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采用超高效液相色谱-串联质谱法同时测定大鼠血浆中的生物活性成分及其在口服黄芩提取物后的药代动力学研究中的应用。

Simultaneous determination of the bioactive components in rat plasma by UPLC-MS/MS and application in pharmacokinetic studies after oral administration of radix Scutellariae extract.

作者信息

Tao Jin-Hua, Xu Jun, Jiang Shu, Ling Yong, Wang Dong-Geng

机构信息

School of Pharmacy, Nantong University, Nantong, People's Republic of China.

Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Nanjing University of Chinese Medicine, Nanjing, People's Republic of China.

出版信息

Biomed Chromatogr. 2017 Sep;31(9). doi: 10.1002/bmc.3961. Epub 2017 Mar 20.

DOI:10.1002/bmc.3961
PMID:28205294
Abstract

A highly sensitive and rapid ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method has been developed and validated for simultaneous quantification of the four main bioactive compounds, i.e. baicalin, baicalein, wogonoside and wogonin, in rat plasma after oral administration of Radix Scutellariae extract. Clarithromycin was used as an internal standard (IS). Plasma samples were processed by protein precipitation with methanol. The separation was performed on an Acquity BEH C column (100 × 2.1 mm, 1.7 μm) at a flow rate of 0.4 mL/min, using 0.1% formic acid-acetonitrile as mobile phase. The MS/MS ion transit ions monitored were 447.5 → 270.1 for baicalin, 270.1 → 168.1 for baicalein, 461.2 → 284.0 for wogonoside, 284.2 → 168.1 for wogonin and 748.5 → 158.1 for IS. Method validation was performed according to US Food and Drug Administration guidelines and the results met the acceptance criteria. The lower limit of quantification (LLOQ) achieved was 1.13 ng/mL for baicalin, 1.23 ng/mL for baicalein, 0.82 ng/mL for wogonoside and 0.36 ng/mL for wogonin. The calibration curves obtained were linear (r > 0.99) over the concentration range ~ 1-1000 ng/mL. The intra- and inter-day precision was <15% and the accuracy was within ±14.7%. After validation, this method was successfully applied to a pharmacokinetic study of Radix Scutellariae extract.

摘要

已开发并验证了一种高灵敏度、快速的超高效液相色谱-串联质谱法(UPLC-MS/MS),用于在大鼠口服黄芩提取物后同时定量测定血浆中四种主要生物活性化合物,即黄芩苷、黄芩素、汉黄芩苷和汉黄芩素。克拉霉素用作内标(IS)。血浆样品通过甲醇蛋白沉淀法处理。采用 Acquity BEH C 柱(100 × 2.1 mm,1.7 μm),以 0.4 mL/min 的流速进行分离,流动相为 0.1% 甲酸-乙腈。监测的 MS/MS 离子跃迁离子分别为:黄芩苷 447.5 → 270.1、黄芩素 270.1 → 168.1、汉黄芩苷 461.2 → 284.0、汉黄芩素 284.2 → 168.1 和内标 748.5 → 158.1。按照美国食品药品监督管理局的指南进行方法验证,结果符合验收标准。黄芩苷的定量下限(LLOQ)为 1.13 ng/mL,黄芩素为 1.23 ng/mL,汉黄芩苷为 0.82 ng/mL,汉黄芩素为 0.36 ng/mL。在约 1 - 1000 ng/mL 的浓度范围内获得的校准曲线呈线性(r > 0.99)。日内和日间精密度 < 15%,准确度在 ±14.7% 以内。验证后,该方法成功应用于黄芩提取物的药代动力学研究。

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