High modulus biodegradable polyurethanes for applications in cardiovascular stents: Evaluation of in-vitro degradation and cell viability

We have recently reported the mechanical properties and hydrolytic degradation behaviour of a series of NovoSorb™ [1] biodegradable polyurethanes (PUs) prepared by varying the hard segment (HS) weight percentage from 60-100. In this study the in-vitro degradation behaviour of the PUs with and withou...

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Main Authors: Melissa eSagarito, Pathiraja A Gunatillake, Raju eAdhikari, Tim eMoore, Francois Clement Malherbe, John ePatterson, Marie-Danielle eNagel
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-05-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fbioe.2015.00052/full
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spelling doaj-48b9296892074628bb6d401efa9b006d2020-11-25T01:51:02ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852015-05-01310.3389/fbioe.2015.00052129346High modulus biodegradable polyurethanes for applications in cardiovascular stents: Evaluation of in-vitro degradation and cell viabilityMelissa eSagarito0Pathiraja A Gunatillake1Raju eAdhikari2Tim eMoore3Francois Clement Malherbe4John ePatterson5Marie-Danielle eNagel64Université de Technologie de CompiègneCSIROCSIROPolyNovo Biomaterials Pty LtdSwinburne University of TechnologySwinburne University of Technology4Université de Technologie de CompiègneWe have recently reported the mechanical properties and hydrolytic degradation behaviour of a series of NovoSorb™ [1] biodegradable polyurethanes (PUs) prepared by varying the hard segment (HS) weight percentage from 60-100. In this study the in-vitro degradation behaviour of the PUs with and without extracellular matrix (ECM) coating was investigated under accelerated hydrolytic degradation (phosphate buffer saline; PBS/70°C) conditions to allow complete degradation. The mass loss at different time intervals and the effect of aqueous degradation products on the viability and growth of Human Umbilical Vein Endothelial Cells (HUVEC) were examined.The results showed that for most PUs in the series the degradation medium turned acidic and the extent of this was dependent on the HS percentage. As the HS decreased, a drop in pH was observed, suggesting that the by-products of soft segment (SS) degradation causing the solution to be acidic. Most of the samples were completely eroded by 18 weeks, except PU containing more than 70% HS which only showed partial degradation with no significant change in appearance. The cytotoxicity tests on HUVEC cells of the aqueous extracts obtained after 18 weeks incubation showed that toxicity was dependent on 3 factors: dose, percentage of HS and degradation time. HUVEC growth is similar to but not identical to that observed with tissue culture polystyrene (TCPS) standard. The results from this in-vitro cytotoxicity study suggest that the mixture of degradation products formed during the accelerated degradation of this PU series are not toxic to cells under the experimental conditions used.http://journal.frontiersin.org/Journal/10.3389/fbioe.2015.00052/fullPolyurethanesStentscardiovascularpropertiesdegradationCell viability
collection DOAJ
language English
format Article
sources DOAJ
author Melissa eSagarito
Pathiraja A Gunatillake
Raju eAdhikari
Tim eMoore
Francois Clement Malherbe
John ePatterson
Marie-Danielle eNagel
spellingShingle Melissa eSagarito
Pathiraja A Gunatillake
Raju eAdhikari
Tim eMoore
Francois Clement Malherbe
John ePatterson
Marie-Danielle eNagel
High modulus biodegradable polyurethanes for applications in cardiovascular stents: Evaluation of in-vitro degradation and cell viability
Frontiers in Bioengineering and Biotechnology
Polyurethanes
Stents
cardiovascular
properties
degradation
Cell viability
author_facet Melissa eSagarito
Pathiraja A Gunatillake
Raju eAdhikari
Tim eMoore
Francois Clement Malherbe
John ePatterson
Marie-Danielle eNagel
author_sort Melissa eSagarito
title High modulus biodegradable polyurethanes for applications in cardiovascular stents: Evaluation of in-vitro degradation and cell viability
title_short High modulus biodegradable polyurethanes for applications in cardiovascular stents: Evaluation of in-vitro degradation and cell viability
title_full High modulus biodegradable polyurethanes for applications in cardiovascular stents: Evaluation of in-vitro degradation and cell viability
title_fullStr High modulus biodegradable polyurethanes for applications in cardiovascular stents: Evaluation of in-vitro degradation and cell viability
title_full_unstemmed High modulus biodegradable polyurethanes for applications in cardiovascular stents: Evaluation of in-vitro degradation and cell viability
title_sort high modulus biodegradable polyurethanes for applications in cardiovascular stents: evaluation of in-vitro degradation and cell viability
publisher Frontiers Media S.A.
series Frontiers in Bioengineering and Biotechnology
issn 2296-4185
publishDate 2015-05-01
description We have recently reported the mechanical properties and hydrolytic degradation behaviour of a series of NovoSorb™ [1] biodegradable polyurethanes (PUs) prepared by varying the hard segment (HS) weight percentage from 60-100. In this study the in-vitro degradation behaviour of the PUs with and without extracellular matrix (ECM) coating was investigated under accelerated hydrolytic degradation (phosphate buffer saline; PBS/70°C) conditions to allow complete degradation. The mass loss at different time intervals and the effect of aqueous degradation products on the viability and growth of Human Umbilical Vein Endothelial Cells (HUVEC) were examined.The results showed that for most PUs in the series the degradation medium turned acidic and the extent of this was dependent on the HS percentage. As the HS decreased, a drop in pH was observed, suggesting that the by-products of soft segment (SS) degradation causing the solution to be acidic. Most of the samples were completely eroded by 18 weeks, except PU containing more than 70% HS which only showed partial degradation with no significant change in appearance. The cytotoxicity tests on HUVEC cells of the aqueous extracts obtained after 18 weeks incubation showed that toxicity was dependent on 3 factors: dose, percentage of HS and degradation time. HUVEC growth is similar to but not identical to that observed with tissue culture polystyrene (TCPS) standard. The results from this in-vitro cytotoxicity study suggest that the mixture of degradation products formed during the accelerated degradation of this PU series are not toxic to cells under the experimental conditions used.
topic Polyurethanes
Stents
cardiovascular
properties
degradation
Cell viability
url http://journal.frontiersin.org/Journal/10.3389/fbioe.2015.00052/full
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