Wu Yun, Ai Yu, Wang Fenrong, Ma Wen, Bian Qiaoxia, Lee David Y-W, Dai Ronghua
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, 110016, China.
Mailman Research Center, McLean Hospital, Harvard Medical School, Boston, MA, United States.
Biomed Chromatogr. 2016 Feb;30(2):97-104. doi: 10.1002/bmc.3519. Epub 2015 Jul 6.
A simple, reliable and rapid ultra-performance liquid chromatography-tandem mass spectrometry method was developed and validated for the simultaneous quantification of four secoiridoid (gentiopicroside, swertiamarin, sweroside) and iridoid glycosides (loganic acid), the bio-active ingredients in rat plasma. After liquid-liquid extraction, chromatographic separation was accomplished on a Shim-pack XR-ODS column with a mobile phase consisting of methanol and 0.1% formic acid in water. A triple quadrupole tandem mass spectrometry equipped with an electrospray ionization source was used as detector operating both in positive and negative ionization mode and operated by multiple-reaction monitoring scanning. The lower limits of quantitation were 0.25-30 ng/mL for all the analytes. Both intra-day and inter-day precision and accuracy of analytes were well within acceptance criteria (±15%). The mean extraction recoveries of analytes and internal standard (amygdalin) from rat plasma were all >71.4%. The validated method was successfully applied to a comparative pharmacokinetic study of four analytes in rat plasma between normal and arthritic rats after oral administration of Huo Luo Xiao Ling Dan and Gentiana macrophylla extract, respectively. Results showed significant differences in pharmacokinetic properties of the analytes among the different groups.
建立并验证了一种简单、可靠且快速的超高效液相色谱-串联质谱法,用于同时定量大鼠血浆中的四种裂环环烯醚萜(龙胆苦苷、獐牙菜苦苷、獐牙菜苷)和环烯醚萜苷(马钱子酸),这些均为生物活性成分。液-液萃取后,在Shim-pack XR-ODS柱上进行色谱分离,流动相由甲醇和0.1%甲酸水溶液组成。配备电喷雾电离源的三重四极杆串联质谱用作检测器,以正离子和负离子模式运行,并通过多反应监测扫描进行操作。所有分析物的定量下限为0.25 - 30 ng/mL。分析物的日内和日间精密度及准确度均在可接受标准(±15%)范围内。大鼠血浆中分析物和内标(苦杏仁苷)的平均萃取回收率均>71.4%。经验证的方法成功应用于分别口服活络效灵丹和秦艽提取物后正常大鼠和关节炎大鼠血浆中四种分析物的比较药代动力学研究。结果表明不同组间分析物的药代动力学性质存在显著差异。