Fenugreek extract and preparation method thereof, pharmaceutical composition containing fenugreek extract and use of pharmaceutical composition
A technology of fenugreek and extract, which is applied in the field of preparation of fenugreek extract, can solve the problems of difficult separation of organic solvents and the like
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preparation example 1
[0045] The water extraction method of preparation example 1 Fenugreek
[0046] Fresh or dried fenugreek seeds are extracted with a water solvent, wherein the weight ratio of the water solvent used is 1 to 20 times that of the fenugreek seeds, preferably 5 to 10 times. The fenugreek seeds soaked in the water solvent are placed at 25°C to 100°C for 0.5 hours to 5 hours, preferably 50°C to 95°C for 0.5 hours to 3 hours, and filtered (by a known physical filtration method) After solid-liquid separation, such as porosity, weight or density), fenugreek extract (abbreviated as YE2) is obtained. The fenugreek extract can be concentrated or dried by known food processing methods.
preparation example 2
[0047] The organic solvent extraction method of preparation example 2 Fenugreek
[0048] Fresh or dried fenugreek seeds are extracted with 50% alcohol solvent, wherein the weight ratio of the alcohol solvent used is 1 to 20 times, preferably 5 to 10 times, that of the fenugreek seeds. Place the fenugreek seeds soaked in alcohol solvent at 25°C to 100°C for 0.5 hours to 5 hours, preferably at 50°C to 95°C for 0.5 hours to 3 hours, and filter (by a known physical filtration method) After solid-liquid separation, such as porosity, weight or density), an alcoholic extract of fenugreek (abbreviated as YE3) is obtained. The fenugreek extract can be concentrated or dried by known food processing methods.
Embodiment 1
[0049] Example 1 Cell Experiment - Dosing and Stimulation Simultaneously, Simultaneously Preventing Mechanism
[0050] (1) Liver hepatocellular carcinoma (HepG2) was planted in each well at 2.5×10 4 cells were cultured for 24 hours.
[0051] (2) It is divided into the following groups:
[0052] Control group: add cell culture medium equal to the volume of the oil droplet inducer and 1% dimethylsulfoxide (DMSO) to the liver cancer cells for 6 hours.
[0053] Oil drop induction group: add 1% DMSO and 500 millimolar concentration (mM) of oil drop inducer [unit fatty acid oleic acid (oleic acid, OA, C18: 1) and saturated fatty acid palmitic acid (paltimic acid, PA, C16: 0), dissolved in cell culture medium at a volume ratio of 2:1 (v / v)] and stimulated in liver cancer cells for 6 hours.
[0054] Positive control group: add phosphoatidylcholine (phosphoatidylcholine) 0.01 microgram per milliliter (μg / mL) and oil drop inducer with 500 millimolar concentration (mM) to stimulate li...
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