Liu Jane, Yuan Long, Liu Guowen, Shen Jim X, Aubry Anne-Françoise, Arnold Mark E, Ji Qin C
Analytical and Bioanalytical Development, Bristol-Myers Squibb, Princeton NJ 08543, United States.
Analytical and Bioanalytical Development, Bristol-Myers Squibb, Princeton NJ 08543, United States.
J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Jun 1;991:85-91. doi: 10.1016/j.jchromb.2015.04.013. Epub 2015 Apr 17.
Herein we report a rapid, accurate and robust UHPLC-MS/MS assay for the quantitation of BMS-911453, a Janus kinase 2 inhibitor under clinical development for the treatment of myeloproliferative disorders, in human plasma. A systematic method development approach was used to optimize the mass spectrometry, chromatography, and sample extraction conditions, and to minimize potential bioanalytical risks. The validated method utilizes stable-isotope labeled (13)C4-BMS-911543 as the internal standard. Liquid-liquid extraction was used for sample preparation. Chromatographic separation was achieved within 2min on a Zorbax Extend-C18 column with an isocratic elution. BMS-911543 and its internal standard were detected by positive ion electrospray tandem mass spectrometry. The assay range was from 1 to 500ng/mL, and the standard curve was fitted with 1/x(2) weighted linear regression. The intra-assay precision was within 5.0% CV and the inter-assay precision was within 2.6% CV. The inter-assay mean accuracy, expressed as percents of theoretical, was between 99.8% and 102.3%. The assay has high recovery (∼80%) and minimal matrix effect (0.95-1.00). BMS-911543 was stable in human plasma for at least 24h at room temperature, 90 days at -20°C, and following three freeze-thaw cycles. The validated method was successfully applied to sample analysis in clinical studies.
在此,我们报告了一种快速、准确且稳健的超高效液相色谱-串联质谱法(UHPLC-MS/MS),用于定量测定人血浆中的BMS-911453,这是一种正在临床开发用于治疗骨髓增殖性疾病的Janus激酶2抑制剂。采用系统的方法开发方法来优化质谱、色谱和样品提取条件,并将潜在的生物分析风险降至最低。验证后的方法使用稳定同位素标记的(13)C4-BMS-911543作为内标。采用液-液萃取进行样品制备。在Zorbax Extend-C18柱上通过等度洗脱在2分钟内实现色谱分离。通过正离子电喷雾串联质谱法检测BMS-911543及其内标。测定范围为1至500ng/mL,标准曲线采用1/x(2)加权线性回归拟合。批内精密度的变异系数(CV)在5.0%以内,批间精密度的CV在2.6%以内。批间平均准确度以理论值的百分比表示,在99.8%至102.3%之间。该测定法具有高回收率(约80%)和最小基质效应(0.95 - 1.00)。BMS-911543在人血浆中于室温下至少稳定24小时,在-20°C下稳定90天,且经过三个冻融循环后仍稳定。验证后的方法已成功应用于临床研究中的样品分析。