CN102911511A - Method for extracting purple pigment and total flavonoids from fresh gynura bicolor - Google Patents

Method for extracting purple pigment and total flavonoids from fresh gynura bicolor Download PDF

Info

Publication number
CN102911511A
CN102911511A CN2011102186853A CN201110218685A CN102911511A CN 102911511 A CN102911511 A CN 102911511A CN 2011102186853 A CN2011102186853 A CN 2011102186853A CN 201110218685 A CN201110218685 A CN 201110218685A CN 102911511 A CN102911511 A CN 102911511A
Authority
CN
China
Prior art keywords
purpurin
subjected
total flavones
liquid
phoenix dish
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.)
Pending
Application number
CN2011102186853A
Other languages
Chinese (zh)
Inventor
李法庆
刘东锋
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Suzhou Baozetang Medical Technology Co Ltd
Original Assignee
Suzhou Baozetang Medical Technology Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Suzhou Baozetang Medical Technology Co Ltd filed Critical Suzhou Baozetang Medical Technology Co Ltd
Priority to CN2011102186853A priority Critical patent/CN102911511A/en
Publication of CN102911511A publication Critical patent/CN102911511A/en
Pending legal-status Critical Current

Links

Abstract

The invention belongs to the technical field of biology, and discloses a method for extracting a purple pigment and total flavonoids from fresh gynura bicolor. The method is characterized in that: (1) fresh gynura bicolor is crushed; 2-4 time amounts of 70-90% of ethanol is added for warm-soaking extraction 2-3 times; the extraction liquid is filtered and is subjected to ultrafiltration in an ultrafiltration membrane system; a permeate is concentrated in a nano-filtration membrane system; a concentrate is subjected to reduced-pressure concentration until no alcohol is left; the concentrate is absorbed by using ion exchange resin; water is used for washing until no sugar color is left; 3-5 BV of a 50-70% ethanol solution is used for eluting; an elution liquid is collected and is subjected to reduced-pressure concentration; and a concentrate is subjected to vacuum drying, such that the purple pigment is obtained; (2) off-column liquid of the ion column and the washing liquid are absorbed by using macroporous resin; 4-6 BV of a 40-60% ethanol solution is used for eluting; an elution liquid is subjected to reduced-pressure concentration; the concentrate is subjected to standing crystallization; and the product is filtered and dried, such that total flavonoids are obtained. The method provided by the invention has the advantages of simple process, easy operation, low energy consumption during the production process, low pollution, high raw material utilization rate, and suitability for industrialized productions.

Description

A kind of method of from new scarlet phoenix dish, extracting purpurin and total flavones
Technical field
The invention belongs to biological technical field, especially relate to a kind of method of from new scarlet phoenix dish, extracting purpurin and total flavones.
Background technology
Red phoenix dish is feverfew, contains abundant mineral substance, vitamins C and amino acid etc., is the traditional hill vegetables of China, and its herb can be adopted the whole year, using fresh herb or dry edible all can, a kind of advantageous green food and dietary supplements are favored by the human consumer deeply.Its flavor is hot, sweet, cool in nature, has clearing heat and cooling blood, invigorates blood circulation, hemostasis, detoxify and promote the subsdence of swelling effect.Being usually used in treating hemoptysis, uterine bleeding, traumatic hemorrhage, dysmenorrhoea, dysentery, sore swollen toxin, wound, ulcer does not restrain for a long time yet.
Modern study shows, contains a large amount of purpurins in the red phoenix dish, has anti-oxidant, effect of scavenging radical, reduces low-density lipoprotein (LDL), and anti-mutation, antitumor improves the eyesight effect.Contain in addition Flavonoid substances.
The method of extracting purpurin and flavones from red phoenix dish has:
Patent (application number CN200910192491) " a kind of extracting method of gynura bicolor purpurin ", the method for this patent disclosure be with water as extraction agent, and in conjunction with purification with macroreticular resin, from red phoenix dish, extract and obtain natural purpurin.
Patent (application number CN201010611189) " a kind of preparation method of red phoenix dish extractive of general flavone ", the method for this patent disclosure is: (1) is with the dry pulverizing of red phoenix dried vegetable; (2) with ethanol or methanol extraction, united extraction liquid, concentrating under reduced pressure becomes medicinal extract; (3) medicinal extract that step (2) is obtained adds water and places cold sinking, the centrifugal precipitation of going, and supernatant liquor is for subsequent use; (4) macroporous adsorbent resin on the supernatant liquor that step (3) is obtained is used ethanol gradient elution; (5) collect step (4) ethanol eluate concentrating under reduced pressure, go up again macroporous resin, use ethanol gradient elution; (6) step (5) ethanol eluate concentrate drying gets red phoenix dish extractive of general flavone.
And from red phoenix dish, extract simultaneously simultaneously the method for these two kinds of compositions, have no through retrieval.Usedly provide a kind of and extract two kinds of compositions, methods from red phoenix dish and be necessary.
Summary of the invention
A kind of method of from new scarlet phoenix dish, extracting purpurin and total flavones of purpose of the present invention.
The objective of the invention is to be achieved through the following technical solutions:
A kind of method of extracting purpurin and total flavones from new scarlet phoenix dish is characterized in that:
1) new scarlet phoenix dish is pulverized, adding the lixiviate of 2-4 times of 70-90% ethanol temperature gets 2-3 time, extracting solution filters and adds ultrafiltration in the ultrafiltration membrane system, seeing through liquid adds in the nanofiltration membrane system concentrated again, concentrated solution is evaporated to without adsorbing in the alcohol adding ion exchange resin, and washing is got 3-5BV50-70% ethanolic soln wash-out without fried sugar, collect the elutriant concentrating under reduced pressure, concentrated solution vacuum-drying namely gets purpurin;
2) adsorb in above-mentioned ion column lower column liquid and the water lotion adding macroporous resin adsorption, get 4-6BV40-60% ethanolic soln wash-out, the elutriant concentrating under reduced pressure, concentrated solution is placed crystallization, leaches and is drying to obtain total flavones.
Step 1) ultra-filtration membrane is the hollow cellulose ultra-filtration membrane of the 3000-10000 of molecular weight cut-off in.
Step 1) nanofiltration membrane is that molecular weight cut-off is the hollow cellulose nanofiltration membrane of 200-300 in.
Step 1) the optional D311 of intermediate ion exchange resin model, 330 and D380 in a kind of.
Step 2) a kind of among the optional HZ816 of macroporous resin model, HPD400 and the AB-8.
Technical superiority of the present invention is: method is extracted two kinds of compositions simultaneously from red phoenix dish, not only improved raw material availability, but also it is high to improve products obtained therefrom purity; Method adopts membrane filtration to belong to remove impurity make use of physics methods, and not only energy consumption is low, pollution is little, can also reduce the Yin Gaowen pigment and decompose, and improves yield.
Further specify the present invention below in conjunction with embodiment, but the scope of protection of present invention is not limited to the following example.
Embodiment
Embodiment 1:
New scarlet phoenix dish is pulverized, take by weighing 20kg add 4 times of 70% ethanol be heated to 50 ℃ the insulation 1 hour, extract 2 times, united extraction liquid filter to add ultrafiltration in the hollow cellulose film system of molecular weight cut-off 3000, sees through liquid and adds nanofiltration in 300 the hollow cellulose film system again, and concentrated solution is evaporated to add in the 2LD311 ion exchange resin without alcohol again and adsorbs, washing is without fried sugar, get 5BV50% ethanolic soln wash-out, collect the elutriant concentrating under reduced pressure, concentrated solution vacuum-drying namely gets purpurin 23g.
Adsorbing in ion column lower column liquid and the water lotion merging adding 1LHZ816 macroporous resin, get 4BV60% ethanolic soln wash-out, the elutriant concentrating under reduced pressure, concentrated solution is placed crystallization, leaches and is drying to obtain total flavones 35g.
Embodiment 2:
New scarlet phoenix dish is pulverized, take by weighing 20kg add 3 times of 90% ethanol be heated to 45 ℃ the insulation 1 hour, extract 3 times, united extraction liquid filter to add ultrafiltration in the hollow cellulose film system of molecular weight cut-off 10000, sees through liquid and adds nanofiltration in 200 the hollow cellulose film system again, and concentrated solution is evaporated to add in the 2.5L330 ion exchange resin without alcohol again and adsorbs, washing is without fried sugar, get 3BV70% ethanolic soln wash-out, collect the elutriant concentrating under reduced pressure, concentrated solution vacuum-drying namely gets purpurin 28g.
Adsorbing in ion column lower column liquid and the water lotion merging adding 1.5LHPD400 macroporous resin, get 5BV50% ethanolic soln wash-out, the elutriant concentrating under reduced pressure, concentrated solution is placed crystallization, leaches and is drying to obtain total flavones 42g.
Embodiment 3:
New scarlet phoenix dish is pulverized, take by weighing 20kg add 2 times of 80% ethanol be heated to 55 ℃ the insulation 1 hour, extract 3 times, united extraction liquid filter to add ultrafiltration in the hollow cellulose film system of molecular weight cut-off 6000, sees through liquid and adds nanofiltration in 300 the hollow cellulose film system again, and concentrated solution is evaporated to add in the 2LD380 ion exchange resin without alcohol again and adsorbs, wash colourless, get 4BV60% ethanolic soln wash-out, collect the elutriant concentrating under reduced pressure, concentrated solution vacuum-drying namely gets purpurin 35g.
Adsorbing in ion column lower column liquid and the water lotion merging adding 2LAB-8 macroporous resin, get 5BV40% ethanolic soln wash-out, the elutriant concentrating under reduced pressure, concentrated solution is placed crystallization, leaches and is drying to obtain total flavones 38g.

Claims (5)

1. method of extracting purpurin and total flavones from new scarlet phoenix dish is characterized in that:
1) new scarlet phoenix dish is pulverized, adding the lixiviate of 2-4 times of 70-90% ethanol temperature gets 2-3 time, extracting solution filters and adds ultrafiltration in the ultrafiltration membrane system, seeing through liquid adds in the nanofiltration membrane system concentrated again, concentrated solution is evaporated to without adsorbing in the alcohol adding ion exchange resin, and washing is got 3-5BV50-70% ethanolic soln wash-out without fried sugar, collect wash-out fluidity concentrating under reduced pressure, concentrated solution vacuum-drying namely gets purpurin;
2) adsorb in above-mentioned ion column lower column liquid and the water lotion adding macroporous resin, get 4-6BV40-60% ethanolic soln wash-out, the elutriant concentrating under reduced pressure, concentrated solution is placed crystallization, leaches and is drying to obtain total flavones.
2. from new scarlet phoenix dish, extract as claimed in claim 1 the method for purpurin and total flavones, it is characterized in that described step 1) in ultra-filtration membrane be the hollow cellulose ultra-filtration membrane of the 3000-10000 of molecular weight cut-off.
3. from new scarlet phoenix dish, extract as claimed in claim 1 the method for purpurin and total flavones, it is characterized in that described step 1) in nanofiltration membrane be that molecular weight cut-off is the hollow cellulose nanofiltration membrane of 200-300.
4. from new scarlet phoenix dish, extract as claimed in claim 1 the method for purpurin and total flavones, it is characterized in that described step 1) the optional D311 of intermediate ion exchange resin model, 330 and D380 in a kind of.
5. from new scarlet phoenix dish, extract as claimed in claim 1 the method for purpurin and total flavones, it is characterized in that described step 2) in a kind of among the optional HZ816 of macroporous resin model, HPD400 and the AB-8.
CN2011102186853A 2011-08-02 2011-08-02 Method for extracting purple pigment and total flavonoids from fresh gynura bicolor Pending CN102911511A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2011102186853A CN102911511A (en) 2011-08-02 2011-08-02 Method for extracting purple pigment and total flavonoids from fresh gynura bicolor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2011102186853A CN102911511A (en) 2011-08-02 2011-08-02 Method for extracting purple pigment and total flavonoids from fresh gynura bicolor

Publications (1)

Publication Number Publication Date
CN102911511A true CN102911511A (en) 2013-02-06

Family

ID=47610101

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2011102186853A Pending CN102911511A (en) 2011-08-02 2011-08-02 Method for extracting purple pigment and total flavonoids from fresh gynura bicolor

Country Status (1)

Country Link
CN (1) CN102911511A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106189349A (en) * 2016-07-15 2016-12-07 广西顺帆投资有限公司 A kind of method extracting dyestuff based on Radix seu Folium Alchorneae trewioidis

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1517343A (en) * 2003-01-13 2004-08-04 大兴安岭华野生物工程有限公司 Extraction method of huckleberry anthocyanidin
JP2005194449A (en) * 2004-01-09 2005-07-21 Ishikawa Pref Gov Method for producing dried kinji herb, and method for producing pigment using the same
CN1896146A (en) * 2005-07-15 2007-01-17 唐肖洪 Extraction of natural edible amaranth pigment
CN101045741A (en) * 2007-04-27 2007-10-03 浙江工商大学 Method for separating preparing anthocyan monomer from mulberry
JP2007289057A (en) * 2006-04-25 2007-11-08 Ishikawa Pref Gov Method for processing kinji-sou, extract comprising kinji-sou active ingredients, and product containing the extract
CN101659793A (en) * 2009-09-18 2010-03-03 华南师范大学 Method for extracting gynura bicolor purpurin
CN102078357A (en) * 2010-12-29 2011-06-01 江苏省中国科学院植物研究所 Preparation method of Gynura bicolor total flavone extract

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1517343A (en) * 2003-01-13 2004-08-04 大兴安岭华野生物工程有限公司 Extraction method of huckleberry anthocyanidin
JP2005194449A (en) * 2004-01-09 2005-07-21 Ishikawa Pref Gov Method for producing dried kinji herb, and method for producing pigment using the same
CN1896146A (en) * 2005-07-15 2007-01-17 唐肖洪 Extraction of natural edible amaranth pigment
JP2007289057A (en) * 2006-04-25 2007-11-08 Ishikawa Pref Gov Method for processing kinji-sou, extract comprising kinji-sou active ingredients, and product containing the extract
CN101045741A (en) * 2007-04-27 2007-10-03 浙江工商大学 Method for separating preparing anthocyan monomer from mulberry
CN101659793A (en) * 2009-09-18 2010-03-03 华南师范大学 Method for extracting gynura bicolor purpurin
CN102078357A (en) * 2010-12-29 2011-06-01 江苏省中国科学院植物研究所 Preparation method of Gynura bicolor total flavone extract

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
于东 等: "花色苷提取、分离纯化及鉴定的研究进展", 《食品与发酵工业》, vol. 35, no. 3, 31 March 2009 (2009-03-31), pages 127 - 133 *
裴咏萍 等: "大孔树脂对红凤菜总黄酮的吸附分离特性研究", 《时珍国医国药》, vol. 21, no. 1, 31 January 2010 (2010-01-31), pages 8 - 9 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106189349A (en) * 2016-07-15 2016-12-07 广西顺帆投资有限公司 A kind of method extracting dyestuff based on Radix seu Folium Alchorneae trewioidis

Similar Documents

Publication Publication Date Title
CN101912480B (en) Method for preparing procyanidin extract of lycium ruthenicum murr
CN102648935A (en) Method for extracting cedrela sinensis total polyphenol
CN102106931B (en) Method for producing diverse extracts of berry tea
CN103467540B (en) A kind of method extracting rhodioside from Root of Kirilow Rhodiola
CN106220693B (en) A method of extracting multiple-ear rock Ke phloridzin
CN106220698A (en) A kind of method of separating high-purity Hesperidin, neohesperidin, naringin and Neosynephrine from Fructus Aurantii Immaturus
CN101177444A (en) Method for extracting momordica grosvenori flavone glycoside from momordica grosvenori
CN104398542A (en) Method for extracting and purifying flavones from plants containing flavones
CN103435588A (en) Novel method for preparing blueberry anthocyanidin
CN105713058A (en) Method for synchronously preparing chlorogenic acid and cynaroside from Lonicera japonica leaves
CN102675398B (en) A kind of method extracting momordica grosvenori glycoside V and farnesol from Grosvenor Momordica
CN104098713B (en) A kind of method simultaneously preparing garlic polysaccharide and alliin
CN102718817A (en) Method for preparing anthocyanin extract from black bean peel
CN105053952B (en) A kind of processing technology of the dried orange peel extracts of no bitter taste
CN110981921B (en) Continuous method for synchronously extracting multiple effective components from figs
CN102675399A (en) Method for extracting mogroside V and mannitol from corsvenor momordica fruit
CN102643315A (en) Method for purifying phlorizin from apple velamen
CN103965096B (en) A kind of preparation method being applicable to industrial 1-DNJ
CN109021046B (en) Method for simultaneously extracting quercetin and kaempferitrin from stem and leaf of momordica grosvenori
CN104292366A (en) Method for simultaneously extracting arabinogalactan and dihydroquercetin from dahurian larch
CN108129532A (en) A kind of method that aurantiin is prepared based on Exocarpium Citri Grandis
CN105085224B (en) A kind of method that hypericin is extracted from hypericum perforatum
CN102911511A (en) Method for extracting purple pigment and total flavonoids from fresh gynura bicolor
CN105616477A (en) Method for purifying polyphenol in lonicera edulis
CN104814987A (en) Method for extracting total flavonoids from hibiscus manihot

Legal Events

Date Code Title Description
DD01 Delivery of document by public notice

Addressee: Suzhou Baozetang Medical Technology Co.,Ltd. Han Shuyu

Document name: Notification of Passing Preliminary Examination of the Application for Invention

C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
DD01 Delivery of document by public notice

Addressee: Suzhou Baozetang Medical Technology Co.,Ltd.

Document name: the First Notification of an Office Action

DD01 Delivery of document by public notice

Addressee: Han Shuyu

Document name: Notification that Application Deemed to be Withdrawn

C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20130206