WO2016071187A1 - Lotion de douche - Google Patents
Lotion de douche Download PDFInfo
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- WO2016071187A1 WO2016071187A1 PCT/EP2015/075071 EP2015075071W WO2016071187A1 WO 2016071187 A1 WO2016071187 A1 WO 2016071187A1 EP 2015075071 W EP2015075071 W EP 2015075071W WO 2016071187 A1 WO2016071187 A1 WO 2016071187A1
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- oil
- acid
- surfactant
- cosmetic
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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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
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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
- A61K8/30—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
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
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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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A61K8/442—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
-
- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
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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
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- 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
Definitions
- the invention is in the field of cosmetics and relates to cosmetic compositions which contain, in addition to a special surfactant mixture, a vegetable oil, an ester and xanthan gum.
- Cosmetic cleaners such as hair shampoos, shower baths or bath preparations, are based on conventional anionic, amphoteric, zwitterionic, nonionic and / or cationic surfactants.
- anionic surfactants if appropriate in the mixture with small amounts of co-surfactants, are used in conventional cleaning agents.
- Surfactants soften the skin during the cleaning process and remove lipids from the outer skin layers. As a result, the skin - especially in the case of very frequent cleaning with commercially available cleaning agents - dry, brittle and sometimes cracked, unless it is fed back after or during cleaning lipids in the form of creams and / or lotions.
- rinse-off body lotions often make it difficult to rinse off the skin and require a high water consumption.
- rinse-off shower creams do not always have satisfactory care properties and rinse-off shower oils are rejected by many consumers because of their low foaming power.
- Another disadvantage is the difficult stabilization of combination preparations over a long period of time, especially storage at extreme temperatures.
- viscosity-stable compositions with non-Newtonian shear behavior have been proposed which have a content of anionic surfactants, alkanolamides and electrolyte salts and ensure the suspension of water-insoluble components.
- anionic surfactants especially anionic surfactants
- electrolyte salts are required, which runs counter to the skin compatibility of the compositions.
- the present invention therefore an object of the invention to produce mild cosmetic cleanser with good foam and care properties.
- Detergents should have an attractive, rich texture, a high content of skin conditioning oils and be stable over a long period of time at extreme temperatures.
- the invention relates to a cosmetic composition which
- the agents according to the invention have the advantage of combining the properties of mild cleansers and nourishing skin lotions in one product. They have excellent foaming and cleaning power and are very well tolerated by the skin due to their high oil content and their moderate surfactant content. They also have a very positive effect on the moisture balance of the skin, which is otherwise attacked during showering (even while showering with water).
- compositions according to the invention have excellent stability and storage properties. Even after storage at extreme temperatures, the detergents according to the invention have a substantially unchanged viscosity and a pleasant, lotion-like texture.
- Another advantage is the very good rinsability of the compositions of the invention.
- the cosmetic agents of the present invention contain the active ingredients a. to d. preferably in a cosmetic carrier, preferably in an aqueous or aqueous-alcoholic carrier.
- the cosmetic carrier particularly preferably contains at least 50% by weight, more preferably at least 55% by weight and particularly preferably at least 60% by weight of water.
- the cosmetic carrier may contain 0.005 to 40% by weight, preferably 0.01 to 30% by weight and in particular 0.05 to 20% by weight of at least one alcohol which may be selected from ethanol, ethyl diglycol, Propanol, 2-propanol, isopropanol, 1, 2-propylene glycol, glycerol, diglycerol, triglycerol, 1-butanol, 2-butanol, 1, 2-butanediol, 1, 3-butanediol, 1-pentanol, 2-pentanol, 1, 2-pentanediol, 1, 5-pentanediol, 1, hexanol, 2-hexanol, 1, 2-hexanediol, 1, 6-hexanediol, polyethylene glycols, sorbitol, sorbitan, benzyl alcohol, phenoxyethanol or mixtures of these alcohols.
- at least one alcohol which may be selected from ethanol, ethy
- ethanol ethyl diglycol
- 1-propanol 2-propanol
- isopropanol 1, 2-propylene glycol
- glycerol benzyl alcohol and / or phenoxyethanol and mixtures of these alcohols.
- glycerin Especially preferred is glycerin.
- compositions of the invention contain the surfactants i., Ii. and iii. preferably in relatively small amounts. This is understood to mean that the proportion by weight of all surfactants in the total weight of the cosmetic agent is preferably not more than 20% by weight, more preferably not more than 18% by weight, particularly preferably not more than 16% by weight and in particular not more than 13% by weight.
- the total weight of the cosmetic agent is preferably 2.0 to 10.0
- Wt .-% more preferably 3.0 to 9.0 wt .-% and in particular 4.0 to 8.0 wt .-%
- the nonionic surfactant iii. on the total weight of the cosmetic agent preferably 0, 1 to 5.0 wt .-%, more preferably 0.5 to 4.0 wt .-% and in particular 1, 0 to 3.0 wt .-%.
- the weight ratio of the anionic surfactant i. to the sum of the amphoteric / zwitterionic and nonionic surfactants is 2.5: 1 to 1: 1, 5, more preferably 2: 1 to 1: 1 and especially 1, 75: 1 to 1: 1 ,
- Suitable anionic surfactants are preferably foamy, mild anionic surfactants, which are preferably selected from the following groups of anionic surfactants:
- linear alkyl sulfonates having 8 to 24 carbon atoms
- linear alpha-olefin sulfonates having 8 to 24 C atoms, - alkyl sulfates and alkyl polyglycol ether sulfates of the formula R- (OCH 2 -CH 2) x -O-SO 3 X, in which R is preferably a linear or branched, saturated or unsaturated alkyl group having 8 to 24 carbon atoms, x is 0 or a number from 1 to 12 and X is an alkali, an alkaline earth, an ammonium or an alkanolamine ion,
- Sulfonates of unsaturated fatty acids having 8 to 24 carbon atoms and 1 to 6 double bonds.
- Particularly preferred anionic surfactants for the purposes of the present invention are alkylpolyglycol ether sulfate salts of the abovementioned formula - preferably those which have an alkyl group having 8 to 24 and in particular 10 to 16 carbon atoms and contain 1 to 6, preferably 1 to 4, ethylene oxide units.
- branched sodium, magnesium and / or triethanolamine salts of lauryl, tridecyl and / or myristyl sulfates which have a degree of ethoxylation of from 1 to 4.
- the agents according to the invention contain as anionic surfactant i. at least one alkyl (ether) sulfate of the general formula R- (O-CH 2 -CH 2) n -OSO 3 X, in which R is a branched alkyl group having 8 to 24 C atoms, n is the number 0 or 1 to 12 and X is an alkali metal , Alkaline earth, ammonium or alkanolamine means.
- R alkyl (ether) sulfate of the general formula R- (O-CH 2 -CH 2) n -OSO 3 X, in which R is a branched alkyl group having 8 to 24 C atoms, n is the number 0 or 1 to 12 and X is an alkali metal , Alkaline earth, ammonium or alkanolamine means.
- the sodium, magnesium and / or triethanolamine salts of tridecyl sulfate which have a degree of ethoxylation of 1 to 4, are particularly preferred.
- anionic surfactants i.
- the anionic surfactants known under the INCI name Sodium Trideceth Sulfates are commercially available from several suppliers (for example from Solvay).
- mixtures of anionic surfactants in the compositions according to the invention.
- Particular preference is given to mixtures of different alkyl ether sulfates of the abovementioned formula, it being of particular advantage if the mixtures each contain at least one anionic surfactant known by the INCI name Sodium Trideceth Sulfate.
- An especially preferred anionic surfactant mixture is, for example, a mixture of the anionic surfactants known under the INCI names Sodium Trideceth Sulfate and Sodium Laureth Sulfate.
- Suitable amphoteric and / or zwitterionic surfactants which can be used in the agents according to the invention include, for example, one or more compounds of the following formulas (I) to (VII) in which the radical R is in each case for one straight-chain or branched, saturated or mono- or polyunsaturated alkyl or alkenyl radical having 7 to 23 carbon atoms (formulas (I) and (II)) or for a straight-chain or branched, saturated or mono- or polyunsaturated alkyl or alkenyl radical with 8 to 24 carbon atoms (formulas (III) to (VII)):
- Preferred amphoteric and / or zwitterionic surfactants ii. one of the abovementioned formulas (I) to (VII) contains, as radical R, predominantly a straight-chain or branched, saturated, mono- or polyunsaturated alkyl radical having 8 to 20, more preferably 8 to 18 and in particular 8 to 16 carbon atoms , Particularly preferred are amphoteric and / or zwitterionic surfactants in which the radical R is derived from coconut oil.
- the agents according to the invention contain as amphoteric or zwitterionic surfactant ii. at least one surfactant from the group of C8-C24-alkylampho (di) acetates and / or C8-C24-Alkylamidopropylbetaine.
- amphoteric / zwitterionic surfactants known under the INCI names Sodium Cocoamphoacetate, Disodium Cocoamphodiacetate, Sodium Lauroamphoacetate, Sodium Lauroamphodiacetate, Sodium Cocoamopropionate, Disodium Cocoamphodipropionate, Cocamidopropyl Betaine and / or Lauramidopropyl Betaine and commercially available from several suppliers.
- sodium lauroampho (di) acetate and / or cocamidopropylbetaine are particularly preferred.
- R is preferably a linear or branched, saturated or unsaturated alkyl or alkenyl radical having 8 to 24 carbon atoms and the radicals R 'are hydrogen or for the
- Alkyl oligoglucosides in particular alkyl oligoglucosides based on hydrogenated C 12/14 cocoalcohol having a DP of 1-3, as commercially available, for example, under the INCI name "coco-glucosides", “decyl glucosides” and / or “lauryl glucosides” are available.
- coco-glucosides "decyl glucosides” and / or “lauryl glucosides” are available.
- agents are characterized in that they contain at least one nonionic surfactant iii. selected from C8-C24 carboxylic acid mono- or dialkanolamides.
- C8-C24-carboxylic acid mono- or dialkanolamides have foam-stabilizing, thickening and nourishing (replenishing) properties.
- R preferably denotes a linear or branched, saturated or unsaturated alkyl or alkenyl radical having 8 to 24 carbon atoms and the radicals R 'stand for hydrogen or for the group - (CH 2) n OH, in which n denotes the numbers 2 or 3, with the proviso that at least one of the radicals R 'is the abovementioned radical - (CH 2) n OH.
- C 8 -C 24 -carboxylic acid mono- or dialkanolamides of the aforementioned formula are the compounds known by the INCI name Cocamide MEA, which are commercially available
- mixtures of nonionic surfactants in the compositions according to the invention.
- Particular preference is given to mixtures of C 8 -C 24 -carboxylic or dialkanolamides and alkyloligoglucosides, and it is of particular advantage if the mixtures each contain at least one nonionic surfactant known by the INCI name Cocamide MEA.
- nonionic surfactant mixtures are, for example, mixtures of the nonionic surfactant known under the INCI name Cocamide MEA with at least one of the nonionic surfactants known under the INCI names Coco-Glucoside, Decyl Glucoside and / or Lauryl Glucoside.
- compositions according to the invention contain, based on their total weight, as the surfactant mixture a.
- alkyl (ether) sulfates of the general formula R- (0-CH2-CH2) n-OSO3X, in the R a branched alkyl group having 8 to 24 carbon atoms, n is the number 0 or 1 to 12 and X is an alkali, alkaline earth, ammonium or alkanolamine.
- amphoteric and / or zwitterionic surfactant selected from the group of C8-C24 alkylampho (di) acetates and / or C8-C24 alkylamidopropyl betaines, and
- agents according to the invention are particularly preferred which (based on their total weight) as surfactant mixture a.
- anionic, amphoteric / zwitterionic and nonionic surfactants i., Ii. and iii. can be used individually in the inventive compositions - as described above - or as a prefabricated surfactant mixture.
- Such surfactant mixtures are commercially available, for example under the name Miracare ® 365 (INCI name: Water, Sodium Sulfate Trideceth, Sodium lauroamphoacetate, Cocamide MEA by Solvay).
- the agents according to the invention contain as compelling component b. the natural thickening and stabilizing agent xanthan gum in an amount of 0.10 to 2.00% by weight.
- xanthan gum gives the inventive compositions a particular good insensitivity to temperature fluctuations (or extremely high and / or low temperatures) and electrolytes.
- compositions according to the invention (based on their weight) contain xanthan gum in amounts of from 0.15 to 1.40% by weight, preferably from 0.20 to 1.20% by weight, more preferably from 0, From 40 to 1, 10 wt .-% and particularly preferably from 0.50 to 1, 00 wt .-%, explicitly 0.50: 0.55: 0.60: 0.65: 0.70, 0.75: 0, 80: 0.85: 0.90: 0.95 or 1.00 wt%.
- the compositions according to the invention contain at least one mono- and / or diester of glycerol and a straight-chain or branched, saturated or unsaturated C 6 -C 24 -carboxylic acid c. in an amount of 0.1 to 10 wt .-%.
- the glyceryl esters have a very positive effect on the build-up of the initial viscosity of the compositions of the invention and, moreover, prevent the loss of viscosity during storage of the compositions, especially at extreme temperatures (e.g., 50-60 ° C or -20 ° C).
- the weight of the at least one mono- and / or diester of glycerol and a straight-chain or branched, saturated or unsaturated Ce-C24-carboxylic acid c. on the total weight of the cosmetic agent 0.2 to 7.5% by weight, more preferably 0.3 to 5 wt .-% and in particular 0.5 to 3 wt .-%.
- Preferred glyceryl esters are the mono- and / or diglycerol esters of caproic acid, caprylic acid. 2-ethylhexanoic acid. Capric acid. Lauric acid, isotridecanoic acid, myristic acid. Palmitic acid, palmitoleic acid, stearic acid, hydroxy stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, elaeostearic acid, arachidic acid, gadoleic acid, behenic acid and erucic acid.
- glyceryl mono- and / or diesters of caproic acid particularly preference is given to the glyceryl mono- and / or diesters of caproic acid, caprylic acid, lauric acid, myristic acid, palmitic acid, stearic acid and oleic acid.
- the agents according to the invention contain as component c. at least one of the glyceryl esters known under the INCI names Glyceryl Caprylate / Caprate, Glyceryl Laurate, Glyceryl Palmitate, Glyceryl Stearate and / or Glyceryl Oleate.
- Suitable vegetable (or natural) oils d. which are added as care components to the compositions according to the invention, are preferably understood to be naturally occurring triglycerides and mixtures of triglycerides.
- Particularly preferred vegetable or natural oils may be selected from amaranth seed oil, apricot kernel oil, argan oil, avocado oil.
- argan oil avocado oil, apricot kernel oil, rose hip kernel oil, jojoba oil, coconut oil, cocoa butter, almond oil, marula oil, olive oil, peach kernel oil, shea butter, sunflower oil and / or grapeseed oil.
- avocado oil, apricot kernel oil, almond oil, olive oil, peach kernel oil, seed oil, safflower oil, soybean oil, sunflower oil and / or grapeseed oil are particularly preferred.
- Too low a content of at least one vegetable oil ( ⁇ 1% by weight) in the compositions of the present invention did not show a satisfactory effect in terms of skin care and skin compatibility of the compositions.
- the proportion by weight of the at least one vegetable oil d preferably 2.0 to 30.0 wt .-%, more preferably 4.0 to 25.0 wt .-% and in particular 5.0 to 20.0 wt .-% of the total weight of the cosmetic composition according to the invention should be.
- the proportion by weight of the at least one vegetable oil is d. Therefore, preferably 2.0 to 30.0 wt .-%, more preferably 4.0 to 25.0 wt .-% and in particular 5.0 to 20.0 wt .-% of the total weight of the cosmetic composition according to the invention.
- compositions according to the invention contain, based on their total weight,
- surfactant mixture a As surfactant mixture a.
- alkyl (ether) sulfates of the general formula R- (0-CH2-CH2) n -OS ⁇ 3X, in which R is a branched alkyl group having 8 to 24 C. Atoms, n is the number 0 or 1 to 12 and X is an alkali, alkaline earth, ammonium or alkanolamine ion.
- amphoteric and / or zwitterionic surfactant selected from the group of C8-C24 alkylampho (di) acetates and / or C8-C24 alkylamidopropyl betaines, and
- xanthan gum 0.1 to 1.5% by weight of xanthan gum, 0.1 to 10% by weight of at least one mono- and / or digiycerin ester of caproic acid, caproic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, hydroxy stearic acid, isostearic acid , Oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, elaeostearic acid, arachic acid, gadoleic acid, behenic acid and erucic acid, and
- agents according to the invention are particularly preferred which (based on their total weight)
- surfactant mixture a As surfactant mixture a.
- compositions according to the invention a. to d. to further increase the skin care (softness and softness of the skin) and to support the deposition of the care agent mixture (c and d.) Contain on the skin at least one cationic polymer.
- the agents according to the invention therefore contain, based on their total weight, preferably 0.01 to 3.00% by weight, more preferably 0.05 to 2.00% by weight and in particular 0, 10 to 1, 50% by weight of at least one cationic polymer.
- Suitable cationic care polymers are:
- hydrophobically modified cellulose derivatives especially Polyquaternium-67, such as are available under the trade name SOFTCAT ® commercially,
- honey for example the commercial product Honeyquat ® 50,
- polymeric dimethyldiallylammonium salts and their copolymers with esters and amides of acrylic acid and methacrylic acid especially Polyquaternium-6 and Polyquaternium-7.
- Synquat ® 100 Poly (dimethyldiallylammonium chloride)
- Merquat ® 550 dimethyldiallylammonium chloride-acrylamide copolymer
- Such compounds are sold under the names Gafquat ® 734 and Gafquat ® 755 commercially,
- Vinylpyrrolidone vinylimidazoliummethochloride copolymers such as those offered under the names Luviquat.RTM ® FC 370, FC 550, FC 905 and HM 552,
- Polyquaternium 2 Polyquaternium 17, Polyquaternium 18, Polyquaternium-24, Polyquaternium 27, Polyquaternium-32, Polyquaternium-37, Polyquaternium 74 and Polyquaternium 89 known polymers.
- Particularly preferred cationic polymers are quaternized cellulose polymers, hydrophobically modified quaternized cellulose polymers, cationic guar derivatives and / or cationic Acrylic acid (derivative) -based polymers, which are particularly preferably selected from the polymers known by the INCI names Guar Hydroxypropyltrimonium Chloride, Polyquaternium-6, Polyquaternium-7, Polyquaternium-10, Polyquaternium-37 and / or Polyquaternium-67.
- compositions according to the invention contain, based on their total weight,
- surfactant mixture a As surfactant mixture a.
- alkyl (ether) sulfates of the general formula R- (0-CH2-CH2) n -OSO3X, in which R is a branched alkyl group having 8 to 24 C. Atoms, n is the number 0 or 1 to 12 and X is an alkali, alkaline earth, ammonium or alkanolamine ion,
- amphoteric and / or zwitterionic surfactant selected from the group of C8-C24 alkylampho (di) acetates and / or C8-C24 alkylamidopropyl betaines, and
- Safflower oil sea buckthorn fruit oil, sea buckthorn seed oil, sasanqua oil, sesame oil.
- compositions according to the invention may also contain further optional components.
- a preferred optional component which can be used in particular to support the stability and the viscosity of the agents according to the invention is at least one electrolyte salt.
- Suitable electrolyte salts may preferably be selected from salts with inorganic and organic anions, such as halide, sulfate, phosphate, carbonate, citrate, benzoate and / or tartrate, and alkali, ammonium and / or alkaline earth cations such as sodium, potassium, ammonium and magnesium cations.
- electrolyte salts are NaCl.
- Na ⁇ SO ,.
- Na citrate ammonium chloride, ammonium sulfate, MgC, MgSO4. and / or CaCb.
- NaCl Especially preferred is NaCl.
- the electrolyte salts may be added to the compositions of the invention both directly and as part of a commercial product.
- compositions according to the invention are preferably 0.01 to 5.00% by weight, more preferably 0.05 to 4.50% by weight, particularly preferably 0, 10 to 4.00% by weight and in particular 0.50 to 3 , 50 wt .-%, wherein the amounts are based on the total weight of the composition.
- compositions according to the invention therefore contain, based on their total weight, at least one electrolyte salt, preferably NaCl, NaaSCU, Na citrate, ammonium chloride, ammonium sulfate, MgCb, MgSO, and / or CaCb and in particular NaCl in a preferred weight fraction of 0 , 01 to 5.00 wt .-%, more preferably 0.05 to 4.50 wt .-%, particularly preferably 0, 10 to 4.00 wt .-% and in particular 0.50 to 3.50 wt .-%.
- electrolyte salt preferably NaCl, NaaSCU, Na citrate, ammonium chloride, ammonium sulfate, MgCb, MgSO, and / or CaCb and in particular NaCl in a preferred weight fraction of 0 , 01 to 5.00 wt .-%, more preferably 0.05 to 4.50 wt .-%, particularly preferably 0, 10 to 4.00
- compositions according to the invention are active substances which have a positive influence on the skin moisture.
- Suitable active ingredients which have a positive influence on the skin moisture are preferably understood as meaning active substances which are selected from the following groups:
- Glycerol can be used in the inventive compositions preferably in a weight fraction of 0, 1 to 10 wt .-%, more preferably 0.2 to 8, particularly preferably 0.5 to 6 and in particular 1 to 5% by weight, wherein the quantities refer to the total weight of the cosmetic product.
- Vitamin A the group of substances called vitamin A includes retinol (vitamin Ai) and 3,4-didehydroretinol (vitamin A2).
- the ß-carotene is the provitamin of retinol.
- vitamin A component for example, vitamin A acid and its esters, vitamin A aldehyde and vitamin A alcohol and its esters such as the palmitate and the acetate into consideration.
- Vitamin B belong to the vitamin B group or to the vitamin B complex among others
- Vitamin B3 • Vitamin B3. Under this name, the compounds nicotinic acid and nicotinamide (niacinamide) are often performed.
- Vitamin Bs pantothenic acid and panthenol.
- panthenol is preferred.
- Useful derivatives of panthenol are, in particular, the esters and ethers of panthenol, as well as cationically derivatized panthenols.
- Individual representatives are, for example, panthenol triacetate, panthenol monoethyl ether and its monoacetate, as well as cationic panthenol derivatives.
- Vitamin ⁇ (pyridoxine plus pyridoxamine and pyridoxal).
- Vitamin C ascorbic acid: use in the form of palmitic acid ester, glucosides or phosphates may be preferred. The use in combination with tocopherols may also be preferred.
- Vitamin E tocopherols, especially a-tocopherol.
- Vitamin F is usually understood as meaning essential fatty acids, in particular linoleic acid, linolenic acid and arachidonic acid.
- Vitamin H is the compound (3aS, 4S, 6aR) -2-oxohexahydrothienol [3,4-d] -imidazole-4-valeric acid, for which, however, the trivial name biotin has meanwhile prevailed.
- the cosmetic compositions according to the invention may preferably contain vitamins, provitamins and vitamin precursors from groups A, B, E and H.
- vitamins, provitamins and vitamin precursors from group B are particularly preferred. Particularly preferred are vitamins, provitamins and vitamin precursors from group B; Particular preference is given to nicotinic acid amide and / or panthenol.
- Vitamins, vitamin derivatives and / or vitamin precursors may be present in the cosmetic compositions of the invention (based on their total weight) preferably in an amount of from 0.001 to 2% by weight, more preferably from 0.005 to 1% by weight and in particular from 0.01 to 0 , 5% by weight are used.
- Suitable plant extracts, milks and / or juices which may be included in the compositions of the invention are preferably selected from green tea, oak bark, nettle, witch hazel, hops, henna, chamomile, burdock, horsetail, hawthorn, lime blossom, Almond, aloe vera, spruce, chestnut, sandalwood, juniper, coconut, mango, apricot, lime, wheat, kiwi, melon, orange, grapefruit, sage, rosemary, birch, mallow, meadowfoam, quenelle, yarrow, thyme, lemon balm, Claw, coltsfoot, vanilla, marshmallow, meristem, ginseng and ginger root included.
- the extracts are prepared by extraction of the whole plant. However, in individual cases it may also be preferred to prepare the extracts exclusively from flowers and / or leaves of the plant.
- alcohols and mixtures thereof can be used as extraction agent for the preparation of said plant extracts water.
- the alcohols are lower alcohols such as ethanol and isopropanol, but especially polyhydric alcohols such as ethylene glycol and propylene glycol, both as sole extractant and in admixture with water, are preferred.
- Plant extracts based on water / propylene glycol in a ratio of 1:10 to 10: 1 have proven to be particularly suitable.
- the plant extracts can be used both in pure and in diluted form. If they are used in diluted form, they usually contain about 2-80 wt .-% of active substance and as a solvent used in their extraction agent or extractant mixture.
- aloe milk aloe vera leaf juice and coconut milk in question.
- the vegetable powders / -säfte can in the cosmetic compositions according to the invention preferably in a weight fraction of 0.01 to 5 wt .-%, preferably 0.02 to 4 wt .-% and in particular 0.05 to 3 wt .-% - based on the total weight of the agent - are used.
- the cosmetic compositions according to the invention preferably have a pH in the range from 3.0 to 6.5, more preferably from 3.5 to 6.0, particularly preferably from 4.0 to 5.8 and in particular from 4.5 to 5, 5 on.
- compositions according to the invention have an excellent viscosity stability on storage (even under extreme conditions).
- the initial viscosity (viscosity immediately after preparation) of the agents according to the invention is preferably 3000 to 15000 mPas (measured at 20 ° C. with a Haake MVII viscometer at 8 rpm (7.2 s)).
- viscosity stability is meant, according to the invention, that the initial viscosity of the compositions according to the invention in storage, i.
- a wide range of the initial viscosity of the compositions according to the invention is preferred in order to adapt the products to the various packaging options (bottle, tube, etc.). This must remain stable even with strong temperature fluctuations to always allow optimal removal of the products from the respective container.
- compositions according to the invention may comprise further components known to the person skilled in the art for such cosmetic compositions.
- Substances for adjusting the pH such as, for example, ⁇ - and ⁇ -hydroxycarboxylic acids, preferably citric acid, lactic acid, malic acid and / or gluconic acid,
- Skin soothing agents such as allantoin and bisabolol
- Propellants such as propane-butane mixtures, N 2 O, dimethyl ether, CO 2 and air,
- Bodying agents such as sugar esters, polyol esters or polyol alkyl ethers,
- Preservatives such as sodium benzoate or salicylic acid
- UV filters such as benzophenone-3 and / or benzophenone-4
- Antioxidants to protect the natural oils such as BHT and / or tocopherol acetate.
- Cosmetic agent according to item 1 characterized in that the proportion by weight of all surfactants in the total weight of the cosmetic agent not more than 20 wt .-%, preferably at most 18 wt .-%, more preferably at most 16 wt .-% and in particular at most 13 wt. -% is.
- the proportion by weight of the anionic surfactant in the total weight of the cosmetic agent is from 2.0 to 10.0% by weight, preferably from 3.0 to 9.0% by weight and in particular from 4.0 to 8.0% by weight,
- the proportion by weight of the amphoteric and / or zwitterionic surfactant in the total weight of the cosmetic agent is from 0.5 to 8.0% by weight, preferably from 1.0 to 6.0% by weight and in particular from 1.5 to 4.0% by weight. % is and
- the proportion by weight of the nonionic surfactant in the total weight of the cosmetic agent is from 0.1 to 5.0% by weight, preferably from 0.5 to 4.0% by weight and in particular from 1.0 to 3.0% by weight.
- Cosmetic agent according to one of the preceding points, characterized in that the weight ratio of the anionic surfactant i. to the sum of the amphoteric / zwitterionic and nonionic surfactants (ii. + iii.) is 2.5: 1 to 1: 1.5, preferably 2: 1 to 1: 1, and more preferably 1.75: 1 to 1: 1.
- Cosmetic agent according to one of the preceding points characterized in that it is used as anionic surfactant i. at least one alkyl (ether) sulfate of the general formula R- (O-CH 2 -CH 2) n-OSO 3 X contains, in the R a branched alkyl group having 8 to 24 carbon atoms, n is the number 0 or 1 to 12 and X is an alkali -, alkaline earth, ammonium or alkanolamine means.
- Cosmetic agent characterized in that as anionic surfactant i. a compound with the INCI name sodium trideceth sulfate is used.
- Cosmetic agent characterized in that as amphoteric and / or zwitterionic surfactant ii. at least one surfactant from the group of C8-C24-alkylampho (di) acetate and / or the C8-C24 alkylamidopropylbetaines is used.
- Cosmetic agent according to one of the preceding points characterized in that as a nonionic surfactant iii. at least one C8-C24-carboxylic acid mono- or dialkanolamide is used.
- Cosmetic composition according to one of the preceding points characterized in that the proportion by weight of xanthan gum in the total weight of the cosmetic agent 0.15 to 1, 40% by weight, preferably 0.20 to 1, 20 wt .-%, especially preferably 0.40 to 1, 10 wt .-% and in particular 0.50 to 1, 00 wt .-% is.
- Cosmetic composition according to one of the preceding points, characterized in that the proportion by weight of the at least one mono- and / or diester of glycerol and a straight-chain or branched, saturated or unsaturated C6-C24-carboxylic acid c. on the total weight of the cosmetic agent 0.2 to 7.5 wt .-%, preferably 0.3 to 5 wt .-% is.
- Cosmetic agent according to one of the preceding points, characterized in that as component c. at least one compound selected from compounds having the INCI names Glyceryl Caprylate / Caprate, Glyceryl Laurate, Glyceryl Palmitate, Glyceryl Stearate and / or Glyceryl Oleate is used.
- Cosmetic composition according to one of the preceding points characterized in that the proportion by weight of the vegetable oil in the total weight of the cosmetic agent 2.0 to 30.0% by weight, preferably 4.0 to 25.0 wt .-% and in particular 5.0 to 20.0 wt .-% is.
- Cosmetic composition according to one of the preceding points characterized in that it is based on its total weight 0.01 to 3.00 wt .-%, preferably 0.05 to 2.00 wt .-% and in particular 0, 10 to 1 Contains 50 wt .-% of at least one cationic polymer.
- composition according to one of the preceding points, characterized in that it is based on its total weight
- alkyl (ether) sulfates of the general formula R- (0-CH2-CH2) n -OSO3X, in which R is a branched alkyl group having 8 to 24 C. Atoms, n is the number 0 or 1 to 12 and X is an alkali, alkaline earth, ammonium or alkanolamine ion,
- amphoteric and / or zwitterionic surfactant selected from the group of C8-C24 alkylampho (di) acetate and / or the C8-C24 alkylamidopropyl betaines, and
- nonionic surfactant selected from C8-C24-carboxylic acid mono- or dialkanolamides,
- At least one cationic polymer selected from quaternized cellulose polymers, hydrophobically modified quaternized cellulose polymers, cationic guar derivatives and / or cationic polymers based on acrylic acid (derivative) basis contains.
- compositions according to the invention have excellent viscosity and stability properties which do not change significantly during the storage of the compositions (even under extreme conditions).
- Compositions according to the invention were prepared according to the following procedure: a) xanthan gum was stirred into water until fully swollen (ie until no visible undissolved particles were present),
- step b) the glyceryl ester was optionally melted, added to the mixture from step b) and the resulting mixture was stirred until homogenized,
- step d) the natural oil was mixed with the perfume oil (and optionally with an antioxidant), added to the mixture of step c), and the resulting mixture stirred for about 15 minutes until homogenized,
Abstract
L'invention concerne des produits cosmétiques qui, par rapport à leur poids total, contiennent a) un mélange de tensioactifs comprenant : i) au moins un tensioactif anionique, ii) au moins un tensioactif amphotère et/ou un tensioactif zwitterionique, et iii) au moins un tensioactif non ionique, b) 0,1à 1,5 % en poids de gomme de xanthane, c) 0,1 à 10 % en poids d'au moins un monoester et/ou diester de glycérine et d'un acide carboxylique C6-C24linéraire ou ramifié, saturé ou insaturé, et d) 1,0 à 40 % en poids d'au moins une huile végétale. Ces produits cosmétiques sont particulièrement stables, même dans des conditions extrêmes, et présentent des propriétés nettoyantes et des propriétés de soin excellentes.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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EP15786970.2A EP3215111A1 (fr) | 2014-11-05 | 2015-10-29 | Lotion de douche |
Applications Claiming Priority (2)
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DE102014222570.1A DE102014222570A1 (de) | 2014-11-05 | 2014-11-05 | Duschlotionen I |
DE102014222570.1 | 2014-11-05 |
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WO2016071187A1 true WO2016071187A1 (fr) | 2016-05-12 |
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PCT/EP2015/075071 WO2016071187A1 (fr) | 2014-11-05 | 2015-10-29 | Lotion de douche |
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EP (1) | EP3215111A1 (fr) |
DE (1) | DE102014222570A1 (fr) |
WO (1) | WO2016071187A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017142626A1 (fr) * | 2016-02-19 | 2017-08-24 | Colgate-Palmolive Company | Compositions de soins d'hygiène personnelle |
US10667513B2 (en) | 2016-01-05 | 2020-06-02 | Solvoluta GmbH | Agent for repelling snails and slugs |
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WO1996031187A2 (fr) * | 1995-04-04 | 1996-10-10 | Imperial Chemical Industries Plc | Compositions tensio-actives |
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EP2881381A1 (fr) * | 2013-12-05 | 2015-06-10 | Evonik Industries AG | Esters partiels de polyglycérol, leur fabrication et leur utilisation |
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MXPA04006002A (es) | 2001-12-21 | 2004-09-27 | Rhodia | Composiciones tensioactivas estables para suspender componentes. |
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2014
- 2014-11-05 DE DE102014222570.1A patent/DE102014222570A1/de not_active Withdrawn
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2015
- 2015-10-29 EP EP15786970.2A patent/EP3215111A1/fr not_active Withdrawn
- 2015-10-29 WO PCT/EP2015/075071 patent/WO2016071187A1/fr active Application Filing
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WO1996031187A2 (fr) * | 1995-04-04 | 1996-10-10 | Imperial Chemical Industries Plc | Compositions tensio-actives |
US20110020253A1 (en) * | 2007-06-06 | 2011-01-27 | Arizona Sunwash, Llc | Body wash with sunscreen system and method |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10667513B2 (en) | 2016-01-05 | 2020-06-02 | Solvoluta GmbH | Agent for repelling snails and slugs |
WO2017142626A1 (fr) * | 2016-02-19 | 2017-08-24 | Colgate-Palmolive Company | Compositions de soins d'hygiène personnelle |
US10391046B2 (en) | 2016-02-19 | 2019-08-27 | Colgate-Palmolive Company | Personal care compositions |
AU2016393718B2 (en) * | 2016-02-19 | 2019-10-10 | Colgate-Palmolive Company | Personal care compositions |
Also Published As
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EP3215111A1 (fr) | 2017-09-13 |
DE102014222570A1 (de) | 2016-05-12 |
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