首页> 外文期刊>Journal of Analytical Methods in Chemistry >Simultaneous Determination of Reserpine, Rescinnamine, and Yohimbine in Human Plasma by Ultraperformance Liquid Chromatography Tandem Mass Spectrometry
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Simultaneous Determination of Reserpine, Rescinnamine, and Yohimbine in Human Plasma by Ultraperformance Liquid Chromatography Tandem Mass Spectrometry

机译:超导液相色谱串联质谱法同时测定人血浆中血浆,rescinnamine和yohimbine

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摘要

A sensitive and selective UPLC-MS/MS method was developed and validated for the determination of three indolic alkaloids (reserpine, rescinnamine, and yohimbine) in human plasma using papaverine as internal standard (IS). After a one step protein precipitationwith acetonitrile, separationwas carried out using C18 column(50 × 2.1 mm,i.d. 1.7 μm) andmobile phase consisting of acetonitrile:water: formic acid (60: 40: 0.1%, v/v/v) pumped at a flow rate of 0.2 mL/min. The mass spectrometric determination was carried out using an electrospray interface operated in the positive mode with multiple reaction monitoring (MRM) mode. The precursor to product ion transitions of m/z 609.32 > 195.01, m/z 635.34 > 221.03, m/z 355.19 > 144, and m/z 340.15 > 202.02 were selected for the quantification of reserpine, rescinnamine, yohimbine, and IS, respectively. The analytical response was found to be linear in the range of 0.36–400, 0.27–300, and 0.23–250 ng/mL with lower limit of quantification of 0.36, 0.27, and 0.23 ng/mL for reserpine, rescinnamine, and yohimbine, respectively. Validation was made following official guidelines. The proposed method enabled reproducible results and hence could be reliable for pharmacokinetic and toxicological analysis.
机译:开发并验证了一种敏感和选择性UPLC-MS / MS方法,用于使用罂粟碱作为内标(IS)中的人血浆中三种吲哚生物碱(Reserpine,rescinamine和Yohimbine)。在乙腈沉淀后,使用C18柱(50×2.1mm,ID1.7μm)和丙二腈:水:甲酸(60:40:0.1%,v / v / v)泵送泵送流速为0.2毫升/分钟。使用以多种反应监测(MRM)模式以正模式操作的电喷雾界面进行质谱法测定。选择M / Z 609.32> 195.01,m / z 635.34> 221.03,m / z 355.19> 144和m / z 340.15> 202.02的前体用于定量血清,rescinamine,yohimbine,以及分别。发现分析响应在0.36-400,0.27-300和0.23-250ng / ml的范围内是线性的,其定量下限为0.36,0.27和0.23ng / ml,用于预殖,rescinnamine和yohimbine,分别。遵循正式指导方针进行验证。所提出的方法使能再生结果,因此可以是药代动力学和毒理学分析的可靠性。

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