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Development and Validation of a Liquid Chromatography-Mass Spectrometry Method for the Determination of Zileuton in Human Plasma

机译:液相色谱-质谱法测定人血浆中齐留通的开发与验证

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摘要

A selective and sensitive liquid chromatography-tandem mass spectrometric method (LC-MS/MS) has been developed and validated for the quantification of zileuton in human plasma. Deuterated internal standard (zileuton D4) was used as the internal standard (ISTD). Zileuton was extracted by liquid-liquid extraction using methyl tert-butyl ether and separated by isocratic elution on a C18 column (100 × 4.6 mm, 5 μm, Discovery C18) with the mobile phase consisting of 1 mM ammonium acetate buffer and methanol in the ratio of 10:90. A flow rate of 1.0 ml/min was used with isocratic elution. Multiple reaction monitoring transitions in positive mode for zileuton and the internal standard were 237.3/161.2 and 241.2/161.1, respectively. The method was validated within the linearity range of 50.5–10,012.7 ng/ml for the bioanalytical method validation parameters like selectivity, accuracy, precision, recovery, stability, and matrix effect.
机译:已经开发出一种选择性灵敏的液相色谱-串联质谱法(LC-MS / MS),并已用于定量测定人血浆中齐留通的有效性。氘代内标(zileuton D4)用作内标(ISTD)。使用甲基叔丁基醚通过液-液萃取来提取齐留通,然后在C18柱(100×4.6 mm,5μm,Discovery C18)上通过等度洗脱进行分离,流动相由1 mM乙酸铵缓冲液和甲醇组成。比例为10:90。等度洗脱使用1.0 ml / min的流速。齐留通和内标物在阳性模式下的多个反应监控跃迁分别为237.3 / 161.2和241.2 / 161.1。对于生物分析方法的验证参数,如选择性,准确性,精密度,回收率,稳定性和基质效应,在线性范围50.5–10,012.7 ng / ml范围内对该方法进行了验证。

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