Suzuki Tsuneharu, Tsukahara Michiko, Akasaka Yuko, Inoue Hideo
Research Laboratory, Minophagen Pharmaceutical Co. Ltd, Kanagawa, Japan.
Biomed Chromatogr. 2017 Dec;31(12). doi: 10.1002/bmc.4032. Epub 2017 Jul 18.
A highly sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method for simultaneous determination of glycyrrhizin (GL) and its active metabolite, glycyrrhetinic acid (GA), from human plasma was validated and applied to a human pharmacokinetic study. The analytes were extracted from human plasma using an Oasis MAX cartridge and chromatographic separation was performed on an Inertsil ODS-3 column. The detection was performed using an API 4000 mass spectrometer operating in the positive electrospray ionization mode. Selected ion monitoring transitions of m/z 823 → 453 for GL and m/z 471 → 149 for GA were obtained. The response was a linear function of concentration over the ranges of 0.5-200 ng/mL for GL and 2-800 ng/mL for GA (both R > 0.998). Using this method, the pharmacokinetics of GL after single oral administration of a clinical dose (75 mg) to six healthy male Japanese volunteers were evaluated. GL was detected in the plasma of all subjects and the average peak concentration was 24.8 ± 12.0 ng/mL. In contrast, peak concentration of GA was 200.3 ± 60.3 ng/mL, i.e. ~8-fold higher than that of GL. This is the first report clarifying pharmacokinetic profiles of GL and GA simultaneously at a therapeutic oral dose of a GL preparation.
建立了一种高灵敏度液相色谱串联质谱(LC-MS/MS)法,用于同时测定人血浆中的甘草酸(GL)及其活性代谢产物甘草次酸(GA),并将其应用于人体药代动力学研究。采用Oasis MAX柱从人血浆中提取分析物,在Inertsil ODS-3柱上进行色谱分离。使用以正电喷雾电离模式运行的API 4000质谱仪进行检测。获得了GL的m/z 823→453和GA的m/z 471→149的选择离子监测跃迁。在GL浓度范围为0.5 - 200 ng/mL和GA浓度范围为2 - 800 ng/mL时,响应与浓度呈线性关系(两者R均>0.998)。使用该方法,对6名健康日本男性志愿者单次口服临床剂量(75 mg)的GL后的药代动力学进行了评估。所有受试者的血浆中均检测到GL,平均峰浓度为24.8±12.0 ng/mL。相比之下,GA的峰浓度为200.3±60.3 ng/mL,即比GL高约8倍。这是第一份在GL制剂治疗口服剂量下同时阐明GL和GA药代动力学特征的报告。