4.6 Article

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

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1234, 期 -, 页码 2-8

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2011.10.046

关键词

Amino acids; Biological samples; Capacitively coupled contactless conductivity detection; Capillary electrophoresis; Sample treatment; Supported liquid membrane

向作者/读者索取更多资源

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 mu M were achieved, corresponding to 3.75-12.5 mu M 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. (C) 2011 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据