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Preparation of novel β-CD/P(AA-co-AM) hydrogels by frontal polymerization
In this paper, betaine (Bet) was used as a hydrogen bond acceptor (HBA), and acrylic acid (AA) and acrylamide (AM) were used as hydrogen bond donors (HBD) and mixed to form a deep eutectic solvent (DES). Different concentrations of β-cyclodextrin (β-CD) were dispersed in the DES, and a novel β-CD/P(...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9929618/ https://www.ncbi.nlm.nih.gov/pubmed/36816088 http://dx.doi.org/10.1039/d2ra07649g |
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author | Li, Bin Qin, Haibo Ma, Ming Xu, Xiaojia Zhou, Mengjing Hao, Wenrui Hu, Zhigang |
author_facet | Li, Bin Qin, Haibo Ma, Ming Xu, Xiaojia Zhou, Mengjing Hao, Wenrui Hu, Zhigang |
author_sort | Li, Bin |
collection | PubMed |
description | In this paper, betaine (Bet) was used as a hydrogen bond acceptor (HBA), and acrylic acid (AA) and acrylamide (AM) were used as hydrogen bond donors (HBD) and mixed to form a deep eutectic solvent (DES). Different concentrations of β-cyclodextrin (β-CD) were dispersed in the DES, and a novel β-CD/P(AA-co-AM) hydrogel was prepared by frontal polymerization (FP). The characteristic structure and morphology of the hydrogels were analyzed using Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM), and the properties of the hydrogels were investigated. The results show that the mechanical properties of the hydrogel were improved by β-CD acting as a second cross-linking agent in the polymerization process, thus increasing the cross-link density of the hydrogel. Because the carboxyl groups contained in the acrylic acid dissociate under alkaline conditions, the composite hydrogel shows excellent pH responsiveness under alkaline conditions. Tetracycline hydrochloride was used as a drug model to test the drug loading and drug release performance of the hydrogels. With the increase of β-CD content, the loading capacity of the hydrogels for tetracycline hydrochloride gradually increased. The data of drug release indicated that the hydrogel has good drug delivery performance and has promising applications in drug delivery systems and other areas. |
format | Online Article Text |
id | pubmed-9929618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-99296182023-02-16 Preparation of novel β-CD/P(AA-co-AM) hydrogels by frontal polymerization Li, Bin Qin, Haibo Ma, Ming Xu, Xiaojia Zhou, Mengjing Hao, Wenrui Hu, Zhigang RSC Adv Chemistry In this paper, betaine (Bet) was used as a hydrogen bond acceptor (HBA), and acrylic acid (AA) and acrylamide (AM) were used as hydrogen bond donors (HBD) and mixed to form a deep eutectic solvent (DES). Different concentrations of β-cyclodextrin (β-CD) were dispersed in the DES, and a novel β-CD/P(AA-co-AM) hydrogel was prepared by frontal polymerization (FP). The characteristic structure and morphology of the hydrogels were analyzed using Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM), and the properties of the hydrogels were investigated. The results show that the mechanical properties of the hydrogel were improved by β-CD acting as a second cross-linking agent in the polymerization process, thus increasing the cross-link density of the hydrogel. Because the carboxyl groups contained in the acrylic acid dissociate under alkaline conditions, the composite hydrogel shows excellent pH responsiveness under alkaline conditions. Tetracycline hydrochloride was used as a drug model to test the drug loading and drug release performance of the hydrogels. With the increase of β-CD content, the loading capacity of the hydrogels for tetracycline hydrochloride gradually increased. The data of drug release indicated that the hydrogel has good drug delivery performance and has promising applications in drug delivery systems and other areas. The Royal Society of Chemistry 2023-02-15 /pmc/articles/PMC9929618/ /pubmed/36816088 http://dx.doi.org/10.1039/d2ra07649g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Li, Bin Qin, Haibo Ma, Ming Xu, Xiaojia Zhou, Mengjing Hao, Wenrui Hu, Zhigang Preparation of novel β-CD/P(AA-co-AM) hydrogels by frontal polymerization |
title | Preparation of novel β-CD/P(AA-co-AM) hydrogels by frontal polymerization |
title_full | Preparation of novel β-CD/P(AA-co-AM) hydrogels by frontal polymerization |
title_fullStr | Preparation of novel β-CD/P(AA-co-AM) hydrogels by frontal polymerization |
title_full_unstemmed | Preparation of novel β-CD/P(AA-co-AM) hydrogels by frontal polymerization |
title_short | Preparation of novel β-CD/P(AA-co-AM) hydrogels by frontal polymerization |
title_sort | preparation of novel β-cd/p(aa-co-am) hydrogels by frontal polymerization |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9929618/ https://www.ncbi.nlm.nih.gov/pubmed/36816088 http://dx.doi.org/10.1039/d2ra07649g |
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