EP3038591A1 - Emulsifier-free, skin conditioning and active ingredient-containing cosmetic or dermatological preparation - Google Patents

Emulsifier-free, skin conditioning and active ingredient-containing cosmetic or dermatological preparation

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Publication number
EP3038591A1
EP3038591A1 EP14755810.0A EP14755810A EP3038591A1 EP 3038591 A1 EP3038591 A1 EP 3038591A1 EP 14755810 A EP14755810 A EP 14755810A EP 3038591 A1 EP3038591 A1 EP 3038591A1
Authority
EP
European Patent Office
Prior art keywords
preparation according
skin
substances
preparation
copolymer
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
Application number
EP14755810.0A
Other languages
German (de)
French (fr)
Inventor
Cathrin Scherner
Inken GROTH
Magdalena VON WEDEL-PARLOW
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beiersdorf AG
Original Assignee
Beiersdorf AG
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
Application filed by Beiersdorf AG filed Critical Beiersdorf AG
Publication of EP3038591A1 publication Critical patent/EP3038591A1/en
Ceased legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/927Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of insects, e.g. shellac
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/31Hydrocarbons
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/342Alcohols having more than seven atoms in an unbroken chain
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35Ketones, e.g. benzophenone
    • A61K8/355Quinones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/66Enzymes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/87Polyurethanes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/004Aftersun preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/02Preparations for care of the skin for chemically bleaching or whitening the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/04Preparations for care of the skin for chemically tanning the skin
    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/30Characterized by the absence of a particular group of ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/30Characterized by the absence of a particular group of ingredients
    • A61K2800/33Free of surfactant

Definitions

  • Emulsifier-free, skin-conditioning and active ingredient-containing cosmetic or dermatological preparation Emulsifier-free, skin-conditioning and active ingredient-containing cosmetic or dermatological preparation
  • the invention comprises an emulsifier-free, skin-conditioning cosmetic or dermatological preparation with active ingredients.
  • the preparation is suitable for application on wet skin without being completely rinsed off and thus allows the creaming and the application of skin care and / or during the shower
  • WO 2013064391 A2 describes cosmetic or dermatological preparations which make it possible to apply cream under the shower.
  • the invention is an emulsifier-free cosmetic or dermatological preparation comprising one or more polyacrylic acid polymers, one or more C14-22 fatty alcohols and one or more waxes and / or a hydrocarbon mixture and one or more active substances.
  • the preparation preferably comprises waxes, in particular Cera Microcristallina, in the range of more than 0.5% by weight, in particular more than 13% by weight, based on the total mass of the preparation.
  • the preferred level refers to both individual waxes and preferably the total amount of multiple waxes.
  • Active ingredients according to the invention include all cosmetically or dermatologically active substances, in particular those substances which have a skin-care and / or skin-protecting property.
  • the active ingredients may preferably be selected from the group of skin care substances, self-tanning agents, cooling substances, warming substances and / or whitening substances.
  • one or more active substances are preferably selected from only one of the abovementioned groups.
  • one or more may be selected from the group of cyclodextrin, ubiquinone, creatine, 1-methylhydantoin-2-imide, glycine soy germ extract, ascorbic acid (vitamin C and its derivatives), ascorbyl palmitate, sodium ascorbyl phosphate, pimpinella anisum Fruit Extract, Arctium Lappa Fruit Extract, Magnolia Officinalis Bark Extract, Sodium Hyaluronate, Taurine, Foil Acid, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Glucosylrutin and Isoquercitrin, Carnitine, Sodium Chloride, Glyceryl Glucoside, Climbazole, Piroctone Olamine, Oryzanol, BHT, Tocopherol, Vitamins, especially Vitamin E and A and their derivatives, Tocopheryl Acetate, Nelumbo Nucifera Leaf Extract, Caffeine, Camellia Sinensis Leaf Extract,
  • Cyanomethylphenyl Menthane Carboxamide Chelidonium Majus Extract, Salicylic Acid, 4-Butylresorcinol, Paullinia Cupana Seed Extract, Butyl Acrylate / Ethyltrimonium Chloride, Methacrylate / Styrene Copolymer, Octenidine HCl, Urea, Octadecenedioic Acid,
  • D-biotin, coenzyme Q10, folic acid and / or derivatives thereof, rucinol, panthenol, niacinamide, alpha-glucosylrutin, carnitine, carnosine, natural and / or synthetic isoflavonoids, creatine, taurine, .beta.-alanine, 1 can be selected as preferred active ingredients -Methylhydantoin-2-imide, N- (4- (2,4-dihydroxyphenyl) thiazol-2-yl) isobutyramide, Glycine Soy Germ Extract, Pimpinella Anisum Fruit Extract, Arctium Lappa Fruit Extract, Magnolia Officinalis Bark Extract, Sodium Hyaluronate, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Glucosylrutin and
  • Q10 should be selected as active ingredient.
  • DHA 1, 3-dihydroxyacetone
  • self-tanning substances as active ingredients in the preparation according to the invention allows a time-saving application and the entire body can be browned so easily for the first time.
  • the circulation stimulating substances such as capsaicinoids as
  • circulation-promoting agents are preferably used
  • Vanilyl butyl ether (0.5 - 2.5%)
  • Nicotinic acid benzyl ester (0.5 - 4.0%)
  • NSAIDs non-steroidal antiinflammatory drugs
  • these are aspirin (acetylsalicylic acid), diflunisal, salsalates, ibuprofen, etofenamate, dexibuprofen, naproxen, fenoprofen, ketoprofen, dexketoprofen, flurbiprofen, oxaprozin, loxoprofen, indomethacin, tolmetin, sulindac, etodolac, ketorolac, diclofenac, nabumetone, piroxicam, meloxicam , Tenoxicam, droxicam, lornoxicam, isoxicam, mefenamic acid, meclofenamic acid,
  • Flufenamic acid Flufenamic acid, tolfenamic acid, celecoxib, rofecoxib, valdecoxib, parecoxib,
  • Menthol is part of the well-known Japanese peppermint oil (CAS: 20747-49-3). The most important isomer is (-) - menthol. Menthol produced when rubbed on the skin due
  • Oleum Eucalypti Oleum Menthae piperitae, Oleum camphoratum, Oleum Rosmarini, Oleum Thymi, Oleum pinis sibricum and Oleum Pini silverstris, as well as the terpenes 1, 8-cineol and levomethanol, as well as oleum Abietis albae, Oleum anisi, Oleum aurantii Floris, can also be used as further preferred essential oils , Oleum Bergamottae, Oleum Calendulae infusum, Oleum Caryophylli, Oleum Chamomillae, Oleum Cinnamomi ceylanici, Oleum Citri, Oleum
  • Citronellae Oleum Cupressi, Oleum Cymbopogonis, Oleum Jecoris, Oleum Lavendulae, Oleum Macidis, Oleum Majoranae, Oleum Melaleucae viridiflorae, Oleum Melissae, Oleum Menthae arvensis, Oleum Millefolium, Oleum Myrrhae, Oleum myrtle, Oleum Pini sibricum, Oleum Pinisilvestris, Oleum Salviae, Oleum Santali, Oleum Terebinthinae rectificat, Oleum Valerianae and Oleum Zingiberis are used.
  • the essential oils are used individually or in combination with others in a proportion of a total of 0.001 to 10 wt.%, In particular 0.01 to 1 wt.% In the preparation, based on the total mass of the preparation without propellant.
  • substances which are known for warming properties such as, for example, HotAct (vanillyl butyl ether) and / or capsicum, can also be used instead of the substances having a seemingly cooling effect.
  • HotAct vanillyl butyl ether
  • capsicum capsicum
  • Whitening fabrics are substances for skin whitening. This refers to the bleaching or coating of human skin to make it lighter for cosmetic purposes.
  • Preferred whitening substances are rucinol, hydroquinones, kojic acid, liquorice root extract, N- (4- (2,4-dihydroxyphenyl) thiazol-2-yl) isobutyramide, Camu Camu, licoriche, acerola or vitamin C.
  • tyrosinase inhibitors and melanin synthesis inhibitors, since the inhibition of tyrosinase results in the inhibition of melanin synthesis, but the inhibition of melanin synthesis does not necessarily mean tyrosinase inhibition.
  • melaninase inhibition For example, rucinol, hydroquinones and kojic acid also inhibit tyrosinase.
  • the use concentration in parts by weight of one or more of the active ingredients in the applied preparation is preferably up to 25% by weight, in particular in the range between 0.001% by weight and 20% by weight, based on the total mass of the preparation.
  • the active compounds from the group of lipophilic compounds.
  • the basic preparation according to the invention is composed of predominantly lipophilic substances, it is thus possible to achieve a longer retention on the skin.
  • the preparation according to the invention preferably comprises as active ingredients Q10 and menthol.
  • the remaining of active ingredients after rinsing and drying on the skin by the preparation according to the invention succeeds.
  • the application of the combination of special fatty alcohols, waxes and advantageously one or more film formers leads to a skin protection and / or skin care even under the shower.
  • the preparations according to the invention advantageously comprise one or more film formers.
  • film formers are advantageously selected from the group hexadecene copolymer, trimethylsiloxysilicate, polypropylsilsesquioxane, polysilicone-25,
  • Acrylate copolymer polyurethane, methacrylate, polyglyceryl stearate, dilinoleate crosspolymer, alkyl acrylate / methacrylic acid crosspolymer, IPDI copolymer, in particular
  • the proportion of film formers is advantageously selected in the range of 0.1% by weight, in particular 0.5% by weight to 10% by weight, based on the total mass of the preparation.
  • the protective film that forms on the skin is examined, once after the application of a rinse off product with integrated skin care aspects (Nivea cream soft shower gel) alone and once after application of the same product (Nivea cream soft shower gel) and subsequent application of the inventive preparation. After both applications, the skin is rinsed with water.
  • the skin refatting measurements were made by IR imaging. The measurement technique is called IR-ATR (InfraRed-Attenuated Total Reflectance).
  • the protective film of the invention comprises a skin-forming film comprising one or more active ingredients.
  • Advantageous and thus longer in the film and thus remaining on the skin are lipophilic drugs to choose.
  • the skin conditioning according to the invention comprises moisturizing
  • the protective film can be detected by means of IR-ATR measurement technology and ideally has a thickness of at least 1 ⁇ m to 10 ⁇ m.
  • the skin conditioning according to the invention is characterized in that the protective film on the skin comprises one or more active substances, one or more lipids and one or more skin moisturizing agents and no skin barrier damaging substances, in particular no emulsifiers and / or surfactants, are included.
  • fatty alcohols In the preparation according to the invention are one or more fatty alcohols and at least one additional wax and / or mixture of liquid and solid
  • Hydrocarbons having a melting range of 5 ° C to 75 ° C, preferably up to 55 ° C (according to DSC), given together, in particular melted.
  • At least one wax is present in addition to at least one fatty alcohol or, in addition to fatty alcohol, at least one mixture of liquid and solid is present
  • hydrocarbons Contain hydrocarbons. Ideally, it contains fatty alcohol, wax and a mixture of hydrocarbons.
  • fatty alcohols are myristyl, cetearyl and / or stearyl alcohols, as waxes Cera Microcristallina, Coco-Glyceride, C18-36 Acid Triglyceride, Synthetic Wax, Cera Alba, Paraffin, Copernicia Cerifera Cera, C18-38 Alkyl Hydroxystearoyl Stearate,
  • Preferred use concentrations of the wax or wax is in the range of 0.5 to 20 wt.%, Based on the total mass of the preparation.
  • the fatty alcohols, waxes and hydrocarbon mixtures advantageously all have a melting range of 5 ° C. to 75 ° C., preferably up to 55 ° C. (according to DSC).
  • DSC Densilic Recanning Calorimetry
  • DSC is a thermal method for measuring emitted / absorbed heat quantity of a sample during isothermal operation, heating or cooling (see DIN 53765, DIN 51007, ASTM E 474, ASTM D 3418).
  • DSC is a comparative measurement method that enables the determination of heat quantities of physical and chemical processes. If a material is his
  • the method runs cyclically, so that after the first heating curve, a defined cooling takes place and then the sample is heated again in the specified temperature range. This gives two different kinds of information: In the first heating curve, all thermal effects, including the prehistory, are discernible. In the second heating curve, the history has been eliminated and the pure thermal behavior of the sample under defined cooling conditions can be evaluated.
  • the melting range of fatty alcohols, waxes or hydrocarbons between 4.5 ° C and 75 ° C according to DSC is the range determined in the first heating curve.
  • Fats and fat-like substances with a waxy consistency can also be used according to the invention as waxes. These include u.a. Fats (triglycerides), mono and diglycerides, natural and synthetic waxes, fatty and wax alcohols, esters of fatty alcohols and fatty acids and fatty acid amides or any mixtures of this substance.
  • Fats triglycerides
  • mono and diglycerides natural and synthetic waxes
  • fatty and wax alcohols esters of fatty alcohols and fatty acids and fatty acid amides or any mixtures of this substance.
  • waxes from the group of fats in particular from the group of natural waxes: Shorea Stenoptera Seed Butter, Hydrogenated Vegetable Oil, Hydrogenated Coco-Glycerides, Butyrospermum Parkii Butter, Theobroma Cocoa (Cocoa) Seed Butter, Mango Butter, Hydrogenated Palm Kernel Glycerides, Hydrogenated Palm Glycerides, Sunflower Seed Wax, Soybean Glycerides, Butyrospermum Parkii
  • Palmitic Acid Stearic Acid
  • the fatty alcohols used are preferably C14 to C22 fatty alcohols.
  • the fatty alcohols are preferably selected from the group consisting of linear fatty alcohols, especially myristyl (C14H 30 O), cetyl alcohol (or palmityl) (C 6 H 34 0), stearyl alcohol (or
  • Octadecyl C 8 H 38 0
  • cetyl stearyl alcohol cetearyl alcohol
  • behenyl alcohol lanolin alcohol
  • lanolin alcohol a mixture of the alcohols cetyl alcohol hexadecanol
  • stearyl alcohol octadecanol
  • the proportion of total C 14-22 fatty alcohols is advantageously from 0.5 to 14% by weight, in particular from 7 to 9% by weight, or in particular from 0.5 to 5%, based on the total mass of the preparation.
  • Hydrocarbon gels or mixtures of liquid and solid paraffin hydrocarbons are preferably used as hydrocarbon mixtures.
  • the content of solid hydrocarbons in the hydrocarbon mixture is preferably between 1 and 50%, particularly preferably between 10 and 30%.
  • Advantageous is the use of
  • Hydrocarbon mixtures which form fringe micelles or paracrystalline structures.
  • the proportion of the total hydrocarbon mixture is advantageously 1 to 50 wt.%, In particular 20 to 30 wt.%, Based on the total mass of the preparation.
  • Fatty alcohol, in particular two or three fatty alcohols, according to the invention are necessarily included in the preparation.
  • one or more waxes are added to the preparation.
  • a hydrocarbon mixture of liquid and solid hydrocarbons which are liquid at room temperature may also be added.
  • the preparation comprises all three building blocks, fatty alcohols, waxes and
  • the preparation and preparation according to the invention may then be admixed with cosmetic or dermatological substances known to the person skilled in the art, the addition of which may not impair the skin-conditioning properties of the preparation obtainable.
  • cosmetic or dermatological substances known to the person skilled in the art, the addition of which may not impair the skin-conditioning properties of the preparation obtainable.
  • thickeners, fillers and neutralizing agents are added to the preparations.
  • Thickeners are advantageously suitable for stabilizing the system and enhance the skin-conditioning properties and the special skin feel of the preparations according to the invention.
  • aluminum Starch Octenylsuccinat is preferably added, which also leads to an optimization of the skin feel by the skin protection film acts a little more velvety.
  • Sodium hydroxide solution is advantageously added as a neutralizing agent so that the thickeners can form their gel network and a stable system is formed.
  • the preparation according to the invention is emulsifier-free. That the optionally acting as emulsifying polyacrylic acid polymers are not understood according to the invention as emulsifiers.
  • Emulgatorhin also includes a minimum content of additional emulsifiers of less than 1 wt.%, Based on the total mass of the preparation, which may be included for example by impurities or entrainment. The influence on the product performance may be irrelevant in these quantity ranges.
  • Polyacrylic acid polymers are understood as meaning the polymers of acrylic and / or methacrylic acid known in cosmetics and acrylate crosspolymers.
  • these are high molecular weight polymers (macromolecules) (> 1 Mg / mole) composed of a backbone of polyacrylic acid and small amounts
  • Polyalkenylether cross-links exist. They are also referred to as carbomers. These water-soluble or dispersible polymers can cause a significant increase in viscosity in the liquid in which they are dissolved or dispersed. This is caused by the formation of carbomer microgels in the water.
  • Particularly preferred polyacrylic acid polymers are, in addition to the carbomers, those acrylate crosspolymers which exert a polymeric emulsifier action.
  • Polymer emulsifiers are mainly high polyacrylic acid polymers
  • emulsifying polyacrylic acid polymers have a small lipophilic portion in addition to the hydrophilic body.
  • acrylate crosspolymers which have the INCI name "Acrylates / C 10-30 Alkyl Acrylate Crosspolymer" have and among the
  • the polyacrylic acid polymers are particularly preferably selected from the group of acrylates / C 10-30 alkyl acrylate crosspolymers and / or carbomers. Especially preferred are acrylates / C 10-30 alkyl acrylate crosspolymer Pemulen® TR-1, e.g. from Lubrizol and Carbopol® 3128 from Lubrizol.
  • a specific combination of polyacrylic acid polymers having an emulsifying action such as the Pemulen TR-1 with other polyacrylic acid polymers, such as Carbopol 3128, which improve the sensory properties and ensure the stability of the preparation, especially at higher temperatures, and a connection with free water.
  • Particularly preferred herein is a combination of three polyacrylic acid polymers wherein a polyacrylic acid polymer has an emulsifying effect, e.g. the pemulen TR-1 or pemulen TR-2, with other polyacrylic acid containing the sensory
  • the preparation according to the invention therefore advantageously comprises at least three polyacrylic acid polymers, in particular three polyacrylic acid polymers, which differ in their properties.
  • the proportion of total polyacrylic acid polymers is preferably 0.05 to 2 wt.%, In particular 0.2 to 1 wt.%, Based on the total mass of the preparation.
  • two polyacrylic acid polymers or three polyacrylic acid polymers are understood to mean that one polyacrylic acid polymer differs from the other in at least one property.
  • the substance group acrylates / C 10-30 alkyl acrylate crosspolymers comprises, for example, the commercial products pemulen TR-1 or TR-2.
  • Carbomers are differentiated, for example, into types A, B and C. Differences here are, for example, their gels with different viscosities (United States Pharmacopoeia, USP). Also essential to the invention and therefore preferred is a proportion of waxes or preferably a mixture of liquid and solid hydrocarbons having a melting range of 4.5 to 75 ° C, in particular up to 55 ° C according to DSC.
  • Preparations according to the invention may be added. Otherwise, the stability is more difficult to adjust due to the absence of emulsifiers.
  • lipids is used as a generic term for fats, oils, waxes and the like, as is well known to the person skilled in the art. Also, the terms “oil phase ,, and” lipid phase , are used interchangeably.
  • oils and fats differ in their polarity. It is proposed to assume the interfacial tension against water as a measure of the polarity index of an oil or an oil phase. In this case, the lower the interfacial tension between this oil phase and water, the greater the polarity of the relevant oil phase. According to the invention, the interfacial tension is considered as a possible measure of the polarity of a given oil component.
  • the interfacial tension is the force acting on an imaginary line of one meter length located in the interface between two phases.
  • the physical unit for this interfacial tension is calculated classically by the force / length relationship and is usually expressed in mN / m (millinewtons divided by meters). It has a positive connotation if it tries to reduce the interface. In the opposite case, it has a negative sign.
  • the preparation according to the invention makes it possible for the first time to apply care in the shower and to apply active ingredients during the showering process.
  • the preparations according to the invention are advantageously formulated only with preservatives which have a water solubility of more than 0.75% at 20 ° C.
  • the preparations according to the invention are furthermore preferably also free of surfactants.
  • Surfactants are substances that are the surface tension of a liquid or the
  • Surfactants cause two actually immiscible liquids, such as oil and water, can be dispersed. Furthermore, surfactants are described as amphiphilic substances that can dissolve organic, nonpolar substances in water. Due to their specific molecular structure, they provide at least one hydrophilic and one hydrophobic one
  • hydrophilic fractions of a surfactant molecule are usually polar functional groups, for example -COO " , -OSO 3 2" , -SO 3 " , while the hydrophobic moieties generally represent nonpolar hydrocarbon radicals
  • Anionic surfactants generally have carboxylate, sulfate or sulfonate groups as functional groups. In aqueous solution they form negatively charged organic ions in an acidic or neutral medium. Cationic surfactants are almost exclusively characterized by the presence of a quaternary ammonium group. In aqueous solution, they form positively charged organic ions in an acidic or neutral environment. Amphoteric surfactants contain both anionic and cationic groups and behave accordingly in aqueous solution depending on the pH as anionic or cationic surfactants. They have a positive charge in a strongly acidic environment and a negative charge in an alkaline environment.
  • washing-active substances such as, for example, cationic surfactants, in particular quaternary ammonium compounds.
  • a detergent substance is used in detergents, dishwashing detergents, shampoos, shower gels and denotes the proportion of the formulation which influences the washing or cleaning performance.
  • Substances increase the "solubility" of fat and dirt particles in water that adhere to the laundry or body, they can be of natural or synthetic origin and are classified according to the nature of their charge in anionic, cationic, ampholytic or nonionic.
  • Emulsifiers cause two immiscible liquids (for example, oil in water) to mix together to form an emulsion. Due to the amphiphilic character, they penetrate into the oil with their fat-soluble part. Through the hydrophilic part For example, the oil droplets produced by stirring can be dispersed in the aqueous environment
  • Emulsifiers and surfactants can damage the skin's barrier layer.
  • Preparations are therefore added neither emulsifiers nor surfactants, so it is advantageous to dispense with the addition of additional washing-active substances.
  • the preparation skin moisturizer, moisturizer, added as an active ingredient.
  • the preparations are used on wet skin and especially for shaving.
  • the preparation according to the invention can be used for skin conditioning.
  • the protective film that forms is ideally at least 1 ⁇ m thick (measured according to IR-ATR measurement technology) and / or does not comprise substances which damage the skin barrier, in particular no emulsifiers, surfactants, PEG 's and / or organohalogen compounds.
  • Preferred embodiments of the preparations according to the invention comprise one or more waxes, a hydrocarbon mixture and an active ingredient from the group of skin moisturizing agents, wherein the fatty alcohols used are myristyl, cetearyl and / or stearyl alcohols, wax Cera Microcristallina and as the hydrocarbon mixture paraffin liquid.
  • Glycerin as well as Ubichinon active ingredient Q10 for skin care and a cooling active substance such as menthol, are advantageous in this preparation as skin moisturizing agent.
  • This triple combination of active ingredients creates a pleasant skin feel and care during both showering and prolonged skin care.
  • sodium hydroxide is preferably contained.
  • Myristyl alcohol 1, 0000 1, 0000 1, 0000 2,0000
  • Phenoxyethanol 0.5000 0.5000 0.5000 0.4000 0.4000
  • Methylisothiazolinone 0.0900 0.0900 0.0900 0.0800 0.0800
  • Carbomer (Carbopol 981) 0,0200 0,0200 0,0200 0,0200 0,0200 0,0200 0,0200
  • Glycyrrhiza Inflata Root Extract 0.0010 0.0250 0.1000

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Abstract

The invention relates to an emulsifier-free, skin conditioning cosmetic or dermatological preparation which contains active ingredients.

Description

Emulgatorfreie, hautkonditionierende und wirkstoffhaltige kosmetische oder dermatologische Zubereitung  Emulsifier-free, skin-conditioning and active ingredient-containing cosmetic or dermatological preparation
Die Erfindung umfasst eine emulgatorfreie, hautkonditionierende kosmetische oder dermatologische Zubereitung mit Wirkstoffen. Die Zubereitung eignet sich für die Applikation auf nasser Haut ohne vollständig abgespült zu werden und ermöglicht damit während des Duschens das Eincremen und das Aufbringen von hautpflegenden und/oder  The invention comprises an emulsifier-free, skin-conditioning cosmetic or dermatological preparation with active ingredients. The preparation is suitable for application on wet skin without being completely rinsed off and thus allows the creaming and the application of skin care and / or during the shower
hautschützenden Wirkstoffen. skin-protecting agents.
Das Eincremen unter feuchten Bedingungen, Hautpflege unter der Dusche, wird  Applying under moist conditions, skincare under the shower, will
zusammenfassend als Hautkonditionierung verstanden. Dies bedeutet u.a.: in summary understood as skin conditioning. This means, inter alia .:
1 . Verwendung eines üblichen Dusch Produktes zur Reinigung der Haut, Abspülung 1 . Use of a standard shower product to cleanse the skin, rinse off
2. Auftragen/Verteilung der erfindungsgemäßen Zubereitung auf nasser Haut 2. Application / distribution of the preparation according to the invention on wet skin
3. Erneutes Abduschen mit warmen oder kaltem Wasser  3. Reapply with warm or cold water
4. Abtrocknen der Haut  4. Drying of the skin
In der WO 2013064391 A2 werden kosmetische oder dermatologische Zubereitungen beschrieben, die ein Eincremen unter der Dusche ermöglichen.  WO 2013064391 A2 describes cosmetic or dermatological preparations which make it possible to apply cream under the shower.
Aufgrund von Zeitmangel wünschen sich viele Menschen eine möglichst effiziente  Due to lack of time, many people want the most efficient
Hautpflege und zeitgleichem Hautschutz. Skin care and simultaneous skin protection.
Wünschenswert ist es eine Zubereitung zur Verfügung zu stellen, die einerseits  It is desirable to provide a preparation, on the one hand
hautverträglich gestaltet ist und andererseits die Möglichkeit eröffnet hautpflegende und/oder hautschützende Wirkstoffe auf die Haut aufzubringen und dabei zeitsparend unter Dusche bzw. auf nasser Haut angewendet werden kann. designed to be skin-friendly and on the other hand opens up the possibility skin-protective and / or skin-protecting agents applied to the skin and can be used to save time under shower or on wet skin.
Die Erfindung ist eine emulgatorfreie kosmetische oder dermatologische Zubereitung umfassend ein oder mehrere Polyacrylsäurepolymere, ein oder mehrere C14-22 Fettalkohole sowie ein oder mehrere Wachse und/oder ein Kohlenwasserstoffgemisch sowie ein oder mehrere Wirkstoffe.  The invention is an emulsifier-free cosmetic or dermatological preparation comprising one or more polyacrylic acid polymers, one or more C14-22 fatty alcohols and one or more waxes and / or a hydrocarbon mixture and one or more active substances.
Bevorzugt umfasst die Zubereitung Wachse, insbesondere Cera Microcristallina, im Bereich von mehr als 0,5 Gew.%, insbesondere mehr als 13 Gew.%, bezogen auf die Gesamtmasse der Zubereitung.  The preparation preferably comprises waxes, in particular Cera Microcristallina, in the range of more than 0.5% by weight, in particular more than 13% by weight, based on the total mass of the preparation.
Der bevorzugte Anteil bezieht sich sowohl auf einzelne Wachse als auch bevorzugt auf die Gesamtmenge an mehreren Wachsen.  The preferred level refers to both individual waxes and preferably the total amount of multiple waxes.
Als erfindungsgemäße Wirkstoffe sind alle kosmetisch oder dermatologisch wirkenden Stoffe umfasst, insbesondere solche Stoffe, die einen hautpflegende und/oder hautschützende Eigenschaft haben. Die Wirkstoffe können bevorzugt aus der Gruppe der hautpflegenden Stoffe, der Selbstbräunungsmittel, der kühlenden (cooling) Substanzen, der wärmenden Substanzen und/oder der whitening (hautaufhellenden) Stoffe gewählt werden. Bevorzugt wird jeweils ein oder mehrere Wirkstoffe aus nur einer der vorstehend genannten Gruppen ausgewählt.Active ingredients according to the invention include all cosmetically or dermatologically active substances, in particular those substances which have a skin-care and / or skin-protecting property. The active ingredients may preferably be selected from the group of skin care substances, self-tanning agents, cooling substances, warming substances and / or whitening substances. In each case one or more active substances are preferably selected from only one of the abovementioned groups.
Als hautpflegende Stoffe sind vorteilhaft diejenigen Stoffe zu wählen, die die Haut geschmeidig machen und glättend wirken, d.h. die Rauhigkeit verringern. Ebenso wie Wirkstoffe, die die Haut in einem gesunden Zustand bewahren, schädigende Einwirkungen auf die Haut durch äußere Einflüsse vermeiden und/oder Feuchtigkeit spenden. As skin-care substances, it is advantageous to choose those substances which make the skin supple and have a smoothing effect, i. reduce the roughness. As well as active ingredients that maintain the skin in a healthy state, avoid damaging effects on the skin due to external influences and / or moisturize.
Als Wirkstoffe können ein oder mehrere gewählt werden aus der Gruppe aus Cyclodextrin, Ubiquinone, Creatine, 1-Methylhydantoin-2-lmide, Glycine Soja Germ Extract, Ascorbic Acid ( Vitamin C und deren Derivate), Ascorbyl Palmitate, Sodium Ascorbyl Phosphate, Pimpinella Anisum Fruit Extract, Arctium Lappa Fruit Extract, Magnolia Officinalis Bark Extract, Sodium Hyaluronate, Taurine, Folie Acid, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Glucosylrutin und Isoquercitrin, Carnitine, Sodium Chloride, Glyceryl Glucoside, Climbazole, Piroctone Olamine, Oryzanol, BHT, Tocopherol, Vitamine, insbesondere Vitamin E und A und deren Derivate, Tocopheryl Acetate, Nelumbo Nucifera Leaf Extract, Caffeine, Camellia Sinensis Leaf Extract, Menthoxypropanediol, Menthane Carboxamide Ethylpyridine,  As active ingredients, one or more may be selected from the group of cyclodextrin, ubiquinone, creatine, 1-methylhydantoin-2-imide, glycine soy germ extract, ascorbic acid (vitamin C and its derivatives), ascorbyl palmitate, sodium ascorbyl phosphate, pimpinella anisum Fruit Extract, Arctium Lappa Fruit Extract, Magnolia Officinalis Bark Extract, Sodium Hyaluronate, Taurine, Foil Acid, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Glucosylrutin and Isoquercitrin, Carnitine, Sodium Chloride, Glyceryl Glucoside, Climbazole, Piroctone Olamine, Oryzanol, BHT, Tocopherol, Vitamins, especially Vitamin E and A and their derivatives, Tocopheryl Acetate, Nelumbo Nucifera Leaf Extract, Caffeine, Camellia Sinensis Leaf Extract, Menthoxypropanediol, Menthane Carboxamide, Ethylpyridine,
Cyanomethylphenyl Menthane Carboxamide, Chelidonium Majus Extract, Salicylic Acid, 4- Butylresorcinol, Paullinia Cupana Seed Extract, Butyl Acrylate/Ethyltrimonium Chloride, Methacrylate/Styrene Copolymer, Octenidine HCl, Urea, Octadecenedioic Acid, Cyanomethylphenyl Menthane Carboxamide, Chelidonium Majus Extract, Salicylic Acid, 4-Butylresorcinol, Paullinia Cupana Seed Extract, Butyl Acrylate / Ethyltrimonium Chloride, Methacrylate / Styrene Copolymer, Octenidine HCl, Urea, Octadecenedioic Acid,
Dihydroxyacetone, Cholesterol, Ceramide 3, Silver Citrate, Arginine HCL, Fucus Vesiculosus Extract, Panthenol, Niacinnamid (Vitamin B3), Retinyl Palmitate/Retinol, Biotin, Bisabolol, Menthol, Alanine, Allantoin, Pyrus Malus Stern Extract, Acetyl Hydroxyproline, Laminaria Ochroleuca Extract, Zingerone, 4-t-Butylcyclohexanol, Garcinia Cambogia Fruit Extract, Epsilon-polylysine, Himbeerketon, Alexidine, N-(4-(2,4-dihydroxyphenyl)thiazol-2- yl)isobutyramide, Dihydromyricetin, Silymarin, 3-(4-Hydroxy-3-methoxy-phenyl)-1-(4-hydroxy- phenyl)-propan-1-on, Pyridoxine-3,4-cyclic phosphate, Oxygen, Dioic Acid, Glycerylglucose.Dihydroxyacetones, Cholesterol, Ceramides 3, Silver Citrate, Arginine HCL, Fucus Vesiculosus Extract, Panthenol, Niacinamide (Vitamin B3), Retinyl Palmitate / Retinol, Biotin, Bisabolol, Menthol, Alanine, Allantoin, Pyrus Malus Star Extract, Acetyl Hydroxyproline, Laminaria Ochroleuca Extract, Zingerone, 4-t-butylcyclohexanol, Garcinia Cambogia Fruit Extract, epsilon-polylysine, raspberry ketone, alexidine, N- (4- (2,4-dihydroxyphenyl) thiazol-2-yl) isobutyramide, dihydromyricetine, silymarin, 3- ( 4-hydroxy-3-methoxy-phenyl) -1- (4-hydroxyphenyl) -propan-1-one, pyridoxine-3,4-cyclic phosphate, oxygen, dioic acid, glycerylglucose.
Als bevorzugte Wirkstoffe sind zu wählen D-Biotin, Coenzym Q10, Folsäure und/oder deren Derivate, Rucinol, Panthenol, Niacinamid, alpha-Glucosylrutin, Carnitin, Carnosin, natürliche und/oder synthetische Isoflavonoide, Kreatin, Taurin, ß-Alanin, 1-Methylhydantoin-2-lmide , N-(4-(2,4-dihydroxyphenyl)thiazol-2-yl)isobutyramide, Glycine Soja Germ Extract, Pimpinella Anisum Fruit Extract, Arctium Lappa Fruit Extract, Magnolia Officinalis Bark Extract, Sodium Hyaluronate, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Glucosylrutin und D-biotin, coenzyme Q10, folic acid and / or derivatives thereof, rucinol, panthenol, niacinamide, alpha-glucosylrutin, carnitine, carnosine, natural and / or synthetic isoflavonoids, creatine, taurine, .beta.-alanine, 1 can be selected as preferred active ingredients -Methylhydantoin-2-imide, N- (4- (2,4-dihydroxyphenyl) thiazol-2-yl) isobutyramide, Glycine Soy Germ Extract, Pimpinella Anisum Fruit Extract, Arctium Lappa Fruit Extract, Magnolia Officinalis Bark Extract, Sodium Hyaluronate, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Glucosylrutin and
Isoquercitrin, Sodium Chloride, Glyceryl Glucoside, Climbazole, Piroctone Olamine, Isoquercitrin, Sodium Chloride, Glyceryl Glucoside, Climbazole, Piroctone Olamine,
Menthoxypropanediol, Menthane Carboxamide Ethylpyridine, Cyanomethylphenyl Menthane Carboxamide und/oder 4-Butylresorcinol. Insbesondere ist als Wirkstoff Q10 zu wählen. Menthoxypropanediol, menthane carboxamides, ethylpyridines, cyanomethylphenyl, menthane carboxamides and / or 4-butylresorcinol. In particular, Q10 should be selected as active ingredient.
Als Selbstbräuner werden erfindungsgemäß vorteilhaft unter anderem eingesetzt:  As a self-tanner advantageously used according to the invention, inter alia:
HC=0 H2C-OHHC = 0 H 2 C-OH
HC=0 HC=0 I I HC = 0 HC = 0 I I
I I CH2 HC-OHII CH 2 HC-OH
HC-OH c=o I I HC-OH c = o I I
I I CH2 C=OII CH 2 C = O
H2C-OH H2c-OH I I H 2 C-OH H 2 c-OH II
HC=0 H2C-OHHC = 0 H 2 C-OH
Glycerolaldehyd Hydroxymethylglyoxal γ-Dialdehyd Erythrulose Glycerol aldehyde hydroxymethylglyoxal γ-dialdehyde erythrulose
6-Aldo-D-Fructose Ninhydrin 6-aldo-D-fructose ninhydrin
Ferner ist das 5-Hydroxy-1 ,4-naphtochinon (Juglon) zu nennen, das aus den Schalen frischer Walnüsse extrahiert wird  Also to be mentioned is 5-hydroxy-1,4-naphthoquinone (juglone) which is extracted from the shells of fresh walnuts
5-Hydroxy-1 ,4-naphtochinon (Juglon)  5-hydroxy-1,4-naphthoquinone (juglone)
sowie das in den Henna-Blättern vorkommende 2-Hydroxy-1 ,4-naphtochinon (Lawson). and 2-hydroxy-1,4-naphthoquinone (Lawson) found in henna leaves.
2-Hydroxy-1 ,4-naphtochinon (Lawson) 2-hydroxy-1,4-naphthoquinone (Lawson)
Ganz besonders bevorzugt im Sinne der Erfindung ist das 1 ,3-Dihydroxyaceton (DHA), im menschlichen Körper vorkommender dreiwertiger Zucker. H2C-OH Very particular preference according to the invention is the 1, 3-dihydroxyacetone (DHA), occurring in the human body trivalent sugars. H 2 C-OH
I  I
C=O  C = O
I  I
H2c-OH H 2 c -OH
1 ,3-Dihydroxyaceton (DHA)  1, 3-dihydroxyacetone (DHA)
Die Anwendung von Selbstbräunungssubstanzen als Wirkstoffe in der erfindungsgemäßen Zubereitung ermöglicht ein zeitsparendes Aufbringen und der gesamte Körper kann so erstmalig problemlos gebräunt werden.  The use of self-tanning substances as active ingredients in the preparation according to the invention allows a time-saving application and the entire body can be browned so easily for the first time.
Als wärmende Stoffe sind die Durchblutung anregende Stoffe, wie Capsaicinoide als  As warming substances are the circulation stimulating substances, such as capsaicinoids as
Wirkstoffe bekannt. Die Wirkweise dieser Produkte beruht zum einen auf der Förderung der Durchblutung in den betroffenen Arealen und zum Anderen auf einen Einfluss auf den Stoffwechsel. So wird zum Beispiel durch Capsaicin die Ausschüttung von Substanz P, ein Neuropeptid aus elf Aminosäuren, angeregt. Dieses Molekül greift aktiv in den Active ingredients known. The mode of action of these products is based on the one hand on the promotion of blood circulation in the affected areas and on the other on an influence on the metabolism. Capsaicin, for example, stimulates the release of substance P, a neuropeptide of eleven amino acids. This molecule actively engages in the
Schmerzkreislauf ein und trägt zu einer Verminderung der wahrgenommenen Schmerzen bei. Pain cycle and contributes to a reduction in the perceived pain.
Als durchblutungsfördernde Wirkstoffe werden bevorzugt eingesetzt  As circulation-promoting agents are preferably used
Capsaicinoide (0,01 - 0,20 %)  Capsaicinoids (0.01 - 0.20%)
Nonivamid (0,01 - 0,15 %)  Nonivamide (0.01-0.15%)
Vanilylbutylether (0,5 - 2,5 %)  Vanilyl butyl ether (0.5 - 2.5%)
Nicotinsäurebenzylester (0,5 - 4,0 %)  Nicotinic acid benzyl ester (0.5 - 4.0%)
Rosmarin Öl (0,5 - 5,0 %)  Rosemary oil (0.5 - 5.0%)
Capsiate (Vanilinsäureester) (0,5 - 2,5 %)  Capsiate (vanilin ester) (0.5 - 2.5%)
Senföle (0,2 - 4,0 %)  Mustard oils (0.2 - 4.0%)
Weitere erfindungsgemäß zu verwendende Wirkstoffe sind aus der Gruppe der nicht wärmenden, entzündungshemmenden Wirkstoffen aus dem Bereich der Nichtsteroidalen Antientzündlichen Wirkstoffe (engl. NSAIDs) zu wählen. Insbesondere sind dies Aspirin (acetylsalicylic acid), Diflunisal, Salsalate, Ibuprofen, Etofenamat, Dexibuprofen, Naproxen, Fenoprofen, Ketoprofen, Dexketoprofen, Flurbiprofen, Oxaprozin, Loxoprofen, Indomethacin, Tolmetin, Sulindac, Etodolac, Ketorolac, Diclofenac, Nabumetone, Piroxicam, Meloxicam, Tenoxicam, Droxicam, Lornoxicam, Isoxicam, Mefenamic acid, Meclofenamic acid, Further active ingredients to be used according to the invention are to be selected from the group of non-heating, anti-inflammatory agents from the field of non-steroidal antiinflammatory drugs (NSAIDs). In particular, these are aspirin (acetylsalicylic acid), diflunisal, salsalates, ibuprofen, etofenamate, dexibuprofen, naproxen, fenoprofen, ketoprofen, dexketoprofen, flurbiprofen, oxaprozin, loxoprofen, indomethacin, tolmetin, sulindac, etodolac, ketorolac, diclofenac, nabumetone, piroxicam, meloxicam , Tenoxicam, droxicam, lornoxicam, isoxicam, mefenamic acid, meclofenamic acid,
Flufenamic acid, Tolfenamic acid, Celecoxib , Rofecoxib, Valdecoxib , Parecoxib, Flufenamic acid, tolfenamic acid, celecoxib, rofecoxib, valdecoxib, parecoxib,
Lumiracoxib, Etoricoxib, Firocoxib, Licofelone, Lysine clonixinate, Hyperforin und/oder Figwort. Bevorzugt sind hierbei Ibuprofen, Diclofenac und dessen Salze, Indomethacin, Flurbiprofen und Etofenamat. Besonders bevorzugt ist die Einarbeitung eines oder mehrerer Substanzen, die für ihre langanhaltenden kühlenden Eigenschaften bekannt sind, z.B. Menthol und dessen Derivate, Campher, Minze, Eukalyptus etc. Lumiracoxib, etoricoxib, firocoxib, licofelone, lysine clonixinate, hyperforin and / or figwort. Preference is given here to ibuprofen, diclofenac and its salts, indomethacin, flurbiprofen and etofenamate. Particularly preferred is the incorporation of one or more substances known for their long-lasting cooling properties, for example menthol and its derivatives, camphor, mint, eucalyptus, etc.
Als besonders bevorzugtes ätherisches Öl hat sich das Menthol erwiesen. Menthol ist Bestandteil des bekannten japanischen Pfefferminzöls (CAS: 20747-49-3). Wichtigstes Isomer ist (-)-Menthol. Menthol erzeugt beim Einreiben auf die Haut infolge  As a particularly preferred essential oil, the menthol has been found. Menthol is part of the well-known Japanese peppermint oil (CAS: 20747-49-3). The most important isomer is (-) - menthol. Menthol produced when rubbed on the skin due
Oberflächenanästhesierung und Reizung der kälteempfindlichen Nerven bei Migräne oder dergleichen ein angenehmes Kältegefühl. Erwiesenermaßen zeigen die betroffenen Surface anesthetization and irritation of cold-sensitive nerves in migraine or the like a pleasant feeling of cold. Proven to show the affected
Hautpartien aber normale bzw. erhöhte Temperatur. Skin but normal or elevated temperature.
Als weitere bevorzugte ätherische Öle können Oleum Eucalypti, Oleum Menthae piperitae, Oleum camphoratum, Oleum Rosmarini, Oleum Thymi, Oleum Pini sibricum und Oleum Pini silverstris sowie die Terpene 1 ,8-Cineol und Levomethanol sowie Oleum Abietis albae, Oleum Anisi, Oleum Aurantii Floris, Oleum Bergamottae, Oleum Calendulae infusum, Oleum Caryophylli, Oleum Chamomillae, Oleum Cinnamomi ceylanici, Oleum Citri, Oleum  Oleum Eucalypti, Oleum Menthae piperitae, Oleum camphoratum, Oleum Rosmarini, Oleum Thymi, Oleum pinis sibricum and Oleum Pini silverstris, as well as the terpenes 1, 8-cineol and levomethanol, as well as oleum Abietis albae, Oleum anisi, Oleum aurantii Floris, can also be used as further preferred essential oils , Oleum Bergamottae, Oleum Calendulae infusum, Oleum Caryophylli, Oleum Chamomillae, Oleum Cinnamomi ceylanici, Oleum Citri, Oleum
Citronellae, Oleum Cupressi, Oleum Cymbopogonis, Oleum Jecoris, Oleum Lavendulae, Oleum Macidis, Oleum Majoranae, Oleum Melaleucae viridiflorae, Oleum Melissae, Oleum Menthae arvensis, Oleum Millefolium, Oleum Myrrhae, Oleum Myrte, Oleum Pini sibricum, Oleum Pinisilvestris, Oleum Salviae, Oleum Santali, Oleum Terebinthinae rectificat, Oleum Valerianae und Oleum Zingiberis eingesetzt werden. Citronellae, Oleum Cupressi, Oleum Cymbopogonis, Oleum Jecoris, Oleum Lavendulae, Oleum Macidis, Oleum Majoranae, Oleum Melaleucae viridiflorae, Oleum Melissae, Oleum Menthae arvensis, Oleum Millefolium, Oleum Myrrhae, Oleum myrtle, Oleum Pini sibricum, Oleum Pinisilvestris, Oleum Salviae, Oleum Santali, Oleum Terebinthinae rectificat, Oleum Valerianae and Oleum Zingiberis are used.
Die ätherischen Öle werden einzeln oder in Kombination mit anderen zu einem Anteil von insgesamt 0,001 bis 10 Gew.%, insbesondere zu 0,01 bis 1 Gew.% in der Zubereitung eingesetzt, bezogen auf die Gesamtmasse der Zubereitung ohne Treibmittel.  The essential oils are used individually or in combination with others in a proportion of a total of 0.001 to 10 wt.%, In particular 0.01 to 1 wt.% In the preparation, based on the total mass of the preparation without propellant.
Vorteilhaft können anstelle der scheinbar kühlend wirkend Substanzen auch Substanzen eingesetzt werden, die für wärmende Eigenschaften bekannt sind, wie beispielsweise HotAct (Vanillyl Buthyl Ether) und/oder Capsicum.  Advantageously, substances which are known for warming properties, such as, for example, HotAct (vanillyl butyl ether) and / or capsicum, can also be used instead of the substances having a seemingly cooling effect.
Whitening Stoffe sind Stoffe zur Hautaufhellung. Darunter versteht man das Ausbleichen oder Beschichten der menschlichen Haut, um diese zu kosmetischen Zwecken heller zu machen.  Whitening fabrics are substances for skin whitening. This refers to the bleaching or coating of human skin to make it lighter for cosmetic purposes.
Bevorzugte whitening Stoffe sind Rucinol, Hydrochinone, Kojisäure, Süßholzwurzelextrakt, N-(4-(2,4-dihydroxyphenyl)thiazol-2-yl)isobutyramide, Camu Camu, Licoriche, Acerola oder Vitamin C.  Preferred whitening substances are rucinol, hydroquinones, kojic acid, liquorice root extract, N- (4- (2,4-dihydroxyphenyl) thiazol-2-yl) isobutyramide, Camu Camu, licoriche, acerola or vitamin C.
Man unterscheidet zwischen Tyrosinasehemmer und Melaninsynthesehemmer, da die Hemmung der Tyrosinase in der Hemmung der Melaninsynthese resultiert, jedoch die Hemmung der Melaninsynthese nicht zwangsläufig Tyrosinasehemmung bedeutet. Rucinol, Hydrochinone und Kojisäure hemmen beispielsweise auch die Tyrosinase. A distinction is made between tyrosinase inhibitors and melanin synthesis inhibitors, since the inhibition of tyrosinase results in the inhibition of melanin synthesis, but the inhibition of melanin synthesis does not necessarily mean tyrosinase inhibition. For example, rucinol, hydroquinones and kojic acid also inhibit tyrosinase.
Die Einsatzkonzentration in Gewichtsanteilen an einem oder mehreren der Wirkstoffe in der aufgebrachten Zubereitung liegt bevorzugt bei bis zu 25 Gew.%, insbesondere im Bereich zwischen 0,001 Gew.% und 20 Gew.%, bezogen auf die Gesamtmasse der Zubereitung. The use concentration in parts by weight of one or more of the active ingredients in the applied preparation is preferably up to 25% by weight, in particular in the range between 0.001% by weight and 20% by weight, based on the total mass of the preparation.
Erfindungsgemäß vorteilhaft ist die Wahl der Wirkstoffe aus der Gruppe der lipophilen Verbindungen zu wählen. According to the invention, it is advantageous to choose the active compounds from the group of lipophilic compounds.
Da die erfindungsgemäße Grundzubereitung aus überwiegend lipophilen Stoffen aufgebaut ist, kann so ein längerer Verbleib auf der Haut realisiert werden.  Since the basic preparation according to the invention is composed of predominantly lipophilic substances, it is thus possible to achieve a longer retention on the skin.
Bevorzugt umfasst die erfindungsgemäße Zubereitung als Wirkstoffe Q10 und Menthol. The preparation according to the invention preferably comprises as active ingredients Q10 and menthol.
Neben einem Kühleffekt während und nach dem Duschen werden gleichzeitig hautpflegende Wirkungen erzielt. In addition to a cooling effect during and after showering skin-caring effects are achieved at the same time.
Erstaunlicherweise gelingt das Zurückbleiben von Wirkstoffen nach dem Abspülen und Abtrocknen auf der Haut durch die erfindungsgemäße Zubereitung. Die Anwendung der Kombination aus speziellen Fettalkoholen, Wachsen und vorteilhaft einem oder mehreren Filmbildnern führt zu einem Hautschutz- und/oder Hautpflege schon unter der Dusche. Surprisingly, the remaining of active ingredients after rinsing and drying on the skin by the preparation according to the invention succeeds. The application of the combination of special fatty alcohols, waxes and advantageously one or more film formers leads to a skin protection and / or skin care even under the shower.
Die erfindungsgemäßen Zubereitungen umfassen vorteilhaft ein oder mehrere Filmbildner.The preparations according to the invention advantageously comprise one or more film formers.
Vorteilhaft werden diese Filmbildner gewählt aus der Gruppe Hexadecencopolymer, Trimethylsiloxysilicat, Polypropylsilsesquioxan, Polysilicone-25, These film formers are advantageously selected from the group hexadecene copolymer, trimethylsiloxysilicate, polypropylsilsesquioxane, polysilicone-25,
Acrylatcopolymer, Polyurethan, Methacrylat, Polyglycerylstearat, Dilinoleat-Crosspolymer, Akyl-Acrylate/Methacrylic Acid Crosspolymer, IPDI Copolymer, insbesondere  Acrylate copolymer, polyurethane, methacrylate, polyglyceryl stearate, dilinoleate crosspolymer, alkyl acrylate / methacrylic acid crosspolymer, IPDI copolymer, in particular
VP/Hexadecene Copolymer, Octyldodecyl Citrate Crosspolymer, Trimethylsiloxysilicat/ Polypropylsilsesquioxan, Polysilicone-25, Ammoniumacrylate - Copolymer, VP / Hexadecenes Copolymer, Octyldodecyl Citrate Crosspolymer, Trimethylsiloxysilicate / Polypropylsilsesquioxane, Polysilicone-25, Ammonium Acrylate Copolymer,
Acrylatcopolymer, Polyurethane-2 und Polymethylmethacrylat, Polyglycerylstearat/ Acrylate copolymer, polyurethane-2 and polymethyl methacrylate, polyglyceryl stearate /
Isostearatdilinoleat - Crosspolymer, Octadecen/MA Copolymer (und) Methylacetylricinoleat (und) Diisooctyladipat, Trimethylsiloxysilicat, Polyurethan-34, C8-22 Alkyl Isostearate dilinoleate - crosspolymer, octadecene / MA copolymer (and) methyl acetylricinoleate (and) diisooctyl adipate, trimethylsiloxysilicate, polyurethane-34, C8-22 alkyl
Acrylate/Methacrylic Acid Crosspolymer und/oder Castor Oil/IPDI Copolymer. Acrylates / Methacrylic Acid Crosspolymer and / or Castor Oil / IPDI Copolymer.
Der Anteil an Filmbildnern wird vorteilhaft im Bereich von 0,1 Gew.%, insbesondere 0,5 Gew.% bis 10 Gew.%., bezogen auf die Gesamtmasse der Zubereitung gewählt.  The proportion of film formers is advantageously selected in the range of 0.1% by weight, in particular 0.5% by weight to 10% by weight, based on the total mass of the preparation.
In einem Vergleich wird der sich bildende Schutzfilm auf der Haut untersucht, einmal nach der Anwendung eines rinse off Produktes mit integrierten Hautpflegeaspekten (Nivea creme soft shower gel) allein und einmal nach Anwendung des gleichen Produktes (Nivea creme soft shower gel) und anschließender Anwendung der erfindungsgemäßen Zubereitung. Nach beiden Anwendungen wird die Haut mit Wasser abgespült. Die durchgeführten Messungen zur Rückfettung der Haut wurden per IR-Imaging gemacht. Die Messtechnik wird IR-ATR (InfraRed-Attenuated Total Reflectance) bezeichnet. In a comparison, the protective film that forms on the skin is examined, once after the application of a rinse off product with integrated skin care aspects (Nivea cream soft shower gel) alone and once after application of the same product (Nivea cream soft shower gel) and subsequent application of the inventive preparation. After both applications, the skin is rinsed with water. The skin refatting measurements were made by IR imaging. The measurement technique is called IR-ATR (InfraRed-Attenuated Total Reflectance).
Es zeigte sich, dass erst nach der Anwendung der erfindungsgemäßen Zubereitung ein mittels der erwähnten Messtechnik sichtbarer Schutzfilm auf der Haut verbleibt und nachweisbar ist. Der Nachweis erfolgt über die Intensität der Kohlenwasserstoff-IR -Banden (CH-IR bands).  It was found that only after application of the preparation according to the invention does a protective film visible by means of the measurement technique mentioned remain on the skin and can be detected. Detection is via the intensity of the hydrocarbon IR bands (CH-IR bands).
Der erfindungsgemäße Schutzfilm umfasst einen auf der Haut sich bildenden Film, der ein oder mehrere Wirkstoffe umfasst. Vorteilhaft und damit länger im Film und damit auf der Haut verbleibend sind lipophile Wirkstoffe zu wählen.  The protective film of the invention comprises a skin-forming film comprising one or more active ingredients. Advantageous and thus longer in the film and thus remaining on the skin are lipophilic drugs to choose.
Die erfindungsgemäße Hautkonditionierung umfasst das Eincremen unter feuchten  The skin conditioning according to the invention comprises moisturizing
Bedingungen, insbesondere der Hautpflege unter der Dusche, wobei ein Schutzfilm auch nach dem Abspülen auf der Haut verbleibt. Der Schutzfilm ist mittels IR-ATR Messtechnik nachweisbar und weist idealerweise eine Dicke von mindestens 1 μηη bis zu 10 μηη auf.Conditions, in particular the skin care in the shower, whereby a protective film remains even after rinsing on the skin. The protective film can be detected by means of IR-ATR measurement technology and ideally has a thickness of at least 1 μm to 10 μm.
Insbesondere ist die erfindungsgemäße Hautkonditionierung dadurch gekennzeichnet, dass im Schutzfilm auf der Haut ein oder mehrere Wirkstoffe, ein oder mehrere Lipide und ein oder mehrere Hautbefeuchtungsmittel umfasst und keine die Hautbarriere schädigenden Stoffe, insbesondere keine Emulgatoren und/oder Tenside, enthalten sind. In particular, the skin conditioning according to the invention is characterized in that the protective film on the skin comprises one or more active substances, one or more lipids and one or more skin moisturizing agents and no skin barrier damaging substances, in particular no emulsifiers and / or surfactants, are included.
Erst dieser auf der Haut verbleibende Film ermöglicht die Aufbringung und auch den Verbleib von Wirkstoffe auf der Haut.  Only this remaining on the skin film allows the application and also the whereabouts of active ingredients on the skin.
Bei der erfindungsgemäßen Zubereitung werden ein oder mehrere Fettalkohole und mindestens ein zusätzliches Wachs und/oder Gemisch aus flüssigen und festen  In the preparation according to the invention are one or more fatty alcohols and at least one additional wax and / or mixture of liquid and solid
Kohlenwasserstoffen, mit einem Schmelzbereich von 5°C bis 75°C, bevorzugt bis 55°C (nach DSC), zusammen gegeben, insbesondere aufgeschmolzen. Hydrocarbons, having a melting range of 5 ° C to 75 ° C, preferably up to 55 ° C (according to DSC), given together, in particular melted.
D.h. vorteilhaft ist neben mindestens einem Fettalkohol mindestens ein Wachs enthalten oder neben Fettalkohol ist mindestens ein Gemisch aus flüssigen und festen  That Advantageously, at least one wax is present in addition to at least one fatty alcohol or, in addition to fatty alcohol, at least one mixture of liquid and solid is present
Kohlenwasserstoffen enthalten. Idealerweise sind Fettalkohol, Wachs und ein Gemisch aus Kohlenwasserstoffen enthalten. Contain hydrocarbons. Ideally, it contains fatty alcohol, wax and a mixture of hydrocarbons.
Vorteilhaft sind als Fettalkohole Myristyl-, Cetearyl- und/oder Stearylalkohole zu wählen, als Wachse Cera Microcristallina, Coco-Glycerid, C18-36 Acid Triglycerid, Synthetic Wax, Cera Alba, Paraffin, Copernicia Cerifera Cera , C18-38 Alkyl Hydroxystearoylstearat,  Preferred as fatty alcohols are myristyl, cetearyl and / or stearyl alcohols, as waxes Cera Microcristallina, Coco-Glyceride, C18-36 Acid Triglyceride, Synthetic Wax, Cera Alba, Paraffin, Copernicia Cerifera Cera, C18-38 Alkyl Hydroxystearoyl Stearate,
Butyrospermum Parkii Butter, Olus oil, C20-40 Alkohol und/oder Bienenwachs und als Kohlenwasserstoffgemisch Paraffinum Liquidum zu wählen. Butyrospermum Parkii Butter, Olus oil, C20-40 alcohol and / or beeswax and as a hydrocarbon mixture to choose Paraffinum Liquidum.
Bevorzugt ist Cera Microcristallina. Bevorzugte Einsatzkonzentrationen des oder der Wachse liegt im Bereich von 0,5 bis 20 Gew.%, bezogen auf die Gesamtmasse der Zubereitung. Preference is given to Cera Microcristallina. Preferred use concentrations of the wax or wax is in the range of 0.5 to 20 wt.%, Based on the total mass of the preparation.
Die Fettalkohole, Wachse und Kohlenwasserstoffgemische weisen dabei vorteilhaft alle einen Schmelzbereich von 5°C bis 75°C, bevorzugt bis 55°C (nach DSC) auf.  The fatty alcohols, waxes and hydrocarbon mixtures advantageously all have a melting range of 5 ° C. to 75 ° C., preferably up to 55 ° C. (according to DSC).
DSC (Differential Scanning Calorimetry) ist ein thermisches Verfahren zur Messung von abgegebener/aufgenommener Wärmemenge einer Probe bei isothermer Arbeitsweise, Aufheizung oder Abkühlung (siehe DIN 53765, DIN 51007, ASTM E 474, ASTM D 3418). DSC ist eine vergleichende Messmethode, die die Bestimmung von Wärmemengen physikalischer und chemischer Prozesse ermöglicht. Wenn ein Material seinen  DSC (Differential Scanning Calorimetry) is a thermal method for measuring emitted / absorbed heat quantity of a sample during isothermal operation, heating or cooling (see DIN 53765, DIN 51007, ASTM E 474, ASTM D 3418). DSC is a comparative measurement method that enables the determination of heat quantities of physical and chemical processes. If a material is his
physikalischen Zustand ändert, wie z.B. Schmelzen oder Umwandlung einer Kristallform in eine andere oder wenn es chemisch reagiert, wird Wärme dabei aufgenommen oder abgegeben. Diese Wärmemengen sind mit Hilfe der DSC quantitativ messbar. Die Methode verläuft zyklisch, so dass nach der ersten Aufheizkurve ein definiertes Abkühlen stattfindet und anschließend die Probe noch einmal im angegebenen Temperaturbereich aufgeheizt wird. Man erhält somit zweierlei Informationen: In der ersten Aufheizkurve sind alle thermische Effekte inklusiv Vorgeschichte erkennbar. In der zweiten Aufheizkurve ist die Vorgeschichte eliminiert worden und das reine thermische Verhalten der Probe unter definierten Abkühlbedingungen ist auswertbar. Der Schmelzbereich der Fettalkohole, Wachse bzw. Kohlenwasserstoffe zwischen 4,5°C und 75°C nach DSC ist der in der ersten Aufheizkurve ermittelte Bereich. physical state changes, such as Melting or transformation of one crystal form into another, or if it reacts chemically, heat is absorbed or released. These amounts of heat can be measured quantitatively with the help of DSC. The method runs cyclically, so that after the first heating curve, a defined cooling takes place and then the sample is heated again in the specified temperature range. This gives two different kinds of information: In the first heating curve, all thermal effects, including the prehistory, are discernible. In the second heating curve, the history has been eliminated and the pure thermal behavior of the sample under defined cooling conditions can be evaluated. The melting range of fatty alcohols, waxes or hydrocarbons between 4.5 ° C and 75 ° C according to DSC is the range determined in the first heating curve.
Als Wachse können erfindungsgemäß auch Fette und fettähnlichen Substanzen mit wachsartiger Konsistenz eingesetzt werden. Hierzu gehören u.a. Fette (Triglyceride), Mono und Diglyceride, natürliche und synthetische Wachse, Fett-und Wachsalkohole, Ester von Fettalkoholen und Fettsäuren sowie Fettsäureamide oder beliebige Gemische dieser Substanz.  Fats and fat-like substances with a waxy consistency can also be used according to the invention as waxes. These include u.a. Fats (triglycerides), mono and diglycerides, natural and synthetic waxes, fatty and wax alcohols, esters of fatty alcohols and fatty acids and fatty acid amides or any mixtures of this substance.
Besonders bevorzugt werden die Wachse aus der Gruppe der Fette , insbesondere aus der Gruppe natürliche Wachse: Shorea Stenoptera Seed Butter, Hydrogenated Vegetable Oil, Hydrogenated Coco-Glycerides, Butyrospermum Parkii Butter, Theobroma Cacao (Cocoa) Seed Butter, Mango Butter, Hydrogenated Palm Kernel Glycerides, Hydrogenated Palm Glycerides, Sunflower Seed Wax, Soybean Glycerides, Butyrospermum Parkii  Particularly preferred are the waxes from the group of fats, in particular from the group of natural waxes: Shorea Stenoptera Seed Butter, Hydrogenated Vegetable Oil, Hydrogenated Coco-Glycerides, Butyrospermum Parkii Butter, Theobroma Cocoa (Cocoa) Seed Butter, Mango Butter, Hydrogenated Palm Kernel Glycerides, Hydrogenated Palm Glycerides, Sunflower Seed Wax, Soybean Glycerides, Butyrospermum Parkii
Unsaponifiables, , Wollwachs , Cera Alba, Beeswax, Zuckerrohrwachs, Cera Carnauba, Candelillawachs, Japanwachs, Hydrogenated Rapeseed Oil, Shellac Wax, Hydrogenated Lecithin, Hydrogenated Soybean Oil, Unsaponifiables,, Wool Wax, Cera Alba, Beeswax, Sugar Cane Wax, Cera Carnauba, Candelilla Wax, Japan Wax, Hydrogenated Rapeseed Oil, Shellac Wax, Hydrogenated Lecithin, Hydrogenated Soybean Oil,
aus der Gruppe synthetischer Wachse, insbesondere aus: from the group of synthetic waxes, in particular:
Cera Microcristallina, Synthetic Beeswax, Synthetic Wax, Polyethylene, Paraffin Wax, Ceresin, Ozokerite aus der Gruppe der Fettsäuren, insbesondere aus: Cera Microcristallina, Synthetic Beeswax, Synthetic Wax, Polyethylene, Paraffin Wax, Ceresin, Ozokerite from the group of fatty acids, in particular:
Palmitic Acid, Stearic Acid, Palmitic Acid, Stearic Acid,
aus der Gruppe der Ester aus Fettsäuren, insbesondere aus from the group of esters of fatty acids, in particular from
Cetearyl Nonanoate, Methyl Palmitate, Glyceryl Tribehenate, Glyceryl Laurate, Glyceryl Stearate, Cetyl Palmitate; Shea Butter Oleyl Esters, PEG-8 Beeswax  Cetearyl Nonanoates, Methyl Palmitates, Glyceryl Tribehenates, Glyceryl Laurates, Glyceryl Stearates, Cetyl Palmitates; Shea Butter Oleyl Esters, PEG-8 Beeswax
gewählt. selected.
Bevorzugte Zusätze sind weiterhin Butyrospermum Parkii Butter, Cocos Nucifera Oil, und/oder Cananga Odorate Flower Oil.  Other preferred additives are Butyrospermum Parkii Butter, Cocos Nucifera Oil, and / or Cananga Odorate Flower Oil.
Als Fettalkohole werden bevorzugt C14 bis C22 Fettalkohole verwendet. Bevorzugt werden die Fettalkohole gewählt aus der Gruppe linearen Fettalkohole, insbesondere Myristylalkohol (C14H30O), Cetylalkohol (oder Palmitylalkohol) (Ci6H340), Stearylalkohol (oder The fatty alcohols used are preferably C14 to C22 fatty alcohols. The fatty alcohols are preferably selected from the group consisting of linear fatty alcohols, especially myristyl (C14H 30 O), cetyl alcohol (or palmityl) (C 6 H 34 0), stearyl alcohol (or
Octadecylalkohol) (Ci8H380) sowie Cetylstearylalkohol (Cetearylalkohol),Behenylalkohol, Lanolin Alcohol, ein Gemisch der Alkohole Cetylalkohol (Hexadecanol) und Stearylalkohol (Octadecanol). Octadecyl) (C 8 H 38 0) and cetyl stearyl alcohol (cetearyl alcohol), behenyl alcohol, lanolin alcohol, (a mixture of the alcohols cetyl alcohol hexadecanol) and stearyl alcohol (octadecanol).
Der Anteil an C14-22 Fettalkoholen insgesamt beträgt vorteilhaft 0,5 bis 14 Gew.%, insbesondere 7 bis 9 Gew.%, bzw. insbesondere 0,5-5% bezogen auf die Gesamtmasse der Zubereitung.  The proportion of total C 14-22 fatty alcohols is advantageously from 0.5 to 14% by weight, in particular from 7 to 9% by weight, or in particular from 0.5 to 5%, based on the total mass of the preparation.
Als Kohlenwasserstoffgemische werden bevorzugt Kohlenwasserstoffgele bzw. Mischungen aus flüssigen und festen Paraffinkohlenwasserstoffen verwendet. Bevorzugt liegt der Gehalt an festen Kohlenwasserstoffen im Kohlenwasserstoffgemisch zwischen 1 und 50%, besonders bevorzugt zwischen 10 und 30%. Vorteilhaft ist die Verwendung von  Hydrocarbon gels or mixtures of liquid and solid paraffin hydrocarbons are preferably used as hydrocarbon mixtures. The content of solid hydrocarbons in the hydrocarbon mixture is preferably between 1 and 50%, particularly preferably between 10 and 30%. Advantageous is the use of
Kohlenwasserstoffgemischen, die Fransenmizellen bzw. parakristalline Strukturen ausbilden.Hydrocarbon mixtures which form fringe micelles or paracrystalline structures.
Der Anteil des Kohlenwasserstoffgemisch insgesamt beträgt vorteilhaft 1 bis 50 Gew.%, insbesondere 20 bis 30 Gew.%, bezogen auf die Gesamtmasse der Zubereitung. The proportion of the total hydrocarbon mixture is advantageously 1 to 50 wt.%, In particular 20 to 30 wt.%, Based on the total mass of the preparation.
Fettalkohol, insbesondere zwei oder drei Fettalkohole, sind erfindungsgemäß zwingend in der Zubereitung enthalten. Zusätzlich wird ein oder mehrere Wachse der Zubereitung hinzugefügt. Bevorzugt kann anstelle des Wachses auch ein Kohlenwasserstoffgemisch aus bei Raumtemperatur flüssigen und festen Kohlenwasserstoffen zugesetzt werden.  Fatty alcohol, in particular two or three fatty alcohols, according to the invention are necessarily included in the preparation. In addition, one or more waxes are added to the preparation. Preferably, instead of the wax, a hydrocarbon mixture of liquid and solid hydrocarbons which are liquid at room temperature may also be added.
Idealerweise umfasst die Zubereitung alle drei Bausteine, Fettalkohole, Wachse und  Ideally, the preparation comprises all three building blocks, fatty alcohols, waxes and
Kohlenwasserstoffgemisch. Hydrocarbon mixture.
Der erfindungsgemäßen Herstellung und Zubereitung können dann dem Fachmann bekannte kosmetische oder dermatologische Stoffe zugegeben werden, wobei deren Zugabe nicht die hautkonditionierenden Eigenschaften der erhältlichen Zubereitung beeinträchtigen darf. Vorteilhaft werden den Zubereitungen Verdicker, Füllstoffe und Neutralisierungsmittel zugesetzt. The preparation and preparation according to the invention may then be admixed with cosmetic or dermatological substances known to the person skilled in the art, the addition of which may not impair the skin-conditioning properties of the preparation obtainable. Advantageously, thickeners, fillers and neutralizing agents are added to the preparations.
Verdicker sind zur Stabilisierung des Systems vorteilhaft geeignet und verstärken die hautkonditionierenden Eigenschaften und das spezielle Hautgefühl der erfindungsgemäßen Zubereitungen.  Thickeners are advantageously suitable for stabilizing the system and enhance the skin-conditioning properties and the special skin feel of the preparations according to the invention.
Als Füllstoff wird bevorzugt Aluminium Starch Octenylsuccinat zugesetzt, was ebenfalls zu einer Optimierung des Hautgefühls führt indem der HautSchutzfilm etwas samtiger wirkt. As a filler, aluminum Starch Octenylsuccinat is preferably added, which also leads to an optimization of the skin feel by the skin protection film acts a little more velvety.
Als Neutralisierungsmittel wird vorteilhaft Natronlauge zugegeben, damit die Verdicker ihr Gelnetzwerk ausbilden können und ein stabiles System entsteht. Sodium hydroxide solution is advantageously added as a neutralizing agent so that the thickeners can form their gel network and a stable system is formed.
Die erfindungsgemäße Zubereitung ist emulgatorfrei. D.h. die ggf. als emulgierend wirkenden Polyacrylsäurepolymere werden erfindungsgemäß nicht als Emulgatoren verstanden.  The preparation according to the invention is emulsifier-free. That the optionally acting as emulsifying polyacrylic acid polymers are not understood according to the invention as emulsifiers.
Anders ausgedrückt, neben den Polyacrylsäurepolymeren werden der Zubereitung keine weiteren Emulgatoren zugesetzt.  In other words, in addition to the polyacrylic acid polymers, no further emulsifiers are added to the formulation.
Emulgatorfrei umfasst auch ein Mindestgehalt an zusätzlichen Emulgatoren von weniger als 1 Gew.%, bezogen auf die Gesamtmasse der Zubereitung, die beispielsweise durch Verunreinigungen oder Einschleppungen enthalten sein können. Der Einfluss auf die Produktperfomance ist in diesen Mengenbereichen ggf. unbeachtlich.  Emulgatorfrei also includes a minimum content of additional emulsifiers of less than 1 wt.%, Based on the total mass of the preparation, which may be included for example by impurities or entrainment. The influence on the product performance may be irrelevant in these quantity ranges.
Bevorzugt wird allerdings ein Gehalt an Emulgatoren von 0 Gew.%.  However, preference is given to a content of emulsifiers of 0% by weight.
Als Polyacrylsäurepolymere werden die in der Kosmetik bekannten Polymere der Acryl- und/oder Methacrylsäure sowie Acrylat-Crosspolymere verstanden.  Polyacrylic acid polymers are understood as meaning the polymers of acrylic and / or methacrylic acid known in cosmetics and acrylate crosspolymers.
Vorzugsweise sind dies Polymere (Makromoleküle) mit hohem Molekulargewicht (> 1 Mg/mol), welche aus einem Gerüst aus Polyacrylsäure und geringen Mengen an  Preferably, these are high molecular weight polymers (macromolecules) (> 1 Mg / mole) composed of a backbone of polyacrylic acid and small amounts
Polyalkenylether-Quervernetzungen bestehen. Sie werden auch als Carbomere bezeichnet. Diese wasserlöslichen oder dispergierbaren Polymere können in der Flüssigkeit, in der sie gelöst oder dispergiert sind, eine bedeutende Viskositätserhöhung hervorrufen. Dies wird durch die Bildung von Carbomer-Mikrogelen im Wasser hervorgerufen. Polyalkenylether cross-links exist. They are also referred to as carbomers. These water-soluble or dispersible polymers can cause a significant increase in viscosity in the liquid in which they are dissolved or dispersed. This is caused by the formation of carbomer microgels in the water.
Besonders bevorzugte Polyacrylsäurepolymere sind neben den Carbomeren diejenigen Acrylat-Crosspolymere, die eine polymere Emulgatorwirkung ausüben.  Particularly preferred polyacrylic acid polymers are, in addition to the carbomers, those acrylate crosspolymers which exert a polymeric emulsifier action.
Polymere Emulgatoren sind hauptsächlich Polyacrylsäurepolymere mit hohem  Polymer emulsifiers are mainly high polyacrylic acid polymers
Molekulargewicht. Diese emulgierend wirkenden Polyacrylsäurepolymere haben einen kleinen lipophilen Anteil zusätzlich zum hydrophilen Hauptteil. Ganz besonders bevorzugt im Sinne der vorliegenden Erfindung sind Acrylat-Crosspolymere, welche die INCI Bezeichnung "Acrylates/C 10-30 Alkyl Acrylate Crosspolymer" haben und unter den Molecular weight. These emulsifying polyacrylic acid polymers have a small lipophilic portion in addition to the hydrophilic body. For the purposes of the present invention, very particular preference is given to acrylate crosspolymers which have the INCI name "Acrylates / C 10-30 Alkyl Acrylate Crosspolymer" have and among the
Handelsbezeichnungen PemulenTR-1 und Pemulen TR-2 sowie Carbopol 1342, Carbopol 1382 und Carbopol ETD 2020 von der Firma NOVEON erhältlich sind. Trade names PemulenTR-1 and Pemulen TR-2 and Carbopol 1342, Carbopol 1382 and Carbopol ETD 2020 are available from NOVEON.
Besonders bevorzugt werden die Polyacrylsäurepolymere gewählt aus der Gruppe der Acrylates/C 10-30 Alkyl Acrylate Crosspolymere und/oder Carbomere. Insbesondere bevorzugt sind Acrylates/C 10-30 Alkyl Acrylate Crosspolymer Pemulen® TR-1 , z.B. von Lubrizol und Carbopol® 3128 von Lubrizol.  The polyacrylic acid polymers are particularly preferably selected from the group of acrylates / C 10-30 alkyl acrylate crosspolymers and / or carbomers. Especially preferred are acrylates / C 10-30 alkyl acrylate crosspolymer Pemulen® TR-1, e.g. from Lubrizol and Carbopol® 3128 from Lubrizol.
Erfindungsgemäß ist hierbei eine spezifische Kombination aus Polyacrylsäurepolymeren mit emulgierender Wirkung, wie das Pemulen TR-1 mit anderen Polyacrylsäurepolymeren, wie Carbopol 3128, die die sensorischen Eigenschaften verbessern und die Stabilität der Zubereitung, insbesondere bei höheren Temperaturen, und eine Verbindung mit freiem Wasser gewährleisten.  In this case, according to the invention, a specific combination of polyacrylic acid polymers having an emulsifying action, such as the Pemulen TR-1 with other polyacrylic acid polymers, such as Carbopol 3128, which improve the sensory properties and ensure the stability of the preparation, especially at higher temperatures, and a connection with free water.
Besonders bevorzugt ist hierbei eine Kombination aus drei Polyacrylsäurepolymeren, wobei ein Polyacrylsäurepolymer eine emulgierende Wirkung aufweist, wie z.B. das Pemulen TR-1 oder Pemulen TR-2, mit anderen Polyacrylsäurepolymeren, die die sensorischen  Particularly preferred herein is a combination of three polyacrylic acid polymers wherein a polyacrylic acid polymer has an emulsifying effect, e.g. the pemulen TR-1 or pemulen TR-2, with other polyacrylic acid containing the sensory
Eigenschaften verbessern und die Stabilität der Zubereitung, insbesondere bei höheren Temperaturen, gewährleisten (z.B. Carbopol 3128) und einem Polyacrylsäurepolymer, das die sensorischen Eigenschaften bei Aufnahme von freiem Wasser verbessern (z.B. Carbopol 981 ). To improve properties and stability of the preparation, especially at higher temperatures (e.g., Carbopol 3128) and a polyacrylic acid polymer, which improve the sensory properties upon ingestion of free water (e.g., Carbopol 981).
Vorteilhaft umfasst die erfindungsgemäße Zubereitung daher bevorzugt mindestens drei Polyacrylsäurepolymere, insbesondere drei Polyacrylsäurepolymere, die sich in ihren Eigenschaften unterscheiden.  The preparation according to the invention therefore advantageously comprises at least three polyacrylic acid polymers, in particular three polyacrylic acid polymers, which differ in their properties.
Der Anteil an Polyacrylsäurepolymeren insgesamt beträgt vorzugsweise 0,05 bis 2 Gew.%, insbesondere 0,2 bis 1 Gew.%, bezogen auf die Gesamtmasse der Zubereitung.  The proportion of total polyacrylic acid polymers is preferably 0.05 to 2 wt.%, In particular 0.2 to 1 wt.%, Based on the total mass of the preparation.
Vorteilhaft zeigte sich die Kombination mindestens zweier Polyacrylsäurepolymere mit mindestens zwei C14-22 Fettalkoholen zur verbesserten Stabilisierung der Zubereitung und vor allem das Hautgefühl bei der Anwendung auf feuchter/nasser Haut ist nicht  The combination of at least two polyacrylic acid polymers with at least two C 14-22 fatty alcohols for improved stabilization of the preparation and, above all, the skin feel when used on wet / moist skin has not proven to be advantageous
unangenehm, nicht wachsig, stumpf oder quietschend. uncomfortable, not waxy, dull or squeaky.
Erfindungsgemäß sind zwei Polyacrylsäurepolymer bzw. drei Polyacrylsäurepolymere so zu verstehen, dass jeweils ein Polyacrylsäurepolymer sich von den jeweils anderen in zumindest einer Eigenschaft unterscheidet. Die Stoffgruppe Acrylates/C 10-30 Alkyl Acrylate Crosspolymere umfasst beispielsweise die Handelsprodukte Pemulen TR-1 bzw. TR-2. According to the invention, two polyacrylic acid polymers or three polyacrylic acid polymers are understood to mean that one polyacrylic acid polymer differs from the other in at least one property. The substance group acrylates / C 10-30 alkyl acrylate crosspolymers comprises, for example, the commercial products pemulen TR-1 or TR-2.
Carbomere werden beispielsweise in die Typen A, B und C unterschieden. Unterschiede sind hierin beispielsweise deren Gele mit unterschiedlichen Viskositäten (United States Pharmacopoeia, USP ). Erfindungswesentlich und damit bevorzugt ist zudem ein Anteil an Wachsen oder bevorzugt eine Mischung aus flüssigen und festen Kohlenwasserstoffen mit einem Schmelzbereich von 4,5 bis 75°C, insbesondere bis 55°C nach DSC. Carbomers are differentiated, for example, into types A, B and C. Differences here are, for example, their gels with different viscosities (United States Pharmacopoeia, USP). Also essential to the invention and therefore preferred is a proportion of waxes or preferably a mixture of liquid and solid hydrocarbons having a melting range of 4.5 to 75 ° C, in particular up to 55 ° C according to DSC.
Als Öle können optional vorteilhaft unpolare bis mittelpolare Lipide in den  As oils may optionally be advantageous nonpolar to medium polar lipids in the
erfindungsgemäßen Zubereitungen zugesetzt werden. Ansonsten ist die Stabilität aufgrund der Emulgatorfreiheit schwieriger einzustellen. Preparations according to the invention may be added. Otherwise, the stability is more difficult to adjust due to the absence of emulsifiers.
Im Rahmen der vorliegenden Offenbarung wird als Oberbegriff für Fette, Öle, Wachse und dergleichen der Ausdruck„Lipide,, verwendet, wie dem Fachmanne durchaus geläufig ist. Auch werden die Begriffe„Ölphase,, und„Lipidphase,, synonym angewandt.  In the context of the present disclosure, the term "lipids" is used as a generic term for fats, oils, waxes and the like, as is well known to the person skilled in the art. Also, the terms "oil phase ,, and" lipid phase ,, are used interchangeably.
Öle und Fette unterscheiden sich unter anderem in ihrer Polarität. Es wird vorgeschlagen, die Grenzflächenspannung gegenüber Wasser als Maß für den Polaritätsindex eines Öls bzw. einer Ölphase anzunehmen. Dabei gilt, dass die Polarität der betreffenden Ölphase umso größer ist, je niedriger die Grenzflächenspannung zwischen dieser Ölphase und Wasser ist. Erfindungsgemäß wird die Grenzflächenspannung als ein mögliches Maß für die Polarität einer gegebenen Ölkomponente angesehen.  Among other things, oils and fats differ in their polarity. It is proposed to assume the interfacial tension against water as a measure of the polarity index of an oil or an oil phase. In this case, the lower the interfacial tension between this oil phase and water, the greater the polarity of the relevant oil phase. According to the invention, the interfacial tension is considered as a possible measure of the polarity of a given oil component.
Die Grenzflächenspannung ist diejenige Kraft, die an einer gedachten, in der Grenzfläche zwischen zwei Phasen befindlichen Linie der Länge von einem Meter wirkt. Die physikalische Einheit für diese Grenzflächenspannung errechnet sich klassisch nach der Beziehung Kraft/Länge und wird gewöhnlich in mN/m (Millinewton geteilt durch Meter) wiedergegeben. Sie hat positives Vorzeichen, wenn sie das Bestreben hat, die Grenzfläche zu verkleinern. Im umgekehrten Falle hat sie negatives Vorzeichen.  The interfacial tension is the force acting on an imaginary line of one meter length located in the interface between two phases. The physical unit for this interfacial tension is calculated classically by the force / length relationship and is usually expressed in mN / m (millinewtons divided by meters). It has a positive connotation if it tries to reduce the interface. In the opposite case, it has a negative sign.
Die erfindungsgemäße Zubereitung ermöglicht erstmals die Anwendung des Pflegens unter der Dusche sowie die Aufbringung von Wirkstoffen schon während des Duschvorgangs.  The preparation according to the invention makes it possible for the first time to apply care in the shower and to apply active ingredients during the showering process.
Die erfindungsgemäßen Zubereitungen werden vorteilhaft nur mit Konservierungsmitteln formuliert, die eine Wasserlöslichkeit von mehr als 0,75% bei 20°C aufweisen. The preparations according to the invention are advantageously formulated only with preservatives which have a water solubility of more than 0.75% at 20 ° C.
Aufgrund des Fehlens von Emulgatoren kann es ansonsten zu Destabilisierungen und zur Auskristallisierung kommen. Due to the lack of emulsifiers, destabilization and crystallization can otherwise occur.
Die erfindungsgemäßen Zubereitungen sind weiterhin bevorzugt auch frei von Tensiden. The preparations according to the invention are furthermore preferably also free of surfactants.
Tenside sind Substanzen, die die Oberflächenspannung einer Flüssigkeit oder die Surfactants are substances that are the surface tension of a liquid or the
Grenzflächenspannung zwischen zwei Phasen herabsetzen und die Bildung von Reduce interfacial tension between two phases and the formation of
Dispersionen ermöglichen oder unterstützen. Tenside bewirken, dass zwei eigentlich nicht miteinander mischbare Flüssigkeiten, wie zum Beispiel Öl und Wasser, dispergiert werden können. Des Weiteren werden Tenside als amphiphile Stoffe beschrieben, die organische, unpolare Substanzen in Wasser lösen können. Sie sorgen, bedingt durch ihren spezifischen Molekülaufbau mit mindestens einem hydrophilen und einem hydrophoben Enable or support dispersions. Surfactants cause two actually immiscible liquids, such as oil and water, can be dispersed. Furthermore, surfactants are described as amphiphilic substances that can dissolve organic, nonpolar substances in water. Due to their specific molecular structure, they provide at least one hydrophilic and one hydrophobic one
Molekülteil, für eine Herabsetzung der Oberflächenspannung des Wassers, die Part of the molecule, for a reduction of the surface tension of the water, the
Benetzung der Haut, die Erleichterung der Schmutzentfernung und -lösung, ein Moisturizing the skin, facilitating the removal of dirt and solution, a
leichtes Abspülen und - je nach Wunsch - für Schaumregulierung. easy rinsing and - as desired - for foam control.
Bei den hydrophilen Anteilen eines Tensidmoleküls handelt es sich meist um polare funktionelle Gruppen, beispielweise -COO", -OS03 2", -S03 ", während die hydrophoben Teile in der Regel unpolare Kohlenwasserstoff reste darstellen. Tenside werden im The hydrophilic fractions of a surfactant molecule are usually polar functional groups, for example -COO " , -OSO 3 2" , -SO 3 " , while the hydrophobic moieties generally represent nonpolar hydrocarbon radicals
Allgemeinen nach Art und Ladung des hydrophilen Molekülteils klassifiziert. Hierbei können vier Gruppen unterschieden werden: Generally classified by type and charge of the hydrophilic part of the molecule. Here four groups can be distinguished:
• anionische Tenside, Anionic surfactants,
• kationische Tenside,  Cationic surfactants,
• amphotere Tenside und  • amphoteric surfactants and
• nichtionische Tenside. • nonionic surfactants.
Anionische Tenside weisen als funktionelle Gruppen in der Regel Carboxylat-, Sulfat- oder Sulfonatgruppen auf. In wäßriger Lösung bilden sie im sauren oder neutralen Milieu negativ geladene organische Ionen. Kationische Tenside sind beinahe ausschließlich durch das Vorhandensein einer quatären Ammoniumgruppe gekennzeichnet. In wäßriger Lösung bilden sie im sauren oder neutralen Milieu positiv geladene organische Ionen. Amphotere Tenside enthalten sowohl anionische als auch kationische Gruppen und verhalten sich demnach in wässriger Lösung je nach pH-Wert wie anionische oder kationische Tenside. Im stark sauren Milieu besitzen sie eine positive und im alkalischen Milieu eine negative Ladung.  Anionic surfactants generally have carboxylate, sulfate or sulfonate groups as functional groups. In aqueous solution they form negatively charged organic ions in an acidic or neutral medium. Cationic surfactants are almost exclusively characterized by the presence of a quaternary ammonium group. In aqueous solution, they form positively charged organic ions in an acidic or neutral environment. Amphoteric surfactants contain both anionic and cationic groups and behave accordingly in aqueous solution depending on the pH as anionic or cationic surfactants. They have a positive charge in a strongly acidic environment and a negative charge in an alkaline environment.
Bekannt sind des Weiteren waschaktive Substanzen, wie beispielsweise kationische Tenside insbesondere quartäre Ammoniumverbindungen. Eine waschaktive Substanz findet in Waschmitteln, Spülmitteln, Shampoos, Duschgels Verwendung und bezeichnet den Anteil der Formulierung, der die Wasch- oder Reinigungsleistung beeinflusst. Waschaktive  Furthermore, washing-active substances, such as, for example, cationic surfactants, in particular quaternary ammonium compounds, are known. A detergent substance is used in detergents, dishwashing detergents, shampoos, shower gels and denotes the proportion of the formulation which influences the washing or cleaning performance. Detergent Active
Substanzen erhöhen die„Löslichkeit" von Fett- und Schmutzpartikeln in Wasser, die in der Wäsche oder am Körper haften. Sie können natürlichen oder synthetischen Ursprungs sein. Sie werden nach der Art ihrer Ladung in anionisch, kationisch, ampholytisch oder nichtionisch unterschieden. Substances increase the "solubility" of fat and dirt particles in water that adhere to the laundry or body, they can be of natural or synthetic origin and are classified according to the nature of their charge in anionic, cationic, ampholytic or nonionic.
Emulgatoren bewirken, dass zwei nicht miteinander mischbare Flüssigkeiten (zum Beispiel Öl in Wasser) sich zu einer Emulsion vermengen können. Aufgrund des amphiphilen Charakters dringen sie mit ihrem fettlöslichen Teil in das Öl ein. Durch den hydrophilen Teil kann das nun durch Rühren entstandene Öltröpfchen in der wässrigen Umgebung dispergiert" werden. Emulgatoren haben primär keinen waschaktiven, tensidischen Emulsifiers cause two immiscible liquids (for example, oil in water) to mix together to form an emulsion. Due to the amphiphilic character, they penetrate into the oil with their fat-soluble part. Through the hydrophilic part For example, the oil droplets produced by stirring can be dispersed in the aqueous environment
Charakter. Character.
Emulgatoren und Tenside können die Barriereschicht der Haut schädigen. Den  Emulsifiers and surfactants can damage the skin's barrier layer. The
Zubereitungen werden daher weder Emulgatoren noch Tenside zugesetzt, also vorteilhaft wird auf den Zusatz zusätzlicher waschaktiver Substanzen verzichtet. Preparations are therefore added neither emulsifiers nor surfactants, so it is advantageous to dispense with the addition of additional washing-active substances.
Vorteilhaft sind den Zubereitungen Hautbefeuchtungsmittel, Moisturizer, als Wirkstoff zugesetzt.  Advantageously, the preparations skin moisturizer, moisturizer, added as an active ingredient.
Die Zubereitungen werden auf nasser Haut verwendet und insbesondere auch zur Rasur. The preparations are used on wet skin and especially for shaving.
Die erfindungsgemäße Zubereitung kann zur Hautkonditionierung verwendet werden. The preparation according to the invention can be used for skin conditioning.
Sie ermöglicht die Erzeugung eines Hautschutzfilms nach Applikation der Zubereitung auf der Haut und anschließendem Abspülen mit Wasser.  It allows the production of a skin protection film after application of the preparation on the skin and subsequent rinsing with water.
Der sich bildende Schutzfilm ist idealerweise mind. 1 μηη dick (gemessen nach IR-ATR Messtechnik) und/oder umfasst keine hautbarriereschädigende Stoffe, insbesondere keine Emulgatoren, Tenside, PEG's und/oder halogenorganische Verbindungen. The protective film that forms is ideally at least 1 μm thick (measured according to IR-ATR measurement technology) and / or does not comprise substances which damage the skin barrier, in particular no emulsifiers, surfactants, PEG 's and / or organohalogen compounds.
Bevorzugte Ausführungsformen der erfindungsgemäßen Zubereitungen umfassen ein oder mehrere Wachse, ein Kohlenwasserstoffgemisch und ein Wirkstoff aus der Gruppe der Hautbefeuchtungsmittel, wobei als Fettalkohole Myristyl-, Cetearyl- und/oder Stearylalkohole, als Wachs Cera Microcristallina und als Kohlenwasserstoffgemisch Paraffinum Liquidum gewählt wird.  Preferred embodiments of the preparations according to the invention comprise one or more waxes, a hydrocarbon mixture and an active ingredient from the group of skin moisturizing agents, wherein the fatty alcohols used are myristyl, cetearyl and / or stearyl alcohols, wax Cera Microcristallina and as the hydrocarbon mixture paraffin liquid.
Vorteilhaft ist in dieser Zubereitung als Hautbefeuchtungswirkstoff Glycerin, sowie Ubichinon Wirkstoff Q10 zur Hautpflege und ein kühlender Wirkstoff wie Menthol zu wählen.  Glycerin, as well as Ubichinon active ingredient Q10 for skin care and a cooling active substance such as menthol, are advantageous in this preparation as skin moisturizing agent.
Diese Dreierkombination an Wirkstoffen verursacht ein angenehmes Hautgefühl und -pflege sowohl während des Duschens als auch eine langanhaltende Hautpflege.  This triple combination of active ingredients creates a pleasant skin feel and care during both showering and prolonged skin care.
Als ein Neutralisierungsmittel ist bevorzugt Natriumhydroxid enthalten.  As a neutralizing agent, sodium hydroxide is preferably contained.
Bei Einschränkungen auf bevorzugt genannte Stoffe, seien es Lipide, Wachse, Wirkstoffe oder Filmbildner oder weitere bevorzugt gennannte Bestandteile, so beziehen sich deren bevorzugten Anteilsbereiche dann auch auf die dann ausgewählten Einzelbestandteile. Die anderen, die durch die Einschränkung ausgeschlossenen Bestandteile, zählen dann nicht mehr zu den aufgeführten Anteilsbereichen hinzu.  In the case of restrictions on substances which are preferred, whether lipids, waxes, active substances or film formers or further preferred components, their preferred ranges of proportions then also relate to the individual constituents then selected. The others, which are excluded from the restriction, will no longer be included in the listed proportions.
Nachfolgende Beispiele veranschaulichen die erfindungsgemäße Herstellung um  The following examples illustrate the preparation according to the invention
erfindungsgemäße Zubereitungen zu erhalten. to obtain preparations according to the invention.
Die Zahlenwerte sind Gewichtsanteile, bezogen auf die Gesamtmasse der Zubereitung. Inhaltststoff 1 2 3 4 5The numerical values are parts by weight, based on the total mass of the preparation. Content substance 1 2 3 4 5
Cera Microcristallina 25,000 16,5000 16,5000 35,000 45,000Cera Microcristallina 25,000 16,5000 16,5000 35,000 45,000
Paraffinium Liquidum 8,5000 8,5000 Paraffinium Liquidum 8.5000 8.5000
Myristylalkohol 1 ,0000 1 ,0000 1 ,0000 2,0000  Myristyl alcohol 1, 0000 1, 0000 1, 0000 2,0000
Cetearylalkohol 5,0000 5,0000 5,0000 4,0000 4,0000 Cetearyl alcohol 5,0000 5,0000 5,0000 4,0000 4,0000
Stearylalkohol 2,0000 2,0000 2,0000 3,0000 3,0000Stearyl alcohol 2,0000 2,0000 2,0000 3,0000 3,0000
Hydrierte Kokosglyceride 3,0000 3,0000 3,0000 2,0000 2,0000Hydrogenated coconut glycerides 3.0000 3.0000 3.0000 2.0000 2.0000
Mandelöl 0,3500 0,7000Almond oil 0,3500 0,7000
Aluminumstärkeoctenylsuccinat 1 ,0000 1 ,0000 1 ,0000 1 ,0000 1 ,0000Aluminum starch octenylsuccinate 1, 0000 1, 0000 1, 0000 1, 0000 1, 0000
Parfüm 0,8000 0,7000 1 ,0000 0,7000 0,7000Perfume 0.8000 0.7000 1, 0000 0.7000 0.7000
Glycerin 5,1000 5,1000 5,1000 15,100 10,100Glycerol 5,1000 5,1000 5,1000 15,100 10,100
Natriumhydroxidlösung 45%ig 0,1600 0,1600 0,1600 0,1600 0,1600Sodium hydroxide solution 45% 0.1600 0.1600 0.1600 0.1600 0.1600
Phenoxyethanol 0,5000 0,5000 0,5000 0,4000 0,4000Phenoxyethanol 0.5000 0.5000 0.5000 0.4000 0.4000
Methylisothiazolinone 0,0900 0,0900 0,0900 0,0800 0,0800Methylisothiazolinone 0.0900 0.0900 0.0900 0.0800 0.0800
Acrylates/C 10-30 Alkyl Acrylate Acrylates / C 10-30 alkyl acrylates
Crosspolymer (Carbopol 3128) 0,1000 0,1000 0,1000 0,1200 Crosspolymer (Carbopol 3128) 0.1000 0.1000 0.1000 0.1200
Carbomer (Carbopol 981 ) 0,0200 0,0200 0,0200 0,0200 0,0200 Carbomer (Carbopol 981) 0,0200 0,0200 0,0200 0,0200 0,0200
Acrylates/C 10-30 Alkyl Acrylate Acrylates / C 10-30 alkyl acrylates
Crosspolymer (Pemulen TR-1 ) 0,1000 0,1000 0,1000 0,1200 0,1400Crosspolymer (Pemulen TR-1) 0.1000 0.1000 0.1000 0.1200 0.1400
Meersalz 0,0100 0,0100 0,0100 0,0500Sea salt 0,0100 0,0100 0,0100 0,0500
Q10 0,0100 0,0050 0,0300 0,005 0,0010Q10 0.0100 0.0050 0.0300 0.005 0.0010
4-Butylresorcin 0,3000 0,0010 0,1000 0,02004-butylresorcinol 0.3000 0.0010 0.1000 0.0200
N-(4-(2,4- dihydroxyphenyl)thiazol-2- yl)isobutyramid 0,1000 0,0250 0,0100 N- (4- (2,4-dihydroxyphenyl) thiazol-2-yl) isobutyramide 0.1000 0.0250 0.0100
Kreatin 0,5000 1 ,0000 0,0010  Creatine 0,5000 1, 0000 0,0010
Niacinamid 0,2000 0,0010 0,1000 Niacinamide 0.2000 0.0010 0.1000
Magnolia Officinalis Bark Magnolia Officinalis Bark
Extract 0,5000 0,1500 0,2500 Arctium Lappa Fruit Extract 0,1000 0,5000 0,0100Extract 0.5000 0.1500 0.2500 Arctium Lappa Fruit Extract 0.1000 0.5000 0.0100
Glycyrrhiza Inflata Root Extract 0,0010 0,0250 0,1000Glycyrrhiza Inflata Root Extract 0.0010 0.0250 0.1000
1 ,3-Dihydroxyaceton 0,1500 1 ,0000 3,5000 0,8000 2,0001, 3-dihydroxyacetone 0.1500 1, 0000 3.5000 0.8000 2,000
Glyceryl Glucoside 5,0000 0,1000 1 ,5000 0,0100Glyceryl Glucosides 5.0000 0.1000 1, 5000 0.0100
Menthoxypropandiol 0,1000 1 ,5000 0,6000 0,2000 0,0100Menthoxypropanediol 0.1000 1, 5000 0.6000 0.2000 0.0100
Panthenol 0,0100 Panthenol 0,0100
Glycin Soja Germ Extrakt 0,2000 0,0500 Glycine Soy Germ Extract 0.2000 0.0500
Glyzyrrhetinsäure 0,0100 0,1000 0,0050 Glycyrrhetinic acid 0.0100 0.1000 0.0050
Wasser ad 100 ad 100 ad 100 ad 100 ad 100  Water ad 100 ad 100 ad 100 ad 100 ad 100
Trisodium EDTA 0,10 0,10 0,10 0,10 Trisodium EDTA 0.10 0.10 0.10 0.10
Q10 0,01 0,005 0,03 0,0045 0,005Q10 0.01 0.005 0.03 0.0045 0.005
4-Butylresorcin 0,30 0,001 0,10 4-butylresorcinol 0.30 0.001 0.10
N-(4-(2,4-dihydroxyphenyl)thiazol-2-yl)isobutyramid 0,10 0,025 0,01 N- (4- (2,4-dihydroxyphenyl) thiazol-2-yl) isobutyramide 0.10 0.025 0.01
Kreatin 0,50 1 ,00 0,001Creatine 0.50 1, 00 0.001
Niacinamid 0,20 0,001 Niacinamide 0.20 0.001
Menthol 0,30  Menthol 0.30
Aqua ad100 ad 100 ad 100 ad 100 ad100  Aqua ad100 ad 100 ad 100 ad 100 ad100

Claims

Patentansprüche claims
1 . Emulgatorfreie kosmetische oder dermatologische Zubereitung umfassend ein oder mehrere Polyacrylsäurepolymere, ein oder mehrere C14-22 Fettalkohole und ein oder mehrere Wachse und/oder ein Kohlenwasserstoffgemisch dadurch gekennzeichnet, dass ein oder mehrere Wirkstoffe enthalten sind.  1 . An emulsifier-free cosmetic or dermatological preparation comprising one or more polyacrylic acid polymers, one or more C 14-22 fatty alcohols and one or more waxes and / or a hydrocarbon mixture, characterized in that one or more active substances are contained.
2. Zubereitung nach Anspruch 1 dadurch gekennzeichnet, dass der oder die Wachse zu einem Anteil von mehr als 0,5 Gew.%, bezogen auf die Gesamtmasse der Zubereitung, gewählt werden.  2. Preparation according to claim 1, characterized in that the wax or waxes to a proportion of more than 0.5 wt.%, Based on the total mass of the preparation, are selected.
3. Zubereitung nach einem der vorstehenden Ansprüche dadurch gekennzeichnet, dass als Fettalkohole Myristyl-, Cetearyl- und/oder Stearylalkohole gewählt werden.  3. Preparation according to one of the preceding claims, characterized in that are selected as fatty alcohols myristyl, cetearyl and / or stearyl alcohols.
4. Zubereitung nach einem der vorstehenden Ansprüche dadurch gekennzeichnet, dass als Wachs Cera Microcristallina, Coco-Glycerid, C18-36 Acid Triglycerid, Synthetic Wax, Cera Alba, Paraffin, Copernicia Cerifera Cera , C18-38 Alkyl Hydroxystearoylstearat, Butyrospermum Parkii Butter, Olus oil, C20-40 Alkohol und/oder Bienenwachs gewählt werden  4. Preparation according to one of the preceding claims, characterized in that as wax Cera Microcristallina, Coco glyceride, C18-36 acid triglyceride, synthetic wax, Cera Alba, paraffin, Copernicia cerifera Cera, C18-38 alkyl hydroxystearoyl stearate, Butyrospermum Parkii butter, Olus oil, C20-40 alcohol and / or beeswax
5. Zubereitung nach einem der vorstehenden Ansprüche dadurch gekennzeichnet, dass ein oder mehrere Filmbildner enthalten sind.  5. Preparation according to one of the preceding claims, characterized in that one or more film formers are included.
6. Zubereitung nach Anspruch 5 dadurch gekennzeichnet, dass als Filmbildner  6. Preparation according to claim 5, characterized in that as a film former
Hexadecencopolymer, Trimethylsiloxysilicat, Polypropylsilsesquioxan, Polysilicone-25, Acrylatcopolymer,Polyurethan, Methacrylat, Polyglycerylstearat, Dilinoleat- Crosspolymer, Akyl-Acrylate/Methacrylic Acid Crosspolymer, IPDI Copolymer, insbesondere VP/Hexadecene Copolymer, Octyldodecyl Citrate Crosspolymer, Trimethylsiloxysilicat/ Polypropylsilsesquioxan, Polysilicone-25, Ammoniumacrylate - Copolymer, Acrylatcopolymer, Polyurethane-2 und Polymethylmethacrylat,  Hexadecene copolymer, trimethylsiloxysilicate, polypropylsilsesquioxane, polysilicone-25, acrylate copolymer, polyurethane, methacrylate, polyglyceryl stearate, dilinoleate crosspolymer, alkyl acrylate / methacrylic acid crosspolymer, IPDI copolymer, especially VP / hexadecenes copolymer, octyldodecyl citrate crosspolymer, trimethylsiloxysilicate / polypropylsilsesquioxane, polysilicone-25 , Ammonium acrylate copolymer, acrylate copolymer, polyurethane-2 and polymethyl methacrylate,
Polyglycerylstearat/ Isostearatdilinoleat - Crosspolymer, Octadecen/MA Copolymer (und) Methylacetylricinoleat (und) Diisooctyladipat, Trimethylsiloxysilicat, Polyurethan-34, C8- 22 Alkyl Acrylate/Methacrylic Acid Crosspolymer und/oder Castor Oil/IPDI Copolymer gewählt werden.  Polyglyceryl stearate / isostearate dilinoleate - crosspolymer, octadecene / MA copolymer (and) methyl acetylricinoleate (and) diisooctyl adipate, trimethylsiloxysilicate, polyurethane-34, C8-22 alkyl acrylate / methacrylic acid crosspolymer and / or castor oil / IPDI copolymer.
7. Zubereitung nach Anspruch 5 oder 6 dadurch gekennzeichnet, dass als Filmbildner Castor Oil/IPDI Copolymer , Trimethylsiloxysilicat/Polypropylsilsesquioxan und/oder Acrylatcopolymer gewählt werden  7. Preparation according to claim 5 or 6, characterized in that as a film former Castor Oil / IPDI copolymer, trimethylsiloxysilicate / Polypropylsilsesquioxan and / or acrylate copolymer can be selected
8. Zubereitung nach Anspruch 5, 6 oder 7 dadurch gekennzeichnet, dass der oder die  8. Preparation according to claim 5, 6 or 7, characterized in that the or
Filmbildner zu einem Anteil von 0,1 - 10 Gew.%, bezogen auf die Gesamtmasse der Zubereitung, gewählt werden.  Film former to a proportion of 0.1 to 10 wt.%, Based on the total mass of the preparation can be selected.
9. Zubereitung nach einem der vorstehenden Ansprüche dadurch gekennzeichnet, dass ein oder mehrere Wirkstoffe aus der Gruppe der hautpflegenden Stoffe, der Selbstbräunungsmittel, der kühlenden Stoffe, der wärmenden Substanzen und/oder der hautaufhellenden Stoffe gewählt werden. 9. Preparation according to one of the preceding claims, characterized in that one or more active substances from the group of skin-care substances, the Self-tanning agents, the cooling substances, the warming substances and / or the skin lightening substances are selected.
10. Zubereitung nach Anspruch 9 dadurch gekennzeichnet, dass ein oder mehrere  10. Preparation according to claim 9, characterized in that one or more
Wirkstoffe aus nur einer der Gruppen der hautpflegenden Stoffe, der  Active substances from only one of the groups of skin-care substances, the
Selbstbräunungsmittel, der kühlenden Stoffe, der wärmenden Substanzen und/oder der hautaufhellenden Stoffe gewählt werden.  Self-tanning agents, the cooling substances, the warming substances and / or the skin lightening substances are selected.
1 1. Zubereitung nach einem der vorstehenden Ansprüche dadurch gekennzeichnet, dass als Wirkstoff D-Biotin, Coenzym Q10, Folsäure und/oder deren Derivate, Rucinol, Panthenol, Niacinamid, alpha-Glucosylrutin, Carnitin, Carnosin, natürliche und/oder synthetische Isoflavonoide, Kreatin, Taurin, ß-Alanin,1-Methylhydantoin-2-lmide , N-(4- (2,4-dihydroxyphenyl)thiazol-2-yl)isobutyramide, Glycine Soja Germ Extract, Pimpinella Anisum Fruit Extract, Arctium Lappa Fruit Extract, Magnolia Officinalis Bark Extract, Sodium Hyaluronate, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Glucosylrutin und Isoquercitrin, Sodium Chloride, Glyceryl Glucoside, Climbazole, Piroctone Olamine, Menthoxypropanediol, Menthane Carboxamide Ethylpyridine, Cyanomethylphenyl Menthane Carboxamide, 1 ,3-Dihydroxyaceton, Glycerylglucose, Menthol und/oder 4- Butylresorcinol gewählt werden.  1 1. A preparation according to any one of the preceding claims, characterized in that as active ingredient D-biotin, coenzyme Q10, folic acid and / or derivatives thereof, rucinol, panthenol, niacinamide, alpha-glucosylrutin, carnitine, carnosine, natural and / or synthetic isoflavonoids, Creatine, Taurine, β-Alanine, 1-Methylhydantoin-2-Imide, N- (4- (2,4-Dihydroxyphenyl) thiazol-2-yl) isobutyramide, Glycine Soy Germ Extract, Pimpinella Anisum Fruit Extract, Arctium Lappa Fruit Extract , Magnolia Officinalis Bark Extract, Sodium Hyaluronate, Glycyrrhiza Inflata Root Extract, Glycyrrhetinic Acid, Glucosylrutin and Isoquercitrin, Sodium Chloride, Glyceryl Glucoside, Climbazole, Piroctone Olamine, Menthoxypropanediol, Menthane Carboxamide Ethylpyridine, Cyanomethylphenyl Menthane Carboxamide, 1, 3-Dihydroxyacetone, Glyceryl Glucose, Menthol and / or 4-butylresorcinol.
12. Zubereitung nach einem der vorstehenden Ansprüche dadurch gekennzeichnet, dass als Wirkstoff Q10 gewählt wird.  12. Preparation according to one of the preceding claims, characterized in that is selected as the active ingredient Q10.
13. Zubereitung nach einem der vorstehenden Ansprüche dadurch gekennzeichnet, dass die Wirkstoffe lipophil sind.  13. Preparation according to one of the preceding claims, characterized in that the active substances are lipophilic.
14. Zubereitung nach einem der vorstehenden Ansprüche dadurch gekennzeichnet, dass ein oder mehrere Hautbefeuchtungsmittel enthalten sind.  14. Preparation according to one of the preceding claims, characterized in that one or more skin moisturizing agents are included.
15. Zubereitung nach einem der vorstehenden Ansprüche dadurch gekennzeichnet, dass die Zubereitung frei von Tensiden ist.  15. Preparation according to one of the preceding claims, characterized in that the preparation is free of surfactants.
16. Zubereitung nach einem der vorstehenden Ansprüche umfassend als Wirkstoffe Q10 und Menthol.  16. Preparation according to one of the preceding claims comprising as active ingredients Q10 and menthol.
17. Verwendung der Zubereitung nach einem der vorstehenden Ansprüche auf nasser Haut.  17. Use of the preparation according to one of the preceding claims on wet skin.
EP14755810.0A 2013-08-29 2014-08-25 Emulsifier-free, skin conditioning and active ingredient-containing cosmetic or dermatological preparation Ceased EP3038591A1 (en)

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DE201310217244 DE102013217244A1 (en) 2013-08-29 2013-08-29 Emulsifier-free, skin-conditioning and active ingredient-containing cosmetic or dermatological preparation
DE201420001438 DE202014001438U1 (en) 2013-08-29 2014-02-19 Emulsifier-free, skin-conditioning and active ingredient-containing cosmetic or dermatological preparation
DE201420001570 DE202014001570U1 (en) 2013-08-29 2014-02-24 Emulsifier-free, skin-conditioning and active ingredient-containing cosmetic or dermatological preparation
PCT/EP2014/067974 WO2015028417A1 (en) 2013-08-29 2014-08-25 Emulsifier-free, skin conditioning and active ingredient-containing cosmetic or dermatological preparation

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DE202014001438U1 (en) 2014-03-05
DE202014001570U1 (en) 2014-03-27

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