Piercing of the Human Parainfluenza Virus by Nanostructured Surfaces.

antiviral surfaces biointerfaces biomimetic surfaces mechanisms of antiviral activity nanostructured surfaces virus−surface interactions

Journal

ACS nano
ISSN: 1936-086X
Titre abrégé: ACS Nano
Pays: United States
ID NLM: 101313589

Informations de publication

Date de publication:
21 Dec 2023
Historique:
medline: 21 12 2023
pubmed: 21 12 2023
entrez: 21 12 2023
Statut: aheadofprint

Résumé

This paper presents a comprehensive experimental and theoretical investigation into the antiviral properties of nanostructured surfaces and explains the underlying virucidal mechanism. We used reactive ion etching to fabricate silicon (Si) surfaces featuring an array of sharp nanospikes with an approximate tip diameter of 2 nm and a height of 290 nm. The nanospike surfaces exhibited a 1.5 log reduction in infectivity of human parainfluenza virus type 3 (hPIV-3) after 6 h, a substantially enhanced efficiency, compared to that of smooth Si. Theoretical modeling of the virus-nanospike interactions determined the virucidal action of the nanostructured substrata to be associated with the ability of the sharp nanofeatures to effectively penetrate the viral envelope, resulting in the loss of viral infectivity. Our research highlights the significance of the potential application of nanostructured surfaces in combating the spread of viruses and bacteria. Notably, our study provides valuable insights into the design and optimization of antiviral surfaces with a particular emphasis on the crucial role played by sharp nanofeatures in maximizing their effectiveness.

Identifiants

pubmed: 38127731
doi: 10.1021/acsnano.3c07099
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Samson W L Mah (SWL)

School of Science, STEM College, RMIT University, Melbourne, Victoria 3000, Australia.
CSIRO Manufacturing, Clayton, Victoria 3168, Australia.

Denver P Linklater (DP)

School of Science, STEM College, RMIT University, Melbourne, Victoria 3000, Australia.
Department of Biomedical Engineering, Graeme Clarke Institute, The University of Melbourne, Parkville, Victoria 3010, Australia.

Vassil Tzanov (V)

Departament de Química Física i Inorgànica, Universitat Rovira i Virgili, C/Marcel.lí Domingo s/n, Tarragona 43007, Spain.

Phuc H Le (PH)

School of Science, STEM College, RMIT University, Melbourne, Victoria 3000, Australia.

Chaitali Dekiwadia (C)

RMIT Microscopy and Microanalysis Facility, STEM College,RMIT University, Melbourne, Victoria 3000, Australia.

Edwin Mayes (E)

RMIT Microscopy and Microanalysis Facility, STEM College,RMIT University, Melbourne, Victoria 3000, Australia.

Ranya Simons (R)

CSIRO Manufacturing, Clayton, Victoria 3168, Australia.

Daniel J Eyckens (DJ)

CSIRO Manufacturing, Clayton, Victoria 3168, Australia.

Graeme Moad (G)

CSIRO Manufacturing, Clayton, Victoria 3168, Australia.

Soichiro Saita (S)

The KAITEKI Institute Inc., Chiyoda-ku, Tokyo 100-8251, Japan.

Saulius Joudkazis (S)

Optical Science Centre, Swinburne University of Technology, Hawthorn, Melbourne, Victoria 3122, Australia.

David A Jans (DA)

Nuclear Signalling Laboratory, Department of Biochemistry and Molecular Biology, Monash University, Monash, Victoria 3800, Australia.

Vladimir A Baulin (VA)

Departament de Química Física i Inorgànica, Universitat Rovira i Virgili, C/Marcel.lí Domingo s/n, Tarragona 43007, Spain.

Natalie A Borg (NA)

School of Health and Biomedical Sciences, RMIT University, Bundoora, Victoria 3083, Australia.

Elena P Ivanova (EP)

School of Science, STEM College, RMIT University, Melbourne, Victoria 3000, Australia.

Classifications MeSH