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Cytotoxicity and Anti-Plasmodium berghei Activity of Emodin Loaded Nanoemulsion
BACKGROUND: Malaria parasites cause a tremendous burden of disease in both the tropics and subtropics areas. Growing of drugs resistance in parasites is one of the most threats to malaria control. The aim of study was to investigate the anti-malarial activity of nano-emodin isolated from Rhamnus cat...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682369/ https://www.ncbi.nlm.nih.gov/pubmed/36466013 http://dx.doi.org/10.18502/ijpa.v17i3.10624 |
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author | Bayat, Fatemeh Motevalli Haghi, Afsaneh Nateghpour, Mehdi Rahimi-Esboei, Bahman Rahimi Foroushani, Abbas Amani, Amir Farivar, Leila Sayyad Talaee, Zahra Faryabi, Aref |
author_facet | Bayat, Fatemeh Motevalli Haghi, Afsaneh Nateghpour, Mehdi Rahimi-Esboei, Bahman Rahimi Foroushani, Abbas Amani, Amir Farivar, Leila Sayyad Talaee, Zahra Faryabi, Aref |
author_sort | Bayat, Fatemeh |
collection | PubMed |
description | BACKGROUND: Malaria parasites cause a tremendous burden of disease in both the tropics and subtropics areas. Growing of drugs resistance in parasites is one of the most threats to malaria control. The aim of study was to investigate the anti-malarial activity of nano-emodin isolated from Rhamnus cathartica on Plasmodium berghei in mice to evaluate parasites inhibition rate using in-vivo test. METHODS: The study was conducted in the School of Public Health, Tehran University of Medical Sciences, during 2020. Nano-emodin particles were prepared from Rhamnus cathartica, and confirmed by Zeta Potential Analyzer, DLS and electron microscopy techniques. Mice were infected with P. berghei and treated by emodin nano-particles. Parasitemia was evaluated in each group in comparison with control group. Toxicity test was done using twice the highest concentration of emodin extract on a separate group of mice and ED50 was calculated. RESULTS: Emodin extract was significantly effective in all concentrations on D4 (P<0.05). The most effective on parasitemia was observed in 400 mg/kg of Liquid Nano-emodin and solid (non-Nano) emodin. ED50 for emodin extract was determined 220 mg/kg. Toxicity test showed no toxic effect on the subjects. CONCLUSION: The emodin extract is safe, lack of side effects. So, it can be used for more and longer period of time and in higher doses. Emodin extract, either in form of liquid and nanoparticle or in a solid form, has the same therapeutic effect on P. berghei in infected Balb/c mice. |
format | Online Article Text |
id | pubmed-9682369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-96823692022-12-02 Cytotoxicity and Anti-Plasmodium berghei Activity of Emodin Loaded Nanoemulsion Bayat, Fatemeh Motevalli Haghi, Afsaneh Nateghpour, Mehdi Rahimi-Esboei, Bahman Rahimi Foroushani, Abbas Amani, Amir Farivar, Leila Sayyad Talaee, Zahra Faryabi, Aref Iran J Parasitol Original Article BACKGROUND: Malaria parasites cause a tremendous burden of disease in both the tropics and subtropics areas. Growing of drugs resistance in parasites is one of the most threats to malaria control. The aim of study was to investigate the anti-malarial activity of nano-emodin isolated from Rhamnus cathartica on Plasmodium berghei in mice to evaluate parasites inhibition rate using in-vivo test. METHODS: The study was conducted in the School of Public Health, Tehran University of Medical Sciences, during 2020. Nano-emodin particles were prepared from Rhamnus cathartica, and confirmed by Zeta Potential Analyzer, DLS and electron microscopy techniques. Mice were infected with P. berghei and treated by emodin nano-particles. Parasitemia was evaluated in each group in comparison with control group. Toxicity test was done using twice the highest concentration of emodin extract on a separate group of mice and ED50 was calculated. RESULTS: Emodin extract was significantly effective in all concentrations on D4 (P<0.05). The most effective on parasitemia was observed in 400 mg/kg of Liquid Nano-emodin and solid (non-Nano) emodin. ED50 for emodin extract was determined 220 mg/kg. Toxicity test showed no toxic effect on the subjects. CONCLUSION: The emodin extract is safe, lack of side effects. So, it can be used for more and longer period of time and in higher doses. Emodin extract, either in form of liquid and nanoparticle or in a solid form, has the same therapeutic effect on P. berghei in infected Balb/c mice. Tehran University of Medical Sciences 2022 /pmc/articles/PMC9682369/ /pubmed/36466013 http://dx.doi.org/10.18502/ijpa.v17i3.10624 Text en Copyright © 2022 Bayat et al. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited. |
spellingShingle | Original Article Bayat, Fatemeh Motevalli Haghi, Afsaneh Nateghpour, Mehdi Rahimi-Esboei, Bahman Rahimi Foroushani, Abbas Amani, Amir Farivar, Leila Sayyad Talaee, Zahra Faryabi, Aref Cytotoxicity and Anti-Plasmodium berghei Activity of Emodin Loaded Nanoemulsion |
title | Cytotoxicity and Anti-Plasmodium berghei Activity of Emodin Loaded Nanoemulsion |
title_full | Cytotoxicity and Anti-Plasmodium berghei Activity of Emodin Loaded Nanoemulsion |
title_fullStr | Cytotoxicity and Anti-Plasmodium berghei Activity of Emodin Loaded Nanoemulsion |
title_full_unstemmed | Cytotoxicity and Anti-Plasmodium berghei Activity of Emodin Loaded Nanoemulsion |
title_short | Cytotoxicity and Anti-Plasmodium berghei Activity of Emodin Loaded Nanoemulsion |
title_sort | cytotoxicity and anti-plasmodium berghei activity of emodin loaded nanoemulsion |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682369/ https://www.ncbi.nlm.nih.gov/pubmed/36466013 http://dx.doi.org/10.18502/ijpa.v17i3.10624 |
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