Magiera Sylwia, Gülmez Şefika
Department of Analytical Chemistry, Silesian University of Technology, 7M. Strzody Str., 44-100 Gliwice, Poland.
Department of Chemistry, Pamukkale University, 20020 Denizli, Turkey.
J Pharm Biomed Anal. 2014 Apr;92:193-202. doi: 10.1016/j.jpba.2014.01.012. Epub 2014 Jan 24.
In this study, a fast, simple and efficient method based on ultrasound-assisted emulsification-microextraction (USAEME) coupled with ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) was successfully developed for the determination of ibuprofen (IBU) and its four metabolites (1-hydroxyibuprofen (1-HIBU), 2-hydroxyibuprofen (2-HIBU), 3-hydroxyibuprofen (3-HIBU), carboxyibuprofen (CIBU)) in human urine. For this purpose, the influence of the different parameters affecting the USAEME procedure was evaluated in order to optimize the efficiency of the process. The optimum conditions were found to be: 100μL of 1-octanol as extraction solvent, 2mL of urine sample, 15% (w/v) NaCl to control the ionic strength, ultrasonication for 10min; and centrifugation for 5min at 6500rpm. After sample preparation, chromatographic separation was achieved on a Zorbax Rapid Resolution High Definition (RRHD) SB-C18 column using the mobile phase consisting of 0.1% formic acid in water and acetonitrile in an elution gradient. Detection was performed in a triple quadrupole tandem mass spectrometer using the multiple reaction monitoring (MRM) mode and negative ionization. The proposed method showed satisfactory linearity over a wide concentration range (correlation coefficients over 0.9994). The lower limit of quantification (LLOQ) was 0.0005ng/mL for IBU and its metabolites. The intra- and inter-day precisions were in the range of 2.19-10.8% and the accuracies were between -5.93% and 6.29%. The mean recovery of analytes ranged from 90.7 to 104%. As a result, this method has been successfully applied for the sensitive determination of IBU and its metabolites in human urine samples.
在本研究中,成功开发了一种基于超声辅助乳化微萃取(USAEME)结合超高效液相色谱-串联质谱(UHPLC-MS/MS)的快速、简单且高效的方法,用于测定人尿液中的布洛芬(IBU)及其四种代谢物(1-羟基布洛芬(1-HIBU)、2-羟基布洛芬(2-HIBU)、3-羟基布洛芬(3-HIBU)、羧基布洛芬(CIBU))。为此,评估了影响USAEME程序的不同参数的影响,以优化该过程的效率。发现最佳条件为:100μL正辛醇作为萃取溶剂,2mL尿液样品,15%(w/v)NaCl以控制离子强度,超声处理10分钟;并在6500rpm下离心5分钟。样品制备后,在Zorbax快速分辨率高清(RRHD)SB-C18柱上进行色谱分离,使用由0.1%甲酸水溶液和乙腈组成的洗脱梯度作为流动相。在三重四极杆串联质谱仪中采用多反应监测(MRM)模式和负离子化进行检测。所提出的方法在宽浓度范围内显示出令人满意的线性(相关系数超过0.9994)。IBU及其代谢物的定量下限(LLOQ)为0.0005ng/mL。日内和日间精密度在2.19 - 10.8%范围内,准确度在-5.93%至6.29%之间。分析物的平均回收率在90.7%至104%之间。因此,该方法已成功应用于人尿液样品中IBU及其代谢物的灵敏测定。