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Biomimetic Nanofibrillation in Two-Component Biopolymer Blends with Structural Analogs to Spider Silk
Despite the enormous potential in bioinspired fabrication of high-strength structure by mimicking the spinning process of spider silk, currently accessible routes (e.g., microfluidic and electrospinning approaches) still have substantial function gaps in providing precision control over the nanofibr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046138/ https://www.ncbi.nlm.nih.gov/pubmed/27694989 http://dx.doi.org/10.1038/srep34572 |
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author | Xie, Lan Xu, Huan Li, Liang-Bin Hsiao, Benjamin S. Zhong, Gan-Ji Li, Zhong-Ming |
author_facet | Xie, Lan Xu, Huan Li, Liang-Bin Hsiao, Benjamin S. Zhong, Gan-Ji Li, Zhong-Ming |
author_sort | Xie, Lan |
collection | PubMed |
description | Despite the enormous potential in bioinspired fabrication of high-strength structure by mimicking the spinning process of spider silk, currently accessible routes (e.g., microfluidic and electrospinning approaches) still have substantial function gaps in providing precision control over the nanofibrillar superstructure, crystalline morphology or molecular orientation. Here the concept of biomimetic nanofibrillation, by copying the spiders’ spinning principles, was conceived to build silk-mimicking hierarchies in two-phase biodegradable blends, strategically involving the stepwise integration of elongational shear and high-pressure shear. Phase separation confined on nanoscale, together with deformation of discrete phases and pre-alignment of polymer chains, was triggered in the elongational shear, conferring the readiness for direct nanofibrillation in the latter shearing stage. The orderly aligned nanofibrils, featuring an ultralow diameter of around 100 nm and the “rigid−soft” system crosslinked by nanocrystal domains like silk protein dopes, were secreted by fine nanochannels. The incorporation of multiscale silk-mimicking structures afforded exceptional combination of strength, ductility and toughness for the nanofibrillar polymer composites. The proposed spider spinning-mimicking strategy, offering the biomimetic function integration unattainable with current approaches, may prompt materials scientists to pursue biopolymer mimics of silk with high performance yet light weight. |
format | Online Article Text |
id | pubmed-5046138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50461382016-10-11 Biomimetic Nanofibrillation in Two-Component Biopolymer Blends with Structural Analogs to Spider Silk Xie, Lan Xu, Huan Li, Liang-Bin Hsiao, Benjamin S. Zhong, Gan-Ji Li, Zhong-Ming Sci Rep Article Despite the enormous potential in bioinspired fabrication of high-strength structure by mimicking the spinning process of spider silk, currently accessible routes (e.g., microfluidic and electrospinning approaches) still have substantial function gaps in providing precision control over the nanofibrillar superstructure, crystalline morphology or molecular orientation. Here the concept of biomimetic nanofibrillation, by copying the spiders’ spinning principles, was conceived to build silk-mimicking hierarchies in two-phase biodegradable blends, strategically involving the stepwise integration of elongational shear and high-pressure shear. Phase separation confined on nanoscale, together with deformation of discrete phases and pre-alignment of polymer chains, was triggered in the elongational shear, conferring the readiness for direct nanofibrillation in the latter shearing stage. The orderly aligned nanofibrils, featuring an ultralow diameter of around 100 nm and the “rigid−soft” system crosslinked by nanocrystal domains like silk protein dopes, were secreted by fine nanochannels. The incorporation of multiscale silk-mimicking structures afforded exceptional combination of strength, ductility and toughness for the nanofibrillar polymer composites. The proposed spider spinning-mimicking strategy, offering the biomimetic function integration unattainable with current approaches, may prompt materials scientists to pursue biopolymer mimics of silk with high performance yet light weight. Nature Publishing Group 2016-10-03 /pmc/articles/PMC5046138/ /pubmed/27694989 http://dx.doi.org/10.1038/srep34572 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Xie, Lan Xu, Huan Li, Liang-Bin Hsiao, Benjamin S. Zhong, Gan-Ji Li, Zhong-Ming Biomimetic Nanofibrillation in Two-Component Biopolymer Blends with Structural Analogs to Spider Silk |
title | Biomimetic Nanofibrillation in Two-Component Biopolymer Blends with Structural Analogs to Spider Silk |
title_full | Biomimetic Nanofibrillation in Two-Component Biopolymer Blends with Structural Analogs to Spider Silk |
title_fullStr | Biomimetic Nanofibrillation in Two-Component Biopolymer Blends with Structural Analogs to Spider Silk |
title_full_unstemmed | Biomimetic Nanofibrillation in Two-Component Biopolymer Blends with Structural Analogs to Spider Silk |
title_short | Biomimetic Nanofibrillation in Two-Component Biopolymer Blends with Structural Analogs to Spider Silk |
title_sort | biomimetic nanofibrillation in two-component biopolymer blends with structural analogs to spider silk |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046138/ https://www.ncbi.nlm.nih.gov/pubmed/27694989 http://dx.doi.org/10.1038/srep34572 |
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