Shandong University of Traditional Chinese Medicine, Jinan 250355, China.
Experimental Center of Shandong University of Traditional Chinese Medicine, Jinan 250355, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2019 Jan 15;1105:15-25. doi: 10.1016/j.jchromb.2018.12.006. Epub 2018 Dec 8.
A simple, sensitive and selective high-performance liquid chromatography electrospray ionization tandem mass spectrometry (HPLC-ESI-MS/MS) method was developed and validated for simultaneous determination and pharmacokinetic study of 15 active compounds (Saikosaponin A, Baicalin, Wogonin, Glycyrrhizic acid, Glycyrrhetinic acid, Albiflorin, Paeoniflorin, Liquiritin, Isoliquiritin, Liquiritigenin, Isoliquiritigenin, Cinnamic acid, Gallic acid, Wogonoside and Oroxylin A) in rat plasma. After a feasible protein precipitation using methanol for sample preparation, chromatographic separation was carried out with a Halo® C column (2.1 × 100 mm, 2.7 μm) at 35 °C, water containing 0.1% formic acid and acetonitrile were used as the mobile phase with a flow rate of 0.3 mL/min. Multiple reaction monitoring (MRM) with positive and negative ion switching mode was performed for the quantification of the standards and internal standard in plasma. All the calibration curves showed good linear regression within the linear range (r > 0.9923). In particular, the results of the method validation including specificity, linearity, accuracy, precision, extraction recovery, matrix effect, and stability of compounds in bio-samples were all within the current acceptance criteria. The established method was successfully applied to the pharmacokinetic study of 15 compounds in rats after oral administration of CGD and laid the foundation for studying the active components and mechanism of CGD in vivo.
建立并验证了一种简单、灵敏且专属的高效液相色谱-电喷雾串联质谱(HPLC-ESI-MS/MS)法,用于同时测定和研究大鼠血浆中 15 种活性化合物(柴胡皂苷 A、黄芩苷、汉黄芩素、甘草酸、甘草次酸、白芍苷、丹皮酚、甘草苷、异甘草苷、甘草素、异甘草素、桂皮酸、没食子酸、甘草苷元和木樨草苷)的浓度及其药代动力学。采用甲醇沉淀蛋白法对样品进行预处理后,采用 Halo® C 柱(2.1×100mm,2.7μm)在 35℃下进行色谱分离,以 0.1%甲酸水和乙腈为流动相进行洗脱,流速为 0.3mL/min。采用正负离子切换模式的多重反应监测(MRM)对标准品和内标物进行定量分析。所有校准曲线在其线性范围内均呈现良好的线性关系(r>0.9923)。方法验证的结果,包括专属性、线性、准确度、精密度、提取回收率、基质效应和生物样本中化合物的稳定性,均符合当前的接受标准。该方法成功应用于 CGD 灌胃给药后大鼠体内 15 种化合物的药代动力学研究,为研究 CGD 体内的活性成分和作用机制奠定了基础。