Application of schisandra fruit in preparation of tyrosine-inhibiting medicine
The technology of tyrosine kinase and Schisandra chinensis is applied in the directions of drug combination, antitumor drug, pharmaceutical formulation, etc., which can solve the problems of drug efficacy and sensitization of tyrosine kinase inhibitory drugs, and achieve the effect of good clinical application prospect.
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Embodiment 1
[0014] Embodiment 1: the preparation of Schisandra chinensis ethanol extract
[0015] Percolation method: take 5000g Schisandra chinensis powder and percolate with 6 times the mass of 90% ethanol at a percolation speed of 15ml / min. Recover the ethanol leachate, recover the ethanol under reduced pressure until there is no ethanol smell, concentrate to obtain an extract with a specific gravity of 1.15 g / ml, and obtain the Schisandra chinensis extract for future use. The ethanol used in the above extraction can also be replaced by various alcohols such as methanol and propanol, and the alcohol concentration can be between 75% and 95%; other organic solvents such as ethyl acetate and ether solvents can also be used instead.
Embodiment 2
[0016] Embodiment 2: supercritical extraction
[0017] Supercritical extraction: crush 1000 g of the schisandra sample into a coarse powder (through a 40-mesh sieve), put 1L of supercritical CO 2 In the extraction kettle, adjust the pressure: 25MPa, temperature: 45°C, flow rate: 30kg / h, extraction time: 2h. A brown extract was collected.
Embodiment 3
[0018] Example 3: Schisandra extract enhances the efficacy of Gleevec in killing leukemia cells.
[0019] Experimental method: Schisandra chinensis ethanol extract and supercritical extract were respectively prepared into 20mg / ml mother liquor with DMSO. Human leukemia cell lines Ku812 and K562 (ATCC, USA). K562 or Ku812 are cultured in RPMI-1640 culture medium containing 10% calf serum, inoculated into 24-well cell culture plates, and the cells in each well are 40,000 cells, and then add Example 1 or Example 1 in each well. 2. For the obtained Schisandra extract, add Gleevec to the wells with the same concentration of the Schisandra ethanol extract to the final concentrations of 0, 6, 12, 25, 50, and 100 ng / ml. After culturing for 3 days, count the number of cells in each well with a flow cytometer (FACScan, Becton Dickinson, USA), and then calculate the half inhibitory concentration IC 50 .
[0020] Experimental results:
[0021] Ku812 and K562 are chronic myeloid leukem...
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