小型毛细管电泳装置中诱导电渗流的研究:控制和逆转策略

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS ELECTROPHORESIS Pub Date : 2024-07-25 DOI:10.1002/elps.202400107
Miyuru De Silva, Prabhavie M. Opallage, Robert C. Dunn
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引用次数: 0

摘要

电渗流(EOF)是指在外加电势的诱导下,溶液在毛细管或微通道中的大量流动。对于毛细管电泳和微芯片电泳,EOF 可以在一次分离中同时分析阳离子和阴离子,并可改变分离速度和分辨率。EOF 来自毛细管壁上的电双电层,通常通过背景缓冲液的 pH 值和离子强度或使用添加剂来控制。因此,了解和控制电双层对于在方法开发过程中保持可接受的重复性至关重要。令人惊讶的是,在低 pH 值的熔融石英毛细管中,即使毛细管表面应该是中性的,研究也能观察到 EOF。之前的研究表明,毛细管壁上产生的径向电场会导致 "诱导电渗流",而诱导电渗流是由毛细管外部的分离电压和接地元件引起的。我们使用薄壁(15 微米)熔融石英分离毛细管来促进径向电场的研究,结果表明 EOF 移动性取决于分离电压和外部接地的位置。这与诱导 EOF 模型一致,即径向电场将正电荷嵌入毛细管壁,形成电双层。这种效应的大小具有长程影响,很难通过将接地元件移离分离毛细管而完全消除。本文讨论了利用外部施加电位的主动 EOF 控制或利用负分离电压的被动方法,作为控制诱导 EOF 的两种可能方法。这两种方法都能逆转 EOF,提高氨基酸分离的分辨率和峰值效率。
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Investigation of induced electroosmotic flow in small-scale capillary electrophoresis devices: Strategies for control and reversal

Electroosmotic flow (EOF) is the bulk flow of solution in a capillary or microchannel induced by an applied electric potential. For capillary and microchip electrophoresis, the EOF enables analysis of both cations and anions in one separation and can be varied to modify separation speed and resolution. The EOF arises from an electrical double layer at the capillary wall and is normally controlled through the pH and ionic strength of the background buffer or with the use of additives. Understanding and controlling the electrical double layer is therefore critical for maintaining acceptable repeatability during method development. Surprisingly, in fused silica capillaries at low pH, studies observe an EOF even though the capillary surface should be neutralized. Previous work has suggested the presence of an “induced electroosmotic flow” from radial electric fields generated across the capillary wall due to the separation voltage and grounded components external to the capillary. Using thin-wall (15 µm) fused silica separation capillaries to facilitate the study of radial fields, we show that the EOF mobility depends on both the separation voltage and the location of external grounds. This is consistent with the induced EOF model, in which radial electric fields embed positive charges at the capillary walls to create an electrical double layer. The magnitude of the effect is characterized and shown to have long-range influences that are difficult to completely null by moving grounded components away from the separation capillary. Instead, active EOF control using externally applied potentials or a passive approach using a negative separation voltage are discussed as two possible methods for controlling the induced EOF. Both methods can reverse the EOF and improve the resolution and peak efficiency in amino acid separations.

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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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