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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Main Authors: Meihui Zhao, Zhenzhen Qi, Xiaosheng Tao, Chad Newkirk, Xiao Hu, Shenzhou Lu
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/8/4136
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spelling doaj-03e18d448fd745ba97f902b9cacf0fdb2021-04-16T23:04:16ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-04-01224136413610.3390/ijms22084136Chemical, Thermal, Time, and Enzymatic Stability of Silk Materials with Silk I StructureMeihui Zhao0Zhenzhen Qi1Xiaosheng Tao2Chad Newkirk3Xiao Hu4Shenzhou Lu5National Engineering Laboratory for Modern Silk, College of Textile and Clothing Engineering, Soochow University, Suzhou 215123, ChinaNational Engineering Laboratory for Modern Silk, College of Textile and Clothing Engineering, Soochow University, Suzhou 215123, ChinaNational Engineering Laboratory for Modern Silk, College of Textile and Clothing Engineering, Soochow University, Suzhou 215123, ChinaDepartment of Physics and Astronomy, Rowan University, Glassboro, NJ 08028, USADepartment of Physics and Astronomy, Rowan University, Glassboro, NJ 08028, USANational Engineering Laboratory for Modern Silk, College of Textile and Clothing Engineering, Soochow University, Suzhou 215123, ChinaThe 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.https://www.mdpi.com/1422-0067/22/8/4136silk fibroinporous materialcrystalline structurestability
collection DOAJ
language English
format Article
sources DOAJ
author Meihui Zhao
Zhenzhen Qi
Xiaosheng Tao
Chad Newkirk
Xiao Hu
Shenzhou Lu
spellingShingle Meihui Zhao
Zhenzhen Qi
Xiaosheng Tao
Chad Newkirk
Xiao Hu
Shenzhou Lu
Chemical, Thermal, Time, and Enzymatic Stability of Silk Materials with Silk I Structure
International Journal of Molecular Sciences
silk fibroin
porous material
crystalline structure
stability
author_facet Meihui Zhao
Zhenzhen Qi
Xiaosheng Tao
Chad Newkirk
Xiao Hu
Shenzhou Lu
author_sort Meihui Zhao
title 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_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_sort chemical, thermal, time, and enzymatic stability of silk materials with silk i structure
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-04-01
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.
topic silk fibroin
porous material
crystalline structure
stability
url https://www.mdpi.com/1422-0067/22/8/4136
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