EP1684872A1 - Substrat contenant des lipides - Google Patents
Substrat contenant des lipidesInfo
- Publication number
- EP1684872A1 EP1684872A1 EP04818153A EP04818153A EP1684872A1 EP 1684872 A1 EP1684872 A1 EP 1684872A1 EP 04818153 A EP04818153 A EP 04818153A EP 04818153 A EP04818153 A EP 04818153A EP 1684872 A1 EP1684872 A1 EP 1684872A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- preparation
- textile
- lipids
- sodium
- 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.)
- Ceased
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0208—Tissues; Wipes; Patches
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
Definitions
- the present invention relates to a cleaning article, its manufacture and use.
- Cleaning the human body means removing (environmental) dirt and thus increasing mental and physical well-being.
- Cleaning the surface of skin and hair is a very complex process that depends on many parameters.
- substances coming from outside such as hydrocarbons or inorganic pigments from a wide variety of environments, as well as residues from cosmetics or undesired microorganisms, should be removed as completely as possible.
- body-specific excretions such as sweat, sebum, skin and hair flakes can be washed off without profound interventions in the physiological balance of the skin.
- Solid cleaning substrates or textiles, in particular wipes are a special product form for cleaning preparations. These can already be impregnated with the cleaning preparation by the manufacturer (a combination for which the term “cleaning article” is also used in the context of the present invention) and thereby have the advantage that the preparation is already specified in the correct dosage in them avoid the disadvantage of preparations stored in bottles, the packaging of which break and the contents "leak".
- cleaning substrates / textiles include the fact that they can be conveniently taken in a counted amount when traveling and that water is generally no longer required for their use.
- Textiles can be woven, knitted or knitted or available as a composite (nonwoven textile). Composites are mostly used (for reasons of cost). In the case of composites, the fabric is not formed by warp and weft or stitch formation, but by intertwining and / or cohesive and / or adhesive bonding of textile fibers. Composites can be differentiated according to DIN 61210 T2 into fleece, paper wadding and felt. Nonwovens are loose materials made of spun fibers (ie fibers with limited length) or filaments (continuous fibers), mostly made of polypropylene, polyester or viscose, their cohesion is generally given by the fibers' own liability.
- the individual fibers can have a preferred direction (oriented or cross-layer nonwovens) or non-directional (tangled nonwovens).
- the nonwovens can be mechanically consolidated by needling, meshing or by swirling using sharp water jets.
- Adhesively bonded nonwovens are created by gluing the fibers with liquid binders (e.g. acrylate polymers, SBR / NBR, polyvinyl esters, polyurethane dispersions) or by melting or dissolving so-called binder fibers that were added to the nonwoven during manufacture.
- liquid binders e.g. acrylate polymers, SBR / NBR, polyvinyl esters, polyurethane dispersions
- binder fibers that were added to the nonwoven during manufacture.
- the fiber surfaces are dissolved by suitable chemicals and connected by pressure or welded at elevated temperatures [J. Falbe, M. Regnitz: Römpp-Chemie-Lexikon, 9th edition. Thieme-Verlag, Stuttgart (19
- a second variant is the "spray process", in which the preparation is sprayed onto the passing cloth. This process is suitable for all textiles, but no highly foaming preparations can be applied to the cloth, since the foam development during the spray process is too great becomes.
- fleece or cloth webs run past scraper plates, beams or nozzles, which are continuously loaded with impregnation solution. Different degrees of impregnation can u. a. by varying the contact pressure and the cloth tension speed.
- wipes with strongly moisturizing preparations eg emulsions, "water-free” lipid impregnations
- a method for producing a cleaning article characterized in that a textile with a preparation containing a) one or more anionic surfactants in a total concentration of 1 to 30% by weight and b) one or more liquid or liquid at room temperature viscous lipids in a total concentration of at least 8% by weight, each based on the total weight of the preparation, by immersing the textile in an immersion bath, spraying the textile with the preparation or by stripping Scraper sheets, bars or nozzles of the textile are impregnated on scraper sheets, bars or nozzles secreting with the preparation, and by using a preparation containing a) one or more anionic surfactants in a total concentration of 1 to 30% by weight and b ) one or more lipids which are liquid or viscous at room temperature in a total concentration of at least 8% by weight, in each case based on the total weight of the preparation, for impregnating cosmetic cleaning wipes which foam when applied to the skin and relubricate the skin with lipids.
- the cleaning articles according to the invention (within the scope of this disclosure also always include the cleaning articles produced by the production process according to the invention and the cleaning articles present after the use according to the invention of the preparation according to the invention) have a high moisturizing effect on the skin when used. They also develop a pleasant, fine-bubble foam when used (“rubbing against the skin”). The foaming that occurs during production is surprisingly low.
- WO 03/005982 and WO 03/005983 describe lipid-soaked wipes which, however, do not contain any surfactants in the preparations.
- WO 97/06306 describes wipes with an emulsion-based impregnation.
- US 3795624 describes wipes which are impregnated with a lipid-containing cleaning preparation based on non-ionic surfactants.
- EP 0934056 and WO 98/18442 describe preparations with an oil component content of up to 6% by weight of the preparation.
- WO 99 55303 describes a two-stage production process for impregnated wipes, in which the active ingredient component of the preparation is applied to the wipe after the previously applied surfactant preparation has dried.
- these documents could not point the way to the present invention.
- the cleaning articles according to the invention preferably contain
- lipids which are liquid or viscous at room temperature in a total concentration of at least 8% by weight in each case based on the total weight of the preparation. It is particularly preferred according to the invention if the preparation according to the invention contains one or more lipids which are liquid or viscous at room temperature in a total concentration of at least 20% by weight, based on the total weight of the preparation.
- Lipids which have a viscosity of less than 10,000 mPas are understood according to the invention to be liquid or viscous at room temperature.
- the viscosities are determined according to the invention with the aid of a Viscotester VT 02 viscometer from Haake (temperature: 25 ° C., spindle diameter 24 mm, rotor speed 62.5 1 / min).
- the textiles according to the invention can be smooth or also surface structured.
- Surface-structured substrates are preferred according to the invention.
- the fabric formation can take place by warp and weft, by stitch formation or by interlacing, and / or cohesive and / or adhesive connection of textile fibers. It is preferred according to the invention if the substrate is a composite.
- textiles in the form of nonwovens, in particular made of water-jet bonded and / or water-jet-embossed nonwoven.
- the substrates can advantageously also be designed as a bulk, perforated fleece or mesh.
- textiles in the form of wipes are particularly preferably used.
- Textiles according to the invention can have macro embossments of any desired pattern.
- the selection to be made depends, on the one hand, on the impregnation to be applied and, on the other hand, on the field of application in which the later textile is to be used.
- the textile has a weight of 20 to 120 g / m 2 , preferably 30 to 80 g / m 2, particularly preferably 40 to 60 g / m 2 (measured at 20 ° C. ⁇ 2 ° C and with a humidity of 65% ⁇ 5% for 24 hours).
- the thickness of the textile is preferably 0.2 mm to 2 mm, in particular 0.4 mm to 1.5 mm, very particularly preferably 0.6 mm to 0.9 mm.
- All organic and inorganic fiber materials on a natural and synthetic basis can generally be used as starting materials for the nonwoven fabric of the textile. Examples include viscose, cotton, cellulose, jute, hemp, sisal, silk, wool, polypropylene, polyester, polyethylene terephthalate (PET), aramid, nylon, polyvinyl derivatives, polyurethanes, polylactide, polyhydroxyalkanoate, cellulose esters and / or polyethylene as well as mineral fibers such as glass fibers or carbon fibers.
- the present invention is not limited to the materials mentioned, but a large number of other fibers can be used to form the nonwoven. For the purposes of the present invention, it is particularly advantageous if the fibers used are not water-soluble.
- the fibers consist of a mixture of 60% to 80% viscose with 40% to 20% PET, in particular 70% viscose and 30% PET.
- 70% viscose and 30% PET is particularly advantageous.
- a textile according to the invention can have a mixture of three different fiber materials.
- a mixture of 10% to 80% viscose with 20% to 90% polyester and 0 to 30% cotton is preferred.
- a mixture of 40% viscose and 50% PET and 10% cotton is particularly preferred according to the invention.
- Fibers made of high-strength polymers such as polyamide, polyester and / or highly stretched polyethylene are also particularly advantageous.
- the fibers can also be colored in order to emphasize and / or increase the visual attractiveness of the fleece.
- the fibers can additionally contain UV stabilizers and / or preservatives.
- the fibers used to form the textile preferably have a water absorption rate of more than 60 mm / [10 min] (measured with the EDANA test 10.1-72), in particular more than 80 mm / [10 min].
- the fibers used to form the textile preferably have a water absorption capacity of more than 5 g / g (measured with the EDANA test 10.1-72), in particular more than 8 g / g.
- Advantageous textiles in the sense of the present invention have a tensile strength of in particular [N / 50mm] in the dry state machine direction> 60, preferably> 80 transverse direction> 20, preferably> 30 in the impregnated state machine direction> 4, preferably> 60 transverse direction> 10, preferably> 20
- the stretchability of advantageous textiles is preferably 15% to 100%, preferably 20% and 50% transverse direction 40% to 120%, preferably 50% and 85% in the soaked state machine direction 15% to 100%, preferably 20% and 40, in the dry state % Transverse direction 40% to 120%, preferably 50% and 85%
- crepe papers or tissues can advantageously also be used as textiles.
- Crepe papers e.g. toilet paper can be stretched and made pliable by wet or dry creping; tissue is a particularly thin, soft, mostly wood-free material with fine (dry) creping, which consists of one or more layers and is very absorbent
- the weight per unit area of the individual layer is generally less than 25 g / m 2 before the crepe.
- the papers can also contain other substances, so-called paper auxiliaries. These include fillers (eg kaolin, chalk, titanium dioxide). to improve smoothness and printability as well as for surface treatment, dyes and pigments for coloring or surface coloring, binders (e.g.
- the impregnation medium has a viscosity of 100 to 2000 mPas, preferably of 200 to 1000 mPas.
- the viscosities are determined according to the invention with the aid of a Viscotester VT 02 viscometer from Haake (temperature: 25 ° C., spindle diameter 24 mm, rotor speed 62.5 1 / min).
- the degree of impregnation of the textile i.e. the weight ratio of impregnation preparation to textile
- the degree of impregnation of the textile is from 100% to 1000% and preferably from 200% to 500%.
- the cleaning articles according to the invention are characterized in that one or more compounds selected from the list of the following compounds are used as anionic surfactants a) in the impregnation preparation: sodium myrethsulfate, sodium laureth sulfate, monoisopropanolamine laureth sulfate, sodium acylglutamate, sodium lauroyl sarcosinate, sodium methyl cocoyl taurate, dioctyl succinate, dioctyl succinate, dioctyl succinate, dioctyl succinate, dioctyl succinate, dioctyl succinate
- preparations can contain further anionic, cationic, amphoteric and non-ionic surfactants. These can be selected from the list of the following connections, for example:
- acylglutamates for example di-TEA-palmitoylaspartate and sodium caprylic / capric glutamate,
- acyl peptides for example palmitoyl-hydrolyzed milk protein, sodium cocoyl-hydrolyzed soy protein and sodium / potassium-cocoyl-hydrolyzed collagen,
- sarcosinates for example myristoyl sarcosin, TEA-lauroyl sarcosinate, and sodium cocoyl sarcosinate,
- taurate for example sodium lauroyl taurate
- alaninate carboxylic acids and derivatives such as 1. carboxylic acids, for example lauric acid, aluminum stearate, magnesium alkanolate and zinc undecylenate, 2. ester carboxylic acids, for example calcium stearoyl lactylate, laureth-6-citrate and sodium PEG-4-lauramide carboxylate, 3. ether carboxylic acids, for example sodium laureth-13 carboxylate and sodium PEG-6 cocamide carboxylate,
- Phosphoric acid esters and salts such as DEA-oleth-10-phosphate and dilureth-4-phosphate
- acyl isethionates e.g. Sodium / ammonium cocoyl isethionate
- alkylarylsulfonates for example sodium cocosmonoglyceride sulfate, sodium C12-14 olefin sulfonate, sodium lauryl sulfoacetate and magnesium PEG-3 cocamide sulfate,
- Sulfosuccinates for example, disodium laureth sulfosuccinate, disodium lauryl sulfosuccinate, disodium undecyleneamido MEA sulfosuccinate and PEG-5 lauryl citrate sulfosuccinate.
- Sulfuric acid esters such as
- alkyl ether sulfate for example ammonium, magnesium, TIPA laureth sulfate, sodium myreth sulfate and sodium C ⁇ 2-13 parethsulfate
- alkyl sulfates for example sodium, ammonium and TEA lauryl sulfate.
- Cationic surfactants to be additionally used are 1. alkylamines, 2. alkylimidazoles,
- Quaternary surfactants contain at least one N atom which is covalently linked to 4 alkyl and / or aryl groups. Regardless of the pH value, this leads to a positive charge.
- Advantageous quaternary surfactants are alkyl betaine, alkyl amidopropyl betaine and alkyl amidopropyl hydroxysulfain.
- Cationic surfactants can furthermore preferably be selected for the purposes of the present invention from the group of the quaternary ammonium compounds, in particular benzyltrialkylammonium chlorides or bromides, such as, for example, benzyldimethylstearylammonium chloride, furthermore alkyltrialkylammonium salts, for example cetyltrimethylammonium chloride or bromide, or alkyldomium chloride, Dialkyldimethylammonium chlorides or bromides, alkylamidethyltrimethylammonium ether sulfates, alkyl pyridinium salts, for example lauryl or cetylpyrimidinium chloride, imidazoline derivatives and compounds with a cationic character such as amine oxides, for example alkyldimethylamine oxides or alkylaminoethyldimethylamine oxides. Cetyltrimethylammonium salts are particularly advantageous.
- acyl- / dialkylethylenediamine for example sodium acylamphoacetate, disodium acylamphodipropionate, disodium alkylamphodiacetate, sodium acylamphohydroxy-propylsulfonate, disodium acylamphodiacetate and sodium acylamphopropionate,
- N-alkylamino acids for example aminopropylalkylglutamide, alkylaminopropionic acid, sodium alkylimidodipropionate and lauroamphocarboxyglycinate.
- alkanolamides such as cocamides MEA / DEA / MIPA
- amine oxides such as cocoamidopropylamine oxide
- esters which are formed by esterification of carboxylic acids with ethylene oxide, glycerol, sorbitan or other alcohols,
- ethers for example ethoxylated / propoxylated alcohols, ethoxylated / propoxylated esters, ethoxylated / propoxylated glycerol esters, ethoxylated / propoxylated cholesterols, ethoxylated / propoxylated triglyceride esters, ethoxylated propoxylated lanolin, ethoxylated / propoxylated polysiloxanes, propoxylated POE ethers and Lauryl glucoside, decyl glycoside and cocoglycoside.
- the cleaning article according to the invention are characterized in that are used in the Imsiegnierzurung as liquid or viscous at room temperature for lipids b) one or more compounds selected from the group mineral oil, C 12 i 5 alkyl benzoate, octyldodecanol, soybean oil, cetyl palmitate.
- the impregnation preparation of the cleaning articles according to the invention can advantageously contain further lipophilic ingredients. These can be selected from the list of the following connections, for example:
- Polar oils are, for example, those from the group of lecithins and fatty acid triglycerides, specifically the triglycerol esters of saturated and / or unsaturated, branched and / or unbranched alkane carboxylic acids with a chain length of 8 to 24, in particular 12 to 18, carbon atoms.
- the fatty acid triglycerides can, for example, advantageously be selected from the group of synthetic, semi-synthetic and natural oils, such as e.g. Olive oil, sunflower oil, soybean oil, peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, castor oil, wheat germ oil, grape seed oil, safflower oil, evening primrose oil, macadamia nut oil and the like.
- Particularly advantageous polar lipids for the purposes of the present invention are all native lipids, such as, for. As olive oil, sunflower oil, soybean oil, peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, castor oil, wheat germ oil, grape seed oil, safflower oil, evening primrose oil, macadamia nut oil, corn oil, avocado oil and the like, and those listed below.
- the oil phase can advantageously be selected from the group of dialkyl ethers, the group of saturated or unsaturated, branched or unbranched alcohols. It is particularly advantageous if the oil phase has a content of C 2- i 5 alkyl benzoate or consists entirely of this.
- the oil phase can advantageously be selected from the group of Guerbet alcohols.
- Guerbet alcohols are named after Marcel Guerbet, who described their production for the first time. They arise according to the reaction equation R ⁇ R - CH 2 --CH 2 - OH R - CH - CH 2 - OH catalyst
- Guerbet alcohols are liquid even at low temperatures and practically cause no skin irritation. They can advantageously be used as greasing, over-greasing and also moisturizing components in skin and hair care products.
- R 1 and R 2 are generally unbranched alkyl radicals.
- the Guerbet alcohol or alcohols are advantageously selected from the
- R1 propyl, butyl, pentyl, hexyl, heptyl or octyl and
- R 2 hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl or tetradecyl.
- Guerbet alcohols preferred according to the invention are 2-butyloctanol - it has the chemical structure
- the total amount of Guerbet alcohols in the finished cosmetic or dermatological preparations is advantageously selected from the range up to 25.0% by weight, preferably 0.5-15.0% by weight, based on the total weight of the preparations.
- any mixtures of such oil and wax components can also be used advantageously for the purposes of the present invention. It may also be advantageous to use waxes, for example cetyl palmitate, as the sole lipid component of the oil phase.
- Nonpolar oils are, for example, those which are selected from the group of branched and unbranched hydrocarbons and waxes, in particular petroleum jelly (Petrolatum), paraffinol, squalane and squalene, polyolefins and hydrogenated polyisobutenes.
- petroleum jelly Petroleum jelly
- paraffinol squalane and squalene
- polyolefins polyolefins
- hydrogenated polyisobutenes are the preferred substances.
- the oil phase can advantageously be selected from the group of branched and unbranched hydrocarbons and waxes, the dialkyl ethers, the group of saturated or unsaturated, branched or unbranched alcohols, and also the fatty acid triglycerides, especially the triglycerol esters of saturated and / or unsaturated, branched and / or unbranched alkane carboxylic acids with a chain length of 8 to 24, in particular 12-18 carbon atoms.
- the fatty acid triglycerides can, for example, advantageously be selected from the group of synthetic, semisynthetic and natural oils, e.g. Olive oil, sunflower oil, soybean oil, peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, palm kernel oil and the like, provided the conditions specified in the main claim are met.
- Fat and / or wax components to be used advantageously according to the invention can be selected from the group of vegetable waxes, animal waxes, mineral waxes and petrochemical waxes.
- Inexpensive according to the invention are, for example, candelilla wax, camamauba wax, japan wax, esparto grass wax, cork wax, guaruma wax, rice germ oil wax, sugar cane wax, berry wax, ouricury wax, montan wax, jojoba wax, shea butter, beeswax, shellac wax, walnut, lanolin (wool wax), pretzel fat, cerium wax Ozokerite (earth wax), paraffin waxes and micro waxes, provided the conditions specified in the main claim are met.
- fat and / or wax components are chemically modified waxes and synthetic waxes, such as those available under the tradenames Syncrowax HRC (glyceryl tribehenate), and Syncrowax AW 1C (C 18- 36 fatty acid) in the CRODA GmbH and Montanesterwachse, sasol waxes, hydrogenated jojoba waxes, synthetic or modified beeswaxes (e.g. dimethicone copolyol beeswax and / or C 30-50- alkyl beeswax), polyalkylene waxes, polyethylene glycol waxes, but also chemically modified fats, e.g. B.
- Syncrowax HRC glycol tribehenate
- Syncrowax AW 1C C 18- 36 fatty acid
- hydrogenated vegetable oils for example hydrogenated castor oil and / or hydrogenated coconut fat glycerides
- triglycerides such as trihydroxystearin, fatty acids, fatty acid esters and glycol esters, such as for example C 20-4 o-alkyl stearate, C 2 o-o-alkylhydroxystearoyl stearate and / or glycol montanate.
- organosilicon compounds which have similar physical properties to the fat and / or wax components mentioned, such as stearoxytrimethylsilane, provided the conditions specified in the main claim are met.
- the fat and / or wax components can be present either individually or in a mixture. Any mixtures of such oil and wax components can also be used advantageously for the purposes of the present invention.
- the oil phase selected from the group of 2-ethyl hexyl isostearate, octyldodecanol, isotridecyl isononanoate, butylene glycol dicaprylate / dicaprate, 2-ethylhexyl cocoate, C 12-1 5-alkyl benzoate, caprylic-capric acid triglyceride, dicaprylyl ether provided the conditions required in the main claim be respected.
- hydrocarbons paraffinol, cycloparaffin, squalane, squalene, hydrogenated polyisobutene or polydecene are to be used advantageously for the purposes of the present invention, provided the conditions specified in the main claim are met.
- silicone oils can be present as monomers, which are usually characterized by structural elements, as follows:
- Silicone oils are high-molecular synthetic polymeric compounds in which silicon atoms are linked in a chain and / or network-like manner via oxygen atoms and the remaining valences of silicon by hydrocarbon residues (mostly methyl, more rarely ethyl, propyl, phenyl groups etc.) are saturated.
- silicon atoms can be substituted with the same or different alkyl radicals and / or aryl radicals, which are generally represented here by the radicals R 1 - R 4 (to say that the number of different radicals is not necessarily limited to up to 4), m can assume values from 2 - 200,000.
- linear silicone oils are systematically referred to as polyorganosiloxanes; the methyl-substituted polyorganosiloxanes, which are the most important compounds of this group in terms of quantity and are distinguished by the following structural formula
- Dimethicone is also known as polydimethylsiloxane or dimethicone (INCI). Dimethicone is available in different chain lengths or with different molecular weights. Dimethicones of different chain lengths and phenyltrimethicones are particularly advantageous linear silicone oils for the purposes of the present invention.
- Particularly advantageous polyorganosiloxanes for the purposes of the present invention are, for example, dimethylpolysiloxanes [poly (dimethylsiloxane)], which, for. B. are available under the trade names ABIL 10 to 10,000 from Th. Goldschmidt.
- phenylmethylpolysiloxanes INCI: phenyl dimethicone, phenyl trimethicone
- cyclic silicones octamethylcyclotetrasiloxane or decamethylcyclopentasiloxane
- amino-modified silicones INCI: Amodimethicone
- silicone waxes e.g. B.
- Polysiloxane-polyalkylene copolymers (INCI: Stearyl Dimethicone and Cetyl Dimethicone) and Dialkoxydimethylpolysiloxane (Stearoxy Dimethicone and Behenoxy Stearyl Dimethicone), which are available as different Abil-Wax types from Th. Goldschmidt.
- n can take values from 3/2 to 20. Broken values for n take into account that there may be odd numbers of siloxyl groups in the cycle.
- Particularly advantageous cyclic silicone oils for the purposes of the present invention are cyclomethicones, in particular cyclomethicones D5 and / or cyclomethicones D6.
- Advantageous silicone oils or silicone waxes in the sense of the present invention are cyclic and / or linear silicone oils and silicone waxes.
- Phenyltrimethicone is advantageously chosen as the silicone oil.
- Other silicone oils for example dimethicone, phenyldimethicone, cyclomethicone (octamethylcyclotetrasiloxane), for example hexamethylcyclotrisiloxane, polydimethylsiloxane, poly (methylphenylsiloxane), cetyldimethicone, behenoxydimethicone, can also be used advantageously for the purposes of the present invention.
- silicone oils of a similar constitution to the compounds described above, the organic side chains of which are derivatized, for example polyethoxylated and / or polypropoxylated.
- these include, for example, poly-siloxane-polyalkyl-polyether copolymers such as the cetyl-dimethicone copolyol and the cetyl-dimethicone copolyol (and) polyglyceryl-4-isostearate (and) hexyl laurate.
- the preparations according to the invention can advantageously contain one or more moisturizing or moisturizing agents.
- moisturizing or moisturizing agents for the purposes of the present invention are, for example, glycerol, lactic acid and / or lactates, in particular sodium lactate, butylene glycol, propylene glycol, biosaccaride Gum-1, glycine soybean, ethylhexyloxyglycerol, pyrrolidonecarboxylic acid and urea.
- polymeric moisturizers from the group of water-soluble and / or water-swellable and / or water-gelable polysaccharides.
- the preparations according to the invention can advantageously contain vitamins and vitamin derivatives and antioxidants. These include vitamins A, B 1-6 , B 12 , C, D, E, F, H, K and PP and their derivatives. According to the invention, these can advantageously be present in a concentration of 0.001 to 10% by weight, preferably 0.05 to 7% by weight, particularly preferably 0.5 to 5% by weight, in each case based on the total weight of the preparation.
- Retinyl palmitate, ascorbyl glucoside, tocopheryl acetate, tocopheryl palmitate, niacinamide, panthenol are used as the preferred vitamin derivatives according to the invention.
- active substances in the sense of the present invention are natural active substances and / or their derivatives, such as.
- other pharmaceutically or dermatologically active substances such as substances that soothe and care for the skin
- substances that soothe and care for the skin include, for example, panthenol, allantoin, tannin as well as plant substances such as azulene and bisabolol, glycyrrhizin, hamamelin and plant extracts such as chamomile, aloe vera, hamazelis and licorice root.
- the amount of the aforementioned active ingredients (one or more compounds) in the preparations is preferably 0.001 to 30% by weight, particularly preferably 0.05-20% by weight, in particular 1-10% by weight, based on the total weight of the Preparation.
- the compositions contain, in addition to the above-mentioned substances, optionally further additives customary in cosmetics, for example perfume, dyes, antimicrobial substances, refatting agents, complexing and sequestering agents, pearlescent agents, plant extracts, self-tanning agents (eg DHA), depigmenting agents, Antidandruff active ingredients, vitamins, other active ingredients, complexes of gamma-oryzanol and calcium salts, niacinamide and its derivatives, panthenol and its derivatives, subtilisin, minerals, preservatives, bactericides, pigments that have a coloring effect, thickeners, softening, moisturizing and / or moisturizing Substances, or other common components of a cosmetic or dermatological formulation such as alcohols, polyols, polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives.
- customary in cosmetics for example perfume, dyes, antimicrobial substances, refatting agents, complexing and sequestering
- the pH of the preparations according to the invention is adjusted in the manner customary for the person skilled in the art with the appropriate acids (lactic acid, citric acid, phosphoric acid etc.) and bases (for example NaOH).
- acids lactic acid, citric acid, phosphoric acid etc.
- bases for example NaOH.
- the following examples are intended to illustrate the compositions according to the invention, but are not intended to limit the invention to these examples.
- the numerical values in the examples mean percentages by weight, based on the total weight of the respective preparations.
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- Cosmetics (AREA)
Abstract
La présente invention concerne un article de nettoyage constitué d'une matière textile imprégnée d'une préparation contenant a) un ou plusieurs agents tensioactifs anioniques, dans une concentration totale de 1 à 30 % en poids, et b) un ou plusieurs lipides liquides ou visqueux à température ambiante, dans une concentration totale d'au moins 8 % en poids, respectivement par rapport au poids total de la préparation. La présente invention concerne également la production de cet article, ainsi que son utilisation.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10352370A DE10352370A1 (de) | 2003-11-10 | 2003-11-10 | Lipidhaltiges Substrat |
PCT/EP2004/052795 WO2005044220A1 (fr) | 2003-11-10 | 2004-11-04 | Substrat contenant des lipides |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1684872A1 true EP1684872A1 (fr) | 2006-08-02 |
Family
ID=34559536
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP04818153A Ceased EP1684872A1 (fr) | 2003-11-10 | 2004-11-04 | Substrat contenant des lipides |
Country Status (4)
Country | Link |
---|---|
US (1) | US20070082033A1 (fr) |
EP (1) | EP1684872A1 (fr) |
DE (1) | DE10352370A1 (fr) |
WO (1) | WO2005044220A1 (fr) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0422026D0 (en) * | 2004-10-05 | 2004-11-03 | Unilever Plc | Laundry product |
ITTO20050788A1 (it) * | 2005-11-09 | 2007-05-10 | Sagitta Srl | Procedimento per il trattamento di tessuti e capi di abbigliamento |
BRPI0910382B1 (pt) | 2008-07-18 | 2021-07-06 | Biomod Concepts Inc | Artigo para aplicar um ingrediente ativo, veículo de aplicação para transferência de micropartículas a um substrato, micropartícula para liberar um ingrediente ativo e método para liberar um ingrediente ativo |
US8071524B2 (en) * | 2009-05-18 | 2011-12-06 | Hoover, Inc. | Biodegradable wipe utilizing bio-based lubricant comprising refined soybean oil |
US9949902B2 (en) | 2012-06-29 | 2018-04-24 | Kimberly-Clark Worldwide, Inc. | Stable emulsion for prevention of skin irritation and items using same |
US9511006B2 (en) | 2012-06-29 | 2016-12-06 | Kimberly-Clark Worldwide, Inc. | Dispersible moist wipe with emulsion for prevention of skin irritation |
US9393197B2 (en) | 2012-06-29 | 2016-07-19 | Kimberly-Clark Worldwide, Inc. | Stable emulsion for prevention of skin irritation and articles using same |
DE102015212822A1 (de) | 2015-07-09 | 2017-01-12 | Beiersdorf Ag | Reinigungstücher getränkt mit Tränkungsmitteln basierend auf einer Mizellentechnologie |
DE102019202723A1 (de) | 2019-02-28 | 2020-09-03 | Beiersdorf Ag | Reinigungstücher getränkt mit Tränkungsmitteln enthaltend Biotenside |
JP7395611B2 (ja) | 2019-04-17 | 2023-12-11 | ザ プロクター アンド ギャンブル カンパニー | カプセル |
EP3956054A1 (fr) | 2019-04-17 | 2022-02-23 | The Procter & Gamble Company | Procédés de fabrication de capsules |
DE102020212222A1 (de) | 2020-09-29 | 2022-03-31 | Beiersdorf Aktiengesellschaft | Reinigungstücher getränkt mit Tränkungsmitteln basierend auf einer Öl-in-Wasser-Emulsion |
DE102020212221B3 (de) | 2020-09-29 | 2022-01-27 | Beiersdorf Aktiengesellschaft | Verbesserte Reinigungstücher getränkt mit Tränkungsmitteln basierend auf Hydrodispersionen |
WO2022082187A1 (fr) | 2020-10-16 | 2022-04-21 | The Procter & Gamble Company | Compositions antitranspirantes et déodorantes comprenant des capsules |
WO2022082192A1 (fr) * | 2020-10-16 | 2022-04-21 | The Procter & Gamble Company | Article de nettoyage à revêtement préférentiel |
MX2023004228A (es) | 2020-10-16 | 2023-04-21 | Procter & Gamble | Particulas aditivas para el cuidado de la ropa. |
US11912961B2 (en) | 2020-10-16 | 2024-02-27 | The Procter & Gamble Company | Liquid fabric care compositions comprising capsules |
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US6440437B1 (en) * | 2000-01-24 | 2002-08-27 | Kimberly-Clark Worldwide, Inc. | Wet wipes having skin health benefits |
EP1470813A2 (fr) * | 2003-04-24 | 2004-10-27 | Beiersdorf AG | Emulsion de nettoyage à taux de matière grasse élevés |
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US3795624A (en) * | 1972-04-07 | 1974-03-05 | Plough | Means for removing cosmetics |
NZ205183A (en) * | 1982-08-13 | 1987-01-23 | Unilever Plc | Wiping cloth includes a liquid"active material" |
US5624676A (en) * | 1995-08-03 | 1997-04-29 | The Procter & Gamble Company | Lotioned tissue paper containing an emollient and a polyol polyester immobilizing agent |
US6028018A (en) * | 1996-07-24 | 2000-02-22 | Kimberly-Clark Worldwide, Inc. | Wet wipes with improved softness |
US5972361A (en) * | 1996-10-25 | 1999-10-26 | The Procter & Gamble Company | Cleansing products |
JP2001503051A (ja) * | 1996-10-25 | 2001-03-06 | ザ、プロクター、エンド、ギャンブル、カンパニー | クレンジング製品 |
US6338855B1 (en) * | 1996-10-25 | 2002-01-15 | The Procter & Gamble Company | Cleansing articles for skin and/or hair which also deposit skin care actives |
US6063397A (en) * | 1996-10-25 | 2000-05-16 | The Procter & Gamble Company | Disposable cleansing products for hair and skin |
US6683041B1 (en) * | 1996-12-05 | 2004-01-27 | The Procter & Gamble Company | Wet-like articles comprising a multi-phase, multi-component emulsion and an activation web |
US5908707A (en) * | 1996-12-05 | 1999-06-01 | The Procter & Gamble Company | Cleaning articles comprising a high internal phase inverse emulsion and a carrier with controlled absorbency |
ZA98828B (en) * | 1997-03-04 | 1999-08-02 | Unilever Plc | System comprising synthetic detergent bar and pouf for holding bar. |
US6326339B1 (en) * | 1997-03-04 | 2001-12-04 | Lever Brothers Company, Division Of Conopco, Inc. | Cleansing system comprising synthetic detergent bar and pouf |
US6132746A (en) * | 1997-05-22 | 2000-10-17 | The Procter & Gamble Company | Cleansing products with improved moisturization |
US6280757B1 (en) * | 1997-05-22 | 2001-08-28 | The Procter & Gamble Company | Cleansing articles for skin or hair |
GB9716273D0 (en) * | 1997-07-31 | 1997-10-08 | Kimberly Clark Ltd | Hand cleanser |
WO1999012519A1 (fr) * | 1997-09-05 | 1999-03-18 | The Procter & Gamble Company | Produits de nettoyage et de conditionnement pour la peau et les cheveux ayant de meilleures qualites d'application des ingredients de conditionnement |
ATE226064T1 (de) * | 1997-09-12 | 2002-11-15 | Procter & Gamble | Hautreinigungs- und konditionierungsartikel für haut und haar |
EP1071396A1 (fr) * | 1998-04-24 | 2001-01-31 | The Procter & Gamble Company | Produits d'hygiene pour la peau et/ou les cheveux deposant de plus des ingredients actifs traitant la peau |
DE10059584A1 (de) * | 2000-11-30 | 2002-06-06 | Beiersdorf Ag | Kosmetische oder dermatologische getränkte Tücher |
EP1275370A1 (fr) * | 2001-07-13 | 2003-01-15 | Johnson and Johnson GmbH | Produits contenant une feuille et une phase aqueuse et lipidique |
EP1275371A1 (fr) * | 2001-07-13 | 2003-01-15 | Johnson and Johnson GmbH | Produits secs comprenant une feuille et deux phases |
-
2003
- 2003-11-10 DE DE10352370A patent/DE10352370A1/de not_active Withdrawn
-
2004
- 2004-11-04 WO PCT/EP2004/052795 patent/WO2005044220A1/fr active Application Filing
- 2004-11-04 EP EP04818153A patent/EP1684872A1/fr not_active Ceased
- 2004-11-04 US US10/578,727 patent/US20070082033A1/en not_active Abandoned
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6440437B1 (en) * | 2000-01-24 | 2002-08-27 | Kimberly-Clark Worldwide, Inc. | Wet wipes having skin health benefits |
EP1470813A2 (fr) * | 2003-04-24 | 2004-10-27 | Beiersdorf AG | Emulsion de nettoyage à taux de matière grasse élevés |
Non-Patent Citations (1)
Title |
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See also references of WO2005044220A1 * |
Also Published As
Publication number | Publication date |
---|---|
DE10352370A1 (de) | 2005-06-23 |
WO2005044220A1 (fr) | 2005-05-19 |
US20070082033A1 (en) | 2007-04-12 |
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