Navegando por Assunto "Isoeleuterina"
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Item Acesso aberto (Open Access) Estudos de citotoxicidade e genotoxicidade de Eleutherine plicata Herb(Universidade Federal do Pará, 2014-09-30) GALUCIO, Natasha Costa da Rocha; BAHIA, Marcelo de Oliveira; http://lattes.cnpq.br/3219037174956649; DOLABELA, Maria Fâni; http://lattes.cnpq.br/0458080121943649The purpose of this study was phytochemical studies of E. plicata, and to evaluate the cytotoxicity, the role of oxidative stress and genotoxicity. The powder of E. plicata bulbs underwent maceration with ethanol, the solution concentrated to residue in rotaevaporator. The ethanol extract was subjected to fractionation by open column chromatography over silica gel, being used as the mobile phase solvents of increasing polarity. The dichloromethane fraction was subjected to fractionation by preparative layer chromatography using dichloromethane as mobile phase, and 3 subfractions obtained. The ethanol extract, fractions and subfractions were subjected to chromatographic and spectrophotometric analysis. All samples were subjected to the tests: cellular viability (MTT), the antioxidant capacity (DPPH), comet and micronucleus assays. From the ethanol extract obtained a rich fraction naphthoquinone (dichloromethane fraction). Fractionation of this led to the isolation of: S1, S2 (major fraction), and fraction of minority S3 (unidentified, not tested). Chromatographic studies and spectrophotometric allowed the identification of S2 (isoeleuterin). Fractionation contributed positively to cytotoxicity on VERO cells, the sample being more cytotoxic to S1. The cytotoxicity in HepG2 cells was concentration dependent, being the fractionation did not contribute positively to this. Also, over time, the longer the exposure time, the lower the cytotoxicity to HepG2 cells. The maximum antioxidant activity was observed for subfraction S1, and this low genotoxicity possessed by both methods and it was the most cytotoxic. The dichloromethane fraction has an intermediate antioxidant capacity, but had a high genotoxicity in micronucleus assay. The isoeleuterin (S2) was lower antioxidant capacity, lower cytotoxicity and genotoxicity conflicting results. The ethanol extract possessed the lowest antioxidant capacity, moderate genotoxicity and lower cytotoxicity. When analyzing the results occur that: a subfraction S1 is the most promising candidate as the antimalarial drug, as have cytotoxicity and genotoxicity rates at acceptable levels. The isoeleuterin needs additional research on 11 genotoxicity. Regarding the dichloromethane fraction was not advisable to use for the development of an antimalarial drug, since it is more genotoxic.Item Acesso aberto (Open Access) Isoeleuterol e isoeleuterina: potenciais marcadores químicos da tintura de Eleutherine plicata Herb (Iridaceae) e atividades microbiológica e antioxidante(Universidade Federal do Pará, 2008-12-30) MALHEIROS, Luiz Claudio da Silva; VIEIRA, José Maria dos Santos; http://lattes.cnpq.br/6807452375674442; BARBOSA, Wagner Luiz Ramos; http://lattes.cnpq.br/1372405563294070Eleutherine plicata Herb. is an Iridaceae, popularly known as marupazinho, widely used by people to treat diarrhea. With the bulb of the plant is about a cup of tea, which is used to treat infestations caused by amoeba. The plant material used in this study was collected in Belém do Pará and their identification by comparison of botany was deposited in exsiccates Paraense Emilio Goeldi Museum under nº 10543. The ethanol extract was prepared by percolation from the bulb previously dried and crushed. After drying the ethanol extract was suspended in a solution hydroalcoholic (1:1) and subjected to partition with solvents of increasing polarity. With the ethanol extract and the fractions were performed eighteen tests to detect classes of secondary metabolites. The ethanol extract and the fractions hexanic and chloroform, showed a positive result for naphthoquinones, anthraquinones and steroids and triperpenoids. The analysis by thin-layer chromatography fractions of ethanol extract and hexane and chloroform, showed areas susceptible to methanolic solution of KOH 10%, indicating the presence of quinones in these samples. The evaluation of the antimicrobial activity of ethanol extract and fractions hexanic and chloroform with strains of C. albicans, S. aureus, E. coli and P. aeruginosa, showed that the chloroform fraction is the most active, presenting the largest halos of inhibition of microbial growth, possibly containing a higher concentration of active constituents. The chemical constituents isoeleutherol and isoeleutherine were isolated from chloroform fraction, and were characterized chemically using RMN 1H e 13C, compared with the literature. The ethanol extract, isoeleutherol and isoeleutherine were submitted to evaluation of their antioxidant activies, and showed weak activity when compared with BHT.