WO2004075866A1 - Conservation de tissus impregnes - Google Patents

Conservation de tissus impregnes Download PDF

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Publication number
WO2004075866A1
WO2004075866A1 PCT/EP2004/001569 EP2004001569W WO2004075866A1 WO 2004075866 A1 WO2004075866 A1 WO 2004075866A1 EP 2004001569 W EP2004001569 W EP 2004001569W WO 2004075866 A1 WO2004075866 A1 WO 2004075866A1
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WO
WIPO (PCT)
Prior art keywords
acid
skin
cosmetic
aqueous
weight
Prior art date
Application number
PCT/EP2004/001569
Other languages
German (de)
English (en)
Inventor
Christian Frisoli
Barbara Heide
Original Assignee
Henkel Kommanditgesellschaft Auf Aktien
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Publication of WO2004075866A1 publication Critical patent/WO2004075866A1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/02—Preparations for cleaning the hair
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0208—Tissues; Wipes; Patches
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36—Carboxylic acids; Salts or anhydrides thereof
    • A61K8/365—Hydroxycarboxylic acids; Ketocarboxylic acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36—Carboxylic acids; Salts or anhydrides thereof
    • A61K8/368—Carboxylic acids; Salts or anhydrides thereof with carboxyl groups directly bound to carbon atoms of aromatic rings
    • 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
    • A61Q1/14—Preparations for removing make-up
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q13/00—Formulations or additives for perfume preparations
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A61Q19/002—Aftershave preparations
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A61Q19/10—Washing or bathing preparations
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/12—Preparations containing hair conditioners
    • 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
    • A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/28—Rubbing or scrubbing compositions; Peeling or abrasive compositions; Containing exfoliants
    • 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
    • A61K2800/52—Stabilizers
    • 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
    • A61K2800/52—Stabilizers
    • A61K2800/524—Preservatives

Definitions

  • the invention relates to a preservation system with which flexible carriers, for example cleaning and care wipes, which are equipped with an aqueous impregnating composition, can be preserved against microbial spoilage over a long period of time.
  • Flexible carriers in particular wipes, sponges and pads, which are impregnated or impregnated with liquid cosmetic compositions, are very popular with consumers. They are time-saving, clean and hygienic to use. Suitable carriers are cloths made of fabrics as well as nonwoven nonwovens made of cotton fibers or of synthetic or mixed fibers, for the manufacture of which mostly polypropylene, polyester or viscose is used. Sponges made of polyurethane, rubber and similar materials are also suitable.
  • the carriers equipped with a cosmetic cleaning and possibly care and active ingredient soaking solution are usually packed in a moist state and can be conveniently transported anywhere and used immediately if necessary, even if, for example, no running water is available for cleaning.
  • preservatives In contrast to disinfectants and fumigants, which have a quick killing effect on microorganisms (microbicidal) and are mostly toxic, preservatives only inhibit the growth and multiplication of the microorganisms over a longer period of time, i.e. they tend to have a microbiostatic effect in the concentrations usually used. However, if the dosage is sufficient, a preservative can kill the microorganisms present within a few days if the initial germ content of the cosmetic product is low and subsequent contamination with microorganisms is excluded. Germination of bacterial spores and the formation of Mycotoxins from mold can also be suppressed by preservatives. Most preservatives are especially effective against yeast and mold (fungistatic). Only a few can be used effectively against bacteria (bacteriostatic).
  • Known preservatives that are approved in the Cosmetics Ordinance are in particular phenoxyethanol, imidazolidinyl urea (Germall ® 115 from ISP), methyldibromo glutaronitrile, polyaminopropyl biguanide, chlorothymol, chloroacetamide, chlorhexidine diacetate, chlorhexidine digluconate, quaternium-15,
  • Known preservatives which are also approved as a food additive and which do not have the disadvantages described above or have them only to a minor extent are salicylic acid, benzoic acid, propionic acid, dehydroacetic acid (3-acetyl-6-methyl-2H-pyran-2,4 (3H) - dione) and sorbic acid.
  • these preservatives react weakly acidic and only neutral, undissociated molecules can pass through the cell membrane and get into the cell interior of the microbes, these preservatives can only be used in more acidic cosmetic compositions.
  • An object of the present invention was to provide a cosmetic product in the form of a flexible carrier which has been provided with an aqueous impregnating composition and is preserved in a long-term stable manner.
  • Another object of the present invention was to provide a cosmetic product in the form of a flexible carrier which is provided with an aqueous impregnating composition and is long-term stable and is compatible with sensitive skin.
  • Another object of the present invention was to provide a cosmetic product in the form of a flexible one, which was provided with an aqueous impregnating composition
  • Carrier which is preserved long-term stable with the gain of a cosmetic additive.
  • a flexible carrier equipped with an aqueous impregnation composition for the non-therapeutic cosmetic or dermatological treatment of the skin, hair, mucous membrane and appendages of the skin the aqueous impregnation composition comprising at least one organic acid effective as a preservative, selected from salicylic acid, Benzoic acid, propionic acid, dehydroacetic acid (3-acetyl-6-methyl-2H-pyran-2,4 (3H) -dione) and sorbic acid as well as the physiologically compatible water-soluble metal salts of these acids, contains and with 0.1-10% by weight of a corresponding acid-base pair is buffered in such a way that it has a pH of 2.5-6.0 both before the carrier is equipped and after two months of storage on the carrier equipped with it.
  • an organic acid effective as a preservative selected from salicylic acid, Benzoic acid, propionic acid, dehydroacetic acid (3-acetyl-6-methyl-2H-pyran-2,4 (3H
  • the present invention furthermore relates to the use of an aqueous impregnating composition which comprises at least one organic acid which acts as a preservative and is selected from salicylic acid, benzoic acid, propionic acid and dehydroacetic acid (3-acetyl-6-methyl-2H-pyran-2,4 (3H) -dione) and sorbic acid as well as the physiologically compatible water-soluble metal salts of these acids, and is buffered with 0.1-10% by weight of a corresponding acid-base pair in such a way that it is used both before the carrier is finished and after two months of storage on the carrier equipped with it has a pH value of 2.5 - 6.0, to equip flexible carriers for non-therapeutic cosmetic or dermatological treatment of the skin, hair, mucous membrane and skin appendages.
  • an organic acid which acts as a preservative and is selected from salicylic acid, benzoic acid, propionic acid and dehydroacetic acid (3-acetyl-6-methyl-2H-pyran-2,4
  • physiologically compatible metal salts include the sodium,
  • water-soluble means a solubility of at least 1 g of salt per
  • the sodium and potassium salts are particularly preferred according to the invention.
  • the salicylic acid, benzoic acid, propionic acid, dehydroacetic acid and sorbic acid and their salts mentioned are used in amounts of 0.02-1% by weight, preferably 0.1-0.8% by weight and particularly preferably 0.1-0. 5% by weight, based in each case on the weight of the impregnation composition.
  • the organic acid effective as a preservative is selected from salicylic acid and its physiologically tolerable water-soluble salts, in particular sodium salicylate.
  • salicylic acid also has cosmetic active properties.
  • the cosmetics specialist uses the keratolytic effect of salicylic acid, for example, to treat blemished skin and acne.
  • Corresponding acid-base pairs suitable according to the invention are aqueous buffer solutions which the aqueous impregnating compositions according to the invention both in the pH range from 2.5 to 6.0, preferably in the pH, before the carrier has been finished and after two months of storage on the carrier equipped with them Stabilize range of 3.5 - 5.5, and particularly preferably in the pH range of 4.0 to 5.0.
  • Aqueous solutions of citric acid and its sodium salts in particular trisodium citrate, tartaric acid and its potassium salts, in particular potassium hydrogen tartrate, and phthalic acid and its potassium salts, in particular potassium hydrogen phthalate, are preferred.
  • a particularly preferred buffer system is formed from citric acid and the sodium toprate.
  • Other buffer systems for example acetic acid / sodium acetate, are in principle also suitable according to the invention. However, due to the smell of vinegar, such a buffer is not acceptable for the production of a cosmetic market product.
  • the long-term stability of the preservation system according to the invention depends crucially on the capacity of the buffer system used.
  • the capacity of the buffer system used is sufficient according to the invention if the aqueous impregnation compositions according to the invention have a pH in the abovementioned ranges both before the carrier has been finished and after two months of storage on the carrier equipped with them.
  • the aqueous impregnation composition according to the invention is first adjusted to the desired pH.
  • the flexible carrier according to the invention is then equipped with the impregnating composition by impregnation or impregnation. Excess impregnation is removed, for example, by squeezing to the desired moisture content.
  • the equipped carrier is then packed airtight and stored at 20 ° C for two months.
  • the impregnation solution is pressed out of the carrier and its pH is determined.
  • This pH must be in the range from 2.5 to 6.0, preferably in the pH range from 3.5 to 5.5, and particularly preferably in the pH range from 4.0 to 5.0.
  • the amount of the suitable buffer system depends on the one hand on the individual constituents of the cosmetic impregnation composition and on the other hand on the acidic or basic character of the carrier material which may be present. It has been shown that the substances acting as buffers within the range of 0.1-10% by weight, preferably 1.0-5.0% by weight and particularly preferably 1.0-4.0% by weight. %, based in each case on the amount of active substance weighed in by the corresponding acid-base pair, per weight of the impregnation composition.
  • the material for the flexible carrier according to the invention which is in cloth or pad form, is selected from woven and non-woven nonwovens made of cotton fibers, plastic and mixed fibers. The nonwoven nonwovens are preferred.
  • Suitable fiber materials are, for example, polypropylene, polyester and viscose.
  • the wipes can be single, two or three layers. Wipes with more than three layers are also suitable according to the invention.
  • the nonwoven can be hydroentangled. Furthermore, the nonwoven fabric can have a structure and / or a pattern and / or holes.
  • the material for the flexible carrier according to the invention which is in the form of a sponge or pad, is selected from natural rubber (polyisoprene), synthetic rubbers and polyurethane.
  • the synthetic rubbers are selected, for example, from styrene-butadiene rubber, isoprene rubber, polybutadiene, butyl rubber, ethylene-propylene rubber, silicone rubber, polyurethane rubber, ethylene-vinyl acetate rubber, polynorbornene rubber and acrylic rubber.
  • Particularly preferred synthetic rubbers are styrene-butadiene rubber, isoprene rubber and polybutadiene.
  • the sponges according to the invention consist of polyurethane foam rubber. They can be produced by the direct reaction of diisocyanates and polyols in a reaction-casting fuel process and subsequent impregnation or impregnation with the cosmetic composition.
  • the foam rubber sponges can be cut or punched in any shape that is optimally adapted to the respective application.
  • the flexible carrier according to the invention can be equipped with the aqueous impregnating composition by spraying or by impregnation. After equipping, the excess liquid can be removed by squeezing.
  • the flexible carriers according to the invention can be in moist form and can be delivered to the end user. Moistening before use is therefore not necessary. Such flexible carriers are convenient and time-saving to use and particularly suitable for on the go.
  • a product is usually supplied as a moist carrier which, in the case of a sponge, contains about 0.1-0.4 g of soaking solution per cm 3 of the dry sponge. In the case of cloths and fleeces, this is Weight ratio of the non-finished cloth to the impregnation composition 1: 1 to 1: 5.
  • the flexible carriers equipped with the aqueous impregnation composition can be dry to a water content of at most 15% by weight, preferably at most 10% by weight and particularly preferably at most 7% by weight.
  • These dried carriers can be moistened with water before use and then used to treat the skin, hair or nails.
  • the flexible carriers according to the invention equipped with the aqueous impregnating composition and optionally dried, are preferably packaged for delivery to the end user in such a way that they are protected against drying out.
  • the flexible carriers can be packed individually or in stacks.
  • the impregnation compositions used to finish the flexible carriers according to the invention are liquid at 20 ° C. based on an aqueous or aqueous-alcoholic solution, emulsion or suspension.
  • the aqueous-alcoholic composition can contain a mono- or polyvalent C 2 -C 9 alcohol as alcohol, preferably ethanol, isopropanol, propylene glycol, glycerol, dipropylene glycol, tripropylene glycol and diglycerol. Because of their skin tolerance, the monohydric C 2 -C 9 alcohols are less preferred.
  • the impregnation compositions are particularly preferably free of monohydric C 2 -C 9 alcohols.
  • the aqueous impregnating compositions used to finish the flexible carriers according to the invention can contain surface-active substances which, depending on the field of application, are called surfactants or emulsifiers and are selected from anionic, cationic, zwitterionic, ampholytic and nonionic surfactants and emulsifiers.
  • Suitable anionic surfactants and emulsifiers for the carriers according to the invention are all anionic surface-active substances suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such as. B. a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group with about 8 to 30 carbon atoms.
  • glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups can be contained in the molecule.
  • suitable anionic surfactants and emulsifiers are, in each case in the form of the sodium, potassium and ammonium and the mono-, di- and trialkanolammonium salts with 2 to 4 carbon atoms in the alkanol group, linear and branched fatty acids with 8 to 30 ° C. -Atoms (soaps),
  • Ether carboxylic acids of the formula RO- (CH 2 -CH 2 O) x -CH 2 -COOH, in which R is a linear one
  • R 1 CO represents a linear or branched acyl radical having 6 to 22 carbon atoms and 0, 1, 2 or 3 double bonds and X represents hydrogen, an alkali metal and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium, for example Acylglutamates derived from fatty acids with 6 to 22, preferably 12 to 18 carbon atoms, such as G 12/14 or Ciz / i ⁇ coconut fatty acid, lauric acid, myristic acid, palmitic acid and / or stearic acid, especially sodium N-cocoyl - and sodium N-stearoyl-L-glutamate,
  • X H or a -CH 2 COOR group
  • R, R 1 and R 2 are independent of each other a hydrogen atom, an alkali or alkaline earth metal cation, an ammonium group, the cation of an ammonium organic base or a radical Z mean, which comes from a polyhydroxylated organic compound which is selected from the group of etherified (C 6 -C 18 ) alkyl polysaccharides with 1 to 6 monomeric saccharide units and / or etherified aliphatic (C 6 -C 6 ) - hydroxyalkyl polyols with 2 to 16 hydroxyl radicals are selected, provided that at least one of the groups R, R 1 or R 2 is a radical Z,
  • Preferred anionic surfactants and emulsifiers are acyl glutamates, acyl isethionates, acyl sarcosinates and acyl taurates, each with a linear or branched acyl radical having 6 to 22 carbon atoms and 0, 1, 2 or 3 double bonds, which in particularly preferred embodiments consist of an octanoyl, decanoyl or lauroyl -, Myristoyl, Palmitoyl and Stearoylrest is selected, esters of tartaric acid, citric acid or Succinic acid or the salts of these acids with alkylated glucose, in particular the products with the INCI name Disodium Coco-Glucoside Citrate, Sodium Coco-Glucoside Tartrate and Disodium Coco-Glucoside Sulfosuccinate, Alkylpolyglycolether Sulfate and Ethercarboxylic acids with 8 to 18 C-atoms in the alkyl group and up to 12 ethoxy groups in the
  • Zwitterionic surfactants and emulsifiers are those surface-active compounds which carry at least one quaternary ammonium group and at least one -COO 9 - or -SO 3 H group in the molecule.
  • Particularly suitable zwitterionic surfactants and emulsifiers are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example the cocoalkyldimethylammonium glycinate, N-acyl-aminopropyl-N, N-dimethylammonium glycinate, for example the cocoacylaminopropyldimethylammonium glycinate 3, and 2 -carboxymethyl-3-hydroxyethylimidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group and the cocoacylaminoethylhydroxyethylcarboxymethylglycinate.
  • a preferred zwitterionic surfactant
  • Ampholytic surfactants and emulsifiers are surface-active compounds which, in addition to a C 8 -C 24 alkyl or acyl group, contain at least one free amino group and at least one -COOH or -SO 3 H group and are capable of forming internal salts
  • suitable ampholytic surfactants are N-alkylglycines, N-alkylaminopropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids each with about 8 to 24 C. Atoms in the alkyl group.
  • Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, cocoacylaminoethyl aminopropionate and C12 C 18 -
  • Nonionic surfactants and emulsifiers contain z as hydrophilic group.
  • B a polyol group, a polyalkylene glycol ether group or a combination of polyol and polyglycol ether group.
  • Such compounds are, for example, adducts of 2 to 50 moles of ethylene oxide and / or 0 to 5 moles of propylene oxide with linear and branched fatty alcohols with 8 to 30 carbon atoms, with fatty acids with 8 to 30 C atoms and on alkylphenols with 8 to 15 C atoms in the
  • Polyol fatty acid (partial) esters such as Hydagen ® HSP (Cognis) or Sovermol ® types
  • Sorbitan fatty acid esters and addition products of ethylene oxide with sorbitan fatty acid esters such as, for example, the polysorbates
  • Z stands for sugar and x for the number of sugar units.
  • Chen consists of C 16 to C 18 alkyl groups.
  • Any mono- or oligosaccharides can be used as the sugar building block Z.
  • Sugar with 5 or 6 carbon atoms and the corresponding oligosaccharides are usually used.
  • sugars are glucose, fructose, galactose, arabinose, ribose, xylose, lyxose, allose, old rose, mannose, gulose, idose, talose and sucrose.
  • Preferred sugar components are glucose, fructose, galactose, arabinose and sucrose; Glucose is particularly preferred.
  • alkyl polyglycosides which can be used according to the invention contain on average 1.1 to 5 sugar units. Alkyl polyglycosides with x values of 1.1 to 2.0 are preferred. Alkyl glycosides in which x is 1.1 to 1.8 are very particularly preferred. - Mixtures of alkyl (oligo) glucosides and fatty alcohols, e.g. B. Montanov ® 68,
  • sterols e.g. B. ergosterol, stigmasterol, sitosterol and mycosterols
  • phospholipids e.g. B. lecithins or phosphatidylcholines
  • Polyglycerols and polyglycerol derivatives such as, for example, polyglycerol poly-12-hydroxystearate (Dehymuls ® PGPH) or triglycerol diisostearate (Lameform ® TGI),
  • alkyl polyglycosides optionally in a mixture with fatty alcohols, alkoxylated polydialkylsiloxanes, alkylene oxide addition products with saturated linear fatty alcohols and fatty acids, each with 2 to 30 moles of ethylene oxide per mole of fatty alcohol or fatty acid, have proven to be preferred nonionic surface-active substances.
  • Cationic surfactants of the type of the quaternary ammonium compounds, the esterquats and the amidoamines can also be used according to the invention.
  • Preferred quaternary ammonium compounds are ammonium halides, in particular chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides.
  • the long alkyl chains of these surfactants preferably have 10 to 18 carbon atoms, such as. B.
  • cetyltrimethylammonium chloride cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, distearyldimethylammonium chloride, lauryldimethylammonium chloride, lauryldimethylbenzylammonium chloride and tricetylmethylammonium chloride.
  • Further preferred cationic surfactants are the imidazolium compounds known under the INCI names Quatemium-27 and Quaternium-83.
  • the aqueous impregnation compositions used for finishing can preferably contain at least one nonionic emulsifier with an HLB value of 3 to 18, according to the 10th edition, Georg Thieme Verlag Stuttgart, in Römpp-Lexikon Chemie (Hrg. J. Falbe, M. Regitz) New York, (1997), page 1764.
  • Nonionic O / W emulsifiers with an HLB value of 10-15 and nonionic W / O emulsifiers with an HLB value of 3-6 can be particularly preferred according to the invention.
  • the cosmetic compositions used to finish the flexible carriers according to the invention can furthermore contain fatty substances selected from fatty acids, fatty alcohols and natural and synthetic waxes which are both solid and can also be in liquid form in aqueous dispersion, and natural and synthetic cosmetic oil components.
  • fatty substances selected from fatty acids, fatty alcohols and natural and synthetic waxes which are both solid and can also be in liquid form in aqueous dispersion, and natural and synthetic cosmetic oil components.
  • Perfume oils and essential oils are also included in the fatty substances according to the invention.
  • Linear and / or branched, saturated and / or unsaturated C 8 can be used as fatty acids. 30 fatty acids. C 10-22 fatty acids are preferred. Examples are the isostearic acids and isopalmitic acids. Further suitable examples are caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoic acid, linolenic acid, arenachidonic acid, gaducenic acid, gadic acid and eradic acid, gadic acid and eradic acid, gadic acid and gaseous acid, gadic acid and gaseous acid, gadic acid and gaseous acid, gadic acid and gaseous acid, gic acid and gaseous acid, gic acid and aric acid, g
  • the amount used is 0.1-15% by weight, preferably 0.5-10% by weight and particularly preferably 1-5% by weight, in each case based on the impregnating composition used to finish the flexible carrier according to the invention.
  • the fatty alcohols which can be used are saturated, mono- or polyunsaturated, branched or unbranched fatty alcohols having 6 to 30, preferably 10 to 22 and very particularly preferably 12 to 22 carbon atoms, e.g.
  • Solid paraffins or isoparaffins plant waxes such as candelilla wax, carnauba wax, esparto grass wax, fruit waxes and sunflower wax, beeswaxes and other insect waxes, ozokerites, ceresin, walnut and microwaxes made of polyethylene or polypropylene can be used according to the invention as natural or synthetic waxes.
  • plant waxes such as candelilla wax, carnauba wax, esparto grass wax, fruit waxes and sunflower wax
  • beeswaxes and other insect waxes ozokerites
  • ceresin ceresin
  • walnut and microwaxes made of polyethylene or polypropylene
  • triglycerides of saturated and optionally hydroxylated C 16-3 o-fatty acids such as. B.
  • hardened triglyceride fats hydrogenated palm oil, hydrogenated coconut oil, hydrogenated castor oil
  • glyceryl tribehenate or glyceryl tri-12-hydroxystearate further synthetic full esters of fatty acids and glycols (e.g. Syncrowachs ® ) or polyols with 2 - 6 C atoms, fatty acid monoalkanolamides with a C 12-22 acyl radical and a C 2- alkanol radical, synthetic fatty acid fatty alcohol esters, e.g. B.
  • stearyl stearate or cetyl palmitate ester waxes from natural fatty acids and synthetic C 20-4 o-fatty alcohols (INCI name C20-40 alkyl stearates) and full esters from fatty alcohols and di- and tricarboxylic acids, eg. B. dicetyl succinate or dicetyl / stearyl adipate, and mixtures of these substances.
  • the natural and synthetic cosmetic oil bodies which can advantageously be used according to the invention include, for example:
  • oils examples include sunflower oil, olive oil, soybean oil, rapeseed oil, almond oil, jojoba oil, orange oil, wheat germ oil, peach seed oil and the liquid components of coconut oil.
  • Other triglyceride oils such as the liquid portions of beef tallow and synthetic triglyceride oils are also suitable.
  • B. 1, 3-di- (2-ethyl-hexyl) cyclohexane (Cetiol ® S) and di-n-alkyl ether with a total of 12 to 36, in particular 12 to 24 carbon atoms, such as. B. di-n-octyl ether, di-n-decyl ether, di-n-nonyl ether, di-n-undecyl ether, n-hexyl-n-octyl ether and n-octyl-n-decyl ether.
  • esters of C 6 - 3 o-fatty acids with C 2-3 o fatty alcohols are preferred.
  • the monoesters of fatty acids with alcohols having 2 to 24 carbon atoms are preferred.
  • Dicarboxylic acid esters such as di-n-butyl adipate, di- (2-ethylhexyl) adipate, di- (2-ethylhexyl) succinate and di-isotridecylacelate as well as diol esters such as ethylene glycol dioleate, ethylene glycol di-isotridecanoate, propylene glycol di (2-ethylhexanoate) , Propylene glycol di-isostearate, propylene glycol di-pelargonate, butanediol di-isostearate, neopentyl glycol di-caprylate,
  • Mono, - di- and trifatty acid esters of saturated and / or unsaturated linear and / or branched fatty acids with glycerin such as.
  • B. Monomuls ® 90-O18, Monomuls ® 90-L12 or Cutina ® MD.
  • the amount used is 0.1-30% by weight, preferably 0.5-15% by weight and particularly preferably 1.0-5% by weight, in each case based on the weight of the impregnating composition used to finish the flexible carrier according to the invention.
  • Further oils which can advantageously be used according to the invention are hydroxycarboxylic acid esters.
  • Preferred hydroxycarboxylic acid esters are full esters of glycolic acid, lactic acid, apple acid, tartaric acid or citric acid.
  • esters of ⁇ -hydroxypropionic acid, tartronic acid, D-gluconic acid, sugar acid, mucic acid or glucuronic acid are esters of ⁇ -hydroxypropionic acid, tartronic acid, D-gluconic acid, sugar acid, mucic acid or glucuronic acid.
  • Primary linear or branched aliphatic alcohols with 8-22 C atoms are suitable as the alcohol component of these esters.
  • the esters of C 12 -C 15 fatty alcohols are particularly preferred. Esters of this type are available under the trademark Cosmacol ® (Eni Chem. Augusta Industriale), for example.
  • Further particularly preferred oil components are the esters of branched in 2-position C12 alkanols ⁇ 3 with 2-ethylhexanoic acid, for example the commercial product Cosmacol ® EOI.
  • the amount of the hydroxycarboxylic acid esters used is 0.1-15% by weight, preferably 0.1-10% by weight and particularly preferably 0.1-5% by weight, in each case based on the weight of the flexible materials used to equip the inventive Carrier used impregnation composition
  • siloxanes can be in the form of oils, resins, elastomers or gums.
  • Preferred siloxanes are polydialkylsiloxanes, such as. B. polydimethylsiloxane, polyalkylarylsiloxanes, such as. B. polyphenylmethylsiloxane, polydialkylsiloxanes containing amine and / or hydroxy groups, and cyclic silicones (INCI name: Cyclomethicone), preferably decamethylcyclopentasiloxane and dodecamethylcyclohexasiloxane.
  • Suitable perfume oils are, for example, mixtures of natural and synthetic fragrances.
  • Natural fragrances are extracts of flowers (lily, lavender, rose, jasmine, neroli, ylang-ylang), stems and leaves (geranium, patchouli, petitgrain), fruits (anise, coriander, caraway, juniper), fruit peel (bergamot, lemon, Oranges), roots (mace, angelica, celery, cardamom, costus, iris, calmus), woods (pine, sandal, guaiac, cedar, rosewood), herbs and grasses (tarragon, sage, lemongrass, thyme), Needles and twigs (spruce, fir, pine, mountain pine), resins and balms (galbanum, elemi, benzoin, myrrh, olibanum, opoponax).
  • Typical synthetic fragrance compounds are products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon type. Fragrance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinylacetate, phenylethyl acetate, linalyl benzoate, benzyl formate, ethyl methylphenyl glycinate, allyl cyclohexyl undyl propyl propionate, styl propyl pentate.
  • the ethers include, for example, benzyl ethyl ether, the aldehydes, for example, the linear alkanals with 8-18 C atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamenaldehyde, Hydroxycitronellal, Lilial and Bourgeonal, to the ketones eg the lonone, ⁇ -isomethylionone and methylcedrylketone, to the alcohols anethole, citronellol, eugenol, isoeugenol, geraniol, linalool, phenylethyl alcohol and terpineol.
  • the hydrocarbons mainly include the terpenes and balms. However, preference is given to using mixtures of different fragrances which together produce an appealing fragrance.
  • Essential oils of lower volatility which are mostly used as aroma components, are also suitable as perfume oils, e.g. Sage oil, chamomile oil, clove oil, lemon balm oil, mint oil, cinnamon leaf oil, linden blossom oil, juniper berry oil, vetiver oil, oliban oil, galbanum oil, labolanum oil and lavandin oil.
  • perfume oils e.g. Sage oil, chamomile oil, clove oil, lemon balm oil, mint oil, cinnamon leaf oil, linden blossom oil, juniper berry oil, vetiver oil, oliban oil, galbanum oil, labolanum oil and lavandin oil.
  • bergamot oil dihydromyrcenol, lilial, lyral, citronellol, phenylethyl alcohol, ⁇ -hexylcinnamaldehyde, geraniol, benzyl acetone, cyclamen aldehyde, linalool, Boisambrene Forte, Ambroxan, indole, hedione, Sandelice, lemon oil, mandarin oil, orange oil, allyl amyl glycolate, Cyclovertal, lavandin oil, muscatel Sage oil, ß-damascone, geranium oil bourbon, cyclohexyl salicylate, Vertofix Coeur, Iso-E-Super, Fixolide NP, evernyl, iraldein gamma, phenylacetic acid, geranyl acetate, benzyl acetate, rose oxide, romilllate, irot
  • the perfume oil and / or essential oil is present in amounts of 0.01-2% by weight, preferably 0.1-1% by weight, in each case based on the weight of the aqueous impregnation composition used to finish the flexible carrier according to the invention , contain.
  • the total amount of oil and fat components is usually 0.01-30% by weight, preferably 0.1-15% by weight and particularly preferably 1-10% by weight, in each case based on the weight of those used to equip the invention flexible carrier used aqueous impregnation composition.
  • the impregnating compositions used to finish the flexible carriers according to the invention may further contain at least one water-soluble polyol.
  • water-soluble polyol include water-soluble diols, triols and higher alcohols, polyglycerols, polyethylene glycols and mono- and disaccharides.
  • water solubility means that at least 5% by weight of the alcohol can be clearly dissolved at 20 ° C or - in the case of long-chain or polymeric alcohols - can be brought into solution by heating the solution to 50-60 ° C.
  • the diols are C 2 -C 12 diols, in particular 1,2-propylene glycol, butylene glycols such as B.
  • Glycerol and polyglycerols, in particular diglycerol and triglycerol, 1,2,6-hexanetriol, and also the polyethylene glycols (PEG) PEG-400, PEG-600, PEG-1000, PEG-1550, PEG-3000 and PEG-4000 are further preferred .
  • Suitable monosaccharides are e.g. B. glucose, fructose, galactose, arabinose, ribose, xylose, lyxose, allose, old rose, mannose, gulose, idose and talose, the deoxy sugar fucose and rhamnose and amino sugar such as. B. glucosamine or galactosamine. Glucose, fructose, galactose, arabinose and fucose are preferred; Glucose is particularly preferred.
  • Suitable oligosaccharides are composed of two to ten monosaccharide units, e.g. B. sucrose, lactose or trehalose. A particularly preferred oligosaccharide is sucrose. The use of honey, which predominantly contains glucose and sucrose, is also particularly preferred.
  • the water-soluble polyol is present in amounts of 0.5-60% by weight, preferably 1.0-30% by weight and particularly preferably 2.0-20% by weight, in each case based on the weight of the equipment used for the impregnating composition used according to the flexible carrier according to the invention.
  • the impregnation compositions used to equip the flexible inventive materials can furthermore contain at least one natural, if desired chemically modified polymer.
  • Such polymers are selected, for example, from cellulose ethers, e.g. B. hydroxypropyl cellulose, carboxymethyl cellulose, hydroxyethyl cellulose and methyl hydroxypropyl cellulose, quaternized cellulose derivatives, such as. B.
  • Celquat ® and Polymer JR ® and particularly preferably Celquat ® H 100, Celquat ® L 200 and Polymer JR ® 400, the polymers known under the names Polyquatemium-24, guar gum, cationic guar derivatives, especially the Products Cosmedia ® Guar and Jaguar ® , alginates, xanthan gum, gum arabic, karaya gum, locust bean gum, linseed gums, dextrans, shellac, starch fractions such as amylose, amylopectin and dextrins, chemically and / or thermally modified starches such as B.
  • the impregnating compositions used for the finishing of the flexible carriers according to the invention can furthermore contain at least one synthetic polymer which can be anionic, cationic, amphoteric or non-ionic.
  • Suitable anionic synthetic polymers contain carboxylate and / or sulfonate groups and as monomers, for example acrylic acid, methacrylic acid, crotonic acid, maleic anhydride and 2-acrylamido-2-methylpropanesulfonic acid.
  • the acidic groups can be present in whole or in part as sodium, potassium, ammonium, mono- or triethanolammonium salt.
  • Preferred monomers are 2-acrylamido-2-methylpropanesulfonic acid and acrylic acid.
  • Very particularly preferred anionic polymers contain 2-acrylamido-2-methylpropanesulfonic acid as the sole monomer or as the comonomer, it being possible for the sulfonic acid group to be wholly or partly in salt form.
  • the homopolymer of 2-acrylamido-2-methylpropanesulfonic acid e.g. B. the product Hostacerin ® AMPS.
  • copolymers of at least one anionic monomer and at least one nonionic monomer are acrylamide, methacrylamide, acrylic acid ester, methacrylic acid ester, vinyl pyrrolidone, vinyl ether and vinyl ester.
  • Preferred anionic copolymers are acrylic acid-acrylamide copolymers and in particular polyacrylamide copolymers with monomers containing sulfonic acid groups, e.g. B.
  • anionic homopolymers are uncrosslinked and crosslinked polyacrylic acids. Allyl ethers of pentaerythritol, sucrose and propylene can be preferred crosslinking agents. Such compounds are, for example, the commercial products Carbopol ® . Further particularly preferred anionic copolymers are those which contain as monomers 80-98% by weight of optionally substituted acrylic acid and 2-20% by weight of C 12 -C 30 fatty alcohol methacrylic acid ester and can be crosslinked. Such connections are e.g. B. the commercial products Pemulen ® .
  • the total amount of natural and / or synthetic polymers is usually 0.1-3% by weight, preferably 0.2-2% by weight and particularly preferably 0.3-1.5 % By weight, in each case based on the weight of the impregnating composition used to equip the inventive inventive in each case based on the weight of the impregnating composition used to equip the flexible carrier.
  • the cosmetic active ingredients that can be used are silicas, natural and synthetic silicates, aluminosilicates, kaolin, talc and apatites, which can be modified with aqueous carboxylic acids having 2 to 3 carbon atoms.
  • the amounts used are 0.1-10% by weight, preferably 0.5-5% by weight, in each case based on the weight of the impregnating composition used to finish the flexible carrier according to the invention.
  • the impregnating compositions used to finish the flexible carriers according to the invention can contain both colored and colorless pigments.
  • the pigments are selected from the oxides of titanium, iron, zinc, zirconium, magnesium, cerium and bismuth, which can be surface-modified if desired, boron nitride particles, water-insoluble pearlescent pigments and water-insoluble organic pigments. Some of the pigments mentioned below also serve as UV absorbers.
  • Particularly preferred colored pigments are selected from the iron oxides with the color index numbers Cl 77491 (iron oxide red), Cl 77492 (iron oxide hydrate yellow) and Cl 77499 (iron oxide black), from Cl 77891 (titanium dioxide) and carbon black.
  • color pigments are selected from Cl 15510, Cl 15585, Cl 15850, Cl 15985, Cl 45170, Cl 45370, Cl 45380, Cl 45425, Cl 45430, Cl 73360, and Cl 75470.
  • the preferred pigments are selected from the oxides of titanium , Zinc, zircon and iron.
  • the preferred inorganic particle substances are hydrophilic or amphiphilic. They can advantageously be surface-coated, in particular surface-treated ("coated"). Examples of these are titanium dioxide pigments coated with aluminum stearate (commercial product MT 100 T from Tayca), zinc oxide coated with dimethylpolysiloxane (Dimethicone), boron nitride coated with Dimethicone (Tres BN ® UHP 1106 from Carborundum), with a mixture of dimethylpolysiloxane and silica gel ( Simethicone) and aluminum oxide hydrate (Alumina) coated titanium dioxide (Eusolex ® T 2000 from Merck), titanium dioxide coated with octylsilanol or spherical polyalkylsesquisiloxane particles (Aerosil ® R972 and Aerosil ® 200V from Degussa). The amounts used are 0.1-20% by weight, preferably 0.5-10% by weight, particularly preferably 0.5-5% by weight
  • the impregnation compositions used to finish the flexible carriers according to the invention can contain at least one organic or inorganic light protection filter.
  • the organic light protection filters which can be oil-soluble or water-soluble, are selected from the derivatives of dibenzoylmethane, cinnamic acid esters, diphenylacrylic acid esters, benzophenone, camphor, p-aminobenzoic acid esters, o-aminobenzoic acid esters, salicylic acid esters, benzimidazoles, 1 , 3,5-triazines, monomeric and oligomeric 4,4-diarylbutadienecarboxylic acid esters and carboxamides, ketotricyclo (5.2.1.0) decane, benzalmalonic acid esters and any mixtures of the components mentioned.
  • oil-soluble light-protection filters preferred are 1- (4-tert-butylphenyl) -3- (4'methoxyphenyl) propane-1,3-dione (Parsol ® 1789), 1-phenyl-3- (4'-ISOPRO pylphenyl) propane-1,3-dione, 3- (4 "-methylbenzylidene) -D, L-camphor, 4- (dimethylamino) -benzoic acid-2-ethylhexyl ester, 4- (dimethylamino) benzoic acid-2-octyl ester, 4- (dimethylamino) benzoic acid amyl ester, 4-methoxycinnamic acid 2-ethylhexyl ester,
  • Preferred water-soluble light protection filters are 2-phenylbenzimidazole-5-sulfonic acid and its alkali, alkaline earth, ammonium, alkylammonium, alkanolammonium and glucammonium salts, sulfonic acid derivatives of benzophenones, preferably 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid and their Salts, sulfonic acid derivatives of 3-benzylidene camphor, such as. B. 4- (2-oxo-3-bornylidene methyl) benzenesulfonic acid and 2-methyl-5- (2-oxo-3-bornylidene) sulfonic acid and their salts.
  • the organic light protection filters are present in amounts of 0.1-20% by weight, preferably 1-15% by weight and particularly preferably 2-10% by weight, in each case based on the flexible carriers used to equip the flexible carriers according to the invention Impregnation composition.
  • the impregnating compositions used to finish the flexible carriers according to the invention can contain self-tanning active ingredients.
  • the self-tanning active ingredients serve to give the skin a darker skin tone even without UV radiation.
  • the self-tanning active ingredients are selected from dihydroxyacetone, erythrulose, monohydroxyindole derivatives and dihydroxyindole derivatives, as are disclosed, for example, in US Pat. No.
  • 5,874,091 in particular 5,6-dihydroxyindole and 6-hydroxyindole, dihydroxyindoline derivatives, as are described in WO 94 / 03148 A2 are disclosed, in particular 5,6-dihydroxyindoline, phenylalanine, tyrosine, dopa and naphthoquinone derivatives, for example Lawson (from henna) or Yuglon (from walnut).
  • the amounts used for the indole derivatives are 0.001-1.5% by weight, preferably 0.01-0.5% by weight, and for the other active ingredients 0.2-5% by weight, based in each case on the Weight of the impregnating composition used to finish the flexible carriers of the invention.
  • the impregnating compositions used to finish the flexible carriers according to the invention can contain cosmetic abrasives, selected from polymer particles and vegetable abrasives, which, if desired, can be coated with fatty substances.
  • Suitable polymeric abrasives are selected from optionally modified starches and starch derivatives, crystalline cellulose, cellulose powders, lactoglobulin derivatives, ground plant parts such as almond bran or wheat bran, hardened jojoba oil (jojoba beads), polymer particles made from polyolefins, polycarbonates, polyurethanes, methacrylates, polyacrylates - Or (meth) acrylate-vinylidene copolymers, which can be crosslinked, polyesters, polyamides, polystyrenes, Teflon or silicones, and micro- or millicapsules, the petrochemical polymers and / or biopolymers such as gelatin, pectin, vegetable gums, alginates and carrageenan and optionally contain cosmetic active
  • Abrasives with average diameters of 90-600 ⁇ m are preferred.
  • Micro- or millicapsules containing active ingredients are also particularly preferred.
  • the commercial capsules are often referred to as aqueous polymer dispersion before, for example, the particularly preferred Millicapsules ® Lipotec SA (INCI name: Aqua, Tocopheryl Acetate, Glycerine, carbomer, Sebacic Acid, agar, Green colourant, Alginic Acid).
  • the impregnating compositions used for the finishing of the flexible carriers according to the invention can contain cosmetic or dermatological active ingredients with sebum-regulating, skin-calming, anti-inflammatory, astringent or circulation-promoting effects.
  • the impregnating compositions used for the finishing of the flexible carriers according to the invention can furthermore contain at least one vegetable or animal protein or protein hydrolyzate.
  • Antioxidants and / or UV absorbers can preferably be added to protect the impregnating compositions used to finish the flexible carriers according to the invention.
  • Particularly suitable antioxidants and / or UV absorbers are tetrabutyl pentaerythrityl hydroxyhydrocinnamate (INCI name), also as neopentanetetrayl tetrakis (3,5-di-tert-butyl-4-hydroxyhydrocinnamate) or
  • Tetrakis [methylene- (3,5-di-tert-butyl-4-hydroxyhydrocinnamate)] methanes are known and commercially available e.g. B. available under the product name Tinogard TT (Ciba), 2-tert-butyl-6- (5-chloro-2H-benzotriazol-2-yl) -p-cresol (INCI name: Bumetrizole), commercially z. B.
  • Tinogard AS (Ciba)
  • Ciba 3- (2H-benzotriazol-2-yl) -5-sec-butyl-4-hydroxybenzenesulfonate sodium salt
  • ICI name sodium benzotriazolyl butylphenol sulfonate
  • B. is available under the product name Tinogard HS or Tinogard H Liquid (Ciba)
  • Tinogard TL (Ciba).
  • the flexible carriers according to the invention can be used in a variety of ways.
  • a preferred embodiment of the invention contains the cosmetic composition in the form of a face or body cleansing composition and can be used as a face or body cleansing wipe or sponge or as a make-up remover.
  • Another preferred embodiment of the invention contains the cosmetic composition in the form of a 2-in-1 cleaning and care composition and can be used as a 2-in-1 cloth or sponge for cleaning and simultaneous care of the facial and / or body skin become.
  • Another preferred embodiment of the invention contains the cosmetic
  • Composition in the form of a skin care milk or lotion can be used as
  • Skin care cloth or sponge can be used.
  • Composition in the form of a facial tonic can be used as a Cleansing Water towel or sponge or Tonic Water towel or sponge for clarifying, refreshing and
  • Toning of the facial and / or body skin can be used.
  • composition of a form of a self-tanning composition and can be used as
  • Self-tanning cloth or sponge can be used.
  • composition in the form of a peeling composition and can be used as a peeling
  • Sponge can be used.
  • Composition and can be used as a hair cleansing or conditioning sponge.
  • Composition in the form of an after-shave can be used as an after-shave sponge.
  • Composition and can be used as a scented sponge.
  • Composition in the form of a pigmented blush or make-up and can be used as
  • Make-up or masking sponge can be used.
  • the impregnation composition according to Example 1 had a pH of 4.3 immediately after the preparation. After finishing a viscose nonwoven with this impregnation composition and storage for two months, the squeezed out impregnation composition had a pH of 4.5.
  • Example 2 represents a soak composition for a lotion and make-up remover wipe.
  • Example 3 represents an impregnation composition for a self-tanning towel.
  • Example 4 represents an impregnation composition for a sun protection towel.
  • Example 5 represents an impregnation composition for a facial cleansing and peeling treatment.
  • Example 6 represents a soaking composition for a skin and hair cleaning wipe.
  • Examples 7-9 are steep soaking compositions for a towel for cleaning and conditioning the hair and skin.

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Abstract

L'invention concerne un support souple comprenant une composition aqueuse d'imprégnation, utilisé pour traiter de manière cosmétique ou dermatologique la peau, les cheveux, les muqueuses et les phanères. Cette invention est caractérisée en ce que la composition aqueuse d'imprégnation contient au moins un acide organique servant d'agent de conservation, cet acide organique étant sélectionné entre de l'acide salicylique, de l'acide benzoïque, de l'acide propionique, de l'acide déhydroacétique (3-acétyl-6-méthyl-2H-pyran-2,4(3H)-dione) et de l'acide sorbique, ainsi que les sels métalliques hydrosolubles physiologiquement acceptables de ces acides. En outre, ladite composition aqueuse d'imprégnation est tamponnée avec 0,1 à 10 % en poids d'un couple acide-base correspondant, de façon à présenter un pH compris entre 2,5 et 6,0, aussi bien avant son introduction dans le support, qu'après un stockage de 2 mois dans le support.
PCT/EP2004/001569 2003-02-28 2004-02-19 Conservation de tissus impregnes WO2004075866A1 (fr)

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US10987292B2 (en) 2013-11-11 2021-04-27 Colgate-Palmolive Company Preservative system
US11252960B2 (en) 2017-01-31 2022-02-22 Kimberly-Clark Worldwide, Inc. Antibacterial composition including benzoic acid ester and methods of inhibiting bacterial growth utilizing the same

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US20070264224A1 (en) * 2004-09-24 2007-11-15 Gelicity (Uk) Limited Exfoliating and Softening Composition
DE102006047247A1 (de) * 2006-10-06 2008-04-10 Evonik Goldschmidt Gmbh Kaltherstellbare, niedrigviskose und langzeitstabile kosmetische Emulsionen mit kationische Gruppen enthaltenden Coemulgatoren
DE102015212822A1 (de) * 2015-07-09 2017-01-12 Beiersdorf Ag Reinigungstücher getränkt mit Tränkungsmitteln basierend auf einer Mizellentechnologie

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