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PROCEDIMIENTO DE PREPARACIÓN DE UNA OLEORRESINA PROVENIENTE DE UN ALGA ROJA, QUE MANTIENE LA CAPACIDAD DE INDUCIR LA ACTIVIDAD TRANSCRIPCIONAL DEL RECEPTOR NUCLEAR PPARy,
专利权人:
PONTIFICIA UNIVERSIDAD CÁTOLICA DE CHILE
发明人:
BRONFMAN, MIGUEL,BRONFMAN, Miguel,BRONFMAN FRANCISCA,BRONFMAN Francisca,PINTO, CLAUDIO,PINTO, Claudio,PISSANI, CLAUDIA,PISSANI, Claudia,PAREDES MARTÍNEZ, MARÍA JOSÉ,PAREDES MARTÍNEZ, María José
申请号:
CLCL2013/000031
公开号:
WO2014/186913A1
申请日:
2013.05.23
申请国别(地区):
WO
年份:
2014
代理人:
摘要:
The present invention relates to a method for preparing an oily extract originating from a red alga, preferably Gracilariachilenis. This process successfully maintains, in the oily extract, a high capacity to induce PPAR-gamma transcriptional activity. This process comprises the steps of: I) Extraction of the fresh alga and transport at low temperature: wherein the live, whole alga is gathered by being torn from its attachment to the seabed substrate in order then to be transferred cold (approximately 4°C) II) Preparation and chopping-up of the alga: comprising the washing of the alga with PBS (pH 7.4), extraction by centrifugation and storage under vacuum at ‑20°C. Thawing to 4°C and further washing with PBS (pH 7.4), drying by centrifugation and chopping-up of the alga with a stainless-steel pound knife into fragments of between 1-3 mm, for subsequent freezing briefly at ‑20°C for lyophilization thereof III) Freeze-drying: lyophilization for 24 hours at ‑50°C and 0.014 mbar and storage under vacuum at ‑20°C IV) Spraying with batchwise solid-liquid extraction of the oleoresin: the lyophilized alga is brought to ambient temperature (20-25°C) and then ground to a fine powder with an average size of less than ½ mm. A quantity of powder is placed in a flask and mixed with an appropriate quantity of solvent (dichloromethane) in order for a batchwise solid-liquid extraction to be performed. This mixture is saturated in a gaseous nitrogen atmosphere and sealed, then undergoing horizontal agitation at 34°C for 30 min. The mixture is then decanted and filtered on paper and the liquid phase is received in a flask. The solid phase is again resuspended in a liposoluble solvent, preferably dichloromethane, the earlier extraction process being repeated. The total liquid phase or extract is concentrated in a rotary evaporator, which removes the solvent, leaving the oleoresin. This product is dried under nitrogen gas to constant weight and is then resuspended in a minimum volume o
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