Pullen R H, Cox J W
J Chromatogr. 1985 Oct 11;343(2):271-83. doi: 10.1016/s0378-4347(00)84597-1.
(15R)-15-Methylprostaglandin E2 (PGE2) is a pro-drug under evaluation for the treatment of acute upper gastrointestinal hemorrhage and gastrointestinal cytoprotection. It is converted in acid (e.g., gastric fluid) to its active 15S epimer. Both epimers are found in human plasma at low pg/ml levels following oral dosing. A high-performance liquid chromatographic (HPLC) method was developed for the simultaneous analysis of (15R)- and (15S)-15-methyl-PGE2 in human plasma. The method combined off-line solid-phase extraction and reversed-phase HPLC clean-up with panacyl bromide derivatization and subsequent analysis using a heteromodal column-switching technique. Assay linearity was demonstrated over a range of 10-200 pg/ml for both 15-methyl-PGE2 epimers (r greater than or equal to 0.995). There were no significant inter-day differences in assay results for either epimer at 50 and 25 pg/ml (p greater than 0.05), with pooled estimates of precision at these levels producing relative standard deviations of less than or equal to 8% and less than or equal to 12%, respectively. The method quantitation limit (signal-to-noise ratio 5:1) for both epimers was 10 pg/ml when processing 3 ml of plasma. The analysis procedure was shown to be useful for quantifying at or below 10% of the (15R)-15-methyl-PGE2 maximum plasma concentration following a 50-micrograms oral dose in three human volunteers. For the same three subjects, however, the plasma concentration of (15S)-15-methyl-PGE2 did not exceed the quantitation limit of 10 pg/ml.
(15R)-15-甲基前列腺素E2(PGE2)是一种正在评估用于治疗急性上消化道出血和胃肠道细胞保护的前体药物。它在酸性环境(如胃液)中转化为其活性15S差向异构体。口服给药后,两种差向异构体在人血浆中的浓度均处于低皮克/毫升水平。开发了一种高效液相色谱(HPLC)方法,用于同时分析人血浆中的(15R)-和(15S)-15-甲基-PGE2。该方法结合离线固相萃取和反相HPLC净化,采用泛酰溴衍生化,随后使用异质柱切换技术进行分析。两种15-甲基-PGE2差向异构体在10 - 200皮克/毫升范围内均显示出测定线性(r大于或等于0.995)。对于50皮克/毫升和25皮克/毫升的两种差向异构体,测定结果的日间差异均无统计学意义(p大于0.05),这些水平的合并精密度估计值产生的相对标准偏差分别小于或等于8%和小于或等于12%。当处理3毫升血浆时,两种差向异构体的方法定量限(信噪比5:1)均为10皮克/毫升。在三名人类志愿者口服50微克剂量后,该分析程序被证明可用于定量(15R)-15-甲基-PGE2最大血浆浓度的10%或以下。然而,对于相同的三名受试者,(15S)-15-甲基-PGE2的血浆浓度未超过10皮克/毫升的定量限。