Shen Jiayuan, Wei Juan, Li Li, Ouyang Huizi, Chang Yanxu, Chen Xiaopeng, He Jun
Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China.
Evid Based Complement Alternat Med. 2018 Sep 26;2018:6460393. doi: 10.1155/2018/6460393. eCollection 2018.
A sensitive and reliable HPLC-MS/MS method has been developed and validated for simultaneous determination of eleven bioactive compounds (rhein, emodin, stilbene glycoside, liquiritin, ononin, verbascoside, gallic acid, schisandrin, liquiritigenin, glycyrrhizic acid, and isoliquiritigenin) in rat plasma after oral administration of Tongmai Yangxin Pill. The collected plasma samples were prepared by liquid-liquid extraction with ethyl acetate after acidification. Eleven compounds were separated on a CORTECS™ C18 column with mobile phases consisting of 0.1% formic acid in deionized water and acetonitrile. The flow rate was 0.3 mL/min. The detection was performed on a tandem mass system with an electrospray ionization (ESI) source in both positive and negative ionization using multiple-reaction monitoring (MRM) mode. The calibration curves were linear over the range of 8-2000 ng/mL for glycyrrhizic acid; 4-1000 ng/mL for liquiritin; 0.8-200 ng/mL for emodin, gallic acid, ononin, schisandrin, and stilbene glycoside; 0.4-100 ng/mL for isoliquiritigenin, liquiritigenin, rhein, and verbascoside, respectively. The intra- and interday precision of the analytes were less than 9.3% and 8.5%. The intra- and interday accuracy were in the range of -14.0% to 10.3% and -6.5% to 9.6%. Meanwhile, the extraction recovery of the analytes in plasma samples ranged from 85.2% to 109.1% and matrix effect from 89.2% to 113.4%. The developed method was successfully applied to the pharmacokinetics of eleven bioactive compounds in rat plasma after oral administration of Tongmai Yangxin Pill prescription.
已建立并验证了一种灵敏可靠的高效液相色谱-串联质谱(HPLC-MS/MS)方法,用于同时测定大鼠口服通脉养心丸后血浆中11种生物活性化合物(大黄酸、大黄素、白藜芦醇苷、甘草苷、鹰嘴豆芽素A、毛蕊花糖苷、没食子酸、五味子醇甲、甘草素、甘草酸和异甘草素)。采集的血浆样品经酸化后用乙酸乙酯液-液萃取进行制备。11种化合物在CORTECS™ C18柱上分离,流动相由0.1%甲酸的去离子水和乙腈组成。流速为0.3 mL/min。采用电喷雾电离(ESI)源在正、负离子模式下通过多反应监测(MRM)模式在串联质谱系统上进行检测。甘草酸的校准曲线在8 - 2000 ng/mL范围内呈线性;甘草苷为4 - 1000 ng/mL;大黄素、没食子酸、鹰嘴豆芽素A、五味子醇甲和白藜芦醇苷为0.8 - 200 ng/mL;异甘草素、甘草素、大黄酸和毛蕊花糖苷分别为0.4 - 100 ng/mL。分析物的日内和日间精密度分别小于9.3%和8.5%。日内和日间准确度分别在-14.0%至10.3%和-6.5%至9.6%范围内。同时,血浆样品中分析物的萃取回收率在85.2%至109.1%之间,基质效应在89.2%至113.4%之间。所建立的方法成功应用于大鼠口服通脉养心丸处方后血浆中11种生物活性化合物的药代动力学研究。