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High-purity salvianolic acid B and preparation method and application thereof

A high-purity salvianolic acid technology, applied in the fields of high-purity salvianolic acid B, preparation and application, can solve the problems of inability to use industrialized production, low purity of salvianolic acid B, many steps, etc. Cost, simple process effect

Inactive Publication Date: 2010-02-03
苑立超
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The disadvantage of the prior art is that the purity of salvianolic acid B obtained is lower than 92%, and there are many steps to obtain more than 92% salvianolic acid B, the cost is very high, and it cannot be used for industrial production

Method used

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  • High-purity salvianolic acid B and preparation method and application thereof

Examples

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Embodiment 1

[0024] Take 1000g of Salvia miltiorrhiza, grind it, add deionized water, heat and extract at 100°C for 1 hour, use water 5 times the weight of Salvia miltiorrhiza, and decoct and extract twice under the condition of pH 4.8, 40 minutes each time, use the weight of Danshen 3 times water. Filter the extract, adjust the pH to 3, use polyamide pre-column chromatography, wash with water to remove impurities, then use 10% ethanol to remove impurities, and 80% ethanol for desorption. The components containing salvianolic acid B were collected and recovered under reduced pressure. The resulting solution was then chromatographed on a polyamide column and desorbed with 95% ethanol to obtain components containing salvianolic acid B. The fractions with a purity greater than 98.5% were collected in sections, concentrated under reduced pressure, and adjusted to pH 4.8. The concentrated solution is passed through a Sephadex column, and the parts with a purity greater than 98.5% are collected...

Embodiment 2

[0026] Take 1500g of Salvia miltiorrhiza, grind it, add deionized water, heat and extract at 100°C for 1 hour, use 5 times of water, then decoct and extract 3 times under the condition of pH4.8, each time for 40 minutes, use 3 times of water . The extract was filtered, the pH was adjusted to 2, and the polyamide pre-column chromatography was used to elute impurities with water, and then 30% ethanol was used to remove impurities, and 90% ethanol was used for desorption. The components containing salvianolic acid B were collected and recovered under reduced pressure. The resulting solution was then chromatographed on a polyamide column and desorbed with 90% ethanol to obtain components containing salvianolic acid B. The fractions with a purity greater than 98% were collected in sections, concentrated under reduced pressure, and adjusted to pH 5. The concentrated solution is passed through a Sephadex column, and the parts with a purity greater than 98.5% are collected in section...

Embodiment 3

[0028] Take 2000g of Salvia miltiorrhiza, grind it, add deionized water, heat and extract at 100°C for 1 hour, use 5 times the water, and then decoct and extract twice under the condition of pH4.8, each time for 40 minutes, use 3 times of water. Filter the extract, adjust the pH to 4, use polyamide pre-column chromatography, wash with water to remove impurities, then use 50% ethanol to remove impurities, use 95% ethanol to desorb, and collect the components containing salvianolic acid B. Ethanol was recovered under reduced pressure. The resulting product was then chromatographed on a polyamide column, desorbed with 95% ethanol, and the fractions with a purity greater than 98% were collected in sections, concentrated under reduced pressure, and adjusted to pH 4.8. The concentrated solution is passed through a Sephadex column, and the parts with a purity greater than 98.5% are collected in sections, concentrated under reduced pressure, and freeze-dried to obtain high-purity salv...

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Abstract

The invention relates to a high-purity salvianolic acid B and a preparation method and application thereof. The method for extracting and separating the salvianolic acid B in the prior art comprises the steps of crushing medicinal materials into powder or performing microwave wall breaking, leaching or decocting extraction, and acquiring the salvianolic acid B by further adopting the methods of macroporous absorbent resin, polyamide chromatography and the like. The defects of the prior art are that the purity of the obtained salvianolic acid B is lower than 92 percent, the steps for obtainingthe salvianolic acid B of which the purity is above 92 percent are quite a lot, the cost is very high, and the prior art cannot be applied to industrial production. The preparation method consists ofthe steps of extraction, polyamide chromatography and collection. The salvianolic acid B is applied to treating cardiovascular and cerebrovascular diseases, kidney diseases, pneumonia, pulmonary heartdiseases, pancreatitis, diabetes, cervical spondylosis, retinal vascular diseases, retinal nerve diseases, migraine headaches, chronic gastritis, dizziness, bone diseases, and Alzheimer's diseases.

Description

Technical field: [0001] The invention relates to a method for extracting and isolating salvianolic acid B from Chinese medicinal material Salvia miltiorrhiza and the application of salvianolic acid B. Background technique: [0002] Salvia miltiorrhiza Bge, a plant of the Labiatae family, is a perennial herb that has the effects of dispelling blood stasis and relieving pain, promoting blood circulation and stimulating menstruation, and clearing heart and annoyance. In modern clinical practice, it is widely used to prevent and treat cardiovascular and cerebrovascular diseases, kidney diseases, liver diseases, etc. Due to the complex ingredients in the extract, it is difficult to promote it to the world. [0003] Salvianolic acid B is a water-soluble phenolic acid isolated from Salvia miltiorrhiza, and its molecular formula is C 36 h 30 o 16 , the molecular weight is 718.614, and the structural formula is: [0004] [0005] Clinical medicine has proved that salvianolic ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D307/84A61K31/343A61P9/00A61P11/00A61P13/12A61P27/02A61P25/28A61K36/53
Inventor 苑立超
Owner 苑立超