Active site of mulberry twig, as well as preparation method and application thereof
A technology of active parts and mulberry branches, which is applied in the field of preparation of active parts of traditional Chinese medicine, can solve the problems of insufficient content determination and quality control of active parts of mulberry branches for hypoglycemia, and achieve industrialization cost saving, good repeatability and high safety. Effect
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Embodiment 1
[0036] Example 1 The preparation method of the active part of Morus twig
[0037] Get mulberry branch 100g, 4 parts, pulverize, sieve. Boil with pure water, 25% ethanol water, 50% ethanol water, and 75% ethanol water respectively, extract twice, the liquid-solid ratio is 10 ml / g, carry out three times in parallel at each concentration level, and pass through strong acidic ion exchange resin 732 (1:20=m / m), then eluted with 0.N ammonia water, collected the eluate and evaporated to dryness, then dissolved in water and slowly passed through strong basic anion exchange resin 201×7, eluted with water, evaporated to dryness The active parts of Mori twigs are obtained by dehydration. Among them, the maximum and average amount of active parts of Mori twig obtained by 50% ethanol water extraction is 0.78g.
Embodiment 2
[0038] Example 2 The preparation method of the active part of Morus twig
[0039] Take 5g of mulberry branches, crush, sieve, heat and reflux twice at 60~80°C with 10~20 times of 50%~80% ethanol, each time for 60~180min, filter and concentrate the extract to recover ethanol to obtain the original solution. The stock solution was adsorbed by a strongly acidic cation exchange resin, and then eluted with 0.5N ammonia water, and the eluate was collected and evaporated to dryness to obtain sample 1. Then sample 1 was dissolved in water, slowly passed through a strong basic anion exchange resin, eluted with water, and the eluate was evaporated to obtain sample 2, which is the active part of Mori twig. The results are shown in Table 1.
[0040] Table 1 The amount of fractions with hypoglycemic activity obtained under different extraction conditions
[0041] coding temperature °C time min Alcohol concentration% Liquid-solid ratioml / g Total alkaloids (g) 1...
Embodiment 3
[0043] Example 3 The content determination method of main component-DNJ of mulberry branch active part
[0044] Take 50 μl of the above sample solution, reference solution, and blank solution respectively in a 1.5ml centrifuge tube, add 200 μl of 0.4mol / L potassium borate buffer solution, then add 250 μl of 5 mmol / L FMOC-Cl (50% acetonitrile), shake well , stand at room temperature for 30 minutes, then add 25 μl of 1mol / L glycine (Gly) to stop the reaction, then add 80 μl of acetic acid solution with a volume fraction of 1%, add water to make up to 1000 μl, and finally filter the solution with an organic membrane to obtain the test solution. The test solution is tested by liquid chromatography, and the conditions of liquid chromatography are: chromatographic column: Ultimate TM XB-C18 chromatographic column (4.6 mm × 250 mm); mobile phase: acetonitrile-0.1% acetic acid (38:62); flow rate: 1ml / min; column temperature: room temperature; wavelength: 254nm; injection volume: ...
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