Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
  • A61K8/34—Alcohols
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
  • A61K8/34—Alcohols
  • A61K8/342—Alcohols having more than seven atoms in an unbroken chain
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
  • A61K8/34—Alcohols
  • A61K8/345—Alcohols containing more than one hydroxy group
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
  • A61K8/35—Ketones, e.g. benzophenone
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
  • A61K8/37—Esters of carboxylic acids
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
  • A61K8/41—Amines
  • A61K8/411—Aromatic amines, i.e. where the amino group is directly linked to the aromatic nucleus
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
  • A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
  • A61K8/4966—Triazines or their condensed derivatives
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P17/00—Drugs for dermatological disorders
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
  • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations

Definitions

• the present invention relates to the field of solid organic ultraviolet (UV) filters and more particularly to that of the solubilization of these filters. It relates more particularly to a composition comprising a combination of solvents and one or more solid organic UV filter (s). The present invention also relates to a process for preparing such a composition and the use of such a composition in the preparation of UV protection products.
• UV solid organic ultraviolet
• UV filters also known as sunscreens or UV filters, protect against the harmful effects of the sun's ultraviolet rays. They are commonly used in cosmetic and / or dermatological products to protect the skin from UV rays (protection against UV-A and / or UV-B). Moreover, more and more textiles containing UV filters are also appearing on the market in order to protect products and the human.
• organic filters also known as chemical filters
• Mineral filters also called physical filters
• organic filters are inert powders whose role is to reflect and diffuse light.
• organic filters some are in solid form (for example in the form of powder) and others in liquid form under normal conditions of temperature and pressure.
• the present invention relates to organic UV filters and more particularly solid organic UV filters and more particularly solid organic UV filters with little or no water-soluble nature.
• organic UV filters and more particularly solid organic UV filters and more particularly solid organic UV filters with little or no water-soluble nature By “little or not soluble in water”, it is more particularly targeted solid organic UV filters which have a solubility of less than 10g / L in water at 30 ° C.
• Solid organic UV filters are compounds generally having aromatic structures conjugated to groups carbonyls or carbon-carbon double bonds. Their UV protection effect is optimal when these filters are evenly distributed on the surface to protect from ultraviolet rays. Moreover, a solid organic UV filter is effective for absorbing UV rays only if it is properly solubilized. Perfect solubilization of the filters must therefore be obtained for optimum absorption of UV radiation. For this, the solubilizers of solid organic UV filters will be chosen so as to optimize the amount of filters that can be solubilized and get a good price / protection ratio. Moreover, most solid organic filters are poorly soluble and tend to crystallize. A good solubilizer of solid organic UV filters must make it possible to avoid recrystallization of the solid organic UV filter in the formulation, which would have the effect of reducing the degree of protection.
• the solubilizing power of the esters is significantly increased by the addition of a limited amount of an alcohol. More particularly, the addition of, for example, 10% alcohol to an ester significantly improves the solubility of solid organic UV filters in the ester. A synergy between the two solvents, alcohol and ester, which makes it possible to obtain high levels of solubilization of solid organic UV filters, has more particularly been demonstrated.
• composition comprising:
• the first solvent being chosen from esters,
• the second solvent being chosen from alcohols, the ratio by weight of the second solvent to the first solvent being between 1: 20 and 1: 2.3,
• solvent means a liquid under normal conditions of temperature and pressure (CNTP), which has the property of dissolving, diluting or extracting other substances without causing chemical modification of these substances and without it - even change.
• the first solvent may consist of a mixture of esters or more preferably of a single ester.
• each ester is liquid in the CNTPs.
• the liquid ester may have a function other than that of a solvent, such as, for example, octyl methoxycinnate, which is a liquid organic UV filter, but which contributes to the solubilization of solid organic UV filters.
• esters the carboxylic acid esters and the dicarboxylic acid diesters are more particularly targeted.
• the esters may be chosen from the group consisting of hexyl laurate, isopropyl myristate, isopropyl stearate, isopropyl palmitate, diethyl succinate, ethylhexyl stearate, dibutyl adipate, diethylhexyl adipate and diisopropyl. adipate, diisopropyl sebacate and isoamyl esters.
• the esters will be chosen from the group consisting of hexyl laurate, isopropyl myristate, isopropyl stearate, isopropyl palmitate, ethylhexyl stearate, dibutyl adipate, diethylhexyl adipate, diisopropyl adipate, diisopropyl sebacate and isoamyl esters.
• isoamyl esters is more particularly targeted isoamyl caprylate, isoamyl caprate, isoamyl laurate, isoamyl myristate, isoamyl palmitate, diisoamyl sebacate, diisoamyl brassylate, diisoamyl thapsate, diisoamyl fumarate, diisoamyl glutaconate, diisoamyl traumatate and mono- or di-isoamyl malonate, succinate, glutarate, adipate, pimelate, suberate and azelate.
• the ester is chosen from the group consisting of isoamyl esters and, more preferably still, from isoamyl laurate and / or diisoamyl sebacate.
• the second solvent may consist of a mixture of alcohols or more preferably of a single alcohol.
• Alcohol is an alcohol in a liquid state under normal conditions of temperature and pressure.
• the alcohol is selected from the group consisting of ethanol, benzyl alcohol, phenoxyethanol and octyldodecanol, more preferably ethanol.
• the synergy between the alcohol and the ester makes it possible to obtain high levels of solubility of solid organic UV filters. Indeed, it has been demonstrated that the solubility obtained by the combination of an ester and an alcohol is greater than that of weighted sums by weight of the theoretical solubility of the solvents used.
• the weight ratio of the second solvent to the first solvent is between 1: 20 and 1: 2.3, preferably between 1: 20 and 1: 4, more preferably between 1: 20 and 1: 5, even more preferably between 1: 15 and 1: 6, and even more preferably between 1: 13 and 1: 7, in particular between 1: 10 and 1: 8, for example 1: 9.
• composition comprising:
• the first solvent being chosen from esters,
• the second solvent being chosen from alcohols, where the ratio by weight of the second solvent to the first solvent is between 1: 10 and 1: 8,
• one or more solid organic UV filter (s) with a content greater than or equal to 15% by weight relative to the total weight of the combination of the first and second solvents.
• the first solvent is chosen from the group consisting of hexyl laurate, isopropyl myristate, isopropyl stearate, isopropyl palmitate, ethylhexyl stearate, dibutyl adipate, diethylhexyl adipate, diisopropyl adipate, diisopropyl sebacate and / or the isoamyl esters, the group may optionally further include diethyl succinate;
• the second solvent is chosen from alcohols, preferably ethanol, benzyl alcohol, phenoxyethanol and / or octyldodecanol.
• Organic UV (s) is / are selected from the group consisting of diethylaminohydrobenzoyl hexyl benzoate, bis-ethylhexyloxyphenol methoxyphenyl triazine and butyl methoxydibenzoyl methane.
• the first solvent will be selected from the group consisting of isoamyl laurate, diisoamyl sebacate, isopropyl myristate and / or diethyl succinate, more preferably still, from the group consisting of isoamyl laurate and / or diisoamyl sebacate.
• the synergy between an alcohol and an ester makes it possible to obtain a composition with a high content of solid organic UV filter (s), which is more stable over time. Indeed, thanks to the combination of solvents as described, the solubility limits of solid organic UV filters are repelled. It is thus easy to solubilize large quantities of solid organic UV filters in the solvent combinations as described, while maintaining a stable composition according to the invention, the UV filters not recrystallizing.
• the composition thus obtained can be stored at room temperature.
• High content means at least 5% of solid organic UV filter (s), the content of 15% to be understood as the total content of all organic solid UV filters on the weight total of the combination of the first and second solvent.
• Such a composition may serve as an intermediate solubilization phase before introduction into a formulation. Indeed, the composition according to the invention appears particularly well suited to the preparation of products requiring a prior step of solubilization of solid organic UV filters.
• Intermediate phase means a preparation, in solid or liquid form, containing one or more ingredient (s), to be mixed with one or more other intermediate phase (s) in order to produce another intermediate phase or a final product.
• each phase A to G is an intermediate phase of the formulation.
• these intermediate phases are mixed (such as, for example, the phases B, C and D of formulas 1 and 2 of this example), these form a new intermediate phase.
• the final product is obtained when all the intermediate phases have been implemented in the formulation.
• the composition concentrated in one or more solid organic UV filter (s) can be used as an intermediate phase and, more particularly, as an intermediate solubilization phase.
• the composition according to the invention as an intermediate phase of solubilization, is then particularly advantageous. Indeed, according to the desired sun protection of the final product, it is sufficient to take a specific amount of the composition according to the invention and introduce it into the product preparation.
• the compositions according to the invention can form a fatty intermediate phase or a final fatty product, that is to say an intermediate phase or a final product having no water.
• each of the phases B, C, D and E of formulas 1 and 2 of example 2 as well as the mixtures of two or more of these phases constitute an intermediate fatty phase within the meaning of the present invention.
• each of the phases A to C of formula 3 of the example, the mixture of two or three of these phases, and formula 3 itself constitute a fatty intermediate phase or a final fat product within the meaning of the invention.
• the solid organic UV filter (s) is / are chosen from the group consisting of:
• the solid organic UV filter (s) is / are chosen from solid organic UV filters which are poorly or not soluble in water, in particular from the group consisting of:
• the solid organic UV filter (s) is / are chosen from the group consisting of lipophilic solid organic UV filters such as benzophenone-3, butyl methoxydibenzoylmethane (BMDBM) ethylhexyl triazone, 4-methylbenzylidene camphor, diethylamino hydroxybenzoyl hexyl benzoate, phenyl salicylate, methylene bis-benzotriazolyl tetramethylbutylphenol, benzophenone-8 and bis-ethylhexyloxyphenol methoxy-phenyl triazine.
• lipophilic solid organic UV filters such as benzophenone-3, butyl methoxydibenzoylmethane (BMDBM) ethylhexyl triazone, 4-methylbenzylidene camphor, diethylamino hydroxybenzoyl hexyl benzoate, phenyl salicylate, methylene bis-benzotri
• the solid organic UV filter (s) is / are chosen from the group consisting of diethylaminohydrobenzoyl hexyl benzoate, bis-ethylhexyloxyphenol methoxyphenyl triazine and butyl methoxydibenzoyl methane.
• the composition comprises
• the first solvent being chosen from the esters
• the second solvent being chosen from alcohols
• the ratio by weight of the second solvent to the first solvent being between 1: 15 and 1: 6
• one or more solid organic UV filter (s) chosen from the group consisting of diethylaminohydrobenzoyl hexyl benzoate, bis-ethylhexyloxyphenol methoxyphenyl triazine and butyl methoxydibenzoyl methane, the filter (s) Organic UV (s) solid (s) being at a content greater than or equal to 15% by weight relative to the total weight of the combination of the first and second solvents.
• the first solvent is selected from the group consisting of hexyl laurate, isopropyl myristate, isopropyl stearate, isopropyl palmitate, ethylhexyl stearate, dibutyl adipate, diethylhexyl adipate, diisopropyl adipate, diisopropyl sebacate and / or isoamyl esters, the group optionally possibly further comprising diethyl succinate; more preferably, the first solvent is chosen from isoamyl esters, isopropyl myristate and / or diethyl succinate, more preferably still, from isoamyl laurate and / or diisoamyl sebacate.
• the second solvent is selected from the group consisting of ethanol, benzyl alcohol, phenoxyethanol and / or octyldodecanol, more preferably ethanol.
• a composition according to the invention may have a content of organic UV filter (s) greater than or equal to 20% by weight relative to the total weight of the combination of solvents.
• the content of organic UV filter (s) is (s) greater than or equal to 25%, more preferably greater than or equal to 30%, even more preferably, the content is greater than or equal to 35%.
• a composition according to the invention may have a content of diethylaminohydrobenzoyl hexyl benzoate greater than or equal to 20% by weight relative to the total weight of the combination of the first and second solvents.
• the content of this solid organic UV filter is greater than or equal to 25%, more preferably greater than or equal to 30, 35, 40, 45 or even 50%, even more preferentially, the content of diethylaminohydrobenzoyl hexyl benzoate is greater or equal to 60%.
• a composition according to the invention may advantageously have a content of bis-ethylhexyloxyphenol methoxyphenyl triazine greater than or equal to 20% by weight relative to the total weight of the combination of solvents.
• a composition according to the invention may advantageously have a content of butyl methoxydibenzoyl methane greater than or equal to 20% by weight relative to the total weight of the solvent combination.
• the composition according to the invention consists of an ester, an alcohol and one or more solid organic UV filter (s), preferably at least one UV filter.
• organic solid little or not soluble in water, more preferably a solid organic lipophilic UV filter.
• the composition according to the invention further comprises at least one additional UV filter.
• the additional UV filter (s) may be organic (s) or mineral / mineral, solid (s) or liquid (s).
• one or more organic UV filter (s) are introduced into the composition according to the invention.
• the UV filters Liquid organic compounds have the advantage of increasing the solubility of solid organic UV filters. Nevertheless, these liquid UV filters may have disadvantages. Their cost is high compared to solvents. They are not of renewable origin, as can be the isoamyic esters for example. In the case of sunscreens for example, they can give the products a sticky feel.
• the liquid organic UV filter may advantageously be chosen from the group consisting of octyl methoxycinnamate, octocrylene, homosalate and polysilicone 15.
• a liquid organic UV filter is an ester
• liquid organic UV filter is considered first, by its ester function, as entering the first solvent.
• a liquid organic UV filter which is a non-preferred ester, is considered as a liquid organic UV filter.
• inorganic UV filters are titanium dioxide and / or zinc oxide.
• the addition of a mineral UV filter may advantageously be accompanied by a mineral UV filter dispersant.
• the mineral filter may be previously dispersed in a mineral filter dispersant before introduction into the composition.
• a mineral UV filter dispersant mention may be made of C12 / C15 alkyl benzoate, isostearyl isostearate and / or pentaerythrityl tetraisostearate.
• composition according to the invention consists of:
• a first solvent chosen from esters
• a second solvent chosen from alcohols the ratio by weight of the second solvent to the first solvent being between 1: 20 and 1: 2.3
• one or more solid organic UV filter preferably at least one solid organic UV filter with little or no water-solubility and / or lipophilic, at a content greater than or equal to 15% by weight relative to the total weight of the combination of the first and second solvents and, optionally,
• the preferential and advantageous modes concerning the first and second solvents, the ratio and the solid organic filters are also applicable to this composition.
• the composition comprises:
• a first solvent chosen from the group consisting of isoamyl laurate, diisoamyl sebacate, isopropyl myristate and / or diethyl succinate, preferentially isoamyl laurate and / or diisoamyl sebacate,
• a second solvent selected from the group consisting of ethanol, benzyl alcohol, phenoxyethanol, octyldodecanol, preferably ethanol,
• organic solid UV screening agents selected from the group consisting of diethylaminohydrobenzoyl hexyl benzoate, bis-ethylhexyloxyphenol methoxyphenyl triazine and / or butyl methoxydibenzoyl methane, and
• the ratio of the second solvent to the first solvent of between 1: 10 and 1: 8.
• the present invention also relates to a method for preparing a composition according to the invention, comprising the following steps:
• step a) comprises mixing the first solvent, the second solvent and the solid organic UV filter (s) of the composition.
• composition according to the invention are as described above.
• the mixing is carried out at a temperature between 75 and 85 ° C, more preferably at about 80 ° C.
• the mixture is made with stirring, such as magnetic stirring, for 10 to 40 minutes, preferably about 15 minutes.
• a composition according to the invention is particularly well suited to a process for preparing a cosmetic and / or dermatological product, comprising the following steps:
• step ii) mixing the composition heated in step i) with a cosmetic and / or dermatological preparation with stirring.
• Cosmetic and / or dermatological preparation means a substance or an intermediate phase in order to obtain a cosmetic and / or dermatological product, such as a fatty intermediate phase.
• the substances introduced into the cosmetic and / or dermatological preparation may advantageously be chosen from emollients, humectants, surfactants, water-resistance agents, preservatives, antimicrobials, thickeners, pigment / coloring agents used for coloring the product or the product. skin and other ingredients commonly used in cosmetics or dermatology. Such substances may be included in an intermediate phase.
• solvents according to the invention are particularly well suited to the solubilization of solid organic UV filter (s), in particular of organic solid UV filter (s) with little or no solubility. (s) in water and / or lipophilic.
• a combination of a first solvent and a second solvent a) the first solvent being selected from esters, b) the second solvent being chosen from alcohols, the ratio by weight of the second solvent to the first solvent being between 1: 20 and 1: 2.3, is particularly useful for solubilizing one or more organic UV filter (s) ( s) solid (s), preferably a solid organic UV filter little or not soluble in water and / or lipophilic.
• the first solvent may consist of a mixture of esters or more preferably of a single ester.
• esters the carboxylic acid esters and the dicarboxylic acid diesters are more particularly targeted.
• the esters may be chosen from the group consisting of hexyl laurate, isopropyl myristate, isopropyl stearate, isopropyl palmitate, diethyl succinate, ethylhexyl stearate, dibutyl adipate, diethyl hexyl adipate, diisopropyl adipate, diisopropyl sebacate and isoamyl esters.
• the esters will be chosen from the group consisting of hexyl laurate, isopropyl myristate, isopropyl stearate, isopropyl palmitate, ethylhexyl stearate, dibutyl adipate, diethylhexyl adipate, diisopropyl adipate, diisopropyl sebacate and isoamyl esters.
• the isoamyl esters more particularly include isoamyl caprylate, isoamyl caprate, isoamyl laurate, isoamyl myristate, isoamyl palmitate, diisoamyl sebacate, diisoamyl brassylate, diisoamyl thapsate, diisoamyl fumarate, diisoamyl glutaconate, diisoamyl traumatate and mono- or di-isoamyl malonate, succinate, glutarate, adipate, pimelate, suberate and azelate.
• the ester is chosen from the group consisting of isoamyl esters, and even more preferably from isoamyl laurate and / or diisoamyl sebacate.
• the second solvent may consist of a mixture of alcohols or more preferably of a single alcohol.
• Alcohol is an alcohol in a liquid state under normal conditions of temperature and pressure.
• the alcohol is selected from the group consisting of ethanol, benzyl alcohol, phenoxyethanol and octyldodecanol, more preferably ethanol.
• the weight ratio of the second solvent to the first solvent is between 1: 20 and 1: 2.3, preferably between 1: 20 and 1: 4, more preferably between 1: 20 and 1: 5, even more preferably between 1: 15 and 1: 6, and even more preferably between 1: 13 and 1: 7, in particular between 1: 10 and 1: 8, for example 1: 9.
• the solid organic UV filter (s) is / are chosen from the group consisting of:
• the organic solid UV filter (s) is / are chosen from the group consisting of:
• the solid organic UV filter (s) is / are chosen from the group consisting of lipophilic solid organic UV filters such as benzophenone-3, butyl methoxydibenzoylmethane (BMDBM) , ethylhexyl triazone, 4-methylbenzylidene camphor, diethylamino hydroxybenzoyl hexyl benzoate, phenyl salicylate, methylene bis-benzotriazolyl tetramethylbutylphenol, benzophenone-8 and bis-ethylhexyloxyphenol methoxy-phenyl triazine
• lipophilic solid organic UV filters such as benzophenone-3, butyl methoxydibenzoylmethane (BMDBM) , ethylhexyl triazone, 4-methylbenzylidene camphor, diethylamino hydroxybenzoyl hexyl benzoate, phenyl salicylate, methylene bis-
• the solid organic UV filter (s) is / are chosen from the group consisting of diethylaminohydrobenzoyl hexyl benzoate, bis-ethylhexyloxyphenol methoxyphenyl triazine and butyl methoxydibenzoyl methane. It will be noted that, more preferably, when one or more of these filters is / are chosen, the ratio of the second solvent to the first solvent is between 1: 15 and 1: 6, preferably between 1: 13 and 1: 7, and even more preferably between 1: 10 and 1: 8, for example 1: 9.
• a composition according to the invention can be used for the preparation of UV protection products.
• UV protection products it is more specifically intended: - cosmetic and / or dermatological products with a UV protection index, applicable on the lips, face, body or hair, such as reds and balms lipsticks, foundations, creams of care, sun products, in all galenic forms such as for example, in the form of creams, lotions, sprays, oils, balms, serum, masks, etc.
• anti-UV products to treat the fabrics of outdoor equipment, such as clothing, shoes, tents, backpack.
• the solubility of the solid organic UV filters is tested in each solvent separately as follows: 1% by weight, based on the total weight of the composition, of a solid organic UV filter is added to the solvent. The solution is heated at 80 ° C for 15 minutes with magnetic stirring and then left standing for 24 hours. If the solution is clear, then an additional 1% by weight of UV filter is added and then treated as before. The addition of solid organic UV filter is repeated every 24 hours until a cloudiness or a precipitate in the solution is observed. The limiting solubility of the filter is then obtained.
• solubility of the UV filter is tested as above by adding 1% by weight, based on the total weight of the solvent combination, of a solid organic UV filter to the solvent combination.
• the synergy is calculated with respect to the respective limit and weighted solubility of the UV filters for the committed solvents.
• Theoretical solubility Solubility of the filter (in the ester) x e% + solubility of the filter (in the alcohol) x a%.
• a composition comprising a combination of isoamyl laurate and ethanol, the ratio by weight of the alcohol to the isoamyl laurate being 1: 9, solubilizes the solid organic UV filter, diethylaminohydrobenzoyl hexyl benzoate to obtain a content 45% by weight on the total weight of the composition, instead of 25.5% with isoamyl alone or 12% in ethanol alone.
• the diethylaminohydrobenzoyl hexyl bezoate filter has a content of 81.8% by weight relative to the total weight of the combination of solvents.
• the synergy observed with the use of the combination isoamyl laurate: ethanol with a 1: 9 ratio is 86.3%.
• the solubility of diethylaminohydrobenzoyl hexyl benzoate in combination of solvents isoamyl laurate: benzyl alcohol in a ratio 9 reaches 39%.
• the diethylaminohydrobenzoyl hexyl benzoate filter has a content of 63.9% by weight relative to the total weight of the combination of solvents.
• the synergy of the solvent combination highlighted in this case is 30.2%.
• the diethylaminohydrobenzoyl hexyl bezoate filter has a content of 81.8% by weight relative to the total weight of the combination of solvents.
• the synergy of the solvent combination highlighted in this case is 80.3%.
• the diethylaminohydrobenzoyl hexyl bezoate filter is at a 44.9% by weight of the total weight of the solvent combination.
• the synergy of the solvent combination highlighted in this case is 28.9%.
• the diethylaminohydrobenzoyl hexyl bezoate filter has a content of 56.2% by weight relative to the total weight of the solvent combination.
• the synergy of the solvent combination highlighted in this case is 23.1%.
• the solubility of diethylaminohydrobenzoyl hexyl benzoate in a combination of diisoamyl sebacate: ethanol solvents in a 9: 1 ratio reaches 36%.
• the diethylaminohydrobenzoyl hexyl bezoate filter has a content of 56.2% by weight relative to the total weight of the solvent combination.
• the synergy of the solvent combination highlighted in this case is 25.6%.
• the diethylaminohydrobenzoyl hexyl bezoate filter has a content of 108.3% by weight relative to the total weight of the solvent combination.
• the synergy of the solvent combination highlighted in this case is 50.9%.
• the solubility of diethylaminohydrobenzoyl hexyl benzoate in a combination of diisoamyl sebacate: phenoxyethanol solvents in a 9: 1 ratio reaches 40%.
• the diethylaminohydrobenzoyl hexyl bezoate filter has a content of 66.6% by weight relative to the total weight of the combination of solvents.
• the synergy of the solvent combination highlighted in this case is 35.8%. * Solubilization in the Diisoamyl sebacate / Octyldodecanol mixture of diethylaminohydrobenzoyl hexyl benzoate
• the solubility of bis-ethylhexyloxyphenol methoxyphenyl triazine in a combination of isoamyl laurate: phenoxyethanol solvents in a 9: 1 ratio reaches 25%.
• the bis-ethylhexyloxyphenol methoxyphenyl triazine filter has a content of 33.3% by weight relative to the total weight of the combination of solvents.
• the synergy of the solvent combination highlighted in this case is 77.3%.
• the solubility of bis-ethylhexyloxyphenol methoxyphenyl triazine in a combination of solvents diethyl succinate: ethanol in a 9: 1 ratio reaches 14%.
• the bis-ethylhexyloxyphenol methoxyphenyl triazine filter has a content of 16.2% by weight relative to the total weight of the combination of solvents.
• the synergy of the solvent combination highlighted in this case is 41.3%.
• the solubility of bis-ethylhexyloxyphenol methoxyphenyl triazine in a combination of solvents diisoamyl sebacate: ethanol in a 9: 1 ratio reaches 21%.
• the bis-ethylhexyloxyphenol methoxyphenyl triazine filter has a content of 26.6% by weight relative to the total weight of the combination of solvents.
• the Synergy of the solvent combination highlighted in this case is 79.4%.
• the bis-ethylhexyloxyphenol methoxyphenyl triazine filter has a content of 38.8% by weight relative to the total weight of the combination of solvents.
• the synergy of the solvent combination highlighted in this case is 113.7%. 5. Tests with butyl methoxydibenzoyl methane as a solid organic UV filter
• the butyl methoxydibenzoyl methane filter has a content of 31.6% weight on the total weight of the solvent combination.
• the synergy ⁇ combination of solvents highlighted in this case is 38.7%.
• the butyl methoxydibenzoyl methane filter has a content of 23% by weight relative to the total weight of the combination of solvents.
• the synergy of the solvent combination highlighted in this case is 22.6%.
• the butyl methoxydibenzoyl methane filter is at a content of 40.8% by weight relative to the total weight of the combination of solvents.
• the synergy of the solvent combination highlighted in this case is 18.3%.
• the solubility of butyl methoxydibenzoyl methane in a combination of diisoamyl sebacate: phenoxyethanol solvents in a 9: 1 ratio reaches 30%.
• the butyl methoxydibenzoyl methane filter has a content of 42.9% by weight relative to the total weight of the solvent combination.
• the synergy of the solvent combination highlighted in this case is 14.1%.
• Example 2 Solar Formulations In order to achieve good solubilization of solid organic UV filters before introducing them into the composition or cosmetic or dermatological formulation, an intermediate phase is prepared (phase C in the examples which follow).
• phase D weigh the ingredients of phase D, mix them, homogenize the phase and check its good dispersion (absence of aggregates). Heat to 75 ° -80 ° C.
• phase F At 40 ° C, introduce the ingredients of phase F, optionally premixed.
• the intermediate phases C and (C + D) are compositions according to the invention. It is advantageous to prepare the intermediate phase of solubilization of solid organic filters C before introducing the mineral filter (s) mineral (s). Indeed, the introduction of a mineral filter in an intermediate phase results in an opacity of said phase.
• One of the methods for evaluating the good solubilization of solid organic filters is to observe the clear nature of the intermediate phase. Therefore, the presence of a mineral filter in the intermediate phase can make this observation difficult.
• UV mineral / mineral filter such as 1-15 titanium dioxide, zinc oxide
• Heat-sensitive materials such as volatile 0.1-10 silicones (5-cyclomethicone), vegetable oils (argan oil), anti-oxidant (s)
• phase D weigh the ingredients of phase D, mix them, homogenize the phase and check its good dispersion (absence of aggregates). Heat to 75 ° -80 ° C.
• a Oil-texturing agent (s) such as dextrin 0.1-3 palmitate, silica
• Hydrophobic agent (s) such as silicone waxes, 0.1-5 polyvinylpyrrolidone derivatives
• hydrophobic (s) such as paraben, 0.1-1, 5 phenoxyethanol Phases Subject family%
• Thermosensitive materials such as 0.1- (5-cyclomethicone) volatile silicones, vegetable oils (argan oil), antioxidants (tocopherol)
• UV filter solubilizer combination of solvents according to the invention and one or more solid organic UV filter (s) such as butylmethoxydibenzoylmethane (BMDBM), ethyl hexyl triazone, acid 4-aminobenzoic acid (PABA).
• solid organic UV filter s
• BMDBM butylmethoxydibenzoylmethane
• PABA acid 4-aminobenzoic acid
• organic UV filter (s) such as octocrylene, octyl methoxy cinnamate,
• polysilicone 15 homosalate.
• phase B During cooling, introduce phase B, then phase D at about 40 ° C.

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