Evidence map›Paper›PMID 39926490›Full record

ArticleACS omega2025

Antiviral Activity of Electrospun Polyamide Ultrathin Fibers Against SARS-CoV-2 Variant.

Moisés V Santana, Gustavo F Sousa, Millena C S Silva, Lays Cordeiro Guimaraes, Leonardo Camilo de Oliveira, Pedro H D M Prazeres, André S A Furtado, Leila S S M Magalhães, Thiago Domingues Stocco, Bartolomeu C Viana and 11 more

Abstract read
In one paragraph

Article in ACS omega, 2025. 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

21 authors.

Moisés V SantanaLIMAV-Interdisciplinary Laboratory for Advanced Materials, UFPI-Federal University of Piaui, Teresina, Piaui 64049-550, Brazil.
Gustavo F SousaLIMAV-Interdisciplinary Laboratory for Advanced Materials, UFPI-Federal University of Piaui, Teresina, Piaui 64049-550, Brazil.
Millena C S SilvaLIMAV-Interdisciplinary Laboratory for Advanced Materials, UFPI-Federal University of Piaui, Teresina, Piaui 64049-550, Brazil.
Lays Cordeiro GuimaraesDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.
Leonardo Camilo de OliveiraDepartment of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, Minas, Gerais 31270-901, Brazil.
Pedro H D M PrazeresDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.ORCID https://orcid.org/0000-0002-1933-3230
André S A FurtadoLIMAV-Interdisciplinary Laboratory for Advanced Materials, UFPI-Federal University of Piaui, Teresina, Piaui 64049-550, Brazil.
Leila S S M MagalhãesLIMAV-Interdisciplinary Laboratory for Advanced Materials, UFPI-Federal University of Piaui, Teresina, Piaui 64049-550, Brazil.
Thiago Domingues StoccoBioengineering Program, Technological and Scientific Institute, Brasil University, São Paulo, São Paulo 08230-030, Brazil.
Bartolomeu C VianaLIMAV-Interdisciplinary Laboratory for Advanced Materials, UFPI-Federal University of Piaui, Teresina, Piaui 64049-550, Brazil.ORCID https://orcid.org/0000-0002-5207-4269
Ramon Raudel Peña-GarciaLIMAV-Interdisciplinary Laboratory for Advanced Materials, UFPI-Federal University of Piaui, Teresina, Piaui 64049-550, Brazil.
Fernanda Roberta MarcianoLIMAV-Interdisciplinary Laboratory for Advanced Materials, UFPI-Federal University of Piaui, Teresina, Piaui 64049-550, Brazil.
Bianca de Sousa LealBiochemistry and Pharmacology Department, Health Sciences Center, UFPI-Federal University of Piauí, Teresina, Piaui 64049-550, Brazil.
Rosimeire Ferreira Dos SantosBiochemistry and Pharmacology Department, Health Sciences Center, UFPI-Federal University of Piauí, Teresina, Piaui 64049-550, Brazil.
João Marcelo de Castro E SouzaBiochemistry and Pharmacology Department, Health Sciences Center, UFPI-Federal University of Piauí, Teresina, Piaui 64049-550, Brazil.
Dalton DitzBiochemistry and Pharmacology Department, Health Sciences Center, UFPI-Federal University of Piauí, Teresina, Piaui 64049-550, Brazil.
Vivian Vasconcelos Costa LitwinskiDepartment of Cellular Biology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.
Mauro Martins TeixeiraDepartment of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, Minas, Gerais 31270-901, Brazil.
Antônio Francisco Machado PereiraNursing Health Sciences Center, UFPI-Federal University of Piauí, Teresina, Piaui 64049-550, Brazil.
Pedro P G GuimarãesDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.
Anderson Oliveira LoboLIMAV-Interdisciplinary Laboratory for Advanced Materials, UFPI-Federal University of Piaui, Teresina, Piaui 64049-550, Brazil.ORCID https://orcid.org/0000-0002-2544-0438

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of new strategies to produce nanomaterials that can be used as personal protective equipment with antiviral activity and low toxicity is crucial. Electrospun ultrathin fibers have attracted considerable attention due to their potential for biomedical applications, including antiviral activity. Herein, we electrospun different grades of commercially available polyamide to produce ultrathin fibers and investigate their antiviral activity against SARS-CoV-2 Gamma lineage (P.1). We evaluated the morphology, chemical composition, and mechanical properties of the ultrathin fibers. We also investigated the in vitro cytotoxicity, hemolytic activity, and antiviral activity against SARS-CoV-2 Gamma lineage (P.1) of the developed ultrathin fibers. The ultrathin fibers had the following diameters and elastic moduli: (i) unmodified crude ultrathin polyamide (PAP) 0.59 μm and 3 MPa, (ii) polyamide Biotech (PAAM) 0.74 μm and 2.2 MPa, and (iii) Amni Virus-Bac OFF polyamide (PAVB) 0.69 μm and 1.06 MPa. The ultrathin PAP fibers showed increased antiviral activity compared to the other ultrathin fibers (PAAM and PAVB). None of the electrospun fibers showed cytotoxicity at the lowest concentration (12.5%). Additionally, hemolysis tests demonstrated a nonhemolytic profile for all fiber groups, reinforcing their biocompatibility and suitability for biomedical applications. The antiviral properties of the electrospun ultrathin PAP fibers, combined with their noncytotoxic and nonhemolytic characteristics, highlight their potential to be used as personal protection against SARS-CoV-2.

Identifiers

PMID39926490
PMCPMC11800004

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.