Abramson F P, Lutz M P
J Chromatogr. 1985 Apr 12;339(1):87-95. doi: 10.1016/s0378-4347(00)84630-7.
A method for the analysis of diethylstilbestrol (DES) which is suitable for pharmacokinetic studies has been developed using capillary gas chromatographic (GC) separation and detection with selected-ion mass spectrometry (MS). This technique has been applied to a variety of samples including human plasma samples and extracts of animal tissues including prostate and liver. To investigate the pharmacokinetics of stilphostrol (diethylstilbestrol diphosphate) we have modified the GC-MS method in two ways. One modification involves a dual assay for DES; the first a direct assay, and the second after hydrolysis of a sample with alkaline phosphatase. The difference in these values is the amount of phosphorylated DES present. The other modification separates stilphostrol and DES using a reversed-phase, ion-paired high-performance liquid chromatographic method followed by alkaline phosphatase hydrolysis followed by the GC-MS method. The details of these three methods are described and some representative data are shown.
已开发出一种适用于药代动力学研究的己烯雌酚(DES)分析方法,该方法采用毛细管气相色谱(GC)分离,并通过选择离子质谱(MS)进行检测。这项技术已应用于多种样品,包括人血浆样品以及动物组织(包括前列腺和肝脏)的提取物。为了研究己烯雌酚二磷酸酯(stilphostrol)的药代动力学,我们对GC-MS方法进行了两方面的改进。一种改进涉及对DES的双重测定;第一种是直接测定,第二种是在样品经碱性磷酸酶水解后进行测定。这些值之间的差异就是存在的磷酸化DES的量。另一种改进是使用反相离子对高效液相色谱法分离己烯雌酚二磷酸酯和DES,随后进行碱性磷酸酶水解,再采用GC-MS方法。描述了这三种方法的详细信息,并展示了一些代表性数据。