Evidence map›Paper›PMID 37619264›Full record

ArticleBiomaterials2023

Facial amphiphilic naphthoic acid-derived antimicrobial polymers against multi-drug resistant gram-negative bacteria and biofilms.

Leman Buzoglu Kurnaz, Swagatam Barman, Xiaoming Yang, Claire Fisher, F Wayne Outten, Prakash Nagarkatti, Mitzi Nagarkatti, Chuanbing Tang

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Recent Advances and Future Prospects in Biological-Membrane-Targeted Polymers.Polymer science & technology (Washington, D.C.) · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. 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 at 1 institution in 1 country.

Leman Buzoglu KurnazDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, United States.
Swagatam BarmanDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, United States.
Xiaoming YangDepartment of Pathology, Microbiology and Immunology, University of South Carolina, School of Medicine, Columbia, SC, 29209, United States.
Claire FisherDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, United States.
F Wayne OuttenDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, United States.
Prakash NagarkattiDepartment of Pathology, Microbiology and Immunology, University of South Carolina, School of Medicine, Columbia, SC, 29209, United States.
Mitzi NagarkattiDepartment of Pathology, Microbiology and Immunology, University of South Carolina, School of Medicine, Columbia, SC, 29209, United States.
Chuanbing TangDepartment of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, United States. Electronic address: tang4@mailbox.sc.edu.
University of South Carolina · 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
NIAID NIH HHS R01 AI149810
6 · The paper itself

Abstract

Inspired by the facial amphiphilic nature and antimicrobial efficacy of many antimicrobial peptides, this work reported facial amphiphilic bicyclic naphthoic acid derivatives with different ratios of charges to rings that were installed onto side chains of poly(glycidyl methacrylate). Six quaternary ammonium-charged (QAC) polymers were prepared to investigate the structure-activity relationship. These QAC polymers displayed potent antibacterial activity against various multi-drug resistant (MDR) gram-negative pathogens such as Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Acinetobacter baumannii. Polymers demonstrated low hemolysis and high antimicrobial selectivity. Additionally, they were able to eradicate established biofilms and kill metabolically inactive dormant cells. The membrane permeabilization and depolarization results indicated a mechanism of action through membrane disruption. Two lead polymers showed no resistance from MDR-P. aeruginosa and MDR-K. pneumoniae. These facial amphiphiles are potentially a new class of potent antimicrobial agents to tackle the antimicrobial resistance for both planktonic and biofilm-related infections.

Indexed as

Anti-Infective AgentsAnti-Bacterial AgentsBiofilmsCarboxylic AcidsEscherichia coliNaphthalenes1-naphthoic acidAnti-Bacterial AgentsAnti-Infective AgentsCarboxylic AcidsNaphthalenesAntimicrobial peptideAntimicrobial polymerAntimicrobial resistanceBiofilmFacial amphiphilicity

Identifiers

PMID37619264
PMCPMC10530118
OpenAlexW4385783803

What OpenQuestion holds

Textmetadata
LicenceTDM
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.