Antiviral functionalization of a polypropylene nonwoven textile structure as a self-decontaminating layer for respiratory masks.


Journal

Biomaterials science
ISSN: 2047-4849
Titre abrégé: Biomater Sci
Pays: England
ID NLM: 101593571

Informations de publication

Date de publication:
16 May 2023
Historique:
medline: 18 5 2023
pubmed: 30 3 2023
entrez: 29 3 2023
Statut: epublish

Résumé

The aim of this work was to develop a filtering biocidal polypropylene (PP) nonwoven textile structure to block and inactivate airborne bacteria and viruses. PP filters were functionalized with a cyclodextrin (CD)-polycarboxylic acid-crosslinked polymer (PP-CD) through a pad/dry/curing process, and were then activated by padding in an alkyl dimethyl benzalkonium chloride (ADBAC) solution. The textile finishing process parameters were optimized with the perspective of mass production, considering the threshold temperature necessary for provoking crosslinking and the limitation of the low thermal stability of PP. The use of an aqueous solution containing hydroxypropyl-β-cyclodextrin (HPβCD), 1,2,3,4-butanetetracarboxylic acid (BTCA), ammonium hypophosphite (AH), and a surfactant allowed immobilization of the optimal quantity of cyclodextrin polymer under curing for 5 minutes at 125 °C without affecting the nonwoven PP structure. The presence of CD drastically increased the sorption of ADBAC on the textiles. There was leaching of ADBAC at the first rinsing and then satisfactory fastness at the second and third rinsings, revealing adsorption mechanisms by weak physical interactions, ionic interactions, and inclusion of ADBAC inside the CD cavities. SEM revealed no clogging of the nonwoven pores, nor any increase in the air flow resistance, as evaluated by pressure drop measurements. The filtration efficiency of particulate matter PM

Identifiants

pubmed: 36988417
doi: 10.1039/d2bm01988d
doi:

Substances chimiques

Polypropylenes 0
Antiviral Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3502-3511

Auteurs

Mickael Maton (M)

Univ. Lille, INSERM, CHU Lille, U1008 - Advanced Drug Delivery Systems, Lille, France. nicolas.blanchemain@univ-lille.fr.

Sarah Gabut (S)

Univ. Lille, INSERM, CHU Lille, U1008 - Advanced Drug Delivery Systems, Lille, France. nicolas.blanchemain@univ-lille.fr.
Univ. Lille, CNRS, INRAE, ENSCL UMR 8207, UMET - Unité Matériaux et Transformations, Lille, France. bernard.martel@univ-lille.fr.

Christel Neut (C)

Univ. Lille, INSERM, CHU Lille, U1286, Institute for Translational Research in Inflammation, Lille, France.

Pascal Odou (P)

Univ. Lille, CHU Lille, ULR 7365 - GRITA - Groupe de Recherche sur les formes Injectables et les Technologies Associées, F-59000 Lille, France.

Camille Sacareau (C)

Institut Pasteur de Lille, Unité de Sécurité Microbiologique, 1 rue du Professeur Calmette, Lille, France.

Anthony Pinon (A)

Institut Pasteur de Lille, Unité de Sécurité Microbiologique, 1 rue du Professeur Calmette, Lille, France.

Michèle Vialette (M)

Institut Pasteur de Lille, Unité de Sécurité Microbiologique, 1 rue du Professeur Calmette, Lille, France.

Gaétan Gerber (G)

Bioserenity, 47 bd de l'Hôpital, Paris, France.

Bernard Martel (B)

Univ. Lille, CNRS, INRAE, ENSCL UMR 8207, UMET - Unité Matériaux et Transformations, Lille, France. bernard.martel@univ-lille.fr.

Nicolas Blanchemain (N)

Univ. Lille, INSERM, CHU Lille, U1008 - Advanced Drug Delivery Systems, Lille, France. nicolas.blanchemain@univ-lille.fr.

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Classifications MeSH