JPH11512477A - 分別植物油 - Google Patents
分別植物油Info
- Publication number
- JPH11512477A JPH11512477A JP9512633A JP51263397A JPH11512477A JP H11512477 A JPH11512477 A JP H11512477A JP 9512633 A JP9512633 A JP 9512633A JP 51263397 A JP51263397 A JP 51263397A JP H11512477 A JPH11512477 A JP H11512477A
- Authority
- JP
- Japan
- Prior art keywords
- oil
- weight
- fractionated
- polar
- water
- 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.)
- Granted
Links
- 235000015112 vegetable and seed oil Nutrition 0.000 title claims abstract description 29
- 239000008158 vegetable oil Substances 0.000 title claims abstract description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 49
- 150000002632 lipids Chemical class 0.000 claims abstract description 47
- 239000010779 crude oil Substances 0.000 claims abstract description 14
- 239000004094 surface-active agent Substances 0.000 claims abstract description 11
- 239000002904 solvent Substances 0.000 claims abstract description 9
- 239000000463 material Substances 0.000 claims abstract description 8
- 239000003921 oil Substances 0.000 claims description 99
- 235000019198 oils Nutrition 0.000 claims description 97
- 238000000034 method Methods 0.000 claims description 53
- 239000000839 emulsion Substances 0.000 claims description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 35
- 239000000203 mixture Substances 0.000 claims description 28
- 238000004519 manufacturing process Methods 0.000 claims description 18
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 16
- KDYAPQVYJXUQNY-OPHDRXFHSA-N 1,2-di-(alpha-linolenoyl)-3-[alpha-D-galactosyl-(1->6)-beta-D-galactosyl]-sn-glycerol Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](OC[C@@H](COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)O[C@@H]1CO[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KDYAPQVYJXUQNY-OPHDRXFHSA-N 0.000 claims description 14
- 244000075850 Avena orientalis Species 0.000 claims description 13
- 235000007319 Avena orientalis Nutrition 0.000 claims description 13
- 235000013339 cereals Nutrition 0.000 claims description 13
- 239000003995 emulsifying agent Substances 0.000 claims description 12
- 150000003904 phospholipids Chemical class 0.000 claims description 11
- 239000002537 cosmetic Substances 0.000 claims description 9
- 235000013305 food Nutrition 0.000 claims description 8
- 241000196324 Embryophyta Species 0.000 claims description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 239000004530 micro-emulsion Substances 0.000 claims description 5
- 235000016709 nutrition Nutrition 0.000 claims description 5
- 230000000699 topical effect Effects 0.000 claims description 5
- VZCCETWTMQHEPK-QNEBEIHSSA-N gamma-linolenic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/CCCCC(O)=O VZCCETWTMQHEPK-QNEBEIHSSA-N 0.000 claims description 4
- 235000020664 gamma-linolenic acid Nutrition 0.000 claims description 4
- -1 inverted vesicles Substances 0.000 claims description 4
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 239000003925 fat Substances 0.000 claims description 3
- 235000019197 fats Nutrition 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 239000002994 raw material Substances 0.000 claims description 3
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 239000013543 active substance Substances 0.000 claims description 2
- 235000021324 borage oil Nutrition 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims description 2
- 239000002552 dosage form Substances 0.000 claims description 2
- VZCCETWTMQHEPK-UHFFFAOYSA-N gamma-Linolensaeure Natural products CCCCCC=CCC=CCC=CCCCCC(O)=O VZCCETWTMQHEPK-UHFFFAOYSA-N 0.000 claims description 2
- 229960002733 gamolenic acid Drugs 0.000 claims description 2
- 235000015097 nutrients Nutrition 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims 1
- 235000013311 vegetables Nutrition 0.000 claims 1
- 238000002156 mixing Methods 0.000 abstract description 11
- 238000001704 evaporation Methods 0.000 abstract description 7
- 239000012454 non-polar solvent Substances 0.000 abstract description 5
- 239000012071 phase Substances 0.000 description 25
- 239000000787 lecithin Substances 0.000 description 21
- 235000010445 lecithin Nutrition 0.000 description 21
- 229930186217 Glycolipid Natural products 0.000 description 19
- 239000000126 substance Substances 0.000 description 17
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 16
- 229940067606 lecithin Drugs 0.000 description 16
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- 241000245063 Primula Species 0.000 description 9
- 235000016311 Primula vulgaris Nutrition 0.000 description 9
- 239000007764 o/w emulsion Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000008346 aqueous phase Substances 0.000 description 8
- 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 description 7
- HVCOBJNICQPDBP-UHFFFAOYSA-N 3-[3-[3,5-dihydroxy-6-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxydecanoyloxy]decanoic acid;hydrate Chemical compound O.OC1C(OC(CC(=O)OC(CCCCCCC)CC(O)=O)CCCCCCC)OC(C)C(O)C1OC1C(O)C(O)C(O)C(C)O1 HVCOBJNICQPDBP-UHFFFAOYSA-N 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
- 238000005194 fractionation Methods 0.000 description 5
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000000284 extract Substances 0.000 description 4
- PZNPLUBHRSSFHT-RRHRGVEJSA-N 1-hexadecanoyl-2-octadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[C@@H](COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCCCCCCCCCC PZNPLUBHRSSFHT-RRHRGVEJSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 240000002791 Brassica napus Species 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 150000008104 phosphatidylethanolamines Chemical class 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 239000008347 soybean phospholipid Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000003222 Helianthus annuus Nutrition 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000287 crude extract Substances 0.000 description 2
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- FROLUYNBHPUZQU-IIZJPUEISA-N (2R,3R,4S,5R)-2-(hydroxymethyl)-6-[3-[3-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropoxy]propoxy]oxane-3,4,5-triol Chemical compound OC[C@H]1OC(OCCCOCCCOC2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@H]1O FROLUYNBHPUZQU-IIZJPUEISA-N 0.000 description 1
- 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 1
- 241001133760 Acoelorraphe Species 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 240000004355 Borago officinalis Species 0.000 description 1
- 235000007689 Borago officinalis Nutrition 0.000 description 1
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 1
- 235000006008 Brassica napus var napus Nutrition 0.000 description 1
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 1
- 244000188595 Brassica sinapistrum Species 0.000 description 1
- 244000020518 Carthamus tinctorius Species 0.000 description 1
- 235000003255 Carthamus tinctorius Nutrition 0.000 description 1
- 241000208818 Helianthus Species 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- QAQJMLQRFWZOBN-LAUBAEHRSA-N L-ascorbyl-6-palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)[C@H]1OC(=O)C(O)=C1O QAQJMLQRFWZOBN-LAUBAEHRSA-N 0.000 description 1
- 239000011786 L-ascorbyl-6-palmitate Substances 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 201000004681 Psoriasis Diseases 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 244000000231 Sesamum indicum Species 0.000 description 1
- 235000003434 Sesamum indicum Nutrition 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 239000001809 ammonium phosphatide Substances 0.000 description 1
- 235000010986 ammonium phosphatide Nutrition 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 235000010385 ascorbyl palmitate Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000002144 chemical decomposition reaction Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 238000013480 data collection Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 150000001982 diacylglycerols Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002296 dynamic light scattering Methods 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- 238000000105 evaporative light scattering detection Methods 0.000 description 1
- 239000011552 falling film Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 235000019629 palatability Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229940083466 soybean lecithin Drugs 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 229940005741 sunflower lecithin Drugs 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B1/00—Production of fats or fatty oils from raw materials
- C11B1/10—Production of fats or fatty oils from raw materials by extracting
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/10—Foods or foodstuffs containing additives; Preparation or treatment thereof containing emulsifiers
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/115—Fatty acids or derivatives thereof; Fats or oils
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
- A61K9/1075—Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
- A61K9/1271—Non-conventional liposomes, e.g. PEGylated liposomes, liposomes coated with polymers
- A61K9/1272—Non-conventional liposomes, e.g. PEGylated liposomes, liposomes coated with polymers with substantial amounts of non-phosphatidyl, i.e. non-acylglycerophosphate, surfactants as bilayer-forming substances, e.g. cationic lipids
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B3/00—Refining fats or fatty oils
- C11B3/006—Refining fats or fatty oils by extraction
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B7/00—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils
- C11B7/0008—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils by differences of solubilities, e.g. by extraction, by separation from a solution by means of anti-solvents
- C11B7/0025—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils by differences of solubilities, e.g. by extraction, by separation from a solution by means of anti-solvents in solvents containing oxygen in their molecule
-
- 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
- Y10S516/917—The agent contains organic compound containing oxygen
- Y10S516/918—The compound contains carboxylic acid ester group
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.植物原料を非極性触媒で抽出し、その溶媒を蒸発させて非極性および極性脂 質を含有する粗製油を得、それをさらに精製することからなり; 粗製油を制御温度でアルコールと混合し、アルコール相を分離し、蒸発させて 極性脂質に富んだ分別植物油を得ることを特徴とする、植物原料から分別植物油 を製造する方法。 2.植物原料は穀物または穀粒、特にカラス麦である、請求項1記載の方法。 3.アルコールはメタノール、エタノール、プロパノールまたはイソプロパノー ルである、請求項1または2記載の方法。 4.アルコールは35重量%までの水、好ましくは2.5〜20重量%の水と混合して 使用される、請求項1〜3の何れかの項記載の方法。 5.粗製油は少なくとも等容量のエタノールと混合される、請求項1〜4の何れ かの項記載の方法。 6.10〜90重量%、好ましくは20〜75重量%の極性脂質と残りは非極性脂質を含 有する、請求項1〜5の何れかの項記載の方法により得られた分別植物油。 7.5重量%以上、好ましくは20重量%以上のリン脂質を含有する、請求項1〜 5の何れかの項記載の方法により得られた分別植物油。 8.3重量%以上、好ましくは15重量%以上のDGDGを含有する、請求項1〜5の 何れかの項記載の方法により得られた分別植物油。 9.水中油形乳濁液、油中水形乳濁液、同様の分散液、逆転ベシクル、微小乳濁 液および他の有機溶液を製造するための界面活性剤としての、請求項1〜5の何 れかの項記載の方法により得られた分別植物油の使用。 10.食品、医薬品、スキンケア製品、あるいは経口、経腸、非経口、局所または 他の投与形態用の製品を製造するための界面活性剤としての、請求項1〜5の何 れかの項記載の方法により得られた分別植物油の使用。 11.請求項1〜5の何れかの項記載の方法により得られた分別植物油を乳化剤と して使用することを特徴とする、トリアシルグリセロール油、好ましくはマツヨ イグサ油またはその画分、ルリヂサ油またはその画分、あるいは他の植物油また はその画分から選択される乳化油を含有する乳濁液組成物。 12.その製造において請求項1〜5の何れかの項記載の方法に従って製造された 分別植物油を使用する、乳濁液、微小乳濁液、逆転ベシクルまたは他の形態の調 整液を含有する食品、栄養物、医薬品、皮膚用品、化粧品または他の組成物。 13.乳化油は遊離酸、その塩またはエステル形態のγ−リノレン酸または他の脂 肪酸からなる請求項12記載の医薬または栄養組成物。 14.さらに他の治療的に活性な物質を含有する請求項13記載の医薬組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE9503296-7 | 1995-09-22 | ||
SE9503296A SE504664C2 (sv) | 1995-09-22 | 1995-09-22 | Sätt att framställa fraktionerad olja, oljan, dess användning samt emulsionskomposition innehållande oljan |
PCT/SE1996/001146 WO1997011141A1 (en) | 1995-09-22 | 1996-09-13 | Fractionated vegetable oil |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH11512477A true JPH11512477A (ja) | 1999-10-26 |
JP3782457B2 JP3782457B2 (ja) | 2006-06-07 |
Family
ID=20399570
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP51263397A Expired - Fee Related JP3782457B2 (ja) | 1995-09-22 | 1996-09-13 | 分別植物油 |
Country Status (13)
Country | Link |
---|---|
US (1) | US6355693B1 (ja) |
EP (1) | EP1027413B1 (ja) |
JP (1) | JP3782457B2 (ja) |
AT (1) | ATE254655T1 (ja) |
AU (1) | AU706577B2 (ja) |
CA (1) | CA2232541C (ja) |
DE (1) | DE69630821T2 (ja) |
DK (1) | DK1027413T3 (ja) |
ES (1) | ES2211974T3 (ja) |
NZ (1) | NZ318909A (ja) |
PT (1) | PT1027413E (ja) |
SE (1) | SE504664C2 (ja) |
WO (1) | WO1997011141A1 (ja) |
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---|---|---|---|---|
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JP2002505272A (ja) * | 1998-03-06 | 2002-02-19 | スコーティア・ホールディングス・ピー・エル・シー | 乳化剤としてガラクト脂質物質からなり、導入された活性物質の持続作用を有する水中油型局所用組成物 |
JP2013146281A (ja) * | 2004-03-17 | 2013-08-01 | Freedom Health Llc | 栄養補助食品 |
JP2019198311A (ja) * | 2018-05-10 | 2019-11-21 | 築野食品工業株式会社 | 食品用乳化用組成物 |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE9702630D0 (sv) * | 1997-07-07 | 1997-07-07 | Scotia Lipidteknik Ab | Satiety product |
FR2792222B1 (fr) * | 1999-04-19 | 2001-06-08 | Lavipharm Lab | Agent emulsifiant, son procede de preparation et son utilisation pour la preparation de compositions cosmetiques, dermatologiques ou pharmacologiques |
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US10351795B2 (en) | 2014-03-19 | 2019-07-16 | Novozymes A/S | Polypeptides having phospholipase C activity and polynucleotides encoding same |
EP3143135B1 (en) | 2014-05-15 | 2019-04-10 | Novozymes A/S | Compositions comprising polypeptides having phospholipase c activity and use thereof |
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FR3049472B1 (fr) | 2016-03-31 | 2021-05-21 | Oleon N V | Procede d'extraction de glycolipides et glycolipides obtenus |
EP3589302A1 (en) * | 2017-03-01 | 2020-01-08 | OAT Services Ltd | Oat lipid extract |
AU2019272730B2 (en) * | 2018-05-22 | 2024-02-01 | Societe Des Produits Nestle S.A. | Creamer |
US11254895B2 (en) * | 2018-09-13 | 2022-02-22 | Bungle Global Innovation, LLC | Oilseed extraction method |
EP3797846B1 (fr) * | 2019-09-26 | 2024-05-22 | Chanel Parfums Beauté | Extraction microfluidique a partir d'extrait vegetal |
GB201916585D0 (en) * | 2019-11-14 | 2020-01-01 | Givaudan Sa | Concentrate |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2554873A (en) * | 1945-07-31 | 1951-05-29 | Musher Foundation Inc | Oat extract composition |
US2636888A (en) * | 1950-02-15 | 1953-04-28 | Quaker Oats Co | Fractionation of oat oil and use of same |
US3734901A (en) | 1970-09-28 | 1973-05-22 | Staley Mfg Co A E | Defatted soybean fractionation by solvent extraction |
US4517120A (en) * | 1983-10-19 | 1985-05-14 | Nestec, S.A. | Coffee oil treatment |
US5026548A (en) * | 1987-04-28 | 1991-06-25 | Cadbury Schweppes Plc | Surfactant |
US4859371A (en) * | 1987-04-29 | 1989-08-22 | The University Of Toronto Innovations Foundation | Extraction of particulate materials |
ATE224704T1 (de) * | 1994-02-04 | 2002-10-15 | Lipocore Holding Ab | Doppelschicht-zusammensetzungen aus digalactosyldiacylglycerol enthaltendem galactolipid |
MY112798A (en) | 1994-02-04 | 2001-09-29 | Karlshamns Lipidteknik Ab | Oil-in-water emulsions |
-
1995
- 1995-09-22 SE SE9503296A patent/SE504664C2/sv not_active IP Right Cessation
-
1996
- 1996-09-13 ES ES96932113T patent/ES2211974T3/es not_active Expired - Lifetime
- 1996-09-13 JP JP51263397A patent/JP3782457B2/ja not_active Expired - Fee Related
- 1996-09-13 AU AU71019/96A patent/AU706577B2/en not_active Ceased
- 1996-09-13 PT PT96932113T patent/PT1027413E/pt unknown
- 1996-09-13 AT AT96932113T patent/ATE254655T1/de not_active IP Right Cessation
- 1996-09-13 WO PCT/SE1996/001146 patent/WO1997011141A1/en active IP Right Grant
- 1996-09-13 NZ NZ318909A patent/NZ318909A/xx not_active IP Right Cessation
- 1996-09-13 DK DK96932113T patent/DK1027413T3/da active
- 1996-09-13 EP EP96932113A patent/EP1027413B1/en not_active Expired - Lifetime
- 1996-09-13 US US09/029,932 patent/US6355693B1/en not_active Expired - Fee Related
- 1996-09-13 CA CA002232541A patent/CA2232541C/en not_active Expired - Fee Related
- 1996-09-13 DE DE69630821T patent/DE69630821T2/de not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002505273A (ja) * | 1998-03-06 | 2002-02-19 | スコーティア・ホールディングス・ピー・エル・シー | 刺激作用を低下させる担体としての水中油型局所用組成物 |
JP2002505272A (ja) * | 1998-03-06 | 2002-02-19 | スコーティア・ホールディングス・ピー・エル・シー | 乳化剤としてガラクト脂質物質からなり、導入された活性物質の持続作用を有する水中油型局所用組成物 |
JP2013146281A (ja) * | 2004-03-17 | 2013-08-01 | Freedom Health Llc | 栄養補助食品 |
JP2019198311A (ja) * | 2018-05-10 | 2019-11-21 | 築野食品工業株式会社 | 食品用乳化用組成物 |
JP2021523687A (ja) * | 2018-05-22 | 2021-09-09 | ソシエテ・デ・プロデュイ・ネスレ・エス・アー | 栄養組成物 |
Also Published As
Publication number | Publication date |
---|---|
SE9503296D0 (sv) | 1995-09-22 |
DK1027413T3 (da) | 2004-03-29 |
US6355693B1 (en) | 2002-03-12 |
EP1027413B1 (en) | 2003-11-19 |
ATE254655T1 (de) | 2003-12-15 |
WO1997011141A1 (en) | 1997-03-27 |
SE504664C2 (sv) | 1997-03-24 |
DE69630821D1 (de) | 2003-12-24 |
NZ318909A (en) | 1999-08-30 |
PT1027413E (pt) | 2004-04-30 |
EP1027413A1 (en) | 2000-08-16 |
AU7101996A (en) | 1997-04-09 |
JP3782457B2 (ja) | 2006-06-07 |
SE9503296L (sv) | 1997-03-23 |
ES2211974T3 (es) | 2004-07-16 |
DE69630821T2 (de) | 2004-12-02 |
AU706577B2 (en) | 1999-06-17 |
CA2232541C (en) | 2005-05-10 |
CA2232541A1 (en) | 1997-03-27 |
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