CN1544455A - Ursolic acid extracting method from privet leaf - Google Patents
Ursolic acid extracting method from privet leaf Download PDFInfo
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- CN1544455A CN1544455A CNA2003101114798A CN200310111479A CN1544455A CN 1544455 A CN1544455 A CN 1544455A CN A2003101114798 A CNA2003101114798 A CN A2003101114798A CN 200310111479 A CN200310111479 A CN 200310111479A CN 1544455 A CN1544455 A CN 1544455A
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- ursolic acid
- glossy privet
- ethanol
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Abstract
The invention discloses a process for extracting ursolic acid from ligustrum lucidum leaves comprising the steps of, A. boiling ligustrum lucidum leaves and waer in an extraction jar, filtering water solution, B. filtering through decompression, C. charging high solubility ethanol and heating for backflow with ligustrum lucidum leaves, B. filtering through decompression to obtain filter liquor, watering to adjust the alcohol concentration of the filter liquor, E. heating the adjusted filter liquor for inverse flow, cooling down, filtering, drying the filtering sediment to obtain the ursolic acid product. The invention realizes simple process and easiness in operation. The ursolic acid prepared can be used as the raw material for making medicament for reducing blood fat and treating cardiovascular diseases.
Description
Technical field
The present invention relates to the extraction of Leaf of Glossy Privet ursolic acid, more specifically relate to a kind of method of from Leaf of Glossy Privet, extracting ursolic acid.
Background technology
Ursolic acid (ursolic acid) has another name called ursonic acid, and urson belongs to triterpene compound.It is very wide in distributed in nature, as is present in the leaf, fruit of Du Juan flower section plant black bearberry, and in the leaf of goatweed royal paulownia, and the leaf of oleaceae plant glossy privet is medium.Ursolic acid has biological effect widely, and it has significantly stable and cooling effect to central nervous system; External all have anti-microbial activity to G+ and G-bacterium and yeast.In addition, it also has the effect of anti-diabetic, antiulcer agent and blood fat reducing.The discovered in recent years ursolic acid not only has resistant function to multiple carcinogenic, short cancer thing, and for example P388 and L1210 leukemia cell, A549 human lung adenocarcinoma cell have the growth of inhibition effect to multiple malignant cell.In addition, ursolic acid also can induce the F9 teratocarcinoma cell to become endoderm cell and angiogenesis inhibitor.Huangshi 999 Pharmaceutical Co., Ltd. is that raw material is researched and developed into national Chinese medicine two kind new medicines with the Leaf of Glossy Privet extract, this product is used for the treatment of hyperlipidemia, has comprehensive comprehensive adjustment human body lipid function, through clinical study, can reduce TC, TG, TC-HDL-C/HDL-C, rising HDL, and can reduce the level of LDL-C, can improve simultaneously the hepatic and renal YIN deficiency, tinnitus, dry that hyperlipemia causes, sleep less, diseases such as irritated irritability, limb fiber crops are afraid of cold, constipation, blood fat curative effect total effective rate is 95%.From the structure bone is the research that raw material extracts ursolic acid technology, modern chemical industries such as Sun Laijiu, 2000,20 (9) 47-48.Present chemosynthesis ursolic acid complex process, the cost height.
Summary of the invention
The objective of the invention is to be to provide a kind of method of extracting ursolic acid from Leaf of Glossy Privet, this method is easy, and is easy to operate, and cost is low, extracts ursolic acid from Leaf of Glossy Privet, is used for Medicines and Health Product, the treatment cardiovascular disease.
In order to achieve the above object, the present invention adopts following technical scheme, the steps include:
1, add dry Leaf of Glossy Privet in extractor, add dry Leaf of Glossy Privet weight 15-20 water doubly again, boiled 40-60 minute, the elimination aqueous solution repeats this step 2-3 time;
2, add dry Leaf of Glossy Privet weight 3-6 30-45% ethanol doubly again in extractor, reflux 1-2 hour, the liquid filtration under diminished pressure in the extractor in concentration tank, is repeated this step 2-3 time, it is stand-by to reclaim ethanol;
3, add dry Leaf of Glossy Privet weight 3-6 70-88% ethanol doubly again in extractor, reflux 1-2 hour, the liquid filtration under diminished pressure in the extractor to concentration tank, is repeated this step 2-3 time, get ethanol extract behind the concentrated filtrate, it is stand-by to reclaim ethanol;
4, add dry Leaf of Glossy Privet weight 0.25-0.5 78-88% ethanol doubly, add ethanol extract weight 0.5-1 activated carbon doubly in the concentration tank of ethanol extract, reflux 1-2 hour, 45-55 ℃ of filtration under diminished pressure gets filtrate, repeating this step adds the above-mentioned filtrate 1 time except that " add dry Leaf of Glossy Privet weight 0.25-0.5 doubly 78-88% ethanol " changes into, filtrate enters in the hold-up vessel, repeat this step 1-2 time then, add water the alcohol concn of filtrate in the hold-up vessel is transferred to 50-75% by 78-88%, get the 50-75% ethanolic soln;
5, with 50-75% ethanolic soln reflux 10-25 minute, be cooled to 20-25 ℃, cooled liquid was placed below 0 ℃ 10-14 hour, and filtration under diminished pressure gets filter residue, dry filter residue, the ursolic acid product.
The present invention compared with prior art has the following advantages and effect: this method is easy, and is easy to operate, and cost is low, and technological method is grasped easily, is particularly suitable for scale operation.Content of ursolic acid just can reach more than 40% by above step.The annual people who suffers from cardiovascular diseases of China becomes the trend of rapid increase, and ursolic acid has unique curative effect of reducing blood-fat, is treatment cardiovascular diseases medical material, and not only technology is simple, obtains from natural plants extensive again.In addition, extract the used plant Leaf of Glossy Privet of ursolic acid and distribution widely, aboundresources are arranged in China.
Embodiment
1, add the dry Leaf of Glossy Privet of 1kg in extractor, add 20kg water again, boiled 45 minutes, the elimination aqueous solution repeats this step and removes " adding in the 1kg drying Leaf of Glossy Privet extractor " 3 times;
2, add 6kg30% ethanol again in extractor, reflux 2 hours in concentration tank, repeats this step 2 time with the liquid filtration under diminished pressure in the extractor, and it is stand-by to reclaim ethanol;
3, add 6kg85%7 alcohol again in extractor, reflux 1 hour to concentration tank, repeats this step 2 time with the liquid filtration under diminished pressure in the extractor, behind the concentrated filtrate ethanol extract, it is stand-by to reclaim ethanol;
4, add 0.5kg85% ethanol, add the 0.03kg activated carbon in the concentration tank of ethanol extract, reflux 1 hour, 55 ℃ of filtration under diminished pressure get filtrate, repeating this step adds the above-mentioned filtrate 1 time except that " adding 0.5kg85% ethanol " changes into, filtrate enters in the hold-up vessel, adds water the alcohol concn of filtrate in the hold-up vessel is transferred to 70% by 85%, gets 70% ethanolic soln;
5, with 70% ethanolic soln reflux 15 minutes, be cooled to 20 ℃, cooled liquid was placed below 0 ℃ 12 hours, and filtration under diminished pressure gets filter residue, and dry filter residue promptly gets ursolic acid product 0.014kg, and yield is 1.4%, and content of ursolic acid is greater than 40%.
Claims (1)
1, a kind of method of extracting ursolic acid from Leaf of Glossy Privet comprises the following steps:
A, add dry Leaf of Glossy Privet in extractor, add dry Leaf of Glossy Privet weight 15-20 water doubly again, boiled 40-60 minute, the elimination aqueous solution repeats this step 2-3 time;
B, add in the dry Leaf of Glossy Privet weight 3-6 30-45% extraction using alcohol jar doubly again, reflux 1-2 hour, the liquid filtration under diminished pressure in the extractor in concentration tank, is repeated this step 2-3 time, recovery ethanol is stand-by;
C, add dry Leaf of Glossy Privet weight 3-6 70-88% ethanol doubly in extractor again, reflux 1-2 hour, the liquid filtration under diminished pressure in the extractor in concentration tank, is repeated this step 2-3 time, behind the concentrated filtrate ethanol extract, recovery ethanol is stand-by;
D, add dry Leaf of Glossy Privet weight 0.25-0.5 70-88% ethanol doubly, add ethanol extract weight 0.5-1 activated carbon doubly in the concentration tank of ethanol extract, reflux 1-2 hour, 45-55 ℃ of filtration under diminished pressure gets filtrate, repeat this step 1-2 time, filtrate enters hold-up vessel, adds water the alcohol concn of filtrate in the hold-up vessel is transferred to 50-75% by 78-88%;
E, with the ethanolic soln reflux of 50-75% 10-25 minute, cooling, cooled solution was placed below 0 ℃ 10-14 hour, filtration under diminished pressure gets filter residue, dry filter residue promptly gets the ursolic acid product.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2003101114798A CN1324044C (en) | 2003-11-28 | 2003-11-28 | Ursolic acid extracting method from privet leaf |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2003101114798A CN1324044C (en) | 2003-11-28 | 2003-11-28 | Ursolic acid extracting method from privet leaf |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1544455A true CN1544455A (en) | 2004-11-10 |
| CN1324044C CN1324044C (en) | 2007-07-04 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2003101114798A Expired - Fee Related CN1324044C (en) | 2003-11-28 | 2003-11-28 | Ursolic acid extracting method from privet leaf |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102028698A (en) * | 2009-12-02 | 2011-04-27 | 山东省中医药研究院 | Medicine for treating colon cancer and preparation method thereof |
| CN102512426A (en) * | 2011-12-26 | 2012-06-27 | 哈尔滨医科大学 | Application of ursolic acid in preparation of health care product with effects of weight loss and fatty liver improvement |
| CN107325150A (en) * | 2017-07-24 | 2017-11-07 | 广东药科大学 | A kind of method of supercritical carbon dioxide extracting fruit of glossy privet ursolic acid |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1126757C (en) * | 2001-12-20 | 2003-11-05 | 武汉大学 | Process for extracting ursolic acid from fructus ligustri lucidi leaf |
| CN1186350C (en) * | 2003-05-19 | 2005-01-26 | 西安交通大学 | Process of extracting and separating ursolic acid from plant |
-
2003
- 2003-11-28 CN CNB2003101114798A patent/CN1324044C/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102028698A (en) * | 2009-12-02 | 2011-04-27 | 山东省中医药研究院 | Medicine for treating colon cancer and preparation method thereof |
| CN102028698B (en) * | 2009-12-02 | 2012-05-23 | 山东省中医药研究院 | Medicine for treating colon cancer and preparation method thereof |
| CN102512426A (en) * | 2011-12-26 | 2012-06-27 | 哈尔滨医科大学 | Application of ursolic acid in preparation of health care product with effects of weight loss and fatty liver improvement |
| CN107325150A (en) * | 2017-07-24 | 2017-11-07 | 广东药科大学 | A kind of method of supercritical carbon dioxide extracting fruit of glossy privet ursolic acid |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1324044C (en) | 2007-07-04 |
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