Method for extracting coptisine
An extraction method and a technology for coptisine are applied in the field of biological extraction, can solve the problems of poor chloroform recrystallization safety, difficult to meet large-scale preparation, unfavorable for industrialized production and the like, and achieve the effects of easy implementation, good utilization rate and low cost
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Embodiment 1
[0028] a) Take 1 kg of Coptidis Rhizoma, pass through a 20-mesh sieve after crushing, then immerse Coptis Rhizoma in 5 liters of sulfuric acid solution with a mass concentration of 1%, heat up to 100° C. and extract for 0.1 hour and then filter to obtain the first acid extract and Residue; in the present embodiment, the concentration of sulfuric acid is 0.05~1%, and the volume is 3-5 times of bulk medicine volume all can realize better acid extraction effect;
[0029] b) According to the method of step a, the residue is acid-extracted three times to obtain the acid-extracted solution of the three-time acid-extracted acid-extracted solution respectively, and the acid-extracted solution obtained for the first acid-extracted and second-time acid-extracted solution is combined and neutralized with milk of lime to pH 10, after standing for 24 hours, discard the precipitation in the acid extract to obtain the supernatant; In this step, the raw materials are subjected to acid extract...
Embodiment 2
[0038] a. Take 1 kg of Cortex Phellodendri, break it through a 20-mesh sieve, then soak Coptidis Rhizome in 15 liters of sulfuric acid solution with a mass concentration of 0.05%, filter it after acid extraction at room temperature for 24 hours, and obtain the first acid extraction solution and residue ;
[0039] b. the residue obtained in step a is acid-extracted with 10 liters of 0.05% sulfuric acid solution, and the extraction conditions are the same as in step a), to obtain the second acid extraction solution and filter residue;
[0040] c. Carry out two acid extractions to the filter residue obtained in step b according to the method of step b again, the first acid extraction and the acid extraction solution of the second acid extraction are combined and neutralized with calcium hydroxide to a pH of 11, and left to stand for 24 After 4 hours, the precipitation in the acid extraction solution was discarded to obtain a supernatant; in the present embodiment, the treatment m...
Embodiment 3
[0049] a. Take 1 kg of the mixture of Coptis chinensis, Cortex Phellodendron and Sanke needles, crush it and pass it through a 20-mesh sieve, then soak the Coptis chinensis in 8 liters of sulfuric acid solution with a mass concentration of 0.3%, raise the temperature of the material to 60°C and extract it with acid for 6 hours Filter to obtain the first acid extract and residue;
[0050] b. The obtained residue was subjected to acid extraction with 5 liters of 0.3% sulfuric acid solution, the acid extraction temperature was 60° C., and the acid extraction time was 2 hours to obtain the second acid extraction solution and filter residue;
[0051] c. Carry out two acid extractions to the obtained filter residue according to the method of step b again, combine the acid extraction solutions of the first acid extraction and the second acid extraction and neutralize with sodium hydroxide to a pH of 12, after standing for 24 hours , discarding the precipitation in the acid extract to...
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