Hybrid polyurea elastomers with enzymatic degradation and tunable mechanical properties

Herein, we report on the synthesis and characterization of enzymatically labile polyureas for use as a tissue-engineered ligament scaffold. Polyureas were selected due to their excellent tensile properties, fatigue resistance, and highly tunable nature. Incorporation of a collagenase-sensitive pepti...

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Main Authors: Nicholas A Sears, Geraldine Pena-Galea, Stacy N Cereceres, Elizabeth Cosgriff-Hernandez
Format: Article
Language:English
Published: SAGE Publishing 2016-12-01
Series:Journal of Tissue Engineering
Online Access:https://doi.org/10.1177/2041731416679363
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spelling doaj-b5852b0971734e8ba7b900e93110f9602020-11-25T03:36:31ZengSAGE PublishingJournal of Tissue Engineering2041-73142016-12-01710.1177/204173141667936310.1177_2041731416679363Hybrid polyurea elastomers with enzymatic degradation and tunable mechanical propertiesNicholas A SearsGeraldine Pena-GaleaStacy N CereceresElizabeth Cosgriff-HernandezHerein, we report on the synthesis and characterization of enzymatically labile polyureas for use as a tissue-engineered ligament scaffold. Polyureas were selected due to their excellent tensile properties, fatigue resistance, and highly tunable nature. Incorporation of a collagenase-sensitive peptide into the backbone of the polyurea provided a means to confer cell-responsive degradation to the synthetic polymer. Chemical, morphological, and mechanical testing were used to confirm incorporation of the peptide and characterize polyurea films. Notably, the incorporation of the peptide resulted in an increase in modulus, elongation, and tensile strength. This was attributed to an increase in phase mixing and an increase in hydrogen bonding between the hard and soft segments. Candidate polyureas with varying levels of collagen-mimetic peptide (0%, 10%, 20%) were then subjected to degradation in collagenase media or buffer at 37°C over 4 weeks. Statistically significant decreases in strength and elongation were observed in polyureas with 20% peptide content after collagenase treatment, whereas specimens in phosphate-buffered saline showed no statistically significant difference. These observations confirmed that enzyme-specific degradation was conferred to the polyurea. Overall, these polyureas hold great promise as a material for ligament reconstruction due to the promising mechanical properties and potential for cell-mediated degradation.https://doi.org/10.1177/2041731416679363
collection DOAJ
language English
format Article
sources DOAJ
author Nicholas A Sears
Geraldine Pena-Galea
Stacy N Cereceres
Elizabeth Cosgriff-Hernandez
spellingShingle Nicholas A Sears
Geraldine Pena-Galea
Stacy N Cereceres
Elizabeth Cosgriff-Hernandez
Hybrid polyurea elastomers with enzymatic degradation and tunable mechanical properties
Journal of Tissue Engineering
author_facet Nicholas A Sears
Geraldine Pena-Galea
Stacy N Cereceres
Elizabeth Cosgriff-Hernandez
author_sort Nicholas A Sears
title Hybrid polyurea elastomers with enzymatic degradation and tunable mechanical properties
title_short Hybrid polyurea elastomers with enzymatic degradation and tunable mechanical properties
title_full Hybrid polyurea elastomers with enzymatic degradation and tunable mechanical properties
title_fullStr Hybrid polyurea elastomers with enzymatic degradation and tunable mechanical properties
title_full_unstemmed Hybrid polyurea elastomers with enzymatic degradation and tunable mechanical properties
title_sort hybrid polyurea elastomers with enzymatic degradation and tunable mechanical properties
publisher SAGE Publishing
series Journal of Tissue Engineering
issn 2041-7314
publishDate 2016-12-01
description Herein, we report on the synthesis and characterization of enzymatically labile polyureas for use as a tissue-engineered ligament scaffold. Polyureas were selected due to their excellent tensile properties, fatigue resistance, and highly tunable nature. Incorporation of a collagenase-sensitive peptide into the backbone of the polyurea provided a means to confer cell-responsive degradation to the synthetic polymer. Chemical, morphological, and mechanical testing were used to confirm incorporation of the peptide and characterize polyurea films. Notably, the incorporation of the peptide resulted in an increase in modulus, elongation, and tensile strength. This was attributed to an increase in phase mixing and an increase in hydrogen bonding between the hard and soft segments. Candidate polyureas with varying levels of collagen-mimetic peptide (0%, 10%, 20%) were then subjected to degradation in collagenase media or buffer at 37°C over 4 weeks. Statistically significant decreases in strength and elongation were observed in polyureas with 20% peptide content after collagenase treatment, whereas specimens in phosphate-buffered saline showed no statistically significant difference. These observations confirmed that enzyme-specific degradation was conferred to the polyurea. Overall, these polyureas hold great promise as a material for ligament reconstruction due to the promising mechanical properties and potential for cell-mediated degradation.
url https://doi.org/10.1177/2041731416679363
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