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An improved blood hemorrhaging treatment using diatoms frustules, by alternating Ca and light levels in cultures

Hemorrhage control requires hemostatic materials that are both effective and biocompatible. Among these, diatom biosilica (DBs) could significantly improve hemorrhage control, but it induces hemolysis (the hemolysis rate > 5%). Thus, the purpose of this study was to explore the influence of Ca(2+...

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Autores principales: Li, Qinfeng, He, Zheng, Rozan, Hussein. E., Feng, Chao, Cheng, Xiaojie, Chen, Xiguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449749/
https://www.ncbi.nlm.nih.gov/pubmed/37637254
http://dx.doi.org/10.1007/s42995-023-00180-3
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author Li, Qinfeng
He, Zheng
Rozan, Hussein. E.
Feng, Chao
Cheng, Xiaojie
Chen, Xiguang
author_facet Li, Qinfeng
He, Zheng
Rozan, Hussein. E.
Feng, Chao
Cheng, Xiaojie
Chen, Xiguang
author_sort Li, Qinfeng
collection PubMed
description Hemorrhage control requires hemostatic materials that are both effective and biocompatible. Among these, diatom biosilica (DBs) could significantly improve hemorrhage control, but it induces hemolysis (the hemolysis rate > 5%). Thus, the purpose of this study was to explore the influence of Ca(2+) biomineralization on DBs for developing fast hemostatic materials with a low hemolysis rate. Here, CaCl(2) was added to the diatom medium under high light (cool white, fluorescent lamps, 67.5 µmol m(−2) s(−1)), producing Ca-DBs-3 with a particle size of 40–50 μm and a Ca(2+) content of Ca-DBs-3 obtained from the higher concentration CaCl(2) group (6.7 mmol L(−1)) of 0.16%. The liquid absorption capacity of Ca-DBs-3 was 30.43 ± 0.57 times its dry weight; the in vitro clotting time was comparable to QuikClot(®) zeolite; the hemostatic time and blood loss using the rat tail amputation model were 36.40 ± 2.52 s and 0.39 ± 0.12 g, which were 40.72% and 19.50% of QuikClot(®) zeolite, respectively. Ca-DBs-3 showed no apparent toxicity to L929 cells (cell viability > 80%) and was non-hemolysis (the hemolysis rate < 2%). This study prepared Ca-DBs-3 with a rapid hemostatic effect and good biocompatibility, providing a path to develop diatom biosilica hemostatic materials. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s42995-023-00180-3.
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spelling pubmed-104497492023-08-26 An improved blood hemorrhaging treatment using diatoms frustules, by alternating Ca and light levels in cultures Li, Qinfeng He, Zheng Rozan, Hussein. E. Feng, Chao Cheng, Xiaojie Chen, Xiguang Mar Life Sci Technol Research Paper Hemorrhage control requires hemostatic materials that are both effective and biocompatible. Among these, diatom biosilica (DBs) could significantly improve hemorrhage control, but it induces hemolysis (the hemolysis rate > 5%). Thus, the purpose of this study was to explore the influence of Ca(2+) biomineralization on DBs for developing fast hemostatic materials with a low hemolysis rate. Here, CaCl(2) was added to the diatom medium under high light (cool white, fluorescent lamps, 67.5 µmol m(−2) s(−1)), producing Ca-DBs-3 with a particle size of 40–50 μm and a Ca(2+) content of Ca-DBs-3 obtained from the higher concentration CaCl(2) group (6.7 mmol L(−1)) of 0.16%. The liquid absorption capacity of Ca-DBs-3 was 30.43 ± 0.57 times its dry weight; the in vitro clotting time was comparable to QuikClot(®) zeolite; the hemostatic time and blood loss using the rat tail amputation model were 36.40 ± 2.52 s and 0.39 ± 0.12 g, which were 40.72% and 19.50% of QuikClot(®) zeolite, respectively. Ca-DBs-3 showed no apparent toxicity to L929 cells (cell viability > 80%) and was non-hemolysis (the hemolysis rate < 2%). This study prepared Ca-DBs-3 with a rapid hemostatic effect and good biocompatibility, providing a path to develop diatom biosilica hemostatic materials. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s42995-023-00180-3. Springer Nature Singapore 2023-08-18 /pmc/articles/PMC10449749/ /pubmed/37637254 http://dx.doi.org/10.1007/s42995-023-00180-3 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 Research Paper
Li, Qinfeng
He, Zheng
Rozan, Hussein. E.
Feng, Chao
Cheng, Xiaojie
Chen, Xiguang
An improved blood hemorrhaging treatment using diatoms frustules, by alternating Ca and light levels in cultures
title An improved blood hemorrhaging treatment using diatoms frustules, by alternating Ca and light levels in cultures
title_full An improved blood hemorrhaging treatment using diatoms frustules, by alternating Ca and light levels in cultures
title_fullStr An improved blood hemorrhaging treatment using diatoms frustules, by alternating Ca and light levels in cultures
title_full_unstemmed An improved blood hemorrhaging treatment using diatoms frustules, by alternating Ca and light levels in cultures
title_short An improved blood hemorrhaging treatment using diatoms frustules, by alternating Ca and light levels in cultures
title_sort improved blood hemorrhaging treatment using diatoms frustules, by alternating ca and light levels in cultures
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449749/
https://www.ncbi.nlm.nih.gov/pubmed/37637254
http://dx.doi.org/10.1007/s42995-023-00180-3
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