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Rapid and sensitive UPLC-MS/MS method for the determination of etodolac in small-volume rat plasma: Application to rat real samples

机译:快速敏感的UPLC-MS / MS / MS方法,用于测定小体积大鼠血浆中eTodolac:对大鼠真实样品的应用

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摘要

A rapid, simple, and sensitive UPLC-MS/MS method was developed and validated for the determination of etodolac in rat plasma using flurbiprofen as an internal standard (IS). Etodolac and IS were detected using electrospray ionization in negative ion multiple reaction monitoring mode by monitoring the transitions (precursor to product) m/z 286.2?12.1 and 243.2?99.2, respectively. The developed new extraction procedure for etodolac in rat plasma does not contain more than one stage. Chromatographic separation was performed on reverse phase C18 column with a gradient mobile phase, which consisted of methanol for solvent A and 5 mM ammonium formate in water solvent B percentages varying at a flow rate of 0.4 mL/min. The LLOQ for etodolac was determined as 1 ng/mL. The calibration curve for etodolac was linear (r > 0.996 for plasma) well within the range of 15000 ng/mL. Quantification of etodolac in rat plasma is possible in a short chromatographic run time (1.91 min) with this method. The proposed method was fully validated by determining specificity, linearity, LLOQ, precision and accuracy, recovery, matrix effect, and stability. The validated method was successfully applied to plasma samples obtained from rats.
机译:开发快速,简单,敏感的UPLC-MS / MS方法,并验证使用Flbiprofen作为内标(IS)的大鼠等离子体中eTodolac的测定。通过监测过渡(前体至产物)M / Z 286.2α12.1和243.2〜99.2,使用电喷雾电离在负离子多反应监测模式中使用电喷雾电离检测eTodolac。在大鼠等离子体中为eTodolac的开发的新提取方法不含超过一个阶段。在具有梯度流动相的反相C18柱上进行色谱分离,其由甲醇组成用于溶剂A和5mM甲酸甲酸铵,在水溶剂B中以0.4ml / min的流速而变化的百分比。替代克的LLOQ确定为1ng / ml。 Etodolac的校准曲线是线性的(浆料的r> 0.996),其在15000ng / ml的范围内。通过该方法在短的色谱研发时间(1.91分钟)中可以在大鼠等离子体中定量etodolac。通过确定特异性,线性,LLOQ,精度和准确度,恢复,矩阵效应和稳定性,完全验证了所提出的方法。已验证的方法已成功应用于从大鼠获得的血浆样品。

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