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Simultaneous Determination of Reserpine, Rescinnamine, and Yohimbine in Human Plasma by Ultraperformance Liquid Chromatography Tandem Mass Spectrometry

机译:超高效液相色谱串联质谱法同时测定人血浆中的利血平,松香胺和育亨宾

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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 precipitation with acetonitrile, separation was carried out using C18 column (50 × 2.1 mm, i.d. 1.7 μm) and mobile 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 ofm/z609.32 > 195.01,m/z635.34 > 221.03,m/z355.19 > 144, andm/z340.15 > 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:开发了一种灵敏且选择性的UPLC-MS / MS方法,并使用罂粟碱作为内标(IS)对人血浆中的三种吲哚生物碱(利血平,Rescinnamine和育亨宾)的测定进行了验证。用乙腈一步沉淀蛋白质后,使用C18色谱柱(50×2.1 mm,内径1.7µm)分离,流动相由乙腈:水:甲酸(60:40:0.1%,v / v / v)组成)以0.2 mL / min的流速泵送。质谱测定是使用以正模式运行且具有多反应监测(MRM)模式的电喷雾接口进行的。选择m / z609.32> 195.01,m / z635.34> 221.03,m / z355.19> 144和m / z340.15> 202.02的产物离子跃迁的前体用于定量利血平,间苯二酚,育亨宾和IS,分别。发现分析响应在0.36–400、0.27–300和0.23–250µng / mL的范围内呈线性,而利血平,Rescinnamine和育亨宾的定量下限为0.36、0.27和0.23µng / mL,分别。验证遵循官方指南。所提出的方法能够再现结果,因此对于药代动力学和毒理学分析可能是可靠的。

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