KR100450501B1 - 인지질조성물 - Google Patents
인지질조성물 Download PDFInfo
- Publication number
- KR100450501B1 KR100450501B1 KR10-1998-0705269A KR19980705269A KR100450501B1 KR 100450501 B1 KR100450501 B1 KR 100450501B1 KR 19980705269 A KR19980705269 A KR 19980705269A KR 100450501 B1 KR100450501 B1 KR 100450501B1
- Authority
- KR
- South Korea
- Prior art keywords
- phospholipid composition
- phospholipid
- solution
- deionized water
- range
- Prior art date
Links
- 150000003904 phospholipids Chemical class 0.000 title claims abstract description 85
- 239000000203 mixture Substances 0.000 title claims abstract description 81
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000008367 deionised water Substances 0.000 claims abstract description 13
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 21
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 15
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims description 14
- 239000003995 emulsifying agent Substances 0.000 claims description 14
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 claims description 11
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 claims description 11
- 150000008104 phosphatidylethanolamines Chemical class 0.000 claims description 11
- 239000003456 ion exchange resin Substances 0.000 claims description 9
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 9
- 235000013345 egg yolk Nutrition 0.000 claims description 8
- 210000002969 egg yolk Anatomy 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 102000002322 Egg Proteins Human genes 0.000 claims description 7
- 108010000912 Egg Proteins Proteins 0.000 claims description 7
- 150000003905 phosphatidylinositols Chemical class 0.000 claims description 5
- PORPENFLTBBHSG-MGBGTMOVSA-N 1,2-dihexadecanoyl-sn-glycerol-3-phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCC PORPENFLTBBHSG-MGBGTMOVSA-N 0.000 claims description 4
- TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 claims description 4
- ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 229940042880 natural phospholipid Drugs 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000000839 emulsion Substances 0.000 description 24
- 235000019441 ethanol Nutrition 0.000 description 13
- 230000001954 sterilising effect Effects 0.000 description 13
- 239000000243 solution Substances 0.000 description 12
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 10
- 238000004659 sterilization and disinfection Methods 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229920001429 chelating resin Polymers 0.000 description 9
- 238000004945 emulsification Methods 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- 230000015556 catabolic process Effects 0.000 description 8
- 230000002378 acidificating effect Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 239000003729 cation exchange resin Substances 0.000 description 5
- 235000012000 cholesterol Nutrition 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 239000003957 anion exchange resin Substances 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 244000068988 Glycine max Species 0.000 description 3
- 235000010469 Glycine max Nutrition 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000008344 egg yolk phospholipid Substances 0.000 description 3
- 229940068998 egg yolk phospholipid Drugs 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- GGQOPZKTDHXXON-UHFFFAOYSA-N hexane;methanol Chemical compound OC.CCCCCC GGQOPZKTDHXXON-UHFFFAOYSA-N 0.000 description 3
- 239000002960 lipid emulsion Substances 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 3
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 240000008415 Lactuca sativa Species 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000013505 freshwater Substances 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 235000012045 salad Nutrition 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000008347 soybean phospholipid Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- DPEYHNFHDIXMNV-UHFFFAOYSA-N (9-amino-3-bicyclo[3.3.1]nonanyl)-(4-benzyl-5-methyl-1,4-diazepan-1-yl)methanone dihydrochloride Chemical compound Cl.Cl.CC1CCN(CCN1Cc1ccccc1)C(=O)C1CC2CCCC(C1)C2N DPEYHNFHDIXMNV-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- 102100031151 C-C chemokine receptor type 2 Human genes 0.000 description 1
- 101710149815 C-C chemokine receptor type 2 Proteins 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000005349 anion exchange Methods 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 235000014198 functional gum Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000008345 purified egg yolk phospholipid Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J7/00—Phosphatide compositions for foodstuffs, e.g. lecithin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/10—Phosphatides, e.g. lecithin
- C07F9/103—Extraction or purification by physical or chemical treatment of natural phosphatides; Preparation of compositions containing phosphatides of unknown structure
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/905—Agent composition per se for colloid system making or stabilizing, e.g. foaming, emulsifying, dispersing, or gelling
- Y10S516/907—The agent contains organic compound containing phosphorus, e.g. lecithin
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Medicinal Preparation (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
시료 No. | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 |
전기전도도(μS/cm) | 16.3 | 110 | 132 | 150 | 198 | 216 | 250 | 580 |
pH | 7.0 | 7.4 | 7.4 | 7.6 | 7.7 | 7.8 | 7.8 | 7.8 |
유적 발생 | ◎ | ◎ | ◎ | ◎ | ◎ | ○ | × | × |
가열살균에 의한pH의 저하 | 2.1 | 1.5 | 0.9 | 0.7 | 0.7 | 0.7 | 0.7 | 0.7 |
주: 유화파괴에 따른 유적발생◎: 전혀 없음○: 극히 약간 있음△: 소량 있음×: 다수 있음 |
시료 No. | 9 | 10 | 11 | 12 | 13 | 14 | 15 |
pH | 6.0 | 6.5 | 7.0 | 8.0 | 9.0 | 9.5 | 10.0 |
전기전도도(μS/cm) | 153 | 159 | 158 | 150 | 155 | 158 | 157 |
유적 발생 | × | ○ | ◎ | ◎ | ◎ | ○ | × |
가열살균에 의한pH의 저하 | 1.2 | 0.9 | 0.7 | 0.7 | 0.7 | 0.8 | 1.5 |
주: 유화파괴에 따른 유적발생◎: 전혀 없음○: 극히 약간 있음△: 소량 있음×: 다수 있음 |
시료 No. | 실시예1 | 16 | 17 | 18 | 19 |
전기전도도(μS/cm) | 172 | 84 | 131 | 168 | 262 |
pH | 7.5 | 7.4 | 7.3 | 7.5 | 7.4 |
유적 발생 | ◎ | × | × | × | × |
가열살균에 의한pH의 저하 | 0.7 | 1.5 | 1.1 | 0.8 | 0.8 |
주: 유화파괴에 따른 유적발생◎: 전혀 없음○: 극히 약간 있음△: 소량 있음×: 다수 있음 |
Claims (10)
- 2종 이상의 인지질을 함유하는 인지질 조성물로서, 탈이온수에 5중량% 농도가 되도록 현탁시킨 액의 전기전도도가 130 내지 220μS/cm 범위에 있고 또 그 액의 pH가 6.5 내지 9.5 범위인 것을 특징으로 하는 인지질 조성물.
- 제 1 항에 있어서, 탈이온수에 5중량% 농도가 되도록 현탁시킨 액의 전기전도도가 150 내지 200μS/cm 범위인 것을 특징으로 하는 인지질 조성물.
- 제 1 항 또는 제 2 항에 있어서, 탈이온수에 5중량% 농도가 되도록 현탁시킨 액의 pH가 7.0 내지 9.0 범위인 것을 특징으로 하는 인지질 조성물.
- 제 1 항에 있어서, 포스파티딜콜린, 포스파티딜에탄올아민, 포스파티딜이노시톨, 포스파티딜세린, 포스파티딘산, 이들의 리조화물 및 스핀고미엘린으로부터 선택된 2종 이상의 인지질을 함유하는 것을 특징으로 하는 인지질 조성물.
- 천연 인지질 함유물에서 추출하여 얻은 정제되지 않은 인지질 조성물을 그대로, 또는 그 정제되지 않은 인지질 조성물을 다시 정제하여 얻은 정제 인지질 조성물을, 용매에 용해시켜서 용해액을 이온교환수지와 접촉시킨 후 용매를 제거하여 제 1 항 내지 제 4 항중 어느 한 항에 기재된 인지질 조성물을 얻는 것을 특징으로하는 인지질 조성물의 제조방법.
- 제 5 항에 있어서, 건조난황을 알콜로 추출하고, 추출액에서 알콜을 제거하여 얻은 정제되지 않은 인지질 조성물을 그대로, 또는 그 정제되지 않은 인지질 조성물을 다시 아세톤 처리하여 얻은 아세톤 불용물에서 아세톤을 제거하여 얻은 정제 인지질 조성물을, 용매에 용해시켜서, 용해액을 이온교환수지와 접촉시킨 후 용매를 제거하여, 제 1 항 내지 제 4 항 중 어느 한 항에 기재된 인지질 조성물을 얻는 것을 특징으로 하는 인지질 조성물의 제조방법.
- 2종 이상의 인지질을 함유하는 인지질 조성물로서, 탈이온수에 5중량% 농도가 되도록 현탁시킨 액의 전기전도도가 130 내지 220μS/cm 범위에 있고, 또, 그 액의 pH가 6.5 내지 9.5 범위에 있는 인지질 조성물로 이루어진 것을 특징으로 하는 유화제.
- 제 7 항에 있어서, 탈이온수에 5중량% 농도가 되도록 현탁시킨 액의 전기전도도가 150 내지 200μS/cm 범위에 있는 인지질 조성물로 이루어진 것을 특징으로 하는 유화제.
- 제 7 항 또는 제 8 항에 있어서, 탈이온수에 5중량% 농도가 되도록 현탁시킨 액의 pH가 7.0 내지 9.0 범위에 있는 인지질 조성물로 이루어진 것을 특징으로 하는 유화제.
- 제 7 항에 있어서, 포스파티딜콜린, 포스파티딜에탄올아민, 포스파티딜이노시톨, 포스파티딜세린, 포스파티딘산, 이들의 리조화물 및 스핀고미엘린으로부터 선택된 2종 이상의 인지질을 함유하는 것을 특징으로 하는 유화제.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP96-302173 | 1996-11-13 | ||
JP30217396 | 1996-11-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR19990077132A KR19990077132A (ko) | 1999-10-25 |
KR100450501B1 true KR100450501B1 (ko) | 2005-01-15 |
Family
ID=17905811
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR10-1998-0705269A KR100450501B1 (ko) | 1996-11-13 | 1997-11-11 | 인지질조성물 |
Country Status (7)
Country | Link |
---|---|
US (1) | US6054494A (ko) |
EP (1) | EP0885896B1 (ko) |
JP (1) | JP3844508B2 (ko) |
KR (1) | KR100450501B1 (ko) |
CN (1) | CN1088461C (ko) |
DE (1) | DE69725969T2 (ko) |
WO (1) | WO1998021215A1 (ko) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1323353B1 (en) * | 2000-10-02 | 2009-04-01 | Fuji Oil Company, Ltd. | Fractionated soybean protein and process for producing the same |
CA2568483A1 (en) * | 2005-11-30 | 2007-05-30 | Meadwestvaco Corporation | Reminder system |
CN101443101A (zh) * | 2006-05-15 | 2009-05-27 | 荷兰联合利华有限公司 | 乳化液的制备方法 |
US20080234376A1 (en) * | 2007-03-21 | 2008-09-25 | Taiwan Liposome Company (A Taiwan Corporation) | Emulsion composition comprising prostaglandin e1 |
JP4959663B2 (ja) * | 2008-09-30 | 2012-06-27 | 富士フイルム株式会社 | 水性化粧料及びその製造方法 |
JP6280557B2 (ja) * | 2012-10-24 | 2018-02-14 | カーギル インコーポレイテッド | リン脂質含有乳化剤組成物 |
AU2014203179C1 (en) * | 2013-06-14 | 2017-05-04 | Aker Biomarine Antarctic As | Lipid extraction processes |
CN105746729B (zh) * | 2014-12-17 | 2021-11-30 | 丰益(上海)生物技术研发中心有限公司 | 乳化剂组合物及其用途 |
WO2018042576A1 (ja) * | 2016-08-31 | 2018-03-08 | キユーピー株式会社 | 卵黄リン脂質組成物およびその製造方法、ならびに該卵黄リン脂質組成物を用いた脂肪乳剤およびリポ化製剤 |
JP2021501149A (ja) | 2017-10-27 | 2021-01-14 | カーギル インコーポレイテッド | パーソナルケア製品 |
CN113201011B (zh) * | 2021-04-27 | 2022-05-24 | 内蒙古铂贝曼科技有限公司 | 一种磷脂加工助剂及其应用 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0259495A1 (en) * | 1986-02-10 | 1988-03-16 | Q.P. Corporation | Process for producing egg yolk lecithin containing a reduced amount of pe and/or containing substantially no impurities |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62281884A (ja) * | 1986-02-10 | 1987-12-07 | Q P Corp | Pe含量が減らされた及び/又は実質上不純物不含の卵黄レシチンの製造法 |
JPS62263109A (ja) * | 1986-05-06 | 1987-11-16 | Pola Chem Ind Inc | リン脂質を安定に配合する方法 |
JPS6333387A (ja) * | 1986-07-28 | 1988-02-13 | Q P Corp | 中性脂質含量が減らされたリゾリン脂質含有リン脂質の製造法 |
JPH0657715B2 (ja) * | 1987-04-09 | 1994-08-03 | キユーピー株式会社 | Lpc以外のリゾ型リン脂質をほとんど含まないリゾリン脂質の製造方法 |
US5064655A (en) * | 1989-02-24 | 1991-11-12 | Liposome Technology, Inc. | Liposome gel composition and method |
US4944948A (en) * | 1989-02-24 | 1990-07-31 | Liposome Technology, Inc. | EGF/Liposome gel composition and method |
US5942639A (en) * | 1991-07-04 | 1999-08-24 | Asta Medica Aktiengesellschaft | Process for the preparation of alkylphosphocholines and the production thereof in pure form |
JPH0544952A (ja) * | 1991-08-08 | 1993-02-23 | Toshiba Corp | ドレンポンプの運転方法 |
JP3100783B2 (ja) * | 1992-10-15 | 2000-10-23 | キユーピー株式会社 | ホスファチジルコリンおよびその製造方法 |
JP3531876B2 (ja) * | 1993-05-13 | 2004-05-31 | 旭化成ケミカルズ株式会社 | ドコサヘキサエン酸を含むリン脂質組成物の取得方法 |
JP3267868B2 (ja) * | 1995-08-29 | 2002-03-25 | キユーピー株式会社 | 卵黄リン脂質組成物 |
-
1997
- 1997-11-11 WO PCT/JP1997/004097 patent/WO1998021215A1/ja active IP Right Grant
- 1997-11-11 EP EP97911511A patent/EP0885896B1/en not_active Expired - Lifetime
- 1997-11-11 US US09/101,302 patent/US6054494A/en not_active Expired - Lifetime
- 1997-11-11 CN CN97191668A patent/CN1088461C/zh not_active Expired - Lifetime
- 1997-11-11 JP JP51149198A patent/JP3844508B2/ja not_active Expired - Lifetime
- 1997-11-11 KR KR10-1998-0705269A patent/KR100450501B1/ko active IP Right Grant
- 1997-11-11 DE DE69725969T patent/DE69725969T2/de not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0259495A1 (en) * | 1986-02-10 | 1988-03-16 | Q.P. Corporation | Process for producing egg yolk lecithin containing a reduced amount of pe and/or containing substantially no impurities |
Also Published As
Publication number | Publication date |
---|---|
KR19990077132A (ko) | 1999-10-25 |
US6054494A (en) | 2000-04-25 |
DE69725969T2 (de) | 2004-09-02 |
EP0885896B1 (en) | 2003-11-05 |
EP0885896A1 (en) | 1998-12-23 |
EP0885896A4 (en) | 2000-11-15 |
JP3844508B2 (ja) | 2006-11-15 |
WO1998021215A1 (fr) | 1998-05-22 |
CN1088461C (zh) | 2002-07-31 |
DE69725969D1 (de) | 2003-12-11 |
CN1208419A (zh) | 1999-02-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DK172721B1 (da) | Fremgangsmåde til fremstilling af æggeblommelecithin i det væsentlige uden urenheder og om ønsket med reduceret phosphatidy | |
KR100450501B1 (ko) | 인지질조성물 | |
CA1092148A (en) | Purification process | |
JP3549598B2 (ja) | ポリグリセリン脂肪酸エステルの製造方法 | |
EP0450769B1 (en) | Functional decholesterolized egg yolks | |
DE69505008T2 (de) | Verfahren zur trennung von lipiden | |
KR19980081133A (ko) | 식물성 라이소레시틴의 제조법 | |
US4323563A (en) | Fat emulsion for intravenous injection | |
CA2676484A1 (en) | Process for producing sphingomyelin and plasmalogen-form glycerophospholipid | |
EP0412624A2 (en) | Method for refining wax esters using amorphous silica | |
JP3100783B2 (ja) | ホスファチジルコリンおよびその製造方法 | |
JP2987682B2 (ja) | 酸性リン脂質の濃縮法 | |
JP4156228B2 (ja) | ホスファチジルセリンの精製方法 | |
Abood et al. | Enhancement of opiate binding by various molecular forms of phosphatidylserine and inhibition by other unsaturated lipids | |
Dewailly et al. | Changes in rat heart phospholipid composition after rapeseed oil feeding | |
JP2005290308A (ja) | リン脂質組成物の製造方法及びこれを用いた医薬品組成物、化粧品組成物、又は食品組成物 | |
JPS63253092A (ja) | Lpc以外のリゾ型リン脂質をほとんど含まないリゾリン脂質の製造方法 | |
JPS63279753A (ja) | 酵素改質レシチンの製造法 | |
KR101412434B1 (ko) | 정제 난황 인 지질 조성물의 제조 방법 및 이로써 얻어진 정제 난황 인 지질 조성물을 사용한 의약품 조성물, 화장품 조성물, 또는 식품 조성물 | |
US3681412A (en) | Glycol phosphatides and the preparation thereof from cephalin | |
GB2065659A (en) | Calciumphosphatidylchlorine- chloride, process for producing the same and pharmaceutical preparations containing the same | |
JP6763521B2 (ja) | 2−dha−リゾホスファチジルコリン含有脂質組成物及びその製造方法 | |
WO1987004711A1 (en) | Process for producing egg yolk lecithin containing a reduced amount of pe and/or containing substantially no impurities | |
JP2717510B2 (ja) | 苦味低減化剤の製造法 | |
JP4887674B2 (ja) | リン脂質組成物の製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20120810 Year of fee payment: 9 |
|
FPAY | Annual fee payment |
Payment date: 20130814 Year of fee payment: 10 |
|
FPAY | Annual fee payment |
Payment date: 20140811 Year of fee payment: 11 |
|
FPAY | Annual fee payment |
Payment date: 20150819 Year of fee payment: 12 |
|
FPAY | Annual fee payment |
Payment date: 20160818 Year of fee payment: 13 |
|
FPAY | Annual fee payment |
Payment date: 20170818 Year of fee payment: 14 |