Shen Jiayuan, Jia Qi, Huang Xuhua, Yao Guangzhe, Ma Wenjuan, Zhang Huamei, Ouyang Huizi, He Jun
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China.
Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China.
Evid Based Complement Alternat Med. 2019 Nov 6;2019:6518528. doi: 10.1155/2019/6518528. eCollection 2019.
This study developed a method for simultaneous determination of 13 elements of (quercitrin, quercetin, hyperoside, caffeic acid, chlorogenic acid, luteolin, apigenin, kaempferol, isoquercitrin, cryptochlorogenic acid, isorhamnetin-3--glucoside, astragalin, and rutin) in rat plasma using high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) in the negative MRM mode. The analytes were analyzed with CORTECS®C column (4.6 × 150 mm, 2.7 m) with mobile phases consisting of 0.1% formic acid in water (A) and acetonitrile (B). The intra- and interday precision of the target compounds were expressed as relative standard deviation (RSD) in the range of 0.5%-10.4%, and the accuracy of the target compounds was expressed as relative error (RE) not exceeding ±14.5% for all analytes. In the meantime, the extraction recovery of the target compounds in plasma samples ranged from 87.4% to 106.2% and matrix effect from 81.0% to 115.5%. The established method was successfully accomplished for the pharmacokinetic study of the analytes in rat plasma samples following oral administration of extract, and the pharmacokinetic parameters of seven compounds were obtained.
本研究建立了一种采用高效液相色谱 - 串联质谱法(HPLC-MS/MS)在负离子多反应监测(MRM)模式下同时测定大鼠血浆中13种成分(槲皮苷、槲皮素、金丝桃苷、咖啡酸、绿原酸、木犀草素、芹菜素、山柰酚、异槲皮苷、隐绿原酸、异鼠李素 - 3 - O - 葡萄糖苷、黄芪苷和芦丁)的方法。分析物采用CORTECS®C柱(4.6×150 mm,2.7 µm)进行分析,流动相由含0.1%甲酸的水溶液(A)和乙腈(B)组成。目标化合物的日内和日间精密度以相对标准偏差(RSD)表示,范围为0.5% - 10.4%,目标化合物的准确度以相对误差(RE)表示,所有分析物的相对误差均不超过±14.5%。同时,血浆样品中目标化合物的提取回收率在87.4%至106.2%之间,基质效应在81.0%至115.5%之间。所建立的方法成功用于大鼠口服提取物后血浆样品中分析物的药代动力学研究,并获得了7种化合物的药代动力学参数。