Patent Application
20230293411
The present invention relates to the field of protection against ultraviolet (UV) radiation. In particular, the present invention relates to compounds of formula (I)
UV radiation causes harmful effects on the human skin. Beside the acute effect of sunburn of the skin, UV radiation is also known to increase the risk of skin cancer. Furthermore, long time exposure to UV-A and UV-B light can cause phototoxic and photo allergenic reactions on the skin and can accelerate skin aging.
To protect the human skin from UV radiation, various sun protecting UV filters (also referred to as UV absorbers) exist including UV-A filter, UV-B filter, and broadband filters. These filters are added to e.g. sunscreen or cosmetic compositions. The UV filters are either organic or inorganic, particulate or non-particulate compounds, of which all have a high absorption efficacy in the UV-light range. In general, UV light can be divided into UV-A radiation (320-400 nm) and UV-B radiation (280-320 nm). Depending on the position of the absorption maxima, UV filters are divided into UV-A and UV-B filters. In case an UV filter absorbs both, UV-A and UV-B light, it is referred to as a broadband absorber.
Since 2006, the EU commission has recommended that all sunscreen or cosmetic compositions should have an UV-A protection factor, which is at least one third of the labelled sun protection factor (SPF), wherein the sun protection factor refers mainly to the UV-B protection.
However, the UV filters known in the prior art, which are used in e.g. sunscreen or cosmetic compositions have certain disadvantages. In particular, it is referred to the disadvantage that the vast majority of cosmetic registered organic UV filters are resistant to environmental degradation through chemical, biological, and photolytic processes. Because of their persistence, they bioaccumulate with potential adverse impact on human health and the environment. Due to their wide release into the environment, and especially in the oceans, the demand for biodegradable UV filters is growing.
Currently, the only two biodegradable UV filters (octyl methoxy cinnamates or ethylhexyl methoxycinnamate—OMC and ethylhexyl salicylate—EHS) are both UV-B absorbers. Therefore, it is not possible to prepare biodegradable formulations able to protect e.g. the skin on the whole UV range including the harmful UV-A rays which are responsible for skin photoaging and cancer.
Croconic acid was found to be an excellent UV-A absorber and readily biodegradable. Croconic acid is also known as 4,5-dihydroxy-4-cyclopentene-1,2,3-trione or 4,5-dihydroxycyclopent-4-ene-1,2,3-trione can be expressed by formula (CA).
The pH of cosmetic or pharmaceutical products desired for everyday application must be compatible with the physiological skin pH which is 3.5 to 5.5. The pH of cosmetic or pharmaceutical compositions usually is adjusted to pH 4.5 to 7.5. Water soluble salts of croconic acid are compatible with the physiological skin pH and can be easily incorporated in typical cosmetic or pharmaceutical compositions.
After applying cosmetic or pharmaceutical compositions (e.g. an emulsion) to the skin, water start to evaporate. Evaporation changes the composition and structure of the cosmetic or pharmaceutical composition (e.g. emulsion) on the skin surface. If exemplarily the UV absorber is dissolved in the water phase, water evaporation can significantly affect the amount of UV absorber remaining in the dissolved state (Baki et al., Introduction to Cosmetic Formulation and Technology, John Wiley & Sons, 2015, p. 244).
The sun protection is negatively impacted by the crystallization of croconic acid salts. In addition, croconic acid salts are known to be photo-instable, i.e. are known undergoing photo-oxidation (Fabre et al., Can. J. Chem., 1995, 73, 1298-1304).
Hence, there is an ongoing need for effective biodegradable UV filters. In particular, it was an object of the present invention to provide an effective biodegradable UV-A filter. In this connection it was a further object to provide biodegradable cosmetic or pharmaceutical compositions comprising ingredients suitable for the whole UV range, in particular wherein the cosmetic or pharmaceutical composition provides for an improved photostability. It was yet another object of the present invention to provide a UV filter (in particular a UV-A filter) which is suitable to use in cosmetic or pharmaceutical compositions, body-care products and/or household cleaning and treating agents.
It has surprisingly been found that at least one of these objects can be achieved by the compound of formula (I) and/or composition according to the present invention.
In particular, the inventors of the present invention have found compounds that effectively absorb light in the UV range relevant for UV protection and which remain dissolved (i.e. do not crystallize) after evaporation of water from aqueous solutions. These compounds are croconic acid salts as defined hereinafter.
In a first aspect, the present invention therefore relates to a compound of formula (I)
or a stereoisomer or tautomer thereof,
wherein
In the following, preferred embodiments of the substituents in the above formula (I) are described in further detail. It is to be understood that each preferred embodiment is relevant on its own as well as in combination with other preferred embodiments. Furthermore, it is to be understood that the preference in each case also apply to the stereoisomer or tautomer of the compound of the invention.
In a preferred embodiment A0 of the first aspect, R3 and R4 are independently C1-C6-hydroxyalkyl, C2-C4-hydroxyalkenyl, C1-C6-aminoalkyl, (CH2O)n—OH, (CH2CH2O)n—OH, or (CH2CH2CH2O)n—OH; or together with the nitrogen to which they are bonded form a 5-membered saturated, partially or fully unsaturated, or aromatic heterocyclic ring, wherein said heterocyclic ring comprises one or more, same of different heteroatoms selected from O, N, or S, wherein said N- and/or S-atoms are independently oxidized or non-oxidized, and wherein each substitutable carbon or heteroatom in the heterocyclic ring is independently unsubstituted or substituted with one or more, same or different substituents RM; or together with the nitrogen to which they are bonded form a double bond to a carbon atom, which is further substituted with two N-atoms, which are independently unsubstituted or substituted with one or more, same or different substituents RN; and
R7, and R8 are independently C1-C6-hydroxyalkyl, C2-C4-hydroxyalkenyl, C1-C6-aminoalkyl, (CH2O)n—OH, (CH2CH2O)n—OH, or (CH2CH2CH2O)n—OH; or together with the nitrogen to which they are bonded form a 5-membered saturated, partially or fully unsaturated, or aromatic heterocyclic ring, wherein said heterocyclic ring comprises one or more, same of different heteroatoms selected from O, N, or S, wherein said N- and/or S-atoms are independently oxidized or non-oxidized, and wherein each substitutable carbon or heteroatom in the heterocyclic ring is independently unsubstituted or substituted with one or more, same or different substituents RM; or together with the nitrogen to which they are bonded form a double bond to a carbon atom, which is further substituted with two N-atoms, which are independently unsubstituted or substituted with one or more, same or different substituents RN.
In a preferred embodiment A1 of the first aspect, R1 and R5 are H.
In a preferred embodiment A2 of the first aspect, R2 to R4 are independently C1-C6-hydroxyalkyl and R6 to R8 are independently C1-C6-hydroxyalkyl.
In a preferred embodiment A3 of the first aspect, R1 and R5 are the same, preferably H; R2 to R4 are the same; and R6 to R8 are the same.
In a preferred embodiment A4 of the first aspect, R2 to R4 and R6 to R8 are hydroxyethyl.
In a preferred embodiment A5 of the first aspect, R1, R2, R5, and R6 are the same;
In a preferred embodiment A6 of the first aspect, R1, R2, R5, and R6 are H;
In a preferred embodiment A7 of the first aspect, R1, R2, R5, and R6 are H;
In a preferred embodiment A8 of the first aspect, the compound according to formula (I) is selected from the group consisting of 4,5-dihydroxy-4-cyclopentene-1,2,3-trione di-triethanolammonium salt, 4,5-dihydroxy-4-cyclopentene-1,2,3-trione di-guanidinium salt, and 4,5-dihydroxy-4-cyclopentene-1,2,3-trione di-argininium salt.
In a preferred embodiment A9 of the first aspect, the compound of formula (I) is selected from the group consisting of
In a second aspect, the present invention relates to a cosmetic or pharmaceutical composition, comprising a compound according to any one of claims 1 to 10 and optionally a dermatologically acceptable emulsifier, thickener, or emollient.
In a preferred embodiment B1 of the second aspect, the cosmetic or pharmaceutical composition further comprises at least one additional UV filter, different to the compound of formula (I), preferably wherein the at least one additional UV filter is a natural and/or biodegradable UV filter.
In a preferred embodiment B2 of the second aspect, the cosmetic or pharmaceutical composition further comprises a photostabilizer, preferably a quencher, wherein preferably the photostabilizer is comprised in the cosmetic or pharmaceutical composition in an amount of at least 0.5 wt.-%, based on the total weight of the cosmetic or pharmaceutical composition.
In a third aspect, the present invention relates to the use of at least one compound of formula (I) as defined in the first aspect (including all embodiments thereof as described herein) or a cosmetic or pharmaceutical composition as defined in the second aspect (including all embodiments thereof as described herein) to protect skin against UV radiations.
In a fourth aspect, the present invention relates to the use of a compound of formula (I) as defined in the first aspect (including all embodiments thereof as described herein) in body-care products or household cleaning and treating agents as a light stabilizer to protect ingredients against photolytic degradation.
In a fifth aspect, the present invention relates to the at least one compound as defined in the first aspect or the cosmetic or pharmaceutical composition as defined in the second aspect for use to protect skin against UV radiations.
Before describing in detail exemplary embodiments of the present invention, definitions important for understanding the present invention are given.
As used in this specification and in the appended claims, the singular forms of “a” and “an” also include the respective plurals unless the context clearly dictates otherwise. In the context of the present invention, the terms “about” and “approximately” denote an interval of accuracy that a person skilled in the art will understand to still ensure the technical effect of the feature in question. The term typically indicates a deviation from the indicated numerical value of ±20%, preferably ±15%, more preferably ±10%, and even more preferably ±5%. It is to be understood that the term “comprising” is not limiting. For the purposes of the present invention the term “consisting of” is considered to be a preferred embodiment of the term “comprising of”. If hereinafter a group is defined to comprise at least a certain number of embodiments, this is meant to also encompass a group which preferably consists of these embodiments only. Furthermore, the terms “first”, “second”, “third” or “(a)”, “(b)”, “(c)”, “(d)” etc. and the like in the description and in the claims, are used for distinguishing between similar elements and not necessarily for describing a sequential or chronological order. It is to be understood that the terms so used are interchangeable under appropriate circumstances and that the embodiments of the invention described herein are capable of operation in other sequences than described or illustrated herein. In case the terms “first”, “second”, “third” or “(a)”, “(b)”, “(c)”, “(d)”, “i”, “ii” etc. relate to steps of a method or use or assay there is no time or time interval coherence between the steps, i.e. the steps may be carried out simultaneously or there may be time intervals of seconds, minutes, hours, days, weeks, months or even years between such steps, unless otherwise indicated in the application as set forth herein above or below. It is to be understood that this invention is not limited to the particular methodology, protocols, reagents etc. described herein as these may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention that will be limited only by the appended claims. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art.
The term “compound(s) according to the invention”, or “compounds of formula (I)” comprises the compound(s) as defined herein as well as a stereoisomer or tautomer thereof.
Depending on the substitution pattern, the compounds according to the invention may have one or more centers of chirality. The invention provides both the single pure enantiomers or pure diastereomers of the compounds according to the invention, and their mixtures and the use according to the invention of the pure enantiomers or pure diastereomers of the compounds according to the invention or their mixtures. Suitable compounds according to the invention also include all possible geometrical stereoisomers (cis/trans isomers or E/Z isomers) and mixtures thereof. Cis/trans isomers may e.g. be present with respect to an amide group. The term “stereoisomer(s)” encompasses both optical isomers, such as enantiomers or diastereomers, the latter existing due to more than one center of chirality in the molecule, as well as geometrical isomers (cis/trans isomers). The present invention relates to every possible stereoisomer of the compounds of formula (I), i.e. to single enantiomers or diastereomers, as well as to mixtures thereof.
The compounds of formula (I) may be amorphous or may exist in one or more different crystalline states (polymorphs) which may have different macroscopic properties such as stability or show different biological properties such as activities. The present invention relates to amorphous and crystalline compounds of formula (I), mixtures of different crystalline states of the respective compound of formula (I).
Tautomers may be formed, if a substituent is present at the compound of formula (I), which allows for the formation of tautomers such as keto-enol tautomers or the like.
The organic moieties mentioned in the above definitions of the variables are—like the term halogen—collective terms for individual listings of the individual group members. The prefix Cn-Cm indicates in each case the possible number of carbon atoms in the group.
The term “halogen” denotes in each case fluorine, bromine, chlorine, or iodine, in particular fluorine, chlorine, or bromine.
The term “alkyl” as used herein denotes in each case a straight-chain or branched alkyl group having usually from 1 to 8 carbon atoms, preferably from 1 to 4 carbon atoms. Examples of an alkyl group are methyl, ethyl, n-propyl, iso-propyl, n-butyl, 2-butyl, iso-butyl, tert-butyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, 1,1-dimethylpropyl, and 1,2-dimethylpropyl. Methyl, ethyl, n-propyl, iso-propyl, and iso-butyl, are particularly preferred.
The term “alkoxy” as used herein denotes in each case a straight-chain or branched alkyl group which is bonded via an oxygen atom and has usually from 1 to 6 carbon atoms, preferably 1 to 2 carbon atoms, more preferably 1 carbon atom. Examples of an alkoxy group are methoxy, ethoxy, n-propoxy, iso-propoxy, n-butyloxy, 2-butyloxy, iso-butyloxy, tert.-butyloxy, and the like.
The term “hydroxyalkyl” as used herein denotes in each case a straight-chain or branched alkyl group having usually from 1 to 8 carbon atoms, preferably from 1 to 6 carbon atoms and being further substituted with 1 to 5, preferably with 1 to 2 hydroxy groups, in particular with 1 hydroxy group. Preferably, the one hydroxy group is terminating the straight-chain or branched alkyl group so that the hydroxy group is bonded to an alkyl bridge, which is bonded to the remainder of the molecule. Examples of an hydroxyalkyl group are hydroxymethyl, hydroxyethyl, n-hydroxypropyl, 2-hydroxypropyl, n-hydroxybutyl, 2-hydroxybutyl, 2-hydroxy-2-methylpropyl, n-hydroxypentyl, and n-hydroxyhexyl. Hydroxymethyl, hydroxyethyl, hydroxypropyl, and hydroxybutyl, are preferred, in particular hydroxyethyl.
The term “hydroxyalkenyl” as used herein denotes in each case an unsaturated hydrocarbon group having usually 2 to 6, preferably 2 to 4 carbon atoms comprising at least one carbon-carbon double bond in any position and being further substituted with 1 to 5, preferably with 1 to 2 hydroxy groups, in particular with 1 hydroxy group. Preferably, the one hydroxy group is terminating the an unsaturated hydrocarbon group so that the hydroxy group is bonded to an alkenyl bridge, which is bonded to the remainder of the molecule. Examples of an hydroxyalkenyl are hydroxyvinyl, hydroxyallyl, hydroxymethallyl, hydroxybuten-1-yl, 2-hydroxy-2-penten-1-yl, 1-hydroxy-3-penten-1-yl and the like. If geometric isomers are possible with regard to the double bond, the present invention relates to both, the E- and Z-isomers.
The term “aminoalkyl” as used herein denotes in each case a straight-chain or branched alkyl group having usually from 1 to 8 carbon atoms, preferably from 1 to 6 carbon atoms and being further substituted with 1 to 5, preferably with 1 to 2 amino groups, in particular 1 amino group. Preferably, the one amino group is terminating the straight-chain or branched alkyl group so that the amino group is bonded to an alkyl bridge, which is bonded to the remainder of the molecule. Examples of an aminoalkyl group are aminomethyl, aminoethyl, n-aminopropyl, 2-aminopropyl, n-aminobutyl, 2-aminobutyl, 2-amino-2-methylpropyl, n-aminopentyl, and n-aminohexyl. Aminomethyl, aminoethyl, aminopropyl, and aminobutyl, are preferred, in particular aminoethyl.
The term “(Cn-Cm-alkyl)” as used herein denotes in each case a linker moiety, wherein the thereto attached moieties are attached to the terminal carbons.
The term “C(═O)” as used therein denotes in each case a carbonyl moiety.
The term “C(═O)—(Cn-Cm-alkyl)” as used herein denotes in each case an alkylcarbonyl, referring to a straight-chain or branched alkyl group as defined above, which is bonded via the carbon atom of a carbonyl group C(═O) to the remainder of the molecule.
The term “aryl” or “aromatic carbocycle” preferably includes 6-membered aromatic carbocyclic rings based on carbon atoms as ring members. A preferred example is phenyl.
The term “heterocyclic” or “heterocyclyl” includes, unless otherwise indicated, in general a 3- to 9-membered, preferably a 4- to 8-membered or 5- to 7-membered, more preferably 5- or 6-membered, in particular 6-membered monocyclic ring. The heterocycle may be saturated, partially or fully unsaturated, or aromatic, wherein saturated means that only single bonds are present, and partially or fully unsaturated means that one or more double bonds may be present in suitable positions, while the Hückel rule for aromaticity is not fulfilled, whereas aromatic means that the Hückel (4n+2) rule is fulfilled. The heterocycle typically comprises one or more, e.g. 1, 2, 3, or 4, preferably 1, 2, or 3 heteroatoms selected from N, O and S as ring members, where S-atoms as ring members may be present as S, SO or SO2. The remaining ring members are carbon atoms. In a preferred embodiment, the heterocycle is an aromatic heterocycle, preferably a 5- or 6-membered aromatic heterocycle comprising one or more, e.g. 1, 2, 3, or 4, preferably 1, 2, or 3 heteroatoms selected from N, O and S as ring members, where S-atoms as ring members may be present as S, SO or SO2. Examples of aromatic heterocycles are provided below in connection with the definition of “hetaryl”. “Hetaryls” or “heteroaryls” are covered by the term “heterocycles”. The saturated or partially or fully unsaturated heterocycles usually comprise 1, 2, 3, 4 or 5, preferably 1, 2 or 3 heteroatoms selected from N, O and S as ring members, where S-atoms as ring members may be present as S, SO or SO2. The skilled person is aware that S, SO or SO2 is to be understood as follows:
Further, a skilled person is aware that resonance structures of the oxidized forms may be possible. Saturated heterocycles include, unless otherwise indicated, in general 3- to 9-membered, preferably 4- to 8-membered or 5- to 7-membered, more preferably 5- or 6-membered monocyclic rings comprising 3 to 9, preferably 4 to 8 or 5 to 7, more preferably 5 or 6 atoms comprising at least one heteroatom, such as pyrrolidine, tetrahydrothiophene, tetrahydrofuran, piperidine, tetrahydropyran, dioxane, morpholine or piperazine.
The term “hetaryl” or “heteroaryl” or “aromatic heterocycle” or “aromatic heterocyclic ring” includes monocyclic 5- or 6-membered aromatic heterocycles comprising as ring members 1, 2, 3 or 4 heteroatoms selected from N, O and S, where S-atoms as ring members may be present as S, SO or SO2. Examples of 5- or 6-membered aromatic heterocycles include pyridyl (also referred to as pyridinyl), i.e. 2-, 3-, or 4-pyridyl, pyrimidinyl, i.e. 2-, 4- or 5-pyrimidinyl, pyrazinyl, pyridazinyl, i.e. 3- or 4-pyridazinyl, thienyl, i.e. 2- or 3-thienyl, furyl, i.e. 2- or 3-furyl, pyrrolyl, i.e. 2- or 3-pyrrolyl, oxazolyl, i.e. 2-, 3- or 5-oxazolyl, isoxazolyl, i.e. 3-, 4- or 5-isoxazolyl, thiazolyl, i.e. 2-, 3- or 5-thiazolyl, isothiazolyl, i.e. 3-, 4- or 5-isothiazolyl, pyrazolyl, i.e. 1-, 3-, 4- or 5-pyrazolyl, i.e. 1-, 2-, 4- or 5-imidazolyl, oxadiazolyl, e.g. 2- or 5-[1,3,4]oxadiazolyl, 4- or 5-(1,2,3-oxadiazol)yl, 3- or 5-(1,2,4-oxadiazol)yl, 2- or 5-(1,3,4-thiadiazol)yl, thiadiazolyl, e.g. 2- or 5-(1,3,4-thiadiazol)yl, 4- or 5-(1,2,3-thiadiazol)yl, 3- or 5-(1,2,4-thiadiazol)yl, triazolyl, e.g. 1H-, 2H- or 3H-1,2,3-triazol-4-yl, 2H-triazol-3-yl, 1H-, 2H-, or 4H-1,2,4-triazolyl and tetrazolyl, i.e. 1H- or 2H-tetrazolyl.
When referring to compositions and the weight percent of the therein comprised ingredients it is to be understood that according to the present invention the overall amount of ingredients does not exceed 100% (±1% due to rounding).
The term “body-care product” refers to any product suitable to apply to the human body, e.g. sunscreen compositions, bath and shower products, preparations containing fragrances and odoriferous substances, hair-care products, dentifrices, decorative preparations, and cosmetic formulations containing active ingredients. Preferred are sunscreen compositions.
The term “sunscreen composition” or “sunscreen” or “skin-care product” refers to any topical product, which reflects and/or absorbs certain parts of UV radiation. Thus, the term “sunscreen composition” is to be understood as not only including sunscreen compositions, but also any cosmetic compositions that provide UV protection. The term “topical product” refers to a product that is applied to the skin and can refer, e.g., to sprays, lotions, creams, oils, foams, powders, or gels. According to the present invention the sunscreen composition may comprise one or more active agents, e.g., organic UV filters, as well as other ingredients or additives, e.g., emulsifiers, emollients, viscosity regulators, stabilizers, preservatives, or fragrances.
The term “pharmaceutical composition” refers to a composition containing at least one active ingredient. Suitable pharmaceutical compositions are hormone preparations, vitamin preparations, vegetable extract preparations, and antibacterial preparations.
Suitable bath and shower additives are, e.g., shower gels, bath-salts, bubble baths and soaps.
Suitable preparations containing fragrances and odoriferous substances are in particular scents, perfumes, toilet waters and shaving lotions (aftershave preparations).
Suitable hair-care products are, e.g., shampoos for humans and animals, in particular dogs, hair conditioners, products for styling and treating hair, perming agents, hair sprays and lacquers, hair gels, hair fixatives and hair dyeing or bleaching agents.
Suitable dentifrices are, e.g., tooth creams, toothpastes, mouth-washes, mouth rinses, anti-plaque preparations and cleaning agents for dentures.
Suitable decorative preparations are, e.g., lipsticks, nail varnishes, eye shadows, mascaras, dry and moist make-up, rouge, powders, depilatory agents and suntan lotions.
Suitable cosmetic formulations containing active ingredients are, e.g., hormone preparations, vitamin preparations, vegetable extract preparations and antibacterial preparations.
The cited body-care products can be in the form of creams, ointments, pastes, foams, gels, lotions, powders, make-ups, sprays, sticks or aerosols. They preferably contain the compound of formula (I) in the aqueous phase.
The term “light stabilizers” as used herein are compounds suitable for protecting body-care and household cleaning and treating agents against photolytic degradation. The light stabilizer is usually present in the body-care product in a concentration of 50 to 1000 ppm.
The term “household cleaning and treating agent” refers to any product suitable to clean or treat household objects, e.g., liquid scouring agents, glass detergents, neutral cleaners (all-purpose cleaners), acid household cleaners (bath), WC cleaners, preferably in washing, rinsing and dishwashing agents, clear rinsing agents, dishwasher detergents, shoe polishes, polishing waxes, floor detergents and polishes, metal, glass and ceramic cleaners, textile-care products, agents for removing rust, color and stains (stain remover salt), furniture and multipurpose polishes and leather dressing agents (leather sprays).
Preferably, household cleaning agents are aqueous or alcoholic (e.g. ethanol or isopropyl alcohol) solutions of one or more of the following components: —anionic, nonionic, amphoteric and/or cationic surfactants—soaps, prepared by saponification of animal and vegetable greases—organic acids, like hydrochloric acid, phosphoric acid, or sulfuric acid, —for basic products inorganic (NaOH or KOH) or organic bases; —abrasives for improved cleaning of surfaces, —waxes and/or silicones for maintenance and protection of surfaces, —polyphosphates, —substances which eliminate hypochlorite or halogens; —peroxides comprising bleaching activators like TAED, for example sodium perborate or H2O2; —enzymes; —in washing detergents discoloration inhibitors, soil-release compounds, grey scale inhibitors, foam inhibitors, fluorescent whitening agents; —cleaning agents based on wax may comprise solvents selected from benzine, turpentine and/or paraffines and emulsifiers based on wax; —filling agents like silicates, polyphosphates, Zeolithes for powdery cleaning agents; —pigments, lakes or soluble dyes; —perfumes; and —light stabilizers, antioxidants and chelating agents.
The term “photostability” refers to the ability of a UV filter or any other molecule, which is exposed to sunlight, to stay stable upon irradiation. In particular, this means that the compound does not undergo a degradation process upon UV radiation.
The term “sun protection factor (SPF)” as used herein indicates how well the skin is protected by a sunscreen composition. In particular, the factor indicates how much longer the protected skin may be exposed to the sun without getting a sunburn in comparison to untreated skin. For example, if a sunscreen composition with an SPF of 15 is evenly applied to the skin of a person usually getting a sunburn after 10 minutes in the sun, the sunscreen allows the skilled person to stay in the sun 15 times longer. In other words, SPF 15 means that 1/15 of the burning UV radiation will reach the skin, assuming sunscreen is applied evenly at a thick dosage of 2 milligrams per square centimeter (mg/cm2).
The term “critical wavelength” is defined as the wavelength at which the area under the UV protection curve (% protection versus wavelength) represents 90% of the total area under the curve in the UV region (280-400 nm). For example, a critical wavelength of 370 nm indicates that the protection of the sunscreen composition is not limited to the wavelengths of UV-B, i.e. wavelengths from 280-320 nm, but extends to 370 nm in such a way that 90% of the total area under the protective curve in the UV region are reached at 370 nm.
The term “ultraviolet filter” or “UV filter” as used herein refers to organic or inorganic compounds, which can absorb and/or reflect UV radiation caused by sunlight. UV filter can be classified based on their UV protection curve as UV-A, UV-B or broadband filters. In the context of the present application, broadband filters may be listed as UV-A filters, as they also provide UV-A protection. In other words, preferred UV-A filters also include broadband filters.
The definition of “broadband” protection (also referred to as broad-spectrum or broad protection) is based on the “critical wavelength”. For broadband coverage, UV-B and UV-A protection must be provided. According to the US requirements, a critical wavelength of at least 370 nm is required for achieving broad spectrum protection. Furthermore, it is recommended by the European Commission that all sunscreen or cosmetic compositions should have an UV-A protection factor, which is at least one third of the labelled sun protection factor (SPF), e.g. if the sunscreen composition has an SPF of 30 the UV-A protection factor has to be at least 10.
The term “biodegradation” as used herein denotes that microorganism metabolize the material completely to CO2, energy, water, and biomass in an aerobic process (according to OECD guideline).
Preferred embodiment regarding the compound of formula (I) as well as the use of the compound of formula (I) to protect skin against UV radiations or as a light stabilizer are described hereinafter. It is to be understood that the preferred embodiments of the invention are preferred alone or in combination with each other. Further, preferred embodiments regarding the cosmetic or pharmaceutical composition comprising a compound of formula (I) as well as the use of such a cosmetic or pharmaceutical composition e.g. in sunscreens are described hereinafter.
As indicated above, the present invention relates in one embodiment to a compound of formula (I)
or a stereoisomer or tautomer thereof,
wherein
It was surprisingly found that the compounds according to the present invention especially benefit from specific advantageous in body-care products (e.g. sunscreen) due to their deliquescent behavior. In this connection, it is to be understood that deliquescent behavior denotes that crystalline substances form a solution when the ambient relative humidity (RH) reaches a certain threshold value.
There are several types of water solid interaction. One type of solid water inaction that is of great importance for highly water soluble crystalline compounds is the phenomenon of deliquescence.
Deliquescence is a first order phase transformation of the solid to a saturated solution which is triggered at a well defined relative humidity which depends on the properties of the solid and the temperature. When this RH is reached, the aqueous solution is the thermodynamically favored phase and dissolution commences. Below this RH, the crystalline solid surrounded by gaseous water is favorable (Mauer et al., Pharmaceutical Development and Technology, 2010, vol. 15, 6, p. 582-594).
After evaporation of water from solutions of the compounds of formula (I) at pH 7±1, the compounds begin to crystallize. In general, water evaporation retardants can be used to slow down the water's evaporation rate as much as possible. However, following this approach there is still a high risk, that the compounds precipitates when water is evaporated.
Compositions, comprising the compounds according to the present invention (pH 7±1), the compounds according to the present invention remain dissolved after evaporation of water from aqueous solutions e.g. from the water phase of a cosmetic or pharmaceutical composition such as an emulsion.
Preferred embodiments regarding the compounds of formula (I), which are relevant for all aspects of the invention, are defined hereinafter.
In one embodiment of the present invention, R1 and R5 are the same, preferably are H.
In one preferred embodiment of the present invention, R3, R4, R7, and R8 are independently C1-C6-hydroxyalkyl, C2-C4-hydroxyalkenyl, C1-C6-aminoalkyl, (CH2O)n—OH, (CH2CH2O)n—OH, or (CH2CH2CH2O)n—OH. Preferrably, R3, R4, R7, and R8 are independently C1-C6-hydroxyalkyl, C2-C4-hydroxyalkenyl, or C1-C6-aminoalkyl.
In one preferred embodiment of the present invention, R1 and R5 are the same, preferably are H; and R2 to R4 are independently C1-C6-hydroxyalkyl, C2-C4-hydroxyalkenyl, C1-C6-aminoalkyl, (CH2O)n—OH, (CH2CH2O)n—OH, or (CH2CH2CH2O)n—OH; and R6 to R8 are independently C1-C6-hydroxyalkyl, C2-C4-hydroxyalkenyl, C1-C6-aminoalkyl, (CH2O)n—OH, (CH2CH2O)n—OH, or (CH2CH2CH2O)n—OH.
In one embodiment of the present invention, R2 to R4 are independently C1-C6-hydroxyalkyl; and R6 to R8 are independently C1-C6-hydroxyalkyl. In a preferred embodiment, R2 to R4 are independently C1-C5-hydroxyalkyl, more preferably C1-C4-hydroxyalkyl, and in particular C1-C3-hydroxyalkyl; and R6 to R8 are independently C1-C5-hydroxyalkyl, more preferably C1-C4-hydroxyalkyl, and in particular C1-C3-hydroxyalkyl.
In one embodiment of the present invention, R1 and R5 are the same, preferably H; R2 to R4 are the same; and R6 to R8 are the same.
In one embodiment of the present invention, R2 to R4 and R6 to R8 are C2-C4-hydroxyalkene, C1-C6-aminoalkyl, (CH2O)n—OH, (CH2CH2O)n—OH, or (CH2CH2CH2O)n—OH. In this connection, it is preferred that R1 and R5 are H.
In one embodiment of the present invention, R2 to R4 and R6 to R8 are hydroxyethyl. In another embodiment of the present invention, R2 to R4 and R6 to R8 are n-hydroxypropyl, n-hydroxybutyl, n-hydroxypentyl, or n-hydroxyhexyl. In this connection, it is preferred that R1 and R5 are H.
In a preferred embodiment of the present invention, R1 and R5 are H; and R2 to R4 and R6 to R8 are hydroxyethyl.
In one embodiment of the present invention, R1, R2, R5, and R6 are the same; R3 and R4 together with the nitrogen to which they are bonded form a double bond to a carbon atom, which is further substituted with two N-atoms, which are independently unsubstituted or substituted with one or more, same or different substituents RN;
In one embodiment of the present invention, R1, R2, R5, and R6 are H;
In a preferred embodiment of the present invention, R1, R2, R5, and R6 are H; R3 and R4 together with the nitrogen to which they are bonded form a double bond to a carbon atom, which is further substituted with two N-atoms, wherein one of these two N-atoms is substituted with RN.
In one embodiment of the present invention, R1, R2, R5, and R6 are H;
In one embodiment of the present invention, R1, R2, R5, and R6 are H;
In one embodiment of the present invention, the compound according to formula (I) is selected from the group consisting of 4,5-dihydroxy-4-cyclopentene-1,2,3-trione di-triethanolammonium salt, 4,5-dihydroxy-4-cyclopentene-1,2,3-trione di-guanidinium salt, and 4,5-dihydroxy-4-cyclopentene-1,2,3-trione di-argininium salt.
In this connection, it is noted that e.g. 4,5-dihydroxy-4-cyclopentene-1,2,3-trione di-triethanolammonium salt may also be known as 4-cyclopentene-1,2,3-trione-4,5-dihydroxy compound with triethanolamine or being expressed as C5H2O5·2 N(CH2CH2OH)3, further illustrated as follows:
Same possible nomenclature variation applies for 4,5-dihydroxy-4-cyclopentene-1,2,3-trione di-guanidinium salt and 4,5-dihydroxy-4-cyclopentene-1,2,3-trione di-argininium salt.
In one embodiment of the present invention, the compound of formula (I) is selected from the group consisting of
In a particular embodiment of the present invention, the compound of formula (I) is
As indicated above, the present invention further relates to cosmetic or pharmaceutical composition, comprising a compound according to the present invention and optionally a dermatologically acceptable emulsifier, thickener, or emollient.
Preferably, the compound of formula (I) is present in the cosmetic or pharmaceutical composition in an amount of from 0.5 to 50 wt.-%, preferably from 1 to 45 wt.-%, more preferably from 2 to 40 wt.-%, and in particular from 3 to 35 wt.-%, based on the total weight of the cosmetic or pharmaceutical composition.
In one embodiment of the present invention, the cosmetic or pharmaceutical composition further comprises at least one additional UV filter, different to the compound of formula (I). The at least one additional UV filter may be an organic or an inorganic UV filter.
Preferably, the at least one additional UV filter is a natural and/or biodegradable UV filter. Thus, in one embodiment of the present invention, the cosmetic or pharmaceutical composition further comprises at least one additional UV filter, different to the compound of formula (I), wherein the at least one additional UV filter is a natural and/or biodegradable UV filter. The at least one additional UV filter may be present in the water or the oil phase. In a preferred embodiment of the present invention, the at least one additional UV filter is present in the oil phase. In connection with this embodiment, the cosmetic or pharmaceutical composition provides an even more improved protection against UV radiation since a UV filter is present in the oil phase and in the water phase, thus providing an improved repartition of the UV filters within the cosmetic or pharmaceutical composition.
In a preferred embodiment, the at least one additional UV filter, different to the compound of formula (I) is a UV-A filter, preferably selected from the group consisting of 2-(4′-diethylamino-2′-hydroxybenzoyl)benzoic acid hexyl ester (also referred to as diethylamino hydroxybenzoyl hexyl benzoate or DHHB), butyl methoxydibenzoylmethane (also known as 4-(tert.-butyl)-4′-methoxydibenzoylmethane or BMDBM), 2,4-bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5 triazine (INCI bis-ethylhexyloxyphenol methoxyphenyl triazine), 2-(2H-benzotriazol-2-yl)-4-methyl-6-[2-methyl-3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]-1-disiloxanyl]propyl]phenol (INCI drometrizole trisiloxane), 2-(2H-benzotriazol-2-yl)-6-(2-ethylhexyloxymethyl)-4-methyl-phenol, methylene bis-benzotriazolyl tetramethylbutylphenol, terephthalylidene dicamphor sulfonic acid, and combinations thereof.
In another preferred embodiment, the at least one additional UV filter, different to the compound of formula (I) is a UV-B filter, preferably selected from the group consisting of octinoxate (also referred to as ethylhexyl methoxycinnamate), ethylhexyl salicylate, 4,4′,4″-(1,3,5-triazin-2,4,6-triyltriimino)tris-benzoic acid-tris(2-ethylhexyl)ester (INCI ethylhexyl triazone), malonate derivatives such as dimethicone diethyl benzalmalonate, diethylhexyl butamido triazone, phenylbenzimidazole sulfonic acid, and combinations thereof.
In another preferred embodiment, the at least one additional UV filter, different to the compound of formula (I) is an inorganic UV filter such as zinc oxide and titanium dioxide.
In yet another preferred embodiment, the at least one additional UV filter, different to the compound of formula (I) is selected from the group consisting of 2-(4′-diethylamino-2′-hydroxybenzoyl)benzoic acid hexyl ester (also referred to as diethylamino hydroxybenzoyl hexyl benzoate or DHHB), butyl methoxydibenzoylmethane (also known as 4-(tert.-butyl)-4′-methoxydibenzoylmethane or BMDBM), 2,4-bis-{[4-(2-ethyl-hexyloxy)-2-hydroxy]-phenyl}-6-(4-methoxyphenyl)-1,3,5 triazine (INCI bis-ethylhexyloxyphenol methoxyphenyl triazine), 2-(2H-benzotriazol-2-yl)-4-methyl-6-[2-methyl-3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]-1-disiloxanyl]propyl]phenol (INCI drometrizole trisiloxane), 2-(2H-benzotriazol-2-yl)-6-(2-ethylhexyloxymethyl)-4-methyl-phenol, methylene bis-benzotriazolyl tetramethylbutylphenol, terephthalylidene dicamphor sulfonic acid, octinoxate (also referred to as ethylhexyl methoxycinnamate), ethylhexyl salicylate, 4,4′,4″-(1,3,5-triazin-2,4,6-triyltriimino)tris-benzoic acid-tris(2-ethylhexyl)ester (INCI ethylhexyl triazone), malonate derivatives such as dimethicone diethyl benzalmalonate, diethylhexyl butamido triazone, phenylbenzimidazole sulfonic acid, zinc oxide, titanium dioxide, and combinations thereof.
In one embodiment of the present invention, the cosmetic or pharmaceutical composition further comprises at least two additional UV filter, different to the compound of formula (I).
In one embodiment of the present invention, the cosmetic or pharmaceutical composition according to the present invention further comprising a photostabilizer. Photostabilizers may be used in a quantity sufficient to obtain a substantial and significant improvement in the photostability of the cosmetic or pharmaceutical composition containing compound of formula (I). This minimum quantity of photostabilizer to be used may vary depending on the starting quantity of compound of formula (I) present in the composition and depending on the nature of the dermatologically acceptable support used in the composition. It may be determined without difficulty using a conventional photostability measuring test.
In a preferred embodiment of the present invention, the photostabilizer is present in the cosmetic or pharmaceutical composition in an amount of at least 0.5 wt.-%, preferably at least 1 wt.-%, more preferably at least 2 wt.-%, and in particular at least 4 wt.-%, based on the total weight of the cosmetic or pharmaceutical composition. In another preferred embodiment, the photostabilizer is present in the cosmetic or pharmaceutical composition in an amount of from 0.5 to 15 wt.-%, preferably from 1 to 12 wt.-%, more preferably from 2 to 10 wt.-%, and in particular from 4 to 8 wt.-%, based on the total weight of the cosmetic or pharmaceutical composition.
In a preferred embodiment, the photostabilizer is a quencher. Preferably, the quencher is present in the cosmetic or pharmaceutical composition in an amount of at least 0.5 wt.-%, preferably at least 1 wt.-%, more preferably at least 1.5 wt.-%, and in particular at least 2 wt.-%, based on the total weight of the cosmetic or pharmaceutical composition. In another preferred embodiment, the quencher is present in the cosmetic or pharmaceutical composition in an amount of from 0.5 to 10 wt.-%, preferably from 1 to 8 wt.-%, more preferably from 1.5 to 6 wt.-%, and in particular from 2 to 5 wt.-%, based on the total weight of the cosmetic or pharmaceutical composition.
In a preferred embodiment of the present invention, the photostabilizer is selected from the group consisting of
Preferred are triplet quencher such as Tinogard Q (comprising tris(tetramethylhydroxypiperidinol) citrate (also known as 4-Piperidinol, 1-hydroxy-2,2,6,6-tetramethyl-, 2-hydroxy-1,2,3-propanetricarboxylate (3:1) (salt) or CAS-Regno. 220410-74-2), water (CAS-Regno. 7732-18-5) and ethanol (CAS-Regno. 64-17-5)). Tinogard Q is an Excited State Quencher, water soluble and is delivered in liquid formulation. Excited State Quencher helps to prevent light induced degradation of formulations in transparent packagings. In combination with UV absorbers it results in highly effective stabilizer systems. In general, Tinogard Q is used to protect personal care products from degradation caused by exposure to UV radiation in transparent packaging. It is applied in e.g. body wash, face wash, liquid hand soap, skin care, shampoo, hair conditioner, and fragrances.
As indicated above, in another aspect, the present invention relates in one embodiment to the use of a compound of formula (I) as defined herein (including all embodiments thereof as described herein) or a cosmetic or pharmaceutical composition as defined herein (including all embodiments thereof as described herein) to protect skin against UV radiations. In connection with this embodiment, the compound of formula (I) as defined herein is used for protecting the skin from UV radiation, in particular for protecting human skin from UV radiation. Preferred is the use of a compound of formula (I) as defined herein (including all embodiments thereof as described herein) or a cosmetic or pharmaceutical composition as defined herein (including all embodiments thereof as described herein) in a sunscreen.
As indicated above, in another aspect, the present invention relates in one embodiment to the at least one compound as defined herein (including all embodiments thereof as described herein) or the cosmetic or pharmaceutical composition as defined herein (including all embodiments thereof as described herein) for use to protect skin against UV radiations.
As indicated above, the present invention further relates to the use of a compound of formula (I) as defined herein (including all embodiments thereof as described herein) in body-care products or household cleaning and treating agents as a light stabilizer to protect ingredients against photolytic degradation.
In connection with the above embodiments, it is to be understood that the compounds of formula (I) are in particularly suitable for use as UV filter and hence for protection of the skin from UV radiation.
Furthermore, in connection with the above embodiments, it is to be understood that the body-care product (e.g. a sunscreen composition) may comprise at least one additive.
In one embodiment, the at least one additive is selected from the group consisting of emulsifier, emollients, viscosity regulators (thickeners), sensory enhancers, adjuvants, preservatives, and combinations thereof.
Preferred emulsifiers include
Preferred emollients include
Preferred thickeners include
Preferred sensory enhancers include
Preferred adjuvants include
Preferred preservatives include
Preferred perfumes are selected from the group consisting of limonene, citral, linalool, alpha-isomethylionon, geraniol, citronellol, 2-isobutyl-4-hydroxy-4-methyltetrahydropyrane, 2-tert.-pentylcyclohexylacetate, 3-methyl-5-phenyl-1-pentanol, 7-acetyl-1,1,3,4,4,6-hexamethyltetraline, adipine acid diester, alpha-amylcinnamaldehyde, alpha-methylionon, amyl C butylphenylmethylpropionalcinnamal, amylsalicylate, amylcinnamylalcohol, anisalcohol, benzoin, benzylalcohol, benzylbenzoate, benzylcinnamate, benzylsalicylate, bergamot oil, bitter orange oil, butylphenylmethylpropioal, cardamom oil, cedrol, cinnamal, cinnamylalcohol, citronnellylmethylcrotonate, lemon oil, coumarin, diethylsuccinate, ethyllinalool, eugenol, evernia furfuracea extracte, evernia prunastri extracte, farensol, guajak wood oil, hexylcinnamal, hexylsalicylate, hydroxycitronellal, lavender oil, lemon oil, linaylacetate, mandarine oil, menthyl PCA, methylheptenone, nutmeg oil, rosemary oil, sweet orange oil, terpineol, tonka bean oil, triethylcitrate, vanillin and combinations thereof.
In connection with the above preferred embodiments, it is to be understood that if the sunscreen or body-care composition comprises two or more additives, combinations of the additives as defined above are also part of the invention.
In connection with the above preferred embodiments, it is to be understood that the body-care product may further comprise water. In case water is present in the body-case product, the body-care product can be an oil in water emulsion (O/W emulsion) or a water in oil emulsion (W/O emulsion). According to a preferred embodiment of the present invention, the cosmetic or pharmaceutical composition comprising a compound of formula (I) is an O/W emulsion or a W/O emulsion.
The present invention is further illustrated by the following examples.
The following abbreviations are used herein:
The compounds of the present invention can be prepared according to the procedures of the following Schemes and Examples, using appropriate materials and are further exemplified by the following specific examples.
Unless otherwise specified, all starting materials are obtained from commercial suppliers and used without further purifications. Unless otherwise specified, all temperatures are expressed in ° C. and all reactions are conducted at rt.
Croconic acid was purchased from abcr GmbH, Germany, purity >95% [CAS Registry Number 488-86-8, 4,5-Dihydroxy-4-cyclopentene-1,2,3-trione].
Tinogard Q was purchased from BASF, Germany. Tinogard Q comprises tris(tetramethylhydroxypiperidinol) citrate in water and ethanol. Tinogard Q is an Excited State Quencher and a water soluble, yellowish-brown liquid.
To a cooled solution of croconic acid (2.02 g, 14.22 mmol) in water (30 ml), a 10% solution of sodium hydroxide in water (11.74 g, 29 mmol) was added slowly at 1° C. until the pH remained stable at 7±1. The resulting sodium salt precipitated partially as yellow crystals. The suspension was transferred to a larger round bottomed flask, 2-butanone (500 ml) was added and water/2-butanone was removed by azeotropic distillation. The resulting yellow crystals were suspended in a few milliliters of 2-butanone, filtered off, washed and dried in vacuo. The di-sodium salt (3.06 g) was obtained as yellow solid.
NMR (13C, 100 MHz, D2O): 188.4 ppm (only one single signal indicating the aromaticity of croconate di-anion).
The di-potassium salt was achieved according to the Comparative Compound 1, whereas potassium hydroxide was used instead of sodium hydroxide.
NMR (13C, 100 MHz, D2O): 188.4 ppm (only one single signal indicating the aromaticity of croconate di-anion).
To a cooled solution of croconic acid (2.02 g, 14.22 mmol) in water (30 ml) a 25% solution of triethanolamine in water (18.2 g, 30.5 mmol) was added dropwise at 1° C. until the pH remained stable at 7±1. The ice bath was removed, and the reaction was warmed to ambient temperature. The suspension was transferred to a larger round bottomed flask, 2-butanone (500 ml) was added and water/2-butanone was removed by azeotropic distillation. The resulting triethanolammonium salt (7.0 g) was obtained as brown oil (highly hygroscopic).
NMR (13C, 100 MHz, D2O): 55.2, 55.3, 188.3 ppm (188.3 ppm signal indicating the aromaticity of croconate di-anion).
The specific extinction coefficient of Comparative (also referred to as Comp.) Compounds 1 and 2 and Compound A was measured using a Perkin Elmer Lambda 650 UV/VIS Spectrophotometer.
A stock solution of concentration c=1 mM of the UV-absorber was prepared in a 100 ml volumetric flask using water. Dilution steps followed in order to adjust the concentration, such that the extinction E at optical pathlength d=1 cm will be 1.0±0.5. UV spectrum was determined in a cuvette of an optical pathlength of d=1 cm at 250 nm to 500 nm. With the Beer-Lambert law one obtains the molar decadic extinction coefficient at any wavelength with:
The respective specific extinction E % 1.1 cm can be obtained via the following equation:
where M=molecular weight of the UV-absorber.
As can be derived from Table 1, all tested compounds are absorbing in an UV region relevant for skin protection. Hence, all tested compounds may be applicable for a cosmetic sun care per se.
In general, the biodegradability is tested on the following concept:
wherein DOC denotes Dissolved organic carbon.
The biodegradation of croconic acid, Myritol 318, Cetiol AB, and glucose was investigated according to OECD 301 (OECD GUIDELINE FOR TESTING OF CHEMICALS No 301) via the OECD 301F manometric respirometry test.
When croconic acid is dissolved in water it dissociates into the di-anion and oxonium ions. Since the di-anion of croconic acid is responsible for UV absorption, only the biodegradation of croconic acid had been tested. It is however also known that 2,2′,2″-nitrilotriethanol is readily biodegradable in water (see e.g. https://www.echa.europa.eu/web/guest/substance-information/-/substanceinfo/100.002.773 and https://www.echa.europa.eu/web/guest/registration-dossier/-/registered-dossier/15134/5/3/2).
Thus, Compound A is biodegradable.
The Formulations 1 to 5 were prepared according to the following manufacturing process with the ingredients as disclosed in Tables 2 and 3.
Part A was heated to 85° C. Part B was heated to 85° C. Part B was added into Part A under homogenization. The mixture was let cooled down to 30° C. under moderate stirring and Part C was added. The mixture was cooled down under moderate stirring to room temperature.
The absorbance of Formulation 1 and 2 was determined as follows:
30 mg milligram of product were evenly spread on roughened PMMA plates (Heliosplate SB6, Helioscreen Creil/France) using a presaturated finger cot. After an equilibration time of 15 minutes transmission measurements between 290 and 400 nm were carried out using a spectrophotometer equipped with an integrating sphere (UV Transmittance Analyzer UV1000-S, Labsphere North Sutton/US).
As can be seen from
Photostability of Formulations 3 to 5 was tested.
30 mg milligram of product were evenly spread on roughened PMMA plates (Heliosplate SB6, Helioscreen Creil/France) using a presaturated finger cot. After an equilibration time of 15 min. transmission measurements between 290 and 400 nm were carried out using a spectrophotometer equipped with an integrating sphere (UV Transmittance Analyzer UV1000-S, Labsphere North Sutton/US).
Afterwards various irradiation doses were applied on the plates using an Atlas CPS+ solar simulator (Atlas Material Testing, Linsengericht/Germany) equipped with a Xenon Arc lamp and special glass filter (Solar Standard 56077759).
Transmission measurements were repeated after irradiation doses of 5, 10, and 20, MED.
The samples of Formulation 3 were irradiated at 5 and 10 MED.
The samples of Formulation 4 were irradiated at 5 MED.
The samples of Formulation 5 were irradiated at 5, 10 and 20 MED.
In this connection it is noted that MED is the Minimal Erythemal Dose and is defined as the threshold dose that may produce sunburn. The susceptibility of skin to damages by a given erythemal effective UV dose depends from the individual skin type and the varying status of skin protection acquired in the course of the year, e.g. by tanning. The MED varies depending from skin.
Weighting of the COLIPA (the European Cosmetics, Toiletries and Perfumeries Association) standard sun spectrum with the erythemal action spectrum leads to the erythemal irradiance of 0.217 W·m−2. Assuming that 1MED is achieved after a UV dose of 250 J·m−2, the time corresponding to 1 MED under COLIPA standard sun conditions would be 19 min. Since the UV intensity of the ATLAS Suntest CPS+ was by a factor of 1.68 higher than the COLIPA standard sun, the UV irradiance of the device may also be expressed as approximately 5 MED·h−1.
As can be seen from
In contrast thereto, Formulation 5 comprising Compound A as single UV filter in combination with the photostabilizer Tinogard Q showed an improved photostability.
| Number | Date | Country | Kind |
|---|---|---|---|
| 20180528.0 | Jun 2020 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2021/066048 | 6/15/2021 | WO |
