Cargando…
Connecting the Stimuli-Responsive Rheology of Biopolymer Hydrogels to Underlying Hydrogen-Bonding Interactions
[Image: see text] Many biopolymer hydrogels are environmentally responsive because they are held together by physical associations that depend on pH and temperature. Here, we investigate how the pH and temperature responses of the rheology of hyaluronan hydrogels are connected to the underlying mole...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735748/ https://www.ncbi.nlm.nih.gov/pubmed/33335340 http://dx.doi.org/10.1021/acs.macromol.0c01742 |
_version_ | 1783622694781059072 |
---|---|
author | Giubertoni, Giulia Burla, Federica Bakker, Huib J. Koenderink, Gijsje H. |
author_facet | Giubertoni, Giulia Burla, Federica Bakker, Huib J. Koenderink, Gijsje H. |
author_sort | Giubertoni, Giulia |
collection | PubMed |
description | [Image: see text] Many biopolymer hydrogels are environmentally responsive because they are held together by physical associations that depend on pH and temperature. Here, we investigate how the pH and temperature responses of the rheology of hyaluronan hydrogels are connected to the underlying molecular interactions. Hyaluronan is an essential structural biopolymer in the human body with many applications in biomedicine. Using two-dimensional infrared spectroscopy, we show that hyaluronan chains become connected by hydrogen bonds when the pH is changed from 7.0 to 2.5 and that the bond density at pH 2.5 is independent of temperature. Temperature-dependent rheology measurements show that because of this hydrogen bonding the stress relaxation at pH 2.5 is strongly slowed down in comparison to pH 7.0, consistent with the sticky reptation model of associative polymers. From the flow activation energy, we conclude that each polymer is cross-linked by multiple (5–15) hydrogen bonds to others, causing slow macroscopic stress relaxation, despite the short time scale of breaking and reformation of each individual hydrogen bond. Our findings can aid the design of stimuli-responsive hydrogels with tailored viscoelastic properties for biomedical applications. |
format | Online Article Text |
id | pubmed-7735748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77357482020-12-15 Connecting the Stimuli-Responsive Rheology of Biopolymer Hydrogels to Underlying Hydrogen-Bonding Interactions Giubertoni, Giulia Burla, Federica Bakker, Huib J. Koenderink, Gijsje H. Macromolecules [Image: see text] Many biopolymer hydrogels are environmentally responsive because they are held together by physical associations that depend on pH and temperature. Here, we investigate how the pH and temperature responses of the rheology of hyaluronan hydrogels are connected to the underlying molecular interactions. Hyaluronan is an essential structural biopolymer in the human body with many applications in biomedicine. Using two-dimensional infrared spectroscopy, we show that hyaluronan chains become connected by hydrogen bonds when the pH is changed from 7.0 to 2.5 and that the bond density at pH 2.5 is independent of temperature. Temperature-dependent rheology measurements show that because of this hydrogen bonding the stress relaxation at pH 2.5 is strongly slowed down in comparison to pH 7.0, consistent with the sticky reptation model of associative polymers. From the flow activation energy, we conclude that each polymer is cross-linked by multiple (5–15) hydrogen bonds to others, causing slow macroscopic stress relaxation, despite the short time scale of breaking and reformation of each individual hydrogen bond. Our findings can aid the design of stimuli-responsive hydrogels with tailored viscoelastic properties for biomedical applications. American Chemical Society 2020-11-18 2020-12-08 /pmc/articles/PMC7735748/ /pubmed/33335340 http://dx.doi.org/10.1021/acs.macromol.0c01742 Text en © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Giubertoni, Giulia Burla, Federica Bakker, Huib J. Koenderink, Gijsje H. Connecting the Stimuli-Responsive Rheology of Biopolymer Hydrogels to Underlying Hydrogen-Bonding Interactions |
title | Connecting the Stimuli-Responsive Rheology of Biopolymer
Hydrogels to Underlying Hydrogen-Bonding Interactions |
title_full | Connecting the Stimuli-Responsive Rheology of Biopolymer
Hydrogels to Underlying Hydrogen-Bonding Interactions |
title_fullStr | Connecting the Stimuli-Responsive Rheology of Biopolymer
Hydrogels to Underlying Hydrogen-Bonding Interactions |
title_full_unstemmed | Connecting the Stimuli-Responsive Rheology of Biopolymer
Hydrogels to Underlying Hydrogen-Bonding Interactions |
title_short | Connecting the Stimuli-Responsive Rheology of Biopolymer
Hydrogels to Underlying Hydrogen-Bonding Interactions |
title_sort | connecting the stimuli-responsive rheology of biopolymer
hydrogels to underlying hydrogen-bonding interactions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735748/ https://www.ncbi.nlm.nih.gov/pubmed/33335340 http://dx.doi.org/10.1021/acs.macromol.0c01742 |
work_keys_str_mv | AT giubertonigiulia connectingthestimuliresponsiverheologyofbiopolymerhydrogelstounderlyinghydrogenbondinginteractions AT burlafederica connectingthestimuliresponsiverheologyofbiopolymerhydrogelstounderlyinghydrogenbondinginteractions AT bakkerhuibj connectingthestimuliresponsiverheologyofbiopolymerhydrogelstounderlyinghydrogenbondinginteractions AT koenderinkgijsjeh connectingthestimuliresponsiverheologyofbiopolymerhydrogelstounderlyinghydrogenbondinginteractions |