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大鼠口服给药后岩白菜素(其主要生物活性成分)的液相色谱-串联质谱测定及药代动力学研究

LC-MS/MS determination and pharmacokinetic study of bergenin, the main bioactive component of after oral administration in rats.

作者信息

Li Bao-Hong, Wu Jin-Dong, Li Xiang-Lu

机构信息

School of Pharmacy, Guangdong Medical College, Dongguan 523808, PR China.

Nature's & US Limited Liability Corporation, St. Louis 63132, USA.

出版信息

J Pharm Anal. 2013 Aug;3(4):229-234. doi: 10.1016/j.jpha.2013.01.005. Epub 2013 Jan 24.

DOI:10.1016/j.jpha.2013.01.005
PMID:29403822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5760982/
Abstract

Bergenin, a -glucoside of 4-O-methyl gallic acid from , is a naturally antitussive and expectorant agent. A rapid and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method has been developed and validated for the determination of the active component-bergenin, in rat plasma after oral administration of aqueous extract. The plasma samples were pretreated by protein precipitation with acetonitrile and chromatographic separation was achieved on a Diamonsil C column (150 mm×4.6 mm, 5 μm) with isocratic elution using a mobile phase consisting of water-methanol (30:70, ) at a flow rate of 0.6 mL/min. The detection was accomplished by a triple-quadrupole tandem mass spectrometer in multiple-reaction monitoring (MRM) scanning an electrospray ionization (ESI) source operating in the negative mode. The optimized mass transition ion-pairs () for quantitation were 327.3/192.0 for bergenin, and 431.1/311.1 for IS. The time for each analysis run was only 3.5 min between injections. The calibration curve exhibited good linearity (>0.99) over a range of 1.00-2000 ng/mL for bergenin. The lower limit of quantitation (LLOQ) was 1.00 ng/mL. The intra- and inter-day precisions were no more than 11.8%, and relative errors (RE) were within the range of 0.0-4.4%. The validated method was successfully applied to investigate the pharmacokinetics of bergenin after oral administration of extract in rats.

摘要

岩白菜素是从[来源未提及]中提取的4-O-甲基没食子酸的α-葡萄糖苷,是一种天然的镇咳祛痰剂。已建立并验证了一种快速灵敏的液相色谱串联质谱法(LC-MS/MS),用于测定大鼠口服[提取物名称未提及]水提取物后血浆中活性成分岩白菜素的含量。血浆样品用乙腈进行蛋白沉淀预处理,在Diamonsil C柱(150 mm×4.6 mm,5μm)上进行色谱分离,采用等度洗脱,流动相为水-甲醇(30:70,[比例单位未提及]),流速为0.6 mL/min。检测通过三重四极杆串联质谱仪在多反应监测(MRM)模式下进行扫描,电喷雾电离(ESI)源在负模式下运行。用于定量的优化质量转移离子对([具体离子对内容未提及]),岩白菜素为327.3/192.0,内标为431.1/311.1。每次进样之间的分析运行时间仅为3.5分钟。岩白菜素的校准曲线在1.00 - 2000 ng/mL范围内呈现良好的线性关系(>0.99)。定量下限(LLOQ)为1.00 ng/mL。日内和日间精密度不超过11.8%,相对误差(RE)在0.0 - 4.4%范围内。该验证方法成功应用于研究大鼠口服[提取物名称未提及]提取物后岩白菜素的药代动力学。

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