Evidence map›Paper›PMID 32355998›Full record

ArticleBiomedical microdevices2020

Rapid lipid bilayer membrane formation on Parylene coated apertures to perform ion channel analyses.

Tanzir Ahmed, Sander van den Driesche, Jayesh Arun Bafna, Martin Oellers, Roland Hemmler, Karsten Gall, Richard Wagner, Mathias Winterhalter, Michael J Vellekoop

Abstract read
In one paragraph

Article in Biomedical microdevices, 2020. 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
  2. Parylenes in bioanalytical and cell culture applications.Analytical and bioanalytical chemistry · 2026
    Review
  3. Article
  4. Article
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.

Tanzir AhmedInstitute for Microsensors, -actuators and -systems (IMSAS), University of Bremen, Microsystems Center Bremen (MCB), Bremen, Germany. tahmed@imsas.uni-bremen.de.
Sander van den DriescheInstitute for Microsensors, -actuators and -systems (IMSAS), University of Bremen, Microsystems Center Bremen (MCB), Bremen, Germany.
Jayesh Arun BafnaDepartment of Life Sciences and Chemistry, Jacobs University Bremen, Bremen, Germany.
Martin OellersInstitute for Microsensors, -actuators and -systems (IMSAS), University of Bremen, Microsystems Center Bremen (MCB), Bremen, Germany.
Roland HemmlerIonovation GmbH, Bissendorf, Germany.
Karsten GallIonovation GmbH, Bissendorf, Germany.
Richard WagnerDepartment of Life Sciences and Chemistry, Jacobs University Bremen, Bremen, Germany.
Mathias WinterhalterDepartment of Life Sciences and Chemistry, Jacobs University Bremen, Bremen, Germany.
Michael J VellekoopInstitute for Microsensors, -actuators and -systems (IMSAS), University of Bremen, Microsystems Center Bremen (MCB), Bremen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a chip design allowing rapid and robust lipid bilayer (LBL) membrane formation using a Parylene coated thin silicon nitride aperture. After bilayer formation, single membrane channels can be reconstituted and characterized by electrophysiology. The ability for robust reconstitution will allow parallelization and enhanced screening of small molecule drugs acting on or permeating across the membrane channel. The aperture was realized on a microfabricated silicon nitride membrane by using standard clean-room fabrication processes. To ensure the lipid bilayer formation, the nitride membrane was coated with a hydrophobic and biocompatible Parylene layer. We tested both Parylene-C and Parylene-AF4. The contact angle measurements on both Parylene types showed very good hydrophobic properties and affinity to lipids. No precoating of the Parylene with an organic solvent is needed to make the aperture lipophilic, in contradiction to Teflon membranes. The chips can be easily placed in an array utilizing a 3D printed platform. Experiments show repetitive LBL formation and destruction (more than 6 times) within a very short time (few seconds). Through measurements we have established that the LBL layers are very thin. This allows the investigation of the fusion process of membrane proteins i.e. outer membrane protein (OmpF) in the LBL within a few minutes.

Indexed as

Biological AssayCell MembraneIon ChannelsKineticsLipid BilayersPermeabilityPerylenePrinting, Three-DimensionalSilicon CompoundsIon ChannelsLipid BilayersPeryleneSilicon Compoundssilicon nitrideLipid Bilayer Membrane (LBL)Parylene-AF4Parylene-CSiliconSilicon Nitride

Identifiers

PMID32355998
PMCPMC7192868

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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.