FI59257C - Foerfarande foer framstaellning av modifierat gelatin - Google Patents
Foerfarande foer framstaellning av modifierat gelatin Download PDFInfo
- Publication number
- FI59257C FI59257C FI2785/74A FI278574A FI59257C FI 59257 C FI59257 C FI 59257C FI 2785/74 A FI2785/74 A FI 2785/74A FI 278574 A FI278574 A FI 278574A FI 59257 C FI59257 C FI 59257C
- Authority
- FI
- Finland
- Prior art keywords
- gelatin
- solution
- heating
- amino acid
- modified
- Prior art date
Links
- 229920000159 gelatin Polymers 0.000 title claims description 80
- 235000019322 gelatine Nutrition 0.000 title claims description 80
- 108010010803 Gelatin Proteins 0.000 title claims description 76
- 235000011852 gelatine desserts Nutrition 0.000 title claims description 76
- 239000008273 gelatin Substances 0.000 title claims description 70
- 238000010438 heat treatment Methods 0.000 claims description 22
- 239000000499 gel Substances 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 18
- 229940024606 amino acid Drugs 0.000 claims description 17
- 235000001014 amino acid Nutrition 0.000 claims description 17
- 238000002844 melting Methods 0.000 claims description 17
- 230000008018 melting Effects 0.000 claims description 17
- 238000002360 preparation method Methods 0.000 claims description 8
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 claims description 7
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims description 7
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims description 7
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims description 7
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 claims description 7
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 claims description 7
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims description 7
- 235000004279 alanine Nutrition 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 229960000310 isoleucine Drugs 0.000 claims description 7
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 6
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 3
- 239000007858 starting material Substances 0.000 claims description 2
- 108010013480 succinylated gelatin Proteins 0.000 claims description 2
- 229940007079 succinylated gelatin Drugs 0.000 claims description 2
- 239000003607 modifier Substances 0.000 claims 2
- 239000000243 solution Substances 0.000 description 33
- 230000006340 racemization Effects 0.000 description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000008280 blood Substances 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 102000008186 Collagen Human genes 0.000 description 3
- 108010035532 Collagen Proteins 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 210000000988 bone and bone Anatomy 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 229920001436 collagen Polymers 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000003058 plasma substitute Substances 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- 239000008156 Ringer's lactate solution Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000003637 basic solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- ZEWYCNBZMPELPF-UHFFFAOYSA-J calcium;potassium;sodium;2-hydroxypropanoic acid;sodium;tetrachloride Chemical compound [Na].[Na+].[Cl-].[Cl-].[Cl-].[Cl-].[K+].[Ca+2].CC(O)C(O)=O ZEWYCNBZMPELPF-UHFFFAOYSA-J 0.000 description 2
- 150000001718 carbodiimides Chemical class 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000000502 dialysis Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004108 freeze drying Methods 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000002504 physiological saline solution Substances 0.000 description 2
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000001223 reverse osmosis Methods 0.000 description 2
- UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical compound O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000011437 continuous method Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- PMMYEEVYMWASQN-UHFFFAOYSA-N dl-hydroxyproline Natural products OC1C[NH2+]C(C([O-])=O)C1 PMMYEEVYMWASQN-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229960002591 hydroxyproline Drugs 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 230000035322 succinylation Effects 0.000 description 1
- 238000010613 succinylation reaction Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/78—Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin or cold insoluble globulin [CIG]
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09H—PREPARATION OF GLUE OR GELATINE
- C09H3/00—Isolation of glue or gelatine from raw materials, e.g. by extracting, by heating
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biophysics (AREA)
- Medicinal Chemistry (AREA)
- Gastroenterology & Hepatology (AREA)
- Biochemistry (AREA)
- Toxicology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Peptides Or Proteins (AREA)
- Medicinal Preparation (AREA)
- Jellies, Jams, And Syrups (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2348294A DE2348294C3 (de) | 1973-09-26 | 1973-09-26 | Modifizierte Gelatine mit erniedrigtem Gelschmelzpunkt |
| DE2348294 | 1973-09-26 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI278574A FI278574A (de) | 1975-03-27 |
| FI59257B FI59257B (fi) | 1981-03-31 |
| FI59257C true FI59257C (fi) | 1981-07-10 |
Family
ID=5893639
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI2785/74A FI59257C (fi) | 1973-09-26 | 1974-09-24 | Foerfarande foer framstaellning av modifierat gelatin |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US3984391A (de) |
| JP (1) | JPS5642635B2 (de) |
| AR (1) | AR200549A1 (de) |
| AT (2) | AT352146B (de) |
| BE (1) | BE820300A (de) |
| CA (1) | CA1030955A (de) |
| CH (1) | CH608025A5 (de) |
| DE (1) | DE2348294C3 (de) |
| ES (1) | ES430297A1 (de) |
| FI (1) | FI59257C (de) |
| FR (1) | FR2244809B1 (de) |
| GB (1) | GB1475364A (de) |
| IE (1) | IE40035B1 (de) |
| LU (1) | LU70987A1 (de) |
| NL (1) | NL182480C (de) |
| RO (1) | RO68605A (de) |
| SE (1) | SE435624B (de) |
| YU (1) | YU35502B (de) |
| ZA (1) | ZA746025B (de) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4495206A (en) * | 1978-04-21 | 1985-01-22 | Canada Packers, Inc. | High protein, solid dietary food product |
| JPS5767521A (en) * | 1980-09-25 | 1982-04-24 | Yamanouchi Pharmaceut Co Ltd | Agent for improving circulation blood vessel |
| JPS61197659A (ja) * | 1985-02-27 | 1986-09-01 | Shiyoubouchiyou Chokan | 泡消火剤組成物 |
| WO1987002047A1 (en) * | 1985-10-04 | 1987-04-09 | Nitta Gelatin Inc. | Process for preparing gelatin having improved solubility |
| US5035896A (en) * | 1988-06-15 | 1991-07-30 | Warner-Lambert Company | Water insoluble drugs coated by coacervated fish gelatin |
| EP1238675A1 (de) * | 2001-03-06 | 2002-09-11 | Fuji Photo Film B.V. | Rekombinante gelatineartige Proteine zur Verwendung als Plasmaexpander |
| GB2388776B (en) * | 2002-05-21 | 2004-08-25 | Croda Int Plc | Succinylated fish gelatin for use as a blood plasma expander |
| JP4841803B2 (ja) * | 2003-09-11 | 2011-12-21 | フジフィルム マニュファクチャリング ユーロプ ビー．ブイ． | 組換えゼラチン様タンパク質の血漿増量剤としての使用法及び代用血漿に適した組成物 |
| US20060057065A1 (en) * | 2004-09-11 | 2006-03-16 | Yanming Wang | Composition and method to prevent and treat brain and spinal cord injuries |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2413815A (en) * | 1941-01-10 | 1947-01-07 | Albert A Epstein | Gelatin preparation |
| US2834683A (en) * | 1956-06-25 | 1958-05-13 | Gen Foods Corp | Method of preparing cold water-soluble gelatin and the resulting product |
| US3057782A (en) * | 1958-01-22 | 1962-10-09 | Hoechst Ag | Cross-linked gelatin plasma substitute and production thereof |
| US3778278A (en) * | 1972-04-26 | 1973-12-11 | Du Pont | Odified gelatin,and a process for their manufacture photographic gelatino-silver halide emulsions containing hydrolyzed m |
| US3763138A (en) * | 1972-05-31 | 1973-10-02 | Du Pont | Process for preparing hydrolyzed modified gelatin followed by reaction with dibasic acid anhydride |
-
1973
- 1973-09-26 DE DE2348294A patent/DE2348294C3/de not_active Expired
-
1974
- 1974-09-23 ES ES430297A patent/ES430297A1/es not_active Expired
- 1974-09-23 ZA ZA00746025A patent/ZA746025B/xx unknown
- 1974-09-23 CA CA209,775A patent/CA1030955A/en not_active Expired
- 1974-09-23 FR FR7431994A patent/FR2244809B1/fr not_active Expired
- 1974-09-24 NL NLAANVRAGE7412588,A patent/NL182480C/xx not_active IP Right Cessation
- 1974-09-24 AR AR255711A patent/AR200549A1/es active
- 1974-09-24 AT AT767574A patent/AT352146B/de not_active IP Right Cessation
- 1974-09-24 RO RO7480051A patent/RO68605A/ro unknown
- 1974-09-24 AT AT767574A patent/ATA767574A/de unknown
- 1974-09-24 FI FI2785/74A patent/FI59257C/fi active
- 1974-09-24 LU LU70987A patent/LU70987A1/xx unknown
- 1974-09-25 CH CH1294874A patent/CH608025A5/xx not_active IP Right Cessation
- 1974-09-25 GB GB4166274A patent/GB1475364A/en not_active Expired
- 1974-09-25 SE SE7412065A patent/SE435624B/xx unknown
- 1974-09-25 BE BE2053885A patent/BE820300A/xx not_active IP Right Cessation
- 1974-09-25 JP JP11039474A patent/JPS5642635B2/ja not_active Expired
- 1974-09-25 US US05/509,213 patent/US3984391A/en not_active Expired - Lifetime
- 1974-09-25 IE IE1989/74A patent/IE40035B1/xx unknown
- 1974-09-26 YU YU2599/74A patent/YU35502B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZA746025B (en) | 1975-09-24 |
| IE40035B1 (en) | 1979-02-28 |
| IE40035L (en) | 1975-03-26 |
| US3984391A (en) | 1976-10-05 |
| FI59257B (fi) | 1981-03-31 |
| SE7412065L (de) | 1975-03-27 |
| CA1030955A (en) | 1978-05-09 |
| ES430297A1 (es) | 1977-02-16 |
| ATA767574A (de) | 1979-02-15 |
| FR2244809A1 (de) | 1975-04-18 |
| FI278574A (de) | 1975-03-27 |
| YU35502B (en) | 1981-04-30 |
| JPS5642635B2 (de) | 1981-10-06 |
| AR200549A1 (es) | 1974-11-15 |
| CH608025A5 (de) | 1978-12-15 |
| NL7412588A (nl) | 1975-04-01 |
| GB1475364A (en) | 1977-06-01 |
| JPS5059400A (de) | 1975-05-22 |
| DE2348294A1 (de) | 1975-04-03 |
| RO68605A (ro) | 1980-08-15 |
| DE2348294C3 (de) | 1980-08-21 |
| FR2244809B1 (de) | 1979-02-16 |
| YU259974A (en) | 1980-10-31 |
| DE2348294B2 (de) | 1979-12-20 |
| NL182480C (nl) | 1988-03-16 |
| NL182480B (nl) | 1987-10-16 |
| LU70987A1 (de) | 1976-08-19 |
| AT352146B (de) | 1979-09-10 |
| BE820300A (fr) | 1975-03-25 |
| SE435624B (sv) | 1984-10-08 |
| AU7367474A (en) | 1976-04-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Sousa et al. | Collagen from Atlantic cod (Gadus morhua) skins extracted using CO2 acidified water with potential application in healthcare | |
| FI59257C (fi) | Foerfarande foer framstaellning av modifierat gelatin | |
| Nan et al. | Effect of ultra-high pressure on molecular structure and properties of bullfrog skin collagen | |
| Shen et al. | Photodynamic crosslinking of proteins II. Photocrosslinking of a model protein-ribonuclease A | |
| KR101020312B1 (ko) | 어류비늘 콜라겐펩타이드의 제조방법 | |
| KR101071338B1 (ko) | 해양 생물 유래 콜라겐 펩타이드의 제조방법 및 그로부터 제조된 콜라겐 펩타이드 | |
| Mirzapour Kouhdasht et al. | Gelatin production using fish wastes by extracted alkaline protease from Bacillus licheniformis | |
| EP1413614A1 (de) | Verfahren zur Herstellung von Peptide von Fischgelatin | |
| JPH06116300A (ja) | ケラチンフラグメントおよびその製造方法 | |
| HU208840B (en) | Process for crosslinking collagens with diphenyl phosphoryl azide | |
| KR100679712B1 (ko) | 불가사리로부터 콜라겐을 제조하는 방법 | |
| Rýglová et al. | The proportion of the key components analysed in collagen-based isolates from fish and mammalian tissues processed by different protocols | |
| Nur et al. | Characterization, antioxidant and α-glucosidase inhibitory activity of collagen hydrolysate from lamuru (caranx ignobilis) fishbone | |
| JPS5931520B2 (ja) | 絹フイブロインペプチド水溶液の製造法 | |
| CN107630058B (zh) | 一种新型自组装胶原蛋白及制备方法 | |
| JP5328077B2 (ja) | 低エンドトキシン化ゼラチンの製造方法 | |
| JP2007023079A (ja) | 架橋性タンパク質およびその製造方法 | |
| Lodhi et al. | Isolation and characterisation of acid-and pepsin-soluble collagen from the skin of Cervus korean TEMMINCK var. mantchuricus Swinhoe | |
| JP4714890B2 (ja) | セリシンハイドロゲル及びセリシン多孔質体の製造方法 | |
| KR100970819B1 (ko) | 눈다랑어 껍질로부터 분리된 콜라겐의 제조방법 | |
| US11028147B2 (en) | Hydrolyzed collagen compositions and methods of making thereof | |
| CN110066315B (zh) | 一种新型水凝胶及其制备方法 | |
| Antunes et al. | Utilisation of oleuropein as a crosslinking agent in collagenic films | |
| CN1405150A (zh) | 蛋白质修饰剂及其制备方法和用途 | |
| Liao et al. | Characterization of three‐spot seahorse (Hippocampus trimaculatus) skin collagen and its fibrillar gel reinforced by EDC: A comparative study |