A Protein Preconcentration Platform Utilizing Dual Gate Structure and Ion-Selective Membrane

Chi Tran Nhu, Phu Nguyen Dang, H. Thanh, T. V. Thi, Loc Do Quang, T. Thanh
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引用次数: 1

Abstract

This study presents a protein preconcentration platform integrated into the microfluidic channel structure. The proposed chip consists of a dual gate preconcentration structure with the main microchannel for sample actuation and two sub-microchannels for depletion region generation. A submicron thick ion-selective membrane was created using the micro-flow patterning technique for electrical connectivity between the main channel and sub-channels. The experimental results show that the proposed chip works stably in two modes: depletion and enrichment. Under capillary electrophoresis and electroosmotic flows, proteins are preconcentrated at the boundary of the depletion region, known as the electro-kinetically trapping zone or concentration zone. Besides, the depletion zone’s size and the concentration region’s fluorescence intensity increased about 2.5 and 3 times according to the voltage difference between the two terminals of the sample channel. The experimental results demonstrate that it is possible to integrate the proposed protein preconcentration structure into a biomicrofluidic chip system for protein detection with low concentration.
利用双门结构和离子选择膜的蛋白质预浓缩平台
本研究提出了一种结合微流控通道结构的蛋白质预浓缩平台。该芯片由双栅预富集结构组成,其中主微通道用于样品驱动,两个子微通道用于耗尽区生成。利用微流图技术在主通道和子通道之间建立了一种亚微米厚的离子选择膜。实验结果表明,该芯片在富集和耗尽两种模式下稳定工作。在毛细管电泳和电渗透流动下,蛋白质在耗尽区边界预浓缩,称为电动捕获区或集中区。此外,根据样品通道两端电压差的变化,耗尽区的大小和浓度区的荧光强度分别增加了约2.5倍和3倍。实验结果表明,将所提出的蛋白质预浓缩结构集成到生物微流控芯片系统中用于低浓度蛋白质检测是可能的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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