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1.
J Chromatogr Sci ; 54(7): 1096-104, 2016 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-27130878

RESUMEN

The dried aerial parts of 12 plants of Cirsium species were extracted with the Soxhlet apparatus using dichloromethane and methanol as solvents. Next, the extracts were separated by TLC methods to obtain the fingerprint chromatograms. The analysis was performed on silica gel or RP-18 layers as stationary phases using the following eluents: ethyl acetate/formic acid/acetic acid/water (12/1.5/1.5/4; v/v) for silica gel, and 5% (v/v) aqueous solution of formic acid/methanol (70/30; v/v) for the first development and the same system in the proportion of 50/50 (v/v) for the second development for RP-18. The double development was applied in the case of RP-18 plates. The analysis was performed for all Cirsium methanolic extracts and five selected standards (naringin, apigenin, rutin, caffeic acid and chlorogenic acid). The results were analyzed using chemometrics. The comparison of individual Cirsium species and the identification of unknown species were performed using the similarity indices (Pearson's correlation coefficient, determination coefficient and congruence coefficient), distance indices (Euclidean distance, Manhattan distance and Chebyshev's distance) and Multi-Scale Structural SIMilarity. Based on chemometric analysis, the first extract of the widely grown species is identified as Cirsium arvense and the second one as Cirsium rivulare.


Asunto(s)
Cromatografía en Capa Delgada/métodos , Cirsium/química , Extractos Vegetales/química , Apigenina/aislamiento & purificación , Ácidos Cafeicos/aislamiento & purificación , Ácido Clorogénico/aislamiento & purificación , Cromatografía en Capa Delgada/normas , Cirsium/clasificación , Flavanonas/aislamiento & purificación , Metanol/química , Cloruro de Metileno/química , Componentes Aéreos de las Plantas/química , Análisis de Componente Principal , Estándares de Referencia , Rutina/aislamiento & purificación , Solventes/química
2.
Molecules ; 21(1): 90, 2016 Jan 14.
Artículo en Inglés | MEDLINE | ID: mdl-26784151

RESUMEN

The amount of secondary metabolites in plants can be enhanced or reduced by various external factors. In this study, the effect of strontium ions on the production of phytoestrogens in soybeans was investigated. The plants were treated with Hoagland's solution, modified with Sr(2+) with concentrations ranging from 0.5 to 3.0 mM, and were grown for 14 days in hydroponic cultivation. After harvest, soybean plants were separated into roots and shoots, dried, and pulverized. The plant material was extracted with methanol and hydrolyzed. Phytoestrogens were quantified by HPLC. The significant increase in the concentration of the compounds of interest was observed for all tested concentrations of strontium ions when compared to control. Sr(2+) at a concentration of 2 mM was the strongest elicitor, and the amount of phytoestrogens in plant increased ca. 2.70, 1.92, 3.77 and 2.88-fold, for daidzein, coumestrol, genistein and formononetin, respectively. Moreover, no cytotoxic effects were observed in HepG2 liver cell models after treatment with extracts from 2 mM Sr(2+)-stressed soybean plants when compared to extracts from non-stressed plants. Our results indicate that the addition of strontium ions to the culture media may be used to functionalize soybean plants with enhanced phytoestrogen content.


Asunto(s)
Glycine max/efectos de los fármacos , Fitoestrógenos/agonistas , Extractos Vegetales/farmacología , Raíces de Plantas/efectos de los fármacos , Brotes de la Planta/efectos de los fármacos , Estroncio/farmacología , Cationes Bivalentes , Supervivencia Celular/efectos de los fármacos , Cromatografía Líquida de Alta Presión , Cumestrol/agonistas , Cumestrol/biosíntesis , Cumestrol/aislamiento & purificación , Genisteína/agonistas , Genisteína/aislamiento & purificación , Genisteína/metabolismo , Células Hep G2 , Humanos , Hidroponía , Isoflavonas/agonistas , Isoflavonas/biosíntesis , Isoflavonas/aislamiento & purificación , Metanol , Fitoestrógenos/aislamiento & purificación , Fitoestrógenos/metabolismo , Extractos Vegetales/química , Raíces de Plantas/crecimiento & desarrollo , Raíces de Plantas/metabolismo , Brotes de la Planta/crecimiento & desarrollo , Brotes de la Planta/metabolismo , Solventes , Glycine max/crecimiento & desarrollo , Glycine max/metabolismo , Estroncio/metabolismo
3.
Med Chem ; 8(1): 118-31, 2012 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-22420560

RESUMEN

Two dimensional thin layer chromatography on DIOL polar bonded stationary phase was performed to optimize the separation of some anioxidant phenolic compounds from Eupatorium cannabinum extracts. Ethyl-methyl ketone mixed with n-heptane and ethyl acetate mixed with n-heptane were used as non-aqueous mobile phases in normal phase separations (1st direction of development in 2D-HPTLC mode) and methanol mixed with water was used as a mobile phase in reversed phase (2nd direction of development in 2D-HPTLC mode). The plates were sprayed by use of Merck TLC sprayer using 2-(diphenylboryoxy)-ethylamine and PEG4000 (Merck, Darmstadt, Germany) or DPPH and photographed in Camag Cabinet UV lamp at 254 nm and 365 nm by use of Fuji 8 mpx camera. Satisfactory separations of antioxidant phenolic compounds in Eupatorium cannabinum extracts were obtained by use of optimized 2D-HPTLC systems.


Asunto(s)
Antioxidantes/aislamiento & purificación , Antioxidantes/farmacología , Eupatorium/química , Fenoles/aislamiento & purificación , Fenoles/farmacología , Extractos Vegetales/química , Antioxidantes/química , Cromatografía en Capa Delgada , Flores/química , Fenoles/química
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