Evidence map›Paper›PMID 39065397›Full record

ArticlePolymers2024

Thermally Stabilised Poly(vinyl alcohol) Nanofibrous Materials Produced by Scalable Electrospinning: Applications in Tissue Engineering.

W Joseph A Homer, Maxim Lisnenko, Sarka Hauzerova, Bohdana Heczkova, Adrian C Gardner, Eva K Kostakova, Paul D Topham, Vera Jencova, Eirini Theodosiou

Abstract read
In one paragraph

Article in Polymers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
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

9 authors.

W Joseph A HomerEngineering for Health Research Centre, College of Engineering and Physical Sciences, Aston University, Birmingham B4 7ET, UK.
Maxim LisnenkoDepartment of Chemistry, Faculty of Science, Humanities and Education, Technical University of Liberec, 461 17 Liberec, Czech Republic.ORCID 0000-0003-4613-7742
Sarka HauzerovaDepartment of Chemistry, Faculty of Science, Humanities and Education, Technical University of Liberec, 461 17 Liberec, Czech Republic.ORCID 0000-0003-1038-7483
Bohdana HeczkovaDepartment of Haematology, Regional Hospital Liberec, 460 01 Liberec, Czech Republic.
Adrian C GardnerThe Royal Orthopaedic Hospital NHS Foundation Trust, Birmingham B31 2AP, UK.ORCID 0000-0001-6532-7950
Eva K KostakovaDepartment of Chemistry, Faculty of Science, Humanities and Education, Technical University of Liberec, 461 17 Liberec, Czech Republic.ORCID 0000-0002-5758-3206
Paul D TophamChemical Engineering and Applied Chemistry, College of Engineering and Physical Sciences, Aston University, Birmingham B4 7ET, UK.ORCID 0000-0003-4152-6976
Vera JencovaDepartment of Chemistry, Faculty of Science, Humanities and Education, Technical University of Liberec, 461 17 Liberec, Czech Republic.ORCID 0000-0001-7391-9526
Eirini TheodosiouEngineering for Health Research Centre, College of Engineering and Physical Sciences, Aston University, Birmingham B4 7ET, UK.ORCID 0000-0001-7068-4434

Funding

Birmingham Orthopaedic Charity N/AEuropean Union CZ.02.01.01/00/22_008/0004562Royal Society IES\R3\183098
6 · The paper itself

Abstract

Electrospinning is a widely employed manufacturing platform for tissue engineering applications because it produces structures that closely mimic the extracellular matrix. Herein, we demonstrate the potential of poly(vinyl alcohol) (PVA) electrospun nanofibers as scaffolds for tissue engineering. Nanofibers were created by needleless direct current electrospinning from PVA with two different degrees of hydrolysis (DH), namely 98% and 99% and subsequently heat treated at 180 °C for up to 16 h to render them insoluble in aqueous environments without the use of toxic cross-linking agents. Despite the small differences in the PVA chemical structure, the changes in the material properties were substantial. The higher degree of hydrolysis resulted in non-woven supports with thinner fibres (285 ± 81 nm c.f. 399 ± 153 nm) that were mechanically stronger by 62% (±11%) and almost twice as more crystalline than those from 98% hydrolysed PVA. Although prolonged heat treatment (16 h) did not influence fibre morphology, it reduced the crystallinity and tensile strength for both sets of materials. All samples demonstrated a lack or very low degree of haemolysis (<5%), and there were no notable changes in their anticoagulant activity (≤3%). Thrombus formation, on the other hand, increased by 82% (±18%) for the 98% hydrolysed samples and by 71% (±10%) for the 99% hydrolysed samples, with heat treatment up to 16 h, as a direct consequence of the preservation of the fibrous morphology. 3T3 mouse fibroblasts showed the best proliferation on scaffolds that were thermally stabilised for 4 and 8 h. Overall these scaffolds show potential as 'greener' alternatives to other electrospun tissue engineering materials, especially in cases where they may be used as delivery vectors for heat tolerant additives.

Indexed as

cross-linkingelectrospinningnon-woven fibrespoly(vinyl alcohol)tissue engineering

Identifiers

PMID39065397
PMCPMC11281220

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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.