Evidence map›Paper›PMID 42623368›Full record

ArticlePloS one2026

Dielectrophoresis and ζ-potential as potential low-cost complements to patch clamp for measurement of cell electrophysiology.

Rashedul Hoque, Fatima H Labeed, Srdjan Cirovic, Michael Pycraft Hughes

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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Rashedul HoqueCentre for Biomedical Engineering, University of Surrey, Guildford, United Kingdom.ORCID https://orcid.org/0000-0001-8821-4115
Fatima H LabeedDepartment of Biology, United Arab Emirates University, Al Ain, United Arab Emirates.
Srdjan CirovicCentre for Biomedical Engineering, University of Surrey, Guildford, United Kingdom.
Michael Pycraft HughesDepartment of Biomedical Engineering and Biotechnology, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates.ORCID https://orcid.org/0000-0001-7385-5876

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell electrophysiology is a useful measure of cell function, including ionic state and channel activity, and the way these are altered by pharmacological intervention. However, measurement of whole-cell electrical properties such as resting membrane potential Vm and membrane whole-cell capacitance and conductance is difficult, which has limited the more widespread adoption of electrophysiology in cell biology and drug discovery. The gold-standard method for acquiring this data is patch clamp, a method of measuring single cells that uses a micromanipulated micropipette in contact with the cell surface. Measurement is difficult, slow, and requires a highly skilled operator, whilst automated alternatives are expensive to run. Other methods such as flow cytometry are unable to provide absolute values of Vm, or measure conductance and capacitance characteristics. Dielectrophoresis (DEP) and electrophoretic light scattering (ELS) have recently been shown to provide useful methods of directly measuring absolute Vm and other parameters, whilst examining many more cells (typically tens of thousands in under a minute). In this paper we use DEP and ELS to examine the electrophysiology of human bladder carcinoma cell line HTB-9 following treatment with ATP, glibenclamide and tetraethylammonium, and compare the results to published data obtained by patch clamp. Results indicate that DEP yields Vm and membrane conductance values that are highly comparable to data from patch clamp, at high speed and low cost, demonstrating the usefulness of techniques such as DEP and ELS for electrophysiological study.

Indexed as

ElectrophoresisElectrophysiological PhenomenaElectrophysiologyPatch-Clamp TechniquesAdenosine TriphosphateCell Line, TumorGlyburideHumansMembrane PotentialsTetraethylammoniumAdenosine TriphosphateGlyburideTetraethylammonium

Identifiers

PMID42623368
PMCPMC13492762

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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.