2017
DOI: 10.1016/j.snb.2016.09.029
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Nanoparticle-based biosensing using interfacial electrokinetic transduction

Abstract: We present a novel label-free electrokinetic method for detecting biomolecular binding on nanoparticles suspended in the vicinity of a laminar microfluidic interface. The sensor is based on the deflection of the liquid interface in an external AC electric field. Biomolecular binding on particles is shown to increase the interfacial electrical conductivity of the suspending electrolyte, which is sensitively transduced as a change in electrokinetic interfacial deflection. Using this approach, we detect the bindi… Show more

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Cited by 8 publications
(5 citation statements)
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“…They created a liquid interface for binding by coflowing two different fluid streams through a microfluidic T-channel and integrated an array of parallel point microelectrodes within the main flow channel. Biotin concentrations could be detected as low as 500 aM by using interfacial electrokinetic transduction [77]. Feldman et al studied ACET enhancement of heterogeneous assays in microfluidics.…”
Section: Biotin Sensorsmentioning
confidence: 99%
“…They created a liquid interface for binding by coflowing two different fluid streams through a microfluidic T-channel and integrated an array of parallel point microelectrodes within the main flow channel. Biotin concentrations could be detected as low as 500 aM by using interfacial electrokinetic transduction [77]. Feldman et al studied ACET enhancement of heterogeneous assays in microfluidics.…”
Section: Biotin Sensorsmentioning
confidence: 99%
“…Nanoparticles are bulk materials that are three dimensional at the nanometer scale. In recent years, nanoparticles have been widely implemented for nanoscience applications . Thus, effective and efficient nanoparticle manipulation are significant for advancement in these fields.…”
Section: Dielectrophoretic Manipulation Of Nanomaterialsmentioning
confidence: 99%
“…Developing a simple, rapid, and highly selective method for the detection of proteins is vital in clinical diagnostics, 1,2 while the need to improve the sensitivity of protein detection is still a barrier for clinical immunoassays. 3 Several label methods for sensitive protein detection have been developed, such as electrochemical, [4][5][6][7] chemiluminescence, 8,9 uorescence, 10,11 radioactive labeling, 12,13 and enzyme-linked immunosorbent assays. 14,15 Compared with conventional detection methods, the label-free and real-time detection of proteins, such as obliqueincidence reectivity difference, 16 surface-enhanced Raman scattering, 17 surface plasmon resonance imaging (SPRI), 18 and ellipsometry, 19 have attracted much attention owing to their more sensitive and more accurate properties.…”
Section: Introductionmentioning
confidence: 99%