WO1994010858A1 - Feeding composition - Google Patents
Feeding composition Download PDFInfo
- Publication number
- WO1994010858A1 WO1994010858A1 PCT/JP1993/001624 JP9301624W WO9410858A1 WO 1994010858 A1 WO1994010858 A1 WO 1994010858A1 JP 9301624 W JP9301624 W JP 9301624W WO 9410858 A1 WO9410858 A1 WO 9410858A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- nutritional supplement
- acid
- supplement composition
- composition
- present
- Prior art date
Links
Classifications
-
- 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
- A23L33/17—Amino acids, peptides or proteins
- A23L33/175—Amino acids
Definitions
- the present invention relates to a nutritional supplement composition, and more specifically, a nutritional supplement composition that is useful for nutritional supplementation during physical exhaustion or fatigue due to exercise, suppression of radical generation due to increased respiration during exercise, and supplementation of bimins. About things.
- drinks and drinks for supplementing water, electrolytes and carbohydrates, and total nutritional foods and drinks containing all nutrients in a well-balanced manner have been known as foods and drinks for supplementing nutrition during exercise and fatigue. Although some of them are commercially available, they are not fully compatible with changes in the living body in special conditions such as physical exhaustion due to exercise and fatigue. There is a demand for the development of nutritional foods that can sufficiently respond to changes in the living body and have a good nutritional supplementing effect.
- the ability of humans to store carbohydrates as glycogen in the liver and muscles, and the amount of heat stored is approximately 1000 to 200 OKca 1 Zbody, which is not sufficient for prolonged exercise or exercise on an empty stomach. . Therefore, during such exercise, lipids are mainly consumed as an energy source instead of carbohydrates. At this time, if a carbohydrate such as glucose is ingested, the above-mentioned lipid metabolism is inhibited, and the carbohydrate is stored as glycogen. The carbohydrates consumed are consumed, which will accelerate glycogen depletion. Exercise cannot be continued if glycogen is depleted.
- glycogen which is a carbohydrate
- the stored glycogen is quickly consumed, and sufficient nutritional support and stamina recovery cannot be expected.
- a main object of the present invention is to provide a new nutritional supplement composition particularly suitable for nutritional supplementation during the above-mentioned exercises and the like.
- Another object of the present invention is to provide the above nutritional supplement composition which can suppress the consumption of glycogen in the body, enhance carbohydrate metabolism, preserve stamina during exercise, and quickly recover from fatigue after exercise. Is to do.
- the present inventors have conducted intensive studies to achieve the above object, and as a result, a nutritional supplement composition containing, as essential components, an insulin secretion-enhancing amino acid and a food material having an antioxidant action, meets the above object.
- a nutritional supplement composition comprising, as essential components, an amino acid that enhances insulin secretion and a food material having an antioxidant action.
- the nutritional supplement composition of the present invention is used in various forms such as a beverage form, a tablet or powder form, and a foaming agent form. That is, in the case of a beverage form, 5-1000 mg of amino acid for enhancing insulin secretion and 10-200 Omg / 10 Oml of a food material having an antioxidant action are contained.
- the nutritional supplement composition in beverage form includes
- It may further contain 1 to 15 g / l Oml of carbohydrate and 0.1 to 30 mg / 100 ml of carotenoid.
- a tablet or a powder In the case of a tablet or a powder, it contains 5 to 1000 mg of an amino acid that enhances insulin secretion and 10 to 200 mg of a food material having an antioxidant effect.
- the nutritional supplement composition in tablet or powder form can also be used in effervescent form.
- a nutritional supplement composition containing 10 Oml is provided. Also, according to another preferred correct embodiments of the present invention, carotene 0. 1 ⁇ 30m gZl 00ml, arginine 5 0 ⁇ 1000m gZl O Om fractionation toast. 3 to 10 gZ 100 ml, Kuen acid 250 ⁇ 800mg / / l 00ml, A nutritional supplement composition is provided that contains vitamin CO-1000 mg / 10 Oml and vitamin E 0-10 Omg / 10 Oml.
- Food materials having an antioxidant activity used in the nutritional supplement composition of the present invention include, for example, carotenoids, vitamin E, vitamins (:, glucanthione, selenium, etc.).
- the carotenoid may be any of various kinds of substances conventionally known in the food and pharmaceutical fields, including purified products derived from natural products (balm carotene, Donariella, etc.).
- --And synthetic products including, but not limited to, one-strength rotin, ⁇ one-strength rotin, 7-strength rotin, lycopene, rutin, canthaxanthin, etc.
- Powders and extracts of various animals and plants may be used. Among them, especially ⁇ -force. Chin is preferred.
- Vitamin ⁇ and vitamin C each of which has been conventionally known in the food and pharmaceutical fields, can be used in the present invention.
- antioxidant vitamins can be incorporated into the composition of the present invention alone or in an appropriate amount alone or in combination of two or more, depending on the form of the composition of the present invention.
- carotenoid can be added and blended in an amount of 0 to 3 Omg, preferably 0.5 to 1 Omg per 10 Oml of the beverage.
- Vitamin C can be added and blended in an amount of 0 to 0.1 lOOmgZl00ml, preferably 50 to 700mgZl0Oml
- vitamin E can be added and blended in an amount of 0 to 100mg0lOm1 and preferably 1 to 10mg0lOm1.
- Selenium can be added and blended at 0 to 10 OgZl0 Oml, preferably 10 to 20 ⁇ g / lOOml, and glucanthione can be added at 1 to 500 mgZl00 ml, preferably 30 to 300 mg / l00 ml.
- the antioxidant bimin has the function of stopping the radical reaction when ingested.
- carotenoids are precursors of vitamin A and act as provitamin A.
- carotenoids have many conjugated double bonds in their chemical structure, so they stop the above radical chain reaction (radical scavenger). Action) is strong, and can exert the effect of preventing accumulation of fatigue substances and, consequently, the effect of preventing carcinogenesis.
- the composition of the present invention prepared by blending the carotenoids and vitamin E contains an oil agent (edible oily material) for dissolving the carotenoid-bimin E. It is necessary to use an emulsifier for emulsifying this.
- the oil and emulsifier are not particularly limited, and any of various oils and emulsifiers conventionally used in the food and beverage fields can be used.
- Specific examples of the emulsifier include, for example, fatty acid esters of polglycerin, fatty acid esters of glycerin, fatty acid esters of propylene glycol, fatty acid esters such as sugar cane, and soybean liquor. And lipids.
- Insulin secretion enhancing amino acids used in combination with the above antioxidant vitamins in the composition of the present invention include, for example, arginine, lysine, leucine, phenylalanine and the like. These amino acids are usually used in a free form, but are not particularly limited to this form.
- metal salt forms such as sodium and calcium, sulfuric acid, hydrochloric acid, and acetic acid
- inorganic or organic acid salt forms such as malic acid, N-acyl derivative forms, and peptide forms in which two or more kinds of amino acids are ester-bonded can be used in the same manner.
- Particularly preferred amino acids include arginine and lysine.
- compositions of the present invention can also be incorporated into the composition of the present invention in an appropriate amount depending on the form of the composition of the present invention.
- the composition should be added to the beverage in an amount of 5 to 100 mg, preferably 50 to 100 mg per 100 ml of the beverage. Can be.
- these insulin secretion enhancing amino acids enhance glycogen synthesis from carbohydrates, enhance lipid metabolism, suppress glycogen consumption, and preserve and exercise sumina during exercise. Enables early recovery from later fatigue.
- the nutritional supplement composition of the present invention is required to contain a predetermined amount of the above-mentioned antioxidant biminamine and insulin secretion-enhancing amino acid as essential components, and is otherwise prepared in the same manner as ordinary foods and drinks.
- Other food materials can be added as appropriate.
- preferable examples include sweeteners such as organic acids and carbohydrates.
- organic acid component examples include citric acid, tartaric acid, malic acid, succinic acid and the like, among which citric acid is preferred. These organic acids are usually added and blended in the range of 100 to 150 Omg / 100 ml, preferably 250 to 800 mg0 Oml, and the composition of the present invention in the form of a beverage is added. Can be prepared.
- saccharide component examples include monosaccharides such as glucose and fructose.
- sugars such as disaccharides such as maltose sucrose; sugar alcohols such as xylitol, sorbitol, glycerin and erythritol; and polysaccharides such as dextrin and cyclodextrin; fructooligosaccharides; galactooligosaccharides; Oligosaccharides such as galactosyl lactose and lactose sucrose are included.
- fructose and glycerin are preferred as those which do not adversely affect lipid metabolism.
- Lactosucrose is preferred as the oligosaccharide.
- the obtained beverage composition of the present invention on the basis of the blend of lactosucrose, enables an increase in bifidobacteria in the body and a decrease in spoilage products, thereby further preventing carcinogenesis and enhancing the immune system. It can be.
- sweeteners other than those described above, natural sweeteners (thomatin, stevia extract (rebaudioside A, etc.), glycyrrhizin, etc.), and synthetic sweeteners (saccharin, aspartame, etc.) can be advantageously used.
- These carbohydrates can, of course, also be added and used as a carbohydrate mixture of isomerized sugar, purified sucrose and the like.
- the amount of the saccharide to be added is about 1 to 15 g, preferably about 3 to 12 g per 100 ml of the beverage composition of the present invention.
- the amount of the oligosaccharide is preferably about 0.5 to 1 Og, more preferably 1 to 3 g.
- the composition of the present invention further includes various nutrients, vitamins, electrolytes (minerals) to trace elements, fragrances such as synthetic fragrances and natural fragrances, coloring agents and flavor substances (cheese, chocolate, etc.).
- fragrances such as synthetic fragrances and natural fragrances, coloring agents and flavor substances (cheese, chocolate, etc.
- the composition of the present invention may be added with natural juice or pulp to make it into a fruit juice beverage or vegetable beverage. These can be used alone or in combination of two or more.
- the mixing ratio of these additives is not particularly limited, but is generally selected from the range of about 0 to 20 parts by weight based on 100 parts by weight of the composition of the present invention. .
- biminamines whether water-soluble or fat-soluble, include various ones such as thiamine, niacin, retinol palmitate, bisbentiamine, riboflavin, pyridoxine hydrochloride, cyanoconolamin, sodium ascorbate, Cholecalciferol, nicotinic acid amide, calcium pantothenate, folic acid, piotin, choline bitartrate and the like can be exemplified, and among these, those belonging to the bimin B group which contributes to metabolic enhancement are preferable.
- electrolytes minerals
- trace elements ordinary ones, for example, sodium chloride, sodium acetate, magnesium sulfate, magnesium chloride, calcium chloride, dipotassium phosphate, monosodium phosphate, calcium glycerate, succinate
- sodium iron oxide, manganese sulfate, copper sulfate, zinc sulfate, sodium iodide, potassium sorbate, zinc, manganese, copper, iodine, and cobalt can be appropriately determined as needed.
- the composition of the present invention is prepared by mixing the above components, and the preparation method is not particularly limited, and all the components may be mixed at the same time, but more preferably as an antioxidant bimin.
- composition can be prepared
- a carotenoid and Z or vitamin E oil solution or crystal are added to water and a suitable emulsifier, and the mixture is emulsified. Then, the resulting emulsion is mixed with an aqueous solution of insulin secretion-enhancing amino acid and other components.
- a suitable emulsifier emulsifier for emulsifying a carotenoid and Z or vitamin E oil solution or crystal
- the mixture is emulsified.
- the resulting emulsion is mixed with an aqueous solution of insulin secretion-enhancing amino acid and other components.
- the mixing operation of the above components may be performed at room temperature, but it is preferable to perform the mixing operation by using a slight heating operation.
- the emulsification can be carried out according to a usual method, using a suitable emulsifier, for example, a homomixer, a high-pressure homogenizer, or the like, in either a complete passage system or a circulation system.
- a suitable emulsifier for example, a homomixer, a high-pressure homogenizer, or the like
- the emulsified liquid after the emulsification can be filtered according to a conventional method, filled in an appropriate container, and sterilized to obtain a desired beverage product.
- the sterilization is performed by heat sterilization or aseptic filtration. it can.
- composition of the present invention When the composition of the present invention is used as a carbonated beverage, a method of injecting carbon dioxide into the emulsifier according to a conventional method may be employed.
- the beverage prepared as described above is
- the osmotic pressure is adjusted to be in the range of about 260 to 60 OmOsmZkg.
- the composition of the present invention can also be prepared in the form of a blowing agent.
- the foaming agent may contain sodium carbonate and / or sodium bicarbonate and a neutralizing agent, in addition to the above-described antioxidant bisamine and insulin secretion-enhancing amino acid, which are essential components of the nutritional supplement composition of the present invention. It is essential that a predetermined amount be blended as a foaming component.
- the neutralizing agent used here refers to an acidic compound capable of neutralizing the above-described sodium carbonate and sodium bicarbonate to generate carbon dioxide gas.
- Such compounds typically include, for example, organic acids such as L-tartaric acid, citric acid, fumaric acid, and ascorbic acid. Of these, ascorbic acid can also simultaneously act as a neutralizing agent and as an antioxidant.
- the foaming agent of the present invention includes, in addition to the above components, various commonly known additive components such as excipients, binders, disintegrants, lubricants, thickeners, surfactants, osmotic pressure adjusting agents, Electrolytes
- Sweeteners, flavors, pigments, pH regulators, etc. can be added and blended as needed.
- examples of the above additives include starches such as wheat starch, potato starch, corn starch and dextrin, sugars such as sucrose, glucose, fructose, maltose, xylose, and lactose; sugars such as sorbitol, mannitol, maltitol, and xylitol.
- Translocation glycosides such as alcohols, coupling sugar, palatinose, etc., excipients such as calcium phosphate, calcium sulfate, starch, sugars, gelatin, gum arabic, dextrin, methylcellulose, polyvinylpyrrolidone, polyvinyl alcohol , Hydroxypropylcellulose, xanthan gum, pectin, tragacanth, binders such as casein, alginic acid and thickeners, leucine, isoleucine, quinolin, sugar ester, hardened oil, stearic acid, magnesia stearate Lubricants such as calcium, sulk, macrogol, etc., disintegrators such as Avicel, CMC, CMC—Na, CMC-Ca, surfactants such as polysorbate and lecithin, sugars, sugar alcohols, aspartame, alitame, etc.
- excipients such as calcium phosphate, calcium sulfate, starch, sugar
- sweeteners of dipeptides, other stevia, and saccharin sugar, and the like can be appropriately selected and used in consideration of the relationship with the essential components, the properties of the preparation, the production method, and the like. Further, various vitamins can be added to the foaming agent.
- the production method of the present invention can be basically the same as the production method of a normal effervescent preparation of this kind, for example, an effervescent tablet. That is, a predetermined amount of each component is mixed and mixed in a small amount, and a direct powder compression method, a dry or wet granulation compression method, or the like can be applied.
- the agent of the present invention (effervescent tablet) thus obtained is simply put into water to obtain a beverage form suitable for oral administration, which is orally administered.
- the dosage is appropriately determined according to the age, sex, weight, degree of disease, etc. of the living body to which the drug is to be applied, and is not particularly limited, but generally, about 1.5 to 6 tablets per tablet. --
- One to two tablets of the tablet of the present invention prepared in a volume of 0.0 g may be taken at once by dissolving in 100 to 30 Om1 of water.
- the preparation of the present invention is not particularly limited to the effervescent tablets described above, and may be dissolved or dispersed in water and taken in an appropriate form, such as granules, powders, capsules, etc., as long as it has the above composition range. It may be in a form.
- various forms such as ame, drop, chocolate, jelly, confectionery, biscuit, and cookie can be arbitrarily adopted. Preparation into these forms can be carried out according to a conventional method by shaping the essential components and necessary additives into an appropriate form using or not using a suitable carrier.
- a suitable carrier for example, flour, rice flour, starch, constarch, soybeans and the like can be used.
- the food and drink of the present invention in various forms prepared as described above are appropriately sterilized or otherwise treated according to a conventional method to obtain a product.
- the nutritional supplement composition of the present invention is ingested during exercise, after exercise, when the physical strength is exhausted, when fatigued, and the like, and can exert effects such as nutritional supplementation, recovery from fatigue, and recovery of stamina.
- the composition of the present invention has a stamina-preserving effect during exercise, a glycogen renewal effect in muscles and liver, an antioxidant effect, a radical scavenger effect, a vitamin supplementation effect, and a lipid metabolism even when ingested during exercise. It has an effect of increasing fat metabolism, an effect of preventing obesity, a function of recovering from fatigue, etc. without adverse effects, and is very useful as a new nutritional supplement composition.
- Antioxidant vitamins ( ⁇ / ⁇ / ⁇ / ⁇ + ⁇ V ⁇ ⁇ ⁇ ⁇ ⁇ 2 ⁇ € ⁇ € € either) either up to insulin secretion-enhancing amino acids (arginine / lysine), emulsifiers (sucrose fatty acid esters), oils (citrus essential oils), sugars (fructose / glucose solution) Sugar, sucrose and fructose), organic acids (cunic acid, tartaric acid), oligosaccharides (fructooligosaccharides, lactosucrose), and flavors, sweeteners, and carbon dioxide shown in Tables 1 and 2 To prepare the composition of the present invention in the form of a beverage.
- Example N Ingredient (in 100 ml), 9 10 11 12 13 14 15 16 Antioxidant vitamin
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- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Mycology (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Non-Alcoholic Beverages (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002127445A CA2127445C (en) | 1992-11-10 | 1993-11-08 | Nutrient composition |
EP93924198A EP0625312B1 (en) | 1992-11-10 | 1993-11-08 | Feeding composition |
DE69323731T DE69323731T2 (de) | 1992-11-10 | 1993-11-08 | Futterzusammensetzung |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4/300075 | 1992-11-10 | ||
JP30007592 | 1992-11-10 | ||
JP6518993 | 1993-03-24 | ||
JP5/65189 | 1993-03-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1994010858A1 true WO1994010858A1 (en) | 1994-05-26 |
Family
ID=26406317
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1993/001624 WO1994010858A1 (en) | 1992-11-10 | 1993-11-08 | Feeding composition |
Country Status (5)
Country | Link |
---|---|
US (1) | US6037375A (ja) |
EP (1) | EP0625312B1 (ja) |
CN (1) | CN1052865C (ja) |
DE (1) | DE69323731T2 (ja) |
WO (1) | WO1994010858A1 (ja) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2745498A1 (fr) * | 1996-02-29 | 1997-09-05 | Giroux Jean Marc | Composition pur augmenter conjointement la tolerance biologique et l'efficacite amincissante des produits hyperproteines hypocaloriques destines au traitement de l'obesite |
US8603546B2 (en) * | 1999-01-11 | 2013-12-10 | Herbaceuticals Inc. | Herbal supplement for increased muscle strength and endurance for athletes |
US6143786A (en) * | 1999-02-02 | 2000-11-07 | Novartis Nutrition Ag | Oral arginine and insulin secretion |
WO2001026642A2 (en) * | 1999-10-08 | 2001-04-19 | Joyce Corinne Bechthold | Methods and compositions for treating neurobehavioral disorders |
US20030134007A1 (en) * | 2002-01-16 | 2003-07-17 | Donhowe Erik Thurman | Product and process of making an alcohol containing sport drink |
WO2005110394A1 (ja) * | 2004-05-19 | 2005-11-24 | Ajinomoto Co., Inc. | 糖尿病治療薬 |
WO2007115131A2 (en) * | 2006-03-29 | 2007-10-11 | Guilford F Timothy | Liposomal reduced glutathione and 1-arginine, including other ingredient(s) |
WO2006081014A2 (en) | 2004-12-23 | 2006-08-03 | Nonomura Arthur M | Cytochrome p450 enzyme complexes and methods of treatment using the same |
US20060263486A1 (en) * | 2005-05-18 | 2006-11-23 | Ralf Jager | Filler material for a beverage container |
US20060211721A1 (en) * | 2005-03-21 | 2006-09-21 | Roberts Alan R | Nutraceutical formulation of a cognitive enhancement system |
JP2007031375A (ja) * | 2005-07-28 | 2007-02-08 | Kyowa Hakko Kogyo Co Ltd | 肌質改善用経口剤 |
CN101312660B (zh) * | 2005-11-23 | 2013-07-17 | 可口可乐公司 | 供体重管理之高效甜味剂以及经彼甜化的组成物 |
US8367137B2 (en) | 2005-11-23 | 2013-02-05 | The Coca-Cola Company | High-potency sweetener composition with fatty acid and compositions sweetened therewith |
US9101160B2 (en) | 2005-11-23 | 2015-08-11 | The Coca-Cola Company | Condiments with high-potency sweetener |
US20100137226A1 (en) * | 2006-06-07 | 2010-06-03 | Kyowa Hakko Bio Co., Ltd | Fatigue-reducing agent |
US8017168B2 (en) | 2006-11-02 | 2011-09-13 | The Coca-Cola Company | High-potency sweetener composition with rubisco protein, rubiscolin, rubiscolin derivatives, ace inhibitory peptides, and combinations thereof, and compositions sweetened therewith |
WO2008115563A1 (en) * | 2007-03-19 | 2008-09-25 | University Of Florida Research Foundation, Inc. | Liquid nutrient composition for improving performance |
EP2330928B1 (en) * | 2008-08-29 | 2016-02-24 | Tropicana Products, Inc. | Naturally sweetened juice beverage products |
RU2469608C2 (ru) * | 2008-08-29 | 2012-12-20 | Тропикана Продактс, Инк. | Натурально подслащенные соковые продукты с бета-глюканом |
EP2362725B1 (en) | 2008-11-04 | 2015-01-07 | Vymedic, Llc | Antiviral supplement formulations |
US8512682B2 (en) | 2009-05-08 | 2013-08-20 | R & B Tooth Armour, Llc | Food product to prevent tooth decay |
US20120171184A1 (en) * | 2010-12-31 | 2012-07-05 | Lajos Szente | Cellular hydration compositions |
US20170281587A1 (en) * | 2014-09-01 | 2017-10-05 | Glico Nutrition Co., Ltd. | Erythrocyte function improving agent |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6078560A (ja) * | 1983-10-04 | 1985-05-04 | Kongo Yakuhin Kk | 無酸味強化栄養剤 |
JPS6094075A (ja) * | 1983-10-31 | 1985-05-27 | Ajinomoto Co Inc | 果汁飲料組成物 |
JPS611111B2 (ja) * | 1983-05-16 | 1986-01-14 | Ajinomoto Kk | |
JPH04126057A (ja) * | 1990-09-17 | 1992-04-27 | Nichii Suishiyou Kouren:Kk | 海水入り清涼飲料水 |
JPH04346770A (ja) * | 1990-10-26 | 1992-12-02 | Maurizio Luca | 栄養補給組成物 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0087068A1 (en) * | 1982-02-12 | 1983-08-31 | Thomas Moses Dr. Beck | Nutritional supplement |
US4871550A (en) * | 1986-09-05 | 1989-10-03 | Millman Phillip L | Nutrient composition for athletes and method of making and using the same |
CA2066951A1 (en) * | 1991-04-26 | 1992-10-27 | Kou Moriyama | Edible composition |
-
1993
- 1993-11-08 DE DE69323731T patent/DE69323731T2/de not_active Expired - Lifetime
- 1993-11-08 EP EP93924198A patent/EP0625312B1/en not_active Expired - Lifetime
- 1993-11-08 WO PCT/JP1993/001624 patent/WO1994010858A1/ja active IP Right Grant
- 1993-11-09 CN CN93114451A patent/CN1052865C/zh not_active Expired - Lifetime
-
1997
- 1997-06-18 US US08/878,063 patent/US6037375A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS611111B2 (ja) * | 1983-05-16 | 1986-01-14 | Ajinomoto Kk | |
JPS6078560A (ja) * | 1983-10-04 | 1985-05-04 | Kongo Yakuhin Kk | 無酸味強化栄養剤 |
JPS6094075A (ja) * | 1983-10-31 | 1985-05-27 | Ajinomoto Co Inc | 果汁飲料組成物 |
JPH04126057A (ja) * | 1990-09-17 | 1992-04-27 | Nichii Suishiyou Kouren:Kk | 海水入り清涼飲料水 |
JPH04346770A (ja) * | 1990-10-26 | 1992-12-02 | Maurizio Luca | 栄養補給組成物 |
Non-Patent Citations (1)
Title |
---|
See also references of EP0625312A4 * |
Also Published As
Publication number | Publication date |
---|---|
DE69323731T2 (de) | 1999-07-22 |
EP0625312A1 (en) | 1994-11-23 |
CN1052865C (zh) | 2000-05-31 |
CN1086682A (zh) | 1994-05-18 |
US6037375A (en) | 2000-03-14 |
EP0625312A4 (en) | 1995-02-08 |
EP0625312B1 (en) | 1999-03-03 |
DE69323731D1 (de) | 1999-04-08 |
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