WO2000032161A1 - Preparations of aqueous-based cleaning agents which form vesicles and which contain active agents, method for their production and their utilisation - Google Patents

Preparations of aqueous-based cleaning agents which form vesicles and which contain active agents, method for their production and their utilisation Download PDF

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Publication number
WO2000032161A1
WO2000032161A1 PCT/EP1999/008595 EP9908595W WO0032161A1 WO 2000032161 A1 WO2000032161 A1 WO 2000032161A1 EP 9908595 W EP9908595 W EP 9908595W WO 0032161 A1 WO0032161 A1 WO 0032161A1
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WO
WIPO (PCT)
Prior art keywords
sterol
preparation according
cleaning
cleaning preparation
fatty alcohol
Prior art date
Application number
PCT/EP1999/008595
Other languages
German (de)
French (fr)
Inventor
Valentina Paspaleeva-Kühn
Silvia Schmandt
Rolf D. Beutler
Original Assignee
Merz + Co. Gmbh & Co.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to KR1020017006662A priority Critical patent/KR20010080615A/en
Priority to EP99957294A priority patent/EP1133276A1/en
Priority to IL14287799A priority patent/IL142877A0/en
Priority to BR9915742-0A priority patent/BR9915742A/en
Priority to AU15051/00A priority patent/AU760248B2/en
Priority to JP2000584858A priority patent/JP2002531389A/en
Priority to EA200100594A priority patent/EA003465B1/en
Priority to NZ511785A priority patent/NZ511785A/en
Application filed by Merz + Co. Gmbh & Co. filed Critical Merz + Co. Gmbh & Co.
Priority to SK709-2001A priority patent/SK7092001A3/en
Priority to PL99347886A priority patent/PL347886A1/en
Priority to CA002352288A priority patent/CA2352288A1/en
Priority to APAP/P/2001/002158A priority patent/AP2001002158A0/en
Priority to HU0104356A priority patent/HUP0104356A3/en
Publication of WO2000032161A1 publication Critical patent/WO2000032161A1/en
Priority to BG105533A priority patent/BG105533A/en
Priority to HR20010400A priority patent/HRP20010400A2/en
Priority to NO20012578A priority patent/NO20012578L/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/94Mixtures with anionic, cationic or non-ionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0008Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/0017Multi-phase liquid compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/14Liposomes; Vesicles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0008Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/0026Structured liquid compositions, e.g. liquid crystalline phases or network containing non-Newtonian phase
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2068Ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/36Organic compounds containing phosphorus
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/382Vegetable products, e.g. soya meal, wood flour, sawdust
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments

Definitions

  • the present invention relates to cleaning preparations on an aqueous basis, in particular shower baths.
  • Foam bath compositions or shampoos containing surfactants and conventional auxiliaries and additives and a proportion of one or more sterols.
  • These aqueous surfactant-containing preparations spontaneously form liposomal structures, especially when used.
  • the invention further relates to a method for producing such surfactant-containing preparations and the use of this preparation as a cleaning agent.
  • Vesicular systems have found widespread use in cosmetics and pharmaceuticals as active ingredient carriers and skin care components.
  • Cosmetic gels and emulsions containing liposomes or vesicles are already known, and dispersions containing liposomes or vesicles are already being produced in the pharmaceutical sector.
  • Liposomal-based cleaning products have also been described.
  • “Mederma Regulativ-Waschlotion Plus” is a commercially available emulsion-based cleaning product with liposomes. This preparation contains O / W emulsifiers and a fat phase, but no washing-active substances.
  • DE-OS 42 05 548 describes bath and shower additives with vesicle-forming properties, which contain fatty oils and / or apolar substances and also have a content of one or more oil-soluble surfactants together with a content of one or more vesicle-forming lipids.
  • the oil-soluble surfactants have an HLB value of 6 to 13 and the vesicle-forming lipids have an HLB value of 2 to 6.
  • DE 196 02 346 7 describes shower oleogels with vesicle-forming properties which contain more than 30% of one or more lipophilic components, 0.1 to 20% vesicle-forming substances and conventional auxiliaries and additives, and furthermore an emulsifier system composed of one or more W / O and one or more O / W emulsifiers, in a ratio of 1 2 to 1 0.2
  • Such hpid-containing cleaning agents which are intended to compensate for the loss of skin lipids which occurs during the removal of dirt, are produced by incorporating prefabricated vesicle dispersions into the preparation or the liposomes, in particular when used as a bath additive, when used by contact with water from the preparation contained lipids arise
  • RA Wumbleter et al describes in perfumee ⁇ e and Cosmetics, 75 Volume, No. 11/94, pages 755 to 759, the use of naturally occurring phytosterols as herbal active ingredients in cosmetics.
  • Phytosterols can be obtained from different oils and fats, such as corn germ, Rapeseed oil, soybean oil, olive oil etc and essentially consist of ß-sitosterol, campesterol and stigmasterol.
  • Generol ® 122 is a soybean mixed product of the three phytosterol components mentioned with a predominant proportion of ß-sitosterol (58.1%) and 29.8% campesterol and 4.5% stigmasterol known
  • ethoxylated product variants of the phytosterols mentioned in particular Generol ® 122.
  • Generol ® 122 E5 5 mol EO
  • Generol ® 122 E5 5 mol EO
  • the latter products have the properties of a typical O / W emulsifier.
  • the latter can be used as corresponding emulsifiers in O / W emulsions and as solubilizers, while the non-ethoxyethered product is suitable as a W / O emulsifier or co-emulsifier in addition to its emulsifying property
  • Phytosterols can also be used positively on damaged or stressed skin, such as constitutional neurodermatitis or sunburn symptoms.
  • such products can also be used as hair conditioners.
  • body cleansing agents contain a proportion of surfactants which are known (cf. DE-PS 42 05 548 and WO 92/04010) that they can have negative effects on the stability of liposomes, since liposomal structures are known to interact with surface-active substances in water Solutions are solubilized So far it has not been possible without special stabilization measures to formulate stable surfactant-containing aqueous systems, as are common for cleaning products, with liposomal components
  • US-A 5688752 describes cleaning and care compositions which, in addition to surfactants, have a lipid composition composed of three components A, B and C in very specific molar ratios, where A ceramides can be phospholipids, pseudoceramides, glycolipids or polyethylene glycol esters, component B long-chain hydrocarbons with polar head groups like fatty acids and component C is an auxiliary component for stabilizing any bilayers that may have formed component C can for example, 3-ß-sterol or cholesterol, sistosterol, stigmasterol or ergosterol. With such products, the loss of the skin of lipids and thus the dehydration should be reduced.
  • a ceramides can be phospholipids, pseudoceramides, glycolipids or polyethylene glycol esters
  • component B long-chain hydrocarbons with polar head groups like fatty acids and component C is an auxiliary component for stabilizing any bilayers that may have formed component C can for example, 3-ß-sterol or cholesterol, sistosterol, stigmasterol
  • the object of the present invention is therefore to formulate an aqueous-based surfactant-containing cleaning system which does not contain any oil-containing components and yet has liposomal structures, in particular when used, which gives all the advantages of cleaning or skin care such as those for surfactant-containing and lipid-containing products are known can be achieved.
  • aqueous-based cleaning preparations containing 1 to 60% of one or more surfactants, which are selected in particular from anionic and / or nonionic and / or amphoteric and / or cationic surfactants, further 0 - 5%, in particular 0, 5 - 2% of one or more conditioning agents, 0 - 5%, in particular 1 - 3% of one or more stabilizers, 0 - 3%, in particular
  • 0.1-1.5% one or more preservatives, 0-5%, in particular 0.1-2%, one or more thickeners, and 0-20%, especially 0.5-3%, active ingredients, 0-1 %, in particular 0.0005-0.01% of dyes and 0-5%, in particular 0.5-2%, of one or more opacifiers or pearlescent agents, and which are characterized by a content of 0.001-15%, in particular 0 , 01-15%, very particularly preferably 0.5-10%, and in particular 0.5-5% of one or more sterols.
  • the cleaning preparation according to the invention preferably contains a mixture of anionic, nonionic and amphoteric, in particular anionic and amphoteric or anionic and nonionic surfactant (s).
  • Anionic surfactants are known for the purpose described and can preferably be selected from alkyl sulfates (for example C10-C18) and / or the corresponding alkyl ether sulfates, in particular with 1-6 ethylene oxide groups in the molecule, sulfosuccinates, sulfosuccinamates, sarcosinates, isethionates, taurides , Ether carboxylic acids, protein-fatty acid condensates, alkyl sulfonates and alkyl benzene sulfonates, monoalkyl phosphates, monoglyceride sulfates, amide ether sulfates, alkyl sulfoacetates, ⁇ -olefin sulfonates
  • alkyl ether sulfates derived from fatty alcohols containing 12 to 18 carbon atoms and a degree of ethoxylation of 2 to 6, such as lauryl / myristyl, Na salt (example Texapon ® K 14 S Special IS, Elfan ® NS 243 S), Ammoni - umlaurylethersulfat (Zetesol ® LA-2) or Monoisopropanolammoniumlaurylethersulfat (Zetesol ® 2056) or alkyl sulphates, eg sodium lauryl sulfate (Texapon ® Z), ammonium lauryl sulfate (Texapon ® ALS) or Monoisopropanolammoniumlaurylsulfat (Sulfetal ® CJOT 60).
  • succinic acid derivatives such as sulfosuccinates and sulfo succinamates having an alkyl group from 8 to 22 carbon atoms, for example WALLASOL ® -L 29 (Disodi- to Laureth-3 Sulfosuccinate).
  • amphoteric surfactant can in particular be selected from alkylaminopropionates, alkyl-, alkylamido- and sulfobetaines and alkylglycinates with a C chain length of C8 to C22. Most preferably, the known co camidopropylbetain under the trade name Dehyton ® K.
  • the nonionic surfactant is particularly selected from alkanolamides, fatty reethoxylaten, fatty alcohol ethoxylates, alkyl polyglucosides, in particular with an alkyl group from 8 to 16 carbon atoms, such as Plantacare ® 2000 UP (Decyl Glucoside), sorbitan esters, such as Tween ® 20 (Polysorbate 20), amine oxides, in particular Fatty amine oxides with a C7 - C26 alkyl chain, e.g. Incromine Oxide ® C30 (Cocamidopropylamine Oxide).
  • sorbitan esters alkylphenol oxyethylates (C8 - C22; possibly 4 - 20 ethylene oxide groups) or mixed condensates made of ethylene oxide and propylene oxide (eg Pluronics® types).
  • Such surfactants suitable for cleaning agents are, for example, also in S ⁇ FW-Journal, 120th year, 2-3 / 94, pp. 115 to 116, in issue 7/94, page 387 and in Cosmetics and Toiletries, vol. 108, 1993 , Pp. 83 - 89, as well as in S ⁇ FW, 117 volume, No. 1 from 1991, pages 3 - 7 or in the monograph by K. Schrader, Basics and Recipes of Cosmetics, 2nd edition (1989, Wilsonhig Buchverlag), Pp. 683 - 691).
  • Suitable cationic surfactants are quaternary ammonium compounds with carbon chain lengths usually between 12 and 22, e.g. Steartrimonium chloride or pyridine salts, e.g. Cetylpyridinium chloride.
  • Particularly suitable sterols are phytosterols such as those derived from corn oil, rapeseed oil, soybean oil, olive oil etc. and mainly consisting of a mixture of ß-sitosterol, campesterol and stigmasterol in different weight proportions, as described, for example, by RA Wumbleter (cf. P. 4, paragraph 4 of this application). Cholesterol and its derivatives, for example dihydrocholesterol or cholesterol esters such as cholesteryl acetate, are also suitable. Particularly suitable as a phytosterol is a product with the trade name Genenerol ® 122 N (refined soyasterol).
  • ethoxylated sterols of the type mentioned with a degree of ethoxylation of 5 to 30, such as.
  • Quantities of 0.5 to 5%, in particular 0.5 to 3% and preferably 0.5 to 2%, of the sterols mentioned are particularly preferred.
  • a mixture of non-ethoxylated phytosterol, for example Generol ® 122 N and one with 5 units of ethoxylated phytosterol, such as, for example, is very particularly preferred.
  • the proportion of ethoxylated sterol is preferably higher than or equal to the proportion of non-ethoxylated sterol, in particular in a ratio of 5: 1% by weight to 1: 1% by weight.
  • a ratio of 3: 1% by weight is particularly preferred.
  • the sole use of a non-ethoxylated sterol, such as Generol ® is 122 N in the specified amounts, such as 1 wt.%.
  • Particularly suitable amounts of surfactant are 5 to 30%, in particular 7.5 to 25% and very particularly preferably 10 to 20% of surfactant or surfactants.
  • composition according to the invention can furthermore contain customary auxiliaries and additives.
  • customary auxiliaries and additives include cationic polymers as conditioning agents, such as polyquaters nium-22 (Merquat ® 280), quaternized protein derivatives such as lauryldimonium hydroxypropyl hydrolized soy protein (part of Prota Flor ® HSQ), silicone derivatives, e.g. Abil ® B 8863, 8843 (Dimethicone Copolyol), protein hydrolyzates or water-soluble proteins.
  • cationic polymers as conditioning agents, such as polyquaters nium-22 (Merquat ® 280), quaternized protein derivatives such as lauryldimonium hydroxypropyl hydrolized soy protein (part of Prota Flor ® HSQ), silicone derivatives, e.g. Abil ® B 8863, 8843 (Dimethicone Copolyol), protein hydrolyzates or water-soluble proteins
  • One or more stabilizers can also be present in small amounts (0 to 5%).
  • complexing agents such as Trilon BD ® (EDTA, sodium salt), agents for pH adjustment, eg citric acid, humectants such as Glycehn, inorganic salts such as sodium chloride as a viscosity regulator.
  • preservatives and thickeners (0 to 5%) can optionally be present.
  • Suitable preservatives are, for example, iodopropynyl butyl carbamate, phenoxyethanol and other common preservatives, such as e.g. p-hydroxybenzoic acid esters, formaldehyde and releasers, sorbic and dehydroacetic acid and their salts, isothiazolinones, 5-bromo-5-nitro-1, 3-dioxane, methyldibromoglutanonitrile, etc.
  • Suitable thickeners are, for example, Volpo ® L 3 are (Laureth-3) or Antil ® 208 (Laureth-3, propylene glycol, acrylates / steareth-50 copolymer) Glucamate DOE 120 ® (PEG-120 Methyl Glu- cose Dioleate), Comperian ® 100 (Cocamide MEA).
  • the cleaning preparation according to the invention can have one or more active ingredients in the amounts specified.
  • active ingredients include, for example, perfume oils or essential oils, active ingredient extracts and / or vitamins.
  • compositions according to the invention can also contain an additional proportion, for example 0.01 to 5%, of one or more vesicle-forming lipids.
  • lecithin examples include in particular lecithin, phospholipids, such as phosphatidylcholine dylcholin, and ceramides such as ceramide 2, -3, -6 and sphingolipids, such as Procera mide ® L, Ceraderm ® S, Ceraveg ®.
  • phospholipids such as phosphatidylcholine dylcholin
  • ceramides such as ceramide 2, -3, -6
  • sphingolipids such as Procera mide ® L, Ceraderm ® S, Ceraveg ®.
  • Lecithin e.g. soy lecithin
  • phosphatidylcholine e.g. soy lecithin
  • phosphatidylserine e.g. phosphatidylcholine
  • diethanolamine e.g. diethanolamine
  • the cleaning preparations according to the invention are produced by melting the sterol or sterols in the aqueous surfactant solution. The preparation is then stirred cold. If necessary, active ingredients and other auxiliaries and additives are then incorporated in the course of production. Suitable temperatures for this are between 60 ° C and 25 ° C.
  • compositions according to the invention spontaneously form liposomal structures, particularly when used. These can be detected by means of transmission electron microscopy (TEM) after freezing fracture.
  • TEM transmission electron microscopy
  • the cleaning preparations according to the invention it is possible to use products with existing liposomes as cleaning and care agents.
  • the preparations according to the invention are very easy to distribute. They have good cleaning and foaming properties, a pleasant feeling on the skin and favorable odor properties. So they meet the requirements for cosmetics.
  • compositions according to the invention can be used in particular as a shower bath, foam bath or shampoo.
  • the individual components can be combined differently.
  • the products according to the invention also have very good stability and can be produced without the use of special and complex apparatus and production processes, as are usually required for the provision of liposomal articles.
  • the consistency of the products can be adjusted as desired using small amounts of additives and auxiliary substances that do not change the feeling on the skin. Due to the special property of sterols, especially phytosterols, namely that they are plant-based In addition to the liposomal effect, raw materials that have a positive influence on hair and skin texture can also achieve a further care effect.
  • Indicative shower compositions can be prepared according to the desired purpose.
  • a hardening shower with eucalyptus oil, mint oil and echinacea extract e.g., a stimulating shower with rosemary oil and lime oil or a muscle relaxation shower with ginger extract, methyl nicotinate, hydroxyethyl salicylate and juniper oil.
  • the invention is illustrated by the following examples. Following the examples, the transmission electron micrographs of the products produced according to the invention are attached. Here one can clearly see the liposomal structures (spherical structures) in the product produced according to the invention after dilution with water 1 T: 20 T at 37 ° C.
  • the products according to the following Examples 1 to 9 were prepared by melting the sterol (s) specified in the aqueous surfactant solution, ie the solution of demineralized water and the specified surfactants, at temperatures between 80 ° C. and 90 ° C. The mixture was then stirred cold and, if appropriate, the further additives, active ingredients and auxiliaries specified were incorporated in the order given at temperatures between 60 ° C. and 25 ° C.
  • FIGS. 1-9 show the liposomal structures (spherical structures) of the preparations according to Examples 1-9 by transmission electron microscopy after freeze fracture.

Abstract

The present invention relates to preparations of aqueous-based cleaning agents, especially shower gels, foam bath preparations or shampoos. Said preparations contain active agents and well-known auxiliary agents and additives and a proprotion of at least one sterol. Said aqueous preparations containing active agents spontaneously form liposomal structures, especially when they are applied. The invention also relates to a method for producing such preparations containing active agents and to their utilisation as cleaning agents.

Description

Vesikelbildende tensidhaltiqe Reinigungszubereitunqen auf wäßriger Basis, Verfahren zu ihrer Herstellung sowie ihre VerwendungWater-based vesicle-forming surfactant-containing cleaning preparations, process for their preparation and their use
Die vorliegende Erfindung betrifft Reinigungszubereitungen auf wäßriger Basis, insbesondere Duschbäder.Schaumbadzusammensetzungen oder Shampoos, enthaltend Tenside sowie übliche Hilfs- und Zusatzstoffe und einen Anteil an einem oder mehreren Sterolen. Diese wäßrigen tensidhaltigen Zubereitungen bilden spontan, insbesondere bei der Anwendung, liposomale Strukturen. Die Erfindung betrifft ferner ein Verfahren zur Herstellung solcher tensidhaltigen Zubereitungen sowie die Verwendung dieser Zubereitung als Reinigungsmittel.The present invention relates to cleaning preparations on an aqueous basis, in particular shower baths. Foam bath compositions or shampoos, containing surfactants and conventional auxiliaries and additives and a proportion of one or more sterols. These aqueous surfactant-containing preparations spontaneously form liposomal structures, especially when used. The invention further relates to a method for producing such surfactant-containing preparations and the use of this preparation as a cleaning agent.
Bisher bekannt sind wasserhaltige tensidische Reinigungsprodukte sowie Öl- und Cremezu- bereitungen zum Duschen oder Baden mit mehr oder weniger stark ausgeprägter Reinigungswirkung bzw. Rückfettung.So far, water-based surfactant cleaning products as well as oil and cream preparations for showering or bathing with a more or less pronounced cleaning effect or regreasing are known.
Vesikuläre Systeme haben als Wirkstoffträger sowie Hautpflegekomponenten eine breite Anwendung in Kosmetik und Pharmazie gefunden. So sind bereits kosmetische Liposomen- bzw. Vesikel-haltige Gele und Emulsionen bekannt, im pharmazeutischen Bereich werden auch bereits Liposomen- bzw. Vesikel-haltige Dispersionen hergestellt. Auch Reinigungsprodukte auf liposomaler Basis sind beschrieben worden. Beispielsweise handelt es sich bei „Mederma Regulativ-Waschlotion Plus" um ein marktübliches Reinigungsprodukt auf Emulsionsbasis mit Liposomen. Dieses Präparat enthält O/W-Emulgatoren und eine Fettphase, allerdings keine waschaktiven Substanzen.Vesicular systems have found widespread use in cosmetics and pharmaceuticals as active ingredient carriers and skin care components. Cosmetic gels and emulsions containing liposomes or vesicles are already known, and dispersions containing liposomes or vesicles are already being produced in the pharmaceutical sector. Liposomal-based cleaning products have also been described. For example, "Mederma Regulativ-Waschlotion Plus" is a commercially available emulsion-based cleaning product with liposomes. This preparation contains O / W emulsifiers and a fat phase, but no washing-active substances.
Die Liposomenbildung im Badewasser aus Ölbad- bzw. Oleogel-Zubereitungen und Badetabletten ist ebenfalls beschrieben worden. So beschreibt die DE-OS 42 05 548 Bade- und Duschzusätze mit vesikelbildenden Eigenschaften, welche fette Öle und/oder apolare Sub- stanzen enthalten und ferner einen Gehalt an einem oder mehreren öllöslichen Tensiden zusammen mit einem Gehalt an einem oder mehreren vesikelbildenden Lipiden aufweist. Die öllöslichen Tenside weisen dabei einen HLB-Wert von 6 bis 13 und die vesikelbildenden Lipide einen HLB-Wert zwischen 2 und 6 auf. Die DE 196 02 346 7 beschreibt Duscholeogele mit vesikelbildenden Eigenschaften, welche mehr als 30% einer oder mehrerer lipophiler Komponenten, 0,1 bis 20% vesikelbildende Substanzen sowie übliche Hilfs- und Zusatzstoffe enthalt und weiterhin ein Emulgatorsystem aus einem oder mehreren W/O- und einem oder mehreren O/W-Emulgatoren aufweist, im Verhältnis von 1 2 bis 1 0,2Liposome formation in bath water from oil bath or oleogel preparations and bath tablets has also been described. For example, DE-OS 42 05 548 describes bath and shower additives with vesicle-forming properties, which contain fatty oils and / or apolar substances and also have a content of one or more oil-soluble surfactants together with a content of one or more vesicle-forming lipids. The oil-soluble surfactants have an HLB value of 6 to 13 and the vesicle-forming lipids have an HLB value of 2 to 6. DE 196 02 346 7 describes shower oleogels with vesicle-forming properties which contain more than 30% of one or more lipophilic components, 0.1 to 20% vesicle-forming substances and conventional auxiliaries and additives, and furthermore an emulsifier system composed of one or more W / O and one or more O / W emulsifiers, in a ratio of 1 2 to 1 0.2
Derartige hpidhaltige Reinigungsmittel, welche den bei der Schmutzentfernung entstehenden Verlust an Hautlipiden ausgleichen sollen, werden hergestellt, indem vorgefertigte Vesikel- Dispersionen in die Zubereitung eingearbeitet werden oder die Liposomen, insbesondere im Falle der Verwendung als Badezusatz, bei der Anwendung durch Wasserkontakt aus den im Präparat enthaltenen Lipiden entstehenSuch hpid-containing cleaning agents, which are intended to compensate for the loss of skin lipids which occurs during the removal of dirt, are produced by incorporating prefabricated vesicle dispersions into the preparation or the liposomes, in particular when used as a bath additive, when used by contact with water from the preparation contained lipids arise
Bei den obengenannten Produkten liegen also entweder keine Tenside vor oder, im Falle daß Tenside vorliegen, besondere Systeme an solchen in Verbindung mit Ölen die die Wechselwirkungen der liposomalen Strukturen mit oberflächenaktiven Substanzen in wäßrigen Losungen derart verhindern sollen, daß sie nicht aufgelost werden Wäßrige tensidhalti- ge Zubereitungen ohne einen Anteil an fetten Ölen bzw ölhaltigen Komponenten, welche liposomale Strukturen ausbilden, liegen derzeit jedoch nicht vor Bisher wurden femer zur Herstellung liposomaler Strukturen in solchen Reinigungsprodukten jeweils vesikelbildende Lipide eingesetzt , wie z B Phospholipide, Sphingolide oder CeramideIn the case of the products mentioned above, there are either no surfactants or, in the event that surfactants are present, special systems on those in combination with oils which are intended to prevent the interactions of the liposomal structures with surface-active substances in aqueous solutions in such a way that they are not dissolved. However, there are currently no preparations without a proportion of fatty oils or oil-containing components which form liposomal structures. Vesicle-forming lipids, such as phospholipids, sphingolides or ceramides, have also been used in the manufacture of liposomal structures in such cleaning products
R A Wächter et al beschreibt in Parfumeπe und Kosmetik, 75 Jahrgang, Nr 11/94, Seite 755 bis 759, die Verwendung natürlich vorkommender Phytosterole als pflanzliche Wirkstoffe in der Kosmetik Phytosterole können dabei aus unterschiedlichen Ölen und Fetten gewonnen werden, wie z B Maiskeimol, Rapsöl, Sojaol, Olivenöl etc und bestehen im wesentlichen aus ß-Sitosterol, Campesterol und Stigmasterol Unter der Produktbezeichnung Generol®122 ist ein aus Sojaol gewonnenes Mischprodukt der genannten drei Phytosterol- komponenten mit überwiegendem Anteil an ß-Sitosterol (58,1 %) sowie 29,8% Campesterol und 4,5% Stigmasterol bekannt Daneben existieren auch ethoxylierte Produktvarianten der genannten Phytosterole, insbesondere von Generol®122 In Abhängigkeit vom Ethoxylie- rungsgrad erhalt man eine Reihe von Produkten mit unterschiedlichen Eigenschaften, wie z B Generol®122 E5 (5 Mol EO) welches überwiegend hydrophob ist sowie solche Produkte mit einem Ethoxylierungsgrad von 10, 16 bzw 25 Letztere Produkte weisen die Eigenschaften eines typischen O/W-Emulgators auf Demzufolge können letztere als entsprechende Emulgatoren in O/W Emulsionen sowie als Solubili- siermittei eingesetzt werden, wahrend das nichtethoxyherte Produkt sich als W/O-Emulgator bzw Coemulgator eignet Neben ihrer emulgierenden Eigenschaft können Phytosterole auch positiv bei geschädigter oder durch Umwelteinflusse belasteter Haut eingesetzt werden, wie z B bei konstitutioneller Neurodermitis oder bei Sonnenbrandsymptomen Ferner können solche Produkte neben der obengenannnten Indikation als Emulsionen auch als Haarspu- lungen eingesetzt werden Durch die Anwendung von Generol-haltigen Shampoos kann die Naßkammbarkeit und der Haarglanz verbessert werden in der genannten Literatursteile werden demnach W/O-Hautcremes für trockene Haut beschrieben, enthaltend neben einem üblichen W/O-Emulgator und verschiedener Olkomponenten sowie Konsistenzgebern und Stabilisatoren einen Gehalt von 1% an Generol®122 als Coemulgator Ferner wird dort eine Haarspuiung beschrieben, welche neben der kationischen Emuisionsgrundlage sowie Konsistenzgebern und Additiven einen Gehalt an einer Olkomponente, einen O/W-Emulgator so- wie Generol® 122 in einer Menge von 1 ,0% aufweist Es wird hierbei ferner festgestellt, daß Generol®122 in Verbindung mit langerkettigen Fettsauren, Fettalkoholen oder Phospho pi- den in der Lage ist, multiiameilare Vesikel oder Schichten aufzubauen Hierbei wird davon ausgegangen, daß sich die Phytosterole in die lamellaren Lipidschichten einlagern Die ethoxylierten Generol-Produkte liegen im Gegensatz zu Generol®122 in einer Schichtanord- nung vor Bei Wassergehalten unter 70% werden dabei lamellare Phasen entwickelt, jedoch bei Erhöhung des Wassergehalts auf über 70% findet ein Übergang zu multilameliaren Ve- sikeln statt, also Liposomen Dabei dürfen jedoch keine Tenside vorliegenRA Wächter et al describes in Parfumeπe and Cosmetics, 75 Volume, No. 11/94, pages 755 to 759, the use of naturally occurring phytosterols as herbal active ingredients in cosmetics. Phytosterols can be obtained from different oils and fats, such as corn germ, Rapeseed oil, soybean oil, olive oil etc and essentially consist of ß-sitosterol, campesterol and stigmasterol. The product name Generol ® 122 is a soybean mixed product of the three phytosterol components mentioned with a predominant proportion of ß-sitosterol (58.1%) and 29.8% campesterol and 4.5% stigmasterol known In addition, there are also ethoxylated product variants of the phytosterols mentioned, in particular Generol ® 122. Depending on the degree of ethoxylation, a number of products with different properties are obtained, such as Generol ® 122 E5 ( 5 mol EO), which is predominantly hydrophobic, and such products with a degree of ethoxylation of 10 , 16 or 25 The latter products have the properties of a typical O / W emulsifier. As a result, the latter can be used as corresponding emulsifiers in O / W emulsions and as solubilizers, while the non-ethoxyethered product is suitable as a W / O emulsifier or co-emulsifier in addition to its emulsifying property Phytosterols can also be used positively on damaged or stressed skin, such as constitutional neurodermatitis or sunburn symptoms. Furthermore, in addition to the above-mentioned indication as emulsions, such products can also be used as hair conditioners. The use of generol-containing shampoos can help Wet combability and hair shine are improved in the cited literature parts accordingly W / O skin creams for dry skin are described, containing in addition to a conventional W / O emulsifier and various oil components as well as consistency agents and stabilizers a content of 1% of Generol ® 1 22 as a co-emulsifier Furthermore, a hair conditioner is described there which, in addition to the cationic emulsion base and consistency enhancers and additives, contains an oil component, an O / W emulsifier and Generol ® 122 in an amount of 1.0% found that Generol ® 122 in combination with long-chain fatty acids, fatty alcohols or phosphides is able to build multiiameilar vesicles or layers. It is assumed that the phytosterols are deposited in the lamellar lipid layers. The ethoxylated generol products are in contrast to Generol ® 122 in a layer arrangement before With water contents below 70%, lamellar phases are developed, but when the water content is increased to over 70%, a transition to multilamelar vesicles takes place, ie liposomes. However, no surfactants may be present
Korperreinigungsmittei enthalten jedoch einen Anteil an Tensiden, von denen bekannt ist (vgl DE-PS 42 05 548 und WO 92/04010), daß sie negative Auswirkungen auf die Stabilität von Liposomen haben können, da liposomale Strukturen bekanntlich durch Wechselwirkungen mit oberflächenaktiven Substanzen in wäßrigen Losungen solubilisiert werden Somit war es ohne besondere Stabilisierungsmaßnahmen bisher nicht möglich, stabile tensidhalti- ge wäßrige Systeme, so wie sie für Reinigungsprodukte üblich sind, mit liposomalen Be- standteilen zu formulierenHowever, body cleansing agents contain a proportion of surfactants which are known (cf. DE-PS 42 05 548 and WO 92/04010) that they can have negative effects on the stability of liposomes, since liposomal structures are known to interact with surface-active substances in water Solutions are solubilized So far it has not been possible without special stabilization measures to formulate stable surfactant-containing aqueous systems, as are common for cleaning products, with liposomal components
US-A 5688752 beschreibt Reinigungs- und Pflegezusammensetzungen, die neben Tensiden eine Lipidzusammensetzung aus drei Komponenten A, B und C in ganz bestimmten molaren Verhaltnissen aufweisen, wobei A Ceramide Phospholipide Pseudoceramide, Giycolipide oder Polyethylenglycolester sein können, die Komponente B langkettige Kohlenwasserstoffe mit polaren Kopfgruppen wie Fettsauren sind und die Komponente C eine Hilfskomponente zur Stabilisierung von eventuell gebildeten Bilayern darstellen Komponente C kann bei- spielsweise 3-ß-Sterol oder Cholesterol, Sistosterol, Stigmasterol oder Ergosterol sein. Mit solchen Produkten soll der Verlust der Haut an Lipiden und damit die Austrocknung reduziert werden.US-A 5688752 describes cleaning and care compositions which, in addition to surfactants, have a lipid composition composed of three components A, B and C in very specific molar ratios, where A ceramides can be phospholipids, pseudoceramides, glycolipids or polyethylene glycol esters, component B long-chain hydrocarbons with polar head groups like fatty acids and component C is an auxiliary component for stabilizing any bilayers that may have formed component C can for example, 3-ß-sterol or cholesterol, sistosterol, stigmasterol or ergosterol. With such products, the loss of the skin of lipids and thus the dehydration should be reduced.
Aufgabe der vorliegenden Erfindung ist es daher, ein tensidhaltiges Reinigungssystem auf wäßriger Basis zu formulieren, welches keine ölhaltigen Komponenten enthält, und dennoch liposomale Strukturen insbesondere bei der Anwendung aufweist, wodurch alle Vorteile der Reinigung bzw. der Hautpflege, wie sie für tensidhaltige sowie lipidhaltige Produkte bekannt sind, erzielt werden können.The object of the present invention is therefore to formulate an aqueous-based surfactant-containing cleaning system which does not contain any oil-containing components and yet has liposomal structures, in particular when used, which gives all the advantages of cleaning or skin care such as those for surfactant-containing and lipid-containing products are known can be achieved.
Diese Aufgabe wird erfindungsgemäß gelöst durch Reinigungszubereitungen auf wäßriger Basis, enthaltend 1 bis 60% eines oder mehrerer Tenside, welche insbesondere ausgewählt sind aus anionischen und/oder nichtionischen und/oder amphoteren und/oder kationischen Tensiden, weiterhin 0 - 5%, insbesondere 0,5 - 2% eines oder mehrerer Konditioniermittel, 0 - 5%, insbesondere 1 - 3% eines oder mehrerer Stabilisatoren, 0 - 3%, insbesondereThis object is achieved according to the invention by aqueous-based cleaning preparations containing 1 to 60% of one or more surfactants, which are selected in particular from anionic and / or nonionic and / or amphoteric and / or cationic surfactants, further 0 - 5%, in particular 0, 5 - 2% of one or more conditioning agents, 0 - 5%, in particular 1 - 3% of one or more stabilizers, 0 - 3%, in particular
0,1 - 1 ,5%, eines oder mehrerer Konservierungsmittel, 0 - 5%, insbesondere 0,1 - 2%, eines oder mehrerer Verdickungsmittel sowie 0 - 20%, insbesondere 0,5 - 3%, Wirkstoffe, 0 - 1%, insbesondere 0,0005 - 0,01 % Farbstoffe und 0 - 5%, insbesondere 0,5 - 2% eines oder mehrerer Trübungs- bzw. Perlglanzmittel aufweisen, und welche gekennzeichnet sind durch einen Gehalt von 0,001 - 15%, insbesondere 0,01 - 15%, ganz besonders bevorzugt 0,5 - 10%, und insbesondere 0,5 - 5% eines oder mehrerer Sterole.0.1-1.5%, one or more preservatives, 0-5%, in particular 0.1-2%, one or more thickeners, and 0-20%, especially 0.5-3%, active ingredients, 0-1 %, in particular 0.0005-0.01% of dyes and 0-5%, in particular 0.5-2%, of one or more opacifiers or pearlescent agents, and which are characterized by a content of 0.001-15%, in particular 0 , 01-15%, very particularly preferably 0.5-10%, and in particular 0.5-5% of one or more sterols.
Überraschenderweise konnte gezeigt werden, daß mit solchen wäßrigen tensidhaltigen Zubereitungen der speziellen angegebenen Zusammensetzung im Laufe der Herstellung bzw. der Anwendung aus den einzelnen Bestandteilen liposomale Strukturen spontan entstehen und beim Reinigungsvorgang als solche vorhanden bleiben. Dies ist in krassem Unterschied zu bekannten ölhaltigen Reinigungszusammensetzungen, aus welchen, wie oben beschrieben, sich beim Einsatz in Wasser Liposomen bilden. Dabei können die durch Tenside bei der Schmutzentfernung auftretenden Verluste an Hautlipiden durch die positive oben be- schhebene Wirkung von Sterolen ausgeglichen werden. Dadurch kann neben der ausgezeichneten Reinigungswirkung der Austrocknung der Haut vorgebeugt werden. Überraschenderweise konnte auf den Einsatz an Ölkomponenten zu diesem Zweck verzichtet werden.Surprisingly, it was possible to show that with such aqueous surfactant-containing preparations of the specific composition specified, liposomal structures arise spontaneously from the individual constituents in the course of production or use and remain as such during the cleaning process. This is in stark contrast to known oil-based cleaning compositions, from which, as described above, liposomes form when used in water. The loss of skin lipids caused by surfactants during dirt removal can be compensated for by the positive effects of sterols, which have been resolved above. In addition to the excellent cleaning effect, this can prevent the skin from drying out. Surprisingly, the use of oil components for this purpose could be dispensed with.
Die erfindungsgemäße Reinigungszubereitung enthält vorzugsweise ein Gemisch aus anionischen, nichtionischen und amphoteren, insbesondere aus anionischen und amphoteren bzw. anionischen und nichtionischen Tensid(en). Anionische Tenside sind für den beschriebenen Zweck bekannt und können vorzugsweise ausgewählt werden aus Alkylsulfaten (z.B. C10-C18) und/oder den entsprechenden Alkyl- ethersulfaten, insbesondere mit 1 - 6 Ethylenoxidgruppen im Molekül, Sulfosuccinaten, Sul- fosuccinamaten, Sarcosinaten, Isethionaten, Tauriden, Ethercarbonsäuren, Eiweiß- Fettsäure-Kondensaten, Alkylsulfonaten sowie Alkylbenzolsulfonaten, Monoalkylphosphaten, Monoglyceridsulfaten, Amidethersulfaten, Alkylsulfoacetaten, α-Olefinsulfonaten. Die Alkyl- ketten in den genannten Tensiden können dabei jeweils acht bis achtzehn Kohlenstoffatome umfassen.The cleaning preparation according to the invention preferably contains a mixture of anionic, nonionic and amphoteric, in particular anionic and amphoteric or anionic and nonionic surfactant (s). Anionic surfactants are known for the purpose described and can preferably be selected from alkyl sulfates (for example C10-C18) and / or the corresponding alkyl ether sulfates, in particular with 1-6 ethylene oxide groups in the molecule, sulfosuccinates, sulfosuccinamates, sarcosinates, isethionates, taurides , Ether carboxylic acids, protein-fatty acid condensates, alkyl sulfonates and alkyl benzene sulfonates, monoalkyl phosphates, monoglyceride sulfates, amide ether sulfates, alkyl sulfoacetates, α-olefin sulfonates. The alkyl chains in the surfactants mentioned can each comprise eight to eighteen carbon atoms.
Besonders bevorzugt sind Alkylethersulfate, die sich von Fettalkoholen mit 12 bis 18 Kohlenstoffatomen und einem Ethoxylierungsgrad von 2 bis 6 ableiten, wie z.B. Lauryl/ Myristylethersulfat, Na-Salz (z.B. Texapon® K 14 S spezial IS, Elfan® NS 243 S), Ammoni- umlaurylethersulfat (Zetesol® LA-2) oder Monoisopropanolammoniumlaurylethersulfat (Zete- sol® 2056) bzw. Alkylsulfate, z.B. Natriumlaurylsulfat (Texapon® Z), Ammoniumlaurylsulfat (Texapon® ALS) oder Monoisopropanolammoniumlaurylsulfat (Sulfetal® CJOT 60).Are particularly preferred alkyl ether sulfates derived from fatty alcohols containing 12 to 18 carbon atoms and a degree of ethoxylation of 2 to 6, such as lauryl / myristyl, Na salt (example Texapon ® K 14 S Special IS, Elfan ® NS 243 S), Ammoni - umlaurylethersulfat (Zetesol ® LA-2) or Monoisopropanolammoniumlaurylethersulfat (Zetesol ® 2056) or alkyl sulphates, eg sodium lauryl sulfate (Texapon ® Z), ammonium lauryl sulfate (Texapon ® ALS) or Monoisopropanolammoniumlaurylsulfat (Sulfetal ® CJOT 60).
Ferner geeignet sind insbesondere Bernsteinsäurederivate, wie Sulfosuccinate und Sulfo- succinamate mit einem Alkylrest von 8 - 22 Kohlenstoffatomen, z.B. Wallasol®-L 29 (Disodi- um Laureth-3 Sulfosuccinate).Also suitable are, in particular succinic acid derivatives, such as sulfosuccinates and sulfo succinamates having an alkyl group from 8 to 22 carbon atoms, for example WALLASOL ® -L 29 (Disodi- to Laureth-3 Sulfosuccinate).
Das amphotere Tensid kann insbesondere ausgewählt werden aus Alkylaminopropionaten, Alkyl-, Alkylamido- und Sulfobetainen und Alkylglycinaten mit einer C-Kettenlänge von C8 bis C22. Insbesondere bevorzugt ist das unter dem Handelsnamen Dehyton® K bekannte Co- camidopropylbetain.The amphoteric surfactant can in particular be selected from alkylaminopropionates, alkyl-, alkylamido- and sulfobetaines and alkylglycinates with a C chain length of C8 to C22. Most preferably, the known co camidopropylbetain under the trade name Dehyton ® K.
Das nichtionische Tensid ist insbesondere ausgewählt aus Alkanolamiden, Fettsäu- reethoxylaten, Fettalkoholethoxylaten, Alkylpolyglucosiden insbesondere mit einem Alkylrest von 8 - 16 Kohlenstoffatomen, z.B. Plantacare®2000 UP (Decyl Glucoside), Sorbitanester, z.B. Tween®20 (Polysorbate 20), Aminoxiden, insbesondere Fettaminoxiden mit einer C7 - C26 Alkylkette, z.B. Incromine Oxide® C30 (Cocamidopropylamine Oxide). Ferner geeignet sind Sorbitanester, Alkylphenoloxethylate ( C8 - C22; ggf. 4 - 20 Ethylenoxidgruppen) oder Mischkondensate aus Ethylenoxid und Propylenoxid (z.B. Pluronics®- Typen). Solche für Reinigunsmittel geeignete Tenside sind beispielsweise auch in SÖFW-Journal, 120. Jahrgang, 2-3/94, S. 115 bis 116, im Heft 7/94, Seite 387 sowie in Cosmetics and Toi- letries, Vol. 108, 1993, S. 83 - 89, sowie in SÖFW, 117 Jahrgang, Nr. 1 aus 1991 , Seite 3 - 7 oder in der Monographie von K. Schrader, Grundlagen und Rezepturen der Kosmetika, 2. Aufl. (1989, Hüthig Buchverlag), S. 683 - 691) beschrieben.The nonionic surfactant is particularly selected from alkanolamides, fatty reethoxylaten, fatty alcohol ethoxylates, alkyl polyglucosides, in particular with an alkyl group from 8 to 16 carbon atoms, such as Plantacare ® 2000 UP (Decyl Glucoside), sorbitan esters, such as Tween ® 20 (Polysorbate 20), amine oxides, in particular Fatty amine oxides with a C7 - C26 alkyl chain, e.g. Incromine Oxide ® C30 (Cocamidopropylamine Oxide). Also suitable are sorbitan esters, alkylphenol oxyethylates (C8 - C22; possibly 4 - 20 ethylene oxide groups) or mixed condensates made of ethylene oxide and propylene oxide (eg Pluronics® types). Such surfactants suitable for cleaning agents are, for example, also in SÖFW-Journal, 120th year, 2-3 / 94, pp. 115 to 116, in issue 7/94, page 387 and in Cosmetics and Toiletries, vol. 108, 1993 , Pp. 83 - 89, as well as in SÖFW, 117 volume, No. 1 from 1991, pages 3 - 7 or in the monograph by K. Schrader, Basics and Recipes of Cosmetics, 2nd edition (1989, Hüthig Buchverlag), Pp. 683 - 691).
Geeignete kationische Tenside sind quatemäre Ammoniumverbindungen mit Kohlenstoffkettenlängen üblicherweise zwischen 12 und 22 wie z.B. Steartrimoniumchlorid oder Pyridi- niumsalze, z.B. Cetylpyridiniumchlorid.Suitable cationic surfactants are quaternary ammonium compounds with carbon chain lengths usually between 12 and 22, e.g. Steartrimonium chloride or pyridine salts, e.g. Cetylpyridinium chloride.
Als Sterol eignen sich insbesondere Phytosterole wie z.B. solche, die aus Maiskeimol, Rapsöl, Sojaöl, Olivenöl etc. gewonnen werden und hauptsächlich aus einem Gemisch von ß-Sitosterol, Campesterol und Stigmasterol in unterschiedlichen Gewichtsanteiien bestehen, wie z.B. von R. A. Wächter beschrieben (vgl. S. 4, Abs. 4 dieser Anmeldung). Ferner geeig- net ist Cholesterol und dessen Derivate, z.B. Dihydrocholesterol oder Cholesterolester wie Cholesterylacetat. Insbesondere ist als Phytosterol ein Produkt mit dem Handelsnamen Ge- nerol®122 N (raffiniertes Sojasterol) geeignet. Weiterhin bevorzugt sind ethoxylierte Sterole der genannten Art mit einem Ethoxylierungsgrad von 5 bis 30, wie z. B. Generol®122 N E5D, E10, E16, E25D (ethoxylierte Sojasterole) oder Nikkol® DHC-15 und -30 (ethoxyiiertes Dihy- drocholesterol).Particularly suitable sterols are phytosterols such as those derived from corn oil, rapeseed oil, soybean oil, olive oil etc. and mainly consisting of a mixture of ß-sitosterol, campesterol and stigmasterol in different weight proportions, as described, for example, by RA Wächter (cf. P. 4, paragraph 4 of this application). Cholesterol and its derivatives, for example dihydrocholesterol or cholesterol esters such as cholesteryl acetate, are also suitable. Particularly suitable as a phytosterol is a product with the trade name Genenerol ® 122 N (refined soyasterol). Also preferred are ethoxylated sterols of the type mentioned with a degree of ethoxylation of 5 to 30, such as. B. Generol ® 122 N E5D, E10, E16, E25D (ethoxylated soy sterols) or Nikkol ® DHC-15 and -30 (ethoxyated dihydrocholesterol).
Insbesondere bevorzugt werden Mengen von 0,5 bis 5%, insbesondere 0,5 bis 3% und vorzugsweise 0,5 bis 2%, des oder der genannten Sterole. Ganz besonders bevorzugt ist eine Mischung aus nichtethoxyliertem Phytosterol, z.B. Generol® 122 N und einem mit 5 Einhei- ten ethoxyliertem Phytosterol, wie z. B. Generol®122 N E5D. Hierbei ist vorzugsweise der Anteil an ethoxyliertem Sterol höher oder gleich dem Anteil an nicht ethoxyliertem Sterol, insbesondere im Verhältnis 5 : 1 Gew.% bis 1 : 1 Gew.%. Besonders bevorzugt ist ein Verhältnis von 3 : 1 Gew.%. Weiterhin bevorzugt ist der alleinige Einsatz von einem nicht- ethoxiliertem Sterol, z.B. Generol® 122 N in den angegebenen Mengen, wie z.B. 1 Gew.%.Quantities of 0.5 to 5%, in particular 0.5 to 3% and preferably 0.5 to 2%, of the sterols mentioned are particularly preferred. A mixture of non-ethoxylated phytosterol, for example Generol ® 122 N and one with 5 units of ethoxylated phytosterol, such as, for example, is very particularly preferred. B. Generol ® 122 N E5D. The proportion of ethoxylated sterol is preferably higher than or equal to the proportion of non-ethoxylated sterol, in particular in a ratio of 5: 1% by weight to 1: 1% by weight. A ratio of 3: 1% by weight is particularly preferred. Further preferably, the sole use of a non-ethoxylated sterol, such as Generol ® is 122 N in the specified amounts, such as 1 wt.%.
Besonders geeignete Tensidmengen sind 5 bis 30%, insbesondere 7,5 bis 25% und ganz besonders bevorzugt 10 bis 20 % an Tensid oder Tensiden.Particularly suitable amounts of surfactant are 5 to 30%, in particular 7.5 to 25% and very particularly preferably 10 to 20% of surfactant or surfactants.
Die erfindungsgemäße Zusammensetzung kann weiterhin übliche Hilfs- und Zusatzstoffe enthalten. Hierzu gehören kationische Polymere als Konditioniermittel, wie z.B. Polyquater nium-22 (Merquat® 280), quaternisierte Proteinderivate wie Lauryldimonium Hydroxypropyl Hydrolized Soy Protein (Bestandteil von Prota Flor® HSQ), Silikonderivate, z.B. Abil® B 8863, 8843 (Dimethicone Copolyol), Eiweiß-Hydrolysate bzw. wasserlösliche Proteine.The composition according to the invention can furthermore contain customary auxiliaries and additives. These include cationic polymers as conditioning agents, such as polyquaters nium-22 (Merquat ® 280), quaternized protein derivatives such as lauryldimonium hydroxypropyl hydrolized soy protein (part of Prota Flor ® HSQ), silicone derivatives, e.g. Abil ® B 8863, 8843 (Dimethicone Copolyol), protein hydrolyzates or water-soluble proteins.
Ferner können ein oder mehrere Stabilisatoren in geringen Mengen (0 bis 5%) enthalten sein. Hier gehören z.B. Komplexbildner wie Trilon®BD (EDTA, Na-Salz), Mittel zur pH- Einstellung, z.B. Zitronensäure, Feuchthaltemittel wie Glycehn, anorganische Salze, z.B. Natriumchlorid als Viskositätsregler.One or more stabilizers can also be present in small amounts (0 to 5%). Here includes, for example complexing agents such as Trilon BD ® (EDTA, sodium salt), agents for pH adjustment, eg citric acid, humectants such as Glycehn, inorganic salts such as sodium chloride as a viscosity regulator.
Daneben können gegebenenfalls ein oder mehrere Konservierungs- und Verdickungsmittel (0 bis 5%) vorhanden sein. Geeignete Konservierungsmittel sind beispielsweise lodopro- pynylbutylcarbamat, Phenoxyethanol und weitere gebräuchliche Konservierungsstoffe, wie z.B. p-Hydroxybenzoesäureester, Formaldehyd und -abspalter, Sorbin- und Dehydracetsäu- re und deren Salze, Isothiazolinone, 5-Brom-5-nitro-1 ,3-dioxan, Methyldibromoglutanonitril, etc..In addition, one or more preservatives and thickeners (0 to 5%) can optionally be present. Suitable preservatives are, for example, iodopropynyl butyl carbamate, phenoxyethanol and other common preservatives, such as e.g. p-hydroxybenzoic acid esters, formaldehyde and releasers, sorbic and dehydroacetic acid and their salts, isothiazolinones, 5-bromo-5-nitro-1, 3-dioxane, methyldibromoglutanonitrile, etc.
Als Verdicker eignen sich z.B. Volpo® L 3 (Laureth-3) oder Antil® 208 (Laureth-3, Propy- lenglykol, Acrylates/Steareth-50 Copolymer), Glucamate® DOE 120 (PEG-120 Methyl Glu- cose Dioleate), Comperian® 100 (Cocamide MEA).Suitable thickeners are, for example, Volpo ® L 3 are (Laureth-3) or Antil ® 208 (Laureth-3, propylene glycol, acrylates / steareth-50 copolymer) Glucamate DOE 120 ® (PEG-120 Methyl Glu- cose Dioleate), Comperian ® 100 (Cocamide MEA).
Insbesondere kann die erfindungsgemäße Reinigungszubereitung ein oder mehrere Wirkstoffe in den angegebenen Mengen aufweisen. Hierzu gehören beispielsweise Parfümöle oder etherische Öle, Wirkstoffextrakte und/oder Vitamine.In particular, the cleaning preparation according to the invention can have one or more active ingredients in the amounts specified. These include, for example, perfume oils or essential oils, active ingredient extracts and / or vitamins.
Hierzu zählen insbesondere Minzöl, Limettenöl, Orangenöl, Wacholderöl, Baldrianöl, Eukalyptusöl, Thymianöl, Palmarosaöl, Rosmarinöl, Lavendelöl, Menthol, Ingwer-, Lindenblüten-, Ringelblumen-, Algen-, Aloevera-, Echinacea-, Efeublätterextrakt und Panthenol, Hydroxy- ethylsalicylat, Nikotinsäureester. Dabei kann je nach beabsichtigtem Wirkungseffekt, wie z.B. der Verbesserung der Haar- bzw. Hautstruktur, Erhöhung der Durchblutung, Entspan- nung, Aromatherapie u.a. eine geeignete Kombination an Wirkstoffen zugesetzt werden. Gegebenenfalls können weitere Rückfetter wie Fettsäureglyceride und deren Ethoxylate, z.B. PEG-6 Caprylic/Capric Glycerides (Softigen® 767) und/oder Farbstoffe wie z.B. Patentblau, Amidoblau, Orange RGL, Cochenillerot, Chinolingelb eingesetzt werden. In einer bevorzugten Ausführungsform können die erfindungsgemäßen Zusammensetzungen auch einen zusätzlichen Anteil, z.B. 0,01 bis 5% eines oder mehrerer vesikelbildender Lipide enthalten. Hierzu gehören insbesondere Lecithin, Phospholipide, wie Phosphati- dylcholin, und Ceramide, wie z.B. Ceramid-2, -3, -6 sowie Sphingolipide, wie z.B. Procera- mide® L, Ceraderm® S, Ceraveg®.These include, in particular, mint oil, lime oil, orange oil, juniper oil, valerian oil, eucalyptus oil, thyme oil, palmarosa oil, rosemary oil, lavender oil, menthol, ginger, linden blossom, marigold, algae, aloe vera, echinacea, ivy leaf extract and panthenol extract , Nicotinic acid ester. Depending on the intended effect, such as improving the hair or skin structure, increasing blood circulation, relaxation, aromatherapy and others, a suitable combination of active ingredients can be added. If necessary, further refatting agents such as fatty acid glycerides and their ethoxylates, for example PEG-6 Caprylic / Capric Glycerides (Softigen ® 767) and / or dyes such as for example patent blue, amido blue, orange RGL, cochineal red, quinoline yellow can be used. In a preferred embodiment, the compositions according to the invention can also contain an additional proportion, for example 0.01 to 5%, of one or more vesicle-forming lipids. These include in particular lecithin, phospholipids, such as phosphatidylcholine dylcholin, and ceramides such as ceramide 2, -3, -6 and sphingolipids, such as Procera mide ® L, Ceraderm ® S, Ceraveg ®.
Besonders bevorzugt sind Lecithin (z.B. Sojalecithin), Phosphatidylcholin, Phosphatidylserin oder- diethanolamin oder Mischungen hiervon.Lecithin (e.g. soy lecithin), phosphatidylcholine, phosphatidylserine or diethanolamine or mixtures thereof are particularly preferred.
Die erfindungsgemäßen Reinigungszubereitungen werden hergestellt, indem das oder die Sterole in der wäßrigen Tensidlösung geschmolzen werden. Anschließend wird die Zubereitung kalt gerührt. Gegebenenfalls werden sodann Wirkstoffe und andere Hilfs- und Zusatzstoffe im Laufe der Herstellung eingearbeitet. Hierfür geeignete Temperaturen liegen zwi- sehen 60°C und 25°C.The cleaning preparations according to the invention are produced by melting the sterol or sterols in the aqueous surfactant solution. The preparation is then stirred cold. If necessary, active ingredients and other auxiliaries and additives are then incorporated in the course of production. Suitable temperatures for this are between 60 ° C and 25 ° C.
Die mit den erfindungsgemäßen Zusammensetzungen erhaltenen Produkte bilden spontan, insbesondere bei der Anwendung, liposomale Strukturen. Diese können mittels Transmissionselektronenmikroskopie (TEM) nach Gefrierbruch nachgewiesen werden.The products obtained with the compositions according to the invention spontaneously form liposomal structures, particularly when used. These can be detected by means of transmission electron microscopy (TEM) after freezing fracture.
Mit den erfindungsgemäßen Reinigungszubereitungen ist es möglich, Produkte mit vorhan- denenen Liposomen als Reinigungs- und Pflegemittel einzusetzen. Die erfindungsgemäßen Präparate sind sehr gut verteilungsfähig. Sie weisen gute Reinigungs- und Schaumeigenschaften, ein angenehmes Hautgefühl sowie günstige geruchliche Eigenschaften auf. Sie genügen also den an Kosmetika zu stellenden Anforderungen.With the cleaning preparations according to the invention, it is possible to use products with existing liposomes as cleaning and care agents. The preparations according to the invention are very easy to distribute. They have good cleaning and foaming properties, a pleasant feeling on the skin and favorable odor properties. So they meet the requirements for cosmetics.
Die erfindungsgemäßen Zusammensetzungen können insbesondere als Duschbad, Schaumbad oder Shampoo angewendet werden. Je nach beabsichtigtem Anwendungszweck können die einzelnen Komponenten unterschiedlich kombiniert werden.The compositions according to the invention can be used in particular as a shower bath, foam bath or shampoo. Depending on the intended application, the individual components can be combined differently.
Die erfindungsgemäßen Produkte verfügen ferner über eine sehr gute Stabilität und können ohne Einsatz spezieller und aufwendiger Apparaturen und Herstellungsverfahren, wie sie üblicherweise zur Bereitstellung liposomaler Artikel erforderlich sind, hergestellt werden. Die Konsistenz der Produkte kann je nach Wunsch mittels geringer Mengen an Zusatz- und Hilfsstoffen eingestellt werden, welche das Hautgefühl nicht verändern. Durch die besondere Eigenschaft der Sterole, insbesondere der Phytosterole, nämlich daß sie als pflanzliche Rohstoffe die Haar- und Hautbeschaffenheit positiv beeinflussen, kann zusätzlich neben dem liposomalen Effekt ein weiterer Pflegeeffekt erzielt werden.The products according to the invention also have very good stability and can be produced without the use of special and complex apparatus and production processes, as are usually required for the provision of liposomal articles. The consistency of the products can be adjusted as desired using small amounts of additives and auxiliary substances that do not change the feeling on the skin. Due to the special property of sterols, especially phytosterols, namely that they are plant-based In addition to the liposomal effect, raw materials that have a positive influence on hair and skin texture can also achieve a further care effect.
Hierbei zeigte sich überraschenderweise, daß insbesondere die Anwesenheit von Tensiden keine negative Auswirkung auf das Vorhandensein bzw. die Ausbildung der Liposomen hat. Dies konnte nicht erwartet werden im Hinblick auf den bereits geschilderten Stand der Technik, worin festgestellt wurde, daß herkömmliche liposomale Strukturen aus z. B. Phospholi- piden durch solche stark oberflächenaktiven O/W-Emulgatoren bzw. Tensiden solubilisiert werden.It was surprisingly found that the presence of surfactants in particular has no negative effect on the presence or formation of the liposomes. This could not be expected in view of the prior art already described, which found that conventional liposomal structures from e.g. B. phospholipids can be solubilized by such highly surface-active O / W emulsifiers or surfactants.
Durch Inkorporierung eines oder mehrerer der obengenannten Wirkstoffe können z.B. Indikationsduschzusammensetzungen je nach gewünschtem Zweck hergestellt werden. So kann z.B. ein Abhärtungsduschbad mit Eukalyptusöl, Minzöl und Echinacea-Extrakt; eine Anregungs-Dusche mit Rosmarinöl und Limettenöl oder eine Muskel-Relax-Dusche mit Ing- wer-Extrakt, Methylnicotinat, Hydroxyethylsalicylat und Wacholderöl hergestellt werden.By incorporating one or more of the above active ingredients e.g. Indicative shower compositions can be prepared according to the desired purpose. For example, a hardening shower with eucalyptus oil, mint oil and echinacea extract; a stimulating shower with rosemary oil and lime oil or a muscle relaxation shower with ginger extract, methyl nicotinate, hydroxyethyl salicylate and juniper oil.
Die Erfindung wird anhand der nachfolgenden Beispiele näher erläutert. Im Anschluß an die Beispiele werden die transmissionselektronenmikroskopischen Aufnahmen der erfindungsgemäß hergestellten Produkte beigefügt. Hierbei kann man deutlich die liposomalen Struktu- ren (kugelförmige Strukturen) im erfindungsgemäß hergestellten Produkt nach Verdünnung mit Wasser 1 T : 20 T bei 37°C sehen. The invention is illustrated by the following examples. Following the examples, the transmission electron micrographs of the products produced according to the invention are attached. Here one can clearly see the liposomal structures (spherical structures) in the product produced according to the invention after dilution with water 1 T: 20 T at 37 ° C.
Herstellung der erfindungsgemäßen Zubereitungen.Preparation of the preparations according to the invention.
Die Produkte gemäß den folgenden Beispielen 1 bis 9 wurden hergestellt, indem das oder die angegebenen Sterole in der wäßrigen Tensidlösung, also der Lösung aus deminerali- siertem Wasser und den angegebenen Tensiden, bei Temperaturen zwischen 80°C und 90°C geschmolzen wurde. Anschließend wurde kalt gerührt und gegebenenfalls die weiteren angegebenen Zusatz-, Wirk- und Hilsstoffe in der angegebenen Reihenfolge bei Temperaturen zwischen 60°C und 25°C eingearbeitet. The products according to the following Examples 1 to 9 were prepared by melting the sterol (s) specified in the aqueous surfactant solution, ie the solution of demineralized water and the specified surfactants, at temperatures between 80 ° C. and 90 ° C. The mixture was then stirred cold and, if appropriate, the further additives, active ingredients and auxiliaries specified were incorporated in the order given at temperatures between 60 ° C. and 25 ° C.
Beispiel 1example 1
Figure imgf000013_0001
Figure imgf000013_0001
Acrylates/Steareth-50 Copolymer + Propylene Glycol + Laureth-3 Acrylates / Steareth-50 Copolymer + Propylene Glycol + Laureth-3
Beispiel 2Example 2
Figure imgf000014_0001
Figure imgf000014_0001
Acrylates/Steareth-50 Copolymer + Propylene Glycol + Laureth-3 Acrylates / Steareth-50 Copolymer + Propylene Glycol + Laureth-3
Beispiel 3Example 3
Figure imgf000015_0001
Figure imgf000015_0001
Beispiel 4Example 4
Figure imgf000016_0001
Figure imgf000016_0001
Beispiel 5Example 5
Figure imgf000017_0001
Beispiel 6
Figure imgf000017_0001
Example 6
Figure imgf000018_0001
Figure imgf000018_0001
Acrylates/Steareth-50 Copolymer + Propylene Glycol + Laureth-3 Beispiel 7Acrylates / Steareth-50 Copolymer + Propylene Glycol + Laureth-3 Example 7
Figure imgf000019_0001
Figure imgf000019_0001
Acrylates/Steareth-50 Copolymer + Propylene Glycol + Laureth-3 Acrylates / Steareth-50 Copolymer + Propylene Glycol + Laureth-3
Beispiel 8Example 8
Figure imgf000020_0001
Figure imgf000020_0001
Acrylates/Steareth-50 Copolymer + Propylene Glycol + Laureth-3 Acrylates / Steareth-50 Copolymer + Propylene Glycol + Laureth-3
Beispiel 9Example 9
Figure imgf000021_0001
Figure imgf000021_0001
Acrylates/Steareth-50 Copolymer + Propylene Glycol + Laureth-3 Nachweis der liposomalen Strukturen in den erfindungsgemäßen ZubereitungenAcrylates / Steareth-50 Copolymer + Propylene Glycol + Laureth-3 Detection of the liposomal structures in the preparations according to the invention
In den folgenden Abbildungen 1 - 9 werden die liposomalen Strukturen (kugelförmige Gebilde) der Zubereitungen gemäß Beispiele 1 - 9 durch Transmissionselektronenmikroskopie nach Gefrierbruch dargestellt.The following Figures 1-9 show the liposomal structures (spherical structures) of the preparations according to Examples 1-9 by transmission electron microscopy after freeze fracture.
Liste der TEM-AufnahmenList of TEM recordings
Beispiel 1 = Nr. 2778Example 1 = No. 2778
Beispiel 2 = Nr. 2831Example 2 = No. 2831
Beispiel 3 = Nr. 2841Example 3 = No. 2841
Beispiel 4 = Nr. 2726Example 4 = No. 2726
Beispiel 5 = Nr. 2922Example 5 = No. 2922
Beispiel 6 = Nr. 2928Example 6 = No. 2928
Beispiel 7 = Nr. 2925Example 7 = No. 2925
Beispiel e = Nr. 2913Example e = No. 2913
Beispiel 9 = Nr. 2952 Example 9 = No. 2952

Claims

Patentansprüche claims
1. Reinigungzubereitungen auf wäßriger Basis, enthaltend 1 bis 60% eines oder mehrerer Tenside, ausgewählt aus anionischen und/oder nichtionischen und/oder amphoteren und/oder kationischen Tensiden, 0 - 5% eines oder mehrerer Konditioniermittel, 0 - 5% eines oder mehrerer Stabilisatoren, 0 - 3% eines oder mehrerer Konservierungsmittel, 0 - 5% eines oder mehrerer Verdickungsmittel sowie 0 - 20% Wirkstoffe, 0 - 1 % Farbstoffe sowie 0 - 5% eines oder mehrerer Trübungs-, bzw. Perlglanzmittel, dadurch gekennzeichnet, daß die Reinigungszubereitung 0,001 -15% eines oder mehrerer Sterole enthält.1. Water-based cleaning preparations containing 1 to 60% of one or more surfactants selected from anionic and / or nonionic and / or amphoteric and / or cationic surfactants, 0-5% of one or more conditioning agents, 0-5% of one or more Stabilizers, 0 - 3% of one or more preservatives, 0 - 5% of one or more thickeners and 0 - 20% active ingredients, 0 - 1% dyes and 0 - 5% of one or more opacifiers or pearlescent agents, characterized in that the cleaning preparation contains 0.001 -15% of one or more sterols.
2. Reinigungszubereitung nach Anspruch 1 , dadurch gekennzeichnet, daß sie ein Duschbad, eine Schaumbadzusammensetzung oder ein Shampoo ist.2. Cleaning preparation according to claim 1, characterized in that it is a shower bath, a foam bath composition or a shampoo.
3. Reinigungszubereitung nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß als Sterol ein oder mehrere Phytosterole enthalten sind.3. Cleaning preparation according to claim 1 or 2, characterized in that one or more phytosterols are contained as sterol.
4. Reinigungszubereitung nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß als Sterol ein ethoxyliertes Sterol mit einem Ethoxylierungsgrad von 5 - 30 (EO) enthalten ist.4. Cleaning preparation according to claim 1 or 2, characterized in that the sterol is an ethoxylated sterol with a degree of ethoxylation of 5-30 (EO).
5. Reinigungszubereitung nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß es eine Mischung aus einem Sterol und einem ethoxylierten Sterol enthält.5. Cleaning preparation according to claim 1 or 2, characterized in that it contains a mixture of a sterol and an ethoxylated sterol.
6. Reinigungszubereitung nach Anspruch 5, dadurch gekennzeichnet, daß der Anteil an ethoxyliertem Sterol höher oder gleich dem Anteil an nicht ethoxyliertem Sterol ist.6. Cleaning preparation according to claim 5, characterized in that the proportion of ethoxylated sterol is higher than or equal to the proportion of non-ethoxylated sterol.
7. Reinigungszubereitung nach einem der Ansprüche 1 bis 6 dadurch gekennzeichnet, daß eine Mischung aus anionischen und amphoteren oder anionischen und nichtionischen Tensiden enthalten ist. 7. Cleaning preparation according to one of claims 1 to 6, characterized in that a mixture of anionic and amphoteric or anionic and nonionic surfactants is contained.
8. Reinigungszubereitung nach einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, daß das anionische Tensid ausgewählt ist aus einem Alkylsulfat, Alkylethersulfat, Sulfosuccinat, Sulfosuccinamat, Sarcosinat, Isethionat, Taurid, Ethercarbonsäure, Eiweiß-Fettsäure-Kondensat, Alkylsulfonat sowie Alkylbenzolsulfonat, Monoalkyl- phosphat, Monoglyceridsulfat, Amidethersulfat, Alkylsulfoacetat, α-Olefinsulfonat, das amphotere Tensid ausgewählt ist aus Alkylaminopropionaten, Alkyl-, Alkylamido-, Sulfobetainen, Alkylglycinaten und das nichtionische Tensid ausgewählt ist aus Alka- nolamiden, Fettsäureethoxylaten, Fettalkoholethoxyiaten, Alkylpolyglucosiden, Aminoxiden, Sorbitanester, Alkylphenoloxethylaten, Mischkondensaten aus Ethylen- oxid und Propylenoxid.8. Cleaning preparation according to one of claims 1 to 7, characterized in that the anionic surfactant is selected from an alkyl sulfate, alkyl ether sulfate, sulfosuccinate, sulfosuccinamate, sarcosinate, isethionate, tauride, ether carboxylic acid, protein fatty acid condensate, alkyl sulfonate and alkylbenzenesulfonate, monoalkyl phosphate, monoglyceride sulfate, amidether sulfate, alkyl sulfoacetate, α-olefin sulfonate, the amphoteric surfactant is selected from alkylaminopropionates, alkyl, alkylamido, sulfobetaines, alkylglycinates and the nonionic surfactant is selected from alkanolamides, fatty acid ethoxylates, fatty alcohol aminoxoxyidoxides, fatty alcohol aminoxoxyidoxides, fatty alcohol ethoxylates, fatty alcohol ethoxy ethoxides, fatty alcohol ethoxylates, fatty alcohol ethoxy ethoxides, fatty alcohol ethoxy ethoxides, Alkylphenol oxyethylates, mixed condensates made from ethylene oxide and propylene oxide.
9. Reinigungszubereitung nach einem der Ansprüche 1 bis 8, dadurch gekennzeichnet, daß sie 10 - 25% an Tensid enthält.9. Cleaning preparation according to one of claims 1 to 8, characterized in that it contains 10-25% of surfactant.
10. Reinigungszubereitung nach einem der Ansprüche 1 bis 9, dadurch gekennzeichnet, daß sie 0,5 bis 5% an Sterol und/oder ethoxyliertem Sterol aufweist.10. Cleaning preparation according to one of claims 1 to 9, characterized in that it has 0.5 to 5% of sterol and / or ethoxylated sterol.
11. Reinigungszubereitung nach einem der Ansprüche 1 bis 10, dadurch gekennzeichnet, daß 0,01 - 5% Lecithin, Phosphatidylcholin, Sphingolipid und/oder Ceramid ent- halten sind.11. Cleaning preparation according to one of claims 1 to 10, characterized in that 0.01 - 5% lecithin, phosphatidylcholine, sphingolipid and / or ceramide are contained.
12. Verfahren zur Herstellung einer Reinigungszubereitung nach einem der Ansprüche 1 bis 11 , dadurch gekennzeichnet, daß man eine Lösung aus Wasser und Tensiden herstellt, diese auf die Schmelztemperatur des oder der Sterole erwärmt, diese darin schmilzt, anschließend die Mischung kalt rührt und danach ggf. weitere Zusatz-, Hilfsund Wirkstoffe bei Temperaturen von 60°C bis 25°C einarbeitet.12. A process for the preparation of a cleaning preparation according to any one of claims 1 to 11, characterized in that a solution of water and surfactants is prepared, heated to the melting temperature of the sterol or sterols, it melts therein, then the mixture is stirred cold and then, if necessary incorporates additional additives, auxiliaries and active ingredients at temperatures from 60 ° C to 25 ° C.
13. Verwendung von Reinigungszubereitungen gemäß einem der Ansprüche 1 bis 11 als Waschgele, Duschbäder, Schaumbäder oder Shampoos. 13. Use of cleaning preparations according to one of claims 1 to 11 as washing gels, shower baths, foam baths or shampoos.
PCT/EP1999/008595 1998-11-27 1999-11-09 Preparations of aqueous-based cleaning agents which form vesicles and which contain active agents, method for their production and their utilisation WO2000032161A1 (en)

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EP99957294A EP1133276A1 (en) 1998-11-27 1999-11-09 Preparations of aqueous-based cleaning agents which form vesicles and which contain active agents, method for their production and their utilisation
PL99347886A PL347886A1 (en) 1998-11-27 1999-11-09 Preparations of aqueous-based cleaning agents which form vesicles and which contain active agents, method for their production and their utilisation
AU15051/00A AU760248B2 (en) 1998-11-27 1999-11-09 Preparations of aqueous-based cleaning agents which form vesicles and which contain active agents, method for their production and their utilisation
JP2000584858A JP2002531389A (en) 1998-11-27 1999-11-09 Aqueous-based sarcoplasmic detergent-containing detergent preparation, process for its preparation and its use
EA200100594A EA003465B1 (en) 1998-11-27 1999-11-09 Aqueous-based cleaning preparations which form vesicles and contain surfactants, process for their preparation and their use
NZ511785A NZ511785A (en) 1998-11-27 1999-11-09 Preparations of aqueous-based cleaning agents which form vesicles and which contain active agents, method for their production and their utilisation
KR1020017006662A KR20010080615A (en) 1998-11-27 1999-11-09 Preparation of aqueous-based cleaning agents which form vesicles and which contain active agents, methods for their production and their utilisation
IL14287799A IL142877A0 (en) 1998-11-27 1999-11-09 Preparations of aqueous-based cleaning agents which form vesicles and which contain active agents, method for their production and their utilization
BR9915742-0A BR9915742A (en) 1998-11-27 1999-11-09 Cleaning preparations containing water-based vesicle-forming surfactants, process for their preparation, as well as their use
CA002352288A CA2352288A1 (en) 1998-11-27 1999-11-09 Aqueous-based cleaning preparations which form vesicles and contain surfactants, process for their preparation and their use
APAP/P/2001/002158A AP2001002158A0 (en) 1998-11-27 1999-11-09 Preparation of aqueous-based cleaning agents which form vesicles and which contain active agents, method for their production their utilisation.
HU0104356A HUP0104356A3 (en) 1998-11-27 1999-11-09 Aqueous-based cleaning composition which form vesicles and which contains tenside method for production and use thereof
BG105533A BG105533A (en) 1998-11-27 2001-05-22 Aqueous based cleaning agent preparations forming vesicules, containing surfactants, method for their production and their utilization
HR20010400A HRP20010400A2 (en) 1998-11-27 2001-05-25 Aqueous-based cleaning agent containing tensid, method of its production and utilization
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MY158895A (en) 2000-05-19 2016-11-30 Monsanto Technology Llc Potassium glyphosate formulations
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DE102010054461A1 (en) 2010-12-14 2012-06-14 Merz Pharma Gmbh & Co. Kgaa Liposome-forming aqueous bath preparations with high active ingredient content and their cosmetic / dermatological / medical application
GB2552864A (en) * 2016-04-26 2018-02-14 Pz Cussons (International) Ltd Aerosol gel composition
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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU1528494A1 (en) * 1987-02-06 1989-12-15 Всесоюзный научно-исследовательский и проектный институт химической промышленности Washing agent for body
EP0557825A2 (en) * 1992-02-24 1993-09-01 Merz & Co. GmbH & Co. Bath and shower additives with vesicle forming properties, preparation and use thereof
US5246693A (en) * 1989-12-13 1993-09-21 L'oreal Cosmetic preparation for the care of the hair and use of the said composition
US5389282A (en) * 1991-04-24 1995-02-14 Kao Corporation Milky detergent composition for hard surfaces
DE4402527A1 (en) * 1994-01-28 1995-08-03 Henkel Kgaa Aqueous solutions of esterquats
US5543074A (en) * 1994-02-18 1996-08-06 Chesebrough-Pond's Usa Co., Div. Of Conopco, Inc. Personal washing compositions

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9421185D0 (en) * 1994-10-20 1994-12-07 Unilever Plc Personal car composition

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU1528494A1 (en) * 1987-02-06 1989-12-15 Всесоюзный научно-исследовательский и проектный институт химической промышленности Washing agent for body
US5246693A (en) * 1989-12-13 1993-09-21 L'oreal Cosmetic preparation for the care of the hair and use of the said composition
US5389282A (en) * 1991-04-24 1995-02-14 Kao Corporation Milky detergent composition for hard surfaces
EP0557825A2 (en) * 1992-02-24 1993-09-01 Merz & Co. GmbH & Co. Bath and shower additives with vesicle forming properties, preparation and use thereof
DE4402527A1 (en) * 1994-01-28 1995-08-03 Henkel Kgaa Aqueous solutions of esterquats
US5543074A (en) * 1994-02-18 1996-08-06 Chesebrough-Pond's Usa Co., Div. Of Conopco, Inc. Personal washing compositions

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch Week 199039, Derwent World Patents Index; Class D21, AN 1990-296104, XP002133701 *

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HUP0104356A3 (en) 2002-12-28
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AU760248B2 (en) 2003-05-08
EA003465B1 (en) 2003-06-26
CN1328444A (en) 2001-12-26
YU36101A (en) 2003-12-31
CA2352288A1 (en) 2000-06-08
HUP0104356A2 (en) 2002-03-28
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AU1505100A (en) 2000-06-19
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EA200100594A1 (en) 2001-12-24
JP2002531389A (en) 2002-09-24
BG105533A (en) 2001-12-31
IL142877A0 (en) 2002-03-10
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NZ511785A (en) 2002-11-26
SK7092001A3 (en) 2001-12-03
EP1133276A1 (en) 2001-09-19
AP2001002158A0 (en) 2001-05-09
BR9915742A (en) 2001-08-14
CZ20011867A3 (en) 2001-10-17
TR200101508T2 (en) 2002-03-21

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