EP2654703A2 - Wirkstoffkombinationen aus glucosylglyceriden und einem oder mehreren partiell hochethoxylierten estern aus polyolen und fettsäuren - Google Patents
Wirkstoffkombinationen aus glucosylglyceriden und einem oder mehreren partiell hochethoxylierten estern aus polyolen und fettsäurenInfo
- Publication number
- EP2654703A2 EP2654703A2 EP11788823.0A EP11788823A EP2654703A2 EP 2654703 A2 EP2654703 A2 EP 2654703A2 EP 11788823 A EP11788823 A EP 11788823A EP 2654703 A2 EP2654703 A2 EP 2654703A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- phase
- polyols
- peg
- fatty acids
- ethoxylated esters
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/60—Sugars; Derivatives thereof
- A61K8/602—Glycosides, e.g. rutin
-
- 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
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/86—Polyethers
-
- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
Definitions
- the present invention relates to active ingredient combinations of glucosylglycerides and one or more partially highly ethoxylated esters of polyols and fatty acids and their use in the field of cosmetic and pharmaceutical dermatology.
- the present invention relates to active ingredients and cosmetic or dermatological preparations containing such combinations of active substances.
- the present invention relates to cosmetic preparations with a content of substances which increase the skin moisture.
- the present invention preferably relates to washing-active cosmetic preparations.
- the outermost layer of the epidermis, the stratum corneum (horny layer), is of particular importance as an important barrier layer, inter alia. for protection against environmental influences and dehydration.
- the horny layer is constantly worn in contact with the environment and must therefore be renewed continuously.
- a skin model widely used today in the art understands the stratum corneum as a two-component system, similar to a brick wall (brick-mortar model).
- the corneocytes horny cells
- the complex composite lipid membrane in the intercellular spaces corresponds to the mortar.
- the epidermal lipids In addition to their barrier effect against external chemical and physical influences, the epidermal lipids also contribute to the cohesion of the horny layer and have influence on the skin smoothness. In contrast to the sebaceous gland lipids, which do not form a closed film on the skin, the epidermal lipids are distributed over the entire horny layer.
- cosmetics usually contain, in addition to balanced lipid mixtures and water, water-binding substances.
- these include u.a. Polyols such as glycerol, sorbitol and xylitol, ethoxylated polyols and hydrolyzed proteins.
- NMF Natural Moisturizing Factor
- Cleaning means the removal of (environmental) dirt and thus causes an increase in mental and physical well-being.
- Cleaning the surface of the skin and hair is a very complex process, depending on many parameters.
- substances coming from the outside such as hydrocarbons or inorganic pigments from a wide variety of environments, as well as residues of cosmetics or unwanted microorganisms, should be removed as completely as possible.
- body excreta such as sweat, sebum, dandruff and hair dandruff are to be washed off without profound interventions in the physiological balance.
- Highly ethoxylated esters of polyols and fatty acids having a degree of ethoxylation of more than 60 are used in aqueous cleaning formulations as thickeners. They are characterized by a good thickening performance, good compatibility, a high salt tolerance and a simple incorporation in aqueous cleaning preparations.
- aqueous cleaning formulations comprising highly ethoxylated esters of polyol and fatty acid, which have a pleasant sensory properties and an improved viscosity ratio at low and high temperatures.
- the preparations according to the invention are distinguished by excellent sensor technology and an improved viscosity ratio at low and high temperatures.
- the highly ethoxylated esters of polyol and fatty acid consist of one or more polyols, preferably glycerol and sugars or derivatives thereof, more preferably glycerol, glucose and sorbitol or derivatives thereof, and a or more fatty acids having a chain length of 8 to 22 C atoms, preferably 10 to 20 C atoms and particularly preferably 12 to 18 C atoms, which may be straight or branched, saturated or unsaturated, and have a degree of ethoxylation of more than 60 , preferably 70 or more, and more preferably 80 or more.
- degree of ethoxylation indicates the number of repeating ethylene oxide units per ester of polyol and fatty acid.
- Particularly preferred highly ethoxylated esters of polyol and fatty acid are PEG-200 hydrogenated glyceryl palmitate (INCI: PEG-200 hydrogenated glyceryl palmate), PEG-90 glyceryl isostearate (INCI: PEG-90 glyceryl isostearate), PEG-120 methyl glucose dioleate (INCI: PEG-120 methyl glucose dioleate) and PEG-80 sorbitan laurate (INCI: PEG-80 sorbitan laurate).
- PEG-200 hydrogenated glyceryl palmitate INCI: PEG-200 hydrogenated glyceryl palmate
- PEG-90 glyceryl isostearate INCI: PEG-90 glyceryl isostearate
- PEG-120 methyl glucose dioleate INCI: PEG-120 methyl glucose dioleate
- PEG-80 sorbitan laurate INCI: PEG-80 sorbitan laurate
- Preferred concentration of highly ethoxylated esters of polyol and fatty acid is 0.001 to 10%, more preferably 0.01-5%, most preferably 0.1% - 3%.
- glucosylglycerides of the general formula are advantageous
- those preparations are particularly advantageous, which are characterized in that the glucosylglyceride or in the water and / or oil phase in concentrations of 0.001 to 40.00 wt .-%, preferably 0.005 to 15.00 wt .-%, especially preferably 0.01 to 12.00 wt .-%, each based on the total weight of the composition.
- the molar ratio of one or more Glucosylglyceriden to one or more highly ethoxylated esters of polyols and fatty acids in the range of 100: 1 to 1: 100, preferably 50: 1 to 1: 50, particularly preferably 20: 1 to 1: 20 to choose.
- the preparations are particularly advantageously characterized in that the one or more highly ethoxylated esters of polyols and fatty acids in concentrations of 0.01 to 10.00 wt .-%, preferably 0.05 to 5.00 wt. -%, particularly preferably 0, 1 - 3.00 wt .-%, in each case based on the total weight of the composition, is present or present.
- the use of the preparation according to the invention as a cosmetic cleansing preparation is advantageous according to the invention.
- the preparation according to the invention is preferably used as a shower gel, foam bath and bath, shampoo and / or facial cleanser.
- the cosmetic preparation according to the invention is stored in a bottle, squeeze bottle, pump spray or aerosol can and applied out of it.
- bottles, squeeze bottles, double-chamber packing, pump spray or aerosol cans containing a preparation according to the invention are also suitable according to the invention.
- the preparation according to the invention advantageously contains one or more anionic surfactants. These are according to the invention advantageously in a concentration of 1 to 20% by weight, and according to the invention preferably in a concentration of 5 to 12% by weight, in each case based on the total weight of the preparation, in the preparation. Particularly preferred according to the invention is the use of narium lauryl ether sulfate as anionic surfactant.
- the preparation advantageously contains one or more amphoteric surfactants.
- amphoteric surfactants are according to the invention advantageously in a concentration of 1 to 20% by weight, and according to the invention preferably in a concentration of 3 to 8% by weight, in each case based on the total weight of the preparation, in the preparation.
- Particularly preferred according to the invention is the use of cocamidopropylbetaine as the amphoteric surfactant.
- the preparation according to the invention may advantageously also contain nonionic surfactants.
- Particularly preferred according to the invention is the use of PEG-7 glyceryl cocoate and / or PEG-40 hydrogenated castor oil as nonionic surfactant.
- PEG-7 glyceryl cocoate and / or PEG-40 hydrogenated castor oil as nonionic surfactant.
- cationic polymers are, for example
- quaternized cellulose derivatives e.g. Polyquaternium-10, as are commercially available under the names Celquat and Polymer JR cationic guar derivatives, in particular those sold under the trade names Cosmedia Guar and Jaguar products
- polymeric dimethyldiallylammonium salts and their copolymers with esters and amides of acrylic acid and methacrylic acid in particular the products sold under the names Merquat 100 and Merquat 550 commercially available.
- cationic polymer or mixtures of cationic polymers in a concentration of 0.01 to 2% by weight, preferably in a concentration of 0.05 to 1.5% by weight and more preferably of 0.1 to 1.0% by weight, in each case based on the total weight of the preparation to use.
- compositions according to the invention contain, in addition to the aforementioned substances optionally additives customary in cosmetics, for example perfume, dyes, antimicrobial agents, lipid-replenishing agents, complexing and sequestering agents, pearlescing agents, plant extracts, vitamins, active ingredients, preservatives, bactericides, pigments containing a have coloring, thickening, softening, wetting and / or moisturizing substances, or other conventional ingredients of a cosmetic or dermatological formulation such as alcohols, polyols, polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives.
- perfume for example perfume, dyes, antimicrobial agents, lipid-replenishing agents, complexing and sequestering agents, pearlescing agents, plant extracts, vitamins, active ingredients, preservatives, bactericides, pigments containing a have coloring, thickening, softening, wetting and / or moisturizing substances, or other conventional ingredients of a cosmetic or dermatological formulation such as alcohols, polyo
- inventively advantageous usable Wrk-, auxiliaries and additives are by no means limited to the substances and compounds mentioned here by name.
- Particularly advantageous active compounds according to the invention are, in particular, niacinamide, panthenol, polidocanol, [gammaj-oryzanol, ubiquinone (in particular Q-10) creatine, creatinine, biotin (vitamin H), vitamin E and vitamin E acetate, plant extracts, such as, for example, bamboo extract, Wasserlilienexschreib, the alpha-hydroxy acids, such as citric acid, tartaric acid, malic acid, salts, such as calcium salts or sea Resmineralien, BHT, Propylgallat and UV filters (eg benzophenone-4 particularly advantageous).
- such active ingredients may advantageously be present in concentrations (individual concentration of an active substance) of from 0.001 to 5% by weight, based in each case on the total weight of the preparation, in the preparations.
- effect substances for example color and / or bulking beads, glitter substances and the like
- effect substances for example color and / or bulking beads, glitter substances and the like
- Opacifying agents / pearlescing agents or mixtures which are advantageous according to the invention include:
- PEG-3 distearate e.g., CUTINA TS from Cognis
- glycol distearate glycerol, laureth-4 and
- Cocamidopropylbetaine e.g., Euperlan PK 3000 and Euperlan PK 4000 the
- glycol distearate coco glucosides, glyceryl oleate and glyceryl stearate (e.g., Lamesoft TM Benz from Cognis).
- Styrene / acrylate copolymers e.g., Acusol OP 301 from Rohm & Haas
- antioxidants which are suitable or customary for cosmetic and / or dermatological applications can be used as favorable antioxidants.
- the amount of antioxidants (one or more compounds) in the preparations is preferably from 0.001 to 30% by weight, particularly preferably from 0.05 to 20% by weight, in particular from 1 to 10% by weight, based on the total weight of the preparation ,
- the cosmetic or dermatological preparation in the sense of the present invention is a solution or emulsion or dispersion, it is possible to use as solvent:
- Oils such as triglycerides of capric or caprylic acid, but preferably castor oil;
- Fats, waxes and other natural and synthetic fats preferably esters of fatty acids with lower C-number alcohols, e.g. with isopropanol, propylene glycol or glycerol, or esters of fatty alcohols with alkanoic acids of low C number or with fatty acids;
- Alcohols, diols or polyols of low C number, and their ethers preferably ethanol, isopropanol, propylene glycol, glycerol, ethylene glycol, ethylene glycol monoethyl or monobutyl ether, propylene glycol monomethyl, monoethyl or monobutyl ether, diethylene glycol monomethyl or monoethyl ether and analog products.
- mixtures of the abovementioned solvents are used.
- alcoholic solvents water can be another ingredient.
- Cosmetic preparations in the context of the present invention may also be present as gels which, in addition to an effective content of the active ingredient according to the invention and solvents used for this purpose, preferably water, also organic thickening agents, e.g. Gum arabic, xanthan gum, sodium alginate, cellulose derivatives, preferably methylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose or inorganic thickening agents, e.g. For example, aluminum silicates such as Benetonite, or a mixture of polyethylene glycol and polyethylene glycol stearate or distearate.
- organic thickening agents e.g. Gum arabic, xanthan gum, sodium alginate
- cellulose derivatives preferably methylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose or inorganic thickening agents, e.g.
- aluminum silicates such as Beneto
- Embodiments of the present invention which are advantageous according to the invention are characterized in that the preparation likewise contains polyacrylates as thickening agent.
- Polyacrylates which are advantageous according to the invention are polymers of acrylic acid, in particular those selected from the group of the so-called carbomers or carbopols (Carbopol ⁇ (R)> is actually a registered trademark of the BF Goodrich Company).
- Advantageous carbopols are for example the types 907, 910, 934, 940, 941, 951, 954, 980, 981, 1342, 1382, 2984 and 5984 or also the types ETD (Easy-to-disperse) 2001, 2020, 2050, Aqua -SF1 wherein these compounds can be present individually or in any desired combinations with one another.
- the copolymers of C10-30-alkyl acrylates and one or more monomers of acrylic acid, methacrylic acid or their esters which are comparable to the acrylate-alkyl acrylate copolymers are advantageous.
- the INCI name for such compounds is "Acrylates / C 10-30 Alkyl Acrylate Crosspolymer”. Particularly advantageous are those available under the trade names Pemulen TR1 and Pemulen TR2 from the BF Goodrich Company.
- the thickener is present in the gel e.g. in an amount between 0, 1 and 30 wt .-%, preferably between 0.5 and 15 wt .-%, included.
- Rewopol SB CS disodium PEG-5 lauryl citrate -30% Evonik Gold Trade name Name Active content Manufacturer
- phase A The ingredients of phase A are mixed until a homogeneous phase is obtained.
- Eumulgin HRE 40 is melted at a temperature of about 40 ° C.
- the remaining Phase B raw materials are added to the Eumulgin HRE 40.
- the phase is mixed homogeneously and added to phase A.
- inventive product A is clearly superior to the comparison product with respect to all features.
- Eumulgin HRE 40 is melted at a temperature of about 40 ° C.
- the perfume is given to Eumulgin HRE 40.
- the phase is mixed homogeneously and added to phase A.
- phase C The addition of the ingredients of phase C is carried out in the order given. It is stirred until a homogeneous shampoo is formed.
- inventive product A is clearly superior to the comparison product with respect to all features.
- the viscosity of the inventive product A remains approximately constant regardless of the storage at -20 ° C, while the viscosity of the comparative product B by storage at -20 ° C falls by about 30%.
- the use of glyceryl glucoside leads to a more uniform viscosity behavior regardless of the temperature at which the products are stored.
- Phase A Index 1 The Inhalants of Phase A Index 1 are mixed together until a homogeneous phase is obtained. The remaining ingredients of phase A are added in the order listed. Carbopol Aqua SF-1 is filtered before addition. It is stirred until a clear phase has emerged. Eumulgin HRE 40 is melted at a temperature of about 40 ° C. The remaining Phase B raw materials are added to the Eumulgin HRE 40. The phase is mixed homogeneously and added to phase A.
- Ucare Polymer JR 400 is sprinkled into the water of phase C.
- the phase C is heated with stirring to about 70 ° C until a clear solution is formed.
- Phase C is cooled and added to Phase A.
- the viscosities of Inventive Product A and Comparative Product B were measured at room temperature (25 ° C) and compared with the viscosity after one day or 7 days storage of the samples at a temperature of -20 ° C (each measured with a HAAKE Viscotester VT02 with rotor 1). Before the measurements of the samples stored at -20 ° C were stored for one day at 25 ° C and measured at this temperature.
- phase A The Inhalstscher of phase A are mixed together until a homogeneous phase is formed.
- Ucare Polymer JR 400 is interspersed in the water of phase B.
- the phase B is heated with stirring to about 70 ° C until a clear solution is formed.
- Phase B is cooled and added to Phase A.
- Eumulgin HRE 40 is melted at a temperature of about 40 ° C.
- the remaining Phase C raw materials are added to the Eumulgin HRE 40.
- the phase is mixed homogeneously and added to phase A.
- phase D The addition of the ingredients of phase D is carried out in the order given. It is stirred until a homogeneous shampoo is formed.
- phase A The Inhalstscher of phase A are mixed together until a homogeneous phase is formed.
- Ucare Polymer JR 400 is interspersed in the water of phase B.
- the phase B is heated with stirring to about 70 ° C until a clear solution is formed.
- Phase B is cooled and added to Phase A.
- phase C The water of phase C is mixed with the sodium hydroxide solution.
- Jaguar Excel is slowly sprinkled while stirring. Subsequently, the mixture is heated to 70 ° C and stirred until a homogeneous phase is formed. With stirring, the citric acid is added. Phase C is cooled and added to phase A.
- Eumulgin HRE 40 is melted at a temperature of about 40 ° C.
- the remaining phase D raw materials are added to the Eumulgin HRE 40.
- the phase is mixed homogeneously and added to phase A.
- phase E The ingredients of phase E are mixed and added to phase A.
- phase F The addition of the ingredients of phase F is carried out in the order given. It is stirred until a homogeneous shampoo is formed.
- phase A The ingredients of phase A are mixed until a homogeneous mixture is obtained.
- Eumulgin HRE 40 is melted at a temperature of about 40 ° C.
- the remaining Phase B raw materials are added to the Eumulgin HRE 40.
- the phase is mixed homogeneously and added to phase A.
- the addition of the ingredients of phase C is carried out with stirring in the order given.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Fats And Perfumes (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE201010055766 DE102010055766A1 (de) | 2010-12-23 | 2010-12-23 | Wirkstoffkombinationen aus Glucosylglyceriden und einem oder mehreren partiell hochethoxylierten Estern aus Polyolen und Fettsäuren |
PCT/EP2011/071159 WO2012084414A2 (de) | 2010-12-23 | 2011-11-28 | Wirkstoffkombinationen aus glucosylglyceriden und einem oder mehreren partiell hochethoxylierten estern aus polyolen und fettsäuren |
Publications (1)
Publication Number | Publication Date |
---|---|
EP2654703A2 true EP2654703A2 (de) | 2013-10-30 |
Family
ID=45063128
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP11788823.0A Withdrawn EP2654703A2 (de) | 2010-12-23 | 2011-11-28 | Wirkstoffkombinationen aus glucosylglyceriden und einem oder mehreren partiell hochethoxylierten estern aus polyolen und fettsäuren |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP2654703A2 (de) |
DE (1) | DE102010055766A1 (de) |
WO (1) | WO2012084414A2 (de) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR112019006334B8 (pt) * | 2016-09-30 | 2021-11-30 | Oreal | Composição cosmética capilar do tipo sem enxágue (leave-on) e método de tratamento capilar |
WO2018058205A1 (en) * | 2016-09-30 | 2018-04-05 | L'oreal | Hair cosmetic compositions containing thiol-based compounds and methods for cleansing and treating hair |
WO2018058208A1 (en) * | 2016-09-30 | 2018-04-05 | L'oreal | Hair cosmetic compositions containing thiol-based compounds and methods for cleansing and treating hair |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102004027325A1 (de) * | 2004-06-03 | 2005-12-22 | Beiersdorf Ag | N-Acylaminosäuren-haltige kosmetische Zubereitung mit ethoxylierten Glycerinen |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19540749A1 (de) * | 1995-11-02 | 1997-05-07 | Beiersdorf Ag | Kosmetische Zubereitungen mit einem wirksamen Gehalt an Glycosylglyceriden |
DE19634021A1 (de) * | 1996-08-23 | 1998-02-26 | Beiersdorf Ag | Antiadhäsive Glycoglycerolipide |
DE19728900A1 (de) * | 1997-07-07 | 1999-01-14 | Henkel Kgaa | Hydrophile Glykoside |
JP2003146884A (ja) * | 2001-11-09 | 2003-05-21 | Kikkoman Corp | 医薬及び抗アレルギー剤 |
JP3770884B2 (ja) * | 2003-05-08 | 2006-04-26 | 株式会社ノエビア | 美白剤 |
JP2004331583A (ja) * | 2003-05-08 | 2004-11-25 | Noevir Co Ltd | 皮膚洗浄料 |
JP4828922B2 (ja) * | 2005-11-22 | 2011-11-30 | 兵庫県 | 抗アレルギー剤 |
JP4817182B2 (ja) * | 2006-07-20 | 2011-11-16 | 花王株式会社 | 毛髪化粧料 |
DE102006055046A1 (de) * | 2006-11-17 | 2008-05-21 | Beiersdorf Ag | Kosmetische Formulierung mit Glucosylglyceriden und Puderrohstoffen |
JP5171206B2 (ja) * | 2007-10-26 | 2013-03-27 | 株式会社ノエビア | 保湿剤及び皮膚外用剤 |
JP2009161475A (ja) * | 2008-01-04 | 2009-07-23 | Tatsuuma-Honke Brewing Co Ltd | インスリン様成長因子−1産生促進剤 |
-
2010
- 2010-12-23 DE DE201010055766 patent/DE102010055766A1/de not_active Withdrawn
-
2011
- 2011-11-28 WO PCT/EP2011/071159 patent/WO2012084414A2/de unknown
- 2011-11-28 EP EP11788823.0A patent/EP2654703A2/de not_active Withdrawn
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102004027325A1 (de) * | 2004-06-03 | 2005-12-22 | Beiersdorf Ag | N-Acylaminosäuren-haltige kosmetische Zubereitung mit ethoxylierten Glycerinen |
Also Published As
Publication number | Publication date |
---|---|
WO2012084414A2 (de) | 2012-06-28 |
WO2012084414A3 (de) | 2013-07-04 |
DE102010055766A1 (de) | 2012-06-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2881381B1 (de) | Polyglycerinpartialester, ihre Herstellung und Verwendung | |
EP3168251B1 (de) | Vernetzte polyglycerinester | |
EP2797571B1 (de) | Wässrige haar- und hautreinigungszusammensetzungen, enthaltend biotenside | |
EP1758548B1 (de) | Stabilisierung von farbstoffen in kosmetischen und dermatologischen zubereitungen | |
US10111825B2 (en) | Oil-in-water emulsions enriched with salt which are highly viscous and stable over time | |
CH698656B1 (de) | Kosmetische Zubereitung in Form einer O/W-Emulsion enthaltend 1,2-Alkandiol(e). | |
EP1470813A2 (de) | Reinigungsemulsion mit hohem Fettgehalt | |
EP2654705A2 (de) | Wirkstoffkombinationen aus glucosylglyceriden und einem oder mehreren milden tensiden | |
EP2328544A2 (de) | Tensidhaltige zusammensetzung mit spezieller emulgatormischung | |
EP2654699B1 (de) | Wirkstoffkombinationen aus glucosylglyceriden und einem oder mehreren konservierungsmitteln | |
EP2654703A2 (de) | Wirkstoffkombinationen aus glucosylglyceriden und einem oder mehreren partiell hochethoxylierten estern aus polyolen und fettsäuren | |
EP2654694A2 (de) | Wirkstoffkombinationen aus glucosylglyceriden und einem oder mehreren perlglanz- und/oder trübungsmitteln | |
WO2012084418A2 (de) | Wirkstoffkombinationen aus glucosylglyceriden und einem oder mehreren sauren konservierungsmitteln | |
WO2012084419A2 (de) | Wirkstoffkombinationen aus glucosylglyceriden und einer oder mehreren gegen kopfschuppen wirksamen substanzen | |
WO2007042410A1 (de) | Desodorierende reinigungszubereitung | |
DE10157543A1 (de) | Emulsionsgetränkte Tücher | |
DE102006030083A1 (de) | Haarpflegereinigungszusammensetzung mit besonderer Trockenhaarsensorik | |
WO2012084424A2 (de) | Wirkstoffkombinationen aus glucosylglyceriden und einem oder mehreren kationischen polymeren | |
EP2440173A2 (de) | Kosmetisches reinigungsmittel mit deo-effekt | |
DE102004027329A1 (de) | Kosmetische Zubereitung mit ethoxylierten Glycerinen und ethoxylierten Glycerin-Fettsäureestern | |
EP3503867B1 (de) | Transparente kosmetische reinigungszusammensetzungen mit verbessertem rheologieprofil | |
DE102004027327A1 (de) | Kosmetische Zubereitung mit ethoxylierten Glycerinen und Lipidphase | |
EP1942863A1 (de) | Kosmetische gelförmige waschaktive zubereitung enthaltend 1,2-alkandiol(en) und ein oder mehrere polyacrylatverdicker | |
WO2004052332A1 (de) | Fettsäuresalze enthaltende reinigungszubereitungen |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: BA ME |
|
17P | Request for examination filed |
Effective date: 20140107 |
|
RBV | Designated contracting states (corrected) |
Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
DAX | Request for extension of the european patent (deleted) | ||
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: HEINS, SABINE Inventor name: FRESE, CHRISTIAN Inventor name: KRAUSS, NICOLE MARIA Inventor name: ZU PUTLITZ, CORINNA Inventor name: SCHERNER, CATHRIN |
|
17Q | First examination report despatched |
Effective date: 20141222 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: A61Q 5/02 20060101ALI20190502BHEP Ipc: A61K 8/60 20060101AFI20190502BHEP Ipc: A61Q 19/10 20060101ALI20190502BHEP Ipc: A61K 8/86 20060101ALI20190502BHEP |
|
INTG | Intention to grant announced |
Effective date: 20190531 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN |
|
18W | Application withdrawn |
Effective date: 20190814 |