WO2020088905A1 - Cosmetic oil-in-water emulsion containing zinc oxide - Google Patents
Cosmetic oil-in-water emulsion containing zinc oxide Download PDFInfo
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- WO2020088905A1 WO2020088905A1 PCT/EP2019/077436 EP2019077436W WO2020088905A1 WO 2020088905 A1 WO2020088905 A1 WO 2020088905A1 EP 2019077436 W EP2019077436 W EP 2019077436W WO 2020088905 A1 WO2020088905 A1 WO 2020088905A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—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
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
-
- 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
- A61K8/0241—Containing particulates characterized by their shape and/or structure
- A61K8/0283—Matrix particles
-
- 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
- A61K8/06—Emulsions
- A61K8/062—Oil-in-water emulsions
-
- 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
- A61K8/27—Zinc; Compounds thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
-
- 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
- A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
- A61K8/585—Organosilicon compounds
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- 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
- A61K2800/30—Characterized by the absence of a particular group of ingredients
-
- 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
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/413—Nanosized, i.e. having sizes below 100 nm
Definitions
- the present invention relates to a cosmetic oil-in-water emulsion (O / W emulsion) containing polyglyceryl-10 stearate (INCI polyglyceryl-10 stearate), sorbitan stearate (INCI sorbitan stearate), zinc oxide and a pH buffer system composed of lactic acid and sodium lactate, wherein the emulsion is free from 3- (4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: oxybenzone), 4-methoxycinnamic acid-2-ethylhexyl ester (INCI octylmethoxycinnamate), propylparaben, butylparaben, methylisothiazolinone, chloromonomethyl isl and DMDM hydantoin, polyethylene glycol ethers and polyethylene glycol esters.
- O / W emulsion containing polyglyceryl-10 stearate (
- UVB range wavelength: 280-320 nm
- UVA radiation wavelength: 320-400 nm
- UVA and UVB filters are in most industrialized countries in the form of positive lists such as Appendix 7 of the
- a particularly interesting UV filter from the UV spectrum is zinc oxide, which is used in the form of fine pigments (micropigments) analogous to titanium dioxide.
- a major reason why zinc oxide, in contrast to titanium dioxide, has so far not been able to establish itself properly in the cosmetic market as a UV filter is due to the fact that the use of zinc oxide leads to the pH value of the preparation being changed storage increases sharply.
- high pH values in cosmetic preparations are problematic not only from a skin physiological point of view, since high pH values destroy the skin's protective acid mantle. Such changes can also make the preparation itself unstable, since many ingredients are sensitive to pH. The emulsion system can be destroyed.
- Emulsion systems of the type oil-in-water emulsion (O / W emulsion), which is why
- Zinc oxide-based sunscreens are primarily offered as a W / O emulsion.
- O / W emulsions on the other hand, delight consumers due to their sensory
- Sulfonic acid function e.g. phenylbenzimidazole sulfonic acid
- Various buffer systems have also been tested. However, such systems usually fall short of expectations in terms of their stability.
- PEG emulsifiers such as PEG-100 stearates (for example in Arlacel 165®) and / or polyacrylates, which are relatively insensitive to pH and contain polyethylene glycol groups .
- PEG emulsifiers such as PEG-100 stearates (for example in Arlacel 165®) and / or polyacrylates, which are relatively insensitive to pH and contain polyethylene glycol groups .
- PEG emulsifiers such as PEG-100 stearates (for example in Arlacel 165®) and / or polyacrylates, which are relatively insensitive to pH and contain polyethylene glycol groups .
- such ingredients are increasingly unpopular with consumers, as they are feared for health and the environment. Whether such concerns are scientifically justified can remain open in
- the object is surprisingly achieved by a cosmetic oil-in-water emulsion (O / W emulsion) containing
- a pH buffer system consisting of lactic acid and sodium lactate
- the emulsion is free from 3- (4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: oxybenzone), 4-methoxycinnamic acid-2-ethylhexyl ester (INCI octylmethoxycinnamate), propylparaben, butylparaben, methylisothiazolinone, chloromonomethyl isl and DMDM hydantoin, polyethylene glycol ethers and polyethylene glycol esters.
- the zinc oxide is coated with triethoxycaprylylsilane.
- Embodiments of the present invention which are advantageous according to the invention are characterized in that the zinc oxide has a primary particle size between 20 and 100 nm.
- the primary particle size can be determined according to SCCS opinion (EC No. 1223/2009, Annex VI,
- No27a and 30a can be determined using a CPS centrifuge or laser scattering method.
- the O / W emulsion contains the zinc oxide in an amount of 0.1 to 20% by weight, based on the total weight of the preparation.
- the O / W emulsion according to the invention contains a mixture of polyglyceryl stearate and sorbitan stearate as the emulsifier system.
- the preparation contains polyglyceryl-10 stearate (INCI polyglyceryl-10 stearate) in a concentration of 1.44 to 2.40% by weight, based on the total weight of the preparation.
- the preparation contains sorbitan stearate (INCI sorbitan stearate) in a concentration of 1.26 to 2.10% by weight, based on the total weight of the preparation.
- the preparation contains lactic acid in a concentration of 0.55 to 0.60% by weight, based on the total weight of the preparation. It is preferred according to the invention to use lactic acid in a concentration of 0.58 to 0.59% by weight, based on the
- the preferred use concentration here is 0.7% by weight, based on the total weight of the preparation.
- the embodiments of the present invention which are advantageous according to the invention are characterized in that the preparation contains no octocrylene (INCI octocrylene) and
- the preparation contains xantham gum (INCI Xantham Gum).
- xantham gum in a concentration of 0.05 to 0.30% by weight, based on the
- the preparation according to the invention can advantageously contain further UV filters. It is preferred according to the invention if the preparation one or more UV filters selected from the group of the compounds 4- (tert-butyl) -4'-methoxydibenzoylmethane (INCI butyl methoxydibenzoylmethane), (2 - [- 4- ( Diethylamino) -2-hydroxybenzoyl]
- Hexyl benzoate (INCI: diethylamino hydroxybenzoyl hexyl benzoate) and 2,4-bis - ⁇ [4- (2-ethylhexyloxy) -2-hydroxy] phenyl ⁇ -6- (4-methoxyphenyl) -1, 3, 5-triazine (INCI bis-ethylhexyloxyphenol methoxyphenyl triazine), 2,2'-methylene-bis- (6- (2H-benzotriazol-2-yl) -4- (1, 1, 3,3-tetramethylbutyl) phenol) , Ethylhexyl salicylate, homomenthyl salicylate,
- Dioctylbutylamidotriazon (INCI: Diethylhexyl-Butamidotriazone), 4,4 ', 4 "- (1, 3,5-Triazin-2,4,6-triyltriimino) -tris-benzoic acid-tris (2-ethylhexyl ester) (also: 2, 4,6-tris [anilino- (p-carbo-2'-ethyl-1'-hexyloxy)] - 1,3,5-triazine (INCI: ethylhexyl triazone), 2,4,6-T ribiphenyl-4 -yl-1, 3,5-triazine, titanium dioxide.
- the preparation according to the invention contains phenoxyethanol, ethylhexylglycerol and / or 4-hydroxyacetophenone.
- the preparation comprises one or more alkanediols from the group of the compounds 1, 2-pentanediol, 1, 2-hexanediol, 1, 2-octanediol, 1, 2-decanediol, 2-methyl-1, Contains 3-propanediol.
- the preparation according to the invention can advantageously one or more compounds selected from the group of the compounds alpha-lipoic acid, folic acid, phytoene, D-biotin, coenzyme Q10, alpha-glucosylrutin, carnitine, carnosine, natural and / or synthetic isoflavonoids, flavonoids, creatine , Creatinine, taurine, b-alanine, panthenol, Magnolol, honokiol, tocopheryl acetate, dihydroxyacetone; 8-Hexadecen-1, 16-dicarboxylic acid, glycerylglycose, (2-hydroxyethyl) urea, vitamin E or its derivatives, glycyrrhetic acid, hyaluronic acid and / or its salts and / or licochalcone A contain.
- the O / W emulsion according to the invention can contain the usual ingredients for such preparations.
- perfumes selected from the group of the compounds limonene, citral, linalool, alpha-isomethylionone, geraniol, citronellol, 2-isobutyl-4-hydroxy-4-methyltetrahydropyran, 2-tert-pentylcyclohexyl acetate, 3-methyl-5-phenyl -1-pentanol, 7-acetyl-1, 1, 3,4,4,6-hexamethyltetralin, adipic diester, alpha-amylcinnamaldehyde, alpha-methylionone, amyl C butylphenylmethylpropionalcinnamal, amylsalicylate, amylcinnamyl alcohol, anise alcohol, benzoin, benzyl benzylamate, benzyl benzyl alcoholate, benzyl benzyl alcoholate , Benzyl salicylate,
- the preparation according to the invention can advantageously contain humectants.
- Moisturisers are substances or mixtures of substances that give cosmetic preparations the property of reducing the release of moisture from the horny layer (also called transepidermal water loss (TEWL)) and / or hydrating the horny layer after application or distribution on the skin surface positive too
- TEWL transepidermal water loss
- moisturizers for the purposes of the present invention are:
- Moisturizers from the group of water-soluble and / or water-swellable and / or water-gelable polysaccharides are particularly advantageous. Particularly advantageous are, for example, hyaluronic acid, chitosan and / or a fucose-rich polysaccharide, which is filed in the Chemical Abstracts under the registration number 178463-23-5 and z. B. is available under the name Fucogel®1000 from the company SOLABIA SA. Moisturizers can also be used advantageously as anti-wrinkle ingredients to protect against skin changes, such as those found in z. B. occur in skin aging, are used.
- the cosmetic preparations according to the invention can furthermore advantageously, although not necessarily, contain fillers which, for. B. the sensory and cosmetic
- compositions Further improve the properties of the formulations and, for example, create or intensify a velvety or silky feeling on the skin.
- Advantageous fillers for the purposes of the present invention are starch and starch derivatives (such as tapioca starch,
- Pigments that have neither primarily UV filtering nor coloring effects such as boron nitride etc.
- / or Aerosile ® CAS No. 7631 -86-9
- / or talc / or polyethylene, nylon, Silica Diemthyl Silyate.
- the preparation according to the invention contains silica dimethyl silylates.
- Embodiments of the present invention which are advantageous according to the invention are characterized in that the preparation comprises one or more oils selected from the group of the compounds butylene glycol dicaprylate / dicaprate, phenethyl benzoate, 012-15 alkyl benzoate, dibutyl adipate; Diisopropyl sebacate, dicaprylyl carbonate, di-C12-13 alkyl tartrate, butyl octyl salicylate, diethylhexyl syringylidenes malonate, hydragenated castor oil dimerate,
- Triheptanoin C12-13 alkyl lactate, C16-17 alkyl benzoate, propylheptyl caprylate,
- Caprylic / Capric Triglyceride Diethylhexyl 2,6-Naphthalate, Octyldodecanol, Caprylic / Capric Triglyceride, Ethylhexyl Cocoate, contains.
- the water phase of the preparations according to the invention can advantageously contain customary cosmetic auxiliaries, such as, for example, electrolytes, self-tanners and in particular one or more thickeners, which one or more can advantageously be selected from the group consisting of silicon dioxide, aluminum silicates, polysaccharides or their derivatives, e.g. B. Hy aluronic acid, hydroxypropylmethyl cellulose.
- customary cosmetic auxiliaries such as, for example, electrolytes, self-tanners and in particular one or more thickeners, which one or more can advantageously be selected from the group consisting of silicon dioxide, aluminum silicates, polysaccharides or their derivatives, e.g. B. Hy aluronic acid, hydroxypropylmethyl cellulose.
- An ethanol content is also advantageous. Examples
- the pH stability (the pH shift) of these preparations was determined at room temperature (20 ° C.).
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Abstract
The invention relates to a cosmetic oil-in-water emulsion (O/W emulsion) containing a) polyglyceryl-10 stearate (INCI: polyglyceryl-10 stearate), b) sorbitan stearate (INCI: sorbitan stearate), c) zinc oxide, and d) a pH buffer system consisting of lactic acid and sodium lactate, wherein the emulsion is free from 3-(4-methylbenzylidene)-camphor, 2-hydroxy-4-methoxybenzophenone (INCI: oxybenzone), 4-methoxycinnamic acid-2-ethylhexyl ester (INCI: octylmethoxycinnamate), propylparaben, butylparaben, methylisothiazolinone, chloromethylisothiazolinone and DMDM-hydantoin, polyethylene glycol ethers and polyethylene glycol esters.
Description
Kosmetische O/W-Emulsion mit Zinkoxid Cosmetic O / W emulsion with zinc oxide
Die vorliegende Erfindung betrifft eine kosmetische Öl-in-Wasser Emulsion (O/W-Emulsion) enthaltend Polyglyceryl-10 Stearat (INCI Polyglyceryl-10 Stearate), Sorbitanstearat (INCI Sorbitan Stearate), Zinkoxid und ein pH-Puffersystem aus Milchsäure und Natriumlactat, wobei die Emulsion frei ist von 3-(4-Methylbenzyliden)-campher, 2-Hydroxy-4- methoxybenzophenon (INCI: Oxybenzon), 4-Methoxyzimtsäure-2-ethylhexylester (INCI Octylmethoxycinnamate), Propylparaben, Butylparaben, Methylisothiazolinon, Chlormethyl- isothiazolinon und DMDM-Hydantoin, Polyethylenglycolethern und Polyethylenglycolestern. The present invention relates to a cosmetic oil-in-water emulsion (O / W emulsion) containing polyglyceryl-10 stearate (INCI polyglyceryl-10 stearate), sorbitan stearate (INCI sorbitan stearate), zinc oxide and a pH buffer system composed of lactic acid and sodium lactate, wherein the emulsion is free from 3- (4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: oxybenzone), 4-methoxycinnamic acid-2-ethylhexyl ester (INCI octylmethoxycinnamate), propylparaben, butylparaben, methylisothiazolinone, chloromonomethyl isl and DMDM hydantoin, polyethylene glycol ethers and polyethylene glycol esters.
Der Trend weg von der vornehmen Blässe hin zur„gesunden, sportlich braunen Haut“ ist seit Jahren ungebrochen. Um diese zu erzielen setzen die Menschen ihre Haut der The trend away from the paleness towards "healthy, sporty brown skin" has been going on for years. To achieve this, people put their skin on the
Sonnenstrahlung aus, da diese eine Pigmentbildung im Sinne einer Melaninbildung hervorruft. Die ultraviolette Strahlung des Sonnenlichtes hat jedoch auch eine schädigende Wirkung auf die Haut. Neben der akuten Schädigung (Sonnenbrand) treten Langzeitschäden wie ein erhöhtes Risiko an Hautkrebs zu erkranken bei übermäßiger Bestrahlung mit Licht aus dem UVB-Bereich (Wellenlänge: 280-320 nm) auf. Die übermäßige Einwirkung der UVB- und UVA- Strahlung (Wellenlänge: 320-400 nm) führt darüber hinaus zu einer Schwächung der elastischen und kollagenen Fasern des Bindegewebes. Dies führt zu zahlreichen Solar radiation, since this causes pigment formation in the sense of melanin formation. However, the ultraviolet radiation from sunlight also has a damaging effect on the skin. In addition to acute damage (sunburn), long-term damage such as an increased risk of developing skin cancer occurs with excessive exposure to light from the UVB range (wavelength: 280-320 nm). The excessive exposure to UVB and UVA radiation (wavelength: 320-400 nm) also leads to a weakening of the elastic and collagen fibers of the connective tissue. This leads to numerous
phototoxischen und photoallergischen Reaktionen und hat eine vorzeitige Hautalterung zur Folge. phototoxic and photoallergic reactions and results in premature skin aging.
Zum Schutz der Haut wurden daher eine Reihe von Lichtschutzfiltersubstanzen entwickelt, die in kosmetischen Zubereitungen eingesetzt werden können. Diese UVA- und UVB-Filter sind in den meisten Industrieländern in Form von Positivlisten wie dem Anlage 7 der To protect the skin, a number of light protection filter substances have therefore been developed that can be used in cosmetic preparations. These UVA and UVB filters are in most industrialized countries in the form of positive lists such as Appendix 7 of the
Kosmetikverordnung zusammengefasst. Cosmetics regulation summarized.
Die Vielzahl an kommerziell erhältlichen Sonnenschutzmitteln darf jedoch nicht darüber hinwegtäuschen, dass diese Zubereitungen des Standes der Technik eine Reihe von However, the large number of commercially available sunscreens must not hide the fact that these preparations of the prior art are a number of
Nachteilen aufweisen.
Ein vom UV-Spektrum her besonders interessanter UV-Filter stellt Zinkoxid dar, dass analog dem Titandioxid in Form feiner Pigmente (Mikorpigmente) eingesetzt wird. Ein wesentlicher Grund dafür, warum sich Zinkoxid, im Gegensatz zum Titandioxid, bisher im kosmetischen Markt als UV-Filter nicht richtig durchsetzen konnte, liegt in der Tatsache begründet, dass der Einsatz von Zinkoxid dazu führt, dass der pH-Wert der Zubereitung im Verlaufe der Lagerung stark ansteigt. Hohe pH-Werte in kosmetischen Zubereitungen sind jedoch nicht nur aus Haut physiologischer Sicht problematisch, da durch hohe pH-Werte der Säureschutzmantel der Haut zerstört wird. Auch die Zubereitung selbst kann durch derartige Veränderungen instabil werden, da viele Inhaltsstoffe pH-empfindlich sind. Das Emulsionssystem kann zerstört werden. Have disadvantages. A particularly interesting UV filter from the UV spectrum is zinc oxide, which is used in the form of fine pigments (micropigments) analogous to titanium dioxide. A major reason why zinc oxide, in contrast to titanium dioxide, has so far not been able to establish itself properly in the cosmetic market as a UV filter is due to the fact that the use of zinc oxide leads to the pH value of the preparation being changed storage increases sharply. However, high pH values in cosmetic preparations are problematic not only from a skin physiological point of view, since high pH values destroy the skin's protective acid mantle. Such changes can also make the preparation itself unstable, since many ingredients are sensitive to pH. The emulsion system can be destroyed.
Das Problem des Anstieges des pH-Wertes durch Zinkoxid tritt vor allem bei Above all, the problem of zinc oxide pH rise occurs
Emulsionssystemen vom Typ ÖI-in-Wasser-Emulsion (O/W-Emulsion) auf, weshalb Emulsion systems of the type oil-in-water emulsion (O / W emulsion), which is why
Sonnenschutzmittel auf Zinkoxid-Basis primär als W/O-Emulsion angeboten werden. O/W- Emulsionen erfreuen sich hingegen beim Verbraucher aufgrund ihrer sensorischen Zinc oxide-based sunscreens are primarily offered as a W / O emulsion. O / W emulsions, on the other hand, delight consumers due to their sensory
Eigenschaften weitaus größerer Beliebtheit als W/O-Emulsionen. Properties far more popular than W / O emulsions.
Es hat im Stande der Technik nicht an Versuchen gemangelt, das Problem des pH-Wert Anstieges in Zinkoxid-Emulsionen in den Griff zu bekommen. So kennt der Fachmann beispielsweise die EP1 102576, bei der Mischungen aus Zinkoxid und UV-Filtern mit There has been no shortage of attempts in the prior art to deal with the problem of the pH increase in zinc oxide emulsions. For example, the person skilled in the art knows EP1 102576, in which mixtures of zinc oxide and UV filters are involved
Sulfonsäure-Funktion (z.B. Phenylbenzimidazolsulfonsäure) eingesetzt werden. Auch wurden verschiedene Puffersysteme getestet. Derartige Systeme bleiben hinsichtlich ihrer Stabilität jedoch meist hinter den Erwartungen zurück. Darüber hinaus lassen sie sich nach dem Stand der Technik nur mit relativ pH-Wert unempfindlichen, Polyethylenglycol-Gruppen enthaltenden O/W-Emulgatoren (sogenannten PEG-Emulgatoren) wie PEG-100 Stearate (z.B. in Arlacel 165®) und/oder Polyacrylaten stabilisieren. Derartige Inhaltsstoffe sind beim Verbraucher jedoch zunehmend unbeliebt, da hier Gefahren für Gesundheit und Umwelt befürchtet werden. Ob derartige Sorgen naturwissenschaftlich berechtigt sind, kann im Rahmen der vorliegenden Offenbarung offen bleiben. Tatsache ist, das Verbraucher zunehmend Produkte nachfragen die derartige Inhaltsstoffe nicht enthalten und beispielsweise ausdrücklich„PEG-freie“ Sulfonic acid function (e.g. phenylbenzimidazole sulfonic acid) can be used. Various buffer systems have also been tested. However, such systems usually fall short of expectations in terms of their stability. In addition, according to the prior art, they can only be stabilized with O / W emulsifiers (so-called PEG emulsifiers), such as PEG-100 stearates (for example in Arlacel 165®) and / or polyacrylates, which are relatively insensitive to pH and contain polyethylene glycol groups . However, such ingredients are increasingly unpopular with consumers, as they are feared for health and the environment. Whether such concerns are scientifically justified can remain open in the context of the present disclosure. The fact is that consumers are increasingly asking for products that do not contain such ingredients and, for example, expressly “PEG-free”
Zubereitungen verlangen. Require preparations.
Es war daher die Aufgabe der vorliegenden Erfindung pH-Wert stabilere, lagerstabile, PEG-freie O/W-Emulsionen mit Zinkoxid als UV-Filter zu entwickeln. It was therefore the object of the present invention to develop pH-stable, storage-stable, PEG-free O / W emulsions with zinc oxide as a UV filter.
Überraschend gelöst wird die Aufgabe durch eine kosmetische Öl-in-Wasser Emulsion (O/W- Emulsion) enthaltend The object is surprisingly achieved by a cosmetic oil-in-water emulsion (O / W emulsion) containing
a) Polyglyceryl-10 Stearat (INCI Polyglyceryl-10 Stearate) a) Polyglyceryl-10 stearate (INCI Polyglyceryl-10 stearate)
b) Sorbitanstearat (INCI Sorbitan Stearate)
c) Zinkoxid b) Sorbitan stearate (INCI sorbitan stearate) c) zinc oxide
d) ein pH-Puffersystem aus Milchsäure und Natriumlactat, d) a pH buffer system consisting of lactic acid and sodium lactate,
wobei die Emulsion frei ist von 3-(4-Methylbenzyliden)-campher, 2-Hydroxy-4- methoxybenzophenon (INCI: Oxybenzon), 4-Methoxyzimtsäure-2-ethylhexylester (INCI Octylmethoxycinnamate), Propylparaben, Butylparaben, Methylisothiazolinon, Chlormethyl- isothiazolinon und DMDM-Hydantoin, Polyethylenglycolethern und Polyethylenglycolestern. wherein the emulsion is free from 3- (4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: oxybenzone), 4-methoxycinnamic acid-2-ethylhexyl ester (INCI octylmethoxycinnamate), propylparaben, butylparaben, methylisothiazolinone, chloromonomethyl isl and DMDM hydantoin, polyethylene glycol ethers and polyethylene glycol esters.
Dabei ist es erfindungsgemäß von Vorteil, wenn das Zinkoxid mit Triethoxycaprylylsilan beschichtet ist. It is advantageous according to the invention if the zinc oxide is coated with triethoxycaprylylsilane.
Erfindungsgemäß vorteilhafte Ausführungsformen der vorliegenden Erfindung sind dadurch gekennzeichnet, dass das Zinkoxid eine Primärpartikelgröße zwischen 20 und 100 nm aufweist. Die Primärpartikelgröße kann dabei gemäß SCCS opinion (EC No. 1223/2009, Annex VI,Embodiments of the present invention which are advantageous according to the invention are characterized in that the zinc oxide has a primary particle size between 20 and 100 nm. The primary particle size can be determined according to SCCS opinion (EC No. 1223/2009, Annex VI,
No27a and 30a) mittels CPS Zentrifuge oder Laser Scattering Methode bestimmt werden. No27a and 30a) can be determined using a CPS centrifuge or laser scattering method.
Vorteilhaft im Sinne der vorliegenden Erfindung ist es, wenn die O/W-Emulsion das Zinkoxid in einer Menge von 0,1 bis 20 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung, enthält. For the purposes of the present invention, it is advantageous if the O / W emulsion contains the zinc oxide in an amount of 0.1 to 20% by weight, based on the total weight of the preparation.
Es ist erfindungsgemäß von Vorteil, wenn die Zubereitung frei ist von Acrylatpolymeren. It is advantageous according to the invention if the preparation is free from acrylate polymers.
Die erfindungsgemäße O/W-Emulsion enthält als Emulgator-System eine Mischung aus Polyg lyceryl- 10 Stearat und Sorbitanstearat. The O / W emulsion according to the invention contains a mixture of polyglyceryl stearate and sorbitan stearate as the emulsifier system.
Dabei ist es erfindungsgemäß von Vorteil, wenn die Zubereitung Polyglyceryl-10 Stearat (INCI Polyg lyceryl- 10 Stearate) in einer Konzentration von 1 ,44 bis 2,40 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung, enthält. It is advantageous according to the invention if the preparation contains polyglyceryl-10 stearate (INCI polyglyceryl-10 stearate) in a concentration of 1.44 to 2.40% by weight, based on the total weight of the preparation.
Im Hinblick auf das Sorbitanstearat ist es erfindungsgemäß von Vorteil, wenn die Zubereitung Sorbitanstearat (INCI Sorbitan Stearate) in einer Konzentration von 1 ,26 bis 2,10 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung, enthält. With regard to the sorbitan stearate, it is advantageous according to the invention if the preparation contains sorbitan stearate (INCI sorbitan stearate) in a concentration of 1.26 to 2.10% by weight, based on the total weight of the preparation.
Im Hinblick auf das Puffer-system hat es sich als erfindungsgemäß vorteilhaft herausgestellt, wenn die Zubereitung Milchsäure in einer Konzentration von 0,55 bis 0,60 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung, enthält. Erfindungsgemäß bevorzugt ist es, die Milchsäure in einer Konzentration von 0,58 bis 0,59 Gewichts-%, bezogen auf das With regard to the buffer system, it has proven advantageous according to the invention if the preparation contains lactic acid in a concentration of 0.55 to 0.60% by weight, based on the total weight of the preparation. It is preferred according to the invention to use lactic acid in a concentration of 0.58 to 0.59% by weight, based on the
Gesamtgewicht der Zubereitung, einzusetzen.
Ferner ist es erfindungsgemäß von Vorteil, wenn die Zubereitung Natriumlactat in einer Total weight of the preparation. It is also advantageous according to the invention if the preparation contains sodium lactate in a
Konzentration von 0,65 bis 0,75 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung, enthält. Die bevorzugte Einsatzkonzentration beträgt hier 0,7 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung. Contains a concentration of 0.65 to 0.75% by weight, based on the total weight of the preparation. The preferred use concentration here is 0.7% by weight, based on the total weight of the preparation.
Die erfindungsgemäß vorteilhaften Ausführungsformen der vorliegenden Erfindung sind dadurch gekennzeichnet, dass die Zubereitung kein Octocrylen (INCI Octocrylene) und The embodiments of the present invention which are advantageous according to the invention are characterized in that the preparation contains no octocrylene (INCI octocrylene) and
Mineralöl enthält. Contains mineral oil.
Es ist vorteilhaft im Sinne der vorliegenden Erfindung, wenn die Zubereitung Xanthamgummi (INCI Xantham Gum) enthält. In einem solchen Falle ist es erfindungsgemäß von Vorteil, wenn Xanthamgummi in einer Konzentration von 0,05 bis 0,30 Gewichts-%, bezogen auf das For the purposes of the present invention, it is advantageous if the preparation contains xantham gum (INCI Xantham Gum). In such a case, it is advantageous according to the invention if xantham gum in a concentration of 0.05 to 0.30% by weight, based on the
Gesamtgewicht der Zubereitung, eingesetzt wird. Total weight of the preparation used.
Neben Zinkoxid kann die erfindungsgemäße Zubereitung vorteilhaft weitere UV-Filter enthalten. Dabei ist es erfindungsgemäß bevorzugt, wenn die Zubereitung ein oder mehrere UV-Filter gewählt aus der Gruppe der Verbindungen 4-(tert.-Butyl)-4’-methoxydibenzoylmethan (INCI Butyl Methoxydibenzoyl-methane), (2-[-4-(Diethylamino)-2-hydroxybenzoyl] In addition to zinc oxide, the preparation according to the invention can advantageously contain further UV filters. It is preferred according to the invention if the preparation one or more UV filters selected from the group of the compounds 4- (tert-butyl) -4'-methoxydibenzoylmethane (INCI butyl methoxydibenzoylmethane), (2 - [- 4- ( Diethylamino) -2-hydroxybenzoyl]
Benzoesäurehexylester (INCI: Diethyl-amino Hydroxybenzoyl Hexyl Benzoate) und 2,4-Bis-{[4- (2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1 ,3,5-triazin (INCI Bis- Ethylhexyloxyphenol Methoxyphenyl Triazine), 2,2’-Methylen-bis-(6-(2H-benzotriazol-2-yl)-4- (1 ,1 ,3,3-tetramethylbutyl)-phenol), Ethylhexylsalicylat, Homomenthylsalicylat, Hexyl benzoate (INCI: diethylamino hydroxybenzoyl hexyl benzoate) and 2,4-bis - {[4- (2-ethylhexyloxy) -2-hydroxy] phenyl} -6- (4-methoxyphenyl) -1, 3, 5-triazine (INCI bis-ethylhexyloxyphenol methoxyphenyl triazine), 2,2'-methylene-bis- (6- (2H-benzotriazol-2-yl) -4- (1, 1, 3,3-tetramethylbutyl) phenol) , Ethylhexyl salicylate, homomenthyl salicylate,
Dioctylbutylamidotriazon (INCI: Diethylhexyl-Butamidotriazone), 4,4',4"-(1 ,3,5-Triazin-2,4,6- triyltriimino)-tris-benzoesäure-tris(2-ethylhexylester) (auch: 2,4,6-Tris-[anilino-(p-carbo-2'-ethyl- 1 '-hexyloxy)]-1 ,3,5-triazin (INCI: Ethylhexyl Triazone), 2,4,6-T ribiphenyl-4-yl-1 ,3,5-triazin, Titandioxid, enthält. Dioctylbutylamidotriazon (INCI: Diethylhexyl-Butamidotriazone), 4,4 ', 4 "- (1, 3,5-Triazin-2,4,6-triyltriimino) -tris-benzoic acid-tris (2-ethylhexyl ester) (also: 2, 4,6-tris [anilino- (p-carbo-2'-ethyl-1'-hexyloxy)] - 1,3,5-triazine (INCI: ethylhexyl triazone), 2,4,6-T ribiphenyl-4 -yl-1, 3,5-triazine, titanium dioxide.
Es ist erfindungsgemäß vorteilhaft, wenn die erfindungsgemäße Zubereitung Phenoxyethanol, Ethylhexylglycerin und/oder 4-Hydroxyacetophenon enthält. It is advantageous according to the invention if the preparation according to the invention contains phenoxyethanol, ethylhexylglycerol and / or 4-hydroxyacetophenone.
Darüber hinaus ist es erfindungsgemäß von Vorteil, wenn die Zubereitung ein oder mehrere Alkandiole aus der Gruppe der Verbindungen 1 ,2-Pentandiol, 1 ,2-Hexandiol, 1 ,2-Octandiol, 1 ,2- Decandiol, 2-Methyl-1 ,3-propandiol enthält. In addition, it is advantageous according to the invention if the preparation comprises one or more alkanediols from the group of the compounds 1, 2-pentanediol, 1, 2-hexanediol, 1, 2-octanediol, 1, 2-decanediol, 2-methyl-1, Contains 3-propanediol.
Außerdem kann die erfindungsgemäße Zubereitung vorteilhafter Weise eine oder mehrere Verbindungen gewählt aus der Gruppe der Verbindungen alpha-Liponsäure, Folsäure, Phytoen, D-Biotin, Coenzym Q10, alpha-Glucosylrutin, Carnitin, Carnosin, natürliche und/oder synthetische Isoflavonoide, Flavonoide, Kreatin, Kreatinin, Taurin, b-Alanin, Panthenol,
Magnolol, Honokiol, Tocopherylacetat, Dihydroxyaceton; 8-Hexadecen-1 ,16-dicarbonsäure, Glycerylglycose, (2-Hydroxyethyl)harnstoff, Vitamin E bzw. seine Derivate, Glycyrrhetinsäure, Hyaluronsäure und/oder deren Salze und/oder Licochalcon A enthalten. In addition, the preparation according to the invention can advantageously one or more compounds selected from the group of the compounds alpha-lipoic acid, folic acid, phytoene, D-biotin, coenzyme Q10, alpha-glucosylrutin, carnitine, carnosine, natural and / or synthetic isoflavonoids, flavonoids, creatine , Creatinine, taurine, b-alanine, panthenol, Magnolol, honokiol, tocopheryl acetate, dihydroxyacetone; 8-Hexadecen-1, 16-dicarboxylic acid, glycerylglycose, (2-hydroxyethyl) urea, vitamin E or its derivatives, glycyrrhetic acid, hyaluronic acid and / or its salts and / or licochalcone A contain.
Darüber hinaus kann die erfindungsgemäße O/W-Emulsion die für derartige Zubereitungen üblichen Inhaltsstoffe enthalten. In addition, the O / W emulsion according to the invention can contain the usual ingredients for such preparations.
So ist es vorteilhaft im Sinne der vorliegenden Erfindung, wenn die erfindungsgemäße For the purposes of the present invention, it is advantageous if the invention
Zubereitung einen oder mehrere Parfümstoffe gewählt aus der Gruppe der Verbindungen Limonen, Citral, Linalool, alpha-lsomethylionon, Geraniol, Citronellol, 2-lsobutyl-4-hydroxy-4- methyltetrahydropyran, 2-tert-Pentylcyclohexylacetat, 3-Methyl-5-phenyl-1 -pentanol, 7-Acetyl- 1 ,1 ,3,4,4,6-hexamethyltetralin, Adipinsäurediester, alpha-Amylcinnamaldehyd, Alpha- Methylionon, Amyl C Butylphenylmethylpropionalcinnamal, Amylsalicylat, Amylcinnamylalkohol, Anisalkohol, Benzoin, Benzylalkohol, Benzylbenzoat, Benzylcinnamat, Benzylsalicylat, Preparation one or more perfumes selected from the group of the compounds limonene, citral, linalool, alpha-isomethylionone, geraniol, citronellol, 2-isobutyl-4-hydroxy-4-methyltetrahydropyran, 2-tert-pentylcyclohexyl acetate, 3-methyl-5-phenyl -1-pentanol, 7-acetyl-1, 1, 3,4,4,6-hexamethyltetralin, adipic diester, alpha-amylcinnamaldehyde, alpha-methylionone, amyl C butylphenylmethylpropionalcinnamal, amylsalicylate, amylcinnamyl alcohol, anise alcohol, benzoin, benzyl benzylamate, benzyl benzyl alcoholate, benzyl benzyl alcoholate , Benzyl salicylate,
Bergamotöl, bitteres Orangenöl, Butylphenylmethylpropioal, Cardamomöl, Cedrol, Cinnamal, Cinnamylalkohol, Citronellylmethylcrotonat, Citronenöl, Coumarin, Diethylsuccinat, Ethyllinalool, Eugenol, Evernia Furfuracea Extract, Evernia Prunastri Extract, Farnesol, Guajakholzöl, Hexylcinnamal, Hexylsalicylat, Hydroxycitronellal, Lavendelöl, Lemonenöl, Linaylacetat, Mandarinenöl, Menthyl PCA, Methylheptenon, Muskatnussöl, Rosmarinöl, süßes Orangenöl, Terpineol, Tonkabohnenöl, Triethylcitrat und/oder Vanillin enthält. Bergamot oil, bitter orange oil, butylphenylmethylpropioal, cardamom oil, cedrol, cinnamal, cinnamyl alcohol, citronellylmethyl crotonate, lemon oil, coumarin, diethylsuccinate, ethyllinalool, eugenol, evernia furfuracea extract, evernia prunastolalolololylololylololylololylololylololylololylololylolaxylololylololylolol, hexafilolololololololol, hexamolololololol, hexalololololol, hexalol oil , Mandarin oil, menthyl PCA, methylheptenone, nutmeg oil, rosemary oil, sweet orange oil, terpineol, tonka bean oil, triethyl citrate and / or vanillin.
Die erfindungsgemäße Zubereitung kann vorteilhaft Feuchthaltemittel enthalten. Als The preparation according to the invention can advantageously contain humectants. As
Feuchthaltemittel (Moisturizer) werden Stoffe oder Stoffgemische bezeichnet, welche kosmeti schen Zubereitungen die Eigenschaft verleihen, nach dem Aufträgen bzw. Verteilen auf der Hautoberfläche die Feuchtigkeitsabgabe der Hornschicht (auch transepidermal water loss (TEWL) genannt) zu reduzieren und/oder die Hydratation der Hornschicht positiv zu Moisturisers are substances or mixtures of substances that give cosmetic preparations the property of reducing the release of moisture from the horny layer (also called transepidermal water loss (TEWL)) and / or hydrating the horny layer after application or distribution on the skin surface positive too
beeinflussen. influence.
Vorteilhafte Feuchthaltemittel (Moisturizer) im Sinne der vorliegenden Erfindung sind Advantageous moisturizers (moisturizers) for the purposes of the present invention are
beispielsweise Glycerin, Butylenglykol, Propylenglykol, Biosaccaride Gum-1 , Glycine Soja, Pyrrolidoncarbonsäure und Harnstoff. Ferner ist es insbesondere von Vorteil, polymere for example glycerin, butylene glycol, propylene glycol, Biosaccaride Gum-1, Glycine soy, pyrrolidone carboxylic acid and urea. Furthermore, it is particularly advantageous to use polymers
Moisturizer aus der Gruppe der wasserlöslichen und/oder in Wasser quellbaren und/oder mit Hilfe von Wasser gelierbaren Polysaccharide zu verwenden. Insbesondere vorteilhaft sind beispielsweise Hyaluronsäure, Chitosan und/oder ein fucosereiches Polysaccharid, welches in den Chemical Abstracts unter der Registraturnummer 178463-23-5 abgelegt und z. B. unter der Bezeichnung Fucogel®1000 von der Gesellschaft SOLABIA S.A. erhältlich ist. Moisturizer können vorteilhaft auch als Antifaltenwirkstoffe zum Schutz vor Hautveränderungen, wie sie z. B. bei der Hautalterung auftreten, verwendet werden.
Die erfindungsgemäßen kosmetischen Zubereitungen können ferner vorteilhaft, wenngleich nicht zwingend, Füllstoffe enthalten, welche z. B. die sensorischen und kosmetischen Moisturizers from the group of water-soluble and / or water-swellable and / or water-gelable polysaccharides. Particularly advantageous are, for example, hyaluronic acid, chitosan and / or a fucose-rich polysaccharide, which is filed in the Chemical Abstracts under the registration number 178463-23-5 and z. B. is available under the name Fucogel®1000 from the company SOLABIA SA. Moisturizers can also be used advantageously as anti-wrinkle ingredients to protect against skin changes, such as those found in z. B. occur in skin aging, are used. The cosmetic preparations according to the invention can furthermore advantageously, although not necessarily, contain fillers which, for. B. the sensory and cosmetic
Eigenschaften der Formulierungen weiter verbessern und beispielsweise ein samtiges oder seidiges Hautgefühl hervorrufen oder verstärken. Vorteilhafte Füllstoffe im Sinne der vorliegenden Erfindung sind Stärke und Stärkederivate (wie z. B. Tapiocastärke, Further improve the properties of the formulations and, for example, create or intensify a velvety or silky feeling on the skin. Advantageous fillers for the purposes of the present invention are starch and starch derivatives (such as tapioca starch,
Distärkephosphat, Aluminium- bzw. Natrium-Stärke Octenylsuccinat und dergleichen), Distarch phosphate, aluminum or sodium starch, octenyl succinate and the like),
Pigmente, die weder hauptsächlich UV-Filter- noch färbende Wirkung haben (wie z. B. Bornitrid etc.) und/oder Aerosile® (CAS-Nr. 7631 -86-9) und /oder Talkum und/oder Polyethylen, Nylon, Silica Diemthyl Silyate. Pigments that have neither primarily UV filtering nor coloring effects (such as boron nitride etc.) and / or Aerosile ® (CAS No. 7631 -86-9) and / or talc and / or polyethylene, nylon, Silica Diemthyl Silyate.
Es ist erfindungsgemäß bevorzugt, wenn die erfindungsgemäße Zubereitung Silica Dimethyl Silylate enthält. It is preferred according to the invention if the preparation according to the invention contains silica dimethyl silylates.
Erfindungsgemäß vorteilhafte Ausführungsformen der vorliegenden Erfindung sind dadurch gekennzeichnet, dass die Zubereitung ein oder mehrere Öle gewählt aus der Gruppe der Verbindungen Butylene Glycol Dicaprylat/Dicaprat, Phenethyl Benzoat, 012-15 Alkyl Benzoat, Dibutyladipat; Diisopropylsebacate, Dicaprylylcarbonat, Di-C12-13 Alkyl Tartrate, Butyloctyl Salicylate, Diethylhexyl Syringylidene Malonate, Hydragenated Castor Oil Dimerate, Embodiments of the present invention which are advantageous according to the invention are characterized in that the preparation comprises one or more oils selected from the group of the compounds butylene glycol dicaprylate / dicaprate, phenethyl benzoate, 012-15 alkyl benzoate, dibutyl adipate; Diisopropyl sebacate, dicaprylyl carbonate, di-C12-13 alkyl tartrate, butyl octyl salicylate, diethylhexyl syringylidenes malonate, hydragenated castor oil dimerate,
Triheptanoin, C12-13 Alkyl Lactate, C16-17 Alkyl Benzoate, Propylheptyl Caprylate, Triheptanoin, C12-13 alkyl lactate, C16-17 alkyl benzoate, propylheptyl caprylate,
Caprylic/Capric Triglyceride, Diethylhexyl 2,6-Naphthalate, Octyldodecanol, Caprylic/Capric Triglyceride, Ethylhexyl Cocoate, enthält. Caprylic / Capric Triglyceride, Diethylhexyl 2,6-Naphthalate, Octyldodecanol, Caprylic / Capric Triglyceride, Ethylhexyl Cocoate, contains.
Dabei ist es erfindugnsgemäß bevorzugt, wenn die Zubereitung Dibutyladipat, It is preferred according to the invention if the preparation dibutyl adipate,
Dicaprylylcarbonat und/oder C12-C15 Alkylbenzoat enthält. Contains dicaprylyl carbonate and / or C12-C15 alkyl benzoate.
Die Wasserphase der erfindungsgemäßen Zubereitungen kann vorteilhaft übliche kosmetische Hilfsstoffe enthalten, wie beispielsweise Elektrolyte, Selbstbräuner sowie insbesondere ein oder mehrere Verdickungsmittel, welches oder welche vorteilhaft gewählt werden können aus der Gruppe Siliciumdioxid, Aluminiumsilikate, Polysaccharide bzw. deren Derivate, z. B. Hy aluronsäure, Hydroxypropylmethylcellulose. Vorteilhaft ist auch ein Gehalt an Ethanol.
Beispiele The water phase of the preparations according to the invention can advantageously contain customary cosmetic auxiliaries, such as, for example, electrolytes, self-tanners and in particular one or more thickeners, which one or more can advantageously be selected from the group consisting of silicon dioxide, aluminum silicates, polysaccharides or their derivatives, e.g. B. Hy aluronic acid, hydroxypropylmethyl cellulose. An ethanol content is also advantageous. Examples
Die nachfolgenden Beispiele sollen die vorliegende Erfindung verdeutlichen, ohne sie einzu schränken. Alle Mengenangaben, Anteile und Prozentanteile sind, soweit nicht anders an- gegeben, auf das Gewicht und die Gesamtmenge bzw. auf das Gesamtgewicht der Zube reitungen bezogen. The following examples are intended to illustrate the present invention without restricting it. Unless otherwise stated, all quantities, proportions and percentages are based on the weight and the total quantity or on the total weight of the preparations.
Von diesen Zubereitungen wurde die pH-Wert Stabilität (der pH Shift) bei Raumtemperatur (20°C) bestimmt. The pH stability (the pH shift) of these preparations was determined at room temperature (20 ° C.).
Fazit: Die erfindungsgemäßen Zubereitungen sind deutlich pH-stabiler als das Conclusion: The preparations according to the invention are significantly more pH-stable than that
Vergleichsbeispiel.
Comparative example.
Claims
1. Kosmetische Öl-in-Wasser Emulsion (O/W-Emulsion) enthaltend 1. Containing cosmetic oil-in-water emulsion (O / W emulsion)
a) Polyglyceryl-10 Stearat (INCI Polyglyceryl-10 Stearate) a) Polyglyceryl-10 stearate (INCI Polyglyceryl-10 stearate)
b) Sorbitanstearat (INCI Sorbitan Stearate) b) Sorbitan stearate (INCI sorbitan stearate)
c) Zinkoxid c) zinc oxide
d) ein pH-Puffersystem aus Milchsäure und Natriumlactat, d) a pH buffer system consisting of lactic acid and sodium lactate,
wobei die Emulsion frei ist von 3-(4-Methylbenzyliden)-campher, 2-Hydroxy-4- methoxybenzophenon (INCI: Oxybenzon), 4-Methoxyzimtsäure-2-ethylhexylester (INCI Octylmethoxycinnamate), Propylparaben, Butylparaben, Methylisothiazolinon, the emulsion being free from 3- (4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone (INCI: oxybenzone), 4-methoxycinnamic acid-2-ethylhexyl ester (INCI octylmethoxycinnamate), propylparaben, butylparaben, methylisothiazolinone,
Chlormethyl-isothiazolinon und DMDM-Hydantoin, Polyethylenglycolethern und Chloromethyl isothiazolinone and DMDM hydantoin, polyethylene glycol ethers and
Polyethylenglycolestern. Polyethylene glycol esters.
2. Kosmetische O/W-Emulsion nach Anspruch 1 , dadurch gekennzeichnet, dass das 2. Cosmetic O / W emulsion according to claim 1, characterized in that the
Zinkoxid mit Triethoxycaprylylsilan beschichtet ist. Zinc oxide is coated with triethoxycaprylylsilane.
3. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 3. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass das Zinkoxid eine Primärpartikelgröße zwischen 20 und 100 nm aufweist. characterized in that the zinc oxide has a primary particle size between 20 and 100 nm.
4. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 4. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung das Zinkoxid in einer Menge von 0,1 bis 20 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung. characterized in that the preparation contains the zinc oxide in an amount of 0.1 to 20% by weight, based on the total weight of the preparation.
5. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 5. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung frei ist von Acrylatpolymeren. characterized in that the preparation is free of acrylate polymers.
6. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 6. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung Polyglyceryl-10 Stearat (INCI Polyglyceryl-10 Stearate) in einer Konzentration von 1 ,44 bis 2,40 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung, enthält. characterized in that the preparation contains polyglyceryl-10 stearate (INCI polyglyceryl-10 stearate) in a concentration of 1.44 to 2.40% by weight, based on the total weight of the preparation.
7. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 7. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung Sorbitanstearat (INCI Sorbitan Stearate) in einer Konzentration von 1 ,26 bis 2,10 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung, enthält. characterized in that the preparation contains sorbitan stearate (INCI sorbitan stearate) in a concentration of 1.26 to 2.10% by weight, based on the total weight of the preparation.
8. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 8. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung Milchsäure in einer Konzentration von 0,55 bis 0,60 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung, enthält characterized in that the preparation contains lactic acid in a concentration of 0.55 to 0.60% by weight, based on the total weight of the preparation
9. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 9. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung Natriumlactat in einer Konzentration von 0,65 bis 0,75 Gewichts-%, bezogen auf das Gesamtgewicht der Zubereitung, enthält characterized in that the preparation contains sodium lactate in a concentration of 0.65 to 0.75% by weight, based on the total weight of the preparation
10. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 10. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung kein Octocrylen (INCI Octocrylene) und Mineralöl enthält.
marked that the preparation contains no octocrylene (INCI octocrylene) and mineral oil.
1 1. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch gekennzeichnet, dass die Zubereitung Xanthamgummi (INCI Xantham Gum) enthält.1 1. Cosmetic O / W emulsion according to one of the preceding claims, characterized in that the preparation contains xantham gum (INCI Xantham gum).
12. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 12. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung einen oder mehrere UV-Filter gewählt aus der Gruppe der Verbindungen 4-(tert.-Butyl)-4’-methoxydibenzoylmethan (INCI Butyl Methoxydibenzoyl-methane), (2-[-4-(Diethylamino)-2-hydroxybenzoyl] characterized in that the preparation one or more UV filters selected from the group of compounds 4- (tert-butyl) -4'-methoxydibenzoylmethane (INCI butyl methoxydibenzoyl methane), (2 - [- 4- (diethylamino) -2 -hydroxybenzoyl]
Benzoesäurehexylester (INCI: Diethyl-amino Hydroxybenzoyl Hexyl Benzoate) und 2,4- Bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1 ,3,5-triazin (INCI Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine), 2,2’-Methylen-bis-(6-(2H- benzotriazol-2-yl)-4-(1 ,1 ,3,3-tetramethylbutyl)-phenol), Ethylhexylsalicylat, Hexyl benzoate (INCI: diethylamino hydroxybenzoyl hexyl benzoate) and 2,4-bis - {[4- (2-ethylhexyloxy) -2-hydroxy] phenyl} -6- (4-methoxyphenyl) -1, 3, 5-triazine (INCI bis-ethylhexyloxyphenol methoxyphenyl triazine), 2,2'-methylene-bis- (6- (2H-benzotriazol-2-yl) -4- (1, 1, 3,3-tetramethylbutyl) phenol) , Ethylhexyl salicylate,
Homomenthylsalicylat, Dioctylbutylamidotriazon (INCI: Diethylhexyl-Butamidotriazone), 4,4',4"-(1 ,3,5-Triazin-2,4,6-triyltriimino)-tris-benzoesäure-tris(2-ethylhexylester) (auch: 2,4,6-Tris-[anilino-(p-carbo-2'-ethyl-1 '-hexyloxy)]-1 ,3,5-triazin (INCI: Ethylhexyl Tria- zone), 2,4,6-T ribiphenyl-4-yl-1 ,3,5-triazin, Titandioxid, enthält. Homomenthyl salicylate, dioctylbutylamidotriazon (INCI: Diethylhexyl-Butamidotriazone), 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'-hexyloxy)] - 1,3,5-triazine (INCI: ethylhexyl triazone), 2,4,6- T contains ribiphenyl-4-yl-1, 3,5-triazine, titanium dioxide.
13. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 13. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung Phenoxyethanol, Ethylhexylglycerin und/oder 4- Hydroxyacetophenon enthält. characterized in that the preparation contains phenoxyethanol, ethylhexylglycerol and / or 4-hydroxyacetophenone.
14. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 14. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung ein oder mehrere Alkandiole aus der Gruppe der Verbindungen 1 ,2-Pentandiol, 1 ,2-Hexandiol, 1 ,2-Octandiol, 1 ,2-Decandiol, 2-Methyl- characterized in that the preparation one or more alkanediols from the group of compounds 1, 2-pentanediol, 1, 2-hexanediol, 1, 2-octanediol, 1, 2-decanediol, 2-methyl
1 ,3-propandiol enthält. 1, 3-propanediol contains.
15. Kosmetische O/W-Emulsion nach einem der vorhergehenden Ansprüche, dadurch 15. Cosmetic O / W emulsion according to one of the preceding claims, characterized
gekennzeichnet, dass die Zubereitung eine oder mehrere Verbindungen gewählt aus der Gruppe der Verbindungen alpha-Liponsäure, Folsäure, Phytoen, D-Biotin, Coenzym characterized in that the preparation one or more compounds selected from the group of the compounds alpha-lipoic acid, folic acid, phytoene, D-biotin, coenzyme
010, alpha-Glucosylrutin, Carnitin, Carnosin, natürliche und/oder synthetische Isoflavo noide, Flavonoide, Kreatin, Kreatinin, Taurin, b-Alanin, Panthenol, Magnolol, Honokiol, Tocopherylacetat, Dihydroxyaceton; 8-Hexadecen-1 ,16-dicarbonsäure, Glycerylglycose, (2-Hydroxyethyl)harnstoff, Vitamin E bzw. seine Derivate, Glycyrrhetinsäure, 010, alpha-glucosylrutin, carnitine, carnosine, natural and / or synthetic isoflavo noide, flavonoids, creatine, creatinine, taurine, b-alanine, panthenol, magnolol, honokiol, tocopheryl acetate, dihydroxyacetone; 8-hexadecen-1, 16-dicarboxylic acid, glycerylglycose, (2-hydroxyethyl) urea, vitamin E or its derivatives, glycyrrhetic acid,
Hyaluronsäure und/oder deren Salze und/oder Licochalcon A enthält.
Contains hyaluronic acid and / or its salts and / or licochalcon A.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102018218740.1A DE102018218740A1 (en) | 2018-11-01 | 2018-11-01 | Cosmetic O / W emulsion with zinc oxide |
DE102018218740.1 | 2018-11-01 |
Publications (1)
Publication Number | Publication Date |
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WO2020088905A1 true WO2020088905A1 (en) | 2020-05-07 |
Family
ID=68233994
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2019/077436 WO2020088905A1 (en) | 2018-11-01 | 2019-10-10 | Cosmetic oil-in-water emulsion containing zinc oxide |
Country Status (2)
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DE (1) | DE102018218740A1 (en) |
WO (1) | WO2020088905A1 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19835691A1 (en) * | 1998-08-07 | 2000-02-10 | Merck Patent Gmbh | pH-stabilized ZnO in sun protection formulations |
DE102012205526A1 (en) * | 2012-04-04 | 2013-10-10 | Beiersdorf Ag | Stable cosmetic preparation with high pigment content |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050220832A1 (en) * | 2004-03-25 | 2005-10-06 | Richard Walton | Gels containing metallic soaps and coupling agents |
US20090257968A1 (en) * | 2004-03-25 | 2009-10-15 | Richard Walton | Gels containing anionic surfactants and coupling agents |
EP2211824B1 (en) * | 2007-10-18 | 2015-09-02 | Unilever PLC | Shaving composition with skincare properties |
-
2018
- 2018-11-01 DE DE102018218740.1A patent/DE102018218740A1/en not_active Withdrawn
-
2019
- 2019-10-10 WO PCT/EP2019/077436 patent/WO2020088905A1/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19835691A1 (en) * | 1998-08-07 | 2000-02-10 | Merck Patent Gmbh | pH-stabilized ZnO in sun protection formulations |
EP1102576A1 (en) | 1998-08-07 | 2001-05-30 | MERCK PATENT GmbH | pH-STABILIZED ZnO IN SUNSCREEN FORMULATIONS |
DE102012205526A1 (en) * | 2012-04-04 | 2013-10-10 | Beiersdorf Ag | Stable cosmetic preparation with high pigment content |
Non-Patent Citations (1)
Title |
---|
"Z-COTE ? and T-Lite TM Microfine Pigments For Broad- Spectrum UV Protection", 17 November 2005 (2005-11-17), pages 1 - 44, XP055104876, Retrieved from the Internet <URL:http://www.atsh.co.ir/Catalogs/articles/NuCelle/Z-COTE & T-LITE Microfine Pigments.pdf> [retrieved on 20140228] * |
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