Evidence map›Paper›PMID 31856234›Full record

ArticlePloS one2019

A lab-on-a-chip for rapid miRNA extraction.

Ole Behrmann, Matthias Hügle, Peter Bronsert, Bettina Herde, Julian Heni, Marina Schramm, Frank T Hufert, Gerald A Urban, Gregory Dame

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. 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
0.8field-weighted citation impact, top 28% of its field
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, 12 citations in OpenAlex.

  1. Detection ofMicroorganisms · 2024
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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

9 authors at 2 institutions in 1 country.

Ole BehrmannDepartment of Microbiology and Virology, Brandenburg Medical School Fontane, Neuruppin, Germany.ORCID 0000-0002-7846-7917
Matthias HügleDepartment of Microbiology and Virology, Brandenburg Medical School Fontane, Neuruppin, Germany.
Peter BronsertInstitute for Surgical Pathology, Medical Center-University of Freiburg, Freiburg, Germany.
Bettina HerdeInstitute for Surgical Pathology, Medical Center-University of Freiburg, Freiburg, Germany.
Julian HeniLaboratory for Sensors, Department of Microsystems Engineering (IMTEK), University of Freiburg, Freiburg, Germany.
Marina SchrammDepartment of Microbiology and Virology, Brandenburg Medical School Fontane, Neuruppin, Germany.
Frank T HufertDepartment of Microbiology and Virology, Brandenburg Medical School Fontane, Neuruppin, Germany.
Gerald A UrbanLaboratory for Sensors, Department of Microsystems Engineering (IMTEK), University of Freiburg, Freiburg, Germany.
Gregory DameDepartment of Microbiology and Virology, Brandenburg Medical School Fontane, Neuruppin, Germany.
University of Freiburg · DEMedizinische Hochschule Brandenburg Theodor Fontane · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a simple to operate microfluidic chip system that allows for the extraction of miRNAs from cells with minimal hands-on time. The chip integrates thermoelectric lysis (TEL) of cells with native gel-electrophoretic elution (GEE) of released nucleic acids and uses non-toxic reagents while requiring a sample volume of only 5 μl. These properties as well as the fast process duration of 180 seconds make the system an ideal candidate to be part of fully integrated point-of-care applications for e.g. the diagnosis of cancerous tissue. GEE was characterized in comparison to state-of-the-art silica column (SC) based RNA recovery using the mirVana kit (Ambion) as a reference. A synthetic miRNA (miR16) as well as a synthetic snoRNA (SNORD48) were subjected to both GEE and SC. Subsequent detection by stem-loop RT-qPCR demonstrated a higher yield for miRNA recovery by GEE. SnoRNA recovery performance was found to be equal for GEE and SC, indicating yield dependence on RNA length. Coupled operation of the chip (TEL + GEE) was characterized using serial dilutions of 5 to 500 MCF7 cancer cells in suspension. Samples were split and cells were subjected to either on-chip extraction or SC. Eluted miRNAs were then detected by stem-loop RT-qPCR without any further pre-processing. The extraction yield from cells was found to be up to ~200-fold higher for the chip system under non-denaturing conditions. The ratio of eluted miRNAs is shown to be dependent on the degree of complexation with miRNA associated proteins by comparing miRNAs purified by GEE from heat-shock and proteinase-K based lysis.

Indexed as

Lab-On-A-Chip DevicesElectrophoresisMicroRNAsRNA, Small NucleolarTime FactorsMicroRNAsRNA, Small Nucleolar

Identifiers

PMID31856234
PMCPMC6922460
OpenAlexW2994854239

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.