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Electrophoretic Separation of Single Particles Using Nanoscale Thermoplastic Columns

机译:纳米级热塑性色谱柱电泳分离单个颗粒

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Phenomena associated with microscale electrophoresis separations cannot, in many cases, be applied to the nanoscale. Thus, understanding the electrophoretic characteristics associated with the nanoscale will help formulate relevant strategies that can optimize the performance of separations carried out on columns with at least one dimension below 150 nm. Electric double layer (EDL) overlap, diffusion, and adsorption/desorption properties and/or dielectrophoretic effects giving rise to stick/slip motion are some of the processes that can play a role in determining the efficiency of nanoscale electrophoretic separations. We investigated the performance characteristics of electrophoretic separations carried out in nanoslits fabricated in poly(methyl methacry-late), PMMA, devices. Silver nanoparticles (AgNPs) were used as the model system with tracking of their transport via dark field microscopy and localized surface plasmon resonance. AgNPs capped with citrate groups and the negatively charged PMMA walls (induced by O-2 plasma modification of the nanoslit walls) enabled separations that were not apparent when these particles were electrophoresed in microscale columns. The separation of AgNPs based on their size without the need for:buffer additives using PMMA nanoslit devices is demonstrated herein. Operational parameters such as the electric field strength, nanoslit dimensions, and buffer composition were evaluated as to their effects on the electrophoretic performance, both in terms of efficiency (plate numbers) and resolution. Electrophoretic separations performed at high electric field strengths (>200 Wcm) resulted in higher plate numbers compared to lower fields due to the absence of stick/slip motion at the higher electric field strengths. Indeed, 60 nm AgNPs could be separated from 100 nm particles in free solution using nanoscale electrophoresis with 100 mu m long columns.
机译:在许多情况下,与微尺度电泳分离相关的现象无法应用于纳米尺度。因此,了解与纳米级相关的电泳特性将有助于制定相关策略,以优化在至少一维低于150 nm的色谱柱上进行的分离性能。双电层(EDL)的重叠,扩散和吸附/解吸特性和/或引起粘着/滑移运动的介电泳效应是某些过程,可在确定纳米级电泳分离效率中发挥作用。我们研究了在聚甲基丙烯酸甲酯(PMMA)器件中制造的纳米缝隙中进行电泳分离的性能特征。银纳米颗粒(AgNPs)被用作模型系统,通过暗场显微镜和局部表面等离子体共振跟踪其传输。用柠檬酸盐基团和带负电的PMMA壁(由纳米缝隙壁的O-2等离子体修饰诱导)覆盖的AgNPs能够实现分离,而这些颗粒在微型柱中电泳时不明显。本文展示了使用PMMA纳米狭缝装置基于AgNP的大小而无需缓冲添加剂的分离。在效率(板数)和分离度两方面,评估了诸如电场强度,纳米缝隙尺寸和缓冲液组成等操作参数对电泳性能的影响。与较高的电场强度相比,在较高的电场强度(> 200 Wcm)下进行的电泳分离产生的板数更高,而较低的电场则更低。实际上,可以使用具有100μm长柱的纳米级电泳在自由溶液中从100 nm颗粒中分离出60 nm AgNP。

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