ZA200501932B - Water in oil emulsion comprising sterolesters - Google Patents

Water in oil emulsion comprising sterolesters Download PDF

Info

Publication number: ZA200501932B
Authority: ZA; South Africa
Prior art keywords: emulsion; water; acid; folic acid; oil
Prior art date: 2002-10-31

Application number

ZA200501932A

Other languages

English (en)

Inventor

Eckhard Floetter

Chiara Garbolino

Adriana Huiberdina Terpstra

Original Assignee

Unilever Plc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2002-10-31

Filing date

2005-03-07

Publication date

2006-05-31

2005-03-07 Application filed by Unilever Plc filed Critical Unilever Plc

2006-05-31 Publication of ZA200501932B publication Critical patent/ZA200501932B/en

Links

239000007762 w/o emulsion Substances 0.000 title claims description 17
OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 claims abstract description 65
239000000839 emulsion Substances 0.000 claims abstract description 42
235000019152 folic acid Nutrition 0.000 claims abstract description 37
239000011724 folic acid Substances 0.000 claims abstract description 35
229930182558 Sterol Natural products 0.000 claims abstract description 33
235000003702 sterols Nutrition 0.000 claims abstract description 33
235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 31
229930195729 fatty acid Natural products 0.000 claims abstract description 31
239000000194 fatty acid Substances 0.000 claims abstract description 31
OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 claims abstract description 30
229960000304 folic acid Drugs 0.000 claims abstract description 30
-1 sterol fatty acid ester Chemical class 0.000 claims abstract description 22
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 8
239000008346 aqueous phase Substances 0.000 claims abstract description 6
LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 claims description 9
239000012071 phase Substances 0.000 claims description 8
235000019163 vitamin B12 Nutrition 0.000 claims description 8
239000011715 vitamin B12 Substances 0.000 claims description 8
235000019158 vitamin B6 Nutrition 0.000 claims description 8
239000011726 vitamin B6 Substances 0.000 claims description 8
229930003779 Vitamin B12 Natural products 0.000 claims description 7
239000000203 mixture Substances 0.000 claims description 7
RADKZDMFGJYCBB-UHFFFAOYSA-N pyridoxal hydrochloride Natural products CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 claims description 7
229940011671 vitamin b6 Drugs 0.000 claims description 7
LGJMUZUPVCAVPU-UHFFFAOYSA-N beta-Sitostanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CC)C(C)C)C1(C)CC2 LGJMUZUPVCAVPU-UHFFFAOYSA-N 0.000 claims description 5
ARYTXMNEANMLMU-UHFFFAOYSA-N 24alpha-methylcholestanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(C)C(C)C)C1(C)CC2 ARYTXMNEANMLMU-UHFFFAOYSA-N 0.000 claims description 4
ARYTXMNEANMLMU-ATEDBJNTSA-N campestanol Chemical compound C([C@@H]1CC2)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CC[C@@H](C)C(C)C)[C@@]2(C)CC1 ARYTXMNEANMLMU-ATEDBJNTSA-N 0.000 claims description 4
239000004615 ingredient Substances 0.000 claims description 4
238000000034 method Methods 0.000 claims description 4
SGNBVLSWZMBQTH-FGAXOLDCSA-N Campesterol Natural products O[C@@H]1CC=2[C@@](C)([C@@H]3[C@H]([C@H]4[C@@](C)([C@H]([C@H](CC[C@H](C(C)C)C)C)CC4)CC3)CC=2)CC1 SGNBVLSWZMBQTH-FGAXOLDCSA-N 0.000 claims description 3
BTEISVKTSQLKST-UHFFFAOYSA-N Haliclonasterol Natural products CC(C=CC(C)C(C)(C)C)C1CCC2C3=CC=C4CC(O)CCC4(C)C3CCC12C BTEISVKTSQLKST-UHFFFAOYSA-N 0.000 claims description 3
SGNBVLSWZMBQTH-PODYLUTMSA-N campesterol 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)CC[C@@H](C)C(C)C)[C@@]1(C)CC2 SGNBVLSWZMBQTH-PODYLUTMSA-N 0.000 claims description 3
235000000431 campesterol Nutrition 0.000 claims description 3
235000016831 stigmasterol Nutrition 0.000 claims description 3
229940032091 stigmasterol Drugs 0.000 claims description 3
BFDNMXAIBMJLBB-UHFFFAOYSA-N stigmasterol Natural products CCC(C=CC(C)C1CCCC2C3CC=C4CC(O)CCC4(C)C3CCC12C)C(C)C BFDNMXAIBMJLBB-UHFFFAOYSA-N 0.000 claims description 3
OILXMJHPFNGGTO-UHFFFAOYSA-N (22E)-(24xi)-24-methylcholesta-5,22-dien-3beta-ol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(C)C(C)C)C1(C)CC2 OILXMJHPFNGGTO-UHFFFAOYSA-N 0.000 claims description 2
OQMZNAMGEHIHNN-UHFFFAOYSA-N 7-Dehydrostigmasterol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)C=CC(CC)C(C)C)CCC33)C)C3=CC=C21 OQMZNAMGEHIHNN-UHFFFAOYSA-N 0.000 claims description 2
HZYXFRGVBOPPNZ-UHFFFAOYSA-N UNPD88870 Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)=CCC(CC)C(C)C)C1(C)CC2 HZYXFRGVBOPPNZ-UHFFFAOYSA-N 0.000 claims description 2
KZJWDPNRJALLNS-VJSFXXLFSA-N sitosterol 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)CC[C@@H](CC)C(C)C)[C@@]1(C)CC2 KZJWDPNRJALLNS-VJSFXXLFSA-N 0.000 claims description 2
HCXVJBMSMIARIN-PHZDYDNGSA-N stigmasterol 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)/C=C/[C@@H](CC)C(C)C)[C@@]1(C)CC2 HCXVJBMSMIARIN-PHZDYDNGSA-N 0.000 claims description 2
FDJOLVPMNUYSCM-WZHZPDAFSA-L cobalt(3+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+3].N#[C-].N([C@@H]([C@]1(C)[N-]\C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C(\C)/C1=N/C([C@H]([C@@]1(CC(N)=O)C)CCC(N)=O)=C\C1=N\C([C@H](C1(C)C)CCC(N)=O)=C/1C)[C@@H]2CC(N)=O)=C\1[C@]2(C)CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@H]1[C@@H](O)[C@@H](N2C3=CC(C)=C(C)C=C3N=C2)O[C@@H]1CO FDJOLVPMNUYSCM-WZHZPDAFSA-L 0.000 claims 2
238000009775 high-speed stirring Methods 0.000 claims 1
239000007764 o/w emulsion Substances 0.000 claims 1
238000002360 preparation method Methods 0.000 claims 1
238000003756 stirring Methods 0.000 claims 1
230000000694 effects Effects 0.000 abstract description 2
150000003432 sterols Chemical class 0.000 description 15
150000004665 fatty acids Chemical class 0.000 description 13
239000003925 fat Substances 0.000 description 11
235000019197 fats Nutrition 0.000 description 11
239000000047 product Substances 0.000 description 11
239000003921 oil Substances 0.000 description 9
235000019198 oils Nutrition 0.000 description 9
235000013305 food Nutrition 0.000 description 7
ZUFQODAHGAHPFQ-UHFFFAOYSA-N pyridoxine hydrochloride Chemical compound Cl.CC1=NC=C(CO)C(CO)=C1O ZUFQODAHGAHPFQ-UHFFFAOYSA-N 0.000 description 6
FFFHZYDWPBMWHY-VKHMYHEASA-N L-homocysteine Chemical compound OC(=O)[C@@H](N)CCS FFFHZYDWPBMWHY-VKHMYHEASA-N 0.000 description 5
AGVAZMGAQJOSFJ-WZHZPDAFSA-M cobalt(2+);[(2r,3s,4r,5s)-5-(5,6-dimethylbenzimidazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2r)-1-[3-[(1r,2r,3r,4z,7s,9z,12s,13s,14z,17s,18s,19r)-2,13,18-tris(2-amino-2-oxoethyl)-7,12,17-tris(3-amino-3-oxopropyl)-3,5,8,8,13,15,18,19-octamethyl-2 Chemical compound [Co+2].N#[C-].[N-]([C@@H]1[C@H](CC(N)=O)[C@@]2(C)CCC(=O)NC[C@@H](C)OP(O)(=O)O[C@H]3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)\C2=C(C)/C([C@H](C\2(C)C)CCC(N)=O)=N/C/2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O AGVAZMGAQJOSFJ-WZHZPDAFSA-M 0.000 description 5
229940014144 folate Drugs 0.000 description 5
229940068065 phytosterols Drugs 0.000 description 5
230000001603 reducing effect Effects 0.000 description 5
208000024172 Cardiovascular disease Diseases 0.000 description 4
239000002253 acid Substances 0.000 description 4
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 4
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
235000020777 polyunsaturated fatty acids Nutrition 0.000 description 4
239000000843 powder Substances 0.000 description 4
235000018102 proteins Nutrition 0.000 description 4
102000004169 proteins and genes Human genes 0.000 description 4
108090000623 proteins and genes Proteins 0.000 description 4
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150000003839 salts Chemical class 0.000 description 4
229920006395 saturated elastomer Polymers 0.000 description 4
235000013311 vegetables Nutrition 0.000 description 4
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102000007544 Whey Proteins Human genes 0.000 description 3
108010046377 Whey Proteins Proteins 0.000 description 3
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239000000796 flavoring agent Substances 0.000 description 3
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150000002224 folic acids Chemical class 0.000 description 3
235000013310 margarine Nutrition 0.000 description 3
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229920001131 Pulp (paper) Polymers 0.000 description 1
240000004808 Saccharomyces cerevisiae Species 0.000 description 1
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235000019486 Sunflower oil Nutrition 0.000 description 1
JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
229940072056 alginate Drugs 0.000 description 1
235000010443 alginic acid Nutrition 0.000 description 1
229920000615 alginic acid Polymers 0.000 description 1
DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
235000020661 alpha-linolenic acid Nutrition 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
239000003529 anticholesteremic agent Substances 0.000 description 1
229940127226 anticholesterol agent Drugs 0.000 description 1
235000010323 ascorbic acid Nutrition 0.000 description 1
239000011668 ascorbic acid Substances 0.000 description 1
229960005070 ascorbic acid Drugs 0.000 description 1
OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
229940116226 behenic acid Drugs 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
229940076810 beta sitosterol Drugs 0.000 description 1
NJKOMDUNNDKEAI-UHFFFAOYSA-N beta-sitosterol Natural products CCC(CCC(C)C1CCC2(C)C3CC=C4CC(O)CCC4C3CCC12C)C(C)C NJKOMDUNNDKEAI-UHFFFAOYSA-N 0.000 description 1
QADVIPISOOQJMJ-WLKYTNTRSA-N beta-stigmasterol Natural products CCC(CC)C=C[C@@H](C)[C@H]1CC[C@@H]2[C@@H]1CC[C@H]3[C@H]2CC=C4C[C@@H](O)CC[C@]34C QADVIPISOOQJMJ-WLKYTNTRSA-N 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000002775 capsule Substances 0.000 description 1
KJDZDTDNIULJBE-QXMHVHEDSA-N cetoleic acid Chemical compound CCCCCCCCCC\C=C/CCCCCCCCCC(O)=O KJDZDTDNIULJBE-QXMHVHEDSA-N 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
235000015165 citric acid Nutrition 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
235000009508 confectionery Nutrition 0.000 description 1
208000029078 coronary artery disease Diseases 0.000 description 1
230000002596 correlated effect Effects 0.000 description 1
230000000875 corresponding effect Effects 0.000 description 1
GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
235000005911 diet Nutrition 0.000 description 1
230000000378 dietary effect Effects 0.000 description 1
235000015872 dietary supplement Nutrition 0.000 description 1
OZRNSSUDZOLUSN-LBPRGKRZSA-N dihydrofolic acid Chemical compound N=1C=2C(=O)NC(N)=NC=2NCC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OZRNSSUDZOLUSN-LBPRGKRZSA-N 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
210000003743 erythrocyte Anatomy 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
235000004426 flaxseed Nutrition 0.000 description 1
235000010492 gellan gum Nutrition 0.000 description 1
239000000216 gellan gum Substances 0.000 description 1
230000036541 health Effects 0.000 description 1
230000006872 improvement Effects 0.000 description 1
238000009884 interesterification Methods 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
150000003903 lactic acid esters Chemical class 0.000 description 1
235000020778 linoleic acid Nutrition 0.000 description 1
OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
229960004488 linolenic acid Drugs 0.000 description 1
KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
210000004185 liver Anatomy 0.000 description 1
235000010420 locust bean gum Nutrition 0.000 description 1
239000000711 locust bean gum Substances 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
229930182817 methionine Natural products 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000011987 methylation Effects 0.000 description 1
238000007069 methylation reaction Methods 0.000 description 1
235000021239 milk protein Nutrition 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
210000000653 nervous system Anatomy 0.000 description 1
235000016709 nutrition Nutrition 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
229960002446 octanoic acid Drugs 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
239000003346 palm kernel oil Substances 0.000 description 1
235000019865 palm kernel oil Nutrition 0.000 description 1
239000002540 palm oil Substances 0.000 description 1
239000000825 pharmaceutical preparation Substances 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
235000002378 plant sterols Nutrition 0.000 description 1
230000008092 positive effect Effects 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
235000010388 propyl gallate Nutrition 0.000 description 1
239000000473 propyl gallate Substances 0.000 description 1
229940075579 propyl gallate Drugs 0.000 description 1
235000019171 pyridoxine hydrochloride Nutrition 0.000 description 1
239000011764 pyridoxine hydrochloride Substances 0.000 description 1
229960004172 pyridoxine hydrochloride Drugs 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
235000020183 skimmed milk Nutrition 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
HCXVJBMSMIARIN-UHFFFAOYSA-N stigmasterol Chemical compound C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(CC)C(C)C)C1(C)CC2 HCXVJBMSMIARIN-UHFFFAOYSA-N 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
235000019157 thiamine Nutrition 0.000 description 1
KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 description 1
229960003495 thiamine Drugs 0.000 description 1
239000011721 thiamine Substances 0.000 description 1
235000010384 tocopherol Nutrition 0.000 description 1
239000011732 tocopherol Substances 0.000 description 1
229960001295 tocopherol Drugs 0.000 description 1
229930003799 tocopherol Natural products 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
229940088594 vitamin Drugs 0.000 description 1
229930003231 vitamin Natural products 0.000 description 1
235000013343 vitamin Nutrition 0.000 description 1
239000011782 vitamin Substances 0.000 description 1
150000003722 vitamin derivatives Chemical class 0.000 description 1
235000019195 vitamin supplement Nutrition 0.000 description 1
235000021119 whey protein Nutrition 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS OR COOKING OILS
- A23D7/00—Edible oil or fat compositions containing an aqueous phase, e.g. margarines
- A23D7/015—Reducing calorie content; Reducing fat content, e.g. "halvarines"
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS OR COOKING OILS
- A23D7/00—Edible oil or fat compositions containing an aqueous phase, e.g. margarines
- A23D7/005—Edible oil or fat compositions containing an aqueous phase, e.g. margarines characterised by ingredients other than fatty acid triglycerides
- A23D7/0056—Spread compositions
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- 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
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
- A23L33/11—Plant sterols or derivatives thereof, e.g. phytosterols
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Food Science & Technology (AREA)
Polymers & Plastics (AREA)
Oil, Petroleum & Natural Gas (AREA)
Botany (AREA)
Health & Medical Sciences (AREA)
Mycology (AREA)
Nutrition Science (AREA)
Edible Oils And Fats (AREA)
Medicinal Preparation (AREA)
Colloid Chemistry (AREA)
Seasonings (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Cosmetics (AREA)

ZA200501932A 2002-10-31 2005-03-07 Water in oil emulsion comprising sterolesters ZA200501932B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP02257560		2002-10-31

Publications (1)

Publication Number	Publication Date
ZA200501932B true ZA200501932B (en)	2006-05-31

Family

ID=32187259

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200501932A ZA200501932B (en)	2002-10-31	2005-03-07	Water in oil emulsion comprising sterolesters

Country Status (12)

Country	Link
US (1)	US20060029622A1 (pl)
EP (1)	EP1555895B8 (pl)
JP (1)	JP2006504419A (pl)
AT (1)	ATE354973T1 (pl)
AU (1)	AU2003271621B2 (pl)
BR (1)	BR0314443B1 (pl)
CA (1)	CA2498957A1 (pl)
DE (1)	DE60312199T2 (pl)
MX (1)	MXPA05004461A (pl)
PL (1)	PL375068A1 (pl)
WO (1)	WO2004039177A1 (pl)
ZA (1)	ZA200501932B (pl)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20050281937A1 (en) *	2004-06-22	2005-12-22	Sarma Monoj K	Reduced-fat flavored edible oil spreads
JP2007106703A (ja) *	2005-10-14	2007-04-26	Nutri Kk	血管障害の予防および治療組成物
EP2067410A1 (en) *	2007-12-07	2009-06-10	Cognis IP Management GmbH	Water-dispersable sterol containing dispersion
JP5253014B2 (ja) *	2008-06-27	2013-07-31	株式会社カネカ	油中水型乳化油脂組成物
EP2149305A1 (en) *	2008-07-31	2010-02-03	DSM IP Assets B.V.	Premix emulsion
CA2954331C (en) *	2014-07-11	2022-01-25	Unilever Bcs Limited	Pourable water-in-oil cooking composition
ES2607715B1 (es)	2015-10-01	2018-01-17	Solutex Na, Lcc	Proceso para la preparación y estabilización de emulsiones con omega-3 mediante redes cristalinas isométricas de derivados de celulosa
DE202017002769U1 (de)	2017-05-24	2017-08-28	Robert Firdaus Grosser	Streichfett mit Fruchtfleisch
CA3209351A1 (en) *	2021-02-23	2022-09-01	Renske Leonarda Margriet Tijssen	Spread composition comprising sterols

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4497800A (en) *	1982-07-06	1985-02-05	Mead Johnson & Company	Stable liquid diet composition
AU664827B2 (en) *	1991-05-03	1995-12-07	Raisio Benecol Ltd.	A substance for lowering high cholesterol level in serum and a method for preparing the same
UA69378C2 (uk) *	1996-11-04	2004-09-15	Райзіо Бенекол Лтд.	Текстуруюча композиція, текстуруючий агент, харчовий продукт, жирові суміші та способи їх одержання
DE59903869D1 (de) *	1998-10-14	2003-01-30	Cognis Deutschland Gmbh	Verwendung von nanoskaligen sterolen und sterolestern
US6274574B1 (en) *	1999-02-26	2001-08-14	Kraft Foods, Inc.	Use of mesophase-stabilized compositions for delivery of cholesterol-reducing sterols and stanols in food products
DE60036374T3 (de) *	1999-05-26	2018-09-20	Adeka Corp.	Pflanzliche sterol-enthaltende fettzusamensetzungen sowie verfahren zur herstellung derselben
BR0001794A (pt) *	2000-05-15	2001-12-26	Laboratorios Biosintetica Ltda	Aplicação de fitosteróides (e seus isÈmeros), ácidofólico, cianocobalamina e piridoxina em fibrasdietéticas (alimentares)
US6576285B1 (en) *	2000-11-14	2003-06-10	Sunpure Ltd.	Cholesterol lowering beverage
US6933291B2 (en) *	2000-12-01	2005-08-23	N.V. Nutricia	Cholesterol lowering supplement

2003
- 2003-09-18 BR BRPI0314443-7A patent/BR0314443B1/pt active IP Right Grant
- 2003-09-18 AU AU2003271621A patent/AU2003271621B2/en not_active Ceased
- 2003-09-18 DE DE60312199T patent/DE60312199T2/de not_active Expired - Lifetime
- 2003-09-18 WO PCT/EP2003/010420 patent/WO2004039177A1/en not_active Ceased
- 2003-09-18 CA CA002498957A patent/CA2498957A1/en not_active Abandoned
- 2003-09-18 AT AT03753429T patent/ATE354973T1/de not_active IP Right Cessation
- 2003-09-18 PL PL03375068A patent/PL375068A1/pl not_active Application Discontinuation
- 2003-09-18 EP EP03753429A patent/EP1555895B8/en not_active Expired - Lifetime
- 2003-09-18 JP JP2004547492A patent/JP2006504419A/ja not_active Withdrawn
- 2003-09-18 US US10/532,954 patent/US20060029622A1/en not_active Abandoned
- 2003-09-18 MX MXPA05004461A patent/MXPA05004461A/es not_active Application Discontinuation
2005
- 2005-03-07 ZA ZA200501932A patent/ZA200501932B/en unknown

Also Published As

Publication number	Publication date
EP1555895A1 (en)	2005-07-27
ATE354973T1 (de)	2006-03-15
AU2003271621B2 (en)	2007-03-29
WO2004039177A1 (en)	2004-05-13
DE60312199D1 (de)	2007-04-12
MXPA05004461A (es)	2005-07-26
CA2498957A1 (en)	2004-05-13
EP1555895B8 (en)	2007-05-30
DE60312199T2 (de)	2007-11-08
BR0314443B1 (pt)	2014-12-16
JP2006504419A (ja)	2006-02-09
US20060029622A1 (en)	2006-02-09
PL375068A1 (pl)	2005-11-14
BR0314443A (pt)	2005-07-19
AU2003271621A1 (en)	2004-05-25
EP1555895B1 (en)	2007-02-28

Publication	Publication Date	Title
US8173160B2 (en)	2012-05-08	Compositions comprising edible oils and vitamins and/or minerals and methods for making the compositions
EP1414314B1 (en)	2011-06-29	Composition for lowering blood cholesterol
EP0828434B1 (en)	2000-02-09	Fat based food products
WO2003055324A1 (en)	2003-07-10	Protein hydrolysate and plant sterol containing composition for improving serum lipid profile and preventing atherosclerosis
US20100040737A1 (en)	2010-02-18	Egg products with components recognized for reducing the levels of cholesterol in people and/or improving their health
AU2009269433A1 (en)	2010-01-14	Taste-improving agent for foods and drinks
HUP0400188A2 (hu)	2004-07-28	Fitoszterinek stabilizált olajos diszperziója, eljárás az előállítására és alkalmazása
EP1555895B8 (en)	2007-05-30	Water in oil emulsion comprising sterolesters
CN101466275A (zh)	2009-06-24	含有甾体糖苷的单位份食欲抑制剂组合物
EP1501367B1 (en)	2011-10-05	Food product comprising a phytosterol
US20050281937A1 (en)	2005-12-22	Reduced-fat flavored edible oil spreads
AU2011254726A1 (en)	2013-01-10	Theobromine for increasing HDL-cholesterol
US20060188635A1 (en)	2006-08-24	Food product comprising phytosterols
US20090181103A1 (en)	2009-07-16	Cholesterol-lowering dairy products and methods for their preparation
CA2673005A1 (en)	2007-06-28	Emulsions comprising non-esterified phytosterols in the aqueous phase
FI125932B (en)	2016-04-15	Foods for use in the prevention and treatment of high cholesterol and blood pressure
RU2268604C1 (ru)	2006-01-27	Пищевой эмульсионный низкокалорийный жировой продукт 40%-ной жирности
RU2264118C1 (ru)	2005-11-20	Пищевой эмульсионный низкокалорийный жировой продукт 30%-ной жирности