Firnau G, Chirakal R, Garnett E S
J Nucl Med. 1984 Nov;25(11):1228-33.
A new synthesis is described for the routine production of 3,4-dihydroxy-6-[18F]fluoro-phenyl-L-alanine (6-[18F]fluoro-L-dopa). The reaction between [18F]fluorine gas and 3,4-dihydroxyphenyl-L-alanine (L-dopa) in liquid hydrogen fluoride gave 2-, 5-, and 6-[18F]fluoro-L-dopa. 6-[18F]Fluoro-L-dopa was isolated by reverse-phase high-pressure liquid chromatography. From 100 mCi [18F]F2, the method produces 3 mCi of 6-[18F]fluoro-L-dopa at the end of synthesis.
描述了一种用于常规生产3,4-二羟基-6-[¹⁸F]氟代苯基-L-丙氨酸(6-[¹⁸F]氟-L-多巴)的新合成方法。在液态氟化氢中,[¹⁸F]氟气与3,4-二羟基苯基-L-丙氨酸(L-多巴)反应生成2-、5-和6-[¹⁸F]氟-L-多巴。通过反相高压液相色谱法分离出6-[¹⁸F]氟-L-多巴。从100毫居里的[¹⁸F]F₂开始,该方法在合成结束时可产生3毫居里的6-[¹⁸F]氟-L-多巴。