Evidence map›Paper›PMID 36275090›Full record

ArticleRSC advances2022

Main-chain flexibility and hydrophobicity of ionenes strongly impact their antimicrobial activity: an extended study on drug resistance strains and

Rafał Jerzy Kopiasz, Anna Zabost, Magdalena Myszka, Aleksandra Kuźmińska, Karolina Drężek, Jolanta Mierzejewska, Waldemar Tomaszewski, Agnieszka Iwańska, Ewa Augustynowicz-Kopeć, Tomasz Ciach and 1 more

Abstract read
In one paragraph

Article in RSC advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Rafał Jerzy KopiaszFaculty of Chemistry, Warsaw University of Technology Noakowskiego 3 Warsaw 00-664 Poland dominik.janczewski@pw.edu.pl.ORCID https://orcid.org/0000-0001-8902-1761
Anna ZabostDepartment of Microbiology, National Tuberculosis and Lung Diseases Research Institute Płocka 26 Warsaw 01-138 Poland.ORCID https://orcid.org/0000-0003-2781-9844
Magdalena MyszkaFaculty of Chemistry, Warsaw University of Technology Noakowskiego 3 Warsaw 00-664 Poland dominik.janczewski@pw.edu.pl.
Aleksandra KuźmińskaFaculty of Chemical and Process Engineering, Warsaw University of Technology Waryńskiego 1 Warsaw 00-645 Poland.
Karolina DrężekFaculty of Chemistry, Warsaw University of Technology Noakowskiego 3 Warsaw 00-664 Poland dominik.janczewski@pw.edu.pl.
Jolanta MierzejewskaFaculty of Chemistry, Warsaw University of Technology Noakowskiego 3 Warsaw 00-664 Poland dominik.janczewski@pw.edu.pl.ORCID https://orcid.org/0000-0002-9298-8794
Waldemar TomaszewskiFaculty of Chemistry, Warsaw University of Technology Noakowskiego 3 Warsaw 00-664 Poland dominik.janczewski@pw.edu.pl.
Agnieszka IwańskaDepartment of Microbiology, National Tuberculosis and Lung Diseases Research Institute Płocka 26 Warsaw 01-138 Poland.
Ewa Augustynowicz-KopećDepartment of Microbiology, National Tuberculosis and Lung Diseases Research Institute Płocka 26 Warsaw 01-138 Poland.
Tomasz CiachFaculty of Chemical and Process Engineering, Warsaw University of Technology Waryńskiego 1 Warsaw 00-645 Poland.
Dominik JańczewskiFaculty of Chemistry, Warsaw University of Technology Noakowskiego 3 Warsaw 00-664 Poland dominik.janczewski@pw.edu.pl.ORCID https://orcid.org/0000-0002-5466-6444

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spread of antibiotic-resistant pathogens and the resurgence of tuberculosis disease are major motivations to search for novel antimicrobial agents. Some promising candidates in this respect are cationic polymers, also known as synthetic mimics of antimicrobial peptides (SMAMPs), which act through the membrane-lytic mechanism. Development of resistance toward SMAMPs is less likely than toward currently employed antibiotics; however, further studies are needed to better understand their structure-activity relationship. The main objective of this work is to understand the cross-influence of hydrophobicity, main-chain flexibility, and the topology of ionenes (polycations containing a cationic moiety within the main-chain) on activity. To fulfill this goal, a library of ionenes was developed and compared with previously investigated molecules. The obtained compounds display promising activity against the model microorganisms and drug-resistance clinical isolates, including

Identifiers

PMID36275090
PMCPMC9477016

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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.