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新型全自动亲水作用/反相柱切换高效液相色谱系统,用于复杂样品中极性和非极性化合物的互补分析。

Novel, fully automatic hydrophilic interaction/reversed-phase column-switching high-performance liquid chromatographic system for the complementary analysis of polar and apolar compounds in complex samples.

作者信息

Wang Yuan, Lehmann Rainer, Lu Xin, Zhao Xinjie, Xu Guowang

机构信息

National Chromatographic R. & A. Center, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, China.

出版信息

J Chromatogr A. 2008 Sep 12;1204(1):28-34. doi: 10.1016/j.chroma.2008.07.010. Epub 2008 Jul 11.

DOI:10.1016/j.chroma.2008.07.010
PMID:18692192
Abstract

In this study we developed and optimized a column-switching high-performance liquid chromatographic (HPLC) system for the complementary analysis of polar and apolar compounds in complex samples. The polar compounds are separated on a hydrophilic interaction chromatographic (HILIC) column; the part of the sample non-retained on HILIC is transferred into and separated on a reversed-phase (RP) column through an interface, thus preventing the loss of analytes eluting at dead time in common single-column mode. The signals are in turn recorded in the same chromatogram either by a UV or by a mass spectrometric detector. Applying a mixture of 25 standard compounds (12 hydrophilic and 13 hydrophobic) the system proves to be reliable, robust and easy-operating. The investigation of urine revealed an increase in the detected metabolite ion masses compared to the single-column HILIC-electrospray ionization (ESI)-MS analysis. Utilizing online the complementary selectivity of HILIC and RPLC in a fully automatic mode, this approach holds out the prospect to enlarge the number of detectable compounds in non-targeted "-omics" studies and sophisticated target-driven approaches by a single injection.

摘要

在本研究中,我们开发并优化了一种柱切换高效液相色谱(HPLC)系统,用于复杂样品中极性和非极性化合物的互补分析。极性化合物在亲水作用色谱(HILIC)柱上分离;HILIC上未保留的样品部分通过接口转移至反相(RP)柱上并在该柱上分离,从而避免了在常规单柱模式下死时间洗脱的分析物损失。信号依次由紫外或质谱检测器记录在同一张色谱图中。应用包含25种标准化合物(12种亲水和13种疏水)的混合物,该系统被证明可靠、稳健且易于操作。尿液研究表明,与单柱HILIC-电喷雾电离(ESI)-MS分析相比,检测到的代谢物离子质量有所增加。以全自动模式在线利用HILIC和RPLC的互补选择性,该方法有望通过一次进样增加非靶向“组学”研究和复杂目标驱动方法中可检测化合物的数量。

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