Usage of total alkaloid of coftis root, phellodendron bark and ÔÇÿSankezhenÔÇÖ as their preparing method
A technology of total alkaloids and three needles, applied in the field of medicine, can solve problems such as drugs that have not been found for diabetes
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Embodiment 1
[0017] Example 1: 1 kg of Coptis chinensis, a Chinese herbal medicine, was cold-soaked with 5 L of 2% sulfuric acid aqueous solution for 24 hours, then filtered through 8 layers of gauze, and the filtrate was neutralized to pH 7.0-8.0 with sodium hydroxide. The neutralized extract was passed through a macroporous adsorption resin column, the inorganic salts and water-soluble impurities were washed away with water, and then 120 g of total alkaloids were obtained by eluting with 60% and 95% ethanol, with a yield of 12%. Its effect on the glucose uptake function of differentiated C2C12 myoblasts is shown in Figure 1:
Embodiment 2
[0018] Example 2: 1 kg of Phellodendron Phellodendri, cold-soaked with 5 L of 2% sulfuric acid aqueous solution for 24 hours, then filtered with 8 layers of gauze, and the filtrate was neutralized to pH 7.0 to 8.0 with sodium hydroxide. The effect of the neutralized extract on the uptake of glucose by differentiated C2C12 cells was firstly washed with water to remove inorganic salts and water-soluble impurities, and then eluted with 60% and 95% ethanol to obtain 67g of total alkaloids, with a yield of 6.7 %. Its effect on the glucose uptake function of differentiated C2C12 cells is shown in Figure 2:.
Embodiment 3
[0019] Example 3: 1 Kg of the three needles of traditional Chinese medicine was cold-soaked with 5 L of 2% sulfuric acid aqueous solution for 24 hours, then filtered through 8 layers of gauze, and the filtrate was neutralized to pH 7.0-8.0 with sodium hydroxide. The neutralized extract was passed through a macroporous adsorption resin column, the inorganic salts and water-soluble impurities were washed away with water, and then 38 g of total alkaloids were obtained by eluting with 60% and 95% ethanol, with a yield of 3.8%. Its effect on the glucose uptake function of differentiated C2C12 myoblasts is shown in Figure 3.
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