CN101659714B - Method for extracting sodium heparin and co-producing amino acid - Google Patents

Method for extracting sodium heparin and co-producing amino acid Download PDF

Info

Publication number
CN101659714B
CN101659714B CN2009100189690A CN200910018969A CN101659714B CN 101659714 B CN101659714 B CN 101659714B CN 2009100189690 A CN2009100189690 A CN 2009100189690A CN 200910018969 A CN200910018969 A CN 200910018969A CN 101659714 B CN101659714 B CN 101659714B
Authority
CN
China
Prior art keywords
resin
amino acid
warmed
weight
filtrate
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.)
Expired - Fee Related
Application number
CN2009100189690A
Other languages
Chinese (zh)
Other versions
CN101659714A (en
Inventor
牛玉娥
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.)
Niu Yue
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CN2009100189690A priority Critical patent/CN101659714B/en
Publication of CN101659714A publication Critical patent/CN101659714A/en
Application granted granted Critical
Publication of CN101659714B publication Critical patent/CN101659714B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

The invention discloses a method for extracting sodium heparin and co-producing amino acid, comprising the following steps: adding refined salt accounting for 1-1.8 weight percent of an intestinal mucosa into small intestinal mucosa; regulating the pH value of a solution to 9.0-9.2; adding fresh porcine pancreas to carry out zymolysis and filtering; carrying out resin absorption, elution and deposition; and drying to obtain the sodium heparin crude product; adding parenzyme into a filtering liquid, keeping the temperature to carry out the zymolysis and filtering to obtain an amino acid solution. The method for extracting sodium heparin and co-producing amino acid co-produces the amino acid solution on the basis of extracting the sodium heparin, thereby improving the economic effect, reducing the waste liquid and lightening the environment pollution.

Description

A kind of method of extracting sodium heparin and co-producing amino acid
Technical field
The present invention relates to a kind of method of from chitterlings, extracting heparin sodium, particularly a kind of method of extracting sodium heparin and co-producing amino acid.
Background technology
Extract heparin sodium and mainly contain salt solution and enzymolysis process from chitterlings: the enzymolysis process yield is higher, and average 1800 chitterlings go out 1 kilogram of heparin sodium crude (tire is 100), but can produce a large amount of waste liquids, mainly contain polypeptide and protein in the waste liquid.Above-mentioned liquid waste disposal is handled very complicated, and environment is polluted.
Summary of the invention
The object of the present invention is to provide a kind of method of extracting sodium heparin and co-producing amino acid, utilize the waste liquid that extracts heparin sodium to prepare amino acid, reduce the generation of waste liquid, the pollution that alleviates environment.
The present invention realizes by following measure:
The invention discloses a kind of method of extracting sodium heparin and co-producing amino acid, it is characterized in that adopting following steps:
A) will scrape the mucous membrane of small intestine suction enzymatic vessel that makes, adding accounts for the refined salt that intestinal mucosa weight is 1%-1.8%, transfers the solution pH value to 9.0-9.2;
Add the fresh pig pancreas when b) solution in the step (a) being warmed to 40 ℃-45 ℃, the add-on of fresh pig pancreas is the 0.4-0.8% of solution weight, continues to be warmed to 50 ℃-55 ℃, insulation enzymolysis 4-5 hour, continue to be warmed to 80 ℃-85 ℃ then, be incubated 10-20 minute after-filtration;
C) filtrate in the step (b) adds the resin that pre-treatment is good, and the resin add-on is the 4-5% of filtrate weight, and whip attachment 6 hours is extracted resin, and the resin of collecting is washed till neutrality in clear water; With 17--18% (weight) strong brine that is equivalent to 1.2 times of weight resins to resin elution 2 times, head times 6 hours, secondary 2 hours is collected this elutriant hybrid filtering of twice, removes particulate contamination; In the elutriant after filtration, adding and elutriant stir a moment with 95% (weight) alcohol of volume, static state deposition, and precipitation is dewatered, and drying gets the heparin crude product;
D) filtrate after the resin absorption in the step (c), transfer pH value to 7-8, add trypsinase when being warmed to 40 ℃-45 ℃, tryptic add-on is the 0.3%-0.4% of filtrate weight, continues to be warmed to 55 ℃-60 ℃, insulation enzymolysis 4-5 hour, continue to be warmed to 80 ℃-85 ℃ then, be incubated 10-20 minute after-filtration, the gac of adding 4% adsorbs in the filtrate, gets amino acid solution.
The method of extraction sodium heparin and co-producing amino acid of the present invention is being extracted on the basis of heparin sodium, coproduction amino acid solution, improved economic benefit, reduce the generation of waste liquid, the pollution that alleviates environment.
Embodiment
One, raw material D254 resin, fresh intestinal mucosa, sodium-chlor (refined salt), alcohol (technical grade, content 95% weight), alkali lye (technical grade, content 30--40%).
Two, operation
1. will scrape the 1000 kilograms of suction enzymatic vessels of mucous membrane of small intestine that make, the refined salt that adds 15 kilograms, transfer the solution pH value to 9.0-9.2, add 6 kilograms of fresh pig pancreases when being warmed to 40 ℃-45 ℃, continue to be warmed to 50 ℃-55 ℃, insulation enzymolysis 5 hours continues to be warmed to 80 ℃-85 ℃ then, is incubated 15 minutes after-filtration; Filtrate adds 45 kilograms of D254 resins that pre-treatment is good, and whip attachment 6 hours is extracted resin, and the resin of collecting is washed till neutrality in clear water; With 54 kilograms of 17--18% (weight) strong brine to resin elution 2 times, head times 6 hours, secondary 2 hours is collected this elutriant hybrid filtering of twice, removes particulate contamination; In the elutriant after filtration, adding and elutriant stir a moment with 95% (weight) alcohol of volume, static state deposition, and precipitation is dewatered, and drying gets heparin crude product 550 grams, and quality meets the heparin sodium standard after testing, tires more than 100.
2. with 900 kilograms of the filtrates after the above-mentioned resin absorption, transfer pH value to 7-8, add 3.2 kilograms of trypsinase when being warmed to 40 ℃-45 ℃, continue to be warmed to 60 ℃, insulation enzymolysis 4 hours continues to be warmed to 85 ℃ then, is incubated 150 minutes after-filtration, the gac of adding 4% adsorbs in the filtrate, gets 850 kilograms of amino acid solutions.After testing, aminoacids content is 5%.Above-mentioned amino acid solution can be used for plant nutrition liquid through being concentrated into 10%, or as the mother liquor of other plant nutrition liquid.

Claims (1)

1. method of extracting sodium heparin and co-producing amino acid is characterized in that adopting following steps:
A) will scrape the mucous membrane of small intestine suction enzymatic vessel that makes, adding accounts for the refined salt that intestinal mucosa weight is 1%-1.8%, transfers the pH value of solution value to 9.0-9.2;
Add the fresh pig pancreas when b) solution in the step (a) being warmed to 40 ℃-45 ℃, the add-on of fresh pig pancreas is the 0.4-0.8% of solution weight, continues to be warmed to 50 ℃-55 ℃, insulation enzymolysis 4-5 hour, continue to be warmed to 80 ℃-85 ℃ then, be incubated 10-20 minute after-filtration;
C) filtrate in the step (b) adds the good resin of pre-treatment, and the resin add-on is the 4-5% of filtrate weight, and whip attachment 6 hours is extracted resin, and the resin of collecting is washed till neutrality in clear water; With 17--18% (weight) strong brine that is equivalent to 1.2 times of weight resins to resin elution 2 times, head times 6 hours, secondary 2 hours is collected this elutriant hybrid filtering of twice, removes particulate contamination; In the elutriant after filtration, adding and elutriant stir a moment with 95% (weight) alcohol of volume, static state deposition, and precipitation is dewatered, and drying gets the heparin crude product;
D) filtrate after the resin absorption in the step (c), adjust pH is to 7-8, add trypsinase when being warmed to 40 ℃-45 ℃, tryptic add-on is the 0.3%-0.4% of filtrate weight, continues to be warmed to 55 ℃-60 ℃, insulation enzymolysis 4-5 hour, continue to be warmed to 80 ℃-85 ℃ then, be incubated 10-20 minute after-filtration, the gac of adding 4% adsorbs in the filtrate, gets amino acid solution;
Described resin is the D254 resin.
CN2009100189690A 2009-09-22 2009-09-22 Method for extracting sodium heparin and co-producing amino acid Expired - Fee Related CN101659714B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2009100189690A CN101659714B (en) 2009-09-22 2009-09-22 Method for extracting sodium heparin and co-producing amino acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2009100189690A CN101659714B (en) 2009-09-22 2009-09-22 Method for extracting sodium heparin and co-producing amino acid

Publications (2)

Publication Number Publication Date
CN101659714A CN101659714A (en) 2010-03-03
CN101659714B true CN101659714B (en) 2011-07-06

Family

ID=41787983

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2009100189690A Expired - Fee Related CN101659714B (en) 2009-09-22 2009-09-22 Method for extracting sodium heparin and co-producing amino acid

Country Status (1)

Country Link
CN (1) CN101659714B (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102286592B (en) * 2011-09-20 2014-03-26 上海杰隆生物制品股份有限公司 Preparation method for pork lung protein peptide
CN102796792A (en) * 2012-08-30 2012-11-28 广元市海鹏生物科技有限公司 Preparation method for chitterlings membrane protein peptide zinc chelate preparation
CN102924626A (en) * 2012-09-19 2013-02-13 杭州龙扬生物科技有限公司 Process for extracting heparin sodium efficiently from small intestines of pigs
CN102911291A (en) * 2012-11-22 2013-02-06 北大荒丰缘集团有限公司 Device suitable for automatic production of extraction industry of casing and sodium heparin
CN104098717A (en) * 2014-07-21 2014-10-15 南通恒阳生物科技有限公司 Method for extracting heparin sodium
CN105265754A (en) * 2014-07-25 2016-01-27 叶青理 Method of extracting proteins and amino acids from enzymolysis waste liquid of porcine small intestinal mucous membrane
CN104498553B (en) * 2014-12-20 2018-06-19 山东绅联生物科技有限公司 A kind of method that coarse amino acid is extracted in the heparin waste liquor of sodium from extraction
CN111995698A (en) * 2020-08-07 2020-11-27 无锡海思瑞科技有限公司 Method for simultaneously extracting heparin sodium and intestinal membrane protein peptide based on enzymolysis method
CN112159486B (en) * 2020-10-15 2023-05-05 河北常山凯库得生物技术有限公司 Method for preparing crude heparin sodium by utilizing low salt of small intestine mucosa of pig

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1291654A (en) * 1999-10-11 2001-04-18 刘中新 Production process for extracting heparin sodium by activated biological enzymolysis method
CN1308088A (en) * 2001-02-28 2001-08-15 灌云县金瑞生物制品有限公司 Zymolysis process of producing heparin sodium
CN1566162A (en) * 2003-07-07 2005-01-19 张国良 Heparin sodium and its preparing process

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1291654A (en) * 1999-10-11 2001-04-18 刘中新 Production process for extracting heparin sodium by activated biological enzymolysis method
CN1308088A (en) * 2001-02-28 2001-08-15 灌云县金瑞生物制品有限公司 Zymolysis process of producing heparin sodium
CN1566162A (en) * 2003-07-07 2005-01-19 张国良 Heparin sodium and its preparing process

Also Published As

Publication number Publication date
CN101659714A (en) 2010-03-03

Similar Documents

Publication Publication Date Title
CN101659714B (en) Method for extracting sodium heparin and co-producing amino acid
CN103030715B (en) Method for separating purified heparin sodium
CN102146144B (en) Method for extracting and refining inulin
CN108602749B (en) Method for producing ferulic acid from corn bran with high purity and high yield
CN101530153B (en) Method by adopting complex enzyme to prepare rice residue protein
CN110684128B (en) Method for extracting and refining polygonatum sibiricum polysaccharide
CN102249896B (en) Method for treating solution containing citric acid
JP2010531639A (en) A one-step process for separating biomass components
CN100522982C (en) Production process for extracting tea saponin from tea-oil tree cake by using water as dissoluent
CN101649336A (en) Novel process for producing sodium heparin
CN106800586A (en) A kind of method of Moringa protein high efficiency extraction
CN103305555B (en) Method for converting geniposide into genipin
CN101597628A (en) The method of preparing xylo-oligosaccharide by corn husk enzymatic hydrolysis
CN102286111A (en) Novel process for extracting pectin from pear skin at normal temperature
KR101170685B1 (en) Method for producing a water-soluble dietary fiber from a rice by-products
CN109942657B (en) Method for extracting dehydroepiandrosterone from sweet potatoes
CN101628922B (en) Oligosaccharide ferulic acid ester preparation method
CN103636917B (en) Utilize Hydrodynamic Cavitation Technology from rice residue, extract the method for rice protein
CN101659713A (en) Method for extracting sodium heparin crude product
CN102838230B (en) Method utilizing cation exchange resin to pretreat citrus processing wastewater
CN105463040A (en) Method for raising yield of xylooligosaccharide
CN102532334B (en) Method for producing flaxseed mucilage
CN105669879A (en) Preparation method of xylooligosaccharide
CN105622782A (en) Preparation method for extracting gracilaria agar by replacing alkaline process with enzymatic method
CN106617115B (en) Method for separating soluble dietary fiber from waste liquid of momordica grosvenori production

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
ASS Succession or assignment of patent right

Owner name: NIU YUE

Free format text: FORMER OWNER: SHI XIN

Effective date: 20110504

C41 Transfer of patent application or patent right or utility model
C53 Correction of patent for invention or patent application
CB03 Change of inventor or designer information

Inventor after: Niu Yue

Inventor before: Shi Xin

COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 250032 NO. 52, SHIFAN ROAD, TIANQIAO DISTRICT, JI NAN CITY, SHANDONG PROVINCE TO: 255200 NURSING DEPARTMENT, ZIBO NO. 1 HOSPITAL, NO. 4, E MEISHAN EAST ROAD, BOSHAN DISTRICT, ZIBO CITY, SHANDONG PROVINCE

Free format text: CORRECT: INVENTOR; FROM: SHI XIN TO: NIU YUE

TA01 Transfer of patent application right

Effective date of registration: 20110504

Address after: 255200 Department of nursing, Zibo first hospital, 4 Mount Emei East Road, Boshan District, Shandong, Zibo

Applicant after: Niu Yue

Address before: 250032 No. 52 normal road, Tianqiao District, Shandong, Ji'nan

Applicant before: Shi Xin

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: 20110706

Termination date: 20110922