首页> 外文期刊>Journal of the Brazilian Chemical Society >Evaluation of Antibacterial Activity, Chromatographic Analysis for Rutin and Quercetin Quantification Using HPLC-UV-Vis from the Hydro-Alcoholic Extract Obtained from Bidens pilosa Linné
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Evaluation of Antibacterial Activity, Chromatographic Analysis for Rutin and Quercetin Quantification Using HPLC-UV-Vis from the Hydro-Alcoholic Extract Obtained from Bidens pilosa Linné

机译:使用HPLC-UV-Vis从Bidens pilosaLinné获得的HPLC-UV-Vis进行抗菌活性的评价,芦丁和槲皮素定量的分析

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Novel and miniaturized technique, a dynamic sonication-assisted solvent extraction before the analysis by high performance liquid chromatography-ultraviolet visible (HPLC-UV-Vis) for isolation, identification and quantification of rutin and quercetin metabolites in alcoholic extracts from Bidens pilosa Linné, was developed. The results showed that the flowers have a greater quantity of both analytes than other parts of the plant (e.g., leaves, stem and roots), the results were corroborated by liquid chromatography-mass spectrometry (LC-MS). In addition, the developed extraction technique against traditional methods for metabolites extraction such as solid-liquid extraction, Soxhlet and rotating-disk sorptive extraction was compared. Under optimal conditions of extraction such as 0.3 mL min -1 of solvent flow, ethanol:water (1:1) as solvent type and 0.5 g of sample amount, it was possible to reach 85% of recovery percentage of target analytes and a limit of detection close to 0.1 μg g -1 with a linear range of 50-400 μg g -1 were also obtained. Finally, the antibacterial evaluation of the flower extract of Bidens pilosa Linné, obtained under above optimal conditions against Gram-positive bacteria, was performed. The higher values of the inhibition diameters when using 1000 mg L -1 and significant differences among Staphylococcus aureus , Bacillus cereus , and Listeria monocytogenes were observed. The tests were performed with different microorganisms inoculated from three different absorbance levels (0.05, 0.5 and 0.1 absorbances), at a lower absorbance of these microorganisms in the growth medium used for evaluating the inhibitory effect of the B. pilosa Linné extract, when using this extract at the concentrations of 500 and 1000 mg L -1 , statistically higher inhibition diameters were noticed.
机译:新颖的和小型化技术,在高效液相色谱 - 紫外线(HPLC-UV-VI)分析之前,进行动态超声辅助溶剂萃取,用于分离,鉴定和定量来自Bidens pilosaLinné的酒精萃取物中的芦丁和槲皮素代谢物的鉴定和定量发达。结果表明,花的两种分析物比植物的其他部分(例如,叶,茎和根)具有更大的分析物,结果通过液相色谱 - 质谱(LC-MS)来证实结果。此外,比较了针对代谢产物提取的传统方法的开发的提取技术,例如固液萃取,SOXHLET和旋转盘吸附萃取。在萃取的最佳条件下,如0.3ml min -1的溶剂流动,乙醇:水(1:1)作为溶剂型和0.5g样品量,可以达到靶分析物的恢复百分比的85%和限制检测接近0.1μgg-1,也得到了50-400μgg-1的线性范围。最后,进行了在高于革兰氏阳性细菌的最佳条件下获得的Bidens pilosaLinné的花提取物的抗菌评价。观察到使用1000mg L -1的抑制直径的较高值,并且观察到金黄色葡萄球菌,芽孢杆菌和Histeria单核细胞生成的显着差异。用来自三种不同的吸光度水平(0.05,0.5和0.1吸收)的不同微生物进行测试,在使用该生长培养基中的这些微生物的较低吸光度下,用于评估B.PilosaLinné提取物的抑制作用的生长培养基浓度为500和1000mg L -1的提取物,注意到统计上更高的抑制直径。

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