Evidence map›Paper›PMID 39460118›Full record

ArticleSensors (Basel, Switzerland)2024

Vertical Microfluidic Trapping System for Capturing and Simultaneous Electrochemical Detection of Cells.

Lilia Bató, Péter Fürjes

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2024. 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. Advances in microfluidic chip technology for cell analysis.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2025
    Review
  2. Article
  3. 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

2 authors.

Lilia BatóMicrosystems Lab, Institute of Technical Physics and Materials Science, HUN-REN Centre for Energy Research, H-1121 Budapest, Hungary.ORCID 0009-0001-9718-3397
Péter FürjesMicrosystems Lab, Institute of Technical Physics and Materials Science, HUN-REN Centre for Energy Research, H-1121 Budapest, Hungary.ORCID 0000-0002-8022-4367

Funding

Nemzeti Kutatási, Fejlesztési és Innovaciós Alap INBIOM TKP2021-EGA-0Nemzeti Kutatási, Fejlesztési és Innovaciós Alap ÚNKPNemzeti Kutatási, Fejlesztési és Innovaciós Alap UNLOOC HORIZON-KDT-JU-2023-1-IA-101140192
6 · The paper itself

Abstract

Electrochemical impedance spectroscopy (EIS) is a non-invasive and label-free method widely used for characterizing cell cultures and monitoring their structure, behavior, proliferation and viability. Microfluidic systems are often used in combination with EIS methods utilizing small dimensions, controllable physicochemical microenvironments and offering rapid real-time measurements. In this work, an electrode array capable of conducting EIS measurements was integrated into a multichannel microfluidic chip which is able to trap individual cells or cell populations in specially designed channels comparable to the size of cells. An application-specific printed circuit board (PCB) was designed for the implementation of the impedance measurement in order to facilitate connection with the device used for taking EIS spectra and for selecting the channels to be measured. The PCB was designed in consideration of the optical screening of trapped cells in parallel with the EIS measurements which allows the comparison of EIS data with optical signals. With continuous EIS measurement, the filling of channels with cell suspension can be followed. Yeast cells were trapped in the microfluidic system and EIS spectra were recorded considering each individual channel, which allows differentiating between the number of trapped cells.

Indexed as

Dielectric SpectroscopyElectrochemical TechniquesElectrodesMicrofluidic Analytical TechniquesMicrofluidicsSaccharomyces cerevisiaecell trappingEISelectrode arraymicrofluidics

Identifiers

PMID39460118
PMCPMC11511429

What OpenQuestion holds

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Registered trials

None linked

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.