Use of total saponins of panax japonicas in preparing medicine for treating rheumatoid arthritis angiogenesis
A technology for total saponins and angiogenesis of Panax ginseng, which can be applied in drug combinations, plant/algae/fungus/moss components, antipyretics, etc., can solve the structural disorder of new blood vessels, cannot change the hypoxic state of synovium, and can not function fully. And other issues
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Embodiment 1
[0026] Embodiment 1: Get the bamboo ginseng medicinal material, accurately weighed, 10 times the amount of 70% ethanol heating and reflux extraction 3 times, each time for 2 hours, 80 ° C water bath concentration, filtering, merging the filtrate, and the filtrate concentrating under reduced pressure to obtain the bamboo joint Ginseng active ingredient.
Embodiment 2
[0027] Embodiment 2: HPLC method detects the content of four kinds of active components in the total saponins of Panax ginseng
[0028] Experimental method: In this experiment, the HPLC method was used to detect whether the total saponins of Panax ginseng contained four active ingredients. The test results showed that it contained ginsenoside Rg2, ginsenoside Ro, Panax ginseng saponin V, and Panax ginseng saponin IVa.
[0029] The experimental system is: chromatographic column Welch Ultimate XB-C18 150×4.6 mm, 5 μm, column temperature 30°C; DAD detector, detection wavelength is 200 nm; mobile phase A is 0.1% phosphoric acid aqueous solution, B is acetonitrile, using the following gradient Elution; flow rate is 1.0 mL / min; injection volume is 10 μL.
[0030] The mobile phase gradient is shown in the table:
[0031]
[0032] See the experimental results figure 1 .
Embodiment 3
[0033] Example 3: Total saponins of Panax japonicus (TSPJ) inhibit angiogenesis in mice with arthritis through the HIF-1α-VEGF-Ang-1 pathway
[0034] Experimental method: 60 male DBA / 1J mice, weighing 16-18g, after one week of adaptive feeding, 8 were randomly selected as the normal group (hereinafter referred to as group C), and the rest of the mice were used as the model group. Dissolve in 10mM acetic acid according to CⅡ, the concentration is 2mg / mL, stir, and fully dissolve overnight at 4°C. Take an equal volume of CII and mix it into a 5mL glass syringe, pump it repeatedly for 30 minutes (operated on ice), until the mixture is completely and fully emulsified, and the emulsion is not loose when it is dripped into the water, and the antigen is made. The mice in the model group were injected with 0.1 mL of antigen on the left side of the base of the tail, and the mice in the normal group were given 0.1 mL of PBS. 14 days after the initial immunization, CII was mixed with an...
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