Preparation method of sweet-scented osmanthus seed extract, sweet-scented osmanthus seed extract and application of sweet-scented osmanthus seed extract
A technology for extracts and seeds, applied in the field of Osmanthus fragrans seed extract and application thereof, and the preparation field of Osmanthus fragrans seed extract, can solve the problem of easy-to-destroy active ingredient espressoside, unfavorable espressoside purity and yield, and preparation instruments Expensive and other problems, to achieve the effect of inhibiting platelet aggregation, preventing and treating heart palsy, and simple process
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Embodiment 1
[0030] A preparation method of osmanthus fragrans seed extract, comprises the following steps:
[0031] S1. Take 5 kg of sweet-scented osmanthus seeds, peel and pulverize, add 50 L of ethanol solution with a volume concentration of 95%, and mix evenly to obtain a mixture.
[0032] S2. Perform percolation extraction on the mixture obtained in step S1, specifically, continuously add ethanol solution with a fresh volume concentration of 95% from above the percolator, and collect percolation liquid at the outlet below the percolator at the same time. 25L. In this step, the number of times of percolation extraction is 3 times, and the time of single percolation extraction is 12h.
[0033] S3. After each percolation extraction is completed, use a rotary evaporator at 40° C. to recover ethanol in the extract under reduced pressure, and combine the obtained concentrates to obtain an osmanthus seed extract.
Embodiment 2
[0035] Evaluation of the Anti-cardiac Activity of Osmanthus fragrans Seed Extract Monomer
[0036] With the sweet-scented osmanthus seed extract that makes in embodiment 1 as tested substance, investigate following experiment:
[0037] Effects on ADP-induced Platelet Aggregation in Rabbits
[0038]Take healthy Japanese big-eared white rabbits weighing 2.5-3.0 kg, and take 3 mL of blood from the ear vein (anticoagulant: blood = 1:9), mix immediately, seal, and centrifuge at 500 rpm for 10 minutes to prepare platelet-rich plasma (PRP). After the PRP was separated, it was centrifuged again (3000rpm / min, 10min) to prepare platelet-poor plasma (PPP). Take the PRP and put it into a 300 μL test cup with magnetic beads, mix the remaining blood, and centrifuge at 3000 rpm for 10 minutes. Take PPP and put it into a 300 μL comparison test cup. After zeroing with PRP, take 200 μL PRP and add 5 μL equimolar concentration of the test substance DMSO (dimethyl sulfoxide) solution, solvent ...
Embodiment 3
[0054] With the sweet-scented osmanthus seed extract that makes in embodiment 1 as tested substance, investigate its effect on rat in vitro cardiomyocyte hypoxic injury protection
[0055] Culture of neonatal rat cardiomyocytes
[0056] Wistar suckling mice aged 1-3d were soaked and sterilized with 75% (unit: v / v) ethanol, and the apical tissue was taken, cut into pieces, placed in a centrifuge tube, and washed with 10 mL, 0.25% (unit: v / v) pancreatic The protease solution was digested in a constant temperature shaker at 37°C in a water bath for 10 minutes, and at the same time, the tissue was pipetted for 2 minutes to allow natural precipitation. After the precipitation is complete, take the supernatant to another tube, add 2mL cold medium to stop the digestion, then centrifuge for 10min, discard the supernatant, add 8mL D-Hanks solution to the precipitation, and finally use 20% (unit It is the DMEM medium of v / v) fetal bovine serum, and the cardiomyocyte pellet is mixed to ...
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