Evidence map›Paper›PMID 39163280›Full record

ArticleACS applied materials & interfaces2024

Bioactivation of Konjac Glucomannan Films by Tannic Acid and Gluconolactone Addition.

Beata Kaczmarek-Szczepańska, Lidia Zasada, Ugo D'Amora, Anna Pałubicka, Anna Michno, Anna Ronowska, Marcin Wekwejt

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. 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

7 authors.

Beata Kaczmarek-SzczepańskaDepartment of Biomaterials and Cosmetics Chemistry, Faculty of Chemistry, Nicolaus Copernicus University in Torun, Gagarina 11, 87-100 Torun, Poland.ORCID 0000-0002-2563-2376
Lidia ZasadaDepartment of Biomaterials and Cosmetics Chemistry, Faculty of Chemistry, Nicolaus Copernicus University in Torun, Gagarina 11, 87-100 Torun, Poland.
Ugo D'AmoraInstitute of Polymers, Composites and Biomaterials, National Research Council, v.le J.F. Kennedy 54, Mostra d'OLtremare Pad. 20, 80125 Naples, Italy.ORCID 0000-0002-6142-059X
Anna PałubickaDepartment of Laboratory Diagnostics and Microbiology with Blood Bank, Specialist Hospital in Kościerzyna, Alojzego Piechowskiego 36, 83-400 Kościerzyna, Poland.
Anna MichnoDepartment of Laboratory Medicine, Medical University of Gdańsk, Marii Skłodowskiej-Curie 3a, 80-210 Gdańsk, Poland.
Anna RonowskaDepartment of Laboratory Medicine, Medical University of Gdańsk, Marii Skłodowskiej-Curie 3a, 80-210 Gdańsk, Poland.
Marcin WekwejtDepartment of Biomaterials Technology, Faculty of Mechanical Engineering and Ship Technology, Gdańsk University of Technology, Gabriela Narutowicza 11/12, 80-229 Gdańsk, Poland.ORCID 0000-0002-6889-7825

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wound healing is a dynamic process that requires an optimal extracellular environment, as well as an accurate synchronization between various cell types. Over the past few years, great efforts have been devoted to developing novel approaches for treating and managing burn injuries, sepsis, and chronic or accidental skin injuries. Multifunctional smart-polymer-based dressings represent a promising approach to support natural healing and address several problems plaguing partially healed injuries, including severe inflammation, scarring, and wound infection. Naturally derived compounds offer unique advantages such as minimal toxicity, cost-effectiveness, and outstanding biocompatibility along with potential anti-inflammatory and antimicrobial activity. Herein, the main driving idea of the work was the design and development of konjac glucomannan d-glucono-1,5-lactone (KG) films bioactivated by tannic acid and d-glucono-1,5-lactone (GL) addition. Our analysis, using attenuated total reflectance-Fourier transform infrared, atomic force microscopy, and surface energy measurements demonstrated that tannic acid (TA) clearly interacted with the KG matrix, acting as its cross-linker, whereas GL was embedded within the polymer structure. All developed films maintained a moist environment, which represents a pivotal property for wound dressing. Hemocompatibility experiments showed that all tested films exhibited no hemolytic impact on human erythrocytes. Moreover, the presence of TA and GL enhanced the metabolic and energetic activity in human dermal fibroblasts, as indicated by the MTT assay, showing results exceeding 150%. Finally, all films demonstrated high antibacterial properties as they significantly reduced the multiplication rate of both

Indexed as

GluconatesLactonesMannansStaphylococcus aureusTanninsAnti-Bacterial AgentsBandagesBiocompatible MaterialsEscherichia coliHumansPolyphenolsWound Healing(1-6)-alpha-glucomannanAnti-Bacterial Agentsbeta-glucono-1,5-lactoneBiocompatible MaterialsGluconatesLactonesMannansPolyphenolstannic acidTanninsbioactivationbioactive propertiesgluconolactonekonjac glucomannantannic acidwound dressing

Identifiers

PMID39163280
PMCPMC11378156

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Registered trials

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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.