Matsuura K, Takashina H
Central Research Laboratories, Santen Pharmaceutical Co., Ltd., Osaka, Japan.
J Chromatogr. 1993 Jul 2;616(2):229-34. doi: 10.1016/0378-4347(93)80390-p.
A gas chromatographic-mass spectrometric method for determining tiopronin, which has a thiol group, in human blood has been described. To prevent the oxidative degradation of tiopronin in the blood, its thiol group was immediately protected by treatment with isobutyl acrylate, which reacted readily with tiopronin in a 0.1 M Na2HPO4 solution (pH 9.1). The reaction was quantitative within 30 min. The blood sample was deproteinized and purified by a combination of liquid-liquid extraction and solid-phase extraction. Finally, the carboxyl moiety of the ester adduct was derivatized to the pentafluorobenzyl ester. The derivatives of tiopronin and the internal standard were analysed with gas chromatography-mass spectrometry. The precision of the method was satisfactory, and the calibration curve had good linearity in the concentration range investigated. The limit of determination of tiopronin in blood was estimated to be ca. 1 ng/ml.
已描述了一种用于测定人体血液中具有硫醇基团的硫普罗宁的气相色谱 - 质谱法。为防止硫普罗宁在血液中发生氧化降解,其硫醇基团通过用丙烯酸异丁酯处理立即得到保护,丙烯酸异丁酯在0.1M磷酸氢二钠溶液(pH 9.1)中能与硫普罗宁迅速反应。该反应在30分钟内定量完成。血液样本通过液 - 液萃取和固相萃取相结合的方法进行脱蛋白和纯化。最后,酯加合物的羧基部分被衍生化为五氟苄酯。硫普罗宁及其内标的衍生物用气相色谱 - 质谱法进行分析。该方法的精密度令人满意,在所研究的浓度范围内校准曲线具有良好的线性。血液中硫普罗宁的测定限估计约为1 ng/ml。