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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Simultaneous stacking of cationic and anionic compounds in single run capillary zone electrophoresis by two-end field amplified sample injection
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Simultaneous stacking of cationic and anionic compounds in single run capillary zone electrophoresis by two-end field amplified sample injection

机译:两端场放大的样品进样在单次运行毛细管区带电泳中同时叠加阳离子和阴离子化合物

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摘要

In order to extend the application of field amplified sample injection (FASI) in high throughput analysis, a convenient and simple procedure, namely two-end field amplified sample injection (TE-FASI), was developed for the simultaneous stacking of cationic and anionic compounds in a single run capillary zone electrophoresis (CZE). Following the capillary-filling with a buffer of high conductivity, water plug was loaded into each end of the capillary; and two high-field strength zones were generated at both heads of the column when high voltage was applied. Therefore, under suppressed EOF cations and anions can be selectively FASI stacked at anode and cathode head, respectively. After separation, the stacked anions and cations are detected by a common detector placed in the center of the capillary. Under the optimized conditions, the limits of detection for the model cationic (matrine and oxymatrine) and anionic (5-sulfosalicylic acid) compounds were determined as 0.2, 0.2 and 0.06. ng/mL, respectively. Compared with non-stacking conditions, the sensitivities of these compounds were enhanced 1003-, 1330- and 1380-fold, respectively. The results of reproducibility, linearity and real sample analysis show that the proposed procedure is promising to be applied for the simultaneous quantification detection of trace cationic and anionic analytes.
机译:为了扩展现场放大样品进样(FASI)在高通量分析中的应用,开发了一种方便,简单的程序,即两端现场放大样品进样(TE-FASI),用于同时堆叠阳离子和阴离子化合物在单次运行毛细管区带电泳(CZE)中进行。用高电导率的缓冲液填充毛细管后,将水塞装入毛细管的两端;当施加高压时,在柱的两个顶部产生两个高场强区。因此,在受到抑制的EOF阳离子和阴离子可以分别选择性地FASI堆叠在阳极和阴极头。分离后,堆积的阴离子和阳离子由放置在毛细管中心的普通检测器检测。在优化的条件下,将阳离子型(苦参碱和氧化苦参碱)和阴离子型(5-磺基水杨酸)化合物的检出限确定为0.2、0.2和0.06。 ng / mL。与非堆积条件相比,这些化合物的敏感性分别提高了1003倍,1330倍和1380倍。再现性,线性和真实样品分析的结果表明,所提出的方法有望用于痕量阳离子和阴离子分析物的同时定量检测。

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