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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...

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Autores principales: Zhao, Meihui, Qi, Zhenzhen, Tao, Xiaosheng, Newkirk, Chad, Hu, Xiao, Lu, Shenzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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