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Exploiting Urazole’s Acidity for Fabrication of Hydrogels and Ion-Exchange Materials
In this study, the acidity of urazole (pKa 5–6) was exploited to fabricate a hydrogel in two simple and scalable steps. Commercially available poly(hexamethylene)diisocyanate was used as a precursor to synthesize an urazole containing gel. The formation of urazole was confirmed by FT-IR and (1)H-NMR...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701905/ https://www.ncbi.nlm.nih.gov/pubmed/34940320 http://dx.doi.org/10.3390/gels7040261 |
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author | Hanay, Saltuk B. Fallah, Ali Senturk, Efsun Yetim, Zeliha Afghah, Ferdows Yilmaz, Hulya Culha, Mustafa Koc, Bahattin Zarrabi, Ali Varma, Rajender S. |
author_facet | Hanay, Saltuk B. Fallah, Ali Senturk, Efsun Yetim, Zeliha Afghah, Ferdows Yilmaz, Hulya Culha, Mustafa Koc, Bahattin Zarrabi, Ali Varma, Rajender S. |
author_sort | Hanay, Saltuk B. |
collection | PubMed |
description | In this study, the acidity of urazole (pKa 5–6) was exploited to fabricate a hydrogel in two simple and scalable steps. Commercially available poly(hexamethylene)diisocyanate was used as a precursor to synthesize an urazole containing gel. The formation of urazole was confirmed by FT-IR and (1)H-NMR spectroscopy. The hydrogel was characterized by microscopy imaging as well as spectroscopic and thermo-gravimetric analyses. Mechanical analysis and cell viability tests were performed for its initial biocompatibility evaluation. The prepared hydrogel is a highly porous hydrogel with a Young’s modulus of 0.91 MPa, has a swelling ratio of 87%, and is capable of exchanging ions in a medium. Finally, a general strategy was demonstrated to embed urazole groups directly into a crosslinked material. |
format | Online Article Text |
id | pubmed-8701905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87019052021-12-24 Exploiting Urazole’s Acidity for Fabrication of Hydrogels and Ion-Exchange Materials Hanay, Saltuk B. Fallah, Ali Senturk, Efsun Yetim, Zeliha Afghah, Ferdows Yilmaz, Hulya Culha, Mustafa Koc, Bahattin Zarrabi, Ali Varma, Rajender S. Gels Article In this study, the acidity of urazole (pKa 5–6) was exploited to fabricate a hydrogel in two simple and scalable steps. Commercially available poly(hexamethylene)diisocyanate was used as a precursor to synthesize an urazole containing gel. The formation of urazole was confirmed by FT-IR and (1)H-NMR spectroscopy. The hydrogel was characterized by microscopy imaging as well as spectroscopic and thermo-gravimetric analyses. Mechanical analysis and cell viability tests were performed for its initial biocompatibility evaluation. The prepared hydrogel is a highly porous hydrogel with a Young’s modulus of 0.91 MPa, has a swelling ratio of 87%, and is capable of exchanging ions in a medium. Finally, a general strategy was demonstrated to embed urazole groups directly into a crosslinked material. MDPI 2021-12-13 /pmc/articles/PMC8701905/ /pubmed/34940320 http://dx.doi.org/10.3390/gels7040261 Text en © 2021 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 Hanay, Saltuk B. Fallah, Ali Senturk, Efsun Yetim, Zeliha Afghah, Ferdows Yilmaz, Hulya Culha, Mustafa Koc, Bahattin Zarrabi, Ali Varma, Rajender S. Exploiting Urazole’s Acidity for Fabrication of Hydrogels and Ion-Exchange Materials |
title | Exploiting Urazole’s Acidity for Fabrication of Hydrogels and Ion-Exchange Materials |
title_full | Exploiting Urazole’s Acidity for Fabrication of Hydrogels and Ion-Exchange Materials |
title_fullStr | Exploiting Urazole’s Acidity for Fabrication of Hydrogels and Ion-Exchange Materials |
title_full_unstemmed | Exploiting Urazole’s Acidity for Fabrication of Hydrogels and Ion-Exchange Materials |
title_short | Exploiting Urazole’s Acidity for Fabrication of Hydrogels and Ion-Exchange Materials |
title_sort | exploiting urazole’s acidity for fabrication of hydrogels and ion-exchange materials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701905/ https://www.ncbi.nlm.nih.gov/pubmed/34940320 http://dx.doi.org/10.3390/gels7040261 |
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