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采用 LC-MS/MS 法测定大鼠血浆中人参皂苷 Rh3 的浓度及其在药代动力学研究中的应用。

Determination of ginsenoside Rh3 in rat plasma by LC-MS/MS and its application to a pharmacokinetic study.

机构信息

School of Pharmacy, North China University of Science and Technology, Tangshan, Hebei, P.R. China.

Canada Royal Enoch Phytomedicine Ltd, Vancouver, BC, Canada.

出版信息

Biomed Chromatogr. 2022 Feb;36(2):e5268. doi: 10.1002/bmc.5268. Epub 2021 Nov 24.

DOI:10.1002/bmc.5268
PMID:34676576
Abstract

Ginsenoside Rh3 (GRh3) is a bacterial metabolite of ginsenoside Rg5, which is the main component of hot-processed ginseng. A simple, efficient and sensitive method was developed and validated for the determination of GRh3 in rat plasma by LC-tandem mass spectrometry. After protein precipitation with methanol/acetonitrile (1:1, vol/vol) using propranolol as the internal standard, the target analytes were separated on an XDB C column, with methanol containing 0.1% formic acid and water containing 0.1% formic acid used as mobile phases for gradient elution. Mass spectrometry was performed in electrospray ion source-positive ion mode and multiple reaction monitoring mode, monitoring the transitions m/z 622.5 → 425.5 and m/z 260.1 → 116.1 for GRh3 and internal standard, respectively. The concentration range of GRh3 was 20-20,000 ng/mL and the correlation coefficient (r ) was greater than 0.99. The accuracy error and relative standard deviation were below 15%. The extraction recovery and matrix effect were 74.2% to 78.7% and 96.9% to 108.4%, respectively. Under different conditions, GRh3 was stable in the range of 1.8%-8.7%. This method has been successfully applied to study the pharmacokinetics of GRh3 with an oral dose of 10.0 mg/kg and an intravenous dose of 2.0 mg/kg in rats, respectively. The absolute bioavailability of GRh3 was 37.6%.

摘要

人参皂苷 Rh3(GRh3)是人参皂苷 Rg5 的细菌代谢产物,是炮制红参的主要成分。建立并验证了一种用于测定大鼠血浆中 GRh3 的 LC-MS/MS 方法。采用甲醇/乙腈(1:1,体积/体积)沉淀蛋白,以普萘洛尔为内标,用甲醇(含 0.1%甲酸)-水(含 0.1%甲酸)作为流动相进行梯度洗脱,在 XDB C 柱上分离目标分析物。质谱采用电喷雾离子源正离子模式和多反应监测模式,监测 GRh3 和内标物的母离子-子离子跃迁 m/z 622.5→425.5 和 m/z 260.1→116.1。GRh3 的浓度范围为 20-20000ng/mL,相关系数(r)大于 0.99。准确度误差和相对标准偏差均低于 15%。提取回收率和基质效应分别为 74.2%-78.7%和 96.9%-108.4%。在不同条件下,GRh3 的稳定性在 1.8%-8.7%范围内。该方法已成功应用于研究大鼠口服 10.0mg/kg 和静脉注射 2.0mg/kg 剂量的 GRh3 的药代动力学,GRh3 的绝对生物利用度为 37.6%。

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