CN1151223C - Hydrolytic collagen - Google Patents

Hydrolytic collagen Download PDF

Info

Publication number
CN1151223C
CN1151223C CNB01113125XA CN01113125A CN1151223C CN 1151223 C CN1151223 C CN 1151223C CN B01113125X A CNB01113125X A CN B01113125XA CN 01113125 A CN01113125 A CN 01113125A CN 1151223 C CN1151223 C CN 1151223C
Authority
CN
China
Prior art keywords
fish
skin
hydrolytic collagen
under
cationic resin
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
CNB01113125XA
Other languages
Chinese (zh)
Other versions
CN1328100A (en
Inventor
陈经国
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.)
Individual
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 CNB01113125XA priority Critical patent/CN1151223C/en
Publication of CN1328100A publication Critical patent/CN1328100A/en
Application granted granted Critical
Publication of CN1151223C publication Critical patent/CN1151223C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Meat, Egg Or Seafood Products (AREA)

Abstract

The present invention relates to hydrolytic collagen. The hydrolytic collagen is prepared in a mode that the skin of a discarded black scraper is mixed with auxiliary materials, such as distilled water, colorless edible hydrochloric acid with the content of 31%, 767 type medical carbon powder, industry ammonia water above 25%, edible sodium hydroxide above 99%, strong acid type cationic resin, acetone, ethanol, etc.; the obtained mixture is prepared into a natural compound amino acid product by the technologies, such as the soaking of a hydrochlric solution, hydrolyzation, decompression for deacidification, decolorization, filtration, column exchange, acid washing, collection, decolorization, filtration, decompression and concentration, vacuum drying, etc. A product of the present invention contains hydroxyproline benefit to human bodies, and the amino acid content is above 90%; therefore, compared with similar products, the present invention has superior quality and low cost.

Description

Hydrolytic collagen
Technical field
The present invention relates to a kind of natural compound amino-acid---manufacturing process of hydrolytic collagen and products thereof.
Background technology
On domestic and international market and the pertinent literature, do not see product and the production technique thereof of making natural compound amino-acid with waste black scraper fish-skin as yet at present.
Summary of the invention
The objective of the invention is to utilize waste black scraper Puffer fish-skin and relevant auxiliary material, production technique of manufacturing natural compound amino-acid---hydrolytic collagen and products thereof.
Hydrolytic collagen of the present invention, by black scraper Puffer fish-skin through the salt acid soak, pyrohydrolysis, medicinal carbon dust decolouring, the strong acid type cationic resin purifying, add acetone, carrying out vacuum-drying behind the ethanol makes, its manufacturing process flow is: fish-skin → about 8 hours → cleaning of immersion drying in the PH2-3 aqueous hydrochloric acid → in the hydrochloric acid soln of concentration 6-10MoI, temperature is that 100 ℃ of-110 ℃ of scopes are carried out hydrolysis in 8-16 hour → at vacuum tightness 0.06Mpa, reduce pressure under temperature 65-75 ℃ of state deacidify → press the fish-skin amount 5%, add activated carbon, under 70 ℃ of conditions of temperature, keep half an hour, decolour processing → filtration → filtrate → carried out upper prop exchange 2 hours → wash acid treatment → usefulness 1.5N ammoniacal liquor wash-out with distilled water with the strong acid type cationic resin of handling, from PH=4, to PH=8, carry out collection and treatment → press 3% of fish-skin amount, add carbon dust, decolour → filter → under vacuum tightness 0.06Mpa, heating 60 ℃-65 ℃ at normal temperatures under the vacuum tightness 0.06Mpa and carrying out the concentrating under reduced pressure processing, after becoming off-white color pasty state xln → and adding ethanol in the 10-15% ratio of fish-skin amount, become faint yellow meal → at vacuum tightness 0.06Mpa, under 70 ℃ of conditions, carry out vacuum-drying → product;
The treatment process of described strong acid type cationic resin is: strong acid type cationic resin → soak half an hour in 4% sodium hydroxide solution, water is flushed to PH=7 → in the hydrochloric acid soln of PH=1 and soaked 8 hours then, uses distilled water flushing PH=5-6 then;
Described to wash sour technology be to be flushed to PH4-5 and to test with silver nitrate solution, until not showing that the chlorion reaction just stops to wash.
Advantage of the present invention is, the natural compound amino-acid hydrolytic collagen that the present invention makes, with domestic like product, compare as hydrolyzed animal protein, hydrolyzed vegetable protein, product of the present invention contains the oxyproline very useful to human body, and the total aminoacids content of the present invention is up to more than 90%, so, compared with similar products, quality is superior, and cost is low.
Embodiment
Embodiment:
Dry, after pure fish-skin weighs, immersion was carried out decalcification processing → cleaning drying back in about 8 hours in the beneficial acid solution of concentration 6-8M01 in the aqueous hydrochloric acid of PH2-3, temperature is that 100 ℃ of-110 ℃ of scopes are carried out hydrolysis in 8-16 hour, hydrochloric acid is food grade more than 99% → at vacuum tightness 0.06Mpa, reduce pressure except that acid treatment under 65 ℃ of-70 ℃ of states of temperature, this processing need be carried out 20% of 2-3 time → dry fish-skin weight, add activated carbon, under 70 ℃ of conditions of temperature, keep half an hour, decolour processing → filtration → filtrate → carried out upper prop exchange 2 hours → wash acid treatment → with carrying out collection and treatment behind 1.5N ammoniacal liquor (technical grade is more than the 25%) wash-out with distilled water with the strong acid type cationic resin of handling, by 3% of dry fish-skin amount, add medicinal carbon dust 767 types, decolour at normal temperatures → under vacuum tightness 0.06Mpa, heat 60 ℃-65 ℃ and carry out concentrating under reduced pressure and handle, after becoming off-white color pasty state xln → and adding ethanol in the 10-15% ratio of fish-skin amount, become faint yellow meal → at vacuum tightness 0.06Mpa, under 70 ℃ of conditions, carry out vacuum-drying → product.

Claims (3)

1, a kind of hydrolytic collagen, it is characterized in that: this hydrolytic collagen, by black scraper Puffer fish-skin through the salt acid soak, pyrohydrolysis, medicinal carbon dust decolouring, the strong acid type cationic resin purifying, add acetone, carrying out vacuum-drying behind the ethanol makes, its manufacturing process flow is: fish-skin → about 8 hours → cleaning of immersion drying in the PH2-3 aqueous hydrochloric acid → in the hydrochloric acid soln of concentration 6-10M, temperature is that 100 ℃ of-110 ℃ of scopes are carried out hydrolysis in 8-16 hour → at vacuum tightness 0.06Mpa, reduce pressure under the temperature 65-75 ℃ of state and deacidify → press 5% of fish-skin amount, add activated carbon, under 70 ℃ of conditions of temperature, keep half an hour, decolour processing → filtration → filtrate → carried out upper prop exchange 2 hours → wash acid treatment → usefulness 1.5N ammoniacal liquor wash-out with distilled water with the strong acid type cationic resin of handling, from PH=4, to PH=8, carry out collection and treatment → press 3% of fish-skin amount, add carbon dust, decolour → filter → under vacuum tightness 0.06Mpa, heating 60 ℃-65 ℃ at normal temperatures under the vacuum tightness 0.06Mpa and carrying out the concentrating under reduced pressure processing, after becoming off-white color pasty state xln → and adding ethanol in the 10-15% ratio of fish-skin amount, become faint yellow meal → at vacuum tightness 0.06Mpa, under 70 ℃ of conditions, carry out vacuum-drying → product.
2, by the described hydrolytic collagen of claim 1, it is characterized in that: the treatment process of described strong acid type cationic resin is: strong acid type cationic resin → soak half an hour in 4% sodium hydroxide solution, water is flushed to PH=7 → in the hydrochloric acid soln of PH=1 and soaked 8 hours then, uses distilled water flushing PH=5-6 then.
3, by the described hydrolytic collagen of claim 1, it is characterized in that: described to wash sour technology be to be flushed to PH4-5 and to test with silver nitrate solution, until not showing that the chlorion reaction just stops to wash.
CNB01113125XA 2001-06-26 2001-06-26 Hydrolytic collagen Expired - Fee Related CN1151223C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB01113125XA CN1151223C (en) 2001-06-26 2001-06-26 Hydrolytic collagen

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB01113125XA CN1151223C (en) 2001-06-26 2001-06-26 Hydrolytic collagen

Publications (2)

Publication Number Publication Date
CN1328100A CN1328100A (en) 2001-12-26
CN1151223C true CN1151223C (en) 2004-05-26

Family

ID=4659867

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB01113125XA Expired - Fee Related CN1151223C (en) 2001-06-26 2001-06-26 Hydrolytic collagen

Country Status (1)

Country Link
CN (1) CN1151223C (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101246140B (en) * 2007-06-16 2012-01-11 中国海洋大学 Novel method for fast measuring collagen hydrolysis degree by biologic sensor
CN101942276A (en) * 2010-08-23 2011-01-12 浙江吉达生物科技有限公司 Process for preparing fish product gelatin
CN103232817B (en) * 2013-04-03 2014-11-26 南昌大学 Fishy smell elimination method for freshwater fish scale gelatin

Also Published As

Publication number Publication date
CN1328100A (en) 2001-12-26

Similar Documents

Publication Publication Date Title
JP7422236B2 (en) Method for producing clam active peptide
CN101289518B (en) Method for preparing chitin and process for preparing chitosan by using chitin
CN104726527A (en) Preparation technology for producing collagen through enzymolysis of fish scales
CN101886106A (en) Method for extracting collagen peptide from fish scales
CN109897101B (en) Collagen tripeptide and production method and application thereof
CN107278208B (en) Chitin, hydrolysate and production of at least one target product from insects by means of enzymatic hydrolysis
JP2004141007A (en) Method for producing gelatine peptide derived from fish
CN101341977A (en) Edible film containing fishskin glue collagen and method of preparing the same
CN101560270A (en) Energy-saving and emission-reducing chitin production method
CN112062834A (en) Deep sea fish skin collagen peptide and extraction and preparation method thereof
CN102732592A (en) Method for preparing freshwater fish bone gelatin by enzyme process
CN1151223C (en) Hydrolytic collagen
CN1582771B (en) Production of collagen peptide from fish skins
CN103627766A (en) Preparation method for silky fowl bioactive peptide powder
CN102643890A (en) Collagen polypeptide and preparation method thereof
CN107629122A (en) The collagen of catfish fish guts protease extraction
CN107056934A (en) A kind of preparation method of high efficiency extraction fish scale collagen
KR100335702B1 (en) Silk peptide and process for the preparation thereof
CN1277845C (en) Clean chitin producing process
CN1313015C (en) Method for producing powder for refining silk
CN113150307B (en) Glycosylated sericin, preparation method and application thereof
KR100408086B1 (en) Process for preparing calcium supplement from starfish
JP2010241708A (en) Elastin-containing soluble peptide and method for producing the same
US11028147B2 (en) Hydrolyzed collagen compositions and methods of making thereof
CN104513842A (en) Production method of odorless moisture-retaining collagen

Legal Events

Date Code Title Description
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C06 Publication
PB01 Publication
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: 20040526

Termination date: 20130626