Extract of potentilla anserina rhizome and medical application thereof
A technology of extracts and rhizomes, which is applied in the field of fernia rhizome extracts and pharmaceutical preparations containing the extracts, can solve the problems of unseen fernia extracts and their use in liver-protecting drugs, and achieve the effect of protecting the liver
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Embodiment 1
[0027] Embodiment 1: preparation of the rhizome extract of Bracken
[0028] Crush 10kg of dried fern rhizomes, extract them under reflux with 75% ethanol (25L×3 times), combine the extracts, concentrate until there is no alcohol smell to obtain a concentrated solution (6L); use petroleum ether (6L×3 times), ethyl acetate (6L×3 times) and water-saturated n-butanol (6L×3 times) to obtain 305g of petroleum ether extract, ethyl acetate extract and n-butanol extract respectively, and n-butanol extraction The substance was dissolved in 5L distilled water and then enriched with AB-8 macroporous resin (2kg, column volume 1.5L). First, 8 column volumes (12L) were washed with 10% ethanol to remove polysaccharides, and then 10 columns were eluted with 65% ethanol. Volume (15L), collect 65% eluate, concentrate under reduced pressure, and spray dry to obtain 185g of Juma rhizome extract extract powder.
Embodiment 2
[0029] Embodiment 2: liquid chromatography analysis
[0030] Preparation of the test solution: Take 5 mg of the extract powder prepared by the method of Example 1 into a 50 mL brown volumetric flask, add 30 mL of 20% acetonitrile aqueous solution for ultrasonic dissolution, and after cooling to room temperature, continue to add 20% acetonitrile aqueous solution to constant volume.
[0031] Analytical method:
[0032] High performance liquid chromatography: Agilent 1260, binary pump;
[0033] Chromatographic column: Diamonsil C18 column (4.6mm×250mm, 5μm);
[0034] Mobile phase: A is acetonitrile, B is 0.1% phosphoric acid solution (adjust the pH value to 6.2 with triethylamine);
[0035] Gradient elution program: 0.01~70min, A 20%→80%;
[0036] Mobile phase flow rate: 1.0mL min -1 ;
[0037] Detection wavelength: 240nm; Column temperature: 30°C;
[0038] Injection volume: 10 μL.
[0039] The extracts prepared from 10 batches of rhizomes from different origins and batche...
Embodiment 3
[0040] Embodiment 3: Pharmacological test of the rhizome extract of Bracken
[0041] 1. Test method
[0042] 1. Cell grouping
[0043]The cells were divided into 6 groups, each with 6 replicate wells: (1) normal culture group (N group): complete culture medium, cultured under normal conditions; (2) ischemia-reperfusion group (IR group): complete culture medium After culturing under normal conditions for 1 hour, simulate hypoxia for 8 hours, and then reperfuse for 4 hours; (3) Bracken extract group: RE1 group: Bracken extract 0.5ng / mL pretreatment for 1 hour; RE2 group: Bracken extract 5ng / mL Pretreatment for 1h; RE3 group: Pretreatment with 50ng / mL Bracken extract for 1h; simulated hypoxia for 8h, reperfusion for 4h; (4) Normal saline group (NS group): pretreatment with the same volume of Bracken extract as normal saline Treat for 1 hour, simulate hypoxia for 8 hours, and reperfuse for 4 hours.
[0044] 2, the pretreatment of fern extract
[0045] (1) Preparation of Bracke...
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