Method for preparing paeonol and paeoniflorin from cortex moutan

A technology for paeonol and paeoniflorin is applied in the field of preparing paeonol and paeoniflorin step by step, which can solve the problems of limited application, waste of raw materials and the like, and achieve the effects of improving purity, low cost and reasonable design.

Inactive Publication Date: 2007-12-12
ZHEJIANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] At present, there are not many patents and literature reports on extracting paeonol from paeonol. In order to increase the yield, more cumbersome methods such as supercritical are often used, which require a certain scale of equipment and equipment, which limits the application in industrial production.

Method used

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  • Method for preparing paeonol and paeoniflorin from cortex moutan

Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0025] Example one

[0026] Take 500kg of decoction pieces of Danpi, dry for 6 hours at 50℃, soak in water for 24 hours, reflux for extraction, collect the distillate to 12 times the volume (6L), freeze at -4℃ for 8 hours, take it out and thawed immediately and filter with suction. The insoluble substance is Dan Dermatol. Add 10 times the amount of 70% ethanol aqueous solution to the dregs and heat and reflux for two extractions, 0.5 hours each time. The extracts are filtered, combined, and concentrated under reduced pressure to 1g / mL (crude drug amount), top D 201 Macroporous resin (0.2-0.6g crude medicinal materials / g wet resin). Rinse with 4BV deionized water, discard, continue to purify with 4BV 20% ethanol aqueous solution, discard, and then eluate with 4BV 40% ethanol aqueous solution, collect the eluate, concentrate under reduced pressure to alcohol-free, freeze-dry, and then obtain Paeonia lactiflora Glycoside part. The extraction rate of paeonol medicinal materials is 2.0...

Example Embodiment

[0027] Example two

[0028] Take 500kg of decoction pieces of Danpi, dry for 6 hours at 50℃, soak in water for 10 hours, reflux for extraction, collect the distillate to 8 times the volume (4L), freeze at -4℃ for 4 hours, take out and melt and filter immediately, the insoluble substance is Dan Dermatol. Add 10 times the amount of 30% ethanol aqueous solution to the dregs and extract once by heating and refluxing for 0.5 hours each time. The extracts are filtered, combined, and concentrated under reduced pressure to 1g / mL (crude drug amount), top D 201 Macroporous resin (0.2-0.6g crude medicinal materials / g wet resin). Rinse with 2BV deionized water, discard, continue to purify with 3BV 10% ethanol aqueous solution, discard, and then eluate with 3BV 30% ethanol aqueous solution, collect the eluate, concentrate under reduced pressure to alcohol-free, freeze-dry, and then obtain peony Glycoside part. The extraction rate of paeonol medicinal material is 1.89% by liquid phase determina...

Example Embodiment

[0029] Example three

[0030] Take 500kg of decoction pieces of Danpi, dry for 6 hours at 50°C, soak in water for 15 hours, reflux for extraction, collect the distillate to 12 times the volume (6L), freeze at -4°C for 6 hours, take out and melt and immediately filter with suction. The insoluble substance is Dan Dermatol. Add 8 times the amount of 50% ethanol aqueous solution to the dregs and heat and reflux for two extractions for 0.5 hours each time. The extracts are filtered, combined, and concentrated under reduced pressure to 1g / mL (crude drug amount), top D 201 Macroporous resin (0.2-0.6g crude medicinal materials / g wet resin). Rinse with 3BV deionized water, discard, continue to purify with 3BV 20% ethanol aqueous solution, discard, and then eluate with 3BV 50% ethanol aqueous solution, collect the eluate, concentrate under reduced pressure to alcohol-free, freeze-dry, and then obtain peony Glycoside part. The extraction rate of paeonol medicinal materials was 1.92% and the ...

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Abstract

The invention relates to a method for preparing paeonol and peony glycosides from root bark of tree peony. It compries following steps: immersing pieces of medical herb of root bark of tree peony in water, extracting through distillation and getting paeonol crystal; extracting dregs of a decoction with alcohol solution, decompressing extract, separating extract with D201 macroporous absorption resin and getting peony glycosides. The invention is characterized by full use of medical herb, increased peony glycosides purity, rational design, low cost, easy operation, good stability and suitability for industrial production.

Description

technical field [0001] The invention belongs to the field of medicine, and in particular relates to a preparation method for obtaining paeonol and paeoniflorin step by step through extraction and refining of traditional Chinese medicine paeonol. Background technique [0002] At present, Chinese herbal medicine has a certain market all over the world. With the increase of people's awareness of health requirements and the aging of the population, sub-health status, people are more eager to return to nature, and use pure natural medicine with high degree of treatment, To prevent problems that cannot be solved by some chemically synthesized drugs, the application of natural herbal medicines is beyond the background of its original national traditional culture. It has become the goal pursued by pharmaceutical companies all over the world to seek medicines with low side effects and high quality and low price from natural medicines. The European Community has carried out unified l...

Claims

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Application Information

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IPC IPC(8): C07C49/255C07H17/04A61K36/71A61K125/00
Inventor 贺庆葛志伟程翼宇水文波窦静
Owner ZHEJIANG UNIV
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