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用于同时测定大鼠血浆中黄酮类化合物和酸浆苦素的液相色谱-串联质谱法:在口服酸浆(灯笼草)提取物后的药代动力学研究中的应用。

LC-MS/MS method for simultaneous determination of flavonoids and physalins in rat plasma: Application to pharmacokinetic study after oral administration of Physalis alkekengi var. franchetii (Chinese lantern) extract.

作者信息

Guo Yaqing, Liu Hongxia, Ding Liqin, Oppong Mahmood, Pan Guixiang, Qiu Feng

机构信息

Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 300193, China.

Tianjin International Joint Academy of Biomedicine, Tianjin, 300457, China.

出版信息

Biomed Chromatogr. 2017 Oct;31(10). doi: 10.1002/bmc.3970. Epub 2017 May 2.

DOI:10.1002/bmc.3970
PMID:28273367
Abstract

A rapid and sensitive liquid chromatography with tandem mass spectrometry (LC-MS/MS) method was developed and validated for the simultaneous determination of luteolin, luteolin-7-O-β-D-glucopyranoside, physalin A, physalin D and physalin L in rat plasma. Scutellarein and dexamethasone were used as the internal standards (IS). Plasma samples were prepared by liquid-liquid extraction with ethyl acetate. The five constituents were separated on an Acquity UPLC BEH C column (100 mm × 2.1 mm, 1.7 μm). A gradient elution procedure was used with acetonitrile (A)-0.1% aqueous formic acid (B). Mass spectrometric detection was performed in negative ion multiple reaction monitoring mode with an electrospray ionization (ESI) source. This method showed good linearity (r  > 0.997) over a concentration range of 2.0-500 ng/mL with a lower limit of quantification of 2.0 ng/mL for all five compounds. The inter- and intra-day accuracy ranged from 91.7 to 104%, and precisions (RSD) were <6.46% for all analytes. The extraction recoveries of all analytes were >85%. This validated method was successfully applied for the first time to the pharmacokinetic study of five ingredients after oral administration of 70% ethanol extract of Chinese lantern in rats.

摘要

建立了一种快速灵敏的液相色谱-串联质谱(LC-MS/MS)法,用于同时测定大鼠血浆中木犀草素、木犀草素-7-O-β-D-葡萄糖苷、酸浆素A、酸浆素D和酸浆素L。以黄芩素和地塞米松作为内标(IS)。血浆样品采用乙酸乙酯液-液萃取法制备。五种成分在Acquity UPLC BEH C柱(100 mm × 2.1 mm,1.7 μm)上分离。采用乙腈(A)-0.1%甲酸水溶液(B)进行梯度洗脱。采用电喷雾电离(ESI)源,在负离子多反应监测模式下进行质谱检测。该方法在2.0-500 ng/mL的浓度范围内具有良好的线性(r > 0.997),所有五种化合物的定量下限均为2.0 ng/mL。日间和日内准确度范围为91.7%至104% , 所有分析物的精密度(RSD)均<6.46%。所有分析物的萃取回收率均>85%。该验证方法首次成功应用于大鼠口服酸浆70%乙醇提取物后五种成分的药代动力学研究。

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