Bristol-Myers Squibb, Research and Development, Bioanalytical and Discovery Analytical Sciences, Route 206 & Provinceline Road, Princeton, NJ 08543, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Jun 1;878(19):1583-9. doi: 10.1016/j.jchromb.2010.04.018. Epub 2010 Apr 24.
BMS-754807 and metformin were co-administered in drug discovery studies which required the quantitation of both compounds in plasma. Since the two compounds are chemically and structurally dissimilar, developing a single bioanalytical method presented a number of chromatographic challenges including the achievement of appropriate retention times and peak shapes on a single analytical column. To address this chromatographic challenge, we investigated different LC columns under different gradient elution schemes using aqueous/organic mobile phases. Using unbonded silica column and aqueous/methanol mobile phase, we were able to obtain robust and well-resolving chromatographic conditions to support the development and implementation of a single LC-MS/MS bioanalytical method. The use of sub-2 micron particle sizes and a high flow rate, which are attainable with UPLC systems, enhanced the method. The method performance evaluation showed that the method easily met the normally used acceptance criteria for bioanalytical methods, namely a deviation of +/-15% from the nominal concentration except at lower limit of quantitation (LLOQ), where +/-20% is accepted. The reported LLOQ of 7.8 ng/ml, for both BMS-754807 and metformin, was adequate to support the pharmacokinetic studies.
在药物发现研究中,联合使用 BMS-754807 和二甲双胍,需要同时定量检测这两种化合物在血浆中的浓度。由于这两种化合物在化学和结构上存在差异,因此开发单一的生物分析方法存在许多色谱挑战,包括在单个分析柱上实现适当的保留时间和峰形。为了解决这个色谱挑战,我们在不同的梯度洗脱方案下研究了不同的 LC 柱,使用水相/有机流动相。我们使用未键合硅胶柱和水/甲醇流动相,能够获得稳健且分辨率良好的色谱条件,支持开发和实施单一的 LC-MS/MS 生物分析方法。使用亚 2 微米粒径和高流速(UPLC 系统可实现)增强了方法的性能。方法性能评估表明,该方法很容易满足生物分析方法通常使用的接受标准,即名义浓度的偏差在 +/-15%以内,除了定量下限(LLOQ)外,接受 +/-20%的偏差。报告的 BMS-754807 和二甲双胍的LLOQ 分别为 7.8ng/ml,足以支持药代动力学研究。