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New technology to improve the thermal stability of botulinum toxin type D by biomimetic mineralization

The advanced biomimetic mineralization technology was applied to protect the Botulinum neurotoxin type D, and the processing of the mineralization granule of botulinum toxin type D was successfully screened. The loss of activity of the toxin protein at different temperatures and the destructive stre...

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Autores principales: Li, Shengqing, Zhang, Xiyun, Hu, Guoyuan, Li, Shuping, Li, Zhining, Fan, Yuxia, Zhang, Yanming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893018/
https://www.ncbi.nlm.nih.gov/pubmed/33603080
http://dx.doi.org/10.1038/s41598-021-83733-9
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author Li, Shengqing
Zhang, Xiyun
Hu, Guoyuan
Li, Shuping
Li, Zhining
Fan, Yuxia
Zhang, Yanming
author_facet Li, Shengqing
Zhang, Xiyun
Hu, Guoyuan
Li, Shuping
Li, Zhining
Fan, Yuxia
Zhang, Yanming
author_sort Li, Shengqing
collection PubMed
description The advanced biomimetic mineralization technology was applied to protect the Botulinum neurotoxin type D, and the processing of the mineralization granule of botulinum toxin type D was successfully screened. The loss of activity of the toxin protein at different temperatures and the destructive strength of the gastrointestinal tract against the toxin were determined biologically. The lethal toxicity of the mineralized toxin to wild rodents was determined by median lethal dose. Protective tests at different temperatures showed that the preservation period of botulinum toxin type D mineralized sample 2 was significantly higher than that of the control group at three different temperatures, and its toxicity loss was significantly reduced. The damage intensity of the mineralized toxin to the gastrointestinal contents of plateau zokor and plateau pika was significantly reduced. The minimum lethal doses of the mineralized toxin particles to plateau zokor, plateau pika, and mice were 5200, 8,600,000, and 25,000 MLD/kg. These results showed that biomimetic mineralization could greatly improve the thermal stability of botulinum toxin type D and reduce the damaging effect of the gastrointestinal contents of target animals to botulinum toxin type D. The mineralized toxin could be used to control the population density of urban rodents. This research provides new insights into the protection of toxin protein substances.
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spelling pubmed-78930182021-02-23 New technology to improve the thermal stability of botulinum toxin type D by biomimetic mineralization Li, Shengqing Zhang, Xiyun Hu, Guoyuan Li, Shuping Li, Zhining Fan, Yuxia Zhang, Yanming Sci Rep Article The advanced biomimetic mineralization technology was applied to protect the Botulinum neurotoxin type D, and the processing of the mineralization granule of botulinum toxin type D was successfully screened. The loss of activity of the toxin protein at different temperatures and the destructive strength of the gastrointestinal tract against the toxin were determined biologically. The lethal toxicity of the mineralized toxin to wild rodents was determined by median lethal dose. Protective tests at different temperatures showed that the preservation period of botulinum toxin type D mineralized sample 2 was significantly higher than that of the control group at three different temperatures, and its toxicity loss was significantly reduced. The damage intensity of the mineralized toxin to the gastrointestinal contents of plateau zokor and plateau pika was significantly reduced. The minimum lethal doses of the mineralized toxin particles to plateau zokor, plateau pika, and mice were 5200, 8,600,000, and 25,000 MLD/kg. These results showed that biomimetic mineralization could greatly improve the thermal stability of botulinum toxin type D and reduce the damaging effect of the gastrointestinal contents of target animals to botulinum toxin type D. The mineralized toxin could be used to control the population density of urban rodents. This research provides new insights into the protection of toxin protein substances. Nature Publishing Group UK 2021-02-18 /pmc/articles/PMC7893018/ /pubmed/33603080 http://dx.doi.org/10.1038/s41598-021-83733-9 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Shengqing
Zhang, Xiyun
Hu, Guoyuan
Li, Shuping
Li, Zhining
Fan, Yuxia
Zhang, Yanming
New technology to improve the thermal stability of botulinum toxin type D by biomimetic mineralization
title New technology to improve the thermal stability of botulinum toxin type D by biomimetic mineralization
title_full New technology to improve the thermal stability of botulinum toxin type D by biomimetic mineralization
title_fullStr New technology to improve the thermal stability of botulinum toxin type D by biomimetic mineralization
title_full_unstemmed New technology to improve the thermal stability of botulinum toxin type D by biomimetic mineralization
title_short New technology to improve the thermal stability of botulinum toxin type D by biomimetic mineralization
title_sort new technology to improve the thermal stability of botulinum toxin type d by biomimetic mineralization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893018/
https://www.ncbi.nlm.nih.gov/pubmed/33603080
http://dx.doi.org/10.1038/s41598-021-83733-9
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