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Microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing
Developing an anti-infective shape-memory hemostatic sponge able to guide in situ tissue regeneration for noncompressible hemorrhages in civilian and battlefield settings remains a challenge. Here we engineer hemostatic chitosan sponges with highly interconnective microchannels by combining 3D print...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342549/ https://www.ncbi.nlm.nih.gov/pubmed/34354068 http://dx.doi.org/10.1038/s41467-021-24972-2 |
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author | Du, Xinchen Wu, Le Yan, Hongyu Jiang, Zhuyan Li, Shilin Li, Wen Bai, Yanli Wang, Hongjun Cheng, Zhaojun Kong, Deling Wang, Lianyong Zhu, Meifeng |
author_facet | Du, Xinchen Wu, Le Yan, Hongyu Jiang, Zhuyan Li, Shilin Li, Wen Bai, Yanli Wang, Hongjun Cheng, Zhaojun Kong, Deling Wang, Lianyong Zhu, Meifeng |
author_sort | Du, Xinchen |
collection | PubMed |
description | Developing an anti-infective shape-memory hemostatic sponge able to guide in situ tissue regeneration for noncompressible hemorrhages in civilian and battlefield settings remains a challenge. Here we engineer hemostatic chitosan sponges with highly interconnective microchannels by combining 3D printed microfiber leaching, freeze-drying, and superficial active modification. We demonstrate that the microchannelled alkylated chitosan sponge (MACS) exhibits the capacity for water and blood absorption, as well as rapid shape recovery. We show that compared to clinically used gauze, gelatin sponge, CELOX™, and CELOX™-gauze, the MACS provides higher pro-coagulant and hemostatic capacities in lethally normal and heparinized rat and pig liver perforation wound models. We demonstrate its anti-infective activity against S. aureus and E. coli and its promotion of liver parenchymal cell infiltration, vascularization, and tissue integration in a rat liver defect model. Overall, the MACS demonstrates promising clinical translational potential in treating lethal noncompressible hemorrhage and facilitating wound healing. |
format | Online Article Text |
id | pubmed-8342549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83425492021-08-20 Microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing Du, Xinchen Wu, Le Yan, Hongyu Jiang, Zhuyan Li, Shilin Li, Wen Bai, Yanli Wang, Hongjun Cheng, Zhaojun Kong, Deling Wang, Lianyong Zhu, Meifeng Nat Commun Article Developing an anti-infective shape-memory hemostatic sponge able to guide in situ tissue regeneration for noncompressible hemorrhages in civilian and battlefield settings remains a challenge. Here we engineer hemostatic chitosan sponges with highly interconnective microchannels by combining 3D printed microfiber leaching, freeze-drying, and superficial active modification. We demonstrate that the microchannelled alkylated chitosan sponge (MACS) exhibits the capacity for water and blood absorption, as well as rapid shape recovery. We show that compared to clinically used gauze, gelatin sponge, CELOX™, and CELOX™-gauze, the MACS provides higher pro-coagulant and hemostatic capacities in lethally normal and heparinized rat and pig liver perforation wound models. We demonstrate its anti-infective activity against S. aureus and E. coli and its promotion of liver parenchymal cell infiltration, vascularization, and tissue integration in a rat liver defect model. Overall, the MACS demonstrates promising clinical translational potential in treating lethal noncompressible hemorrhage and facilitating wound healing. Nature Publishing Group UK 2021-08-05 /pmc/articles/PMC8342549/ /pubmed/34354068 http://dx.doi.org/10.1038/s41467-021-24972-2 Text en © The Author(s) 2021 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Du, Xinchen Wu, Le Yan, Hongyu Jiang, Zhuyan Li, Shilin Li, Wen Bai, Yanli Wang, Hongjun Cheng, Zhaojun Kong, Deling Wang, Lianyong Zhu, Meifeng Microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing |
title | Microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing |
title_full | Microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing |
title_fullStr | Microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing |
title_full_unstemmed | Microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing |
title_short | Microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing |
title_sort | microchannelled alkylated chitosan sponge to treat noncompressible hemorrhages and facilitate wound healing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342549/ https://www.ncbi.nlm.nih.gov/pubmed/34354068 http://dx.doi.org/10.1038/s41467-021-24972-2 |
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