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Haemostatic Nanoparticles-Derived Bioactivity of from Selaginella tamariscina Carbonisata

High-temperature carbonisation is used to prepare many traditional Chinese medicine charcoal drugs, but the bioactive haemostatic substances of these medicines and their mechanisms are still unknown. This study developed and evaluated nanoparticles (NPs) derived from Selaginella pulvinate Carbonisat...

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Autores principales: Zhao, Yusheng, Zhang, Yue, Kong, Hui, Zhang, Meiling, Cheng, Jinjun, Luo, Juan, Zhao, Yan, Qu, Huihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036756/
https://www.ncbi.nlm.nih.gov/pubmed/31973222
http://dx.doi.org/10.3390/molecules25030446
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author Zhao, Yusheng
Zhang, Yue
Kong, Hui
Zhang, Meiling
Cheng, Jinjun
Luo, Juan
Zhao, Yan
Qu, Huihua
author_facet Zhao, Yusheng
Zhang, Yue
Kong, Hui
Zhang, Meiling
Cheng, Jinjun
Luo, Juan
Zhao, Yan
Qu, Huihua
author_sort Zhao, Yusheng
collection PubMed
description High-temperature carbonisation is used to prepare many traditional Chinese medicine charcoal drugs, but the bioactive haemostatic substances of these medicines and their mechanisms are still unknown. This study developed and evaluated nanoparticles (NPs) derived from Selaginella pulvinate Carbonisata (STC) for the first time. The haemostatic effect of STC-NPs prepared at 300, 350, and 400 °C were investigated in mouse tail amputation and liver scratch experiments. STC-NPs obtained at 400 °C had the strongest haemostatic effect, and were accordingly characterised by ultraviolet–visible spectroscopy, fluorescence spectroscopy, Fourier transform infrared spectroscopy, transmission electron microscopy, high resolution transmission electron microscopy, X-ray diffractometry, and X-ray photoelectron spectroscopy. STC-NPs averaged 1.4–2.8 nm and exhibited a quantum yield of 6.06% at a maximum excitation wavelength of 332 nm and emission at 432 nm. STC-NPs displayed low toxicity against mouse monocyte macrophage RAW 264.7 cells by CCK-8 assay, and STC-NP treatment significantly shortened bleeding time in rat and mouse models. Coagulation assays showed that the haemostatic effects of STC-NPs were related to improving the fibrinogen and platelet contents, as well as decreasing the prothrombin time that resulted from stimulating extrinsic blood coagulation and activating the fibrinogen system. The STC-NPs had remarkable haemostatic effects in the tail amputation and liver scratch models; these effects may be associated with the exogenous coagulation pathway and activation of the brinogen system, according to the evaluation of the mouse coagulation parameters. This novel evaluation supports the material basis of STC use in traditional Chinese medicine, and this article is worthy of study by authors of clinical pharmacy.
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spelling pubmed-70367562020-03-11 Haemostatic Nanoparticles-Derived Bioactivity of from Selaginella tamariscina Carbonisata Zhao, Yusheng Zhang, Yue Kong, Hui Zhang, Meiling Cheng, Jinjun Luo, Juan Zhao, Yan Qu, Huihua Molecules Article High-temperature carbonisation is used to prepare many traditional Chinese medicine charcoal drugs, but the bioactive haemostatic substances of these medicines and their mechanisms are still unknown. This study developed and evaluated nanoparticles (NPs) derived from Selaginella pulvinate Carbonisata (STC) for the first time. The haemostatic effect of STC-NPs prepared at 300, 350, and 400 °C were investigated in mouse tail amputation and liver scratch experiments. STC-NPs obtained at 400 °C had the strongest haemostatic effect, and were accordingly characterised by ultraviolet–visible spectroscopy, fluorescence spectroscopy, Fourier transform infrared spectroscopy, transmission electron microscopy, high resolution transmission electron microscopy, X-ray diffractometry, and X-ray photoelectron spectroscopy. STC-NPs averaged 1.4–2.8 nm and exhibited a quantum yield of 6.06% at a maximum excitation wavelength of 332 nm and emission at 432 nm. STC-NPs displayed low toxicity against mouse monocyte macrophage RAW 264.7 cells by CCK-8 assay, and STC-NP treatment significantly shortened bleeding time in rat and mouse models. Coagulation assays showed that the haemostatic effects of STC-NPs were related to improving the fibrinogen and platelet contents, as well as decreasing the prothrombin time that resulted from stimulating extrinsic blood coagulation and activating the fibrinogen system. The STC-NPs had remarkable haemostatic effects in the tail amputation and liver scratch models; these effects may be associated with the exogenous coagulation pathway and activation of the brinogen system, according to the evaluation of the mouse coagulation parameters. This novel evaluation supports the material basis of STC use in traditional Chinese medicine, and this article is worthy of study by authors of clinical pharmacy. MDPI 2020-01-21 /pmc/articles/PMC7036756/ /pubmed/31973222 http://dx.doi.org/10.3390/molecules25030446 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhao, Yusheng
Zhang, Yue
Kong, Hui
Zhang, Meiling
Cheng, Jinjun
Luo, Juan
Zhao, Yan
Qu, Huihua
Haemostatic Nanoparticles-Derived Bioactivity of from Selaginella tamariscina Carbonisata
title Haemostatic Nanoparticles-Derived Bioactivity of from Selaginella tamariscina Carbonisata
title_full Haemostatic Nanoparticles-Derived Bioactivity of from Selaginella tamariscina Carbonisata
title_fullStr Haemostatic Nanoparticles-Derived Bioactivity of from Selaginella tamariscina Carbonisata
title_full_unstemmed Haemostatic Nanoparticles-Derived Bioactivity of from Selaginella tamariscina Carbonisata
title_short Haemostatic Nanoparticles-Derived Bioactivity of from Selaginella tamariscina Carbonisata
title_sort haemostatic nanoparticles-derived bioactivity of from selaginella tamariscina carbonisata
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036756/
https://www.ncbi.nlm.nih.gov/pubmed/31973222
http://dx.doi.org/10.3390/molecules25030446
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