首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >A liquid chromatography,/atmospheric pressure ionization tandem mass spectrometry quantitation method for nevirapine and its two oxidative metabolites, 2-hydroxynevirapine and nevirapine 4-carboxylic acid, and pharmacokinetics in baboons
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A liquid chromatography,/atmospheric pressure ionization tandem mass spectrometry quantitation method for nevirapine and its two oxidative metabolites, 2-hydroxynevirapine and nevirapine 4-carboxylic acid, and pharmacokinetics in baboons

机译:奈韦拉平及其两种氧化代谢产物2-羟基奈韦拉平和奈韦拉平4-羧酸的液相色谱/大气压电离串联质谱定量方法以及狒狒的药代动力学

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摘要

A rapid highly sensitive and specific electrospray ionization (ESI) liquid chromatography/tandem mass spectrometry (LC/MS/MS) method for quantification of nevirapine (NVP) and its two metabolites, 2-hydroxynevirapine (2-OHNVP) and nevirapine 4-carboxylic acid (4-CANVP), in baboon serum was developed and validated. Nevirapine, 2-OHNVP, 4-CANVP, and the internal standard, hesperetin, were extracted from baboon serum with ethyl acetate. Components in the extract were separated on a 50 X 2.1 mm Aquasil C-18 5 mu m stainless steel column by isocratic elution with 40% acetonitrile/0.1% formic acid at a flow rate of 0.2mL/min. The liquid flow was passed through a pre-source splitter and 5% of the eluant was introduced into the atmospheric pressure ionization (API) source. The components were analyzed in the multiple-reaction monitoring (MRM) mode as the precursor/product ion pair of m/z 267.2/226.2 for NVP, 283.0/161.2 for 2-OHNVP, 297.2/279.2 for 4-CANVP, and 303.2/177.2 for hesperetin. Linear calibration curves were obtained in the range of 1-1000 ng/mL for NVP and 2-OHNVP and 5-1000 ng/mL for 4-CANVP, using 0.2 mL baboon serum, respectively. The within-day and between-day precisions were < 10% for NVP and 2-OHNVP, and < 11.5% for 4-CANVP. Due to the similar structures and fragmentation patterns of 2-OHNVP and 3-OHNVP, it is not expected that the LC/MS/MS can differentiate 2-OHNVP and 3-OHNVP and they were assayed as a composite. The method was applied to a single-dose escalation study of NVP in non-pregnant baboons (Papio anubis) to characterize the pharmacokinetics of NVP, 2-OHNVP plus 3-OHNVP, and 4-CANVP, and to determine the appropriate dose necessary to achieve comparable peak serum concentration of NVP as reported in healthy human adults. Copyright (c) 2007 John Wiley & Sons, Ltd.
机译:快速,灵敏,特异的电喷雾电离(ESI)液相色谱/串联质谱(LC / MS / MS)方法用于定量测定奈韦拉平(NVP)及其两种代谢物2-羟基奈韦拉平(2-OHNVP)和奈韦拉平4-羧酸开发并验证了狒狒血清中的乙酸(4-CANVP)。用乙酸乙酯从狒狒血清中提取奈韦拉平,2-OHNVP,4-CANVP和内标橙皮素。提取物中的成分在50 X 2.1 mm Aquasil C-18 5μm不锈钢柱上通过40%乙腈/0.1%甲酸的等度洗脱以0.2mL / min的流速进行分离。使液体流通过预源分离器,并将5%的洗脱液引入大气压电离(API)源。在多反应监测(MRM)模式下分析了这些组分,分别为m / z对NVP为267.2 / 226.2,对2-OHNVP为283.0 / 161.2,对4-CANVP为297.2 / 279.2和303.2 /橙皮素为177.2。使用0.2 mL狒狒血清分别在NVP和2-OHNVP的1-1000 ng / mL和4-CANVP的5-1000 ng / mL范围内获得线性校准曲线。 NVP和2-OHNVP的日内和日间精度为<10%,而4-CANVP为<11.5%。由于2-OHNVP和3-OHNVP的结构和片段化模式相似,因此,预计LC / MS / MS不能区分2-OHNVP和3-OHNVP,因此将它们分析为复合物。该方法用于非妊娠狒狒(Papio anubis)中NVP的单次剂量递增研究,以表征NVP,2-OHNVP加3-OHNVP和4-CANVP的药代动力学,并确定所需的适当剂量在健康成年人中达到可比较的NVP峰值血清浓度。版权所有(c)2007 John Wiley&Sons,Ltd.

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