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A Simple Method for Synthesis of Chitosan Nanoparticles with Ionic Gelation and Homogenization
Chitosan nanoparticles (CNPs) are known to have great utility in many fields (pharmaceutical, agricultural, food industry, wastewater treatment, etc.). In this study we aimed to synthesize sub-100 nm CNPs as a precursor of new biopolymer-based virus surrogates for water applications. We present a si...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254159/ https://www.ncbi.nlm.nih.gov/pubmed/37298804 http://dx.doi.org/10.3390/molecules28114328 |
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author | Van Bavel, Nicolas Issler, Travis Pang, Liping Anikovskiy, Max Prenner, Elmar J. |
author_facet | Van Bavel, Nicolas Issler, Travis Pang, Liping Anikovskiy, Max Prenner, Elmar J. |
author_sort | Van Bavel, Nicolas |
collection | PubMed |
description | Chitosan nanoparticles (CNPs) are known to have great utility in many fields (pharmaceutical, agricultural, food industry, wastewater treatment, etc.). In this study we aimed to synthesize sub-100 nm CNPs as a precursor of new biopolymer-based virus surrogates for water applications. We present a simple yet efficient synthesis procedure for obtaining high yield, monodisperse CNPs with size 68–77 nm. The CNPs were synthesized by ionic gelation using low molecular weight chitosan (deacetylation 75–85%) and tripolyphosphate as crosslinker, under rigorous homogenization to decrease size and increase uniformity, and purified by passing through 0.1 μm polyethersulfone syringe filters. The CNPs were characterized using dynamic light scattering, tunable resistive pulse sensing, and scanning electron microscopy. We demonstrate reproducibility of this method at two separate facilities. The effects of pH, ionic strength and three different purification methods on the size and polydispersity of CNP formation were examined. Larger CNPs (95–219) were produced under ionic strength and pH controls, and when purified using ultracentrifugation or size exclusion chromatography. Smaller CNPs (68–77 nm) were formulated using homogenization and filtration, and could readily interact with negatively charge proteins and DNA, making them an ideal precursor for the development of DNA-labelled, protein-coated virus surrogates for environmental water applications. |
format | Online Article Text |
id | pubmed-10254159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102541592023-06-10 A Simple Method for Synthesis of Chitosan Nanoparticles with Ionic Gelation and Homogenization Van Bavel, Nicolas Issler, Travis Pang, Liping Anikovskiy, Max Prenner, Elmar J. Molecules Article Chitosan nanoparticles (CNPs) are known to have great utility in many fields (pharmaceutical, agricultural, food industry, wastewater treatment, etc.). In this study we aimed to synthesize sub-100 nm CNPs as a precursor of new biopolymer-based virus surrogates for water applications. We present a simple yet efficient synthesis procedure for obtaining high yield, monodisperse CNPs with size 68–77 nm. The CNPs were synthesized by ionic gelation using low molecular weight chitosan (deacetylation 75–85%) and tripolyphosphate as crosslinker, under rigorous homogenization to decrease size and increase uniformity, and purified by passing through 0.1 μm polyethersulfone syringe filters. The CNPs were characterized using dynamic light scattering, tunable resistive pulse sensing, and scanning electron microscopy. We demonstrate reproducibility of this method at two separate facilities. The effects of pH, ionic strength and three different purification methods on the size and polydispersity of CNP formation were examined. Larger CNPs (95–219) were produced under ionic strength and pH controls, and when purified using ultracentrifugation or size exclusion chromatography. Smaller CNPs (68–77 nm) were formulated using homogenization and filtration, and could readily interact with negatively charge proteins and DNA, making them an ideal precursor for the development of DNA-labelled, protein-coated virus surrogates for environmental water applications. MDPI 2023-05-25 /pmc/articles/PMC10254159/ /pubmed/37298804 http://dx.doi.org/10.3390/molecules28114328 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Van Bavel, Nicolas Issler, Travis Pang, Liping Anikovskiy, Max Prenner, Elmar J. A Simple Method for Synthesis of Chitosan Nanoparticles with Ionic Gelation and Homogenization |
title | A Simple Method for Synthesis of Chitosan Nanoparticles with Ionic Gelation and Homogenization |
title_full | A Simple Method for Synthesis of Chitosan Nanoparticles with Ionic Gelation and Homogenization |
title_fullStr | A Simple Method for Synthesis of Chitosan Nanoparticles with Ionic Gelation and Homogenization |
title_full_unstemmed | A Simple Method for Synthesis of Chitosan Nanoparticles with Ionic Gelation and Homogenization |
title_short | A Simple Method for Synthesis of Chitosan Nanoparticles with Ionic Gelation and Homogenization |
title_sort | simple method for synthesis of chitosan nanoparticles with ionic gelation and homogenization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254159/ https://www.ncbi.nlm.nih.gov/pubmed/37298804 http://dx.doi.org/10.3390/molecules28114328 |
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