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Structure and Dynamics of a Temperature-Sensitive Hydrogel
[Image: see text] Polyisocyanotripeptides (TriPIC) are biomimetic polymers which consist of a β-helical backbone stabilized by hydrogen bonds between amide groups. Their oligoethylene glycol side chains give aqueous TriPIC solutions a thermoresponsive behavior: at 50 °C the solution becomes a hydrog...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327313/ https://www.ncbi.nlm.nih.gov/pubmed/34279949 http://dx.doi.org/10.1021/acs.jpcb.1c03121 |
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author | van Dam, Eliane P. Yuan, Hongbo Kouwer, Paul H. J. Bakker, Huib J. |
author_facet | van Dam, Eliane P. Yuan, Hongbo Kouwer, Paul H. J. Bakker, Huib J. |
author_sort | van Dam, Eliane P. |
collection | PubMed |
description | [Image: see text] Polyisocyanotripeptides (TriPIC) are biomimetic polymers which consist of a β-helical backbone stabilized by hydrogen bonds between amide groups. Their oligoethylene glycol side chains give aqueous TriPIC solutions a thermoresponsive behavior: at 50 °C the solution becomes a hydrogel. In this paper we study the molecular structure and water dynamics of TriPIC aqueous solutions while undergoing gelation using FT-IR spectroscopy and polarization-resolved femtosecond infrared spectroscopy (fs-IR). We find evidence that the oligoethylene glycol side chains trap part of the water molecules upon gel formation, and we propose that the interaction between the oligoethylene glycol side chains and water plays an essential role in the bundling of the polymers and thus in the formation of a hydrogel. |
format | Online Article Text |
id | pubmed-8327313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-83273132021-08-03 Structure and Dynamics of a Temperature-Sensitive Hydrogel van Dam, Eliane P. Yuan, Hongbo Kouwer, Paul H. J. Bakker, Huib J. J Phys Chem B [Image: see text] Polyisocyanotripeptides (TriPIC) are biomimetic polymers which consist of a β-helical backbone stabilized by hydrogen bonds between amide groups. Their oligoethylene glycol side chains give aqueous TriPIC solutions a thermoresponsive behavior: at 50 °C the solution becomes a hydrogel. In this paper we study the molecular structure and water dynamics of TriPIC aqueous solutions while undergoing gelation using FT-IR spectroscopy and polarization-resolved femtosecond infrared spectroscopy (fs-IR). We find evidence that the oligoethylene glycol side chains trap part of the water molecules upon gel formation, and we propose that the interaction between the oligoethylene glycol side chains and water plays an essential role in the bundling of the polymers and thus in the formation of a hydrogel. American Chemical Society 2021-07-19 2021-07-29 /pmc/articles/PMC8327313/ /pubmed/34279949 http://dx.doi.org/10.1021/acs.jpcb.1c03121 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | van Dam, Eliane P. Yuan, Hongbo Kouwer, Paul H. J. Bakker, Huib J. Structure and Dynamics of a Temperature-Sensitive Hydrogel |
title | Structure and Dynamics of a Temperature-Sensitive
Hydrogel |
title_full | Structure and Dynamics of a Temperature-Sensitive
Hydrogel |
title_fullStr | Structure and Dynamics of a Temperature-Sensitive
Hydrogel |
title_full_unstemmed | Structure and Dynamics of a Temperature-Sensitive
Hydrogel |
title_short | Structure and Dynamics of a Temperature-Sensitive
Hydrogel |
title_sort | structure and dynamics of a temperature-sensitive
hydrogel |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327313/ https://www.ncbi.nlm.nih.gov/pubmed/34279949 http://dx.doi.org/10.1021/acs.jpcb.1c03121 |
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