Phase Behaviour and Miscibility Studies of Collagen/Silk Fibroin Macromolecular System in Dilute Solutions and Solid State

Detalhes bibliográficos
Autor(a) principal: Ghaeli, Ima
Data de Publicação: 2017
Outros Autores: de Moraes, Mariana A. [UNIFESP], Beppu, Marisa M., Lewandowska, Katarzyna, Sionkowska, Alina, Ferreira-da-Silva, Frederico, Ferraz, Maria P., Monteiro, Fernando J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/51439
http://dx.doi.org/10.3390/molecules22081368
Resumo: Miscibility is an important issue in biopolymer blends for analysis of the behavior of polymer pairs through the detection of phase separation and improvement of the mechanical and physical properties of the blend. This study presents the formulation of a stable and one-phase mixture of collagen and regenerated silk fibroin (RSF), with the highest miscibility ratio between these two macromolecules, through inducing electrostatic interactions, using salt ions. For this aim, a ternary phase diagram was experimentally built for the mixtures, based on observations of phase behavior of blend solutions with various ratios. The miscibility behavior of the blend solutions in the miscible zones of the phase diagram was confirmed quantitatively by viscosimetric measurements. Assessing the effects of biopolymer mixing ratio and salt ions, before and after dialysis of blend solutions, revealed the importance of ion-specific interactions in the formation of coacervate-based materials containing collagen and RSF blends that can be used in pharmaceutical, drug delivery, and biomedical applications. Moreover, the conformational change of silk fibroin from random coil to beta sheet, in solution and in the final solid films, was detected by circular dichroism (CD) and Fourier transform infrared spectroscopy (FTIR), respectively. Scanning electron microscopy (SEM) exhibited alterations of surface morphology for the biocomposite films with different ratios. Surface contact angle measurement illustrated different hydrophobic properties for the blended film surfaces. Differential scanning calorimetry (DSC) showed that the formation of the beta sheet structure of silk fibroin enhances the thermal stability of the final blend films. Therefore, the novel method presented in this study resulted in the formation of biocomposite films whose physico-chemical properties can be tuned by silk fibroin conformational changes by applying different component mixing ratios.
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spelling Ghaeli, Imade Moraes, Mariana A. [UNIFESP]Beppu, Marisa M.Lewandowska, KatarzynaSionkowska, AlinaFerreira-da-Silva, FredericoFerraz, Maria P.Monteiro, Fernando J.2019-08-19T11:49:56Z2019-08-19T11:49:56Z2017Molecules. Basel, v. 22, n. 8, p. -, 2017.1420-3049http://repositorio.unifesp.br/handle/11600/51439http://dx.doi.org/10.3390/molecules22081368WOS000408602900131.pdf10.3390/molecules22081368WOS:000408602900131Miscibility is an important issue in biopolymer blends for analysis of the behavior of polymer pairs through the detection of phase separation and improvement of the mechanical and physical properties of the blend. This study presents the formulation of a stable and one-phase mixture of collagen and regenerated silk fibroin (RSF), with the highest miscibility ratio between these two macromolecules, through inducing electrostatic interactions, using salt ions. For this aim, a ternary phase diagram was experimentally built for the mixtures, based on observations of phase behavior of blend solutions with various ratios. The miscibility behavior of the blend solutions in the miscible zones of the phase diagram was confirmed quantitatively by viscosimetric measurements. Assessing the effects of biopolymer mixing ratio and salt ions, before and after dialysis of blend solutions, revealed the importance of ion-specific interactions in the formation of coacervate-based materials containing collagen and RSF blends that can be used in pharmaceutical, drug delivery, and biomedical applications. Moreover, the conformational change of silk fibroin from random coil to beta sheet, in solution and in the final solid films, was detected by circular dichroism (CD) and Fourier transform infrared spectroscopy (FTIR), respectively. Scanning electron microscopy (SEM) exhibited alterations of surface morphology for the biocomposite films with different ratios. Surface contact angle measurement illustrated different hydrophobic properties for the blended film surfaces. Differential scanning calorimetry (DSC) showed that the formation of the beta sheet structure of silk fibroin enhances the thermal stability of the final blend films. Therefore, the novel method presented in this study resulted in the formation of biocomposite films whose physico-chemical properties can be tuned by silk fibroin conformational changes by applying different component mixing ratios.FEDER funds through the Programa Operacional Factores de Competitividade (COMPETE)Portuguese funds through FCT (Fundação para a Ciencia e a Tecnologia)European Cooperation in Science and Technology (COST)Univ Porto, i3S, Rua Alfredo Allen 208, P-4200135 Oporto, PortugalUniv Porto, INEB Inst Engn Biomed, Rua Alfredo Allen 208, P-4200135 Oporto, PortugalUniv Porto, Dept Engn Met & Mat, FEUP, Fac Engn, P-4200465 Oporto, PortugalUniv Estadual Campinas, Sch Chem Engn, BR-13083852 Campinas, SP, BrazilUniv Fed São Paulo, Dept Chem Engn, BR-09913030 Diadema, BrazilNicolaus Copernicus Univ Torun, Dept Chem Biomat & Cosmet, Fac Chem, Ul Gagarina 7, PL-87100 Torun, PolandUniv Porto, IBMC, Rua Alfredo Allen 208, P-4200135 Oporto, PortugalUniv Fernando Pessoa, Energy Environm & Hlth Res Unit, FP ENAS CEBIMED, Biomed Res Ctr, P-200150 Oporto, PortugalUniv Fed São Paulo, Dept Chem Engn, BR-09913030 Diadema, BrazilFEDER: POCI/01/0145/FEDER/007265FCT: PT2020 UID/QUI/50006/2013European Cooperation in Science and Technology (COST): Action MP1301Web of Science-engMdpibiopolymersprotein-protein interactionsilk fibroinmiscibilitycoacervationPhase Behaviour and Miscibility Studies of Collagen/Silk Fibroin Macromolecular System in Dilute Solutions and Solid Stateinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALWOS000408602900131.pdfapplication/pdf6492493${dspace.ui.url}/bitstream/11600/51439/1/WOS000408602900131.pdf6f23e1cf4f7f7a7f9067183eaa16ecd4MD51open accessTEXTWOS000408602900131.pdf.txtWOS000408602900131.pdf.txtExtracted texttext/plain72173${dspace.ui.url}/bitstream/11600/51439/8/WOS000408602900131.pdf.txt176a83e3ba11275f8c04681a5dbe27deMD58open accessTHUMBNAILWOS000408602900131.pdf.jpgWOS000408602900131.pdf.jpgIM Thumbnailimage/jpeg6790${dspace.ui.url}/bitstream/11600/51439/10/WOS000408602900131.pdf.jpgc7e77656cf72484de07a0c345700eb0eMD510open access11600/514392023-06-05 19:32:09.007open accessoai:repositorio.unifesp.br:11600/51439Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-06-05T22:32:09Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Phase Behaviour and Miscibility Studies of Collagen/Silk Fibroin Macromolecular System in Dilute Solutions and Solid State
title Phase Behaviour and Miscibility Studies of Collagen/Silk Fibroin Macromolecular System in Dilute Solutions and Solid State
spellingShingle Phase Behaviour and Miscibility Studies of Collagen/Silk Fibroin Macromolecular System in Dilute Solutions and Solid State
Ghaeli, Ima
biopolymers
protein-protein interaction
silk fibroin
miscibility
coacervation
title_short Phase Behaviour and Miscibility Studies of Collagen/Silk Fibroin Macromolecular System in Dilute Solutions and Solid State
title_full Phase Behaviour and Miscibility Studies of Collagen/Silk Fibroin Macromolecular System in Dilute Solutions and Solid State
title_fullStr Phase Behaviour and Miscibility Studies of Collagen/Silk Fibroin Macromolecular System in Dilute Solutions and Solid State
title_full_unstemmed Phase Behaviour and Miscibility Studies of Collagen/Silk Fibroin Macromolecular System in Dilute Solutions and Solid State
title_sort Phase Behaviour and Miscibility Studies of Collagen/Silk Fibroin Macromolecular System in Dilute Solutions and Solid State
author Ghaeli, Ima
author_facet Ghaeli, Ima
de Moraes, Mariana A. [UNIFESP]
Beppu, Marisa M.
Lewandowska, Katarzyna
Sionkowska, Alina
Ferreira-da-Silva, Frederico
Ferraz, Maria P.
Monteiro, Fernando J.
author_role author
author2 de Moraes, Mariana A. [UNIFESP]
Beppu, Marisa M.
Lewandowska, Katarzyna
Sionkowska, Alina
Ferreira-da-Silva, Frederico
Ferraz, Maria P.
Monteiro, Fernando J.
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Ghaeli, Ima
de Moraes, Mariana A. [UNIFESP]
Beppu, Marisa M.
Lewandowska, Katarzyna
Sionkowska, Alina
Ferreira-da-Silva, Frederico
Ferraz, Maria P.
Monteiro, Fernando J.
dc.subject.eng.fl_str_mv biopolymers
protein-protein interaction
silk fibroin
miscibility
coacervation
topic biopolymers
protein-protein interaction
silk fibroin
miscibility
coacervation
description Miscibility is an important issue in biopolymer blends for analysis of the behavior of polymer pairs through the detection of phase separation and improvement of the mechanical and physical properties of the blend. This study presents the formulation of a stable and one-phase mixture of collagen and regenerated silk fibroin (RSF), with the highest miscibility ratio between these two macromolecules, through inducing electrostatic interactions, using salt ions. For this aim, a ternary phase diagram was experimentally built for the mixtures, based on observations of phase behavior of blend solutions with various ratios. The miscibility behavior of the blend solutions in the miscible zones of the phase diagram was confirmed quantitatively by viscosimetric measurements. Assessing the effects of biopolymer mixing ratio and salt ions, before and after dialysis of blend solutions, revealed the importance of ion-specific interactions in the formation of coacervate-based materials containing collagen and RSF blends that can be used in pharmaceutical, drug delivery, and biomedical applications. Moreover, the conformational change of silk fibroin from random coil to beta sheet, in solution and in the final solid films, was detected by circular dichroism (CD) and Fourier transform infrared spectroscopy (FTIR), respectively. Scanning electron microscopy (SEM) exhibited alterations of surface morphology for the biocomposite films with different ratios. Surface contact angle measurement illustrated different hydrophobic properties for the blended film surfaces. Differential scanning calorimetry (DSC) showed that the formation of the beta sheet structure of silk fibroin enhances the thermal stability of the final blend films. Therefore, the novel method presented in this study resulted in the formation of biocomposite films whose physico-chemical properties can be tuned by silk fibroin conformational changes by applying different component mixing ratios.
publishDate 2017
dc.date.issued.fl_str_mv 2017
dc.date.accessioned.fl_str_mv 2019-08-19T11:49:56Z
dc.date.available.fl_str_mv 2019-08-19T11:49:56Z
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dc.identifier.citation.fl_str_mv Molecules. Basel, v. 22, n. 8, p. -, 2017.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/51439
http://dx.doi.org/10.3390/molecules22081368
dc.identifier.issn.none.fl_str_mv 1420-3049
dc.identifier.file.none.fl_str_mv WOS000408602900131.pdf
dc.identifier.doi.none.fl_str_mv 10.3390/molecules22081368
dc.identifier.wos.none.fl_str_mv WOS:000408602900131
identifier_str_mv Molecules. Basel, v. 22, n. 8, p. -, 2017.
1420-3049
WOS000408602900131.pdf
10.3390/molecules22081368
WOS:000408602900131
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http://dx.doi.org/10.3390/molecules22081368
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