WO2013064609A1 - Préparation cosmétique contenant des matières pulvérisées pour améliorer la tenue du parfum - Google Patents

Préparation cosmétique contenant des matières pulvérisées pour améliorer la tenue du parfum Download PDF

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Publication number
WO2013064609A1
WO2013064609A1 PCT/EP2012/071677 EP2012071677W WO2013064609A1 WO 2013064609 A1 WO2013064609 A1 WO 2013064609A1 EP 2012071677 W EP2012071677 W EP 2012071677W WO 2013064609 A1 WO2013064609 A1 WO 2013064609A1
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WO
WIPO (PCT)
Prior art keywords
oil
perfume
substances
liquid
substance
Prior art date
Application number
PCT/EP2012/071677
Other languages
German (de)
English (en)
Inventor
Katja MÄTZOLD
Svenja Lena Möllgaard
Stefan Biel
Katrin Counradi
Ina Schornstein
Heike Miertsch
Horst Argembeaux
Original Assignee
Beiersdorf Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beiersdorf Ag filed Critical Beiersdorf Ag
Priority to BR112014007410A priority Critical patent/BR112014007410A2/pt
Priority to EP12780740.2A priority patent/EP2773310A1/fr
Publication of WO2013064609A1 publication Critical patent/WO2013064609A1/fr

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Classifications

    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/731—Cellulose; Quaternized cellulose derivatives
    • 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
    • A61K8/0241—Containing particulates characterized by their shape and/or structure
    • 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
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/25—Silicon; Compounds thereof
    • 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
    • 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
    • A61K2800/41—Particular ingredients further characterized by their size
    • A61K2800/412—Microsized, i.e. having sizes between 0.1 and 100 microns
    • 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
    • A61K2800/56—Compounds, absorbed onto or entrapped into a solid carrier, e.g. encapsulated perfumes, inclusion compounds, sustained release forms
    • 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
    • A61K2800/60—Particulates further characterized by their structure or composition
    • A61K2800/65—Characterized by the composition of the particulate/core
    • A61K2800/654—The particulate/core comprising macromolecular material
    • 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

Definitions

  • the invention comprises cosmetic preparations comprising perfume on one
  • the active substance (s) is present homogeneously, ie uniformly distributed, within the amorphous matrix of a particle.
  • These matrix capsules can be prepared, for example, by spray drying.
  • the core-shell encapsulation is preferably used for applications requiring a sudden release or release over a very long period of time.
  • WO 2008 025640 A1 describes processes for the production of microparticles.
  • EP 1 858 387 A1 describes products for the directed release of active substances with two different chambers.
  • the active substances can be present as a solid and / or as a liquid in one of the chambers. Preferably, they are in the solid state, which in liquid active substances optionally by absorption / adsorption on suitable
  • Carrier substances can be achieved.
  • the active ingredients may thus be in the form of powder, granules, flakes, tablets, microencapsulated liquids or solids, CPF (concentrated powder form) powders, d. H. as a free-flowing powder having a liquid content of at least 10%, preferably at least 30%, on a powdered carrier.
  • CPF concentrated powder form
  • the preparation of these CPF powders can be carried out according to WO 99/17868 A1, to which reference is made in full.
  • Polyamide particles for improving perfume transfer in cosmetic or dermatological deodorant or antiperspirant compositions are provided.
  • US 2007 0248553 A1 describes anhydrous antiperspirant compositions which contain a second perfume which is incorporated in an emulsifier-free, cyclodextrin-containing matrix and released by water. Similar publications are US 2006026331 1 A1, US 2006 0263312 A1, US 2006 0263313 A1.
  • EP 0 493 578 A1 describes a process for the preparation of a water-soluble or water-dispersible formulation of a biologically active ingredient (eg pesticides for agriculture) and a carrier. Active ingredient and carrier are mixed and solubilized in liquid carbon dioxide, the carbon dioxide is converted to the gaseous state by pressure reduction and then removed to provide an intimate mixture of the formulation.
  • WO 2005 073300 A1 describes an improvement in the solubility of primary
  • Production of the porous body is carried out by separation of freeze-dried emulsions in disperse and continuous phases.
  • liquid is not brought to a carrier particle but liquid is removed by freeze-drying, so that cavities are formed.
  • WO 2006 082536 A1 describes spray-dried preparations of active ingredients which are present in a gum arabic carrier mixed with a surfactant.
  • the technology is used to encapsulate menthol for chewing gum and tablets.
  • WO 2008 041 196 A1 describes a pulverized, non-liquid
  • Hair conditioning product wherein the liquid conditioner is absorbed on a solid carrier.
  • the powdered product is mixed with water before use.
  • EP 0 279 328 A2 describes a perfume composition which, because of the particular choice of ingredients present in the composition (film-forming substrates and emulsifiers), enables a reversible "re-encapsulation" of the active deodorizing ingredients to result in various successive activations enter the skin without the user having to make another application.
  • the re-encapsulation occurs during drying of the skin following a perspiration period.
  • Another technology to encapsulate substances such as flavors is extrusion.
  • the carrier z.
  • WO 2006 082536 A1 describes the preparation of spray-dried hydrophobic
  • WO 2005 032503 A1 describes a system for the controlled release of perfume, which is water-based and contains a film-forming material (acrylate / hydroxyacrylate copolymer).
  • WO 2003 088894 A2 describes the controlled release in anhydrous systems in which various types of perfumes, drugs and combinations can be encapsulated. It is a free-flowing powder, which consists of solid
  • hydrophobic nanoparticles encapsulated in moisture-sensitive microspheres.
  • EP 1 183 003 A1 describes the so-called spray-drying
  • WO 2005 073300 A1 describes freeze-drying
  • WO 2005 014704 A1 describes CO 2 drying and in WO 95 21688 A1 the so-called PGSS process.
  • a powdered carrier is added to the droplet spray.
  • the addition of carrier is the difference to the PGSS method.
  • This carrier binds the fine droplets and a free-flowing powder is formed. That so resulting powder may have a liquid content of up to a maximum of 80 wt.%, Based on the total mass of the powder.
  • the CPF technology makes it possible to produce free-flowing powders with a high liquid content.
  • any gas can be used which dissolves in the liquid to be pulverized. The higher the melting temperature of the liquid, the less carrier material is needed to stabilize the powdered liquid. The proportion of the carrier may therefore be between 1 and 90% by weight.
  • any solid, powdery substance can be used, but it is advantageous if its particle size is smaller than 100 ⁇ m, or if one of the carriers has a porosity, such as activated carbon or zeolites.
  • the advantages of the CPF process are that the low temperatures during the pulverization slow down or prevent degradation reactions, there is only low odor nuisance and the inert C02 acts as a protective gas for reactive substances.
  • the CPF process is already used in food technology, detergents, paints and adhesives technology.
  • component (A) to be adsorbed is an oil-soluble compound
  • Stabilizers polysaccharides, chelators, glycerides or emulsifiers used.
  • perfume oils are named.
  • Carrier (C) may also be polysaccharides, in which case various stabilizers B) of C) different polysaccharides are used.
  • perfume oils it is desirable to be able to incorporate perfume oils in a cosmetic formulation so that they are released as evenly as possible over a long time regardless of the necessary external triggers for their release.
  • the invention is therefore a cosmetic or dermatological preparation comprising one or more pulverulent products comprising or consisting of one or more liquid at room temperature, pasty and / or up to a temperature of 150 ° C meltable substance or mixtures (a.) Containing or consisting of Perfume and / or perfume ingredients absorbed on one or more particulate carriers (b.).
  • the substance or mixture of substances (a.) May, in a preferred embodiment, consist entirely of one or more perfume or perfume ingredients.
  • the supports (a.) are characterized by an average particle size in the range of 5 nm to 2 mm, a tamped density of 50 kg / m 3 to 1400 kg / m 3 and a spherical, fibrous, flaky and / or sponge-like particle shape.
  • Powders which have a minimum of 5 nm and a maximum of 2 mm in the average particle size.
  • the tamped density is 50 kg / m 3 to 1400 kg / m 3 .
  • the tamped density is determined by the determination of the volume, wherein the tamping volume represents the smallest volume of a fixed amount of filler, which after stomping or compaction according to standardized
  • the porosity of the carrier is freely selectable from non-porous to highly porous.
  • the carriers are usually used in cosmetics powder substances.
  • they are selected from the group of polysaccharides and silicic acids and their derivatives, as well as powder materials such as those in decorative cosmetics as a filler and
  • Sensoric additive can be used are possible.
  • the following list of advantageous carrier materials to be used should in no way be limiting: polysaccharides:
  • Rice starch Rice starch, wheat starch and their derivatives (eg trade names: Amylogum CLS from Avebe, C * EmCap from Cerestar, DryFlo types from Akzo Nobel
  • the powdery products include the perfume-containing substances or mixtures (a.) And the particulate carriers (b.) On which they are absorbed, or preferably consist only of these two components a.) And b.).
  • emulsifiers or stabilizers in the powdery products can be dispensed with.
  • Another preferred criterion is that the powdered products are produced according to the CPF process.
  • the substance or the substance mixture is hydrophilic. Then it is preferably characterized in that it alone is not soluble or sparingly soluble in a hydrophobic preparation.
  • a hydrophilic substance or a hydrophilic substance mixture is characterized in that it is miscible with water. Solubility is the property of a substance to dissolve homogeneously in a liquid or melt.
  • Substance or mixtures of substances which can not be completely or only inhomogeneously dissolved in the solvent are said to be insoluble or poorly soluble.
  • perfume-containing, hydrophilic substances / substance mixtures in hydrophobic preparations perfume-containing, hydrophilic substances / substance mixtures in hydrophobic preparations.
  • the substance or the mixture of substances is hydrophobic. Then it is preferably characterized in that it alone is not soluble or sparingly soluble in a hydrophilic preparation.
  • a hydrophobic substance or mixture of substances is characterized in that it is immiscible with water. Solubility is the property of a substance to dissolve homogeneously in a liquid or melt. Substance or mixtures of substances which can not be completely or only inhomogeneously dissolved in the solvent are said to be insoluble or poorly soluble.
  • perfume-containing, hydrophobic substances / substance mixtures in hydrophilic preparations to provide perfume-containing, hydrophobic substances / substance mixtures in hydrophilic preparations to provide.
  • Perfume oils can thus be incorporated into a cosmetic formulation so that they are released as evenly as possible over a long period of time and no external influences are necessary.
  • Standard capsule systems of the prior art allow release by external trigger, either by the addition of water (sugar capsules) or mechanical shear (melamine capsules).
  • the inventively preferred CPF systems release the fragrance of perfume on the skin simply via classical equilibrium reactions.
  • the CPF process makes it possible to produce powdery solids from liquids.
  • the process principle is to dissolve a gas in the liquid to be pulverized under elevated pressure, preferably until a gas-saturated solution is obtained. Compared to pure liquid, such a solution has a number of favorable
  • the pressurized liquid / gas solution is then a
  • Relaxation organ in the relaxation organ or after, in particular shortly after the relaxation organ, a solid, powdery excipient, the particulate carrier admixed.
  • any gas which dissolves sufficiently in the liquid substance or substance mixture to be pulverized can be used as the gas.
  • the gas carbon dioxide, a hydrocarbon, in particular methane, ethane, propane, butane, ethene, propene or a halogenated hydrocarbon, an ether, an inert gas, in particular nitrogen, helium or argon, a gaseous oxide, in particular nitrous oxide or sulfur dioxide, and ammonia be used.
  • a mixture of two or more of the aforementioned gases may be used.
  • the increased pressure at which the gas is dissolved in the liquid or mixture of substances may be in the range of 5 bar to 800 bar, but preferably the pressure is in the range of 10 bar to 350 bar and more preferably in the range of 20 bar to 250 bar.
  • the dissolution of the gas in the liquid or mixture of substances is accelerated by mixing the gas with the liquid or mixture of substances.
  • This mixing can be achieved, for example, by shaking or rolling the pressure vessel, in which the liquid to be pulverized is placed.
  • the CPF process works in principle with any solid, powdery carrier.
  • Perfume ingredients is bound by adhesion, impregnation and / or agglomeration of the carrier particle. Surprisingly, the CPF process does not cause a closed shell to form. There are no capsules. Thus, the substance or mixture containing perfume and / or perfume ingredients may be released from the particulate carrier as soon as the loaded particles enter an environment in which the substance or mixture containing perfume and / or perfume ingredients is soluble. Even if a part of the perfume or perfume ingredients can already dissolve in the surrounding formulation, the binding to the carrier particle surprisingly leads to a delayed release. Thus, the use of these systems thus leads to a long-lasting product effect.
  • the advantage here is that the perfume is released by delayed diffusion on the skin surface, without the supply of external trigger such as water or mechanical stress is necessary.
  • all materials which are liquid at room temperature, pasty and / or meltable up to a temperature of 150 ° C. are to be understood as substances to be pulverized, mixtures of substances, active ingredients or active solutions.
  • mixtures of substances containing perfume or perfume ingredients include solvents for perfume or perfume ingredients, eg. As ethanol, propylene glycol,
  • Hydrocarbons, ethers and volatile silicones for incorporation of the perfume raw substances into the substance mixture can surface-active substances such as emulsifiers and
  • Solubilizers can be used.
  • Preferred solvents for perfumes and perfume ingredients are in particular oils, low-melting fats and waxes.
  • the mixture is preferably liquid at room temperature, but may also be pasty to solid, if it is then melted at a temperature up to 150 ° C.
  • Preferred cosmetic active ingredients which may additionally be present in the preparation and are preferably pulverized by means of CPF, are to be selected from the group of antibacterial, antiperspirant, anti-aging, skin-calming and / or
  • deodorant agents such as ethylhexylglycerol, methyl phenylbutanol, butyloctanoic acid, polyglyceryl-2 caprate, polyaminopropyl biguanide, octenidine HCl, silver citrate or other active ingredients such as Q10, panthenol, bisabolol, ubiquinones, calcium pantothenates, niacinamide, oryzanol and / or piroctone Olamine be chosen.
  • active ingredients such as Q10, panthenol, bisabolol, ubiquinones, calcium pantothenates, niacinamide, oryzanol and / or piroctone Olamine be chosen.
  • Suitable humectants are glycerol and glycols.
  • Other active ingredients may be selected from the group of extracts such as Cymbopogon Citratus, Persea Gratissima, Pearl, Maris Limus, Ostrea Shell, Fucus Vesiculosus, Hamamelis Virginiana, Chamomilla Recutita Flower Extract, Silk, Cotton Seed Oil, Green Tea Extract (Camelia), Magnolia, Rice, Cashmere, Simmondsia Chinensis (Jojoba) Oil, Cucumber, Menthol, Glycyrrhiza Inflata.
  • Extracts such as Cymbopogon Citratus, Persea Gratissima, Pearl, Maris Limus, Ostrea Shell, Fucus Vesiculosus, Hamamelis Virginiana, Chamomilla Recutita Flower Extract, Silk, Cotton Seed Oil, Green Tea Extract (Camelia), Magnolia, Rice, Cashmere, Simmondsia Chinensis (Jojoba) Oil, Cucumber, Menthol, Glycyrrhiza
  • perfumes or perfume ingredients according to the invention in particular perfume oils, it is possible to add:
  • phenoxyacetates alpha-amylcinnamaldehyde, alpha-butylcinnamaldehyde, alpha-hexylcinnamaldehyde, alpha-ionone, alpha-isomethylionone, alpha-methyionantheme, alpha-methyl-3,4-methylene dioxyhydrocinnamic aldehyde, alpha-methylbenzylacetate, alpha-pinene, alpha-terpineol , Aluminum magnesium hydroxide stearate, amaranthus extract, ammonium lactate, ammonium polyacrylate, ammonium polyacryloyl dimethyl taurate, amyl acetate, amyl salicylate, andrographolides, anethole, anisic acid, aniseed oil, anisyl acetate, anisyl alcohol, annatto, anthemis nobilis flower, arginine PCA, ascorbyl tocopheryl maleate,
  • Cedrenol Cedrenyl Acetate, Cedrol, Cedrol Methyl Ether, Cedryl Acetate, Chlorhexidine Digluconate, Chrysanthenum Parthenium, Cinnamic Alcohol, Cinnamic Aldehyde, Cis-3 Hexenyl Salicylate, Citral, Citronella Oil, Citronellal, Citronellyl Acetate, Citrus Aurantium Dulcis Blossoms, Citrus Oil distilled, clove bud oil, cocoglucoside, coffea robusta, cognac oil, coleus barbatus extract, coumarin, cyclamen aldehyde, cyclohexyl salicylate, d-camphor, decanal, delta-3-carene, diacetin, diethyl malonate, diethyl phthalate, diethylene glycol monoethyl ether , Dihydromyrcenyl acetate, dihydrotinyl acetate, dimethoxy
  • Bisiminomethylguaiacol manganese chlorides ethyl butyrate, ethyl glucoside, ethyl maltol, ethyl vanillin, ethyl-2-methyl-1,3-dioxolane-2-acetate, ethylenea brassylate, ethyllinalool, ethyllinyllyl acetate, ethylvanillin, ethyl methylphenyl glycidate, eucalyptol, eucalyptus oil, eugenol, Melissa leaves extract, fir needle oil, formaldehyde cyclododecyl ethyl acetal, galbanum oil, gamma-decalactone, gamma-nonalactone, gamma-terpinene, gamma-undecalactone, garden grape, geranium oil, geranyl acetate, glucosylrutin
  • Cumin Seed Extract Cumin Oil, Copper Gluconate, Labdanum Oil, Lagerstroemia Indica Extract, Lauric Aldehyde, Lauryl Alcohol, Lauryl Dimonium Hydroxypropyl Hydrolyzed Soy Protein, Lauryl Polyglucoside Sodium Hydroxypropyl Starch Phosphate, Lavandin Oil, Lavender Oil, Lemon Oil, Lemon Oil Terpenes, Lemon Terpenes, Lemongrass Oil, Lovage oil, Lime oil, Linalool, Linalyl acetate, Linseed acid, Linseed acid magnesium aspartate, l-menthol, Laurel oil, Lupinus luteus extract, Majantol, maltol isobutyrate, mandarin oil, melibiose, menthanyl acetate, menthol, menthol liquid, menthone, menthyl acetate, menthyl lactate, menthyl salicylate, methyl 2-nonenoates, methyl abietates, methyl cedryl keto
  • Octyldodecanol Melissa leaf oil, Oleyl erucate, Omega pentadecalactone, Orange oil, Orange terpenes, Orange terpenes (natural), Orange blossom oil,
  • Granatum Fruit Juice Pyracantha Fortuneana Extract, Pyrus Malus Water, Rhodinol, Rosemary Oil, Rose Extract, Rose Oil, Rosemary Oil, Sabinene, Sage Oil, Sandalwood Oil, Sandalwood Oil, Sarcosine, Sassafras Tree Oil, Saxifraga Sarmentosa Extract, Yarrow Oil, Sclareoate, Scutellaria Baicalensis Extract, Selaginella Tamariscina Extract, Shorea
  • Alkylcitrates triacetin, trichloromethylphenyl carbinyl acetate, tricyclodecenyl propionates, trideceth-6, triethyl citrate, trioctyldodecyl citrate, trioxaundecanedioic acid, undecanal, 2- methyl-, vanilla, vanillin, vetiver oil, juniper tar, incense resin, frankincense extract, xymenynic acid, ylang ylang oil, cinnamon oil, cinnamic acid, zinc gluconate, lemongrasol, lemon oil,
  • the substance or mixture comprises only one or more of the listed perfume ingredients.
  • the preparations according to the invention are preferably anhydrous. However, a residual amount of water may be present in the preparation according to the invention as a result of the raw material and may therefore be unavoidable. As anhydrous therefore be within the meaning of the invention
  • compositions containing less than 5% by weight of water (not including water of crystallization), preferably less than 2% by weight of water and in particular less than 1% by weight of water, based on the total mass of the preparation.
  • the cosmetic and dermatological preparations according to the invention may further contain cosmetic adjuvants and other active ingredients such as are commonly used in such preparations, for.
  • cosmetic adjuvants and other active ingredients such as are commonly used in such preparations, for.
  • Color pigments, thickeners, moisturizing and / or moisturizing substances, fats, oils, waxes or other customary constituents of a cosmetic or dermatological formulation such as alcohols, polyols, polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives if the additive does not have the required solubility properties impaired.
  • the proportions relate to parts by weight, based on the total mass of the preparation, unless otherwise disclosed.
  • Carrier particles (microcrystalline cellulose) 7,00 14,00
  • Examples 2 and 3 according to the invention show an improved, because prolonged perfume release compared to the comparative example.
  • the z-Nose measuring system is capable of chromatographing gas space samples within a very short time.
  • the process is as follows:
  • Tubes were placed with the lid open for 4 h at a possible draft-free, open place
  • Figure 1 illustrates the release of the perfume into the gas space.
  • the amount of perfume in the gas space (in% by weight, based on the total in the

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Cosmetics (AREA)
  • Fats And Perfumes (AREA)

Abstract

Préparation cosmétique ou dermatologique contenant un ou plusieurs produits pulvérulents comportant une ou plusieurs matières ou mélanges de matières fluides, pâteux et/ou fusibles jusqu'à une température de 150°C, ces matières ou mélanges de matières contenant ou étant composés de parfum et/ou de constituants de parfum, le mélange ou la matière étant absorbés sur un ou plusieurs supports particulaires. La préparation selon l'invention présente une libération prolongée du parfum (longue tenue).
PCT/EP2012/071677 2011-11-03 2012-11-02 Préparation cosmétique contenant des matières pulvérisées pour améliorer la tenue du parfum WO2013064609A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
BR112014007410A BR112014007410A2 (pt) 2011-11-03 2012-11-02 preparação cosmética compreendendo substâncias pulverizadas para melhorar a fixação do perfume
EP12780740.2A EP2773310A1 (fr) 2011-11-03 2012-11-02 Préparation cosmétique contenant des matières pulvérisées pour améliorer la tenue du parfum

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102011085685A DE102011085685A1 (de) 2011-11-03 2011-11-03 Kosmetische Zubereitung mit pulverisierten Stoffen zur Verbesserung der Parfümhaftung
DE102011085685.4 2011-11-03

Publications (1)

Publication Number Publication Date
WO2013064609A1 true WO2013064609A1 (fr) 2013-05-10

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Country Link
EP (1) EP2773310A1 (fr)
BR (1) BR112014007410A2 (fr)
DE (1) DE102011085685A1 (fr)
WO (1) WO2013064609A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE202016001339U1 (de) 2016-03-03 2016-03-14 Beiersdorf Ag Kosmetische Reinigungszubereitung enthalten Peeling-Partikel und Rheosmin
WO2017180440A1 (fr) * 2016-04-11 2017-10-19 Amcol International Corporation Système de distribution à base de microparticules naturelles pour utilisation dans des soins personnels et d'autres applications topiques
WO2020015880A1 (fr) * 2018-07-16 2020-01-23 Beiersdorf Ag Composition cosmétique désodorisante biphase

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