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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Ultrasound-assisted emulsification microextractioe combined with ultra-high performance liquid chromatography-tandem mass spectrometry for the analysis of ibuprofeo and its metabolites ie human urine
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Ultrasound-assisted emulsification microextractioe combined with ultra-high performance liquid chromatography-tandem mass spectrometry for the analysis of ibuprofeo and its metabolites ie human urine

机译:超声辅助乳化微萃取与超高效液相色谱-串联质谱联用分析布洛芬及其代谢物即人尿

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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: 100 jxL of 1-octanol as extraction solvent, 2 mL of urine sample, 15% (w/v) NaCl to control the ionic strength, ultrasonication for 10 min; and centrifugation for 5 min at 6500 rpm. 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 0.0005 ng/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.
机译:本研究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,有效的方法来测定布洛芬的方法(IBU)及其四种代谢物(人尿中的1-羟基布洛芬(1-HIBU),2-羟基布洛芬(2-HIBU),3-羟基布洛芬(3-HIBU)和羧基布洛芬(CIBU))。为此,评估了影响USAEME程序的不同参数的影响,以优化流程效率。发现最佳条件为:100 jxL 1-辛醇作为提取溶剂,2 mL尿液样品,15%(w / v)NaCl以控制离子强度,超声处理10分钟;并以6500 rpm离心5分钟。样品制备后,在Zorbax快速分离高清(RRHD)SB-C18色谱柱上进行色谱分离,使用流动相,该流动相由0.1%的甲酸水溶液和乙腈组成,洗脱梯度。采用多反应监测(MRM)模式和负电离在三重四极杆串联质谱仪中进行检测,该方法在宽浓度范围内均具有令人满意的线性(相关系数超过0.9994)。 IBU及其代谢物的定量下限(LLOQ)为0.0005 ng / mL。日内和日间精度在2.19-10.8%范围内,精度在-5.93%和6.29%之间。分析物的平均回收率在90.7%至104%之间。结果,该方法已成功应用于人尿样中IBU及其代谢物的灵敏测定。

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