A Study on Preparation of 3'-18FFluoro-3'-deoxythymidine and Its Biodistribution in 9L Glioma Bearing Rats.
- Author:
Ah Young SHIM
1
;
Byung Seok MOON
;
Tae Sup LEE
;
Kyo Chul LEE
;
Gwang Il AN
;
Seung Dae YANG
;
Kook Hyun YU
;
Gi Jeong CHEON
;
Chang Woon CHOI
;
Sang Moo LIM
;
Kwon Soo CHUN
Author Information
1. Laboratory of Radiopharmaceuticals, Korea Institute of Radiological and Medical Sciences, Seoul, Korea. yukook@dgu.ac.kr
- Publication Type:Original Article
- Keywords:
[18F]FLT;
PET;
brain tumor;
tumor imaging
- MeSH:
Animals;
Brain;
Brain Neoplasms;
Cell Proliferation;
Chromatography, High Pressure Liquid;
Glioma*;
Half-Life;
Injections, Intravenous;
Metabolism;
Rats*;
Thymidine
- From:Nuclear Medicine and Molecular Imaging
2006;40(5):263-270
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Several radioisotope-labeled thymidine derivatives such as [11C]thymidine was developed to demonstrate cell proliferation in tumor. But it is difficult to track metabolism with [11C]thymidine due to rapid in vivo degradation and its short physical half-life. 3'-[18F]fluoro-3'-deoxythymidine ([18F]FLT) was reported to have the longer half life of fluorine-18 and the lack of metabolic degradation in vivo. Here, we described the synthesis of the 3'-[18F]fluoro-3'-deoxythymidine ([18F]FLT) and compared with [18F]FET and [18F]FDG in cultured 9L cell and obtained the biodistribution and PET image in 9L tumor bearing rats. MATERIAL AND METHOD: For the synthesis of [18F]FLT, 3-N-tert-butoxycarbonyl-(5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-deoxy-3'-O-(4-nitrobenzenesulfonyl)-beta-D-threopentofuranosyl)thymine was used as a FLT precursor, on which the tert-butyloxycarbonyl group was introduced to protect N3-position and nitrobenzenesulfonyl group. Radiolabeling of nosyl substitued precursor with 18F was performed in acetonitrile at 120 degrees C and deproteced with 0.5 N HCl. The cell uptake was measured in cultured 9L glioma cell. The biodistribution was evaluated in 9L tumor bearing rats after intravenous injection at 10 min, 30 min, 60 min and 120 min and obtained PET image 60 minutes after injection. RESULTS: The radiochemical yield was about 20-30% and radiochemical purity was more than 95% after HPLC purification. Cellular uptake of [18F]FLT was increased as time elapsed. At 120 min post-injection, the ratios of tumor/blood, tumor/muscle and tumor/brain were 1.61+/-0.34, 1.70+/-0.30 and 9.33+/-2.22, respectively. The 9L tumor was well visualized at 60 min post injection in PET image. CONCLUSION: The uptake of [18F]FLT in tumor was higher than in normal brain and PET image of [18F]FLT was acceptable. These results suggest the possibility of [18F]FLT as an imaging agent for brain tumor.
