Gelatin-Modified Polyurethanes for Soft Tissue Scaffold

Recently, in the field of biomaterials for soft tissue scaffolds, the interest of their modification with natural polymersis growing. Synthetic polymers are often tough, and many of them do not possess fine biocompatibility. On the other hand, natural polymers are biocompatible but weak when used al...

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Main Authors: Justyna Kucińska-Lipka, Iga Gubańska, Helena Janik
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1155/2013/450132
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spelling doaj-f23858bc2b0444c8b329d8218aeab7d42020-11-25T01:09:31ZengHindawi LimitedThe Scientific World Journal1537-744X2013-01-01201310.1155/2013/450132450132Gelatin-Modified Polyurethanes for Soft Tissue ScaffoldJustyna Kucińska-Lipka0Iga Gubańska1Helena Janik2Department of Polymer Technology, Chemical Faculty, Gdansk University of Technology, Narutowicza Street 11/12, 80-233 Gdansk, PolandDepartment of Polymer Technology, Chemical Faculty, Gdansk University of Technology, Narutowicza Street 11/12, 80-233 Gdansk, PolandDepartment of Polymer Technology, Chemical Faculty, Gdansk University of Technology, Narutowicza Street 11/12, 80-233 Gdansk, PolandRecently, in the field of biomaterials for soft tissue scaffolds, the interest of their modification with natural polymersis growing. Synthetic polymers are often tough, and many of them do not possess fine biocompatibility. On the other hand, natural polymers are biocompatible but weak when used alone. The combination of natural and synthetic polymers gives the suitable properties for tissue engineering requirements. In our study, we modified gelatin synthetic polyurethanes prepared from polyester poly(ethylene-butylene adipate) (PEBA), aliphatic 1,6-hexamethylene diisocyanate (HDI), and two different chain extenders 1,4-butanediol (BDO) or 1-ethoxy-2-(2-hydroxyethoxy)ethanol (EHEE). From a chemical point of view, we replaced expensive components for building PU, such as 2,6-diisocyanato methyl caproate (LDI) and 1,4-diisocyanatobutane (BDI), with cost-effective HDI. The gelatin was added in situ (in the first step of synthesis) to polyurethane to increase biocompatibility and biodegradability of the obtained material. It appeared that the obtained gelatin-modified PU foams, in which chain extender was BDO, had enhanced interactions with media and their hydrolytic degradation profile was also improved for tissue engineering application. Furthermore, the gelatin introduction had positive impact on gelatin-modified PU foams by increasing their hemocompatibility.http://dx.doi.org/10.1155/2013/450132
collection DOAJ
language English
format Article
sources DOAJ
author Justyna Kucińska-Lipka
Iga Gubańska
Helena Janik
spellingShingle Justyna Kucińska-Lipka
Iga Gubańska
Helena Janik
Gelatin-Modified Polyurethanes for Soft Tissue Scaffold
The Scientific World Journal
author_facet Justyna Kucińska-Lipka
Iga Gubańska
Helena Janik
author_sort Justyna Kucińska-Lipka
title Gelatin-Modified Polyurethanes for Soft Tissue Scaffold
title_short Gelatin-Modified Polyurethanes for Soft Tissue Scaffold
title_full Gelatin-Modified Polyurethanes for Soft Tissue Scaffold
title_fullStr Gelatin-Modified Polyurethanes for Soft Tissue Scaffold
title_full_unstemmed Gelatin-Modified Polyurethanes for Soft Tissue Scaffold
title_sort gelatin-modified polyurethanes for soft tissue scaffold
publisher Hindawi Limited
series The Scientific World Journal
issn 1537-744X
publishDate 2013-01-01
description Recently, in the field of biomaterials for soft tissue scaffolds, the interest of their modification with natural polymersis growing. Synthetic polymers are often tough, and many of them do not possess fine biocompatibility. On the other hand, natural polymers are biocompatible but weak when used alone. The combination of natural and synthetic polymers gives the suitable properties for tissue engineering requirements. In our study, we modified gelatin synthetic polyurethanes prepared from polyester poly(ethylene-butylene adipate) (PEBA), aliphatic 1,6-hexamethylene diisocyanate (HDI), and two different chain extenders 1,4-butanediol (BDO) or 1-ethoxy-2-(2-hydroxyethoxy)ethanol (EHEE). From a chemical point of view, we replaced expensive components for building PU, such as 2,6-diisocyanato methyl caproate (LDI) and 1,4-diisocyanatobutane (BDI), with cost-effective HDI. The gelatin was added in situ (in the first step of synthesis) to polyurethane to increase biocompatibility and biodegradability of the obtained material. It appeared that the obtained gelatin-modified PU foams, in which chain extender was BDO, had enhanced interactions with media and their hydrolytic degradation profile was also improved for tissue engineering application. Furthermore, the gelatin introduction had positive impact on gelatin-modified PU foams by increasing their hemocompatibility.
url http://dx.doi.org/10.1155/2013/450132
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AT igagubanska gelatinmodifiedpolyurethanesforsofttissuescaffold
AT helenajanik gelatinmodifiedpolyurethanesforsofttissuescaffold
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