WO2003084352A1 - Aliment liquide/boisson contenant une vitamine liposoluble et procede de stabilisation de cette vitamine liposoluble - Google Patents
Aliment liquide/boisson contenant une vitamine liposoluble et procede de stabilisation de cette vitamine liposoluble Download PDFInfo
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- WO2003084352A1 WO2003084352A1 PCT/JP2003/004564 JP0304564W WO03084352A1 WO 2003084352 A1 WO2003084352 A1 WO 2003084352A1 JP 0304564 W JP0304564 W JP 0304564W WO 03084352 A1 WO03084352 A1 WO 03084352A1
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- Prior art keywords
- vitamin
- pigment
- fat
- liquid food
- drink
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- 235000009464 menaquinone-7 Nutrition 0.000 description 1
- 239000011700 menaquinone-7 Substances 0.000 description 1
- RAKQPZMEYJZGPI-LJWNYQGCSA-N menaquinone-7 Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CCC=C(C)C)=C(C)C(=O)C2=C1 RAKQPZMEYJZGPI-LJWNYQGCSA-N 0.000 description 1
- LXKDFTDVRVLXFY-WQWYCSGDSA-N menaquinone-8 Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CCC=C(C)C)=C(C)C(=O)C2=C1 LXKDFTDVRVLXFY-WQWYCSGDSA-N 0.000 description 1
- WCRXHNIUHQUASO-UVZVDVBNSA-N menaquinone-9 Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CCC=C(C)C)=C(C)C(=O)C2=C1 WCRXHNIUHQUASO-UVZVDVBNSA-N 0.000 description 1
- 235000021239 milk protein Nutrition 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 235000013923 monosodium glutamate Nutrition 0.000 description 1
- RJMUSRYZPJIFPJ-UHFFFAOYSA-N niclosamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=CC=C([N+]([O-])=O)C=C1Cl RJMUSRYZPJIFPJ-UHFFFAOYSA-N 0.000 description 1
- 235000019520 non-alcoholic beverage Nutrition 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 235000015205 orange juice Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 1
- 238000004810 partition chromatography Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229930002330 retinoic acid Natural products 0.000 description 1
- 229960003471 retinol Drugs 0.000 description 1
- 239000011607 retinol Substances 0.000 description 1
- 235000020944 retinol Nutrition 0.000 description 1
- 229950001574 riboflavin phosphate Drugs 0.000 description 1
- 150000003287 riboflavins Chemical class 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 235000020254 sheep milk Nutrition 0.000 description 1
- 229940073490 sodium glutamate Drugs 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000014214 soft drink Nutrition 0.000 description 1
- 235000013322 soy milk Nutrition 0.000 description 1
- 235000013555 soy sauce Nutrition 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000012134 supernatant fraction Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- 229930003802 tocotrienol Natural products 0.000 description 1
- 235000019148 tocotrienols Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 229960001727 tretinoin Drugs 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 235000015192 vegetable juice Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 235000001892 vitamin D2 Nutrition 0.000 description 1
- 239000011653 vitamin D2 Substances 0.000 description 1
- 235000005282 vitamin D3 Nutrition 0.000 description 1
- 239000011647 vitamin D3 Substances 0.000 description 1
- 229940021056 vitamin d3 Drugs 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 235000014101 wine Nutrition 0.000 description 1
- 235000004835 α-tocopherol Nutrition 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
- 235000007680 β-tocopherol Nutrition 0.000 description 1
- 239000011590 β-tocopherol Substances 0.000 description 1
- 239000002478 γ-tocopherol Substances 0.000 description 1
- QUEDXNHFTDJVIY-DQCZWYHMSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-DQCZWYHMSA-N 0.000 description 1
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
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B5/00—Preserving by using additives, e.g. anti-oxidants
- C11B5/0021—Preserving by using additives, e.g. anti-oxidants containing oxygen
-
- 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
- A23D7/00—Edible oil or fat compositions containing an aqueous phase, e.g. margarines
- A23D7/003—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, 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, COOKING OILS
- A23D7/00—Edible oil or fat compositions containing an aqueous phase, e.g. margarines
- A23D7/01—Other fatty acid esters, e.g. phosphatides
- A23D7/011—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, COOKING OILS
- A23D7/00—Edible oil or fat compositions containing an aqueous phase, e.g. margarines
- A23D7/06—Preservation of finished products
-
- 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
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
-
- 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
- A23L33/15—Vitamins
-
- 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
- A23L33/15—Vitamins
- A23L33/155—Vitamins A or D
-
- 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
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
- A23L5/40—Colouring or decolouring of foods
- A23L5/42—Addition of dyes or pigments, e.g. in combination with optical brighteners
- A23L5/43—Addition of dyes or pigments, e.g. in combination with optical brighteners using naturally occurring organic dyes or pigments, their artificial duplicates or their derivatives
-
- 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
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
- A23L5/40—Colouring or decolouring of foods
- A23L5/42—Addition of dyes or pigments, e.g. in combination with optical brighteners
- A23L5/43—Addition of dyes or pigments, e.g. in combination with optical brighteners using naturally occurring organic dyes or pigments, their artificial duplicates or their derivatives
- A23L5/44—Addition of dyes or pigments, e.g. in combination with optical brighteners using naturally occurring organic dyes or pigments, their artificial duplicates or their derivatives using carotenoids or xanthophylls
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Definitions
- the present invention relates to a liquid food or drink containing a fat-soluble vitamin, a method for stabilizing fat-soluble vitamins, and a composition used in the method.
- fat-soluble vitamins are unstable to light, heat or oxidation, and stabilization of fat-soluble vitamins in liquid foods and beverages containing fat-soluble vitamins has been a challenge.
- Foods and drinks containing fat-soluble vitamins include foods and drinks containing vitamin K (JP-A-11-127816), milk and dairy products enriched with vitamin K and calcium (JP-A-11-56232), and ubiquinone.
- Non-alcoholic beverages Table 2001-504343
- vitamin A or vitamin E-containing beverage compositions W096 / 04801 and the like are known. Disclosure of the invention
- An object of the present invention is to provide a liquid food or drink containing a fat-soluble vitamin, a method for stabilizing a fat-soluble vitamin, and a composition used in the method.
- the present invention relates to the following (1) to (20).
- a liquid food or drink comprising a suspension and an antioxidant.
- the antioxidant selected from the group consisting of polyphenol, tocopherol or a derivative thereof or a salt thereof, ascorbic acid or a salt thereof, rutin, force phain, and isoflavone; ) Liquid food and drink.
- vitamin K is filoquinone (vitamin Ki), menaquinone (vitamin K 2 ) or menadione (vitamin 3 ).
- carotenoid pigment is a carotenoid pigment selected from the group consisting of carotene, gardenia pigment, marigold pigment, and lycopene.
- Liposome is added to a solution or liquid food or beverage containing fat-soluble vitamins. Stability of fat-soluble vitamins characterized by adding flavin or a derivative thereof, a salt thereof, a carotenoid dye, a cochineal dye and a safflower dye, a dye or an emulsion, and an antioxidant. Method.
- the antioxidant selected from the group consisting of polyphenol, tocopherol or a derivative thereof or a salt thereof, ascorbic acid or a salt thereof, rutin, caffeine, and isoflavone; ) A method for stabilizing fat-soluble vitamins.
- vitamin K is filoquinone (vitamine Kj), menaquinone (vitamin K 2 ) or menadione (vitamin ⁇ 3 ).
- carotenoid pigment is a lipstick tenoid pigment selected from the group consisting of carotenes, gardenia pigments, marigold pigments, and copenens. Stabilization method.
- a solution containing a fat-soluble vitamin or a liquid food and drink 'product The emulsion is added so that the content of the emulsion per 100m1 is 1g or more.
- Any one of the stabilization methods Any one of the stabilization methods.
- Dyes or emulsions selected from the group consisting of riboflavin or its derivatives or salts thereof, carotenoid dyes, cochineal dyes and safflower dyes, as well as polyphenols and tocophore Or a derivative thereof or a salt thereof, ascorbic acid or a salt thereof, a composition comprising an antioxidant selected from the group consisting of rutin, caffeine, and isoflavone.
- composition according to the above (19), wherein the carotenoid pigment is a carotenoid pigment selected from the group consisting of carotenes, gardenia pigments, and marigold pigments.
- Examples of the fat-soluble vitamin in the present invention include vitamin, vitamin D, vitamin A, ubiquinone and the like.
- the fat-soluble vitamin can be obtained by extraction and purification from a natural product by a known method, or can be obtained by chemical synthesis by a known method. Any one can be used, even if obtained by law. 'Also, commercially available products can be used.
- vitamin K examples include, for example, quinoquinone (vitamin K, menaquinone (vitamin K 2 ), menadione (vitamin K 3 ), and the like.
- menaquinone examples include menaquinone-4, menaquinone-1, menaquinone-6, menaquinone_7, menaquinone-8, menaquinone-9, and the like. Menaquinone-14 and menaquinone-17 are preferably used.
- vitamin D examples include ergocalciferol (vitamin D 2 ), cholecalciferol (vitamin D 3 ), and derivatives of these such as estenol sulfate.
- Vitamin E includes-tocopherol, ⁇ -tocopherol, ⁇ -tocopherol / re, ⁇ -tocopherolone, ⁇ -tocotrienole,-tocotrienol, ⁇ y- Examples include tocotrienol, ⁇ -tocotrienolate, derivatives thereof such as acetate, nicotinic acid ester / ester, and esteroline phosphate. In addition, these salts can be given. For example, ⁇ -tocopherol ninatrium can be mentioned.
- Vitamin ⁇ includes retinol (vitamin A, 3-dehydro Tino monophosphate (vitamin A 2 ), retino monophosphate, 3-dehydro retino monophosphate, retinoic acid, 3-dehydro retinoic acid, and derivatives thereof such as acetates and palmitates Can be.
- ubiquinone those having 1 to 12 isoprene residues in ubiquinone are preferably used, those having 6 to 12 are more preferably used, and those having 10 (hereinafter referred to as ubidecarenone) are preferable. Is particularly preferably used.
- Examples of the dye used in the present invention include riboflavin or a derivative thereof, a salt thereof, a carotenoid dye, a cochineal dye, and a safflower dye.
- the above dyes may be used alone or in combination of two or more dyes.
- riboflavin derivative examples include riboflavin phosphate, riboflavin butyrate, and the like.
- salt of riboflavin or a derivative thereof examples include a sodium salt and a lithium salt.
- riboflavin 5, ester monatophosphate can be mentioned.
- carotenoid pigment examples include carotene, gardenia pigment, marigold pigment, and lycopene.
- carotene examples include ⁇ -carotene, / 3-carotene, 0 / -force mouth, and the like, and j3—power mouth is preferably used.
- the pigment used in the present invention may be a commercially available pigment, but may be a pigment containing the pigment or an extract obtained by extracting the pigment containing these pigments with a solvent or the like. It may be a concentrated or dried product of the extract, or a purified product obtained by purifying the extract by a conventional method.
- Examples of a substance containing riboflavin or a derivative thereof or a salt thereof include, for example, a substance containing sodium riboflavin 5′-phosphate, and a substance containing, for example, Saccharomyces ′ cerevisiae. (Saccharomyces cerevisiae).
- those containing j3—Rokutoten include, for example, green-yellow vegetables such as carrots and cabochias, and microalgae such as Dunaliella salina.
- examples of those containing a gardenia pigment include gardenia gardenia (Gardenia asminoides Ellis).
- examples of those containing a marigold dye include, for example, flowers of Tagetes erecta WILLD.
- Examples of lycopene-containing substances include I! J Eho, Solanaceae tomato (Lycopersicon esculentum MILL.), And the like.
- cochineal dye examples include coccinellidae (Coccus cacti L.).
- safflower pigment containing for example, Asteraceae safflower
- the solvent used for solvent extraction of the dye may be any solvent that can extract these dyes, such as an aqueous medium or an organic solvent. Further, the solvent may be used alone or as a mixed solvent obtained by combining a plurality of solvents.
- aqueous medium examples include water, purified water, deionized water, and distilled water.
- organic solvents alkyl acetates, monohydric aliphatic alcohols, and aliphatic ketones are preferable, and ethyl acetate, ethanol, and acetone are more preferable. From the viewpoint of use in foods and drinks, ethanol is particularly preferable. Masure,
- Extraction can be performed using a stirrer, ultrasonic generator, reflux extractor, Soxhlet extractor, or the like. After extraction, the obtained extract may be used as an extract, or the extraction residue may be further extracted with an extraction solvent, and the obtained extract may be used as the extract.
- Concentration or drying of the extract can be performed by a conventional method such as heating concentration, concentration under reduced pressure, freeze drying, natural drying, ventilation drying, etc., and is obtained by these operations.
- Purification from extracts is performed by membrane separation, liquid membrane separation, solvent partitioning, or partition chromatography, adsorption chromatography, ion chromatography, affinity chromatography, gel chromatography, dialysis, etc. Can be performed by a conventional method such as a fractionation method.
- the emulsion used in the present invention can be used for foods and drinks, and is an artificially produced one that is derived from natural products as long as it gives turbidity to liquid foods and drinks. There may be.
- Emulsions derived from natural products include, for example, milk of mammals such as milk, goat milk, sheep milk, and horse milk, skim milk, partially skim milk, fermented milk, lactic acid beverages, milk drinks, concentrated milk, and skim milk. Concentrated milk and the like can be given.
- artificially produced emulsions include aqueous media, fats and oils (such as animal oils such as essential oils, vegetable oils and butter oils), and emulsifiers (glycerin fatty acid esters, sucrose fatty acid esters, lecithin, saboyun, milk) Protein, gum arabic, etc.) and emulsified using a high-speed stirring emulsifier, an ultrasonic homogenizer, a high-pressure homogenizer, an ultra-high-pressure homogenizer, etc. according to a conventional method. it can.
- milk protein casein or casein sodium is preferably used.
- Examples of the aqueous medium used for preparing an emulsion include water, purified water, deionized water, and distilled water.
- oils and fats vegetable oils are preferably used.
- arabia gum or sucrose fatty acid ester is preferably used.
- the emulsion may be an oil-in-water (0 / W) type or an oil-in-water (W / 0) type, but is preferably an oil-in-water type.
- An example of the emulsion is an emulsion obtained by adding arabia gum and sucrose fatty acid ester as an emulsifier to a mixture of water and vegetable oil and emulsifying the mixture.
- the ratio of vegetable oil to water is preferably 0.5 to 50%, more preferably 0.5 to 20% by volume.
- the emulsifier is 10 to 40 ° / volume to water. Les, preferably to be.
- Examples of emulsions include Cloudy Base (manufactured by Ogawa Kofu), Neokura B-2 (manufactured by San-Ei Gen F'F 'A), and Neo-Cla B 19 (San Ei Gen F'F' I) Neikokura No. 3380 (manufactured by San-Eigen FFI Inc.).
- antioxidant used in the present invention examples include polyphenol, tocopherol or a derivative thereof or a salt thereof, ascorbic acid or a salt thereof, rutin, caffeine, isoflavone and the like.
- antioxidants may be used alone or in combination of two or more.
- polyphenols examples include catechin and proanthocyanidin.
- Tocopheronore is Hitokoferonore, j3 — Tocophero
- ⁇ -Tocophero / Le ⁇ -Tocophero / Le
- CK-Tocotrieno / Le ⁇ -Tocotrieno / Le
- ⁇ -Tocotori Nore, ⁇ -Tocotriol and the like.
- these derivatives include acetates, gluconates, phosphates and the like.
- These salts include, for example, arninadium sodium.
- Examples of the salt of ascorbic acid include a sodium salt and a potassium salt.
- the antioxidant used in the present invention may be an extract obtained by extracting the antioxidant containing these antioxidants with a solvent or the like, or may be a concentrate or a dried product of the extract. It may be a purified product obtained by purifying the extract by a conventional method.
- the extraction method can be performed according to the method described above for the extraction of the pigment.
- antioxidants include polyphenols such as coffee beans, seeds of buddu, immature lingos, and Labiatae Examples include leaves or flowers of rosemary (rosmary) (Rosmarinus of ic inal is) and leaves of camellia spp. (Came llias inens is). Examples of caffeine-containing substances include coffee beans, leaves of Camellia spp. (Camellia s inens is), and the like. Examples of isoflavone-containing substances include soybeans.
- a pigment or an emulsion and an antioxidant to a solution or a liquid food or beverage containing fat-soluble vitamins, fat-soluble vitamins can be stabilized.
- the pigment or emulsion used in this case and the antioxidant may contain the same compound as the fat-soluble vitamin to be stabilized, but usually does not.
- a solution obtained by adding fat-soluble vitamin to an aqueous medium such as water, purified water, deionized water, distilled water, or an organic solvent such as ethanol is used. I can give it.
- One fat-soluble vitamin may be used alone, or two or more fat-soluble vitamins may be used in combination.
- fat-soluble vitamins When fat-soluble vitamins are added to an aqueous medium, fat-soluble vitamins are insoluble in water, so fats-soluble vitamins contain water, glycerol, or propylene glycol, and emulsifiers (such as sorbitan, gum arabic, and sucrose fatty acids). Ester, lecithin, etc.), and using a high-speed stirrer, an ultrasonic homogenizer, a high-pressure homogenizer, an ultra-high-pressure homogenizer, or the like, and emulsifying in a conventional manner, using a fat-soluble vitamin-containing emulsion, or It is preferable to use a commercially available emulsified fat-soluble vitamin preparation.
- emulsifiers such as sorbitan, gum arabic, and sucrose fatty acids. Ester, lecithin, etc.
- the above-mentioned emulsifier may be added, and the solution obtained by emulsification may be used as the solution containing the fat-soluble vitamin.
- Liquid foods and drinks containing fat-soluble vitamins include fruit juice or pulp drinks such as orange juice, soft drinks such as cola, milk drinks such as milk, lactic acid bacteria drinks, soy milk drinks, tea drinks, tea drinks, coffee drinks, etc. Alcoholic beverages such as wine, energy drinks, vegetable juices such as tomatoes There may be mentioned those in the form of a liquid such as sauce, noodle soup, ramen soup, liquid dressing, soup, miso soup, etc., but are not limited to these as long as they are drinkable.
- Liquid foods and drinks containing fat-soluble vitamins can be produced by using a general method for producing liquid foods and drinks except for adding fat-soluble vitamins.
- One fat-soluble vitamin may be used alone, or two or more fat-soluble vitamins may be used in combination.
- the fat-soluble vitamins need not always be added to the liquid food or drink containing the fat-soluble vitamins.
- a solution or liquid food or drink obtained by adding a dye or an emulsion and an antioxidant to a solution or liquid food or drink containing a fat-soluble vitamin can be used as the liquid food or drink of the present invention.
- Liquid food or drink of the present invention, the liquid in the food and drink of the c the present invention can be suitably used as a health food containing a fat-soluble vitamins.
- a liquid food or drink of the present invention as a health food When used, it is preferable that the fat-soluble vitamin is contained at a high concentration.
- the content of fat-soluble vitamin in 100 ml of the liquid food or drink of the present invention is preferably 8 g or more, more preferably 10 g or more, and more preferably 50 ⁇ g or more in the case of vitamin K. Is more preferred.
- the amount is preferably 0.1 ⁇ g or more, more preferably 0.5 / ig or more.
- the amount is preferably 1 mg or more, more preferably 5 mg or more.
- the amount is preferably 0.1 mg or more, more preferably 0.5 mg or more.
- the amount is preferably 1 mg or more, more preferably 10 mg or more, and even more preferably 30 mg or more.
- the stability of the fat-soluble vitamin is measured, for example, by measuring the concentration of the fat-soluble vitamin after irradiating 20 ml of the liquid food or drink of the present invention with a white fluorescent lamp at 2,000 lux. Determined as the percentage of the concentration of fat-soluble vitamins after light irradiation with respect to the previous concentration (hereinafter referred to as the residual ratio) Can be.
- the amount of the pigment to be added is preferably 0.1 mg or more, more preferably 0.5 mg or more, and even more preferably 1 mg or more, in 100 ml of the liquid food or drink of the present invention.
- the amount of the emulsion to be added is preferably at least lg, more preferably at least 5 g , in 100 ml of the liquid food or drink of the present invention.
- the amount of the antioxidant to be added is preferably 0.1 mg or more, more preferably 0.5 mg or more, more preferably 1 mg or more, in 100 ml of the liquid food or drink of the present invention.
- the liquid foods and drinks of the present invention include, in addition to fat-soluble vitamins, pigments, emulsions, and antioxidants, food additives generally used in foods and drinks, such as sweeteners, coloring agents, and preservatives. , Thickening stabilizers, antioxidants, coloring agents, bleaching agents, fungicides, gum bases, bittering agents, enzymes, brighteners, acidulants, seasonings, emulsifiers, strengthening agents, manufacturing agents, fragrances, spice extracts Things and the like may be added.
- composition obtained by mixing the above dye or emulsion and an antioxidant can be used as a stabilizer for fat-soluble vitamins.
- the composition may be used as a powder, or may be dissolved in an aqueous medium in which the fat-soluble vitamin is dissolved, an aqueous medium similar to an organic solvent, an organic solvent, or the like, and used as a solution.
- composition may be added with various additives that can be used in foods and drinks, such as seasonings, spices, inorganic salts, acids, amino acids, nucleic acids, and sugars, if necessary.
- Examples of inorganic salts include salt, potassium chloride, ammonium chloride, magnesium oxide, dolomite, and the like.
- Examples of the acid include carboxylic acids such as fumaric acid, linoleic acid, tartaric acid, citric acid, and fatty acids, and salts thereof.
- Examples of the salt include sodium and potassium salts.
- Examples of the amino acid include sodium glutamate, glycine and the like.
- Examples of the nucleic acid include sodium inosinate and sodium guanylate.
- Sugars include sucrose, glucose, milk bran and the like. I can do it.
- Examples of seasonings include natural seasonings such as soy sauce, miso, and extract, and examples of spices include various spices. The addition amount of these substances can be appropriately set according to the purpose of use. It is preferably up to 500 parts by weight.
- Reagents or preparations containing the dyes or antioxidants shown in Tables 1 to 9 were added to the aqueous solution so that the content of the dyes and antioxidants was as shown in Tables 1 to 9, respectively.
- the resulting mixture was mixed with stirring to prepare an aqueous solution containing vitamin 1 ⁇ 2 .
- Each dye was dissolved in an aqueous solution of vitamin K 2 and added in such an amount that the transmittance per 1 cm of optical path length was 12% when irradiated with light having a wavelength of 430 ⁇ .
- Riboflavin 5'-monophosphate sodium manufactured by Nippon Kuchi Co., Ltd.
- ⁇ -Rikiflavin water-soluble biocarotene
- Flaper Holder RC (manufactured by Hasegawa Koryo; contains 30% polyphenol), and as a polyphenol, Theafran 9 OS (manufactured by ITO EN; contains 92% of total polyphenol, of which catechin 63%) or polyphenol OPC Kyowa (manufactured by Kyowa Hakko Kogyo Co., Ltd .; 90% total polyphenols, of which at least 60% proanthocyanidin), and RM-21 (Mitsubishi Chemical Corporation) as a rosemary extract Water-soluble vitamin E04 (manufactured by Kyowa Hakko Kogyo Co., Ltd .; Hiichi d-tocopheronole containing 4%), sodium ascorbic acid (as Nippon Roche Co., Ltd.) Glycosyltransferase rutin (manufactured by San-Ei Gen F.F.I .; contains 15% of rutin), caffeine, caffeine (Junsei Chemical Co.,
- a transparent glass bottle was filled with 20 mL of the aqueous solution containing the vitamin K 2 , the dye and the antioxidant, and irradiated with light at 2,000 lux for 72 hours using a white fluorescent lamp (15 watts, manufactured by Hitachi). .
- Catalytic power ram Platinum power ram IRICA RC ⁇ 10-1 (4 X 10mm), manufactured by Medical Science Equipment Power ram Temperature: 40 ° C : Methanore
- Fluorescence detector (Ex. 320nm Em. 430nm)
- the residual ratio of vitamin K 2 was determined by the following equation.
- Vitamin 2 remaining (%) Vitamin 2 concentration after light irradiation / Vitamin before light irradiation ⁇ 2 concentration (4 mg / l.) X 100
- Tables 1 to 9 show the content of the dye and the antioxidant in the solution and the residual ratio of vitamin 2 .
- the content of the dye and the antioxidant is shown as the weight in 100 ml of the solution.
- Marigold dye 0 0.0 0.0 0.0 0.0
- Coenzym Q10 water-soluble CoQ10 AQUAN0VA; contains 3 ° /. Of ubide force lenon) in 300 mL of water, and dissolve ubidecarenone.
- Table 2 shows the content of your Yopibi residual ratio of glutamic K 2 of dye and antioxidant in solution. The same reagent or preparation containing a dye or an antioxidant as in Example 1 was used.
- the content of the dye and the antioxidant is shown as the weight in 100 ml of the solution.
- Emulsion in the first Table 3 shows the content and vitamin 1 2 residual ratio in an aqueous solution of an antioxidant.
- the content of the antioxidant in the emulsion was calculated based on the weight in 100 ml of the solution and Table 13.
- Emulsion content (g) Star (mg) 0 6 Isofura / pon 0 0 0
- Vitamin K 2 emulsified powders manufactured by Kyowa Hakko Kogyo Co., Ltd. 30 mg, the water-soluble Baiokarote emissions 0 2 (Kyowa Hakko Kogyo Co., Ltd .; - carotene containing 2%)] 20 mg, Sanme phosphorus (San-Ei Gen F. 'F' manufactured by Eye Corporation; Rutin 15%) 100mg, Vita
- Mi emissions manufactured by Nippon Roche; thia Mi emissions hydrochloride 1. 0 mg, Vita Mi emissions B 12 (Japan port Gerhard Ltd .; Shiano Kobara 0.1% containing Mi emissions) lmg, Naiashin (manufactured by Nippon Roche Nicotinic acid amide) 8.45 mg, calcium pantothenate (manufactured by Kawai Pharmaceutical Co., Ltd.) 5 mg, vitamin C (manufactured by Nippon Roche; 9 mg of sodium ascorbate), apple juice concentrate (manufactured by Sanofizu Co., Ltd.) 60 g of water is added to 5 g, glucose / fructose syrup (manufactured by Sanmatsu Kogyo Co., Ltd.) and 0.4 ml of apple flavor (manufactured by Ogawa Koryo Co., Ltd.), and mixed.
- Mi emissions manufactured by Nippon Roche; thia Mi emissions hydrochloride 1. 0 mg, Vita Mi emissions B
- Dry Vitamin A (manufactured by Sankyo) 4mg, Riboflavin 5, Sternate sodium monophosphate (manufactured by Nipponguchi Shu Co.) 5.0mg, Flavor Holder Rc (manufactured by Hasegawa Koryo; contains polyphenol 30 ° /.) 100mg, Vita Mi emissions B t (Japan port Gerhard Co., thiamine hydrochloride) 1. 0 mg, vitamin B 12 (manufactured by Nippon Roche;. Shianokoparami down the 0.
- Doraibita Mi emissions D 3 (Sankyo Co., Ltd.) 0. 5 mg, San'ero 2 SFU (Mi Sakae source F 'F' manufactured by Eye Corporation; base - banner dye 60% containing) 100 mg, poly Hue Nord OPC Kyowa (Kyowa Hakko Kogyo Co., Made; 90% total polyphenol Of Puroantoshia - containing Gin 60% or more) 2 0 mg, vitamin (manufactured by Nippon Roche; thia Mi emissions hydrochloride) 1.
- Vita Mi emissions B 12 (manufactured by Nippon Roche; Shianokobarami down the 0.1% containing) lmg, niacin (Nippon Roche; nicotinic acid amide) 8.45 mg, calcium pantothenate (Kawai Pharmaceutical) 5 mg, vitamin C (Nippon Roche; sodium ascorbate) 9 mg, apple concentrate 60 ml of water is added to 0.4 g of fruit juice (manufactured by Sanyo Foods), 15 g of glucose fructose syrup (manufactured by Sanmatsu Kogyo), and 0.4 ml of apple flapper (manufactured by Ogawa Perfume), and mixed.
- Coenzym Q10 (AQUAN0VA; contains 3% water-soluble ubide lenone) 333 mg, riboflavin 5'-sodium phosphate ester (Nipponguchi Shu) 5.0 mg , Theafran 9 OS (Itoen; total poly phenol 92% containing, 63% of the out catechin-containing) 20 mg, vitamin (Nippon Roche, thiamine hydrochloride) 1.
- Vita Mi emissions B 12 (manufactured by Nippon Roche; Xia Nokobarami down the 0.1 Lmg, niacin (Nihonguchi Shu Co., Ltd .; nicotinic acid amide) 8.45 mg, calcium pantothenate (Kawai Pharmaceutical Co., Ltd.) 5 mg, vitamin C (Nippon Roche Co., Ltd., sodium ascorbate) 9 mg, 60 ml of water is added to 5 g of apple concentrated juice (manufactured by Sanyo Foods), 15 g of glucose fructose syrup (manufactured by Sanmatsu Kogyo), and 0.4 ml of apple flavor (manufactured by Ogawa Koryo), and 60 ml of water is added.
- the dyes or emulsions and antioxidants listed in Table 14 are listed in Table 14 And water to 1000 ml to prepare a stabilizer for liquid foods and beverages containing fat-soluble vitamins. The same reagent or preparation containing a dye or an antioxidant as in Example 1 is used.
- a liquid food or drink containing a fat-soluble vitamin, a method for stabilizing fat-soluble vitamin, and a composition used in the stabilization method.
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- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Mycology (AREA)
- Biochemistry (AREA)
- Emergency Medicine (AREA)
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Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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JP2003581608A JP4257934B2 (ja) | 2002-04-11 | 2003-04-10 | ビタミンk2の安定化方法 |
KR1020047015915A KR100989536B1 (ko) | 2002-04-11 | 2003-04-10 | 지용성 비타민을 함유하는 액상 음식품 및 지용성비타민의 안정화 방법 |
US10/510,772 US7501138B2 (en) | 2002-04-11 | 2003-04-10 | Liquid food/drink containing fat-soluble vitamin and method of stabilizing fat-soluble vitamin |
AU2003236052A AU2003236052A1 (en) | 2002-04-11 | 2003-04-10 | Liquid food/drink containing fat-soluble vitamin and method of stabilizing fat-soluble vitamin |
Applications Claiming Priority (2)
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JP2002108787 | 2002-04-11 | ||
JP2002-108787 | 2002-04-11 |
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WO2003084352A1 true WO2003084352A1 (fr) | 2003-10-16 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/JP2003/004564 WO2003084352A1 (fr) | 2002-04-11 | 2003-04-10 | Aliment liquide/boisson contenant une vitamine liposoluble et procede de stabilisation de cette vitamine liposoluble |
Country Status (6)
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US (1) | US7501138B2 (ja) |
JP (1) | JP4257934B2 (ja) |
KR (1) | KR100989536B1 (ja) |
CN (1) | CN100574639C (ja) |
AU (1) | AU2003236052A1 (ja) |
WO (1) | WO2003084352A1 (ja) |
Cited By (4)
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JP2007125018A (ja) * | 2005-11-04 | 2007-05-24 | Pepsico Inc | 飲料中のビタミン類の分解を防止する飲料組成物および方法 |
JP2007159572A (ja) * | 2005-11-21 | 2007-06-28 | Riken Vitamin Co Ltd | 飲料用ビタミンe含有組成物 |
WO2013058301A1 (ja) * | 2011-10-21 | 2013-04-25 | 株式会社明治 | 乳性食品およびその製造方法 |
WO2016098562A1 (ja) * | 2014-12-19 | 2016-06-23 | グリコ栄養食品株式会社 | π共役系の難溶性又は不溶性物質の可溶化又は分散化組成物 |
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US8480797B2 (en) | 2005-09-12 | 2013-07-09 | Abela Pharmaceuticals, Inc. | Activated carbon systems for facilitating use of dimethyl sulfoxide (DMSO) by removal of same, related compounds, or associated odors |
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AU2007237685B2 (en) * | 2006-03-15 | 2012-08-09 | Suntory Holdings Limited | Compositions containing riboflavin and sesamin-class compounds |
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US20090018186A1 (en) * | 2006-09-06 | 2009-01-15 | The Coca-Cola Company | Stable beverage products comprising polyunsaturated fatty acid emulsions |
WO2008032006A1 (en) * | 2006-09-11 | 2008-03-20 | Overseal Natural Ingredients Ltd. | Naturally derived colours with bioactive compounds |
EP1972571A1 (en) * | 2007-03-08 | 2008-09-24 | Unilever N.V. | Beverage container holding an aqueous liquid and an oleogenous liquid |
WO2008126587A1 (ja) * | 2007-03-15 | 2008-10-23 | Suntory Holdings Limited | 抗疲労剤 |
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CN115078586A (zh) * | 2022-06-28 | 2022-09-20 | 广州汇元医药科技有限公司 | 一种高效液相色谱法测定维生素D3粉中dl-α-生育酚含量的方法 |
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2003
- 2003-04-10 JP JP2003581608A patent/JP4257934B2/ja not_active Expired - Fee Related
- 2003-04-10 KR KR1020047015915A patent/KR100989536B1/ko not_active IP Right Cessation
- 2003-04-10 CN CN03808167A patent/CN100574639C/zh not_active Expired - Fee Related
- 2003-04-10 AU AU2003236052A patent/AU2003236052A1/en not_active Abandoned
- 2003-04-10 US US10/510,772 patent/US7501138B2/en not_active Expired - Fee Related
- 2003-04-10 WO PCT/JP2003/004564 patent/WO2003084352A1/ja active Application Filing
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WO1993004598A1 (en) * | 1991-09-06 | 1993-03-18 | Betatene Limited | Carotenoid composition |
WO1994006310A1 (en) * | 1992-09-15 | 1994-03-31 | Smithkline Beecham Plc | Novel compositions |
JPH0767574A (ja) * | 1993-08-31 | 1995-03-14 | Takeda Chem Ind Ltd | カロチノイド類組成物 |
JPH07241181A (ja) * | 1994-03-04 | 1995-09-19 | Ezaki Glico Co Ltd | 着色料及び/又はビタミンを含む食品等の安定化法 |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007125018A (ja) * | 2005-11-04 | 2007-05-24 | Pepsico Inc | 飲料中のビタミン類の分解を防止する飲料組成物および方法 |
JP2007159572A (ja) * | 2005-11-21 | 2007-06-28 | Riken Vitamin Co Ltd | 飲料用ビタミンe含有組成物 |
WO2013058301A1 (ja) * | 2011-10-21 | 2013-04-25 | 株式会社明治 | 乳性食品およびその製造方法 |
JPWO2013058301A1 (ja) * | 2011-10-21 | 2015-04-02 | 株式会社明治 | 乳性食品およびその製造方法 |
WO2016098562A1 (ja) * | 2014-12-19 | 2016-06-23 | グリコ栄養食品株式会社 | π共役系の難溶性又は不溶性物質の可溶化又は分散化組成物 |
JPWO2016098562A1 (ja) * | 2014-12-19 | 2017-09-28 | グリコ栄養食品株式会社 | π共役系の難溶性又は不溶性物質の可溶化又は分散化組成物 |
Also Published As
Publication number | Publication date |
---|---|
JPWO2003084352A1 (ja) | 2005-08-11 |
US20050158424A1 (en) | 2005-07-21 |
US7501138B2 (en) | 2009-03-10 |
JP4257934B2 (ja) | 2009-04-30 |
AU2003236052A1 (en) | 2003-10-20 |
KR100989536B1 (ko) | 2010-10-25 |
CN100574639C (zh) | 2009-12-30 |
KR20040106324A (ko) | 2004-12-17 |
CN1646033A (zh) | 2005-07-27 |
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