Augmented antiviral activity of chlorhexidine gluconate on herpes simplex virus type 1, H1N1 influenza A virus, and adenovirus in combination with salicylic acid.


Journal

Archives of virology
ISSN: 1432-8798
Titre abrégé: Arch Virol
Pays: Austria
ID NLM: 7506870

Informations de publication

Date de publication:
30 Nov 2023
Historique:
received: 25 02 2023
accepted: 18 09 2023
medline: 4 12 2023
pubmed: 1 12 2023
entrez: 30 11 2023
Statut: epublish

Résumé

The excessive usage of chlorhexidine gluconate (CHG) as a broad-spectrum antimicrobial reagent can have a negative impact on the environment and on human health. The aim of this study was to investigate the effectiveness of some plant-derived compounds in reducing the CHG concentration required to exert its antiviral activity. Antiviral assays were conducted according to EN 14476 (2019) against herpes simplex virus type 1 (HSV-1), H1N1 influenza A virus, and adenovirus type 5 (Ad-5) as enveloped and non-enveloped viral models to assess the synergistic interaction of CHG and natural additive compounds. The effective concentration of 0.247 mM CHG against HSV-1 was decreased tenfold in combination with 0.0125 mM salicylic acid, with a titer reduction of 1.47 ⋅ 10 Our supplemented CHG formulation showed immediate antiviral effectiveness, which is important for management of the infections. CHG can be combined with salicylic acid to exhibit synergistic antiviral activity at lower concentrations and reduce the time required for inactivation. Furthermore, in the presence of interfering substances, the combination has higher antiviral activity than CHG alone.

Sections du résumé

BACKGROUND BACKGROUND
The excessive usage of chlorhexidine gluconate (CHG) as a broad-spectrum antimicrobial reagent can have a negative impact on the environment and on human health. The aim of this study was to investigate the effectiveness of some plant-derived compounds in reducing the CHG concentration required to exert its antiviral activity.
METHODS METHODS
Antiviral assays were conducted according to EN 14476 (2019) against herpes simplex virus type 1 (HSV-1), H1N1 influenza A virus, and adenovirus type 5 (Ad-5) as enveloped and non-enveloped viral models to assess the synergistic interaction of CHG and natural additive compounds.
RESULTS RESULTS
The effective concentration of 0.247 mM CHG against HSV-1 was decreased tenfold in combination with 0.0125 mM salicylic acid, with a titer reduction of 1.47 ⋅ 10
CONCLUSION CONCLUSIONS
Our supplemented CHG formulation showed immediate antiviral effectiveness, which is important for management of the infections. CHG can be combined with salicylic acid to exhibit synergistic antiviral activity at lower concentrations and reduce the time required for inactivation. Furthermore, in the presence of interfering substances, the combination has higher antiviral activity than CHG alone.

Identifiants

pubmed: 38036721
doi: 10.1007/s00705-023-05932-1
pii: 10.1007/s00705-023-05932-1
doi:

Substances chimiques

chlorhexidine gluconate MOR84MUD8E
Salicylic Acid O414PZ4LPZ
Antiviral Agents 0
Anti-Infective Agents, Local 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

302

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.

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Auteurs

Niloofar Jamshidinia (N)

Pharmaceutical Biotechnology Lab, School of Biology and Center of Excellence in Phylogeny of Living Organisms, College of Science, University of Tehran, Tehran, 14155-6455, Iran.

Fatemeh Saadatpour (F)

Molecular Virology Lab, Department of Microbiology, School of Biology, College of Science, University of Tehran, Tehran, 14155-6455, Iran.

Ehsan Arefian (E)

Molecular Virology Lab, Department of Microbiology, School of Biology, College of Science, University of Tehran, Tehran, 14155-6455, Iran. arefian@ut.ac.ir.

Fatemeh Mohammadipanah (F)

Pharmaceutical Biotechnology Lab, School of Biology and Center of Excellence in Phylogeny of Living Organisms, College of Science, University of Tehran, Tehran, 14155-6455, Iran. fmohammadipanah@ut.ac.ir.

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