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通过固相萃取和三通分流接口实现尺寸排阻色谱与毛细管电泳的在线联用。

On-line coupling of size exclusion chromatography and capillary electrophoresis via solid-phase extraction and a Tee-split interface.

作者信息

Tempels F W Alexander, Wiese Gerard, Underberg Willy J M, Somsen Govert W, de Jong Gerhardus J

机构信息

Department of Biomedical Analysis, Faculty of Pharmaceutical Sciences, Utrecht University, Sorbonnelaan 16, NL-3584 CA Utrecht, The Netherlands.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Jul 24;839(1-2):30-5. doi: 10.1016/j.jchromb.2006.02.003. Epub 2006 Mar 2.

Abstract

An on-line size exclusion chromatography (SEC)-solid-phase extraction (SPE)-capillary electrophoresis (CE) system using a Tee-split interface has been developed for the analysis of peptides in biological fluids. The SEC column fractionates the sample by molecular size and the low-molecular-weight fraction, which contains the peptides, is directed to a C(18) SPE microcolumn, where the peptides are trapped and concentrated. The SPE column is desorbed with 425 nL acetonitrile and the effluent is sent to the Tee-split interface, which hydrodynamically splits (1:40) the flow and, thus, allows appropriate injection of analytes into the CE system. The performance of the system is investigated by the analysis of enkephalins in cerebrospinal fluid (CSF). It is demonstrated that the SEC step efficiently removes potentially interfering proteins, permitting reproducible SPE and CE. The total system provides efficient separations of the enkephalins with plate numbers up to 100,000. Concentration limits of detection (S/N = 3) for the peptides are about 100 ng/mL for injection of 20 microL spiked CSF samples. Plots of enkephalin peak areas versus concentration showed good linearity over the 0.25-10 microg/mL range (R2 > or = 0.985). Repeatability of migration time and peak area was within 2% and 10% R.S.D., respectively.

摘要

已开发出一种使用三通分流接口的在线尺寸排阻色谱(SEC)-固相萃取(SPE)-毛细管电泳(CE)系统,用于分析生物流体中的肽。SEC柱按分子大小对样品进行分级分离,含有肽的低分子量级分被导向C(18) SPE微柱,肽在该微柱上被捕获并浓缩。用425 nL乙腈解吸SPE柱,流出物被送至三通分流接口,该接口以流体动力学方式分流(1:40)流动,从而允许将分析物适当注入CE系统。通过分析脑脊液(CSF)中的脑啡肽来研究该系统的性能。结果表明,SEC步骤能有效去除潜在干扰蛋白,使SPE和CE具有可重复性。整个系统能高效分离脑啡肽,塔板数高达100,000。对于注入20 μL加标CSF样品的肽,检测限(S/N = 3)的浓度约为100 ng/mL。脑啡肽峰面积与浓度的曲线在0.25 - 10 μg/mL范围内显示出良好的线性(R2≥0.985)。迁移时间和峰面积的重复性分别在2%和10%相对标准偏差(R.S.D.)以内。

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