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1.
Int J Mol Sci ; 22(16)2021 Aug 16.
Artículo en Inglés | MEDLINE | ID: mdl-34445465

RESUMEN

Cordyline terminalis leaf extract (aqCT) possesses abundant polyphenols and other bioactive compounds, which are encapsulated in gelatin-polyethylene glycol-tyramine (GPT)/alpha-cyclodextrin (α-CD) gels to form the additional functional materials for biomedical applications. In this study, the gel compositions are optimized, and the GPT/α-CD ratios equal to or less than one half for solidification are found. The gelation time varies from 40.7 min to 5.0 h depending on the increase in GPT/α-CD ratios and aqCT amount. The aqCT extract disturbs the hydrogen bonding and host-guest inclusion of GPT/α-CD gel networks, postponing the gelation. Scanning electron microscope observation shows that all gels with or without aqCT possess a microarchitecture and porosity. GPT/α-CD/aqCT gels could release polyphenols from 110 to 350 nmol/mL at the first hour and sustainably from 5.5 to 20.2 nmol/mL for the following hours, which is controlled by feeding the aqCT amount and gel properties. GPT/α-CD/aqCT gels achieved significant antioxidant activity through a 100% scavenging DPPH radical. In addition, all gels are non-cytotoxic with a cell viability more than 85%. Especially, the GPT3.75α-CD10.5aqCT gels with aqCT amount of 3.1-12.5 mg/mL immensely enhanced the cell proliferation of GPT3.75α-CD10.5 gel without extract. These results suggest that the inherent bioactivities of aqCT endowed the resulting GPT/α-CD/aqCT gels with effective antioxidant and high biocompatibility, and natural polyphenols sustainably release a unique platform for a drug delivery system or other biomedical applications.


Asunto(s)
Cordyline/química , Dermis/efectos de los fármacos , Fibroblastos/efectos de los fármacos , Geles/química , Extractos Vegetales/farmacología , Hojas de la Planta/química , Polifenoles/farmacología , Células Cultivadas , Liberación de Fármacos , Geles/administración & dosificación , Humanos
2.
J Nat Prod ; 82(10): 2809-2817, 2019 10 25.
Artículo en Inglés | MEDLINE | ID: mdl-31596585

RESUMEN

Antibacterial-activity-guided fractionation of a dichloromethane extract from the fruit of Cordyline manners-suttoniae and subsequent structure-activity investigations resulted in the identification of 10 new (1-10) and one known (11) 5α-spirostane saponin. The structures of the new compounds were established by 1D and 2D NMR analyses. The absolute configurations of the isolated compounds were determined by X-ray diffraction analysis or chemical derivatizations. The most active compound, suttonigenin F (6), inhibited the Gram-positive bacteria Staphylococcus aureus with MIC75 values that were comparable to those of the antibiotic chloramphenicol. Structure-activity relationships were also obtained from the assessment of antibacterial and cytotoxic activities of the isolated saponins.


Asunto(s)
Antibacterianos/aislamiento & purificación , Cordyline/química , Saponinas/aislamiento & purificación , Antibacterianos/química , Antibacterianos/farmacología , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Frutas/química , Humanos , Estructura Molecular , Extractos Vegetales/análisis , Saponinas/química , Saponinas/farmacología , Relación Estructura-Actividad
3.
Fitoterapia ; 134: 454-458, 2019 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-30910736

RESUMEN

A new sulfated steroidal derivative (fruticogenin A: 1-sulfo-australigenin-3-sodium sulphate, 1) and three new steroidal saponins named fruticoside K (3-sulfo-spirostan-25(27)-ene-1ß,3ß-diol-1-O-[α-L-rhamnopyranosyl-(1 → 4)-ß-D-fucopyranoside], 2), fruticoside L (3-sulfo-spirostan-25(27)-ene-1ß,3ß,6α-triol-1-O-[α-L-rhamnopyranosyl-(1 → 4)-ß-D-fucopyranoside], 3) and fruticoside M (spirostan-25(27)-ene-1ß,3α-diol-1-O-[α-L-rhamnopyranosyl-(1 → 2)-α-L-rhamnopyranoside], 4) were isolated from the aerial parts of Cordyline fruticosa L. var. strawberries. Their structures were established on the basis of 1D and 2D NMR data, mass spectrometry and chemical methods. Compounds 2 and 4 exhibited weak cytotoxicity against melanoma (A375), breast adenocarcinoma (MDA-MB-231), and colon carcinoma (HCT116) human tumor cell lines.


Asunto(s)
Cordyline/química , Fitosteroles/farmacología , Saponinas/farmacología , Antineoplásicos Fitogénicos/aislamiento & purificación , Antineoplásicos Fitogénicos/farmacología , Camerún , Línea Celular Tumoral , Humanos , Estructura Molecular , Fitoquímicos/aislamiento & purificación , Fitoquímicos/farmacología , Fitosteroles/aislamiento & purificación , Componentes Aéreos de las Plantas/química , Saponinas/aislamiento & purificación
4.
Artículo en Inglés | MEDLINE | ID: mdl-28213142

RESUMEN

Current study employs mixture of chlorophyll-anthocyanin dye extracted from leaves of Cordyline fruticosa as new sensitizers for dye-sensitized solar cell (DSSCs), as well as betalains dye obtained from fruit of Hylocereus polyrhizus. Among ten pigments solvents, the ethanol and methanol extracts revealed higher absorption spectra of pigments extracted from C. fruticosa and H. polyrhizus respectively. A major effect of temperature increase was studied to increase the extraction yield. The results indicated that extraction temperature between 70 and 80°C exhibited a high dye concentration of each plant than other temperatures. The optimal temperature was around 80°C and there was a sharp decrease of dye concentration at temperatures higher than this temperature. According to experimental results, the conversion efficiency of DSSC fabricated by mixture of chlorophyll and anthocyanin dyes from C. fruticosa leaves is 0.5% with short-circuit current (Isc) of 1.3mA/cm-2, open-circuit voltage (Voc) of 0.62V and fill factor (FF) of 60.16%. The higher photoelectric conversion efficiency of the DSSC prepared from the extract of H. polyrhizus was 0.16%, with Voc of 0.5V, Isc of 0.4mA/cm-2 and FF of 79.16%. The DSSC based betalain dye extracted from fruit of H. polyrhizus shows higher maximum IPCE of 44% than that of the DSSCs sensitized with mixed chlorophyll-anthocyanin dye from C. fruticosa (42%).


Asunto(s)
Cactaceae/química , Colorantes/química , Cordyline/química , Pigmentos Biológicos/aislamiento & purificación , Energía Solar , Clorofila/química , Electroquímica , Electrones , Fotones , Solventes , Espectrometría por Rayos X , Espectroscopía Infrarroja por Transformada de Fourier , Propiedades de Superficie , Temperatura , Titanio/química , Difracción de Rayos X
5.
Artículo en Inglés | MEDLINE | ID: mdl-25483560

RESUMEN

Nine solvents, namely, n-hexane, ethanol, acetonitrile, chloroform, ethyl-ether, ethyl-acetate, petroleum ether, n-butyl alcohol, and methanol were used to extract natural dyes from Cordyline fruticosa, Pandannus amaryllifolius and Hylocereus polyrhizus. To improve the adsorption of dyes onto the TiO2 particles, betalain and chlorophyll dyes were mixed with methanol or ethanol and water at various ratios. The adsorption of the dyes mixed with titanium dioxide (TiO2) was also observed. The highest adsorption of the C.fruticosa dye mixed with TiO2 was achieved at ratio 3:1 of methanol: water. The highest adsorption of P.amaryllifolius dye mixed with TiO2 was observed at 2:1 of ethanol: water. H.polyrhizus dye extracted by water and mixed with TiO2 demonstrated the highest adsorption among the solvents. All extracted dye was adsorbed onto the surface of TiO2 based on Fourier Transform Infrared Spectroscopy (FTIR) analysis. The inhibition of crystallinity of TiO2 was likewise investigated by X-ray analysis. The morphological properties and composition of dyes were analyzed via SEM and EDX.


Asunto(s)
Cactaceae/química , Cordyline/química , Pandanaceae/química , Pigmentos Biológicos/aislamiento & purificación , Solventes/química , Titanio/química , Adsorción , Betacianinas/aislamiento & purificación , Clorofila/aislamiento & purificación , Suministros de Energía Eléctrica , Ácidos Picolínicos/aislamiento & purificación , Energía Solar
6.
Chem Pharm Bull (Tokyo) ; 60(2): 275-9, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22293491

RESUMEN

Four new cholestane glycosides (1-4) were isolated from the leaves of Cordyline terminalis (Agavaceae). The structures of the new compounds were determined on the basis of spectroscopic analysis and a few chemical transformations followed by chromatographic and spectroscopic analyses.


Asunto(s)
Colestanos/química , Cordyline/química , Glicósidos/química , Hojas de la Planta/química , Supervivencia Celular/efectos de los fármacos , Colestanos/farmacología , Glicósidos/farmacología , Células HL-60 , Humanos , Concentración 50 Inhibidora , Espectroscopía de Resonancia Magnética , Estructura Molecular
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