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Chitosan Grafted with Thermoresponsive Poly(di(ethylene glycol) Methyl Ether Methacrylate) for Cell Culture Applications

Chitosan is a polysaccharide extracted from animal sources such as crab and shrimp shells. In this work, chitosan films were modified by grafting them with a thermoresponsive polymer, poly(di(ethylene glycol) methyl ether methacrylate) (PMEO(2)MA). The films were modified to introduce functional gro...

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Autores principales: Dasgupta, Natun, Sun, Duo, Gorbet, Maud, Gauthier, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10051194/
https://www.ncbi.nlm.nih.gov/pubmed/36987295
http://dx.doi.org/10.3390/polym15061515
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author Dasgupta, Natun
Sun, Duo
Gorbet, Maud
Gauthier, Mario
author_facet Dasgupta, Natun
Sun, Duo
Gorbet, Maud
Gauthier, Mario
author_sort Dasgupta, Natun
collection PubMed
description Chitosan is a polysaccharide extracted from animal sources such as crab and shrimp shells. In this work, chitosan films were modified by grafting them with a thermoresponsive polymer, poly(di(ethylene glycol) methyl ether methacrylate) (PMEO(2)MA). The films were modified to introduce functional groups useful as reversible addition–fragmentation chain transfer (RAFT) agents. PMEO(2)MA chains were then grown from the films via RAFT polymerization, making the chitosan films thermoresponsive. The degree of substitution of the chitosan-based RAFT agent and the amount of monomer added in the grafting reaction were varied to control the length of the grafted PMEO(2)MA chain segments. The chains were cleaved from the film substrates for characterization using (1)H NMR and a gel permeation chromatography analysis. Temperature-dependent contact angle measurements were used to demonstrate that the hydrophilic–hydrophobic nature of the film surface varied with temperature. Due to the enhanced hydrophobic character of PMEO(2)MA above its lower critical solution temperature (LCST), the ability of PMEO(2)MA-grafted chitosan films to serve as a substrate for cell growth at 37 °C (incubation temperature) was tested. Interactions with cells (fibroblasts, macrophages, and corneal epithelial cells) were assessed. The modified chitosan films supported cell viability and proliferation. As the temperature is lowered to 4 °C (refrigeration temperature, below the LCST), the grafted chitosan films become less hydrophobic, and cell adhesion should decrease, facilitating their removal from the surface. Our results indicated that the cells were detached from the films following a short incubation period at 4 °C, were viable, and retained their ability to proliferate.
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spelling pubmed-100511942023-03-30 Chitosan Grafted with Thermoresponsive Poly(di(ethylene glycol) Methyl Ether Methacrylate) for Cell Culture Applications Dasgupta, Natun Sun, Duo Gorbet, Maud Gauthier, Mario Polymers (Basel) Article Chitosan is a polysaccharide extracted from animal sources such as crab and shrimp shells. In this work, chitosan films were modified by grafting them with a thermoresponsive polymer, poly(di(ethylene glycol) methyl ether methacrylate) (PMEO(2)MA). The films were modified to introduce functional groups useful as reversible addition–fragmentation chain transfer (RAFT) agents. PMEO(2)MA chains were then grown from the films via RAFT polymerization, making the chitosan films thermoresponsive. The degree of substitution of the chitosan-based RAFT agent and the amount of monomer added in the grafting reaction were varied to control the length of the grafted PMEO(2)MA chain segments. The chains were cleaved from the film substrates for characterization using (1)H NMR and a gel permeation chromatography analysis. Temperature-dependent contact angle measurements were used to demonstrate that the hydrophilic–hydrophobic nature of the film surface varied with temperature. Due to the enhanced hydrophobic character of PMEO(2)MA above its lower critical solution temperature (LCST), the ability of PMEO(2)MA-grafted chitosan films to serve as a substrate for cell growth at 37 °C (incubation temperature) was tested. Interactions with cells (fibroblasts, macrophages, and corneal epithelial cells) were assessed. The modified chitosan films supported cell viability and proliferation. As the temperature is lowered to 4 °C (refrigeration temperature, below the LCST), the grafted chitosan films become less hydrophobic, and cell adhesion should decrease, facilitating their removal from the surface. Our results indicated that the cells were detached from the films following a short incubation period at 4 °C, were viable, and retained their ability to proliferate. MDPI 2023-03-18 /pmc/articles/PMC10051194/ /pubmed/36987295 http://dx.doi.org/10.3390/polym15061515 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
Dasgupta, Natun
Sun, Duo
Gorbet, Maud
Gauthier, Mario
Chitosan Grafted with Thermoresponsive Poly(di(ethylene glycol) Methyl Ether Methacrylate) for Cell Culture Applications
title Chitosan Grafted with Thermoresponsive Poly(di(ethylene glycol) Methyl Ether Methacrylate) for Cell Culture Applications
title_full Chitosan Grafted with Thermoresponsive Poly(di(ethylene glycol) Methyl Ether Methacrylate) for Cell Culture Applications
title_fullStr Chitosan Grafted with Thermoresponsive Poly(di(ethylene glycol) Methyl Ether Methacrylate) for Cell Culture Applications
title_full_unstemmed Chitosan Grafted with Thermoresponsive Poly(di(ethylene glycol) Methyl Ether Methacrylate) for Cell Culture Applications
title_short Chitosan Grafted with Thermoresponsive Poly(di(ethylene glycol) Methyl Ether Methacrylate) for Cell Culture Applications
title_sort chitosan grafted with thermoresponsive poly(di(ethylene glycol) methyl ether methacrylate) for cell culture applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10051194/
https://www.ncbi.nlm.nih.gov/pubmed/36987295
http://dx.doi.org/10.3390/polym15061515
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