Evidence map›Paper›PMID 26392836›Full record

ArticleBiomicrofluidics2015

Dielectrophoretic capture of low abundance cell population using thick electrodes.

Julien Marchalot, Jean-François Chateaux, Magalie Faivre, Hichem C Mertani, Rosaria Ferrigno, Anne-Laure Deman

Abstract read
In one paragraph

Article in Biomicrofluidics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Julien MarchalotInstitut des Nanotechnologies de Lyon (INL), CNRS UMR 5270, Université de Lyon 1, Université de Lyon , Villeurbanne F-69622, France.
Jean-François ChateauxInstitut des Nanotechnologies de Lyon (INL), CNRS UMR 5270, Université de Lyon 1, Université de Lyon , Villeurbanne F-69622, France.
Magalie FaivreInstitut des Nanotechnologies de Lyon (INL), CNRS UMR 5270, Université de Lyon 1, Université de Lyon , Villeurbanne F-69622, France.
Hichem C MertaniCentre de Recherche en Cancérologie de Lyon (CRCL), Centre Léon Bérard, INSERM U1052-CNRS UMR5286, Université de Lyon 1, Université de Lyon , Lyon 69008, France.
Rosaria FerrignoInstitut des Nanotechnologies de Lyon (INL), CNRS UMR 5270, Université de Lyon 1, Université de Lyon , Villeurbanne F-69622, France.
Anne-Laure DemanInstitut des Nanotechnologies de Lyon (INL), CNRS UMR 5270, Université de Lyon 1, Université de Lyon , Villeurbanne F-69622, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enrichment of rare cell populations such as Circulating Tumor Cells (CTCs) is a critical step before performing analysis. This paper presents a polymeric microfluidic device with integrated thick Carbon-PolyDimethylSiloxane composite (C-PDMS) electrodes designed to carry out dielectrophoretic (DEP) trapping of low abundance biological cells. Such conductive composite material presents advantages over metallic structures. Indeed, as it combines properties of both the matrix and doping particles, C-PDMS allows the easy and fast integration of conductive microstructures using a soft-lithography approach while preserving O2 plasma bonding properties of PDMS substrate and avoiding a cumbersome alignment procedure. Here, we first performed numerical simulations to demonstrate the advantage of such thick C-PDMS electrodes over a coplanar electrode configuration. It is well established that dielectrophoretic force ([Formula: see text]) decreases quickly as the distance from the electrode surface increases resulting in coplanar configuration to a low trapping efficiency at high flow rate. Here, we showed quantitatively that by using electrodes as thick as a microchannel height, it is possible to extend the DEP force influence in the whole volume of the channel compared to coplanar electrode configuration and maintaining high trapping efficiency while increasing the throughput. This model was then used to numerically optimize a thick C-PDMS electrode configuration in terms of trapping efficiency. Then, optimized microfluidic configurations were fabricated and tested at various flow rates for the trapping of MDA-MB-231 breast cancer cell line. We reached trapping efficiencies of 97% at 20 μl/h and 78.7% at 80 μl/h, for 100 μm thick electrodes. Finally, we applied our device to the separation and localized trapping of CTCs (MDA-MB-231) from a red blood cells sample (concentration ratio of 1:10).

Identifiers

PMID26392836
PMCPMC4560720

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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.