Suppr超能文献

使用碳纳米电极阵列对痘苗病毒进行交流介电泳操控和电穿孔

AC dielectrophoretic manipulation and electroporation of vaccinia virus using carbon nanoelectrode arrays.

作者信息

Madiyar Foram Ranjeet, Haller Sherry L, Farooq Omer, Rothenburg Stefan, Culbertson Christopher, Li Jun

机构信息

Department of Physical Sciences, Embry-Riddle Aeronautical University, Daytona Beach, FL, USA.

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

出版信息

Electrophoresis. 2017 Jun;38(11):1515-1525. doi: 10.1002/elps.201600436. Epub 2017 Mar 8.

Abstract

This paper reports the capture and detection of vaccinia virus particles based on AC dielectrophoresis (DEP) and electrochemical impedance measurements employing an embedded vertically aligned carbon nanofiber (VACNF) nanoelectrode array (NEA) versus a macroscopic indium-tin-oxide (ITO) transparent electrode in a "points-and-lid" configuration. The nano-DEP device was fabricated by bonding two SU-8 covered electrodes patterned using photolithography. The bottom electrode contains a 200 × 200 μm active region on a randomly distributed NEA and the top electrode contains a microfluidic channel in SU-8 spin-coated on ITO to guide the flow of the virus solution. The real-time impedance change was measured during DEP capture and validated with fluorescence microscopy measurements. The NEA was able to capture virus particles with a rather low AC voltage (∼8.0 V peak-to-peak) at 1.0 kHz frequency as the particles were passed through the fluidic channel at high flow velocities (up to 8.0 mm/s). A concentration detection limit as low as ∼2.58 × 10 particles/mL was obtained via impedance measurements after only 54 sec of DEP capture. At the low AC frequencies (50.0 Hz or less), the high electric field at the exposed VACNF tips induced electroporation of the DEP-captured virus particles, which was validated by fluorescence emission from the dyes staining lipophilic membrane and internal nucleic acid, respectively. This study suggests the possibility of integration of a fully functional electronic device for rapid, reversible and label-free capture and detection of pathogenic viruses, with a potential of generating electroporation to the captured the virus particles for further biochemical study.

摘要

本文报道了基于交流介电泳(DEP)和电化学阻抗测量,采用嵌入式垂直排列碳纳米纤维(VACNF)纳米电极阵列(NEA)与宏观铟锡氧化物(ITO)透明电极以“点盖”配置捕获和检测痘苗病毒颗粒的方法。纳米DEP装置通过将两个采用光刻图案化的SU-8覆盖电极键合而成。底部电极在随机分布的NEA上包含一个200×200μm的有源区域,顶部电极在ITO上旋涂的SU-8中包含一个微流体通道,以引导病毒溶液的流动。在DEP捕获过程中测量实时阻抗变化,并用荧光显微镜测量进行验证。当病毒颗粒以高流速(高达8.0mm/s)通过流体通道时,NEA能够在1.0kHz频率下以相当低的交流电压(约8.0V峰峰值)捕获病毒颗粒。仅经过54秒的DEP捕获后,通过阻抗测量获得了低至约2.58×10颗粒/mL的浓度检测限。在低交流频率(50.0Hz或更低)下,暴露的VACNF尖端处的高电场诱导DEP捕获的病毒颗粒发生电穿孔,这分别通过对亲脂性膜和内部核酸染色的染料发出的荧光得到验证。这项研究表明,有可能集成一种全功能电子设备,用于快速、可逆和无标记地捕获和检测致病病毒,并有可能对捕获的病毒颗粒进行电穿孔以进行进一步的生化研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验