Application of ginkgo seed extract
A technology of extracts and ginkgo kernels, which can be used in the fields of medicine, food or health care products, can solve problems such as aplastic anemia, colchicine with large side effects, leukopenia, etc., and achieve strong inhibitory effect and good anti-gout effect Effect
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Embodiment 1
[0024] Example 1 , the preparation of ginkgo kernel extract
[0025] Appropriate amount of coarse powder of medicinal materials, 10 times the amount of 70% ethanol, heated and refluxed for 3 times, 2h each time, filtered and combined the filtrate, concentrated the filtrate under reduced pressure, and dried the concentrated solution to obtain the extract powder.
Embodiment 2
[0026] Example 2 Inhibitory effect of ginkgo kernel extract on xanthine oxidase
[0027] Experimental Materials:
[0028] Drug to be tested: ginkgo kernel extract (sample prepared in Example 1), dissolved in DMSO to prepare a 60 mg / mL mother solution.
[0029] Xanthine oxidase: Sigma, Cat.:X1875
[0030] Xanthine: Sigma, Cat.: X7375
[0031] Positive control drug: Allopurinol (Jiangsu Fangqiang Pharmaceutical)
[0032] experimental method:
[0033] Potassium phosphate buffer was used as the diluent to prepare different working concentrations of drug solution, xanthine oxidase (0.04U / mL) and xanthine solution (0.8mM), and 50 μL of drug solution and 50 μL of yellow purine solution were added to a 96-well assay plate. Purine oxidase and 100 μL xanthine solution were detected with a microplate reader at 290 nm, and the values of absorbance and absorbance increase were recorded every 5 seconds for a total of 10 minutes.
[0034] The experimental results are shown in Table ...
Embodiment 3
[0038] Example 3, the inhibitory effect of ginkgo kernel extract on tumor necrosis factor alpha
[0039] Experimental Materials:
[0040] Drug to be tested: ginkgo kernel extract (sample prepared in Example 1), dissolved in DMSO to prepare a 60 mg / mL mother solution.
[0041] TNFαELISA Kit: R&D, Cat.:DY210
[0042] Positive control drug: IKK-2 inhibitor IV (Santa cruz, Cat.:sc-203083)
[0043] Lipopolysaccharide (LPS): Sigma, Cat.:L6529
[0044] experimental method:
[0045] Fresh healthy adult whole blood was taken, and human peripheral blood mononuclear cells (PBMC) were separated by density gradient centrifugation. After counting, they were seeded in 96-well cell culture plates, and drugs of different concentrations were added. After pretreatment for 30 minutes, lipopolysaccharide (LPS) stimulation overnight, the next day, according to the method of TNFαELISA kit ELISA test detection of TNFα protein content.
[0046] The experimental results are shown in Table 2 below:...
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