ArticleBiomicrofluidics2016
Preconcentration of diluted mixed-species samples following separation and collection in a micro-nanofluidic device.
Article in Biomicrofluidics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
9 citing papers in PubMed.
- Ion Concentration Polarization in Branched Microchannels: Effect of Membrane Thickness and Applied Voltage.Membranes · 2025Article
- Fabrication of High Aspect Ratio Nano-Channels by Thermal Nano-Imprinting and Parylene Deposition.Micromachines · 2023Article
- Eco friendly nanofluidic platforms using biodegradable nanoporous materials.Scientific reports · 2021Article
- Direct Visualization of Perm-Selective Ion Transportation.Scientific reports · 2020Article
- Free Flow Ion Concentration Polarization Focusing (FF-ICPF).Analytical chemistry · 2020Article
- Nanoelectrokinetic bufferchannel-less radial preconcentrator and online extractor by tunable ion depletion layer.Biomicrofluidics · 2019Article
- A Multiwell-Based Detection Platform with Integrated PDMS Concentrators for Rapid Multiplexed Enzymatic Assays.Scientific reports · 2018Article
- Article
- A simple electrokinetic protein preconcentrator utilizing nano-interstices.Biomicrofluidics · 2016Article
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A microfluidic device consisting of a nanoscale Nafion membrane and a polydimethylsiloxane microchannel is proposed for the preconcentration of diluted multi-mixed species samples then following separation and collection. When an electric field is applied across the microchip, an accumulation of the mixed-species sample occurs at the junction between the microchannel and the membrane by means of ion concentration polarization effect. A separation of the sample then takes place due to the difference in the electrophoretic mobilities of the sample components. Finally, the component of interest is guided to a collection reservoir by manipulating the external potential configuration and is trapped in place by means of a magnetically actuated valve. The preconcentration performance of the proposed device is evaluated in both straight and convergent microchannels using a fluorescein isothiocyanate labeled bovine serum albumin (FITC-BSA) sample. It is shown that a preconcentration factor of 40 times can be achieved using a straight microchannel. By contrast, the preconcentration factor increases to 50 times when using a convergent channel. The practical feasibility of the proposed device is demonstrated by performing the preconcentration, separation, and collection of a mixed FITC-BSA and Tetramethylrhodamine sample.
Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.