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Thrombin@Fe(3)O(4) nanoparticles for use as a hemostatic agent in internal bleeding
Bleeding remains one of the main causes of premature mortality at present, with internal bleeding being the most dangerous case. In this paper, magnetic hemostatic nanoparticles are shown for the first time to assist in minimally invasive treatment of internal bleeding, implying the introduction dir...
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/PMC5762673/ https://www.ncbi.nlm.nih.gov/pubmed/29321571 http://dx.doi.org/10.1038/s41598-017-18665-4 |
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author | Shabanova, Emiliya M. Drozdov, Andrey S. Fakhardo, Anna F. Dudanov, Ivan P. Kovalchuk, Marina S. Vinogradov, Vladimir V. |
author_facet | Shabanova, Emiliya M. Drozdov, Andrey S. Fakhardo, Anna F. Dudanov, Ivan P. Kovalchuk, Marina S. Vinogradov, Vladimir V. |
author_sort | Shabanova, Emiliya M. |
collection | PubMed |
description | Bleeding remains one of the main causes of premature mortality at present, with internal bleeding being the most dangerous case. In this paper, magnetic hemostatic nanoparticles are shown for the first time to assist in minimally invasive treatment of internal bleeding, implying the introduction directly into the circulatory system followed by localization in the bleeding zone due to the application of an external magnetic field. Nanoparticles were produced by entrapping human thrombin (THR) into a sol-gel derived magnetite matrix followed by grinding to sizes below 200 nm and subsequent colloidization. Prepared colloids show protrombotic activity and cause plasma coagulation in in vitro experiments. We also show here using a model blood vessel that the THR@ferria composite does not cause systematic thrombosis due to low activity, but being concentrated by an external magnetic field with simultaneous fibrinogen injection accelerates local hemostasis and stops the bleeding. For instance, a model vessel system with circulating blood at the puncture of the vessel wall and the application of a permanent magnetic field yielded a hemostasis time by a factor of 6.5 shorter than that observed for the control sample. Biocompatibility of composites was tested on HELF and HeLa cells and revealed no toxic effects. |
format | Online Article Text |
id | pubmed-5762673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57626732018-01-17 Thrombin@Fe(3)O(4) nanoparticles for use as a hemostatic agent in internal bleeding Shabanova, Emiliya M. Drozdov, Andrey S. Fakhardo, Anna F. Dudanov, Ivan P. Kovalchuk, Marina S. Vinogradov, Vladimir V. Sci Rep Article Bleeding remains one of the main causes of premature mortality at present, with internal bleeding being the most dangerous case. In this paper, magnetic hemostatic nanoparticles are shown for the first time to assist in minimally invasive treatment of internal bleeding, implying the introduction directly into the circulatory system followed by localization in the bleeding zone due to the application of an external magnetic field. Nanoparticles were produced by entrapping human thrombin (THR) into a sol-gel derived magnetite matrix followed by grinding to sizes below 200 nm and subsequent colloidization. Prepared colloids show protrombotic activity and cause plasma coagulation in in vitro experiments. We also show here using a model blood vessel that the THR@ferria composite does not cause systematic thrombosis due to low activity, but being concentrated by an external magnetic field with simultaneous fibrinogen injection accelerates local hemostasis and stops the bleeding. For instance, a model vessel system with circulating blood at the puncture of the vessel wall and the application of a permanent magnetic field yielded a hemostasis time by a factor of 6.5 shorter than that observed for the control sample. Biocompatibility of composites was tested on HELF and HeLa cells and revealed no toxic effects. Nature Publishing Group UK 2018-01-10 /pmc/articles/PMC5762673/ /pubmed/29321571 http://dx.doi.org/10.1038/s41598-017-18665-4 Text en © The Author(s) 2017 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 Shabanova, Emiliya M. Drozdov, Andrey S. Fakhardo, Anna F. Dudanov, Ivan P. Kovalchuk, Marina S. Vinogradov, Vladimir V. Thrombin@Fe(3)O(4) nanoparticles for use as a hemostatic agent in internal bleeding |
title | Thrombin@Fe(3)O(4) nanoparticles for use as a hemostatic agent in internal bleeding |
title_full | Thrombin@Fe(3)O(4) nanoparticles for use as a hemostatic agent in internal bleeding |
title_fullStr | Thrombin@Fe(3)O(4) nanoparticles for use as a hemostatic agent in internal bleeding |
title_full_unstemmed | Thrombin@Fe(3)O(4) nanoparticles for use as a hemostatic agent in internal bleeding |
title_short | Thrombin@Fe(3)O(4) nanoparticles for use as a hemostatic agent in internal bleeding |
title_sort | thrombin@fe(3)o(4) nanoparticles for use as a hemostatic agent in internal bleeding |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762673/ https://www.ncbi.nlm.nih.gov/pubmed/29321571 http://dx.doi.org/10.1038/s41598-017-18665-4 |
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