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Direct and Indirect Cationization of Cellulose Nanocrystals: Structure–Properties Relationship and Virus Capture Activity

[Image: see text] Due to increasing public concern over hygiene, there have been many studies investigating antimicrobial and antiviral agents recently. With the aim of developing biobased virucidal/virus capture agents, we report a chemical modification of the cellulose nanocrystals (CNCs) surface...

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Autores principales: Madani, Maryam, Borandeh, Sedigheh, Teotia, Arun Kumar, Seppälä, Jukka V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565721/
https://www.ncbi.nlm.nih.gov/pubmed/36464847
http://dx.doi.org/10.1021/acs.biomac.2c01045
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author Madani, Maryam
Borandeh, Sedigheh
Teotia, Arun Kumar
Seppälä, Jukka V.
author_facet Madani, Maryam
Borandeh, Sedigheh
Teotia, Arun Kumar
Seppälä, Jukka V.
author_sort Madani, Maryam
collection PubMed
description [Image: see text] Due to increasing public concern over hygiene, there have been many studies investigating antimicrobial and antiviral agents recently. With the aim of developing biobased virucidal/virus capture agents, we report a chemical modification of the cellulose nanocrystals (CNCs) surface with poly(2-dimethylamino) ethyl acrylate) methyl chloride quaternary salt (Q-PDMAEA) to introduce the positively charged functional groups. The surface of CNCs was modified through direct and indirect graft polymerization. Subsequently, the direct and indirect cationization effect on the degree of functionalization, thermal stability, crystallinity, and antiviral activity of CNCs was investigated. Indirect cationization produced the highest degree of polymer grafting, increasing particle size and thermal stability. Further, the modified CNCs were tested for their ability to capture nonenveloped bacteriophages PhiX174 (ΦX174) and MS2. We observed a significant (>4.19 log(10)) reduction in total viral load by specific functionalized CNCs. However, the activity depended on the structure of functional groups, surface charge density, and the type of virus under study. Overall, the direct and indirect cationization of CNC leads to biobased agents with immobilized cationic charge, with good virus capture activity. Such agents can be used for various applications including textiles, packaging, wastewater treatment, etc.
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spelling pubmed-105657212023-10-12 Direct and Indirect Cationization of Cellulose Nanocrystals: Structure–Properties Relationship and Virus Capture Activity Madani, Maryam Borandeh, Sedigheh Teotia, Arun Kumar Seppälä, Jukka V. Biomacromolecules [Image: see text] Due to increasing public concern over hygiene, there have been many studies investigating antimicrobial and antiviral agents recently. With the aim of developing biobased virucidal/virus capture agents, we report a chemical modification of the cellulose nanocrystals (CNCs) surface with poly(2-dimethylamino) ethyl acrylate) methyl chloride quaternary salt (Q-PDMAEA) to introduce the positively charged functional groups. The surface of CNCs was modified through direct and indirect graft polymerization. Subsequently, the direct and indirect cationization effect on the degree of functionalization, thermal stability, crystallinity, and antiviral activity of CNCs was investigated. Indirect cationization produced the highest degree of polymer grafting, increasing particle size and thermal stability. Further, the modified CNCs were tested for their ability to capture nonenveloped bacteriophages PhiX174 (ΦX174) and MS2. We observed a significant (>4.19 log(10)) reduction in total viral load by specific functionalized CNCs. However, the activity depended on the structure of functional groups, surface charge density, and the type of virus under study. Overall, the direct and indirect cationization of CNC leads to biobased agents with immobilized cationic charge, with good virus capture activity. Such agents can be used for various applications including textiles, packaging, wastewater treatment, etc. American Chemical Society 2022-12-05 /pmc/articles/PMC10565721/ /pubmed/36464847 http://dx.doi.org/10.1021/acs.biomac.2c01045 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Madani, Maryam
Borandeh, Sedigheh
Teotia, Arun Kumar
Seppälä, Jukka V.
Direct and Indirect Cationization of Cellulose Nanocrystals: Structure–Properties Relationship and Virus Capture Activity
title Direct and Indirect Cationization of Cellulose Nanocrystals: Structure–Properties Relationship and Virus Capture Activity
title_full Direct and Indirect Cationization of Cellulose Nanocrystals: Structure–Properties Relationship and Virus Capture Activity
title_fullStr Direct and Indirect Cationization of Cellulose Nanocrystals: Structure–Properties Relationship and Virus Capture Activity
title_full_unstemmed Direct and Indirect Cationization of Cellulose Nanocrystals: Structure–Properties Relationship and Virus Capture Activity
title_short Direct and Indirect Cationization of Cellulose Nanocrystals: Structure–Properties Relationship and Virus Capture Activity
title_sort direct and indirect cationization of cellulose nanocrystals: structure–properties relationship and virus capture activity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565721/
https://www.ncbi.nlm.nih.gov/pubmed/36464847
http://dx.doi.org/10.1021/acs.biomac.2c01045
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