Department of Chemistry, The University of Kansas, Lawrence, Kansas, USA.
Center of Biomodular Multiscale Systems for Precision Medicine, The University of Kansas, Lawrence, Kansas, USA.
Electrophoresis. 2020 Oct;41(18-19):1627-1640. doi: 10.1002/elps.202000109. Epub 2020 Aug 7.
Electrophoresis or electrochromatography carried out in nanometer columns (width and depth) offers some attractive benefits compared to microscale columns. These advantages include unique separation mechanisms that are scale dependent, fast separation times, and simpler workflow due to the lack of a need for column packing and/or wall coatings to create a stationary phase. We report the use of thermoplastics, in this case PMMA, as the substrate for separating single-stranded DNAs (ssDNAs). Electrophoresis nanochannels were created in PMMA using nanoimprint lithography (NIL), which can produce devices at lower cost and in a higher production mode compared to the fabrication techniques required for glass devices. The nanochannel column in PMMA was successful in separating ssDNAs in free solution that was not possible using microchip electrophoresis in PMMA. The separation could be performed in <1 s with resolution >1.5 when carried out using at an electric field strength of 280 V/cm and an effective column length of 60 μm (100 nm × 100 nm, depth and width). The ssDNAs transport through the PMMA column was driven electrokinetically under the influence of an EOF. The results indicated that the separation was dominated by chromatographic effects using an open tubular nano-electrochromatography (OT-NEC) mode of separation. Interesting to these separations was that no column packing was required nor a wall coating to create the stationary phase; the separation was affected using the native polymer that was UV/O activated and an aqueous buffer mobile phase.
与微尺度柱相比,在纳米柱(宽度和深度)中进行电泳或电色谱分析具有一些吸引人的优势。这些优点包括依赖于尺度的独特分离机制、快速的分离时间以及由于不需要柱填充和/或壁涂层来创建固定相而简化的工作流程。我们报告了使用热塑性塑料(在这种情况下为 PMMA)作为分离单链 DNA(ssDNA)的基板。使用纳米压印光刻(NIL)在 PMMA 中创建电泳纳米通道,与制造玻璃器件所需的制造技术相比,NIL 可以以更低的成本和更高的生产模式生产器件。PMMA 中的纳米通道柱成功地分离了在 PMMA 微芯片电泳中不可能分离的游离溶液中的 ssDNA。当在 280 V/cm 的电场强度和 60 μm(100nm×100nm,深度和宽度)的有效柱长下进行分离时,分离可以在 <1 s 内完成,分辨率>1.5。ssDNA 通过 PMMA 柱的传输是在 EOF 的影响下通过电动驱动的。结果表明,分离主要是通过使用开放管型纳米电色谱(OT-NEC)分离模式的色谱效应来实现的。这些分离的一个有趣之处是不需要柱填充也不需要壁涂层来创建固定相;分离受到使用 UV/O 激活的天然聚合物和水缓冲移动相的影响。