DE10307467A1 - Stabilized and non-sticky cosmetic and dermatological emulsions contain siloxane elastomers in addition to surfactants and pigments - Google Patents

Abstract

Cosmetic and dermatological emulsions contain (A) one or more surfactants; (B) one or more pigmentary organic substances; and (C) one or more siloxane elastomers.

Description

The present invention relates to cosmetic and dermatological emulsions containing organic Solids and surfactants and a method for stabilization of such emulsions.

Cosmetic preparations are mainly used to care for the skin. As the largest human organ, the human skin performs numerous vital functions. With an average surface area of around 2 m ² in adults, it has an outstanding role as a protective and sensory organ. Among its many functions (for example for heat regulation), the most important is the barrier function that prevents the skin (and ultimately the entire organism) from drying out. At the same time, the skin acts as a protective device against the penetration and absorption of external substances (e.g. dirt, chemicals, microorganisms). It also has an important role as a regulatory and target organ in human metabolism.

The cosmetic skin care serves primarily to the natural Function of the skin as a barrier against environmental influences and against the loss of endogenous Fabrics (in addition to water, also natural Fats, electrolytes etc.) or restore.

The aim of skin care is also to that by daily Washing to compensate for the loss of fat and water in the skin. This is especially important when the natural regeneration ability is not sufficient. Moreover skin care products are intended to protect against environmental influences, especially from the sun and wind, protect and delay skin aging.

The harmful effects of the ultraviolet Part of the solar radiation on the skin is generally known. In dependence from their respective wavelength the rays have different effects on the organ skin: the So-called UV-C radiation with a wavelength that is less than 290 nm is absorbed by the ozone layer in the earth's atmosphere and has none physiological importance. In contrast, cause rays in the area between 290 nm and 320 nm, the so-called UV-B range, an erythema, a simple sunburn or even more or less severe Burns. UV-A radiation (320 to 400 nm) is more photodynamic in terms of triggering, special phototoxic reactions and chronic changes in the skin dangerous as UV-B radiation. So even the UV-A radiation is enough normal everyday conditions to quickly reduce the collagen and damage elastin fibers. Also the injurious one Influence of UV-B radiation can be intensified by UV-A radiation.

Furthermore, very low doses of radiation can be generated trigger photochemical reactions. Which also includes especially the formation of free radicals, which in turn are due to their high reactivity can trigger uncontrolled subsequent reactions. To such reactions can prevent cosmetic or dermatological formulations in addition to UV filter substances additionally Antioxidants and / or radical scavengers added become.

Medical topical compositions usually contain one or more drugs in effective Concentration. For the sake of simplicity, it becomes a clear distinction between cosmetic and medical application and corresponding Products on the legal provisions of the Federal Republic of Germany referenced (e.g. cosmetics regulation, food and drug law).

By far the most important product type in the area of skin care products are emulsions. Emulsions are disperse two- or multi-phase systems, whereby cosmetic emulsions from at least one fat phase (fats and mineral oils, fatty acid esters, Fatty alcohols etc.) and at least one water phase (water, glycerin, Glycols, etc.) are made with the help of emulsifiers in the finest form droplet can be distributed into each other. If the oil phase is finely distributed in the Water phase, it is an oil-in-water emulsion (O / W emulsion, z. B. milk). The basic character of an O / W emulsion is characterized by the water, i. H. it is less greasy on the skin, is rather mattifying and is absorbed into the skin faster than a W / O emulsion.

Although emulsions from the thermodynamic From a standpoint, systems are unstable, cosmetic ones succeed To produce emulsions with years of stability. An emulsion is said to be stable if over a given period of time no measurable away temporal and local changes the drop size distribution have it determined.

The stability or instability of emulsions depends on various factors. For one, the water phase, for example, tends a W / O emulsion because the water and oil phases have different densities have sedimentation. The oil phase an O / W emulsion accordingly has a tendency to record.

Furthermore, droplet aggregation can occur between the finely divided droplets of the disperse phase due to the attractive forces, the individual droplets of an aggregate initially remaining separated from one another by a thin film of continuous phase. The original drop size ver The division changes only apparently and can be restored by stirring or shaking.

However, the touching droplet Furthermore also flow together resulting in a real change the drop size distribution leads, which can only be changed by adding energy. This process is called coalescence. The process of coalescence runs all the more slower, the more viscous the outer phase the emulsion is.

The processes described can be done individually or run together. One process often initiates or reinforces the other. So z. B. by the formation of aggregates in O / W emulsions the recording of the oil phase accelerated. The disperse state of an emulsion goes partially or even completely lost, the two phases separate, and one speaks of breaking the emulsion.

To stabilize emulsions over a longer Accordingly, aids are needed over a period of time that prevent the two phases from separating, at least in this way long delay until the emulsion fulfills its purpose Has.

On the one hand, these tools should the interface stabilize by preventing the droplets of the disperse phase flow together. Ideally, these substances also cause a rejection of the Droplet, which prevents that approximate these, so that one Aggregation (aggregate formation) can be avoided.

On the other hand, auxiliary substances are used used to counteract the creaming or sedimentation of the phases.

Emulsifiers are surface-active Substances capable of interfacial tension between the oil and water phases to decrease by preferentially at the interface between these two. This is due to their amphiphilic molecular structure allows: Emulsifiers have at least one polar (hydrophilic) group and at least one non-polar (lipophilic) group. With that they are soluble in both the hydrophilic and lipophilic phases. The Part that is more soluble in the corresponding phase projects into it and thereby reduces the interfacial tension between the two phases.

Trying to classify Emulsifiers are difficult because they are chemically very different Categories belong. The faster an emulsifier lowers the interfacial tension, the more effective it is and the lower the equilibrium value of the interfacial tension is.

In addition, emulsifiers stabilize also through the formation of interface films and thus "physical" barriers, whereby aggregation and coalescence of the emulsified particles is prevented. Due to the deposition of the emulsifier on the interface the droplets either charged so they repel each other, or it becomes a stable, often highly viscous or even solid protective layer around the droplets educated.

• – feinste Verteilung der beiden Phasen ineinander Je kleiner die dispergierten Teilchen sind, umso stabiler ist die Emulsion.
• – hohe Viskosität der äußeren Phase
• – ein stabiler Grenzflächenfilm
• – ein ausgewogenes Phasenvolumenverhältnis

However, the use of one or more emulsifiers is generally not sufficient for the practical production of cosmetic or dermatological emulsions. Essential factors for the stability of cosmetic or dermatological preparations are also:

• Finest distribution of the two phases into one another The smaller the dispersed particles, the more stable the emulsion.
• - high viscosity of the outer phase
• - a stable interfacial film
• - a balanced phase volume ratio

The emulsifier system must therefore mostly additional contain another component for the actual emulsifier, as a co-emulsifier, stabilizer or depending on the mechanism of action also as a consistency agent, thickener or protective colloid etc. referred to as.

Through these substances, in the following The stability of an emulsion is called stabilizers for the sake of simplicity elevated. Stabilizers need not surface active, can but be amphiphilic connections.

One way to stabilize emulsions is to increase the viscosity of the outer phase according to the above. This Viscosity increase causes usually a significant decrease in mobility dispersed droplets, whereby the sedimentation or creaming speed is reduced. Along with this, the droplets also meet less frequently, which results in a lower tendency to coalesce.

The viscosity of the outer phase can be for example by adding thickeners, which z. B. gels and / or lamellar liquid crystals form. In principle, emulsifiers are also able to Formation of emulsifier gel networks to increase the viscosity of a liquid. Indeed will do this a comparatively high amount of emulsifier is required because gel networks are then be formed when using the entire interface between the phases emulsifier molecules is occupied.

Breakage of an emulsion can also be prevented by choosing an appropriate phase volume ratio. To illustrate this fact, consider an emulsion as a system made of metal balls same diameter (inner phase) and a liquid (outer phase). In this simple model, sedimentation or creaming can no longer take place if the entire liquid is filled with metal balls. This is - assuming a densest packing of spheres as a distribution - the case with a ratio of 1: 2, ie if 2/3 of the emulsion consists of an internal phase. It is evident that the viscosity of an emulsion increases with an increasing proportion of the inner phase, since this limits the mobility of the dispersed droplets.

Of course, the expert is one Variety of possibilities known, stable emulsions for cosmetic or dermatological Formulate application, for example in the form of creams and Ointments that are spreadable from room to skin temperature, or as lotions and milks that tend to be in this temperature range are flowable. In addition to choosing the "right" emulsifier or emulsifier system, this is particularly important also on the further composition of the preparation.

A disadvantage of emulsions, however, is their lack of stability across from higher Concentrations of surfactants, which manifests itself, for example, in a phase separation. The The state of the art knows surfactant-containing preparations based on emulsions. However, these are common formulated in such a way that the Emulsion first stabilized with emulsifiers and then a surfactant system is adapted. Since emulsions are generally destroyed by the addition of surfactants, the choice of surfactant system and the preparations obtained are severely restricted are based on expensive and complicated recipes.

Often the emulsion destroying effect of the surfactants through further components of the emulsion - such as, for example (Organic) solids and the like - still increased.

On the other hand, it is often desirable use certain surfactants to reduce their other physical, to be able to use chemical or physiological properties.

An object of the present invention So it was cosmetic or dermatological emulsions - especially O / W emulsions - too find which opposite Surfactants - especially in combination with other emulsion-destroying substances - stable are.

• A. ein oder mehrere Tenside,
• B. eine oder mehrere pigmentäre organische Substanzen und
• C. ein oder mehrere Siloxanelastomere

den Nachteilen des Standes der Technik abhelfen würden.It has been shown to be surprising, and this is the solution to these problems that cosmetic and dermatological emulsions containing

• A. one or more surfactants,
• B. one or more pigmentary organic substances and
• C. one or more siloxane elastomers

would remedy the disadvantages of the prior art.

The preparations according to the present Invention are extremely satisfactory preparations in every respect, which is not limited to one Raw material selection are limited. Accordingly, they are quite suitable especially to as a basis for Forms of preparation with diverse To serve applications. The preparations according to the present Invention show very good sensory and cosmetic properties, such as the spreadability on the skin or the ability to draw into the skin. In particular, the preparations according to the invention are notable for excellent skin feel out. Leave emulsions with an excellent skin feel a velvety feeling and dry residue, which is not greasy, greasy or sticky.

oder auch durch Reaktion von Hydroxy-endständigem Dimethylpolysiloxan und Trimethylsiloxy-endständigem Methylpolysiloxan:

The use of solid elastomeric polyorganosiloxanes or organopolysiloxanes, hereinafter referred to as siloxane elastomers, in cosmetic preparations is known per se and has become increasingly important in recent years. In addition to their use in cosmetics, these substances were used in food and feed, pharmaceuticals, impregnating agents, lubricants and so on. Siloxal elastomers are partially or completely cross-linked and mostly have a three-dimensional structure. They are obtainable by a reaction of vinyl-terminated polymethylsiloxane and methylhydrodimethylsiloxane

or also by reaction of hydroxy-terminated dimethylpolysiloxane and trimethylsiloxy-terminated methylpolysiloxane:

These siloxane elastomers are, for example for setting the rheological properties of a preparation used. Such siloxane elastomers are described, for example in the European U.S. Patent No. 295,886 and U.S. Patent No. 5,266,321, which the use of these substances in facial cleansers or oils Reveal makeup products. Nature is also in these writings of the siloxane elastomers described. The siloxane elastomers are used in cosmetics Preparations especially because of their pleasant sensory Properties, the resulting products are considered velvety, powdery and / or described matting.

• (a) Siloxanelastomere, welche die Einheiten R₂SiO und RSiO_1,5 und/oder R₃SiO_0,5 und/oder SiO₂ enthalten, wobei die einzelnen Reste R jeweils unabhängig voneinander Wasserstoff, C_{1 -24}-Alkyl (wie beispielsweise Methyl, Ethyl, Propyl) oder Aryl (wie beispielsweise Phenyl oder Tolyl), Alkenyl (wie beispielsweise Vinyl) bedeuten und das Gewichtsverhältnis der Einheiten R₂SiO zu RSiO_1,5 aus dem Bereich von 1 : 1 bis 30 : 1 gewählt wird;
• (b) Siloxanelastomere, welche in Silikonöl unlöslich und quellfähig sind, die durch die Additionsreaktion eines Organopolysiloxans (1), das siliciumbebundenen Wasserstoff enthält, mit einem Organopolysiloxan (2), das ungesättigte aliphatische Gruppen enthält, erhältlich sind, wobei die verwendeten Mengenateile so gewählt werden, daß die Menge des Wasserstoffes des Organopolysiloxans (1) oder der ungesättigten aliphatischen Gruppen des Organopolysiloxans (2) – im Bereich von 1 bis 20 mol-% liegt, wenn das Organopolysiloxan nicht cyclisch ist und – im Bereich von 1 bis 50 mol-% liegt, wenn das Organopolysiloxan cyclisch ist.

The siloxane elastomer (s) according to the present invention are advantageously selected from one or more of the following groups:

• (a) Siloxane elastomers which contain the units R ₂ SiO and RSiO _1.5 and / or R ₃ SiO _0.5 and / or SiO ₂ , the individual radicals R each independently of one another being hydrogen, C _{1 -24} -alkyl (such as for example methyl, ethyl, propyl) or aryl (such as phenyl or tolyl), alkenyl (such as vinyl) and the weight ratio of the units R ₂ SiO to RSiO _{1.5 is selected} from the range from 1: 1 to 30: 1 ;
• (b) Siloxane elastomers which are insoluble and swellable in silicone oil and which can be obtained by the addition reaction of an organopolysiloxane (1) containing silicon-bonded hydrogen with an organopolysiloxane (2) containing unsaturated aliphatic groups, the proportions used being chosen so the amount of hydrogen of the organopolysiloxane (1) or the unsaturated aliphatic groups of the organopolysiloxane (2) - is in the range from 1 to 20 mol% if the organopolysiloxane is not cyclic and - in the range from 1 to 50 mol% % is when the organopolysiloxane is cyclic.

Advantageous in the sense of the present Invention are the or the siloxane elastomers in the form of spherical Powder or in the form of gels.

According to the invention advantageous in the form of spherical Powder present siloxane elastomers are those with the INCI name Dimethicone / Vinyl Dimethicone crosspolymer, for example that by DOW CORNING under the trade names DOW CORNING 9506 Powder available.

It is particularly preferred if the siloxane elastomer in combination with oils from hydrocarbons of animal and / or vegetable origin, synthetic oils, synthetic Esters, synthetic ethers or mixtures thereof is used.

It is very particularly preferred when the siloxane elastomer in combination with unbranched at room temperature liquid or pasty silicone oils or cyclic silicone oils or mixtures thereof are used. Are particularly advantageous Organopolysiloxane elastomers with the INCI name Polysilicone-11 in a mixture with dimethicone or dimethiconol, cyclomethicone, cyclopentasiloxane, especially those available from Grant Industries Inc. Gransil types GCM, GCM-5, DMG-6, CSE Gel, PM-Gel, LTX, ININ Gel, AM-18 Gel and / or DMCM fifth Elastomer blends with the INCI name Cyclomethicone are also preferred (and) Dimethicone crosspolymers, available from Dow Corning at the trade name Dow Corning 9040 and / or 9041 Silicone Elastomer blend.

The siloxane elastomers are also advantageous containing gels, which are sold under the trade names KSG-15, -16, -17, -18, -20 from Shin-Etsu or Gransil 5CYCgel, Gransil SR DMF 10gel, Gransil SR DC 556gel from Grant Chemical, SF 839, SF1204, JK113 from General Electric and Lauryl Dimeticon / Vinyldimethicon crosspolymers, as described under the designations KSG41, -42, -43, -44 by the company Shin-Etsu available are. Another advantageous siloxane elastomer is cyclomethicone + Vinyldimethicon / Methicon Crosspolymer or the chemically related Elastomer Crosslinked Stearyl Methyl Dimethyl Siloxane Elastomer, as for example by the company Grant Chemical under the Designation SR-CYC Tobe offered.

It is exceptionally preferred if the siloxane elastomer in the form of a gel made of siloxane elastomer and a lipid phase is used, the content of the siloxane elastomer in the gel is 1 to 80% by weight, preferably 0.1 to 60% by weight, in each case based on the total weight of the gel.

It is advantageous in the sense of the present Invention, the total amount of siloxane elastomers (active content) the range from 0.01 to 20% by weight, advantageously from 0.1 to 10% by weight, based on the total weight of the formulation.

Pigmentary organic substances (= organic pigments) for the purposes of the present invention are, for example, organic UV filter substances which are used in the finished cosmetic or dermatological Preparation present as solids.

gekennzeichnet ist und unter der Handelsbezeichnung Tinosorb^® M bei der CIBA-Chemikalien GmbH erhältlich ist.An advantageous organic pigment for the purposes of the present invention is 2,2'-methylene-bis- (6- (2H-benzotriazol-2-yl) -4- (1,1,3,3-tetramethylbutyl) phenol) [INCI : Methylene Bis-Benztriazolyl Tetramethylbutylphenol], which is characterized by the chemical structural formula

and is available under the trade name Tinosorb ^® M from CIBA-Chemicals GmbH.

According to the invention contain cosmetic or dermatological preparations 0.001 to 30 wt .-%, advantageously 0.05 up to 15% by weight, very particularly preferably 0.1 to 10% by weight of pigmentary organic Substances.

"Surfactant" in the sense of the present invention Amphiphilic substances are referred to as organic, non-polar substances dissolve in water can. They care, due to their specific molecular structure with at least one hydrophilic and one hydrophobic part of the molecule, for a reduction the surface tension of the water. There are anionic, cationic, amphoteric and non-ionic Surfactants that have different functional groups.

Anionic surfactants generally have carboxylate, sulfate or sulfonate groups as functional groups. In an aqueous solution they form negatively charged organic ions in an acidic or neutral environment. Cationic surfactants are characterized almost exclusively by the presence of a quaternary ammonium group. In aqueous solution they form positively charged organic ions in an acidic or neutral environment. Amphoteric surfactants contain both anionic and cationic groups and accordingly behave like anionic or cationic surfactants in aqueous solution depending on the pH. They have a positive charge in a strongly acidic environment and a negative charge in an alkaline environment. In the neutral pH range, however, they are zwitterionic, as the following example should illustrate:

Are typical for non-ionic surfactants Polyether chains. Non-ionic surfactants form in an aqueous medium no ions.

wobei R einen verzweigten oder unverzweigten Alkylrest mit 4 bis 24 Kohlenstoffatomen darstellt und wobei DP einen mittleren Glucosylierungsgrad von bis zu 2 bedeutet.Non-ionic surfactants are particularly advantageous for the purposes of the present invention. Non-ionic surfactants which are particularly advantageous according to the invention are characterized by the following chemical structure

where R is a branched or unbranched alkyl radical having 4 to 24 carbon atoms and where DP is an average degree of glucosylation of up to 2.

The value DP represents the degree of glucosylation of the alkyl glucosides used according to the invention and is defined as

Here, p ₁ , p ₂ , p ₃ ... and, p _{i represent} the proportion of single, double, triple ... i times glucosylated products in percentages by weight. Products with degrees of glucosylation of 1 - 2, in particular advantageous, are advantageous according to the invention 1.1 to 1.5, very particularly advantageously selected from approximately 1.3.

The value DP takes into account the fact that alkyl glucosides are usually mixtures of mono- and oligoglucosides due to their production. A relatively high content of monoglucosides, typically in the order of 40 to 70% by weight, based on the total weight of the mixture, is advantageous according to the invention.

R is advantageously selected from the group of unbranched alkyl radicals, the myristyl radical, the cetyl group, the stearyl group and the eicosyl group are preferred. Lauryl glucoside and cocoglucoside are preferred. Particularly preferred is decyl glucoside.

Alkyl glucosides (also: alkyl polyglycosides) used according to the invention can be obtained by processes such as those described in DE-OS 40 40 655 and other writings. They are commercially available from various manufacturers.

According to the invention contain cosmetic or dermatological preparations 0.001 to 15% by weight, advantageously 0.005 up to 5% by weight, very particularly preferably 0.01 to 1% by weight of surfactants.

The preparations in the sense of the present Invention can preferably one or more water phases in addition to one or more oil phases included and for example in the form of W / O, O / W, W / O / W or O / W / O emulsions are present. Such formulations can preferably also microemulsions, sticks, foams (so-called mousse), solid emulsions (i.e. emulsions stabilized by solids, e.g. B. Pickering emulsions) or sprayable emulsions.

Also (macroscopically) two or more phases Systems are advantageous according to the invention. "Two or multiphase "in the sense The present invention means that two or more phases are separate one above the other layered. It is particularly advantageous in the sense of present invention if at least one of the macroscopically visible Phases represents a (W / O, O / W, micro) emulsion. The emulsion will perceived as a phase in this (macroscopic) view, although of course to the professional it is known that emulsions itself formed from two or more phases homogenized with one another become. The "emulsion phase" is long-term stable, so that it also about a longer one Period (months, years) not to segregate respectively Phase separation comes within the emulsion.

The macroscopically visible phases or layers can be advantageous - for example by shaking - at short notice emulsify to a homogeneous emulsion, which is not long-term stable is, but rather about back to two or a period of minutes, hours or days more layered on top of each other Phases segregated. It is particularly advantageous in the sense of the present Invention if at least one of the macroscopically visible phases a microemulsion and at least one other the macroscopic visible phases an oil phase represents.

Sprayable emulsions, in particular microemulsions

Sprayable O / W emulsions, in particular, are particularly advantageous for the purposes of the present invention special O / W microemulsions.

The droplet diameters of the usual "simple", i.e. non-multiples Emulsions range from approx. 1 μm to approx. 50 μm. Such "macroemulsions" are without further coloring Additions, colored milky white and opaque. Finer "macro emulsions", their droplet diameter in the range of approx. 0.5 μm to approx. 1 μm lie, are, again without coloring Additions, bluish white colored and opaque. Such "macro emulsions" usually have one high viscosity.

The droplet diameter of microemulsions however, in the sense of the present invention lies in the range of about 50 to about 500 nm. Such microemulsions are colored bluish white to translucent and mostly low viscosity. The viscosity of many Microemulsions of the O / W type are comparable to that of water.

The advantage of microemulsions is that in the disperse phase active ingredients are present in much finer disperse can than in the disperse phase of "macroemulsions". Another advantage is, that you are sprayable due to their low viscosity. Become microemulsions Used as cosmetics, corresponding products are characterized high cosmetic elegance.

O / W microemulsions which are obtainable with the aid of so-called phase inversion temperature technology and contain at least one emulsifier (emulsifier A), which is selected from the group of emulsifiers with the following properties, are particularly advantageous according to the invention:
- Their lipophilicity depends on the temperature, such that the lipophilicity increases by increasing the temperature and the lipophilicity of the emulsifier decreases by lowering the temperature.

Advantageous emulsifiers A are e.g. B. polyethoxylated fatty acids (PEG-100 stearate, PEG-20 Stearate, PEG-150 Laurath, PEG-8 distearate and the like) and / or polyethoxylated fatty alcohols (Cetearath-12, Cetearath-20, Isoceteth-20, Beheneth-20, Laureth-9 etc.) and / or alkyl polyglycosides (cetearyl Glycoside, Stearyl Glycoside, Palmityl Glycoside etc.).

If the phase inversion essentially by varying the temperature are O / W emulsions, especially O / W microemulsions available, the size of the oil droplets in the essentially by the concentration of the emulsifier (s) used is determined in such a way that a higher Emulsifier concentration causes smaller droplets and fewer Emulsifier concentration leads to larger droplets. The Droplet sizes are usually between 20 and 500 nm.

In the sense of the present invention, it may be advantageous to use further W / O and / or O / W emulsifiers that do not fall under the definition of emulsifier A, for example to increase the water resistance of the preparations according to the present invention. Here z. B. alkyl methicone copolyols and / or alkyl dimethicone copolyols (in particular cetyl dimethicone copolyol, lauryl methicone copolyol), W / O emulsifiers (such as, for example, sorbitan stearate, glyceryl stearate, glycerol stearate, sorbitan oleate, lecithin, glyceryl isostearate 3-polyglycerol, polyglyceryl glyceryl, polyglyceryl glyceryl, polyglyceryl glyceryl, polyglyceryl glyceryl) -3 diisostearate, PEG-7 hydrogenated castor oil, polyglyceryl 4-isostearate, acrylate / C _10-30 alkyl acrylate crosspolymer, sorbitan isostearate, poloxamer 101, polyglyceryl-2-dipolyhydroxystearate, polyglyceryl-3-diisostearate, polyglyceryl-4-dip , PEG-30-dipolyhydroxystearate, diisostearoylpolyglyceryl-3-diisostearate, glycol distearate, polyglyceryl-3-dipolyhydroxystearate) and / or fatty acid esters of sulfuric or phosphoric acid (cetyl phosphate, trilaureth-4 phosphate, trioleth-8-phosphate, stearyl phosphate, etc.) ) be used.

Further advantageous sprayable O / W emulsions For the purposes of the present invention, low-viscosity cosmetic or dermatological Hydrodispersions, which have at least one oil phase and at least one Contain water phase, the preparation by at least one Gelling agent is stabilized and not necessarily emulsifiers must contain but can contain one or more emulsifiers.

Advantageous gel formers for such preparations are, for example, copolymers of C _10-30 alkyl acrylates and one or more monomers of acrylic acid, methacrylic acid or their esters. The INCI name for such compounds is "Acrylics / C 10-30 Alkyl Acrylate Crosspolymer". The Pemulen ^® types TR 1, TR 2 and TRZ from Goodrich (Noveon) are particularly advantageous.

Carbopole are also advantageous Gelling agent for such preparations. Carbopole are polymers of acrylic acid, in particular also acrylate-alkyl acrylate copolymers. Carbopole are advantageous e.g. types 907, 910, 934, 940, 941, 951, 954, 980, 981, 1342, 1382, 2984 and 5984. likewise the ETD types 2020, 2050 and Carbopol Ultrez 10. Other advantageous gelling agents for such Preparations are xanthan gum, cellulose derivatives and locust bean gum.

As possible (optional) emulsifiers can ethoxylated fatty alcohols or ethoxylated fatty acids (especially PEG-100 stearate, ceteareth-20) and / or other nonionic surfactants Substances are used.

• – mindestens einen Silikonemulgator (W/S) mit einem HLB-Wert ≤ 8 und/oder mindestens einen W/O-Emulgator mit einem HLB-Wert < 7 und
• – mindestens einen O/W-Emulgator mit einem HLB-Wert > 10 enthalten.

Furthermore, the very low viscosity to sprayable emulsions can also be W / O or water-in-silicone oil (W / S) emulsions. W / O or W / S emulsions are particularly advantageous

• - At least one silicone emulsifier (W / S) with an HLB value ≤ 8 and / or at least one W / O emulsifier with an HLB value <7 and
• - Contain at least one O / W emulsifier with an HLB value> 10.

Such preparations contain furthermore at least 20% by weight of lipids, the lipid phase being advantageous also silicone oils contain or even consist entirely of such.

The silicone emulsifier (s) can advantageously be selected from the group of alkyl methicon copolyols and / or alkyl dimethicone copolyols (e.g. dimethicone copolyols, which are available from Goldschmidt AG under the trade names ABIL ^® B 8842, ABIL ^® B 8843, ABIL ^® B 8847, ABIL ^® B 8851, ABIL ^® B 8852, ABIL ^® B 8863, ABIL ^® B 8873 and ABIL ^® B 88183, cetyl dimethicone copolyol [Goldschmidt AG / ABIL ^® EM 90], cyclomethicone dimethicone copolyol [Goldschmidt AG / ABIL ^® EM 97], lauryl [Dow Corning Ltd. / Dow Corning ^® 5200 Formulation Aid], octyl dimethicone ethoxy glucoside [Wacker].

The W / O emulsifier (s) with an HLB value of <7 can advantageously be selected from the following group: sorbitan stearate, sorbitan oleate, lecithin, glyceryl alcoholate, lanolin, hydrogenated castor oil, glyceryl isostearate, polyglyceryl 3-oleate, pentaerythrithyl isostearate, methylglucose dioleate Mixture with hydroxystearate and beeswax, PEG-7 hydrogenated castor oil, polyglyceryl 4-isostearate, hexyl laurate, acrylate / C _10-30 alkyl acrylate cross-polymer, sorbitan isostearate, polyglyceryl 2-dipolyhydroxystearate, polyglyceryl-3-diisostearate, PEG dipolyhydroxystearate, diisostearoylpolyglyceryl-3-diisostearate, polyglyceryl-3-dipolyhydroxystearate, polyglyceryl-4-dipolyhydroxystearate, polyglyceryl-3-dioleate.

The or the O / W emulsifiers with an HLB value> 10 can advantageously be selected from the following group: glyceryl stearate in a mixture with ceteareth-20, ceteareth-25, ceteareth-6 in a mixture with stearyl alcohol, cetylstearyl alcohol mixed with PEG-40 castor oil and sodium cetylstearyl sulfate, Triceteareth-4 phosphate, glyceryl stearate, sodium cetyl stearyl sulfate, Lecithin trilaureth-4 phosphate, laureth-4 phosphate, stearic acid, propylene glycol stearate SE, PEG-9 stearate, PEG-20 stearate, PEG-30 stearate, PEG-40 stearate, PEG-100 stearate, Ceteth-2, Ceteth-20, Polysorbate-20, Polysorbate-60, Polysorbate-65, Polysorbate-100, glyceryl stearate in a mixture with PEG-100 stearate, Ceteareth-3, isostearylglyceryl ether, cetylstearyl alcohol in a mixture with sodium cetyl stearyl sulfate, PEG-40 stearate, glycol distearate, PEG-22-dodecyl glycol copolymer, polyglyceryl-2-PEG-4 stearate, ceteareth-12, Ceteareth-20, ceteareth-30, methyl glucose sesquistearate, steareth-10, PEG-20 stearate, Steareth-21, Steareth-20, Isosteareth-20, PEG-45 / Dodecyl glycol copolymer, methoxy-PEG-22 / dodecyl glycol copolymer, Glyceryl stearate SE, ceteth-20, PEG-20-methylglucose sesquistearate, Glyceryl stearate citrate, cetyl phosphate, cetearyl sulfate, sorbitan sesquioleate, Triceteareth-4-phosphate, trilaureth-4-phosphate, polyglyceryl-methylglucose distearate, Potassium cetyl phosphate, isosteareth-10, polyglyceryl-2-sesquiisostearate, Ceteth-10, isoceteth-20, glyceryl stearate in a mixture with ceteareth-20, Ceteareth-12, cetyl stearyl alcohol and cetyl palmitate, PEG-30 stearate, PEG-40 stearate, PEG-100 stearate.

The preparations according to the present Invention can also advantageous as cosmetic or dermatological impregnation solutions, with which in particular water-insoluble substrates - such as. B. woven or non-woven cloths - moistened are used. Such impregnation solutions are preferably thin, in particular sprayable (such as PIT emulsions, W / O emulsions, etc.) and preferably a viscosity less than 2000 mPas, in particular less than 1,500 mPa · s (measuring device: Haake Viskotester VT-02 at 25 ° C). With their help, for example, cosmetic sun protection wipes, wipes and the like available which combines the soft, water-insoluble material with the low-viscosity cosmetic and dermatological impregnation solution.

foams

Particularly advantageous in the sense of The present invention are also self-foaming, foam-like, post-foaming or expandable cosmetic and dermatological preparations.

Preparations are to be found under “self-foaming”, “foam-like”, “post-foaming” or “foamable” understand which foams - be it already during of the manufacturing process, be it in the application by the consumer or otherwise - by Entry of one or more gases can be produced in principle. In such foams are the gas bubbles (arbitrarily) distributed in one (or more) liquid phase (s), where the (foamed) Preparations macroscopically do not necessarily have the appearance of a foam. Cosmetic according to the invention (foamed) or dermatological preparations (hereinafter the simplicity for the sake of foams referred to) z. B. macroscopically visible dispersed systems in liquids represent dispersed gases. The foam character can, for example only become visible under a (light) microscope. Beyond that foams according to the invention - in particular then when the gas bubbles are too small to be recognized under a light microscope - even at the strong increase in volume of the system can be seen.

• A. mindestens einem Emulgator A, gewählt aus der Gruppe der ganz-, teil- oder nicht neutralisierten, verzweigten und/oder unverzweigten, gesättigten und/oder ungesättigten Fettsäuren mit einer Kettenlänge von 10 bis 40 Kohlenstoffatomen,
• B. mindestens einem Emulgator B, gewählt aus der Gruppe der polyethoxylierten Fettsäurester mit einer Kettenlänge von 10 bis 40 Kohlenstoffatomen und mit einem Ethoxylierungsgrad von 5 bis 100 und
• C. mindestens einem Coemulgator C, gewählt aus der Gruppe der gesättigten und/oder ungesättigten, verzweigten und/oder unverzweigten Fettalkohole mit einer Kettenlänge von 10 bis 40 Kohlenstoffatomen besteht.

For the purposes of the present invention, such preparations advantageously contain an emulsifier system which consists of

• A. at least one emulsifier A, selected from the group of fully, partially or not neutralized, branched and / or unbranched, saturated and / or unsaturated fatty acids with a chain length of 10 to 40 carbon atoms,
• B. at least one emulsifier B, selected from the group of polyethoxylated fatty acid esters with one Chain length of 10 to 40 carbon atoms and with a degree of ethoxylation of 5 to 100 and
• C. at least one co-emulsifier C, selected from the group consisting of saturated and / or unsaturated, branched and / or unbranched fatty alcohols with a chain length of 10 to 40 carbon atoms.

The one or more emulsifiers preferably chosen from the group of fatty acids, which in whole or in part with usual Alkalis (such as sodium and / or potassium hydroxide, sodium and / or Potassium carbonate and mono- and / or triethanolamine) neutralized are. For example, stearic acid and Stearates, isostearic acid and isostearates, palmitic acid and palmitates and myristic acid and myristates.

The or the emulsifiers B are preferably chosen from the following group: PEG-9 stearate, PEG-8 distearate, PEG-20 stearate, PEG-8 stearate, PEG-8 oleate, PEG-25 glyceryl trioleate, PEG-40 sorbitan lanolate, PEG-15 glyceryl ricinoleate, PEG-20 glyceryl stearate, PEG-20 glyceryl isostearate, PEG-20 glyceryl oleate, PEG-20 stearate, PEG-20 methylglucose sesquistearate, PEG-30 glyceryl isostearate, PEG-20 glyceryl laurate, PEG-30 stearate, PEG-30 glyceryl stearate, PEG-40 stearate, PEG-30 glyceryl laurate, PEG-50 stearate, PEG-100 stearate, PEG-150 laurate. For example, polyethoxylated ones are particularly advantageous Stearic.

According to the invention, the co-emulsifier (s) C are preferably selected from the following group: behenyl alcohol (C ₂₂ H ₄₅ OH), cetearyl alcohol [a mixture of cetyl alcohol (C ₁₆ H ₃₃ OH) and stearyl alcohol (C ₁₈ H ₃₇ OH)], lanolin alcohols (wool wax alcohols , which represent the unsaponifiable alcohol fraction of the wool wax which is obtained after the saponification of wool wax). Cetyl and cetylstearyl alcohol are particularly preferred.

According to the invention, it is advantageous the weight ratios from emulsifier A to emulsifier B to coemulsifier C (A: B: C) as to choose a: b: c, where a, b and c are independent rational numbers from 1 to 5, preferably from 1 to 3 can represent. A weight ratio of approximately 1: 1: 1 is particularly preferred.

It is advantageous in the sense of the present Invention, the total amount of emulsifiers A and B and the coemulsifier C in the range from 2 to 20% by weight, advantageously from 5 to 15 % By weight, in particular from 7 to 13% by weight, in each case based on the Total weight of the formulation to choose.

Pickering / solids stabilized emulsions

Particularly advantageous in the sense of The present invention is also cosmetic or dermatological Preparations made only by finely divided solid particles are stabilized. Such "emulsifier-free" emulsions also known as Pickering emulsions.

It happens in Pickering emulsions for an enrichment of the solid substance at the oil / water phase boundary in the form of a layer, which prevents the disperse phases from flowing together becomes. The surface properties are of particular importance the solid particles, which are both hydrophilic and lipophilic Should show properties.

The stabilizing solid particles can be advantageous also superficial treated to be water-repellent ("coated"), whereby a amphiphilic character of these solid particles are formed or should be preserved. The surface treatment can consist of that the Solid particles according to known methods with a thin hydrophobic or hydrophilic layer.

The average particle diameter the microfine solid particles used as the stabilizer is preferred smaller than 100 μm, selected particularly advantageously less than 50 microns. It is essentially irrelevant in what form (platelets, Rod, globule etc.) or modification of the solid particles used.

• – Titandioxide (gecoatet und ungecoatet): z. B. Eusolex T-2000 von der Fa. Merck, Titandioxid MT-100 Z von der Fa. Tayca Corporation
• – Zinkoxide z. B. Z-Cote und Z-Cote HP1 von der BASF AG, MZ -300, MZ -500 und MZ-505M von der Fa. Tayca Corporation
• – Eisenoxide

The microfine solid particles are preferably selected from the group of the amphiphilic metal oxide pigments. The following are particularly advantageous:

• - Titanium dioxides (coated and uncoated): e.g. B. Eusolex T-2000 from Merck, titanium dioxide MT-100 Z from Tayca Corporation
• - Zinc oxides e.g. B. Z-Cote and Z-Cote HP1 from BASF AG, MZ-300, MZ-500 and MZ-505M from Tayca Corporation
• - iron oxides

Furthermore, it is advantageous if the microfine solid particles from the following group chosen are: boron nitrides, starch derivatives (Tapioca Starch, Sodium Corn Starch Octynylsuccinat etc.), talc, latex particles.

According to the invention, it is advantageous if the solid-stabilized emulsions are significantly less than Contain or even contain 0.5% by weight of one or more emulsifiers completely are free of emulsifiers.

pencils

Also watery stick-like preparations are known per se, these also in the form of W / O emulsions can be present.

Application and others Ingredients:

The cosmetic or dermatological invention Formulations can as usual be composed and the cosmetic or dermatological Sun protection, also for the treatment, care and cleaning of the skin and / or hair and as a make-up product in decorative cosmetics serve.

Depending on their structure, cosmetic or topical dermatological compositions in the sense of the present Invention, used for example as a skin protection cream, Cleansing milk, day or night cream, etc. It may be possible and advantageous, the compositions according to the invention as a basis for pharmaceutical Use wording.

The cosmetic are used and dermatological preparations in the usual for cosmetics Sufficiently applied to the skin and / or hair.

The cosmetic and dermatological Preparations according to the invention can Contain cosmetic auxiliaries, as is usually the case in such preparations are used, e.g. B. preservatives, preservation aids, Complexing agents, bactericides, perfumes, substances for preventing or increasing foaming, Dyes, pigments that have a coloring Have effect thickeners, moisturizing and / or moisturizing Substances, fillers, which the skin feeling improve fats, oils, Waxes or other usual Components of a cosmetic or dermatological formulation such as alcohols, polyols, polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives.

Advantageous preservatives for the purposes of the present invention are, for example, formaldehyde releasers (such as, for example, DMDM hydantoin, which is available, for example, from Lonza under the trade name Glydant ^™ ), iodopropyl butyl carbamates (for example those under the trade names Glycacil-L, Glycacil -S available from Lonza and / or Dekaben LMB from Jan Dekker), parabens (ie alkyl p-hydroxybenzoate such as methyl, ethyl, propyl and / or butyl paraben), phenoxyethanol, ethanol, benzoic acid and the like. According to the invention, the preservation system usually also advantageously comprises preservation aids, such as, for example, octoxyglycerol, glycine soya, etc.

Advantageous complexing agents in the sense The present invention includes, for example, EDTA, [S, S] ethylenediamine disuccinate (EDDS), which, for example, under the trade name Octaquest available from Octel and / or iminodisuccinic acid, which u. a. from Bayer AG under the trade name Iminodisuccinat VP OC 370 (approx. 30% solution) and Baypure CX 100 permanently available is.

Particularly advantageous preparations are also obtained when antioxidants as additives or active ingredients be used. Included according to the invention the preparations advantageously one or more antioxidants. As cheap, but still optional antioxidants can all for cosmetic and / or dermatological applications suitable or customary Antioxidants are used.

Particularly advantageous in the sense of present invention can water-soluble Antioxidants are used, such as vitamins, e.g. B. ascorbic acid and their derivatives.

Preferred antioxidants are also Vitamin E and its derivatives as well as Vitamin A and its derivatives.

The amount of antioxidants (a or more compounds) in the preparations is preferably 0.001 to 30% by weight, particularly preferably 0.05 to 20% by weight, in particular 0.1 to 10 wt .-%, based on the total weight of the preparation.

If vitamin E and / or its Derivatives that are antioxidants are advantageous their respective concentrations from the range of 0.001 to 10 % By weight, based on the total weight of the formulation.

If vitamin A or vitamin A derivatives, or carotenes or their derivatives represent the antioxidant (s), is advantageous, their respective concentrations from the range from 0.001 to 10% by weight, based on the total weight of the formulation, to choose.

It is particularly advantageous when the cosmetic preparations according to the present invention contain cosmetic or dermatological active ingredients, preferred Active ingredients are antioxidants that protect the skin from oxidative stress protect can.

Other advantageous active ingredients in For the purposes of the present invention, natural active substances and / or their derivatives, such as. B. alpha-lipoic acid, phytoene, D-biotin, coenzyme Q10, alpha-glucosylrutin, carnitine, carnosine, natural and / or synthetic isoflavonoids, creatine, taurine and / or β-alanine and 8-hexadecen-1,16-dicarboxylic acid (Dioic acid, CAS number 20701-68-2; provisional INCI name Octadecendioic acid).

Recipes according to the invention, which, for. B. known anti-wrinkle active ingredients such as flavone glycosides (in particular α-glycosyl rutin), Coenzyme Q10, vitamin C and / or derivatives, vitamin A and / or derivatives, Containing vitamin E and / or derivatives and the like are suitable particularly advantageous for the prophylaxis and treatment of cosmetic or dermatological skin changes, as they e.g. B. occur in skin aging (such as Dryness, roughness and formation of dry wrinkles, Itching, reduced regreasing (e.g. after washing), visible vasodilation (telangiectasia, Cuperosis), flaccidity and formation of wrinkles and fine lines, local hyper, hypo and incorrect pigmentation (e.g. age spots), increased vulnerability across from mechanical stress (e.g. cracking) and the like). Farther They are particularly suitable against the appearance of dry or rough skin.

The water phase of the preparations according to the present Invention can advantageously be conventional contain cosmetic auxiliaries, such as alcohols, in particular those with a low C number, preferably ethanol and / or Isopropanol, diols or polyols with a low C number and their ethers, preferably propylene glycol, glycerin, butylene glycol, ethylene glycol, Ethylene glycol monoethyl or monobutyl ether, propylene glycol monomethyl, -monoethyl or monobutyl ether, diethylene glycol monomethyl or monoethyl ether and analog products, polymers, foam stabilizers, Electrolytes and in particular one or more thickeners, which one or which can advantageously be chosen from from the group silicon dioxide, aluminum silicates, polysaccharides or their derivatives, e.g. B. hyaluronic acid, Xanthan gum, hydroxypropylmethyl cellulose, particularly advantageous from the group of polyacrylates, preferably a polyacrylate from the Group of the so-called Carbopole [from Bf. Goodrich], for example Carbopole types 980, 981, 1382, 2984, 5984, ETD 2020, ETD 2050, Ultrez 10, individually or in combination.

The preparations according to the present Invention can also advantageously self-tanning substances contain, such as dihydroxyacteon and / or melanin derivatives in concentrations of 1 wt .-% up to 8 wt .-%, based on the Total weight of the preparation.

The preparations according to the present invention can also advantageously contain repellents for protection against mosquitoes, ticks and spiders and the like. Z are advantageous. B. N, N-diethyl-3-methylbenzamide (trade name: Metadelphene, "DEET"), dimethyl phthalate (trade name: Palatinol M, DMP) and in particular 3- (Nn-butyl-N-acetylamino) propionic acid ethyl ester (under the Insect Repellent ^® 3535 (available from Merck). The repellents can be used both individually and in combination.

Fabrics or Mixtures of substances referred to which cosmetic or dermatological Give preparations the property after application or Spread the on the skin surface Release of moisture from the horny layer (also trans epidermal water loss (TEWL)) and / or the hydration of the horny layer to positively influence.

Advantageous moisturizers for the purposes of the present invention are, for example, glycerol, lactic acid and / or lactates, in particular sodium lactate, butylene glycol, propylene glycol, biosaccaride gum-1, glycine soya, ethylhexyloxyglycerol, pyrrolidonecarboxylic acid and urea. Furthermore, it is particularly advantageous to use polymeric 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 advantageously be used as anti-wrinkle agents for the prophylaxis and treatment of cosmetic or dermatological skin changes, such as those described for example in US Pat. B. occur in skin aging, are used.

The cosmetic or dermatological preparations according to the invention can furthermore advantageously, although not necessarily, contain fillers which, for. B. further improve the sensory and cosmetic properties of the formulations and, for example, cause 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, distarch phosphate, aluminum or sodium starch, octenyl succinate and the like), pigments which have neither mainly UV filter nor coloring effects (such as e.g. B. boron nitride etc.) and / or Aerosile ^® (CAS No. 7631-86-9).

The oil phase of the formulations according to the invention is chosen advantageously from the group of polar oils, for example from the group of lecithins and fatty acid triglycerides, namely the triglycerol esters of saturated and / or unsaturated, branched and / or unbranched alkane carboxylic acids with a chain length of 8 to 24, especially 12 to 18 carbon atoms. The fatty acid triglycerides can for example, advantageously chosen are from the group of synthetic, semi-synthetic and natural oils, such as z. B. cocoglyceride, olive oil, Sunflower oil, Soybean oil, Peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, castor oil, wheat germ oil, grape seed oil, safflower oil, evening primrose oil, macadamia nut oil and the like more.

According to the invention, z. B. natural Waxes of animal and vegetable origin, such as Beeswax and other insect waxes as well as berry wax, shea butter and / or Lanolin (wool wax).

Other advantageous polar oil components can in the sense of the present invention can also be selected from the group of Esters from saturated and / or unsaturated, branched and / or unbranched alkane carboxylic acids with a chain length of 3 to 30 carbon atoms and saturated and / or unsaturated, branched and / or unbranched alcohols with a chain length of 3 to 30 carbon atoms and from the group of esters from aromatic carboxylic acids and saturated and / or unsaturated, branched and / or unbranched alcohols with a chain length of 3 to 30 carbon atoms. Such ester oils can then advantageously chosen are selected from the group octyl palmitate, octyl cocoate, octyl isostearate, Octyldodeceyl myristate, octyl dodecanol, cetearyl isononanoate, isopropyl myristate, Isopropyl palmitate, isopropyl stearate, isopropyl oleate, n-butyl stearate, n-hexyl laurate, n-decyl oleate, Isooctyl stearate, isononyl stearate, isononyl isononanoate, 2-ethylhexyl palmitate, 2-ethylhexyl laurate, 2-hexyldecyl stearate, 2-octyldodecyl palmitate, Stearyl heptanoate, oleyl oleate, olerlerucate, erucyl oleate, erucylerucate, Tridecyl stearate, tridecyl trimellitate, as well as synthetic, semi-synthetic and natural Mixtures of such esters, such as. B. Jojoba oil.

Furthermore, the oil phase can advantageously be chosen from the group of dialkyl ethers and dialkyl carbonates, advantageous are z. B. dicaprylyl ether (Cetiol OE) and / or dicaprylyl carbonate, for example that under the trade name Cetiol CC at Cognis available.

It is further preferred oil components from the group consisting of isoeicosane, neopentyl glycol, propylene glycol dicaprylate / dicaprate, caprylic / capric / diglyceryl succinate, butylene glycol dicaprylate / dicaprate, C _12-13 alkyl lactate, di-C _12-13 -Alkyltartrat, triisostearin, Dipentaerythrityl Hexacaprylat / Hexacaprat To use propylene glycol monoisostearate, tricaprylin, dimethyl isosorbide. It is particularly advantageous if the oil phase of the formulations according to the invention has a content of C _12-15 alkyl benzoate.

Advantageous oil components are also e.g. B. butyl octyl salicylate (for example, under the trade name Hallbrite BHB available from CP Hall), Hexadecylben zoat and butyl octyl benzoate and mixtures thereof (Hallstar AB) and / or Diethylhexyl naphthalate (Hallbrite TQ or Corapan TQ from H&R).

Any mix of such oil and wax components are to be used advantageously for the purposes of the present invention.

Particularly advantageous wax components, which can additionally increase the water resistance, especially of light protection formulations, are also acetylated glycol stearate with tristearin (e.g. Unitwix from ISP with the INCI: Acetylated Glycol Stearate and Tristearin), C _18-36 fatty acid triglyceride (e.g.: Syncrowax HGLC from Crode GmbH with INCI: C18-36 Acid Triglyceride) as well as those under the trade names "Performa V 1608" (INCI: C30-38 Olefin / Isopropyl Maleate / MA Copolymer) and "Perfroma V 825" (synthetic wax ) substances available from New Phase Technologies.

Other beneficial substances which in the oil phase of the preparations according to the present invention be incorporated and contribute to increasing water resistance can, are PEG-45 dodecyl glycol copolymer (INCI: PEG-45 dodecyl glycol Copolymer) and methoxy PEG-22 dodecyl glycol copolymer (INCI: methoxy PEG-22 Dodecyl Glycol Copolymer), both from AKZO Noble are available.

Furthermore, the oil phase can also be advantageous also non-polar oils contain, for example those which are selected from the group of branched and unbranched hydrocarbons and waxes, in particular Mineral oil, Vaseline (petrolatum), paraffin oil, Squalane and squalene, polyolefins, hydrogenated polyisobutenes and Isohexadecane. Among the polyolefins, polydecenes are the preferred Substances.

The oil phase can also be advantageous have a content of cyclic or linear silicone oils or completely such oils exist, although it is preferred, except the silicone oil or silicone oils one additional Content of other oil phase components to use.

werden auch als Polydimethylsiloxan bzw. Dimethicon (INCI) bezeichnet. Dimethicone gibt es in verschiedenen Kettenlängen bzw. mit verschiedenen Molekulargewichten.Silicone oils are high-molecular synthetic polymeric compounds in which silicon atoms are linked in a chain and / or network-like manner via oxygen atoms and the remaining valences of silicon by hydrocarbon residues (mostly methyl, more rarely ethyl, propyl, phenyl groups, etc.) ) are saturated. The silicone oils are systematically referred to as polyorganosiloxanes. The methyl-substituted polyorganosiloxanes, which are the most important compounds of this group in terms of quantity and are characterized by the following structural formula

are also known as polydimethylsiloxane or dimethicone (INCI). Dimethicone is available in different chain lengths or with different molecular weights.

Particularly advantageous polyorganosiloxanes for the purposes of the present invention are, for example, dimethylpolysiloxanes [poly (dimethylsiloxane)], which are available, for example, under the trade names Abil 10 to 10,000 from Th. Goldschmidt. Phenylmethylpolysiloxanes (INCI: phenyl Dimethicone, phenyl trimethicone), cyclic silicones (octamethylcyclotetrasiloxane or decamethylcyclopentasiloxane), which according to INCI are also called cyclomethicones, amino-modified silicones (INCI: amodimethicone) and silicone waxes, e.g. B. Polysiloxane-polyalkylene copolymers (INCI: Stearyl Dimethicone and Cetyl Dimethicone) and Dialkoxydimethylpolysiloxane (Stearoxy Dimethicone and Behenoxy Stearyl Dimethicone), which are available as different Abil-Wax types from Th. Goldschmidt. However, other silicone oils can also be used advantageously for the purposes of the present invention, for example cetyldimethicone, hexamethylcyclotrisiloxane, polydimethylsiloxane, poly (methylphenylsiloxane).

The cosmetic and dermatological preparations according to the invention can contain dyes and / or color pigments, in particular if they are in the form of decorative cosmetics. The dyes and pigments can be selected from the corresponding positive list in the Cosmetics Ordinance or the EC list of cosmetic colorants. In most cases, they are identical to the colorants approved for food. Advantageous color pigments are, for example, titanium dioxide, mica, iron oxides (for example Fe ₂ O ₃ , Fe ₃ O ₄ , FeO (OH)) and / or tin oxide. Advantageous dyes are, for example, carmine, Berlin blue, chrome oxide green, ultramarine blue and / or manganese violet. It is particularly advantageous to choose the dyes and / or color pigments from the Rowe Color Index, 3rd edition, Society of Dyers and Colorists, Bradford, England, 1971.

If the formulations according to the invention in the form of products that are used on the face, is it convenient as a dye one or more substances from the following group to choose: 2,4-dihydroxyazobenzene, 1- (2'-chloro-4'-nitro-1'phenylazo) -2-hydroxynaphthalene, Ceres red, 2- (sulfo-l-naphthylazo) -1-naphthol-4-sulfonic acid, calcium salt the 2-hydroxy-1,2'-azonaphthalene-1'-sulfonic acid, calcium and barium salts of 1- (2-sulfo-4-methyl-1-phenylazo) -2-naphthylcarboxylic acid, calcium salt 1- (2-sulfo-1-naphthylazo) -2-hydroxynaphthalene-3-carboxylic acid, aluminum salt 1- (4-sulfo-1-phenylazo) -2-naphthol-6-sulfonic acid, aluminum salt 1- (4-sulfo-1-naphthylazo) -2-naphthol-3,6-disulfonic acid, 1- (4-sulfo-1-naphthylazo) -2-naphthol-6,8-disulfonic acid, aluminum salt 4- (4-sulfo-1-phenylazo) -1- (4-sulfophenyl) -5-hydroxy-pyrazolone-3-carboxylic acid, aluminum and zirconium salts of 4,5-dibromofluorescein, aluminum and zirconium salts of 2,4,5,7-tetrabromofluorescein, 3 ', 4', 5 ', 6'-tetrachloro-2,4,5,7-tetrabromofluorescein and his aluminum salt, aluminum salt of 2,4,5,7-tetraiodofluorescein, Aluminum salt of quinophthalone disulfonic acid, aluminum salt of indigo disulfonic acid, red and black iron oxide (CIN: 77 491 (red) and 77 499 (black)), Iron oxide hydrate (CIN: 77 492), manganese ammonium diphosphate and titanium dioxide.

Oil-soluble natural dyes are also advantageous, such as B. paprika extracts, β-carotene or cochineal.

• 1. Natürliche Perlglanzpigmente, wie z. B. – „Fischsilber" (Guanin/Hypoxanthin-Mischkristalle aus Fischschuppen) und – „Perlmutt" (vermahlene Muschelschalen)
• 2. Monokristalline Perlglanzpigmente wie z. B. Bismuthoxychlorid (BiOCl)
• 3. Schicht-Substrat Pigmente: z. B. Glimmer / Metalloxid

Formulations containing pearlescent pigments are also advantageous for the purposes of the present invention. The types of pearlescent pigments listed below are particularly preferred:

• 1. Natural pearlescent pigments, such as. B. - "fish silver" (guanine / hypoxanthine mixed crystals from fish scales) and - "mother-of-pearl" (milled mussel shells)
• 2. Monocrystalline pearlescent pigments such as B. Bismuth oxychloride (BiOCl)
• 3. Layer-substrate pigments: e.g. B. mica / metal oxide

The basis for pearlescent pigments are, for example powdery Pigments or castor oil dispersions from Bismuth oxychloride and / or titanium dioxide and bismuth oxychloride and / or titanium dioxide on mica. Particularly advantageous is e.g. B. under the CIN 77163 listed gloss pigment.

The following pearlescent pigment types based on mica / metal oxide are also advantageous:

Z are particularly preferred. B. the from Merck under the trade names Timiron, Colorona or Dichrona available Pearlescent pigments.

The list of the pearlescent pigments mentioned is of course not intended to be limiting. Pearlescent pigments which are advantageous in the sense of the present invention can be obtained in numerous ways known per se. For example, other substrates besides mica can be coated with other metal oxides, such as. B. silica and the like. Z are advantageous. B. with TiO ₂ and Fe ₂ O ₃ coated SiO ₂ particles ("Ronaspheren"), which are sold by Merck and are particularly suitable for the optical reduction of fine wrinkles.

It can also be an advantage completely to do without a substrate like mica. Particularly preferred are iron pearlescent pigments, which without the use of mica getting produced. Such pigments are e.g. B. under the trade name Sicopearl Kupfer 1000 available from BASF.

Are also particularly advantageous also effect pigments sold under the trade name Metasomes Standard / slide in different colors (yello, red, green, blue) are available from Flora Tech. The glitter particles are in mixtures with different ones Auxiliaries and dyes (such as the dyes with the Color Index (CI) numbers 19140, 77007, 77289, 77491).

The dyes and pigments can both individually and in a mixture and mutually be coated, with different coating thicknesses different color effects are generally produced. The The total amount of dyes and coloring pigments is advantageous from the range of z. B. 0.1 wt .-% to 30 wt .-%, preferably from 0.5 to 15% by weight, in particular from 1.0 to 10% by weight, in each case based on the total weight of the preparations.

It is also beneficial in the sense of the present invention, cosmetic and dermatological preparations to create whose main The purpose of protection from sunlight is not, but it still does Contain the content of other UV protection substances. So z. B. in day creams or makeup products usually UV-A or UV-B filter substances incorporated. Also provide UV protection substances, as well as antioxidants and, if desired, Preservatives, effective protection of the preparations themselves against spoilage. Favorable are also cosmetic and dermatological preparations that in in the form of a sunscreen.

Accordingly, the preparations contain in the sense of the present invention preferably at least one further UV-A, UV-B and / or broadband filter substance. The wording can, although not necessary, if necessary in addition to the above organic pigmentary Substance also one or more organic and / or inorganic Contain pigments as UV filter substances, which in the water and / or the oil phase can be present.

The preparations according to the present Invention can also advantageously in the form of so-called oil-free cosmetic or dermatological Emulsions are present which have a water phase and at least one liquid at room temperature UV filter substance included as a further phase and which is particularly advantageous also free of other oil components could be.

Particularly advantageous UV filter substances which are liquid at room temperature in the sense of the present Invention are homomenthyl salicylate (INCI: homosalate), 2-ethylhexyl-2-cyano-3,3-diphenylacrylate (INCI: octocrylene), 2-ethylhexyl-2-hydroxybenzoate (2-ethylhexyl salicylate, octyl salicylate, INCI: ethylhexyl salicylate) and esters Cinnamic acid, preferably 4-methoxycinnamic acid (2-ethylhexyl) ester (2-ethylhexyl-4-methoxycinnamate, INCI: ethylhexyl methoxycinnamate) and 4-methoxycinnamic acid isopentyl ester (isopentyl-4-methoxycinnamate, INCI: isoamyl p-methoxycinnamate) (2,2-bis ethoxycarbonylvinyl) phenoxy) propenyl) -methoxysiloxan / dimethylsiloxane - copolymer which is obtainable for example under the trade name Parsol ^® SLX from Hoffmann La Roche.

Preferred inorganic pigments are metal oxides and / or other metal compounds which are sparingly soluble or insoluble in water, in particular oxides of titanium (TiO ₂ ), zinc (ZnO), iron (e.g. Fe ₂ O ₃ ), zirconium (ZrO ₂ ), silicon ( SiO ₂ ), manganese (e.g. MnO), aluminum (Al ₂ O ₃ ), cerium (e.g. Ce ₂ O ₃ ), mixed oxides of the corresponding metals as well as mixtures of such oxides and the sulfate of barium (BaSO ₄ ).

The pigments can be advantageous in the sense of present invention also in the form of commercially available oily or aqueous predispersions come into use. These predispersions can advantageously be used as dispersants and / or solubilizing agents may be added.

The pigments can be advantageous according to the invention superficial treated ("coated"), for example a hydrophilic, amphiphilic or hydrophobic character is formed will or should be preserved. This surface treatment can consist of that the Pigments according to known methods with a thin hydrophilic and / or hydrophobic inorganic and / or organic layer be provided. The various surface coatings can be in According to the present invention also contain water.

Inorganic surface coatings in the sense of the present invention can consist of aluminum oxide (Al ₂ O ₃ ), aluminum hydroxide Al (OH) ₃ , or aluminum oxide hydrate (also: alumina, CAS no .: 1333-84-2), sodium hexametaphosphate (NaPO ₃ ) ₆ , sodium metaphosphate (NaPO ₃ ) _n , silicon dioxide (SiO ₂ ) (also: silica, CAS No .: 7631-86-9), or iron oxide (Fe ₂ O ₃ ). These inorganic surface coatings can occur alone, in combination and / or in combination with organic coating materials.

Organic surface coatings in the sense of the present invention consist of vegetable or animal aluminum stearate, vegetable or animal stearic acid, Lauric acid, Dimethylpolysiloxane (also: Dimethicone), methylpolysiloxane (Methicone), Simethicone (a mixture of dimethylpolysiloxane with an average chain length from 200 to 350 dimethylsiloxane units and silica gel) or alginic acid. This organic surface coatings can alone, in combination and / or in combination with inorganic Coating materials occur.

Zinc oxide particles and predispersions of zinc oxide particles suitable according to the invention are available under the following trade names from the listed companies:

Suitable titanium dioxide particles and predispersions of titanium dioxide particles are available under the following trade names from the companies listed:

Other advantageous pigments are latex particles. Latex particles which are advantageous according to the invention are those described in the following documents: US 5,663,213 respectively. EP 0 761 201 , Particularly advantageous latex particles are those which are formed from water and styrene / acrylate copolymers and, for. B. are available under the trade name "Alliance SunSphere" from Rohm & Haas.

Advantageous UV-A filter substances for the purposes of the present invention are dibenzoylmethane derivatives, in particular 4- (tert-butyl) -4'-methoxydibenzoylmethane (CAS-Nr. 70356-09-1), marketed by Givaudan under the trade name Parsol ^® 1789 and is sold by Merck under the trade name Eusolex ^® 9020.

• – Phenylen-1,4-bis-(2-benzimidazyl)-3,3'-5,5'-tetrasulfonsäure 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 mit der INCI-Bezeichnung Disodium Phenyl Dibenzimidazol Tetrasulfonat (CAS-Nr.: 180898-37-7), welches beispielsweise unter der Handelsbezeichnung Neo Heliopan AP bei Haarmann & Reimer erhältlich ist;
• – Salze der 2-Phenylbenzimidazol-5-sulfonsäure, wie ihr Natrium-, Kalium- oder ihr Triethanolammonium-Salz sowie die Sulfonsäure selbst mit der INCI Bezeichnung Phenylbenzimidazole Sulfonsäure (CAS.-Nr. 27503-81-7), welches beispielsweise unter der Handelsbezeichnung Eusolex 232 bei Merck oder unter Neo Heliopan Hydro bei Haarmann & Reimer erhältlich ist;
• – 1,4-di(2-oxo-10-Sulfo-3-bornylidenmethyl)-Benzol (auch: 3,3'-(1,4-Phenylendimethylene)-bis-(7,7-dimethyl-2-oxo-bicyclo-[2.2.1]hept-1-ylmethan Sulfonsäure) und dessen Salze (besonders die entprechenden 10-Sulfato-verbindungen, insbesondere das entsprechende Natrium-, Kalium- oder Triethanolammonium-Salz), das auch als Benzol-1,4-di(2-oxo-3-bornylidenmethyl-10-sulfonsäure) bezeichnet wird. Benzol-1,4- di(2-oxo-3-bornylidenmethyl-10-sulfonsäure) hat die INCI-Bezeichnung Terephtalidene Dicampher Sulfonsäure (CAS.-Nr.: 90457-82-2) und ist beispielsweise unter dem Handelsnamen Mexoryl SX von der Fa. Chimex erhältlich;
• – Sulfonsäure-Derivate des 3-Benzylidencamphers, wie z. B. 4-(2-Oxo-3-bornylidenmethyl)benzolsulfonsäure, 2-Methyl-5-(2-oxo-3-bornylidenmethyl)sulfonsäure und deren Salze.

Advantageous further UV filter substances in the sense of the present invention are sulfonated, water-soluble UV filters, such as. B .:

• - Phenylene-1,4-bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid and its 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 with the INCI name Disodium Phenyl Dibenzimidazole Tetrasulfonate (CAS No .: 180898-37-7), which, for example, under the Trade name Neo Heliopan AP is available from Haarmann &Reimer;
• - Salts of 2-phenylbenzimidazole-5-sulfonic acid, such as its sodium, potassium or triethanolammonium salt and the sulfonic acid itself with the INCI name phenylbenzimidazole sulfonic acid (CAS No. 27503-81-7), which, for example, under the Trade name Eusolex 232 is available from Merck or under Neo Heliopan Hydro from Haarmann &Reimer;
• - 1,4-di (2-oxo-10-sulfo-3-bornylidenemethyl) -benzene (also: 3,3 '- (1,4-phenylenedimethylene) -bis- (7,7-dimethyl-2-oxo- bicyclo- [2.2.1] hept-1-ylmethane sulfonic acid) and its salts (especially the corresponding 10-sulfato compounds, especially the corresponding sodium, potassium or triethanolammonium salt), which is also called benzene-1,4- di (2-oxo-3-bornylidenemethyl-10-sulfonic acid) Benzene-1,4-di (2-oxo-3-bornylidenemethyl-10-sulfonic acid) has the INCI name Terephtalidene Dicampher Sulfonic Acid (CAS no .: 90457-82-2) and is available, for example, under the trade name Mexoryl SX from Chimex;
• - Sulfonic acid derivatives of 3-benzylidene camphor, such as. B. 4- (2-oxo-3-bornylidene methyl) benzenesulfonic acid, 2-methyl-5- (2-oxo-3-bornylidene methyl) sulfonic acid and salts thereof.

worin R¹, R² und R³ unabhängig voneinander gewählt werden aus der Gruppe der verzweigten oder unverzweigten, gesättigten oder ungesättigten Alkylreste mit 1 bis 10 Kohlenstoffatomen. Es ist erfindungsgemäß besonders vorteilhaft, die Reste R¹ und R² gleich zu wählen, insbesondere aus der Gruppe der verzweigten Alkylreste mit 3 bis 5 Kohlenstoffatomen. Es ist ferner besonders vorteilhaft im Sinne der vorliegenden Erfindung, wenn R³ einen unverzweigten oder verzweigten Alkylrest mit 8 Kohlenstoffatomen, insbesondere den 2-Ethylhexylrest darstellt.Advantageous UV filter substances in the sense of the present invention are also benzoxazole derivatives, which are characterized by the following structural formula,

wherein R ¹ , R ² and R ^{3 are} independently selected from the group of branched or unbranched, saturated or unsaturated alkyl radicals having 1 to 10 carbon atoms. It is particularly advantageous according to the invention to choose the radicals R ¹ and R ^{2 the} same, in particular from the group of the branched alkyl radicals having 3 to 5 carbon atoms. It is furthermore particularly advantageous for the purposes of the present invention if R ^{3 is} an unbranched or branched alkyl radical having 8 carbon atoms, in particular the 2-ethylhexyl radical.

auszeichnet und bei 3V Sigma unter der Handelsbezeichnung Uvasorb^® K2A erhältlich ist.According to the invention, particularly preferred benzoxazole derivative is 2,4-bis- [5-1 (dimethylpro pyl) benzoxazol-2-yl- (4-phenyl) -imino] -6- (2-ethylhexyl} -imino-1,3,5-triazine with CAS No. 288254-16-0, which is characterized by the structural formula

distinguished and is available from 3V Sigma under the trade name Uvasorb ^® K2A.

That or the benzoxazole derivatives are advantageously in dissolved Form in the cosmetic according to the invention Preparations. However, it may also be advantageous if the benzoxazole derivative or derivatives in pigmentary, d. H. undissolved form - for example in particle sizes of 10 nm up to 300 nm.

worin
– R¹ und R² unabhängig voneinander Wasserstoff, C₁-C₂₀-Alkyl, C₃-C₁₀-Cycloalkyl oder C₃-C₁₀-Cycloalkenyl bedeuten, wobei die Substituenten R¹ und R² gemeinsam mit dem Stickstoffatom, an das sie gebunden sind, einen 5- oder 6-Ring bilden können und
– R³ einen C₁-C₂₀-Alkyl Rest bedeutet.Advantageous UV filter substances in the sense of the present invention are also so-called hydroxybenzophenones. Hydroxybenzophenones are characterized by the following structural formula:

wherein
- R ¹ and R ² independently of one another are hydrogen, C ₁ -C ₂₀ alkyl, C ₃ -C ₁₀ cycloalkyl or C ₃ -C ₁₀ cycloalkenyl, where the substituents R ¹ and R ² together with the nitrogen atom to which they are bound, can form a 5 or 6 ring and
- R ^{3 is} a C ₁ -C ₂₀ alkyl radical.

und unter dem Uvinul A Plus bei der Fa. BASF erhältlich ist.A particularly advantageous hydroxybenzophenone in the context of the present invention is 2- (4'-diethylamino-2'-hydoxybenzoyl) benzoic acid hexyl ester (also: aminobenzophenone), which is distinguished by the following structure:

and is available under the Uvinul A Plus from BASF.

Advantageous UV filter substances In the sense of the present invention, so-called broadband filters are also i.e. Filter substances that contain both UV-A and UV-B radiation absorb.

• – 2,4-Bis-{[4-(2-Ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5-triazin (INCI: Bis-Ethylhexyloxylphenol Methoxyphenyl Triazin), welches unter der Handelsbezeichnung Tinosorb^® S bei der CIBA-Chemikalien GmbH erhältlich ist;
• – Dioctylbutylamidotriazon (INCI: Diethylhexyl Butamido Triazone), welches unter der Handelsbezeichnung UVASORB HEB bei Sigma 3V erhältlich ist;
• – 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), welches von der BASF Aktiengesellschaft unter der Warenbezeichnung UVI-NUL^® T 150 vertrieben wird;
• – 2-[4,6-Bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy)phenol (CAS Nr.: 2725-22-6).

Advantageous broadband filters or UV-B filter substances are, for example, triazine derivatives, such as, for. B.

• - 2,4-bis - {[4- (2-ethylhexyloxy) -2-hydroxy] phenyl} -6- (4-methoxyphenyl) -1,3,5-triazine (INCI: bis-ethylhexyloxyphenol methoxyphenyl triazine ), which is available under the trade name Tinosorb ^® S from CIBA-Chemicals GmbH;
• - Dioctylbutylamidotriazon (INCI: Diethylhexyl Butamido Triazone), which is available under the trade name UVASORB HEB from Sigma 3V;
• - 4,4 ', 4''- (1,3,5-triazine-2,4,6-triyltriimino) -tris-benzoic acid tris (2-ethylhexyl ester), also: 2,4,6-tris- [ anilino- (p-carbo-2'-ethyl-1'-hexyloxy)] - 1,3,5-triazine (INCI: ethylhexyl triazone), which is sold by BASF Aktiengesellschaft under the trade name UVI-NUL ^® T 150;
• - 2- [4,6-bis (2,4-dimethylphenyl) -1,3,5-triazin-2-yl] -5- (octyloxy) phenol (CAS No .: 2725-22-6).

Advantageous broadband filter in For the purposes of the present invention, 2- (2H-benzotriazol-2-yl) -4-methyl-6- [2-methyl-3- [1,3,3,3-tetramethyl-1 - [(trimethylsilyl) oxy ] disiloxanyl] propyl] phenol (CAS No .: 155633-54-8) with the INCI name Drometrizole Trisiloxane.

• – 3-Benzylidencampher-Derivate, vorzugsweise 3-(4-Methylbenzyliden)campher, 3-Benzylidencampher;
• – 4-Aminobenzoesäure-Derivate, vorzugsweise 4-(Dimethylamino)-benzoesäure(2-ethylhexyl)ester, 4-(Dimethylamino)benzoesäureamylester;
• – 2,4,6-Trianilino-(p-carbo-2'-ethyl-1'-hexyloxy)-1,3,5-triazin;
• – Ester der Benzalmalonsäure, vorzugsweise 4-Methoxybenzalmalonsäuredi(2-ethylhexyl)ester;
• – Ester der Zimtsäure, vorzugsweise 4-Methoxyzimtsäure(2-ethylhexyl)ester, 4-Methoxyzimtsäureisopentylester;
• – Derivate des Benzophenons, vorzugsweise 2-Hydroxy-4-methoxybenzophenon, 2-Hydroxy-4-methoxy-4'-methylbenzophenon, 2,2'-Dihydroxy-4-methoxybenzophenon sowie
• – an Polymere gebundene UV-Filter.

The other UV filter substances can be oil-soluble or water-soluble. Advantageous oil-soluble filter substances are e.g. B .:

• - 3-benzylidene camphor derivatives, preferably 3- (4-methylbenzylidene) camphor, 3-benzylidene camphor;
• - 4-aminobenzoic acid derivatives, preferably 4- (dimethylamino) benzoic acid (2-ethylhexyl) ester, 4- (dimethylamino) benzoic acid amyl ester;
• - 2,4,6-trianilino- (p-carbo-2'-ethyl-1'-hexyloxy) -1,3,5-triazine;
• - Esters of benzalmalonic acid, preferably 4-methoxybenzalmalonic acid di (2-ethylhexyl) ester;
• - Esters of cinnamic acid, preferably 4-methoxycinnamic acid (2-ethylhexyl) ester, 4-methoxycinnamic acid isopentyl ester;
• - Derivatives of benzophenone, preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone and
• - UV filters bound to polymers.

Advantageous water-soluble filter substances are z. E.g .: sulfonic acid derivatives the 3-benzylidene camphor, such as. B. 4- (2-oxo-3-bornylidene methyl) benzenesulfonic acid, 2-methyl-5- (2-oxo-3-bornylidene methyl) sulfonic acid and their salts.

A further light protection filter substance according to the invention to be used advantageously is ethylhexyl-2-cyano-3,3-diphenyl acrylate, sold under the name Uvinul ^® N 539 T is available (octocrylene) from BASF.

Particularly advantageous preparations in the sense of the present ending, which is characterized by a high or very high UV-A protection, included in addition to the or filter substances according to the invention) furthermore preferably further UV-A and / or broadband filters, in particular Dibenzoylmethane derivatives [for example the 4- (tert-butyl) -4'-methoxydibenzoylmethane] and / or that 2,4-bis - {[4- (2-ethyl-hexyloxy) -2-hydroxy] phenyl} -6- (4-methoxyphenyl) -1,3,5-triazine and / or phenylene-1,4-bis (2-benzimidazyl) -3,3'-5,5'-tetrasulfonic acid bis-sodium salt individually or in any combination with each other.

The list of UV filters mentioned, which can be used within the meaning of the present invention Of course not be limiting.

The preparations advantageously contain according to the present Invention the substances that UV radiation in the UV-A and / or UV-B range absorb, in a total amount of e.g. B. 0.1% by weight to 30% by weight, preferably 0.5 to 20% by weight, in particular 1.0 to 15.0% by weight, in each case based on the total weight of the preparations, for cosmetic Preparations available to place the hair or skin in front of the entire area protect from ultraviolet radiation.

The following examples are intended illustrate the present invention without restricting it. The Numerical values in the examples mean percentages by weight, based on on the total weight of the respective preparations.

1. PIT - emulsions (spray)

2. Hydrodispersion and O / W sprays

3. W / O emulsion

4. W / O - sun protection emulsions

5. O / W emulsions

6. O / W emulsions

7. foaming emulsions

Claims (13)

Containing cosmetic and dermatological emulsions A. one or more surfactants, B. one or more pigmentary organic Substances and C. one or more siloxane elastomers. Use of siloxane elastomers to achieve or Increase of stability of emulsions the presence of surfactants. Emulsions according to claim 1 or use according to claim 2, characterized in that the emulsion 0.01 to 20 wt .-%, advantageously from 0.1 to 10 wt .-% - each based on the total weight of the preparation - on one or more siloxane elastomer (s) contains. Emulsions according to claim 1 or use according to claim 2, characterized in that the emulsion 0.001 to 15 wt .-%, advantageously 0.005 to 5 wt .-%, very particularly preferably 0.01 to 1 wt .-% - each based on the total weight of the preparation - on one or more surfactants contains. Emulsions according to claim 1 or use according to claim 2, characterized in that as a surfactant at least one alkyl polyglycoside is used. Emulsions according to claim 1 or use according to claim 2, characterized in that the emulsion is an O / W formulation. Emulsions according to claim 1 or use according to claim 2, characterized in that the Preparation at least one UV filter substance selected from the group of triazines, camphor derivatives and organic and / or inorganic Pigments. Emulsions according to claim 1 or use according to claim 2, characterized in that the Preparation of at least one UV-A filter substance and / or a broadband filter, chosen from the group dibenzoylmethane derivatives [in particular the 4- (tert-butyl) -4'-methoxydibenzoylmethane], 2,2'-methylene-bis- (6- (2H-benzotriazol-2-yl) -4- (1,1,3,3-tetramethylbutyl) -phenol), 1,4-di (2-oxo-10-sulfo-3-bornylidenemethyl) benzene and its salts and 2,4-bis - {[4- (2-ethylhexyloxy) -2-hydroxy] phenyl} - 6- (4-methoxyphenyl) -1,3,5-triazine, contains the further filter substances individually or in any Combinations with each other can exist. Emulsions according to claim 1 or use according to claim 2, characterized in that the Preparation of at least one flavone glycoside, in particular α-glucosylrutin, and / or contains vitamin E and / or its derivatives. Use of preparations according to claim 5 or 6 to protect the skin from premature aging. Use of preparations according to one of the preceding Expectations for moisturizing the skin. Use of material combination of siloxane elastomers and surfactants to improve the sensory properties of cosmetic emulsions. Use of material combination of siloxane elastomers and surfactants to reduce the stickiness of cosmetic emulsions.