AU7155100A - Micromilling plant sterols and emulsifiers - Google Patents
Micromilling plant sterols and emulsifiers Download PDFInfo
- Publication number
- AU7155100A AU7155100A AU71551/00A AU7155100A AU7155100A AU 7155100 A AU7155100 A AU 7155100A AU 71551/00 A AU71551/00 A AU 71551/00A AU 7155100 A AU7155100 A AU 7155100A AU 7155100 A AU7155100 A AU 7155100A
- Authority
- AU
- Australia
- Prior art keywords
- emulsifier
- plant sterol
- dispersion
- oil
- percent
- 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.)
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- 235000002378 plant sterols Nutrition 0.000 title claims description 208
- 239000003995 emulsifying agent Substances 0.000 title claims description 205
- 239000006185 dispersion Substances 0.000 claims description 197
- 235000013305 food Nutrition 0.000 claims description 136
- 241000196324 Embryophyta Species 0.000 claims description 121
- 239000000203 mixture Substances 0.000 claims description 112
- 239000008157 edible vegetable oil Substances 0.000 claims description 64
- 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 62
- 239000003921 oil Substances 0.000 claims description 52
- 235000019198 oils Nutrition 0.000 claims description 51
- 239000002245 particle Substances 0.000 claims description 50
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 50
- 238000000034 method Methods 0.000 claims description 45
- 229930182558 Sterol Natural products 0.000 claims description 35
- 150000003432 sterols Chemical class 0.000 claims description 35
- 235000003702 sterols Nutrition 0.000 claims description 35
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 claims description 30
- 150000002148 esters Chemical class 0.000 claims description 28
- 235000010958 polyglycerol polyricinoleate Nutrition 0.000 claims description 26
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical group CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 24
- 229920000223 polyglycerol Polymers 0.000 claims description 24
- 239000002904 solvent Substances 0.000 claims description 23
- 239000000787 lecithin Substances 0.000 claims description 21
- 235000010445 lecithin Nutrition 0.000 claims description 21
- 238000002156 mixing Methods 0.000 claims description 20
- 230000002411 adverse Effects 0.000 claims description 17
- 238000010348 incorporation Methods 0.000 claims description 15
- 235000019519 canola oil Nutrition 0.000 claims description 13
- 239000000828 canola oil Substances 0.000 claims description 13
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 12
- 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 claims description 11
- 235000019197 fats Nutrition 0.000 claims description 11
- 229940067606 lecithin Drugs 0.000 claims description 11
- 108090000623 proteins and genes Proteins 0.000 claims description 11
- 102000004169 proteins and genes Human genes 0.000 claims description 11
- 150000002168 ethanoic acid esters Chemical class 0.000 claims description 10
- 229920000136 polysorbate Polymers 0.000 claims description 10
- ODFAPIRLUPAQCQ-UHFFFAOYSA-M sodium stearoyl lactylate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C([O-])=O ODFAPIRLUPAQCQ-UHFFFAOYSA-M 0.000 claims description 10
- 229940080352 sodium stearoyl lactylate Drugs 0.000 claims description 10
- 150000003445 sucroses Chemical class 0.000 claims description 10
- DNISEZBAYYIQFB-PHDIDXHHSA-N (2r,3r)-2,3-diacetyloxybutanedioic acid Chemical compound CC(=O)O[C@@H](C(O)=O)[C@H](C(O)=O)OC(C)=O DNISEZBAYYIQFB-PHDIDXHHSA-N 0.000 claims description 9
- 229940110456 cocoa butter Drugs 0.000 claims description 9
- 235000019868 cocoa butter Nutrition 0.000 claims description 9
- 229920000728 polyester Polymers 0.000 claims description 8
- 235000019483 Peanut oil Nutrition 0.000 claims description 6
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 6
- 229930006000 Sucrose Natural products 0.000 claims description 6
- 235000014121 butter Nutrition 0.000 claims description 6
- 235000005687 corn oil Nutrition 0.000 claims description 6
- 239000002285 corn oil Substances 0.000 claims description 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- 239000004006 olive oil Substances 0.000 claims description 6
- 235000008390 olive oil Nutrition 0.000 claims description 6
- 239000000312 peanut oil Substances 0.000 claims description 6
- 239000003549 soybean oil Substances 0.000 claims description 6
- 235000012424 soybean oil Nutrition 0.000 claims description 6
- 239000005720 sucrose Substances 0.000 claims description 6
- -1 sucrose fatty acid Chemical class 0.000 claims description 6
- 235000020238 sunflower seed Nutrition 0.000 claims description 6
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 6
- 239000008158 vegetable oil Substances 0.000 claims description 5
- 239000002655 kraft paper Substances 0.000 claims description 2
- 239000003996 polyglycerol polyricinoleate Substances 0.000 claims 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 2
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 claims 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims 1
- 239000011975 tartaric acid Substances 0.000 claims 1
- 235000002906 tartaric acid Nutrition 0.000 claims 1
- 235000013311 vegetables Nutrition 0.000 claims 1
- 235000012000 cholesterol Nutrition 0.000 description 19
- 239000000839 emulsion Substances 0.000 description 17
- 239000003925 fat Substances 0.000 description 17
- 238000002844 melting Methods 0.000 description 16
- 230000008018 melting Effects 0.000 description 16
- 235000013861 fat-free Nutrition 0.000 description 15
- 235000015071 dressings Nutrition 0.000 description 14
- 235000004213 low-fat Nutrition 0.000 description 13
- 239000013078 crystal Substances 0.000 description 10
- 239000012071 phase Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000693 micelle Substances 0.000 description 6
- 239000004533 oil dispersion Substances 0.000 description 6
- 229940068065 phytosterols Drugs 0.000 description 6
- 239000002002 slurry Substances 0.000 description 6
- 244000299461 Theobroma cacao Species 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 5
- 239000008346 aqueous phase Substances 0.000 description 5
- 235000013351 cheese Nutrition 0.000 description 5
- 235000019219 chocolate Nutrition 0.000 description 5
- 235000005911 diet Nutrition 0.000 description 5
- 150000002632 lipids Chemical class 0.000 description 5
- 235000013618 yogurt Nutrition 0.000 description 5
- 229920001214 Polysorbate 60 Polymers 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 4
- 239000003833 bile salt Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000001906 cholesterol absorption Effects 0.000 description 4
- 239000006071 cream Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 235000013336 milk Nutrition 0.000 description 4
- 239000008267 milk Substances 0.000 description 4
- 210000004080 milk Anatomy 0.000 description 4
- 210000004877 mucosa Anatomy 0.000 description 4
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 4
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 4
- 229940113124 polysorbate 60 Drugs 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- 150000003839 salts Chemical group 0.000 description 4
- 239000011324 bead Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 235000013365 dairy product Nutrition 0.000 description 3
- 235000011850 desserts Nutrition 0.000 description 3
- 230000037213 diet Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000265 homogenisation Methods 0.000 description 3
- 210000000936 intestine Anatomy 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 210000002966 serum Anatomy 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000000052 vinegar Substances 0.000 description 3
- 235000021419 vinegar Nutrition 0.000 description 3
- VGSSUFQMXBFFTM-UHFFFAOYSA-N (24R)-24-ethyl-5alpha-cholestane-3beta,5,6beta-triol Natural products C1C(O)C2(O)CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CC)C(C)C)C1(C)CC2 VGSSUFQMXBFFTM-UHFFFAOYSA-N 0.000 description 2
- 235000005979 Citrus limon Nutrition 0.000 description 2
- 244000131522 Citrus pyriformis Species 0.000 description 2
- 108010011756 Milk Proteins Proteins 0.000 description 2
- 102000014171 Milk Proteins Human genes 0.000 description 2
- LGJMUZUPVCAVPU-JFBKYFIKSA-N Sitostanol Natural products O[C@@H]1C[C@H]2[C@@](C)([C@@H]3[C@@H]([C@H]4[C@@](C)([C@@H]([C@@H](CC[C@H](C(C)C)CC)C)CC4)CC3)CC2)CC1 LGJMUZUPVCAVPU-JFBKYFIKSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 230000003143 atherosclerotic effect Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 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 description 2
- 229940093761 bile salts Drugs 0.000 description 2
- 238000007385 chemical modification Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 208000029078 coronary artery disease Diseases 0.000 description 2
- 235000015142 cultured sour cream Nutrition 0.000 description 2
- 235000021185 dessert Nutrition 0.000 description 2
- 230000000378 dietary effect Effects 0.000 description 2
- 235000014505 dips Nutrition 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 210000004347 intestinal mucosa Anatomy 0.000 description 2
- 235000013310 margarine Nutrition 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 239000013081 microcrystal Substances 0.000 description 2
- 235000021239 milk protein Nutrition 0.000 description 2
- 230000002572 peristaltic effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 235000014438 salad dressings Nutrition 0.000 description 2
- 235000015067 sauces Nutrition 0.000 description 2
- 230000007928 solubilization Effects 0.000 description 2
- 238000005063 solubilization Methods 0.000 description 2
- 235000014347 soups Nutrition 0.000 description 2
- 235000013599 spices Nutrition 0.000 description 2
- LGJMUZUPVCAVPU-HRJGVYIJSA-N stigmastanol 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](CC)C(C)C)[C@@]2(C)CC1 LGJMUZUPVCAVPU-HRJGVYIJSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000725 suspension 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
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 208000037260 Atherosclerotic Plaque Diseases 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 208000035150 Hypercholesterolemia Diseases 0.000 description 1
- 238000008214 LDL Cholesterol Methods 0.000 description 1
- 108010055297 Sterol Esterase Proteins 0.000 description 1
- 102000000019 Sterol Esterase Human genes 0.000 description 1
- 108010046377 Whey Proteins Proteins 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 238000002288 cocrystallisation Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001687 destabilization Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 210000002249 digestive system Anatomy 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000000260 hypercholesteremic effect Effects 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000010226 intestinal metabolism Effects 0.000 description 1
- 239000003264 margarine Substances 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 208000010125 myocardial infarction Diseases 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000021590 normal diet Nutrition 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000012053 oil suspension Substances 0.000 description 1
- 238000009928 pasteurization Methods 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 229950005143 sitosterol Drugs 0.000 description 1
- 210000000813 small intestine Anatomy 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 208000037816 tissue injury Diseases 0.000 description 1
- 230000007723 transport mechanism Effects 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 235000021119 whey protein Nutrition 0.000 description 1
- 235000008939 whole milk Nutrition 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
- A23D7/005—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
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/12—Fermented milk preparations; Treatment using microorganisms or enzymes
- A23C9/13—Fermented milk preparations; Treatment using microorganisms or enzymes using additives
-
- 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
- A23D7/0053—Compositions other than spreads
-
- 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
- A23D9/04—Working-up
- A23D9/05—Forming free-flowing pieces
-
- 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Botany (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Edible Oils And Fats (AREA)
- General Preparation And Processing Of Foods (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Description
AUSTRALIA
Patents Act 1990 COMPLETE SPECIFICATION STANDARD PATENT Applicant(s): KRAFT FOODS, INC.
Invention Title: MICROMILLING PLANT STEROLS AND EMULSIFIERS The following statement is a full description of this invention, including the best method of performing it known to me/us: CASE 67034-1 MICROMILLING PLANT STEROLS AND EMULSIFIERS RELATED APPLICATIONS This application is based on, and claims benefit of, United States Provisioral Patent Application Serial Number 60/165/338, filed on November 12, 1999.
FIELD OF THE INVENTION The present invention relates to micromilling of free plant sterols and/or plant stanols in the presence of emulsifiers to provide oil or aqueous suspensions or dispersions which can be used directly in food compositions.
Such oil or aqueous dispersions of plant sterols and/or plant stanols may be used as cholesterol-reducing agents to generate full fat, low-fat, fat-free, and triglyceride-free food products which deliver relatively high levels of the cholesterol-reducing agents.
BACKGROUND OF THE INVENTION 15 Cholesterol has been known for many years to be a component of atherosclerotic plaques. Mounting evidence indicates diets high in cholesterol may increase the levels of cholesterol in the blood which, in turn, increase the risk of atherosclerotic disease and its attendant manifestations of heart attack, stroke and other tissue injuries resulting from atherosclerosis.
20 Cholesterol absorbed from dietary sources is thought to increase the risk of atherosclerotic disease.
Other than avoidance or reduced consumption of high cholesterol foods, measures available without prescription to the general public to reduce the absorption of cholesterol from the diet have met with little success.
Furthermore, in many cases, high serum cholesterol cannot be reduced by lowering dietary cholesterol. However, high cholesterol levels in serum can be lowered effectively by altering the intestinal metabolism of lipids. !nrecent years, it has become known that certain plant sterols and plant stanols such as 1-sitosterol (24-ethyl-5-cholestene-33-ol) and its hydrogenated form (13- Docket 67034 sitostanol (24-ethyl-5a-cholestane-3p-ol) can help lower serum cholesterol by inhibiting cholesterol absorption in the digestive system. Plant stanols are the hydrogenated form of plant sterols. See, "Reduction of Serum Cholesterol With Sito Stanol-Ester Margarine in a Mildly Hypercholesterolemic Population", New England Journal of Medicine, Nov. 16, 1995, pp. 1308- 1312; "Short- Term Administration of Tall Oil Phytosterols Improves Plasma Lipid Profiles in Subjects with Different Cholesterol Levels," Metabolism, Vol.47, No. 6 (June), 1998, pp.751-756; and "Cholesterol-lowering Efficiency of a Sitostanol-containing Phytosterol Mixture with a Prudent Diet in Hyperlipidemic Men," Am. J. Clin. Nutr., 1999, 1144-50.
The use of plant sterols, which are natural components of vegetable fats and oils, in food products is considered safe. Plant sterols themselves are not absorbed or only absorbed in very small amounts from the intestines. A decreased incidence of coronary disease is clearly associated with a decrease in serum cholesterol and, in particular, a decrease in LDL cholesterol. A high serum cholesterol level is one of the most significant indicators of risk of coronary disease. There are a variety of naturally occurring plant sterols which have been reported to have a cholesterolreducing effect, although not all have equivalent action.
Although the mechanism by which plant sterols achieve the effect of lowering serum cholesterol has not been fully elucidated and not wishing to be limited by theory, it is believed that plant sterols interfere with cholesterol absorption by competition-type mechanisms. Cholesterol absorption appears to take place primarily in the proximal third of the small intestine. Cholesterol 25 esters must be converted to their free hydroxyl form by the action of cholesterol esterases before they can be absorbed. The free cholesterol requires bile salts for solubilization and absorption. Bile salts form an aqueous dispersion of micelles in which the cholesterol is solubilized along with phospholipids and hydrolysis products of other dietary lipids. Micelles transport the cholesterol across the hydrophilic barrier (the unstirred water layer) to reach the surface of the intestinal mucosa. At the mucosa, it is thought that the cholesterol dissociates from the micelle and is transported Docket 67034 into the mucosa cells by a process which has not yet been fully defined but may include passive exchange diffusion or by protein-mediated transport.
Plant sterols could interfere with cholesterol absorption by either of, or by both of, the following general mechanisms: competition with cholesterol for absorption into the bile-salt micelles or competition with the transport mechanism into the mucosa cells.
Conventionally, plant sterols have been incorporated into food products by melting a sterol or stanol, incorporating it into an oil phase, and blending the oil phase with other components to result in a plant sterolcontaining food product. However, the plant sterols generally have high melting points about 130-180 0 C) which can result in significant crystallization of the plant sterols within the oil phase of such food products.
Such crystallization results in food products with a gritty and unacceptable texture. This gritty texture is especially detectable when the oil/plant sterol phase is incorporated at high levels in the food product. The high melting points and hydrophobic nature of such plant sterols also makes it difficult to blend such plant sterols with an aqueous phase. Furthermore, actual melting of the plant sterol for incorporation into food products is energy intensive.
Attempts have been made to solve these problems using, for example, chemical modification of the plant sterols. For example, esterification of plant sterols generally results in lowered melting temperatures. Thus, such plant sterol esters generally may be incorporated into food products more readily due to the lower melting points and can provide food products without significant gritty texture.
25 More recently, several different approaches have been used to incorporate plant sterols into food products. For example, copending U.S.
Application Serial No. 09/324,702 (filed June 2, 1999) provides plant sterol and/or plant stanol complexes or blends which are generated by cocrystallization of the plant sterols or plant stanols with one or more emulsifiers. More specifically, the plant sterol-emulsifier complexes were prepared by mixing plant sterol and emulsifier in the ratio of about two parts plant sterol to about one part emulsifier to a ratio of about one part plant Docket 67034 sterol to about two parts emulsifier, adding about 0 to about 80 percent of a triglyceride oil, heating the mixture until it melts, and co-crystallizing the melted mixture to form the plant sterol-emulsifier complex. Such plant sterolemulsifier complexes have melting temperatures at least 30 0 C bel6O that of the plant sterol and can be incorporated into food products without the grittiness normally associated with plant sterols or plant stanols.
European Patent Application EP 0 896 671 A (published February 24, 1999) provides an aqueous dispersion of phytosterols by melting the phytosterols and emulsifiers to form a molten mixture and then dispersing the molten mixture in water using high shear. It was reported "that the step of melting the high melting phytosterols with surfactant prior to dispersion in water with or without surfactant contributes importantly to the ability to prepare a very fine dispersion with the use of high shear mixing or homogenization of the phytosterol or other melting lipid." The phytosterols are reported to have particle sizes of less than 15 microns and preferably less than 10 microns in aqueous dispersions. Such phytosterol dispersions could be incorporated into food products without the grittiness normally associated with phytosterols.
It would be desirable, therefore, to provide additional forms of plant sterols which can be incorporated into food products at relatively high levels without adversely affecting texture or other organoleptic properties. It would also be desirable to provide forms of plant sterols which can more easily be incorporated into food products. It would also be desirable to provide forms of plant sterols which can more easily be incorporated into food products without 25 requiring significant modification of existing food production lines or methods, It would also be desirable to provide methods for preparing such plant sterols without chemical modification of the plant sterol itself. It would also be desirable to provide methods for preparing such plant sterols without heating or melting of the plant sterols. It would also be desirable to provide forms of plant sterols in either aqueous or oil dispersions as desired. The present invention provides such plant sterols and methods for preparing them.
Docket 67034 SUMMARY OF THE INVENTION The present invention relates to full-fat, low-fat, fat-free, and triglyceride-free food products which incorporate plant sterols as cholesterolreducing compounds. The cholesterol-reducing compounds are incorporated into such food products by adding them as oil or aqueous dispersions of micromilled plant sterol and emulsifier mixtures. The micromilled plant sterol and emulsifier blends can be incorporated into full-fat, low-fat, fat-free, and triglyceride-free food products. Methods for making such micromilled plant sterols and food products which incorporate such micromilled plant sterols are also provided. These methods can also be used to prepare oil or aqueous dispersions of high melting lipids The micromilled sterols of this invention can be prepared using sterols, esterified sterols, and mixtures thereof. The invention, however, appears to be used to its greatest advantage when employing non-esterified sterols. The 15 plant sterol esters have relatively lower melting points than the plant sterols themselves and can more readily be dissolved in oil phases. To a large extent, they do not pose significant problems of solubilization and dispersion in food products comprising water-in-oil or oil-in-water emulsions. However, more of the esterified plant sterols by weight are required, in comparison with the free plant sterols, to lower serum cholesterol because the ester portion of the molecule does not appear to be effective in the lowering of serum cholesterol. Thus, the present invention is important as it allows the use of unmodified plant sterols free sterols) in food products in a form micromilled particles) that competes more effectively with cholesterol for 25 absorption by the intestinal mucosa. The present invention can be used, however and if desired, to incorporate higher levels of esterified plant sterols than has generally been possible in the past.
The plant sterol-emulsifier mixtures of the present invention can be prepared by mixing about 75 to about 99.9 percent plant sterol and about 0.1 to about 25 percent emulsifier, dispersing the plant sterol and emulsifier mixture in an aqueous phase or an oil phase, and then micromilling the aqueous or oil phase to provide an aqueous or oil dispersion of the plant Docket 67034 sterol. If desired, the aqueous phase or oil phase can be mixed with the emulsifier followed by addition of the plant sterol; the resulting mixture is then micromilled. When preparing the plant sterol-emulsifier mixtures of this invention using water as the solvent, the emulsifier and plant sterol should be co-micromilled. However, when preparing plant sterol-emulsifier mixtures of this invention using edible oil as the solvent, the emulsifier can be added to the plant sterol/edible oil mixtures either before or after the micromilling step.
It is generally preferred, however, that the emulsifier is present in the oil mixtures during micromilling. Preferably, the average particle size of the micromilled plant sterol/emulsifier dispersion is about 1 to about 40 microns, more preferably about 1 to about 20 microns, and most preferably about 1 to about 10 microns. It is generally preferred that the temperature during micromilling be kept at, close to, or below ambient temperature about to about 50°C, more preferably about 20 to 30°C, and even more preferably about 23 to about 270C for at, close to, or below ambient temperature; and below about 200°C, and more preferably at about 0 to about 150°C for temperatures below ambient). In some cases, micromilling at temperatures below ambient temperatures may provide lower particle sizes. Temperature control, if needed, can be provided using any conventional technique or apparatus coolant jacketed micromilling apparatus, heat exchangers, cooling baths, and the like). Plant sterol-emulsifier dispersions in water or edible oil can be prepared with plant sterols as well as esterified plant sterols.
Preferably the plant sterol-emulsifier dispersions are prepared with the nonesterified plant sterols.
25 For purposes of this invention, "plant sterols" is intended to include both plant sterols and plant stanols; the term "sterols" alone is intended to include only the plant sterols; and the term "stanols" alone is intended to include only the plant stanols. The inherently non-absorbable sterols are not necessarily limited to the conventional plant sterols sterols and stanols) but encompass all nontoxic sterols and like compounds which compete with cholesterol for occupancy in the oil droplets of the bile-salt micelles, according to current theory, thereby promoting crystallization of cholesterol in the -6- Docket 67034 intestine so that it may be excreted without absorption. Furthermore, for purposes of this invention, the term "plant sterols" is intended to include both the non-esterified and the esterified form of any of the plant sterols mentioned herein above.
Due to their small average particle size and large surface to mass ratio, the micromilled plant sterol dispersions of this invention are ideally suited for use as cholesterol-reducing agents. The present invention provides such micromilled plant sterols as either aqueous-based or oil-based dispersions.
The plant sterol-emulsifier dispersions may be added directly to food products. Moreover, such plant sterol-emulsifier dispersions can generally be added to food products without requiring significant modification to either the food products or to the existing production line used for preparing such food products. Indeed, the plant sterol dispersions of this invention can supply at least a portion of the water and/or oil normally used in preparation of the food product. For food products containing both aqueous and oil phases, both aqueous plant sterol dispersion and oil-based plant sterol dispersions can be used if desired. Generally, the amount of bulk water and/or edible oil component added can be adjusted to account for the amounts added in the form of the plant sterol dispersions to maintain the water/oil content in the desired range. The present invention provides plant sterol-containing food products wherein the plant sterol is present in an amount sufficient to reduce serum cholesterol levels in a human consuming such food products. In addition, the present invention provides methods for generating plant sterolemulsifier aqueous or oil dispersions for use in food products. Moreover, the 25 present invention provides food products generated by incorporating the plant .5 sterol-emulsifier dispersions into the food products.
It is, therefore, an object of the present disclosure to provide a plant sterol-emulsifier dispersion suitable for incorporation into food products, said plant sterol-emulsifier dispersion comprising about 20 to about 80 percent of a mixture of plant sterol and emulsifier, and about 20 to about 80 percent of a solvent, wherein the mixture is micromilled at, close to, or below ambient temperatures to form the plant sterol-emulsifier dispersion having an average Docket 67034 particle size of about 1 to about 40 microns, wherein the solvent is water or an edible oil, and wherein the plant sterol-emulsifier dispersion can be incorporated into food products in an amount effective to reduce serum cholesterol levels in a human consuming the food products without 'adversely modifying the texture of the food products. Preferably, the average particle size of the plant sterol in the plant sterol-emulsifier dispersion is about 1 to about 20 microns and, more preferably, about 1 to about 10 microns.
It is another object of the present invention to provide a plant sterolemulsifier dispersion suitable for incorporation into food products, wherein a blend of about 75 to about 99.9 percent plant sterol and about 0.1 to about percent emulsifier is micromilled in water or an edible oil and at, close to, or below ambient temperature to form the plant sterol-emulsifier dispersion having an average particle size of about I to about 40 microns, wherein the plant sterol-emulsifier dispersion can be directly incorporated into food products in an amount effective to reduce serum cholesterol levels in a a human consuming such food products, without adversely modifying the i texture of the food products. Preferably, the average particle size of the plant sterol in the plant sterol-emulsifier dispersion is about 1 to about 20 microns 0 and, more preferably, about 1 to about 10 microns.
It is another object of the present invention to provide a plant sterolemulsifier dispersion suitable for incorporation into food products, said plant sterol-emulsifier dispersion comprising about 0.1 to about 80 percent plant sterol, about 0.1 to about 15 percent emulsifier, and about 20 to about 99 percent edible oil, wherein the plant sterol and the edible oil are micromilled 25 at, close to, or below ambient temperature to form an edible oil dispersion o.
having an average particle size of about 1 to about 40 microns and wherein the emulsifier is then incorporated into the edible oil dispersion to form the plant sterol-emulsifier dispersion; whereby the plant sterol-emulsifier dispersion can be directly incorporated into food products in an amount effective to reduce serum cholesteroQl levels in a buman consuming such food products, without adversely modifying the texture of the food products.
Preferably, the average particle size of the plant sterol in the plant sterol- Docket 67034 emulsifier dispersion is about 1 to about 20 microns and, more preferably, about 1 to about 10 microns.
It is a further object of the present disclosure to provide a method of forming a plant sterol-emulsifier dispersion for use in a food product- said method comprising forming a first mixture of about 75 to about 99.9 percent plant sterol and about 0.1 to about 25 percent emulsifier, mixing the first mixture with water or an edible oil to form a second mixture, and (3) micromilling the second mixture at, close to, or below ambient temperature to form the plant sterol-emulsifier dispersion, wherein the average particle size of the plant sterol-emulsifier dispersion is about 1 to about 40 microns, wherein the plant sterol-emulsifier dispersion can be directly incorporated into the food product in an amount effective to reduce serum cholesterol levels in a human consuming such food product, without adversely modifying the texture of the food product.
It is a further object of the present disclosure to provide a method of forming a plant sterol-emulsifier dispersion for use in a food product, said method comprising forming a mixture of about 0.1 to about 80 percent •plant sterol, about 0.1 to about 15 percent emulsifier, and about 20 to about 99 percent of water or an edible oil and micromilling the mixture at, close 20 to, or below ambient temperature to form the plant sterol-emulsifier dispersion, wherein the average particle size of the plant sterol-emulsifier dispersion is about 1 to about 40 microns, wherein the plant sterol-emulsifier dispersion can be directly incorporated into the food product in an amount effective to reduce serum cholesterol levels in a human consuming such food product, without adversely modifying the texture of the food product.
Still yet another object of the present invention is to provide a food product containing a cholesterol-reducing amount of a plant sterol wherein the plant sterol is incorporated into the food product using a water or edible oil dispersion of plant sterol, wherein the dispersion is prepared by micromilling a mixture of the plant sterol and an emulsifier in water or edible oil at, close to, or below ambient temperature to achieve an average particle size of about 1 to about 40 microns, and wherein the plant sterol dispersion does not Docket 67034 adversely affect the texture of the food product. It is also an object of the present invention to provide a food product containing a cholesterol-reducing amount of a plant sterol wherein the plant sterol is incorporated as a plant sterol-emulsifier dispersion and the plant sterol is in a form that is rdadily available in the intestines to exchange with micellar cholesterol. Plant sterols incorporated into the plant sterol-emulsifier dispersions of this invention, whether aqueous or edible oil dispersions, appear to remain, to a large extent, in a form that can readily be exchanged with micellar cholesterol and can effectively compete for cholesterol either at the micelle or at the mucosa surface.
Still another object of the present invention is to provide a plant sterolemulsifier dispersion suitable for incorporation into a food product, said plant sterol-emulsifier dispersion comprising a dispersion of about 75 to about 99.9 percent plant sterol and about 0.1 to about 25 percent emulsifier, wherein the plant sterol and emulsifier are micromilled in water or the edible oil at, close to, or below ambient temperature to form the plant sterol-emulsifier dispersion, wherein the plant sterol-emulsifier dispersion has an average particle size of about 1 to about 40 microns, and wherein the plant sterolemulsifier dispersion can be incorporated into the food product in an amount o 20 effective to reduce serum cholesterol levels in a human consuming the food product without adversely modifying the texture of the food product.
Another object of the present invention is to provide a method of forming a plant sterol-emulsifier dispersion in water or an edible oil suitable for use in a food product, said method comprising: forming a mixture of a 25 blend of about 75 to about 99.9 percent plant sterol and about 0.1 to about percent emulsifier in an aqueous or oil phase, wherein the mixture includes .i about 1 to about 80 percent of the blend and about 20 to about 99 percent water or edible oil; and micromilling the mixture at, close to, or below ambient temperature to form the plant sterol-emulsifier dispersion, wherein the plant sterol-emulsifier dispersion has an average particle size of about 1 to about 40 microns and wherein the plant sterol-emulsifier dispersion can be incorporated into the food product in an amount effective to reduce serum Docket 67034 cholesterol levels in a human consuming the food product without adversely modifying the texture of the food product. Preferably the mixture includes about 70 to about 90 percent water or edible oil.
These and other objects and advantages of the present inveintion will be apparent to those skilled in the art upon a consideration of the present specification.
DETAILED DESCRIPTION OF THE INVENTION The present invention provides full-fat, low-fat, fat-free, and triglyceride-free food products which incorporate plant sterols as cholesterolreducing compounds. The cholesterol-reducing compounds are incorporated into food products by adding them as micromilled plant sterol dispersions.
These dispersions can be aqueous dispersions or edible oil dispersions. To form the desired aqueous plant sterol dispersions, the plant sterol is mixed with an emulsifier in a water solvent to form a coarse dispersion and then the coarse dispersion is micromilled at, close to, or below ambient temperature to S•form the desired plant sterol dispersion having an average plant sterol particle i size of about 1 to about 40 microns. To form the desired plant sterol oil o..dispersion, the plant sterol is mixed an edible oil solvent to form a coarse dispersion and then the coarse dispersion is micromilled at, close to, or below ambient temperature to form, after the addition of the emulsifier, the desired plant sterol dispersion having an average plant sterol particle size of about 1 to about 40 microns. In preparing such plant sterol oil dispersions, the emulsifier may be added to the coarse dispersion and micromilled with the plant sterol or added to the micromilled plant sterol. Generally, it is preferred 25 that the emulsifier is micromilled with the plant sterol in order to ensure homogenous distribution of the emulsifier. Preferably the average plant sterol particle size is about 1 to about 20 microns, and more preferably about 1 to about 10 microns.
The plant sterol dispersions, whether aqueous. or oil based, can be directly incorporated into full-fat, low-fat, fat-free, and triglyceride-free food products in a cholesterol-reducing amount without imparting gritty texture or -11 Docket 67034 other undesirable organoleptic properties to the resulting food products. Such food products include, but are not limited to, pourable dressings, spoonable dressings, drinks, confections, ice creams, whipped desserts, whipped toppings, frozen dairy foods, dairy products milk, yogurt, cheese, cream cheese; process cheese, and the like), dips, sauces, soups, deserts, dessert toppings, chocolate products, spreads, sour cream products, cream cheese products, and the like. The use of such micromilled plant sterol dispersion (in either water or edible oil systems) allows the incorporation of the plant sterol in food products at a relatively high level without producing a gritty texture.
Moreover, since these dispersions can be water- or edible oil-based, they provide great flexibility in the manufacturing process. Aqueous dispersions of micromilled plant sterols, for example, can be used to produce low-fat or fatfree food products. In most cases, such plant sterol dispersions can be added to the desired food product with only minimal modification to existing food production lines. Although the micromilled plant sterol dispersions of this i invention are mainly intended to be used in food products, they can, of course, also be used in pharmaceutical preparations for their cholesterolreducing effect.
The plant sterol-emulsifier dispersion of this invention can be used in V, 20 full-fat, reduced fat, low-fat, fat-free, or triglyceride-free food products. For purposes of this invention, the term "full-fat" is generally used as it is currently defined by the FDA Standards of Identity. In addition, the term "low-fat" includes "reduced-fat," "light," "low-fat," and "fat-free" as defined by the o Standards of Identity. In addition, for purposes of this invention, "low-fat" also 25 encompasses triglyceride-free products although they are not included in the Standards of Identity. However, the term "fat-free" is intended to include only "fat-free" as defined by the Standards of Identity. In addition, the terms "fullfat", "low-fat" and "fat-free" are intended to include full-fat, low-fat, and fat-free food products that do not fall into the categories defined by the Standards of Identity (as of the time of this disclosure) but deliverto the consumer either full-fat or reduced levels of fat per serving. Furthermore, a composition containing high levels of plant sterols in an aqueous dispersion may be -12- Docket 67034 described as "triglyceride-free" for purposes of this invention even though they may not be termed "fat-free" under the current Standards of Identity.
In one embodiment of the invention, an aqueous plant sterol-emulsifier dispersion suitable for incorporation into food products is provided, w'erein a mixture of a plant sterol and an emulsifier in an aqueous medium is micromilled at, close to, or below ambient temperatures to form the aqueous dispersion having an average particle size of about 1 to about 40 microns. In another embodiment of the invention, an edible oil based plant sterolemulsifier dispersion suitable for incorporation into food products is provided, wherein a mixture of a plant sterol and an emulsifier in an edible oil medium is micromilled at, close to, or below ambient temperatures to form the edible oil based dispersion having an average particle size of about 1 to about microns. In still another embodiment of the invention, an edible oil based plant sterol-emulsifier dispersion suitable for incorporation into food products is provided, wherein a mixture of a plant sterol in an edible oil medium is micromilled at, close to, or below ambient temperatures to form the edible oil based dispersion having an average particle size of about 1 to about o microns, after which the emulsifier is added and blended into the dispersion.
In other words, the edible oil-based dispersion can be prepared by micromilling the plant sterol with the edible oil in the presence or absence of the emulsifier. Where the emulsifier is not present during micromilling, it can be added directly to the plant sterol-edible oil dispersion. Of course, a portion of the emulsifier may be added to the coarse plant sterol dispersion before micromilling and the remainder added after micromilling.
00.6: 25 Generally such plant-sterol emulsifier dispersions comprise a mixture of about 75 to about 99.9 percent plant sterol and about 0.1 to about :".**percent emulsifier in the desired solvent system. Preferably, mixture contains about 90 to about 99.8 percent plant sterol and about 0.2 to about 10 percent emulsifier. The plant sterol and the emulsifier are mixed together to form a mixture in the desired solvent system and then micromilledto achieve the desired average particle size. The plant sterol-emulsifier dispersions can be incorporated into food products to provide an amount of the plant sterol -13- Docket 67034 effective to reduce serum cholesterol levels in a human consuming such food products without adversely modifying the texture of the food products.
In another important embodiment of the invention, a plant sterolemulsifier dispersion comprises about 1 to about 80 percent of a plant sterol/emulsifier blend and about 20 to about 99 percent of a solvent water or edible oil). Preferably, the plant sterol-emulsifier dispersion comprises about 1 to about 60 percent of the plant sterol/emulsifier blend and about 40 to about 99 percent of the solvent water or edible oil). The plant sterol-dispersion generally comprises about 10 to about 30 percent plant sterol/emulsifier blend and about 70 to about 90 percent solvent. Preferably, the plant sterol/emulsifier blend contains about 75 to about 99.9 percent plant sterol and about 0.1 to about 25 percent emulsifier. More preferably, the plant sterol/emulsifier blend about 90 to about 99.8 percent plant sterol and about 0.2 to about 10 percent emulsifier. The plant sterol, the emulsifier, and the solvent are mixed together to form a mixture. The mixture is then micromilled at, close to, or below ambient temperatures to form the desired plant sterol dispersion.
Suitable emulsifiers include propylene glycol monoester, polyglycerol esters, polyglycerol polyricinoleates, lecithin, modified lecithins, lactylated 20 monoglycerides, sodium stearoyl lactylate, citric acid esters, diacetyl tartaric acid monoesters, acetic acid esters of monoglycerides, polyoxyethylene sorbitan esters, sucrose esters, monoglycerides, protein emulsifiers eggs, milk proteins, whey proteins, and the like), and mixtures thereof. The dispersion may be water or oil based. For water- and especially for oil-based 25 dispersions, polyglycerol esters and polyglycerol polyricinoleates are preferred. Suitable edible oils for use in preparing the oil-based dispersions include, for example, vegetable oil, olive oil, corn oil, soybean oil, canola oil, sunflower seed oil, peanut oil, rapeseed oil, sucrose fatty acid polyesters, and the like, as well as mixtures thereof. Other known edible oils may also be used. A single edible oil or mixtures of such edible oils may be used. For purposes of this invention, edible oils also include fats such as cocoa butter, -14- Docket 67034 butter fat, and the like. For use in the present invention, such fats are generally melted before micromilling.
The micromilled plant sterol dispersion can be prepared using any conventional micromilling apparatus. Generally, the plant sterol, eiulsifier, and solvent water or edible oil) are mixed together and then introduced into the micromilling apparatus. The dispersion is formed by micromilling the mixture for a sufficient time to form the desired average particle size. Suitable micromilling techniques and equipment include, for example, ball mills, horizontal media mills, ring mills, colloid mills, and the like. The mixture is micromilled until a dispersion having an average particle size of about 1 to about 40 microns is obtained. Using a horizontal media mill equipped with 1 to 2.5 mm diameter zirconia/silica balls, a suitable dispersion can generally be obtained using a single pass through the mill. Of course, other equipment or parameters can be employed so long as the desired average particle size is 15 obtained in a reasonable time period. Generally, a relatively narrow particle size distribution is preferred so that the number of particles having a diameter greater than about 60 microns is minimized generally such large .°particles should be less than about 10 percent, and preferably less than about 1 percent). The inclusion of significant numbers of such larger particles could 20 result in a "gritty" texture or mouthfeel and may adversely affect emulsion S: stability. If desired, filtering equipment or apparatus could be used to remove such large particles. The micromilling should be carried out either at or close to ambient temperatures about 20 to about 50 0 C, preferably about 20 to 30'C, and more preferably about 23 to about 270C) or below 25 ambient temperatures below about 200C and more preferably at about 0 to about 150C). Preferably temperature control is used during the micromilling process to maintain the temperature within these ranges.
Temperature control is especially important when using oil as the solvent since significantly increased temperatures may increase the amount of plant sterol dissolved in the oil which could later form large undesirable crystals in the food product. Needle-like crystal formation is especially undesirable as they can lead to emulsion destabilization by bridging the oil droplets. It has Docket 67034 been found that certain polyglycerol esters and polyglycerol polyricinoleates Grindsted PGE 55 AK polyglycerol esters and Grindsted PGPR polyglycerol polyricinoleates, both of which are available from Danisco A/S) are especially beneficial in retarding undesirable crystal growth, esp"ecially the needle-like crystal growth, when either water- or oil-based dispersions are incorporated into an emulsion-based food product salad dressings, mayonnaise-type products, margarines, table spreads, and the like).
Although not wished to be limited by theory, it is believed that these specific emulsifiers have the proper hydrophobic-hydrophillic properties that allow them to coat any micro-crystals that may be present and effectively retard their growth, thereby more effectively preventing the formation of needleshaped crystals. Thus, plant-sterol emulsifier dispersions prepared using these emulsifiers provide, when incorporated into emulsion-based food products, an even smoother mouthfeel and texture as well as more stable 15 emulsions.
A wide variety of food products may be generated utilizing the present invention. The food products may range in fat content from full-fat to fat-free or triglyceride-free food products. In recent years, many efforts have been made to reduce the fat content of various foods, such as salad dressing, sour 20 cream and frozen desserts. Using the present invention, if desired, large amounts of plant sterols up to about 12 percent of the total food product) can be incorporated without adversely affecting the texture or other organoleptic properties of the food product. Thus, the plant sterol can be incorporated into food products and, thus, into normal diets, at cholesterol- :o 25 reducing levels. Generally, it is preferred that the plant sterol dispersions are included in food products at levels which provide about 0.5 to about grams plant sterol per serving.
The plant sterol dispersions as provided by the present invention allow the incorporation of the plant sterol into food products at cholesterol-reducing levels while avoiding the grittiness that arises in the use of conventional plant sterol compounds. Thus, the present invention allows the 'use of plant sterols in formulating food products and in amounts which are effective in reducing -16- Docket 67034 the serum cholesterol of humans who consume such food products. The present invention allows the incorporation of cholesterol-reducing amount of plant sterols in a form the plant sterol-emulsifier dispersion) without the gritty textural qualities normally associated with plant sterols. ThuslYthe use of plant sterols in the plant sterol-emulsifier dispersions achieves healthpromoting characteristics, higher levels of plant sterol incorporation, and desirable textural attributes.
Not only are the textural characteristics of the resulting food products improved by use of the plant sterol-emulsifier dispersions of the present invention, the stability of the resulting plant sterol-containing food compositions especially when in the form of an emulsion is also improved with the use of the plant sterol-emulsifier dispersions of the present invention.
Often, plant sterols added alone to an oil-in-water emulsion composition will destabilize the emulsion, as evidenced by the release of free oil. In contrast, 15 the addition of the plant sterol-emulsifier dispersions of this invention results in ready incorporation of the plant sterol into the emulsion, as evidenced by the lack of free oil released upon homogenization or during the normal shelf life. Indeed, greater stability is generally observed if the aqueous sterol slurry or dispersion is added after formation of the desired emulsion after the 20 homogenization step) since such later-added sterol particles do not interfere S: with the initial formation of the oil-in-water emulsions. Both simulated and o: actual shipping test confirm the desired emulsion stability of the micromilled sterol-containing emulsions.
The plant sterol-emulsifier complexes of this invention generally 25 contain about 1 to about 80 percent of a blend of plant sterol and emulsifier and about 20 to about 99 of a solvent system water or an edible oil).
Preferably, the plant sterol-emulsifier complexes of this invention generally contain about 1 to about 60 percent of the blend of plant sterol and emulsifier and about 40 to about 99 of the solvent system water or an edible oil).
More preferably, the solvent system is included at about 70 to 90 percent.
The plant sterol-emulsifier complexes of this invention may be prepared as water dispersions or as oil dispersions. The plant sterol-emulsifier -17- Docket 67034 dispersions and methods to formulate them may be used to generate a variety of full-fat, low-fat, fat-free and triglyceride-free products pourable dressings, spoonable dressings, whipped desserts, whipped toppings, frozen dairy foods, dips, sauces, soups, yogurts, dessert toppings, spread', sour cream products, cream cheese products, chocolate products, and the like.) The examples that follows are intended to further describe and not to limit the invention. All percentages and ratios used in the present specification are by weight, unless otherwise indicated. All references cited in the present specification are incorporated by reference.
Example 1. An emulsifier-plant sterol aqueous dispersion was prepared using plant sterols (melting temperature of about 120-130°C) from Cargill, Incorporated (Minneapolis, Minnesota). Polysorbate 60 (12g) was heated in a microwave oven until clear. The heated Polysorbate 60 was then dispersed in water (3388g) at a temperature of about 70 0 C. Free sterols 15 (600g) were then added and dispersed while maintaining the temperature at about room temperature. The resulting slurry was then pumped (about 180 g/min) through a pilot plant media mill (Model KDL Pilot from Willy A.
Bachofen AG Maschinefabrik, Basel, Switzerland). The mill was loaded at about 85 percent of its volume with 2 mm zirconia-silica beads Les 20 Mirois, Cedex, France) and was operated at its maximum rotational speed.
:o The temperature of the mixture passing through the mill was maintained :l below about 500C. After two passes through the mill, a water dispersion 0: 0. having an average particle size of about 10 microns was obtained. The water dispersion contained about 0.3 percent emulsifier and about 15 percent 25 sterols, with the balance being water.
Example 2. This examples illustrates the use of the plant sterol aqueous dispersion of Example 1 to produce a pourable emulsion dressing containing about 3.3 percent plant sterols (equivalent to about 1g plant sterols per 30g serving). Salt (about 0.37 Ibs) and sugar (about 0.87 Ibs) were added to water (about 8.9 Ibs) with mixing. A separate mixture of xanthan gum (about 35g) and canola oil (about 200g) was prepared and blended to ensure that the gum was well dispersed. The gum/oil slurry was then added to the -18- Docket 67034 water mixture with mixing; mixing was continued for about 3 minutes to allow the gum to hydrate. Polysorbate 60 (about 1.6 Ibs) and additional canola oil (about 2.6 Ibs) were then added with mixing Vinegar (120 grain; 1.6 Ibs) and lemon juice (about 53 g) were added; mixing was continued for at least one minutes. The resulting mixture was then homogenized by passage through a high shear hydroshear device (180 psi backpressure). The resulting oil-inwater emulsion (about 6.2 Ibs) was placed in a Hobart mixture to which an aqueous plant sterol dispersion (about 1.8 Ibs) as prepared in Example 1 was added with agitation. Appropriate spices and/or other additives can then be added; mixing was continued for about 3 minutes. The pourable dressing was dispensed into appropriate bottles and stored under conventional conditions.
The resulting pourable dressing had good storage stability and i organoleptic properties as compared to conventional pourable dressings 15 without gritty or other undesirable textures or mouthfeel. Additionally, the resulting pourable dressing contained plant sterols in amounts reported to be cholesterol reducing.
Example 3. An emulsifier-plant sterol oil dispersion was prepared using plant sterols (melting temperature of about 120-1300C) from Cargill, 20 Incorporated (Minneapolis, Minnesota). Polysorbate 60 (12g) was dispersed in canola oil (3388g) at about 30°C using a mixer equipped with a three bladed stir rod. Free sterols (800g) were then added to the emulsifier oil o*o *mixture with continued stirring at about 30°C to form a slurry. Using a peristaltic pump, the slurry was pumped through a pilot plant media mill 25 (Model KDL Pilot from Willy A. Bachofen AG Maschinefabrik, Basel, Switzerland) at a rate of 180g/min. The mill was loaded at about 85 percent of its volume with 2mm zirconia-silica beads Les Mirois, Cedex, France) and was operated at its maximum rotational speed. The temperature of the mixture passing through the mill was maintained below about 500C.
After two passes through the mill, an oil water dispersion having an average particle size of about 10 microns was obtained. The oil dispersion contained -19- Docket 67034 about 0.3 percent emulsifier and about 20 percent sterols, with the balance being oil.
Example 4. This examples illustrates the use of the plant sterol oil dispersion of Example 3 to produce a pourable emulsion dressing dontaining about 3.3 percent plant sterols (equivalent to aboutlg plant sterols per serving). Salt (about 0.28 Ibs) and sugar (about 0.66 Ibs) were added to water (about 9.7 Ibs) with mixing. A separate mixture of xanthan gum (about 26g) and canola oil (about 200g) was prepared and blended to ensure that the gum was well dispersed. The gum/oil slurry was then added to the water mixture with mixing; mixing was continued for about 3 minutes to allow the gum to hydrate. The emulsifier/plant sterol/oil dispersion from Example 3 was then added to the water containing the hydrated gum. Additional canola oil (about 0.5 Ibs) was then added with mixing Vinegar (120 grain; 1.6 Ibs) and lemon juice (about 53 g) were added; mixing was continued for at least one S 15 minutes. The resulting mixture was then homogenized by passage through a high shear hydroshear device (180 psi backpressure). Appropriate spices and/or other additives can then be added; mixing was continued for about 3 minutes. The pourable dressing was dispensed into appropriate bottles and stored under conventional conditions.
o o 000 20 The resulting pourable dressing had good storage stability and organoleptic properties as compared to conventional pourable dressings without gritty or other undesirable textures or mouthfeel. Additionally, the resulting pourable dressing contained plant sterols in amounts reported to be 0 o 0 0cholesterol reducing Example 5. This example illustrates the use of an aqueous plant sterol-emulsifier dispersion for the preparation of a yogurt product. Plant sterols (about 10 percent) were mixed with 2% whole milk, milk powder (about 2 percent), and gelatin (about 6 percent) and then micromilled at about 300C using essentially the same milling procedure as described in Example 1 to obtain an aqueous plant sterol-emulsifier dispersion having an average particle size of about 10 microns. Milk proteins from the milk provided the Docket 67034 required emulsifiers. About 0.2 liters of the aqueous plant sterol-emulsifier dispersion was mixed with about 1.8 liters of 2% milk and pasteurized using conventional pasteurization conditions. After cooling to room temperature, about 100ml yogurt containing active cultures was stirred into the mi~iure.
The mixture was then held at about 70°F for about 1 hour, stirred, and then held at about 70oF for about an additional 14 hours. The resulting yogurt had good organoleptic properties while providing beneficial plant sterols.
Example 6. A mixture of 30 percent free sterols and 4.2 percent lecithin (Lucas Meyer, Hamburg, German) was dispersed in melted cocoa butter with agitation. The resulting dispersion was fed to a micromill (Model KDL Pilot from Willy A. Bachofen AG Maschinefabrik, Basel, Switzerland) using a peristaltic pump at a rate of 180 g/min. The micromill was filled to about 70 percent volume with 2.0 to 2.5 mm Zirconia beads. The mixture was kept at 50°C during the micromilling process. After two passes, the average S 15 particle size was about 20 microns. The resulting cocoa butter suspension S was thick, creamy, and opaque. The cocoa butter suspension (about percent sterol) was then mixed into a melted and conched chocolate mixture at 50°C and tempered to produce a plant sterol-containing chocolate have mouthfeel and flavor comparable to conventional chocolate products.
Example 7. A plant sterol (25 percent) and canola oil (75 percent) dispersion was micromilled using essentially the same procedure as in Example 3 (except that an emulsifier was not included). The resulting plant o sterol/oil dispersion had an average particle size of about 20 microns.
Various emulsifiers (about 10 percent) in canola oil were incorporated into the 25 plant sterol/oil dispersions with through mixing. An aqueous phase (2 percent salt, 2 percent sugar, and vinegar to adjust the pH to about 3.5) was added to each emulsifier/plant sterol/oil mixture with thorough mixing and then examined using a polarizing microscope to determine to what extent the emulsifiers might retard crystal growth and especially long, needle-like crystal growth. The aqueous phase and plant sterol/oil dispersions were combined at about a 1/1 ratio.
When added at levels of about 0.01 to about 0.75 percent, two emulsifiers Grindsted PGE 55 AK polyglycerol esters and Grindsted -21 Docket 67034 PGPR 90 polyglycerol polyricinoleates, both of which are available from Danisco A/S) gave significantly improved retardation of crystal growth. Other similar emulsifiers, even those having similar HLB values about 2-4) or those of the same chemical type, did not perform as well with regard to prevention of crystal growth and/or increased emulsion stability. Although not wishing to be limited by theory, it is believed that these emulsifiers are able to coat any microcrystals that might form and prevent, or at least significantly retard, further crystal growth.
It is to be understood that a reference herein to a prior art document does not constitute an admission that the document forms part of the common general knowledge in the art in Australia or in any other country.
In the claims which follow and in the preceding description of the invention, except where the context requires otherwise due to express language or necessary implication, the words "comprises" and "comprising" are used in the sense of "includes" and "including", i.e. the features specified may be associated with further features in various embodiments of the invention.
9 o• 2 22
Claims (47)
1. A plant sterol-emulsifier dispersion suitable for incorporation into food products, said plant sterol-emulsifier dispersion comprising a mixture of about 1 to about 80 percent of an plant sterol-emulsifier blend and about to about 99 percent of a solvent, wherein the plant sterol-emulsifier blend comprises about 75 to about 99.9 percent of a plant sterol and about 0.1 to about 25 percent of an emulsifier, wherein the mixture is micromilled at, or close to, or below ambient temperatures to form the plant sterol-emulsifier dispersion having an average particle size of about 1 to about 40 microns, wherein the solvent is water or an edible oil, and wherein the plant sterol- emulsifier dispersion can be incorporated into food products in an amount effective to reduce serum cholesterol levels in a human consuming the food products without adversely modifying the texture of the food products. 99* 9*2. The plant sterol-emulsifier dispersion as defined in claim 1, wherein the mixture comprises about 10 to about 30 percent of the plant sterol- emulsifier blend and about 70 to about 90 percent of the solvent and wherein the plant sterol-emulsifier blend comprises about 90 to about 99.8 percent of the plant sterol and about 0.2 to about 10 percent of the emulsifier.
3. The plant sterol-emulsifier dispersion as defined in claim 1, wherein the solvent is water and the dispersion has an average particle size of about 1 to about 20 microns.
4. The plant sterol-emulsifier dispersion as defined in claim 1, wherein the solvent is the edible oil and the dispersion has an average particle size of about 1 to about 20 microns. The plant sterol-emulsifier dispersion as define d in claim 4, wherein the edible oil is selected from the group consisting of soy bean oil, vegetable -23- Docket 67034 oil, olive oil, corn oil, canola oil, sunflower seed oil, peanut oil, rapeseed oil, sucrose fatty acid polyesters, cocoa butter, butter fat, and mixtures thereof.
6. The plant sterol-emulsifier dispersion as defined in claim wherein the emulsifier is selected from the group consisting of propylene glycol monoester, polyglycerol esters, polyglycerol polyricinoleates, lecithin, modified lecithins, lactylated monoglycerides, sodium stearoyl lactylate, citric acid esters, diacetyl tartaric acid monoesters, acetic acid esters of monoglycerides, polyoxyethylene sorbitan esters, sucrose esters, monoglycerides, protein emulsifiers, and mixtures thereof.
7. The plant sterol-emulsifier dispersion as defined in claim 5, wherein the emulsifier is selected from the group consisting of propylene glycol monoester, polyglycerol esters, polyglycerol polyricinoleates, lecithin, modified lecithins, lactylated monoglycerides, sodium stearoyl lactylate, citric acid esters, diacetyl tartaric acid monoesters, acetic acid esters of monoglycerides, polyoxyethylene sorbitan esters, sucrose esters, monoglycerides, protein emulsifiers, and mixtures thereof. 0***CC
8. The plant sterol-emulsifier dispersion as defined in claim 6, wherein the emulsifier is a polyglycerol ester or a polyglycerol polyricinoleate.
9. The plant sterol-emulsifier dispersion as defined in claim 7, wherein the emulsifier is a polyglycerol ester or a polyglycerol polyricinoleate. 0 l
10. The plant sterol-emulsifier dispersion as defined in claim 1, S* wherein the plant sterol is a sterol.
11. The plant sterol-emulsifier dispersion as defined in claim 1, wherein the plant sterol is a stanol.
12. The plant sterol-emulsifier dispersion as defined in claim 1, wherein the plant sterol is a mixture of a sterol and a stanol. -24- Docket 67034
13. A method of forming a plant sterol-emulsifier dispersion for use in a food product, said method comprising forming a first mixture of about to about 99.9 percent of a plant sterol and about 0.1 to about 25 percent of an emulsifier, mixing the first mixture with water or an edible oil to form a second mixture, and micromilling the second mixture at, or close to, or below ambient temperature to form the plant sterol-emulsifier dispersion, wherein the average particle size of the plant sterol-emulsifier dispersion is about 1 to about 40 microns, wherein the plant sterol-emulsifier dispersion can be directly incorporated into the food product in an amount effective to reduce serum cholesterol levels in a human consuming such food product, without adversely modifying the texture of the food product.
14. The method as defined in claim 13, wherein the first mixture contains about 90 to about 99.8 percent of the plant sterol and about 0.2 to about 10 percent of the emulsifier and wherein the second mixture contains about 1 to about 80 percent of the first mixture and about 20 to about 99 percent of the solvent. *5.16. S.. The method as defined in claim 13, wherein the second mixture is formed using water and the dispersion has an average particle size of about 1 to about 20 microns. *ooo
16. The method as defined in claim 13, wherein the second mixture is formed using the edible oil and the dispersion has an average particle size of •about 1 to about 20 microns.
17. The method as defined in claim 16, wherein the edible oil is selected from the group consisting of soy bean oil, vegetable oil, olive oil, corn oil, canola oil, sunflower seed oil, peanut oil, rapeseed oil, sucrose fatty acid polyesters, cocoa butter, butter fat, and mixtures thereof.
18. The method as defined in claim 14, wherein the emulsifie' is selected from the group consisting of propylene glycol monoester, polyglycerol esters, polyglycerol polyricinoleates, lecithin, modified lecithins, Docket 67034 lactylated monoglycerides, sodium stearoyl lactylate, citric acid esters, diacetyl tartaric acid monoesters, acetic acid esters of monoglycerides, polyoxyethylene sorbitan esters, sucrose esters, monoglycerides, protein emulsifiers, and mixtures thereof.
19. The method as defined in claim 17, wherein the emulsifier is selected from the group consisting of propylene glycol monoester, polyglycerol esters, polyglycerol polyricinoleates, lecithin, modified lecithins, lactylated monoglycerides, sodium stearoyl lactylate, citric acid esters, diacetyl tartaric acid monoesters, acetic acid esters of monoglycerides, polyoxyethylene sorbitan esters, sucrose esters, monoglycerides, protein emulsifiers, and mixtures thereof. The method as defined in claim 18, wherein the emulsifier is a polyglycerol ester or a polyglycerol polyricinoleate. 0O
21. The method as defined in claim 19, wherein the emulsifier is a polyglycerol ester or a polyglycerol polyricinoleate. 6
22. The method as defined in claim 13, wherein the plant sterol is a sterol.
23. The method as defined in claim 13, wherein the plant sterol is a o** stanol. 23. The method as defined in claim 13, wherein the plant sterol is a mixture of a sterol and a stanol. A food product containing a cholesterol-reducing amount of a plant 0
24. The method as defined in claim 13, wherein the plant sterol is a mixture of a sterol and a stanol. A food product containing a cholesterol-reducing amount of a plant sterol wherein the plant sterol is incorporated into the food product using a water or edible oil dispersion of a mixture of a plant sterol and an emulsifier, wherein the dispersion is prepared by micromilling,a mixture.of about 75 to about 99.9 percent plant sterol and about 0.1 to about 25 percent of the emulsifier in water or the edible oil and at a temperature at, close to, or below 26 Docket 67034 ambient temperature, wherein the dispersion has an average particle size of about 1 to about 40 microns, and wherein the dispersion does not adversely affect the texture of the food product.
26. The food product as defined in claim 25, wherein the dispersion is a water dispersion and the dispersion has an average particle size of about 1 to about 20 microns.
27. The food product as defined in claim 25, wherein the dispersion is an edible oil dispersion and the dispersion has an average particle size of about 1 to about 20 microns.
28. The food product as defined in claim 27, wherein the edible oil is selected from the group consisting of soy bean oil, vegetable oil, olive oil, corn oil, canola oil, sunflower seed oil, peanut oil, rapeseed oil, sucrose fatty acid polyesters, cocoa butter, butter fat, and mixtures thereof.
29. The food product as defined in claim 27, wherein the emulsifier is selected from the group consisting of propylene glycol monoester, polyglycerol esters, polyglycerol polyricinoleates, lecithin, modified lecithins, lactylated monoglycerides, sodium stearoyl lactylate, citric acid esters, diacetyl tartaric acid monoesters, acetic acid esters of monoglycerides, polyoxyethylene sorbitan esters, sucrose esters, monoglycerides, protein emulsifiers, and mixtures thereof
30. The food product as defined in claim 28, wherein the emulsifier is e selected from the group consisting of propylene glycol monoester, *polyglycerol esters, polyglycerol polyricinoleates, lecithin, modified lecithins, lactylated monoglycerides, sodium stearoyl lactylate, citric acid esters, diacetyl tartaric acid monoesters, acetic acid esters of monoglycerides, polyoxyethylene sorbitan esters, sucrose esters, monoglycerides, protein emulsifiers, and mixtures thereof. -27- Docket 67034
31. The food product as defined in claim 29, wherein the emulsifier is a polyglycerol ester or a polyglycerol polyricinoleate.
32. The food product dispersion as defined in claim 30, wherein the emulsifier is a polyglycerol ester or a polyglycerol polyricinoleate.
33. The food product as defined in claim 25, wherein the plant sterol is a sterol.
34. The food product as defined in claim 25, wherein the plant sterol is a stanol. The food product as defined in claim 25, wherein the plant sterol is a mixture of a sterol and a stanol.
36. The food product as defined in claim 25, wherein the mixture contains about 90 to about 99.8 percent of the plant sterol and about 0.2 to :i about 10 percent of the emulsifier and wherein water or edible oil dispersion contains about 1 to about 80 percent of the mixture and about 20 to about 99 percent of the water or edible oil.
37. The food product as defined in claim 36, wherein water or edible oil dispersion contains about 10 to about 30 percent of the mixture and about 70 to about 90 percent of the water or edible oil.
38. A plant sterol-emulsifier dispersion suitable for incorporation into food products, said plant sterol-emulsifier dispersion comprising about 0.1 to about 80 percent plant sterol, about 0.1 to about 15 percent emulsifier, and about 20 to about 99 percent edible oil, wherein the plant sterol and the edible oil are micromilled at, close to, or below ambient temperature to form an edible oil dispersion having an average particle size of about 1 to about microns and wherein the emulsifier is then incorporated into the,edible oil dispersion to form the plant sterol-emulsifier dispersion; whereby the plant sterol-emulsifier dispersion can be directly incorporated into food products in -28 Docket 67034 an amount effective to reduce serum cholesterol levels in a human consuming such food products, without adversely modifying the texture of the food products.
39. The plant sterol-emulsifier dispersion as defined in claim 38, wherein the dispersion has an average particle size of about 1 to about microns. The plant sterol-emulsifier dispersion as defined in claim 38, wherein the edible oil is selected from the group consisting of soy bean oil, vegetable oil, olive oil, corn oil, canola oil, sunflower seed oil, peanut oil, rapeseed oil, sucrose fatty acid polyesters, cocoa butter, butter fat, and mixtures thereof.
41. The plant sterol-emulsifier dispersion as defined in claim 38, wherein the emulsifier is selected from the group consisting of propylene :glycol monoester, polyglycerol esters, polyglycerol polyricinoleates, lecithin, modified lecithins, lactylated monoglycerides, sodium stearoyl lactylate, citric acid esters, diacetyl tartaric acid monoesters, acetic acid esters of monoglycerides, polyoxyethylene sorbitan esters, sucrose esters, monoglycerides, protein emulsifiers, and mixtures thereof.
42. The plant sterol-emulsifier dispersion as defined in claim wherein the emulsifier is selected from the group consisting of propylene l* *o glycol monoester, polyglycerol esters, polyglycerol polyricinoleates, lecithin, modified lecithins, lactylated monoglycerides, sodium stearoyl lactylate, citric acid esters, diacetyl tartaric acid monoesters, acetic acid esters of monoglycerides, polyoxyethylene sorbitan esters, sucrose esters, monoglycerides, protein emulsifiers, and mixtures thereof.
43. The plant sterol-emulsifier dispersion as defined in claim 41, wherein the emulsifier is a polyglycerol ester or a polyglycerol polyricinoleate. S' -29- Docket 67034
44. The plant sterol-emulsifier dispersion as defined in claim 42, wherein the emulsifier is a polyglycerol ester or a polyglycerol polyricinoleate. The plant sterol-emulsifier dispersion as defined in clairfi'38, wherein the plant sterol is a sterol.
46. The plant sterol-emulsifier dispersion as defined in claim 38, wherein the plant sterol is a stanol.
47. The plant sterol-emulsifier dispersion as defined in claim 38, wherein the plant sterol is a mixture of a sterol and a stanol.
48. A method of forming a plant sterol-emulsifier dispersion for use in a food product, said method comprising micromilling a plant sterol in an edible oil at, close to, or below ambient temperature to form a plant sterol dispersion, wherein the average particle size of the plant sterol dispersion is about 1 to about 40 microns; and incorporating an emulsifier into the plant sterol dispersion to form the plant sterol-emulsifier dispersion, wherein the plant sterol-emulsifier dispersion contains about 0.1 to about 80 percent plant sterol, about 0.1 to about 15 percent emulsifier, and about 20 to about 99 percent edible oil and wherein the plant sterol-emulsifier dispersion can be directly incorporated into the food product in an amount effective to reduce serum cholesterol levels in a human consuming such food product, without adversely modifying the texture of the food product.
49. The method as defined in claim 48, wherein average particle size of the plant sterol dispersion is about 1 to about 20 microns. The method as defined in claim 48, wherein the edible oil is selected from the group consisting of soy bean oil, vegetable oil, olive oil, corn oil, canola oil, sunflower seed oil, peanut oil, rapeseed oil, sucrose fatty acid polyesters, cocoa butter, butter fat, and mixtures thereof. Docket 67034
51. The method as defined in claim 50, wherein the emulsifier is selected from the group consisting of propylene glycol monoester, polyglycerol esters, polyglycerol polyricinoleates, lecithin, modified lecithins, lactylated monoglycerides, sodium stearoyl lactylate, citric acid estdrs, diacetyl.tartaric acid monoesters, acetic acid esters of monoglycerides, polyoxyethylene sorbitan esters, sucrose esters, monoglycerides, protein emulsifiers, and mixtures thereof.
52. The method as defined in claim 50, wherein the emulsifier is a polyglycerol ester or a polyglycerol polyricinoleate.
53. The method as defined in claim 51, wherein the emulsifier is a polyglycerol ester or a polyglycerol polyricinoleate.
54. The method as defined in claim 51, wherein the plant sterol is a sterol.
55. The method as defined in claim 51, wherein the plant sterol is a S• stanol.
56. The plant sterol-emulsifier dispersion as defined in claim 51, wherein the plant sterol is a mixture of a sterol and a stanol. KRAFT FOODS, INC. ateBy its Patent Attorneys GRIFFITH HACK -31
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16533899P | 1999-11-12 | 1999-11-12 | |
| US60/165338 | 1999-11-12 | ||
| US09/543946 | 2000-04-06 | ||
| US09/543,946 US6391370B1 (en) | 1999-11-12 | 2000-04-06 | Micromilling plant sterols and emulsifiers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU7155100A true AU7155100A (en) | 2001-05-17 |
| AU779365B2 AU779365B2 (en) | 2005-01-20 |
Family
ID=26861300
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU71551/00A Ceased AU779365B2 (en) | 1999-11-12 | 2000-11-10 | Micromilling plant sterols and emulsifiers |
Country Status (2)
| Country | Link |
|---|---|
| AU (1) | AU779365B2 (en) |
| CA (1) | CA2325336C (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0118225D0 (en) * | 2001-07-26 | 2001-09-19 | Nestle Sa | Milk product comprising unesterfied sterol |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4195084A (en) * | 1977-01-07 | 1980-03-25 | Eli Lilly And Company | Taste-stable aqueous pharmaceutical suspension of tall oil sitosterols and a method for the preparation thereof |
| US6423363B1 (en) * | 1997-08-22 | 2002-07-23 | Lipton, Division Of Conopco, Inc. | Aqueous dispersion |
| CA2334449A1 (en) * | 1998-06-05 | 1999-12-16 | Radka K. Milanova | Compositions comprising phytosterol, phytostanol or mixtures of both having enhanced solubility and dispersability and incorporation thereof into foods, beverages, pharmaceuticals, nutraceuticals and the like |
-
2000
- 2000-11-09 CA CA002325336A patent/CA2325336C/en not_active Expired - Fee Related
- 2000-11-10 AU AU71551/00A patent/AU779365B2/en not_active Ceased
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| Publication number | Publication date |
|---|---|
| CA2325336A1 (en) | 2001-05-12 |
| CA2325336C (en) | 2004-10-05 |
| AU779365B2 (en) | 2005-01-20 |
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