Li Kun-Yan, Zhou Yan-Gang, Ren Hua-Yi, Wang Feng, Zhang Bi-Kui, Li Huan-De
Clinical Pharmaceutical Research Institute, XiangYa Second Hospital, Central South University, Changsha 410011, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 May 1;850(1-2):581-5. doi: 10.1016/j.jchromb.2006.12.051. Epub 2007 Jan 12.
The ultra-performance liquid chromatography-electrospray tandem mass spectrometry (UPLC-ESI-MS/MS) method has been developed to perform the determination of quetiapine, perospirone, aripiprazole and quetiapine sulfoxide in in vitro samples in less than 3 min. The UPLC separation was carried out using an Acquity UPLC BEH C18 column (100 mm x 2.1mm i.d., 1.7 microm particle size) that provided high efficiency and resolution in combination with high linear velocities. The UPLC system was coupled to a Waters Micromass Quattro Premier XE tandem quadrupole mass spectrometer. This system permits high-speed data acquisition without peak intensity degradation, and produces sharp and narrow chromatographic peaks (w(h) about 2.5s) of compounds. The determination was performed in multiple reaction monitoring (MRM) mode. The quantification parameters of the developed method were established, obtaining instrumental LODs lower than 0.005 microg/l and a repeatability at a low concentration level lower than 10% CV (n=10). Finally, the method was successfully applied to the analysis of atypical antipsychotics and some metabolites in in vitro samples.
已开发出超高效液相色谱 - 电喷雾串联质谱(UPLC - ESI - MS/MS)方法,可在不到3分钟的时间内测定体外样品中的喹硫平、哌罗匹隆、阿立哌唑和喹硫平亚砜。使用Acquity UPLC BEH C18柱(100 mm×2.1mm内径,1.7微米粒径)进行UPLC分离,该柱结合高线性速度可提供高效率和分辨率。UPLC系统与Waters Micromass Quattro Premier XE串联四极杆质谱仪相连。该系统允许高速数据采集而不会出现峰强度下降,并产生尖锐且狭窄的化合物色谱峰(半高宽约2.5秒)。测定在多反应监测(MRM)模式下进行。建立了所开发方法的定量参数,获得的仪器检测限低于0.005微克/升,低浓度水平下的重复性低于10%变异系数(n = 10)。最后,该方法成功应用于体外样品中抗非典型精神病药物及其一些代谢物的分析。