Evidence map›Paper›PMID 41835594›Full record

ArticleACS omega2026

Advanced Biomaterials in Tissue Engineering Based on Antibacterial and Antibiofilm Nanocomposites for Multidrug-Resistant Wound Pathogens.

Aizhan B Talipova, Volodymyr Buranych, Irina S Savitskaya, Inara Abashidze, Fyodor I Malchik, Dina H Shokatayeva, Martin Sahul, Krzysztof Rokosz, Mária Čaplovičová, Alexander D Pogrebnjak

Abstract read
In one paragraph

Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Aizhan B TalipovaDepartment of Biotechnology, Al-Farabi Kazakh National University, Almaty 050040, Kazakhstan.
Volodymyr BuranychInstitute of Electrical Engineering, Slovak Academy of Sciences Dúbravská cesta 9, 84104 Bratislava, Slovakia.ORCID https://orcid.org/0000-0002-5831-8754
Irina S SavitskayaDepartment of Biotechnology, Al-Farabi Kazakh National University, Almaty 050040, Kazakhstan.
Inara AbashidzeHealth Policy and Management Department, Al-Farabi Kazakh National University, Almaty 050040, Kazakhstan.
Fyodor I MalchikLaboratory of Electrochemical Production Technologies, Al-Farabi Kazakh National University, Almaty 050040, Kazakhstan.ORCID https://orcid.org/0000-0001-6381-0738
Dina H ShokatayevaDepartment of Biotechnology, Al-Farabi Kazakh National University, Almaty 050040, Kazakhstan.
Martin SahulInstitute of Materials Science, Faculty of Materials Science and Technology, Slovak University of Technology, J. Bottu 25, 917 24 Trnava, Slovakia.
Krzysztof RokoszFaculty of Electronics and Computer Science, Koszalin University of Technology, Śniadeckich 2, PL 75-453 Koszalin, Poland.
Mária ČaplovičováCentre for Nanodiagnostics of Materials, Slovak University of Technology in Bratislava, 5 Vazovova Street, Bratislava 812 43, Slovakia.
Alexander D PogrebnjakInstitute of Materials Science, Faculty of Materials Science and Technology, Slovak University of Technology, J. Bottu 25, 917 24 Trnava, Slovakia.ORCID https://orcid.org/0000-0002-9218-6492

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment of chronic wounds is critically challenged by resilient biofilms formed by multidrug-resistant (MDR) pathogens, which are largely impervious to conventional antibiotics. This study addresses this challenge by engineering a multifunctional hydrogel dressing that synergistically integrates bacterial cellulose (BC), MXene nanosheets, and hydroxyapatite (HAp). Plays a critical dual role in the composite, significantly boosting bioactivity while also stabilizing the MXene to prevent oxidation and maintain its antibacterial properties. As a result, the BC/MXene/HAp composite achieved a near-total (98%) eradication of viable cells in mature biofilms of challenging MDR pathogens, including MRSA and FQRPA. Such activity is driven by a dual-mechanism that effectively disrupts both the initial attachment of bacteria and the structural scaffold of established biofilms. Complementing this efficacy, in vitro assays with NIH-3T3 fibroblasts confirm that the composite supports excellent cell adhesion, proliferation, and metabolic activity, highlighting its high biocompatibility. This work demonstrates a nonantibiotic strategy to combat biofilms through a synergistically designed biomaterial. Given its robust performance and multifunctionality, this platform is a promising candidate for the development of advanced therapeutic dressings in regenerative wound care.

Identifiers

PMID41835594
PMCPMC12980239

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.