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利用碳纳米纤维纳米电极阵列的介电泳操纵噬菌体。

Manipulation of bacteriophages with dielectrophoresis on carbon nanofiber nanoelectrode arrays.

机构信息

Department of Chemistry, Kansas State University, Manhattan, KS 66506, USA.

出版信息

Electrophoresis. 2013 Apr;34(7):1123-30. doi: 10.1002/elps.201200486. Epub 2013 Mar 11.

Abstract

This work describes efficient manipulation of bacteriophage virus particles using a nanostructured DEP device. The nonuniform electric field for DEP is created by utilizing a nanoelectrode array (NEA) made of vertically aligned carbon nanofibers versus a macroscopic indium tin oxide electrode in a "points-and-lid" configuration integrated in a microfluidic channel. The capture of the virus particles has been systematically investigated versus the flow velocity, sinusoidal AC frequency, peak-to-peak voltage, and virus concentration. The DEP capture at all conditions is reversible and the captured virus particles are released immediately when the voltage is turned off. At the low virus concentration (8.9 × 10(4) pfu/mL), the DEP capture efficiency up to 60% can be obtained. The virus particles are individually captured at isolated nanoelectrode tips and accumulate linearly with time. Due to the comparable size, it is more effective to capture virus particles than larger bacterial cells with such NEA-based DEP devices. This technique can be potentially utilized as a fast sample preparation module in a microfluidic chip to capture, separate, and concentrate viruses and other biological particles in small volumes of dilute solutions in a portable detection system for field applications.

摘要

这项工作描述了使用纳米结构 DEP 装置对噬菌体病毒颗粒进行有效操作。DEP 的非均匀电场是通过利用由垂直排列的碳纤维纳米纤维制成的纳米电极阵列(NEA)与“点和盖”配置中的宏观氧化铟锡电极相对于集成在微流道中的宏观氧化铟锡电极来创建的。系统地研究了病毒颗粒的捕获与流速、正弦交流频率、峰峰值电压和病毒浓度的关系。在所有条件下,DEP 捕获都是可逆的,当电压关闭时,捕获的病毒颗粒会立即释放。在低病毒浓度(8.9×10(4)pfu/mL)下,DEP 捕获效率可高达 60%。病毒颗粒在孤立的纳米电极尖端上被单独捕获,并随时间线性积累。由于尺寸相当,与基于这种 NEA 的 DEP 装置相比,用这种装置捕获比更大的细菌细胞更有效。这种技术可以用作微流控芯片中的快速样品制备模块,以在便携式检测系统中用于现场应用的小体积稀释溶液中捕获、分离和浓缩病毒和其他生物颗粒。

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