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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Ion-pair solid phase extraction for the simultaneous separation and quantitation of metformin and canagliflozin in human plasma by LC-MS/MS
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Ion-pair solid phase extraction for the simultaneous separation and quantitation of metformin and canagliflozin in human plasma by LC-MS/MS

机译:LC-MS / MS对人血浆中二甲双胍和蜜甲杆素同时分离和定量的离子对固相提取

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摘要

A high-throughput and sensitive liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) has been developed for the simultaneous determination of metformin and canagliflozin in human plasma. The optimized ion-pair solid phase extraction of the analytes was carried out using 100 mu L plasma, followed by reversed-phase chromatography on COSMOSIL 5CN-MS (150 x 4.6 mm, 5 mu m) column. An isocratic mobile phase consisting of methanol-20 mM ammonium formate in water, pH 5 (75:25, v/v) was used for separation of the analytes with a resolution factor of 2.18. Mass spectrometer was operated in the multiple reaction monitoring mode at unit mass resolution. Electro spray ionization was used for mass transition of m/z 130.1/60.1 and m/z 462.1/267.1 for metformin and canagliflozin, respectively. The method was successfully validated for the concentration range of 2.50-2500 ng/mL for both the analytes. The intra- and inter-batch precision determinations for metformin and canagliflozin, expressed as coefficient of variation were lower than 5.5% at all the test concentrations. Recovery of both the drugs was in the range of 78-90% and was reproducible in the quality control samples. No significant matrix effects were observed for the analytes as evident from the IS normalized matrix factors. Stability of the drugs in whole blood and plasma samples was ascertained under different conditions. The assay showed acceptable performance when applied to clinical samples generated from healthy Indian subjects.
机译:已经开发出与串联质谱(LC-MS / MS)偶联的高通量和敏感的液相色谱,用于同时测定人血浆中的二甲双胍和蜜菌素。使用100μl等离子体进行分析物的优化离子对固相提取,然后在Cosmosil 5CN-MS(150×4.6mm,5μm)塔上反相色谱法进行反相色谱。将由水中甲醇-20mM氨基铵组成的等离子流动相,使用pH5(75:25,v / v)来分离分析物,分辨率为2.18。质谱仪以单位质量分辨率在多反应监测模式中操作。电镀电离分别用于M / Z 130.1 / 60.1和M / Z 462.1 / 267.1的质量转变,分别用于二甲双胍和蜜碳醇酶。对于分析物,该方法已成功验证2.50-2500ng / ml的浓度范围。在所有测试浓度下,二甲双胍和蜜碳基团的批量素素和蜜甲杆菌素的粒子素和蜜菌菌酶的内部和蜜菌素的谱系齐率低于5.5%。两种药物的回收率在78-90%的范围内,在质量控制样品中可重现。由于来自归一化矩阵因子的显而易见的分析物未观察到显着的基质效应。在不同条件下确定全血和血浆样品中药物的稳定性。当应用于从健康印度受试者产生的临床样本时,测定显示出可接受的性能。

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