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Pullulan/Poly(Vinyl Alcohol) Composite Hydrogels for Adipose Tissue Engineering

Composite hydrogels based on pullulan (HP) and poly(vinyl alcohol) (PVA) were both prepared by simple chemical crosslinking with sodium trimethaphosphate (STMP) or by dual crosslinking (simultaneously chemical crosslinking with STMP and physical crosslinking by freeze-thaw technique). The resulting...

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Autores principales: Samoila, Iuliana, Dinescu, Sorina, Pircalabioru, Gratiela Gradisteanu, Marutescu, Luminita, Fundueanu, Gheorghe, Aflori, Magdalena, Constantin, Marieta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804089/
https://www.ncbi.nlm.nih.gov/pubmed/31581444
http://dx.doi.org/10.3390/ma12193220
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author Samoila, Iuliana
Dinescu, Sorina
Pircalabioru, Gratiela Gradisteanu
Marutescu, Luminita
Fundueanu, Gheorghe
Aflori, Magdalena
Constantin, Marieta
author_facet Samoila, Iuliana
Dinescu, Sorina
Pircalabioru, Gratiela Gradisteanu
Marutescu, Luminita
Fundueanu, Gheorghe
Aflori, Magdalena
Constantin, Marieta
author_sort Samoila, Iuliana
collection PubMed
description Composite hydrogels based on pullulan (HP) and poly(vinyl alcohol) (PVA) were both prepared by simple chemical crosslinking with sodium trimethaphosphate (STMP) or by dual crosslinking (simultaneously chemical crosslinking with STMP and physical crosslinking by freeze-thaw technique). The resulting hydrogels and cryogels were designed for tissue engineering applications. PVA, with two different molecular weights (47,000 and 125,000 g/mol; PVA(47) and PVA(125), respectively), as well as different P/PVA weight ratios were tested. The physico-chemical characterization of the hydrogels was performed by FTIR spectroscopy and scanning electron microscopy (SEM). The swelling kinetics, dissolution behavior, and degradation profiles in simulated physiological conditions (phosphate buffer at pH 7.4) were investigated. Pullulan concentration and the crosslinking method had significant effects on the pore size, swelling ratio, and degradation profiles. Cryogels exhibit lower swelling capacities than the conventional hydrogels but have better stability against hydrolitic degradation. Biocompatibility of the hydrogels was also investigated by both MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) and LDH (lactaten dehydrogenase) assay. The MTT and LDH assays proved that dual crosslinked HP/PVA(125) (75:25, w/w) scaffolds are more biocompatible and promote to a greater extent the adhesion and proliferation of L929 murine fibroblast cells than chemically crosslinked HP/PVA(47) (50/50, w/w) scaffolds. Moreover, the HP/PVA(125) cryogel had the best ability for the adipogenic differentiation of cells. The overall results demonstrated that the HP/PVA composite hydrogels or cryogels are suitable biomaterials for tissue engineering applications.
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spelling pubmed-68040892019-11-18 Pullulan/Poly(Vinyl Alcohol) Composite Hydrogels for Adipose Tissue Engineering Samoila, Iuliana Dinescu, Sorina Pircalabioru, Gratiela Gradisteanu Marutescu, Luminita Fundueanu, Gheorghe Aflori, Magdalena Constantin, Marieta Materials (Basel) Article Composite hydrogels based on pullulan (HP) and poly(vinyl alcohol) (PVA) were both prepared by simple chemical crosslinking with sodium trimethaphosphate (STMP) or by dual crosslinking (simultaneously chemical crosslinking with STMP and physical crosslinking by freeze-thaw technique). The resulting hydrogels and cryogels were designed for tissue engineering applications. PVA, with two different molecular weights (47,000 and 125,000 g/mol; PVA(47) and PVA(125), respectively), as well as different P/PVA weight ratios were tested. The physico-chemical characterization of the hydrogels was performed by FTIR spectroscopy and scanning electron microscopy (SEM). The swelling kinetics, dissolution behavior, and degradation profiles in simulated physiological conditions (phosphate buffer at pH 7.4) were investigated. Pullulan concentration and the crosslinking method had significant effects on the pore size, swelling ratio, and degradation profiles. Cryogels exhibit lower swelling capacities than the conventional hydrogels but have better stability against hydrolitic degradation. Biocompatibility of the hydrogels was also investigated by both MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) and LDH (lactaten dehydrogenase) assay. The MTT and LDH assays proved that dual crosslinked HP/PVA(125) (75:25, w/w) scaffolds are more biocompatible and promote to a greater extent the adhesion and proliferation of L929 murine fibroblast cells than chemically crosslinked HP/PVA(47) (50/50, w/w) scaffolds. Moreover, the HP/PVA(125) cryogel had the best ability for the adipogenic differentiation of cells. The overall results demonstrated that the HP/PVA composite hydrogels or cryogels are suitable biomaterials for tissue engineering applications. MDPI 2019-10-01 /pmc/articles/PMC6804089/ /pubmed/31581444 http://dx.doi.org/10.3390/ma12193220 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Samoila, Iuliana
Dinescu, Sorina
Pircalabioru, Gratiela Gradisteanu
Marutescu, Luminita
Fundueanu, Gheorghe
Aflori, Magdalena
Constantin, Marieta
Pullulan/Poly(Vinyl Alcohol) Composite Hydrogels for Adipose Tissue Engineering
title Pullulan/Poly(Vinyl Alcohol) Composite Hydrogels for Adipose Tissue Engineering
title_full Pullulan/Poly(Vinyl Alcohol) Composite Hydrogels for Adipose Tissue Engineering
title_fullStr Pullulan/Poly(Vinyl Alcohol) Composite Hydrogels for Adipose Tissue Engineering
title_full_unstemmed Pullulan/Poly(Vinyl Alcohol) Composite Hydrogels for Adipose Tissue Engineering
title_short Pullulan/Poly(Vinyl Alcohol) Composite Hydrogels for Adipose Tissue Engineering
title_sort pullulan/poly(vinyl alcohol) composite hydrogels for adipose tissue engineering
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804089/
https://www.ncbi.nlm.nih.gov/pubmed/31581444
http://dx.doi.org/10.3390/ma12193220
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