Dai Bin, Hu Zhiqiang, Li Haiyan, Yan Chong, Zhang Liwei
Department of Neurosurgery, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.
School of Pharmacy, Guangdong Medical College, Dongguan 523808, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Jan 26;978-979:54-61. doi: 10.1016/j.jchromb.2014.11.021. Epub 2014 Dec 3.
A simple, rapid and sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for simultaneous determination of six components including apigenin, quercetin, apigenin-7-O-β-D-glucoside, quercetin-3-O-β-D-glucoside, 3'-methoxyluteolin-7-O-β-D-glucoside, and tricin-7-O-β-D-glucopyranoside in rat plasma using formononetin as the internal standard (IS). The plasma samples were pretreated by a one-step liquid-liquid extraction with dichloromethane. The chromatographic separation was carried out on a ZORBAX SB-Aq column with a gradient mobile phase consisting of acetonitrile and 2mM aqueous ammonium acetate. All analytes and IS were quantitated through electrospray ionization in negative ion multiple reaction monitoring mode. The mass transitions were as follows: m/z 269.1→117.2 for apigenin, m/z 301.2→151.2 for quercetin, m/z 431.3→311.2 for apigenin-7-O-β-D-glucoside, m/z 463.2→300.2 for quercetin-3-O-β-D-glucoside, m/z 461.3→283.1 for 3'-methoxyluteolin-7-O-β-D-glucoside, m/z 491.3→313.1 for tricin-7-O-β-D-glucopyranoside, and m/z 267.2→252.2 for IS, respectively. All calibration curves exhibited good linearity with correlation coefficient (r)>0.995. The intra-day and inter-day precisions (RSD) at three QC levels were both less than 14.0% and the accuracies ranged from 89.8% to 113.8%. The extraction recoveries of six compounds ranged from 82.3% to 92.5%. The validated method was successfully applied to pharmacokinetic study of the six components in male rat plasma after oral administration of Paulownia tomentosa flower extract.
建立了一种简单、快速且灵敏的液相色谱-串联质谱(LC-MS/MS)方法,并进行了验证,该方法以刺芒柄花素为内标,同时测定大鼠血浆中包括芹菜素、槲皮素、芹菜素-7-O-β-D-葡萄糖苷、槲皮素-3-O-β-D-葡萄糖苷、3'-甲氧基木犀草素-7-O-β-D-葡萄糖苷和小麦黄素-7-O-β-D-吡喃葡萄糖苷在内的六种成分。血浆样品通过二氯甲烷一步液-液萃取进行预处理。色谱分离在ZORBAX SB-Aq柱上进行,流动相为乙腈和2mM乙酸铵水溶液组成的梯度洗脱。所有分析物和内标通过电喷雾电离在负离子多反应监测模式下进行定量。质谱转换如下:芹菜素m/z 269.1→117.2,槲皮素m/z 301.2→151.2,芹菜素-7-O-β-D-葡萄糖苷m/z 431.3→311.2,槲皮素-3-O-β-D-葡萄糖苷m/z 463.2→300.2,3'-甲氧基木犀草素-7-O-β-D-葡萄糖苷m/z 461.3→283.1,小麦黄素-7-O-β-D-吡喃葡萄糖苷m/z 491.3→313.1,内标m/z 267.2→252.2。所有校准曲线均呈现良好的线性,相关系数(r)>0.995。三个质量控制水平下的日内和日间精密度(RSD)均小于14.0%,准确度范围为89.8%至113.8%。六种化合物的萃取回收率范围为82.3%至92.5%。该验证方法成功应用于雄性大鼠口服泡桐花提取物后血浆中六种成分的药代动力学研究。