Zhang Nan, Li Rui, Yu Haiyao, Shi Dan, Dong Ning, Zhang Sixi, Wang Helei
Department of Emergency Medicine, the First Hospital of Jilin University, Changchun, 130021, China.
Biomed Chromatogr. 2013 Dec;27(12):1754-8. doi: 10.1002/bmc.2989. Epub 2013 Jul 11.
A sensitive and rapid LC-MS/MS method was developed and validated for the determination of kadsurenone in rat plasma using lysionotin as the internal standard (IS). The analytes were extracted from rat plasma with acetonitrile and separated on a SB-C18 column (50 × 2.1 mm, i.d.; 1.8 µm) at 30 °C. Elution was achieved with a mobile phase consisting of methanol-water-formic acid (65:35:0.1, v/v/v) at a flow rate of 0.30 mL/min. Detection and quantification for analytes were performed by mass spectrometry in the multiple reaction monitoring mode with positive electrospray ionization m/z at 357.1 → 178.1 for kadsurenone, and m/z 345.1 → 315.1 for IS. Calibration curves were linear over a concentration range of 4.88-1464 ng/mL with a lower limit of quantification of 4.88 ng/mL. The intra- and inter-day accuracies and precisions were <8.9%. The LC-MS/MS assay was successfully applied for oral pharmacokinetic evaluation of kadsurenone using the rat as an animal model.
建立了一种灵敏、快速的液相色谱-串联质谱(LC-MS/MS)方法,并以裂环马钱子碱为内标(IS)对大鼠血浆中卡苏烯酮进行了测定和方法验证。用乙腈从大鼠血浆中提取分析物,并在30℃下于SB-C18柱(50×2.1mm,内径;1.8μm)上进行分离。以甲醇-水-甲酸(65:35:0.1,v/v/v)为流动相,流速为0.30mL/min进行洗脱。通过质谱在多反应监测模式下对分析物进行检测和定量,卡苏烯酮的正电喷雾电离m/z为357.1→178.1,内标的m/z为345.1→315.1。校准曲线在4.88-1464ng/mL的浓度范围内呈线性,定量下限为4.88ng/mL。日内和日间准确度和精密度均<8.9%。以大鼠为动物模型,该LC-MS/MS测定法成功应用于卡苏烯酮的口服药代动力学评价。