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Combination of extracts from Aristolochia cymbifera with streptomycin as a potential antibacterial drug

The appearance of new antibiotic-resistant bacteria is a societal problem that requires the development of new alternative treatments. Therefore, this work evaluated the antibacterial activity of ethanolic (EHI), dichloromethanic (EDI) and hexanic (EHE) extracts from Aristolochia cymbifera stems and...

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Autores principales: Silva, Willer F, Cecílio, Samyra G, Magalhães, Cintia LB, Ferreira, Jaqueline MS, Tótola, Antonio H, de Magalhaes, Jose C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771021/
https://www.ncbi.nlm.nih.gov/pubmed/24040585
http://dx.doi.org/10.1186/2193-1801-2-430
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author Silva, Willer F
Cecílio, Samyra G
Magalhães, Cintia LB
Ferreira, Jaqueline MS
Tótola, Antonio H
de Magalhaes, Jose C
author_facet Silva, Willer F
Cecílio, Samyra G
Magalhães, Cintia LB
Ferreira, Jaqueline MS
Tótola, Antonio H
de Magalhaes, Jose C
author_sort Silva, Willer F
collection PubMed
description The appearance of new antibiotic-resistant bacteria is a societal problem that requires the development of new alternative treatments. Therefore, this work evaluated the antibacterial activity of ethanolic (EHI), dichloromethanic (EDI) and hexanic (EHE) extracts from Aristolochia cymbifera stems and the combination of these extracts with an antimicrobial drug to develop a new antibacterial therapy. The EDI, EHE and EHI extracts were obtained by maceration using three different solvents. The minimal inhibitory concentrations (MIC) of these extracts were determined using the microdilution test to determine the antibacterial potential of these extracts and their combination with streptomycin against Staphylococcus aureus, Bacillus cereus, Klebsiella pneumoniae and Shigella flexneri. The extract dose leading to the cytotoxicity of 50% of the cells (CC50) was evaluated using mammalian cells MA104 and the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay. The extracts had a MIC under 500 mg/L and a CC50 lower than 50 mg/L. The antibiotic/extract proportion influenced the antibacterial activity of the mixtures, and the proportion that optimized the antibacterial activity of streptomycin was a mixture that contained 75 percent of extract. This composition included less than 6.5 mg/L of extract and 2.5 mg/L of streptomycin and has potential as a new antibacterial therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2193-1801-2-430) contains supplementary material, which is available to authorized users.
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spelling pubmed-37710212013-09-13 Combination of extracts from Aristolochia cymbifera with streptomycin as a potential antibacterial drug Silva, Willer F Cecílio, Samyra G Magalhães, Cintia LB Ferreira, Jaqueline MS Tótola, Antonio H de Magalhaes, Jose C Springerplus Research The appearance of new antibiotic-resistant bacteria is a societal problem that requires the development of new alternative treatments. Therefore, this work evaluated the antibacterial activity of ethanolic (EHI), dichloromethanic (EDI) and hexanic (EHE) extracts from Aristolochia cymbifera stems and the combination of these extracts with an antimicrobial drug to develop a new antibacterial therapy. The EDI, EHE and EHI extracts were obtained by maceration using three different solvents. The minimal inhibitory concentrations (MIC) of these extracts were determined using the microdilution test to determine the antibacterial potential of these extracts and their combination with streptomycin against Staphylococcus aureus, Bacillus cereus, Klebsiella pneumoniae and Shigella flexneri. The extract dose leading to the cytotoxicity of 50% of the cells (CC50) was evaluated using mammalian cells MA104 and the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay. The extracts had a MIC under 500 mg/L and a CC50 lower than 50 mg/L. The antibiotic/extract proportion influenced the antibacterial activity of the mixtures, and the proportion that optimized the antibacterial activity of streptomycin was a mixture that contained 75 percent of extract. This composition included less than 6.5 mg/L of extract and 2.5 mg/L of streptomycin and has potential as a new antibacterial therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2193-1801-2-430) contains supplementary material, which is available to authorized users. Springer International Publishing 2013-09-03 /pmc/articles/PMC3771021/ /pubmed/24040585 http://dx.doi.org/10.1186/2193-1801-2-430 Text en © Silva et al.; licensee Springer. 2013 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Silva, Willer F
Cecílio, Samyra G
Magalhães, Cintia LB
Ferreira, Jaqueline MS
Tótola, Antonio H
de Magalhaes, Jose C
Combination of extracts from Aristolochia cymbifera with streptomycin as a potential antibacterial drug
title Combination of extracts from Aristolochia cymbifera with streptomycin as a potential antibacterial drug
title_full Combination of extracts from Aristolochia cymbifera with streptomycin as a potential antibacterial drug
title_fullStr Combination of extracts from Aristolochia cymbifera with streptomycin as a potential antibacterial drug
title_full_unstemmed Combination of extracts from Aristolochia cymbifera with streptomycin as a potential antibacterial drug
title_short Combination of extracts from Aristolochia cymbifera with streptomycin as a potential antibacterial drug
title_sort combination of extracts from aristolochia cymbifera with streptomycin as a potential antibacterial drug
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771021/
https://www.ncbi.nlm.nih.gov/pubmed/24040585
http://dx.doi.org/10.1186/2193-1801-2-430
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