Xiaowen Li, Ling Tong, Yunfei Li, Guoxiang Sun, Dailin Yang, Herry Sun
School of Pharmacy, Shenyang Pharmaceutical University, Wenhua Road 103, Shenyang 110016, China.
Tasly R&D Institute, Tianjin Tasly Group Co., Ltd., Tianjin 300402, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Apr 1;1017-1018:28-35. doi: 10.1016/j.jchromb.2016.01.062. Epub 2016 Feb 26.
An ultra fast liquid chromatography-tandem mass sepectrometry (UFLC-MS/MS) method was developed for simultaneous determination of seven active alkaloid components (tetrahydropalmatine, corydaline, α-allocryptopine, tetrahydroberberine, tetrahydrocoptisine, tetrahydrocolumbamine and dehydrocorydaline) in rat plasma after oral administration of Cerebralcare Granule. Plasma samples were pretreated by protein precipitation with acetronitrile containing the internal standard diazepam. Chromatographic separation was achieved on a Phenomenex Kinetex C18 column (100×2.1mm, 2.6μm) with gradient elution using mobile phase consisting of acetonitrile -0.1% formic acid in water at a flow rate of 0.3mL/min. The detection was performed on an electrospray ionization triple quadrupole tandem mass spectrometer using multiple reaction monitoring (MRM) with positive ionization mode. The established method was fully validated and proved to be sensitive and specific with lower limits of quantification (LLOQs) all less than 0.0265ng/mL in rat plasma. Good linearities of seven alkaloids were obtained in respective concentration ranges (r>0.9923). The intra- and inter-day precisions were below of 15% for all the seven alkaloids in terms of relative standard deviation (RSD), and the accuracies were ranged from -2.7% to 8.3% in terms of relative error (RE). Extraction recovery, matrix effect and stability were within the required limits in rat plasma. The validated method was successfully applied to investigate the pharmacokinetics of the seven alkaloids in rat plasma after oral administration of Cerebralcare Granule (CG).
建立了一种超快速液相色谱-串联质谱法(UFLC-MS/MS),用于同时测定大鼠口服脑心康颗粒后血浆中7种活性生物碱成分(延胡索乙素、紫堇碱、α-别隐品碱、四氢小檗碱、四氢黄连碱、四氢掌叶防己碱和脱氢紫堇碱)。血浆样品采用含内标地西泮的乙腈进行蛋白沉淀预处理。色谱分离采用Phenomenex Kinetex C18柱(100×2.1mm,2.6μm),以乙腈-0.1%甲酸水溶液为流动相进行梯度洗脱,流速为0.3mL/min。采用电喷雾电离三重四极杆串联质谱仪,以正离子模式进行多反应监测(MRM)检测。所建立的方法经过全面验证,结果表明该方法灵敏、特异,大鼠血浆中各成分的定量下限(LLOQ)均低于0.0265ng/mL。7种生物碱在各自的浓度范围内具有良好的线性关系(r>0.9923)。7种生物碱的日内和日间精密度相对标准偏差(RSD)均低于15%,准确度相对误差(RE)在-2.7%至8.3%之间。大鼠血浆中的提取回收率、基质效应和稳定性均在规定范围内。该验证方法成功应用于研究大鼠口服脑心康颗粒(CG)后血浆中7种生物碱的药代动力学。