Pungetmongkol Porpin, Yamamoto Takatoki
International School of Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand.
Department of Mechanical Engineering, Tokyo Institute of Technology, Tokyo 152-8550, Japan.
Micromachines (Basel). 2019 Mar 15;10(3):189. doi: 10.3390/mi10030189.
Many researchers have fabricated micro and nanofluidic devices incorporating optical, chemical, and electrical detection systems with the aim of achieving on-chip analysis of macromolecules. The present study demonstrates a label-free detection of DNA using a nanofluidic device based on impedance measurements that is both sensitive and simple to operate. Using this device, the electrophoresis and dielectrophoresis effect on DNA conformation and the length dependence were examined. A low alternating voltage was applied to the nanogap electrodes to generate a high intensity field (>0.5 MV/m) under non-faradaic conditions. In addition, a 100 nm thick gold electrode was completely embedded in the substrate to allow direct measurements of a solution containing the sample passing through the gap, without any surface modification required. The high intensity field in this device produced a dielectrophoretic force that stretched the DNA molecule across the electrode gap at a specific frequency, based on back and forth movements between the electrodes with the DNA in a random coil conformation. The characteristics of 100 bp, 500 bp, 1 kbp, 5 kbp, 10 kbp, and 48 kbp λ DNA associated with various conformations were quantitatively analyzed with high resolution (on the femtomolar level). The sensitivity of this system was found to be more than about 10 orders of magnitude higher than that obtained from conventional linear alternating current (AC) impedance for the analysis of bio-polymers. This new high-sensitivity process is expected to be advantageous with regard to the study of complex macromolecules and nanoparticles.
许多研究人员制造了包含光学、化学和电学检测系统的微纳流体装置,旨在实现对大分子的芯片上分析。本研究展示了一种基于阻抗测量的纳米流体装置对DNA的无标记检测,该检测既灵敏又易于操作。利用该装置,研究了电泳和介电泳对DNA构象及长度依赖性的影响。在非法拉第条件下,向纳米间隙电极施加低交流电压以产生高强度场(>0.5 MV/m)。此外,将一个100 nm厚的金电极完全嵌入基底中,以便直接测量通过间隙的含样品溶液,无需任何表面修饰。该装置中的高强度场产生了介电泳力,基于DNA呈无规卷曲构象时在电极间的来回移动,该力在特定频率下将DNA分子拉伸穿过电极间隙。对100 bp、500 bp、1 kbp、5 kbp、10 kbp和48 kbp λ DNA与各种构象相关的特性进行了高分辨率(飞摩尔水平)定量分析。结果发现,该系统的灵敏度比用于生物聚合物分析的传统线性交流(AC)阻抗高出约10个数量级以上。这种新的高灵敏度方法有望在复杂大分子和纳米颗粒的研究方面具有优势。