WO2014208613A1 - Powder composition, method for producing same, and beverage - Google Patents
Powder composition, method for producing same, and beverage Download PDFInfo
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- WO2014208613A1 WO2014208613A1 PCT/JP2014/066880 JP2014066880W WO2014208613A1 WO 2014208613 A1 WO2014208613 A1 WO 2014208613A1 JP 2014066880 W JP2014066880 W JP 2014066880W WO 2014208613 A1 WO2014208613 A1 WO 2014208613A1
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- starch hydrolyzate
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- fat
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Classifications
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- 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
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- 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
- A23D9/02—Other edible oils or fats, e.g. shortenings, cooking oils characterised by the production or working-up
- A23D9/04—Working-up
- A23D9/05—Forming free-flowing pieces
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F3/00—Tea; Tea substitutes; Preparations thereof
- A23F3/06—Treating tea before extraction; Preparations produced thereby
- A23F3/14—Tea preparations, e.g. using additives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F5/00—Coffee; Coffee substitutes; Preparations thereof
- A23F5/10—Treating roasted coffee; Preparations produced thereby
- A23F5/14—Treating roasted coffee; Preparations produced thereby using additives, e.g. milk, sugar; Coating, e.g. for preserving
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F5/00—Coffee; Coffee substitutes; Preparations thereof
- A23F5/24—Extraction of coffee; Coffee extracts; Making instant coffee
- A23F5/36—Further treatment of dried coffee extract; Preparations produced thereby, e.g. instant coffee
- A23F5/40—Further treatment of dried coffee extract; Preparations produced thereby, e.g. instant coffee using organic additives, e.g. milk, sugar
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- 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
- A23L2/385—Concentrates of non-alcoholic beverages
- A23L2/39—Dry compositions
-
- 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
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/10—Foods or foodstuffs containing additives; Preparation or treatment thereof containing emulsifiers
Definitions
- the present invention relates to a powder composition containing a fat-soluble substance, a starch hydrolyzate, and a low molecular surfactant, and a method for producing the powder composition, which are particularly preferably used for beverages.
- the invention also relates to a beverage containing this powder composition.
- milk proteins such as skim milk, casein and its salts
- a technique for producing a protein-free powdered oil and fat composition having equal or better stability and dispersibility.
- a protein-free powdery fat composition comprising edible fats and oils, octenyl succinic esterified starch, and trehalose as main components (Patent Document 1); edible fats and oils having a melting point of 20 ° C.
- Protein-free powdery fat composition comprising starch, lactose and dextrin as main components
- Patent Document 2 group consisting of glycerin fatty acid ester, sucrose fatty acid ester, sorbitan fatty acid ester, propylene glycol fatty acid ester and lecithin 20 to 80% by mass of an emulsifier in the form of a paste or liquid at room temperature of one or more selected from the following, and starch or a hydrolyzate thereof and an organic acid glycerin fatty acid ester (mass ratio 100: 0.1 to 50), and / Or emulsifiable starch derivatives
- a powder emulsifier comprising 80 to 20% by mass of a powdering agent comprising hydrolyzate thereof (Patent Document 3); 6.6 to 10 parts by mass of hemicellulose and 100% by mass for 100 parts by mass of edible fats and oils Powdered oil composition containing 34-60 parts by mass of branched cyclic dextrin (Patent
- Oily powder characterized by being grade 2 to grade 5 (Patent Document 5); comprising an oily component, gum arabic and sugar, wherein the mass ratio of oily component to gum arabic is 2: 1 to 1: 5, and Mass of gum arabic and sugar 5: 1 to 1: 100 powder oil composition (Patent Document 6); amphiphile that spontaneously forms closed endoplasmic reticulum in aqueous system or sugar polymer that forms sugar polymer particles And an oil / fat component and an excipient, and when mixed with water, the powdered oil / fat forms an O / W emulsion by the action of the closed vesicles or the particles of the sugar polymer.
- Patent Document 7 There is a composition (Patent Document 7).
- the characteristic pulverized base material affects the taste quality of the food used due to the viscosity and specific odor when dissolved, and is special and expensive, so it is versatile and reduces costs. It is difficult to put it into practical use.
- the powder manufacturing method is characteristic, the existing spray drying equipment suitable for mass production cannot be used, and new manufacturing equipment and manufacturing ingenuity are required. was there.
- Powdered oil and fat composition having a dextrose equivalent of 2 to 30 (Patent Document 8); a fat-soluble material-dispersed oil in which a fat-soluble material is dispersed in fat and oil and a lipophilic emulsifier; A fat-sugar coating dispersion is prepared by mixing with an aqueous sugar-dispersed solution, and optionally dried to obtain a fat-sugar coating dispersion or an oil-sugar powder raw material.
- a manufacturing method using a starch hydrolyzate having a glucose equivalent (DE) of 5 to 15 as a saccharide (Patent Document 9) is known. .
- Japanese Unexamined Patent Publication No. 11-318332 Japanese Laid-Open Patent Publication No. 2003-73691 Japanese Unexamined Patent Publication No. 6-245719 Japanese Unexamined Patent Publication No. 2006-14629 Japanese Unexamined Patent Publication No. 2000-109882 Japanese Unexamined Patent Publication No. 2000-119686 International Publication No. 2012/081546 Japanese Unexamined Patent Publication No. 6-33087 Japanese Unexamined Patent Publication No. 2008-188010
- dextrose equivalent glucose equivalent
- dextrose equivalent glucose equivalent
- starch hydrolysates with a complex molecular weight distribution may have different molecular weight compositions, even with the same dextrose equivalent, and interact with low molecular weight surfactants such as fats and organic acid monoglycerides. It is not an appropriate parameter to understand the action essentially. Therefore, in order to prepare a protein-free powdered oil and fat composition by using a general-purpose powdered base material and spray-drying manufacturing method, further studies are required.
- the present invention has been made in view of the above-described conventional situation, and uses a general-purpose powdered base material to provide a beverage particularly suitable for the spray drying method and having excellent long-term emulsion stability. It is an object of the present invention to provide a powder oil composition that can be used.
- the gist of the present invention is as follows.
- a powder composition containing a fat-soluble substance, a starch hydrolyzate and a low molecular surfactant The powder composition, wherein the starch hydrolyzate has a peak area ratio in the range of molecular weight of 8500 to 18500 with respect to the total peak area when the molecular weight distribution is measured by gel permeation chromatography is 15% or less.
- the fat-soluble substance is an edible fat.
- the low molecular surfactant is a food emulsifier.
- a method for producing a powder composition comprising a fat-soluble substance, a starch hydrolyzate and a low molecular surfactant, As the starch hydrolyzate, a starch hydrolyzate in which the ratio of the peak area in the molecular weight range of 8500 to 18500 is 15% or less with respect to the total peak area when the molecular weight distribution is measured by gel permeation chromatography, Mixing the starch hydrolyzate, fat-soluble substance, low molecular surfactant and water to prepare a mixture, After emulsifying the mixture to obtain an emulsion, A method for producing a powder composition, characterized in that the emulsion is spray-dried or freeze-dried.
- the powder composition of the present invention is suitable for production by a spray drying method, using existing spray drying equipment suitable for mass production, without requiring new production equipment or production devices, A powder composition that can be used as a good protein-free powdery fat composition can be provided.
- the powder composition of the present invention is a powder composition containing a fat-soluble substance, a starch hydrolyzate, and a low molecular surfactant, and the starch hydrolyzate has a molecular weight distribution measured by gel permeation chromatography.
- the ratio of the peak area in the molecular weight range of 8500 to 18500 with respect to the total peak area is 15% or less.
- the fat-soluble substance is not particularly limited as long as it is hydrophobic and lipophilic, insoluble or hardly soluble in water, and easily soluble or dispersible in an organic solvent. Since the powder composition of the present invention is particularly suitably used for beverages, edible substances are preferred as the fat-soluble substance.
- the fat-soluble substance that can be used in the present invention is not limited to liquid, and may be semi-solid or solid, and these can be used by melting.
- Vegetable oils such as rapeseed oil, corn oil, soybean oil, palm oil, palm kernel oil, palm oil, sunflower oil, safflower oil, macadamia seed oil, camellia seed oil, tea seed oil, rice bran oil, olive oil, cottonseed oil;
- Animal fats such as beef tallow, milk fat, pork tallow, sheep fat, fish oil;
- Processed fats and oils such as refined, deodorized, fractionated, hardened and transesterified from these vegetable oils or animal oils or liquids (processed oils and fats, animal oils and processed oils, etc.
- edible oils and fats are “edible oils and fats”) Called;); Hydrocarbons such as squalene, squalane, liquid paraffin; Sterols such as cholesterol and plant sterols; Higher alcohols such as jojoba oil; Oil-soluble vitamins such as vitamin E, vitamin A, vitamin D, vitamin K, beta carotene, alpha carotene; Oil-soluble dyes; Oil-soluble perfume; Complex lipids such as glycolipids and phospholipids; unsaturated fatty acids such as polyunsaturated fatty acids such as ⁇ and ⁇ linolenic acid, linoleic acid, arachidonic acid, DHA, EPA; Examples thereof include waxes. These can be used individually by 1 type or in combination of 2 or more types. Among these, edible fats and oils, sterols, oil-soluble pigments, oil-soluble fragrances, oil-soluble vitamins and unsaturated fatty acids are preferable as edible fat-soluble substances.
- the rising melting point is 25 to 45 ° C., since a rich oil and fat flavor can be felt.
- palm kernel oil and coconut oil are preferable, and especially hardened palm kernel oil and cured coconut oil are preferable.
- the proportion of fatty acids having 12 or less carbon atoms in the constituent fatty acids is preferably 50% by mass or more, and from the viewpoint of oxidation stability, the proportion of unsaturated fatty acids is 15% by mass. Is preferably 10% by mass or less, more preferably 5% by mass or less, and most preferably 1% by mass or less.
- starch hydrolyzate is a general term for polysaccharides such as amylose and amylopectin that are hydrolyzed with heat, acid, alkali, enzyme, etc. in starch, also called dextrin, and glucose is ⁇ -1,4 or 1
- the main component is polysaccharides linked by 6 bonds.
- examples of the starch hydrolyzate include soluble starch, thin starch, amylodextrin, white dextrin, yellow dextrin, britesh gum, erythrodextrin, acrodextrin, maltodextrin and the like. These can be used individually by 1 type or in combination of 2 or more types.
- Starch as a raw material for the starch hydrolyzate is collected from a plant containing starch. At this time, as plant varieties, varieties that are mass-produced as agricultural products are economically advantageous. Moreover, the ratio of amylose and amylopectin contained in starch differs depending on the variety of plant. Amylose mainly has a structure in which glucose is connected in a straight chain by ⁇ -1,4 bonds, and amylopectin has a structure mainly in which glucose is connected while being branched by ⁇ -1,6 bonds.
- amylose has a strong interaction with low-molecular-weight surfactants, so when the degree of hydrolysis is high, such as when the DE value of dextrin is greater than 8, there are no particular restrictions on the varieties of starch-derived plants.
- a plant derived from starch having a higher ratio of amylopectin is preferable, and as such a plant, waxy species, that is, waxy corn, glutinous rice, or the like, or , Tapioca and sweet potato are preferable, and one kind thereof may be used, or two or more kinds may be mixed and used as a raw material starch.
- the starch hydrolyzate used in the present invention is a ratio of the peak area in the range of molecular weight 8500 to 18500 with respect to the total peak area when the molecular weight distribution is measured by gel permeation chromatography (GPC) (hereinafter simply referred to as “peak area ratio”). Is 15% or less.
- the ratio of the peak area is usually 15% or less, preferably 10% or less, more preferably 9% or less, further preferably 7% or less, and particularly preferably 5% or less.
- the peak area ratio is not more than the upper limit, the influence of the interaction with the low molecular surfactant is small, and the overall emulsion stability is improved. The smaller the peak area ratio, the better.
- the lower limit is not particularly limited.
- the measurement of the molecular weight distribution by gel permeation chromatography is usually carried out using the GPC apparatus under the following conditions.
- Detector Differential refractometer
- Sample injection volume 200 ⁇ l
- Calibration curve Pullulan standard (9 types of molecular weight between 2350,000 and 5,900) and glucose (molecular weight of 180)
- the peak area ratio is calculated as the ratio to the total peak area by converting the measurement result of the molecular weight distribution obtained by the above method into a differential molecular weight distribution curve and then summing the peak areas corresponding to the molecular weight of 8500 to 18500. can do.
- the starch hydrolyzate having a peak area ratio of 15% or less is, for example, a membrane separation using a reverse osmosis membrane, a nanofiltration membrane, an ultrafiltration membrane, a microfiltration membrane, or a column packed with silica gel or an ion exchange resin.
- the fraction hydrolyzate is separated and purified to remove components with a molecular weight of 8500 or more and 18500 or less by using fractionation treatment with, and low molecular weight treatment with starch-degrading enzymes such as ⁇ -amylase, ⁇ -amylase and glucoamylase. Can be manufactured.
- starch hydrolyzate having a peak area ratio of 15% or less As a starch hydrolyzate having a peak area ratio of 15% or less, “Paindex # 3” and “Paindex # 100” manufactured by Matsutani Chemical Industry Co., Ltd. “Fuji Oligo G67” manufactured by Nippon Shokuhin Kako Co., Ltd., Sanwa Starch Industries, Ltd. “Sandeck # 30”, “Sandeck # 70”, “Sandeck # 150”, “Sandeck # 180”, “Sandeck # 250”, “Sandeck # 300”, and the like are commercially available, and these can be used.
- the starch hydrolyzate used in the present invention may have a peak area ratio of 15% or less, and may be in a powder state or a liquid state. Moreover, although there is no restriction
- the dextrose equivalent is an index indicating the degree of starch hydrolysis measured by the Lane Einon method or the Somogy method.
- the dextrose equivalent of the starch hydrolyzate used in the present invention is 8 or less, preferably 7 or less, more preferably 5 or less, or 15 or more, preferably 18 or more, more preferably 20 or more. This is preferable.
- the weight average molecular weight of the starch hydrolyzate used in the present invention is preferably 9000 or less or 12000 or more. In particular, it is preferably 7000 or less, more preferably 6000 or less, and even more preferably 5000 or less. Also, it is preferably 15000 or more, more preferably 20000 or more, further preferably 50000 or more, particularly preferably 60000 or more, and most preferably 70000 or more. Among them, it is preferably 1000 to 5000, or 70000 to 300000. It is preferable that the weight average molecular weight of the starch hydrolyzate is within this range in order to obtain the above peak area ratio of 15% or less.
- the low molecular surfactant is a substance having a hydrophilic part and a lipophilic part in the molecular structure, an amphiphilic substance having a surface activity, and preferably a substance having a molecular weight of 5000 or less.
- Low molecular surfactants do not include macromolecules such as proteins, polysaccharides, and synthetic polymers.
- the low molecular surfactant used in the present invention may be in any form such as powder, solid, liquid, paste, etc., but is preferably dissolved in water.
- the molecular weight of the low molecular surfactant is more preferably 3000 or less, and most preferably 2000 or less. The smaller the molecular weight of the low molecular surfactant, the larger the number of moles per weight, and the more the number of molecules contributing to the emulsion stability is more preferable.
- limiting in particular as a minimum of the molecular weight of a low molecular surfactant Since the hydrophilic part and lipophilic part are included in molecular structure, the molecular weight is 200 or more normally.
- low molecular surfactant examples include lecithin and lysolecithin, monoglycerin organic acid fatty acid ester, fatty acid salt, monoalkylsulfate, alkylpolysiloxane whose hydrophilic portion is ionic (cationic / anionic / zwitterionic).
- a food emulsifier that can be used for foods and drinks is preferable, and among food emulsifiers, those that have been confirmed to be safe for eating and drinking and are soluble in water are preferable.
- Examples of food emulsifiers include lecithin and lysolecithin, monoglycerin organic acid fatty acid ester, sucrose fatty acid ester, glycerin fatty acid ester, polyglycerin fatty acid ester, sorbitan fatty acid ester, polysorbate, propylene glycol fatty acid ester, and saponin.
- Lysolecithin, monoglycerin organic acid fatty acid ester, sucrose fatty acid ester, polyglycerin fatty acid ester, polysorbate are preferred, sucrose fatty acid ester, polyglycerin fatty acid ester are more preferred, and sucrose fatty acid is preferred because of its high solubility in water Esters are most preferred.
- sucrose fatty acid ester from the viewpoint of stabilizing the emulsification of the oil-in-water emulsion, those having an HLB of 5 or more are preferable, 7 or more are more preferable, 18 or less are preferable, and 11 or less are more preferable. . Further, from the viewpoint of efficiently adsorbing to the oil droplet interface and strengthening the interface film, the carbon number of the fatty acid of the sucrose fatty acid ester is preferably 12 or more, more preferably 14 or more, preferably 20 or less, and more preferably 18 or less. .
- a relatively hydrophobic low molecular surfactant capable of controlling the physical properties and phase state of a fat-soluble substance is used in combination with a hydrophilic low molecular surfactant that dissolves in water. It is preferable.
- a hydrophobic low-molecular surfactant food emulsifiers that can be used for foods and drinks are preferred, among food emulsifiers, and safety that can be eaten and eaten has been confirmed and dispersed in a fat-soluble substance. Those that dissolve are preferred.
- hydrophobic food emulsifiers examples include lecithin, monoglycerin organic acid fatty acid ester, sucrose fatty acid ester, glycerin fatty acid ester, polyglycerin fatty acid ester, sorbitan fatty acid ester, and propylene glycol fatty acid ester.
- Monoglycerin organic acid fatty acid ester, sucrose fatty acid ester, glycerin fatty acid ester, and polyglycerin fatty acid ester are preferred because of their large action on fat-soluble substances, and sucrose fatty acid ester, glycerin fatty acid ester, and polyglycerin fatty acid ester are More preferred is sucrose fatty acid ester.
- sucrose fatty acid ester and polyglycerin fatty acid ester those having an HLB of 5 or less are preferred, those having 4 or less are more preferred, and those having 0 or more are preferred from the viewpoint of effectively controlling the physical properties and phase state of the fat-soluble substance.
- one or more is more preferable, and 2-3 is most preferable.
- the number of carbon atoms of the fatty acid of the sucrose fatty acid ester and the polyglycerol fatty acid ester is preferably 12 or more, more preferably 16 or more, and most preferably 18 or more.
- the powder composition of the present invention contains the above-mentioned fat-soluble substance, starch hydrolyzate, and low-molecular surfactant as essential components, but in a range that does not interfere with the effects of the present invention, Components other than the starch hydrolyzate and the low molecular surfactant, for example, proteins, carbohydrates, aroma components, anti-caking agents, and the like may be contained. Therefore, the liquid mixture for producing the powder composition of the present invention described later may contain these other components.
- Examples of other components that may be contained in the powder composition of the present invention include protein derived from dairy products such as casein, sodium caseinate, whey protein, skim milk powder, and milk, animal proteins such as gelatin, isolated soy protein, Vegetable proteins such as protein extracted from corn or wheat; starch and processed starch, soy polysaccharides, gum arabic, etc.
- dairy products such as casein, sodium caseinate, whey protein, skim milk powder, and milk
- animal proteins such as gelatin, isolated soy protein, Vegetable proteins such as protein extracted from corn or wheat; starch and processed starch, soy polysaccharides, gum arabic, etc.
- Microorganisms, plants, dietary fibers and gums obtained by synthesis polysaccharides such as oligosaccharides, sugars and lactose Carbohydrates such as disaccharides, monosaccharides such as glucose and fructose, or mixtures thereof; fruit juice obtained by squeezing apples, bananas, grapes, mandarin oranges; flavorings; vitamins represented by vitamin B group, iron , Minerals such as magnesium and calcium; organic acids such as citric acid, malic acid and lactic acid Colors to improve appearance; flavors to improve flavor; magnesium carbonate, fine silicon dioxide, magnesium stearate, calcium stearate, ammonium iron citrate, ferrocyanide, anhydrous sodium phosphate, anhydrous magnesium sulfate, Examples of the anti-caking agent such as calcium phosphate and calcium silicate include, but are not limited to these.
- the powder composition of the present invention preferably contains substantially no sodium caseinate in terms of emulsion stability when used as a beverage.
- Casein sodium here refers to casein sodium added to the casein separated from the milk of mammals such as cattle by precipitation with acid, fermentation, enzyme treatment, etc. Refers to products that have been refined, dried, packaged and distributed.
- “Not containing sodium caseinate” means that the content of sodium caseinate in the powder composition is 0.1 or less, preferably 0.05 or less in terms of mass ratio when the low molecular surfactant is 1. , More preferably 0.01 or less, most preferably 0.005 or less.
- the content of sodium caseinate is 1.0% by mass or less, preferably 0.5% by mass or less, more preferably 0.3% by mass or less, Particularly preferably, it means 0.1% by mass or less, and most preferably means that it is not contained at all.
- the powder composition of the present invention may contain water
- the powder composition of the present invention is a powder, so that even if it contains water, it maintains the form as a powder.
- the water content is preferably 5.0% by mass or less, more preferably 4.0% by mass or less, and most preferably 3.0% by mass or less.
- the preferable content of each component of the powder composition of the present invention is as follows. Content of fat-soluble substance in the composition: 10% by mass or more is preferable, 20% by mass or more is more preferable, 70% by mass or less is preferable, and 50% by mass or less is more preferable. Content of starch hydrolyzate in the composition: 30% by mass or more is preferable, 50% by mass or more is more preferable, 90% by mass or less is preferable, and 80% by mass or less is more preferable. Content of low molecular surfactant in the composition: 0.1% by mass or more is preferable, 0.5% by mass or more is more preferable, 1.0% by mass or more is particularly preferable, and 10% by mass or less is preferable.
- the content ratio of the low molecular surfactant and the starch hydrolyzate is more preferably 1: 1 to 1: 4.
- the content ratio of the low molecular surfactant: starch hydrolyzate (mass ratio) 1: 3 to 1: 900.
- the range is 1:10 to 1: 160.
- the content of the fat-soluble substance in the composition is in the range above the lower limit, the amount of the fat-soluble substance per cost of the powder composition is appropriate and economical, and is in the range below the upper limit.
- Emulsification is good, emulsification is difficult to break when pulverized or when the powder composition is dissolved, and the content of other components is relatively appropriate, and functions by other components are sufficiently obtained be able to.
- the content of the starch hydrolyzate in the composition is in the range above the lower limit, pulverization becomes good, and the obtained powder composition has low adhesion, good flowability, and good handling powder.
- the amount of the fat-soluble substance per cost of the powder composition is appropriate and economical, and the content of other components is relatively appropriate, depending on the other components The function can be fully obtained.
- the content of the low-molecular-weight surfactant in the composition is in the range of the above lower limit or more, the emulsification stabilization becomes good, and the emulsification is difficult to break when powdered or when the powder composition is dissolved,
- the taste of the low molecular surfactant itself does not become strong, and when used in foods, the flavor is hardly impaired.
- the low molecular surfactant is expensive, it is economical because the price of the powder composition itself is appropriate because it is in the range below the above upper limit, and the content of other components is relatively appropriate. The function by other components can be sufficiently obtained.
- the content of the starch hydrolyzate with respect to the fat-soluble substance is in the range above the lower limit, so that pulverization is good, and the obtained powder composition has low adhesion, good fluidity, and good handling.
- the amount of the fat-soluble substance per cost of the powder composition is appropriate and economical.
- the content ratio of the starch hydrolyzate with respect to the low molecular surfactant is within the above-mentioned lower limit, the taste of the low molecular surfactant itself is appropriate, and when used in foods, the flavor is hardly impaired.
- the low-molecular surfactant is expensive, it is economical because the price of the powder composition itself is appropriate because it is in the range of the upper limit or less, the emulsion stabilization is good, When the powder composition is dissolved, the emulsification is not easily broken.
- the method for producing the powder composition of the present invention is not particularly limited, but preferably, according to the method for producing the powder composition of the present invention, a starch hydrolyzate having a peak area ratio of 15% or less, a fat-soluble substance, and a low molecular interface.
- the mixture is prepared by mixing an activator and water to prepare a mixed solution, emulsifying the mixed solution to obtain an emulsion, and then spray-drying or freeze-drying the obtained emulsion.
- the viscosity and solid content of the emulsion obtained in the next step is spray drying described later, or It is preferably used so as to have a suitable viscosity and solid content suitable for freeze-drying.
- a method of emulsifying a mixed solution obtained by mixing starch hydrolyzate, fat-soluble substance, low molecular surfactant and water it can be adopted without any limitation as long as it is a homogeneous emulsification method usually used for foods.
- any of a method using a homogenizer, a method using a colloid mill, a method using a homomixer, and the like are applicable.
- the drying method of the emulsion spray drying method, air flow drying method, drum drying method, cylindrical drying method, freeze drying method such as vacuum freeze drying method, vacuum drying method and the like can be used, but suitable for mass production. Spray drying is preferred.
- the emulsion may be heated as necessary.
- the emulsion to be subjected to spray drying has a viscosity of 5 to 200 mPa ⁇ s at the temperature at the time of spraying, in view of emulsification efficiency, emulsion stability, and dischargeability of the emulsion from the nozzle in the spray drying process. Is preferable.
- the solid content of the emulsified liquid is preferably 5% or more, more preferably 10% or more, further preferably 15% or more, and 70% or less on a mass basis in order to ensure dischargeability from the nozzle during spray drying. Is preferably 60% or less, and more preferably 50% or less.
- the powder composition obtained by spray drying of the emulsion may be pulverized, classified, granulated, etc. as necessary.
- the powder composition of the present invention is contained in beverages such as coffee beverages, tea beverages, various tea beverages other than black tea, and preferably used in milk beverages such as milk coffee, cafe au lait, and milk tea.
- a milk drink is a drink containing milk fat, milk protein, and the like, which are milk components.
- the beverage containing the powder composition of the present invention is produced, for example, as follows.
- a mixed solution is prepared by mixing the powder composition of the present invention, milk components, coffee, tea or tea extract, emulsifier, and water as necessary.
- a known compounding agent such as a pH adjuster such as sugar, fragrance, vitamin, and sodium bicarbonate, a sweetener, a thickening stabilizer, an antioxidant, and an enzyme may be added to the mixed solution.
- milk components such as nonfat dry milk, nonfat concentrated milk, WPC, WPI, MPC, TMP, buttermilk powder, lactose, and whey minerals are milk components. It is preferable to use a raw material containing non-fat milk solids such as. However, milk components such as milk, concentrated milk, whole milk powder, fresh cream and cheese, and milk fat such as butter and butter oil may be added as necessary.
- the emulsification method can be used without particular limitation as long as it is a homogeneous emulsification method usually used for foods.
- any of a method using a homogenizer, a method using a colloid mill, a method using a homomixer, etc. can be used. it can.
- This homogeneous emulsification treatment is usually carried out under heating conditions of 40 to 80 ° C., and the emulsification step using a homogenizer is usually carried out under high pressure conditions of 5 to 200 MPa, preferably 10 to 100 MPa.
- sterilization treatment such as UHT sterilization and retort sterilization is performed.
- retort sterilization is performed at 121 ° C. for 20 to 40 minutes.
- UHT sterilization used for beverages for PET bottles is ultra-high temperature sterilization at a higher temperature, for example, a sterilization temperature of 130 to 150 ° C. and a sterilization value (Fo) at 121 ° C. corresponding to 10 to 50.
- UHT sterilization is a known method such as a direct injection method such as a steam injection method in which water vapor is directly blown into a beverage, a steam infusion method in which a beverage is injected into the water vapor, and an indirect heating method using a surface heat exchanger such as a plate or tube.
- a plate type sterilizer can be used.
- the manufactured drink of this invention is suitable for a container-packed drink, for example, can be used as a can drink or a plastic bottle drink.
- the content of the powder composition of the present invention in the beverage of the present invention thus produced varies depending on the amount of milk component, coffee, tea or tea extract added at the same time, but is usually 0.1% by mass. Preferably, it is 0.5% by mass or more, more preferably 1.0% by mass or more, preferably 30% by mass or less, and 20% by mass or less. Is more preferable, and it is further more preferable that it is 10 mass% or less.
- the content of the milk component in the milk beverage is preferably 5% by mass or more, more preferably 10% by mass or more, and 60% by mass or less in terms of milk. Preferably, it is 40% by mass or less, more preferably 25% by mass or less.
- the emulsifier is not particularly limited as long as it can be used in foods.
- fatty acid esters such as sucrose fatty acid ester, polysorbate (polyoxyethylene sorbitan acid ester), glycerin fatty acid ester (monoglyceride, organic acid monoglyceride, polyglycerin fatty acid ester), sorbitan fatty acid ester, propylene glycol fatty acid ester, etc.
- fatty acid esters such as sucrose fatty acid ester, polysorbate (polyoxyethylene sorbitan acid ester), glycerin fatty acid ester (monoglyceride, organic acid monoglyceride, polyglycerin fatty acid ester), sorbitan fatty acid ester, propylene glycol fatty acid ester, etc.
- Sodium stearoyl lactate calcium stearoyl lactate, enzymatically decomposed lecithin, lecithin, saponin and the like.
- sucrose fatty acid ester, organic acid monoglyceride, polyglycerin fatty acid ester, sorbitan fatty acid ester, polysorbate (polyoxyethylene sorbitan acid ester) are preferable, and sucrose fatty acid ester, organic acid monoglyceride, polyglycerin fatty acid ester are It is more preferable since the emulsion stability of the milk beverage is good.
- food emulsifiers ie, bacteriostatic emulsifiers
- food emulsifiers that are effective against heat-resistant bacteria that are harmful bacteria in beverages
- any emulsifier for food having the effect can be used without particular limitation, but sucrose fatty acid ester, polyglycerin fatty acid ester, and organic acid monoglyceride include Particularly preferred are sucrose fatty acid esters, polyglycerin fatty acid esters, and organic acid monoglycerides having 14 to 22 carbon atoms in the constituent fatty acids, and sucrose fatty acid esters and polyglycerin fatty acids in which the constituent fatty acids have 16 to 18 carbon atoms.
- Esters are more preferred, and these are preferred because of their high effectiveness against bacteria.
- sucrose fatty acid ester and polyglycerin fatty acid ester to be used a monoester content of 50% by mass or more, preferably 60% by mass or more, more preferably 70% by mass or more is preferable because of its high effectiveness against bacteria. It is.
- the polyglycerol fatty acid ester the average degree of polymerization of polyglycerol is preferably 2 to 5, and more preferably 2 to 3 because of its high effectiveness against bacteria.
- the content of the emulsifier in the milk beverage is usually preferably 0.005% by mass or more, more preferably 0.01% by mass or more, preferably 0.5% by mass or less, and more preferably 0.3% by mass or less.
- the beverage containing the powder composition of the present invention is preferably a beverage containing a bacteriostatic emulsifier, substantially not containing sodium caseinate, particularly from the viewpoint of emulsion stability. That is, it is preferable that sodium caseinate is not substantially contained in the powder composition, and further, it is preferable that sodium caseinate is not substantially contained in the production of beverages.
- the content of sodium caseinate is 0.3% by mass or less, preferably 0.1% by mass or less, more preferably 0.05% by mass or less. More preferably, it means 0.01% by mass or less, particularly preferably 0.001% by mass or less. Most preferably, it does not contain at all.
- the beverage containing the powder composition of the present invention is a beverage having high emulsification stability while having bacteriostatic properties.
- Example 1 Hardened coconut oil (“Hardened coconut oil” manufactured by Fuji Oil Co., Ltd.) 15% by mass, sucrose fatty acid ester (sucrose stearate “Ryoto (registered trademark) sugar ester S-570” manufactured by Mitsubishi Chemical Foods, HLB5) 1 0.0% by mass, starch hydrolyzate A (manufactured by Matsutani Chemical Industry Co., Ltd., Paindex # 3, derived from corn starch) and 50% by mass of water were mixed. This mixed solution was dispersed at 50 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier. The obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”). A-1 ”) was obtained.
- Example 2 A powder composition (hereinafter referred to as “powder composition”) was used in the same manner as in Example 1 except that the starch hydrolyzate A was changed to starch hydrolyzate B (manufactured by Matsutani Chemical Industry Co., Ltd., Paindex # 100, derived from waxy corn starch). This was referred to as product B-1 ".
- Example 1 A powder composition (hereinafter referred to as “powder composition”) was used in the same manner as in Example 1 except that the starch hydrolyzate A was changed to starch hydrolyzate C (manufactured by Matsutani Chemical Industry Co., Ltd., Paindex # 2, derived from corn starch). C-1 ").
- Hardened coconut oil (“Hardened coconut oil” manufactured by Fuji Oil Co., Ltd.) 20% by mass, sucrose fatty acid ester (sucrose stearate “Ryoto (registered trademark) sugar ester S-570” manufactured by Mitsubishi Chemical Foods, HLB5) 2 0.5% by mass, 27.5% by mass of starch hydrolyzate A and 50% by mass of water were mixed.
- This mixed solution was dispersed at 50 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier.
- the obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”).
- A-2 was obtained.
- Example 4 A powder composition (hereinafter referred to as “powder composition B-2”) was obtained in the same manner as in Example 3 except that starch hydrolyzate A was changed to starch hydrolyzate B.
- powder composition C-2 A powder composition (hereinafter referred to as “powder composition C-2”) was obtained in the same manner as in Example 3 except that the starch hydrolyzate A was changed to the starch hydrolyzate C.
- Test Example 2 1.1 g of powder compositions A-2, B-2, and C-2 were dissolved in 100 ml of water, and the degree of layer separation over time when stored at 30 ° C or 50 ° C was observed to stabilize the emulsion. The properties were evaluated in the same manner as in Test Example 1. The results are shown in Table 3. When 1.1 g of the powder compositions A-2, B-2 and C-2 are dissolved in 100 ml of water and stored at 20 ° C., 30 ° C., 35 ° C., 40 ° C. and 50 ° C. for 3 days. The average particle diameter increase rate of the emulsion was evaluated according to the following criteria. The average particle size was measured using a nanoparticle size distribution measuring device (SALD-7100 manufactured by Shimadzu Corporation). The results are shown in Table 4.
- Increase rate average particle diameter after storage / average particle diameter before storage is less than 1.3 ⁇ : the increase rate is 1.3 or more and less than 1.5 ⁇ : the increase rate is 1.5 or more and less than 1.7 ⁇ : The increase rate is 1.7 or more
- Test Example 3 From the results of Test Examples 1 and 2, there was no difference in the powder composition at the time of obtaining the powder composition, and there was a difference in the emulsion in which the powder composition was dispersed and dissolved in water. The particle diameter increase rate of the emulsion was considered to reflect the emulsion stability when the powder composition was dissolved again. Therefore, an emulsion containing a starch hydrolyzate was prepared, and the emulsion was not powdered, diluted with water to the same concentration as in Test Examples 1 and 2, and the particle diameter increase rate of the diluted emulsion was confirmed.
- the median diameter increase rate of the particles of the diluted emulsion was as follows: It was evaluated with. The median diameter was measured using a laser diffraction / scattering particle size distribution analyzer (Horiba, Ltd., LA-950V2). The results are shown in Table 6.
- Increase rate median diameter of particles after storage / median diameter of particles before storage is less than 2.5 ⁇ : the increase rate is 2.5 or more and less than 3.5 ⁇ : increase above The rate is 3.5 or more and less than 4.5.
- X The increase rate is 4.5 or more.
- Hardened coconut oil (“Hardened coconut oil” manufactured by Fuji Oil Co., Ltd.) 20% by mass, sucrose fatty acid ester (sucrose stearate “Ryoto (registered trademark) sugar ester S-570” manufactured by Mitsubishi Chemical Foods, HLB5) 2 0.5% by mass, sodium caseinate (manufactured by Tatua) 2.5% by mass, starch hydrolyzate A 27.5% by mass and water 47.5% by mass were mixed.
- This mixed solution was dispersed at 50 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier.
- the obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”).
- A-3 was obtained.
- powder composition C-3 A powder composition (hereinafter referred to as “powder composition C-3”) was obtained in the same manner as in Example 5 except that the starch hydrolyzate A was changed to the starch hydrolyzate C.
- Test Example 4 1.1 g of the powder compositions A-3 and C-3 were each dissolved in 100 ml of water and evaluated in the same manner as in Test Example 1. The results are shown in Table 7.
- Hardened coconut oil (“Hardened coconut oil” manufactured by Fuji Oil Co., Ltd.) 16% by mass, sucrose fatty acid ester (sucrose stearate “Ryoto (registered trademark) sugar ester S-1170” manufactured by Mitsubishi Chemical Foods, HLB11) 1 .25% by mass, starch hydrolyzate A 32.75% by mass and water 50% by mass were mixed.
- This mixed solution was dispersed at 50 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier.
- the obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”).
- A-4 was obtained.
- Example 7 A powder composition A-5 was obtained in the same manner as in Example 6 except that 0.1% by mass of monoglycerin fatty acid ester was added to the hardened coconut oil to make water 49.9% by mass.
- Example 8 0.1% by mass of sucrose laurate ("Ryoto (registered trademark) sugar ester L-195" manufactured by Mitsubishi Chemical Foods Co., Ltd., HLB1) was added to the hardened coconut oil to make water 49.9% by mass. Obtained a powder composition A-6 in the same manner as in Example 6.
- Example 9 Example 6 except that 0.1% by mass of sucrose stearate (“Ryoto® Sugar Ester S-370”, HLB3) was added to the hydrogenated coconut oil to make 49.9% by mass of water. In the same manner as above, a powder composition A-7 was obtained.
- Example 10 0.1% by mass of polyglycerin behenic acid ester (“Ryoto (registered trademark) polyglycerin B-100D, manufactured by Mitsubishi Chemical Foods Co., Ltd., HLB3)” is added to the hardened coconut oil, and 49.9% by mass of water.
- a powder composition A-8 was obtained in the same manner as in Example 6 except that
- Hardened coconut oil (“Hardened coconut oil” manufactured by Fuji Oil Co., Ltd.) 16% by mass, sucrose fatty acid ester (sucrose stearate “Ryoto (registered trademark) sugar ester S-770” manufactured by Mitsubishi Chemical Foods, HLB11) 1 .25% by mass, starch hydrolyzate A 32.75% by mass and water 50% by mass were mixed.
- This mixed solution was dispersed at 70 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier.
- the obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”).
- A-9 was obtained.
- Hardened coconut oil (“hardened coconut oil”) in which 0.08% by mass of sucrose fatty acid ester (sucrose stearate “Ryoto (registered trademark) sugar ester S-370” manufactured by Mitsubishi Chemical Foods Co., Ltd., HLB3) was previously dispersed.
- Sucrose fatty acid ester (sucrose stearate “Ryoto (registered trademark) sugar ester S-770", Mitsubishi Chemical Foods, Ltd., HLB11) 1.25% by mass, starch hydrolyzate A 32.67 mass% and 50 mass% water were mixed. This mixed solution was dispersed at 70 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier. The obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”). A-10 ").
- Test Example 7 2.0 g of powder compositions A-9 and A-10 were each dissolved in 100 ml of water and the average particle diameter increase rate when stored at 20 ° C., 25 ° C., 30 ° C., 40 ° C. and 50 ° C. for 3 days Evaluation was performed according to the same criteria as in Test Example 2. The average particle size was measured using SALD-7100 manufactured by Shimadzu Corporation. The results are shown in Table 10.
- Example 13 In the same manner as in Test Example 3, the effect of adding a hydrophobic low molecular surfactant was confirmed. Specifically, hydrogenated coconut oil (“Sucrose stearate“ Ryoto (registered trademark) Sugar ester S-370 ”manufactured by Mitsubishi Chemical Foods, Ltd., HLB3) 0.08% by mass in advance is dispersed in advance.
- sucrose fatty acid ester sucrose stearate “Ryoto (registered trademark) sugar ester S-770”, Mitsubishi Chemical Foods Co., Ltd., HLB11
- Starch hydrolyzate A 32.67% by mass and water 50% by mass were mixed.
- This mixed solution was dispersed at 70 ° C. using a homomixer and then emulsified at 100 MPa using an ultrahigh pressure emulsifier, and a diluted emulsion was prepared by dispersing 4.0 g of the obtained emulsion in 100 ml of water. did.
- the remaining emulsion was dried with a spray dryer to obtain a powder composition A-11.
- the average particle diameter increase rate when the obtained diluted emulsion was stored at 20 ° C., 25 ° C., 30 ° C., 40 ° C., and 50 ° C. for 4 days was evaluated according to the same criteria as in Test Example 2.
- the average particle size was measured using a nanoparticle size distribution measuring device (SALD-7100 manufactured by Shimadzu Corporation). The results are shown in Table 11.
- Example 14 Instant tea 0.15% by mass, sugar 7.0% by mass, skim milk powder 1.9% by mass, powder composition A-1 3.2% by mass, sucrose fatty acid ester (sucrose palmitate ester “Ryoto (registered) (Trademark) Sugar Ester P-1570 (Mitsubishi Chemical Foods Co., Ltd.) 0.03% by mass and water (remainder) were mixed, sufficiently stirred and dissolved, and then emulsified with a high-pressure homogenizer. This was UHT sterilized and then filled into a PET bottle to obtain a PET bottled milk tea containing milk components. This milk tea was in good stability after refrigeration and storage at room temperature for 2 months.
- sucrose fatty acid ester sucrose palmitate ester “Ryoto (registered) (Trademark) Sugar Ester P-1570 (Mitsubishi Chemical Foods Co., Ltd.) 0.03% by mass and water (remainder) were mixed, sufficiently stirred and dissolved, and then emulsified with a high
- Example 15 A PET bottled milk tea was obtained in the same manner as in Example 13 except that the powder composition A-1 was changed to A-10. This milk tea was in good stability after refrigeration and storage at room temperature for 2 months.
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Abstract
Description
〔1〕
脂溶性物質、澱粉加水分解物及び低分子界面活性剤を含有する粉末組成物であって、
前記澱粉加水分解物が、ゲル浸透クロマトグラフィーで分子量分布を測定した際の総ピーク面積に対する分子量8500以上18500以下の範囲のピーク面積の割合が15%以下であることを特徴とする粉末組成物。
〔2〕
前記脂溶性物質が食用油脂である、上記〔1〕に記載の粉末組成物。
〔3〕
前記低分子界面活性剤が食品用乳化剤である、上記〔1〕または〔2〕に記載の粉末組成物。
〔4〕
前記澱粉加水分解物の重量平均分子量が9000以下である、上記〔1〕~〔3〕のいずれか一に記載の粉末組成物。
〔5〕
前記澱粉加水分解物の重量平均分子量が50000以上である、上記〔1〕~〔3〕のいずれか一に記載の粉末組成物。
〔6〕
実質的にカゼインナトリウムを含有しない、上記〔1〕~〔5〕のいずれか一に記載の粉末組成物。
〔7〕
上記〔1〕~〔6〕のいずれか一に記載の粉末組成物を含有する、飲料。
〔8〕
さらに、乳成分を含有する、上記〔7〕に記載の飲料。
〔9〕
さらに、静菌性乳化剤を含有する上記〔7〕または〔8〕に記載の飲料。
〔10〕
コーヒーまたは紅茶飲料である、上記〔7〕~〔9〕のいずれか一に記載の飲料。
〔11〕
脂溶性物質、澱粉加水分解物及び低分子界面活性剤を含有する粉末組成物の製造方法であって、
前記澱粉加水分解物として、ゲル浸透クロマトグラフィーで分子量分布を測定した際の総ピーク面積に対する、分子量8500以上18500以下の範囲のピーク面積の割合が15%以下である澱粉加水分解物を用い、
前記澱粉加水分解物、脂溶性物質、低分子界面活性剤及び水を混合して混合液を調製し、
前記混合液を乳化して乳化液を得た後、
前記乳化液を噴霧乾燥または凍結乾燥することを特徴とする、粉末組成物の製造方法。 That is, the gist of the present invention is as follows.
[1]
A powder composition containing a fat-soluble substance, a starch hydrolyzate and a low molecular surfactant,
The powder composition, wherein the starch hydrolyzate has a peak area ratio in the range of molecular weight of 8500 to 18500 with respect to the total peak area when the molecular weight distribution is measured by gel permeation chromatography is 15% or less.
[2]
The powder composition according to [1] above, wherein the fat-soluble substance is an edible fat.
[3]
The powder composition according to [1] or [2] above, wherein the low molecular surfactant is a food emulsifier.
[4]
The powder composition according to any one of [1] to [3] above, wherein the starch hydrolyzate has a weight average molecular weight of 9000 or less.
[5]
The powder composition according to any one of [1] to [3] above, wherein the starch hydrolyzate has a weight average molecular weight of 50,000 or more.
[6]
The powder composition according to any one of [1] to [5], which contains substantially no sodium caseinate.
[7]
A beverage comprising the powder composition according to any one of [1] to [6] above.
[8]
Furthermore, the drink as described in said [7] containing a milk component.
[9]
The beverage according to [7] or [8] above, further comprising a bacteriostatic emulsifier.
[10]
The beverage according to any one of [7] to [9] above, which is a coffee or tea beverage.
[11]
A method for producing a powder composition comprising a fat-soluble substance, a starch hydrolyzate and a low molecular surfactant,
As the starch hydrolyzate, a starch hydrolyzate in which the ratio of the peak area in the molecular weight range of 8500 to 18500 is 15% or less with respect to the total peak area when the molecular weight distribution is measured by gel permeation chromatography,
Mixing the starch hydrolyzate, fat-soluble substance, low molecular surfactant and water to prepare a mixture,
After emulsifying the mixture to obtain an emulsion,
A method for producing a powder composition, characterized in that the emulsion is spray-dried or freeze-dried.
ここで、本明細書において“質量%”と“重量%”、“質量ppm”と“重量ppm”、及び“質量部”と“重量部”とは、それぞれ同義である。また、単に“ppm”と記載した場合は、“重量ppm”のことを示す。 Embodiments of the present invention will be described in detail below, but the description of the constituent elements described below is an example (representative example) of an embodiment of the present invention, and the present invention does not exceed the gist thereof. The content of is not specified.
Here, in the present specification, “mass%” and “weight%”, “mass ppm” and “weight ppm”, and “mass part” and “weight part” are synonymous, respectively. In addition, when “ppm” is simply described, it indicates “weight ppm”.
脂溶性物質としては、疎水性かつ親油性であり、水に不溶又は難溶で、有機溶媒に可溶又は分散しやすい物質であれば、特に制限はない。本発明の粉末組成物は、特に飲料に好適に用いられることから、脂溶性物質としては食用可能なものが好ましい。 [Fat-soluble substances]
The fat-soluble substance is not particularly limited as long as it is hydrophobic and lipophilic, insoluble or hardly soluble in water, and easily soluble or dispersible in an organic solvent. Since the powder composition of the present invention is particularly suitably used for beverages, edible substances are preferred as the fat-soluble substance.
ナタネ油、コーン油、大豆油、パーム油、パーム核油、ヤシ油、ヒマワリ油、サフラワー油、マカデミア種子油、ツバキ種子油、茶実油、米糠油、オリーブ油、綿実油等の植物性油脂;
牛脂、乳脂、豚脂、羊脂、魚油等の動物性油脂;
これら植物性油脂又は動物性油脂の液状又は固体状物を精製や脱臭、分別、硬化、エステル交換といった油脂加工した加工油脂(上記植物性油脂、動物性油脂及びその加工油脂等を「食用油脂」という。);
スクワレン、スクワラン、流動パラフィン等の炭化水素;
コレステロール、植物ステロール等のステロール類;
ホホバ油等の高級アルコール;
ビタミンE、ビタミンA、ビタミンD、ビタミンK、ベータカロチン、アルファカロチン等の油溶性ビタミン;
油溶性色素;
油溶性香料;
糖脂質、リン脂質等の複合脂質;
αおよびγリノレン酸、リノール酸、アラキドン酸、DHA、EPA等の多価不飽和脂肪酸などの不飽和脂肪酸;
ワックス類
等が挙げられる。
これらは1種を単独で又は2種以上を組み合わせて用いることができる。
これらのうち、食用可能な脂溶性物質として、食用油脂、ステロール類、油溶性色素、油溶性香料、油溶性ビタミン、不飽和脂肪酸が好ましい。 As a fat-soluble substance that can be used in the present invention, for example,
Vegetable oils such as rapeseed oil, corn oil, soybean oil, palm oil, palm kernel oil, palm oil, sunflower oil, safflower oil, macadamia seed oil, camellia seed oil, tea seed oil, rice bran oil, olive oil, cottonseed oil;
Animal fats such as beef tallow, milk fat, pork tallow, sheep fat, fish oil;
Processed fats and oils such as refined, deodorized, fractionated, hardened and transesterified from these vegetable oils or animal oils or liquids (processed oils and fats, animal oils and processed oils, etc. are “edible oils and fats”) Called;);
Hydrocarbons such as squalene, squalane, liquid paraffin;
Sterols such as cholesterol and plant sterols;
Higher alcohols such as jojoba oil;
Oil-soluble vitamins such as vitamin E, vitamin A, vitamin D, vitamin K, beta carotene, alpha carotene;
Oil-soluble dyes;
Oil-soluble perfume;
Complex lipids such as glycolipids and phospholipids;
unsaturated fatty acids such as polyunsaturated fatty acids such as α and γ linolenic acid, linoleic acid, arachidonic acid, DHA, EPA;
Examples thereof include waxes.
These can be used individually by 1 type or in combination of 2 or more types.
Among these, edible fats and oils, sterols, oil-soluble pigments, oil-soluble fragrances, oil-soluble vitamins and unsaturated fatty acids are preferable as edible fat-soluble substances.
また、食用油脂の中でもパーム核油、ヤシ油が好ましく、特に硬化したパーム核油、硬化したヤシ油が好ましい。
パーム核油、ヤシ油としては、構成脂肪酸のうち、炭素数が12以下の脂肪酸の割合が50質量%以上であることが好ましく、酸化安定性の面から、不飽和脂肪酸の割合が15質量%以下であることが好ましく、10質量%以下であることがより好ましく、5質量%以下であることがさらに好ましく、1質量%以下であることが最も好ましい。 As an edible oil and fat, it is particularly preferable that the rising melting point is 25 to 45 ° C., since a rich oil and fat flavor can be felt.
Among the edible oils and fats, palm kernel oil and coconut oil are preferable, and especially hardened palm kernel oil and cured coconut oil are preferable.
As the palm kernel oil and coconut oil, the proportion of fatty acids having 12 or less carbon atoms in the constituent fatty acids is preferably 50% by mass or more, and from the viewpoint of oxidation stability, the proportion of unsaturated fatty acids is 15% by mass. Is preferably 10% by mass or less, more preferably 5% by mass or less, and most preferably 1% by mass or less.
澱粉加水分解物とは、澱粉中のアミロースやアミロペクチン等の多糖類を、熱、酸、アルカリ、酵素等で加水分解したものの総称であり、デキストリンとも呼ばれ、グルコースがα-1,4または1,6結合で連なった多糖類が主成分である。
澱粉加水分解物としては、可溶性澱粉、薄手のり澱粉、アミロデキストリン、白色デキストリン、黄色デキストリン、ブリテシュガム、エリトロデキストリン、アクロデキストリン、マルトデキストリン等が挙げられる。これらは1種を単独で又は2種以上を組み合わせて用いることができる。
澱粉加水分解物の原料となる澱粉は、澱粉を含有する植物から採取される。この際、植物の品種としては、農産物として大量生産される品種が経済的に有利である。また、植物の品種により、澱粉中に含まれるアミロースとアミロペクチンの比率が異なる。アミロースはグルコースがα-1,4結合で直鎖状につながった構造を主としており、アミロペクチンはグルコースがα-1,6結合で分岐しながらつながった構造を主としている。一般的には、アミロースは低分子界面活性剤との相互作用が強いため、デキストリンのDE値が8より大のように加水分解度が高い場合には、澱粉の由来植物の品種に特に制限はないが、DEが8以下のように加水分解度が低い場合は、よりアミロペクチンの比率が高い澱粉を持つ由来植物が好ましく、そのような植物として、ワキシー種、すなわちワキシーコーンやもち米など、または、タピオカ、甘薯が好ましく、それらを1種類用いてもよいし、2種類以上を混合し、原料澱粉として用いてもよい。 [Starch hydrolyzate]
The starch hydrolyzate is a general term for polysaccharides such as amylose and amylopectin that are hydrolyzed with heat, acid, alkali, enzyme, etc. in starch, also called dextrin, and glucose is α-1,4 or 1 The main component is polysaccharides linked by 6 bonds.
Examples of the starch hydrolyzate include soluble starch, thin starch, amylodextrin, white dextrin, yellow dextrin, britesh gum, erythrodextrin, acrodextrin, maltodextrin and the like. These can be used individually by 1 type or in combination of 2 or more types.
Starch as a raw material for the starch hydrolyzate is collected from a plant containing starch. At this time, as plant varieties, varieties that are mass-produced as agricultural products are economically advantageous. Moreover, the ratio of amylose and amylopectin contained in starch differs depending on the variety of plant. Amylose mainly has a structure in which glucose is connected in a straight chain by α-1,4 bonds, and amylopectin has a structure mainly in which glucose is connected while being branched by α-1,6 bonds. In general, amylose has a strong interaction with low-molecular-weight surfactants, so when the degree of hydrolysis is high, such as when the DE value of dextrin is greater than 8, there are no particular restrictions on the varieties of starch-derived plants. However, when the degree of hydrolysis is low such that DE is 8 or less, a plant derived from starch having a higher ratio of amylopectin is preferable, and as such a plant, waxy species, that is, waxy corn, glutinous rice, or the like, or , Tapioca and sweet potato are preferable, and one kind thereof may be used, or two or more kinds may be mixed and used as a raw material starch.
このピーク面積の割合は、通常15%以下であり、中でも10%以下が好ましく、9%以下がより好ましく、7%以下がさらに好ましく、5%以下が特に好ましい。ピーク面積割合が上限以下であることにより、低分子界面活性剤との相互作用の影響が少なく、全体の乳化安定性が良好となる。ピーク面積割合は小さいほど好ましく、その下限については特に制限はない。 The starch hydrolyzate used in the present invention is a ratio of the peak area in the range of molecular weight 8500 to 18500 with respect to the total peak area when the molecular weight distribution is measured by gel permeation chromatography (GPC) (hereinafter simply referred to as “peak area ratio”). Is 15% or less.
The ratio of the peak area is usually 15% or less, preferably 10% or less, more preferably 9% or less, further preferably 7% or less, and particularly preferably 5% or less. When the peak area ratio is not more than the upper limit, the influence of the interaction with the low molecular surfactant is small, and the overall emulsion stability is improved. The smaller the peak area ratio, the better. The lower limit is not particularly limited.
カラム:TSKgelG2500PWXL、GMPWXL(東ソー(株)製)
カラム温度:40℃
移動相:0.2M 硝酸ナトリウム水溶液
流速:1.0ml/min
検出器:示差屈折率計
サンプル注入量:200μl
検量線:プルラン標準品(分子量2,350,000~5,900の間の9種類)、及びグルコース(分子量180)
また、ピーク面積割合は、上記の方法で求めた分子量分布の測定結果を、微分分子量分布曲線に変換した後、分子量8500以上18500以下に相当するピーク面積を合計し、総ピーク面積に対する割合として算出することができる。 Here, the measurement of the molecular weight distribution by gel permeation chromatography is usually carried out using the GPC apparatus under the following conditions.
Column: TSKgel G2500PWXL, GMPWXL (manufactured by Tosoh Corporation)
Column temperature: 40 ° C
Mobile phase: 0.2 M sodium nitrate aqueous solution Flow rate: 1.0 ml / min
Detector: Differential refractometer Sample injection volume: 200 μl
Calibration curve: Pullulan standard (9 types of molecular weight between 2350,000 and 5,900) and glucose (molecular weight of 180)
The peak area ratio is calculated as the ratio to the total peak area by converting the measurement result of the molecular weight distribution obtained by the above method into a differential molecular weight distribution curve and then summing the peak areas corresponding to the molecular weight of 8500 to 18500. can do.
また、ピーク面積割合が15%以下である澱粉加水分解物として、松谷化学工業社製「パインデックス#3」、「パインデックス#100」、日本食品化工社製「フジオリゴG67」、三和澱粉工業社製「サンデック#30」「サンデック#70」「サンデック#150」「サンデック#180」「サンデック#250」「サンデック#300」などが市販されており、これらを用いることができる。 The starch hydrolyzate having a peak area ratio of 15% or less is, for example, a membrane separation using a reverse osmosis membrane, a nanofiltration membrane, an ultrafiltration membrane, a microfiltration membrane, or a column packed with silica gel or an ion exchange resin. The fraction hydrolyzate is separated and purified to remove components with a molecular weight of 8500 or more and 18500 or less by using fractionation treatment with, and low molecular weight treatment with starch-degrading enzymes such as α-amylase, β-amylase and glucoamylase. Can be manufactured.
Moreover, as a starch hydrolyzate having a peak area ratio of 15% or less, “Paindex # 3” and “Paindex # 100” manufactured by Matsutani Chemical Industry Co., Ltd. “Fuji Oligo G67” manufactured by Nippon Shokuhin Kako Co., Ltd., Sanwa Starch Industries, Ltd. “Sandeck # 30”, “Sandeck # 70”, “Sandeck # 150”, “Sandeck # 180”, “Sandeck # 250”, “Sandeck # 300”, and the like are commercially available, and these can be used.
低分子界面活性剤とは、分子構造内に親水性部分と親油性部分をもち、両親媒性で界面活性を持つ物質であり、分子量が5000以下の物質であることが好ましい。低分子界面活性剤にはタンパク質や多糖類、合成ポリマーなどの高分子は含まれない。 [Low molecular surfactant]
The low molecular surfactant is a substance having a hydrophilic part and a lipophilic part in the molecular structure, an amphiphilic substance having a surface activity, and preferably a substance having a molecular weight of 5000 or less. Low molecular surfactants do not include macromolecules such as proteins, polysaccharides, and synthetic polymers.
疎水性の低分子界面活性剤としては、中でも、飲食品に使用可能な食品用乳化剤が好ましく、食品用乳化剤の中でも、飲食可能な安全性が確認されているもので、かつ脂溶性物質に分散、溶解するものが好ましい。
そのような疎水性の食品用乳化剤としては、例えば、レシチン、モノグリセリン有機酸脂肪酸エステル、ショ糖脂肪酸エステル、グリセリン脂肪酸エステル、ポリグリセリン脂肪酸エステル、ソルビタン脂肪酸エステル、プロピレングリコール脂肪酸エステルが挙げられ、中でも、脂溶性物質への作用が大きいことから、モノグリセリン有機酸脂肪酸エステル、ショ糖脂肪酸エステル、グリセリン脂肪酸エステル、ポリグリセリン脂肪酸エステルが好ましく、ショ糖脂肪酸エステル、グリセリン脂肪酸エステル、ポリグリセリン脂肪酸エステル、がさらに好ましく、ショ糖脂肪酸エステルが最も好ましい。
ショ糖脂肪酸エステル、ポリグリセリン脂肪酸エステルとしては、脂溶性物質の物性、相状態を効果的に制御するという観点からHLBが5以下のものが好ましく、4以下がより好ましく、また0以上のものが好ましく、1以上のものがより好ましく、2~3が最も好ましい。また、脂溶性物質の相状態、すなわち結晶状態を安定化するという観点からショ糖脂肪酸エステル、ポリグリセリン脂肪酸エステルの脂肪酸の炭素数は12以上が好ましく、16以上がより好ましく、18以上が最も好ましい。 In addition, as a low molecular surfactant, a relatively hydrophobic low molecular surfactant capable of controlling the physical properties and phase state of a fat-soluble substance is used in combination with a hydrophilic low molecular surfactant that dissolves in water. It is preferable.
As the hydrophobic low-molecular surfactant, food emulsifiers that can be used for foods and drinks are preferred, among food emulsifiers, and safety that can be eaten and eaten has been confirmed and dispersed in a fat-soluble substance. Those that dissolve are preferred.
Examples of such hydrophobic food emulsifiers include lecithin, monoglycerin organic acid fatty acid ester, sucrose fatty acid ester, glycerin fatty acid ester, polyglycerin fatty acid ester, sorbitan fatty acid ester, and propylene glycol fatty acid ester. Monoglycerin organic acid fatty acid ester, sucrose fatty acid ester, glycerin fatty acid ester, and polyglycerin fatty acid ester are preferred because of their large action on fat-soluble substances, and sucrose fatty acid ester, glycerin fatty acid ester, and polyglycerin fatty acid ester are More preferred is sucrose fatty acid ester.
As the sucrose fatty acid ester and polyglycerin fatty acid ester, those having an HLB of 5 or less are preferred, those having 4 or less are more preferred, and those having 0 or more are preferred from the viewpoint of effectively controlling the physical properties and phase state of the fat-soluble substance. Preferably, one or more is more preferable, and 2-3 is most preferable. Further, from the viewpoint of stabilizing the phase state of the fat-soluble substance, that is, the crystalline state, the number of carbon atoms of the fatty acid of the sucrose fatty acid ester and the polyglycerol fatty acid ester is preferably 12 or more, more preferably 16 or more, and most preferably 18 or more. .
本発明の粉末組成物は、上記の脂溶性物質、澱粉加水分解物、及び低分子界面活性剤を必須成分として含有するものであるが、本発明の効果を妨げない範囲で、脂溶性物質、澱粉加水分解物及び低分子界面活性剤以外の成分、例えば、タンパク質、糖質、香気成分、固結防止剤などが含まれていてもよい。従って、後述の本発明の粉末組成物を製造するための混合液には、これらの他の成分が含まれていてもよい。 [Other ingredients]
The powder composition of the present invention contains the above-mentioned fat-soluble substance, starch hydrolyzate, and low-molecular surfactant as essential components, but in a range that does not interfere with the effects of the present invention, Components other than the starch hydrolyzate and the low molecular surfactant, for example, proteins, carbohydrates, aroma components, anti-caking agents, and the like may be contained. Therefore, the liquid mixture for producing the powder composition of the present invention described later may contain these other components.
カゼインナトリウムを含有しないとは、粉末組成物中において、カゼインナトリウムの含有量が、低分子界面活性剤を1としたとき、質量比で、0.1以下であること、好ましくは0.05以下であること、さらに好ましくは0.01以下であること、最も好ましくは0.005以下であることを意味する。または、粉末組成物中において、カゼインナトリウムの含有量が、1.0質量%以下であること、好ましくは0.5質量%以下であること、さらに好ましくは0.3質量%以下であること、特に好ましくは0.1質量%以下であることを意味し、最も好ましくは全く含有しないことを意味する。 The powder composition of the present invention preferably contains substantially no sodium caseinate in terms of emulsion stability when used as a beverage. Casein sodium here refers to casein sodium added to the casein separated from the milk of mammals such as cattle by precipitation with acid, fermentation, enzyme treatment, etc. Refers to products that have been refined, dried, packaged and distributed.
“Not containing sodium caseinate” means that the content of sodium caseinate in the powder composition is 0.1 or less, preferably 0.05 or less in terms of mass ratio when the low molecular surfactant is 1. , More preferably 0.01 or less, most preferably 0.005 or less. Or, in the powder composition, the content of sodium caseinate is 1.0% by mass or less, preferably 0.5% by mass or less, more preferably 0.3% by mass or less, Particularly preferably, it means 0.1% by mass or less, and most preferably means that it is not contained at all.
本発明の粉末組成物の各成分の好ましい含有量は、以下の通りである。
組成物中の脂溶性物質の含有量:10質量%以上が好ましく、20質量%以上がより好ましく、70質量%以下が好ましく、50質量%以下がより好ましい。
組成物中の澱粉加水分解物の含有量:30質量%以上が好ましく、50質量%以上がより好ましく、90質量%以下が好ましく、80質量%以下がより好ましい。
組成物中の低分子界面活性剤の含有量:0.1質量%以上が好ましく、0.5質量%以上がより好ましく、1.0質量%以上が特に好ましく、10質量%以下が好ましく、5.0質量%以下がより好ましく、3.0質量%以下が特に好ましい。
また、組成物中の脂溶性物質と澱粉加水分解物の含有割合は、脂溶性物質:澱粉加水分解物(質量比)=1:0.43~1:9の範囲であることが好ましく、1:1~1:4であることがより好ましく、低分子界面活性剤と澱粉加水分解物の含有割合は、低分子界面活性剤:澱粉加水分解物(質量比)=1:3~1:900の範囲であることが好ましく、1:10~1:160であることがより好ましい。 [Ingredient composition]
The preferable content of each component of the powder composition of the present invention is as follows.
Content of fat-soluble substance in the composition: 10% by mass or more is preferable, 20% by mass or more is more preferable, 70% by mass or less is preferable, and 50% by mass or less is more preferable.
Content of starch hydrolyzate in the composition: 30% by mass or more is preferable, 50% by mass or more is more preferable, 90% by mass or less is preferable, and 80% by mass or less is more preferable.
Content of low molecular surfactant in the composition: 0.1% by mass or more is preferable, 0.5% by mass or more is more preferable, 1.0% by mass or more is particularly preferable, and 10% by mass or less is preferable. 0.0 mass% or less is more preferable, and 3.0 mass% or less is particularly preferable.
The content ratio of the fat-soluble substance and the starch hydrolyzate in the composition is preferably in the range of fat-soluble substance: starch hydrolyzate (mass ratio) = 1: 0.43 to 1: 9. The content ratio of the low molecular surfactant and the starch hydrolyzate is more preferably 1: 1 to 1: 4. The content ratio of the low molecular surfactant: starch hydrolyzate (mass ratio) = 1: 3 to 1: 900. Preferably, the range is 1:10 to 1: 160.
低分子界面活性剤に対する澱粉加水分解物の含有割合が、上記下限以上の範囲であることにより、低分子界面活性剤自体の味が適切であり、食品に用いた場合には風味を損ねにくい。また、低分子界面活性剤は高価であるため、上記上限以下の範囲であることにより、粉末組成物自体の価格が適切となり経済的であり、乳化安定化も良好であり、粉末化の際や、粉末組成物を溶解した際に乳化が壊れにくい。 In addition, the content of the starch hydrolyzate with respect to the fat-soluble substance is in the range above the lower limit, so that pulverization is good, and the obtained powder composition has low adhesion, good fluidity, and good handling. The amount of the fat-soluble substance per cost of the powder composition is appropriate and economical.
When the content ratio of the starch hydrolyzate with respect to the low molecular surfactant is within the above-mentioned lower limit, the taste of the low molecular surfactant itself is appropriate, and when used in foods, the flavor is hardly impaired. In addition, since the low-molecular surfactant is expensive, it is economical because the price of the powder composition itself is appropriate because it is in the range of the upper limit or less, the emulsion stabilization is good, When the powder composition is dissolved, the emulsification is not easily broken.
本発明の粉末組成物を製造する方法は特に制限はないが、好ましくは本発明の粉末組成物の製造方法に従って、ピーク面積割合が15%以下の澱粉加水分解物、脂溶性物質、低分子界面活性剤及び水を混合して混合液を調製し、この混合液を乳化して乳化液を得た後、得られた乳化液を噴霧乾燥、または凍結乾燥することにより製造される。 [Production Method of Powder Composition]
The method for producing the powder composition of the present invention is not particularly limited, but preferably, according to the method for producing the powder composition of the present invention, a starch hydrolyzate having a peak area ratio of 15% or less, a fat-soluble substance, and a low molecular interface. The mixture is prepared by mixing an activator and water to prepare a mixed solution, emulsifying the mixed solution to obtain an emulsion, and then spray-drying or freeze-drying the obtained emulsion.
噴霧乾燥法により乳化液中の水分を除去して粉末組成物を製造する場合、必要に応じて乳化液を加熱してもよい。また、噴霧乾燥に供される乳化液は、噴霧時点の温度における粘度が5~200mPa・sであることが、乳化効率、乳化安定性及び噴霧乾燥工程における乳化液のノズルからの吐出性の点で好ましい。また、乳化液の固形分量は、噴霧乾燥時におけるノズルからの吐出性を確保するために、質量基準で5%以上が好ましく、10%以上がより好ましく、15%以上がさらに好ましく、70%以下が好ましく、60%以下がより好ましく、50%以下がさらに好ましい。 As the drying method of the emulsion, spray drying method, air flow drying method, drum drying method, cylindrical drying method, freeze drying method such as vacuum freeze drying method, vacuum drying method and the like can be used, but suitable for mass production. Spray drying is preferred.
When producing a powder composition by removing moisture in the emulsion by spray drying, the emulsion may be heated as necessary. In addition, the emulsion to be subjected to spray drying has a viscosity of 5 to 200 mPa · s at the temperature at the time of spraying, in view of emulsification efficiency, emulsion stability, and dischargeability of the emulsion from the nozzle in the spray drying process. Is preferable. The solid content of the emulsified liquid is preferably 5% or more, more preferably 10% or more, further preferably 15% or more, and 70% or less on a mass basis in order to ensure dischargeability from the nozzle during spray drying. Is preferably 60% or less, and more preferably 50% or less.
本発明の粉末組成物は、特に制限はないが、好ましくは飲食品に含有され、さらに好ましくは飲料に含有される。 [Beverages]
Although there is no restriction | limiting in particular in the powder composition of this invention, Preferably it contains in food-drinks, More preferably, it contains in a drink.
尚、製造された本発明の飲料は、容器詰め飲料に好適であり、例えば、缶飲料、ペットボトル飲料として用いられることができる。 After this homogeneous emulsification treatment, sterilization treatment such as UHT sterilization and retort sterilization is performed. Usually, retort sterilization is performed at 121 ° C. for 20 to 40 minutes. On the other hand, UHT sterilization used for beverages for PET bottles is ultra-high temperature sterilization at a higher temperature, for example, a sterilization temperature of 130 to 150 ° C. and a sterilization value (Fo) at 121 ° C. corresponding to 10 to 50. UHT sterilization is a known method such as a direct injection method such as a steam injection method in which water vapor is directly blown into a beverage, a steam infusion method in which a beverage is injected into the water vapor, and an indirect heating method using a surface heat exchanger such as a plate or tube. For example, a plate type sterilizer can be used.
In addition, the manufactured drink of this invention is suitable for a container-packed drink, for example, can be used as a can drink or a plastic bottle drink.
また、乳成分を含む乳飲料の場合、乳飲料中の乳成分の含有量は、牛乳換算で5質量%以上であることが好ましく、10質量%以上であることがより好ましく、60質量%以下であることが好ましく、40質量%以下であることが、より好ましく、25質量%以下であることがさらに好ましい。 The content of the powder composition of the present invention in the beverage of the present invention thus produced varies depending on the amount of milk component, coffee, tea or tea extract added at the same time, but is usually 0.1% by mass. Preferably, it is 0.5% by mass or more, more preferably 1.0% by mass or more, preferably 30% by mass or less, and 20% by mass or less. Is more preferable, and it is further more preferable that it is 10 mass% or less.
In the case of a milk beverage containing a milk component, the content of the milk component in the milk beverage is preferably 5% by mass or more, more preferably 10% by mass or more, and 60% by mass or less in terms of milk. Preferably, it is 40% by mass or less, more preferably 25% by mass or less.
本発明の粉末組成物を含有する飲料は、静菌性を有しながらも、高い乳化安定性を有する飲料である。 The beverage containing the powder composition of the present invention thus obtained is preferably a beverage containing a bacteriostatic emulsifier, substantially not containing sodium caseinate, particularly from the viewpoint of emulsion stability. That is, it is preferable that sodium caseinate is not substantially contained in the powder composition, and further, it is preferable that sodium caseinate is not substantially contained in the production of beverages. In addition, in the composition or beverage, the content of sodium caseinate is 0.3% by mass or less, preferably 0.1% by mass or less, more preferably 0.05% by mass or less. More preferably, it means 0.01% by mass or less, particularly preferably 0.001% by mass or less. Most preferably, it does not contain at all.
The beverage containing the powder composition of the present invention is a beverage having high emulsification stability while having bacteriostatic properties.
硬化ヤシ油(「硬化ヤシ油」不二製油社製)15質量%、ショ糖脂肪酸エステル(ショ糖ステアリン酸エステル「リョートー(登録商標)シュガーエステルS-570」三菱化学フーズ社製、HLB5)1.0質量%、澱粉加水分解物A(松谷化学工業社製、パインデックス#3、コーンスターチ由来)34質量%および水50質量%を混合した。この混合液を50℃でホモミキサーを用いて分散させた後、高圧乳化機を用いて乳化し、得られた乳化液を噴霧乾燥機で乾燥して、粉末組成物(以下、「粉末組成物A-1」と称す。)を得た。 [Example 1]
Hardened coconut oil ("Hardened coconut oil" manufactured by Fuji Oil Co., Ltd.) 15% by mass, sucrose fatty acid ester (sucrose stearate "Ryoto (registered trademark) sugar ester S-570" manufactured by Mitsubishi Chemical Foods, HLB5) 1 0.0% by mass, starch hydrolyzate A (manufactured by Matsutani Chemical Industry Co., Ltd., Paindex # 3, derived from corn starch) and 50% by mass of water were mixed. This mixed solution was dispersed at 50 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier. The obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”). A-1 ") was obtained.
澱粉加水分解物Aを、澱粉加水分解物B(松谷化学工業社製、パインデックス#100、ワキシーコーンスターチ由来)に変更した以外は、実施例1と同様にして粉末組成物(以下、「粉末組成物B-1」と称す。)を得た。 [Example 2]
A powder composition (hereinafter referred to as “powder composition”) was used in the same manner as in Example 1 except that the starch hydrolyzate A was changed to starch hydrolyzate B (manufactured by Matsutani Chemical Industry Co., Ltd., Paindex # 100, derived from waxy corn starch). This was referred to as product B-1 ".
澱粉加水分解物Aを、澱粉加水分解物C(松谷化学工業社製、パインデックス#2、コーンスターチ由来)に変更した以外は、実施例1と同様にして粉末組成物(以下、「粉末組成物C-1」と称す。)を得た。 [Comparative Example 1]
A powder composition (hereinafter referred to as “powder composition”) was used in the same manner as in Example 1 except that the starch hydrolyzate A was changed to starch hydrolyzate C (manufactured by Matsutani Chemical Industry Co., Ltd., Paindex # 2, derived from corn starch). C-1 ").
硬化ヤシ油(「硬化ヤシ油」不二製油社製)20質量%、ショ糖脂肪酸エステル(ショ糖ステアリン酸エステル「リョートー(登録商標)シュガーエステルS-570」三菱化学フーズ社製、HLB5)2.5質量%、澱粉加水分解物A27.5質量%および水50質量%を混合した。この混合液を50℃でホモミキサーを用いて分散させた後、高圧乳化機を用いて乳化し、得られた乳化液を噴霧乾燥機で乾燥して、粉末組成物(以下、「粉末組成物A-2」と称す。)を得た。 [Example 3]
Hardened coconut oil ("Hardened coconut oil" manufactured by Fuji Oil Co., Ltd.) 20% by mass, sucrose fatty acid ester (sucrose stearate "Ryoto (registered trademark) sugar ester S-570" manufactured by Mitsubishi Chemical Foods, HLB5) 2 0.5% by mass, 27.5% by mass of starch hydrolyzate A and 50% by mass of water were mixed. This mixed solution was dispersed at 50 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier. The obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”). A-2 ") was obtained.
澱粉加水分解物Aを、澱粉加水分解物Bに変更した以外は、実施例3と同様にして粉末組成物(以下、「粉末組成物B-2」と称す。)を得た。 [Example 4]
A powder composition (hereinafter referred to as “powder composition B-2”) was obtained in the same manner as in Example 3 except that starch hydrolyzate A was changed to starch hydrolyzate B.
澱粉加水分解物Aを、澱粉加水分解物Cに変更した以外は、実施例3と同様にして粉末組成物(以下、「粉末組成物C-2」と称す。)を得た。 [Comparative Example 2]
A powder composition (hereinafter referred to as “powder composition C-2”) was obtained in the same manner as in Example 3 except that the starch hydrolyzate A was changed to the starch hydrolyzate C.
1.1gの粉末組成物A-1、B-1、C-1をそれぞれ100mlの水に溶解し、30℃又は50℃で保存したときの経時的な層分離の度合いを観察し、乳化安定性を以下の基準で評価した。結果を表2に示す。
<乳化安定性の評価>
○: 層分離がない、または、ごくわずかに認められる。
△: 層分離が認められる。
×: 明確に層分離している。または、オイル粒やオイル層が多量に認められ、乳化が破壊されている。 [Test Example 1]
1.1 g of powder compositions A-1, B-1, and C-1 were each dissolved in 100 ml of water and the degree of layer separation over time when stored at 30 ° C. or 50 ° C. was observed to stabilize the emulsion. Sex was evaluated according to the following criteria. The results are shown in Table 2.
<Evaluation of emulsion stability>
○: No or no layer separation.
Δ: Layer separation is observed.
X: The layers are clearly separated. Alternatively, a large amount of oil particles and oil layer are observed, and the emulsification is broken.
1.1gの粉末組成物A-2、B-2、C-2をそれぞれ100mlの水に溶解し、30℃又は50℃で保存したときの経時的な層分離の度合いを観察し、乳化安定性を、試験例1と同様に評価した。結果を表3に示す。
また、1.1gの粉末組成物A-2、B-2、C-2をそれぞれ100mlの水に溶解した液を20℃、30℃、35℃、40℃、50℃で3日間保存したときのエマルションの平均粒子径増加率を以下の基準で評価した。平均粒子径は、ナノ粒子径分布測定装置(島津製作所社製SALD-7100)を用いて測定した。結果を表4に示す。 [Test Example 2]
1.1 g of powder compositions A-2, B-2, and C-2 were dissolved in 100 ml of water, and the degree of layer separation over time when stored at 30 ° C or 50 ° C was observed to stabilize the emulsion. The properties were evaluated in the same manner as in Test Example 1. The results are shown in Table 3.
When 1.1 g of the powder compositions A-2, B-2 and C-2 are dissolved in 100 ml of water and stored at 20 ° C., 30 ° C., 35 ° C., 40 ° C. and 50 ° C. for 3 days. The average particle diameter increase rate of the emulsion was evaluated according to the following criteria. The average particle size was measured using a nanoparticle size distribution measuring device (SALD-7100 manufactured by Shimadzu Corporation). The results are shown in Table 4.
◎: 増加率=保存後の平均粒子径/保存前の平均粒子径が、1.3未満である
○: 上記増加率が、1.3以上、1.5未満である
△: 上記増加率が、1.5以上、1.7未満である
×: 上記増加率が、1.7以上である <Average particle diameter increase rate of emulsion after storage>
A: Increase rate = average particle diameter after storage / average particle diameter before storage is less than 1.3 ○: the increase rate is 1.3 or more and less than 1.5 Δ: the increase rate is 1.5 or more and less than 1.7 ×: The increase rate is 1.7 or more
試験例1、2の結果から、いずれの粉末組成物も、粉末組成物を得る時点では差異はなく、水に粉末組成物を分散、溶解したエマルションで差異がみられたことから、保存後のエマルションの粒子径増加率が、粉末組成物を再度溶解した際の乳化安定性を反映していると考えられた。そのため、澱粉加水分解物を含有する乳化液を調製し、それを粉末化せず、試験例1、2と同濃度に水で希釈し、その希釈エマルションの粒子径増加率を確認した。 [Test Example 3]
From the results of Test Examples 1 and 2, there was no difference in the powder composition at the time of obtaining the powder composition, and there was a difference in the emulsion in which the powder composition was dispersed and dissolved in water. The particle diameter increase rate of the emulsion was considered to reflect the emulsion stability when the powder composition was dissolved again. Therefore, an emulsion containing a starch hydrolyzate was prepared, and the emulsion was not powdered, diluted with water to the same concentration as in Test Examples 1 and 2, and the particle diameter increase rate of the diluted emulsion was confirmed.
◎: 増加率=保存後の粒子のメジアン径/保存前の粒子のメジアン径が、2.5未満である
○: 上記増加率が、2.5以上、3.5未満である
△: 上記増加率が、3.5以上、4.5未満である
×: 上記増加率が、4.5以上である <Median diameter increase rate of emulsion particles after storage>
A: Increase rate = median diameter of particles after storage / median diameter of particles before storage is less than 2.5 ○: the increase rate is 2.5 or more and less than 3.5 Δ: increase above The rate is 3.5 or more and less than 4.5. X: The increase rate is 4.5 or more.
硬化ヤシ油(「硬化ヤシ油」不二製油社製)20質量%、ショ糖脂肪酸エステル(ショ糖ステアリン酸エステル「リョートー(登録商標)シュガーエステルS-570」三菱化学フーズ社製、HLB5)2.5質量%、カゼインナトリウム(Tatua社製)2.5質量%、澱粉加水分解物A27.5質量%および水47.5質量%を混合した。この混合液を50℃でホモミキサーを用いて分散させた後、高圧乳化機を用いて乳化し、得られた乳化液を噴霧乾燥機で乾燥して、粉末組成物(以下、「粉末組成物A-3」と称す。)を得た。 [Example 5]
Hardened coconut oil ("Hardened coconut oil" manufactured by Fuji Oil Co., Ltd.) 20% by mass, sucrose fatty acid ester (sucrose stearate "Ryoto (registered trademark) sugar ester S-570" manufactured by Mitsubishi Chemical Foods, HLB5) 2 0.5% by mass, sodium caseinate (manufactured by Tatua) 2.5% by mass, starch hydrolyzate A 27.5% by mass and water 47.5% by mass were mixed. This mixed solution was dispersed at 50 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier. The obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”). A-3 ”) was obtained.
澱粉加水分解物Aを、澱粉加水分解物Cに変更した以外は、実施例5と同様にして粉末組成物(以下、「粉末組成物C-3」と称す。)を得た。 [Comparative Example 3]
A powder composition (hereinafter referred to as “powder composition C-3”) was obtained in the same manner as in Example 5 except that the starch hydrolyzate A was changed to the starch hydrolyzate C.
1.1gの粉末組成物A-3、C-3をそれぞれ100mlの水に溶解し、試験例1と同様に評価した。結果を表7に示す。 [Test Example 4]
1.1 g of the powder compositions A-3 and C-3 were each dissolved in 100 ml of water and evaluated in the same manner as in Test Example 1. The results are shown in Table 7.
試験例3と同様の方法で、カゼインナトリウムの添加量の影響を確認した。
具体的には、硬化ヤシ油(「硬化ヤシ油」不二製油社製)20質量%、ショ糖脂肪酸エステル(ショ糖ステアリン酸エステル「リョートー(登録商標)シュガーエステルS-570」三菱化学フーズ社製、HLB5)2.5質量%、澱粉加水分解物H27.5質量%、および、0.001~1.0質量%のカゼインナトリウムを水で100質量%となるよう調製し、混合した。この混合液を65℃でホモミキサーを用いて分散させた後、高圧乳化機を用いて乳化し、得られた乳化液2.2gを100mlの水に分散した希釈エマルションを調製した。得られた希釈乳化液を、40℃で保存したときの経時的な層分離の度合いを観察し、乳化安定性を試験例1の基準で評価した。結果を表8に示す。 [Test Example 5]
In the same manner as in Test Example 3, the effect of the amount of sodium caseinate added was confirmed.
Specifically, 20% by mass of hydrogenated coconut oil (“Hardened coconut oil” manufactured by Fuji Oil Co., Ltd.), sucrose fatty acid ester (sucrose stearate “Ryoto (registered trademark) sugar ester S-570”, Mitsubishi Chemical Foods, Inc. HLB5) 2.5 mass%, starch hydrolyzate H27.5 mass%, and 0.001 to 1.0 mass% sodium caseinate were prepared to 100 mass% with water and mixed. The mixture was dispersed at 65 ° C. using a homomixer and then emulsified using a high-pressure emulsifier, and a diluted emulsion was prepared by dispersing 2.2 g of the obtained emulsion in 100 ml of water. The degree of layer separation over time when the obtained diluted emulsion was stored at 40 ° C. was observed, and the emulsion stability was evaluated according to the criteria of Test Example 1. The results are shown in Table 8.
硬化ヤシ油(「硬化ヤシ油」不二製油社製)16質量%、ショ糖脂肪酸エステル(ショ糖ステアリン酸エステル「リョートー(登録商標)シュガーエステルS-1170」三菱化学フーズ社製、HLB11)1.25質量%、澱粉加水分解物A32.75質量%および水50質量%を混合した。この混合液を50℃でホモミキサーを用いて分散させた後、高圧乳化機を用いて乳化し、得られた乳化液を噴霧乾燥機で乾燥して、粉末組成物(以下、「粉末組成物A-4」と称す。)を得た。 [Example 6]
Hardened coconut oil ("Hardened coconut oil" manufactured by Fuji Oil Co., Ltd.) 16% by mass, sucrose fatty acid ester (sucrose stearate "Ryoto (registered trademark) sugar ester S-1170" manufactured by Mitsubishi Chemical Foods, HLB11) 1 .25% by mass, starch hydrolyzate A 32.75% by mass and water 50% by mass were mixed. This mixed solution was dispersed at 50 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier. The obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”). A-4 ") was obtained.
硬化ヤシ油に対し、モノグリセリン脂肪酸エステルを0.1質量%加え、水を49.9質量%にした以外は、実施例6と同様にして、粉末組成物A-5を得た。 [Example 7]
A powder composition A-5 was obtained in the same manner as in Example 6 except that 0.1% by mass of monoglycerin fatty acid ester was added to the hardened coconut oil to make water 49.9% by mass.
硬化ヤシ油に対し、ショ糖ラウリン酸エステル(「リョートー(登録商標)シュガーエステルL-195」三菱化学フーズ社製、HLB1)を0.1質量%加え、水を49.9質量%にした以外は、実施例6と同様にして、粉末組成物A-6を得た。 [Example 8]
0.1% by mass of sucrose laurate ("Ryoto (registered trademark) sugar ester L-195" manufactured by Mitsubishi Chemical Foods Co., Ltd., HLB1) was added to the hardened coconut oil to make water 49.9% by mass. Obtained a powder composition A-6 in the same manner as in Example 6.
硬化ヤシ油に対し、ショ糖ステアリン酸エステル(「リョートー(登録商標)シュガーエステルS-370」、HLB3)を0.1質量%加え、水を49.9質量%にした以外は、実施例6と同様にして、粉末組成物A-7を得た。 [Example 9]
Example 6 except that 0.1% by mass of sucrose stearate (“Ryoto® Sugar Ester S-370”, HLB3) was added to the hydrogenated coconut oil to make 49.9% by mass of water. In the same manner as above, a powder composition A-7 was obtained.
硬化ヤシ油に対し、ポリグリセリンベヘニン酸エステル(「リョートー(登録商標)ポリグリエステルB-100D」三菱化学フーズ社製、HLB3)を0.1質量%加え、水を49.9質量%にした以外は、実施例6と同様にして、粉末組成物A-8を得た。 [Example 10]
0.1% by mass of polyglycerin behenic acid ester (“Ryoto (registered trademark) polyglycerin B-100D, manufactured by Mitsubishi Chemical Foods Co., Ltd., HLB3)” is added to the hardened coconut oil, and 49.9% by mass of water. A powder composition A-8 was obtained in the same manner as in Example 6 except that
1.1gの粉末組成物A-4~8をそれぞれ100mlの水に溶解し、30℃又は50℃で保存したときの経時的な層分離の度合いを観察し、乳化安定性を以下の基準で評価した。結果を表9に示す。 [Test Example 6]
1.1 g of the powder composition A-4 to 8 was dissolved in 100 ml of water, and the degree of layer separation over time when stored at 30 ° C. or 50 ° C. was observed. evaluated. The results are shown in Table 9.
硬化ヤシ油(「硬化ヤシ油」不二製油社製)16質量%、ショ糖脂肪酸エステル(ショ糖ステアリン酸エステル「リョートー(登録商標)シュガーエステルS-770」三菱化学フーズ社製、HLB11)1.25質量%、澱粉加水分解物A32.75質量%および水50質量%を混合した。この混合液を70℃でホモミキサーを用いて分散させた後、高圧乳化機を用いて乳化し、得られた乳化液を噴霧乾燥機で乾燥して、粉末組成物(以下、「粉末組成物A-9」と称す。)を得た。 [Example 11]
Hardened coconut oil ("Hardened coconut oil" manufactured by Fuji Oil Co., Ltd.) 16% by mass, sucrose fatty acid ester (sucrose stearate "Ryoto (registered trademark) sugar ester S-770" manufactured by Mitsubishi Chemical Foods, HLB11) 1 .25% by mass, starch hydrolyzate A 32.75% by mass and water 50% by mass were mixed. This mixed solution was dispersed at 70 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier. The obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”). A-9 ") was obtained.
あらかじめ、ショ糖脂肪酸エステル(ショ糖ステアリン酸エステル「リョートー(登録商標)シュガーエステルS-370」三菱化学フーズ社製、HLB3)0.08質量%を分散した硬化ヤシ油(「硬化ヤシ油」不二製油社製)16質量%に、ショ糖脂肪酸エステル(ショ糖ステアリン酸エステル「リョートー(登録商標)シュガーエステルS-770」三菱化学フーズ社製、HLB11)1.25質量%、澱粉加水分解物A32.67質量%および水50質量%を混合した。この混合液を70℃でホモミキサーを用いて分散させた後、高圧乳化機を用いて乳化し、得られた乳化液を噴霧乾燥機で乾燥して、粉末組成物(以下、「粉末組成物A-10」と称す。)を得た。 [Example 12]
Hardened coconut oil (“hardened coconut oil”) in which 0.08% by mass of sucrose fatty acid ester (sucrose stearate “Ryoto (registered trademark) sugar ester S-370” manufactured by Mitsubishi Chemical Foods Co., Ltd., HLB3) was previously dispersed. Sucrose fatty acid ester (sucrose stearate "Ryoto (registered trademark) sugar ester S-770", Mitsubishi Chemical Foods, Ltd., HLB11) 1.25% by mass, starch hydrolyzate A 32.67 mass% and 50 mass% water were mixed. This mixed solution was dispersed at 70 ° C. using a homomixer, and then emulsified using a high-pressure emulsifier. The obtained emulsion was dried using a spray dryer to obtain a powder composition (hereinafter referred to as “powder composition”). A-10 ").
2.0gの粉末組成物A-9、A-10をそれぞれ100mlの水に溶解し、20℃、25℃、30℃、40℃、50℃で3日間保存したときの平均粒子径増加率を試験例2と同様の基準で評価した。平均粒子径は、島津製作所社製SALD-7100を用いて測定した。
結果を表10に示す。 [Test Example 7]
2.0 g of powder compositions A-9 and A-10 were each dissolved in 100 ml of water and the average particle diameter increase rate when stored at 20 ° C., 25 ° C., 30 ° C., 40 ° C. and 50 ° C. for 3 days Evaluation was performed according to the same criteria as in Test Example 2. The average particle size was measured using SALD-7100 manufactured by Shimadzu Corporation.
The results are shown in Table 10.
試験例3と同様の方法で、疎水性低分子界面活性剤添加の影響を確認した。
具体的には、あらかじめ、ショ糖脂肪酸エステル(ショ糖ステアリン酸エステル「リョートー(登録商標)シュガーエステルS-370」三菱化学フーズ社製、HLB3)0.08質量%を分散した硬化ヤシ油(「硬化ヤシ油」不二製油社製)16質量%に、ショ糖脂肪酸エステル(ショ糖ステアリン酸エステル「リョートー(登録商標)シュガーエステルS-770」三菱化学フーズ社製、HLB11)1.25質量%、澱粉加水分解物A32.67質量%および水50質量%を混合した。この混合液を70℃でホモミキサーを用いて分散させた後、超高圧乳化機を用いて、100MPaで乳化し、得られた乳化液4.0gを100mlの水に分散した希釈乳化液を調製した。残りの乳化液は、噴霧乾燥機で乾燥して、粉末組成物A-11を得た。
得られた希釈乳化液を、20℃、25℃、30℃、40℃、50℃で4日間保存したときの平均粒子径増加率を試験例2と同様の基準で評価した。平均粒子径は、ナノ粒子径分布測定装置(島津製作所社製SALD-7100)を用いて測定した。結果を表11に示す。 [Example 13]
In the same manner as in Test Example 3, the effect of adding a hydrophobic low molecular surfactant was confirmed.
Specifically, hydrogenated coconut oil (“Sucrose stearate“ Ryoto (registered trademark) Sugar ester S-370 ”manufactured by Mitsubishi Chemical Foods, Ltd., HLB3) 0.08% by mass in advance is dispersed in advance. 16% by mass of hardened coconut oil “Fuji Oil Co., Ltd.” and 1.25% by mass of sucrose fatty acid ester (sucrose stearate “Ryoto (registered trademark) sugar ester S-770”, Mitsubishi Chemical Foods Co., Ltd., HLB11) , Starch hydrolyzate A 32.67% by mass and water 50% by mass were mixed. This mixed solution was dispersed at 70 ° C. using a homomixer and then emulsified at 100 MPa using an ultrahigh pressure emulsifier, and a diluted emulsion was prepared by dispersing 4.0 g of the obtained emulsion in 100 ml of water. did. The remaining emulsion was dried with a spray dryer to obtain a powder composition A-11.
The average particle diameter increase rate when the obtained diluted emulsion was stored at 20 ° C., 25 ° C., 30 ° C., 40 ° C., and 50 ° C. for 4 days was evaluated according to the same criteria as in Test Example 2. The average particle size was measured using a nanoparticle size distribution measuring device (SALD-7100 manufactured by Shimadzu Corporation). The results are shown in Table 11.
インスタントティー0.15質量%、砂糖7.0質量%、脱脂粉乳1.9質量%、粉末組成物A-1を3.2質量%、ショ糖脂肪酸エステル(ショ糖パルミチン酸エステル「リョートー(登録商標)シュガーエステルP-1570」三菱化学フーズ社製)0.03質量%、及び水(残部)を混合し、充分に撹拌して溶解させた後、高圧ホモジナイザーで乳化した。これを、UHT殺菌した後、PETボトルに充填し、乳成分を含有するPETボトル詰めミルクティーを得た。このミルクティーは冷蔵および室温2ヶ月保管後も良好な安定性であった。 [Example 14]
Instant tea 0.15% by mass, sugar 7.0% by mass, skim milk powder 1.9% by mass, powder composition A-1 3.2% by mass, sucrose fatty acid ester (sucrose palmitate ester “Ryoto (registered) (Trademark) Sugar Ester P-1570 (Mitsubishi Chemical Foods Co., Ltd.) 0.03% by mass and water (remainder) were mixed, sufficiently stirred and dissolved, and then emulsified with a high-pressure homogenizer. This was UHT sterilized and then filled into a PET bottle to obtain a PET bottled milk tea containing milk components. This milk tea was in good stability after refrigeration and storage at room temperature for 2 months.
粉末組成物A-1をA-10とした以外は、実施例13と同様にして、PETボトル詰めミルクティーを得た。このミルクティーは冷蔵および室温2ヶ月保管後も良好な安定性であった。 [Example 15]
A PET bottled milk tea was obtained in the same manner as in Example 13 except that the powder composition A-1 was changed to A-10. This milk tea was in good stability after refrigeration and storage at room temperature for 2 months.
Claims (11)
- 脂溶性物質、澱粉加水分解物及び低分子界面活性剤を含有する粉末組成物であって、
前記澱粉加水分解物が、ゲル浸透クロマトグラフィーで分子量分布を測定した際の総ピーク面積に対する分子量8500以上18500以下の範囲のピーク面積の割合が15%以下であることを特徴とする粉末組成物。 A powder composition containing a fat-soluble substance, a starch hydrolyzate and a low molecular surfactant,
The powder composition, wherein the starch hydrolyzate has a peak area ratio in the range of molecular weight of 8500 to 18500 with respect to the total peak area when the molecular weight distribution is measured by gel permeation chromatography is 15% or less. - 前記脂溶性物質が食用油脂である、請求項1に記載の粉末組成物。 The powder composition according to claim 1, wherein the fat-soluble substance is an edible fat.
- 前記低分子界面活性剤が食品用乳化剤である、請求項1または2に記載の粉末組成物。 The powder composition according to claim 1 or 2, wherein the low molecular surfactant is a food emulsifier.
- 前記澱粉加水分解物の重量平均分子量が9000以下である、請求項1~3のいずれか一項に記載の粉末組成物。 The powder composition according to any one of claims 1 to 3, wherein the starch hydrolyzate has a weight average molecular weight of 9000 or less.
- 前記澱粉加水分解物の重量平均分子量が50000以上である、請求項1~3のいずれか一項に記載の粉末組成物。 The powder composition according to any one of claims 1 to 3, wherein the starch hydrolyzate has a weight average molecular weight of 50,000 or more. *
- 実質的にカゼインナトリウムを含有しない、請求項1~5のいずれか一項に記載の粉末組成物。 The powder composition according to any one of claims 1 to 5, which contains substantially no sodium caseinate.
- 請求項1~6のいずれか一項に記載の粉末組成物を含有する、飲料。 A beverage containing the powder composition according to any one of claims 1 to 6. *
- さらに、乳成分を含有する、請求項7に記載の飲料。 Furthermore, the drink of Claim 7 containing a milk component.
- さらに、静菌性乳化剤を含有する請求項7または8に記載の飲料。 The beverage according to claim 7 or 8, further comprising a bacteriostatic emulsifier.
- コーヒーまたは紅茶飲料である、請求項7~9のいずれか一項に記載の飲料。 The beverage according to any one of claims 7 to 9, which is a coffee or tea beverage.
- 脂溶性物質、澱粉加水分解物及び低分子界面活性剤を含有する粉末組成物の製造方法であって、
前記澱粉加水分解物として、ゲル浸透クロマトグラフィーで分子量分布を測定した際の総ピーク面積に対する、分子量8500以上18500以下の範囲のピーク面積の割合が15%以下である澱粉加水分解物を用い、
前記澱粉加水分解物、脂溶性物質、低分子界面活性剤及び水を混合して混合液を調製し、
前記混合液を乳化して乳化液を得た後、
前記乳化液を噴霧乾燥または凍結乾燥することを特徴とする、粉末組成物の製造方法。 A method for producing a powder composition comprising a fat-soluble substance, a starch hydrolyzate and a low molecular surfactant,
As the starch hydrolyzate, a starch hydrolyzate in which the ratio of the peak area in the molecular weight range of 8500 to 18500 is 15% or less with respect to the total peak area when the molecular weight distribution is measured by gel permeation chromatography,
Mixing the starch hydrolyzate, fat-soluble substance, low molecular surfactant and water to prepare a mixture,
After emulsifying the mixture to obtain an emulsion,
A method for producing a powder composition, characterized in that the emulsion is spray-dried or freeze-dried.
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JP2017158499A (en) * | 2016-03-10 | 2017-09-14 | ミヨシ油脂株式会社 | Powder oil and fat and beverage and food |
JP2018507206A (en) * | 2015-02-20 | 2018-03-15 | ペプシコ・インク | Stabilization of sorbic acid in beverage syrup |
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CN114222503A (en) * | 2019-10-17 | 2022-03-22 | 森永乳业株式会社 | Composition, method of manufacture and use |
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