School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
J Pharm Biomed Anal. 2013 Apr 15;77:120-7. doi: 10.1016/j.jpba.2013.01.029. Epub 2013 Jan 28.
Schisandra chinensis (Turcz.) Baill., a traditional Chinese medicine, has been used for treating insomnia for centuries. This paper was designed to study on the plasma pharmacokinetic for its absorption process, and to compare the pharmacokinetics of its active ingredients in normal and insomnic rats orally administrated with the prescription. Therefore, an efficient, sensitive and selective ultra fast liquid chromatography/tandem mass spectrometry (UFLC-MS/MS) method for the simultaneous determination of six sedative and hypnotic lignans (schisandrin, schisandrol B, schisantherin A, deoxyshisandrin, γ-schisandrin and gomisin N) of Schisandra chinensis (Turcz.) Baill. in rat plasma has been developed and validated. The analysis was performed on a Shim-pack XR-ODS column (75mm×3.0mm, 2.2μm) using gradient elution with the mobile phase consisting of acetonitrile and 0.1% formic acid waterat a flow rate of 0.4ml/min. The detection of the analytes was performed on 4000Q UFLC-MS/MS system with turbo ion spray source in the positive ion and multiple reaction-monitoring mode. The method was validated in plasma samples, which showed good linearity over a wide concentration range (r(2)>0.99), and obtained lower limits of quantification were 10, 1.2, 1.2, 1.2, 1.0 and 1.2ngmL(-1) for the analytes. The intra- and inter-day assay variability was less than 15% for all analytes. The mean extraction recoveries of analytes and IS from rats plasma were all more than 85.0%. The validated method has been successfully applied to comparing pharmacokinetic profiles of analytes in rat plasma. The results indicated that significant difference in pharmacokinetic parameters of the analytes was observed between two groups, while absorptions of these analytes in insomnic group were all significantly higher than those in normal group.
北五味子(Turcz.)Baill.,一种传统的中药,几个世纪以来一直被用于治疗失眠。本文旨在研究其吸收过程的血浆药代动力学,并比较正常和失眠大鼠口服该方剂后其活性成分的药代动力学。因此,建立并验证了一种同时测定大鼠血浆中北五味子(Turcz.)Baill.的六种镇静催眠木脂素(五味子酯、五味子醇 B、五味子甲素、五味子乙素、γ-五味子素和戈米辛 N)的高效、灵敏和选择性的超快速液相色谱/串联质谱法(UFLC-MS/MS)。分析采用 Shim-pack XR-ODS 柱(75mm×3.0mm,2.2μm),以乙腈和 0.1%甲酸水为流动相,梯度洗脱,流速为 0.4ml/min。采用 4000Q UFLC-MS/MS 系统,以正离子和多反应监测模式,涡轮离子喷雾源进行检测。该方法在血浆样品中进行了验证,结果表明,在较宽的浓度范围内(r(2)>0.99)具有良好的线性关系,定量下限为 10、1.2、1.2、1.2、1.0 和 1.2ngmL(-1)。所有分析物的日内和日间测定变异性均小于 15%。分析物和 IS 从大鼠血浆中的平均提取回收率均大于 85.0%。验证后的方法已成功应用于比较大鼠血浆中分析物的药代动力学特征。结果表明,两组之间分析物的药代动力学参数存在显著差异,而失眠组中这些分析物的吸收均明显高于正常组。