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Preparation and characterization of silk fibroin as a biomaterial with potential for drug delivery

BACKGROUND: Degummed silk fibroin from Bombyx mori (silkworm) has potential carrier capabilities for drug delivery in humans; however, the processing methods have yet to be comparatively analyzed to determine the differential effects on the silk protein properties, including crystalline structure an...

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Autores principales: Zhang, Hao, Li, Ling-ling, Dai, Fang-yin, Zhang, Hao-hao, Ni, Bing, Zhou, Wei, Yang, Xia, Wu, Yu-zhang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538618/
https://www.ncbi.nlm.nih.gov/pubmed/22676291
http://dx.doi.org/10.1186/1479-5876-10-117
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author Zhang, Hao
Li, Ling-ling
Dai, Fang-yin
Zhang, Hao-hao
Ni, Bing
Zhou, Wei
Yang, Xia
Wu, Yu-zhang
author_facet Zhang, Hao
Li, Ling-ling
Dai, Fang-yin
Zhang, Hao-hao
Ni, Bing
Zhou, Wei
Yang, Xia
Wu, Yu-zhang
author_sort Zhang, Hao
collection PubMed
description BACKGROUND: Degummed silk fibroin from Bombyx mori (silkworm) has potential carrier capabilities for drug delivery in humans; however, the processing methods have yet to be comparatively analyzed to determine the differential effects on the silk protein properties, including crystalline structure and activity. METHODS: In this study, we treated degummed silk with four kinds of calcium-alcohol solutions, and performed secondary structure measurements and enzyme activity test to distinguish the differences between the regenerated fibroins and degummed silk fibroin. RESULTS: Gel electrophoresis analysis revealed that Ca(NO(3))(2)-methanol, Ca(NO(3))(2)-ethanol, or CaCl(2)-methanol treatments produced more lower molecular weights of silk fibroin than CaCl(2)-ethanol. X-ray diffraction and Fourier-transform infrared spectroscopy showed that CaCl(2)-ethanol produced a crystalline structure with more silk I (α-form, type II β-turn), while the other treatments produced more silk II (β-form, anti-parallel β-pleated sheet). Solid-State (13)C cross polarization and magic angle spinning-nuclear magnetic resonance measurements suggested that regenerated fibroins from CaCl(2)-ethanol were nearly identical to degummed silk fibroin, while the other treatments produced fibroins with significantly different chemical shifts. Finally, enzyme activity test indicated that silk fibroins from CaCl(2)-ethanol had higher activity when linked to a known chemotherapeutic drug, L-asparaginase, than the fibroins from other treatments. CONCLUSIONS: Collectively, these results suggest that the CaCl(2)-ethanol processing method produces silk fibroin with biomaterial properties that are appropriate for drug delivery.
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spelling pubmed-35386182013-01-10 Preparation and characterization of silk fibroin as a biomaterial with potential for drug delivery Zhang, Hao Li, Ling-ling Dai, Fang-yin Zhang, Hao-hao Ni, Bing Zhou, Wei Yang, Xia Wu, Yu-zhang J Transl Med Research BACKGROUND: Degummed silk fibroin from Bombyx mori (silkworm) has potential carrier capabilities for drug delivery in humans; however, the processing methods have yet to be comparatively analyzed to determine the differential effects on the silk protein properties, including crystalline structure and activity. METHODS: In this study, we treated degummed silk with four kinds of calcium-alcohol solutions, and performed secondary structure measurements and enzyme activity test to distinguish the differences between the regenerated fibroins and degummed silk fibroin. RESULTS: Gel electrophoresis analysis revealed that Ca(NO(3))(2)-methanol, Ca(NO(3))(2)-ethanol, or CaCl(2)-methanol treatments produced more lower molecular weights of silk fibroin than CaCl(2)-ethanol. X-ray diffraction and Fourier-transform infrared spectroscopy showed that CaCl(2)-ethanol produced a crystalline structure with more silk I (α-form, type II β-turn), while the other treatments produced more silk II (β-form, anti-parallel β-pleated sheet). Solid-State (13)C cross polarization and magic angle spinning-nuclear magnetic resonance measurements suggested that regenerated fibroins from CaCl(2)-ethanol were nearly identical to degummed silk fibroin, while the other treatments produced fibroins with significantly different chemical shifts. Finally, enzyme activity test indicated that silk fibroins from CaCl(2)-ethanol had higher activity when linked to a known chemotherapeutic drug, L-asparaginase, than the fibroins from other treatments. CONCLUSIONS: Collectively, these results suggest that the CaCl(2)-ethanol processing method produces silk fibroin with biomaterial properties that are appropriate for drug delivery. BioMed Central 2012-06-07 /pmc/articles/PMC3538618/ /pubmed/22676291 http://dx.doi.org/10.1186/1479-5876-10-117 Text en Copyright ©2012 Zhang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Zhang, Hao
Li, Ling-ling
Dai, Fang-yin
Zhang, Hao-hao
Ni, Bing
Zhou, Wei
Yang, Xia
Wu, Yu-zhang
Preparation and characterization of silk fibroin as a biomaterial with potential for drug delivery
title Preparation and characterization of silk fibroin as a biomaterial with potential for drug delivery
title_full Preparation and characterization of silk fibroin as a biomaterial with potential for drug delivery
title_fullStr Preparation and characterization of silk fibroin as a biomaterial with potential for drug delivery
title_full_unstemmed Preparation and characterization of silk fibroin as a biomaterial with potential for drug delivery
title_short Preparation and characterization of silk fibroin as a biomaterial with potential for drug delivery
title_sort preparation and characterization of silk fibroin as a biomaterial with potential for drug delivery
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538618/
https://www.ncbi.nlm.nih.gov/pubmed/22676291
http://dx.doi.org/10.1186/1479-5876-10-117
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