US20080021112A1 - Long chain alcohols provided in edible oils - Google Patents
Long chain alcohols provided in edible oils Download PDFInfo
- Publication number
- US20080021112A1 US20080021112A1 US11/763,748 US76374807A US2008021112A1 US 20080021112 A1 US20080021112 A1 US 20080021112A1 US 76374807 A US76374807 A US 76374807A US 2008021112 A1 US2008021112 A1 US 2008021112A1
- Authority
- US
- United States
- Prior art keywords
- long chain
- oil
- edible oil
- high molecular
- policosanol
- 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.)
- Abandoned
Links
- 150000001298 alcohols Chemical class 0.000 title claims abstract description 30
- 239000008157 edible vegetable oil Substances 0.000 title claims abstract description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims abstract description 16
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 7
- 239000004094 surface-active agent Substances 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 34
- 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 claims description 18
- 241000251539 Vertebrata <Metazoa> Species 0.000 claims description 5
- 235000012000 cholesterol Nutrition 0.000 claims description 5
- 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 claims description 4
- 235000020661 alpha-linolenic acid Nutrition 0.000 claims description 4
- 229960004488 linolenic acid Drugs 0.000 claims description 4
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 claims description 4
- 150000003626 triacylglycerols Chemical class 0.000 claims description 4
- 229940057917 medium chain triglycerides Drugs 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 230000001804 emulsifying effect Effects 0.000 claims 1
- 229930195729 fatty acid Natural products 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 10
- 235000013305 food Nutrition 0.000 abstract description 9
- 239000003921 oil Substances 0.000 description 35
- 235000019198 oils Nutrition 0.000 description 35
- 229960001109 policosanol Drugs 0.000 description 32
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 32
- 235000013310 margarine Nutrition 0.000 description 14
- 239000000047 product Substances 0.000 description 14
- 239000003264 margarine Substances 0.000 description 13
- 239000003549 soybean oil Substances 0.000 description 11
- 235000012424 soybean oil Nutrition 0.000 description 11
- 150000002148 esters Chemical class 0.000 description 10
- 235000015071 dressings Nutrition 0.000 description 9
- 239000000839 emulsion Substances 0.000 description 8
- 239000012071 phase Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 240000008415 Lactuca sativa Species 0.000 description 5
- 239000008346 aqueous phase Substances 0.000 description 5
- 235000013361 beverage Nutrition 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- 235000012045 salad Nutrition 0.000 description 5
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 4
- CHHHXKFHOYLYRE-UHFFFAOYSA-M 2,4-Hexadienoic acid, potassium salt (1:1), (2E,4E)- Chemical compound [K+].CC=CC=CC([O-])=O CHHHXKFHOYLYRE-UHFFFAOYSA-M 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 4
- 240000000111 Saccharum officinarum Species 0.000 description 4
- 235000007201 Saccharum officinarum Nutrition 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000004302 potassium sorbate Substances 0.000 description 4
- 235000010241 potassium sorbate Nutrition 0.000 description 4
- 229940069338 potassium sorbate Drugs 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
- 244000126608 Ruta angustifolia Species 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 239000001201 calcium disodium ethylene diamine tetra-acetate Substances 0.000 description 3
- 235000011188 calcium disodium ethylene diamine tetraacetate Nutrition 0.000 description 3
- SHWNNYZBHZIQQV-UHFFFAOYSA-L calcium;disodium;2-[2-[bis(carboxylatomethyl)azaniumyl]ethyl-(carboxylatomethyl)azaniumyl]acetate Chemical compound [Na+].[Na+].[Ca+2].[O-]C(=O)C[NH+](CC([O-])=O)CC[NH+](CC([O-])=O)CC([O-])=O SHWNNYZBHZIQQV-UHFFFAOYSA-L 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 229960001484 edetic acid Drugs 0.000 description 3
- 150000002632 lipids Chemical class 0.000 description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 description 3
- 239000008158 vegetable oil Substances 0.000 description 3
- 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 2
- 235000005979 Citrus limon Nutrition 0.000 description 2
- 244000131522 Citrus pyriformis Species 0.000 description 2
- 102000002322 Egg Proteins Human genes 0.000 description 2
- 108010000912 Egg Proteins Proteins 0.000 description 2
- 229920001214 Polysorbate 60 Polymers 0.000 description 2
- HDSBZMRLPLPFLQ-UHFFFAOYSA-N Propylene glycol alginate Chemical compound OC1C(O)C(OC)OC(C(O)=O)C1OC1C(O)C(O)C(C)C(C(=O)OCC(C)O)O1 HDSBZMRLPLPFLQ-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
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- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000011648 beta-carotene Substances 0.000 description 2
- 235000013734 beta-carotene Nutrition 0.000 description 2
- TUPZEYHYWIEDIH-WAIFQNFQSA-N beta-carotene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2=CCCCC2(C)C TUPZEYHYWIEDIH-WAIFQNFQSA-N 0.000 description 2
- 229960002747 betacarotene Drugs 0.000 description 2
- 235000014121 butter Nutrition 0.000 description 2
- 235000015155 buttermilk Nutrition 0.000 description 2
- 235000019519 canola oil Nutrition 0.000 description 2
- 239000000828 canola oil Substances 0.000 description 2
- 235000019219 chocolate Nutrition 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 235000014510 cooky Nutrition 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000013345 egg yolk Nutrition 0.000 description 2
- 210000002969 egg yolk Anatomy 0.000 description 2
- 235000019197 fats Nutrition 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 235000011194 food seasoning agent Nutrition 0.000 description 2
- 235000003599 food sweetener Nutrition 0.000 description 2
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 2
- 125000005456 glyceride group Chemical group 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000008173 hydrogenated soybean oil Substances 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000000787 lecithin Substances 0.000 description 2
- 235000010445 lecithin Nutrition 0.000 description 2
- 229940067606 lecithin Drugs 0.000 description 2
- 239000008268 mayonnaise Substances 0.000 description 2
- 235000010746 mayonnaise Nutrition 0.000 description 2
- CNNRPFQICPFDPO-UHFFFAOYSA-N octacosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCO CNNRPFQICPFDPO-UHFFFAOYSA-N 0.000 description 2
- 150000003904 phospholipids Chemical class 0.000 description 2
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 2
- 229920000053 polysorbate 80 Polymers 0.000 description 2
- 235000014438 salad dressings Nutrition 0.000 description 2
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 2
- 239000004299 sodium benzoate Substances 0.000 description 2
- 235000010234 sodium benzoate Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000003765 sweetening agent Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 239000000052 vinegar Substances 0.000 description 2
- 235000021419 vinegar Nutrition 0.000 description 2
- 235000019155 vitamin A Nutrition 0.000 description 2
- 239000011719 vitamin A Substances 0.000 description 2
- 239000000230 xanthan gum Substances 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- 229940082509 xanthan gum Drugs 0.000 description 2
- 235000010493 xanthan gum Nutrition 0.000 description 2
- 235000013618 yogurt Nutrition 0.000 description 2
- 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 2
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- 229960002666 1-octacosanol Drugs 0.000 description 1
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241001132374 Asta Species 0.000 description 1
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 1
- 235000006008 Brassica napus var napus Nutrition 0.000 description 1
- 240000000385 Brassica napus var. napus Species 0.000 description 1
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 244000020518 Carthamus tinctorius Species 0.000 description 1
- 235000003255 Carthamus tinctorius Nutrition 0.000 description 1
- 241000938605 Crocodylia Species 0.000 description 1
- CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 description 1
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
- 239000011627 DL-alpha-tocopherol Substances 0.000 description 1
- 235000001815 DL-alpha-tocopherol Nutrition 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- RUSIZKKQGFQEHZ-UHFFFAOYSA-N OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O Chemical compound OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O RUSIZKKQGFQEHZ-UHFFFAOYSA-N 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 229930182558 Sterol Natural products 0.000 description 1
- -1 Sterol Compounds Chemical class 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
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- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
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- 235000008429 bread Nutrition 0.000 description 1
- 235000012970 cakes Nutrition 0.000 description 1
- 239000001325 capsicum annuum l. var. longum oleoresin Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
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- ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 description 1
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- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
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- 239000012669 liquid formulation Substances 0.000 description 1
- 235000004213 low-fat Nutrition 0.000 description 1
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- 235000012658 paprika extract Nutrition 0.000 description 1
- DYUUPIKEWLHQGQ-SDXBLLFJSA-N paprika oleoresin Chemical compound C(\[C@]12[C@@](O1)(C)C[C@@H](O)CC2(C)C)=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=C[C@H]1C(C)=C[C@H](O)CC1(C)C DYUUPIKEWLHQGQ-SDXBLLFJSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
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- 230000000704 physical effect Effects 0.000 description 1
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- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
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- 229940068968 polysorbate 80 Drugs 0.000 description 1
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- 230000001953 sensory effect Effects 0.000 description 1
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- 239000007921 spray Substances 0.000 description 1
- 230000007103 stamina Effects 0.000 description 1
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- 229960000984 tocofersolan Drugs 0.000 description 1
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- 229930003799 tocopherol Natural products 0.000 description 1
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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
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS OR COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings or cooking oils
- A23D9/007—Other edible oils or fats, e.g. shortenings or cooking oils characterised by ingredients other than fatty acid triglycerides
-
- 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
- A23D9/00—Other edible oils or fats, e.g. shortenings or cooking oils
- A23D9/02—Other edible oils or fats, e.g. shortenings or cooking oils characterised by the production or working-up
-
- 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
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/60—Salad dressings; Mayonnaise; Ketchup
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
Definitions
- the present invention describes a method of obtaining uniform distribution of a long chain alcohol or a mixture of such alcohols in a comestible product by dissolving or suspending the long chain alcohol in an edible oil.
- long chain alcohols have important properties for improving the health of humans and animals. These beneficial properties include improving stamina, lowering blood cholesterol levels, and decreasing platelet aggregation.
- One desirable route for ingesting these alcohols is in food or beverage products.
- these long chain alcohols are very insoluble in water, and the very small amounts of these long chain alcohols needed to produce beneficial health effects makes content uniformity of long chain alcohols in a dry blending operation very difficult to achieve. Therefore, a means is needed for incorporating these long chain alcohols into food or beverage products in a manner that yields a uniform and consistent distribution of these materials in the comestible product.
- EP 801904 A1 describes the use of long chain alcohols (defined as alcohols having more than 20 carbon atoms) in continuous fat phase compositions containing particulate sweeteners.
- the incorporation of the long chain alcohols at about 0.1% to about 0.4% was reported to decrease the viscosity of confectionery coatings made with this composition.
- All of the described compositions contained a particulated sweetener in addition to a chocolate material and a vegetable oil.
- WO 98/47385 discloses a fat emulsion with a blend of emulsifiers created by the blending of a partial glyceride with a phospholipid and a long chain alcohol having a chain length of greater than C 20 .
- the total weight of the glyceride and phospholipid in the composition must be greater than about 0.02 weight percent.
- the present invention provides a method of providing a desirable distribution of long chain alcohols in a food or beverage product. More specifically, this process comprises dissolving or suspending the long chain alcohol in an edible oil, and then incorporating this edible oil into a food or beverage product.
- the present invention is a method for preparing a long chain alcohol in an edible oil material comprising: providing an edible oil substantially free of medium chain triglycerides composed of C 8 -C 10 triglycerides and less than about 12 weight percent linolenic acid; providing a long chain alcohol; admixing said edible oil and long chain alcohol in the presence of an energy source such that the long chain alcohol is admixed in the oil; said long chain alcohol/edible oil admixture is stable and substantially free of an emulsifier or surfactant and having a viscosity of less than about 200 centipoise as measured at 70° F. at 60 revolutions per minute.
- a second embodiment of the invention provides the composition made by the method of the invention. In
- the present invention provides a method for incorporating long chain alcohols into an oil matrix without the need to add emulsifiers, surfactants or penetrant enhancers.
- the method includes the use of heat or mechanical energy or other suitable energy sources in order to make the long chain alcohols soluble in the lipid matrix.
- the lipid matrix is an oil, preferably an oil derived from a vegetable source. Suitable oil sources include sunflower, safflower, corn, soybean, canola, mixtures of these oils and the like.
- long chain alcohols are understood to include saturated and unsaturated alcohols which contain more than about 90 weight percent C 20 or longer, primarily aliphatic alcohol materials. For the greatest health benefit it is preferred that the long chain alcohols be predominately, greater than 50 weight, percent octacosanol (C 28 ), preferably more than 65 percent and more preferably greater than about 70 weight percent.
- C 28 percent octacosanol
- policosanol is understood to be a mixture of long chain alcohols ranging from C 20 to C 36 preferably with greater than 65 weight percent C 28 . Common distribution and concentration ranges of the various components of policosanol are found in U.S. Pat. No. 5,856,316, the contents of which are incorporated by reference as set forth in its entirety. These long chain alcohols are available from various natural sources, most preferably from sugar cane wax. The long chain alcohols can also be synthesized using techniques well known in the art.
- Policosanol is soluble at about 160-180° F. in suitable lipid matrices such as vegetable oils and fat-soluble emulsifiers, vitamins and the like.
- suitable lipid matrices such as vegetable oils and fat-soluble emulsifiers, vitamins and the like.
- Suitable methods for incorporating policosanol or other long chain alcohol into the oil include heating by conventional means such as: heating elements or open flame; radiation sources and other ultrasonic wave generating equipment; as well as mechanical means such as agitation, homogenization, and the like.
- the long chain alcohol is ground into a microcrystalline form in order to improve the stability of the oil/long chain alcohol mixture.
- Suitable grinding techniques include hammermill, cryogenic rotary mills and the like.
- the particle size of the ground material is less than about 100 microns, preferably from about 20 to about 80 and most preferably from about 30 to about 60 microns.
- the level of long chain alcohol incorporated into the oil is from about 0.1 to about 5 percent, preferably from about 0.5 to about 3 and most preferably from about 0.8 to about 2 weight percent.
- concentration of the long chain alcohol will vary depending on various factors such as the dosage desired, the serving size and the solubility of the long chain alcohol in a particular oil.
- One advantage of the present invention is that the long chain alcohol remains stable in the edible oil.
- stable is understood to mean that the long chain alcohol does not precipitate, crystallize out, or separate when dissolved in the edible oil.
- the viscosity of the policosanol-enriched oil is such that the admixture remains suitable for many applications. Unlike other disclosures, the present invention does not have to be made into a high viscosity paste before being incorporated in a comestible.
- the long chain alcohol/edible oil mixture has a viscosity of less than about 200 centipoise, preferably from about 10 to about 150 and most preferably from 50 to about 130 centipoise. The viscosity is measured at 70° F. using a Brookfield Viscometer Model DV-II + , spindle #2 at 60 revolutions per minute for 10 seconds.
- the long chain alcohol/oil preparations can be used as a spray oil for cookies and crackers or can be used to formulate a number of cholesterol lowering food products including salad dressings, mayonnaise dressings, nutrition bars, beverages, juices, low fat ice creams, yogurts and frozen yogurts, non-dairy creamers, cheese spreads, milk products, confectioneries, chocolate-containing products such as cakes and cookies, margarine, and other spreads suitable for application on breads and the like.
- the long chain alcohol/oil preparations can also be formulated into pharmaceutical preparations, including tablets, soft gelatin capsules, especially those containing liquid formulations, such as suspensions, emulsions, solutions and the like.
- the present invention can be provided in foods in which water is the continuous phase, such as salad dressings and mayonnaise.
- the long chain alcohol/edible oil product of the present invention is incorporated into a product which has a continuous oil phase such as spreads and margarines.
- the long chain alcohol typically comprises from about 0.0001% to about 0.4% of the comestible product, preferably from about 0.007 to about 0.14 and most preferably from about 0.018 to about 0.071 weight percent of the comestible product.
- the level of the long chain alcohol is from 0.1 to about 100 milligrams/servings; preferably from about 0.5 to about 20 milligrams/serving and most preferably from about 2 to about 10 milligrams/servings.
- the present invention provides an edible oil/ long chain alcohol mixture that does not require the incorporation of high levels of linolenic acid in the edible oil as was previously disclosed in the art. Further the present invention does not require the addition of triglycerides, particularly C 8 -C 10 triglycerides; or other surfactants or emulsifiers in order to form the admixture. Because the edible oil/long chain alcohol does not need to incorporate these other agents, the admixture can be more readily formulated into other comestible products. Substantially free as used herein is understood to mean less than 1.0 weight percent, preferably less than 0.5 and most preferably less than 0.1 weight percent.
- the comestible product of the present invention can be used to reduce the cholesterol level of vertebrates that consume the comestible.
- Vertebrates include reptiles, mammals, fish and the like, with humans being most preferred.
- One percent policosanol in a vegetable oil was prepared by adding 2.0 g policosanol (CHOLESSTANOL (95% pure sugarcane wax material from Garuda International)) to 198.0 g soybean salad oil in a 400-ml PYREX glass beaker.
- the beaker was placed in a waterbath on a stove. The stove was turned on and the soybean oil/policosanol mixture was stirred gently by hand with a stainless steel spatula.
- the policosanol/soybean oil dispersion was heated and stirred until policosanol melted and solubilized in the oil at 160-180° F.
- the viscosity of the policosanol soybean oil preparation was measured at 170, 120, 80 and 70° F. using the Brookfield Viscometer Model DV-II, Spindle #2 (60 rpm for 10 seconds. This viscosity data is presented in Table 1. Table 1 also presents results on soybean salad oil preparations containing 0, 0.1, 0.2, 0.4 and 0.6 weight % policosanol made by similar processes.
- a policosanol preparation from the preceding example containing 1.0% policosanol in soybean oil was used to produce cholesterol lowering regular and light (reduced fat) margarine spreads containing plant stanol esters.
- the formulations are shown in Table 2.
- the oil phase ingredients, liquid soy bean oil (#9196 Ventura) and partially hydrogenated soybean oil (# 9494 Ventura), Canola oil, plant stanol esters, monoglycerides, lecithin and hexaglycerols were blended together in a margarine emulsion tank. The blend was mixed slowly and heated to 160° F. to melt into a clear liquid oil blend.
- the policosanol preparation, butter flavor, vitamins A & D blend and beta-carotene were added and blended into the oil phase.
- the aqueous phase was prepared by blending potassium sorbate, ethylenediaminetetra acetic acid (EDTA), citric acid and salt in the water in an aqueous phase tank or in a stainless steel container. While stirring the oil phase at high speed, about 800 rpm, the aqueous phase was poured slowly into the oil phase to produce the margarine spread emulsion at approximately 130 ⁇ 5° F.
- the margarine was prepared by processing the emulsion through a scrape surface heat exchanger (A-unit) and then through a pin worker (B-unit) and finally through a filler unit. The finished margarine spread was filled into suitable containers.
- the cooling system was adjusted during the processing of the margarine spread emulsion to maintain the temperature of the finished spread at the filler unit at about 40-60° F.
- the margarine spreads processed as indicated exhibited physical and sensory properties characteristic of regular and light margarine spreads.
- TABLE 2 Composition of a Typical Cholesterol-Lowering Margarine Spread Containing Policosanol. Regular Light Margarine Margarine Spread Spread Wt. Pounds Wt.
- Both the regular and light margarine spreads contained approximately 3.5 milligrams of policosanol per 8 gram serving size.
- the policosanol preparation 1.0% policosanol in soybean oil, was used to prepare ranch, French, creamy Italian and thousand island dressings containing plant stanol esters. Table 3 showed the composition of a ranch dressing produced.
- the process for preparing the ranch dressing in the pilot plant involved the following processing steps.
- the preservatives potassium sorbate and sodium benzoate
- EDTA were dissolved in the dressing emulsion tank on a pilot plant size Charlotte Colloid Mill unit.
- KELTROL T xanthan gum and KELCOLOID LVF both from Kelco
- KELTROL T xanthan gum and KELCOLOID LVF both from Kelco
- the gum dispersion was hydrated in the water for 10 minutes using medium speed agitation.
- the oil blend containing stanol esters (if present), CAPROL ET, policosanol oil blend, vitamin E and tocopherol preparation were added slowly to form the dressing emulsion.
- the coarse emulsion produced was then milled through a colloid mill with 0.02′′ gap opening. After the viscosity, titratable acidity, salt and pH were determined and approved, the milled dressing was pumped through a filling unit and bottled.
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Abstract
The present invention provides a method for incorporating long chain alcohols into edible oils. The long chain alcohol/edible oil admixture is then suitable for use in preparation of various foods. The long chain alcohol is added by the introduction of energy and in a preferred embodiment in the absence of surfactants and emulsifiers.
Description
- This application is being concurrently filed with two additional applications. These related applications are entitled Encapsulated Long Chain Alcohols, U.S. Ser. No. yy/yyy,yyy (Attorney Docket MCP-234) and Long Chain Alcohols Admixed in Sterol Compounds, U.S. Ser. No. zz/zzz,zzz (Attorney Docket MCP-235), the contents of these applications incorporated by reference as if set forth in their entirety.
- The present invention describes a method of obtaining uniform distribution of a long chain alcohol or a mixture of such alcohols in a comestible product by dissolving or suspending the long chain alcohol in an edible oil.
- Long chain alcohols are known to have beneficial effects on human health. Researchers have reported that a blend of long chain alcohols obtained from sugar cane wax was effective in lowering serum cholesterol in rats. Sho, H., Chinen, I., and Fukuda, N., J. Nutr. Sci. Vitaminol. 30:553 (1984). In addition, U.S. Pat. No. 5,856,316 discloses the use of a mixture of long chain alcohols from sugar cane wax for lowering serum cholesterol in humans.
- From the above disclosures it is apparent that long chain alcohols have important properties for improving the health of humans and animals. These beneficial properties include improving stamina, lowering blood cholesterol levels, and decreasing platelet aggregation. One desirable route for ingesting these alcohols is in food or beverage products. However, these long chain alcohols are very insoluble in water, and the very small amounts of these long chain alcohols needed to produce beneficial health effects makes content uniformity of long chain alcohols in a dry blending operation very difficult to achieve. Therefore, a means is needed for incorporating these long chain alcohols into food or beverage products in a manner that yields a uniform and consistent distribution of these materials in the comestible product.
- Expensive and difficult measures have been disclosed to overcome these problems. For example, EP 801904 A1, describes the use of long chain alcohols (defined as alcohols having more than 20 carbon atoms) in continuous fat phase compositions containing particulate sweeteners. The incorporation of the long chain alcohols at about 0.1% to about 0.4% was reported to decrease the viscosity of confectionery coatings made with this composition. All of the described compositions contained a particulated sweetener in addition to a chocolate material and a vegetable oil.
- Similarly, WO 98/47385 discloses a fat emulsion with a blend of emulsifiers created by the blending of a partial glyceride with a phospholipid and a long chain alcohol having a chain length of greater than C20. The total weight of the glyceride and phospholipid in the composition must be greater than about 0.02 weight percent.
- Despite the teachings of these disclosures, there is an ongoing need to easily incorporate long chain alcohols into food products so that the advantageous effects of these alcohols can be achieved.
- The present invention provides a method of providing a desirable distribution of long chain alcohols in a food or beverage product. More specifically, this process comprises dissolving or suspending the long chain alcohol in an edible oil, and then incorporating this edible oil into a food or beverage product. In one embodiment the present invention is a method for preparing a long chain alcohol in an edible oil material comprising: providing an edible oil substantially free of medium chain triglycerides composed of C8-C10 triglycerides and less than about 12 weight percent linolenic acid; providing a long chain alcohol; admixing said edible oil and long chain alcohol in the presence of an energy source such that the long chain alcohol is admixed in the oil; said long chain alcohol/edible oil admixture is stable and substantially free of an emulsifier or surfactant and having a viscosity of less than about 200 centipoise as measured at 70° F. at 60 revolutions per minute. A second embodiment of the invention provides the composition made by the method of the invention. In a third embodiment the composition of the present invention is employed to reduce the cholesterol level of a vertebrate that consumes an effective amount of the composition.
- The present invention provides a method for incorporating long chain alcohols into an oil matrix without the need to add emulsifiers, surfactants or penetrant enhancers. The method includes the use of heat or mechanical energy or other suitable energy sources in order to make the long chain alcohols soluble in the lipid matrix. In a preferred embodiment the lipid matrix is an oil, preferably an oil derived from a vegetable source. Suitable oil sources include sunflower, safflower, corn, soybean, canola, mixtures of these oils and the like.
- As used herein, long chain alcohols are understood to include saturated and unsaturated alcohols which contain more than about 90 weight percent C20 or longer, primarily aliphatic alcohol materials. For the greatest health benefit it is preferred that the long chain alcohols be predominately, greater than 50 weight, percent octacosanol (C28), preferably more than 65 percent and more preferably greater than about 70 weight percent. As used herein policosanol is understood to be a mixture of long chain alcohols ranging from C20 to C36 preferably with greater than 65 weight percent C28. Common distribution and concentration ranges of the various components of policosanol are found in U.S. Pat. No. 5,856,316, the contents of which are incorporated by reference as set forth in its entirety. These long chain alcohols are available from various natural sources, most preferably from sugar cane wax. The long chain alcohols can also be synthesized using techniques well known in the art.
- Policosanol is soluble at about 160-180° F. in suitable lipid matrices such as vegetable oils and fat-soluble emulsifiers, vitamins and the like. Suitable methods for incorporating policosanol or other long chain alcohol into the oil, include heating by conventional means such as: heating elements or open flame; radiation sources and other ultrasonic wave generating equipment; as well as mechanical means such as agitation, homogenization, and the like.
- In a preferred embodiment of the present invention, the long chain alcohol is ground into a microcrystalline form in order to improve the stability of the oil/long chain alcohol mixture. Suitable grinding techniques include hammermill, cryogenic rotary mills and the like. The particle size of the ground material is less than about 100 microns, preferably from about 20 to about 80 and most preferably from about 30 to about 60 microns.
- Typically the level of long chain alcohol incorporated into the oil is from about 0.1 to about 5 percent, preferably from about 0.5 to about 3 and most preferably from about 0.8 to about 2 weight percent. Those with skill in the art will appreciate that the concentration of the long chain alcohol will vary depending on various factors such as the dosage desired, the serving size and the solubility of the long chain alcohol in a particular oil.
- One advantage of the present invention is that the long chain alcohol remains stable in the edible oil. As used herein, stable is understood to mean that the long chain alcohol does not precipitate, crystallize out, or separate when dissolved in the edible oil.
- Another advantage of the present invention is that the viscosity of the policosanol-enriched oil is such that the admixture remains suitable for many applications. Unlike other disclosures, the present invention does not have to be made into a high viscosity paste before being incorporated in a comestible. The long chain alcohol/edible oil mixture has a viscosity of less than about 200 centipoise, preferably from about 10 to about 150 and most preferably from 50 to about 130 centipoise. The viscosity is measured at 70° F. using a Brookfield Viscometer Model DV-II+, spindle #2 at 60 revolutions per minute for 10 seconds.
- Once the long chain alcohol has been suspended or dissolved into the oil matrix, those with skill in the art will readily understand how to incorporate the long chain alcohol/oil matrix into food products designed to lower cholesterol. The long chain alcohol/oil preparations can be used as a spray oil for cookies and crackers or can be used to formulate a number of cholesterol lowering food products including salad dressings, mayonnaise dressings, nutrition bars, beverages, juices, low fat ice creams, yogurts and frozen yogurts, non-dairy creamers, cheese spreads, milk products, confectioneries, chocolate-containing products such as cakes and cookies, margarine, and other spreads suitable for application on breads and the like. The long chain alcohol/oil preparations can also be formulated into pharmaceutical preparations, including tablets, soft gelatin capsules, especially those containing liquid formulations, such as suspensions, emulsions, solutions and the like.
- The present invention can be provided in foods in which water is the continuous phase, such as salad dressings and mayonnaise. In a preferred embodiment of the invention the long chain alcohol/edible oil product of the present invention is incorporated into a product which has a continuous oil phase such as spreads and margarines. The long chain alcohol typically comprises from about 0.0001% to about 0.4% of the comestible product, preferably from about 0.007 to about 0.14 and most preferably from about 0.018 to about 0.071 weight percent of the comestible product.
- Typically the level of the long chain alcohol is from 0.1 to about 100 milligrams/servings; preferably from about 0.5 to about 20 milligrams/serving and most preferably from about 2 to about 10 milligrams/servings.
- The present invention provides an edible oil/ long chain alcohol mixture that does not require the incorporation of high levels of linolenic acid in the edible oil as was previously disclosed in the art. Further the present invention does not require the addition of triglycerides, particularly C8-C10 triglycerides; or other surfactants or emulsifiers in order to form the admixture. Because the edible oil/long chain alcohol does not need to incorporate these other agents, the admixture can be more readily formulated into other comestible products. Substantially free as used herein is understood to mean less than 1.0 weight percent, preferably less than 0.5 and most preferably less than 0.1 weight percent.
- The comestible product of the present invention can be used to reduce the cholesterol level of vertebrates that consume the comestible. Vertebrates include reptiles, mammals, fish and the like, with humans being most preferred.
- The following examples are provided as specific embodiments of the present invention. Other modifications of this invention will be readily apparent to those skilled in these arts without departing from the scope of the present invention.
- One percent policosanol in a vegetable oil was prepared by adding 2.0 g policosanol (CHOLESSTANOL (95% pure sugarcane wax material from Garuda International)) to 198.0 g soybean salad oil in a 400-ml PYREX glass beaker. The beaker was placed in a waterbath on a stove. The stove was turned on and the soybean oil/policosanol mixture was stirred gently by hand with a stainless steel spatula. The policosanol/soybean oil dispersion was heated and stirred until policosanol melted and solubilized in the oil at 160-180° F. The viscosity of the policosanol soybean oil preparation was measured at 170, 120, 80 and 70° F. using the Brookfield Viscometer Model DV-II, Spindle #2 (60 rpm for 10 seconds. This viscosity data is presented in Table 1. Table 1 also presents results on soybean salad oil preparations containing 0, 0.1, 0.2, 0.4 and 0.6 weight % policosanol made by similar processes.
- The results showed no significant differences between the viscosities of the samples at 120° F. and also at 176° F. regardless of the policosanol concentration. However, at 80 and 70° F., the viscosities of the samples increased as the concentration of policosanol in the oil samples increased. The samples were stored at room temperature and observed the next day. The policosanol preparations developed translucent gel-like precipitates. After a few days at room temperature, the gel-like materials developed layers and gel-like precipitates. The gel-like precipitates dissolved when the samples were heated to about 180° F.
TABLE 1 Effect of Policosanol Concentration on Viscosity of Soybean Oil % Policosanol Viscosity @ Viscosity @ Viscosity @ Viscosity @ Concentration 176° F. 120° F. 80° F. 70° F. 0 15.0 cP 26.0 cP 43.3 cP 59.5 cP 0.10 14.5 cP 27.0 cP 43.5 cP 64.5 cP 0.20 14.5 cP 28.0 cP 46.5 cP 82.0 cP 0.40 15.0 cP 28.0 cP 49.5 cP 119.0 cP 0.60 15.0 cP 28.0 cP 53.5 cP 112.0 cP 1.00 14.5 cP 28.0 cP 105.0 cP 129.0 cP - A policosanol preparation from the preceding example containing 1.0% policosanol in soybean oil was used to produce cholesterol lowering regular and light (reduced fat) margarine spreads containing plant stanol esters. The formulations are shown in Table 2. The oil phase ingredients, liquid soy bean oil (#9196 Ventura) and partially hydrogenated soybean oil (# 9494 Ventura), Canola oil, plant stanol esters, monoglycerides, lecithin and hexaglycerols were blended together in a margarine emulsion tank. The blend was mixed slowly and heated to 160° F. to melt into a clear liquid oil blend. The policosanol preparation, butter flavor, vitamins A & D blend and beta-carotene were added and blended into the oil phase.
- The aqueous phase was prepared by blending potassium sorbate, ethylenediaminetetra acetic acid (EDTA), citric acid and salt in the water in an aqueous phase tank or in a stainless steel container. While stirring the oil phase at high speed, about 800 rpm, the aqueous phase was poured slowly into the oil phase to produce the margarine spread emulsion at approximately 130±5° F. The margarine was prepared by processing the emulsion through a scrape surface heat exchanger (A-unit) and then through a pin worker (B-unit) and finally through a filler unit. The finished margarine spread was filled into suitable containers. The cooling system was adjusted during the processing of the margarine spread emulsion to maintain the temperature of the finished spread at the filler unit at about 40-60° F. The margarine spreads processed as indicated exhibited physical and sensory properties characteristic of regular and light margarine spreads.
TABLE 2 Composition of a Typical Cholesterol-Lowering Margarine Spread Containing Policosanol. Regular Light Margarine Margarine Spread Spread Wt. Pounds Wt. Pounds Oil Phase Ingredients Liquid Soybean Oil 7.44225 23.64125 Partially Hydrogenated Soybean Oil 11.00000 0 Liquid Canola Oil 30.00000 0 Plant Stanol Esters (Raisio) 21.55000 21.55000 Mono-glycerides 0.30000 0.40000 Lecithin 0.20000 0.30000 Hexaglycerol Distearate, POLYALDO 0.10000 0.10000 6-2-S (Lonza) Hexaglycerol Mixed Esters, 0 0.10000 CAPROL ET (A. C. Humko) Butter Flavor (Firmenich) 0.05000 0.05000 Vitamin A &D Blend (Roche) 0.00625 0.00625 Beta-Carotene 0.00150 0.00250 Policosanol/Oil Blend, (1:99 w/w) 4.35000 4.35000 (CHOLESSTANOL Policosanol from Garuda International) Aqueous Phase Ingredients Water 22.88550 47.38300 Salt 2.00000 2.00000 Citric Acid 0.00750 0.01000 Calcium Disodium EDTA 0.00700 0.00700 Potassium Sorbate 0.10000 0.10000 TOTAL 100.00000 100.00000 - Both the regular and light margarine spreads contained approximately 3.5 milligrams of policosanol per 8 gram serving size.
- The policosanol preparation, 1.0% policosanol in soybean oil, was used to prepare ranch, French, creamy Italian and thousand island dressings containing plant stanol esters. Table 3 showed the composition of a ranch dressing produced. The process for preparing the ranch dressing in the pilot plant involved the following processing steps. The preservatives (potassium sorbate and sodium benzoate) and EDTA were dissolved in the dressing emulsion tank on a pilot plant size Charlotte Colloid Mill unit. KELTROL T xanthan gum and KELCOLOID LVF (both from Kelco) were dispersed in a portion of the soybean oil (one part gums and 2-5 parts oil). The gum dispersion was hydrated in the water for 10 minutes using medium speed agitation. This was followed by blending in the vinegar and lemon juice, sugar, salt, ranch seasonings, buttermilk solids and titanium dioxide. After mixing the blend at high speed for 10 minutes, the polysorbates were melted and added with the liquid egg yolk and mixed for about one minute. The policosanol oil blend was mixed into the salad oil. The stanol esters (if present) and CAPROL ET (A. C. Humko) were added to the soybean salad oil and the mixture was heated to approximately 130° F. to melt and dissolve CAPROL and stanol esters. While mixing the aqueous phase blend at high speed, the oil blend containing stanol esters (if present), CAPROL ET, policosanol oil blend, vitamin E and tocopherol preparation were added slowly to form the dressing emulsion. The coarse emulsion produced was then milled through a colloid mill with 0.02″ gap opening. After the viscosity, titratable acidity, salt and pH were determined and approved, the milled dressing was pumped through a filling unit and bottled.
TABLE 3 Compositions of Typical Cholesterol-Lowering Ranch Dressings Containing Policosanol with or without Stanol Esters Without With Stanol Stanol Esters Ester Weight Weight Ingredient Composition (Pounds) (Pounds) Water 33.0807 36.6479 Vinegar, 120 Grain, White distilled 7.0000 7.0000 Sugar, Fine Granulated 4.9000 4.9000 Ranch Seasoning #139 (Ventura) 4.2000 4.2000 Cultured Buttermilk Solids #64414 1.6000 1.6000 (Armour) Salt 0.7000 0.7000 Calcium Disodium EDTA 0.0060 0.0060 Egg Yolk, Liquid, 10% Salt 0.3600 0.3600 KELTROL T Xanthan Gum (Kelco) 0.3500 0.3500 Polysorbate 60, Tween 60 0.3000 0.3000 Lemon Juice Concentrate, 400 GPL 0.2500 0.2500 KELCOLOID LVF, (Kelco) 0.1750 0.1750 Polysorbate 80, TWEEN 80 0.1600 0.1600 Titanium Dioxide 0.1400 0.1400 Potassium Sorbate 0.0800 0.0800 Sodium Benzoate 0.0800 0.0800 Vitamin E Acetate (Roche) 0.0183 0.0183 Policosanol/soybean oil blend (1:99 1.2000 1.2000 w/w) (CHOLESSTANOL policosanol from Garuda International) DL-Alpha-Tocopherol (Roche) 0.0082 0.0082 Calcium Disodium EDTA 0.0060 0.0060 Paprika Oleoresin 1000 ASTA 0.0019 0.0019 Soybean Oil, Salad Oil 38.8186 41.1967 Stanol Esters (Raisio) 5.9453 0.0000 CAPROL ET (A. C. Humko) 0.6200 0.6200 TOTAL 100.0000 100.0000
Both dressings contained approximately, 3.5 milligram of policosanol per 30 gram serving size.
Claims (4)
1-19. (canceled)
20. A method of reducing cholesterol in vertebrate comprising: providing an effective amount of the comestible product containing high molecular weight alcohols made by a process comprising:
providing a high molecular weight alcohol;
providing an edible oil containing less than about 12 weight percent linolenic acid that is substantially free of medium chain triglycerides composed of C8 to C10 fatty acids;
admixing said high molecular alcohols in said edible oil to form a high molecular weight alcohol/edible oil admixture that contains less than two weight percent high molecular weight alcohol; and combining said admixture with other components to form the comestible product.
21. The method of claim 20 wherein the comestible contains about 0.1 to about 100 milligrams of high molecular weight alcohol per serving size.
22. A method of reducing cholesterol in a vertebrate comprising administering an effective amount of a composition comprising a stable edible oil/long chain alcohol admixture substantially free of an emulsifying or surfactant agent, the edible oil substantially free of medium chain triglycerides composed of C8-C10 triglycerides and containing less than about 10 weight percent linolenic acid
the admixture having a viscosity of less than about 200 centipoise as measured at 70° F.
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|---|---|---|---|---|
| US6355274B1 (en) | 1999-12-15 | 2002-03-12 | Mcneil-Ppc, Inc. | Encapsulated long chain alcohols |
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| US8703209B2 (en) | 2003-06-17 | 2014-04-22 | Edward Larry McCleary | Composition and method for modulating hydrogen ion physiology |
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| US8017153B2 (en) | 2006-02-07 | 2011-09-13 | U.S. Nutraceuticals, LLC | Dietary supplement composition for blood lipid health |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5952393A (en) * | 1998-02-12 | 1999-09-14 | Sorkin, Jr.; Harlan Lee | Composition for reducing serum cholesterol levels |
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-
1999
- 1999-12-15 US US09/461,887 patent/US7232574B1/en not_active Expired - Lifetime
-
2000
- 2000-12-07 NZ NZ519139A patent/NZ519139A/en unknown
- 2000-12-07 NZ NZ508688A patent/NZ508688A/en unknown
- 2000-12-11 AU AU72163/00A patent/AU7216300A/en not_active Abandoned
- 2000-12-14 CA CA002328304A patent/CA2328304A1/en not_active Abandoned
- 2000-12-14 AR ARP000106643A patent/AR026957A1/en unknown
- 2000-12-14 JP JP2000380986A patent/JP2001211827A/en active Pending
- 2000-12-14 MX MXPA00012493A patent/MXPA00012493A/en unknown
- 2000-12-14 EP EP00311174A patent/EP1108363A1/en not_active Withdrawn
- 2000-12-14 NO NO20006369A patent/NO317591B1/en unknown
- 2000-12-14 BR BR0005882-3A patent/BR0005882A/en not_active IP Right Cessation
-
2007
- 2007-06-15 US US11/763,748 patent/US20080021112A1/en not_active Abandoned
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5952393A (en) * | 1998-02-12 | 1999-09-14 | Sorkin, Jr.; Harlan Lee | Composition for reducing serum cholesterol levels |
Also Published As
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| US7232574B1 (en) | 2007-06-19 |
| NO20006369L (en) | 2001-06-18 |
| BR0005882A (en) | 2001-08-21 |
| CA2328304A1 (en) | 2001-06-15 |
| MXPA00012493A (en) | 2004-06-18 |
| NO20006369D0 (en) | 2000-12-14 |
| JP2001211827A (en) | 2001-08-07 |
| AR026957A1 (en) | 2003-03-05 |
| NO317591B1 (en) | 2004-11-15 |
| AU7216300A (en) | 2001-06-21 |
| NZ519139A (en) | 2004-12-24 |
| NZ508688A (en) | 2003-02-28 |
| EP1108363A1 (en) | 2001-06-20 |
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