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采用填充吸附剂微萃取和亲水作用色谱-超高效液相色谱-串联质谱法测定人尿中的肉碱和酰基肉碱。

Determination of carnitine and acylcarnitines in human urine by means of microextraction in packed sorbent and hydrophilic interaction chromatography-ultra-high-performance liquid chromatography-tandem mass spectrometry.

作者信息

Magiera Sylwia, Baranowski Jacek

机构信息

Department of Inorganic, Analytical Chemistry and Electrochemistry, Silesian University of Technology, 7 M. Strzody Str., 44-100 Gliwice, Poland.

Department of Clinical Physiology, University Hospital, SE-581 85 Linköping, Sweden.

出版信息

J Pharm Biomed Anal. 2015 May 10;109:171-6. doi: 10.1016/j.jpba.2015.02.044. Epub 2015 Feb 28.

Abstract

A method using semi-automatic microextraction by packed sorbent (eVol®-MEPS) and hydrophilic interaction chromatography-ultra-high-performance liquid chromatography-tandem mass spectrometry (HILIC-UHPLC-MS/MS) was described for the simultaneous determination of carnitine and acylcarnitines in human urine. The optimal conditions of MEPS extraction were obtained using C2 of M1 (C8+SCX) phase as a sorbent. Chromatographic separation of the analytes was achieved within 2.5min on Acquity UPLC BEH HILIC column using a gradient elution program with water containing 5mM ammonium acetate and acetonitrile as the mobile phase. The detection was performed on a triple-quadrupole tandem mass spectrometer in a positive ion mode via electrospray ionization (ESI). The linearity of the calibration curves for all compounds was found over a range from 0.1ng/mL to 500ng/mL. The method afforded satisfactory results in terms of sensitivity, specificity, precision, accuracy, recovery as well as stability of the analyte under various conditions. The method was used successfully for determination of carnitine and acylcarnitines in human urine.

摘要

描述了一种使用填充吸附剂的半自动微萃取方法(eVol®-MEPS)和亲水相互作用色谱-超高效液相色谱-串联质谱法(HILIC-UHPLC-MS/MS)同时测定人尿中肉碱和酰基肉碱的方法。以M1(C8+SCX)相的C2作为吸附剂,获得了MEPS萃取的最佳条件。使用含5mM醋酸铵的水和乙腈作为流动相的梯度洗脱程序,在Acquity UPLC BEH HILIC柱上于2.5分钟内实现了分析物的色谱分离。在三重四极杆串联质谱仪上通过电喷雾电离(ESI)以正离子模式进行检测。所有化合物校准曲线的线性范围为0.1ng/mL至500ng/mL。该方法在灵敏度、特异性、精密度、准确度、回收率以及分析物在各种条件下的稳定性方面均获得了令人满意的结果。该方法成功用于人尿中肉碱和酰基肉碱的测定。

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