US20030143252A1 - Inorganic/organic complexes for reducing skin irritation - Google Patents
Inorganic/organic complexes for reducing skin irritation Download PDFInfo
- Publication number
- US20030143252A1 US20030143252A1 US10/330,355 US33035502A US2003143252A1 US 20030143252 A1 US20030143252 A1 US 20030143252A1 US 33035502 A US33035502 A US 33035502A US 2003143252 A1 US2003143252 A1 US 2003143252A1
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- strontium
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 210000000720 eyelash Anatomy 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 230000004761 fibrosis Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 208000024963 hair loss Diseases 0.000 description 1
- 230000003676 hair loss Effects 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000002887 hydroxy group Chemical class [H]O* 0.000 description 1
- 206010021198 ichthyosis Diseases 0.000 description 1
- 229910021432 inorganic complex Inorganic materials 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000003410 keratolytic agent Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 229960000485 methotrexate Drugs 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 201000002266 mite infestation Diseases 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 230000002207 retinal effect Effects 0.000 description 1
- NCYCYZXNIZJOKI-OVSJKPMPSA-N retinal group Chemical group C\C(=C/C=O)\C=C\C=C(\C=C\C1=C(CCCC1(C)C)C)/C NCYCYZXNIZJOKI-OVSJKPMPSA-N 0.000 description 1
- 229930002330 retinoic acid Natural products 0.000 description 1
- 229960003471 retinol Drugs 0.000 description 1
- 235000020944 retinol Nutrition 0.000 description 1
- 239000011607 retinol Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 230000009759 skin aging Effects 0.000 description 1
- 230000037393 skin firmness Effects 0.000 description 1
- 231100000019 skin ulcer Toxicity 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000002887 superconductor Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229960004907 tacalcitol Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 229960001727 tretinoin Drugs 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 239000011653 vitamin D2 Substances 0.000 description 1
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
- 239000011647 vitamin D3 Substances 0.000 description 1
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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
- A61K8/35—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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/58—Metal complex; Coordination compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/74—Biological properties of particular ingredients
- A61K2800/75—Anti-irritant
Definitions
- the present invention relates to a method or regime/regimen for reducing skin irritation, notably that irritation attributed to the topical application of certain active species onto the skin, or due to exposure to the environment.
- This invention especially relates to reducing skin irritation by treating the skin with effective amounts of certain inorganic/organic complexes, or compositions comprised thereof.
- a wide variety of compounds are formulated into cosmetics to, inter alia, improve the appearance of the skin, to beautify the skin, to treat skin conditions, or to render the skin less dry or more supple. Unfortunately, certain of these compounds may cause irritation when they are topically applied onto the skin or mucous membranes.
- Salicylic acid derivatives are of great value, given their biological effects on the skin, in particular on the principal clinical signs of skin aging, namely, fine lines and wrinkles, disorganization of the “grain” of the skin, modification of the skin's complexion and loss of skin firmness and tonicity.
- administration of these derivatives presents a problem since they can cause stinging, itching and tautness after they have been applied, which may result in considerable discomfort. Users, and more particularly those having sensitive skin, are thus often discouraged from using these compounds.
- Sensitive skin and the signs which are characteristic of sensitive skin are described in EP-0680749.
- the irritation may be characterized by stinging, itching or tautness, which too may cause considerable discomfort.
- WO-A-96/19184, WO-A-96/19182 and WO-A-96/19228 describe the administration of water-soluble divalent strontium, manganese, magnesium and calcium salts to reduce the irritation of compounds which have an irritant effect, in particular of exfoliants such as hydroxy acids.
- the present invention features therapeutically/cosmetically treating skin irritation by topical application onto the afflicted skin of at least one compound having the formula (I):
- radicals R which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl or perfluoroalkyl radical having from 1 to 12 carbon atoms;
- radicals R′ which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl, alkoxy or perfluoroalkyl radical having from 1 to-12 carbon atoms;
- X is an element selected from among magnesium, strontium, barium, zinc, manganese, palladium and copper.
- the subject compounds of formula (I) are either in hydrated or nonhydrated state and, advantageously, constitute organic/inorganic complexes.
- the present invention thus also features a cosmetic method or regime/regimen comprising topically applying onto the skin, the keratin fibers, the nails, or the mucous membranes, at least one compound of formula (I) or composition comprised thereof.
- this invention features formulating at least one compound of formula (I):
- radicals R which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl or perfluoroalkyl radical having from 1 to 12 carbon atoms;
- radicals R′ which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl, alkoxy or perfluoroalkyl radical having from 1 to 12 carbon atoms;
- X is an element of column IIA of the Periodic Table (CAS version), zinc, manganese, palladium or copper, whether hydrated or nonhydrated, into a topically applicable, physiologically acceptable medium (vehicle, diluent or carrier) and thus producing a dermatological or pharmaceutical composition, effective as an agent which reduces skin irritation.
- the subject compounds/compositions are particularly useful soothing agents and can be formulated as cosmetic products.
- linear or branched alkyl radical having from 1 to 12 carbon atoms are especially intended methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, hexyl, 2-ethylhexyl, octyl, nonyl, dodecyl, 2-methylbutyl, 2-methylpentyl, 1-methylhexyl and 3-methylheptyl radicals.
- R is a linear or branched, saturated alkyl or perfluoroalkyl radical having from 1 to 6 carbon atoms.
- R′ is advantageously a linear or branched, saturated alkyl, alkoxy or perfluoroalkyl radical having from 1 to 6 carbon atoms.
- the substituents R and R′ are linear and/or saturated.
- the substituents R and R′ preferably comprise a difference of at most two carbon atoms with respect to each other.
- Exemplary derivatives according to the invention include strontium 2,4-pentanedionate, bis(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato)strontium hydrate, bis(2,2,6,6-tetramethyl-3,5-heptanedionato)strontium hydrate, strontium hexafluoroacetylacetonate, calcium 2,4-pentanedionate, bis(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato)calcium, calcium hexafluoroacetylacetonate dihydrate, calcium 2,2,6,6-tetramethyl-3,5-heptanedionate, and mixtures thereof.
- the substituents R and R′ are methyl radicals.
- X is selected from among strontium, calcium, magnesium, manganese, barium, copper, zinc and palladium, and more especially is selected from among strontium, calcium, copper and zinc.
- compositions according to the invention are well suited for topical application onto the skin, keratin fibers, nails or mucous membranes; in particular, the subject compositions are cosmetic and/or dermatological compositions.
- physiologically acceptable medium a medium which is compatible with the skin, mucous membranes (including the inside of the eyelids and the lips), nails and/or keratin fibers (head hair and/or body hairs).
- this physiologically acceptable medium contains no reaction by-product or residual product, since the compounds of formula (I) are the result of a clean synthesis technique.
- these compounds are prepared via a method employing a carbonated or hydroxylated activated cation which will react with a ⁇ -diketone (the starting organic compound).
- the reaction by-products formed during the reaction are carbon dioxide or water, and they are eliminated from the reaction medium, in particular, in the form of gas or are easily eliminated after reaction (in particular with the washing water).
- these reaction by-products remain present in trace amounts, they are nontoxic and/or nonreactive with respect to the compounds of formula (I).
- the present invention also features compositions in which the compound of formula (I) is the result of the reaction between a P-diketone and a hydroxylated or carbonated activated cation.
- the compounds of formula (I) according to the invention are advantageously present in an effective amount to ensure the desired result, i.e., to reduce or eliminate the irritation. They can be, for example, present in a composition according to the invention in a weight amount advantageously ranging from 0.001% to 30%, preferably from 0.01% to 20% and more preferably from 0.1% to 10%, of the total weight of the composition.
- compositions containing a compound according to the invention can be in any pharmaceutical form normally employed, and, in particular, one which is suitable for topical application, for example in the form of an oily solution, an oily gel, a liquid, pasty or solid anhydrous product, an emulsion of the water-in-oil (W/O), oil-in-water (O/W) or multiple (W/O/W or O/W/0) type, a microemulsion or a vesicle dispersion of ionic and/or nonionic type.
- W/O water-in-oil
- O/W oil-in-water
- O/W oil-in-water
- O/W oil-in-water
- a microemulsion or a vesicle dispersion of ionic and/or nonionic type formulated according to the usual techniques.
- the compounds of formula (I) are more particularly in the fatty phase of the compositions according to the invention.
- compositions can be more or less fluid and can have the appearance of a white or colored cream, an ointment, a milk, a lotion, a serum, a paste or a mousse. They can optionally be applied onto the skin in the form of an aerosol. They can also be in solid form and, for example, in stick form.
- the subject compositions can also comprise at least one additive or adjuvant selected from among water, fatty substances, preservatives, gelling agents, surfactants and emulsifiers, antioxidants, fillers, solvents, fragrances, dyestuffs, and colorants, UV-screening agents, cosmetic and/or dermatological active agents such as moisturizers, vitamins and anti-aging active agents, and mixtures thereof.
- additives and adjuvants selected from among water, fatty substances, preservatives, gelling agents, surfactants and emulsifiers, antioxidants, fillers, solvents, fragrances, dyestuffs, and colorants, UV-screening agents, cosmetic and/or dermatological active agents such as moisturizers, vitamins and anti-aging active agents, and mixtures thereof.
- additives and adjuvants selected from among water, fatty substances, preservatives, gelling agents, surfactants and emulsifiers, antioxidants, fillers, solvents, fragrances, dyestuffs, and colorants, UV-
- the fatty substances can be selected from among synthetic oils, oils of animal origin, oils of plant origin, mineral oils (liquid petroleum jelly), silicone oils, fluoro oils, and mixtures thereof. Fatty alcohols, fatty acids and waxes can also be used.
- the proportion of the fatty phase can range from 5% to 80% by weight, and preferably from 5% to 50% by weight, relative to the total weight of the composition.
- the oils, waxes, emulsifiers and co-emulsifiers included in the composition in emulsion form are selected from among those conventional in the cosmetic field.
- the emulsifier and the co-emulsifier are advantageously present in the composition in a proportion ranging from 0.3% to 30% by weight, and preferably from 0.5% to 20% by weight, relative to the total weight of the composition.
- the fatty phase can represent more than 90% of the total weight of the composition.
- Representative emulsifiers according to the invention include, for example, polyethylene glycol oleyl ethers such as the products marketed under the trademarks BRIJ92 and BRIJ96 by ICI.
- compositions according to the invention are those conventional in the fields under consideration.
- the nature of the additives and adjuvants and their amounts should be such that they do not modify the properties of the compounds of formula (I) according to the invention.
- compositions of the invention can be used as cleansing, protective, treatment or care products and/or as makeup products for facial and/or body skin, mucous membranes and/or keratin fibers.
- They in particular constitute treatment or care creams for the face, for the hands or for the body (for example day creams, night creams, antisun or sunscreen creams), protective or care body milks, lotions (cleansing lotions, antisun or sunscreen lotions), skincare mousses or gels, or bath compositions.
- They can also constitute makeup products, in particular, for the cheeks, the lips, the eyelashes and the eyelids, such as foundations, lipsticks and eyeshadows: to this end, they can contain dyestuffs and in particular chemical dyes or pigments.
- haircare compositions such as shampoos, treating lotions, restructuring lotions for the hair, lotions or gels for combating hair loss, antiparasitic shampoos, etc.
- compositions according to the invention can also be formulated as solid preparations constituting cleansing bars or soaps.
- compositions comprising the compound of formula (I) can also comprise the product or active agent/species which can cause an irritation of the skin.
- compositions preferably cosmetic, which comprise, formulated into a physiologically acceptable medium, at least one compound of formula (I) and at least one product which can cause an irritation of the skin.
- the amount of the at least one compound of formula (I) according to the invention is preferably a sufficient amount such that the skin irritant effect decreases, or even disappears.
- this amount can be varied in particular as a function of the amount and of the nature of the product with an irritant nature which is applied.
- a composition according to the invention can comprise at least one compound of formula (I) at an amount ranging from 0.001% to 30%, preferably from 0.01% to 20% and more preferably still from 0.1% to 10%, of the total weight of the composition.
- the amount of the product which can cause an irritation of the skin can thus correspond to an amount which is sufficient to cause an irritation of the skin if it is present alone (without the compound of formula (I)).
- the present invention presents, indeed, the advantage of being able to increase the amount of active agents, which are conventionally of irritant nature, in compositions with respect to the amount normally employed, with a view to improved effectiveness of the latter.
- the amount of active agent which can be used in the composition advantageously ranges from 5% to 50% of the total weight of the composition.
- the products which can cause an irritation of the skin are typically preservatives, surfactants, fragrances, solvents, propellants and active agents, and mixtures thereof.
- the products which are considered to be inert in a cosmetic composition can have an irritant nature when they are applied to the skin, the scalp, the nails or the mucous membranes, such as, in particular, preservatives, surfactants, fragrances, solvents or propellants.
- products considered as active agents in cosmetic compositions can have an irritant nature when they are applied to the skin, the scalp, the nails or the mucous membranes. This can be referred to as an irritant side effect exhibited by these products, which are, in particular, active agents such as, especially, certain sunscreens, hydroxy acids, in particular ⁇ -hydroxy acids (glycolic, lactic, malic, citric, tartaric, mandelic, etc.) and ⁇ -hydroxy acids, especially salicylic acid and its derivatives, keto acids, in particular in ⁇ - and ⁇ -form, derivatives of hydroxy or keto acids, especially in ⁇ - and ⁇ -form, retinoids (retinol and its esters, retinal, retinoic acid and its derivatives, retinoids, in particular those described in FR-A-2570377, EP-A-0199636, EP-A-0325540 and EP-A-0402072), anthralins (dioxyanthranol), anthran
- vitamin D and derivatives thereof particularly exemplary as vitamin D 3 , vitamin D 2 , 1,25-dihydroxy vitamin D 3 (calcitriol), calcipotriol, 1,24-dihydroxy vitamin D 3 (such as tacalcitol), 24,25-dihydroxy vitamin D 3 , 1-hydroxy vitamin D 2 and 1,24-dihydroxy vitamin D 2 .
- vitamin D 3 particularly exemplary as vitamin D 3 , vitamin D 2 , 1,25-dihydroxy vitamin D 3 (calcitriol), calcipotriol, 1,24-dihydroxy vitamin D 3 (such as tacalcitol), 24,25-dihydroxy vitamin D 3 , 1-hydroxy vitamin D 2 and 1,24-dihydroxy vitamin D 2 .
- salicylic acid derivatives particularly exemplary are 5-n-octanoylsalicylic acid and 5-n-dodecanoylsalicylic acid, and their salts and esters thereof.
- the present invention also features administering at least one compound of formula (I) formulated into a nonirritant cosmetic composition or a cosmetic composition suited for individuals with sensitive skin.
- compositions which comprise at least one compound of formula (I) and at least one active agent which causes irritation of the skin are particularly suitable for caring for and/or for treating and/or making up human skin and/or mucous membranes and/or keratin fibers, and in particular for combating the signs of aging of the skin and/or for improving the radiance of the complexion and/or for smoothing facial and/or body skin and/or for treating and reducing wrinkles and fine lines on the skin and/or for stimulating the process of epidermal renewal and/or for treating acne and/or for treating skin conditions/afflications.
- this invention features the use of at least one compound of formula (I) in a cosmetic composition containing an active agent which causes irritation of the skin, destined for caring for human skin and/or mucous membranes and/or keratin fibers, and, in particular, intended for improving the radiance of the complexion and/or smoothing facial and/or body skin and/or combating the signs of aging of the skin and/or acne.
- this invention features the manufacture or production of a dermatological or therapeutic composition containing at least one compound of formula (I) and an active agent which causes irritation of the skin and which is suited for combating the signs of aging of the skin and/or treating and reducing wrinkles and fine lines on the skin and/or stimulating the process of epidermal renewal and/or treating acne and/or skin conditions.
- skin conditions are intended, in particular, shingles, burns, eczema, demodectic acariasis, skin ulcers, fibrosis, controlling healing, psoriasis, pruritus, dermatitis, ichthyosis, corns and verrucae.
- the milk thus formulated was soft, had a good exfoliant property for the skin and did not irritate the skin. It is well suited for use by individuals with sensitive skin.
- the Episkin system is a model of human epidermis reconstituted in vitro, which was manufactured by the company Episkin.
- the epidermis contained only one cell type: keratinocytes.
- the keratinocytes were seeded onto a dermis equivalent which was composed of various types of collagen.
- the assignee hereof has studied the cytotoxicity of the keratinocytes (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide test) after applying to this reconstructed skin model various compositions in a proportion of 150 2 mg/cm, and maintaining same in an incubator at 37° C./5% CO 2 for a period of 18 hours. Each composition was tested on two epidermides of 1.13 cm .
- the basic composition A was: BRIJ95 2.5% BRIJ92 2.5% liquid petroleum jelly 30% water qs 100%
- compositions tested corresponded to this composition A to which 5-n-octanoylsalicylic acid, alone or in admixture with a compound of formula (I) according to the invention, was added.
- composition A was not cytotoxic.
- composition A was prepared by adding a compound of formula (I) to composition A in the presence of 0.5%, 0.75% or 1% of 5-n-octanoylsalicyclic acid did not render the composition A cytotoxic.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
β-Diketone/hydroxylated or carbonated activated cation inorganic/organic complexes are well suited for preventing, avoiding or reducing skin irritation, notably that elicited by exposure to irritant active agents/species or to the external environment.
Description
- This application is a divisional of application Ser. No. 09/671,627, filed Sep. 28, 2000, now allowed, incorporated by reference herein in its entirety and relied upon, which claims priority under 35 U.S.C. §119 of FR-99/12057, filed Sep. 28, 1999, hereby expressly incorporated by reference.
- 1. Technical Field of the Invention
- The present invention relates to a method or regime/regimen for reducing skin irritation, notably that irritation attributed to the topical application of certain active species onto the skin, or due to exposure to the environment.
- This invention especially relates to reducing skin irritation by treating the skin with effective amounts of certain inorganic/organic complexes, or compositions comprised thereof.
- 2. Description of the Prior Art
- A wide variety of compounds are formulated into cosmetics to, inter alia, improve the appearance of the skin, to beautify the skin, to treat skin conditions, or to render the skin less dry or more supple. Unfortunately, certain of these compounds may cause irritation when they are topically applied onto the skin or mucous membranes.
- It is known to this art to administer salicylic acid derivatives as keratolytic agents for treating acne; these are also useful anti-aging agents in cosmetic and/or dermatological compositions. Thus, FR-A-2581542 and EP-A-0378936 describe such salicylic acid compounds.
- Salicylic acid derivatives are of great value, given their biological effects on the skin, in particular on the principal clinical signs of skin aging, namely, fine lines and wrinkles, disorganization of the “grain” of the skin, modification of the skin's complexion and loss of skin firmness and tonicity. However, administration of these derivatives presents a problem since they can cause stinging, itching and tautness after they have been applied, which may result in considerable discomfort. Users, and more particularly those having sensitive skin, are thus often discouraged from using these compounds. Sensitive skin and the signs which are characteristic of sensitive skin are described in EP-0680749.
- The same also holds true for exfoliants such as hydroxy acids. Concerning these compounds, it has been proposed, in EP-0413528, to combine them with amphoteric species in order to decrease the discomfort that they may cause.
- It is also widely described that some users of cosmetic products comprising surfactants, preservatives, fragrances, solvents or propellants complain that their skin is irritated after applying one or more of the above substrates thereto.
- However, because of their irritant nature, these products are generally employed at very low doses. Formulation of these products in small amounts may, therefore, prove to be relatively disadvantageous with respect to administration of other active species which are less active, but which are formulated in greater amounts since they are less or not irritant.
- It is also known to this art that the skin of certain individuals is irritated when it has been exposed to a specific or unusual chemical or physical environment, in particular when it is exposed to considerable variations in temperature, to wind or to a very polluted environment. Thus, the skin may react with itching, tautness or stinging.
- Thus, the irritation may be characterized by stinging, itching or tautness, which too may cause considerable discomfort.
- WO-A-96/19184, WO-A-96/19182 and WO-A-96/19228 describe the administration of water-soluble divalent strontium, manganese, magnesium and calcium salts to reduce the irritation of compounds which have an irritant effect, in particular of exfoliants such as hydroxy acids.
- It has now unexpectedly and surprisingly been determined that certain inorganic/organic complexes are useful for reducing the irritation induced, in particular, by certain species or products topically applied onto the skin, or by exposure to the environment.
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- in which the radicals R, which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl or perfluoroalkyl radical having from 1 to 12 carbon atoms; the radicals R′, which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl, alkoxy or perfluoroalkyl radical having from 1 to-12 carbon atoms; and X is an element selected from among magnesium, strontium, barium, zinc, manganese, palladium and copper.
- The subject compounds of formula (I) are either in hydrated or nonhydrated state and, advantageously, constitute organic/inorganic complexes.
- The present invention thus also features a cosmetic method or regime/regimen comprising topically applying onto the skin, the keratin fibers, the nails, or the mucous membranes, at least one compound of formula (I) or composition comprised thereof.
-
- in which the radicals R, which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl or perfluoroalkyl radical having from 1 to 12 carbon atoms; the radicals R′, which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl, alkoxy or perfluoroalkyl radical having from 1 to 12 carbon atoms; and X is an element of column IIA of the Periodic Table (CAS version), zinc, manganese, palladium or copper, whether hydrated or nonhydrated, into a topically applicable, physiologically acceptable medium (vehicle, diluent or carrier) and thus producing a dermatological or pharmaceutical composition, effective as an agent which reduces skin irritation.
- The subject compounds/compositions are particularly useful soothing agents and can be formulated as cosmetic products.
- More particularly, according to the present invention, by “linear or branched alkyl radical having from 1 to 12 carbon atoms” are especially intended methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, hexyl, 2-ethylhexyl, octyl, nonyl, dodecyl, 2-methylbutyl, 2-methylpentyl, 1-methylhexyl and 3-methylheptyl radicals.
- Preferably, R is a linear or branched, saturated alkyl or perfluoroalkyl radical having from 1 to 6 carbon atoms. In addition, R′ is advantageously a linear or branched, saturated alkyl, alkoxy or perfluoroalkyl radical having from 1 to 6 carbon atoms.
- Preferably, the substituents R and R′ are linear and/or saturated.
- In particular, the substituents R and R′ preferably comprise a difference of at most two carbon atoms with respect to each other.
- These compounds of formula (I) are water-insoluble, unlike the compounds described in WO-A-96/19184, WO-A-96/19182 and WO-A-96/19228. Their property of reducing the irritation which is, in particular, induced by certain products applied onto the skin, which are generally hydrophilic, such as hydroxy acids, is thus all the more surprising.
- Exemplary derivatives according to the invention include strontium 2,4-pentanedionate, bis(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato)strontium hydrate, bis(2,2,6,6-tetramethyl-3,5-heptanedionato)strontium hydrate, strontium hexafluoroacetylacetonate, calcium 2,4-pentanedionate, bis(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato)calcium, calcium hexafluoroacetylacetonate dihydrate, calcium 2,2,6,6-tetramethyl-3,5-heptanedionate, and mixtures thereof.
- Certain of these compounds have been described as catalysts of chemical reactions or as reagents of methods for obtaining inorganic compounds, such as superconductors (WO 91/13051 or “Preparation and properties of beta-diketone and beta-keto ester complexes of bismuth (III), strontium (II) and calcium (II)” by Doi Masura et al., in Nippon Kagaku Kaishi (1995), (10), 802-8).
- Preferably, the substituents R and R′ are methyl radicals.
- Advantageously, X is selected from among strontium, calcium, magnesium, manganese, barium, copper, zinc and palladium, and more especially is selected from among strontium, calcium, copper and zinc.
- The compositions according to the invention are well suited for topical application onto the skin, keratin fibers, nails or mucous membranes; in particular, the subject compositions are cosmetic and/or dermatological compositions.
- By the expression “physiologically acceptable medium” is intended a medium which is compatible with the skin, mucous membranes (including the inside of the eyelids and the lips), nails and/or keratin fibers (head hair and/or body hairs). In addition, this physiologically acceptable medium contains no reaction by-product or residual product, since the compounds of formula (I) are the result of a clean synthesis technique.
- Specifically, these compounds are prepared via a method employing a carbonated or hydroxylated activated cation which will react with a β-diketone (the starting organic compound). The reaction by-products formed during the reaction are carbon dioxide or water, and they are eliminated from the reaction medium, in particular, in the form of gas or are easily eliminated after reaction (in particular with the washing water). Furthermore, if these reaction by-products remain present in trace amounts, they are nontoxic and/or nonreactive with respect to the compounds of formula (I).
- Thus, the present invention also features compositions in which the compound of formula (I) is the result of the reaction between a P-diketone and a hydroxylated or carbonated activated cation.
- The compounds of formula (I) according to the invention are advantageously present in an effective amount to ensure the desired result, i.e., to reduce or eliminate the irritation. They can be, for example, present in a composition according to the invention in a weight amount advantageously ranging from 0.001% to 30%, preferably from 0.01% to 20% and more preferably from 0.1% to 10%, of the total weight of the composition.
- The compositions containing a compound according to the invention can be in any pharmaceutical form normally employed, and, in particular, one which is suitable for topical application, for example in the form of an oily solution, an oily gel, a liquid, pasty or solid anhydrous product, an emulsion of the water-in-oil (W/O), oil-in-water (O/W) or multiple (W/O/W or O/W/0) type, a microemulsion or a vesicle dispersion of ionic and/or nonionic type. These compositions are formulated according to the usual techniques.
- As indicated above, the compounds of formula (I) are more particularly in the fatty phase of the compositions according to the invention.
- These compositions can be more or less fluid and can have the appearance of a white or colored cream, an ointment, a milk, a lotion, a serum, a paste or a mousse. They can optionally be applied onto the skin in the form of an aerosol. They can also be in solid form and, for example, in stick form.
- The subject compositions can also comprise at least one additive or adjuvant selected from among water, fatty substances, preservatives, gelling agents, surfactants and emulsifiers, antioxidants, fillers, solvents, fragrances, dyestuffs, and colorants, UV-screening agents, cosmetic and/or dermatological active agents such as moisturizers, vitamins and anti-aging active agents, and mixtures thereof. The amounts of these various additives and adjuvants are those conventionally used in the cosmetic and/or dermatological field.
- The fatty substances can be selected from among synthetic oils, oils of animal origin, oils of plant origin, mineral oils (liquid petroleum jelly), silicone oils, fluoro oils, and mixtures thereof. Fatty alcohols, fatty acids and waxes can also be used.
- When the composition is formulated as an emulsion, the proportion of the fatty phase can range from 5% to 80% by weight, and preferably from 5% to 50% by weight, relative to the total weight of the composition. The oils, waxes, emulsifiers and co-emulsifiers included in the composition in emulsion form are selected from among those conventional in the cosmetic field. The emulsifier and the co-emulsifier are advantageously present in the composition in a proportion ranging from 0.3% to 30% by weight, and preferably from 0.5% to 20% by weight, relative to the total weight of the composition.
- When the composition is an oily gel or solution, the fatty phase can represent more than 90% of the total weight of the composition.
- Representative emulsifiers according to the invention include, for example, polyethylene glycol oleyl ethers such as the products marketed under the trademarks BRIJ92 and BRIJ96 by ICI.
- The amounts of the various constituents of the compositions according to the invention are those conventional in the fields under consideration. The nature of the additives and adjuvants and their amounts should be such that they do not modify the properties of the compounds of formula (I) according to the invention.
- The compositions of the invention can be used as cleansing, protective, treatment or care products and/or as makeup products for facial and/or body skin, mucous membranes and/or keratin fibers. They in particular constitute treatment or care creams for the face, for the hands or for the body (for example day creams, night creams, antisun or sunscreen creams), protective or care body milks, lotions (cleansing lotions, antisun or sunscreen lotions), skincare mousses or gels, or bath compositions. They can also constitute makeup products, in particular, for the cheeks, the lips, the eyelashes and the eyelids, such as foundations, lipsticks and eyeshadows: to this end, they can contain dyestuffs and in particular chemical dyes or pigments.
- They can also be used for the hair in the form of solutions, creams, gels, emulsions or mousses, and in particular as haircare compositions such as shampoos, treating lotions, restructuring lotions for the hair, lotions or gels for combating hair loss, antiparasitic shampoos, etc.
- The compositions according to the invention can also be formulated as solid preparations constituting cleansing bars or soaps.
- The compositions comprising the compound of formula (I) can also comprise the product or active agent/species which can cause an irritation of the skin.
- In this instance, the present invention also features compositions, preferably cosmetic, which comprise, formulated into a physiologically acceptable medium, at least one compound of formula (I) and at least one product which can cause an irritation of the skin.
- The amount of the at least one compound of formula (I) according to the invention is preferably a sufficient amount such that the skin irritant effect decreases, or even disappears. Thus, this amount can be varied in particular as a function of the amount and of the nature of the product with an irritant nature which is applied. However, by way of illustration, and as indicated above, a composition according to the invention can comprise at least one compound of formula (I) at an amount ranging from 0.001% to 30%, preferably from 0.01% to 20% and more preferably still from 0.1% to 10%, of the total weight of the composition.
- In the compositions according to the invention, the amount of the product which can cause an irritation of the skin can thus correspond to an amount which is sufficient to cause an irritation of the skin if it is present alone (without the compound of formula (I)).
- The present invention presents, indeed, the advantage of being able to increase the amount of active agents, which are conventionally of irritant nature, in compositions with respect to the amount normally employed, with a view to improved effectiveness of the latter. Thus, the amount of active agent which can be used in the composition advantageously ranges from 5% to 50% of the total weight of the composition. In particular, it is possible to formulate hydroxy acids at up to 50% of the total weight of the composition, salicylic acid or derivatives thereof at up to 10%, or retinoids at up to 5%, without any discomfort for the user.
- Many topically applied products have an irritant nature, especially for individuals (users) with skin which is easily irritated. Thus, these products, as described above, cause stinging, itching or tautness, which result in discomfort to the user which discourages further use.
- The products which can cause an irritation of the skin are typically preservatives, surfactants, fragrances, solvents, propellants and active agents, and mixtures thereof.
- Thus, even the products which are considered to be inert in a cosmetic composition can have an irritant nature when they are applied to the skin, the scalp, the nails or the mucous membranes, such as, in particular, preservatives, surfactants, fragrances, solvents or propellants.
- Too, products considered as active agents in cosmetic compositions can have an irritant nature when they are applied to the skin, the scalp, the nails or the mucous membranes. This can be referred to as an irritant side effect exhibited by these products, which are, in particular, active agents such as, especially, certain sunscreens, hydroxy acids, in particular α-hydroxy acids (glycolic, lactic, malic, citric, tartaric, mandelic, etc.) and β-hydroxy acids, especially salicylic acid and its derivatives, keto acids, in particular in α- and β-form, derivatives of hydroxy or keto acids, especially in α- and β-form, retinoids (retinol and its esters, retinal, retinoic acid and its derivatives, retinoids, in particular those described in FR-A-2570377, EP-A-0199636, EP-A-0325540 and EP-A-0402072), anthralins (dioxyanthranol), anthranoids (for example those described in EP-A-0319028), peroxides (in particular benzoyl peroxide), minoxidil and its derivatives, lithium salts, antiproliferating agents such as 5-fluorouracil or methotrexate, certain vitamins such as vitamin D and its derivatives and vitamin B9 and its derivatives, hair tints or dyes (para-phenylenediamine and its derivatives, aminophenols), perfuming alcoholic solutions (fragrances, eaux de toilette, aftershave and deodorants), antiperspirants (some aluminum salts), hair-removing or permanent-waving active agents (thiols), depigmenting agents (hydroquinone), capsaicin, antilouse active agents (pyrethrin), ionic and nonionic detergent agents and propigmenting agents (dihydroxyacetone, psoralens and methylangecilins), and mixtures thereof.
- Among vitamin D and derivatives thereof, particularly exemplary as vitamin D 3, vitamin D2, 1,25-dihydroxy vitamin D3 (calcitriol), calcipotriol, 1,24-dihydroxy vitamin D3 (such as tacalcitol), 24,25-dihydroxy vitamin D3, 1-hydroxy vitamin D2 and 1,24-dihydroxy vitamin D2.
- Among the salicylic acid derivatives, particularly exemplary are 5-n-octanoylsalicylic acid and 5-n-dodecanoylsalicylic acid, and their salts and esters thereof.
- The present invention also features administering at least one compound of formula (I) formulated into a nonirritant cosmetic composition or a cosmetic composition suited for individuals with sensitive skin.
- The compositions which comprise at least one compound of formula (I) and at least one active agent which causes irritation of the skin are particularly suitable for caring for and/or for treating and/or making up human skin and/or mucous membranes and/or keratin fibers, and in particular for combating the signs of aging of the skin and/or for improving the radiance of the complexion and/or for smoothing facial and/or body skin and/or for treating and reducing wrinkles and fine lines on the skin and/or for stimulating the process of epidermal renewal and/or for treating acne and/or for treating skin conditions/afflications.
- Thus, this invention features the use of at least one compound of formula (I) in a cosmetic composition containing an active agent which causes irritation of the skin, destined for caring for human skin and/or mucous membranes and/or keratin fibers, and, in particular, intended for improving the radiance of the complexion and/or smoothing facial and/or body skin and/or combating the signs of aging of the skin and/or acne.
- In addition, this invention features the manufacture or production of a dermatological or therapeutic composition containing at least one compound of formula (I) and an active agent which causes irritation of the skin and which is suited for combating the signs of aging of the skin and/or treating and reducing wrinkles and fine lines on the skin and/or stimulating the process of epidermal renewal and/or treating acne and/or skin conditions.
- By the term “skin conditions” are intended, in particular, shingles, burns, eczema, demodectic acariasis, skin ulcers, fibrosis, controlling healing, psoriasis, pruritus, dermatitis, ichthyosis, corns and verrucae.
- In order to further illustrate the present invention and the advantages thereof, the following specific examples are given, it being understood that same are intended only as illustrative and in nowise limitative.
- In said examples to follow, all parts and percentages are given by weight, unless otherwise indicated.
- Milk for the skin, having exfoliating activity:
5-n-octanoylsalicylic acid 0.5% strontium 2,4-pentanedionate 0.5% BRIJ95 2.5% BRIJ92 2.5% liquid petroleum jelly 30% water qs 100% - The milk thus formulated was soft, had a good exfoliant property for the skin and did not irritate the skin. It is well suited for use by individuals with sensitive skin.
- Test on Reconstructed Skin:
- The Episkin system is a model of human epidermis reconstituted in vitro, which was manufactured by the company Episkin. The epidermis contained only one cell type: keratinocytes. The keratinocytes were seeded onto a dermis equivalent which was composed of various types of collagen.
- After a period of proliferation of the keratinocytes immersed in the culture medium, the system was raised up to the air/liquid interface. This step of immersing the cultures induced the differentiation of the keratinocytes towards the terminal stage of corneocytes in 13 days, thus allowing the reconstruction, in vitro, of an epidermis which possessed a basal layer, a spiny layer, a granular layer and a horny layer.
- The assignee hereof has studied the cytotoxicity of the keratinocytes (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide test) after applying to this reconstructed skin model various compositions in a proportion of 150 2 mg/cm, and maintaining same in an incubator at 37° C./5% CO 2 for a period of 18 hours. Each composition was tested on two epidermides of 1.13 cm .
- The basic composition A was:
BRIJ95 2.5% BRIJ92 2.5% liquid petroleum jelly 30% water qs 100% - The other compositions tested corresponded to this composition A to which 5-n-octanoylsalicylic acid, alone or in admixture with a compound of formula (I) according to the invention, was added.
- The measurement of cell viability was carried out immediately after rinsing of the compositions with phosphate buffered saline (PBS).
- Thus, composition A was not cytotoxic. The addition of 0.3% (w/V) of 5-n-octanoylsalicylic acid to this composition rendered it cytotoxic.
- The various compositions tested provided the results obtained which are collated in the Table below:
TABLE Concentration as % (w/V) of Concentration the Compound of as % (w/V) of 5-n-octanoyl-salicylic formula (I) the compound of acid added to formula (I) added to % of cell composition A added composition A viability — 0 0.5 7.8 Strontium 2,4- 0.54 0.5 95.5 pentanedionate Strontium 2,4- 0.8 0.75 125.6 pentanedionate Strontium 2,4- 1.08 1 113.4 pentanedionate - The addition of a compound of formula (I) to composition A in the presence of 0.5%, 0.75% or 1% of 5-n-octanoylsalicyclic acid did not render the composition A cytotoxic.
- While the invention has been described in terms of various specific and preferred embodiments, the skilled artisan will appreciate that various modifications, substitutions, omissions, and changes may be made without departing from the spirit thereof. Accordingly, it is intended that the scope of the present invention be limited solely by the scope of the following claims, including equivalents thereof.
Claims (65)
1. A topically applicable cosmetic/dermatological composition for reducing mammalian skin irritation, comprising an anti-skin-irritant effective amount of at least one compound having the formula (I):
in which the radicals R, which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl or perfluoroalkyl radical having from 1 to 12 carbon atoms; the radicals R′, which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl, alkoxy or perfluoroalkyl radical having from 1 to 12 carbon atoms; and X is magnesium, strontium, barium, zinc, manganese or palladium, said compound being in hydrated or nonhydrated form, and a topically applicable, physiologically acceptable medium therefor.
2. A composition according to claim 1 , wherein, in the compound of formula (I), each radical R is a linear or branched, saturated alkyl or perfluoroalkyl radical having from 1 to 6 carbon atoms.
3. A composition according to claim 1 , wherein, in the compound of formula (I), each radical R′ is a linear or branched, saturated alkyl, alkoxy or perfluoroalkyl radical having from 1 to 6 carbon atoms.
4. A composition according to claim 1 , wherein, in the compound of formula (I), R′ is a linear or branched, saturated alkyl, alkoxy or perfluoroalkyl radical having from 1 to 6 carbon atoms.
5. A composition according to claim 1 , wherein, in the compound of formula (I), the substituents R and R′ are linear.
6. A composition according to claim 2 , wherein, in the compound of formula (I), the substituents R and R′ are linear.
7. A composition according to claim 3 , wherein, in the compound of formula (I), the substituents R and R′ are linear.
8. A composition according to claim 4 , wherein, in the compound of formula (I), the substituents R and R′ are linear.
9. A composition according to claim 1 , wherein, in the compound of formula (I), the substituents R and R′ are saturated.
10. A composition according to claim 2 , wherein, in the compound of formula (I), the substituents R and R′ are saturated.
11. A composition according to claim 1 , wherein, in the compound of formula (I), the substituents R and R′ comprise a difference of at most two carbon atoms with respect to each other.
12. A composition according to claim 2 , wherein, in the compound of formula (I), the substituents R and R′ comprise a difference of at most two carbon atoms with respect to each other.
13. A composition according to claim 3 , wherein, in the compound of formula (I), the substituents R and R′ comprise a difference of at most two carbon atoms with respect to each other.
14. A composition according to claim 4 , wherein, in the compound of formula (I), the substituents R and R′ comprise a difference of at most two carbon atoms with respect to each other.
15. A composition according to claim 1 , wherein, in the compound of formula (I), X is strontium or zinc.
16. A composition according to claim 2 , wherein, in the compound of formula (I), X is strontium or zinc.
17. A composition according to claim 3 , wherein, in the compound of formula (I), X is strontium or zinc.
18. A composition according to claim 4 , wherein, in the compound of formula (I), X is strontium or zinc.
19. A composition according to claim 5 , wherein, in the compound of formula (I), X is strontium or zinc.
20. A composition according to claim 6 , wherein, in the compound of formula (I), X is strontium or zinc.
21. A composition according to claim 7 , wherein, in the compound of formula (I), X is strontium or zinc.
22. A composition according to claim 8 , wherein, in the compound of formula (I), X is strontium or zinc.
23. A composition according to claim 9 , wherein, in the compound of formula (I), X is strontium or zinc.
24. A composition according to claim 10 , wherein, in the compound of formula (I), X is strontium or zinc.
25. A composition according to claim 11 , wherein, in the compound of formula (I), X is strontium or zinc.
26. A composition according to claim 12 , wherein, in the compound of formula (I), X is strontium or zinc.
27. A composition according to claim 13 , wherein, in the compound of formula (I), X is strontium or zinc.
28. A composition according to claim 14 , wherein, in the compound of formula (I), X is strontium or zinc.
29. A composition according to claim 1 , wherein, in the compound of formula (I), R and R′ are methyl radicals.
30. A composition according to claim 15 , wherein, in the compound of formula (I), R and R′ are methyl radicals.
31. The composition according to claim 1 , wherein said at least one compound of formula (I) is selected from the group consisting of strontium 2,4-pentanedionate, bis(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato)strontium hydrate, bis(2,2,6,6-tetramethyl-3,5-heptanedionato)strontium hydrate and strontium hexafluoroacetylacetonate and mixtures thereof.
32. A topically applicable cosmetic/dermatological composition for substantially inhibiting or reducing mammalian skin irritation, comprising an irritant amount of at least one normally skin-irritating active species/product and an anti-irritant effective amount of at least one compound having the formula (I):
in which the radicals R, which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl or perfluoroalkyl radical having from 1 to 12 carbon atoms; the radicals R′, which may be identical or different, are each a linear or branched, saturated or unsaturated, optionally hydroxylated alkyl, alkoxy or perfluoroalkyl radical having from 1 to 12 carbon atoms; and X is magnesium, strontium, barium, zinc, manganese or palladium, said compound being in hydrated or nonhydrated form, and a topically applicable, physiologically acceptable medium therefor.
33. A composition according to claim 32 , wherein, in the compound of formula (I), each radical R is a linear or branched, saturated alkyl or perfluoroalkyl radical having from 1 to 6 carbon atoms.
34. A composition according to claim 32 , wherein, in the compound of formula (I), each radical R′ is a linear or branched, saturated alkyl, alkoxy or perfluoroalkyl radical having from 1 to 6 carbon atoms.
35. A composition according to claim 32 , wherein, in the compound of formula (I), the substituents R and R′ are linear.
36. A composition according to claim 32 , wherein, in the compound of formula (I), the substituents R and R′ are saturated.
37. A composition according to claim 32 , wherein, in the compound of formula (I), the substituents R and R′ comprise a difference of at most two carbon atoms with respect to each other.
38. A composition according to claim 32 , wherein, in the compound of formula (I), X is strontium or zinc.
39. A composition according to claim 32 , wherein, in the compound of formula (I), R and R′ are methyl radicals.
40. A composition according to claim 38 , wherein, in the compound of formula (I), R and R′ are methyl radicals.
41. The composition according to claim 32 , wherein said at least one compound of formula (I) is selected from the group consisting of strontium 2,4-pentanedionate, bis(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato)strontium hydrate, bis(2,2,6,6-tetramethyl-3,5-heptanedionato)strontium hydrate and strontium hexatluoroacetylacetonate and mixtures thereof.
42. A composition according to claim 32 , wherein said at least one normally skin-irritating active species/product is selected from the group consisting of a preservative, surfactant, fragrance, solvent, propellant, active agent, and mixtures thereof.
43. A composition according to claim 32 , wherein said at least one normally skin-irritating active species/product is selected from the group consisting of a sunscreen, hydroxy acid, keto acid, retinoid, anthralin, anthranoid, peroxide, minoxidil, lithium salt, antiproliferating agent, vitamin, hair tint, hair dye, perfuming alcoholic solution, antiperspirant, hair-removing active agent, permanent-waving active agent, depigmenting agent, capsaicin, antilouse active agent, ionic detergent agent, nonionic detergent agent, propigmenting agent and mixtures thereof.
44. A composition according to claim 32 , wherein said at least one normally skin-irritating active species/product is selected from the group consisting of an α-hydroxy acid, a β-hydroxy acid, an α-keto acid, a β-keto acid, 5-fluorouracil, methothrexate, vitamin B9, vitamin D or a derivative thereof and mixtures thereof.
45. A composition according to claim 32 , wherein said at least one normally skin-irritating active species/product is a p-hydroxy acid.
46. A composition according to claim 32 , wherein said at least one normally skin-irritating active species/product is salicylic acid or a derivative thereof.
47. A composition according to claim 32 , wherein said at least one normally skin-irritating active species/product is selected from the group consisting of 5-n-octanoylsalicylic acid, 5-n-dodecanoylsalicylic acid, a salt thereof, and an ester thereof.
48. A composition according to claim 1 , which is in liquid form.
49. A composition according to claim 1 , which is selected from the group consisting of an oily solution, gel, anhydrous liquid, anhydrous solid, anhydrous paste, emulsion, microemulsion, vesicular dispersion, cream, lotion, milk, ointment, serum, mousse, aerosol, stick, makeup, shampoo and soap.
50. A composition according to claim 49 , which is other than a cream or soap.
51. A composition according to claim 32 , which is in liquid form.
52. A composition according to claim 32 , which is selected from the group consisting of an oily solution, gel, anhydrous liquid, anhydrous solid, anhydrous paste, emulsion, microemulsion, vesicular dispersion, cream, lotion, milk, ointment, serum, mousse, aerosol, stick, makeup, shampoo and soap.
53. A composition according to claim 52 , which is other than a cream or soap.
54. A composition according to claim 1 , wherein said at least one compound of formula (I) is present in an amount of from 0.001% to 30% by weight of the total weight of the composition.
55. A composition according to claim 1 , wherein said at least one compound of formula (I) is present in an amount of from 0.01% to 20% by weight of the total weight of the composition.
56. A composition according to claim 1 , wherein said at least one compound of formula (I) is present in an amount of from 0.1% to 10% by weight of the total weight of the composition.
57. A composition according to claim 32 , wherein said at least one compound of formula (I) is present in an amount of from 0.001% to 30% by weight of the total weight of the composition.
58. A composition according to claim 32 , wherein said at least one compound of formula (I) is present in an amount of from 0.01% to 20% by weight of the total weight of the composition.
59. A composition according to claim 32 , wherein said at least one compound of formula (I) is present in an amount of from 0.1% to 10% by weight of the total weight of the composition.
60. A composition according to claim 32 , wherein said at least one normally skin-irritating active species/product is present in an amount of from 5% to 50% by weight of the total weight of the composition.
61. A composition according to claim 57 , wherein said at least one normally skin-irritating active species/product is present in an amount of from 5% to 50% by weight of the total weight of the composition.
62. A composition according to claim 58 , wherein said at least one normally skin-irritating active species/product is present in an amount of from 5% to 50% by weight of the total weight of the composition.
63. A composition according to claim 59 , wherein said at least one normally skin-irritating active species/product is present in an amount of from 5% to 50% by weight of the total weight of the composition.
64. A composition according to claim 1 , wherein the compound of formula (I) is the product of the reaction of a β-diketone and a hydroxylated or carbonated activated cation.
65. A composition according to claim 32 , wherein the compound of formula (I) is the product of the reaction of a P-diketone and a hydroxylated or carbonated activated cation.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/330,355 US20030143252A1 (en) | 1999-09-28 | 2002-12-30 | Inorganic/organic complexes for reducing skin irritation |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9912057A FR2798855B1 (en) | 1999-09-28 | 1999-09-28 | USE OF INORGANIC-ORGANIC COMPLEXES IN A COMPOSITION FOR TOPICAL USE |
| FR9912057 | 1999-09-28 | ||
| US09/671,627 US6521222B1 (en) | 1999-09-28 | 2000-09-28 | Inorganic/organic complexes for reducing skin irritation |
| US10/330,355 US20030143252A1 (en) | 1999-09-28 | 2002-12-30 | Inorganic/organic complexes for reducing skin irritation |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/671,627 Division US6521222B1 (en) | 1999-09-28 | 2000-09-28 | Inorganic/organic complexes for reducing skin irritation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20030143252A1 true US20030143252A1 (en) | 2003-07-31 |
Family
ID=9550295
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/671,627 Expired - Fee Related US6521222B1 (en) | 1999-09-28 | 2000-09-28 | Inorganic/organic complexes for reducing skin irritation |
| US10/330,355 Abandoned US20030143252A1 (en) | 1999-09-28 | 2002-12-30 | Inorganic/organic complexes for reducing skin irritation |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/671,627 Expired - Fee Related US6521222B1 (en) | 1999-09-28 | 2000-09-28 | Inorganic/organic complexes for reducing skin irritation |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US6521222B1 (en) |
| EP (1) | EP1092426A1 (en) |
| JP (1) | JP2001114625A (en) |
| CA (1) | CA2319849C (en) |
| FR (1) | FR2798855B1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060034779A1 (en) * | 2004-08-02 | 2006-02-16 | Agis Industries (1983) Ltd. | Foamable compositions containing vitamin D3 analogues, processes for preparing same and methods of treatment utilizng same |
| US20110008267A1 (en) * | 2004-08-02 | 2011-01-13 | Perrigo Israel Pharmaceuticals Ltd. | Pharmaceutical and Cosmeceutical Wash-Off Mousse Shampoo Compositions, Processes for Preparing the Same and Uses Thereof |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6242434B1 (en) * | 1997-08-08 | 2001-06-05 | Bone Care International, Inc. | 24-hydroxyvitamin D, analogs and uses thereof |
| US20020128240A1 (en) * | 1996-12-30 | 2002-09-12 | Bone Care International, Inc. | Treatment of hyperproliferative diseases using active vitamin D analogues |
| US6566353B2 (en) * | 1996-12-30 | 2003-05-20 | Bone Care International, Inc. | Method of treating malignancy associated hypercalcemia using active vitamin D analogues |
| US6087350A (en) * | 1997-08-29 | 2000-07-11 | University Of Pittsburgh Of The Commonwealth System Of Higher Education | Use of pretreatment chemicals to enhance efficacy of cytotoxic agents |
| US6521608B1 (en) * | 1998-03-27 | 2003-02-18 | Oregon Health & Science University | Vitamin D and its analogs in the treatment of tumors and other hyperproliferative disorders |
| WO2002006218A2 (en) | 2000-07-18 | 2002-01-24 | Bone Care International, Inc. | STABILIZED 1α-HYDROXY VITAMIN D |
| US7147873B2 (en) * | 2002-01-16 | 2006-12-12 | 3M Innovative Properties Company | Antiseptic compositions and methods |
| US20060003950A1 (en) * | 2004-06-30 | 2006-01-05 | Bone Care International, Inc. | Method of treating prostatic diseases using a combination of vitamin D analogues and other agents |
| US7094775B2 (en) * | 2004-06-30 | 2006-08-22 | Bone Care International, Llc | Method of treating breast cancer using a combination of vitamin D analogues and other agents |
| FR2885802A1 (en) * | 2005-05-17 | 2006-11-24 | Oreal | COSMETIC USE OF VITAMIN K TO ENHANCE THE BARRIER FUNCTION OF THE SKIN |
| MX2008011236A (en) * | 2006-03-01 | 2009-02-10 | Tristrata Inc | Composition and method for topical treatment of tar-responsive dermatological disorders. |
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-
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- 1999-09-28 FR FR9912057A patent/FR2798855B1/en not_active Expired - Fee Related
-
2000
- 2000-09-13 EP EP00402525A patent/EP1092426A1/en not_active Withdrawn
- 2000-09-22 CA CA002319849A patent/CA2319849C/en not_active Expired - Fee Related
- 2000-09-27 JP JP2000295105A patent/JP2001114625A/en active Pending
- 2000-09-28 US US09/671,627 patent/US6521222B1/en not_active Expired - Fee Related
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2002
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| US4322441A (en) * | 1979-10-15 | 1982-03-30 | Minnesota Mining And Manufacturing Company | Use of fluorinated beta-diketones as bacteriocides and fungicides |
| US5178869A (en) * | 1990-01-31 | 1993-01-12 | Lion Corporation | Liquid dentifrice compositions |
| US6126996A (en) * | 1990-07-06 | 2000-10-03 | Advanced Technology Materials, Inc. | Metal complex source reagents for chemical vapor deposition |
| US5820664A (en) * | 1990-07-06 | 1998-10-13 | Advanced Technology Materials, Inc. | Precursor compositions for chemical vapor deposition, and ligand exchange resistant metal-organic precursor solutions comprising same |
| US5328914A (en) * | 1990-07-20 | 1994-07-12 | L'oreal | Use of pyrimidine 3-oxide derivatives for slowing down hair loss and topical compositions used |
| US5372850A (en) * | 1992-02-17 | 1994-12-13 | Mitsubishi Denki Kabushiki Kaisha | Method of manufacturing an oxide-system dielectric thin film using CVD method |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060034779A1 (en) * | 2004-08-02 | 2006-02-16 | Agis Industries (1983) Ltd. | Foamable compositions containing vitamin D3 analogues, processes for preparing same and methods of treatment utilizng same |
| US20110008267A1 (en) * | 2004-08-02 | 2011-01-13 | Perrigo Israel Pharmaceuticals Ltd. | Pharmaceutical and Cosmeceutical Wash-Off Mousse Shampoo Compositions, Processes for Preparing the Same and Uses Thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2319849A1 (en) | 2001-03-28 |
| EP1092426A1 (en) | 2001-04-18 |
| FR2798855B1 (en) | 2003-04-25 |
| FR2798855A1 (en) | 2001-03-30 |
| JP2001114625A (en) | 2001-04-24 |
| CA2319849C (en) | 2006-11-14 |
| US6521222B1 (en) | 2003-02-18 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |