Evidence map›Paper›PMID 37565371›Full record

ArticleAdvanced healthcare materials2023

Membrane-Active Metallopolymers: Repurposing and Rehabilitating Antibiotics to Gram-Negative Superbugs.

JiHyeon Hwang, Swagatam Barman, Ruixuan Gao, Xiaoming Yang, Andrea O'Malley, Prakash Nagarkatti, Mitzi Nagarkatti, Maksymilian Chruszcz, Chuanbing Tang

Open access · hybridAbstract read
In one paragraph

Article in Advanced healthcare materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

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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.

JiHyeon HwangDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, USA.ORCID 0000-0001-5782-7496
Swagatam BarmanDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, USA.
Ruixuan GaoDepartment of Chemistry, University of South Florida, Tampa, FL, 33620, USA.
Xiaoming YangDepartment of Pathology, Microbiology and Immunology, University of South Carolina, School of Medicine, Columbia, SC, 29209, USA.
Andrea O'MalleyDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, USA.
Prakash NagarkattiDepartment of Pathology, Microbiology and Immunology, University of South Carolina, School of Medicine, Columbia, SC, 29209, USA.
Mitzi NagarkattiDepartment of Pathology, Microbiology and Immunology, University of South Carolina, School of Medicine, Columbia, SC, 29209, USA.
Maksymilian ChruszczDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, USA.
Chuanbing TangDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, USA.ORCID 0000-0002-0242-8241
University of South Carolina · USUniversity of South Florida · US

Funding

Control of Facial Amphiphilicity to Tune Macromolecular Interactions with BacteriaR01AI149810 · NIAID · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI TANG, CHUANBING · 2020 to 2024
$1.8M
Metallopolymer and Antibiotic Bioconjugates against Multidrug Resistant BacteriaR01AI120987 · NIAID · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI TANG, CHUANBING · 2016 to 2019
$1.4M
NIAID NIH HHS R01 AI120987NIAID NIH HHS R01 AI149810NIH HHS R01AI149810
6 · The paper itself

Abstract

Among multiple approaches to combating antimicrobial resistance, a combination therapy of existing antibiotics with bacterial membrane-perturbing agents is promising. A viable platform of metallopolymers as adjuvants in combination with traditional antibiotics is reported in this work to combat both planktonic and stationary cells of Gram-negative superbugs and their biofilms. Antibacterial efficacy, toxicity, antibiofilm activity, bacterial resistance propensity, and mechanisms of action of metallopolymer-antibiotic combinations are investigated. These metallopolymers exhibit 4-16-fold potentiation of antibiotics against Gram-negative bacteria with negligible toxicity toward mammalian cells. More importantly, the lead combinations (polymer-ceftazidime and polymer-rifampicin) eradicate preformed biofilms of MDR E. coli and P. aeruginosa, respectively. Further, β-lactamase inhibition, outer membrane permeabilization, and membrane depolarization demonstrate synergy of these adjuvants with different antibiotics. Moreover, the membrane-active metallopolymers enable the antibiotics to circumvent bacterial resistance development. Altogether, the results indicate that such non-antibiotic adjuvants bear the promise to revitalize the efficacy of existing antibiotics to tackle Gram-negative bacterial infections.

Indexed as

Anti-Bacterial AgentsEscherichia coliAnimalsDrug Resistance, Multiple, BacterialGram-Negative BacteriaMammalsMicrobial Sensitivity TestsPolymersAnti-Bacterial AgentsPolymersadjuvantsantimicrobial resistancebiofilmsmetallopolymersstationary phase

Identifiers

PMID37565371
PMCPMC10842942
OpenAlexW4385751471

What OpenQuestion holds

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LicenceCC BY-NC
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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.