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首页> 外文期刊>Phytotherapy research: PTR >Determination of Ginsenoside-Rg(1) in Human Plasma and its Application to Pharmacokinetic Studies Following Intravenous Administration of 'Shenmai' Injection
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Determination of Ginsenoside-Rg(1) in Human Plasma and its Application to Pharmacokinetic Studies Following Intravenous Administration of 'Shenmai' Injection

机译:参麦注射液静脉给药后人血浆中人参皂苷-Rg(1)的测定及其在药代动力学研究中的应用

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摘要

'Shemnai' injection is derived from traditional Chinese medicine 'Shenmaisan' and made from Radix ginseng Rubra and Radix Ophiopogonis. Ginsenoside-Rg(1), as a major constituent of Radix ginseng Rubra, is considered responsible for the efficacy of this injection. A rapid, simple and accurate method has been established for determination of ginsenoside-Rg(1) in Shenmai injection and human plasma using LG-ESI-MS/MS, and to study the pharmacokinetics of Rg(1) in ten healthy volunteers after intravenous single dosing of 60 nil, of Shenmai injection. Following solid-phase extraction (SPE), samples were separated on a C, column coupled with electrospray ionization mass spectrometry. The protonated analyte was quantified by multiple reaction monitoring (MRM) with a quadruple mass spectrometer in positive mode. Linearity was confirmed in the concentration range of 1 to 1000 ng/mL for Rg(1), and the lower limit of quantification (LLOQ, S/N > 10) was I ng/mL. The intraday and interday RSDs were within 15% and mean extraction recoveries ranged from 98.6% to 104.9%. The pharmacokinetics of Rg(1) in healthy volunteers conforms to the two-compartment open model. The main pharmacokinetics parameters were as follows: t(1/2 beta), 2.09 +/- 1.89 h; CL, 0.03 +/- 0.01 L kg(-1) h(-1); AUC (0 similar to infinity), 124.4 +/- 35.9 2 ng mL(-1) h and AUC (0 similar to infinity), 127.9 +/- 37.2 ng mL(-1) h, respectively. Copyright (c) 2008 John Wiley & Sons, Ltd.
机译:“ Shemnai”注射液源自中药“ Shenmaisan”,由人参Rubra和麦冬制成。人参皂甙Rg(1)作为人参卢布的主要成分,被认为是该注射剂功效的原因。建立了一种快速,简单,准确的方法,使用LG-ESI-MS / MS测定参麦注射液和人血浆中的人参皂甙Rg(1),并研究了十名健康志愿者在静脉注射后Rg(1)的药代动力学单剂60毫升,参麦注射液。固相萃取(SPE)之后,将样品在C柱上与电喷雾电离质谱联用。质子化分析物通过多反应监测(MRM)用四重质谱仪以正模式进行定量。 Rg(1)的浓度范围为1至1000 ng / mL,线性得到证实,定量下限(LLOQ,S / N> 10)为I ng / mL。日内和日间RSD均在15%以内,平均提取回收率在98.6%至104.9%之间。 Rg(1)在健康志愿者中的药代动力学符合两室开放模型。主要药代动力学参数如下:t(1/2 beta),2.09 +/- 1.89 h; CL,0.03 +/- 0.01 L kg(-1)h(-1); AUC(0类似于无穷大),分别为124.4 +/- 35.9 2 ng mL(-1)h和AUC(0类似于无穷大),分别为127.9 +/- 37.2 ng mL(-1)h。版权所有(c)2008 John Wiley&Sons,Ltd.

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