Department of Pharmacology, Institute of Medical Sciences, Shanghai Jiaotong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2012 Jan 15;881-882:126-30. doi: 10.1016/j.jchromb.2011.12.010. Epub 2011 Dec 16.
A rapid, simple and sensitive LC-MS/MS method was developed and validated for the determination of Bis(9)-(-)-Meptazinol (B9M) in rat plasma. Protein precipitation method was used for sample preparation, using five volumes of methanol as the precipitation agent. The analytes were separated by a Zorbax Extend-C18 column with the mobile phase of methanol-water (containing 5mM ammonium formate, pH 9.8) (95:5, v/v), and monitored by positive electrospray ionization in multiple reaction monitoring (MRM) mode. Retention time of IS (Bis(5)-(-)-Meptazinol) and B9M were 1.9 min and 3.3 min, respectively. The limit of detection was 0.1 ng/ml and the linear range was 1-500 ng/ml. The relative standard deviation (RSD) of intra-day and inter-day variation was 4.4-6.2% and 6.2-8.9%, respectively. The extraction recoveries of B9M in plasma were over 95%. The method proved to be applicable to the pharmacokinetic study of B9M in rat after intravenous and subcutaneous administration.
建立并验证了一种用于测定大鼠血浆中双(9)-(-)-美普他酚(B9M)的快速、简单、灵敏的 LC-MS/MS 方法。样品制备采用蛋白沉淀法,以五倍量甲醇作为沉淀剂。采用甲醇-水(含 5mM 甲酸铵,pH9.8)(95:5,v/v)作为流动相,在 Zorbax Extend-C18 柱上进行分离,采用正电喷雾电离多反应监测(MRM)模式进行检测。内标(双(5)-(-)-美普他酚)和 B9M 的保留时间分别为 1.9 分钟和 3.3 分钟。检测限为 0.1ng/ml,线性范围为 1-500ng/ml。日内和日间变异的相对标准偏差(RSD)分别为 4.4-6.2%和 6.2-8.9%。B9M 在血浆中的提取回收率均超过 95%。该方法适用于 B9M 静脉注射和皮下给药后在大鼠体内的药代动力学研究。