CN1810797A - Prepn of flavone compound with guava leaf - Google Patents
Prepn of flavone compound with guava leaf Download PDFInfo
- Publication number
- CN1810797A CN1810797A CN 200610041855 CN200610041855A CN1810797A CN 1810797 A CN1810797 A CN 1810797A CN 200610041855 CN200610041855 CN 200610041855 CN 200610041855 A CN200610041855 A CN 200610041855A CN 1810797 A CN1810797 A CN 1810797A
- Authority
- CN
- China
- Prior art keywords
- guava leaf
- extract
- guava
- compound
- flavones
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
The present invention relates to technology of producing flavone compound with guava leaf. The production process of extracting flavone compound with guava leaf includes the steps of: drying, eliminating impurity, crushing, coarse extraction, refining, cooling, concentration, separation, recovering, defatting, stoving, detecting, etc. Through the advanced technological process, brown or yellow flavone powder is obtained. The produced flavone compound contains flavonoid, terpene, phenol, amino acid, phosphoric acid and other bioactive matter, and may be used as the material for oral liquid to treat type-II diabetes and complications.
Description
Affiliated field
The present invention relates to a kind of technology of producing flavone compound with guava leaf, specifically is a kind of preparation of flavone compound of Guava Leaf.
Background technology
Background study prompting adopts advanced extractive technique that natural plant resource is processed abroad, and exploitation becomes the novel medicine product and becoming a kind of development trend, does not appear in the newspapers for the effective constituent preparation method that extracts from Guava Leaf.
Pharmacological studies show that, the effective constituent of extracting in the Guava Leaf is effective to the diabetes B patient, and to point out its pharmacological action be not the secreting function that directly improves human insulin β cell, but has improved the utilization of human body surrounding tissue to sugar.
Clinical and experimental study shows, the effective constituent of extracting in the Guava Leaf is for treatment diabetes B total effective rate 〉=85%, and has hypotensive simultaneously and effect reducing blood-fat, has treatment to have the diabetes B patient's of above complication obvious curative effects concurrently.
Fitochemical studies shows that the effective constituent of extracting in the Guava Leaf belongs to flavonoid compound.The preparation technique of at present existing other plant flavonoid compound, and the problem that the preparation technique of existing other plant flavonoid compound exists is low, the poor stability of pick-up rate.The method of extracting flavonoid compound at present from Guava Leaf still belongs to blank at home.
Technology contents
Purpose of the present invention:
The objective of the invention is to propose extract in a kind of new raw material the method for flavonoid compound, promptly from Guava Leaf, extract the method for flavonoid compound; Realize industrialized production, for treatment diabetes B and relevant complication, improve the raw material extracting method that body immunity provides new pure natural plant medicines.
Technical solution of the present invention:
The preparation of flavone compound of Guava Leaf is characterized in that: forms by following steps,
The elementary processing of A, Guava Leaf
(1) drying: get the ripe Guava Leaf of collecting and adopt daylight airing or furnace drying method to be dried to contain moisture≤10%;
(2) impurity elimination: will promptly also be that the Guava Leaf of the pure piscidia foline of medicinal flavones (transient name) content 〉=5 ‰ standards is handled, separated the elimination nonmetallic impurity through vibration letter sorting sieve through dried Guava Leaf;
(3) pulverize: will pulverize grinding particle size 〉=100 orders through the standard compliant Guava Leaf of above processes;
The extraction of B, Guava Leaf chromocor compound
(1) slightly carries: will be through the Guava Leaf powder after the elementary processing, adopt 0.5～2 ton stainless-steel vacuum to extract equipment, under the condition of 110～120 ℃ of temperature, its Guava Leaf powder and be 〉=90% edible ethanol as solvent strength, by the solid solution ratio is 1: 5, an extraction time is 30～45 minutes, produces the extracting solution of Guava Leaf flavones;
(2) essence is carried: extract repeatedly 3～4 times by above extraction process, finish until substantially the flavonoid compound in the Guava Leaf powder being extracted;
(3) quicken: when first, second time extracted, for accelerating extraction rate, can add a small amount of pure water, add-on is pressed 1%～20% of Guava Leaf grain weight amount and is selected arbitrarily; 10%～20%;
Concentrating of the extracting solution of C, Guava Leaf chromocor compound
(1) concentrate: Guava Leaf flavonoid compound extracting solution is poured in 0.5～2 ton the stainless steel thickening equipment, under normal pressure, temperature is condensed into medicinal extract with it under 110 ℃～120 ℃ condition;
(2) cooling: the Guava Leaf flavonoid compound extract after will concentrating cooled off after 2～4 hours,, temperature is less than 30 ℃～40 ℃, and it is stand-by to put into bucket;
(3) reclaim: adopt the alcohol recovery device on the thickening equipment, alcohol is reclaimed after alcohol content tester detects at 〉=75% o'clock, can be used as and extract solvent and continue stand-byly,, can be separately fall it and concentrate and reach more than the standard back and collect stand-by with thickening equipment if do not reach above standard.
The powder process of D, Guava Leaf chromocor compound concentrated extract
(1) separates: will concentrate cooled Guava Leaf flavonoid compound extract and adopt butterfly type whizzer to separate, and isolate solid and liquid;
(2) degreasing: concerning isolated liquid, pack into behind the container with holes with commercially available oil suction base, put into spissated Guava Leaf flavonoid compound extract parting liquid, its grease absorption is clean, and rest part can be used as raw material and adds in the extracting solution;
Isolated solid is carried out the degreasing of non-ethers solvent, promptly use the pharmaceutical grade chloroform with low-temperature defatted in dynamic degreasing tank to isolated Guava Leaf flavonoid compound extract solid, maintain the temperature at 45 ℃～55 ℃, the time obtains Guava Leaf flavones wet-milling after stirring degreasing in 45～60 minutes;
(3) oven dry: Guava Leaf flavones wet-milling is Tumblied Dry, then use the pulverizing mill abrasive dust, dry powder moisture≤10%, granularity≤200 orders, outward appearance is brown-green;
(4) detect: adopt the instrument after the examination criteria product are proofreaied and correct to detect to the Guava Leaf chromocor compound dry powder after the oven dry, its content should reach the pure Guava Leaf cellulose content of medicinal flavones 〉=10%, then packs standby.
Advantage of the present invention and effect:
Employing is sorted sieve processing, separation, extraction, the concentrated intermediate medicinal extract that obtains through vibrating, and intermediate medicinal extract is obtained Guava Leaf flavones dry powder through the degreasing of non-ethers solvent, oven dry, and outward appearance is brown-green.Not only kept the flavonoid element in the Guava Leaf, terpene, biologically active substances such as phenols, amino acid and phosphoric acid, and can improve 5～10 times of pick-up rates, safe and reliable, realize industrialized production, become a kind of raw material for the treatment of the novel hypoglycemic oral pure natural plant medicines of diabetes B, be used for the treatment of diabetes B and relevant complication.
Specific embodiment
Implementation of the present invention is: a kind of production technology of flavonoid compound of Guava Leaf.It is characterized in that by elementary processing, extraction, concentrate, powder process and the parameter index in each stage constitute.
The particular content of implementation of the present invention comprises: the preparation method of Guava Leaf flavonoid compound is characterized in that: form by following steps,
The elementary processing of A, Guava Leaf
The Guava Leaf that to collect the mature period is processed by the following method:
(1) drying: get the ripe Guava Leaf of collecting and adopt daylight airing or furnace drying method to be dried to contain moisture≤10%;
(2) impurity elimination: will be through dried Guava Leaf, the Guava Leaf of the pure piscidia foline of promptly medicinal flavones (transient name) content 〉=5 ‰ standards is handled, is separated the elimination nonmetallic impurity through vibration letter sorting sieve;
(3) pulverize: will pulverize grinding particle size 〉=100 orders through the standard compliant Guava Leaf of above processes;
The extraction of B, Guava Leaf chromocor compound
(1) slightly carries: will be through the Guava Leaf powder after the elementary processing, adopt 0.5～2 ton stainless-steel vacuum to extract equipment, under normal pressure, choose under the condition of 110,112,113,114,115,116,117,118,119 or 120 ℃ of temperature, its Guava Leaf powder and be 〉=90% edible ethanol as solvent strength, by the solid solution ratio is 1: 5, and an extraction time is 30～45 minutes, produces the extracting solution of Guava Leaf flavones.
(2) essence is carried: extract repeatedly 3～4 times by above extraction process, finish until substantially the flavonoid compound in the Guava Leaf powder being extracted.
(3) quicken: when first, second time extracted, for accelerating extraction rate, can add a small amount of pure water, add-on is pressed 1%～20% of Guava Leaf grain weight amount and is selected arbitrarily, all can as 1%, 3%, 5%, 8%, 10%, 12%, 14%, 15%, 17%, 19% or 20%.
Concentrating of the extracting solution of C, Guava Leaf chromocor compound
(1) concentrates: Guava Leaf flavonoid compound extracting solution is poured in 0.5～2 ton the stainless steel thickening equipment, temperature can be chosen following 110,111,112,113,114,115,116,117,118,119 ℃ or 120 ℃, under normal pressure, under the condition, it is condensed into medicinal extract.
(2) cooling: the cooling of Guava Leaf flavonoid compound extract after will concentrating is after 2～4 hours, and temperature reduces to＜and 30 ℃～40 ℃, it is stand-by to put into bucket.
(3) reclaim: adopt the alcohol recovery device on the thickening equipment, alcohol is reclaimed after alcohol content tester detects at 〉=75% o'clock, can be used as and extract solvent and continue stand-byly,, can be separately fall it and concentrate and reach more than the standard back and collect stand-by with thickening equipment if do not reach above standard.
The powder process of D, Guava Leaf chromocor compound concentrated extract
(1) separates: will concentrate cooled Guava Leaf flavonoid compound extract and adopt butterfly type whizzer to separate, and isolate solid and liquid at normal temperatures and pressures;
(2) degreasing: concerning isolated liquid, pack into behind the container with holes, put into spissated Guava Leaf flavonoid compound extract parting liquid with commercially available oil suction base, with its grease absorption clean after, can be used as raw material and add in the extracting solution;
Isolated solid is carried out the degreasing of non-ethers solvent, promptly use the pharmaceutical grade chloroform with low-temperature defatted in dynamic degreasing tank to isolated Guava Leaf flavonoid compound extract solid, remain temperature between 45 ℃～55 ℃, the time obtains Guava Leaf flavones wet-milling after stirring degreasing in 45～60 minutes;
(3) oven dry: Guava Leaf flavones wet-milling is Tumblied Dry, then use the pulverizing mill abrasive dust, require dry powder moisture≤10%, granularity≤200 orders, outward appearance is brown-green;
(4) detect: adopt the instrument after the examination criteria product are proofreaied and correct to detect to the Guava Leaf chromocor compound dry powder after the oven dry, its content should reach the pure piscidia foline of medicinal flavones (transient name also is an effective constituent) content 〉=10%, then packs standby.
Below concrete inventive embodiment:
The production technique of preparation Guava Leaf chromocor compound (to produce 500Kg) is as follows:
Adopt methods such as daylight airing or oven dry to be dried to the ripe Guava Leaf of collecting and contain moisture≤10%.To handle, separate elimination nonmetallic impurity and metal species impurity through vibration letter sorting sieve (150 mesh sieve) through the Guava Leaf that reaches the pure piscidia foline of flavones (transient name) content 〉=5 ‰ standards after daylight airing or the oven dry.To pulverize through the standard compliant Guava Leaf of aforesaid method processing.Grinding particle size 〉=100 orders.
Will be through the Guava Leaf powder after the processing, adopt 0.5～2 ton stainless-steel vacuum to extract equipment, 110 ℃～120 ℃ of temperature, its Guava Leaf powder and as solvent 〉=90% edible ethanol, by the solid solution ratio is 1: 5, an extraction time is 30～45 minutes, produces the extracting solution of Guava Leaf flavones.Extract repeatedly 3～4 times by above extraction process, for accelerating extraction rate, can add a small amount of pure water when first, second time extracted, add-on is no more than Guava Leaf grain weight amount 10%～20%.Finish until substantially the flavonoid compound in the Guava Leaf powder being extracted.Pack in the bucket Guava Leaf powder flavonoid compound extracting solution and number record, outwell after the waste residue after Guava Leaf is extracted is emitted.
Pour Guava Leaf flavonoid compound extracting solution into 0.5～2 ton stainless steel thickening equipment, under vacuum condition, it is condensed into medicinal extract.After 2～4 hours, it is stand-by to put into bucket with the Guava Leaf flavonoid compound extract cooling after concentrating.
Adopt butterfly type whizzer that the Guava Leaf flavonoid compound extract after concentrating is carried out solid and liquid separation the Guava Leaf flavonoid compound extract after concentrating.Isolated liquid with commercially available oil suction base, behind its container with holes of packing into, is put into spissated Guava Leaf flavonoid compound extract parting liquid, its grease absorption is clean.Rest part can be used as raw material and adds in the extracting solution.Isolated solid is carried out the degreasing of non-ethers solvent, promptly use the pharmaceutical grade chloroform with low-temperature defatted in dynamic degreasing tank to isolated Guava Leaf flavonoid compound extract solid.Keep 45 ℃～55 ℃ of temperature.After stirring degreasing in 45～60 minutes, obtain Guava Leaf flavones wet-milling.Guava Leaf flavones wet-milling is Tumblied Dry, then use the pulverizing mill abrasive dust.Dry powder moisture≤10%, granularity≤200 orders.Adopt the instrument after the examination criteria product are proofreaied and correct to detect to the Guava Leaf chromocor compound dry powder after the oven dry, its content should reach the pure piscidia foline of medicinal flavones (transient name also is an effective constituent) content 〉=10%.
After the Guava Leaf chromocor compound dry powder of making sterilized, and packed for standby use.
Claims (1)
1, the preparation of flavone compound of Guava Leaf is characterized in that: forms by following steps,
The elementary processing of A, Guava Leaf
(1) drying: get the ripe Guava Leaf of collecting and adopt daylight airing or furnace drying method to be dried to contain moisture≤10%;
(2) impurity elimination: will promptly also be that the Guava Leaf of the pure piscidia foline of medicinal flavones (transient name) content 〉=5 ‰ standards is handled, separated the elimination nonmetallic impurity through vibration letter sorting sieve through dried Guava Leaf;
(3) pulverize: will pulverize grinding particle size 〉=100 orders through the standard compliant Guava Leaf of above processes;
The extraction of B, Guava Leaf chromocor compound
(1) slightly carries: will be through the Guava Leaf powder after the elementary processing, adopt 0.5～2 ton stainless-steel vacuum to extract equipment, under the condition of 110～120 ℃ of temperature, its Guava Leaf powder and be 〉=90% edible ethanol as solvent strength, by the solid solution ratio is 1: 5, an extraction time is 30～45 minutes, produces the extracting solution of Guava Leaf flavones;
(2) essence is carried: extract repeatedly 3～4 times by above extraction process, finish until substantially the flavonoid compound in the Guava Leaf powder being extracted;
(3) quicken: when first, second time extracted, for accelerating extraction rate, can add a small amount of pure water, add-on is pressed 1%～20% of Guava Leaf grain weight amount and is selected arbitrarily; 10%～20%;
Concentrating of the extracting solution of C, Guava Leaf chromocor compound
(1) concentrate: Guava Leaf flavonoid compound extracting solution is poured in 0.5～2 ton the stainless steel thickening equipment, under normal pressure, temperature is condensed into medicinal extract with it under 110 ℃～120 ℃ condition;
(2) cooling: the Guava Leaf flavonoid compound extract after will concentrating cooled off after 2～4 hours,, temperature is less than 30 ℃～40 ℃, and it is stand-by to put into bucket;
(3) reclaim: adopt the alcohol recovery device on the thickening equipment, alcohol is reclaimed after alcohol content tester detects at 〉=75% o'clock, can be used as and extract solvent and continue stand-byly,, can be separately fall it and concentrate and reach more than the standard back and collect stand-by with thickening equipment if do not reach above standard.
The powder process of D, Guava Leaf chromocor compound concentrated extract
(1) separates: will concentrate cooled Guava Leaf flavonoid compound extract and adopt butterfly type whizzer to separate, and isolate solid and liquid;
(2) degreasing: concerning isolated liquid, pack into behind the container with holes with commercially available oil suction base, put into spissated Guava Leaf flavonoid compound extract parting liquid, its grease absorption is clean, and rest part can be used as raw material and adds in the extracting solution;
Isolated solid is carried out the degreasing of non-ethers solvent, promptly use the pharmaceutical grade chloroform with low-temperature defatted in dynamic degreasing tank to isolated Guava Leaf flavonoid compound extract solid, maintain the temperature at 45 ℃～55 ℃, the time obtains Guava Leaf flavones wet-milling after stirring degreasing in 45～60 minutes;
(3) oven dry: Guava Leaf flavones wet-milling is Tumblied Dry, then use the pulverizing mill abrasive dust, dry powder moisture≤10%, granularity≤200 orders, outward appearance is brown-green;
(4) detect: adopt the instrument after the examination criteria product are proofreaied and correct to detect to the Guava Leaf chromocor compound dry powder after the oven dry, its content should reach the pure Guava Leaf cellulose content of medicinal flavones 〉=10%, then packs standby.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100418554A CN100516060C (en) | 2006-03-01 | 2006-03-01 | preparation of flavone compound with guava leaf |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100418554A CN100516060C (en) | 2006-03-01 | 2006-03-01 | preparation of flavone compound with guava leaf |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1810797A true CN1810797A (en) | 2006-08-02 |
| CN100516060C CN100516060C (en) | 2009-07-22 |
Family
ID=36843936
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006100418554A Expired - Fee Related CN100516060C (en) | 2006-03-01 | 2006-03-01 | preparation of flavone compound with guava leaf |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100516060C (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101883575B (en) * | 2007-04-27 | 2013-07-17 | 欧博康有限公司 | Guava extract |
| CN103768579A (en) * | 2012-10-18 | 2014-05-07 | 刘晓峰 | Traditional Chinese medicine for reducing blood sugar and preparation method thereof |
| CN105250487A (en) * | 2015-10-19 | 2016-01-20 | 潘勤霞 | Method for extracting flavone from eggplants |
| CN109007834A (en) * | 2018-08-31 | 2018-12-18 | 华南理工大学 | A kind of Fructus psidii guajavae immaturus leaf extract cyclodextrin inclusion compound and the preparation method and application thereof |
-
2006
- 2006-03-01 CN CNB2006100418554A patent/CN100516060C/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101883575B (en) * | 2007-04-27 | 2013-07-17 | 欧博康有限公司 | Guava extract |
| CN103768579A (en) * | 2012-10-18 | 2014-05-07 | 刘晓峰 | Traditional Chinese medicine for reducing blood sugar and preparation method thereof |
| CN105250487A (en) * | 2015-10-19 | 2016-01-20 | 潘勤霞 | Method for extracting flavone from eggplants |
| CN109007834A (en) * | 2018-08-31 | 2018-12-18 | 华南理工大学 | A kind of Fructus psidii guajavae immaturus leaf extract cyclodextrin inclusion compound and the preparation method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100516060C (en) | 2009-07-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100590109C (en) | Technique for extracting cynamorlum herba cistanches medicinal materials effective component | |
| CN1281628C (en) | Method for extracting edible tree fungi polysaccharide | |
| CN102372761A (en) | Method for extracting tea saponin from sasanglla cake | |
| CN1733785A (en) | Method for extracting chimonin | |
| CN110272932A (en) | A kind of preparation method of lucid ganoderma spore powder polysaccharide peptide | |
| CN101265303B (en) | Method for extracting lentinan by using discarded mushroom culture medium as raw material | |
| CN101049328A (en) | Technique for producing extractive of olive growing leaves | |
| CN102106928B (en) | Method for preparing high-purity oil tea saponins | |
| CN102993329A (en) | Method for comprehensively extracting saponin, polysaccharides and polyphenol from camellia oleifera abel defatted cakes | |
| CN1557841A (en) | Process for synthetic extraction of polysaccharides, tea-polyphenol, theanine, caffeine from tea | |
| CN101067146A (en) | Biological extraction process of main chemical components in licorice | |
| CN1291669C (en) | Method extracting waste tobacco at subcritical DMC | |
| CN1810797A (en) | Prepn of flavone compound with guava leaf | |
| CN1850979A (en) | Chinese starjasmine stem lignin aglycone total extract and its extracting process | |
| CN1321735A (en) | Method for extracting onion oil | |
| CN102038044A (en) | Supercritical CO2 extraction process of onion oil | |
| CN1942109A (en) | Method for extracting active components of ginseng by mechanical means | |
| CN1290554A (en) | Extracting method for effective active matter of lucid ganoderma spore | |
| CN1281600C (en) | Method for extracting high purity seabuckthorn flavone aglycone | |
| CN101613278A (en) | A kind of from Folium Ipomoea the industrial technology of rapid extraction high-purity chlorogenic acid | |
| CN101638404B (en) | High-purity salvianolic acid B and preparation method and application thereof | |
| CN110003985A (en) | A kind of combination sound wave extracting method of borneol essential oil | |
| CN1485324A (en) | Method of membrane separation technique for producing seabuckthorn flavone | |
| CN1858045A (en) | Extracting method for Chinese toon old leaf flavone and saponin | |
| CN1244566C (en) | Method of preparing taxadol from leaf and twing of planted taxus chinensis |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20090722 Termination date: 20120301 |