EP3962436A1 - Cosmetic o/w emulsion with scleroglucan and hydrophilic uv filter substances - Google Patents

Cosmetic o/w emulsion with scleroglucan and hydrophilic uv filter substances

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Publication number
EP3962436A1
EP3962436A1 EP20725691.8A EP20725691A EP3962436A1 EP 3962436 A1 EP3962436 A1 EP 3962436A1 EP 20725691 A EP20725691 A EP 20725691A EP 3962436 A1 EP3962436 A1 EP 3962436A1
Authority
EP
European Patent Office
Prior art keywords
emulsion
weight
emulsifiers
emulsions according
hydrophilic
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.)
Pending
Application number
EP20725691.8A
Other languages
German (de)
French (fr)
Inventor
Keti Piradashvili
Thomas Raschke
Lisa Peschke
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
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Filing date
Publication date
Application filed by Beiersdorf AG filed Critical Beiersdorf AG
Publication of EP3962436A1 publication Critical patent/EP3962436A1/en
Pending legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • A61K8/062Oil-in-water emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier 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
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations

Definitions

  • the present invention relates to a cosmetic preparation containing scleroglucan and hydrophilic UV filter substances.
  • Emulsions are generally understood to mean heterogeneous systems which consist of two liquids which are immiscible or only partially miscible with one another, which are usually referred to as phases and in which one of the two liquids is dispersed in the other liquid in the form of very fine droplets. Externally and with the naked eye, emulsions appear homogeneous.
  • the two liquids are water and oil and if oil droplets are finely distributed in water, then it is an oil-in-water emulsion (O / W emulsion, e.g. milk).
  • O / W emulsion oil-in-water emulsion
  • the basic character of an O / W emulsion is shaped by the water.
  • W / O emulsion water-in-oil emulsion, e.g. butter
  • so-called emulsifiers are added to the emulsions.
  • Emulsifiers are usually molecules with a polar, hydrophilic structural element and a non-polar, lipophilic structural element.
  • a so-called HLB value (a dimensionless number between 0 and 20) is assigned to each emulsifier, which indicates whether the water or oil solubility is preferred. Numbers under 8 indicate oil-soluble, hydrophobic emulsifiers, numbers over 8 indicate water-soluble, hydrophilic emulsifiers.
  • the water phase is combined with the lipid phase (oil phase) with stirring, the droplets of the inner phase of the emulsion having to be broken down to a size of less than 10 ⁇ m so that the emulsion becomes stable.
  • UVA and UVB filters are summarized in most industrialized countries in the form of positive lists such as Annex 7 of the Cosmetics Ordinance.
  • O / W emulsions cosmetic oil-in-water emulsions (O / W emulsions) containing, in addition to a water phase, one or more oil phases dispersed therein as well
  • Scleroglucan is released into the surrounding medium as a microbial exopolysaccharide by fungal species of the genus Sclerotium (Basidiomycota, Agariomycetes). Sclerotium delphinii, for example, is a major pest of plants. Scleroglucan is also known as Sclerotium Gum (INCI: Sclerotium Gum).
  • Scleroglucan is a (1—> 3; 1—> 6) - ⁇ -D-glucan. Its mean molecular weight is about
  • Scleroglucan consists of a linear (1—> 3) - ⁇ -D-glucan chain (O d HioO d OQHIOOd) ⁇ , on which statistically every third glucose unit with a single (1—> 6) - ⁇ -D- Glcp residue is branched.
  • Scleroglucan is readily soluble in water and can be used as a thickener.
  • the use of scleroglucan in cosmetic emulsions is known per se to the person skilled in the art, but the prior art could not point the way to the present invention.
  • DE 10 2014 015 554 discloses the use of scleroglucan in UV filters containing cosmetic preparations to reduce the contamination and / or discoloration of textiles caused by the UV filters in the preparation.
  • EP 1 132 076 describes thickened hair compositions containing scleroglucan.
  • the emulsion according to the invention is characterized in that the content of scleroglucan in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.01 and 1.5% by weight, particularly preferably between 0.1 and 1.0% by weight, each based on the total weight of the emulsion.
  • the emulsion contains one or more oil-in-water emulsifiers (O / W emulsifiers) in a total concentration of 0.05 to 5.0% by weight and preferably in a total concentration of 2.0 to 4.0% by weight, based in each case on the total weight of the emulsion.
  • O / W emulsifiers oil-in-water emulsifiers
  • the emulsion according to the invention is characterized in that the content of one or more anionic emulsifiers in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and
  • the emulsion according to the invention is characterized in that the content of one or more nonionic emulsifiers in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and
  • the emulsion according to the invention is characterized in that the content of one or more hydrophilic UV filter substances in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and 3% by weight , particularly preferably between 0.1 and 2% by weight, based in each case on the total weight of the emulsion.
  • Advantageous hydrophilic UV-A filter substances for the purposes of the present invention are, for. B. the salts of 2-phenylbenzimidazole-5-sulfonic acid, such as their sodium, potassium or their trietha nolammonium salt, as well as the sulfonic acid itself; also phenylene-1,4-bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid
  • 1,4-di (2-oxo-10-sulfo-3-bornylidenemethyl) benzene and its salts are also advantageous ), which is also known as benzene-1,4-di (2-oxo-3-bornylidenemethyl-10-sulfonic acid) and is characterized by the following structure:
  • the emulsion according to the invention is characterized in that hydrophilic emulsifiers with an HLB value of greater than or equal to 8 are used as O / W emulsifiers.
  • HLB value of emulsifiers can be found in the usual standard works (e.g. Fiedler, Lexicon of Auxiliaries for Pharmacy, Cosmetics and Neighboring Areas, Editio Cantor Verlag, Aulendorf).
  • the emulsion according to the invention is characterized in that, as O / W emulsifiers, glyceryl stearate citrate (CAS 39175-72-9, INCI Glyceryl Stearate Citrate, e.g. Imwitor 370 from Hüls), polyglyceryl-3 methylglucose distearate (INCI Polyglyceryl Methyl Glucose Distearate, e.g. Tego Care 450 from Evonik) and / or polyethylene glycol (2000) monostearate (INCI; PEG-40 stearate) can be used.
  • O / W emulsifiers glyceryl stearate citrate (CAS 39175-72-9, INCI Glyceryl Stearate Citrate, e.g. Imwitor 370 from Hüls), polyglyceryl-3 methylglucose distearate (INCI Polyglyceryl Methyl Glucose Distearate, e
  • the emulsion according to the invention contains potassium cetyl phosphate, sodium cetearyl sulfate, sodium stearyl glutamate, alkali salts of saturated fatty acids of chain length C14-C22, in particular sodium stearate, as an anionic emulsifier.
  • the emulsion according to the invention contains one or more polyglyceryl fatty acid esters as nonionic emulsifiers.
  • the polyglyceryl fatty acid ester particularly preferred according to the invention is polyglyceryl-10 stearate (INCI polyglyceryl-10 stearate).
  • the emulsion according to the invention is characterized in that the content of one or more anionic emulsifiers in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and 2% by weight, particularly is preferably between 0.1 and 1.0% by weight, based in each case on the total weight of the emulsion.
  • the emulsion according to the invention is characterized in that the content of one or more nonionic emulsifiers, in particular one or more polyglyceryl fatty acid esters, especially polyglyceryl-10 stearate, in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and
  • the emulsion according to the invention can have the consistency of an ointment, cream or low-viscosity lotion or represent an ointment, cream or low-viscosity lotion. It is preferred according to the invention if the process according to the invention is carried out in the form of the hot-hot process. In this process, a hot oil and water phase are combined with one another.
  • the emulsion can advantageously be in the form of an ointment, cream or lotion (optionally sprayable).
  • the emulsion can advantageously also be used as a spray or as a soaking medium for a plaster or cloth. Therefore, plasters and tissues soaked with the emulsion according to the invention are also according to the invention.
  • the water phase of the emulsion according to the invention can advantageously contain conventional cosmetic auxiliaries, such as alcohols, in particular those with a low carbon number, preferably ethanol and / or isopropanol, diols or polyols with a low carbon number, and their ethers, preferably propylene glycol, glycerol, ethylene glycol, ethylene glycol monoethyl - or monobutyl ether, hexanediol, octanediol, glyceryl caprylate, ethylhexylglycerol, methylpropanediol, propylene glycol monomethyl, monoethyl or monobutyl ether, diethylene glycol monomethyl or monoethyl ether, and analogous products, as well as phenoxyethanol, hydrochloride, benzethylacetophenol, benzethonium alcohol , Foam stabilizers, electrolytes, self-tanner
  • the oil phase according to the invention can contain all conventional constituents of oil, fat and wax components used in cosmetics.
  • the emulsion according to the invention can advantageously contain cosmetic active and care substances, for example the UV light protection filters approved according to the Cosmetics Ordinance.
  • active ingredients can advantageously be contained therein in concentrations of 0.01 to 30% by weight, based on the total weight of the preparation.
  • esters unsaturated fatty acids and their esters, in particular special di- and triglycerides (e.g. g-linolenic acid, linoleic acid, oleic acid), mannose, magnolia bark extract, magnolol, honokiol, glycyrrhetinic acid in concentrations of 0.001 up to 5% by weight, based on the total weight of the preparation.
  • di- and triglycerides e.g. g-linolenic acid, linoleic acid, oleic acid
  • mannose magnolia bark extract
  • magnolol magnolol
  • honokiol glycyrrhetinic acid in concentrations of 0.001 up to 5% by weight, based on the total weight of the preparation.
  • the preparation according to the invention particularly preferably contains alpha-hydroxy acids and / or salts thereof as further constituents.
  • lactic acid / lactates or citric acid / citrates are preferably used in a concentration of 0.01 to 5% by weight, based on the total weight of the preparation.
  • the preparation according to the invention can contain perfumes in any desired composition and amount.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Birds (AREA)
  • Emergency Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Dispersion Chemistry (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

The invention relates to cosmetic oil-in-water emulsions (O/W emulsions) having, in addition to a water phase, one or more oil phases dispersed therein and a) scleroglucan and b) one or more hydrophilic UV filter substances.

Description

Beschreibung description
Kosmetische O/W-Emulsion mit Skleroglucan und hydrophilen UV-Filtersubstanzen Cosmetic O / W emulsion with scleroglucan and hydrophilic UV filter substances
Die vorliegende Erfindung betrifft eine kosmetische Zubereitung enthaltend Skleroglucan und hydrophile UV-Filtersubstanzen. The present invention relates to a cosmetic preparation containing scleroglucan and hydrophilic UV filter substances.
Der Wunsch, schön und attraktiv auszusehen, ist von Natur aus im Menschen verwurzelt. Auch wenn das Schönheitsideal im Laufe der Zeit Wandlungen erfahren hat, so ist das Stre ben nach einem makellosen Äußeren immer das Ziel der Menschen gewesen. Einen wesent lichen Anteil an einem schönen und attraktiven Äußeren haben dabei der Zustand und das Aussehen der Haut. The desire to look beautiful and attractive is inherently rooted in people. Even if the ideal of beauty has changed in the course of time, striving for a flawless appearance has always been the goal of people. The condition and appearance of the skin play a key role in a beautiful and attractive appearance.
Damit die Haut ihre biologischen Funktionen im vollen Umfang erfüllen kann, bedarf sie der regelmäßigen Reinigung und Pflege. Die Reinigung der Haut dient dabei der Entfernung von Schmutz, Schweiß und Resten abgestorbener Hautpartikel, die einen idealen Nährboden für Krankheitserreger und Parasiten aller Art bilden. Hautpflegeprodukte dienen meist der Be feuchtung und Rückfettung der Haut. Häufig sind ihnen Wirkstoffe zugesetzt, welche die Haut regenerieren und beispielsweise ihre vorzeitige Alterung (z. B. das Entstehen von Fält- chen, Falten) verhindern und vermindern sollen. In order for the skin to be able to fully fulfill its biological functions, it needs regular cleaning and care. The cleaning of the skin serves to remove dirt, sweat and residues of dead skin particles, which form an ideal breeding ground for pathogens and parasites of all kinds. Skin care products are mostly used to moisturize and re-oil the skin. Often, active ingredients are added to them that regenerate the skin and, for example, are intended to prevent and reduce its premature aging (eg the appearance of fine lines and wrinkles).
Hautpflegeprodukte bestehen in der Regel aus Emulsionen. Unter Emulsionen versteht man im Allgemeinen heterogene Systeme, die aus zwei nicht oder nur begrenzt miteinander mischbaren Flüssigkeiten bestehen, die üblicherweise als Phasen bezeichnet werden und bei denen eine der beiden Flüssigkeiten in Form feinster Tröpfchen in der anderen Flüssig keit dispergiert ist. Äußerlich und mit bloßem Auge betrachtet erscheinen Emulsionen homo gen. Skin care products are usually made up of emulsions. Emulsions are generally understood to mean heterogeneous systems which consist of two liquids which are immiscible or only partially miscible with one another, which are usually referred to as phases and in which one of the two liquids is dispersed in the other liquid in the form of very fine droplets. Externally and with the naked eye, emulsions appear homogeneous.
Sind die beiden Flüssigkeiten Wasser und Öl und liegen Öltröpfchen fein verteilt in Wasser vor, so handelt es sich um eine ÖI-in-Wasser-Emulsion (O/W-Emulsion, z. B. Milch). Der Grundcharakter einer O/W-Emulsion ist durch das Wasser geprägt. Bei einer Wasser-in-ÖI- Emulsion (W/O-Emulsion, z. B. Butter) handelt es sich um das umgekehrte Prinzip, wobei der Grundcharakter hier durch das Öl bestimmt wird. Um Emulsionen über einen längeren Zeitraum stabil zu halten und eine Entmischung der Phasen zu verhindern, werden den Emulsionen sogenannte Emulgatoren zugesetzt. Bei Emulgatoren handelt es sich in der Regel um Moleküle mit einem polaren, hydrophilen Struk turelement und einem unpolaren, lipophilen Strukturelement. Ende der vierziger Jahre wurde ein System entwickelt, das die Auswahl von Emulgatoren erleichtern sollte. Jedem Emulga tor wird ein so genannter HLB-Wert (eine dimensionslose Zahl zwischen 0 und 20) zuge schrieben, der angibt, ob eine bevorzugte Wasser- oder Öllöslichkeit vorliegt. Zahlen unter 8 kennzeichnen öllösliche, hydrophobe Emulgatoren, Zahlen über 8 wasserlösliche, hydrophi le. If the two liquids are water and oil and if oil droplets are finely distributed in water, then it is an oil-in-water emulsion (O / W emulsion, e.g. milk). The basic character of an O / W emulsion is shaped by the water. In the case of a water-in-oil emulsion (W / O emulsion, e.g. butter), the principle is reversed, the basic character being determined here by the oil. In order to keep emulsions stable over a longer period of time and to prevent the phases from separating, so-called emulsifiers are added to the emulsions. Emulsifiers are usually molecules with a polar, hydrophilic structural element and a non-polar, lipophilic structural element. At the end of the 1940s a system was developed to make the selection of emulsifiers easier. A so-called HLB value (a dimensionless number between 0 and 20) is assigned to each emulsifier, which indicates whether the water or oil solubility is preferred. Numbers under 8 indicate oil-soluble, hydrophobic emulsifiers, numbers over 8 indicate water-soluble, hydrophilic emulsifiers.
Bei der Herstellung einer Emulsion wird die Wasserphase mit der Lipidphase (Ölphase) unter Rühren vereinigt, wobei die Tröpfchen der inneren Phase der Emulsion auf eine Größe von unter 10 pm zerkleinert werden müssen, damit die Emulsion stabil wird. In the production of an emulsion, the water phase is combined with the lipid phase (oil phase) with stirring, the droplets of the inner phase of the emulsion having to be broken down to a size of less than 10 μm so that the emulsion becomes stable.
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 Sonnenstrah lung aus, da diese eine Pigmentbildung im Sinne einer Melaninbildung hervorruft. Die ultra violette Strahlung des Sonnenlichtes hat jedoch auch eine schädigende Wirkung auf die Haut. Neben der akuten Schädigung (Sonnenbrand) treten Langzeitschäden wie ein erhöh tes 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 elasti schen und kollagenen Fasern des Bindegewebes. Dies führt zu zahlreichen phototoxischen und photoallergischen Reaktionen und hat eine vorzeitige Hautalterung zur Folge. The trend away from elegant paleness towards "healthy, sporty brown skin" has been unbroken for years. To achieve this, people expose their skin to solar radiation, as this causes pigment formation in the sense of melanin. However, the ultra violet radiation of 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 when exposed to 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 phototoxic and photoallergic reactions and leads to premature skin aging.
Zum Schutz der Haut wurde 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 der Anlage 7 der Kosmetikver ordnung zusammengefasst. 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 summarized in most industrialized countries in the form of positive lists such as Annex 7 of the Cosmetics Ordinance.
Der Einsatz von hydrophilen UV-Filtern in Emulsionen führt häufig zu einer Destabilisierung dieser Systeme und einer daraus resultierenden Trennung der Phasen. Eine Langzeitstabi- liserung von O/W Emulsionen mit UV-Filtern auch bei erhöhter Temperatur ist daher wün schenswert. Überraschend gelöst wird die Aufgabe durch kosmetische ÖI-in-Wasser-Emulsionen (O/W- Emulsionen) enthaltend neben einer Wasserphase eine oder mehrere darin dispergierte Öl phasen sowie The use of hydrophilic UV filters in emulsions often leads to a destabilization of these systems and a resulting separation of the phases. Long-term stabilization of O / W emulsions with UV filters, even at elevated temperatures, is therefore desirable. The object is surprisingly achieved by cosmetic oil-in-water emulsions (O / W emulsions) containing, in addition to a water phase, one or more oil phases dispersed therein as well
a) Skleroglucan a) scleroglucan
und and
b) eine oder mehrere hydrophile UV-Filtersubstanzen. b) one or more hydrophilic UV filter substances.
Skleroglucan wird von Pilzarten der Gattung Sclerotium (Basidiomycota, Agariomycetes) als mikrobielles Exopolysaccharid in das umgebende Medium abgegeben. Sclerotium delphinii beispielsweise ist ein bedeutender Pflanzenschädling. Skleroglucan wird auch als Scleroti umgummi (INCI: Sclerotium Gum) bezeichnet. Scleroglucan is released into the surrounding medium as a microbial exopolysaccharide by fungal species of the genus Sclerotium (Basidiomycota, Agariomycetes). Sclerotium delphinii, for example, is a major pest of plants. Scleroglucan is also known as Sclerotium Gum (INCI: Sclerotium Gum).
Skleroglucan ist ein (1— >3; 1— >6)-ß-D-Glucan. Seine mittlere Molmasse beträgt etwa Scleroglucan is a (1—> 3; 1—> 6) -β-D-glucan. Its mean molecular weight is about
5,7 *106 g/mol, sein durchschnittlicher Polymerisationsgrad etwa 35.000. 5.7 * 10 6 g / mol, its average degree of polymerization about 35,000.
Die chemische Struktur des Skleroglucans wird wie folgt veranschaulicht: The chemical structure of scleroglucan is illustrated as follows:
Skleroglucan besteht aus einer linearen (1— >3)-ß-D-Glucan-Kette (OdHioOdOQHIOOd)^, an der statistisch jede dritte Glucose-Einheit mit einem einzelnen (1— >6)-ß-D-Glcp-Rest ver zweigt ist. Scleroglucan consists of a linear (1—> 3) -β-D-glucan chain (O d HioO d OQHIOOd) ^, on which statistically every third glucose unit with a single (1—> 6) -β-D- Glcp residue is branched.
Skleroglucan ist in Wasser gut löslich und kann als Verdicker eingesetzt werden. Der Einsatz von Skleroglucan in kosmetischen Emulsionen ist dem Fachmann an sich bekannt, doch konnte der Stand der Technik nicht den Weg zur vorliegenden Erfindung weisen. Beispielsweise offenbart die DE 10 2014 015 554 die die Verwendung von Skleroglucan in UV-Filter enthaltenden kosmetischen Zubereitungen, zur Reduzierung der durch die UV- Filter in der Zubereitung hervorgerufenen Verunreinigung und/oder Verfärbung von Textilien. Scleroglucan is readily soluble in water and can be used as a thickener. The use of scleroglucan in cosmetic emulsions is known per se to the person skilled in the art, but the prior art could not point the way to the present invention. For example, DE 10 2014 015 554 discloses the use of scleroglucan in UV filters containing cosmetic preparations to reduce the contamination and / or discoloration of textiles caused by the UV filters in the preparation.
Die EP 1 132 076 beschreibt verdickte Haarzusammensetzungen mit einem Gehalt an Skleroglucan. EP 1 132 076 describes thickened hair compositions containing scleroglucan.
Es ist erfindungsgemäß vorteilhaft, wenn die erfindungsgemäße Emulsion dadurch gekenn zeichnet ist, dass der Gehalt an Skleroglucan in der Emulsion von 0,001 bis 5,0 Gew.-% und bevorzugt zwischen 0,01 und 1 ,5 Gew.-%, besonders bevorzugt zwischen 0,1 und 1 ,0 Gew.- %, jeweils bezogen auf das Gesamtgewicht der Emulsion, beträgt. It is advantageous according to the invention if the emulsion according to the invention is characterized in that the content of scleroglucan in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.01 and 1.5% by weight, particularly preferably between 0.1 and 1.0% by weight, each based on the total weight of the emulsion.
Es ist erfindungsgemäß vorteilhaft, wenn die die Emulsion einen oder mehrere Öl-in-Wasser- Emulgatoren (O/W-Emulgatoren) in einer Gesamtkonzentration von 0,05 bis 5,0 Gew.-% und bevorzugt in einer Gesamtkonzentration von 2,0 bis 4,0 Gew.-%, jeweils bezogen auf das Gesamtgewicht der Emulsion, beträgt. According to the invention, it is advantageous if the emulsion contains one or more oil-in-water emulsifiers (O / W emulsifiers) in a total concentration of 0.05 to 5.0% by weight and preferably in a total concentration of 2.0 to 4.0% by weight, based in each case on the total weight of the emulsion.
Es ist erfindungsgemäß besonders vorteilhaft, wenn die erfindungsgemäße Emulsion dadurch gekennzeichnet ist, dass der Gehalt an einem oder mehreren anionischen Emulga toren in der Emulsion von 0,001 bis 5,0 Gew.-% und bevorzugt zwischen 0,05 und According to the invention it is particularly advantageous if the emulsion according to the invention is characterized in that the content of one or more anionic emulsifiers in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and
2 Gew.-%, besonders bevorzugt zwischen 0,1 und 1 ,0 Gew.-%, jeweils bezogen auf das Gesamtgewicht der Emulsion, beträgt. 2% by weight, particularly preferably between 0.1 and 1.0% by weight, based in each case on the total weight of the emulsion.
Es ist erfindungsgemäß besonders vorteilhaft, wenn die erfindungsgemäße Emulsion dadurch gekennzeichnet ist, dass der Gehalt an einem oder mehreren nichtionischen Emul gatoren in der Emulsion von 0,001 bis 5,0 Gew.-% und bevorzugt zwischen 0,05 und According to the invention it is particularly advantageous if the emulsion according to the invention is characterized in that the content of one or more nonionic emulsifiers in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and
3 Gew.-%, besonders bevorzugt zwischen 0,1 und 2 Gew.-%, jeweils bezogen auf das Ge samtgewicht der Emulsion, beträgt. 3% by weight, particularly preferably between 0.1 and 2% by weight, in each case based on the total weight of the emulsion.
Es ist erfindungsgemäß besonders vorteilhaft, wenn die erfindungsgemäße Emulsion dadurch gekennzeichnet ist, dass der Gehalt an einem oder mehreren hydrophilen UV- Filtersubstanzen in der Emulsion von 0,001 bis 5,0 Gew.-% und bevorzugt zwischen 0,05 und 3 Gew.-%, besonders bevorzugt zwischen 0,1 und 2 Gew.-%, jeweils bezogen auf das Gesamtgewicht der Emulsion, beträgt. According to the invention, it is particularly advantageous if the emulsion according to the invention is characterized in that the content of one or more hydrophilic UV filter substances in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and 3% by weight , particularly preferably between 0.1 and 2% by weight, based in each case on the total weight of the emulsion.
Vorteilhafte hydrophile UV-A-Filtersubstanzen im Sinne der vorliegenden Erfindung sind z. B. die Salze der 2-Phenylbenzimidazol-5-sulfonsäure, wie ihr Natrium-, Kalium- oder ihr Trietha- nolammonium-Salz, sowie die Sulfonsäure selbst; ferner die Phenylen-1 ,4-bis-(2-benzimi- dazyl)-3,3’-5,5’-tetrasulfonsäure Advantageous hydrophilic UV-A filter substances for the purposes of the present invention are, for. B. the salts of 2-phenylbenzimidazole-5-sulfonic acid, such as their sodium, potassium or their trietha nolammonium salt, as well as the sulfonic acid itself; also phenylene-1,4-bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid
und ihre Salze, besonders die entsprechenden Natrium-, Kalium- oder Triethanolammonium- Salze, insbesondere das Phenylen-1 ,4-bis-(2-benzimidazyl)-3,3’-5,5’-tetrasulfonsäure-bis- natriumsalz and their salts, especially the corresponding sodium, potassium or triethanolammonium salts, especially the phenylene-1,4-bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid-bis-sodium salt
mit der INCI-Bezeichnung Bisi idazylate, welches beispielsweise unter der Handelsbe zeichnung Neo Heliopan AP bei Haarmann & Reimer erhältlich ist. with the INCI name Bisi idazylate, which is available from Haarmann & Reimer, for example, under the trade name Neo Heliopan AP.
Ferner vorteilhaft sind das 1 ,4-di(2-oxo-10-Sulfo-3-bornylidenmethyl)-Benzol und dessen Salze (besonders die entprechenden 10-Sulfato-verbindungen, insbesondere das ent sprechende Natrium-, Kalium- oder Triethanolammonium-Salz), das auch als Benzol-1 ,4- di(2-oxo-3-bornylidenmethyl-10-sulfonsäure) bezeichnet wird und sich durch die folgende Struktur auszeichnet: 1,4-di (2-oxo-10-sulfo-3-bornylidenemethyl) benzene and its salts (especially the corresponding 10-sulfato compounds, especially the corresponding sodium, potassium or triethanolammonium salt) are also advantageous ), which is also known as benzene-1,4-di (2-oxo-3-bornylidenemethyl-10-sulfonic acid) and is characterized by the following structure:
Es ist erfindungsgemäß vorteilhaft, wenn die erfindungsgemäße Emulsion dadurch gekenn zeichnet ist, dass als O/W-Emulgatoren hydrophile Emulgatoren mit einem HLB-Wert von größer/gleich 8 eingesetzt werden. Der HLB-Wert von Emulgatoren kann dabei den üblichen Standartwerken (z. B. Fiedler, Lexikon der Hilfsstoffe für Pharmazie, Kosmetik und angren zende Gebiete, Editio Cantor Verlag, Aulendorf) entnommen werden. It is advantageous according to the invention if the emulsion according to the invention is characterized in that hydrophilic emulsifiers with an HLB value of greater than or equal to 8 are used as O / W emulsifiers. The HLB value of emulsifiers can be found in the usual standard works (e.g. Fiedler, Lexicon of Auxiliaries for Pharmacy, Cosmetics and Neighboring Areas, Editio Cantor Verlag, Aulendorf).
Es ist erfindungsgemäß bevorzugt, wenn die erfindungsgemäße Emulsion dadurch gekenn zeichnet ist, dass als O/W-Emulgatoren Glycerylstearatcitrat (CAS 39175-72-9, INCI Glyceryl Stearate Citrate, z. B. Imwitor 370 der Firma Hüls), Polyglyceryl-3 Methylglucosedistearat (INCI Polyglyceryl Methyl Glucose Distearate, z. B. Tego Care 450 der Firma Evonik) und/oder Polyethylenglycol(2000)monostearat (INCI; PEG-40 stearate) eingesetzt werden. It is preferred according to the invention if the emulsion according to the invention is characterized in that, as O / W emulsifiers, glyceryl stearate citrate (CAS 39175-72-9, INCI Glyceryl Stearate Citrate, e.g. Imwitor 370 from Hüls), polyglyceryl-3 methylglucose distearate (INCI Polyglyceryl Methyl Glucose Distearate, e.g. Tego Care 450 from Evonik) and / or polyethylene glycol (2000) monostearate (INCI; PEG-40 stearate) can be used.
In einer erfindungsgemäß bevorzugten Ausführungsform enthält die erfindungsgemäße Emulsion Kalium Cetylphosphat, Natrium Cetearylsulfat, Natrium Stearylglutamat, Alkalisal ze von gesättigten Fettsäuren der Kettenlänge C14-C22, insbesondere Natrium Stearat als anionischen Emulgator. In a preferred embodiment according to the invention, the emulsion according to the invention contains potassium cetyl phosphate, sodium cetearyl sulfate, sodium stearyl glutamate, alkali salts of saturated fatty acids of chain length C14-C22, in particular sodium stearate, as an anionic emulsifier.
In einer weiteren erfindungsgemäß bevorzugten Ausführungsform enthält die erfindungsge mäße Emulsion einen oder mehrere Polyglycerylfettsäureester als nichtionische Emulgato ren. Der erfindungsgemäß besonders bevorzugte Polyglycerylfettsäureester ist dabei Poly- glyceryl-10 Stearat (INCI Polyglyceryl-10 Stearate). In a further embodiment preferred according to the invention, the emulsion according to the invention contains one or more polyglyceryl fatty acid esters as nonionic emulsifiers. The polyglyceryl fatty acid ester particularly preferred according to the invention is polyglyceryl-10 stearate (INCI polyglyceryl-10 stearate).
Es ist erfindungsgemäß besondersvorteilhaft, wenn die erfindungsgemäße Emulsion dadurch gekennzeichnet ist, dass der Gehalt an ein oder mehreren anionischen Emulgatoren in der Emulsion von 0,001 bis 5,0 Gew.-% und bevorzugt zwischen 0,05 und 2 Gew.-%, be sonders bevorzugt zwischen 0,1 und 1 ,0 Gew.-%, jeweils bezogen auf das Gesamtgewicht der Emulsion, beträgt. It is particularly advantageous according to the invention if the emulsion according to the invention is characterized in that the content of one or more anionic emulsifiers in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and 2% by weight, particularly is preferably between 0.1 and 1.0% by weight, based in each case on the total weight of the emulsion.
Es ist erfindungsgemäß besonders vorteilhaft, wenn die erfindungsgemäße Emulsion dadurch gekennzeichnet ist, dass der Gehalt an ein oder mehreren nichtionischen Emulgato ren, insbesondere einen oder mehrere Polyglycerylfettsäureester, besonders Polyglyceryl-10 Stearat in der Emulsion von 0,001 bis 5,0 Gew.-% und bevorzugt zwischen 0,05 und According to the invention, it is particularly advantageous if the emulsion according to the invention is characterized in that the content of one or more nonionic emulsifiers, in particular one or more polyglyceryl fatty acid esters, especially polyglyceryl-10 stearate, in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and
3 Gew.-%, besonders bevorzugt zwischen 0,1 und 2,0 Gew.-%, jeweils bezogen auf das Gesamtgewicht der Emulsion, beträgt. 3% by weight, particularly preferably between 0.1 and 2.0% by weight, based in each case on the total weight of the emulsion.
Die erfindungsgemäße Emulsion kann die Konsistenz einer Salbe, Creme oder dünnflüssi gen Lotion aufweisen bzw. eine Salbe, Creme oder dünnflüssige Lotion darstellen. Es ist erfindungsgemäß bevorzugt, wenn das erfindungsgemäße Verfahren in Form des Hot- Hot-Verfahrens durchgeführt wird. Bei diesem Verfahren werden eine heiße Öl- und Was serphase miteinander vereinigt. The emulsion according to the invention can have the consistency of an ointment, cream or low-viscosity lotion or represent an ointment, cream or low-viscosity lotion. It is preferred according to the invention if the process according to the invention is carried out in the form of the hot-hot process. In this process, a hot oil and water phase are combined with one another.
Dabei ist es erfindungsgemäß besonders bevorzugt, wenn das Verfahren bei einer Tempera tur nicht über 85 °C durchgeführt wird. It is particularly preferred according to the invention if the process is carried out at a temperature not above 85.degree.
Die Emulsion kann erfindungsgemäß vorteilhaft als Salbe, Creme oder Lotion (ggf. sprühbar) vorliegen. According to the invention, the emulsion can advantageously be in the form of an ointment, cream or lotion (optionally sprayable).
Die Emulsion kann erfindungsgemäß vorteilhaft auch als Spray oder als Tränkungsmedium für ein Pflaster oder Tuch eingesetzt werden. Daher sind auch Pflaster und Tücher getränkt mit der erfindungsgemäßen Emulsion, erfindungsgemäß. According to the invention, the emulsion can advantageously also be used as a spray or as a soaking medium for a plaster or cloth. Therefore, plasters and tissues soaked with the emulsion according to the invention are also according to the invention.
Die Wasserphase der erfindungsgemäßen Emulsion kann vorteilhaft übliche kosmetische Hilfsstoffe enthalten, wie beispielsweise Alkohole, insbesondere solche niedriger C-Zahl, vorzugsweise Ethanol und/oder Isopropanol, Diole oder Polyole niedriger C-Zahl sowie de ren Ether, vorzugsweise Propylenglykol, Glycerin, Ethylenglykol, Ethylenglykolmonoethyl- oder -monobutylether, Hexandiol, Octandiol, Glycerylcaprylat, Ethylhexylglycerin, Methylpro- pandiol, Propylenglykolmonomethyl, -monoethyl- oder -monobutylether, Diethylenglykolmo- nomethyl- oder monoethylether, und analoge Produkte, außerdem Phenoxyethanol, Hydro- xyacetophenone, Benzylalkohol, Benzethonium Chlorid, Polymere, Schaumstabilisatoren, Elektrolyte, Selbstbräuner, Repellentien sowie insbesondere ein oder mehrere Verdickungs mittel, welches oder welche vorteilhaft gewählt werden können aus der Gruppe der Polysac charide bzw. deren Derivate, z.B. Xanthangummi, Carrageenan, Gellangummi, Stärken und Cellulosen, Hyaluronsäure. The water phase of the emulsion according to the invention can advantageously contain conventional cosmetic auxiliaries, such as alcohols, in particular those with a low carbon number, preferably ethanol and / or isopropanol, diols or polyols with a low carbon number, and their ethers, preferably propylene glycol, glycerol, ethylene glycol, ethylene glycol monoethyl - or monobutyl ether, hexanediol, octanediol, glyceryl caprylate, ethylhexylglycerol, methylpropanediol, propylene glycol monomethyl, monoethyl or monobutyl ether, diethylene glycol monomethyl or monoethyl ether, and analogous products, as well as phenoxyethanol, hydrochloride, benzethylacetophenol, benzethonium alcohol , Foam stabilizers, electrolytes, self-tanners, repellants and, in particular, one or more thickening agents, which or which can advantageously be selected from the group of polysaccharides or their derivatives, eg Xanthan gum, carrageenan, gellan gum, starches and celluloses, hyaluronic acid.
Die erfindungsgemäße Ölphase kann alle herkömmlichen Bestandteile von in der Kosmetik eingesetzten Öl-, Fett- und Wachskomponenten enthalten. The oil phase according to the invention can contain all conventional constituents of oil, fat and wax components used in cosmetics.
Die erfindungsgemäße Emulsion kann erfindungsgemäß vorteilhaft kosmetische Wirk- und Pflegestoffe enthalten, beispielsweise die nach der Kosmetikverordnung zugelassenen UV- Lichtschutzfilter. Derartige Wirkstoffe können erfindungsgemäß vorteilhaft in Konzentrationen von 0,01 bis 30 Gew.-%, bezogen auf das Gesamtgewicht der Zubereitung in dieser enthal ten sein. Als weitere Pflegestoffe können insbesondere Niacinamid, Panthenol, Aloe vera, Vitamin E, Vitamin A, Vitamin A-Derivate, Retinylpalmitat, Vitamin C, Vitamin C-Derivate, Ascorbylp- hosphat, Ascorbylpalmitat, Harnstoff, Taurin, Folsäure, Aminosäuren (z.B. Glycin, Histidin, Alanin, Arginin), Dipeptide (z.B. Carnosin), ungesättigte Fettsäuren und deren Ester, insbe sondere Di- und Triglyceride (z.B. g-Linolensäure, Linolsäure, Ölsäure), Mannose, Magnolia Rindenextrakt, Magnolol, Honokiol, Glycyrrhetinsäure in Konzentrationen von 0,001 bis 5 Gew.-%, bezogen auf das Gesamtgewicht der Zubereitung eingesetzt werden. According to the invention, the emulsion according to the invention can advantageously contain cosmetic active and care substances, for example the UV light protection filters approved according to the Cosmetics Ordinance. According to the invention, such active ingredients can advantageously be contained therein in concentrations of 0.01 to 30% by weight, based on the total weight of the preparation. As further care substances, niacinamide, panthenol, aloe vera, vitamin E, vitamin A, vitamin A derivatives, retinyl palmitate, vitamin C, vitamin C derivatives, ascorbyl phosphate, ascorbyl palmitate, urea, taurine, folic acid, amino acids (e.g. glycine, Histidine, alanine, arginine), dipeptides (e.g. carnosine), unsaturated fatty acids and their esters, in particular special di- and triglycerides (e.g. g-linolenic acid, linoleic acid, oleic acid), mannose, magnolia bark extract, magnolol, honokiol, glycyrrhetinic acid in concentrations of 0.001 up to 5% by weight, based on the total weight of the preparation.
Erfindungsgemäß besonders bevorzugt enthält die erfindungsgemäße Zubereitung als weite re Bestandteile Alpha-Hydroxysäuren und/oder deren Salze. Dabei werden erfindungsgemäß bevorzugt Milchsäure/Lactate oder Zitronensäure/Citrate in einer Konzentration von 0,01 bis 5 Gew.-%, bezogen auf das Gesamtgewicht der Zubereitung eingesetzt. According to the invention, the preparation according to the invention particularly preferably contains alpha-hydroxy acids and / or salts thereof as further constituents. According to the invention, lactic acid / lactates or citric acid / citrates are preferably used in a concentration of 0.01 to 5% by weight, based on the total weight of the preparation.
Die erfindungsgemäße Zubereitung kann Parfümstoffe in beliebiger Zusammensetzung und Menge enthalten. The preparation according to the invention can contain perfumes in any desired composition and amount.
Die nachfolgenden Beispiele sollen die vorliegende Erfindung verdeutlichen ohne sie einzu schränken. Die Angaben beziehen sich stets auf Gew.-%, sofern nicht andere Angaben ge macht werden. The following examples are intended to illustrate the present invention without restricting it. The data always relate to% by weight, unless otherwise stated.
Rezepturbeispiele Recipe examples
pH 7,0 pH 7.0
pH 7,0 pH 7.0

Claims

Patentansprüche Claims
1. Kosmetische ÖI-in-Wasser-Emulsionen (O/W-Emulsionen) enthaltend neben einer Wasserphase eine oder mehrere darin dispergierte Ölphasen sowie 1. Cosmetic oil-in-water emulsions (O / W emulsions) containing one or more oil phases dispersed therein in addition to a water phase
a) Skleroglucan a) scleroglucan
und and
b) ein oder mehrere hydrophile UV-Filtersubstanzen. b) one or more hydrophilic UV filter substances.
2. O/W-Emulsionen nach Anspruch 1 , dadurch gekennzeichnet, dass der Gehalt an Skleroglucan in der Emulsion von 0,01 bis 1 ,0 Gew.-%, bezogen auf das Gesamtge wicht der Emulsion, beträgt. 2. O / W emulsions according to claim 1, characterized in that the content of scleroglucan in the emulsion is from 0.01 to 1, 0 wt .-%, based on the total weight of the emulsion.
3. O/W-Emulsionen nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass der Gehalt an einem oder mehreren hydrophilen UV-Filtersubstanzen in der Emulsion von 0,001 bis 5,0 Gew.-% und bevorzugt zwischen 0,05 und 3 Gew.-%, be sonders bevorzugt zwischen 0,1 und 2,0 Gew.-%, jeweils bezogen auf das Gesamtge wicht der Emulsion, beträgt. 3. O / W emulsions according to one of the preceding claims, characterized in that the content of one or more hydrophilic UV filter substances in the emulsion of 0.001 to 5.0 wt .-% and preferably between 0.05 and 3 wt. -%, particularly preferably between 0.1 and 2.0% by weight, based in each case on the total weight of the emulsion.
4. O/W-Emulsionen nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass die hydrophile UV-A-Filtersubstanz oder die -Substanzen gewählt wird oder wer den aus der Gruppe der Salze der 2-Phenylbenzimidazol-5-sulfonsäure, wie ihr Natri um-, Kalium- oder ihr Triethanolammonium-Salz, sowie der Sulfonsäure selbst; ferner der Phenylen-1 ,4-bis-(2-benzimidazyl)-3,3’-5,5’-tetrasulfonsäure 4. O / W emulsions according to one of the preceding claims, characterized in that the hydrophilic UV-A filter substance or substances is selected or who is selected from the group of salts of 2-phenylbenzimidazole-5-sulfonic acid, such as sodium um, potassium or its triethanolammonium salt, as well as the sulfonic acid itself; also phenylene-1,4-bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid
und ihrer Salze, besonders der entsprechenden Natrium-, Kalium- oder Triethanolam- monium-Salze, insbesondere des Phenylen-1 ,4-bis-(2-benzimidazyl)-3,3’-5,5’-tetrasul- fonsäure-bis-natriumsalzes mit der INCI-Bezeichnung Bisimidazylate, bzw des das 1 ,4-di(2-oxo-10-Sulfo-3- bornylidenmethylj-Benzols und dessen Salzen (besonders die entprechenden 10- Sulfato-verbindungen, insbesondere das entsprechende Natrium-, Kalium- oder Tri- ethanolammonium-Salz), das auch als Benzol- 1 ,4-di(2-oxo-3-bornylidenmethyl- 10- sulfonsäure) (INCI: Terephthalylidene dicamphor sulfonic acid) bezeichnet wird und sich durch die folgende Struktur auszeichnet: and their salts, especially the corresponding sodium, potassium or triethanolammonium salts, especially phenylene-1,4-bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid-bis -sodium salt with the INCI name bisimidazylate, or the 1,4-di (2-oxo-10-sulfo-3-bornylidenemethylj-benzene and its salts (especially the corresponding 10 sulfato compounds, in particular the corresponding sodium, potassium or triethanolammonium salt), which is also known as benzene-1,4-di (2-oxo-3-bornylidenemethyl-10-sulfonic acid) (INCI: Terephthalylidene dicamphor sulfonic acid) and is characterized by the following structure:
5. O/W-Emulsionen nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass die Emulsion einen oder mehrere ÖI-in-Wasser-Emulgatoren (O/W- Emulgatoren) in einer Gesamtkonzentration von 0,05 bis 5,0%, bezogen auf das Ge samtgewicht der Emulsion, beträgt. 5. O / W emulsions according to one of the preceding claims, characterized in that the emulsion is based on one or more oil-in-water emulsifiers (O / W emulsifiers) in a total concentration of 0.05 to 5.0% on the total weight of the emulsion.
6. O/W-Emulsionen nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass der Gehalt an einem oder mehreren anionischen Emulgatoren in der Emulsion von 0,001 bis 5,0 Gew.-% und bevorzugt zwischen 0,05 und 2 Gew.-%, besonders bevorzugt zwischen 0, 1 und 1 ,0 Gew.-%, jeweils bezogen auf das Gesamtgewicht der Emulsion, beträgt. 6. O / W emulsions according to one of the preceding claims, characterized in that the content of one or more anionic emulsifiers in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and 2% by weight , particularly preferably between 0.1 and 1.0% by weight, based in each case on the total weight of the emulsion.
7. O/W-Emulsionen nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass der Gehalt an einem oder mehreren nichtionischen Emulgatoren in der Emulsion von 0,001 bis 5,0 Gew.-% und bevorzugt zwischen 0,05 und 3 Gew.-%, besonders bevorzugt zwischen 0, 1 und 2,0 Gew.-%, jeweils bezogen auf das Gesamtgewicht der Emulsion, beträgt. 7. O / W emulsions according to one of the preceding claims, characterized in that the content of one or more nonionic emulsifiers in the emulsion is from 0.001 to 5.0% by weight and preferably between 0.05 and 3% by weight , particularly preferably between 0.1 and 2.0% by weight, based in each case on the total weight of the emulsion.
8. O/W-Emulsionen nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass als O/W-Emulgatoren hydrophile Emulgatoren mit einem HLB-Wert von grö ßer/gleich 8 eingesetzt werden. 8. O / W emulsions according to one of the preceding claims, characterized in that hydrophilic emulsifiers with an HLB value of greater than / equal to 8 are used as O / W emulsifiers.
9. O/W-Emulsionen nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass als O/W-Emulgatoren Polyglyceryl-3 Methylglucosedistearat (z. B. Tego Care 450 der Firma Evonik), Kalium Cetylphosphate, Natrium Cetearylsulfat, Natrium Stea- rylglutamat, Kalium Cetylphosphate, Glycerylstearatcitrat, Alkalisalze von gesättigten Fettsäuren der Kettenlänge C14-C22, insbesondere Natrium Stearat und/oder Po- lyethylglycolester von gesättigten Fettsäuren wie zum Beispiel Polyethylengly- col(2000)monostearat (INCI; PEG-40 stearate) und PEG-100 stearat eingesetzt wer den. 9. O / W emulsions according to any one of the preceding claims, characterized in that the O / W emulsifiers are polyglyceryl-3 methylglucose distearate (e.g. Tego Care 450 from Evonik), potassium cetyl phosphate, sodium cetearyl sulfate, sodium stearyl glutamate , Potassium cetyl phosphate, glyceryl stearate citrate, alkali salts of saturated fatty acids of chain length C14-C22, in particular sodium stearate and / or polyethylglycol esters of saturated fatty acids such as polyethylene glycol (2000) monostearate (INCI; PEG-40 stearate) and PEG-100 stearate are used.
10. O/W-Emulsionen nach einem der vorstehenden Ansprüche, dadurch gekennzeichnet, dass als O/W-Emulgatoren ein oder mehrere Polyglycerylfettsäureester gewählt wer den, insbesondere bevorzugt Polyglyceryl-10 Stearat. 10. O / W emulsions according to any one of the preceding claims, characterized in that one or more polyglyceryl fatty acid esters are selected as O / W emulsifiers, particularly preferably polyglyceryl-10 stearate.
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WO2008155382A2 (en) * 2007-06-20 2008-12-24 Henkel Ag & Co. Kgaa Cosmetic stick based on a congealed oil-in-water dispersion/emulsion having a hydrogel former
US20140004058A1 (en) * 2012-06-28 2014-01-02 Johnson & Johnson Consumer Companies, Inc. Sunscreen compositions containing an ultraviolet radiation-absorbing polyester
WO2015066194A1 (en) * 2013-10-29 2015-05-07 Mary Kay Inc. Cosmetic compositions
DE102014015554A1 (en) 2014-10-22 2016-04-28 Beiersdorf Ag Polysaccharide-containing sunscreens with reduced tendency to textile staining
JP2016117666A (en) * 2014-12-19 2016-06-30 ロレアル Non-adhesive stable composition

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