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Thiolation and characterization of regenerated Bombyx mori silk fibroin films with reduced glutathione
Bombyx mori silk fibroin-based materials have good biocompatibility and biodegradability. In order to maximize their utility while maintain appropriate features, silk fibroin (SF) films were modified with reduced glutathione (GSH) (NH(2))–ECG–(COOH), using the carbodiimide chemistry method, for the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661838/ https://www.ncbi.nlm.nih.gov/pubmed/31384810 http://dx.doi.org/10.1186/s13065-019-0583-x |
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author | Zhang, Xiaoning Bao, Hong Donley, Carrie Liang, Jianwei Yang, Sha Xu, Shui |
author_facet | Zhang, Xiaoning Bao, Hong Donley, Carrie Liang, Jianwei Yang, Sha Xu, Shui |
author_sort | Zhang, Xiaoning |
collection | PubMed |
description | Bombyx mori silk fibroin-based materials have good biocompatibility and biodegradability. In order to maximize their utility while maintain appropriate features, silk fibroin (SF) films were modified with reduced glutathione (GSH) (NH(2))–ECG–(COOH), using the carbodiimide chemistry method, for the introduction of thiol groups onto surfaces. The effects of this modification on SF films’ chemical and physical properties, and cytotoxicity were assessed. The chemical and elemental composition analysis results suggested that reduced glutathione (GSH) was covalently coupled onto the surface of silk fibroin films. Atomic force microscopy (AFM) results indicated the surface roughness of silk fibroin film was increased after the modification by GSH. The GSH-modified silk fibroin films also showed the smaller contact angle due to the hydrophilic peptides coupled on the film surface. Through MTT assay, it was shown that the chemically modified SF film was not cytotoxic to HEK293 cells, and it had no adverse influence on the growth of HEK293 cells. Our approach provides a new option to engineer SF-based material surface with thiol groups in order to allow for secondary reactions and holds great promise for applications of SF-based materials in the biomedical field. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13065-019-0583-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6661838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-66618382019-08-05 Thiolation and characterization of regenerated Bombyx mori silk fibroin films with reduced glutathione Zhang, Xiaoning Bao, Hong Donley, Carrie Liang, Jianwei Yang, Sha Xu, Shui BMC Chem Research Article Bombyx mori silk fibroin-based materials have good biocompatibility and biodegradability. In order to maximize their utility while maintain appropriate features, silk fibroin (SF) films were modified with reduced glutathione (GSH) (NH(2))–ECG–(COOH), using the carbodiimide chemistry method, for the introduction of thiol groups onto surfaces. The effects of this modification on SF films’ chemical and physical properties, and cytotoxicity were assessed. The chemical and elemental composition analysis results suggested that reduced glutathione (GSH) was covalently coupled onto the surface of silk fibroin films. Atomic force microscopy (AFM) results indicated the surface roughness of silk fibroin film was increased after the modification by GSH. The GSH-modified silk fibroin films also showed the smaller contact angle due to the hydrophilic peptides coupled on the film surface. Through MTT assay, it was shown that the chemically modified SF film was not cytotoxic to HEK293 cells, and it had no adverse influence on the growth of HEK293 cells. Our approach provides a new option to engineer SF-based material surface with thiol groups in order to allow for secondary reactions and holds great promise for applications of SF-based materials in the biomedical field. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13065-019-0583-x) contains supplementary material, which is available to authorized users. Springer International Publishing 2019-05-10 /pmc/articles/PMC6661838/ /pubmed/31384810 http://dx.doi.org/10.1186/s13065-019-0583-x Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Zhang, Xiaoning Bao, Hong Donley, Carrie Liang, Jianwei Yang, Sha Xu, Shui Thiolation and characterization of regenerated Bombyx mori silk fibroin films with reduced glutathione |
title | Thiolation and characterization of regenerated Bombyx mori silk fibroin films with reduced glutathione |
title_full | Thiolation and characterization of regenerated Bombyx mori silk fibroin films with reduced glutathione |
title_fullStr | Thiolation and characterization of regenerated Bombyx mori silk fibroin films with reduced glutathione |
title_full_unstemmed | Thiolation and characterization of regenerated Bombyx mori silk fibroin films with reduced glutathione |
title_short | Thiolation and characterization of regenerated Bombyx mori silk fibroin films with reduced glutathione |
title_sort | thiolation and characterization of regenerated bombyx mori silk fibroin films with reduced glutathione |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661838/ https://www.ncbi.nlm.nih.gov/pubmed/31384810 http://dx.doi.org/10.1186/s13065-019-0583-x |
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