2018
DOI: 10.1049/mnl.2018.5206
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Development of in‐flow label‐free single molecule sensors using planar solid‐state nanopore integrated microfluidic devices

Abstract: Nanopore biosensors have attracted attention due to their label-free single molecule detection capability. To date, different materials and applications have been shown in the field, varying from Si 3 N 4 to graphene and biomolecule sensing to DNA sequencing. Classical nanopore devices are composed of Si 3 N 4 material supported on a Si wafer and the detection is largely based on electrochemical sensing using chambers of ml volumes on both sides of the nanopore device. In this study, inflow label-free electroc… Show more

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Cited by 12 publications
(7 citation statements)
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“…Microfluidic devices and lab-on-a-chip systems are widely used nowadays in chemical and biological sciences [1][2][3][4] for applications ranging from the synthesis of nanoparticles and colloidal systems [5][6][7] to molecular diagnostics [8,9] and cell biology [10,11], owing to their reduced consumption of reactants [12], better control over reaction variables such as the reactant concentration and temperature [13,14], and the ability to spatially control liquid composition with cellular resolution [11,15]. Virtually any use of these devices in chemical analysis and fabrication or biological assays/bioengineering requires the ability to mix well and predictably two or more chemical or biological components [16,17].…”
Section: Introductionmentioning
confidence: 99%
“…Microfluidic devices and lab-on-a-chip systems are widely used nowadays in chemical and biological sciences [1][2][3][4] for applications ranging from the synthesis of nanoparticles and colloidal systems [5][6][7] to molecular diagnostics [8,9] and cell biology [10,11], owing to their reduced consumption of reactants [12], better control over reaction variables such as the reactant concentration and temperature [13,14], and the ability to spatially control liquid composition with cellular resolution [11,15]. Virtually any use of these devices in chemical analysis and fabrication or biological assays/bioengineering requires the ability to mix well and predictably two or more chemical or biological components [16,17].…”
Section: Introductionmentioning
confidence: 99%
“…Consequently, the back cover structure with the equivalent effect of noise suppression was recommended for its relatively small corresponding delay. The synergistic effect of flow velocity and drift velocity exist in solid-state nanopore integrated microfluidic devices, which is a universal task for all nanopore-microfluidic devices, was presented by Guzel and coworkers [31]. The author gave the DNA capture regime as three parts: the diffusion-limited regime, transitional regime, and flow-limited regime, and they had different regions of action, which are determined by the location of the distance from the nanopore (within 500 nm or not), the driven speed of the electrical field and microfluidic flow.…”
Section: Fundamental Configuration Of a Nanopore-based Microfluidic Systemmentioning
confidence: 98%
“…This advanced technology benefits from the advantages of lab on‐chip technologies consisting of sophisticated, but often very basic, microfluidic channel networks. Microfluidic systems have gone through many developments to perform complex and time‐consuming biological functions in a much effective and shorter time [ 23 , 24 , 25 , 26 ]. These systems are also cost effective and automated while consuming small fluid volume [ 27 , 28 , 29 ].…”
Section: Introductionmentioning
confidence: 99%