Exploring the Gelation Mechanisms and Cytocompatibility of Gold (III)-Mediated Regenerated and Thiolated Silk Fibroin Hydrogels

Accelerating the gelation of silk fibroin (SF) solution from several days or weeks to minutes or few hours is critical for several applications (e.g., cell encapsulation, bio-ink for 3D printing, and injectable controlled release). In this study, the rapid gelation of SF induced by a gold salt (Au&l...

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Main Authors: Chavee Laomeephol, Helena Ferreira, Supansa Yodmuang, Rui L. Reis, Siriporn Damrongsakkul, Nuno M. Neves
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:Biomolecules
Subjects:
Online Access:https://www.mdpi.com/2218-273X/10/3/466
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spelling doaj-2310b8926a764f339ace1a5aeee0332b2020-11-25T03:29:28ZengMDPI AGBiomolecules2218-273X2020-03-0110346610.3390/biom10030466biom10030466Exploring the Gelation Mechanisms and Cytocompatibility of Gold (III)-Mediated Regenerated and Thiolated Silk Fibroin HydrogelsChavee Laomeephol0Helena Ferreira1Supansa Yodmuang2Rui L. Reis3Siriporn Damrongsakkul4Nuno M. Neves5Biomedical Engineering Research Center, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand3B’s Research Group, I3Bs-Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark-Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco, Guimarães, PortugalBiomedical Engineering Research Center, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand3B’s Research Group, I3Bs-Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark-Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco, Guimarães, PortugalBiomedical Engineering Research Center, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand3B’s Research Group, I3Bs-Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark-Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco, Guimarães, PortugalAccelerating the gelation of silk fibroin (SF) solution from several days or weeks to minutes or few hours is critical for several applications (e.g., cell encapsulation, bio-ink for 3D printing, and injectable controlled release). In this study, the rapid gelation of SF induced by a gold salt (Au<sup>3+</sup>) as well as the cytocompatibility of Au<sup>3+</sup>-mediated SF hydrogels are reported. The gelation behaviors and mechanisms of regenerated SF and thiolated SF (tSF) were compared. Hydrogels can be obtained immediately after mixing or within three days depending on the types of silk proteins used and amount of Au<sup>3+</sup>. Au<sup>3+</sup>-mediated SF and tSF hydrogels showed different color appearances. The color of Au-SF hydrogels was purple-red, whereas the Au-tSF hydrogels maintained their initial solution color, indicating different gelation mechanisms. The reduction of Au<sup>3+</sup> by amino groups and further reduction to Au by tyrosine present in SF, resulting in a dityrosine bonding and Au nanoparticles (NPs) production, are proposed as underlying mechanisms of Au-SF gel formation. Thiol groups of the tSF reduced Au<sup>3+</sup> to Au<sup>+</sup> and formed a disulfide bond, before a formation of Au<sup>+</sup>-S bonds. Protons generated during the reactions between Au<sup>3+</sup> and SF or tSF led to a decrease of the local pH, which affected the chain aggregation of the SF, and induced the conformational transition of SF protein to beta sheet. The cytocompatibility of the Au-SF and tSF hydrogels was demonstrated by culturing with a L929 cell line, indicating that the developed hydrogels can be promising 3D matrices for different biomedical applications.https://www.mdpi.com/2218-273X/10/3/466silk fibrointhiolated silk fibroingoldhydrogelcytocompatibility
collection DOAJ
language English
format Article
sources DOAJ
author Chavee Laomeephol
Helena Ferreira
Supansa Yodmuang
Rui L. Reis
Siriporn Damrongsakkul
Nuno M. Neves
spellingShingle Chavee Laomeephol
Helena Ferreira
Supansa Yodmuang
Rui L. Reis
Siriporn Damrongsakkul
Nuno M. Neves
Exploring the Gelation Mechanisms and Cytocompatibility of Gold (III)-Mediated Regenerated and Thiolated Silk Fibroin Hydrogels
Biomolecules
silk fibroin
thiolated silk fibroin
gold
hydrogel
cytocompatibility
author_facet Chavee Laomeephol
Helena Ferreira
Supansa Yodmuang
Rui L. Reis
Siriporn Damrongsakkul
Nuno M. Neves
author_sort Chavee Laomeephol
title Exploring the Gelation Mechanisms and Cytocompatibility of Gold (III)-Mediated Regenerated and Thiolated Silk Fibroin Hydrogels
title_short Exploring the Gelation Mechanisms and Cytocompatibility of Gold (III)-Mediated Regenerated and Thiolated Silk Fibroin Hydrogels
title_full Exploring the Gelation Mechanisms and Cytocompatibility of Gold (III)-Mediated Regenerated and Thiolated Silk Fibroin Hydrogels
title_fullStr Exploring the Gelation Mechanisms and Cytocompatibility of Gold (III)-Mediated Regenerated and Thiolated Silk Fibroin Hydrogels
title_full_unstemmed Exploring the Gelation Mechanisms and Cytocompatibility of Gold (III)-Mediated Regenerated and Thiolated Silk Fibroin Hydrogels
title_sort exploring the gelation mechanisms and cytocompatibility of gold (iii)-mediated regenerated and thiolated silk fibroin hydrogels
publisher MDPI AG
series Biomolecules
issn 2218-273X
publishDate 2020-03-01
description Accelerating the gelation of silk fibroin (SF) solution from several days or weeks to minutes or few hours is critical for several applications (e.g., cell encapsulation, bio-ink for 3D printing, and injectable controlled release). In this study, the rapid gelation of SF induced by a gold salt (Au<sup>3+</sup>) as well as the cytocompatibility of Au<sup>3+</sup>-mediated SF hydrogels are reported. The gelation behaviors and mechanisms of regenerated SF and thiolated SF (tSF) were compared. Hydrogels can be obtained immediately after mixing or within three days depending on the types of silk proteins used and amount of Au<sup>3+</sup>. Au<sup>3+</sup>-mediated SF and tSF hydrogels showed different color appearances. The color of Au-SF hydrogels was purple-red, whereas the Au-tSF hydrogels maintained their initial solution color, indicating different gelation mechanisms. The reduction of Au<sup>3+</sup> by amino groups and further reduction to Au by tyrosine present in SF, resulting in a dityrosine bonding and Au nanoparticles (NPs) production, are proposed as underlying mechanisms of Au-SF gel formation. Thiol groups of the tSF reduced Au<sup>3+</sup> to Au<sup>+</sup> and formed a disulfide bond, before a formation of Au<sup>+</sup>-S bonds. Protons generated during the reactions between Au<sup>3+</sup> and SF or tSF led to a decrease of the local pH, which affected the chain aggregation of the SF, and induced the conformational transition of SF protein to beta sheet. The cytocompatibility of the Au-SF and tSF hydrogels was demonstrated by culturing with a L929 cell line, indicating that the developed hydrogels can be promising 3D matrices for different biomedical applications.
topic silk fibroin
thiolated silk fibroin
gold
hydrogel
cytocompatibility
url https://www.mdpi.com/2218-273X/10/3/466
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