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Ultrasensitive (Co)polymers Based on Poly(methacrylamide) Structure with Fining-Tunable pH Responsive Value

Novel pH responsive copolymers with tertiary amine groups were prepared by free radical polymerization with 2-(dialkylamino)ethyl methacrylate monomers. These polymers were pH sensitive with the ability to be responsively fine-tuned in aqueous solution, which was proven through titration, transmitta...

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Detalles Bibliográficos
Autores principales: Fan, Haiming, Li, Po, Li, Wei, Li, Hui, Huang, Xiaonan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222650/
https://www.ncbi.nlm.nih.gov/pubmed/30060442
http://dx.doi.org/10.3390/molecules23081870
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author Fan, Haiming
Li, Po
Li, Wei
Li, Hui
Huang, Xiaonan
author_facet Fan, Haiming
Li, Po
Li, Wei
Li, Hui
Huang, Xiaonan
author_sort Fan, Haiming
collection PubMed
description Novel pH responsive copolymers with tertiary amine groups were prepared by free radical polymerization with 2-(dialkylamino)ethyl methacrylate monomers. These polymers were pH sensitive with the ability to be responsively fine-tuned in aqueous solution, which was proven through titration, transmittance measurements, and proton nuclear magnetic resonance spectroscopy. The polymers were soluble in water at low pH values, induced by electrostatic repulsion between amine groups, and aggregated above their pK(a) value due to the hydrophobic effect of the alkyls. The pH responsive values were precisely tuned from 7.4 to 4.8 by increasing the hydrophobic monomer ratio. Our work provides a novel approach for the development of ultrasensitive pH-responsive polymers for application in biomedical materials.
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spelling pubmed-62226502018-11-13 Ultrasensitive (Co)polymers Based on Poly(methacrylamide) Structure with Fining-Tunable pH Responsive Value Fan, Haiming Li, Po Li, Wei Li, Hui Huang, Xiaonan Molecules Article Novel pH responsive copolymers with tertiary amine groups were prepared by free radical polymerization with 2-(dialkylamino)ethyl methacrylate monomers. These polymers were pH sensitive with the ability to be responsively fine-tuned in aqueous solution, which was proven through titration, transmittance measurements, and proton nuclear magnetic resonance spectroscopy. The polymers were soluble in water at low pH values, induced by electrostatic repulsion between amine groups, and aggregated above their pK(a) value due to the hydrophobic effect of the alkyls. The pH responsive values were precisely tuned from 7.4 to 4.8 by increasing the hydrophobic monomer ratio. Our work provides a novel approach for the development of ultrasensitive pH-responsive polymers for application in biomedical materials. MDPI 2018-07-27 /pmc/articles/PMC6222650/ /pubmed/30060442 http://dx.doi.org/10.3390/molecules23081870 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fan, Haiming
Li, Po
Li, Wei
Li, Hui
Huang, Xiaonan
Ultrasensitive (Co)polymers Based on Poly(methacrylamide) Structure with Fining-Tunable pH Responsive Value
title Ultrasensitive (Co)polymers Based on Poly(methacrylamide) Structure with Fining-Tunable pH Responsive Value
title_full Ultrasensitive (Co)polymers Based on Poly(methacrylamide) Structure with Fining-Tunable pH Responsive Value
title_fullStr Ultrasensitive (Co)polymers Based on Poly(methacrylamide) Structure with Fining-Tunable pH Responsive Value
title_full_unstemmed Ultrasensitive (Co)polymers Based on Poly(methacrylamide) Structure with Fining-Tunable pH Responsive Value
title_short Ultrasensitive (Co)polymers Based on Poly(methacrylamide) Structure with Fining-Tunable pH Responsive Value
title_sort ultrasensitive (co)polymers based on poly(methacrylamide) structure with fining-tunable ph responsive value
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222650/
https://www.ncbi.nlm.nih.gov/pubmed/30060442
http://dx.doi.org/10.3390/molecules23081870
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