WO2015144329A1

WO2015144329A1 - Active-ingredient combinations consisting of ethylhexyl-2-cyano-3,3-diphenyl acrylate and 4-hydroxyacetophenone, and cosmetic or dermatological preparations containing said active-ingredient combinations

Info

Publication number: WO2015144329A1
Application number: PCT/EP2015/051547
Authority: WO
Inventors: Julia Pruns; Bente Nissen; Thomas Raschke; Magdalena VON WEDEL-PARLOW
Original assignee: Beiersdorf Ag
Priority date: 2014-03-26
Filing date: 2015-01-27
Publication date: 2015-10-01
Also published as: DE102014104257A1

Abstract

The invention relates to active-ingredient combinations consisting of ethylhexyl-2-cyano-3,3-diphenyl acrylate and 4-hydroxyacetophenone, and to cosmetic or dermatological preparations containing said active-ingredient combinations.

Description

Beiersdorf AG

Hamburg

Active ingredient combinations of ethylhexyl 2-cyano-3,3-diphenylacrylate and 4-hydroxyacetophenone and cosmetic or dermatological preparations, these

Containing active ingredient combinations

The present invention relates to active ingredient combinations of ethylhexyl 2-cyano-3,3-diphenyl-acrylate and 4-hydroxyacetophenone and cosmetic or dermatological preparations containing these drug combinations.

The present invention relates to cosmetic or dermatological preparations containing active ingredients for the care and protection of the skin, in particular the sensitive skin as well as especially in the foreground standing by intrinsic and / or extrinsic factors aged or aging skin and the use of such agents and combinations of such active ingredients in the field of cosmetic and dermatological skin care.

Cosmetic skincare is primarily understood as strengthening or restoring the skin's natural function as a barrier against environmental influences (e.g., dirt, chemicals, microorganisms) and against the loss of endogenous substances (e.g., water, natural fats, electrolytes).

If this function is disturbed, it may lead to increased absorption of toxic or allergenic substances or the infestation of microorganisms and as a result to toxic or allergic skin reactions.

In the case of old skin, for example, the regenerative renewal slows down, whereby in particular the water-binding capacity of the horny layer subsides. It therefore becomes inflexible, dry and cracked ("physiologically" dry skin). A barrier damage is the result. The skin becomes susceptible to negative environmental influences such as the invasion of microorganisms, toxins and allergens. As a result, even toxic or allergic skin reactions may occur.

In the case of pathologically dry and sensitive skin, barrier damage is a priori. Epidermal intercellular lipids are defective or inadequate or formed. The consequence is an increased permeability of the horny layer and insufficient protection of the skin from loss of hygroscopic substances and water.

The barrier effect of the skin can be quantified by determining transepidermal water loss (TEWL). It is the evaporation of water from the inside of the body without the inclusion of water loss during sweating. The determination of the TEWL value has proved extremely informative and can be used for the diagnosis of chapped or chapped skin, for the determination of the compatibility of chemically different surfactants and the like.

For the beauty and care of the skin, the water content in the uppermost layer of skin is of utmost importance. It can be favorably influenced to a limited extent by introducing moisture regulators.

Anionic surfactants, which are generally components of cleansing formulations, can increase the pH in the horny layer for a long time, severely hampering regenerative processes that serve to restore and renew the barrier function of the skin. In this case, in the horny layer between regeneration and the loss of essential substances by regular extraction, a new, often very unfavorable equilibrium state, which significantly affects the appearance of the skin and the physiological functioning of the horny layer.

Even with a simple water bath without the addition of surfactants, there is initially a swelling of the horny layer of the skin, wherein the degree of this swelling depends, for example, on the duration of the bath and its temperature. At the same time, water-soluble substances, e.g. Water-soluble dirt components, but also skin-own substances, which are responsible for the water-binding capacity of the horny layer, washed off or washed out. In addition, skin fats are to a certain extent dissolved and washed out by the skin's own surface-active substances. This causes after initial swelling a subsequent significant dehydration of the skin, which can be enhanced by detergent additives.

In healthy skin, these processes are generally irrelevant, as the protective mechanisms of the skin can readily compensate for such minor disorders of the upper layers of the skin. But even in the case of non-pathological deviations from the normal status, eg due to environmental wear or irritation, photodamage, aging skin etc., the protective mechanism of the skin surface is disturbed. Under certain circumstances, he is then unable to fulfill his task on his own and must be regenerated by external measures.

In addition, it is known that the lipid composition and amount of the horny layer of the pathologically altered, dry and dry but non-diseased skin of younger and older people deviates from the normal state found in the healthy, normally hydrated skin of an equal age group. The changes in the lipid pattern of the very dry, non-eczematous skin of patients with atopic eczema represent an extreme case for the deviations that are found in the dry skin of healthy people.

The effect of ointments and creams on barrier function and hydration of the horny layer is usually not in restoring or strengthening the physico-chemical properties of the lamellae from intercellular lipids. A significant partial effect is based on the mere coverage of the treated skin areas and the resulting water retention in the underlying horny layer. Co-applied hygroscopic substances bind the water, resulting in a measurable increase in the water content in the horny layer. However, this purely physical barrier can be removed relatively easily. After discontinuation of the product, the skin then returns very quickly to the state before the start of treatment. In addition, the skin care effect may be reduced with regular treatment, so that the status quo is finally reached even during the treatment. For certain products, the condition of the skin may temporarily worsen after weaning. A sustainable product effect is usually not achieved or only to a limited extent.

In order to support the deficient skin in its natural regeneration and to strengthen its physiological function, topical preparations are increasingly being added intercellular lipid mixtures, which are to be used by the skin to rebuild the natural barrier. However, these lipids, especially the ceramides, are very expensive raw materials. In addition, their effect is usually much less than hoped.

The aim of the present invention was therefore to find ways to avoid the disadvantages of the prior art. In particular, the effect of the skin care products should be physiological, fast and sustained. Skincare in the sense of the present invention is primarily to be understood as meaning the natural function of the skin as a barrier against environmental influences (eg dirt, chemicals, microorganisms) and against the loss of endogenous substances (eg water, lipids , Electrolytes) is strengthened or restored.

Products for the care, treatment and cleaning of dry and stressed skin are known per se. However, their contribution to the regeneration of a physiologically intact, hydrated and smooth horny layer is extensive and time-limited.

The effect of ointments and creams on the barrier function and the hydration of the horny layer is based essentially on the coverage (occlusion) of the treated skin areas. The ointment or cream is, so to speak, a (second) artificial barrier that is supposed to prevent the loss of water from the skin. Accordingly, this physical barrier - for example, with cleaning agents - can be removed again, whereby the original, impaired state is reached again. In addition, the skin care effect may decrease with regular treatment. After discontinuation of the product application, the skin returns to its pre-treatment state very quickly. For certain products, the condition of the skin may even temporarily deteriorate. A sustainable product effect is usually not achieved or only to a limited extent.

The effect of some pharmaceutical preparations on the barrier function of the skin even exists in a selective barrier damage which is supposed to enable active substances to penetrate into or through the skin into the body. A disturbed appearance of the skin is partially accepted as a side effect.

The effect of nourishing cleansing products consists essentially in an efficient refatting with sebum lipid-like substances. By simultaneously reducing the surfactant content of such preparations, the damage to the horny layer barrier can be further limited.

Antioxidants, preferably those which are used in skin-care cosmetic or dermatological preparations. In particular, the invention also relates to cosmetic and dermatological preparations containing such antioxidants. In a preferred embodiment, the present invention relates to cosmetic and dermatological Preparations for the prophylaxis and treatment of skin aging, in particular the skin aging caused by oxidative processes.

Antioxidants are substances which prevent oxidation processes or which prevent the autoxidation of unsaturated compounds containing fats. Antioxidants which are also used in the field of cosmetics and pharmacy are, for example, α-tocopherol, sesamol, bile acid derivatives, butylhydroxyanisole and butylhydroxytoluene.

Mainly antioxidants are used as protective substances against spoilage of preparations containing them. Nevertheless, it is known that undesirable oxidation processes can also occur in human and animal skin. Such processes play an essential role in skin aging.

In the article "Skin Diseases Associated with Oxidative Injury" in "Oxidative Stress in Dermatology", p. 323 and following (Marcel Decker Inc., New York, Basel, Hong Kong, publishers: Jürgen Fuchs, Frankfurt, and Lester Packer, Berkeley, California), oxidative damage to the skin and its nearer causes are listed.

UV radiation, for example, can lead to photo-oxidative reactions, in which case the photochemical reaction products intervene in the skin metabolism.

Predominantly, such photochemical reaction products are free-radical compounds, e.g. Hydroxy radicals, hydroperoxy radicals and superoxide ions. Undefined radical photoproducts, which are formed in the skin itself, can also show uncontrolled sequelae due to their high reactivity. However, singlet oxygen, a non-radical excited state of the oxygen molecule, can also occur on UV irradiation, as do short-lived epoxides and many others. Singlet oxygen, for example, is distinguished from the normally present triplet oxygen (radical ground state) by increased reactivity. However, there are also excited, reactive (radical) triplet states of the oxygen molecule.

For the reason of preventing such reactions, antioxidants and / or radical scavengers may additionally be incorporated into cosmetic or dermatological formulations. In addition to UV radiation, other environmental pollutants such as ozone, cigar smoke, oxidizing chemicals, metal ions (iron, nickel, copper, etc.) also induce oxidative stress in the skin of sulfur and nitrogen oxides, thus promoting premature skin aging.

Also, exposure to heat can result in a significant increase in the lipid peroxide level of the affected skin, and even normal metabolic processes can induce oxidative stress.

The object of the present invention was to remedy the disadvantages of the prior art. In particular, it was an object of the present invention to provide active ingredients and products which act as antioxidants in vivo and / or counteract skin aging caused by oxidative stress.

A well-known and highly effective antioxidant is 4-hydroxyacetophenone, which is sold by Symrise under the trade name "SymSave® H." It has the CAS No. 99-93-4 and is characterized by the following chemical structure:

A disadvantage of this substance is that its solubility in cosmetic solvents such as oils or lipids is only moderate, which limits their use in - mostly oily - cosmetic or dermatological preparations.

It was therefore an object of the present invention to remedy this situation and to suggest ways in which the use concentration of 4-hydroxyacetophenone in dissolved form can be increased.

It was surprising and unforeseeable for a person skilled in the art that combinations of ethylhexyl 2-cyano-3,3-diphenylacrylate and 4-hydroxyacetophenone as well as cosmetic or dermatological preparations containing these combinations of active ingredients would remedy the disadvantages of the prior art. Ethylhexyl 2-cyano-3,3-diphenylacrylate is also called octocrylene and is a UV-B filter substance, which is available from BASF under the name Uvinul® N 539 T and is characterized by the following structure:

Octocrylene absorbs light mainly in the UV-B and little in the short-wave UV-A range. The filter effect is not very strong. Octocrylene is usually used in combination with other filter substances, while at the same time increasing the photostability of certain UV-A filters and stabilizing their protective effect as a result.

The solubility experiments were carried out at 2 different temperatures: at room temperature (about 20 ° C) and at 35 ° C.

The crystalline 4-hydroxyacetophenone was added in small portions slowly (over several hours) to the respective solvent with stirring until no further material could be dissolved. Here the solubility limit was reached. Undissolved material was clearly recognizable as a milky precipitate or individual crystals.

The experiments at 35 ° C were carried out in a water bath. The temperature was kept constant by means of a temperature probe, which was connected to the heating stirrer. The solubility experiments with octocrylene could be carried out only at 35 ° C, since the substance is very tough at room temperature.

The experiments were carried out in screwed 15 ml glasses to prevent evaporation of the solvent.

The solubility was measured 12 to 24 hours after the last addition of the substance so that the system could equilibrate.

Octocrylene surprisingly dissolves 4-hydroxyacetophenone significantly better than the known cosmetic oils dicaprylyl ether and alkyl benzoates.

Advantageously, weight ratios of octocrylene to 4-hydroxyacetophenone are selected from the range of 100 to 1 to 1 to 20, preferably from 50 to 1 to 1 to 10, particularly preferably from 20 to 1 to 1 to 5.

Preferred use concentrations of 4-hydroxyacetophenone in cosmetic or dermatological preparations are selected from the range of 0.001% to 3%, preferably from 0.01 to 2%, particularly preferably from 0.01 to 1%, in each case based on the total weight of the preparations.

The active compound combinations used according to the invention can be readily incorporated into common cosmetic or dermatological formulations, advantageously in pump sprays, aerosol sprays, creams, ointments, tinctures, lotions, nail care products (for example nail varnishes, nail polish removers, nail balms) and the like.

It may also be advantageous to buffer the compositions according to the invention. A pH range of 3.5 to 7.5 is advantageous. It is particularly favorable to choose the pH in a range of 4.0-6.5.

The cosmetic and / or dermatological formulations according to the invention may be composed as usual and used for the treatment of the skin and / or the hair in the sense of a dermatological treatment or a treatment in the sense of nourishing cosmetics. But they can also be used in make-up products in decorative cosmetics. For use, the cosmetic and / or dermatological formulations according to the invention are applied to the skin and / or the hair in a sufficient amount in the manner customary for cosmetics and dermatological agents.

Advantageous are those cosmetic and dermatological preparations that are in the form of a sunscreen. Advantageously, these additionally contain at least one UVA filter and / or at least one UVB filter and / or at least one inorganic pigment.

Cosmetic preparations according to the invention for protecting the skin from UV rays may be in various forms, such as e.g. Usually used for this type of preparations. So they can e.g. a solution, a water-in-oil (W / O) or oil-in-water (O / W) type emulsion, or a multiple emulsions, such as water-in-oil-in-water (W / O / W), a gel, a hydrodispersion, a solid stick or even an aerosol.

The cosmetic preparations according to the invention may contain cosmetic adjuvants such as are commonly used in such preparations, e.g. Preservatives, bactericides, antioxidants, perfumes, antifoaming agents, dyes, pigments which have a coloring effect, thickeners, surface-active substances, emulsifiers, emollients, moisturizing and / or moisturizing substances, fats, oils, waxes or other common ingredients a cosmetic formulation such as alcohols, polyols, polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives.

Emulsions are advantageous according to the invention and contain e.g. the said fats, oils, waxes and other fatty substances, as well as water and an emulsifier, as commonly used for such a type of formulation.

Gels according to the invention usually contain lower C-number alcohols, for example ethanol, isopropanol, 1,2-propanediol, glycerol and water or an abovementioned oil in the presence of a thickener, which in the case of oily-alcoholic gels is preferably silicon dioxide or an aluminum silicate in aqueous-alcoholic or alcoholic gels, preferably a polyacrylate. Solid sticks according to the invention contain, for example, natural or synthetic waxes, fatty alcohols or fatty acid esters. Preference is given to lip balms and deodorant sticks ("deodorant sticks").

Suitable propellants for cosmetic or dermatological preparations which can be sprayed from aerosol containers according to the invention are the customary known highly volatile, liquefied propellants, e.g. Hydrocarbons (propane, butane, isobutane) suitable, which can be used alone or in combination with each other. Also, compressed air is advantageous to use.

Advantageously, the preparations according to the invention may additionally contain substances which absorb UV radiation in the UVB range, the total amount of filter substances being e.g. 0.1 wt .-% to 30 wt .-%, preferably 0.5 to 10 wt .-%, in particular 1 to 6 wt .-%, based on the total weight of the preparation to provide cosmetic preparations, which protect the skin from the entire range of ultraviolet radiation.

Cosmetic preparations for the care of the hair are, for example, shampooing agents, preparations which are used to rinse the hair before or after shampooing, before or after the permanent wave treatment, before or after dyeing or discoloring the hair, to make-up preparations or Inserting the hair, preparations for dyeing or decolorizing, a hairdressing and treatment lotion, a hair lacquer or permanent waving agent.

The cosmetic preparations contain active ingredients and adjuvants such as are commonly used for this type of preparations for hair care and hair treatment.

As auxiliaries are preservatives, surface-active substances, substances for preventing foaming, emulsifiers, thickeners, fats, oils, waxes, organic solvents, bactericides, perfumes, dyes or pigments, whose job is to dye the hair or the preparation itself, electrolytes , Preparations against the greasing of the hair.

Cosmetic preparations which are a shampoo or a washing, shower or bath preparation preferably comprise at least one anionic, nonionic or amphoteric surfactant or mixtures thereof. The following examples are intended to illustrate the embodiments of the present inventions. The information always refers to weight%, unless otherwise stated.

Taqescreme

O / W Taqescreme

Sunblock

O / W Taqescreme

O / W cream

Claims

1. active ingredient combinations of ethylhexyl-2-cyano-3,3-diphenylacrylate (octocrylene) and 4-hydroxyacetophenone. 2. active compound combinations according to claim 1, in which weight ratios of octocrylene to 4-hydroxyacetophenone selected from the range of from 100 to 1 to 1 to 20, preferably from 50 to 1 to 1 to 10, particularly preferably from 20 to 1 to 1 to 5 3. Cosmetic or dermatological preparations containing active ingredient combinations according to claim 1 or 2. 4. Preparations according to claim 3, in which 4-hydroxyacetophenone is present in weight concentrations selected from the range of 0.001% to 3%, preferably from 0.01 to 2%. , particularly preferably from 0.01 to 1%, in each case based on the total weight of the preparations.