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Self-anticoagulant sponge for whole blood auto-transfusion and its mechanism of coagulation factor inactivation
Clinical use of intraoperative auto-transfusion requires the removal of platelets and plasma proteins due to pump-based suction and water-soluble anticoagulant administration, which causes dilutional coagulopathy. Herein, we develop a carboxylated and sulfonated heparin-mimetic polymer-modified spon...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423252/ https://www.ncbi.nlm.nih.gov/pubmed/37573353 http://dx.doi.org/10.1038/s41467-023-40646-7 |
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author | Xu, Tao Ji, Haifeng Xu, Lin Cheng, Shengjun Liu, Xianda Li, Yupei Zhong, Rui Zhao, Weifeng Kizhakkedathu, Jayachandran N. Zhao, Changsheng |
author_facet | Xu, Tao Ji, Haifeng Xu, Lin Cheng, Shengjun Liu, Xianda Li, Yupei Zhong, Rui Zhao, Weifeng Kizhakkedathu, Jayachandran N. Zhao, Changsheng |
author_sort | Xu, Tao |
collection | PubMed |
description | Clinical use of intraoperative auto-transfusion requires the removal of platelets and plasma proteins due to pump-based suction and water-soluble anticoagulant administration, which causes dilutional coagulopathy. Herein, we develop a carboxylated and sulfonated heparin-mimetic polymer-modified sponge with spontaneous blood adsorption and instantaneous anticoagulation. We find that intrinsic coagulation factors, especially XI, are inactivated by adsorption to the sponge surface, while inactivation of thrombin in the sponge-treated plasma effectively inhibits the common coagulation pathway. We show whole blood auto-transfusion in trauma-induced hemorrhage, benefiting from the multiple inhibitory effects of the sponge on coagulation enzymes and calcium depletion. We demonstrate that the transfusion of collected blood favors faster recovery of hemostasis compared to traditional heparinized blood in a rabbit model. Our work not only develops a safe and convenient approach for whole blood auto-transfusion, but also provides the mechanism of action of self-anticoagulant heparin-mimetic polymer-modified surfaces. |
format | Online Article Text |
id | pubmed-10423252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104232522023-08-14 Self-anticoagulant sponge for whole blood auto-transfusion and its mechanism of coagulation factor inactivation Xu, Tao Ji, Haifeng Xu, Lin Cheng, Shengjun Liu, Xianda Li, Yupei Zhong, Rui Zhao, Weifeng Kizhakkedathu, Jayachandran N. Zhao, Changsheng Nat Commun Article Clinical use of intraoperative auto-transfusion requires the removal of platelets and plasma proteins due to pump-based suction and water-soluble anticoagulant administration, which causes dilutional coagulopathy. Herein, we develop a carboxylated and sulfonated heparin-mimetic polymer-modified sponge with spontaneous blood adsorption and instantaneous anticoagulation. We find that intrinsic coagulation factors, especially XI, are inactivated by adsorption to the sponge surface, while inactivation of thrombin in the sponge-treated plasma effectively inhibits the common coagulation pathway. We show whole blood auto-transfusion in trauma-induced hemorrhage, benefiting from the multiple inhibitory effects of the sponge on coagulation enzymes and calcium depletion. We demonstrate that the transfusion of collected blood favors faster recovery of hemostasis compared to traditional heparinized blood in a rabbit model. Our work not only develops a safe and convenient approach for whole blood auto-transfusion, but also provides the mechanism of action of self-anticoagulant heparin-mimetic polymer-modified surfaces. Nature Publishing Group UK 2023-08-12 /pmc/articles/PMC10423252/ /pubmed/37573353 http://dx.doi.org/10.1038/s41467-023-40646-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Xu, Tao Ji, Haifeng Xu, Lin Cheng, Shengjun Liu, Xianda Li, Yupei Zhong, Rui Zhao, Weifeng Kizhakkedathu, Jayachandran N. Zhao, Changsheng Self-anticoagulant sponge for whole blood auto-transfusion and its mechanism of coagulation factor inactivation |
title | Self-anticoagulant sponge for whole blood auto-transfusion and its mechanism of coagulation factor inactivation |
title_full | Self-anticoagulant sponge for whole blood auto-transfusion and its mechanism of coagulation factor inactivation |
title_fullStr | Self-anticoagulant sponge for whole blood auto-transfusion and its mechanism of coagulation factor inactivation |
title_full_unstemmed | Self-anticoagulant sponge for whole blood auto-transfusion and its mechanism of coagulation factor inactivation |
title_short | Self-anticoagulant sponge for whole blood auto-transfusion and its mechanism of coagulation factor inactivation |
title_sort | self-anticoagulant sponge for whole blood auto-transfusion and its mechanism of coagulation factor inactivation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423252/ https://www.ncbi.nlm.nih.gov/pubmed/37573353 http://dx.doi.org/10.1038/s41467-023-40646-7 |
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