Inhibition of influenza virus infection in mice by pulmonary administration of a spray dried antiviral.

Aerosol science Antiviral drugs Broad spectrum Cyclodextrin Dry powder inhaler Entry inhibitor In vivo Influenza virus Inhalation Intratracheal administration Pulmonary drug delivery Respiratory viruses Rodents Spray drying

Journal

European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
ISSN: 1873-3441
Titre abrégé: Eur J Pharm Biopharm
Pays: Netherlands
ID NLM: 9109778

Informations de publication

Date de publication:
18 Sep 2024
Historique:
received: 05 04 2024
revised: 11 08 2024
accepted: 17 09 2024
medline: 21 9 2024
pubmed: 21 9 2024
entrez: 20 9 2024
Statut: aheadofprint

Résumé

Increasing resistance to antiviral drugs approved for the treatment of influenza urges the development of novel compounds. Ideally, this should be complemented by a careful consideration of the administration route. 6'siallyllactosamine-functionalized β-cyclodextrin (CD-6'SLN) is a novel entry inhibitor that acts as a mimic of the primary attachment receptor of influenza, sialic acid. In this study, we aimed to develop a dry powder formulation of CD-6'SLN to assess its in vivo antiviral activity after administration via the pulmonary route. By means of spray drying the compound together with trileucine, a dispersion enhancer, we created a powder that retained the antiviral effect of the drug, remained stable under elevated temperature conditions and performed well in a dry powder inhaler. To test the efficacy of the dry powder drug against influenza infection in vivo, infected mice were treated with CD-6'SLN using an aerosol generator that allowed for the controlled administration of powder formulations to the lungs of mice. CD-6'SLN was effective in mitigating the course of the disease compared to the control groups, reflected by lower disease activity scores and by the prevention of virus-induced IL-6 production. Our data show that CD-6'SLN can be formulated as a stable dry powder that is suitable for use in a dry powder inhaler and is effective when administered via the pulmonary route to influenza-infected mice.

Identifiants

pubmed: 39303952
pii: S0939-6411(24)00333-3
doi: 10.1016/j.ejpb.2024.114507
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

114507

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Francesco Stellacci is inventor on patent number WO 2018/015465 A1 − Virucidal compounds and uses thereof. Francesco Stellacci and Paulo H. Jacob Silva are co-founders of Asterivir, a start-up company that focuses on developing novel antivirals. The employer of Henderik W. Frijlink holds a license agreement with PureIMS on the Twincer and Cyclops dry powder inhalers. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; nor in the writing of the manuscript or in the decision to submit the article for publication.

Auteurs

Rick Heida (R)

Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, 9713 AV Groningen, the Netherlands.

Paulo H Jacob Silva (PH)

Institute of Materials, Ecole Polytechnique Fédérale de Lausanne, Lausanne 1015 Switzerland.

Renate Akkerman (R)

Department of Medical Microbiology and Infection Prevention, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, the Netherlands.

Jill Moser (J)

Department of Critical Care, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9700 RB Groningen, the Netherlands; Department of Pathology and Medical Biology, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9700 RB Groningen, the Netherlands.

Jacqueline de Vries-Idema (J)

Department of Medical Microbiology and Infection Prevention, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, the Netherlands.

Aurélien Bornet (A)

Institute of Materials, Ecole Polytechnique Fédérale de Lausanne, Lausanne 1015 Switzerland.

Sujeet Pawar (S)

Institute of Materials, Ecole Polytechnique Fédérale de Lausanne, Lausanne 1015 Switzerland.

Francesco Stellacci (F)

Institute of Materials, Ecole Polytechnique Fédérale de Lausanne, Lausanne 1015 Switzerland.

Henderik W Frijlink (HW)

Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, 9713 AV Groningen, the Netherlands.

Anke L W Huckriede (ALW)

Department of Medical Microbiology and Infection Prevention, University of Groningen, University Medical Center Groningen, 9700 RB Groningen, the Netherlands.

Wouter L J Hinrichs (WLJ)

Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, 9713 AV Groningen, the Netherlands. Electronic address: w.l.j.hinrichs@rug.nl.

Classifications MeSH