Novel probes for imaging amyloid-β:: F-18 and C-11 labeling of 2-(4-aminostyryl)benzoxazole derivatives

被引:23
作者
Shimadzu, H [1 ]
Suemoto, T [1 ]
Suzuki, M [1 ]
Shiomitsu, T [1 ]
Okamura, N [1 ]
Kudo, Y [1 ]
Sawada, T [1 ]
机构
[1] Natl Cardiovasc Ctr, BF Res Inst Inc, Suita, Osaka 5650873, Japan
关键词
fluorine-18; 2-(4-methylaminostyryl)-6-(2-[F-18]fluoroethoxy)benzoxazole; BF-168; 2-(4-[N-methyl-C-11]methylaminostyryl)-5-fluorobenzoxazole; BF-145; amyloid-beta; PET;
D O I
10.1002/jlcr.811
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
2-(4-Methylaminostyryl)-6-(2-[F-18]fluoroethoxy)benzoxazole ([F-18]BF-168) was prepared and found to be a potential probe for imaging amyloid-beta. The precursor, a 6-(2-tosyloxyethoxy)benzoxazole derivative, was fluorinated with [F-18]KF and Kryptofix 222 in acetonitrile, and the crude product purified by semi-preparative HPLC to give [F-18]BF-168. The radiochemical purity was > 95% and the maximum specific activity was 106 TBq/mmol at the end of synthesis. The synthesis time was 110 min from the end of bombardment. 2-(4-[N-methyl-C-11]methylaminostyryl)-5-fluorobenzoxazole ([C-11]BF-145) was also prepared from 2-(4-aminostyryl)-5-fluorobenzoxazole, [C-11]MeI and 5 N NaOH in DMSO, and purified by semi-preparative HPLC. The radiochemical purity was >95% and the specific activity was 40-70TBq/mmol at the end of synthesis. The synthesis time was 45 min from the end of bombardment. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:181 / 190
页数:10
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