Bello Julian, Shim Jiwook
Department of Biomedical Engineering, Henry M. Rowan College of Engineering, Rowan University, 201 Mullica Hill Road, Glassboro, NJ, 08028, USA.
Biomed Microdevices. 2018 Apr 21;20(2):38. doi: 10.1007/s10544-018-0281-9.
Nanopore fabrication via the controlled dielectric breakdown (CDB) method offers an opportunity to create solid-state nanopores directly in salt solution with sub-nanometer precision. Driven by trap assisted current tunneling, the method uses localized defects, or traps, in the dielectric material to isolate a breakdown point and fabricate a single pore in less than 10 minutes. Here we present an approach to controlled dielectric breakdown of SiNx in which the nanopore is fabricated in LiCl buffer instead of the traditional KCl buffer. Direct fabrication in LiCl buffer promotes a uniform, symmetric, cylindrical nanopore structure that is fully wet and can be used for experiments in situ. We have shown that fabrication in LiCl reduces the necessity for overnight pore stabilization and allows for the desired analyte to be added in significantly less time than it would take if fabrication was performed in KCl. Pores created by this approach can be used for biosensing applications, including the detection of double-stranded DNA. DNA translocation experiments were conducted in both LiCl and KCl buffer. Experiments conducted in LiCl buffer resulted in about a 2-fold increase in dsDNA transport duration when compared to experiments conducted in KCl buffer of the same concentration. An increase in transport duration of over 10-fold in comparison to KCl was observed when the concentration of the LiCl buffer was increased by a factor of 3.
通过可控介电击穿(CDB)方法制造纳米孔,为在盐溶液中直接以亚纳米精度创建固态纳米孔提供了契机。在陷阱辅助电流隧穿的驱动下,该方法利用介电材料中的局部缺陷或陷阱来隔离击穿点,并在不到10分钟的时间内制造出单个孔。在此,我们展示了一种用于SiNx可控介电击穿的方法,其中纳米孔是在LiCl缓冲液而非传统的KCl缓冲液中制造的。在LiCl缓冲液中直接制造可促进形成均匀、对称的圆柱形纳米孔结构,该结构完全湿润且可用于原位实验。我们已经表明,在LiCl中制造减少了过夜孔稳定化的必要性,并且与在KCl中制造相比,能够在显著更短的时间内添加所需的分析物。通过这种方法创建的孔可用于生物传感应用,包括双链DNA的检测。在LiCl和KCl缓冲液中都进行了DNA转位实验。与在相同浓度的KCl缓冲液中进行的实验相比,在LiCl缓冲液中进行的实验导致双链DNA运输持续时间增加了约2倍。当LiCl缓冲液的浓度增加3倍时,观察到与KCl相比运输持续时间增加了10倍以上。