Neoplasm metastasis suppressing pharmaceutical composition prepared by DMGF (7,7''-Dimethoxyagastisflavone) and application of neoplasm metastasis suppressing pharmaceutical composition
A pharmaceutical composition and tumor metastasis technology, applied in the direction of drug combination, antineoplastic drugs, medical preparations containing active ingredients, etc., can solve the problems of unknown mechanism and application, failure to make further breakthroughs, and few studies on DMGF mechanism and efficacy , to achieve the effect of inhibiting tumor metastasis
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experiment example 1
[0031] Experimental Example 1: Preparation of DMGF
[0032] The DMGF used in the present invention is an extract containing DMGF obtained by high performance liquid chromatography (High Performance Liquid Chromatography, HPLC), and the purity of the DMGF is above 98%. In this experimental example, DMGF was extracted in a Waters high-performance liquid chromatography system (Waters2796Bio-separationModule), wherein the column used in this experimental example is the column of the system, which is C18 with a particle size of 5mm TM Symmetry column (250mmx4.6mm), and by means of 30% methanol aqueous solution to wash the column at a speed of 0.5mL / min, and take the eluate that has a significant change in the absorbance at 254nm, which is Contains DMGF extract. Next, weigh about 5 mg of the aforementioned DMGF-containing extract at room temperature, and use this as a unit dose. Next, it is packaged in the form of a powder or cachet and stored at room temperature.
experiment example 2
[0033] Experimental example 2: DMGF has the effect of inhibiting the ability of tumor cells to degrade the extracellular matrix and inhibiting tumor metastasis
[0034] Using tissue culture techniques, mouse melanoma was cultured in cell culture medium DMEM (Gibco / Invitrogen, Carlsbad, CA, USA) containing 10% fetal bovine serum (Gibco / Invitrogen, Carlsbad, CA, USA) and 1% antibiotics (mousemelanomacells) cell line B16F10 to an appropriate number, wherein the antibiotics are preferably penicillin / streptomycin / amphotericin. Next, take the containing quantity 3×10 4 The suspension of B16F10 cells was seeded in the upper chamber of two transwell culture dishes, one of which was added with DMGF at a final concentration of 1 μg / ml; the other was not added with DMGF as a control Group. In addition, cell culture medium DMEM was added to the upper and lower chambers of the permeable culture dish, and fetal bovine serum (FBS) was additionally added to the lower chamber. Then, put it ...
experiment example 3
[0038] Experimental Example 3: DMGF can inhibit the expression of matrix metalloproteinase-2 and inhibit the ability of tumor cells to degrade extracellular matrix
[0039] B16F10 cells were cultured by tissue culture technology, and the culture conditions were the same as those in Experimental Example 2. Take the containing quantity 1×10 6 The suspension of B16F10 cells was inoculated in at least three culture dishes, and two culture dishes were selected, and after adding the disulfonone compound DMGF with a final concentration of 1 μg / ml to the suspension of B16F10 cells, they were placed back in a 37°C Continue to cultivate in the incubator. After culturing for 12 and 24 hours respectively, the culture medium and the added compounds in the culture dish were sucked off, washed with phosphate buffered saline (PBS), and collected with trypsin-EDTA. B16F10 cells. And one of the dishes was not added with DMGF, and B16F10 cells were harvested according to the aforementioned met...
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