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Method for the Destruction of Endotoxin in Synthetic Spider Silk Proteins
Although synthetic spider silk has impressive potential as a biomaterial, endotoxin contamination of the spider silk proteins is a concern, regardless of the production method. The purpose of this research was to establish a standardized method to either remove or destroy the endotoxins present in s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093939/ https://www.ncbi.nlm.nih.gov/pubmed/30111805 http://dx.doi.org/10.1038/s41598-018-29719-6 |
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author | Decker, Richard E. Harris, Thomas I. Memmott, Dylan R. Peterson, Christopher J. Lewis, Randolph V. Jones, Justin A. |
author_facet | Decker, Richard E. Harris, Thomas I. Memmott, Dylan R. Peterson, Christopher J. Lewis, Randolph V. Jones, Justin A. |
author_sort | Decker, Richard E. |
collection | PubMed |
description | Although synthetic spider silk has impressive potential as a biomaterial, endotoxin contamination of the spider silk proteins is a concern, regardless of the production method. The purpose of this research was to establish a standardized method to either remove or destroy the endotoxins present in synthetic spider silk proteins, such that the endotoxin level was consistently equal to or less than 0.25 EU/mL, the FDA limit for similar implant materials. Although dry heat is generally the preferred method for endotoxin destruction, heating the silk proteins to the necessary temperatures led to compromised mechanical properties in the resultant materials. In light of this, other endotoxin destruction methods were investigated, including caustic rinses and autoclaving. It was found that autoclaving synthetic spider silk protein dopes three times in a row consistently decreased the endotoxin level 10–20 fold, achieving levels at or below the desired level of 0.25 EU/mL. Products made from triple autoclaved silk dopes maintained mechanical properties comparable to products from untreated dopes while still maintaining low endotoxin levels. Triple autoclaving is an effective and scalable method for preparing synthetic spider silk proteins with endotoxin levels sufficiently low for use as biomaterials without compromising the mechanical properties of the materials. |
format | Online Article Text |
id | pubmed-6093939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60939392018-08-20 Method for the Destruction of Endotoxin in Synthetic Spider Silk Proteins Decker, Richard E. Harris, Thomas I. Memmott, Dylan R. Peterson, Christopher J. Lewis, Randolph V. Jones, Justin A. Sci Rep Article Although synthetic spider silk has impressive potential as a biomaterial, endotoxin contamination of the spider silk proteins is a concern, regardless of the production method. The purpose of this research was to establish a standardized method to either remove or destroy the endotoxins present in synthetic spider silk proteins, such that the endotoxin level was consistently equal to or less than 0.25 EU/mL, the FDA limit for similar implant materials. Although dry heat is generally the preferred method for endotoxin destruction, heating the silk proteins to the necessary temperatures led to compromised mechanical properties in the resultant materials. In light of this, other endotoxin destruction methods were investigated, including caustic rinses and autoclaving. It was found that autoclaving synthetic spider silk protein dopes three times in a row consistently decreased the endotoxin level 10–20 fold, achieving levels at or below the desired level of 0.25 EU/mL. Products made from triple autoclaved silk dopes maintained mechanical properties comparable to products from untreated dopes while still maintaining low endotoxin levels. Triple autoclaving is an effective and scalable method for preparing synthetic spider silk proteins with endotoxin levels sufficiently low for use as biomaterials without compromising the mechanical properties of the materials. Nature Publishing Group UK 2018-08-15 /pmc/articles/PMC6093939/ /pubmed/30111805 http://dx.doi.org/10.1038/s41598-018-29719-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Decker, Richard E. Harris, Thomas I. Memmott, Dylan R. Peterson, Christopher J. Lewis, Randolph V. Jones, Justin A. Method for the Destruction of Endotoxin in Synthetic Spider Silk Proteins |
title | Method for the Destruction of Endotoxin in Synthetic Spider Silk Proteins |
title_full | Method for the Destruction of Endotoxin in Synthetic Spider Silk Proteins |
title_fullStr | Method for the Destruction of Endotoxin in Synthetic Spider Silk Proteins |
title_full_unstemmed | Method for the Destruction of Endotoxin in Synthetic Spider Silk Proteins |
title_short | Method for the Destruction of Endotoxin in Synthetic Spider Silk Proteins |
title_sort | method for the destruction of endotoxin in synthetic spider silk proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093939/ https://www.ncbi.nlm.nih.gov/pubmed/30111805 http://dx.doi.org/10.1038/s41598-018-29719-6 |
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