Sedative and hypnotic active saponin components of spina date seed, as well as separation and purification method and application of sedative and hypnotic active saponin components
A technology for separation and purification of jujube seed, which is applied in the field of saponin components of soothe the nerves and hypnotic activity and its separation and purification.
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Embodiment 1
[0037] Example 1 Preparation of saponins of soothing hypnotic active saponin from Jujube seed
[0038] A sample of wild jujube seed powder (after frying and crushing, the wild jujube seed is passed through a 40-mesh sieve, and dried at 60°C for 24h), placed in a Soxhlet extractor with 10 times the volume of petroleum ether and defatted at 60°C for 4 hours to obtain residue and wild jujube seed oil; The residue was taken out, dried, crushed, and passed through a 40-mesh sieve to obtain defatted jujube seed powder. The defatted jujube seed powder was extracted with 25 times the volume of 70% ethanol in a 90°C water bath for 3 hours, and filtered to obtain residue I and alcohol. Liquid; evaporate the alcohol liquid to a paste under reduced pressure at 60°C, add water to dissolve it, filter and remove impurities to obtain an aqueous solution, add 1 volume of water-saturated n-butanol to the aqueous solution to extract, discard the water layer, and obtain n-butyl Alcohol layer I; alka...
Embodiment 2
[0039] Example 2 Separation and Purification of Saponins from Jujube Seed Soothing Hypnotic Activity
[0040] Due to the large polarity of saponin, low-activity alumina or silica gel is generally used as the adsorbent, and then solvents of different polarity are used for elution according to different saponin. Dry 100-200 mesh silica gel for column chromatography at 110°C for 1 hour, then rinse with distilled water to remove impurities; then soak in 95% ethanol for 24 hours; after vacuum degassing, wet it into chromatography Column (36mm×80mm). Column packing method: first add a certain amount of water to the column, then pour the silica gel with water into the column, discharge excess water through the column, keep the water surface above the silica gel layer by more than 3cm, until the silica gel layer is 7cm from the top of the column~ 8cm, spare. Load the saponin sample solution with a concentration of 25mg / ml, a sample volume of 10ml, 60% ethanol solution as the eluent, ad...
Embodiment 3
[0043] Example 3 Experimental determination of hypnotic activity
[0044] (1) Influence on the autonomous and coordinated movement of mice
[0045] (1) Autonomous movement
[0046] Suanzaoren soothing hypnotic active saponins components Ⅰ and Ⅱ were mixed into 10mg / ml medicinal solution. Thirty mice, half male and half male, were randomly divided into three groups with 10 mice in each group. Each group was given 0.15ml / 10g·d of liquid medicine (equivalent to 17g / kg·d of crude drug, about 50 times the clinical adult dose). The blank group was given the same volume of normal saline once a day for 3 consecutive days. Fasting for 24h before the last dose. 45 minutes after the last administration, the mice were placed in a cardboard box and allowed to adapt for 5 minutes, and the number of activities within 5 minutes was recorded (measure the walking time of the mice and the number of times the forelimbs were raised). Compared with the blank group, there is a very significant differen...
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