Evidence map›Paper›PMID 38165478›Full record

ArticleApplied microbiology and biotechnology2024

Chitosan-based matrix as a carrier for bacteriophages.

Monika Sikora, Sławomir Wąsik, Jacek Semaniak, Zuzanna Drulis-Kawa, Maria Wiśniewska-Wrona, Michał Arabski

Open access · goldAbstract read
In one paragraph

Article in Applied microbiology and biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

9 citing papers in PubMed, 13 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

6 authors at 3 institutions in 1 country.

Monika SikoraDepartment of Medical Biology, Institute of Biology, Jan Kochanowski University in Kielce, Kielce, Poland.
Sławomir WąsikInstitute of Physics, Jan Kochanowski University in Kielce, Kielce, Poland.
Jacek SemaniakInstitute of Physics, Jan Kochanowski University in Kielce, Kielce, Poland.
Zuzanna Drulis-KawaDepartment of Pathogen Biology and Immunology, University of Wroclaw, Wroclaw, Poland.
Maria Wiśniewska-WronaLukasiewicz Research Network-Lodz Institute of Technology, Lodz, Poland.
Michał ArabskiDepartment of Medical Biology, Institute of Biology, Jan Kochanowski University in Kielce, Kielce, Poland. arabski@ujk.edu.pl.ORCID http://orcid.org/0000-0002-9712-9286
Jan Kochanowski University · PLLodz University of Technology · PLUniversity of Wrocław · PL

Funding

Narodowe Centrum Nauki 2016/21/B/NZ6/01157
6 · The paper itself

Abstract

Wound healing is a dynamic and complex process where infection prevention is essential. Chitosan, thanks to its bactericidal activity against gram-positive and gram-negative bacteria, as well as anti-inflammatory and hemostatic properties, is an excellent candidate to design dressings for difficult-to-heal wound treatment. The great advantage of this biopolymer is its capacity to be chemically modified, which allows for the production of various functional forms, depending on the needs and subsequent use. Moreover, chitosan can be an excellent polymer matrix for bacteriophage (phage) packing as a novel alternative/supportive antibacterial therapy approach. This study is focused on the preparation and characteristics of chitosan-based material in the form of a film with the addition of Pseudomonas lytic phages (KTN4, KT28, and LUZ19), which would exhibit antibacterial activity as a potential dressing that accelerates the wound healing. We investigated the method of producing a polymer based on microcrystalline chitosan (MKCh) to serve as the matrix for phage deposition. We described some important parameters such as average molar mass, swelling capacity, surface morphology, phage release profile, and antibacterial activity tested in the Pseudomonas aeruginosa bacterial model. The chitosan polysaccharide turned out to interact with phage particles immobilizing them within a material matrix. Nevertheless, with the high hydrophilicity and swelling features of the prepared material, the external solution of bacterial culture was absorbed and phages went in direct contact with bacteria causing their lysis in the polymer matrix. KEY POINTS: • A novel chitosan-based matrix with the addition of active phages was prepared • Phage interactions with the chitosan matrix were determined as electrostatic • Phages in the matrix work through direct contact with the bacterial cells.

Indexed as

BacteriophagesChitosanPseudomonas PhagesAnti-Bacterial AgentsGram-Negative BacteriaGram-Positive BacteriaPolymersAnti-Bacterial AgentsChitosanPolymersAntibacterial dressingBacteriophagesChitosanPseudomonas aeruginosaWound healing

Identifiers

PMID38165478
PMCPMC10761466
OpenAlexW4390496425

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.