Zhang Juanhong, Wang Rong, Xie Hua, Meng Xiandong, Jia Zhengping, Ma Jun, Zhang Junli, Wang Juan
Base for Clinical Pharmacology, Lanzhou General Hospital of Lanzhou Military Region, Lanzhou 730050, China.
Se Pu. 2011 Jan;29(1):26-30. doi: 10.3724/sp.j.1123.2011.00026.
A rapid and sensitive method was developed and validated using a normal phase liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) for determination of propranolol enantiomers in pharmaceuticals. Sample preparation involved a single extraction step by the addition of methanol. Separation of propranolol enantiomers was achieved on a Chiralcel OD-H chiral column using a mobile phase consisting of n-hexane-ethanol-ammonia (70:30:0.4, v/v/v), and the flow rate was 0.40 mL/min for 20 min. The analyte was monitored by tandem mass spectrometry with electrospray positive ionization in multiple reaction monitoring (MRM) mode, using the transitions of m/z 260.2 --> 116.0. Propranolol enantiomers can be completely separated. The linear range was 2.5-1000 microg/L, and the limit of quantification (LOQ) was 2.5 microg/L. The values for within day and between day precisions and accuracies were well within the generally accepted criteria for analytical methods. The relative standard deviations (RSDs) were less than 2.64%, and the recoveries of the two enantiomers were 99.08%-102.58% and 100.21%-103.16%, respectively. The separation method is accurate, convenient, reliable, efficient, and can be subsequently used for quality control of propranolol enantiomers in pharmaceuticals.
建立了一种快速灵敏的方法,并通过正相液相色谱-串联质谱联用(LC-MS/MS)进行验证,用于测定药品中普萘洛尔对映体。样品制备包括通过添加甲醇进行单一萃取步骤。普萘洛尔对映体在Chiralcel OD-H手性柱上分离,流动相由正己烷-乙醇-氨(70:30:0.4,v/v/v)组成,流速为0.40 mL/min,持续20分钟。通过串联质谱在多反应监测(MRM)模式下以电喷雾正离子化监测分析物,使用m/z 260.2 --> 116.0的跃迁。普萘洛尔对映体能够完全分离。线性范围为2.5 - 1000 μg/L,定量限(LOQ)为2.5 μg/L。日内和日间精密度及准确度值均完全符合分析方法的普遍接受标准。相对标准偏差(RSD)小于2.64%,两种对映体的回收率分别为99.08% - 102.58%和100.21% - 103.16%。该分离方法准确、方便、可靠、高效,可随后用于药品中普萘洛尔对映体的质量控制。