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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >On-line coupling of a clean-up device with supported liquid membrane to capillary electrophoresis for direct injection and analysis of serum and plasma samples
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On-line coupling of a clean-up device with supported liquid membrane to capillary electrophoresis for direct injection and analysis of serum and plasma samples

机译:在线清洗设备与支持的液膜的在线耦合至毛细管电泳,可直接进样并分析血清和血浆样品

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A simple sample clean-up device with planar supported liquid membrane (SLM) was developed and coupled on-line to capillary electrophoresis (CE) for direct injection of human body fluids. Donor and acceptor compartments of the device were filled with diluted body fluid and deionized water, respectively, and the two solutions were separated by a thin SLM. Analytes of interest were selectively transported from the donor solution through the SLM into the acceptor solution by diffusion whereas interfering matrix components were efficiently retained on the SLM. Equilibrium between the concentrations of analytes at the SLM was obtained typically in 5. min. Then a CE separation capillary was inserted into the acceptor compartment to firmly touch the SLM and the pretreated sample was hydrodynamically injected into the capillary. The analytical procedure was demonstrated by rapid pretreatment, on-line injection, and CE determination of selected amino acids in human serum and plasma samples. 1-Ethyl-2-nitrobenezene and bis(2-ethylhexyl) phosphate (15%, v/v) was used as the selective SLM for clean-up of the body fluids and 0.5. M acetic acid was used as a background electrolyte solution for CE analysis of the pretreated amino acids. Concentrations of amino acids on acceptor side of the SLM reached 40-58% of their original concentrations in donor solution after 5. min equilibration time and then remained constant proving that equilibrium was achieved at the SLM. Injection of the pretreated samples was highly repeatable with RSD values of peak areas 2.4-8.4% and 3.4-10.5% for standard solutions and real samples, respectively. Limits of detection between 0.75 and 2.5. μM were achieved, corresponding to 3.75-12.5. μM in 1:4 diluted real samples, which ensure sensitive determination of most amino acids in the body fluids. The developed method is fast, simple, efficient, cheap and selective and may be applied to determination of a wide range of analytes in various samples with complex matrices.
机译:开发了一种简单的带有平面支撑液膜(SLM)的样品净化装置,并将其在线耦合到毛细管电泳(CE)上以直接注入人体液体。装置的供体室和受体室分别充满稀释的体液和去离子水,两种溶液通过稀薄的SLM分开。感兴趣的分析物通过扩散从供体溶液通过SLM选择性转移到受体溶液中,而干扰基质成分则有效地保留在SLM上。通常在5分钟内即可获得SLM上分析物浓度之间的平衡。然后将CE分离毛细管插入受体隔室以牢固地接触SLM,然后将经过预处理的样品以流体动力学方式注入毛细管中。通过快速预处理,在线注射和CE测定人血清和血浆样品中所选氨基酸,证明了该分析方法。 1-乙基-2-硝基苯和双(2-乙基己基)磷酸酯(15%,v / v)用作选择性的SLM,用于清除体液和0.5。 M乙酸用作背景电解质溶液,用于预处理氨基酸的CE分析。在5分钟的平衡时间后,供体溶液中SLM受体侧的氨基酸浓度达到其原始浓度的40-58%,然后保持恒定,证明在SLM上达到了平衡。预处理样品的进样可高度重复,标准溶液和真实样品的峰面积的RSD值分别为2.4-8.4%和3.4-10.5%。检出限在0.75到2.5之间。达到μM,对应于3.75-12.5。 1:4稀释的真实样品中的μM,可确保灵敏地测定体液中的大多数氨基酸。所开发的方法快速,简单,高效,便宜且选择性强,可用于测定具有复杂基质的各种样品中的多种分析物。

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