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A New Bioanalytical Method for the Determination of Alprazolam in Human Plasma

机译:测定人血浆中阿普唑仑的新生物分析方法

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摘要

A new liquid chromatography-tandem mass spectrometry method has been developed and validated for the determination of alprazolam in human plasma, using lorazepam as internal standard. Detection was performed using positive ion electrospray tandem mass spectrometry on an Agilent 1200 Triple Ouad 6410A system. The mass transition ion-pair was followed as m/z 309→ 281 for alprazolam and m/z 321→275 for lorazepam, in multiple-reaction monitoring mode. The plasma samples were extracted with tert-buthyl methyl ether and separated by liquid chromatography. Alprazolam and the internal standard were separated on a Zorbax SB-CN column using a mobile phase consisting in 70:30 (v/v) mixture of acetonitrile and 0.5% formic acid aqueous solution, with a flow rate of 0.8 mL/min. The proposed method has been validated for the concentration range in between 0.1 and 50 ng/mL and a correlation coefficient of 0.9991. The precision and accuracy were within 12% for intra-day and inter-days assays. The overall recoveries for alprazolam and lorazepam were 76% and 88%, respectively. The overall time of one analysis was 4 minutes. The assay has proven to be sensitive, specific and reproducible, suitable for the quantitative determination of alprazolam in human plasma.
机译:开发了一种新型液相色谱-串联质谱法,并以劳拉西m为内标,用于测定人血浆中阿普唑仑的有效性。使用正离子电喷雾串联质谱法在Agilent 1200 Triple Ouad 6410A系统上进行检测。在多反应监测模式下,阿普唑仑的m / z 309→281和劳拉西m的m / z 321→275为质量过渡离子对。用叔丁基甲基甲醚提取血浆样品,并通过液相色谱分离。在Zorbax SB-CN色谱柱上使用流动相分离阿普唑仑和内标,该流动相由乙腈和0.5%甲酸水溶液的70:30(v / v)混合物组成,流速为0.8 mL / min。所提出的方法在0.1至50 ng / mL的浓度范围内得到验证,相关系数为0.9991。日内和日间分析的准确性和准确性均在12%以内。阿普唑仑和劳拉西m的总回收率分别为76%和88%。一项分析的总时间为4分钟。该测定方法被证明是灵敏,特异和可重复的,适用于定量测定人血浆中的阿普唑仑。

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