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手性毛细管电色谱与电喷雾电离质谱联用:方法开发及人血浆中华法林对映体的测定

Combination of chiral capillary electrochromatography with electrospray ionization mass spectrometry: method development and assay of warfarin enantiomers in human plasma.

作者信息

Zheng Jack, Shamsi Shahab A

机构信息

Department of Chemistry, Center of Biotechnology and Drug Design, Georgia State University, Atlanta, Georgia 30303, USA.

出版信息

Anal Chem. 2003 Nov 15;75(22):6295-305. doi: 10.1021/ac030193j.

DOI:10.1021/ac030193j
PMID:14616014
Abstract

The hyphenation of chiral capillary electrochromatography (CEC) with electrospray ionization mass spectrometry (ESI-MS) is very challenging but promising due to the fact that it combines sensitivity with high specificity and selectivity. In this work, CEC capillaries packed with (3R,4S)-Whelk-O1 chiral stationary phase were used for simultaneous enantioseparation of (+/-)-warfarin and its internal standard, (+/-)-coumachlor. Furthermore, both the chiral CEC separation and MS detection parameters were examined in detail. First, the influence of different column fabrication was investigated. Second, enantioseparation was optimized by varying CEC parameters, including acetonitrile concentration, buffer pH, and ionic strength. Under the optimum chiral CEC conditions, ESI-MS parameters such as sheath liquid pH and composition, sheath liquid flow rate, drying gas flow rate, drying gas temperature, nebulizer pressure, and fragmentor voltage were investigated to achieve maximum MS signals of the separated enantiomers. Finally, using solid-phase extraction as sample preparation method, (+/-)-warfarin spiked in 100-microL human plasma samples were analyzed. The calibration curves showed good linearity for both (R)-warfarin (R = 0.9979) and (S)-warfarin (R = 0.9978) enantiomers. The experimental limit of detection was approximately 25 ng/mL for both enantiomers. Even though the data are still preliminary, we can state with confidence that chiral CEC-ESI-MS has the potential to establish itself as a very powerful technique for the determination of enantiomeric ratios in human body fluid.

摘要

手性毛细管电色谱(CEC)与电喷雾电离质谱(ESI-MS)联用极具挑战性,但前景广阔,因为它兼具高灵敏度、高特异性和高选择性。在本研究中,使用填充有(3R,4S)-Whelk-O1手性固定相的CEC毛细管同时对(+/-)-华法林及其内标(+/-)-香豆氯进行对映体分离。此外,还详细研究了手性CEC分离和MS检测参数。首先,考察了不同柱制备方法的影响。其次,通过改变CEC参数(包括乙腈浓度、缓冲液pH值和离子强度)优化对映体分离。在最佳手性CEC条件下,研究了ESI-MS参数,如鞘液pH值和组成、鞘液流速、干燥气流速、干燥气温度、雾化器压力和碎裂电压,以实现分离对映体的最大MS信号。最后,采用固相萃取作为样品制备方法,分析了加样于100 μL人血浆样品中的(+/-)-华法林。校准曲线显示(R)-华法林(R = 0.9979)和(S)-华法林(R = 0.9978)对映体均具有良好的线性。两种对映体的实验检测限约为25 ng/mL。尽管数据仍属初步,但我们可以有信心地说,手性CEC-ESI-MS有潜力成为测定人体液中对映体比例的一项非常强大的技术。

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