Evidence map›Paper›PMID 31527873›Full record

ArticlePloS one2019

Scope and efficacy of the broad-spectrum topical antiseptic choline geranate.

Joshua R Greene, Kahla L Merrett, Alexanndra J Heyert, Lucas F Simmons, Camille M Migliori, Kristen C Vogt, Rebeca S Castro, Paul D Phillips, Joseph L Baker, Gerrick E Lindberg and 3 more

Abstract 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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Tropical life sciences research · 2023
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. 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

13 authors.

Joshua R GreeneDepartment of Chemistry, Northern Arizona University, Flagstaff, AZ, United States of America.
Kahla L MerrettDepartment of Chemistry, Northern Arizona University, Flagstaff, AZ, United States of America.
Alexanndra J HeyertDepartment of Chemistry, Northern Arizona University, Flagstaff, AZ, United States of America.
Lucas F SimmonsDepartment of Chemistry, Northern Arizona University, Flagstaff, AZ, United States of America.
Camille M MiglioriDepartment of Chemistry, Dixie State University, St. George, UT, United States of America.
Kristen C VogtDepartment of Chemistry, The College of New Jersey, Ewing, NJ, United States of America.
Rebeca S CastroDepartment of Chemistry, The College of New Jersey, Ewing, NJ, United States of America.
Paul D PhillipsDepartment of Chemistry, Northern Arizona University, Flagstaff, AZ, United States of America.
Joseph L BakerDepartment of Chemistry, The College of New Jersey, Ewing, NJ, United States of America.
Gerrick E LindbergDepartment of Chemistry, Northern Arizona University, Flagstaff, AZ, United States of America.ORCID 0000-0002-5292-4200
David T FoxChemistry Division, Los Alamos National Laboratory, Los Alamos, NM, United States of America.
Rico E Del SestoDepartment of Chemistry, Dixie State University, St. George, UT, United States of America.
Andrew T KoppischDepartment of Chemistry, Northern Arizona University, Flagstaff, AZ, United States of America.ORCID 0000-0002-3818-0030

Funding

SSCIMA: Integrating Analysis of Socio-economic Sub-population Dynamics to Improve Spatial Models of Infectious DiseaseU54MD012388 · NIMHD · NORTHERN ARIZONA UNIVERSITY · PI Julie A. Baldwin · 2017 to 2026
$49.7M
NIMHD NIH HHS U54 MD012388
6 · The paper itself

Abstract

Choline geranate (also described as Choline And GEranic acid, or CAGE) has been developed as a novel biocompatible antiseptic material capable of penetrating skin and aiding the transdermal delivery of co-administered antibiotics. The antibacterial properties of CAGE were analyzed against 24 and 72 hour old biofilms of 11 clinically isolated ESKAPE pathogens (defined as Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumanii, Pseudomonas aeruginosa, and Enterobacter sp, respectively), including multidrug resistant (MDR) isolates. CAGE was observed to eradicate in vitro biofilms at concentrations as low as 3.56 mM (0.156% v:v) in as little as 2 hours, which represents both an improved potency and rate of biofilm eradication relative to that reported for most common standard-of-care topical antiseptics in current use. In vitro time-kill studies on 24 hour old Staphylococcus aureus biofilms indicate that CAGE exerts its antibacterial effect upon contact and a 0.1% v:v solution reduced biofilm viability by over three orders of magnitude (a 3log10 reduction) in 15 minutes. Furthermore, disruption of the protective layer of exopolymeric substances in mature biofilms of Staphylococcus aureus by CAGE (0.1% v:v) was observed in 120 minutes. Insight into the mechanism of action of CAGE was provided with molecular modeling studies alongside in vitro antibiofilm assays. The geranate ion and geranic acid components of CAGE are predicted to act in concert to integrate into bacterial membranes, affect membrane thinning and perturb membrane homeostasis. Taken together, our results show that CAGE demonstrates all properties required of an effective topical antiseptic and the data also provides insight into how its observed antibiofilm properties may manifest.

Indexed as

Anti-Bacterial AgentsAnti-Infective Agents, LocalBacteriaBiofilmsCholineMicrobial Sensitivity TestsAnti-Bacterial AgentsAnti-Infective Agents, LocalCholine

Identifiers

PMID31527873
PMCPMC6748422

What OpenQuestion holds

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LicenceCC BY
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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.