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Electrokinetic injection for stacking neutral analytes in capillary andmicrochip electrophoresis

机译:电动注射用于在毛细管电泳和微芯片电泳中堆叠中性分析物

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An on-column mechanism for electrokinetically injecting long sample plugs with simultaneous stacking of neutral analytes in capillary electrokinetic chromatography is presented. On-column stacking methods allow for the direct injection of long sample plugs into the capillary, with narrowing of the analyte peak width to allow for an increase in the detected signal. Low-pressure injections (similar to 50 mbar) are commonly used to introduce sample plugs containing neutral analytes. We demonstrate that injection can be accomplished by applying an electric field from the sample vial directly into the capillary, with neutral analytes injected by electroosmotic now at up to 1 order of magnitude faster than the corresponding pressure injections, Since stacking occurs simultaneously with electrokinetic injection, stacking is initiated at the capillary inlet, resulting in an increased length of capillary remaining for separation. Reproducibility obtained for peak height and peak area with electroosmotic flow injection is comparable to that obtained with the pressure injection mode, while reproducibility of analysis time is markedly improved. Electrokinetic stacking of neutral analytes utilizing electroosmotic flow is demonstrated with discontinuous (high conductivity, high mobility) as well as continuous (equal conductivity, equal mobility) sample electrolytes, Injecting neutral analytes by electroosmotic now affords a 10-fold or greater decrease. in analysis times when capillaries of 50-mum i.d. or smaller are used. This stacking method should be exportable to dynamic pH junction stacking and electrokinetic chromatography with capillary arrays. Equations describing this electrokinetic injection mode are introduced and stacking of a neutral analyte on a microchip by electrokinetic injection using a simple cross-T channel configuration is demonstrated.
机译:提出了一种在电动毛细管色谱中电动注入长样品塞并同时堆叠中性分析物的柱上机理。柱上堆积方法允许将长样品塞直接注入毛细管中,同时使分析物峰宽变窄,从而增加检测到的信号。低压注入(类似于50 mbar)通常用于引入包含中性分析物的样品塞。我们证明,可以通过将样品瓶中的电场直接施加到毛细管中来完成注入,而电渗析中性分析物现在的注入速度比相应的压力注入快了1个数量级。由于堆叠与电动注入同时发生,在毛细管入口处开始堆积,导致剩余的毛细管长度增加以进行分离。通过电渗流进样获得的峰高和峰面积的重现性可与压力注入模式获得的重现性相媲美,而分析时间的重现性得到了显着提高。在不连续(高电导率,高迁移率)以及连续(等电导率,等迁移率)样品电解质的情况下,利用电渗流对中性分析物进行了电动堆积,现在通过电渗析注入中性分析物可减少10倍或更多倍。分析时间内径为50毫米的毛细管或更小。这种堆叠方法应可用于动态pH连接堆叠和带有毛细管阵列的电动色谱。引入描述该电动注入模式的方程式,并演示了使用简单的交叉T通道配置通过电动注入将中性分析物堆叠在微芯片上的过程。

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