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1.
China Journal of Chinese Materia Medica ; (24): 227-231, 2007.
Artículo en Chino | WPRIM | ID: wpr-246003

RESUMEN

<p><b>OBJECTIVE</b>Analysis of the constituents of the essential oil extracted from the flowers of the Chrysanthemum morifolium processed by the microwave-airflow and the calefaction after steam process from the State Chrysanthemum GAP bases in Zhejiang Province and to provide scientific basis for quality control.</p><p><b>METHOD</b>The essential oil was extracted by water-steam distillation and separated by GC capillary column chromatography. The components were quantitatively determined with normalization method, and identified by GC-MS.</p><p><b>RESULT</b>From the microwave-airflow dried sample and the calefactively dried sample after steam process, 119 and 175 components were detected, among them fifty and fifty-five components were identified, which were composed of 67.89% and 63.64% of the total essential oil, respectively.</p><p><b>CONCLUSION</b>The yield of the essential oil extracted from the microwave-airflow dried sample was 0.40%, and that from the calefactively dried sample after steam process was 0. 19%. The former is 2.1 times higher than the latter. The components of the essential oil are similar and there are differences between the content of corresponding compounds in the two samples. The results showed that application of microwave-airflow combined drying technology remained original and essential constituents. The production benefit was improved greatly. The grade and quality of C. morifolium enhanced, and it's market selling price was increased compared to the traditional drying calefaction after steam process.</p>


Asunto(s)
Chrysanthemum , Química , Flores , Química , Cromatografía de Gases y Espectrometría de Masas , Métodos , Cetonas , Química , Microondas , Aceites Volátiles , Química , Plantas Medicinales , Química , Reproducibilidad de los Resultados , Sesquiterpenos , Química , Vapor , Tecnología Farmacéutica , Métodos
2.
China Journal of Chinese Materia Medica ; (24): 1755-1759, 2007.
Artículo en Chino | WPRIM | ID: wpr-287903

RESUMEN

<p><b>OBJECTIVE</b>To study the bioactive constituents of the fresh rhizome of Pinellia ternata, and provide the scientific basis for quality control.</p><p><b>METHOD</b>Various chromatographic techniques were used to separate and purify the chemical constituents, and their chemical structures were determined on the basis of physical-chemical properties and spectroscopic analysis. The inhibitory effects of the isolated compounds on tumor necrosis factor (TNF)-alpha production in the peritoneal macrophages of mice stimulated with lipopolysaccharide (LPS) were assayed in vitro by microplate colorimetric method.</p><p><b>RESULT</b>Nine compounds were isolated and identified as (E)-p-coumaryl alcohol (1), 3, 4-dihydroxycinnamyl alcohol (2), ferulic acid (3), lariciresinol (4), erythro-guaiacylglycerol-beta-O-4'-sinapyl ether (5), dehydrodiconiferyl alcohol (6) , isolariciresinol (7) , sachaliside 1 (8) and coniferin (9). The inhibitory effect of compounds 1, 2, 3, 8, and 9 were 24.1% , 57.6% , 40.2% , 82.7% , and 62.0% , respectively, against the TNF-alpha production in the peritoneal macrophages of mice stimulated with LPS at a concentration of 10(-5) mol L(-1) in vitro.</p><p><b>CONCLUSION</b>The compounds 1, 2 and 4-8 from genera Pinellia Ten. and compound 9 from P. ternata were isolated for the first time. The compounds 1, 2, 8 and 9 were phenylpropanoids, and 4-7 were lignanoids. The anti-inflammatory effects of the rhizome of P. ternata might relate at the least to compounds 1, 2, 3, 8 and 9.</p>


Asunto(s)
Animales , Masculino , Ratones , Antiinflamatorios no Esteroideos , Farmacología , Células Cultivadas , Cinamatos , Química , Farmacología , Ácidos Cumáricos , Química , Farmacología , Furanos , Química , Farmacología , Lignanos , Química , Farmacología , Macrófagos Peritoneales , Biología Celular , Metabolismo , Ratones Endogámicos C57BL , Estructura Molecular , Pinellia , Química , Plantas Medicinales , Química , Rizoma , Química , Factor de Necrosis Tumoral alfa , Metabolismo
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