Medicinal composition having immunity-regulating function
A technology for medicines and extracts, applied in the field of Bupleurum edulis extracts, can solve problems such as researches or literatures on the regulation of immune function of Bupleurum edulis that have come out yet.
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Embodiment 1
[0047] Embodiment 1 screening plant material
[0048] Select the roots of various Bupleurum plants and grind them into plant powder.
[0049] Get above-mentioned plant powder 0.5g, after shaking overnight at room temperature with 25ml of 95wt% ethanol, redissolve into 2ml with 95wt% alcohol after drying and concentrating, carry out high performance liquid chromatography (HPLC) analysis, HPLC analysis condition is as follows:
[0050] Column: SymmetryShield TM (Waters), RP 18, 5μm, 250×4.6mmlD
[0051] Mobile phase: A: H 2 O, B: Acetonitrile, C: Methanol
[0052] Detection: UV / λ=237nm.
[0053] Among these Bupleurum extracts, select and standard dibenzylbutyrolactone type lignan (kaerophyllin) ( figure 1 Middle (a) line) has the same peak ( figure 1 The peak in the frame) Bupleurum, figure 1 The (b) line represents (b) Bupleurum (i.e., sequence identification number 1); (c) line represents Altai Bupleurum (i.e., the sequence identification number 2 Bupleurum); (d) line ...
Embodiment 2
[0054] Embodiment 2 extracts active ingredient
[0055] Grind the Altai Bupleurum krylovianum plant selected in Example 1, take 2kg of powder and add it to 16L of 95wt% ethanol aqueous solution, after 5 hours at room temperature, dry and concentrate to obtain an extract with an extraction rate of 6.7±0.1%. Perform high performance liquid chromatography (HPLC) analysis, such as figure 2 As shown, there is a peak between 30-40 minutes.
[0056] HPLC analysis conditions:
[0057] Column: SymmetryShield TM (Waters), RP 18, 5μm, 250×4.6mmlD
[0058] Mobile phase: A: H 2 O, B: Acetonitrile, C: Methanol
[0059]Detection: UV / λ=237nm
Embodiment 3
[0060] Example 3 Identification of active ingredients
[0061] 18.5 kg of Bupleurum krylovianum screened in Example 1 was added to 25 L of methanol, and after 4 hours at room temperature, it was concentrated and dried to obtain 18.5 kg of a residue. Take this residue 500mg, carry out column chromatography, with SiO 2 As the stationary phase, use hexane, ethyl acetate, methanol (6 / 4 / 1-3 / 2 / 1-0 / 0 / 1 to adjust different volume ratios) as the mobile phase, and after washing the column with a polar gradient, They were collected separately and analyzed by thin layer chromatography (TLC) to obtain 12 fractions. These 12 parts are carried out following HLPC analysis, and 12 parts are dissolved in methanol respectively, and concentration is adjusted to 1mg / ml, selects the part that has identical peak with standard product dibenzylbutyrolactone type lignan (kaerophyllin), will This part was subjected to the above-mentioned column chromatography again to separate the extract with higher ...
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