Patent Application
20130108565
The invention relates to the use of at least one compound of the formula I and/or salt thereof as self-tanning substance or as tanning enhancer for dihydroxyacetone or for a mixture of self-tanning substances comprising dihydroxyacetone. The invention furthermore relates to the use of at least one compound of the formula I and/or salt thereof for the modulation of the hue which is achieved on tanning with dihydroxyacetone or by the mixture or preparation comprising dihydroxyacetone. The invention furthermore relates to the use of at least one compound of the formula I and/or salt thereof in a mixture or preparation comprising at least one self-tanning substance as contrast-reduction agent. The invention likewise furthermore relates to a preparation comprising a compound of the formula I and/or salt thereof and at least dihydroxyacetone (DHA) as self-tanning substance and to a process for the preparation of a preparation of this type.
The trend away from refined paleness towards “healthy, sporty brown skin” has been uninterrupted for years. In order to achieve a tanned complexion, people expose their skin to sunlight, since this causes pigmentation due to melanin formation. However, the UV radiation in sunlight also has a damaging effect on the skin. Besides acute damage (sunburn), long-term damage occurs on excessive irradiation with light from the UVB region (wavelength 280-320 nm), such as, for example, an increased risk of contracting skin cancer. Excessive exposure to UVB and UVA radiation (wavelength: 320-400 nm) generates highly reactive free-radical species, which multiply further even after termination of the irradiation, and wrinkling and skin ageing occur as a consequence thereof.
Tanning (pigmentation) of the skin offers natural protection against the adverse consequences of sunlight. The epidermis contains individual pigment-forming cells, the melanocytes, besides the basal cells in its lowest layer, the basal layer. UV light stimulates the production of melanin in these cells, which is transported into the kerantinocytes (horny cells), where it becomes visible as a brown skin colour. Melanin protects the cell nuclei against further irradiation and the adverse effects it causes on the cell DNA. It wraps around the cell nucleus like a parasol and thus protects it against harmful UV radiation.
Depending on the chemical composition of the pigments formed biochemically, a distinction is made between brownish-black eumelanin and reddish-yellow pheomelanin. The skin hue observed is determined by the ratio of these two types of melanin.
This pigment formation starting from the amino acid tyrosine is initiated predominantly by UVB radiation and is known as “indirect pigmentation”. Its development runs over a number of days; the suntan obtained in this way lasts a few weeks. In the case of “direct pigmentation”, which commences with the solar irradiation, predominantly colourless melanin precursors are oxidised by UVA radiation to dark-coloured melanin. Since this oxidation is reversible, it results in skin tanning which only lasts briefly.
Artificial tanning of the skin can be produced externally with the aid of make-up and orally by taking carotenoids.
Much more popular, however, is artificial tanning of the skin which can be achieved by the application of so-called self-tanners. The substance most frequently employed worldwide for these purposes is 1,3-dihydroxyacetone (dihydroxyacetone, DHA), which is used in an amount of 700 t/a. Self-tanners can be reacted with the proteins and amino acids of the horny layer of the skin in the sense of a Maillard reaction or via a Michael addition, where polymers which give the skin a brownish hue form via a reaction route which has not yet been clarified completely. This reaction is complete after about 4 to 6 hours. The tan achieved in this way cannot be washed off and is only removed with the normal skin desquamation.
Various substances are already known which are employed as self-tanners and which are described below.
DHA is a water-soluble crystalline solid which is unstable under neutral to basic conditions. This instability is also accompanied by the development of cosmetically undesired malodours.
A problem which can frequently occur on use with self-tanner substances, in particular with 1,3-dihydroxyacetone, is that the tanning of the skin is discoloured towards orange by the dominance of the yellow component.
There also continues to be a demand for dermatologically tolerated skin-colouring substances, in particular for combination with dihydroxyacetone, which are suitable for use in cosmetic and/or dermatological preparations or medical devices.
The present invention is concerned with the object of improving the colouring of protein-containing matrices, in particular the skin, with respect to a more natural hue.
This problem is solved in accordance with the invention by the subject-matters of the independent claims. Advantageous embodiments are the subject-matter of the dependent claims.
Surprisingly, it has now been found that compounds of the formula I and/or salts thereof together with DHA colour the skin darker than the self-tanner DHA alone and the colour result appears more natural.
The invention accordingly relates to the use of at least one compound of the formula I
Z—X I
The invention furthermore relates to the use of at least one compound of the formula I
Z—X I
The invention furthermore relates to the use of at least one compound of the formula I
Z—X I
A C1 to C4-alkyl group here encompasses methyl, ethyl, propyl-, isopropyl, butyl, x-methylpropyl (x=1 ;2) and tert-butyl.
In the case of a combination of at least one of the compounds of the formula I, as described above, with dihydroxyacetone for use in cosmetic formulations which serve for colouring the skin, a preferred red shift of the hue achieved is observed.
The self-tanning can thus be carried out with a natural appearing coloration without the undesired yellow cast of the coloured skin with dihydroxyacetone or with a mixture of self-tanning substances comprising dihydroxyacetone as self-tanner and on use of at least one compound of the formula I, as described above.
EP 0 715 845 A1 discloses a cosmetic composition comprising dihydroxyacetone, at least one alkyl polyglycoside, at least one fatty alcohol, optionally at least one polysugar and at least one cosmetically acceptable vehicle.
WO 98/38977 A1 describes a cosmetic preparation for use as self-tanning agent comprising a combination of erythrulose in the D or L form, optionally also as racemate, and a reducing sugar, for example dihydroxyacetone, glucose, xylose, fructose, reose, ribose, arabinose, allose, tallose, altrose, mannose, galactose, lactose, sucrose, erythrose and glyceraldehyde.
The cosmetic preparation of U.S. Pat. No. 6,231,837 B1, which can be employed as self-tanning agent, comprises at least one self-tanner, in particular dihydroxyacetone, at least one polyethoxyglycol, in particular ethoxydiglycol, at least one polyol and at least one suitable cosmetic vehicle. Polyols from the group 1,2,6-hexanetriol, isopropylideneglycerol, polyoxyethylenesorbitol, glycerol, diglycerol, erythritol, mannitol, xylitol, D- and L-sorbitol, glucose, fructose, galactose, mannose, sucrose, lactose, trehalose, maltose and inositol are described as suitable, in particular D-sorbitol.
The ability of the specific group of the compounds of the formula I to enhance the tanning of dihydroxyacetone cannot be derived from the prior art.
Throughout the document, the term self-tanner or self-tanning substance or self-tanner substance is used synonymously. These terms denote a substance which colours the skin and react with the proteins and/or amino acids of the protein-containing matrix in the sense of a Maillard reaction or via a Michael addition and thus form melanoids. The melanoids are yellow-brown to virtually black organic compounds which can essentially arise through the reaction of carbonyl groups with amino or thio functions. The principle of colouring with formation of melanoids is the basic colouring principle of the self-tanning substances. The colouring capacity of such self-tanning substances, in particular of dihydroxyacetone, can be enhanced through the use of at least one compound of the formula I, as described above.
Dihydroxyacetone, which can be used, inter alia, as self-tanner, colours the skin in accordance with a colouring principle of this type. The use of compounds of the formula I enables the colouring process with dihydroxyacetone to be enhanced and the hue achieved to be improved. Accordingly, a tanning enhancer is taken to mean a compound of the formula I which is capable, on colouring of the skin with dihydroxyacetone, of achieving a darker hue which is shifted more towards red than with dihydroxyacetone or a mixture of self-tanning substances comprising dihydroxyacetone alone.
Furthermore, the use of a tanning enhancer of this type or a compound of the formula I, as described above or as described as preferred, on application to the skin reduces the drying-out thereof compared with the use of dihydroxyacetone or a mixture of self-tanning substances comprising dihydroxyacetone alone.
In addition, compounds of the formula I can have a contrast-reduction effect, which reduces an uneven skin coloration in use with dihydroxyacetone or with a mixture of self-tanning substances comprising dihydroxyacetone and thus reduces the contrast between relatively strongly coloured and less strongly coloured areas of the skin. An uneven skin coloration of this type may arise through uneven pigmentation and/or a different distribution of the horny skin. A contrast-reduction agent is accordingly a substance which reduces an uneven skin coloration by reducing the contrast between relatively strongly coloured and less strongly coloured areas of the skin.
Compounds of the formula I, as described above, in particular isomaltulose, act/acts as tanning enhancer(s) for dihydroxyacetone and at the same time also reduce/reduces melanin production, as surprisingly observed in cell culture tests with B16V mouse melanoma cells.
The invention accordingly furthermore relates to the use of at least one compound of the formula I
Z—X I
In particular, the at least one compound of the formula I, as described above, acts in mixtures or preparations comprising at least dihydroxyacetone. The at least one compound of the formula I, the compounds indicated as preferred or particularly preferably isomaltulose, particularly preferably acts in a preparation comprising dihydroxyacetone as self-tanning substance.
A reduction in contrast can therefore be achieved, in particular, by preparations in which combinations according to the invention of dihydroxyacetone or a mixture of self-tanning substances comprising dihydroxyacetone and at least one compound of the formula I, as described above or described as preferred, are additionally combined with a substance which inhibits the biochemical formation of melanin. The combination of tanning mixtures which are based on the Maillard reaction or Michael addition with melanogenesis-inhibiting substances has the effect that skin areas which are already hyperpigmented lose their high melanin concentrations and the hue generated by the colorant on the skin surface imposes itself over a large area.
Suitable for combination are commercially available melanogenesis inhibitors, such as, for example, ascorbic acid and derivatives thereof, niacin-amide, emblica, ellagic acid, mulberry extract, kojic acid, liquorice extract, rucinol, hydroquinone, azelaic acid, arbutin or magnesium ascorbyl phosphate.
The invention therefore likewise relates to a preparation comprising at least one compound of the formula I, as described above, and a melanogenesis inhibitor.
Uneven pigmentation is really not uncommon in the population and is based on different degrees of melanin production by the melanocytes or an irregular distribution of the melanocytes in the skin. Melanin production is triggered by the enzyme tyrosinase, which ultimately sets the colour of the skin, the eyes and the hair.
In combination with dihydroxyacetone, colouring of the skin with more natural skin colorations, in particular shifted into the red colour region, can be achieved, where in addition an advantageous reduction in contrast of unevenly coloured areas of the skin is possible. In addition, in the case of the skin, drying-out of the skin is likewise advantageously reduced by compounds of the formula I.
A compound of the formula I encompasses specific disaccharides or derivatives thereof, whose OH groups and/or CH2OH groups may be substituted. The compound of the formula I can be divided into an aldose or ketose radical Z and a fructofuranose, fructopyranose or mannitol radical X.
An aldose radical having five to six C atoms here is taken to mean a monosaccharide containing an aldehyde group or an aldose having five to six C atoms without the anomeric OH group. The anomeric OH group is the OH group bonded to the anomeric carbon atom. The term aldose encompasses the aldopentoses and aldohexoses. Accordingly, the aldose radical is in a fully acetalic form.
The term aldose having five to six C atoms here encompasses the following monosaccharides:
The aldose radicals may each be in their α- or β-anomeric form or in the form of a mixture of the two anomeric forms. Furthermore, the aldose radicals can be in the furanoid or pyranoid form or in the form of a mixture of the two forms.
A ketose radical having five to six C atoms is taken to mean a monosaccharide containing a keto group or a ketose having five to six C atoms without the anomeric OH group. The anomeric OH group is the OH group bonded to the anomeric carbon atom. The term ketose encompasses the ketopentoses and ketohexoses. Accordingly, the ketose radical is in a fully acetalic form.
The term ketose having five to six C atoms here encompasses the following monosaccharides:
The ketose radicals may each be in their α- or β-anomeric form or in the form of a mixture of the two anomeric forms. Furthermore, the ketose radicals can be in the furanoid or pyranoid form or in the form of a mixture of the two forms.
Particular preference is given to an aldose or ketose radical having 6 C atoms.
A fructofuranose radical is taken to mean a fructofuranose in the α- or β-anomeric form without the H atom of one of the OH groups. A fructopyranose radical is taken to mean a fructopyranose in the α- or β-anomeric form without the H atom of one of the OH groups. A mannitol radical is taken to mean mannitol in the open-chain or a cyclic form without the H atom of one of the OH groups.
X particularly preferably stands for a fructofuranose or mannitol radical.
A glycosidic bond denotes the chemical bond between the anomeric carbon atom of a monosaccharide and an oxygen atom (generally heteroatom) of a further monosaccharide or aglycone. If a monoglycosidic bond is present, then, for the purposes of the invention, only the anomeric carbon atom of the aldose radical or ketose radical is connected to a non-anomeric carbon atom of the fructofuranose, fructopyranose, or mannitol radical via an oxygen bridge. If a diglycosidic bond is present, then, for the purposes of the invention, the anomeric carbon atom of the aldose radical or ketose radical is connected to the anomeric carbon atom of the fructofuranose or fructopyranose radical via an oxygen bridge.
The glycosidic bond of the compounds of the formula I can accordingly be formed as a diglycosidic or as a monoglycosidic bond.
Furthermore, at least one of the OH groups of the respective disaccharide or of the compound of the formula I may be substituted by OAlk, OAcy or OKt+ and/or two OH groups of the respective disaccharide may be protected by benzylidene, isopropylidene, 4-hydroxy-3-methoxybenzylidene or 4-methoxybenzylidene.
Alk here preferably stands for methyl, ethyl, propyl-, isopropyl, tert-butyl or benzyl, particularly preferably for methyl, ethyl, or benzyl and very particularly preferably for methyl or benzyl. Acy very particularly preferably stands for acetyl.
Two adjacent OH groups in the cis position may also be connected to one another in the form of a cyclic acetal or ketal. Acetals with benzaldehyde, anisaldehyde and vanillin and ketals with acetone are preferred here and particular preference is given to acetals with benzaldehyde and ketals with acetone.
The hydroxyl groups are particularly preferably unsubstituted or replaced by OKt+. The hydroxyl groups are very particularly preferably unsubstituted.
At least one CH2OH group of the compound of the formula I may be replaced by COOH, by COOKt+ or by CH3. Particularly preferably, the CH2OH group(s) of X is (are) in unsubstituted form. If the CH2OH group of Z has been replaced by COOH, the aldose or ketose radical present is thus an alduronic acid or keturonic acid radical respectively.
The following individual compounds are indicated by formulae in each of which the aldose or ketose radical Z is on the left of the bracket and the fructofuranose, fructopyranose or mannitol radical X is on the right of the bracket. The C atom of the respective radical connected to one another via an oxygen bridge is indicated in the brackets on the right and left of the arrow. If a monosaccharide is in the form of a full acetal, the respective configuration of the anomeric centre is also indicated in this case. If a monosaccharide can be in the form of a semiacetal, the open-chain form, and/or the cyclic α- and/or β-form of above individual compounds is also encompassed in this case. The disaccharide here can be in the form of a mixture of all open-chain and/or cyclic structures which are in each case conceivable to the person skilled in the art. The ratio of the respectively involved structures is, as is known, determined here by solvent and temperature.
Preferred individual compounds of the compounds of the formula I are:
Preference is given to compounds of the formula I in which Z is connected to X by a monoglycosidic connection. X very particularly preferably stands for a fructofuranose radical.
From the group of the individual compounds, isomaltulose (palatinose), isomalt or palatin-C6′-uronic acid are particularly preferably used in accordance with the invention. Isomaltulose is very particularly preferably employed.
Advantageous self-tanners which can be employed in a dihydroxyacetone-containing mixture or preparation are, inter alia:
The at least one compound of the formula I, as described above or described as preferred, can also be used in accordance with the invention together with a mixture of self-tanning substances comprising at least dihydroxyacetone and a further self-tanner selected from the above-mentioned group. By way of example, the mixture to be used in accordance with the invention consists of dihydroxyacetone and at least one further self-tanning substance, as described above. This mixture can then be combined in accordance with the invention with at least one compound of the formula I and employed in cosmetic, dermatological or pharmaceutical preparations, as described below.
Dihydroxyacetone is very particularly preferably employed without further self-tanning substances from the above-mentioned group.
The invention furthermore relates to preparations comprising at least one vehicle which is suitable for cosmetic, pharmaceutical, dermatological preparations, at least dihydroxyacetone and at least one compound of the formula I, as described above or preferably described.
The preparation preferably comprises at least dihydroxyacetone in an amount of 0.01 to 20% by weight, particularly preferably in an amount of 0.5 to 15% by weight and very particularly preferably in an amount of 1 to 8% by weight, based on the total amount of the preparation.
The preparation preferably comprises the at least one compound of the formula I, as described above and described as preferred, in an amount of 0.01 to 20% by weight, particularly preferably in an amount of 0.5 to 15% by weight and very particularly preferably in an amount of 1 to 8% by weight, based on the total amount of the preparation.
The percent by weight ratio of the at least one compound of the formula I to dihydroxyacetone on use as tanning enhancer and/or colour modulator is 1:20 to 20:1, preferably 1:10 or 10:1, particularly preferably 1:3 to 3:1 and very particularly preferably 1:1.
Preparations having self-tanner properties, in particular those which comprise dihydroxyacetone, tend towards malodours on application to the human skin, which are thought to be caused by degradation products of dihydroxyacetone itself or by products of side reactions and which are regarded as unpleasant by some users. It has been found that these malodours are prevented on use of formaldehyde scavengers and/or flavonoids. The preparation according to the invention comprising at least one compound of the formula I, as described above with the substituents indicated and also preferably mentioned and the individual compounds and at least dihydroxyacetone as self-tanner, can therefore preferably also comprise formaldehyde scavengers and optionally flavonoids for improving the odour. However, the reducing disaccharides of the formula I claimed for preparations according to the invention, and the corresponding individual compounds, may also themselves contribute to the improvement in odour, since, as is known, they can form semiacetals and full acetals with formaldehyde.
The formaldehyde scavenger is preferably selected from the group alkali metal, alkaline-earth metal or ammonium disulfite. Particular preference is given to a preparation which comprises, in combination DHA Plus, a mixture of DHA, sodium disulfite and magnesium stearate.
DHA Plus is a product mixture which comprises sodium metabisulfite, synonymous with Na2S2O5 or INCI: sodium disulfite, for the masking, elimination or neutralisation of formaldehyde. The addition of sodium metabisulfite in finished formulations results in significant reduction or suppression of the unpleasant odour. DHA Plus is marketed by Merck, Darmstadt.
The preparation according to the invention comprising at least one compound of the formula I, as described above with the substituents indicated and also preferably mentioned and the individual compounds and at least dihydroxyacetone as self-tanner, may particularly preferably comprise flavonoids for improving the odour and optionally for accelerating tanning.
The flavonoid here additionally acts as stabiliser for the self-tanner or the self-tanning substances and/or reduces or prevents or improves storage-dependent malodours, which may also arise due to additives or assistants present.
It is preferably a flavonoid in which one or more phenolic hydroxyl groups have been blocked by etherification or esterification. For example, hydroxyethyl-substituted flavonoids, such as, preferably, troxerutin, troxequercetin, troxeisoquercetin or troxeluteolin, and flavonoid sulfates or flavonoid phosphates, such as, preferably, rutin sulfates, have proven to be particularly highly suitable flavonoids here. Particular preference is given in the sense of the use according to the invention to rutin sulfate and troxerutin. Very particular preference is given to the use of troxerutin.
The preferred flavonoids have a non-positively charged flavan skeleton. It is thought that metal ions, such as, for example, Fe2+/Cu2+, are complexed by these flavonoids and autooxidation processes in the case of fragrances or compounds whose degradation results in malodours are thus prevented or reduced.
Particular preference is given to a preparation which, besides at least one compound of the formula I, comprises DHA Rapid. DHA Rapid is a product mixture comprising dihydroxyacetone and troxerutin, from Merck, Darmstadt. This particularly preferred preparation may optionally also comprise a formaldehyde scavenger, for example sodium disulfite.
Corresponding premixes and preparations which comprise formaldehyde scavengers and optionally flavonoids in order to improve the odour on the skin are described in the German patent application DE 10 2007 013 368A1, the contents of which in this respect expressly also belong to the disclosure content of the present application.
The preparations here are usually preparations which can be applied topically, for example cosmetic or dermatological formulations or medical devices. In this case, the preparations comprise a cosmetically or dermatologically suitable vehicle and, depending on the desired property profile, optionally further suitable ingredients. In the case of pharmaceutical preparations, the preparations in this case comprise a pharmaceutically tolerated vehicle and optionally further pharmaceutical active compounds.
“Can be applied topically” in the sense of the invention means that the preparation is applied externally and locally, i.e. that the preparation must be suitable for, for example, application to the skin.
In the sense of the present invention, the term agent or formulation is also used synonymously alongside the term preparation.
The preparations may include or comprise, essentially consist of or consist of the said requisite or optional constituents. All compounds or components which can be used in the preparations are either known and commercially available or can be synthesised by known processes.
Further preferred combinations of embodiments are disclosed in the claims.
The invention also relates to a process for the preparation of a preparation, as described above, in which at least one compound of the formula I as described above or described as preferred, is mixed with a vehicle and optionally with further active compounds or assistants. At least one further self-tanner substance is optionally then added and mixed, and finally dihydroxyacetone is added and mixed. Dihydroxyacetone is preferably added at a maximum of 40° C. Suitable vehicles and active compounds or assistants are described in detail in the following part.
In the preparations described, which, in accordance with the invention, comprise at least one compound of the formula I or preferred compounds of the formula I, as described above, and dihydroxyacetone, coloured pigments may furthermore also be present, where the layer structure of the pigments is not limited.
The coloured pigment should preferably be skin-coloured or brownish on use of 0.1 to 5% by weight. The choice of a corresponding pigment is familiar to the person skilled in the art.
Besides the compounds of the formula I, as described above or described as preferred, at least dihydroxyacetone as self-tanning substance and the optional other ingredients, preferred preparations may comprise organic UV filters, so-called hydrophilic or lipophilic sun-protection filters, which are effective in the UVA region and/or UVB region and(/or IR and/or VIS region (absorbers). These substances can be selected, in particular, from cinnamic acid derivatives, salicylic acid derivatives, camphor derivatives, triazine derivatives, β,β-diphenylacrylate derivatives, p-aminobenzoic acid derivatives and polymeric filters and silicone filters, which are described in the application WO-93/04665. Further examples of organic filters are indicated in the patent application EP-A 0 487 404. The said UV filters are usually named below in accordance with INCI nomenclature.
Particularly suitable for a combination are:
Salicylates: Homosalate marketed by Merck under the name “Eusolex HMS”; Ethylhexyl salicylate, for example marketed by Symrise under the name “Neo Heliopan OS”, Dipropylene glycol salicylate, for example marketed by Scher under the name “Dipsal”, TEA salicylate, for example marketed by Symrise under the name “Neo Heliopan TS”.
β,β-Diphenylacrylate derivatives: Octocrylene, for example marketed by Merck under the name “Eusolex® OCR”, “Uvinul N539” from BASF, Etocrylene, for example marketed by BASF under the name “Uvinul N35”.
Benzophenone derivatives: Benzophenone-1, for example marketed under the name “Uvinul 400”; Benzophenone-2, for example marketed under the name “Uvinul D50”; Benzophenone-3 or Oxybenzone, for example marketed under the name “Uvinul M40”; Benzophenone-4, for example marketed under the name “Uvinul MS40”; Benzophenone-9, for example marketed by BASF under the name “Uvinul DS-49”, Benzophenone-5, Benzophenone-6, for example marketed by Norquay under the name “Helisorb 11”, Benzophenone-8, for example marketed by American Cyanamid under the name “Spectra-Sorb UV-24”, Benzophenone-12 n-hexyl 2-(4-diethylamino-2-hydroxybenzoyl) benzoate or 2-hydroxy-4-methoxybenzophenone, marketed by Merck, Darmstadt, under the name Eusolex® 4360.
Benzylidenecamphor derivatives: 3-Benzylidenecamphor, for example marketed by Chimex under the name “Mexoryl SD”, 4-Methylbenzylidenecamphor, for example marketed by Merck under the name “Eusolex 6300”, benzylidenecamphorsulfonic acid, for example marketed by Chimex under the name “Mexoryl SL”, Camphor benzalkonium methosulfate, for example marketed by Chimex under the name “Mexoryl SO”, terephthalylidene-dicamphorsulfonic acid, for example marketed by Chimex under the name “Mexoryl SX”, Polyacrylamidomethylbenzylidenecamphor marketed by Chimex under the name “Mexoryl SW”.
Phenylbenzimidazole derivatives: phenylbenzimidazolesulfonic acid, for example marketed by Merck under the name “Eusolex 232”, disodium phenyl dibenzimidazole tetrasulfonate, for example marketed by Symrise under the name “Neo Heliopan AP”.
Phenylbenzotriazole derivatives: Drometrizole trisiloxane, for example marketed by Rhodia Chimie under the name “Silatrizole”, Methylenebis(benzotriazolyl)tetramethylbutylphenol in solid form, for example marketed by Fairmount Chemical under the name “MIXXIM BB/100”, or in micronised form as an aqueous dispersion, for example marketed by BASF under the name “Tinosorb M”.
Triazine derivatives: ethylhexyltriazone, for example marketed under the name “Uvinul T150” by BASF, diethylhexylbutamidotriazone, for example marketed under the name “Uvasorb HEB” by Sigma 3V, 2,4,6-tris(diisobutyl 4′-aminobenzalmalonate)-s-triazine or 2,4,6-tris(biphenyl)-1,3,5-triazine marketed as Tinosorb A2B by BASF, 2,2′-[6-(4-methoxyphenyl)- 1,3,5-triazine-2,4-diyl]bis[5-(2-ethylhexyl)oxy]phenol, marketed as Tinosorb S by BASF, N2,N4-bis[4-[5-(1,1-dimethylpropyl)-2-benzoxazolyl]phenyl]- N6-(2-ethylhexyl)-1,3,5-triazine-2,4,6-triamine marketed as Uvasorb K 2A by Sigma 3V.
Anthraniline derivatives: Menthyl anthranilate, for example marketed by Symrise under the name “Neo Heliopan MA”.
Imidazole derivatives: Ethylhexyldimethoxybenzylidenedioxoimidazoline propionate.
Benzalmalonate derivatives: polyorganosiloxanes containing functional benzalmalonate groups, such as, for example, polysilicone-15, for example marketed by Hoffmann LaRoche under the name “Parsol SLX”.
4,4-Diarylbutadiene derivatives: 1,1-Dicarboxy(2,2′-dimethylpropyl)-4,4-diphenylbutadiene.
Benzoxazole derivatives: 2,4-bis[5-(1-dimethylpropyl)benzoxazol-2-yl(4-phenyl) imino]-6-(2-ethylhexyl)imino-1,3,5-triazine, for example marketed by Sigma 3V under the name Uvasorb K2A, and mixtures comprising this.
Piperazine derivatives, such as, for example, the compound
or the UV filters of the following structures
It is also possible to use UV filters based on polysiloxane copolymers having a random distribution in accordance with the following formula, where, for example, a=1.2; b=58 and c=2.8:
The compounds listed should only be regarded as examples. It is of course also possible to use other UV filters.
Suitable organic UV-protecting substances can preferably be selected from the following list: Ethylhexyl salicylate, Phenylbenzimidazolesulfonic acid, Benzophenone-3, Benzophenone-4, Benzophenone-5, n-Hexyl 2-(4- diethylamino-2-hydroxybenzoyl)benzoate, 4-Methylbenzylidenecamphor, Terephthalylidenedicamphorsulfonic acid, Disodium phenyldibenzimidazoletetrasulfonate, Methylenebis(benzotriazolyl)tetramethylbutylphenol, Ethylhexyl Triazone, Diethylhexyl Butamido Triazone, Drometrizole trisiloxane, Polysilicone-15, 1,1-Dicarboxy(2,2′-dimethylpropyl)-4,4-diphenylbutadiene, 2,4-bis[5-1(dimethylpropyl)benzoxazol-2-yl(4-phenyl) imino]-6-(2-ethylhexyl)imino-1,3,5-triazine and mixtures thereof.
These organic UV filters are generally incorporated into formulations in an amount of 0.01 percent by weight to 20 percent by weight, preferably 1% by weight-10% by weight.
Besides the compounds of the formula I, at least dihydroxyacetone as self-tanning substance and the optional other ingredients, as described above, the preparations may comprise further inorganic UV filters, so-called particulate UV filters.
These combinations with particulate UV filters are possible both as powder and also as dispersion or paste of the following types.
Preference is given here both to those from the group of the titanium dioxides, such as, for example, coated titanium dioxide (for example Eusolex® T-2000, Eusolex®T-AQUA, Eusolex®T-AVO, Eusolex®T-OLEO), zinc oxides (for example Sachtotec®), iron oxides or also cerium oxides and/or zirconium oxides.
Furthermore, combinations with pigmentary titanium dioxide or zinc oxide are also possible, where the particle size of these pigments are greater than or equal to 200 nm, for example Hombitan® FG or Hombitan® FF-Pharma.
It may furthermore be preferred for the preparations to comprise inorganic UV filters which have been aftertreated by conventional methods, as described, for example, in Cosmetics & Toiletries 1990, 105, 53. One or more of the following aftertreatment components can be selected here: amino acids, beeswax, fatty acids, fatty acid alcohols, anionic surfactants, lecithin, phospholipids, sodium, potassium, zinc, iron or aluminium salts of fatty acids, polyethylenes, silicones, proteins (particularly collagen or elastin), alkanolamines, silicon dioxide, aluminium oxide, further metal oxides, phosphates, such as sodium hexametaphosphate, or glycerine.
Particulate UV filters which are preferably employed here are:
The treated micronised titanium dioxides employed for the combination may also be aftertreated with:
aluminium and silicone oils, such as, for example, the product UV-Titan M262 from Sachtleben,
The combination with the following products may furthermore also be advantageous:
By way of example, it is also possible to employ mixtures of various metal oxides, such as, for example, titanium dioxide and cerium oxide, with and without aftertreatment, such as, for example, the product Sunveil A from Ikeda. In addition, also mixtures of aluminium oxide, silicon dioxide and silicone-aftertreated titanium dioxide, zinc oxide mixtures, such as, for example, the product UV-Titan M261 from Sachtleben.
These inorganic UV filters are generally incorporated into the preparations in an amount of 0.1 percent by weight to 25 percent by weight, preferably 2% by weight-10% by weight.
By combination of one or more of the said compounds having a UV filter action, the protective action against harmful effects of the UV radiation can be optimised.
All said UV filters can also be employed in encapsulated form. In particular, it is advantageous to employ organic UV filters in encapsulated form.
The capsules in preparations to be employed in accordance with the invention are preferably present in amounts which ensure that the encapsulated UV filters are present in the preparation in the percent by weight ratios indicated above.
Preferred preparations may also comprise at least one further cosmetic active compound, for example selected from antioxidants, anti-ageing active compounds, anti-wrinkle, anti-flake, anti-acne, deodorants, anti-cellulite active compounds, self-tanning substances, skin-lightening active compounds or vitamins.
The protective action of preparations against oxidative stress or against the effect of free radicals can be improved if the preparations comprise one or more antioxidants, the person skilled in the art being presented with absolutely no difficulties in selecting antioxidants which act suitably quickly or with a time delay.
There are many proven substances known from the specialist literature which can be used as antioxidants, for example amino acids (for example glycine, histidine, tyrosine, tryptophan) and derivatives thereof, imidazoles, (for example urocanic acid) and derivatives thereof, peptides, such as D,L-carnosine, D-carnosine, L-carnosine and derivatives thereof (for example anserine), carotinoids, carotenes (for example α-carotene, β-carotene, lycopene) and derivatives thereof, chlorogenic acid and derivatives thereof, lipoic acid and derivatives thereof (for example dihydrolipoic acid), aurothioglucose, propylthiouracil and other thiols (for example thioredoxin, glutathione, cysteine, cystine, cystamine and the glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl and lauryl, palmitoyl, oleyl, γ-linoleyl, cholesteryl and glyceryl esters thereof) and salts thereof, dilauryl thiodipropionate, distearyl thiodipropionate, thiodipropionic acid and derivatives thereof (esters, ethers, peptides, lipids, nucleotides, nucleosides and salts), and sulfoximine compounds (for example buthionine sulfoximines, homocysteine sulfoximine, buthionine sulfones, penta-, hexa- and heptathionine sulfoximine) in very low tolerated doses (for example pmol to μmol/kg), and also (metal) chelating agents, (for example α-hydroxyfatty acids, palmitic acid, phytic acid, lactoferrin), α-hydroxy acids (for example citric acid, lactic acid, malic acid), humic acid, bile acid, bile extracts, bilirubin, biliverdin, EDTA, EGTA and derivatives thereof, unsaturated fatty acids and derivatives thereof, vitamin C and derivatives (for example ascorbyl palmitate, magnesium ascorbyl phosphate, ascorbyl acetate), tocopherols and derivatives (for example vitamin E acetate), vitamin A and derivatives (for example vitamin A palmitate) and conifervl benzoate of benzoin resin, rutinic acid and derivatives thereof, α-glycosylrutin, ferulic acid, furfurylideneglucitol, carnosine, butylhydroxytoluene, butylhydroxyanisole, nordihydroguaiaretic acid, trihydroxybutyrophenone, quercetin, uric acid and derivatives thereof, mannose and derivatives thereof, zinc and derivatives thereof (for example ZnO, ZnSO4), selenium and derivatives thereof (for example selenomethionine), stilbenes and derivatives thereof (for example stilbene oxide, trans-stilbene oxide).
Suitable antioxidants are also compounds of the formulae A or B
in which
The terms R1 to R6 and X only apply here to the radicals of the formulae A and B and do not apply to the radicals of the formula I.
Mixtures of antioxidants are likewise suitable for use in the cosmetic preparations according to the invention. Known and commercial mixtures are, for example, mixtures comprising, as active ingredients, lecithin, L-(+)-ascorbyl palmitate and citric acid, natural tocopherols, L-(+)-ascorbyl palmitate, L-(+)-ascorbic acid and citric acid (for example Oxynex® K LIQUID), tocopherol extracts from natural sources, L-(+)-ascorbyl palmitate, L-(+)-ascorbic acid and citric acid (for example Oxynex® L LIQUID), DL-α-tocopherol, L-(+)-ascorbyl palmitate, citric acid and lecithin (for example Oxynex® LM) or butylhydroxytoluene (BHT), L-(+)-ascorbyl palmitate and citric acid (for example Oxynex® 2004). Antioxidants of this type are usually employed in such preparations with the compounds according to the invention in percent by weight ratios in the range from 1000:1 to 1:1000, preferably in percent by weight ratios of 100:1 to 1:100.
Of the phenols, the polyphenols, some of which are naturally occurring, are of particular interest for applications in the pharmaceutical, cosmetic or nutrition sector. For example, the flavonoids or bioflavonoids, which are principally known as plant dyes, frequently have an antioxidant potential. K. Lemanska, H. Szymusiak, B. Tyrakowska, R. Zielinski, I. M. C. M. Rietjens; Current Topics in Biophysics 2000, 24, 101, are concerned with effects of the substitution pattern of mono- and dihydoxyflavones. It is observed therein that dihydroxyflavones containing an OH group adjacent to the keto function or OH groups in the 3′4′- or 6,7- or 7,8-position have antioxidative properties, while other mono- and dihydroxyflavones in some cases do not have antioxidative properties.
Quercetin (cyanidanol, cyanidenolon 1522, meletin, sophoretin, ericin, 3,3′,4′,5,7-pentahydroxyflavone) is frequently mentioned as a particularly effective antioxidant (for example C. A. Rice-Evans, N. J. Miller, G. Paganga, Trends in Plant Science 1997, 2, 152. K. Lemanska, H. Szymusiak, B. Tyrakowska, R. Zielinski, A. E. M. F. Soffers and I. M. C. M. Rietjens (Free Radical Biology & Medicine 2001, 31, 869, have investigated the pH dependence of the antioxidant action of hydroxyflavones. Quercetin exhibits the highest activity amongst the structures investigated over the entire pH range.
Suitable anti-ageing active compounds, in particular for skin-care preparations, are preferably so-called compatible solutes. These are substances which are involved in the osmosis regulation of plants or microorganisms and can be isolated from these organisms. The generic term compatible solutes here also encompasses the osmolytes described in German patent application DE-A-10133202. Suitable osmolytes are, for example, the polyols, methylamine compounds and amino acids and respective precursors thereof. Osmolytes in the sense of German patent application DE-A-10133202 are taken to mean, in particular, substances from the group of the polyols, such as, for example, myo-inositol, mannitol or sorbitol, and/or one or more of the osmolytically active substances mentioned below: taurine, choline, betaine, phosphorylcholine, glycerophosphorylcholines, glutamine, glycine, α-alanine, glutamate, aspartate, proline and taurine. Precursors of these substances are, for example, glucose, glucose polymers, phosphatidylcholine, phosphatidylinositol, inorganic phosphates, proteins, peptides and polyamino acids. Precursors are, for example, compounds which are converted into osmolytes by metabolic steps.
Compatible solutes which are preferably employed in accordance with the invention are substances selected from the group consisting of pyrimidine-carboxylic acids (such as ectoin and hydroxyectoin), proline, betaine, glutamine, cyclic diphosphoglycerate, N.-acetylornithine, trimethylamine N-oxide di-myo-inositol phosphate (DIP), cyclic 2,3-diphosphoglycerate (cDPG), 1,1-diglycerol phosphate (DGP), β-mannosyl glycerate (firoin), β-mannosyl glyceramide (firoin-A) or/and dimannosyl diinositol phosphate (DMIP) or an optical isomer, derivative, for example an acid, a salt or ester, of these compounds, or combinations thereof.
Of the pyrimidinecarboxylic acids, particular mention should be made here of ectoin ((S)-1,4,5,6-tetrahydro-2-methyl-4-pyrimidinecarboxylic acid) and hydroxyectoin ((S,S)-1,4,5,6-tetrahydro-5-hydroxy-2-methyl-4-pyrimidine-carboxylic acid) and derivatives thereof.
Additionally, anti-aging active compounds which can be used are products from Merck, such as, for example, 5,7-dihydroxy-2-methylchromone, marketed under the trade name RonaCare® Luremine or the commercial products RonaCare® Isoquercetin, RonaCare® Tilirosid or RonaCare® Cyclopeptide 5.
The preparations may also comprise one or more further skin-lightening active compounds or synonymously depigmentation active compounds. Skin-lightening active compounds can in principle be all active compounds known to the person skilled in the art. Examples of compounds having skin-lightening activity are hydroquinone, kojic acid, arbutin, aloesin, niacinamide, azelaic acid, elagic acid, mulberry extract, magnesium ascorbyl phosphate, liquorice extract, emblica, ascorbic acid or rucinol.
The preparations to be employed may comprise vitamins as further ingredients. Preference is given to vitamins and vitamin derivatives selected from vitamin A, vitamin A propionate, vitamin A palmitate, vitamin A acetate, retinol, vitamin B, thiamine chloride hydrochloride (vitamin B1), riboflavin (vitamin B2), nicotinamide, vitamin C (ascorbic acid), vitamin D, ergocalciferol (vitamin D2), vitamin E, DL-α-tocopherol, tocopherol E acetate, tocopherol hydrogensuccinate, vitamin K1; esculin (vitamin P active compound), thiamine (vitamin B1), nicotinic acid (niacin), pyridoxine, pyridoxal, pyridoxamine, (vitamin B6), pantothenic acid, biotin, folic acid and cobalamine (vitamin B12), particularly preferably vitamin A palmitate, vitamin C and derivatives thereof, DL-α-tocopherol, tocopherol E acetate, nicotinic acid, pantothenic acid and biotin. In the case of cosmetic application, vitamins are usually added with the flavonoid-containing premixes or preparations in ranges from 0.01 to 5.0% by weight, based on the total weight. Nutrition-physiological applications are oriented towards the respective recommended vitamin requirement.
The retinoids described are at the same time also effective anti-cellulite active compounds. A likewise known anti-cellulite active compound is caffeine.
The said constituents of the preparation can be incorporated in the usual manner, with the aid of techniques which are well known to the person skilled in the art.
Suitable preparations are those for external application, for example can be sprayed onto the skin as cream or milk (O/W, W/O, O/W/O, W/O/W), as lotion or emulsion, in the form of oily-alcoholic, oily-aqueous or aqueous-alcoholic gels or solutions. They can be in the form of solid sticks or formulated as an aerosol.
Examples which may be mentioned of application forms of the preparations to be employed are: solutions, suspensions, emulsions, PIT emulsions, pastes, ointments, gels, creams, lotions, powders, soaps, surfactant-containing cleansing preparations, oils, aerosols, plasters, compresses, bandages and sprays.
Preferred assistants originate from the group of preservatives, stabilisers, solubilisers, colorants, odour improvers.
Ointments, pastes, creams and gels may comprise the customary vehicles which are suitable for topical application, for example animal and vegetable fats, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silica, talc and zinc oxide, or mixtures of these substances.
Powders and sprays may comprise the customary vehicles, for example lactose, talc, silica, aluminium hydroxide, calcium silicate and polyamide powder, or mixtures of these substances. Sprays may additionally comprise the customary readily volatile, liquefied propellants, for example chlorofluorocarbons, propane/butane or dimethyl ether. Compressed air can also advantageously be used.
Solutions and emulsions may comprise the customary vehicles, such as solvents, solubilisers and emulsifiers, for example water, ethanol, isopropanol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butyl glycol, oils, in particular cottonseed oil, peanut oil, wheatgerm oil, olive oil, castor oil and sesame oil, glycerol fatty acid esters, polyethylene glycols and fatty acid esters of sorbitan, or mixtures of these substances.
A preferred solubiliser in general is 2-isopropyl-5-methylcyclohexane-carbonyl-D-alanine methyl ester.
Suspensions may comprise the customary vehicles, such as liquid diluents, for example water, ethanol or propylene glycol, suspension media, for example ethoxylated isostearyl alcohols, polyoxyethylene sorbitol esters and polyoxyethylene sorbitan esters, microcrystalline cellulose, aluminium metahydroxide, bentonite, agar-agar and tragacanth, or mixtures of these substances.
Soaps may comprise the customary vehicles, such as alkali metal salts of fatty acids, salts of fatty acid monoesters, fatty acid protein hydrolysates, isothionates, lanolin, fatty alcohol, vegetable oils, plant extracts, glycerol, sugars, or mixtures of these substances.
Surfactant-containing cleansing products may comprise the customary vehicles, such as salts of fatty alcohol sulfates, fatty alcohol ether sulfates, sulfosuccinic acid monoesters, fatty acid protein hydrolysates, isothionates, imidazolinium derivatives, methyl taurates, sarcosinates, fatty acid amide ether sulfates, alkylamidobetaines, fatty alcohols, fatty acid glycerides, fatty acid diethanolamides, vegetable and synthetic oils, lanolin derivatives, ethoxylated glycerol fatty acid esters, or mixtures of these substances.
Face and body oils may comprise the customary vehicles, such as synthetic oils, such as fatty acid esters, fatty alcohols, silicone oils, natural oils, such as vegetable oils and oily plant extracts, paraffin oils, lanolin oils, or mixtures of these substances.
Further typical cosmetic application forms are also lipsticks, lip-care sticks, powder make-up, emulsion make-up and wax make-up, and sunscreen, pre-sun and after-sun preparations.
The preferred preparation forms also include, in particular, emulsions.
Emulsions are advantageous and comprise, for example, the said fats, oils, waxes and other fatty substances, as well as water and an emulsifier, as usually used for a preparation of this type.
The lipid phase may advantageously be selected from the following group of substances:
For the purposes of the present invention, the oil phase of the emulsions, oleogels or hydrodispersions or lipodispersions is advantageously selected from the group of esters of saturated and/or unsaturated, branched and/or unbranched alkanecarboxylic acids having a chain length of 3 to 30 C atoms and saturated and/or unsaturated, branched and/or unbranched alcohols having a chain length of 3 to 30 C atoms, or from the group of esters of aromatic carboxylic acid and saturated and/or unsaturated, branched and/or unbranched alcohols having a chain length of 3 to 30 C atoms. Ester oils of this type can then advantageously be selected from the group 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, oleyl oleate, oleyl erucate, erucyl oleate, erucyl erucate and synthetic, semisynthetic and natural mixtures of esters of this type, for example jojoba oil.
The oil phase may furthermore advantageously be selected from the group branched and unbranched hydrocarbons and hydrocarbon waxes, silicone oils, dialkyl ethers, the group of saturated or unsaturated, branched or unbranched alcohols, and fatty acid triglycerides, specifically the triglycerol esters of saturated and/or unsaturated, branched and/or unbranched alkanecarboxylic acids having a chain length of 8 to 24, in particular 12-18C atoms. The fatty acid triglycerides may, for example, advantageously be selected from the group of synthetic, semi-synthetic and natural oils, for example olive oil, sunflower oil, soya oil, peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, palm kernel oil and the like.
Any desired mixtures of oil and wax components of this type may also advantageously be employed for the purposes of the present invention. It may also be advantageous to employ waxes, for example cetyl palmitate, as sole lipid component of the oil phase.
The aqueous phase of the preparations to be employed optionally advantageously comprises alcohols, diols or polyols having a low carbon number, and ethers thereof, preferably ethanol, isopropanol, propylene glycol, glycerol, ethylene glycol, ethylene glycol monoethyl or monobutyl ether, propylene glycol monomethyl, monoethyl or monobutyl ether, diethylene glycol monomethyl or monoethyl ether and analogous products, furthermore alcohols having a low carbon number, for example ethanol, isopropanol, 1,2-propanediol, glycerol, and, in particular, one or more thickeners, which may advantageously be selected from the group silicon dioxide, aluminium silicates, polysaccharides and derivatives thereof, for example hyaluronic acid, xanthan gum, hydroxypropylmethylcellulose, particularly advantageously from the group of the polyacrylates, preferably a polyacrylate from the group of the so-called Carbopols, for example Carbopol grades 980, 981, 1382, 2984, 5984, in each case individually or in combination.
In particular, mixtures of the above-mentioned solvents are used. In the case of alcoholic solvents, water may be a further constituent.
Emulsions are advantageous and comprise, for example, the said fats, oils, waxes and other fatty substances, as well as water and an emulsifier, as usually used for a formulation of this type.
In a preferred embodiment, the preparations to be employed comprise hydrophilic surfactants. The hydrophilic surfactants are preferably selected from the group of the alkylglucosides, acyl lactylates, betaines and coconut amphoacetates.
It is likewise advantageous to employ natural or synthetic raw materials and assistants or mixtures which are distinguished by an effective content of the active compounds used in accordance with the invention, for example Plantaren® 1200 (Henkel KGaA), Oramix® NS 10 (Seppic). The cosmetic and dermatological preparations may exist in various forms. Thus, they may be, for example, a solution, a water-free preparation, an emulsion or microemulsion of the water-in-oil (W/O) type or of the oil-in-water (O/W) type, a multiple emulsion, for example of the water-in-oil-in-water (W/O/W) type, a gel, a solid stick, an ointment or an aerosol. It is also advantageous to administer ectoins in encapsulated form, for example in collagen matrices and other conventional encapsulation materials, for example as cellulose encapsulations, in gelatine, wax matrices or liposomally encapsulated. In particular, wax matrices, as described in DE-A-43 08 282, have proven favourable. Preference is given to emulsions. O/W emulsions are particularly preferred. Emulsions, W/O emulsions and O/W emulsions are obtainable in a conventional manner.
Emulsifiers that can be used are, for example, the known W/O and O/W emulsifiers. It is advantageous to use further conventional co-emulsifiers in the preferred O/W emulsions.
The co-emulsifiers selected are advantageously, for example, O/W emulsifiers, principally from the group of substances having HLB values of 11-16, very particularly advantageously having HLB values of 14.5-15.5, so long as the O/W emulsifiers have saturated radicals R and R′. If the O/W emulsifiers have unsaturated radicals R and/or R′, or if isoalkyl derivatives are present, the preferred HLB value of such emulsifiers may also be lower or higher.
It is advantageous to select the fatty alcohol ethoxylates from the group of the ethoxylated stearyl alchols, cetyl alcohols, cetylstearyl alcohols (cetearyl alcohols).
It is furthermore advantageous to select the fatty acid ethoxylates from the following group:
An ethoxylated alkyl ether carboxylic acid or salt thereof which can advantageously be used is sodium laureth-11 carboxylate. An alkyl ether sulfate which can advantageously be used is sodium laureth 1-4 sulfate. An ethoxylated cholesterol derivative which can advantageously be used is polyethylene glycol (30) cholesteryl ether. Polyethylene glycol (25) soyasterol has also proven successful. Ethoxylated triglycerides which can advantageously be used are the polyethylene glycol (60) evening primrose glycerides.
It is furthermore advantageous to select the polyethylene glycol glycerol fatty acid esters from the group polyethylene glycol (20) glyceryl laurate, polyethylene glycol (21) glyceryl laurate, polyethylene glycol (22) glyceryl laurate, polyethylene glycol (23) glyceryl laurate, polyethylene glycol (6) glyceryl caprate/cprinate, polyethylene glycol (20) glyceryl oleate, polyethylene glycol (20) glyceryl isostearate, polyethylene glycol (18) glyceryl oleate (cocoate).
It is likewise favourable to select the sorbitan esters from the group polyethylene glycol (20) sorbitan monolaurate, polyethylene glycol (20) sorbitan monostearate, polyethylene glycol (20) sorbitan monoisostearate, polyethylene glycol (20) sorbitan monopalmitate, polyethylene glycol (20) sorbitan monooleate.
The following can be employed as optional W/O emulsifiers, but ones which may nevertheless be advantageous in accordance with the invention:
Particularly advantageous W/O emulsifiers are glyceryl monostearate, glyceryl monoisostearate, glyceryl monomyristate, glyceryl monooleate, diglyceryl monostearate, diglyceryl monoisostearate, propylene glycol monostearate, propylene glycol monoisostearate, propylene glycol monocaprylate, propylene glycol monolaurate, sorbitan monoisostearate, sorbitan monolaurate, sorbitan monocaprylate, sorbitan monoisooleate, sucrose distearate, cetyl alcohol, stearyl alcohol, arachidyl alcohol, behenyl alcohol, isobehenyl alcohol, selachyl alcohol, chimyl alcohol, polyethylene glycol (2) stearyl ether (steareth-2), glyceryl monolaurate, glyceryl monocaprinate, glyceryl monocaprylate or PEG-30 dipolyhydroxystearate.
The preparation may comprise cosmetic adjuvants which are usually used in this type of preparation, such as, for example, thickeners, softeners, moisturisers, surface-active agents, emulsifiers, preservatives, antifoams, perfumes, waxes, lanolin, propellants, dyes and/or pigments, and other ingredients usually used in cosmetics.
The dispersant or solubiliser used can be an oil, wax or other fatty bodies, a short-chain, monohydric monoalcohol or a short-chain low-molecular-weight polyol or mixtures thereof. Particularly preferred monoalcohols or polyols include ethanol, i-propanol, propylene glycol, glycerol and sorbitol.
A preferred embodiment of the invention is an emulsion which is in the form of a protective cream or milk and comprises, for example, fatty alcohols, fatty acids, fatty acid esters, in particular triglycerides of fatty acids, lanolin, natural and synthetic oils or waxes and emulsifiers in the presence of water.
Further preferred embodiments are oily lotions based on natural or synthetic oils and waxes, lanolin, fatty acid esters, in particular triglycerides of fatty acids, or oily-alcoholic lotions based on a lower alcohol, such as ethanol, or a glycerol, such as propylene glycol, and/or a polyol, such as glycerol, and oils, waxes and fatty acid esters, such as triglycerides of fatty acids.
The preparation may also be in the form of an alcoholic gel which comprises one or more low-molecular-weight alcohols or polyols, such as ethanol, propylene glycol or glycerol, and a thickener, such as siliceous earth. The oily-alcoholic gels also comprise natural or synthetic oil or wax. The solid sticks consist of natural or synthetic waxes and oils, fatty alcohols, fatty acids, fatty acid esters, lanolin and other fatty substances.
If a preparation is formulated as an aerosol, use is generally made of the customary propellants, such as alkanes, air, nitrogen, dinitrogen monoxide, preferably alkanes.
Even without further comments, it is assumed that a person skilled in the art will be able to utilise the above description in the broadest scope. The preferred embodiments and examples should therefore merely be regarded as descriptive disclosure which is absolutely not limiting in any way. The complete disclosure content of all applications and publications mentioned above and below is incorporated into this application by way of reference. The percent by weight ratios of the individual ingredients in the preparations of the examples expressly belong to the disclosure content of the description and can therefore be utilised as features.
Further important features and advantages of the invention arise from the sub-claims and from the examples.
It goes without saying that the features mentioned above and still to be explained below can be used not only in the respective combination indicated, but also in other combinations or in isolation without leaving the framework of the present invention.
Preferred embodiments of the invention are described in the examples and are explained in greater detail in the following description without restricting the scope of the present invention.
Four participants (female and male) were selected for the study. In order to carry out the study, test fields measuring 4×4.5 cm2 were marked on both forearms of each participant.
The following test formulation was used:
For comparison, the above-mentioned test formulation was used with 6 percent by weight of dihydroxyacetone without addition of isomaltulose. One test field was treated with 2 μl/cm2 of the O/W formulation described above comprising 6 percent by weight of DHA, the other test field was treated with 2 μl/cm2 of the O/W formulation described above comprising 5 percent by weight of DHA and 5 percent by weight of isomaltulose. For this purpose, the sample was applied in a grid, so that the test amount is distributed uniformly on the test field. Using a glove finger, the sample was rubbed uniformly with gentle pressure, so that the entire test area was treated and the preparation was absorbed (about 30 seconds). In each case, one treatment was carried out per forearm. A colour measurement was carried out in the test field before treatment and 24 h after the treatment. The colour measurements were carried out using a Minolta cr-300 Chroma-meter, and the L, a and b values in accordance with the CIE (Commission Internationale de l'Eclairage) definition were determined. The decrease in luminance and the increase in the colour having a red and yellow wavelength were determined compared with the colour of the skin before the treatment. The following values were obtained:
Description of the performance of the B16 V mouse melanoma cell test:
B16V mouse melanoma cells (manufacturer: DSMZ; Article No.: ACC370) in RPMI medium (Invitrogen, Article No.: 31870), to which 10% of FBS (foetal bovine serum, Invitrogen, Article No: 10499044), 2 mM L-glutamine (Invitrogen, Article No: 25030) and 1 mM sodium pyruvate (Invitrogen, Article No: 11360) had additionally been added (modified RPMI medium), are transferred into a culture bottle and incubated at 37° C. and 5% CO2 for 72 h. The medium is separated off, and the cells are washed with 10 ml of D-PBS (Invitrogen, Article No. 14190) and subsequently filtered off with suction. 1 ml of HyQtase cell detachment solution (Hyclone, Article No. SV30030.01) is added to the cells. The bottle is swirled a number of times, and the HyQtase cell detachment solution is subsequently removed by suction. The cells are then incubated in the incubator at 37° C. and 5% CO2for 5 min. The cells are taken up in the modified RPMI medium (Invitrogen, Article No.: 31870), and the cell count is determined. To this end, the cells are stained with Tryptan Blue and counted in a Neubauer chamber. The cells are subsequently sown out again in the modified RPMI medium in a defined cell count of 80,000 cells per well (6-well clear plate, TCT, PS (Nunc)).
The plate is subsequently incubated at 37° C. and 5% CO2 for 24 h, the medium is then removed. 1980 μl of the isomaltulose dilution are subsequently added. For this substance dilution, the isomaltulose is dissolved in DMSO and subsequently filtered through a sterile filter (0.2 μm, Millipore, Article No. SLLG013SL). The solution is then diluted with the modified RPMI medium (in this case the FBS content in the RPMI medium is only 5%) in such a way that the isomaltulose concentration is 1 mM or 5 mM. 20 μl of an alpha-MSH solution in DMSO (alpha-melanocyte-stimulating hormone=alpha-MSH) (DMSO, Sigma, Article No.:D2650) are then added, so that the alpha-MSH concentration in the well is 10−8 M. The plate is subsequently incubated again at 37° C. and 5% CO2 for 24 h. The process described in this section is repeated a further twice in total.
After the final incubation period, the medium is removed by suction, and the cells are washed with 1000 μl of D-PBS (Invitrogen, Article No. 14190). The medium is again removed by suction 250 μl of HyQtase cell detachment solution (Hyclone, Article No. SV30030.01) are added to the cells. The 6-well plate is swirled a number of times, and the HyQtase cell detachment solution is subsequently removed by suction. The cells are then incubated in the incubator at 37° C. and 5% CO2 for 5 min. The cells are then taken up in 1.5 ml of DPBS (Invitrogen, Article No. 14190) and transferred into a cup (SARSTEDT, Ref. 72.692.005). The cell count is subsequently determined. To this end, the cells are stained with Tryptan Blue and counted in a Neubauer chamber. The cells are then centrifuged for 1 min at 3500 g. The pellets obtained are photographed, and the supernatant is subsequently removed by suction. The pellets are dissolved in 1 ml of 1N NaOH at 80° C. for 1 h and then cooled to RT. 200 μl are then pipetted as quadruple determination (per cup) into a 96-well plate (VWR, Article No. 4100636981), and the absorption at a wavelength of 405 nm is determined. (Satire, Tecan). The content of melanin can be determined in this way by means of a calibration line.
The following table shows the results of the determination of the melanin concentration obtained for the substance dilutions indicated. The other values were determined relative to the blank sample with dimethyl sulfoxide (DMSO) and α-MSH, whose measurement was set at 100%
12 explants from the stomach tissue of a 49-year-old pale-skinned woman (Caucasian type) having an average diameter of 10 mm are prepared (reference: P831-AB49).
The explants are kept in a BEM medium (BIO-EC's explants medium) at 37° C. in a moist atmosphere comprising 5% of CO2.
The following samples are tested: (in each case 3 explants), where the solutions of the corresponding substances used comprise 90% of water and 10% of ethanol.
2 μl of the respective sample are added to the explants and distributed for the first time (DO), 1 day later (D1), 2 days later (D2), 3 days later (D3) and 4 days later (D4). The colour of the explants is determined chromametrically. The measurements are carried out on addition (DO), on day 1 (D1), on day 5 (D5) and on day 11 (D11). The colour measurements are carried out using a Minolta CR-300 Chroma-meter, and the L, a and b values are read off correspondingly on the instrument.
Principle of the Chromametric Measurement:
The following parameters are set:
In 1931, a test series was carried out by the CIE (Commision Internationale de L'Eclairage), where the “2-degree standard observer” was defined. A colour area is present here which is viewed at a viewing angle of 2 degrees. This viewing angle is used as standard in the chromametric measurement.
The sample is placed on the bearing rail with the epidermis facing downwards. The irradiation is carried out from the underside through the area indicated (3 mm).
Contrast Study:
In the colorimetric determinations <L a b>, the L value determines the contrast of the skin. If the L value drops, the skin appears darker.
Results:
Table 1 shows the measurement values of the explants for samples TO, R, P1 and P2 (in each case n=3):
In comparison with the untreated sample, isomaltulose exhibits a darkening of the skin (falling L values) and generates a more natural skin shade, confirmed by the increasing values of a red-brown shift (a value). Isomaltulose is a self-tanning substance.
In comparison with the positive control, the DHA/isomaltulose mixture exhibits a more natural skin colour (increasing a value confirms the red/brown shift). After 11 days, the DHA/isomaltulose mixture causes a darker colour compared with the colour generated by the positive control.
Preparation Process:
Firstly, phase A is warmed to 75° C. and phase B to 80° C. Phase B is then slowly added to phase A with stirring and stirred until a homogeneous mixture forms. After homogenisation, phase C is added to the formulation at 40° C.
Sources of Supply:
(1) Sasol Germany GmbH (2) Cognis GmbH (3) BASF AG (4) Degussa-Goldschmidt AG (5) Merck KGaA/Rona® (6) Sigma-Aldrich (7) Merck KGaA/Rona®
Preparation Process:
Firstly, phases A and B are warmed separately to 75° C. Phase A is then slowly added to phase B with careful stirring. The mixture is homogenised at 65° C. for one minute. The mixture is subsequently cooled to 40° C. with stirring, and phase C is added with stirring, the mixture is cooled to 35° C., and phase D is added, and cooling is continued.
Sources of Supply:
(1) Degussa-Goldschmidt AG (2) Sasol Germany GmbH (3) Cognis GmbH (4) Merck KGaA/Rona® (5) Sigma-Aldrich (6) Merck KGaA/Rona®
Preparation Process:
Firstly, phases A and B are warmed to 80° C. Phase B is then slowly added to phase A with stirring and homogenised. The mixture is then cooled, and phase C is added at 40 ° C.
Sources of Supply:
(1) Degussa-Goldschmidt AG, (2) Cognis GmbH, (3) BASF AG, (4) Sasol Germany GmbH, (5) Merck KGaA/Rona® (6) Dow Corning (7) Kuhs GmbH & Co. KG, (8) Merck KGaA/Rona®, (9) Sigma-Aldrich
Preparation Process:
Firstly, phases A and B are mixed separately and warmed to 75° C. Phase C is then added to phase B and added to phase A with stirring. The mixture is homogenised. The mixture is then cooled with stirring, and phases D and E are added at 40° C.
Sources of Supply:
(1)Seppic (2) Uniqema (3) Cognis GmbH (4) Condea Chinica D.A.C.S.p.A. (5) Merck KGaA/Rona® (6) Dow Corning (7) Rhodia GmbH (8) Kuhs GmbH & Co. KG (9) Drom (10) Merck KGaA/Rona® (11) Sigma-Aldrich
Preparation Process:
Firstly, phase B is dissolved and then added to phase A. The pH is adjusted to the value pH=6.0 using sodium hydroxide solution or citric acid.
Sources of Supply:
(1) Dow Corning (2) Merck KGaA/Rona® (3) Merck KGaA/Rona® (4) Sigma-Aldrich
Preparation Process:
Firstly, phases A and B are mixed separately and warmed to 80° C. Phase B is then slowly added to phase A with stirring. The mixture is homogenised and cooled to 40° C, and phase C is added, then cooled to room temperature.
Sources of Supply:
(1) Merck KGaA/Rona® (2) Degussa-Goldschmidt AG (3) Cognis GmbH (4) BASF AG (5) Sasol Germany GmbH (6) Dow Corning (7) Sigma-Aldrich (8) Merck KGaA/Rona®
Preparation Process:
Firstly, phases A and B are warmed separately to 75° C. Phase A is then slowly added to phase B with stirring. Phase C is added to A/B at 60° C., and the mixture is homogenised. The mixture is subsequently cooled to 40° C., and phases D and E are added successively.
Sources of Supply:
(1)Seppic (2) Uniqema (3) Cognis GmbH (4) Condea Chimica D.A.C.S.p.A. (5) Dow Corning (6) Merck KGaA/Rona® (7) D. D. Williamson (8) Les Colorants Wackherr SA (9) Drom (10) Merck KGaA/Rona® (11) Sigma-Aldrich
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2010 026 776.7 | Jul 2010 | DE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP11/03129 | 6/24/2011 | WO | 00 | 1/9/2013 |
