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反相和亲水相互作用液相色谱的串联耦合,以拓宽药物化合物分析的洗脱窗口。

Serial coupling of reversed-phase and hydrophilic interaction liquid chromatography to broaden the elution window for the analysis of pharmaceutical compounds.

作者信息

Louw Stefan, Pereira Alberto S, Lynen Frédéric, Hanna-Brown Melissa, Sandra Pat

机构信息

Pfizer Analytical Research Centre - Ghent University, Krijgslaan 281 S4-bis, B-9000 Ghent, Belgium.

出版信息

J Chromatogr A. 2008 Oct 24;1208(1-2):90-4. doi: 10.1016/j.chroma.2008.08.058. Epub 2008 Aug 20.

Abstract

It is presently a common practice in drug discovery to analyse samples by reversed-phase liquid chromatography (RPLC) and hydrophilic interaction chromatography (HILIC). To increase throughput, HILIC was connected in series to RPLC by means of a T-piece with make-up flow. The first column is a 2mm I.D. column having an optimal flow between 0.1 and 0.2mL/min. Via the T-piece, the flow for the second dimension column with an I.D. of 4.6mm is adjusted to 1.5-2.0mL/min with a high acetonitrile content (i.e. >/=80%) mobile phase. Therefore, even in gradient RPLC analysis starting with a mobile phase with high water content, the HILIC column is always operated at high acetonitrile concentration which is required to obtain retention on the HILIC column. The performance of the hyphenated RPLC/HILIC set-up is illustrated with the analysis of two model samples of pharmaceutical interest. Optimization of the conditions in the HILIC dimension is discussed.

摘要

目前在药物发现过程中,通过反相液相色谱(RPLC)和亲水相互作用色谱(HILIC)分析样品是一种常见的做法。为了提高通量,HILIC通过带有补充流的T型接头与RPLC串联连接。第一根柱是内径为2mm的柱,最佳流速在0.1至0.2mL/min之间。通过T型接头,将内径为4.6mm的二维柱的流速用高乙腈含量(即≥80%)的流动相调整至1.5 - 2.0mL/min。因此,即使在以高水含量流动相开始的梯度RPLC分析中,HILIC柱也始终在高乙腈浓度下运行,这是在HILIC柱上获得保留所必需的。通过对两种具有药物研究价值的模型样品的分析来说明联用的RPLC/HILIC装置的性能。讨论了HILIC维度条件的优化。

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