Lee Heon-Woo, Seo Ji-Hyung, Kim Yong-Won, Jeong Seo-Young, Lee Kyung-Tae
College of Pharmacy, Kyung-Hee University, Dongdaemun-Ku, Seoul 130-701, Korea.
Rapid Commun Mass Spectrom. 2006;20(18):2675-80. doi: 10.1002/rcm.2638.
In the present study, we developed a method coupling liquid-liquid extraction (LLE) to high-performance liquid chromatography (HPLC) with positive ion electrospray ionization tandem mass spectrometry (ESI-MS/MS) to determine zaltoprofen levels in human plasma, using enalapril as internal standard (IS). The high sensitivity and specificity of MS/MS detection enabled the use of small plasma volumes (250 microL) and a simple LLE procedure. Furthermore, the short run-times (2 min) involved are compatible with the requirements of large-scale clinical studies. Ion acquisition was performed in multiple reaction monitoring (MRM) mode by monitoring the transitions m/z 299.3 > 225.0 for zaltoprofen and m/z 377.4 > 234.2 for the IS enalapril. The limit of detection (LOD) was 0.01 microg/mL and the lower limit of quantitation (LLOQ) was 0.05 microg/mL. The devised method was linear over the studied range (0.05-20 microg/mL), with r2 > 0.99 and a run-time of 2 min. Intra-day precisions fell in the range 2.0-13.8%, inter-day precisions in the range 2.1-3.9%, and intra- and inter-day accuracies in the range 102.8-114.1%. The described method provides a fast and sensitive analytical tool for zaltoprofen and was successfully applied to a 24-subject pharmacokinetic study.
在本研究中,我们开发了一种将液-液萃取(LLE)与高效液相色谱(HPLC)联用,并结合正离子电喷雾电离串联质谱(ESI-MS/MS)的方法,以依那普利为内标(IS)来测定人血浆中扎托洛芬的含量。MS/MS检测的高灵敏度和特异性使得能够使用少量血浆(250微升)并采用简单的液-液萃取程序。此外,所涉及的短运行时间(2分钟)符合大规模临床研究的要求。通过监测扎托洛芬的m/z 299.3 > 225.0和内标依那普利的m/z 377.4 > 234.2的跃迁,在多反应监测(MRM)模式下进行离子采集。检测限(LOD)为0.01微克/毫升,定量下限(LLOQ)为0.05微克/毫升。所设计的方法在所研究的范围(0.05 - 20微克/毫升)内呈线性,r2 > 0.99,运行时间为2分钟。日内精密度在2.0 - 13.8%范围内,日间精密度在2.1 - 3.9%范围内,日内和日间准确度在102.8 - 114.1%范围内。所描述的方法为扎托洛芬提供了一种快速且灵敏的分析工具,并成功应用于一项24名受试者的药代动力学研究。