ZA200106813B - Lipase-catalysed esterification of marine oil. - Google Patents
Lipase-catalysed esterification of marine oil. Download PDFInfo
- Publication number
- ZA200106813B ZA200106813B ZA200106813A ZA200106813A ZA200106813B ZA 200106813 B ZA200106813 B ZA 200106813B ZA 200106813 A ZA200106813 A ZA 200106813A ZA 200106813 A ZA200106813 A ZA 200106813A ZA 200106813 B ZA200106813 B ZA 200106813B
- Authority
- ZA
- South Africa
- Prior art keywords
- dha
- epa
- process according
- lipase
- fatty acids
- Prior art date
Links
- 238000005886 esterification reaction Methods 0.000 title claims description 49
- 230000032050 esterification Effects 0.000 title claims description 26
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 144
- 108090001060 Lipase Proteins 0.000 claims description 77
- 102000004882 Lipase Human genes 0.000 claims description 77
- 239000004367 Lipase Substances 0.000 claims description 76
- 235000019421 lipase Nutrition 0.000 claims description 76
- 235000021588 free fatty acids Nutrition 0.000 claims description 67
- 238000000034 method Methods 0.000 claims description 47
- 230000008569 process Effects 0.000 claims description 44
- 239000000203 mixture Substances 0.000 claims description 34
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 21
- 229930195729 fatty acid Natural products 0.000 claims description 21
- 239000000194 fatty acid Substances 0.000 claims description 21
- 150000004665 fatty acids Chemical class 0.000 claims description 21
- 239000003054 catalyst Substances 0.000 claims description 13
- 238000000199 molecular distillation Methods 0.000 claims description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 6
- 230000007062 hydrolysis Effects 0.000 claims description 5
- 238000006460 hydrolysis reaction Methods 0.000 claims description 5
- 241000235402 Rhizomucor Species 0.000 claims description 2
- MBMBGCFOFBJSGT-KUBAVDMBSA-N docosahexaenoic acid Natural products CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 description 95
- 235000020669 docosahexaenoic acid Nutrition 0.000 description 94
- 235000020673 eicosapentaenoic acid Nutrition 0.000 description 80
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 description 79
- 239000003921 oil Substances 0.000 description 33
- 235000019198 oils Nutrition 0.000 description 33
- 125000005456 glyceride group Chemical group 0.000 description 30
- 238000006243 chemical reaction Methods 0.000 description 29
- 239000000047 product Substances 0.000 description 17
- 235000021323 fish oil Nutrition 0.000 description 16
- 239000012141 concentrate Substances 0.000 description 13
- 230000000694 effects Effects 0.000 description 13
- 239000002253 acid Substances 0.000 description 9
- 238000002474 experimental method Methods 0.000 description 9
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 9
- 125000004494 ethyl ester group Chemical group 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 101001003495 Pseudomonas fluorescens Lipase Proteins 0.000 description 7
- 101001064559 Pseudomonas fluorescens Lipase Proteins 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
- 241000252203 Clupea harengus Species 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 238000004821 distillation Methods 0.000 description 6
- 235000019514 herring Nutrition 0.000 description 6
- 238000011084 recovery Methods 0.000 description 6
- 238000004448 titration Methods 0.000 description 6
- 229940013317 fish oils Drugs 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 241001125048 Sardina Species 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 235000019512 sardine Nutrition 0.000 description 4
- 235000003441 saturated fatty acids Nutrition 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 241000589774 Pseudomonas sp. Species 0.000 description 3
- 241000235403 Rhizomucor miehei Species 0.000 description 3
- 101000966371 Rhizopus niveus Lipase Proteins 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 150000004671 saturated fatty acids Chemical class 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 150000003626 triacylglycerols Chemical class 0.000 description 3
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 2
- 241000228245 Aspergillus niger Species 0.000 description 2
- 241000222175 Diutina rugosa Species 0.000 description 2
- 108010048733 Lipozyme Proteins 0.000 description 2
- 241001661345 Moesziomyces antarcticus Species 0.000 description 2
- 241000498617 Mucor javanicus Species 0.000 description 2
- 101000968489 Rhizomucor miehei Lipase Proteins 0.000 description 2
- 239000000061 acid fraction Substances 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000005194 fractionation Methods 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- FCCDDURTIIUXBY-UHFFFAOYSA-N lipoamide Chemical compound NC(=O)CCCCC1CCSS1 FCCDDURTIIUXBY-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 235000020660 omega-3 fatty acid Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012746 preparative thin layer chromatography Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000000526 short-path distillation Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 241000589540 Pseudomonas fluorescens Species 0.000 description 1
- 240000005384 Rhizopus oryzae Species 0.000 description 1
- 235000013752 Rhizopus oryzae Nutrition 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000008130 destillate Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 229940090949 docosahexaenoic acid Drugs 0.000 description 1
- 229960005135 eicosapentaenoic acid Drugs 0.000 description 1
- JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000005639 glycero group Chemical group 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 235000019626 lipase activity Nutrition 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000011987 methylation Effects 0.000 description 1
- 238000007069 methylation reaction Methods 0.000 description 1
- 235000021281 monounsaturated fatty acids Nutrition 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 108010072641 thermostable lipase Proteins 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6409—Fatty acids
- C12P7/6427—Polyunsaturated fatty acids [PUFA], i.e. having two or more double bonds in their backbone
- C12P7/6434—Docosahexenoic acids [DHA]
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/02—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fatty acids with glycerol
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6409—Fatty acids
- C12P7/6427—Polyunsaturated fatty acids [PUFA], i.e. having two or more double bonds in their backbone
- C12P7/6432—Eicosapentaenoic acids [EPA]
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
- C12P7/6445—Glycerides
- C12P7/6458—Glycerides by transesterification, e.g. interesterification, ester interchange, alcoholysis or acidolysis
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
- C12P7/6445—Glycerides
- C12P7/6472—Glycerides containing polyunsaturated fatty acid [PUFA] residues, i.e. having two or more double bonds in their backbone
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Fats And Perfumes (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO19990739A NO312973B1 (no) | 1999-02-17 | 1999-02-17 | Lipase-katalysert forestring av marine oljer |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200106813B true ZA200106813B (en) | 2002-08-19 |
Family
ID=19902972
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200106813A ZA200106813B (en) | 1999-02-17 | 2001-08-17 | Lipase-catalysed esterification of marine oil. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US6518049B1 (fr) |
| EP (1) | EP1153114B1 (fr) |
| JP (1) | JP2002537442A (fr) |
| AT (1) | ATE348140T1 (fr) |
| AU (1) | AU757203B2 (fr) |
| CA (1) | CA2362212C (fr) |
| DE (1) | DE60032337T2 (fr) |
| ES (1) | ES2276669T3 (fr) |
| NO (1) | NO312973B1 (fr) |
| NZ (1) | NZ513574A (fr) |
| WO (1) | WO2000049117A1 (fr) |
| ZA (1) | ZA200106813B (fr) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002293774A (ja) * | 2001-03-29 | 2002-10-09 | Kuraray Co Ltd | ５−（メタ）アクリロイルオキシ−２，６−ノルボルナンカルボラクトンの製造方法 |
| EP2295529B2 (fr) * | 2002-07-11 | 2022-05-18 | Basf As | Procédé de diminution des polluants environnementaux dans une huile ou une graisse et produit d'alimentation pour poissons |
| SE0202188D0 (sv) * | 2002-07-11 | 2002-07-11 | Pronova Biocare As | A process for decreasing environmental pollutants in an oil or a fat, a volatile fat or oil environmental pollutants decreasing working fluid, a health supplement, and an animal feed product |
| NO319194B1 (no) * | 2002-11-14 | 2005-06-27 | Pronova Biocare As | Lipase-katalysert forestringsfremgangsmate av marine oljer |
| WO2005084129A2 (fr) * | 2004-03-04 | 2005-09-15 | Htl High-Tech Lipids Ltd. | Triglycerides structures et emulsions contenant ces triglycerides |
| DE102004015781A1 (de) * | 2004-03-31 | 2005-10-20 | Cognis Ip Man Gmbh | Verfahren zur enzymatischen Synthese von Triglyceriden ungesättigter Fettsäuren |
| US20060135610A1 (en) * | 2004-12-22 | 2006-06-22 | Bortz Jonathan D | Cardiovascular compositions |
| CA2609341C (fr) * | 2005-05-23 | 2011-10-04 | Natural Asa | Concentration d'esters alkyliques d'acides gras produite par des reactions enzymatiques avec du glycerol |
| ES2559959T3 (es) * | 2005-06-16 | 2016-02-16 | Dsm Nutritional Products Ag | Enzimas inmovilizadas y métodos para usar las mismas |
| ES2292341B1 (es) * | 2006-03-13 | 2009-03-16 | Universidad De Almeria | "procedimiento para la purificacion de acido eicosapentaenoico (epa)". |
| EP1978102B1 (fr) * | 2007-04-02 | 2010-07-07 | Cognis IP Management GmbH | Un mélange comprenant des glycérides d'acides gras |
| EP1978101A1 (fr) | 2007-04-02 | 2008-10-08 | Cognis IP Management GmbH | Procédé d'enrichissement en acides gras polyinsaturés |
| JP2008278781A (ja) * | 2007-05-09 | 2008-11-20 | Osaka City | ２位よりも１，３位のｄｈａ含有率が高いトリアシルグリセロールの製造方法 |
| CL2008002020A1 (es) | 2007-07-12 | 2008-11-14 | Ocean Nutrition Canada Ltd | Metodo de modificacion de un aceite, que comprende hidrolizar gliceridos con una solucion de lipasa thermomyces lanuginosus, separar la fraccion de acido graso saturado de la fraccion de glicerido hidrolizado y esterificar los gliceridos hidrolizados en la presencia de candida antarctica lipasa b; y composicion de aceite. |
| KR101357298B1 (ko) * | 2008-06-20 | 2014-01-28 | 에이케이 앤 엠엔 바이오팜 주식회사 | 오메가-3계 고도불포화 지방산의 고순도 정제방법 |
| DK2349250T3 (en) | 2008-10-31 | 2017-07-03 | Lipid Pharmaceuticals Ehf | Fatty acids for use as a medicament |
| US8362080B2 (en) | 2008-12-18 | 2013-01-29 | Baylor College Of Medicine | Increasing glutathione levels for therapy |
| WO2011067666A1 (fr) | 2009-12-03 | 2011-06-09 | Blt Berg Lipidtech As | Procédé de production de compositions d'acides gras enrichis |
| ES2862980T3 (es) | 2009-12-30 | 2021-10-08 | Basf Pharma Callanish Ltd | Composiciones de ácido graso poliinsaturado obtenibles mediante un proceso de separación cromatográfica en lecho móvil simulado |
| WO2012095749A1 (fr) | 2011-01-14 | 2012-07-19 | Pharma Marine As | Élimination de monoglycérides de concentrés d'acides gras |
| GB201111595D0 (en) | 2011-07-06 | 2011-08-24 | Equateq Ltd | Improved process |
| GB201111594D0 (en) | 2011-07-06 | 2011-08-24 | Equateq Ltd | New improved process |
| GB201111591D0 (en) | 2011-07-06 | 2011-08-24 | Equateq Ltd | Further new process |
| GB201111589D0 (en) | 2011-07-06 | 2011-08-24 | Equateq Ltd | New modified process |
| GB201111601D0 (en) | 2011-07-06 | 2011-08-24 | Equateq Ltd | New process |
| WO2013035113A1 (fr) | 2011-09-06 | 2013-03-14 | Lipid Pharmaceuticals Ehf. | Suppositoires enrobés |
| SI2800563T1 (sl) | 2012-01-06 | 2018-11-30 | Omthera Pharmaceuticals Inc. | Z DPA obogateni sestavki omega-3 polinenasičenih maščobnih kislin v obliki proste kisline |
| EP2846779A4 (fr) | 2012-05-07 | 2015-12-16 | Omthera Pharmaceuticals Inc | Compositions de statines et d'acides gras oméga-3 |
| GB201300354D0 (en) | 2013-01-09 | 2013-02-20 | Basf Pharma Callanish Ltd | Multi-step separation process |
| US8802880B1 (en) | 2013-05-07 | 2014-08-12 | Group Novasep | Chromatographic process for the production of highly purified polyunsaturated fatty acids |
| US9428711B2 (en) | 2013-05-07 | 2016-08-30 | Groupe Novasep | Chromatographic process for the production of highly purified polyunsaturated fatty acids |
| EP3118186B1 (fr) | 2013-12-11 | 2022-02-09 | Novasep Process | Installation chromatographique de production d acides gras polyinsatures |
| US10975031B2 (en) | 2014-01-07 | 2021-04-13 | Novasep Process | Method for purifying aromatic amino acids |
| US10722542B2 (en) | 2016-06-16 | 2020-07-28 | Ambo Innovations, Llc | Non-winterized, standardized marine source oil products and methods of making thereof |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02303492A (ja) | 1989-05-19 | 1990-12-17 | Nippon Oil & Fats Co Ltd | 長鎖高度不飽和脂肪酸グリセリドの濃縮法 |
| DK95490D0 (da) * | 1990-04-18 | 1990-04-18 | Novo Nordisk As | Fremgangsmaade til fremstilling af triglycerid og triglyceridsammensaetning |
| JPH07203979A (ja) | 1994-01-25 | 1995-08-08 | Maruha Corp | 高度不飽和脂肪酸グリセリドの製造方法 |
| GB9404483D0 (en) * | 1994-03-08 | 1994-04-20 | Norsk Hydro As | Refining marine oil compositions |
| WO1996037586A1 (fr) * | 1995-05-24 | 1996-11-28 | Loders Croklaan B.V. | Procede de production de matiere grasse contenant des acides gras polyinsatures a longue chaine |
| AU6610996A (en) * | 1995-05-24 | 1996-12-11 | Loders Croklaan B.V. | Production of materials high in long chain polyunsaturated f atty acids |
| WO1998018952A1 (fr) | 1996-10-30 | 1998-05-07 | Nippon Suisan Kaisha, Ltd. | Procede de production de matieres grasses contenant des acides gras hautement insatures contenant eux-memes un acide docosahexaenoique a concentration selective |
-
1999
- 1999-02-17 NO NO19990739A patent/NO312973B1/no not_active IP Right Cessation
-
2000
- 2000-02-16 AT AT00906778T patent/ATE348140T1/de not_active IP Right Cessation
- 2000-02-16 EP EP00906778A patent/EP1153114B1/fr not_active Expired - Lifetime
- 2000-02-16 DE DE60032337T patent/DE60032337T2/de not_active Expired - Lifetime
- 2000-02-16 CA CA002362212A patent/CA2362212C/fr not_active Expired - Lifetime
- 2000-02-16 WO PCT/NO2000/000056 patent/WO2000049117A1/fr active IP Right Grant
- 2000-02-16 AU AU28338/00A patent/AU757203B2/en not_active Ceased
- 2000-02-16 ES ES00906778T patent/ES2276669T3/es not_active Expired - Lifetime
- 2000-02-16 JP JP2000599845A patent/JP2002537442A/ja active Pending
- 2000-02-16 US US09/913,585 patent/US6518049B1/en not_active Expired - Lifetime
- 2000-02-16 NZ NZ513574A patent/NZ513574A/xx unknown
-
2001
- 2001-08-17 ZA ZA200106813A patent/ZA200106813B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002537442A (ja) | 2002-11-05 |
| ES2276669T3 (es) | 2007-07-01 |
| NZ513574A (en) | 2002-12-20 |
| EP1153114B1 (fr) | 2006-12-13 |
| CA2362212A1 (fr) | 2000-08-24 |
| AU757203B2 (en) | 2003-02-06 |
| NO990739D0 (no) | 1999-02-17 |
| NO312973B1 (no) | 2002-07-22 |
| EP1153114A1 (fr) | 2001-11-14 |
| NO990739L (no) | 2000-08-18 |
| CA2362212C (fr) | 2009-10-27 |
| DE60032337T2 (de) | 2007-07-12 |
| ATE348140T1 (de) | 2007-01-15 |
| DE60032337D1 (de) | 2007-01-25 |
| AU2833800A (en) | 2000-09-04 |
| WO2000049117A1 (fr) | 2000-08-24 |
| US6518049B1 (en) | 2003-02-11 |
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