WO2001013733A1 - Fat or oil composition - Google Patents
Fat or oil composition Download PDFInfo
- Publication number
- WO2001013733A1 WO2001013733A1 PCT/JP2000/005633 JP0005633W WO0113733A1 WO 2001013733 A1 WO2001013733 A1 WO 2001013733A1 JP 0005633 W JP0005633 W JP 0005633W WO 0113733 A1 WO0113733 A1 WO 0113733A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fat
- oil
- amount
- oil composition
- fatty acid
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings, cooking oils
- A23D9/007—Other edible oils or fats, e.g. shortenings, 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, COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings, cooking oils
- A23D9/007—Other edible oils or fats, e.g. shortenings, cooking oils characterised by ingredients other than fatty acid triglycerides
- A23D9/013—Other fatty acid esters, e.g. phosphatides
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- 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 COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
- A23L33/11—Plant sterols or derivatives thereof, e.g. phytosterols
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/115—Fatty acids or derivatives thereof; Fats or oils
- A23L33/12—Fatty acids or derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
- A61K31/201—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having one or two double bonds, e.g. oleic, linoleic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
- A61K31/202—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having three or more double bonds, e.g. linolenic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/575—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of three or more carbon atoms, e.g. cholane, cholestane, ergosterol, sitosterol
Definitions
- the present invention relates to a fat or oil composition capable of reducing arteriosclerotic factors in blood when taken, similarly to a usual fat or oil, in the daily life.
- BACKGROUND ART Arteriosclerosis is a risk factor of various circulatory diseases such as hypertension and thrombosis. Arteriosclerosis is caused by hypercholesterolemia, formation of thrombus or the like. The state of a high total cholesterol level is generally called hypercholesterolemia. The cholesterol in blood is classified into HDL, LDL, VLDL and the like by specific gravity. Among them, LDL is a principal risk factor of arteriosclerosis, while HDL is said to be useful for the prevention of arteriosclerosis. It is therefore important to increase the HDL cholesterol level in blood for the prevention of arteriosclerosis.
- PAI-1 plasminogen activator inhibitor type 1
- arteriosclerosis prevention by the daily dietary control is more important than treatment. There is accordingly a demand for a substance which can be taken easily in the daily life and at the same time, can reduce the above-described arteriosclerotic factor.
- a fat or oil composition which comprises at least 35 wt .
- % of a diacylglycerol the constituent fatty acids of said diacylglycerol satisfying the following equation: (an amount of a cis-form unsaturated fatty acid) / (an amount of a saturated fatty acid + an amount of a trans-form unsaturated fatty acid) > 6, wherein the amount of the trans-form unsaturated acid is not greater than 5 wt . % based on the constituent fatty acids of said diacylglycerol.
- a fat or oil processed food comprising the above-described fat or oil composition.
- an HDL-cholesterol-level elevating agent and PAI-1-activity lowering agent each comprising the above-described fat or oil composition.
- a method for elevating the HDL cholesterol level in blood and a method for lowering the activity of PAI-1 each of which comprises administering the above-described fat or oil composition.
- Intake of the fat or oil composition of the present invention usually as an edible oil makes it possible to reduce the blood level of an arteriosclerotic factor, leading to the prevention of arteriosclerosis and furthermore, various geriatric diseases.
- the fat or oil composition according to the present invention contains at least 35 wt . % (which will hereinafter be indicated simply as "%") of a diacylglycerol.
- the diacylglycerol content is preferably at least 50%, with at least 60% being more preferred and with at least 80% being particularly preferred.
- the constituent fatty acids of the diacylglycerol contained in the fat or oil composition of the present invention satisfy the following equation: (an amount of a cis-form unsaturated fatty acid) / (an amount of a saturated fatty acid + an amount of a trans-form unsaturated fatty acid) > 6.
- this weight ratio of [ (cis) / (trans + saturated) ] is less than 6, the HDL cholesterol elevating effects and PAI-1 lowering effects both lower.
- the weight ratio of [(cis) / (trans + saturated) ] is preferably at least 8 and more preferably at least 9.
- the amount of the trans-form unsaturated fatty acid not greater than 5% is particularly preferred and also the amount of the saturated fatty acid not greater than 5% is particularly preferred, each based on the amount of the constituent fatty acids of the diacylglycerol.
- the weight ratio of [(cis) / (trans + saturated)] is preferably less than 20, with the most preferred weight ratio being 9.4 to 19.1.
- the cis-form unsaturated fatty acid include oleic acid, ⁇ -linoleic acid, ⁇ -linolenic acid, cis-dihomo-
- trans-form unsaturated fatty acid means an unsaturated fatty acid having, in the molecule thereof, at least one trans-form double bond.
- saturated fatty acids include palmitic acid, stearic acid and arachic acid.
- Fatty acids having 8 to 24 carbon atoms are preferred, with those having 16 to 22 carbon atoms being particularly preferred.
- a phytosterol is a component having effects for lowering the cholesterol level and is contained in the conventional plant oil in an amount of about 0.05 to 1.2%. With a view to obtaining the cholesterol lowering effects equivalent to those of such a plant oil, the content of phytosterol is preferably at least 0.05%, with at least
- the phytosterol content in the fat or oil composition containing a diacylglycerol differs depending on the preparation process of the composition.
- a commercially available fatty acid obtained by distillation is used as a raw material, the phytosterol content in the composition inevitably lowers. In such a case, it is preferred to add a phytosterol to give an amount of 0.05% or greater.
- No particular limitation is imposed on the upper limit of the phytosterol content.
- the phytosterol content falling within a range of 0.05 to 1.2% is sufficient.
- at least 1.2% of phytosterol can be added.
- the phytosterol include phytosterols in the free form such as ⁇ -sitosterol,
- ⁇ -sitosterol stigmasterol, campesterol, ⁇ -sitostanol , ⁇ - sitostanol, stigmastanol, campestanol and cycloartenol and esters thereof such as fatty acid esters, ferulic acid esters, and cinnamic acid esters.
- the other components contained in the fat or oil composition of the present invention are a triacyl glycerol and a monoacyl glycerol.
- the monoacyl glycerol content not greater than 2%, particularly not greater than 1.5% is preferred. Most of the remaining part is composed of a triacyl glycerol.
- the fat or oil composition according to the present invention can be prepared, for example, by subjecting fat or oil containing desired constituent fatty acids and glycerin to transesterification; or by acting lipase on a mixture of desired constituent fatty acids or ester thereof with glycerin, thereby carrying out esterification .
- the esterification using lipase is preferred for preventing isomerization during the reaction. Even in the esterification by using lipase, with a view to preventing isomerization upon purification after completion of the reaction, it is preferred to carry the purification under conditions mild enough not to cause isomerization of the fatty acids.
- a component contained in the conventional fat or oil composition for example, an antioxidant such as tocopherol, ascorbyl palmitate, ascorbyl stearate, BHT, BHA or phospholipid and/or emulsifier such as sucrose fatty acid ester, polyglycerin fatty acid ester or organic acid monoglyceride .
- an antioxidant such as tocopherol, ascorbyl palmitate, ascorbyl stearate, BHT, BHA or phospholipid and/or emulsifier such as sucrose fatty acid ester, polyglycerin fatty acid ester or organic acid monoglyceride .
- the fat or oil composition according to the present invention has HDL cholesterol elevating action and PAI-1 lowering action.
- the use of a diacylglycerol ordinarily causes an increase in the melting point compared with the use of a triacyl glycerol composed of the same fatty acids
- the fat or oil composition according to the present invention is able to have a liquid form at room temperature, which brings about an advantage that it is usable widely as an edible oil.
- the fat or oil composition according to the present invention can therefore be used suitably as a cooking oil.
- processed foods such as potato chips, snacks, cakes, cookies, pies, bread or chocolates; bakery mix; processed meat products; frozen entree; frozen foods; or the like.
- the amount of the fat or oil (total amount of edible oil and diacylglycerol) in the food is 3 to 95% and the amount of phytosterol is at least 0.05% based on the total amount of the fat or oil.
- the diacylglycerol content in the fat or oil is at least 35%, more preferably at least 50%.
- fat or oil processed food as used herein means a processed food obtained by adding, to the above- described fat or oil composition, the other food raw materials.
- the following raw materials are usable as components for the fat or oil processed food.
- edible fat or oil used in the present invention is a commonly used edible fat or oil.
- examples include natural animal or vegetable fats or oils; and processed fats or oils obtained by subjecting them to transesterification, hydrogenation, fractionation or the like.
- Preferred examples include vegetable oils such as soybean oil, rapeseed oil, rice bran oil, corn oil, sunflower oil, palm oil, palm kernel oil and coconut oil; and processed fats or oils thereof.
- the emulsifier insofar as it is commonly used for food.
- examples include sucrose fatty acid esters, sorbitan fatty acid esters, glycerin fatty acid esters, lecithin and decomposed product thereof; and proteins such as egg protein, soybean protein and milk protein and various proteins available therefrom by separation or hydrolysis.
- thickener insofar as it is commonly used for food.
- examples include xanthan gum, gellan gum, guar gum, carrageenan, pectin, tragacanth gum, polysaccharides such as various starches and proteins such as gelatin and albumen .
- seasonings such as salt, sugar and vinegar.
- Antioxidants such as tocopherol and natural antioxidant components .
- Acidic oil-in-water type fat or oil processed food • oil phase / water phase : 20/80 to 80/20 • amount of diacylglycerol: at least 35% (preferably at least 50%) based on the amount of the fat or oil in the oil phase
- amount of phytosterol at least 0.05% based on the amount of the fat or oil in the oil phase
- amount of emulsifier 0.05 to 5%
- the pH is adjusted by an organic acid such as citric acid or salt thereof, or an acidifier such as lemon juice.
- an organic acid such as citric acid or salt thereof
- an acidifier such as lemon juice.
- oil phase / water phase 90/10 to 10/90 (preferably 85/15 to 50/50) • amount of diacylglycerol: at least 35% (preferably at least 50%) based on the amount of the fat or oil in the oil phase
- amount of phytosterol at least 0.05% based on the amount of the fat or oil in the oil phase • melting point of the fat or oil in the oil phase: 20 to 50°C (preferably 20 to 40°C).
- amount of diacylglycerol at least 35% (preferably at least 50%) relative to the amount of the fat or oil
- baking powder 0 to 1% From the above-described materials, various baked cakes such as short bread which have HDL elevating effects and PAI-1 lowering effects can be prepared in a conventional manner.
- Short bread Flour 60 parts by weight
- Example 1 The fatty acid obtained by hydrolysis of a commercially available soybean oil having a trans fatty acid content of 0.8% was winterized to reduce the content of the saturated fatty acid. The resulting fatty acid was reacted with glycerin at 40°C in the presence of a commercially available immobilized 1,3-specific lipase ("Lipozyme 3A"; product of Novo Nordisk A/S) as a catalyst. After the lipase preparation was filtered off, the residue was subjected to molecular distillation, followed by purification in a conventional manner, whereby a fat or oil composition A was obtained.
- Lipozyme 3A immobilized 1,3-specific lipase
- a fat or oil composition C was obtained by mixing the fat or oil composition A and fat or oil composition B at a ratio of 7:3.
- a fat or oil composition D was obtained by mixing the fat or oil composition A and a commercially available soybean oil at a ratio of 6:4. Comparative Example 1
- the fatty acid obtained by hydrolysis of a commercially available rapeseed oil having a trans fatty acid content of 2.8% was reacted with glycerin at 40°C in the presence of a commercially available immobilized 1,3- specific lipase as a catalyst. After the lipase preparation was filtered off, the residue was subjected to molecular distillation, followed by purification in a conventional manner, whereby a fat or oil composition F was obtained.
- the glyceride composition and constituent fatty acids of the diacylglycerol of each of the fat or oil compositions obtained in Examples 1 to 4 and Comparative Examples 1 and 2, and a soybean oil (Comparative Example 3) are shown in Tables 1 and 2. [Measurement of glyceride distribution]
- each of the fat or oil compositions was silylated by a silylating agent ("silylating agent TH", product of Kanto Chemical), followed by analysis through gas chromatography by using a capillary column ("DBTM-1", trade name; product of J&W Scientific Incorporated) .
- silylating agent TH product of Kanto Chemical
- DBTM-1 capillary column
- Diacylglycerol fractions in each of the fat or oil compositions were collected by column chromatogram [after the removal of the triglyceride fractions by using "Wakogel C-200" (product of Wako Pure Chemicals Co., Ltd.) and hexane, diacylglycerol fractions were obtained using a 70:30 mixed solvent of hexane and ether]. After methyl- esterification in a conventional manner, analysis was carried out by gas chromatography with a capillary column ("CP-SIL88", trade name; product of Chrompack International BV) .
- CP-SIL88 capillary column
- each of the fat or oil compositions was used for three months. Daily intake of it was 12.5 g. Male and female adults, 10 in total, whose total cholesterol level tended to be high were tested. Effects, on the total cholesterol level and HDL cholesterol level, of each of the fat or oil compositions obtained in Examples and Comparative Examples are shown in Table 3. The effects are indicated by a value relative to the initial value set at 100. In each group, no change was observed from the total cholesterol level before the test to that after the test.
- each of the fat or oil compositions was used for three months. Daily intake of it was 12.5 g. Male and female adults, 8 in total, whose total cholesterol level tended to be high were tested. Effects, on PAI-1, of each of the fat or oil compositions obtained in Examples and Comparative Examples are shown in Table 4. The effects are indicated by a value relative to the initial value set at 100.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Nutrition Science (AREA)
- Botany (AREA)
- Mycology (AREA)
- Edible Oils And Fats (AREA)
- Fats And Perfumes (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE60034356T DE60034356T2 (en) | 1999-08-24 | 2000-08-23 | FAT OR OIL COMPOSITION |
EP00954919A EP1221861B1 (en) | 1999-08-24 | 2000-08-23 | Fat or oil composition |
BRPI0012320-0A BR0012320B1 (en) | 1999-08-24 | 2000-08-23 | composition of fats or oils. |
AU67259/00A AU6725900A (en) | 1999-08-24 | 2000-08-23 | Fat or oil composition |
CA2382223A CA2382223C (en) | 1999-08-24 | 2000-08-23 | Fat or oil composition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23755699A JP3779505B2 (en) | 1999-08-24 | 1999-08-24 | Oil composition |
JP11/237556 | 1999-08-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2001013733A1 true WO2001013733A1 (en) | 2001-03-01 |
Family
ID=17017080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2000/005633 WO2001013733A1 (en) | 1999-08-24 | 2000-08-23 | Fat or oil composition |
Country Status (11)
Country | Link |
---|---|
US (2) | US6495536B1 (en) |
EP (2) | EP1702515B1 (en) |
JP (1) | JP3779505B2 (en) |
CN (2) | CN1679403B (en) |
AT (2) | ATE358982T1 (en) |
AU (1) | AU6725900A (en) |
BR (1) | BR0012320B1 (en) |
CA (1) | CA2382223C (en) |
DE (1) | DE60034356T2 (en) |
ES (2) | ES2283310T3 (en) |
WO (1) | WO2001013733A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002011552A2 (en) * | 2000-08-08 | 2002-02-14 | Kao Corporation | Oil/fat composition |
US7517544B2 (en) | 2001-09-28 | 2009-04-14 | Kao Corporation | Production method for fried foods |
WO2011103151A2 (en) | 2010-02-17 | 2011-08-25 | Bunge Oils, Inc. | Oil compositions of stearidonic acid |
US8158184B2 (en) | 2004-03-08 | 2012-04-17 | Bunge Oils, Inc. | Structured lipid containing compositions and methods with health and nutrition promoting characteristics |
WO2014092531A2 (en) | 2012-12-13 | 2014-06-19 | Sime Darby Malaysia Berhad | Bakery shortenings from palm diacylglycerol |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3662445B2 (en) | 1999-06-30 | 2005-06-22 | 花王株式会社 | Water-in-oil emulsified fat composition |
US6762203B2 (en) * | 1999-08-03 | 2004-07-13 | Kao Corporation | Oil composition |
JP3779505B2 (en) * | 1999-08-24 | 2006-05-31 | 花王株式会社 | Oil composition |
JP3621610B2 (en) | 1999-08-30 | 2005-02-16 | 花王株式会社 | Water-in-oil emulsified fat composition |
JP4911815B2 (en) * | 2000-04-28 | 2012-04-04 | 株式会社Adeka | Plant sterol-containing oil and fat composition |
JP3774110B2 (en) * | 2000-07-19 | 2006-05-10 | 花王株式会社 | Edible oil and fat and method for producing the same |
JP4391673B2 (en) * | 2000-08-08 | 2009-12-24 | 花王株式会社 | Oil composition |
BR0113108A (en) * | 2000-08-08 | 2003-06-10 | Kao Corp | Oil / fat composition |
US6956058B2 (en) | 2001-04-26 | 2005-10-18 | Kao Corporation | Method for improving insulin resistance |
JP4995377B2 (en) * | 2001-04-26 | 2012-08-08 | 花王株式会社 | Oil composition |
BR0309705A (en) * | 2002-05-06 | 2005-03-15 | Archer Daniels Midland Co | Foods and beverages containing diacylglycerol |
US8029847B2 (en) * | 2002-07-12 | 2011-10-04 | General Mills Marketing, Inc. | Trans fat replacement system and method of making a baked good with a trans fat replacement system |
US20050042332A1 (en) * | 2002-07-12 | 2005-02-24 | Lonergan Dennis A. | Method of making a laminated dough product and a product produced thereby |
TWI331017B (en) * | 2002-09-13 | 2010-10-01 | Kao Corp | Oil or fat compositions |
GB0311081D0 (en) | 2003-05-14 | 2003-06-18 | Btg Internat Limted | Treatment of neurodegenerative conditions |
JP2005015425A (en) * | 2003-06-27 | 2005-01-20 | Kao Corp | Agent for ameliorating lipid metabolism |
WO2005018632A1 (en) | 2003-08-18 | 2005-03-03 | Btg International Limited | Treatment of neurodegenerative conditions |
JP4568585B2 (en) * | 2003-11-18 | 2010-10-27 | 花王株式会社 | Oil composition |
JP5100974B2 (en) * | 2004-04-28 | 2012-12-19 | 花王株式会社 | Oil composition |
US20080069932A1 (en) * | 2004-04-28 | 2008-03-20 | Kao Corporation | Oil or Fat Composition |
KR101162136B1 (en) | 2004-04-28 | 2012-07-03 | 카오카부시키가이샤 | Fat composition |
JP4823558B2 (en) * | 2004-04-28 | 2011-11-24 | 花王株式会社 | Oil composition |
MY146635A (en) * | 2004-09-01 | 2012-09-14 | Malaysian Palm Oil Board | Specialty palm oil products and other specialty vegetable oil products |
DK1804589T3 (en) * | 2004-10-08 | 2012-01-02 | Aarhuskarlshamn Denmark As | fat Compositions |
GB0504362D0 (en) | 2005-03-02 | 2005-04-06 | Btg Int Ltd | Cytokine modulators |
KR101201267B1 (en) * | 2005-07-13 | 2012-11-14 | 카오카부시키가이샤 | Fat-and-oil containing composition for bakery product |
US20080063782A1 (en) * | 2006-09-13 | 2008-03-13 | Kerry Group Services International, Ltd. | Zero-trans fat shortening for laminated dough applications |
DK2177608T3 (en) * | 2007-07-31 | 2015-12-14 | Fuji Oil Co Ltd | Immobilized lipase and process for producing the same |
JP2012207041A (en) * | 2012-07-23 | 2012-10-25 | Kao Corp | Lipid metabolism improving agent |
CN110934196A (en) * | 2019-11-11 | 2020-03-31 | 暨南大学 | Method for preparing ultra-stable temperature-sensitive nutritional oil foam by molecular assembly and application |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0171112A1 (en) * | 1984-07-17 | 1986-02-12 | Unilever N.V. | Fat containing diglycerides |
JPS63104917A (en) * | 1986-10-22 | 1988-05-10 | Kao Corp | Oral administration composition |
WO1996032022A1 (en) * | 1995-04-13 | 1996-10-17 | Unilever N.V. | Edible plastic spread |
WO1998001461A1 (en) * | 1996-07-03 | 1998-01-15 | Maurel Sante | Diglycerid and sterol based organometallic complexes and pharmaceutical compositions and dietetic products containing them |
EP0836805A1 (en) * | 1996-10-18 | 1998-04-22 | Kao Corporation | General-purpose oils composition |
US6025348A (en) * | 1998-04-30 | 2000-02-15 | Kao Corporation | Oil and fat composition containing phytosterol |
EP0990391A1 (en) * | 1998-03-24 | 2000-04-05 | Kao Corporation | Phytosterol-containing fat composition |
Family Cites Families (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6043270A (en) * | 1986-06-11 | 2000-03-28 | Procyon Pharmaceuticals, Inc. | Protein kinase C modulators V |
JPH07121196B2 (en) | 1987-01-23 | 1995-12-25 | 花王株式会社 | Water-in-oil type emulsion oil composition |
JP2531201B2 (en) | 1987-10-08 | 1996-09-04 | 日本油脂株式会社 | Mixed crystal triglyceride |
JPH0738771B2 (en) | 1989-01-17 | 1995-05-01 | 花王株式会社 | Liquid edible oil composition |
JP2862981B2 (en) | 1989-10-31 | 1999-03-03 | 花王株式会社 | Oil-in-oil-in-oil double emulsified fat composition |
US5077069A (en) | 1991-01-07 | 1991-12-31 | Kabi Pharmacia Ab | Composition of natural antioxidants for the stabilization of polyunsaturated oils |
US5260077A (en) | 1991-02-12 | 1993-11-09 | The Lubrizol Corporation | Vegetable oil compositions |
DK166650B1 (en) | 1991-03-15 | 1993-06-28 | Aarhus Oliefabrik As | FAT BASES AND THE USE OF THESE IN COSMETIC AND PHARMACEUTICAL EMULSION PRODUCTS |
US6262022B1 (en) | 1992-06-25 | 2001-07-17 | Novartis Ag | Pharmaceutical compositions containing cyclosporin as the active agent |
JP3540015B2 (en) | 1993-06-15 | 2004-07-07 | 株式会社リコー | Pyrenylamine compound and method for producing the same |
DK0719091T3 (en) | 1993-09-14 | 1998-08-24 | Unilever Nv | Natural triglyceride fats |
US5786019A (en) | 1993-09-14 | 1998-07-28 | Loders-Croklaan B.V. | Healthy spread fats |
AU1705595A (en) | 1994-02-18 | 1995-09-04 | Loders Croklaan B.V. | Fat blends containing diglycerides |
DE69505235T2 (en) | 1994-02-18 | 1999-04-29 | Loders Croklaan B.V., Wormerveer | DIGLYCERIDE CONTAINING FAT BLENDS |
ES2133655T3 (en) | 1994-03-31 | 1999-09-16 | Unilever Nv | OILS WITH A LOW CONTENT OF SATURATED FATTY ACIDS. |
CA2186012C (en) * | 1994-04-29 | 2000-05-30 | Frederick William Cain | Ice-cream coating fats |
JP3596134B2 (en) | 1995-12-21 | 2004-12-02 | 三菱化学株式会社 | Oil composition |
JP3761984B2 (en) | 1996-03-12 | 2006-03-29 | 三菱化学株式会社 | Oil composition for frying |
US5998396A (en) * | 1996-11-05 | 1999-12-07 | Riken Vitamin Co., Ltd. | Oil solubilized solutions and foods containing phytosterols and process for their production |
WO1998047385A1 (en) | 1997-04-24 | 1998-10-29 | Unilever N.V. | Fat emulsions |
US6423363B1 (en) | 1997-08-22 | 2002-07-23 | Lipton, Division Of Conopco, Inc. | Aqueous dispersion |
DK0898896T3 (en) | 1997-08-22 | 2004-10-18 | Unilever Nv | Foods based on fats containing sterols |
US6139897A (en) * | 1998-03-24 | 2000-10-31 | Kao Corporation | Oil or fat composition containing phytosterol |
US6087353A (en) | 1998-05-15 | 2000-07-11 | Forbes Medi-Tech Inc. | Phytosterol compositions and use thereof in foods, beverages, pharmaceuticals, nutraceuticals and the like |
JP3720194B2 (en) | 1998-07-09 | 2005-11-24 | 花王株式会社 | Method for producing partial glycerides |
NZ509976A (en) * | 1998-08-03 | 2003-08-29 | Ronald E | Prostate formula |
JP3662445B2 (en) * | 1999-06-30 | 2005-06-22 | 花王株式会社 | Water-in-oil emulsified fat composition |
US6762203B2 (en) * | 1999-08-03 | 2004-07-13 | Kao Corporation | Oil composition |
JP3779505B2 (en) * | 1999-08-24 | 2006-05-31 | 花王株式会社 | Oil composition |
JP3621610B2 (en) * | 1999-08-30 | 2005-02-16 | 花王株式会社 | Water-in-oil emulsified fat composition |
US20020132035A1 (en) | 2001-01-10 | 2002-09-19 | Dov Tamarkin | Synthetic fat composition |
CA2407833A1 (en) | 2000-05-04 | 2001-11-08 | Unilever Plc | Pourable frying composition |
BR0116179A (en) | 2000-12-07 | 2003-10-14 | Unilever Nv | Disposable composition, process of preparing a disposable composition and use of the composition |
JP3735070B2 (en) * | 2001-03-26 | 2006-01-11 | 花王株式会社 | Container-packed emulsified beverage |
JP4995377B2 (en) * | 2001-04-26 | 2012-08-08 | 花王株式会社 | Oil composition |
JP2003102301A (en) | 2001-08-28 | 2003-04-08 | Sagaken Chiiki Sangyo Shien Center | Method for producing diacylglycerol and gene inactivating function of gene encoding diacylglycerolacyltransferase |
BR0309705A (en) | 2002-05-06 | 2005-03-15 | Archer Daniels Midland Co | Foods and beverages containing diacylglycerol |
TWI331017B (en) * | 2002-09-13 | 2010-10-01 | Kao Corp | Oil or fat compositions |
US20040229805A1 (en) | 2002-10-28 | 2004-11-18 | Ardies C. Murray | Agents for producing the health-benefits of repeated exercise |
US20040209953A1 (en) | 2002-12-06 | 2004-10-21 | Wai Lee Theresa Siu-Ling | Glyceride compositions and methods of making and using same |
-
1999
- 1999-08-24 JP JP23755699A patent/JP3779505B2/en not_active Expired - Fee Related
- 1999-10-26 US US09/427,081 patent/US6495536B1/en not_active Expired - Lifetime
-
2000
- 2000-08-23 CN CN2005100672796A patent/CN1679403B/en not_active Expired - Fee Related
- 2000-08-23 DE DE60034356T patent/DE60034356T2/en not_active Expired - Lifetime
- 2000-08-23 EP EP06011348A patent/EP1702515B1/en not_active Expired - Lifetime
- 2000-08-23 CA CA2382223A patent/CA2382223C/en not_active Expired - Fee Related
- 2000-08-23 ES ES00954919T patent/ES2283310T3/en not_active Expired - Lifetime
- 2000-08-23 CN CNB008118302A patent/CN1204819C/en not_active Expired - Fee Related
- 2000-08-23 BR BRPI0012320-0A patent/BR0012320B1/en not_active IP Right Cessation
- 2000-08-23 AT AT00954919T patent/ATE358982T1/en not_active IP Right Cessation
- 2000-08-23 EP EP00954919A patent/EP1221861B1/en not_active Expired - Lifetime
- 2000-08-23 WO PCT/JP2000/005633 patent/WO2001013733A1/en active IP Right Grant
- 2000-08-23 AT AT06011348T patent/ATE548919T1/en active
- 2000-08-23 ES ES06011348T patent/ES2380782T3/en not_active Expired - Lifetime
- 2000-08-23 AU AU67259/00A patent/AU6725900A/en not_active Abandoned
-
2002
- 2002-09-17 US US10/244,736 patent/US7514472B2/en not_active Expired - Fee Related
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0171112A1 (en) * | 1984-07-17 | 1986-02-12 | Unilever N.V. | Fat containing diglycerides |
JPS63104917A (en) * | 1986-10-22 | 1988-05-10 | Kao Corp | Oral administration composition |
WO1996032022A1 (en) * | 1995-04-13 | 1996-10-17 | Unilever N.V. | Edible plastic spread |
WO1998001461A1 (en) * | 1996-07-03 | 1998-01-15 | Maurel Sante | Diglycerid and sterol based organometallic complexes and pharmaceutical compositions and dietetic products containing them |
EP0836805A1 (en) * | 1996-10-18 | 1998-04-22 | Kao Corporation | General-purpose oils composition |
EP0990391A1 (en) * | 1998-03-24 | 2000-04-05 | Kao Corporation | Phytosterol-containing fat composition |
US6025348A (en) * | 1998-04-30 | 2000-02-15 | Kao Corporation | Oil and fat composition containing phytosterol |
Non-Patent Citations (5)
Title |
---|
DATABASE BIOSIS BIOSCIENCES INFORMATION SERVICE, PHILADELPHIA, PA, US; XP002153095 * |
KOOISTRA, T., BOSMA, P. J., TOET, K., COHEN, L. H., GRIFFIOEN, M., VAN DEN BERG, E., LE CLERQ, L., AND VAN HINSBERGH, V. W. M.: "Role of protein kinase C and cyclic AMP in the regulation of tissue-type plasminogen activator, plasminogen activator inhibitor-1 and platelet-derived growth factor messenger RNA levels in human endothelial cells possible involvement of proto-oncogenes C-JUN and C-FOS", ARTERIOSCLEROSIS AND THROMBOSIS., vol. 11, no. 4, 1991, AMERICAN HEART ASSOCIATION., US, pages 1042 - 1052, ISSN: 1049-8834 * |
LING W H ET AL: "ENHANCED EFFICACY OF SITOSTANOL-CONTAINING VERSUS SITOSTANOL-FREE PHYTOSTEROL MIXTURES IN ALTERING LIPOPROTEIN CHOLESTEROL LEVELS ANDSYNTHESIS IN RATS", ATHEROSCLEROSIS,NL,AMSTERDAM, vol. 118, no. 2, 1995, pages 319 - 331, XP002044615, ISSN: 0021-9150 * |
PATENT ABSTRACTS OF JAPAN vol. 012, no. 349 (C - 529) 20 September 1988 (1988-09-20) * |
WESTSTRATE J A ET AL: "PLANT STEROL-ENRICHED MARGARINES AND REDUCTION OF PLASMA TOTAL-AND LDL-CHOLESTEROL CONCENTRATIONS IN NORMOCHOLESTEROLAEMIC AND MILDLY HYPERCHOLESTEROLAEMIC SUBJECTS", EUROPEAN JOURNAL OF CLINICAL NUTRITION., vol. 52, no. 5, May 1998 (1998-05-01), pages 334 - 343, XP000884738 * |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002011552A2 (en) * | 2000-08-08 | 2002-02-14 | Kao Corporation | Oil/fat composition |
WO2002011552A3 (en) * | 2000-08-08 | 2002-04-18 | Kao Corp | Oil/fat composition |
US7090886B2 (en) | 2000-08-08 | 2006-08-15 | Kao Corporation | Oil/fat composition |
US7517544B2 (en) | 2001-09-28 | 2009-04-14 | Kao Corporation | Production method for fried foods |
US8158184B2 (en) | 2004-03-08 | 2012-04-17 | Bunge Oils, Inc. | Structured lipid containing compositions and methods with health and nutrition promoting characteristics |
US8221818B2 (en) | 2004-03-08 | 2012-07-17 | Bunge Oils, Inc. | Composition with health and nutrition promoting characteristics, containing interestified lipids and phytosterol, and related methods |
WO2011103151A2 (en) | 2010-02-17 | 2011-08-25 | Bunge Oils, Inc. | Oil compositions of stearidonic acid |
US8372465B2 (en) | 2010-02-17 | 2013-02-12 | Bunge Oils, Inc. | Oil compositions of stearidonic acid |
US8685484B2 (en) | 2010-02-17 | 2014-04-01 | Bunge Oils, Inc. | Oil compositions of stearidonic acid |
WO2014092531A2 (en) | 2012-12-13 | 2014-06-19 | Sime Darby Malaysia Berhad | Bakery shortenings from palm diacylglycerol |
Also Published As
Publication number | Publication date |
---|---|
CN1370050A (en) | 2002-09-18 |
DE60034356D1 (en) | 2007-05-24 |
EP1702515A3 (en) | 2006-11-29 |
EP1702515A2 (en) | 2006-09-20 |
EP1702515B1 (en) | 2012-03-14 |
CA2382223C (en) | 2010-08-03 |
BR0012320A (en) | 2002-05-21 |
DE60034356T2 (en) | 2007-12-20 |
EP1221861A1 (en) | 2002-07-17 |
ES2380782T3 (en) | 2012-05-18 |
ATE548919T1 (en) | 2012-03-15 |
CN1679403A (en) | 2005-10-12 |
US20030096867A1 (en) | 2003-05-22 |
ES2283310T3 (en) | 2007-11-01 |
JP2001064671A (en) | 2001-03-13 |
AU6725900A (en) | 2001-03-19 |
US6495536B1 (en) | 2002-12-17 |
ATE358982T1 (en) | 2007-05-15 |
EP1221861B1 (en) | 2007-04-11 |
CN1204819C (en) | 2005-06-08 |
CA2382223A1 (en) | 2001-03-01 |
JP3779505B2 (en) | 2006-05-31 |
US7514472B2 (en) | 2009-04-07 |
BR0012320B1 (en) | 2012-10-02 |
CN1679403B (en) | 2010-04-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7514472B2 (en) | Fat or oil composition | |
CN100421565C (en) | Oil/fat composition | |
US8524309B2 (en) | Oil or fat composition | |
US8685484B2 (en) | Oil compositions of stearidonic acid | |
JP5100974B2 (en) | Oil composition | |
JP2004359784A (en) | Oil-and-fat composition | |
JP3752127B2 (en) | Oil composition | |
JP3997043B2 (en) | Oil composition and processed oil product | |
JP3597437B2 (en) | Edible fats and oils with blood lipid improving function | |
JP4629818B2 (en) | HDL cholesterol raising agent | |
JP2003221332A (en) | Oil-in-water type emulsion composition | |
JP4049503B2 (en) | Oil composition | |
JP4629817B2 (en) | PAI-1 lowering agent | |
JP4612930B2 (en) | Remnant-like lipoprotein lowering agent | |
JP2007284457A (en) | Pai-1 depressant | |
JP2006062973A (en) | LDL-C AND Lp(a)-LOWERING AGENT |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CR CU CZ DE DK DM DZ EE ES FI GB GD GE GH GM HR HU ID IL IN IS KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG UZ VN YU ZA ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2000954919 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 008118302 Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2382223 Country of ref document: CA |
|
WWP | Wipo information: published in national office |
Ref document number: 2000954919 Country of ref document: EP |
|
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
WWG | Wipo information: grant in national office |
Ref document number: 2000954919 Country of ref document: EP |