WO2007119492A1 - ロックイン型粉末 - Google Patents
ロックイン型粉末 Download PDFInfo
- Publication number
- WO2007119492A1 WO2007119492A1 PCT/JP2007/055895 JP2007055895W WO2007119492A1 WO 2007119492 A1 WO2007119492 A1 WO 2007119492A1 JP 2007055895 W JP2007055895 W JP 2007055895W WO 2007119492 A1 WO2007119492 A1 WO 2007119492A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- lock
- powder
- starch
- type powder
- polyphenols
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0216—Solid or semisolid forms
- A61K8/022—Powders; Compacted Powders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/347—Phenols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/368—Carboxylic acids; Salts or anhydrides thereof with carboxyl groups directly bound to carbon atoms of aromatic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9755—Gymnosperms [Coniferophyta]
- A61K8/9761—Cupressaceae [Cypress family], e.g. juniper or cypress
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9794—Liliopsida [monocotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/01—Deodorant compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/261—Alcohols; Phenols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
- A61K2800/522—Antioxidants; Radical scavengers
Definitions
- the present invention relates to a lock-in type powder containing polyphenols and a solid preparation containing the same. More specifically, the present invention is a lock-in type powder containing polyphenols and excellent in long-term stability, and even after storage for a long period of time, no deterioration in color tone or discoloration is substantially observed, and The present invention relates to the lock-in type powder and a solid preparation containing the same, which can maintain good effects over a long period of time without any change in fragrance, deodorant effect, and decrease in anti-oxidation effect. In particular, the present invention relates to solid preparations that are not easily altered by basic components such as sodium sulfate sodium hydrogencarbonate and surfactants and enzymes contained in bathing agents and detergents.
- a deodorant composition in which an alkali component is allowed to coexist with polyphenols that are known to exist in a product has an excellent deodorizing effect and also has the feature that it can be used with confidence as in the case of the deodorant. So, we got the knowledge and started research to apply this knowledge.
- a lock-in type powder in which a flavor component is encapsulated is, for example, in an amorphous matrix material obtained by heating a carbohydrate such as a carbohydrate together with a small amount of water as necessary.
- the liquid flavor component is mechanically dispersed and contained (Locked-in), solidified by cooling as it is, and then finely pulverized, or the contained one is used with a single screw or twin screw extruder, It is manufactured by extruding into a coolant such as a refrigerant through a die and solidifying it, and then cutting or pulverizing it, which is already known.
- the lock-in type powder is conventionally used for imparting a flavor to various foods, and is widely used particularly in the production of candy, chewing gum and the like.
- Patent Documents 4 to 4) 7 A method in which a mixture of sugars such as sucrose, starch hydrolyzate and emulsifier is heated and mixed with a flavor component, extruded into a cold solvent, molded, and then pulverized (Patent Documents 4 to 4) 7).
- Patent Documents 4 to 4 Method of fixing essential oils with sorbitol aqueous solution or melt.
- Patent Document 1 Japanese Patent Laid-Open No. 9 290014
- Patent Document 2 JP-A-9-290026
- Patent Document 3 Japanese Patent Publication No. 34-5600
- Patent Document 4 Japanese Patent Laid-Open No. 49-62677
- Patent Document 5 JP-A 52-94452
- Patent Document 6 Japanese Patent Laid-Open No. 61-12248
- Patent Document 7 JP-T 61-502656
- Patent Document 8 JP-A-49-132251
- Non-Patent Document 1 Jhon M. deMAN, "PRINCIPLES OF FOOD CHEMIST RY” Second Edition, Van No strand Reinhold (New York), 1990, 167-168
- An object of the present invention is to provide a solid preparation that has excellent storage stability, does not undergo discoloration, color tone deterioration, or change in fragrance even after long-term storage, and that retains a deodorizing function. It is in. Furthermore, even after a standard period from the time the consumer uses the product to the end of use after the product has been shipped, the product is discolored and the color tone is reduced.
- the object is to provide a solid preparation effective in the production of a cosmetic product which does not have a change in fragrance and a deodorant function or a decrease in antioxidant function. Furthermore, it is providing the lock-in type powder which has the deodorizing function contained in the said solid formulation for cosmetics mixing
- the solid preparation means an agent having a certain shape such as a tablet, a pill, a capsule, a granule, a fine granule or a powder.
- the solid preparation of the present invention means a cosmetic product or a raw material for producing a cosmetic product.
- a cosmetic product can be obtained by applying, for example, conventional means to a solid preparation that is a raw material for producing a cosmetic product.
- the subject of the present invention is, for example, a basic component such as sodium sulfate, sodium carbonate, sodium phosphate, sodium bicarbonate, or an enzyme, which is often used as a base component of cosmetics such as bathing agents or detergents. It is to provide a solid preparation for cosmetics that does not cause discoloration, color tone deterioration, or fragrance change of cosmetics, and that also retains a deodorizing function.
- a basic component such as sodium sulfate, sodium carbonate, sodium phosphate, sodium bicarbonate, or an enzyme
- cosmetics such as bathing agents or detergents. It is to provide a solid preparation for cosmetics that does not cause discoloration, color tone deterioration, or fragrance change of cosmetics, and that also retains a deodorizing function.
- lock-in type powder in which polyphenols are encapsulated in saccharides is prepared with difficulty, and the lock-in type powder is prepared.
- the solid preparation for cosmetics after long-term storage has a deodorizing function and an antioxidant function.
- the present invention relates to the following (1) to (10).
- the invention according to the above (1) is a lock-in type powder characterized by containing polyphenols. It is also a lock-in type powder for cosmetics, characterized in that it contains polyphenols. Furthermore, it can be said that the invention according to the above (1) is a lock-in type powder characterized in that polyphenols are encapsulated in a saccharide or a saccharide matrix.
- the invention according to the above (1) is also a lock-in capsule powder characterized by containing polyphenols.
- the invention according to the above (1) is also a lock-in type capsule powder characterized by containing polyphenols in a saccharide or a saccharide matrix.
- the saccharide used here is not particularly limited as long as it is a saccharide capable of producing a lock-in type powder.
- polyphenols hereinafter sometimes referred to as polyphenol which are essential components of the present invention will be described.
- the polyphenol used in the present invention is not particularly limited as long as it is a polyphenol capable of achieving the intended purpose.
- the polyphenol used in the present invention means a compound in which two or more hydroxyl groups are substituted with hydrogen atoms in the same benzene ring, and the glycoside is also a polyphenol. Including. Of these, hydroquinone and polyphenol having an o-diphenol structure are preferred.
- the o-diphenol structure means a structure in which a hydroxyl group is directly substituted on the benzene ring and the force is adjacent to the hydroxyl group.
- polyphenols include, for example, apigenin, apigenin glycoside, acacetin, isorhamnetin, isorhamnetin glycoside, isoquercitrin, epicatechin, epicatechin gallate, epigallocatechin, epigallocatechin gallate, esculetin, ethi Luprotocatechuate, ellagic acid, catechol, gamma acid, catechin, gardenine, gallocatechin, caffeic acid, caffeic acid ester, chlorogenic acid, kaempferol, kaempferol glycoside, quercetin, quercetin glycoside, quercetagenin, ge-cetin , Ge-cetin glycoside, gosipetin, gosipetin glycoside, gosiponole, 4-dihydroxyanthraquinone, 1,4 dihydroxynaphthalene, cyadin, cyadin glycoside, sinensetin, diosmethine , Diosmethin
- flavonoids such as quercetin, epicatechin, and epigallocatechin and their glycosides, gallic acid, gallic acid ester, chlorogenic acid, caffeic acid, caffeic acid ester, tan
- polyphenols having an o-diphenol structure such as acid, pyrocatechol, nordihydrogualectic acid, L-dopa, 4-methylcatechol, 5-methylcatechol, 4-methoxycatechol, 5-methoxycatechol, and hydroquinone are particularly preferred.
- polyphenols may be used alone or in combination of two or more.
- the said polyphenol can be prepared by a well-known method, you may purchase a commercial item. Alternatively, it may be prepared by synthesis. Furthermore, a high-concentration polyphenol fraction prepared with plant power can also be used.
- the content of polyphenols varies depending on the type of solid preparation to be blended, the components contained, etc., and thus cannot be defined unconditionally.
- the content of polyphenols relative to the total weight of the lock-in type powder is 0.2 to 20% by weight, preferably 1 to 15% by weight.
- the amount of the plant extract may be the same as described above.
- matrix material of the lock-in type powder of the present invention include, for example, monosaccharides, disaccharides, polysaccharides, sugar alcohols, polyols, sugar derivatives, modified starches, modified starches, and rubbers.
- lactitonor manolecitore, pentato monole, arabinose, pentose, xylose, galactose, starch, hydrogenated starch hydrolysate, maltodextrin, monosaccharide, force lagenan, polydextrose and derivatives and mixtures thereof.
- Each of the matrix materials is a matrix of a lock-in type powder used in the present invention.
- An example of the power that is preferred as a squeeze material is a mixture of carbohydrates contained in a weight ratio of 1:99 to 30:70 in terms of solids and hydrogenated products of sugar and sugar.
- the hydrogenated product of the saccharide is preferably xylitol, lactitol, maltitol, isomalt, or one or more selected from the hydrogenation treatment and hydrogenated corn syrup force.
- ⁇ starch is chemically treated starch, such as starch treated with acid (eg, dextrin), starch treated with enzyme (eg, dextrin), heated starch (eg, dextrin).
- a starch starch
- oxidized starch cross-linked starch and other starch derivatives (for example, see Non-Patent Document 1).
- DE DE extrose Equivalent
- the dextrin those having a low DE (D extrose Equivalent) value, particularly about 20 or less are preferably used. If the DE value is greater than about 20, the moisture stability will be poor. However, if the DE value is less than about 5, the viscosity when mixing with polyphenol may be too high.
- a starch derivative is a highly modified starch in which the side chain of starch is modified with a hydrophilic group or a hydrophobic group.
- starch derivatives such as starch phosphate, starch carboxy
- starch ethers such as methyl ether
- cross-linked starches such as phosphate cross-linked starch.
- These starch derivatives are preferably used because they are superior in stability to moisture during storage of the resulting capsules compared to other modified starches.
- another factor that increases the moisture stability of the capsule is the use of a modified starch having a high average molecular weight and a branched structure.
- the modified starch having a branched structure include a modified starch containing amylopectin in a high ratio. In particular, starch containing about 80% by weight or more of amylopectin is preferably used.
- modified starches include modified starches derived from amika starch, tapio force starch, waxy maize and the like. Among them, a modified starch derived from Kusushi-Maze is particularly preferable.
- the most preferably used modified starch is a modified starch derived from cocoon rice cake, and a starch derivative having a bulky steric structure that has a stronger interaction between the side chains of starch.
- modified starches include PURITY GUM 59, PURITY GUM BE, PURITY GUM 1773, N-LOK (all trade names, edible chemical starch produced by National Starch and Chemical Company) and the like.
- modified pregelatinized starch having a viscosity equal to or higher than that (hereinafter referred to as “modified pregelatinized starch ( ⁇ 50 cps)”) is used as at least a part of the matrix material.
- Modified pregelatinized starch is obtained by rapidly dehydrating and drying a paste-like product prepared by swelling or dissolving the modified starch in water or hot water in the state of glue. Dispersion ⁇ Swells and can easily reproduce paste.
- modified starch that forms the base of the modified pregelatinized starch
- modified starches such as oxidized starch and derivative starch (starch acetate ester, starch phosphate ester, various starch ether phosphates, cross-linked starch, etc.).
- the modified pregelatinized starch ( ⁇ 50 x 5) is known in the prior art, and various products are sold. These commercially available products may be used as appropriate. For example, “Ne Creamer 46” manufactured by National 'Starch & Chemical Co., Ltd.' is a commercially available product. These modified pregelatinized starches ( ⁇ 50 x 5) may be used with other modified pregelatinized starches.
- the modified pregelatinized starch used together with the modified pregelatinized starch ( ⁇ 50 cps) is, for example, less than 50 cps (mPa-s) when measured at 30 ° C after heating at 80 ° C for 5 minutes in a 20% aqueous solution.
- Modified pregelatinized starch (hereinafter referred to as “modified pregelatinized starch ( ⁇ 50 cps)”).
- Modified pregelatinized starch ( ⁇ 50cps) is a variety of modified starches such as hydrolyzed starch, oxidized starch, and derivative starches (denpene acetate, starch phosphate, various starch ether phosphates, cross-linked starch, etc.).
- Modified starch obtained by swollen or dissolved in water or hot water, and rapidly dehydrated and dried in the state of glue
- modified pregelatinized starch ( ⁇ 50 x 3) a variety of products have been marketed.
- Examples of commercially available products include “Pirity Gum BE” and “Capsule” manufactured by National 'Starch' And Chemical Co., Ltd. By using these in combination, it is possible to gradually release polyphenol over a longer period of time when using cosmetics, and to maintain a deodorizing function and an antioxidant function over a long period of time.
- the volatilization rate and volatilization pattern of the lock-in powder are improved. Can be adjusted. In addition, it prevents deterioration of polyphenol due to base materials (e.g., sulfuric acid marking sheet thorium and sodium hydrogen carbonate) contained in bathing agents and detergents, changes over time, etc., and has a longer deodorizing function and antioxidant function. It can be held over time.
- base materials e.g., sulfuric acid marking sheet thorium and sodium hydrogen carbonate
- the blending ratio of the modified pregelatinized starch to the total amount of matrix material is based on the ease of production of the lock-in type powder, long-term storage, deodorization and antioxidant functions, release performance, and feel during use.
- the matrix base material is preferably 50% by mass or more, more preferably 60 to: LOO% by mass, still more preferably 70 to 95% by mass or more.
- the blending ratio of the modified pregelatinized starch ( ⁇ 50 cps) is preferably 15% by mass or more, more preferably 20% by mass or more, and 20 to 80% by mass with respect to the total amount of the matrix material. Is more preferable.
- the ratio of use is generally a mass ratio of 10:90 to 80:20. More preferred is a mass ratio of 20:80 to 70: 30! /.
- the modified pregelatinized starch may be used in combination with other components such as sugars.
- saccharides that can be used in combination include monosaccharides such as glucose, fructose, mannose, galactose, xylose, arabinose, and ribose, disaccharides such as mannose, ratatose, and sucrose, and starch hydrolyzed with acid or enzyme.
- Dextrins sugar alcohols such as mannitol, sorbit and malbit. Of these, dextrin is preferred.
- modified pregelatinized starch ( ⁇ 50 x 5) is used as a matrix material, for example, the formed lock-in type powder is powdered.
- the viscosity value of the 20% aqueous solution of the modified pregelatinized starch is as described above, and 40 g of the modified pregelatinized starch is added to 160 g of water at a temperature of 20 ° C to form a 20% aqueous solution.
- the aqueous solution was heated to 80 ° C with stirring, maintained at 80 ° C for 5 minutes with stirring, then cooled to 30 ° C, and the viscosity of the aqueous solution immediately after reaching 30 ° C was measured using a viscometer It is a value when measured using “Tokimec Viscmeter BM TypeJ; Spindle No. 1 30 rpm, Spin die No. 2 30 rpm) manufactured by Tokimec.
- Flavors and / or fertilal lances encapsulated in the lock-in type powder of the present invention may be those that can be used for flavoring cosmetic products, including those conventionally used in solid formulations for cosmetic products. Any of them is not particularly limited.
- the fragrance used may be in any state such as liquid, paste or solid which may be synthetic fragrance or natural essential oil.
- flavors used in the present invention include esters, alcohols, aldehydes, ketones, acetals, phenols, ethers, latatones, furans, carbonization.
- Synthetic fragrances such as hydrogen and acids, natural fragrances and the like.
- fragments examples include hydrocarbons, alcohols, funols, aldehydes and Z or acetals, ketones and / or ketals, ethers, synthesis Examples include musks, acids, ratatones, esters, nitrogen-containing products, logene compounds, and natural fragrances.
- a fragrance having a desired fragrance or fragrance can be used according to the fragrance or fragrance required for the cosmetic product.
- a single product may be a synthetic product, or a natural source such as a plant may be introduced.
- Essential oils, resinoids, balsams, absolutes, concretes, tinctures, and the like can be prepared by known methods and used with strength.
- fragrance component examples include hydrocarbon-based fragrances such as limonene, binene, y-tvenene and caryophyllene; phenol ethyl alcohol, tvneol, pakdanol, gera-ol, nerol, linalool, cis 3 Alcoholic fragrances such as xenol; Aldelic fragrances such as lilyal, citral, aldehyde C-8, aldehyde C-9, aldehyde C-11, hexylcinnamic aldehyde, vanillin, helioto mouth pin; onon, mouth zu phenon, woody flow, Ketone-based fragrances such as Damascon and Iso Super; other fragrances such as musk, eugenol and coumarin; essential oils such as lemon oil, orange oil and peppermint oil; essences such as apple essence and strawberry essence be able toIn the present invention, one or more of hydrocarbon-based fragrances
- the matrix material, polyphenols, and an additive containing flavor and Z or fertillance used as needed are made into a lock-in type powder by the following method, for example.
- polyphenols dispersed in water are added to the matrix material.
- a fragrance and other additives may be added as necessary.
- the amount of added phenol in polyphenols can be about 0.2 to 20% by weight, preferably 1 to 15% by weight, based on the matrix material. wear.
- the stability of the resulting powder with respect to moisture varies depending on the content of moisture, polyphenols, fragrances, other additives, etc., and the content becomes too high during molding, resulting in poor stability. For this reason, the amount of polyphenols added is preferably about 20% by weight or less based on the matrix material. If the amount of polyphenols added is too small, the effect cannot be obtained.
- the blending ratio of polyphenols with respect to the matrix material is usually about 0.2 to 20% by weight, preferably about 1 to 15% by weight.
- the amount of the fragrance added varies depending on the solid preparation for blending cosmetics and cannot be generally specified. For example, it is usually about 0.2 to 20% by weight based on the matrix material.
- the amount of water in which the polyphenols are dispersed be the minimum amount that allows the polyphenols to be uniformly dispersed.
- the amount is preferably about 3 to 40% by weight based on the type and amount of polyphenol used and the force that varies depending on the type and amount of matrix material used. If the amount of water added is too large, it is not preferred because it takes too much time to reduce the water content by subsequent heating.
- the heating temperature is preferably in the range of about 110 to 200 ° C., which depends on the composition.
- the heating time is until the matrix material melts and the moisture content becomes lower. Preferably, it is boiled in a boiling pot etc. until the water content is about 0.5 to 6% by weight. If the residual water content is too high at this point, the water content of the resulting powder increases and the stability to water deteriorates, which is not preferable. By force, a homogeneous mixture of matrix material and polyphenols can be obtained.
- a uniform mixture of matrix material and polyphenols can be obtained by a method different from the above. That is, water is added to the matrix material as necessary and heated to form a matrix material melt.
- the amount is preferably the minimum amount in which the matrix material is uniformly dispersed, for example about 3 to 40% by weight with respect to the matrix material. If the amount of water added is too large, it takes too much time to reduce the water content by subsequent heating, which is not preferable.
- the heating temperature is within the range of about 110 to 200 ° C. depending on the composition until the matrix material is melted and the water content is lowered to some extent. Preferably, boil in a boiling pot until the water content is about 0.5 to 6% by weight.
- the method of mixing the matrix material melt and the polyphenols is not particularly limited as long as it is a method capable of obtaining a uniform mixture.
- an apparatus such as a high-speed stirrer (Home Disperser) is used.
- polyphenols and the like are added to the place where the melt of the matrix material is being stirred, and stirring is continued to make it uniform.
- a dispersant or an emulsifier is blended in the polyphenols or the like, a uniform dispersion of the polyphenols or the like is easily obtained.
- the homogeneous mixture obtained by the above method is transferred to an extruder, and after sealing, pressure is applied and extruded from the injection port (die) of the extruder.
- an extruder that can perform heating, mixing, and extrusion in the same container and has a pressure vessel with an extrusion plate can also be used.
- matrix material, added water, polyphenols, fragrance, etc. are introduced into the extruder using a feeding device comprising a metering pump, etc., and these are heated, mixed, and then extruded in the extruder.
- a series of steps can be continuously performed without changing the container, and the production amount per hour can be increased.
- those having a structure hereinafter referred to as “barrel” that can be heated and mixed at the same time when the raw materials are conveyed are more preferable.
- an extruder having a pressure vessel force having two or more screws is preferably used.
- An extruder having two or more screws has a superior conveying force and mixing force compared to an extruder having a single screw force, and enables more stable production.
- An extruder having two or more screws in the barrel is particularly preferably used.
- solidification of the matrix mixture is usually performed using a cooled refrigerant.
- a refrigerant put a refrigerant in the cooling tank and cool it appropriately to a low temperature. It is desirable to select a refrigerant that does not harm humans, does not dissolve the matrix material, and can be easily removed from the surface of the resulting powder.
- alcohols such as ethanol and isopropyl alcohol.
- the cooling method for these refrigerants can be freely selected according to the equipment, such as cooling with dry ice or the like, or cooling with an apparatus such as a cooler.
- the cooling temperature is a temperature sufficient to rapidly cool and solidify the homogeneous mixture extruded by the die force of the extruder, and a temperature at which the obtained solid does not soften.
- the temperature should be about 1-10-30 ° C.
- the solid material obtained here is a product obtained by rapidly cooling and solidifying a matrix material encapsulating polyphenol.
- the extrusion pressure is different depending on the type of raw material and the type of extruder. If the matrix material containing polyphenol is continuously extruded in the form of a filament, the die force of the extruder is sufficient. Specifically, when using an extruder with a pressure vessel with an extrusion plate, it is better to apply a pressure of about 5 to 50 psig by means such as introducing nitrogen gas after sealing the extruder.
- the solid obtained by rapidly cooling while extruding the uniform mixture is cut or pulverized by means such as stirring to form a lock-in type powder.
- the obtained powder is separated into powder and refrigerant by means such as centrifugal separation.
- An anti-caking agent should be added to prevent re-consolidation of the powder.
- silicon dioxide, tricalcium sulfate, tricalcium phosphate and the like can be used as the anti-caking agent.
- the amount of anti-caking agent added should be about 0.1 to 1% by weight based on the total weight.
- the powder is dried.
- the drying method is not particularly limited, but it is necessary to select a method that does not destroy the particle structure of the powder.
- vacuum drying by means such as a vacuum rotary dryer is preferred.
- the water content of the powder thus obtained is preferably about 6% by weight or less.
- sieving or the like can be performed to obtain a lock-in type powder.
- the average particle size of the lock-in type powder is not particularly limited, but it is homogeneously mixed with a cosmetic base material, etc., and retains the deodorizing function and antioxidant function when using polyphenol. From the tactile sensation at the time of use, the size is usually about 2 to 250 / ⁇ ⁇ .
- the lock-in type powder thus obtained is powder pack, whitening powder, powder bath, tablet bath, bubble bath, deodorant powder, powder detergent, dishwasher detergent, powder bleach, slime remover, denture wash It is blended into cosmetics made into various solid preparations such as pills. Its main purpose is to impart a deodorizing effect when using cosmetics. In addition, if polyphenols coexist with a fragrance, the fragrance will be added during use. It is also a purpose. In particular, in powder baths or tablet-type baths, sodium sulfate is used as the base material, or sodium sulfate and sodium hydrogen carbonate in the case of foaming baths. In detergents, surfactants are used.
- sodium sulfate, sodium carbonate, sodium phosphate, and the like are used as builders, and additives such as enzymes are also used.
- a lock-in type powder in which polyphenols are encapsulated since the polyphenols are not affected by such a base material compound, it can be used well after long-term storage. Has odor function.
- cosmetics containing alkali components, especially bathing agents or detergents retain a good deodorizing function. For this reason, examples of preferable cosmetics include bathing agents and detergents.
- the basic substance (alkali component), which is a component used in the present invention, is a known chemical substance and is not particularly limited as long as the intended purpose of the present invention can be achieved.
- Specific basic substances include carbonates such as sodium carbonate, potassium carbonate, sodium bicarbonate, hydrogen carbonate, ammonium carbonate and guanidine carbonate; or bicarbonates; boric acid such as potassium borate and sodium borate.
- Salt Potassium silicate, No. 1 sodium silicate, No. 2 sodium silicate, No.
- the blending amount of the basic substance is not particularly limited in the present invention.
- the aqueous solution strength of a solid preparation containing a lock-in type powder exceeds H7 and is 13 or less, and further, pH 8-13. I prefer to do that.
- the solid preparation of the present invention may further contain an enzyme.
- This enzyme may be an enzyme having a deodorizing function, such as degrading malodorous components that are commonly used in detergents, or a phenolic compound acid-enzyme. These enzymes are known. Examples of these enzymes include carbohydrase, lipase, protease, phytase, laccase and the like.
- the amount of the enzyme blended varies depending on the type and amount of polyphenol used. However, it cannot be specified in general, and is not particularly limited as long as the intended purpose can be achieved.
- Examples of the surfactant include a non-one type (such as polyoxyethylene alkyl ether and fatty acid alkylolamide), and an acyl glutamate type. One or two of these surfactants can be used. It is preferable to use in combination.
- Examples of polyoxyethylene alkyl ethers include polyoxyethylene stearyl and polyoxyethylene hydrogenated castor oil.
- Examples of fatty acid alkylolamides include pear oil fatty acid diethanolamide.
- the acyl glutamic acid type includes saturated and unsaturated fatty acids having 12 to 18 carbon atoms, coconut oil fatty acid, hydrogenated palm oil fatty acid, palm oil fatty acid, hydrogenated palm oil fatty acid, beef tallow fatty acid, hydrogenated beef tallow fatty acid which are a mixture thereof.
- glutamic acid esters such as N-coconut oil fatty acid acyl-L-glutamic acid triethanolamine, lauroyl-L-glutamic acid triethanolamine, N-coconut oil fatty acid acyl-L sodium glutamate, N-lauroyl-L -Sodium Daltamate, N Myristoyl- L Glutamate, N Palm Oil Fatty Acid 'Hardened Beef Fatty Acid Fatty Acid-L-Glutamic Acid Sodium L, N Palm Oil Fatty Acid Fatty Acid L-Potassium Glutamate
- the lock-in type powder is used as a base material which also has sodium hydrogen carbonate power as sodium sulfate or a foaming agent.
- the cosmetic solid preparation of the present invention is a powder or tablet-type detergent
- the lock-in powder and the fragrance as well as the moisturizing agent and the enzyme agent as necessary are added to the surfactant and the builder.
- Disintegrating agents, coloring agents, buffering agents, alkali agents, bleaching agents, softening agents, anti-deposition agents, powdering agents and the like can be blended.
- the polyphenols are encapsulated in a lock-in capsule, the polyphenols are stably retained and can be used even after being stored for a long time. It is possible to maintain an excellent appearance that the cosmetic is not colored. Moreover, incense Deodorizing effect and antioxidant function are maintained when using cosmetics. There is also a characteristic that it is hardly affected by the base material used in cosmetics. When the cosmetic is a bath agent, a particularly excellent effect can be obtained when it is a detergent. Further, when an alkaline component is blended in the cosmetic product, it can exhibit an excellent deodorizing effect and antioxidant function in cooperation with polyphenols released from the lock-in type powder.
- the fragrance when a fragrance is used in the cosmetic product or solid preparation of the present invention, the fragrance is contained in a lock-in capsule, so that the fragrance is hardly affected by the base material used in the cosmetic product. As a result, it is possible to obtain a solid preparation for cosmetics V which does not cause a decrease in scent or change in fragrance during storage.
- a bathing agent containing a fragrance containing a fragrance
- a bathing agent base comprising 49.0 parts by weight of sodium sulfate, 49.0 parts by weight of sodium hydrogen carbonate, 1.0 part by weight of anhydrous caustic acid and 1.0 part by weight of fragrance.
- 90.0 parts by weight of catechin, gallic acid and green coffee bean extract of the present invention each containing 0.1 part by weight of polyphenol-containing lock-in type powder 1.0 parts by weight are added and mixed uniformly.
- a uniform melt was obtained by heating together with 10 parts by weight of gallic acid (manufactured by Pure Chemical Co., Ltd.) dispersed in 27 mL of exchange water. Next, the melt was extruded into an isopropyl alcohol cooled to 10 ° C. using an extruder in the form of a filament, rapidly cooled, stirred and pulverized. Subsequently, isopropyl alcohol was removed by centrifugation to obtain a uniform lock-in type powder B.
- a uniform melt was obtained by heating together with 10 parts by weight of coffee bean extract (Production Example 1) dispersed in 27 mL of exchange water. Next, the melt was extruded in a filament form into isopropyl alcohol cooled to 10 ° C. using an extruder, rapidly cooled, stirred and pulverized. Next, isopropyl alcohol was removed by centrifugation to obtain a uniform lock-in type powder C.
- Dishwasher powder detergent (Chiami: Lion) 90.0 parts by weight of lock-in type powder A prepared in Example 1 was added and mixed uniformly.
- Dishwasher machine powder detergent (Chiami: manufactured by Lion) 99.0 parts by weight manufactured in Example 2 0 parts by weight of lock-in type powder Bl. was added and mixed uniformly.
- Dishwashing machine powder detergent (Chiami: manufactured by Lion) 91.0 parts by weight of lock-in type powder C prepared in Example 3 was added and mixed uniformly.
- Dishwasher powder detergent (Chi-Imi: Lion) 99.9 parts by weight of gallic acid 0.1 part by weight was added and mixed uniformly.
- Dishwasher powder detergent (L) to (N), (P), (Q) immediately after manufacture and after storing them in a container at 5 ° C, 25 ° C, 50 ° C for 1 month
- the appearance and odor of each dishwasher powder detergent (L) to (N), (P), (Q) were evaluated by sensory evaluation based on the following evaluation criteria. The evaluation result was based on the average score of five people.
- the powder "1.0" of Example 1 contains 0.1 part by weight of polyphenol (the same applies to other examples).
- the dishwasher powder detergent manufactured by the conventional method has a high degree of coloring (discoloration) and a very bad appearance and a change in odor after storage at 50 ° C for 1 month.
- the dishwasher powder detergent formulated with the lock-in type powder of the present invention has an appearance and odor before storage even after storage at 50 ° C for 1 month. You can see that the appearance looks similar to scent.
- Powder detergent for clothes 99. 9 parts by weight of catechin (Polyphenol powder GTP90: manufactured by Aya) 0.1 part by weight was added and mixed uniformly.
- Powder detergent for clothes 99. 9 parts by weight of 0.1% by weight of the raw coffee extract from Production Example 1 was added and mixed uniformly.
- Powder detergent for clothing (P)-(R), (L)-(N) immediately after production and after storing them in a container at 5 ° C, 25 ° C, 50 ° C for 1 month, The appearance and odor of each of the powder detergents for clothing (P) to (R) and (L) to (N) were evaluated in the same manner as in Test Example 1.
- the powder detergent for clothing manufactured by the conventional method has a high degree of coloring (discoloration) after storage at 50 ° C for 1 month, and the appearance becomes extremely bad, and the odor also changes.
- the laundry detergent containing the lock-in type powder of the present invention has the same appearance and odor before storage even after storage at 50 ° C for 1 month. Appearance retains odor and can be divided.
- the polyphenols are encapsulated in a lock-in capsule, the polyphenols are stably retained and can be used even after being stored for a long period of time. It is possible to maintain an excellent appearance that the cosmetic is not colored. In addition, the deodorizing effect and antioxidant function are retained when using cosmetics. There is also a characteristic that it is hardly affected by the base material used in cosmetics. When the cosmetic is a bath agent, a particularly excellent effect can be obtained when it is a detergent. Further, when an alkaline component is blended in the cosmetic product, it can exhibit an excellent deodorizing effect and antioxidant function in cooperation with polyphenols released from the lock-in type powder.
- the fragrance when used in the cosmetic or solid preparation of the present invention, the fragrance is used in the cosmetic because it is contained in the lock-in capsule. It is possible to obtain a V ⁇ cosmetic solid preparation that is hardly affected by the base material and does not deteriorate the fragrance or change the fragrance during storage.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Botany (AREA)
- Biotechnology (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Detergent Compositions (AREA)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/282,740 US20090092644A1 (en) | 2006-03-22 | 2007-03-22 | Locked-in type powder |
EP07739338A EP2002848A4 (en) | 2006-03-22 | 2007-03-22 | POWDER OF IMMOBILIZED TYPE |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006-079796 | 2006-03-22 | ||
JP2006079796A JP2007254339A (ja) | 2006-03-22 | 2006-03-22 | ロックイン型粉末 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2007119492A1 true WO2007119492A1 (ja) | 2007-10-25 |
Family
ID=38609277
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2007/055895 WO2007119492A1 (ja) | 2006-03-22 | 2007-03-22 | ロックイン型粉末 |
Country Status (6)
Country | Link |
---|---|
US (1) | US20090092644A1 (ja) |
EP (1) | EP2002848A4 (ja) |
JP (1) | JP2007254339A (ja) |
KR (1) | KR20090003250A (ja) |
CN (1) | CN101405035A (ja) |
WO (1) | WO2007119492A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011040424A1 (ja) * | 2009-09-30 | 2011-04-07 | ダイヤアクアソリューションズ株式会社 | 除菌機能付き脱臭剤、除菌機能付き脱臭材料、除菌機能付き脱臭剤の滴下供給装置、除菌機能付き脱臭剤の噴霧方法 |
JP2011184315A (ja) * | 2010-03-05 | 2011-09-22 | Fancl Corp | プレストパウダー |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102007062323A1 (de) * | 2007-12-21 | 2009-06-25 | Siemens Healthcare Diagnostics Products Gmbh | Langzeitstabiles Thromboplastin-Reagenz |
JP5800446B2 (ja) * | 2008-02-13 | 2015-10-28 | 株式会社ロッテ | 弱酸性下の消臭組成物 |
CA2743427A1 (en) * | 2008-11-26 | 2010-06-03 | Perio Sciences, Llc | Antioxidant compositions for soft oral tissue and methods of formulation and use thereof |
WO2011028495A1 (en) * | 2009-08-24 | 2011-03-10 | The Board Of Governors For Higher Education, State Of Rhode Island And Providence Plantations | Hot-melt extruded compositions containing plant-derived phenolic materials and processes for the preparation thereof |
JP5499932B2 (ja) * | 2010-06-21 | 2014-05-21 | ライオンハイジーン株式会社 | 自動洗浄機用固型洗浄剤組成物及びその製造方法 |
CA2849910A1 (en) | 2011-09-30 | 2013-04-04 | Perio Sciences, Llc | Antioxidant compositions for treatment of inflammation or oxidative damage |
CN103845268B (zh) * | 2014-03-21 | 2016-03-30 | 吴加英 | 一种婴儿用浴泡球及其制备方法 |
CN114405252B (zh) * | 2022-01-17 | 2024-06-18 | 山东华辰制药有限公司 | 一种除臭颗粒剂及其制备方法 |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4962677A (ja) | 1972-10-12 | 1974-06-18 | ||
JPS49132251A (ja) | 1973-04-24 | 1974-12-18 | ||
JPS5294452A (en) | 1975-12-12 | 1977-08-09 | Mallinckrodt Chemical Works | Production of fine taste composition particle |
JPS6112248A (ja) | 1984-06-27 | 1986-01-20 | Takasago Corp | 食用油脂含有カプセルの製造法 |
JPS61502656A (ja) | 1984-07-16 | 1986-11-20 | フィルムニッシュ ソシエテ アノニム | 固形精油風味剤組成物およびその製造方法 |
JPH09290026A (ja) | 1996-04-26 | 1997-11-11 | Kyocera Corp | 脳外科用バーホールキャップ |
JPH09290014A (ja) | 1996-12-27 | 1997-11-11 | Sanei Gen F F I Inc | 消臭剤 |
JP2002113080A (ja) * | 2000-08-11 | 2002-04-16 | Takasago Internatl Corp | 消臭剤組成物およびその使用方法 |
JP2002363106A (ja) * | 2001-03-05 | 2002-12-18 | New Food Creation Gijutsu Kenkyu Kumiai | 徐放性基材及び徐放性物品 |
JP2005194419A (ja) | 2004-01-08 | 2005-07-21 | Takasago Internatl Corp | 香料カプセルおよびそれを含有する入浴剤 |
JP2006079796A (ja) | 2004-08-13 | 2006-03-23 | Renesas Technology Corp | 不揮発性半導体記憶装置および半導体記憶装置 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2809895A (en) * | 1955-07-05 | 1957-10-15 | Sunkist Growers Inc | Solid flavoring composition and method of preparing the same |
US4919962A (en) * | 1988-08-12 | 1990-04-24 | General Foods Corporation | Coffee flakes and process |
WO1996002609A1 (fr) * | 1994-07-15 | 1996-02-01 | Otsuka Pharmaceutical Co., Ltd. | Agent gonflant contenant un antioxydant |
US6241975B1 (en) * | 1999-07-24 | 2001-06-05 | Pacific Corporation | Method for preparation of plant extract powder |
FR2808681B1 (fr) * | 2000-05-10 | 2002-09-06 | Michel Fauvel | Produit cosmetique, notamment pour les soins de la peau |
US20030206978A1 (en) * | 2001-11-29 | 2003-11-06 | Bob Sherwood | Agglomerated particles including an active agent coprocessed with silicified microcrystalline cellulose |
JP3662550B2 (ja) * | 2002-05-08 | 2005-06-22 | 高砂香料工業株式会社 | 粉末組成物 |
US7115283B2 (en) * | 2003-05-06 | 2006-10-03 | Access Business Group International Llc | Preparations for sustained release of nutraceuticals and methods of controllably releasing nutraceuticals |
JP5171038B2 (ja) * | 2003-10-10 | 2013-03-27 | エティファルム | イチョウ・エキスを含む放出持続性の微小顆粒およびそのような顆粒の製造方法 |
US8257751B2 (en) * | 2003-11-03 | 2012-09-04 | Beauté Pacifique ApS | Composition for the cosmetic treatment of age-related dermatological symptoms |
SG10201502232SA (en) * | 2006-03-22 | 2015-05-28 | Takasago Perfumery Co Ltd | Deodorant composition |
-
2006
- 2006-03-22 JP JP2006079796A patent/JP2007254339A/ja not_active Withdrawn
-
2007
- 2007-03-22 WO PCT/JP2007/055895 patent/WO2007119492A1/ja active Application Filing
- 2007-03-22 CN CNA2007800099956A patent/CN101405035A/zh active Pending
- 2007-03-22 EP EP07739338A patent/EP2002848A4/en not_active Withdrawn
- 2007-03-22 KR KR1020087023004A patent/KR20090003250A/ko not_active Application Discontinuation
- 2007-03-22 US US12/282,740 patent/US20090092644A1/en not_active Abandoned
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4962677A (ja) | 1972-10-12 | 1974-06-18 | ||
JPS49132251A (ja) | 1973-04-24 | 1974-12-18 | ||
JPS5294452A (en) | 1975-12-12 | 1977-08-09 | Mallinckrodt Chemical Works | Production of fine taste composition particle |
JPS6112248A (ja) | 1984-06-27 | 1986-01-20 | Takasago Corp | 食用油脂含有カプセルの製造法 |
JPS61502656A (ja) | 1984-07-16 | 1986-11-20 | フィルムニッシュ ソシエテ アノニム | 固形精油風味剤組成物およびその製造方法 |
JPH09290026A (ja) | 1996-04-26 | 1997-11-11 | Kyocera Corp | 脳外科用バーホールキャップ |
JPH09290014A (ja) | 1996-12-27 | 1997-11-11 | Sanei Gen F F I Inc | 消臭剤 |
JP2002113080A (ja) * | 2000-08-11 | 2002-04-16 | Takasago Internatl Corp | 消臭剤組成物およびその使用方法 |
JP2002363106A (ja) * | 2001-03-05 | 2002-12-18 | New Food Creation Gijutsu Kenkyu Kumiai | 徐放性基材及び徐放性物品 |
JP2005194419A (ja) | 2004-01-08 | 2005-07-21 | Takasago Internatl Corp | 香料カプセルおよびそれを含有する入浴剤 |
JP2006079796A (ja) | 2004-08-13 | 2006-03-23 | Renesas Technology Corp | 不揮発性半導体記憶装置および半導体記憶装置 |
Non-Patent Citations (5)
Title |
---|
"Nihon ni Okeru Syokuhin Kouryou Kagoubutu no Shiyou Jittai Cyousa", 2000, JAPAN FLAVOR & FRAGRANCE MATERIALS ASSOCIATION |
"Syuuchi Kanyou Gijyutsusyu (Kouryou) Daiichibu, Kouryou Ippan", 29 January 1999, JAPAN PATENT OFFICE |
JHON M. DEMAN: "PRINCIPLES OF FOOD CHEMISTRY", 1990, VAN NOSTRAND REINHOLD, pages: 167 - 168 |
MOTOICHI INDO: "Gousei Kouryou, Kagaku to Syouhin Chishiki", 6 March 1996, THE CHEMICAL DAILY CO., LTD. |
PERFUME AND FLAVOR CHEMICALS (AROMA CHEMICALS) 1, 2, vol. 1,2, 1969 |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011040424A1 (ja) * | 2009-09-30 | 2011-04-07 | ダイヤアクアソリューションズ株式会社 | 除菌機能付き脱臭剤、除菌機能付き脱臭材料、除菌機能付き脱臭剤の滴下供給装置、除菌機能付き脱臭剤の噴霧方法 |
JPWO2011040424A1 (ja) * | 2009-09-30 | 2013-02-28 | ダイヤアクアソリューションズ株式会社 | 除菌機能付き脱臭剤、除菌機能付き脱臭材料、除菌機能付き脱臭剤の滴下供給装置、除菌機能付き脱臭剤の噴霧方法 |
JP2011184315A (ja) * | 2010-03-05 | 2011-09-22 | Fancl Corp | プレストパウダー |
Also Published As
Publication number | Publication date |
---|---|
EP2002848A4 (en) | 2009-04-15 |
EP2002848A9 (en) | 2009-04-22 |
EP2002848A2 (en) | 2008-12-17 |
US20090092644A1 (en) | 2009-04-09 |
JP2007254339A (ja) | 2007-10-04 |
CN101405035A (zh) | 2009-04-08 |
KR20090003250A (ko) | 2009-01-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2007119492A1 (ja) | ロックイン型粉末 | |
US6932982B2 (en) | Encapsulated flavor and/or fragrance composition | |
JP6023946B2 (ja) | 消臭剤組成物 | |
JP5546129B2 (ja) | フレーバーおよび/またはフレグランスカプセル | |
EP1753307B1 (en) | Particulate flavouring composition | |
JP5090588B2 (ja) | 芳香成分のための固体運搬系 | |
EP1523339B2 (en) | Composition for controlled release of perfumes and flavours | |
US20070128234A1 (en) | Process for the incorporation of a flavor or fragrance ingredient or composition into a carbohydrate matrix | |
US20070031582A1 (en) | Oxigen stable active containing compositions | |
BRPI0212783B1 (pt) | composição secada por borrifo, método para a preparação de um produto particulado, sistema de suprimento granular, método para aromatizar um produto alimentício ou de bebida, método para aperfeiçoar, aumentar ou modificar as propriedades de fragrância de uma composição, produto alimentício ou de bebida, e, produto ou artigo aromatizante | |
RU2323595C2 (ru) | Некристаллическая система доставки вкусоароматических веществ или отдушки, способ ее приготовления (варианты), вкусоароматизированный продукт, изделие с отдушкой и способ улучшения, усиления или модификации органолептических свойств вкусоароматической композиции или композиции с отдушкой | |
MX2007007181A (es) | Acidos grasos poliinsaturados encapsulados. | |
JP2019523314A (ja) | フレーバーを含む固体カプセルの製造 | |
JP6426080B2 (ja) | 物質混合物 | |
JP2006083071A (ja) | 香粧品用固形製剤 | |
Barra et al. | Normand et al.(43) Pub. Date: Jul. 14, 2005 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 07739338 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 12282740 Country of ref document: US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 200780009995.6 Country of ref document: CN Ref document number: 2007739338 Country of ref document: EP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020087023004 Country of ref document: KR |