EP1861170A1 - Utilisation de preparations cosmetiques contenant une quantite d'oxygene libre non lie moleculairement - Google Patents

Utilisation de preparations cosmetiques contenant une quantite d'oxygene libre non lie moleculairement

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Publication number
EP1861170A1
EP1861170A1 EP05850370A EP05850370A EP1861170A1 EP 1861170 A1 EP1861170 A1 EP 1861170A1 EP 05850370 A EP05850370 A EP 05850370A EP 05850370 A EP05850370 A EP 05850370A EP 1861170 A1 EP1861170 A1 EP 1861170A1
Authority
EP
European Patent Office
Prior art keywords
skin
acid
preparations
present
advantageous
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP05850370A
Other languages
German (de)
English (en)
Inventor
Andreas Bleckmann
Uta Meiring
Ludger Kolbe
Thomas Blatt
Christopher Mummert
Jens Treu
Jutta Kunert
Frank Teuber
Guido Heinsohn
Jessica Rathsack
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beiersdorf AG
Original Assignee
Beiersdorf AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beiersdorf AG filed Critical Beiersdorf AG
Publication of EP1861170A1 publication Critical patent/EP1861170A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/22—Peroxides; Oxygen; Ozone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00—Medicinal preparations containing inorganic active ingredients
    • 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
    • A61K8/04—Dispersions; Emulsions
    • A61K8/046—Aerosols; Foams
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • 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
    • A61Q19/08—Anti-ageing preparations

Definitions

  • the present invention relates to the use of cosmetic preparations having a cosmetically effective content of non-molecularly bound free oxygen for increasing skin cell regeneration.
  • the object of the present invention was to provide skin-care preparations and preparations for the care of naturally aged skin, wherein the preparations should care for and beautify the external appearance of the body.
  • ⁇ increases skin cell regeneration
  • the preparations preferably contain from 5 to 20% by volume, more preferably from 7.5 to 15% by volume, of free oxygen.
  • the use according to the invention thus represents, so to speak, the extra breath of pure oxygen for a healthy and rejuvenated skin.
  • “regeneration of the skin cells” or “skin cell regeneration” is to be understood as meaning that, when used according to the invention, the epidermal renewal rate ("epidermal turnover") of the skin is increased. ) is, for example, the area change of the corneocytes ..
  • the skin cell regeneration can be detected / detected with the aid of a fully automated microscope robot system.
  • the procedure is explained in the following point-wise:
  • the epidermis of the skin is renewed by the constant re-production of keratinocytes, their differentiation / cornification and desquamation every 28 days.
  • These dander are out Horn cells composed essentially of keratin, so from amino acids exist.
  • the measuring area is first pre-stripped once. Subsequently, two D-Squames are applied to this area and after a single roll back and forth with the weight roller removed from the skin surface and fixed on a slide with barcodes.
  • the slide is then fixed in the special robot holder.
  • the robot evaluates the dermal samples by image analysis, i. the corneocyte area is determined.
  • the essential basis of the present invention is the pulsed short-term topical application of molecular oxygen.
  • a short-term pulse up to 1 hour
  • the present invention differs fundamentally from the prior art.
  • a short-term, pulse- or bolus-like stimulation of the intracellular and extracellular oxygen content has a signaling function for the cells of the skin in that various mechanisms are stimulated, as a result of which the cells as a whole are activated cell physiologically without the disadvantages associated with associated with long-term oxygen use.
  • a permanent compensation of oxygen deficiency conditions in the skin should not be achieved according to the invention.
  • the pulse-like application of molecular oxygen regularly -. B. 2-3 times a day - to repeat.
  • a particular advantage of the present invention is that the molecular oxygen is not bound to support structures. This has the consequence that a rapid influx and drainage of the gas through the various layers of the skin is possible. Long periods of residence and the associated risks of oxidative and degenerative processes, which can occur within a few hours in a strongly oxygen-containing atmosphere. would run counter to the inventive idea, are thus excluded.
  • the data underlying this invention clearly demonstrate the advantage of a pulsed application with pure molecular oxygen over a permanent supply of oxygen or the application via carrier molecules.
  • “Self-foaming”, “foam-like”, “post-foaming” or “foamable” are to be understood as preparations from which foams - either during the manufacturing process, either in the consumer's application or otherwise - by the entry of or several gases can be produced in principle.
  • the gas bubbles are (randomly) distributed in one (or more) liquid phase (s), wherein the (foamed) preparations macroscopically need not necessarily have the appearance of a foam.
  • foams may, for. B. represent macroscopically visible dispersed systems of dispersed gases in liquids.
  • the foam character can also be visible only under a (light) microscope, for example.
  • foams according to the invention - in particular when the gas bubbles are too small to be detected under a light microscope - can also be recognized by the large volume increase of the system.
  • At least one emulsifier A selected from the group of fully, partially or not neutralized, branched and / or unbranched, saturated fatty acids having a chain length of 10 to 40 carbon atoms,
  • At least one emulsifier B selected from the group of polyethoxylated fatty acid esters having a chain length of 10 to 40 carbon atoms and with a degree of ethoxylation of 5 to 100 and
  • co-emulsifier C selected from the group of saturated, branched and / or unbranched fatty alcohols having a chain length of 10 to 40 carbon atoms.
  • the emulsifier or emulsifiers A are preferably selected from the group of fatty acids which are completely or partially neutralized with customary alkalis (such as, for example, sodium and / or potassium hydroxide, sodium and / or potassium carbonate and also mono- and / or triethanolamine) ,
  • customary alkalis such as, for example, sodium and / or potassium hydroxide, sodium and / or potassium carbonate and also mono- and / or triethanolamine
  • stearic acid and stearates, isostearic acid and isostearates, palmitic acid and palmitates as well as myristic acid and myristates are particularly advantageous.
  • the emulsifier (s) B are preferably selected from the following group: PEG-9 stearate, PEG-8 distearate, PEG-20 stearate, PEG-8 stearate, PEG-25 glyceryl trioleate, PEG-15 glyceryl ricinoleate, PEG- 20-glyceryl stearate, PEG-20 glyceryl isostearate, PEG-20 stearate, PEG-20 methyl glucose sesquistearate, PEG-30 glyceryl isostearate, PEG-20 glyceryl laurate, PEG-30 stearate, PEG-30 glyceryl stearate, PEG- 40-stearate, PEG-30 glyceryl laurate, PEG-50 stearate, PEG-100 stearate, PEG-150 laurate.
  • polyethoxylated stearic acid esters are particularly advantageous.
  • the co-emulsifier (s) C are preferably selected according to the invention from the following group: behenyl alcohol (C 22 H 45 OH), cetearyl alcohol [a mixture of cetyl alcohol (C 16 H 33 OH) and stearyl alcohol (C 18 H 37 OH)], lanolin alcohols (Wool wax alcohols, which are the unsaponifiable alcohol fraction of wool wax obtained after saponification of wool wax). Particularly preferred are cetyl and cetylstearyl alcohol.
  • the total amount of the emulsifiers A and B and the Coemulgators C from the range of 2 to 10 wt .-%, preferably from 2.5 to 7 wt .-%, each based on the total weight of Formulation, to choose.
  • preparations which are in the form of emulsions and contain one or more O / W emulsifiers having an HLB value of more than 6.
  • the one or more O / W emulsifiers are particularly advantageously selected from the group of ethoxylated fatty acids and / or ethoxylated fatty alcohols.
  • Especially advantageous are ceteareth-n, steareth-n, PEG-n-stearates and polysorbates n, where n can assume values between 20 and 100 (corresponding to 20 to 100 ethoxy units).
  • O / W emulsifiers for the purposes of the present invention are glyceryl stearate citrate, polyglyceryl-3-methylglucose distearate and PEG-40 Castor OiI optionally in combination with sodium cetearyl sulfate and / or cetearyl alcohol.
  • O / W emulsions for the purposes of the present invention in addition to one or more O / W emulsifiers also co-emulsifiers selected from the group glyceryl stearate, fatty acids and fatty alcohols.
  • the self-foaming, foam-like, post-foaming or foamable cosmetic emulsions may also contain substances which stabilize the gas-emulsion interface.
  • Such interfacial stabilizers may e.g. B. be selected from the group of fillers.
  • the fillers may also z. B. further improve the sensory and cosmetic properties of the formulations and, for example, cause or enhance a velvety or silky feel on the skin.
  • Advantageous fillers for the purposes of the present invention are polymethyl methacrylates, methacrylate copolymers, starch and starch derivatives (such as, for example, tapioca starch, distarch phosphate, aluminum or sodium starch, octenyl succinate and the like), pigments which have neither primary UV filter nor dyeing action have (such as. for example, boron nitride etc.) and / or Aerosils ® (CAS no. 7631-86-9). Particularly advantageous is talc. Further advantageously, the one or more interface stabilizers can be selected from the group of rheological additives. Aluminum and / or magnesium silicates are particularly advantageous.
  • the emulsions may also contain hydrocolloids (also referred to as thickeners or gel formers), which may stabilize the preparations.
  • hydrocolloids also referred to as thickeners or gel formers
  • hydrocolloids which are advantageous according to the invention.
  • Hydrocolloids which are preferred according to the invention are: magnesium and / or aluminum silicates and, for example, methylcelluloses, which are referred to as the methyl ethers of cellulose. They are characterized by the following structural formula
  • R can represent a hydrogen or a methyl group.
  • cellulose mixed ethers which are generally also referred to as methylcelluloses and, in addition to a dominating content of methyl, additionally contain 2-hydroxyethyl, 2-hydroxypropyl or 2-hydroxybutyl groups.
  • Particularly preferred are (hydroxypropyl) methylcelluloses, for example those available under the trade name Methocel E4M from Dow Chemical Comp.
  • the cosmetic preparations according to the invention may contain cosmetic adjuvants, such as are commonly used in such preparations, for.
  • preservatives preservatives, complexing agents, bactericides, perfumes, substances to increase the foaming, dyes, pigments that have a coloring effect, thickeners, moisturizing and / or moisturizing substances, fillers that improve the feel on the skin, fats, oils, waxes or other common ingredients of a cosmetic formulation such as alcohols, polyols, polymers, foam stabilizers, electrolyte, organic solvents or silicone derivatives.
  • Advantageous preservatives for the purposes of the present invention are, for example, iodopropylbutylcarbamates (for example those available under the trade names Glycacil-L, Glycacil-S from Lonza and / or Dekaben LMB from Jan Dekker), parabens (ie p-hydroxybenzoic acid alkyl esters, such as Methyl, ethyl, propyl and / or butylparaben), phenoxyethanol, ethanol, benzoic acid and the like.
  • the preservation system according to the invention also advantageously also preserving aids, such as octoxyglycerol, glycine soy etc.
  • EDTA 1 [S, S] -Ethylendiamindisuccinat (EDDS), which is available, for example, under the trade name Octaquest from the company.
  • Octel pentasodium ethylenediamine tetramethylene phosphonate, which z. B. under the trade name Dequest 2046 from the company.
  • Monsanto is available and / or iminodisuccinic, which among other things from the company.
  • Bayer AG under the trade name Iminodisuccinat VP OC 370 (about 30% solution) and Baypure CX 100 is permanently available.
  • compositions are also obtained when antioxidants are used as additives or active ingredients.
  • the preparations advantageously contain one or more antioxidants.
  • antioxidants all suitable or common for cosmetic applications antioxidants can be used.
  • water-soluble antioxidants can be used, such as vitamins.
  • antioxidants are vitamin E and its derivatives as well as vitamin A and its derivatives.
  • the amount of the antioxidants (one or more compounds) in the preparations is preferably 0.001 to 30 wt .-%, particularly preferably 0.05 to 20 wt .-%, in particular 0.1 to 10 wt .-%, based on the total weight the preparation.
  • vitamin E and / or its derivatives represent the antioxidant (s)
  • vitamin A or vitamin A derivatives or carotenes or their derivatives represent the antioxidant (s)
  • beneficial agents to be used in the context of the present invention are those which have a positive effect on the condition of the skin, such as, in particular, active ingredients for positively influencing the aging skin, the formation of wrinkles or even existing ones Reduce wrinkles.
  • biochinones in particular ubiquinone (Q10) and ubiquinol, folic acid and its derivatives (in particular tetrahydrofolic acid and dihydrofolic acid), niacin and its derivatives (in particular niacinamide), creatine and creatinine, carnitine, biotin, isoflavone, cardiolipin, lipoic acid, anti-freezing proteins , Hops and hops malt extracts.
  • agents that promote the restructuring of connective tissue such as natural and / or synthetic isoflavonoids and isoflavonoid-containing plant extracts - such.
  • soy and clover extracts - can be used very well in the formulations of the invention.
  • active ingredients for aiding the skin functions in dry skin such as vitamin C, biotin, carnitine, propionic acid, green tea extracts, eucalyptus oil, urea and mineral salts (such as. For example, NaCl 1 Marine minerals) as well as osmolytes (such as inositol, betaine, quaternary ammonium compounds)).
  • agents such as sericosides, various extracts of licorice, licochalcone, especially licochalcone A, silymarin, silyphos, dexpanthenol, inhibitors of prostaglandin metabolism, in particular cyclooxygenase and the leukotriene metabolism, in particular 5-lipoxygenase, but also 5-lipoxvgenase Inhibitor protein, FLAP.
  • creatine and creatinine are suitable active ingredients to create and / or renew an (energy) depot and to activate the repair of various cellular structures, in particular the DNA.
  • modulators of pigmentation also proved to be advantageous.
  • agents that reduce the pigmentation of the skin and thus lead to a cosmetically desired lightening of the skin and / or reduce the occurrence of age spots and / or lighten existing age spots are also proved to be advantageous.
  • Examples include tyrosine sulfate, dioic acid (8-hexadecene-1, 16-dicarboxylic acid) and lipoic acid and lipoamide, various extracts of licorice, kojic acid, hydroquinone, arbutin, alpha-arbutin, deoxyarbutin, fruit acids, especially alpha-hydroxy acids (AHAs ), Bearberry (Uvae ursi), ursolic acid, ascorbic acid, green tea extracts, aminoguanidine, pyridoxamine, niacinamide, inhibitors of Proteinase Activated Receptor 2 (PAR-2).
  • various extracts of licorice kojic acid, hydroquinone, arbutin, alpha-arbutin, deoxyarbutin, fruit acids, especially alpha-hydroxy acids (AHAs ), Bearberry (Uvae ursi), ursolic acid, ascorbic acid, green tea extracts, aminoguanidine, pyridoxamine, n
  • formulations according to the invention which contain other active ingredients which bring about increased or faster tanning of the skin (advanced glycation end products (AGE), lipofuscins, nucleic acid oligonucleotides, purines and pyrimidines, NO-releasing substances), tyrosine and its derivatives (in particular N - Acetyl-tyrosine), phenylalanine and its derivatives (especially N-acetyl-phenylalanine), activators of Proteinase Activated Receptor 2 (PAR-2), either with or without the influence of UV light.
  • active ingredients which bring about increased or faster tanning of the skin
  • AGE glycation end products
  • lipofuscins nucleic acid oligonucleotides
  • purines and pyrimidines purines and pyrimidines
  • NO-releasing substances NO-releasing substances
  • tyrosine and its derivatives in particular N - Acetyl-tyrosine
  • Inventive formulations which z. B. known anti-wrinkle active ingredients such as Flavonglyco- side (especially ⁇ -glycosyl rutin), coenzyme Q10, vitamin E and / or derivatives and the like, are particularly advantageous for the prophylaxis and treatment of cosmetic or dermatological lesions, as z. Skin aging (such as dryness, roughness and formation of dryness lines, itching, reduced refatting (eg after washing), visible vascular dilations (telangiectasia, cuperosis), flaccidity and development of wrinkles and wrinkles, local Hyper-, hypo- and false pigmentation (eg, age spots), increased susceptibility to mechanical stress (eg, cracking), and the like). Furthermore, they are advantageously suitable against the appearance of dry or rough skin.
  • known anti-wrinkle active ingredients such as Flavonglyco- side (especially ⁇ -glycosyl rutin), coenzyme Q10, vitamin E and / or derivatives and the like, are particularly advantageous for the
  • Moisturizers are substances or substance mixtures which give cosmetic preparations the property of reducing the moisture release of the horny layer (also called transepidermal water loss (TEWL) after application or spreading on the skin surface and / or positively influencing the hydration of the horny layer
  • Advantageous moisturizers for the purposes of the present invention are, for example, glycerol, lactic acid and / or lactates, in particular sodium lactate, butylene glycol, propylene glycol, biosaccharide gum-1, glycine soya, ethylhexyloxyglycerol, pyrrolidonecarboxylic acid and urea.
  • the oil phase of the preparations according to the present invention advantageously contains nonpolar, for example those which are selected from the group of branched and unbranched hydrocarbons and waxes, in particular mineral oil, Vaseline (petrolatum), paraffin oil, squalane, polyolefins, hydrogenated polyisobutenes and iso - hexadecane.
  • nonpolar for example those which are selected from the group of branched and unbranched hydrocarbons and waxes, in particular mineral oil, Vaseline (petrolatum), paraffin oil, squalane, polyolefins, hydrogenated polyisobutenes and iso - hexadecane.
  • polyolefins polydecenes are the preferred substances.
  • the oil phase may further comprise a content of cyclic or linear silicone oils or consist entirely of such oils, although it is preferred to use an additional content of other oil phase components in addition to the silicone oil or silicone oils.
  • Silicone oils are synthetic compounds in which silicon atoms via oxygen atoms chain and / or net-like linked and the remaining valences of silicon by hydrocarbon radicals (usually methyl, more rarely ethyl, propyl, phenyl groups, etc.) are saturated , Systematically, the silicone oils are called polyorganosiloxanes.
  • the methyl-substituted polyorganosiloxanes which are the quantitatively most important compounds of this group and are characterized by the following structural formula
  • Dimethicones are available in different chain lengths or with different molecular weights.
  • cyclomethicone octamethylcyclotetrasiloxane
  • silicone oils are also advantageous for the purposes of the present invention, for example hexamethylcyclotrisiloxane, polydimethylsiloxane, poly (methylphenylsiloxane).
  • Particularly advantageous polyorganosiloxanes in the context of the present invention are, for example, dimethylpolysiloxanes [poly (dimethylsiloxane)], which are obtainable, for example, under the trade names Abil 10 to 10 000 from Th. Goldschmidt.
  • phenylmethylpolysiloxanes INCI: phenyl dimethicone, phenyl trimethicone
  • cyclic silicones octamethylcyclotetrasiloxane or decamethylcyclopentasiloxane
  • amino-modified silicones INCI: amodimethicones
  • silicone waxes eg.
  • polysiloxane-polyalkylene copolymers ICI: stearyl dimethicone and cetyl dimethicone
  • dialkoxydimethylpolysiloxanes stearoxy dimethicones and behenoxy stearyl dimethicone
  • cetyl dimethicone hexamethylcyclotrisiloxane
  • polydimethylsiloxane poly (methylphenylsiloxane).
  • the preparations according to the present invention may also advantageously contain one or more substances from the following group of siloxane elastomers, for example in order to increase the water resistance and / or the sun protection factor of the products:
  • Siloxane elastomers which are insoluble and swellable in silicone oil obtainable by the addition reaction of an organopolysiloxane (1) containing silicon-bonded hydrogen with an organopolysiloxane (2) containing unsaturated aliphatic groups, the proportions used being such be such that the amount of hydrogen of the organopolysiloxane (1) or the unsaturated aliphatic groups of the organopolysiloxane (2)
  • the siloxane elastomer (s) are in the form of spherical powders or in the form of gels.
  • siloxane elastomers are those with the INCI name dimethicone / vinyl dimethicone crosspolymer, for example that available from DOW CORNING under the trade names DOW CORNING 9506 Powder available.
  • siloxane elastomer is used in combination with oils of hydrocarbons of animal and / or vegetable origin, synthetic oils, synthetic esters, synthetic ethers or mixtures thereof. It is very particularly preferred if the siloxane elastomer is used in combination with unbranched silicone oils or cyclic silicone oils or mixtures thereof which are liquid or pasty at room temperature. Especially advantageous are organopolysiloxane elastomers with the INCI name Dimethicone / Polysilicone-11, in particular the Gransil types GCM, GCM-5, DMG-6, CSE gel, PM-GeI, LTX, ININ available from Grant Industries Inc. Gel, AM-18 gel and / or DMCM-5.
  • siloxane elastomer is used in the form of a gel of siloxane elastomer and a lipid phase, wherein the content of the siloxane elastomer in the gel is 1 to 80% by weight, preferably 0.1 to 60% by weight , in each case based on the total weight of the gel.
  • the total amount of Siloxanelasto- mers (active content) from the range of 0.01 to 10 wt .-%, preferably from 0.1 to 5 wt .-%, each based on the total weight of Formulation, to choose.
  • the preparations according to the present invention preferably contain at least one further UV-A, UV-B and / or broad-spectrum filter substance.
  • the formulations may, although not necessary, optionally also contain one or more organic and / or inorganic pigments as UV filter substances, which may be present in the water and / or the oil phase.
  • the preparations according to the present invention may also advantageously be in the form of so-called oil-free cosmetic emulsions which have a water phase and at least one UV filter substance which is liquid at room temperature as a white Tere phase and which may be particularly advantageous also free of other oil components.
  • Preferred inorganic pigments are metal oxides and / or other water-insoluble or insoluble metal compounds, in particular oxides of titanium (TiO 2 ), zinc (ZnO), iron (eg Fe 2 O 3 ), zirconium (ZrO 2 ), silicon ( SiO 2 ), manganese (for example MnO), aluminum (Al 2 O 3 ), cerium (for example Ce 2 O 3 ), mixed oxides of the corresponding metals and mixtures of such oxides and also the sulfate of barium ( BaSO 4 ).
  • the pigments can also be used advantageously in the form of commercially available oily or aqueous predispersions.
  • dispersants and / or solubilizers can be added to these predispersions.
  • the pigments may advantageously be surface-treated ("coated"), whereby, for example, a hydrophilic, amphiphilic or hydrophobic character is to be formed or retained.
  • This surface treatment may consist in using a thin hydrophilic and hydrophilic pigment according to methods known per se or hydrophobic inorganic and / or organic layer
  • the various surface coatings may also contain water for the purposes of the present invention.
  • Suitable titanium dioxide particles and predispersions of titanium dioxide particles are available from the following companies under the following trade names:
  • UV-A filter substances for the purposes of the present invention are dibenzoyl methane derivatives, in particular 4- (tert-butyl) -4'-methoxydibenzoylmethane (CAS No. 70356-09-1), which has been sold by Givaudan under the trademark Parsol ® 1789 and sold by Merck under the trade name Eusolex® 9020.
  • Salts of 2-phenylbenzimidazole-5-sulfonic acid such as its sodium, potassium or triethanolammonium salt, and also the sulfonic acid itself with the INCI name phenylbenzimidazole sulfonic acid (CAS No. 27503-81-7), which is available, for example, under the trade name Eusolex 232 from Merck or under Neo Heliopan Hydro from Symrise;
  • Benzene 1, 4-di (2-oxo-3-bomylidenemethyl-10-sulfonic acid) is called.
  • Benzene 1, 4-di (2-oxo-3-bornylidenemethyl-10-sulfonic acid) has the INCI name Terephtalidene Dicampher Sulfonic acid (CAS No.: 90457-82-2) and is available, for example, under the trade name Mexoryl SX from Chimex;
  • Sulfonic acid derivatives of 3-Benzylidencamphers such as. B. 4- (2-oxo-3-bornylidenme- thyl) benzenesulfonic acid, 2-methyl-5- (2-oxo-3-bomylidenemethyl) sulfonic acid and salts thereof.
  • Benzoxazole derivatives such as.
  • Hydroxybenzophenones e.g. B. 2- (4'-diethylamino-2'-hydroxybenzoyl) -benzoeklar (also: aminobenzophenone), which is available under the trade name Uvinul A Plus in the company. BASF.
  • Triazine derivatives such as. B. 2,4-bis - ⁇ [4- (2-ethyl-hexyloxy) -2-hydroxy] -phenyl ⁇ -6- (4-methoxyphenyl) -1, 3,5-triazine (INCI: Bis- Ethylhexyloxylphenol methoxyphenyl triazine), which is available under the trade name Tinosorb® S from CIBA-Chemikalien GmbH; Dioctylbutylamidotriazone (INCI: Diethylhexyl Butamido Triazone), which is available under the trade name UVASORB HEB from Sigma 3V; 4,4 ', 4 "- (1,3,5-triazine-2,4,6-triyltriimino) tris-benzoic acid tris (2-ethylhexyl ester), also: 2,4,6-tris [anilino- (p-carbo-2'-ethyl-1'-hex
  • Benzotriazoles such as. B. 2,2'-methylene-bis (6- (2H-benzotriazol-2-yl) -4- (1,1,3,3-tetramethylbutyl) -phenol) (INCI: Methylene bis-benztriazolyl tetramethylbutylphenol ), which z. B. under the trade name Tinosorb® M at CIBA-Chemikalien GmbH is available.
  • 3-Benzylidene camphor derivatives preferably 3- (4-methylbenzylidene) camphor, 3-benzylidene camphor;
  • 4-aminobenzoic acid derivatives preferably (2-ethylhexyl) 4- (dimethylamino) benzoate, 4- (dimethylamino) benzoic acid amyl ester;
  • Esters of benzalmalonic acid preferably di (2-ethylhexyl) 4-methoxybenzalmalonate
  • Esters of cinnamic acid preferably 4-methoxycinnamic acid (2-ethylhexyl) ester, 4-methoxycinnamic acid isopentyl ester;
  • benzophenone preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone and
  • Particularly advantageous preparations in the sense of the present invention which are distinguished by a high or very high UV-A protection, preferably contain further UV-A and / or broadband filters, in particular dibenzoylmethane derivatives, in addition to the filter substance (s) according to the invention.
  • UV filters which can be used in the context of the present invention is of course not intended to be limiting.
  • the total amount of the filter substances is from the range of 0.1 to 30 wt .-%, preferably 0.5 to 10 wt .-%, in particular 1, 0 to 6.0 wt .-% - each based on the total weight of the preparations - chosen to provide cosmetic preparations that protect the hair or the skin from the entire range of ultraviolet radiation.
  • Such packaging are z. B. from the two-chamber technology known.
  • the so-called. Bag-on-valve systems consisting of a valve which is hermetically sealed to a foil bag.
  • the foil bag is optimally multi-layered with at least one or more barrier layers.
  • the bag valve is hermetically sealed before being filled with an aerosol container (aluminum, tinplate or plastic).
  • the bag is located in an aerosol container and is connected to the valve and the aerosol container when closing.
  • the container is preferably supplied with environmentally friendly propellant gases, such as nitrogen or noble gases, wherein the propellant gas between the bag and sealed aerosol container is, whereas the cosmetic is in the bag.
  • environmentally friendly propellant gases such as nitrogen or noble gases
  • the propellant surrounds the bag filled with the cosmetic.
  • the nozzle the spray or application head of the system
  • the pressure on the bag will cause the contents to leak in varying amounts depending on the diameter of the nozzle.
  • the preparation contained in the bag must be matched to the packaging in order to achieve the correct output in terms of viscosity at given can pressure.
  • the dispensing head optimally includes a closing mechanism at the exit opening which reduces potential contamination of the product between the valve opening and the exit opening.
  • the self-closing dispensing head can z.
  • an aerosol valve is opened, the product flows through a channel to the outlet opening.
  • the elastic element eg made of a thermoplastic elastomer (TPE), polyethylene, polypropylene, polyoxymethylene (POM)
  • TPE thermoplastic elastomer
  • POM polyoxymethylene
  • the pressure between the aerosol valve and the outlet reduced to complete sealing.
  • the elastic element is lowered into the product-carrying channel, and the remaining contents are applied until the channel has been completely closed.
  • Thesverschliessende dispensing head may also z. B. be carried out as follows:
  • an aerosol valve By actuating the applicator, an aerosol valve is opened, an elastic membrane springs opposite to the product flow. An inseparable plug connected to the membrane follows this movement and the exit port / ring slit nozzle is opened.
  • Predispersion of the inorganic gelling agent and swelling of the hydrocolloid with stirring in the water phase Combination of heated to 75 C C fatty phase with the heated to 70 0 C water phase. Addition of the particulate hydrophobic, hydrophobicized solid substances with stirring. Homogenization by means of a Zahnkranz- dispersing machine (rotor-stator principle) at 65 0 C. 45 min stirring under vacuum and cooling. Addition of the additives at 30 ° C. (perfume, active ingredients). Homogenization by means of a Zahnkranzdispergiermaschine (rotor-stator principle) at 27 0 C. Fumigation of the emulsion at 7-8 bar by means of a dynamic foam generator (eg from HANSA INDUSTRIE MIXER) with oxygen.
  • a dynamic foam generator eg from HANSA INDUSTRIE MIXER
  • 85% by volume of the emulsion IV are foamed with 5% by volume of oxygen and 5% by volume of propane / butane a .
  • Vitamin E acetate 2.00
  • Emulsion I 80-97% by volume of Emulsion I is foamed with 3-20% by volume of a suitable gas (e.g., propane / butane, compressed air, nitrogen).
  • a suitable gas e.g., propane / butane, compressed air, nitrogen.

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Abstract

L'invention concerne l'utilisation de préparations cosmétiques se présentant sous la forme d'émulsions huile dans eau et comprenant entre 2,5 et 25 parts de volume d'oxygène libre par rapport au volume totale de la préparation, pour accroître la régénération de cellules cutanées.
EP05850370A 2005-03-08 2005-12-29 Utilisation de preparations cosmetiques contenant une quantite d'oxygene libre non lie moleculairement Withdrawn EP1861170A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102005011498A DE102005011498A1 (de) 2005-03-08 2005-03-08 Verwendung kosmetischer Zubereitungen mit einem Gehalt an nicht molekular gebundenem freien Sauerstoff
PCT/EP2005/014106 WO2006094550A1 (fr) 2005-03-08 2005-12-29 Utilisation de preparations cosmetiques contenant une quantite d'oxygene libre non lie moleculairement

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EP1861170A1 true EP1861170A1 (fr) 2007-12-05

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EP (1) EP1861170A1 (fr)
DE (1) DE102005011498A1 (fr)
WO (1) WO2006094550A1 (fr)

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Publication number Priority date Publication date Assignee Title
DE102007028025A1 (de) 2007-06-14 2008-12-18 Beiersdorf Ag Kosmetische oder dermatologische Zubereitungen mit einem Gehalt an molekularem Sauerstoff, grenzflächenaktiven Glucosederivaten und vorteilhafterweise einer oder mehreren UV-Licht absorbierenden Substanzen
DE102007028022A1 (de) 2007-06-14 2008-12-18 Beiersdorf Ag Kosmetische oder dermatologische Zubereitungen mit einem Gehalt an molekularem Sauerstoff und Panthenol
DE102007028028A1 (de) 2007-06-14 2008-12-18 Beiersdorf Ag Sauerstoff in kosmetischen oder dermatologischen Zubereitungen
DE102007028027A1 (de) 2007-06-14 2008-12-18 Beiersdorf Ag Schnell Sauerstoff freisetzende kosmetische Zubereitungen
DE102007028024A1 (de) 2007-06-14 2008-12-18 Beiersdorf Ag Kosmetische oder dermatologische Zubereitungen mit einem Gehalt an molekularem Sauerstoff und Parfümstoffen
DE102007028026A1 (de) 2007-06-14 2008-12-18 Beiersdorf Ag Langsam Sauerstoff freisetzende kosmetische Zubereitungen
DE102007032664A1 (de) 2007-07-13 2009-01-15 Beiersdorf Ag Kosmetische oder dermatologische Zubereitungen enthaltend ein oder mehrere Apiogalacturonane oder einen oder mehrere Apiogalacturonane enthaltenden Extrakt aus Zostera marina und einem Gehalt an molekularem Sauerstoff
DE102010044674B9 (de) 2010-09-08 2014-05-15 Meddrop Technology Ag Perkutanes Applikationssystem
DE102014220452A1 (de) * 2014-10-09 2016-04-14 Beiersdorf Ag Kosmetisches Emulsionsspray

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US3330730A (en) * 1962-08-03 1967-07-11 Colgate Palmolive Co Pressurized emulsion quick breaking foam compositions
EP0379765A1 (fr) * 1989-01-27 1990-08-01 Varix Ag Méthode et composition pour promouvoir la santé de la peau
US5874093A (en) * 1996-11-15 1999-02-23 Eliaz; Isaac Cosmetic composition containing molecular oxygen
DE10144061A1 (de) * 2001-09-07 2003-04-17 Beiersdorf Ag Selbstschäumende oder schaumförmige Zubereitungen mit anorganischen Gelbildnern, organischen Hydrokolloiden und partikulären hydrophoben und/oder hydrophobisierten und/oder ölabsorbierenden Festkörpersubstanzen
DE10216503A1 (de) * 2002-04-11 2004-02-19 Beiersdorf Ag Selbstschäumende oder schaumförmige Zubereitungen, enthaltend ein oder mehrere vorgelatinisierte, quervernetzte Stärkederivate
DE20220553U1 (de) * 2002-09-05 2003-12-11 Hallmann, Paul-Alexander, Dr.rer.nat. Pflanzenpigmente aus Leguminosen zur Revitalisierung und Stabilisierung
DE10342449A1 (de) * 2003-09-13 2005-04-07 Beiersdorf Ag Verwendung von Sauerstoff in kosmetischen oder dermatologischen Zubereitungen

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DE102005011498A1 (de) 2006-09-21
WO2006094550A1 (fr) 2006-09-14

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