Evidence map›Paper›PMID 32256069›Full record

ArticleInternational journal of nanomedicine2020

Correlative ex situ and Liquid-Cell TEM Observation of Bacterial Cell Membrane Damage Induced by Rough Surface Topology.

David J Banner, Emre Firlar, Justas Jakubonis, Yusuf Baggia, Jodi K Osborn, Reza Shahbazian-Yassar, Constantine M Megaridis, Tolou Shokuhfar

Abstract read
In one paragraph

Article in International journal of nanomedicine, 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. Review
  2. Article
  3. Marine Algae Extract (Bioinorganic chemistry and applications · 2022
    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

8 authors.

David J BannerDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0001-8399-6074
Emre FirlarDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0003-0190-6528
Justas JakubonisDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA.
Yusuf BaggiaDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0003-1134-6851
Jodi K OsbornDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0002-3713-6126
Reza Shahbazian-YassarDepartment of Mechanical and Industrial Engineering, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0002-7744-4780
Constantine M MegaridisDepartment of Mechanical and Industrial Engineering, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0002-6339-6933
Tolou ShokuhfarDepartment of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0002-7905-2748

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNanoscale surface roughness has been suggested to have antibacterial and antifouling properties. Several existing models have attempted to explain the antibacterial mechanism of nanoscale rough surfaces without direct observation. Here, conventional and liquid-cell TEM are implemented to observe nanoscale bacteria/surface roughness interaction. The visualization of such interactions enables the inference of possible antibacterial mechanisms. METHODS AND

resultsNanotextures are synthesized on biocompatible polymer microparticles (MPs) via plasma etching. Both conventional and liquid-phase transmission electron microscopy observations suggest that these MPs may cause cell lysis via bacterial binding to a single protrusion of the nanotexture. The bacterium/protrusion interaction locally compromises the cell wall, thus causing bacterial death. This study suggests that local mechanical damage and leakage of the cytosol kill the bacteria first, with subsequent degradation of the cell envelope.

conclusionNanoscale surface roughness may act via a penetrative bactericidal mechanism. This insight suggests that future research may focus on optimizing bacterial binding to individual nanoscale projections in addition to stretching bacteria between nanopillars. Further, antibacterial nanotextures may find use in novel applications employing particles in addition to nanotextures on fibers or films.

Indexed as

Anti-Bacterial AgentsBacterial Outer MembraneDrug CarriersEscherichia coliMicroplasticsMicroscopy, Electron, TransmissionPolylactic Acid-Polyglycolic Acid CopolymerSurface PropertiesAnti-Bacterial AgentsDrug CarriersMicroplasticsPolylactic Acid-Polyglycolic Acid Copolymerantibacterial microparticlesantibacterial nanopatternsantibacterial surface topologygraphene liquid cellliquid TEM

Identifiers

PMID32256069
PMCPMC7093104

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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.