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1. 广东省人民医院核医学科PET中心
2. 南方医科大学放射医学教研室广州,510515
3. 南方医科大学放射医学教研室,广州,510080
Published:01 May 2006
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[1]陈立光,唐安戊,王淑侠,何山震,丁振华.~(11)C-CH_3I合成条件的优化[J].核技术,2006(05):376-379.
CHEN Liguang1, 2 TANG Anwu1 WANG Shuxia1 HE Shanzhen1 DING Zhenhua2 1. Optimization of radiosynthesis of 11C-CH3I[J]. Nuclear techniques, 2006, (5): 376-379.
碳-11碘代甲烷(11C-CH3I)是正电子药物甲基化不可缺少的重要标记试剂
它广泛用于合成11C-蛋氨酸、11C-胆碱、11C-Raclopride等碳标记正电子药物。我们利用11C-CH3I自动化合成模块对合成条件进行了优化
提高了合成设备产率和合成的稳定性。经过30批次的条件优化实验
获得了较高而且稳定的产率。产物总合成时间11min
放化产率(90.2±2.5)%
放化纯度>98%
合成成功率100%。
The [11C]methyl iodide (11C-CH3I ) is a very important methylated precursor in 11C labeled PET tracer synthesis. In order to get higher and more stable radiosynthesis yield of 11C-CH3I
this research aims at optimizing the key steps over the radiosynthesis procedure. After the system temperature of the module was optimized
a higher synthesis yield of 11C-CH3I (90.2 ±2.5)% was got
and 100% success rate of the synthesis was obtained at the same time. The synthesis time was 11min
and the radiochemical purity of the precursor was over 98%. Thus optimization of the system can lead to producing 11C-CH3I with higher and more stable yield.
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