Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
  • A61Q1/02—Preparations containing skin colorants, e.g. pigments
  • A61Q1/025—Semi-permanent tattoos, stencils, e.g. "permanent make-up"
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
  • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
  • A61K8/8105—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
  • A61K8/8117—Homopolymers or copolymers of aromatic olefines, e.g. polystyrene; Compositions of derivatives of such polymers
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
  • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
  • A61K8/8141—Compositions 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
  • A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
  • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
  • A61K8/85—Polyesters
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
  • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
  • A61K8/87—Polyurethanes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
  • A61Q1/02—Preparations containing skin colorants, e.g. pigments
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
  • A61Q1/02—Preparations containing skin colorants, e.g. pigments
  • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
  • A61Q1/02—Preparations containing skin colorants, e.g. pigments
  • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
  • A61Q1/06—Lipsticks
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
  • A61Q1/02—Preparations containing skin colorants, e.g. pigments
  • A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
  • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
  • A61K2800/59—Mixtures
  • A61K2800/594—Mixtures of polymers

Definitions

• the invention relates to a preparation for application to the skin or skin appendages and to the use thereof, a method for the production thereof and a device for the application thereof.
• the preparation according to the invention can be used for decorative purposes, for applying make-up to the skin, the semi-mucous membranes or for skin regions in the vicinity of mucous membranes. It can also be applied to skin appendages.
• skin appendages There are products that are applied to the skin appendages, such as hair, eyelashes and eyebrows, or their artificial replicas, to give them the desired properties.
• hair, eyelashes and eyebrows or their artificial replicas, to give them the desired properties.
• eyelashes can be provided with a colored coating that highlights them, shapes them and, if necessary, extends them.
• hair it is known to provide hair with a coating which smoothes the hair, gives it volume or, if necessary, also stains individual strands.
• Pens or pastes are usually in anhydrous form as mixtures of vegetable, animal or synthetic oils, fats and waxes, in which a powder phase of pigments approved for cosmetics, pearlescent agents and fillers such as talc, kaolin or amorphous silicon dioxide is dispersed.
• Loose or pressed powders usually consist of mixtures of pigments approved for cosmetics, pearlescent agents and fillers, which are brought into a manageable or processable form by means of an oil-based binder or in the form of an emulsion.
• GA Nowak in "The Cosmetic Preparations", 1st edition 1969 on pages 588 and 589, describes various recipes for eyeliners or liquid make-up, which are based on synthetic film formers such as polyvinylpyrrolidone (PVP) or carboxymethyl cellulose or natural film formers such as shellac, tragacanth On page 441, GA Nowak describes lip varnishes based on solvents such as ethyl alcohol or isopropanol, which contain ethyl cellulose, cellulose acetate, shellac, methyl abietate or PVP as film formers, but such preparations have obviously been used in practice because of their solvent content
• EP-A 0 793 957 describes a composition which can be applied to the skin, the semi-mucous membranes or the mucous membranes, which contains an aqueous dispersion of particles of a film-forming polymer which on a carrier has a film with a hardness below 110 (determined from NF-T-30-016).
• compositions are said to form a film which adheres well to the base, which is soft and flexible, follows the movements of the skin and does not become cracked and does not come off. These compositions should not migrate to the skin and should not be transferred to other materials.
• a wax-free gel composition is known from EP-A 10 104 18, which contains polyurethane polymers as film formers. This composition is used as a mascara and is said to stick to the eyelashes for more than a day. To adjust the viscosity, a pyrogenic silica is preferably used for these compositions, which, however, leads to a crumbling off of the mass, particularly when applied more heavily.
• EP-A 12 492 25 also describes a wax-free gel composition which is said to be waterproof and should last for more than two days. This composition is to be used in particular as a colorant for hair, eyelashes and eyebrows and is intended to form a smooth coating after application and drying.
• the pyrogenic silica contained in the recipe thickens the composition even in a low concentration and makes the dried film appear dull. Since it is also not hydrophobic, it promotes the water absorption of the film and thus reduces the water resistance and thus its durability.
• US Pat. No. 6,458,390 describes a makeup composition which contains iron oxide pigments and film formers and is said to be long-lasting. However, for this composition it is necessary that a special silicone acrylate copolymer is used dissolved in a volatile solvent. In contrast, an aqueous dispersion is used according to the invention. Water-based products can contain the ingredients either dissolved or dispersed. In the latter case, care must be taken to ensure that in the case of undissolved ingredients, e.g. Pigments that do not settle over time and therefore lead to unusable products.
• the products should be stable even when bathing or showering, i.e. in contact with water, possibly also in connection with shampoos, shower preparations or soap.
• the coating should be constructed in such a way that it holds the ingredients so that portions of it cannot migrate and the surrounding area can stain.
• Make-up can be applied to the skin, on semi-mucous membranes and / or near mucous membranes.
• Preparations for make-up are to be understood in particular as lip rouge, cheek rouge, make-up, eyeshadow, lip liner, eyeliner, concealer and body paint such as so-called temporary tattoos or mehndi painting.
• Another object of the invention was to provide a cosmetic preparation which can be applied to skin appendages and which can be used there for a long time, e.g. adheres for more than 8 hours and in particular for more than a day, remains in the place where it is applied, without being removed by water, sweat or contact with objects, but is also easily removable again. Furthermore, it was an object of the invention to provide a wax-free composition which provides a permanent and glossy coating. In addition, a composition should be provided that is easy to apply and has a long shelf life.
• a mixture of at least two aqueous dispersions of film-forming polymers is used according to the invention, which leads to better adhesion and longer shelf life.
• the preparation according to the invention for application to the skin or skin appendages on an aqueous basis thus contains a mixture of at least two aqueous dispersions of flame-forming polymers, one of which is a polyurethane-based polymer and the other an acrylic-based polymer, and optionally conventional ingredients.
• the preparation has a viscosity, measured at 25 ° C. and with 200 s "1 , in
• the preparation according to the invention is in the form of an aqueous dispersion which dries after application to form a waterproof film and adheres excellently to the applied site.
• This film is elastic and stretchable and can therefore follow the movements of the skin and semi-mucous membranes or the hair. On the other hand, it neither contracts nor shrinks significantly when it dries, so that it does not create a feeling of tension on the skin or lips and does not crumble away. It also does not become cracked or granular and is so elastic and durable that it does not detach from the edge of the application or even as a whole - rather, it remains "like a second skin" at the application site.
• the film usually shows a high surface gloss and high reflectivity when it is dried, but at the latest after it has dried completely Stable so that it is not adversely affected by a possible second application of the preparation.
• the dry film must not stick or give a sticky feeling.
• the preparation according to the invention contains colorants, they must have such grain sizes, surface properties and shapes that the colorants do not adversely affect the film formation, although they - to a certain extent as “foreign bodies” - interfere with the formation of the film.
• Inorganic pigments can be suitable as colorants for cosmetic preparations , e.g. yellow, red or black iron oxides, ultramarine, chrome oxide green, chrome oxide hydrate green, carbon black (carbon black) and / or possibly organic pigments, lacquers of organic dyes, platelet-shaped metal powders, e.g.
• a composition which is very easy to apply and, once applied, adheres in place for a long time without changing in a negative way, passing over to other objects, migrating to adjacent areas or staining or crumbling off.
• the composition can be stored for a very long time without ingredients settling.
• the coating or film obtained with the composition according to the invention has the gloss which is desirable for a cosmetic.
• the content of an aqueous dispersion of at least one polycondensate is therefore selected for the preparation according to the invention selected from the anionic, cationic, nonionic or amphoteric polyurethane polymers or copolymers.
• the polyurethane can advantageously be selected from the group of polyester polyurethanes, polyether polyurethanes, polyurethane polyvinyl pyrrolidones, acrylic polyurethanes and silicone-containing polyurethanes and mixtures thereof.
• the polyurethane is in the aqueous phase in the form of particles, the size of which is preferably in a range from 10 to 1000 nm, particularly preferably 15 to 300 nm and in particular 30 to 100 nm.
• polyurethane dispersions that form a film after application are suitable.
• Such polyurethane polymers are known to the person skilled in the art.
• polyester-polyurethanes e.g. by the company Noveon (formerly BF Goodrich) under the name Avalure, e.g. Avalure UR-425, Avalure UR-430, Avalure UR-405 and Avalure UR-410, or products such as those offered by Zeneca under the name Neorez.
• the polyurethane polymer is preferably one designated by the CTFA name Polyurethane-2.
• the polyurethane polymer is used as an aqueous dispersion.
• a dispersion of the polymer with a proportion of polymer of 10 to 80%, preferably 30 to 60% in water is preferably used.
• Mixtures of the polyurethane polymers listed above, in particular mixtures of polyester polyurethanes and polyether polyurethanes, or else mixtures of polyurethane polymers with polyureas, silicone acrylates, PEG / PPG-25/25 and / or dimethicone / acrylates copolymer are also suitable.
• the proportion of the aqueous polyurethane dispersion in the total composition should be in a range from 1 to 60%, preferably 15 to 50%. All percentages in this description, examples and claims are always by weight unless otherwise noted.
• the polyurethane component ensures, among other things, water resistance in the film formed. The desired effect of the polymer no longer occurs below a proportion of 1%. With more than 60%, the adjustment of the viscosity and the incorporation of colorants is difficult.
• the second essential component of the composition according to the invention is at least one acrylic-based polymer which ensures the adhesion of the composition, gloss and abrasion resistance.
• it is a polymer obtained by radical polymerization, which is preferably an acrylate Copolymer or acrylic and / or vinyl polymer and / or acrylic and / or vinyl copolymer.
• These polymers are obtained in particular by the radical polymerization of suitable monomers, preferably by means of emulsion polymerization.
• Acrylic acid, crotonic acid, maleic anhydride or methacrylic acid may be mentioned as examples of suitable monomers.
• acrylic polymers and copolymers can also be obtained by polymerizing or copolymerizing monomers which are selected, for example, from monomers such as methyl acrylate, ethyl acrylate, butyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, butyl acrylamide, ethylhexyl acrylamide and the like.
• Acrylic polymers are also used as aqueous dispersions, the particle size of which is in the same range as that of the polyurethane polymer. Both aryl acrylate copolymers and alkyl acrylate copolymers can be used as the acrylic polymer or acrylate copolymer, in which case the alkyl portion may have 1 to 30 carbon atoms.
• the acrylate copolymer is a polymer which is preferably selected by polymerization of at least one monomer which contains an ethylenically unsaturated bond and is selected from ⁇ , ⁇ -ethylenically unsaturated carboxylic acids, ⁇ , ⁇ -ethylenically unsaturated carboxylic acid esters and ⁇ , ⁇ -ethylenically unsaturated carboxylic acid amides and Combinations of two or more of these monomers are obtained.
• the preferred ⁇ , ⁇ -ethylenically unsaturated carboxylic acids are acrylic acid, methacrylic acid and their esters and amides, and crotonic acid, maleic acid and itaconic acid. (Meth) acrylic acid and crotonic acid are preferably used. Acrylic acid and methacrylic acid and their esters are particularly preferred.
• Suitable ⁇ , ⁇ -ethylenically unsaturated carboxylic acid esters are, in particular, (meth) acrylic acid esters, the ester fraction of which is a CrC 30 alkyl radical or C 6 -C 10 aryl radical.
• the alkyl or aryl moieties can be additionally substituted, for example with
• Preferred acrylates that can be used include Methyl methacrylate, ethyl methacrylate, butyl methacrylate, isobutyl methacrylate, 2-ethylhexyl methacrylate, lauryl methacrylate and cyclohexyl methacrylate.
• Preferred aryl methacrylates that can be used include benzyl acrylate and phenyl acrylate. Copolymers of styrene and (meth) acrylic acid (esters) are particularly suitable.
• Carboxylic acid amides can also be used.
• N-alkyl- or N-aryl (meth) acrylamides can preferably be mentioned, the alkyl portion of which can have 2 to 15 C atoms or the aryl portion can have 6 to 10 C atoms.
• N-Ethylacrylamide, N-t-butylacrylamide, N-t-octylacrylamide and N-undecylacrylamide can be mentioned as preferred here.
• Copolymers of the monomers mentioned with other olefinically unsaturated monomers can also be used.
• examples include acrylic copolymers which have been obtained by copolymerizing acrylic acid or methacrylic acid with monomers such as butadiene, styrene or vinyl esters such as vinyl acetate or vinyl benzoate.
• Copolymers which are obtained by copolymerizing acrylic acid or methacrylic acid with styrene or vinyl compounds are preferably used.
• the acrylate copolymer is used in the form of an aqueous dispersion, the aqueous dispersion containing the copolymer in a proportion of 20 to 70%, particularly preferably 25 to 40%.
• the proportion of the acrylate copolymer or of the aqueous dispersion of the acrylate copolymer in the total composition is 1 to 60%, in each case based on the weight of the total composition and preferably 15 to 35%.
• the desired abrasion resistance is not achieved if the proportion is less than 1%. With a proportion of more than 60%, the swelling capacity of the dried film is increased and thus its water resistance is reduced, which leads to poor performance properties. In addition, the incorporation of colorants is very difficult.
• a mixture of at least two different acrylic-based polymers is used as the acrylic component, one of which is preferably an acrylate copolymer and the other is a copolymer of acrylic acid / methacrylic acid monomers and ethylenically unsaturated aryl monomers.
• the latter acrylic polymer is preferably a styrene-containing acrylate copolymer. Styrene acrylates ammonium methacrylate copolymer is particularly preferably used here.
• This component is also preferably used in the form of an aqueous dispersion, the dispersion generally containing 30 to 50% polymer in water.
• the proportion of this special aryl / acrylate copolymer in the total composition is 1 to 60%, a proportion in the range from 15 to 35% and in particular 20 to 30% being particularly preferred.
• the aqueous polymer dispersions form 50 to 90%, preferably 55 to 75% of the total composition.
• a polyurethane dispersion, an acrylate copolymer dispersion and a styrene / acrylic dispersion are preferably used. This combination is particularly preferably used in such proportions that the polymer portion is formed from approximately 35 to 55% polyurethane, approximately 15 to 25% acrylate copolymer dispersion and the rest from styrene / acrylic dispersion.
• the polymers are preferably selected such that 30 to 60% of the polymer dispersions of polymers or copolymers which are water-resistant in the dried state have a glass transition temperature below 10.degree. With 5 to 30% of one or more of the dispersions of random or block copolymers, a block or section in the dried state particularly preferably shows a glass transition temperature of more than 30 ° C.
• the preparation according to the invention can be in addition to those mentioned above
• Polymer components still contain other polymers as long as they are compatible and the properties of the components according to the invention are not affect.
• So-called hybrid polymers which can be obtained by copolymerization as acrylic or vinyl polymers with silicone segments or silicone groups, may also be present.
• Polycondensates with silicone segments or silicone groups are also known and commercially available.
• Polyesters polyester amides or polyamides are also suitable. Polyesters can be obtained by the methods known to those skilled in the art by polycondensation of aliphatic or aromatic dicarboxylic acids with aliphatic or aromatic diols or polyhydric alcohols.
• Examples include polycondensates of adipic acid, succinic acid, glutaric acid, sebacic acid, terephthalic acid or isoterephthalic acid with diols, such as ethylene glycol, diethylene glycol, propylene glycol or polyhydric alcohols, such as glycerol, trimethylolpropane, pentaerythritol, mannitol, sorbitol or soft segment or xylene segment or xylene segment or xylene segment.
• Polyesteramides are obtained accordingly by the polycondensation of dicarboxylic acids with diamines or amino alcohols.
• Suitable natural polymers may only be mentioned by way of example: shellac, dammar resin, Kopal, Elemi, tragacanth, gum arabic, xanthan or cellulose dehvates, which may or may not be chemically modified, and mixtures thereof.
• composition according to the invention is the viscosity, which is in a range from 0.02 to 3.8 Pa s, measured at 25 ° C. and 200 s "1.
• the viscosity can be determined in a manner known per se using a rheometer The measurement is suitably measured with a rheometer, type BOHLIN CVOR (plate / plate measuring system) at 25 ° C and at a shear rate of 200 s-1 without shear.
• a rheometer type BOHLIN CVOR (plate / plate measuring system) at 25 ° C and at a shear rate of 200 s-1 without shear.
• DIN 53018 part 1 and Part 2.
• composition according to the invention despite the low viscosity, was very durable and long is storable and, due to its structure, can also keep particulate ingredients in dispersion, so that no separation or settling of the colorants occurs.
• composition according to the invention can contain other customary ingredients, depending on the desired properties and the field of use.
• composition according to the invention is intended for staining, e.g. for coloring hair, including eyelashes and / or eyebrows, or as decorative eye cosmetics, e.g. as an eyeliner, it also contains colorants. Colorants for such compositions are known per se and those suitable for cosmetics can also be used for the composition according to the invention.
• inorganic pigments such as titanium dioxide, zinc oxide, iron oxides, chromium oxide green, chromium oxide hydrate green, ultramarine, carbon black, organic pigments such as carmine and its salts or phthalocyanine, mica, coated with metal oxides such as titanium dioxide, iron oxide, chromium oxide Mica, bismuth oxychloride or bismuth oxychloride coated with metal oxides, platelet-like preparations based on silicon dioxide, aluminum oxide or glass, which may also be coated with metal oxides, e.g.
• titanium dioxide, iron oxides, titanium dioxide, iron oxides, chromium oxide, chromium oxide hydrate, platelet-shaped metal powders such as passivated aluminum, bronze , Brass, copper, silver, gold, barium, aluminum, strontium, calcium or zirconium lacquers of organic dyes or mixtures thereof can be used.
• national or regional legislation for the manufacture of cosmetics should also be observed, since in some countries colorants that come into contact with the mucous membranes of the eye must be approved. In Germany, for example, the admissibility of colorants is regulated by Appendix 3 to Section 3 of the Cosmetics Regulation. Both organic soluble dyes and pigments can be used to dye keratin fibers, in particular eyelashes, eyebrows and hair.
• Pigments are preferred for the composition according to the invention. Both normal pigments and coated pigments can be used.
• the pigments preferably have a small particle size, preferably in a range from 20 nm to 150 ⁇ m. For this purpose, the pigments are finely ground in the usual way or, if necessary, used micronized.
• the pigments include, for example, black iron oxide or ultramarine blue suitable colorants.
• the proportion of the pigment depends on the desired color and suitable amounts are known per se to the person skilled in the art.
• a share of 0 to 30%, in particular 5 to 25% are known per se to the person skilled in the art.
• proportions outside of these ranges are also possible, however.
• the shelf life of the products according to the invention can be improved by preferably using pigments with a hydrophobic, physically or chemically adhesive coating.
• Coatings for pigments are known per se and do not require any further explanation here.
• silicone-containing coatings with dimethicone or other silicones or coatings with titanium triisostearate are suitable.
• the use of coated pigments has the further advantage that wetting or swelling of the film formed on contact with water is minimized. This further increases the durability and durability of the film formed. Even if the film swells somewhat when in contact with water, if it is not subjected to mechanical friction in the swollen state, it remains completely intact and stable.
• a surface-active substance When using highly hydrophobically coated pigments, it is advisable to also add a surface-active substance to the composition, if appropriate in combination with a polymeric wetting agent.
• a surface-active substance and wetting agents contribute to the water compatibility of the particles.
• suitable surface-active agents are low molecular weight surfactants, such as sarcosinates, nonionic and or anionic surfactants, such as PEG-modified fatty acids and fatty alcohols, sodium laureth sulfate, solubilizers, as are also customary for the compatibility of UV substances, and / or ester oils.
• the low molecular weight surfactant if present, is preferably used in a proportion of 0.1 to 3%, in each case based on the weight of the total composition.
• Suitable polymeric wetting agents are, for example, silicone surfactants and amphiphilic silicone acrylates, and PVP derivatives, for example VP / eicosen and VP / hexadecene copolymers, fluorosurfactants, cholesterol esters, lecithin, and acrylate copolymers, for example an acrylate block copolymer and other known polymer surfactants.
• An acrylic wetting agent is particularly preferably used as the polymer wetting agent in order to improve the compatibility.
• the polymeric wetting agent if present, is suitably used in an amount of 0.05 to 5%, preferably 0.1 to 3%.
• a nonionic wetting agent in particular a dimethicone copolyol or a nonionic polymeric wetting agent, such as an acrylate or polyethylene block copolymer, is used in a small amount, preferably 0.05 to 3% by weight, very particularly preferably 0.3 to 1, 5 wt .-% used.
• This causes the colorant particles to be well wetted on the one hand and to be incorporated into the polymer structure on the other by molecular interactions. At the same time, this causes the film to run particularly smoothly on drying and thereby form a high surface gloss.
• This can also be achieved by using polymer segments with a known good reflectivity and a higher glass transition temperature T g , such as polystyrene.
• thickeners are preferably used together with the pigments, which ensures even better storage stability.
• the mass obtained should not become crumbly, but must be applied smoothly, not all known thickeners are suitable for this.
• pyrogenic Silica is unsuitable as it will crumble away after the composition has been applied.
• the preparation according to the invention should have such a low viscosity that it is free-flowing and can therefore also be stored in vessels of very different geometries without there being a problem with the removal.
• a low-viscosity preparation can be obtained if a thickener mixture is used which contains at least one inorganic layered silicate combined with a xanthan gum.
• Suitable mixtures are those of natural and synthetic and modified polysaccharides, mineral and modified mineral thickeners, silicate thickeners, celluloses and modified celluloses, nonionic associative thickeners, copolymer thickeners, such as hydroxyethyl acrylates / sodium acryloyl dimethyl taurate copolymer, sodium acrylate acryloyl dimethyl taurate copolymer, sodium , VP / Dimethiconyl Acrylate / Polycarbamoyl / Polyglycolester.
• a mixture of a larger proportion of a hydrocolloid or vegetable gum, for example xanthan gum, a smaller proportion of a silicate thickener and a small proportion of a polysaccharide, in particular cellulose, which may also be chemically modified is used.
• a mixture of 40 to 70% xanthan gum, 10 to 40% mineral thickener and the rest cellulose or cellulose derivative is an example.
• a mixture of cellulose, silicate and xantham rubber in a ratio of in the range from 1: 1: 4 to 1: 2: 6 is particularly preferably used as the thickener.
• the thickener mixture can be added in a proportion of up to 20%.
• proportions in the range from 0.2 to 5%, based in each case on the weight of the overall composition, have proven suitable. If a lower viscosity is desired, the lower portion of the thickener is of course used, while if the viscosity is to be increased, the portion of the thickener is increased.
• the thickener mixture used according to the invention stabilizes the pigments and thus essentially prevents the pigments from settling. Stay with it the pigments are homogeneously distributed even after prolonged storage and do not have to be redispersed by shaking before each use.
• the low viscosity that can be achieved despite the use of the thickener mixture ensures that the mass does not apply to the eyelash and nevertheless colors well.
• the disadvantage of a thicker application is that stresses form during drying, which lead to the mass flaking off after some time.
• a coating is achieved which, due to its elasticity and its uniform layer thickness, remains in place for a long time and permanently.
• the preparation according to the invention can also contain one or more conventional and known sunscreens or UV-absorbing agents in order to protect the skin or hair from the sun.
• sunscreens are used in the usual amounts for cosmetics.
• composition according to the invention all common preservatives can be used for this, including carbamates, e.g. lodpropinylbutylcarbamat. These preservatives are used up to the amounts permitted by law, such as those specified in Germany by Appendix 6 to Section 3a of the Cosmetics Ordinance in the currently valid version.
• cosolvents ie water-miscible solvents
• Suitable here are, for example, monohydric and / or polyhydric alcohols with 2 to 20 carbon atoms, esters and ethers thereof, liquid, water-miscible or easily dispersible compounds such as N-methyl-pyrrolidinone, dimethylacetamide, glycerol, diglycerol, triglycerol, butylene glycol , Hexanetriol, propylene glycol, dipropylene glycol, hexylene glycols, mixtures of dimethicone copolymer and caprylic / capric triglycerides or other suitable silicone surfactants, as well as solutions of water-soluble solid substances which are known as However, humectants do not serve as co-solvents, such as urea, xylitol, inosito
• the film-forming polymers used according to the invention have a glass transition temperature in a range which allows a soft and elastic film to be formed even without a plasticizer.
• a plasticizer known for cosmetic compositions can also be added. Suitable here are both low molecular weight and higher molecular weight plasticizers, which are optionally dissolved or solubilized in a co-solvent. Silicone surfactants, but also short-chain ester oils are suitable.
• the hardness of the film formed from the preparation according to the invention can also be influenced by adding benzoyl benzoate, tributyl citrate, trihydroxypropyl citrate or laureth-2-benzoate.
• the plasticizers are used in a manner known per se, e.g. in a share of 0 to 5%.
• defoamers known per se can be used to a lesser extent Amount added.
• silicone compounds as are also used for other cosmetic compositions.
• Such a silicone compound is usually used as an emulsion in a proportion of approximately 0 to 5%, preferably 0.1 to 1%.
• the applied mass is to be removed again, this can be achieved in a simple manner by applying water at a higher temperature, ie at a temperature above 25 ° C., preferably between 30 and 38 ° C., to the applied film and then the film is removed by mechanical friction, for example with a cotton pad.
• the preparation according to the invention can be produced in a manner known per se.
• the preparation is preferably carried out by first preparing the polymer dispersions and heating them to an elevated temperature, preferably in the range between 45 and 60 ° C.
• a thickener mixture is used, this is preferably in a cosolvent which can be mixed with water as desired, but is different from water, e.g. a polyhydric alcohol, glycerin or ester oil.
• a cosolvent which can be mixed with water as desired, but is different from water, e.g. a polyhydric alcohol, glycerin or ester oil.
• the two mixtures are then mixed together and the other constituents are added in the customary manner.
• the colorants can then be incorporated into the homogeneous dispersion and distributed evenly therein.
• composition according to the invention is so stable that it does not separate or settle even without stirring. Possibly. the composition can also be filled hot into the containers provided for it immediately after production.
• auxiliaries such as plasticizers, brighteners, leveling agents, etc. can be added after the composition has been finished.
• the composition according to the invention can be used for the treatment of skin and skin appendages.
• the composition according to the invention is suitable on the one hand for applying makeup to the eyes and on the other hand for treating keratinous material, in particular eyelashes, eyebrows and hair.
• Another object of the invention is therefore the use of the preparation according to the invention for applying makeup to the eyes, preferably the eyelids, eyelid edges, eyelashes and eyebrows.
• Another object of the invention is the use of the preparation according to the invention for the treatment of keratinous material, in particular hair, eyelashes and eyebrows, both in their natural state and in their artificial replicas.
• the preparation according to the invention is preferably used in order to provide keratinous material with a coating, in particular a coloring coating.
• a coating in particular a coloring coating.
• This coating has a long shelf life and remains even in contact with water.
• the coloring remains up to 4 days.
• the coating can be removed at any time by applying water, preferably at a higher temperature, and removing the coating after a few minutes by mechanical rubbing.
• the application can preferably be applied with an application system which comprises a container and a removable element for closing, the element for closing preferably being an element for application, i.e. is an applicator.
• Another object of the invention is therefore also a device for applying a preparation, as described above, which comprises a container which can hold the preparation and has a neck piece with thread and seal, and an applicator element which has a brush and at its other end has a handle which forms a closure cap, the brush head having a diameter in the range from 5.5 and 6.5 mm and a Has length in the range from 12.5 to 17.5 mm and the bristles are arranged in a helical arrangement radially around a centerpiece with a high number of turns.
• the application system has a container which contains the composition according to the invention and is provided with a neck piece.
• the neck piece has an annular scraper.
• the element for closing the container carries an applicator which has a handle and is provided with a brush as an application element at its first end and is connected to a handle at its second end.
• the closure element closes the container, the applicator attached to the closure element being immersed in the preparation.
• the closure element is pulled out, the applicator moving over the ring-shaped scraper and thereby scraping off excess material.
• the preparation can then be applied with a brush.
• the preparation according to the invention has an extremely low viscosity, it is possible to design the container in a wide variety of geometries, which is not possible with the known applicator systems for mascara.
• Usual mascara has a relatively high viscosity and can therefore only be kept in cylindrical containers into which the applicator can be inserted so that it can take off the mass. Since the preparation according to the invention has such a viscosity that the mass is free flowing, the preparation can also be filled into bulky vessels or vessels of any geometry.
• the applicator for applying the preparation fulfills the following conditions so that the application is homogeneous and stable.
• the applicator is a brush with soft bristles, so that when applied repeatedly, the bristles do not damage the layer that has already been applied and can therefore be attacked by water.
• the brush is short with a large diameter, so that individual eyelash areas can be specifically colored.
• a brush with a large number of turns is particularly preferably used.
• a preparation which can be applied permanently and permanently to the skin and skin appendages and can remain there for a very long time. As soon as the preparation has been applied to the desired area and has dried, which takes only a short time, it sticks to the applied location without being transferred to objects in contact with it, without migrating or crumbling off in close areas.
• the preparation is therefore ideally suited for application to keratinous material, especially eyelashes, eyebrows and hair.
• the preparation can be applied to hair to give it a protective coating and at the same time fullness and momentum.
• the preparation is provided with colorants and is used for coloring the keratinous material.
• a preparation produced according to the comparative example - not according to the invention - sticks has insufficient opacity, is unevenly applied and fails in the preservation load test - despite an apparently sufficient amount of preservative which corresponds to the content in the examples according to the invention.
• Hydrophobically modified pigment 10.0 VP / hexadecene copolymer 0.30
• a mascara is produced from the above components, in which the acrylate copolymer dispersion and the polyurethane dispersion are placed and preheated to 50 to 55 ° C., and the other ingredients are then mixed in. The mixture is stirred until a homogeneous mass is obtained. This mass can then be filled as it is or cooled.
• the viscosity was determined as follows.
• Measuring device Bohlin CVOR rheometer, shear stress ramp 1 to 1000 Pa upwards for recording a yield point
• Measuring system plate / plate 20 to 0.4 mm gap distance
• Measuring time 120 s plus 60 s preheating to 25 ° C. Conversion to viscosity curve is done electronically

Landscapes

• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Birds (AREA)
• Epidemiology (AREA)
• Cosmetics (AREA)

Priority Applications (9)

Applications Claiming Priority (2)

Publications (1)

Family

ID=7970981

Family Applications (1)

Country Status (12)

Cited By (5)

Families Citing this family (36)

Citations (3)

Family Cites Families (16)

• 2002
  • 2002-05-10 DE DE20207329U patent/DE20207329U1/de not_active Expired - Lifetime
• 2003
  • 2003-03-06 AU AU2003210430A patent/AU2003210430A1/en not_active Abandoned
  • 2003-03-06 EP EP03749851A patent/EP1505946B2/de not_active Expired - Lifetime
  • 2003-03-06 JP JP2004502955A patent/JP3984259B2/ja not_active Expired - Lifetime
  • 2003-03-06 BR BR0307962-7A patent/BR0307962A/pt not_active Application Discontinuation
  • 2003-03-06 WO PCT/EP2003/002327 patent/WO2003094868A1/de not_active Ceased
  • 2003-03-06 MX MXPA04009330A patent/MXPA04009330A/es active IP Right Grant
  • 2003-03-06 DE DE50307767T patent/DE50307767D1/de not_active Expired - Lifetime
  • 2003-03-06 CN CNB038100452A patent/CN100408014C/zh not_active Expired - Lifetime
  • 2003-03-06 KR KR1020047016240A patent/KR100854566B1/ko not_active Expired - Lifetime
  • 2003-03-06 CA CA2479106A patent/CA2479106C/en not_active Expired - Lifetime
  • 2003-03-06 US US10/509,193 patent/US20050163741A1/en not_active Abandoned
  • 2003-03-06 AT AT03749851T patent/ATE367798T1/de not_active IP Right Cessation
• 2007
  • 2007-03-08 JP JP2007058318A patent/JP2007145864A/ja active Pending

Patent Citations (3)

Also Published As

Similar Documents

Legal Events