/PET Centre Rossendorf, University Hospital Carl Gustav Carus, Dresden, Germany

198

Objectives: This study describes the radiosynthesis of [18F]fluoroacetate (18F-FAC), radiopharmacological characterization, and molecular imaging of oxidative metabolism in tumor bearing mice using 18F-FAC in comparison with 11C-ACE.

Methods: The radiosynthesis of n.c.a. sodium 18F-FAC was performed in two step reaction sequence and subsequent SPE purification in a remotely controlled synthesis module. Biodistribution, metabolism and small animal PET studies of 18F-FAC and 11C-ACE were carried out in rats and HT-29 tumor-bearing mice.

Results: 18F-FAC was obtained in radiochemical yields of 20-25% within 50 min. Biodistribution data showed higher initial radioactivity uptake in most organs and tissues for 18F-FAC; the initial brain uptake of 0.67 %ID/g at 5 min p.i. followed by a 22% clearance at 60 min p.i. Both radiotracers can clearly delineate the tumor. The tumor-to-muscle ration was 1.8 for 18F-FAC and 1.5 for 11C-ACE. Unlike 11C-ACE, 18F-FAC shows a slow transport of the free radiotracer from the blood pool into the tumor, and 10% of the free fraction of 18F-FAC is trapped in tumor tissue.

Conclusions: The highly reproducible remotely-controlled two step/one pot synthesis of 18F-FAC represents an alternative to previously published synthesis routes. The successful PET imaging of xenotransplanted human colorectal adenocarcinoma tumor HT-29 by means of 18F-FAC shows that the radiotracer may not only be restricted for imaging of previously reported prostate cancer tumors. However, the exact mechanism of 18F-FAC tissue uptake remains unclear and should be subject of further studies.

Research Support: Supported in part by the EU FP6 ‘‘BioCare’’, proposal #505785.





This Article
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by Bergmann, R.
Right arrow Articles by Wuest, F.
PubMed
Right arrow Articles by Bergmann, R.
Right arrow Articles by Wuest, F.