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New Nanofibers Based on Protein By-Products with Bioactive Potential for Tissue Engineering

Concentrated collagen hydrolysate (HC10CC), rabbit collagen glue (RCG), and keratin hydrolysate (KH) were investigated in terms of their extraction from mammalian by-products and processing by electrospinning. The electrospun nanofibers were characterized by scanning electron microscopy coupled with...

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Autores principales: Râpă, Maria, Gaidău, Carmen, Stefan, Laura Mihaela, Matei, Ecaterina, Niculescu, Mihaela, Berechet, Mariana Daniela, Stanca, Maria, Tablet, Cristina, Tudorache, Mădălina, Gavrilă, Raluca, Predescu, Cristian, Vidu, Ruxandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412532/
https://www.ncbi.nlm.nih.gov/pubmed/32679796
http://dx.doi.org/10.3390/ma13143149
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author Râpă, Maria
Gaidău, Carmen
Stefan, Laura Mihaela
Matei, Ecaterina
Niculescu, Mihaela
Berechet, Mariana Daniela
Stanca, Maria
Tablet, Cristina
Tudorache, Mădălina
Gavrilă, Raluca
Predescu, Cristian
Vidu, Ruxandra
author_facet Râpă, Maria
Gaidău, Carmen
Stefan, Laura Mihaela
Matei, Ecaterina
Niculescu, Mihaela
Berechet, Mariana Daniela
Stanca, Maria
Tablet, Cristina
Tudorache, Mădălina
Gavrilă, Raluca
Predescu, Cristian
Vidu, Ruxandra
author_sort Râpă, Maria
collection PubMed
description Concentrated collagen hydrolysate (HC10CC), rabbit collagen glue (RCG), and keratin hydrolysate (KH) were investigated in terms of their extraction from mammalian by-products and processing by electrospinning. The electrospun nanofibers were characterized by scanning electron microscopy coupled with the energy dispersive X-ray spectroscopy (SEM/EDS), attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), differential scanning calorimetry (DSC), and indentation tests. The cytotoxicity of the electrospun nanofibers was conducted on L929 fibroblast cells using MTT and LDH assays and cell morphology observations. The electrospun RCG and KH nanofibers morphology showed an average size of nanofibers ranging between 44 and 410 nm, while the electrospun HC10CC nanofibers exhibited higher sizes. The ATR-FTIR spectra performed both on extracted proteins and electrospun nanofibers showed that the triple helix structure of collagen is partially preserved. The results were in agreement with the circular dichroism analysis for protein extracts. Furthermore, the viscoelastic properties of electrospun KH nanofibers were superior to those of electrospun RCG nanofibers. Based on both in vitro quantitative and qualitative analysis, the electrospun nanofibers were not cytotoxic, inducing a healthy cellular response. The results of new electrospun protein-based nanofibers may be useful for further research on bioactive properties of these nanofibers for tissue engineering.
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spelling pubmed-74125322020-08-26 New Nanofibers Based on Protein By-Products with Bioactive Potential for Tissue Engineering Râpă, Maria Gaidău, Carmen Stefan, Laura Mihaela Matei, Ecaterina Niculescu, Mihaela Berechet, Mariana Daniela Stanca, Maria Tablet, Cristina Tudorache, Mădălina Gavrilă, Raluca Predescu, Cristian Vidu, Ruxandra Materials (Basel) Article Concentrated collagen hydrolysate (HC10CC), rabbit collagen glue (RCG), and keratin hydrolysate (KH) were investigated in terms of their extraction from mammalian by-products and processing by electrospinning. The electrospun nanofibers were characterized by scanning electron microscopy coupled with the energy dispersive X-ray spectroscopy (SEM/EDS), attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), differential scanning calorimetry (DSC), and indentation tests. The cytotoxicity of the electrospun nanofibers was conducted on L929 fibroblast cells using MTT and LDH assays and cell morphology observations. The electrospun RCG and KH nanofibers morphology showed an average size of nanofibers ranging between 44 and 410 nm, while the electrospun HC10CC nanofibers exhibited higher sizes. The ATR-FTIR spectra performed both on extracted proteins and electrospun nanofibers showed that the triple helix structure of collagen is partially preserved. The results were in agreement with the circular dichroism analysis for protein extracts. Furthermore, the viscoelastic properties of electrospun KH nanofibers were superior to those of electrospun RCG nanofibers. Based on both in vitro quantitative and qualitative analysis, the electrospun nanofibers were not cytotoxic, inducing a healthy cellular response. The results of new electrospun protein-based nanofibers may be useful for further research on bioactive properties of these nanofibers for tissue engineering. MDPI 2020-07-15 /pmc/articles/PMC7412532/ /pubmed/32679796 http://dx.doi.org/10.3390/ma13143149 Text en © 2020 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
Râpă, Maria
Gaidău, Carmen
Stefan, Laura Mihaela
Matei, Ecaterina
Niculescu, Mihaela
Berechet, Mariana Daniela
Stanca, Maria
Tablet, Cristina
Tudorache, Mădălina
Gavrilă, Raluca
Predescu, Cristian
Vidu, Ruxandra
New Nanofibers Based on Protein By-Products with Bioactive Potential for Tissue Engineering
title New Nanofibers Based on Protein By-Products with Bioactive Potential for Tissue Engineering
title_full New Nanofibers Based on Protein By-Products with Bioactive Potential for Tissue Engineering
title_fullStr New Nanofibers Based on Protein By-Products with Bioactive Potential for Tissue Engineering
title_full_unstemmed New Nanofibers Based on Protein By-Products with Bioactive Potential for Tissue Engineering
title_short New Nanofibers Based on Protein By-Products with Bioactive Potential for Tissue Engineering
title_sort new nanofibers based on protein by-products with bioactive potential for tissue engineering
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412532/
https://www.ncbi.nlm.nih.gov/pubmed/32679796
http://dx.doi.org/10.3390/ma13143149
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