A kind of Garcinia cambogia seed extract with antitumor activity and preparation method thereof
An anti-tumor activity and anti-tumor technology, which is applied in the field of medicine, can solve the problems that there is no patent disclosure of Garcinia japonica seeds, tumor cells are prone to drug resistance, and anti-tumor cells have not been reported, so as to promote protection and reproducibility. Effects of continuous use, easy purchase, and shortened extraction time
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Embodiment 1
[0035] Embodiment one: the preparation embodiment of extract
[0036] A preparation method of garcinia cambogia seed extract with anti-tumor activity ( figure 1 ), including the following detailed steps:
[0037] (1) Seed peeling: Rinse the picked fresh ripe fruit with clean water, then cut it open, take out the seed, wash the surface of the seed with distilled water to remove the residual juice, then remove the seed coat to obtain the peeled seed, and break the seed into Crumble, place in a clean tray.
[0038] (2) Drying and crushing: Place the seed fragments in a vacuum freeze dryer for freeze-drying treatment. The drying conditions are as follows: temperature is -80°C, vacuum pressure is less than 0.140 mbar, and the drying time is 48 hours. The dried seed fragments are pulverized with an electric pulverizer, and the seed powder is obtained after passing through a 40-mesh sieve, and the powder is placed in a cool and dry place.
[0039](3) Extraction and drying: Weigh ...
Embodiment 2
[0041] Example 2: Example of Activity Verification of the Extract
[0042] The following is the in vitro anti-tumor cell experiment of the Garcinia macrophylla seed extract obtained according to the present invention.
[0043] The CCK8 method was used to measure the growth inhibitory activity of the Garcinia cambogia seed extract obtained in the above-mentioned embodiment 1 to 3 kinds of tumor cells, including lung cancer cell A549, cervical cancer cell Hela and gastric cancer cell HGC-27, specifically including the following steps:
[0044] (1) Cell recovery: Take out the frozen tumor cells from the -80°C refrigerator, take one tube for each type of tumor cells, and quickly transfer them to the intercellular space with an ice box, and place the cryopreserved tubes in a water bath at 37°C. Thaw the cells. In an ultra-clean workbench, transfer the thawed cells to a 50 mL centrifuge tube, add 10 mL of LDME / F-12 complete culture solution (containing 10% fetal bovine serum and 1%...
Embodiment 3
[0057] Embodiment three: the chemical composition analysis of extract
[0058] Take 200 g of the total extract prepared in Example 1, add an appropriate amount of distilled water for suspension, then add petroleum ether to remove the seed oil, then add ethyl acetate for extraction, and concentrate the extract to dryness to obtain an ethyl acetate layer extract 63.3 g. The ethyl acetate layer extract was subjected to silica gel column chromatography and gradient elution with dichloromethane / methanol (100:0~0:100, v / v) to obtain 5 main components. Purified by repeated silica gel and dextran gel (Sephadex LH-20) column chromatography, the silica gel column chromatography used dichloromethane and methanol solvent system for gradient elution, and the Sephadex LH-20 column chromatography used dichloromethane Methane / methanol (1:1, v / v) was used as the mobile phase for isocratic elution, and the obtained main components were further prepared and purified by circulating preparative l...
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