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Simultaneous determination of pioglitazone and its two active metabolites in human plasma by LC-MS/MS.

机译:LC-MS / MS同时测定人血浆中吡格列酮及其两种活性代谢物。

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摘要

A liquid chromatography/tandem mass spectrometry (LC-MS/MS) method was developed and validated for the simultaneous determination of pioglitazone (PIO) and its two metabolites: M-III (keto-derivative) and M-IV (hydroxy-derivative) in human plasma. Human plasma samples of 0.2 ml were extracted by a single step liquid-liquid extraction procedure and analyzed using a high performance liquid chromatography (HPLC) electrospray tandem mass spectrometer system. The compounds were eluted isocratically on a C-18 column, ionized using a positive ion atmospheric pressure electrospray ionization source and analyzed using multiple reaction monitoring mode. The ion transitions monitored were m/z 357-->134 for PIO, m/z 371-->148 for M-III, m/z 373-->150 for M-IV and m/z 413-->178 for the internal standard. The chromatographic run time was 2.5 min per injection, with retention times of 1.45, 1.02 and 0.95 min for PIO, M-III and M-IV, respectively. The calibration curves of pioglitazone, M-III and M-IV were well fit over the range of 0.5-2000 ng/ml (r(2)>0.998759) by using a weighted (1/x(2)) quadratic regression. The inter-day precisions of the quality control samples (QCs) were
机译:建立了液相色谱/串联质谱(LC-MS / MS)方法并验证了该方法可同时测定吡格列酮(PIO)及其两种代谢物:M-III(酮基衍生物)和M-IV(羟基衍生物)在人类血浆中。通过一步液-液提取程序提取0.2 ml人体血浆样品,并使用高效液相色谱(HPLC)电喷雾串联质谱仪系统进行分析。化合物在C-18色谱柱上等度洗脱,使用正离子大气压电喷雾电离源进行离子化,并使用多种反应监测模式进行分析。对于PIO,监测的离子跃迁为m / z 357-> 134,对于M-III为m / z 371-> 148,对于M-IV为m / z 373-> 150和m / z 413-> 178用于内部标准。每次进样的色谱运行时间为2.5分钟,PIO,M-III和M-IV的保留时间分别为1.45、1.02和0.95分钟。使用加权(1 / x(2))二次回归,吡格列酮,M-III和M-IV的校准曲线在0.5-2000 ng / ml的范围内(r(2)> 0.998759)非常吻合。对于PIO,质量控制样品(QC)的日间精度为

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