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A polymer-based systemic hemostatic agent
Uncontrolled noncompressible hemorrhage is a major cause of mortality following traumatic injuries in civilian and military populations. An injectable hemostat for point-of-care treatment of noncompressible hemorrhage represents an urgent medical need. Here, we describe an injectable hemostatic agen...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394519/ https://www.ncbi.nlm.nih.gov/pubmed/32775633 http://dx.doi.org/10.1126/sciadv.aba0588 |
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author | Gao, Yongsheng Sarode, Apoorva Kokoroskos, Nikolaos Ukidve, Anvay Zhao, Zongmin Guo, Shihui Flaumenhaft, Robert Gupta, Anirban Sen Saillant, Noelle Mitragotri, Samir |
author_facet | Gao, Yongsheng Sarode, Apoorva Kokoroskos, Nikolaos Ukidve, Anvay Zhao, Zongmin Guo, Shihui Flaumenhaft, Robert Gupta, Anirban Sen Saillant, Noelle Mitragotri, Samir |
author_sort | Gao, Yongsheng |
collection | PubMed |
description | Uncontrolled noncompressible hemorrhage is a major cause of mortality following traumatic injuries in civilian and military populations. An injectable hemostat for point-of-care treatment of noncompressible hemorrhage represents an urgent medical need. Here, we describe an injectable hemostatic agent via polymer peptide interfusion (HAPPI), a hyaluronic acid conjugate with a collagen-binding peptide and a von Willebrand factor–binding peptide. HAPPI exhibited selective binding to activated platelets and promoted their accumulation at the wound site in vitro. In vivo studies in mouse tail vein laceration model demonstrated a reduction of >97% in both bleeding time and blood loss. A 284% improvement in the survival time was observed in the rat inferior vena cava traumatic model. Lyophilized HAPPI could be stably stored at room temperature for several months and reconstituted during therapeutic intervention. HAPPI provides a potentially clinically translatable intravenous hemostat. |
format | Online Article Text |
id | pubmed-7394519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-73945192020-08-07 A polymer-based systemic hemostatic agent Gao, Yongsheng Sarode, Apoorva Kokoroskos, Nikolaos Ukidve, Anvay Zhao, Zongmin Guo, Shihui Flaumenhaft, Robert Gupta, Anirban Sen Saillant, Noelle Mitragotri, Samir Sci Adv Research Articles Uncontrolled noncompressible hemorrhage is a major cause of mortality following traumatic injuries in civilian and military populations. An injectable hemostat for point-of-care treatment of noncompressible hemorrhage represents an urgent medical need. Here, we describe an injectable hemostatic agent via polymer peptide interfusion (HAPPI), a hyaluronic acid conjugate with a collagen-binding peptide and a von Willebrand factor–binding peptide. HAPPI exhibited selective binding to activated platelets and promoted their accumulation at the wound site in vitro. In vivo studies in mouse tail vein laceration model demonstrated a reduction of >97% in both bleeding time and blood loss. A 284% improvement in the survival time was observed in the rat inferior vena cava traumatic model. Lyophilized HAPPI could be stably stored at room temperature for several months and reconstituted during therapeutic intervention. HAPPI provides a potentially clinically translatable intravenous hemostat. American Association for the Advancement of Science 2020-07-31 /pmc/articles/PMC7394519/ /pubmed/32775633 http://dx.doi.org/10.1126/sciadv.aba0588 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Gao, Yongsheng Sarode, Apoorva Kokoroskos, Nikolaos Ukidve, Anvay Zhao, Zongmin Guo, Shihui Flaumenhaft, Robert Gupta, Anirban Sen Saillant, Noelle Mitragotri, Samir A polymer-based systemic hemostatic agent |
title | A polymer-based systemic hemostatic agent |
title_full | A polymer-based systemic hemostatic agent |
title_fullStr | A polymer-based systemic hemostatic agent |
title_full_unstemmed | A polymer-based systemic hemostatic agent |
title_short | A polymer-based systemic hemostatic agent |
title_sort | polymer-based systemic hemostatic agent |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394519/ https://www.ncbi.nlm.nih.gov/pubmed/32775633 http://dx.doi.org/10.1126/sciadv.aba0588 |
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