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Enzymatically Degradable Mussel-Inspired Adhesive Hydrogel
[Image: see text] Mussel-inspired adhesive hydrogels represent innovative candidate medical sealants or glues. In the present work, we describe an enzyme-degradable mussel-inspired adhesive hydrogel formulation, achieved by incorporating minimal elastase substrate peptide Ala-Ala into the branched p...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235916/ https://www.ncbi.nlm.nih.gov/pubmed/22059927 http://dx.doi.org/10.1021/bm201261d |
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author | Brubaker, Carrie E. Messersmith, Phillip B. |
author_facet | Brubaker, Carrie E. Messersmith, Phillip B. |
author_sort | Brubaker, Carrie E. |
collection | PubMed |
description | [Image: see text] Mussel-inspired adhesive hydrogels represent innovative candidate medical sealants or glues. In the present work, we describe an enzyme-degradable mussel-inspired adhesive hydrogel formulation, achieved by incorporating minimal elastase substrate peptide Ala-Ala into the branched poly(ethylene glycol) (PEG) macromonomer structure. The system takes advantage of neutrophil elastase expression upregulation and secretion from neutrophils upon recruitment to wounded or inflamed tissue. By integrating adhesive degradation behaviors that respond to cellular cues, we expand the functional range of our mussel-inspired adhesive hydrogel platforms. Rapid (<1 min) and simultaneous gelation and adhesion of the proteolytically active, catechol-terminated precursor macromonomer was achieved by addition of sodium periodate oxidant. Rheological analysis and equilibrium swelling studies demonstrated that the hydrogel is appropriate for soft tissue-contacting applications. Notably, hydrogel storage modulus (G′) achieved values on the order of 10 kPa, and strain at failure exceeded 200% strain. Lap shear testing confirmed the material’s adhesive behavior (shear strength: 30.4 ± 3.39 kPa). Although adhesive hydrogel degradation was not observed during short-term (27 h) in vitro treatment with neutrophil elastase, in vivo degradation proceeded over several months following dorsal subcutaneous implantation in mice. This work represents the first example of an enzymatically degradable mussel-inspired adhesive and expands the potential biomedical applications of this family of materials. |
format | Online Article Text |
id | pubmed-3235916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-32359162011-12-12 Enzymatically Degradable Mussel-Inspired Adhesive Hydrogel Brubaker, Carrie E. Messersmith, Phillip B. Biomacromolecules [Image: see text] Mussel-inspired adhesive hydrogels represent innovative candidate medical sealants or glues. In the present work, we describe an enzyme-degradable mussel-inspired adhesive hydrogel formulation, achieved by incorporating minimal elastase substrate peptide Ala-Ala into the branched poly(ethylene glycol) (PEG) macromonomer structure. The system takes advantage of neutrophil elastase expression upregulation and secretion from neutrophils upon recruitment to wounded or inflamed tissue. By integrating adhesive degradation behaviors that respond to cellular cues, we expand the functional range of our mussel-inspired adhesive hydrogel platforms. Rapid (<1 min) and simultaneous gelation and adhesion of the proteolytically active, catechol-terminated precursor macromonomer was achieved by addition of sodium periodate oxidant. Rheological analysis and equilibrium swelling studies demonstrated that the hydrogel is appropriate for soft tissue-contacting applications. Notably, hydrogel storage modulus (G′) achieved values on the order of 10 kPa, and strain at failure exceeded 200% strain. Lap shear testing confirmed the material’s adhesive behavior (shear strength: 30.4 ± 3.39 kPa). Although adhesive hydrogel degradation was not observed during short-term (27 h) in vitro treatment with neutrophil elastase, in vivo degradation proceeded over several months following dorsal subcutaneous implantation in mice. This work represents the first example of an enzymatically degradable mussel-inspired adhesive and expands the potential biomedical applications of this family of materials. American Chemical Society 2011-11-07 2011-12-12 /pmc/articles/PMC3235916/ /pubmed/22059927 http://dx.doi.org/10.1021/bm201261d Text en Copyright © 2011 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Brubaker, Carrie E. Messersmith, Phillip B. Enzymatically Degradable Mussel-Inspired Adhesive Hydrogel |
title | Enzymatically Degradable
Mussel-Inspired Adhesive
Hydrogel |
title_full | Enzymatically Degradable
Mussel-Inspired Adhesive
Hydrogel |
title_fullStr | Enzymatically Degradable
Mussel-Inspired Adhesive
Hydrogel |
title_full_unstemmed | Enzymatically Degradable
Mussel-Inspired Adhesive
Hydrogel |
title_short | Enzymatically Degradable
Mussel-Inspired Adhesive
Hydrogel |
title_sort | enzymatically degradable
mussel-inspired adhesive
hydrogel |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235916/ https://www.ncbi.nlm.nih.gov/pubmed/22059927 http://dx.doi.org/10.1021/bm201261d |
work_keys_str_mv | AT brubakercarriee enzymaticallydegradablemusselinspiredadhesivehydrogel AT messersmithphillipb enzymaticallydegradablemusselinspiredadhesivehydrogel |