WO2013156647A1 - Composición para la limpieza y/o hidratación de la piel - Google Patents
Composición para la limpieza y/o hidratación de la piel Download PDFInfo
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- WO2013156647A1 WO2013156647A1 PCT/ES2013/070237 ES2013070237W WO2013156647A1 WO 2013156647 A1 WO2013156647 A1 WO 2013156647A1 ES 2013070237 W ES2013070237 W ES 2013070237W WO 2013156647 A1 WO2013156647 A1 WO 2013156647A1
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- component
- skin
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- composition according
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Classifications
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- 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
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
-
- 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
- A61K8/37—Esters of carboxylic acids
-
- 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
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/062—Oil-in-water emulsions
-
- 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
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
-
- 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
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
-
- 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
- A61Q19/007—Preparations for dry skin
-
- 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
- A61Q19/10—Washing or bathing preparations
-
- 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
- A61K2800/59—Mixtures
-
- 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
- A61K2800/59—Mixtures
- A61K2800/592—Mixtures of compounds complementing their respective functions
- A61K2800/5922—At least two compounds being classified in the same subclass of A61K8/18
Definitions
- the present invention relates to cosmetic or dermatological compositions for cleaning and / or hydrating the skin, especially cosmetic or dermatological compositions for cleaning and / or hydrating the skin in the bath or shower, characterized by its high oil content and low water content
- the process of cleaning the skin can produce certain aggressions on the skin that can cause a slight swelling of its most superficial layer. In general, this process of superficial irritation is compensated by the skin's own protective mechanisms. However, in the case of skins prone to dryness, or subject to some wear, due to the effect of factors such as sunlight or cold, such natural protection mechanisms may not be sufficient. It is for this reason that the formulations used for body washing must contain, in addition to the least aggressive cleaning agents possible, specific components added in order to protect the skin, such as oils.
- shower oils One of the types of skin cleansing formulations that meet this type of requirement are so-called shower oils. This type of composition is characterized by containing a mixture of mild surfactants combined with oils present in relatively high proportions. These compositions clean gently and, thanks to oils, relax, soften and protect the skin against drying out.
- the main technical difficulty in obtaining shower oils is the solubility in the surfactant system of the relatively high percentage of oil required. That is, obtaining stable and preferably transparent single-phase formulations, capable of producing a suitable foam, in quantity and quality.
- TIPA triisopropanolamine lauryl ether sulfate
- the prior art includes some alternatives to the TIPA lauryl ether sulfate based system.
- Document US4371548 describes a bath or shower composition, consisting of a mixture of surfactants (10% to 90% by weight of fatty alcohol amine sulfate (C8-C18) optionally ethoxylated in the fatty alcohol sulfate anion (C8- C18), where preferably the amines are mixtures of diethylamine and monobutylethanolamine, and a metal or ammonium sulfate of C8-18 ethoxylated fatty alcohol) with a cosmetically acceptable oil (from 20% to 60% by weight).
- a mixture of surfactants (10% to 90% by weight of fatty alcohol amine sulfate (C8-C18) optionally ethoxylated in the fatty alcohol sulfate anion (C8- C18), where preferably the amines are mixtures of diethylamine and monobutylethanolamine, and a metal or ammonium sulfate of C8-18 ethoxylated fatty alcohol) with
- US4130497 describes a cosmetic composition in a single liquid phase, which can be used for bathing and showering and that provides the skin with a layer of a beneficial agent for the skin that is Maintains after bath or shower.
- Said composition contains oil and a mixture of anhydrous anionic surfactants, the first surfactant being an anhydrous fatty alcohol amine salt (C8-C18) sulfate, containing on average 0 to 4 moles of ethylene oxide, preferably mono or diethylene ethanolamine sulfate of lauryl ether with 2 or 3 moles of ethylene oxide, diethylamine and monobutylethanolamine sulfate of lauryl ether and the amyl of nonylphenyl and octylphenyl sulfate, and the second surfactant an alkyl ether carboxylic acid or a sodium or aminic salt thereof
- document US6306410 is relevant for the present invention.
- This document describes cosmetic compositions for makeup removal, transparent, single phase, easy to spread and remove with water.
- the compositions contain up to 80% by weight of oleaginous bodies and ethoxylated partial glycerides. Description of the invention
- compositions for skin cleansing in particular in the field of bath and especially shower preparations
- cleaning compositions with a high content of oil solubilized in the system surfactant such compositions being therefore monophasic compositions, stable and preferably transparent, capable of providing a high degree of oil deposition on the skin, adequate foam production, good application capacity and satisfactory cleaning power.
- the present invention offers an efficient solution to the aforementioned requirements, providing a cosmetic or dermatological composition comprising:
- component (c) characterized in that it contains a minimum of 20% by weight, preferably 30% by weight, of component (c) with respect to the total weight of active material of the composition of the invention.
- the shower or bath compositions according to the invention are transparent, allow a good deposition of oil on the skin, have a foaming power and are not irritating.
- the present invention also provides a method for cleaning and / or moisturizing the skin, which comprises the steps of (1) wetting or moistening the skin; (2) apply on the skin a sufficient amount of a composition according to the present invention and, finally, (3) rinse the skin with water.
- the present invention also provides the use of a composition according to the invention for cleaning and / or moisturizing the skin, in particular for cleaning and / or hydrating the skin during the shower or bath.
- the present invention also provides a method for the preparation of the compositions of the invention.
- compositions of the invention which provide a cosmetic or dermatological composition for cleaning and / or moisturizing the skin, preferably compositions used for showering or bathing, comprise:
- composition of the invention comprises a component (a) comprising at least one alkyl ether carboxylate.
- R is an alkyl or alkenyl group having 6 to 22 carbon atoms, linear or branched, saturated or unsaturated
- Ri is an alkyl group having 1 to 4 carbon atoms
- n has a value in the range of 0 to 20
- m has a value in the range of 0 to 6
- M + is a cation, preferably selected from the group consisting of hydrogen, an alkali metal, a metal alkaline earth, ammonium, an alkylammonium, an alkanolammonium or a glucamonium.
- the carboxylate ether may be ethoxylated and propoxylated, the value of n and m being therefore in formula (I) greater than 0.
- the order or sequence of the ethylene oxide and oxide groups of Propylene is not critical to the invention. Therefore, both carboxylate ethers according to formula (I) containing ethylene oxide and propylene oxide in separate blocks and those carboxylate ethers according to formula (I) in which ethylene oxide and propylene oxide They are distributed randomly and can be used in the compositions according to the invention.
- the carboxylate ethers of formula (I) are free of propylene oxide.
- alkyl ether carboxylates of formula (I) free of commercially available propylene oxide are those that correspond to the commercial reference AKYPO® RLM 45 CA (INCI designation Laureth-6 Carboxylic Acid) and AKYPO® RO 20 (INCI designation Oleth-3 Carboxylic Acid), AKYPO® RLM 25 (INCI designation Sodium Laureth-6 Carboxylate), AKYPO® RLM 45N (INCI designation Sodium Laureth-6 Carboxylate), AKYPO® RLM 100 (INCI designation Laureth-11 Carboxylic Acid), AKYPO® LF- 1 (INCI designation Capryleth-6 Carboxylic Acid), AKYPO® LF-2 (INCI designation Capryleth- 9 Carboxylic Acid), AKYPO® RO50 (INCI designation Oleth-6 Carboxylic Acid), AKYPO® RO90 (IN
- alkyl ether carboxylates with a chain are preferred R-alkyl containing between 6 and 22 carbon atoms, more preferably between 10 and 18; with a value of n between 1 and 15, preferably between 1 and 6; and with a value of m between 0 and 3, preferably between 0 and 2, more preferably m is 0.
- the carboxylate ether of formula (I) is characterized by an alkyl chain R containing between 10 and 14 carbon atoms, n between 3 and 6 moles of ethylene oxide per mole of alkyl ether carboxylate and m the same to 0.
- the carboxylate ether of formula (I) is characterized by an alkyl chain R containing between 16 and 18 carbon atoms, n between 1 and 5 moles of ethylene oxide per mole of alkyl ether carboxylate, preferably n between 1 and 3 and m equal to 0.
- Ethoxylated glycerin esters are characterized by an alkyl chain R containing between 16 and 18 carbon atoms, n between 1 and 5 moles of ethylene oxide per mole of alkyl ether carboxylate, preferably n between 1 and 3 and m equal to 0.
- the present invention comprises an ethoxylated glycerin ester (component (b)) having the formula (II).
- formula (II) where said formula (II) comprises the components of formula i), ii), iii) and / or iv), being i) component represented by formula (II), where, independently, one of the symbols Bi, B 2 , B 3 represents an acyl group represented by -CO-R and the rest represents H
- B 3 represents an acyl group represented by -CO-R
- each of m, n or 1 independently represents a number from 0 to 40, the sum of m, n, l being in the range of 1 to 40.
- R ' represents H or CH 3 , preferably H.
- R represents a linear or branched alkyl or alkenyl group, of 3 to 21 carbon atoms, preferably 5 to 17 carbon atoms, more preferably 5 to 11 atoms of carbon.
- component b) according to the invention comprises at least two different components of formula (II): one of formula (i), (ii) or (iii), and another of formula (iv); the proportion by weight of the components [(i) + (ii) + (iii)] / (iv) between 3.0: 0.3 and 0.5: 3.0.
- component b) according to the invention comprises components of formulas (i), (ii), (iii) and (iv); the proportion by weight of the components [(i) + (ii) + (iii)] / (iv) between 3.0: 0.3 and 0.5: 3.0, and the weight ratio between components (i) / (ii) / (iii) of 60-90 / 10-35 / less than 10.
- R represents an alkyl or alkenyl group of 5 to 9 carbon atoms.
- the degree of alkoxylation that is, the sum of m, n and 1 is between 1 and 20, more preferably between 5 and 12, even more preferably between 5 and 9.
- component (b) comprises at least one component of each formula (i), (ii), (iii) or (iv);
- R of the -CO-R group represents an alkyl group of 5 to 9 carbon atoms; the degree of ethoxylation, that is, the sum of m, n and 1 is between 5 and 9 and, finally, the weight ratio of [(i) + (ii) + (iii)] / (iv) is in the range 2.0: 0.5 to 0.5: 3, preferably 1.5: 0.8 to 0.8: 2.5.
- Examples of commercially available ethoxylated glycerin esters according to the invention are those that correspond to the commercial reference Emanon-EVE (INCI designation Glycereth-7 Caprate / Caprylate), Levenol® C-201 (INCI designation Glycereth-17 Cocoate), Levenol ® C-301 (INCI designation Glycereth-7 Cocoate), Levenol® C-421 (INCI designation Glycereth-2 Cocoate), Levenol® H&B (INCI designation Glycereth-2 Cocoate), Levenol® N-242 (INCI designation PEG-6 Caprylic / Capric Glycerides), Levenol® N-661 (INCI designation Glycereth-7
- Oily substance The present invention comprises a component (c) comprising at least one oily substance.
- the oily substances according to the invention are defined as liquids, at room temperature, cosmetically acceptable and substantially immiscible in water.
- the oily substance of the invention may comprise natural oils, defined as glyceryl esters of fatty acids (triglycerides) that are normally found in animal or plant tissues, including those that have been hydrogenated to reduce or eliminate unsaturations.
- the oily substance of the invention may also include synthetic oils, obtained from glycerin and fatty acid preparations.
- the oily substances can be selected, among others, from oils of animal or vegetable origin, hydrocarbons, esters of a higher alcohol and a higher fatty acid, fatty acids, triglycerides, esters of cholesterol fatty acids, scented oils and mixtures of any of the components mentioned above.
- component c) is a vegetable oil.
- vegetable oils according to the invention are soybean oil, palm oil, rapeseed oil, sunflower oil, wheat germ oil, coconut oil, olive oil, castor oil, rapeseed oil, oil of safflower, peanut oil, palm nut oil, cottonseed oil, corn oil, grapeseed oil, hazelnut oil, linseed oil, rice bran oil, sesame oil or mixtures of same. It is especially preferable to choose the oils of the invention from soybean oil, sunflower oil, castor oil and wheat germ oil, or mixtures thereof.
- the composition of the invention is especially preferable to choose the oils of the invention from soybean oil, sunflower oil, castor oil and wheat germ oil, or mixtures thereof.
- compositions according to the invention provide a cosmetic or dermatological composition for cleaning and / or moisturizing the skin, preferably compositions used for showering or bathing, comprising:
- component (c) characterized in that it contains a minimum of 20% by weight, preferably 30% by weight, of component (c) with respect to the total weight of active material of the composition of the invention.
- Active matter means the set of specific components responsible for a given action; Within the scope of the present application, this is a cosmetic or dermatological composition that cleanses and / or moisturizes the skin, the active material is all the surfactants present in the composition. All surfactants are understood to mean, within the scope of the present invention, the sum of components a, b and f.
- compositions according to the invention comprise:
- component c - between 9% and 30%, preferably between 20% and 28%, of component b), and - between 20% and 50%, preferably between 30% and 45%, of component c);
- each of the indicated amounts being expressed as a percentage by weight of the referred component with respect to the total active weight of the composition.
- the weight ratio between component (a) and component (b) is between 0.3: 1 and 4: 1
- the weight ratio between component (a) and component (c) is between 0.3: 1 and 0.9: 1.
- component (b) and component (c) be between 0.2: 1 and 0.8: 1.
- a cosmetic or dermatological composition is preferred for cleaning and / or moisturizing the skin, preferably compositions used for showering or bathing, comprising:
- a component (a) comprising an alkyl ether carboxylate of formula (I) with an alkyl chain R containing between 10 and 14 carbon atoms, n between 3 and 6 ym equal to 0.
- a component (b) comprising at least one ethoxylated glycerin ester according to formula (II), in which the R group of the -CO group -R represents an alkyl group of 5 to 9 carbon atoms, and the degree of ethoxylation, that is, the sum of n, m and 1 is between 5 and 9.
- At least one component c) comprising at least one oily substance, preferably soybean oil, sunflower oil, castor oil, wheat germ oil or mixtures thereof,
- compositions used for the shower comprising, with respect to the total weight of active material of said composition:
- component (a) comprising at least one alkyl ether carboxylate with an alkyl chain containing between 16 and 18 carbon atoms, n between 1 and 5, and m equal to 0.
- a component (b) comprising at least one ethoxylated glycerin ester according to formula (II), in which the group R of the group -CO-R represents an alkyl group of 5 to 9 carbon atoms, and the degree of ethoxylation, that is, the sum of n, m and 1 is between 5 and 9.
- At least one component c) comprising at least one oily substance, preferably soybean oil, sunflower oil, castor oil, wheat germ oil or mixtures thereof.
- the pH of the shower or bath compositions according to the invention is preferably between 5 and 6.5.
- compositions of the invention also contain water (component d)).
- the water used is distilled water. He Minimum water content is 1% by weight with respect to the total composition.
- the compositions of the invention contain one or more emulsifiers (component e)), additional surfactants (component f)) and cosmetically or pharmaceutically acceptable excipients or active ingredients (component g)).
- emulsifiers component e
- additional surfactants component f
- cosmetically or pharmaceutically acceptable excipients or active ingredients component g
- Emulsifiers such as glyceryl monostearate, glyceryl monostearate, glyceryl monomiristate, glyceryl monooleate, diglyceryl monostearate, diglyceryl monostearate, propylene glycol monostearate, propylene glycol monostearate, propylene glycol monostearate monostearate, sorchatelate monostearate monostearate monostearate , sorbitan monocaprylate, sorbitan monoisoleate, sucrose distearate, cetyl alcohol, stearyl alcohol, arachidic alcohol, behenyl alcohol, isobehenyl alcohol, selakyl alcohol, chimeric alcohol, polyethylene glycol (2) stearyl ether (INCI name Steareth-2), monolaurate glyceryl
- Mild surfactants are polyglycol ether sulfates of fatty alcohols, monoglycerides sulfates, mono- and / or dialkylsulphosuccinates, fatty acid isethionates, fatty acid sarcosinates, fatty acid taurides, fatty acid glutamates, fatty acid alkyl glycosides, , alkylamidobetains and / or protein fatty acid condensates.
- Cosmetically or pharmaceutically acceptable excipients are polyglycol ether sulfates of fatty alcohols, monoglycerides sulfates, mono- and / or dialkylsulphosuccinates, fatty acid isethionates, fatty acid sarcosinates, fatty acid taurides, fatty acid glutamates, fatty acid alkyl glycosides, , alkylamidobetains and / or protein fatty acid condensates.
- Hydrotropes such as short chain alkyl aryl sulfonates, sulfosuccinates.
- Suitable thickening agents are hydrophilic silicas, polysaccharides, more particularly: cellulose, guar gum, starch, "pullulan” (-1, 4-; -l, 6-glucan), “dextran”, “fructan” , “mannan” (“glucomannan”), agar, “carrageenan”, chitin, chitosan, pectin, algic acid, and hyaluronic acid; and its derivatives having substituent groups such as methyl groups, ethyl groups, hydroxyethyl groups, hydroxypropyl groups or the like; polysaccharide derivatives such as hydroxyethylcellulose, hydroxyethyl ethylcellulose, hydroxyethyl guar gum, hydroxyethyl starch, methylcellulose, methyl guar gum, methyl allylamide, ethyl cellulose, ethyl guar gum, ethylamidon,
- Distearate Distearate
- alkyl oligoglycosides fatty amides ethoxylated, such as the ethoxylated amide of rapeseed fatty acid that responds to the INCI designation PEG-4 Rapeseedamide
- alkyl carboxylic acid amides such as that which corresponds to the INCI designation Trideceth-2 Carboxamide MEA.
- excipients that the invention may contain are perfumes, solubilizers, silicones, deodorants, antimicrobial substances, agents of complex ation, cationic, anionic, amphoteric and non-ionic preservative agents, plant extracts, vitamins, antioxidants.
- Cosmetically or pharmaceutically acceptable active ingredients that the invention may contain would be, for example, aloe vera, zinc pyrithione, urea, etc.
- the invention provides a method for cleaning and / or hydrating the skin, which comprises the steps of:
- composition of the present invention can be applied directly to the skin, or it can be applied to the skin by means of a cleansing instrument, as examples of cleansing instruments are included, not exclusively, brushes, sponges and meshes; and finally
- the invention provides the use of a composition according to the invention for cleaning and / or hydration, in particular for cleaning and / or hydrating the skin during the shower or bath.
- the invention provides the use of a composition according to the invention for the preparation of a cosmetic or dermatological composition for cleaning and / or moisturizing the skin, in particular for cleaning and / or hydrating the skin during showering. or bathroom
- the invention provides a method for the preparation of the compositions of the invention comprising first mixing components a), b) and e), and optionally e), f) and g); adjust the pH with NaOH solution and finally add water.
- Table 1 shows the compositions A, B and C prepared for comparative purposes, as well as examples D to G which correspond to compositions according to the invention.
- compositions are obtained by mixing the surfactant components with the corresponding oils and propylene glycol.
- the pH of the composition is adjusted with NaOH (50%) and finally the addition of water is compensated.
- formulas containing alkyl carboxylic ether ie the compositions according to the invention
- the mixing of the components of the formulas takes place at room temperature and with constant stirring.
- Table 1 The data shown in Table 1 represent percentages by weight of active matter (% MA).
- compositions according to the invention D-G are transparent, with a light yellow hue and show stability at 30 days.
- Comparative compositions B and C show a cloudy appearance and separation at 30 days. Stability was measured at 24 hours and 30 days, at controlled temperatures of 5 ° C, ambient T and 40 ° C.
- the capacity for deposition of oil on the skin is one of the advantageous characteristics of the compositions according to the invention.
- the oil deposition was determined by the following method. A deer skin with 1 g of the shower oil composition and 4 g of water was stirred for 5 minutes, using a red dye (0.1% Sudan III) for oil marking. Subsequently the deer skin was rinsed under the tap for 30 seconds (T approx. 40 ° C) and dried for 24 hours at 20 ° C and 60% relative humidity. The dye was extracted (stirring with 5 ml of acetone, 4 times. The solvent was allowed to evaporate and the dye extracted was dissolved in 5 ml of acetone. The absorbance of the solution was measured at 502 nm (maximum absorption). He performed the same process by washing a deer skin only with oil and dye, that is, in the absence of the surfactant system.The concentration of dye extracted was calculated by Beer-Lamber law.
- compositions according to the invention show oil deposition values greater than the oil deposition of the comparative composition A based on the laureth-TIPA.
- compositions according to the invention represent an adequate alternative to those based on the laureth-TIPA, obtaining formulas that match the parameters of appearance and stability and that exhibit advantages in relation to the ability to favor the deposition of the oil on the skin.
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Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES13727957.6T ES2644305T3 (es) | 2012-04-16 | 2013-04-15 | Composición para limpiar y/o hidratar la piel |
BR112014025808-2A BR112014025808B1 (pt) | 2012-04-16 | 2013-04-15 | composição de limpeza e/ou hidratação da pele |
EP13727957.6A EP2839827B1 (en) | 2012-04-16 | 2013-04-15 | Composition for skin hygiene and/or hydration |
US14/394,436 US10583079B2 (en) | 2012-04-16 | 2013-04-15 | Composition for skin hygiene and/or hydration |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES201200412A ES2425998B1 (es) | 2012-04-16 | 2012-04-16 | Composición para la limpieza y/o hidratación de la piel |
ESP201200412 | 2012-04-16 |
Publications (1)
Publication Number | Publication Date |
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WO2013156647A1 true WO2013156647A1 (es) | 2013-10-24 |
Family
ID=48579132
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/ES2013/070237 WO2013156647A1 (es) | 2012-04-16 | 2013-04-15 | Composición para la limpieza y/o hidratación de la piel |
Country Status (6)
Country | Link |
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US (1) | US10583079B2 (es) |
EP (1) | EP2839827B1 (es) |
BR (1) | BR112014025808B1 (es) |
ES (2) | ES2425998B1 (es) |
PL (1) | PL2839827T3 (es) |
WO (1) | WO2013156647A1 (es) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109069373A (zh) | 2015-10-01 | 2018-12-21 | 雷克特本克斯尔有限责任公司 | 个人清洁组合物和稳定微生物的方法 |
US20170312198A1 (en) * | 2016-04-27 | 2017-11-02 | Elc Management Llc | Cleansing Compositions And Methods |
ES2894690T3 (es) * | 2018-12-20 | 2022-02-15 | Chanel Inc | Perfumes acuosos |
CN113332159B (zh) * | 2020-02-18 | 2024-07-30 | 香奈儿公司 | 水性香水 |
EP4442327A1 (en) * | 2023-04-05 | 2024-10-09 | Kao Corporation, S.A. | Composition which contains a mixture of mono-, di-, and triglycerides and glycerine |
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US4130497A (en) | 1976-01-16 | 1978-12-19 | Lever Brothers Company | Detergent composition |
US4371548A (en) | 1979-09-22 | 1983-02-01 | Lingner And Fischer Gmbh | Detergent-oil bath additives |
US6132738A (en) | 1997-03-26 | 2000-10-17 | Beiersdorf Aktiengesellschaft | Shower preparations having a high oil content |
US6306410B1 (en) | 1997-09-24 | 2001-10-23 | Cognis Deutschland Gmbh | Cosmetic formulations containing ethoxylated partial glycerides |
EP1213007A2 (en) * | 2000-12-06 | 2002-06-12 | Johnson & Johnson Consumer Companies, Inc. | Personal care formulations |
DE10261110A1 (de) * | 2002-12-20 | 2004-07-01 | Hans Schwarzkopf & Henkel Gmbh & Co. Kg | Ölduschbad mit spezieller Tensidkombination |
US20060165616A1 (en) * | 2002-07-22 | 2006-07-27 | Michael Brock | Microemulsion containing anti-uv filters and/or anti-dandruff agents |
Family Cites Families (5)
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FR2789575B1 (fr) * | 1999-02-16 | 2001-03-30 | Oreal | Compositions cosmetiques detergentes contenant un tensioactif hydroxyalkylether anionique et une gomme de guar cationique et leurs utilisations |
DK1045021T3 (da) * | 1999-04-13 | 2004-04-05 | Kao Corp Sa | Sammensætning omfattende en blanding af alkoxylerede mono- di- og triglycerider og glycerol |
ES2185497B1 (es) * | 2001-07-30 | 2004-03-16 | Kao Corp Sa | Composiciones nacarantes acuosas concentradas. |
US20050124705A1 (en) * | 2002-03-28 | 2005-06-09 | Beiersdorf Ag | Cosmetic or pharmaceutical, low-viscosity oil-in-water emulsions containing phospholipids |
EP2438904A1 (en) * | 2010-10-05 | 2012-04-11 | Kao Corporation | Cleansing composition |
-
2012
- 2012-04-16 ES ES201200412A patent/ES2425998B1/es not_active Expired - Fee Related
-
2013
- 2013-04-15 EP EP13727957.6A patent/EP2839827B1/en active Active
- 2013-04-15 ES ES13727957.6T patent/ES2644305T3/es active Active
- 2013-04-15 BR BR112014025808-2A patent/BR112014025808B1/pt active IP Right Grant
- 2013-04-15 PL PL13727957T patent/PL2839827T3/pl unknown
- 2013-04-15 US US14/394,436 patent/US10583079B2/en active Active
- 2013-04-15 WO PCT/ES2013/070237 patent/WO2013156647A1/es active Application Filing
Patent Citations (7)
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US4130497A (en) | 1976-01-16 | 1978-12-19 | Lever Brothers Company | Detergent composition |
US4371548A (en) | 1979-09-22 | 1983-02-01 | Lingner And Fischer Gmbh | Detergent-oil bath additives |
US6132738A (en) | 1997-03-26 | 2000-10-17 | Beiersdorf Aktiengesellschaft | Shower preparations having a high oil content |
US6306410B1 (en) | 1997-09-24 | 2001-10-23 | Cognis Deutschland Gmbh | Cosmetic formulations containing ethoxylated partial glycerides |
EP1213007A2 (en) * | 2000-12-06 | 2002-06-12 | Johnson & Johnson Consumer Companies, Inc. | Personal care formulations |
US20060165616A1 (en) * | 2002-07-22 | 2006-07-27 | Michael Brock | Microemulsion containing anti-uv filters and/or anti-dandruff agents |
DE10261110A1 (de) * | 2002-12-20 | 2004-07-01 | Hans Schwarzkopf & Henkel Gmbh & Co. Kg | Ölduschbad mit spezieller Tensidkombination |
Non-Patent Citations (1)
Title |
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"Cosmetic and dermatologic formulations containing the polymeric rheology modifier Polyurethane-39", IP.COM JOURNAL, IP.COM INC., WEST HENRIETTA, NY, US, 8 June 2009 (2009-06-08), XP013132198, ISSN: 1533-0001 * |
Also Published As
Publication number | Publication date |
---|---|
EP2839827B1 (en) | 2017-08-02 |
BR112014025808B1 (pt) | 2020-11-03 |
PL2839827T3 (pl) | 2017-11-30 |
EP2839827A1 (en) | 2015-02-25 |
US20150118328A1 (en) | 2015-04-30 |
ES2644305T3 (es) | 2017-11-28 |
US10583079B2 (en) | 2020-03-10 |
ES2425998B1 (es) | 2014-09-29 |
ES2425998A1 (es) | 2013-10-18 |
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