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Chemical, Thermal, Time, and Enzymatic Stability of Silk Materials with Silk I Structure
The crystalline structure of silk fibroin Silk I is generally considered to be a metastable structure; however, there is no definite conclusion under what circumstances this crystalline structure is stable or the crystal form will change. In this study, silk fibroin solution was prepared from B. Mor...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073524/ https://www.ncbi.nlm.nih.gov/pubmed/33923636 http://dx.doi.org/10.3390/ijms22084136 |
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author | Zhao, Meihui Qi, Zhenzhen Tao, Xiaosheng Newkirk, Chad Hu, Xiao Lu, Shenzhou |
author_facet | Zhao, Meihui Qi, Zhenzhen Tao, Xiaosheng Newkirk, Chad Hu, Xiao Lu, Shenzhou |
author_sort | Zhao, Meihui |
collection | PubMed |
description | The crystalline structure of silk fibroin Silk I is generally considered to be a metastable structure; however, there is no definite conclusion under what circumstances this crystalline structure is stable or the crystal form will change. In this study, silk fibroin solution was prepared from B. Mori silkworm cocoons, and a combined method of freeze-crystallization and freeze-drying at different temperatures was used to obtain stable Silk I crystalline material and uncrystallized silk material, respectively. Different concentrations of methanol and ethanol were used to soak the two materials with different time periods to investigate the effect of immersion treatments on the crystalline structure of silk fibroin materials. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman scattering spectroscopy (Raman), Scanning electron microscope (SEM), and Thermogravimetric analysis (TGA) were used to characterize the structure of silk fibroin before and after the treatments. The results showed that, after immersion treatments, uncrystallized silk fibroin material with random coil structure was transformed into Silk II crystal structure, while the silk material with dominated Silk I crystal structure showed good long-term stability without obvious transition to Silk II crystal structure. α-chymotrypsin biodegradation study showed that the crystalline structure of silk fibroin Silk I materials is enzymatically degradable with a much lower rate compared to uncrystallized silk materials. The crystalline structure of Silk I materials demonstrate a good long-term stability, endurance to alcohol sterilization without structural changes, and can be applied to many emerging fields, such as biomedical materials, sustainable materials, and biosensors. |
format | Online Article Text |
id | pubmed-8073524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80735242021-04-27 Chemical, Thermal, Time, and Enzymatic Stability of Silk Materials with Silk I Structure Zhao, Meihui Qi, Zhenzhen Tao, Xiaosheng Newkirk, Chad Hu, Xiao Lu, Shenzhou Int J Mol Sci Article The crystalline structure of silk fibroin Silk I is generally considered to be a metastable structure; however, there is no definite conclusion under what circumstances this crystalline structure is stable or the crystal form will change. In this study, silk fibroin solution was prepared from B. Mori silkworm cocoons, and a combined method of freeze-crystallization and freeze-drying at different temperatures was used to obtain stable Silk I crystalline material and uncrystallized silk material, respectively. Different concentrations of methanol and ethanol were used to soak the two materials with different time periods to investigate the effect of immersion treatments on the crystalline structure of silk fibroin materials. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman scattering spectroscopy (Raman), Scanning electron microscope (SEM), and Thermogravimetric analysis (TGA) were used to characterize the structure of silk fibroin before and after the treatments. The results showed that, after immersion treatments, uncrystallized silk fibroin material with random coil structure was transformed into Silk II crystal structure, while the silk material with dominated Silk I crystal structure showed good long-term stability without obvious transition to Silk II crystal structure. α-chymotrypsin biodegradation study showed that the crystalline structure of silk fibroin Silk I materials is enzymatically degradable with a much lower rate compared to uncrystallized silk materials. The crystalline structure of Silk I materials demonstrate a good long-term stability, endurance to alcohol sterilization without structural changes, and can be applied to many emerging fields, such as biomedical materials, sustainable materials, and biosensors. MDPI 2021-04-16 /pmc/articles/PMC8073524/ /pubmed/33923636 http://dx.doi.org/10.3390/ijms22084136 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhao, Meihui Qi, Zhenzhen Tao, Xiaosheng Newkirk, Chad Hu, Xiao Lu, Shenzhou Chemical, Thermal, Time, and Enzymatic Stability of Silk Materials with Silk I Structure |
title | Chemical, Thermal, Time, and Enzymatic Stability of Silk Materials with Silk I Structure |
title_full | Chemical, Thermal, Time, and Enzymatic Stability of Silk Materials with Silk I Structure |
title_fullStr | Chemical, Thermal, Time, and Enzymatic Stability of Silk Materials with Silk I Structure |
title_full_unstemmed | Chemical, Thermal, Time, and Enzymatic Stability of Silk Materials with Silk I Structure |
title_short | Chemical, Thermal, Time, and Enzymatic Stability of Silk Materials with Silk I Structure |
title_sort | chemical, thermal, time, and enzymatic stability of silk materials with silk i structure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073524/ https://www.ncbi.nlm.nih.gov/pubmed/33923636 http://dx.doi.org/10.3390/ijms22084136 |
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