Evidence map›Paper›PMID 24404035›Full record

ArticleBiomicrofluidics2013

Microarray of non-connected gold pads used as high density electric traps for parallelized pairing and fusion of cells.

Feriel S Hamdi, Olivier Français, Frederic Subra, Elisabeth Dufour-Gergam, Bruno Le Pioufle

Abstract read
In one paragraph

Article in Biomicrofluidics, 2013. 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.

  1. Article
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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

5 authors.

Feriel S HamdiEcole Normale Supérieure de Cachan, CNRS, SATIE, UMR 8029, Cachan, France ; Univ Paris-Sud, CNRS, Institut d'Electronique Fondamentale, UMR 8622, Orsay, France.
Olivier FrançaisEcole Normale Supérieure de Cachan, CNRS, SATIE, UMR 8029, Cachan, France.
Frederic SubraEcole Normale Supérieure de Cachan, CNRS, LBPA, UMR 8113, Cachan, France.
Elisabeth Dufour-GergamUniv Paris-Sud, CNRS, Institut d'Electronique Fondamentale, UMR 8622, Orsay, France.
Bruno Le PioufleEcole Normale Supérieure de Cachan, CNRS, SATIE, UMR 8029, Cachan, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell fusion consists of inducing the formation of a hybridoma cell containing the genetic properties of the progenitor cells. Such an operation is usually performed chemically or electrically. The latter method, named electrofusion, is considered as having a strong potential, due to its efficiency and non-toxicity, but deserves further investigations prior to being applicable for key applications like antibody production and cancer immunotherapy. Indeed, to envision such applications, a high amount of hybrid cells is needed. In this context, we present in this paper a device for massive cell pairing and electrofusion, using a microarray of non-connected conductive pads. The electrofusion chamber--or channel--exposes cells to an inhomogeneous electric field, caused by the pads array, enabling the trapping and pairing of cells with dielectrophoresis (DEP) forces prior to electrofusion. Compared to a mechanical trapping, such electric trapping is fully reversible (on/off handling). The DEP force is contactless and thus eases the release of the produced hybridoma. Moreover, the absence of wire connections on the pads permits the high density trapping and electrofusion of cells. In this paper, the electric field mapping, the effect of metallic pads thickness, and the transmembrane potential of cells are studied based on a numerical model to optimize the device. Electric calculations and experiments were conducted to evaluate the trapping force. The structure was finally validated for cell pairing and electrofusion of arrays of cells. We believe that our approach of fully electric trapping with a simple structure is a promising method for massive production of electrofused hybridoma.

Identifiers

PMID24404035
PMCPMC3716780

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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.