WO2011074141A1 - Procédé de traitement de fibres de kératine - Google Patents

Procédé de traitement de fibres de kératine Download PDF

Info

Publication number
WO2011074141A1
WO2011074141A1 PCT/JP2009/071732 JP2009071732W WO2011074141A1 WO 2011074141 A1 WO2011074141 A1 WO 2011074141A1 JP 2009071732 W JP2009071732 W JP 2009071732W WO 2011074141 A1 WO2011074141 A1 WO 2011074141A1
Authority
WO
WIPO (PCT)
Prior art keywords
keratin fibers
derivatives
composition
process according
filter
Prior art date
Application number
PCT/JP2009/071732
Other languages
English (en)
Inventor
Maxime De Boni
Hiroshi Takahashi
Original Assignee
L'oreal
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by L'oreal filed Critical L'oreal
Priority to JP2012528136A priority Critical patent/JP2013514262A/ja
Priority to PCT/JP2009/071732 priority patent/WO2011074141A1/fr
Publication of WO2011074141A1 publication Critical patent/WO2011074141A1/fr

Links

Classifications

    • A—HUMAN NECESSITIES
    • A45—HAND OR TRAVELLING ARTICLES
    • A45D—HAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D7/00—Processes of waving, straightening or curling hair
    • A45D7/06—Processes of waving, straightening or curling hair combined chemical and thermal
    • 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
    • A61K8/416—Quaternary ammonium compounds
    • 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
    • A61K8/4946—Imidazoles or their condensed derivatives, e.g. benzimidazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • 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
    • A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/805—Corresponding aspects not provided for by any of codes A61K2800/81 - A61K2800/95

Definitions

  • the present invention relates to a process for treating keratin fibers such as hair, as well as a composition and a kit to be used for the process.
  • the repairing treatment should be effective against various stresses, as mentioned before.
  • compositions and/or processes known as treatments for damaged keratin fibers that have been proposed are still insufficient insofar as they are often temporary and do not achieve proper recovery of keratin fiber integrity. In addition, there is still a strong interest in finding efficient protective systems for keratin fibers.
  • UV filters are widely used in skin care products and are known to be effective in the protection of the skin, which is sensitive to UV rays, against solar stresses and aggressions.
  • the keratin fibers such as hair are also sensitive to UV rays. Therefore, there is a real need for compositions and processes that help prevention hair damage by UV rays.
  • an objective of the present invention is to provide a new treatment process for keratin fibers such as hair, using a UV filter, even with a relatively small amount thereof, which provides the keratin fibers with good cosmetic effects, in particular superior UV protecting effects as well as superior repairing or recovering effects, which can be effective against various stresses for a long time.
  • composition comprising at least one UV filter
  • composition contains neither a reducing agent nor a source o carbonate ions of the formula:
  • X is a group selected from the group consisting of 0 “ , OH, NH 2 , 0- OH, and O-COO " .
  • the above process may further comprise the step of rinsing the keratin fibers after the step of applying the composition onto the keratin fibers and/or after the step of heating the keratin fibers .
  • Mechanical tension may be provided to the keratin fibers.
  • the mechanical tension may be provided by using at least one
  • reshaping means selected from the group consisting of a curler, a roller, a plate and an iron.
  • the occlusive space may be formed by at least one coating means.
  • the coating means may be rigid or flexible.
  • the coating means may comprise at least one member selected from the group
  • the keratin fibers may be heated at 45°C to 250°C during the step of heating the keratin fibers.
  • the keratin fibers may be heated by at least one heater providing at least one selected from the group consisting of hot air, hot steam, high frequency induction heating, microwave heating, infrared ray irradiation, laser, and flash lamp irradiation.
  • the coating means and/or the reshaping means may comprise the heater.
  • the UV filter may be an organic UV filter.
  • the UV filter may be selected from the group consisting of anthranilates;
  • dibenzoylmethane derivatives dibenzoylmethane derivatives; cinnamic derivatives; salicylic derivatives; camphor derivatives; benzophenone derivatives; ⁇ , ⁇ - diphenylacrylate derivatives; triazine derivatives; benzotriazole derivatives; benzalmalonate derivatives; benzimidazole
  • the UV filter may be selected from the group consisting of:
  • the composition may comprise the UV filter in an amount of 0.01 to 40% by weight relative to the total weight of the composition.
  • the pH of the composition may range from 6 to 11.
  • compositions for treating keratin fibers to be heated in an occlusive space comprising at least one UV filter,
  • composition contains neither a reducing agent nor a source carbonate ions of the formula:
  • X is a group selected from the group consisting of 0 " , OH, NH 2 , O- OH, and O-COO " .
  • the present invention also relates to a kit for treating keratin fibers, comprising:
  • At least one coating means to form an occlusive space, and at least one heater to heat the keratin fibers in the occlusive space;
  • composition comprising at least one UV filter
  • composition contains neither a reducing agent nor a source of carbonate ions of the formula:
  • X is a group selected from the group consisting of 0 " , OH, NH 2 , 0- 0H, and 0-COO " .
  • cosmetic effects using a UV filter, and in particular superior UV protecting effects as well as superior repairing or recovering effects, which can be effective against various stresses for a long time, by using a composition comprising a UV filter in association with a specific heating process for the keratin fibers .
  • the above specific heating process is performed in a closed or occlusive environment, which limits the evaporation of water or moisture from the keratin fibers and maintains the keratin fibers at higher temperature preferably in the wet state. Accordingly, the keratin fibers can be evenly heated, and the UV filter can easily penetrate into or deposit onto the keratin fibers such that it can remain in or on the keratin fibers for a long time even after some stresses such as shampooing.
  • the process according to the present invention can exhibit good cosmetic effects by using even a relatively small amount of UV filter as compared to a conventional process in which it is difficult for a UV filter to stay on or in the keratin fibers.
  • composition used in the present invention may not contain any reducing agents such as thiol-compounds . Therefore, malodor derived from the reducing agents can be prevented. Furthermore, the composition used in the present invention may not contain any carbonate ion source as defined above. Therefore, cosmetic treatment may be more effective, because there is no possibility of producing carbon dioxide which may form a foam that may
  • composition used for the present invention comprises at least one UV filter.
  • UV here comprises the UVB region (260-320nm in
  • UVA region (320-400nm in wavelength) and the UVA region (320-400nm in wavelength) .
  • a UV filter means any material which has filtering effects in the wavelength of UV, in particular the UVA and UVB regions .
  • the UV filter may be an organic and/or inorganic UV filter active in the UV-A and/or UV-B region which is hydrophilic and/or
  • the UV filter is an organic UV filter.
  • the hydrophilic, lipophilic or insoluble organic UV filter may be selected in particular from anthranilates; dibenzoylmethane derivatives; cinnamic derivatives; salicylic derivatives; camphor derivatives; benzophenone derivatives; ⁇ , ⁇ -diphenylacrylate derivatives; triazine derivatives; benzotriazole derivatives;
  • benzalmalonate derivatives in particular those cited in U.S. Pat. No. 5,624,663; benzimidazole derivatives; imidazolines; bis- benzoazolyl derivatives, such as described in EP-669,323 and U.S. Pat. No. 2,463,264; p-aminobenzoic acid (PABA) derivatives;
  • PABA p-aminobenzoic acid
  • methylenebis (hydroxyphenylbenzotriazole) derivatives such as described in U.S. Pat. Nos. 5,237,071, 5,166,355, GB-2, 303, 549, DE-197, 26, 184 and EP-893,119; benzoxazole derivatives, such as described in EP-0, 832 , 642 , EP-1, 027, 883, EP-1,300,137 and DE- 10162844; screening polymers and screening silicones, such as those described in particular in WO 93/04665; dimers derived from a-alkylstyrene, such as those described in DE-19855649; 4,4- diarylbutadienes, such as described in EP-0, 967, 200, DE-19746654, DE-19755649, EP-A-1, 008, 586, EP-1, 133, 980 and EP-133,981; and their mixtures.
  • Para-Aminobenzoic acid derivatives PABA, Ethyl PABA, Ethyl
  • Salicylic Derivatives Homosalate, marketed under the trademark “Eusolex HMS” by Rona/EM Industries, Ethylhexyl Salicylate, marketed under the trademark “Neo Heliopan OS” by Haarmann and Reimer, Dipropyleneglycol Salicylate, marketed under the trademark “Eusolex HMS” by Rona/EM Industries, Ethylhexyl Salicylate, marketed under the trademark “Neo Heliopan OS” by Haarmann and Reimer, Dipropyleneglycol Salicylate, marketed under the
  • Cinnamic Derivatives Ethylhexyl Methoxycinnamate, marketed in particular under the trademark "Parsol MCX” by Hoffmann-LaRoche, Isopropyl Methoxycinnamate, Isoamyl Methoxycinnamate, marketed under the trademark "Neo Heliopan E 1000" by Haarmann and Reimer, Cinoxate, DEA Methoxycinnamate, Diisopropyl Methylcinnamate, and Glyceryl Ethylhexanoate Dimethoxycinnamate;
  • Etocrylene marketed in particular under the trademark "Uvinul N35" by BASF;
  • Benzophenone Derivatives Benzophenone-1, marketed under the trademark "Uvinul 400" by BASF, Benzophenone-2 , marketed under the trademark “Uvinul D50” by BASF, Benzophenone-3 or Oxybenzone, marketed under the trademark “Uvinul M40" by BASF, Benzophenone-4 , marketed under the trademark “Uvinul MS40” by BASF, Benzophenone- 5, Benzophenone-6, marketed under the trademark “Helisorb 11" by Norquay, Benzophenone-8 , marketed under the trademark "Spectra- Sorb UV-24” by American Cyanamid, Benzophenone-9, marketed under the trademark "Uvinul DS-49” by BASF, Benzophenone-12 , and n- Hexyl 2- ( 4-diethylamino-2-hydroxybenzoyl ) benzoate;
  • Phenylbenzimidazole Derivatives Phenylbenzimidazole Sulfonic Acid, marketed in particular under the trademark “Eusolex 232” by Merck, and Disodium Phenyl Dibenzimidazole Tetrasulfonate,
  • Phenylbenzotriazole Derivatives Drometrizole Trisiloxane
  • Triazine Derivatives Bis-Ethylhexyloxyphenol Methoxyphenyl
  • Triazine marketed under the trademark "Tinosorb S” by Ciba-Geigy
  • Ethylhexyl Triazone marketed in particular under the trademark “Uvinul T150” by BASF
  • Diethylhexyl Butamido Triazone marketed under the trademark “Uvasorb HEB” by Sigma 3V
  • 2,4,6- Tris (dineopentyl 4 ' -aminobenzalmalonate) -s-triazine the trademark "Tinosorb S” by Ciba-Geigy
  • Ethylhexyl Triazone marketed in particular under the trademark “Uvinul T150” by BASF
  • Diethylhexyl Butamido Triazone marketed under the trademark "Uvasorb HEB” by Sigma 3V
  • 2,4,6- Tris (dineopentyl 4 ' -aminobenzalmalonate) -s-triazine the
  • Benzalmalonate Derivatives Dineopentyl 4 ' -methoxybenzalmalonate, and Polyorganosiloxane comprising benzalmalonate functional groups, such as Polysilicone-15, marketed under the trademark "Parsol SLX” by Hoffmann-La Roche;
  • Benzoxazole Derivatives 2,4-bis[5-l (dimethylpropyl ) benzoxazol- 2-yl- (4-phenyl) imino] -6- (2-ethylhexyl) imino-1, - 3, 5-triazine, marketed under the trademark of Uvasorb K2A by Sigma 3V
  • the preferred organic UV screening agents are selected from:
  • Ethylhexyl Methoxycinnamate Homosalate, Ethylhexyl Salicylate, Octocrylene, Phenylbenzimidazole Sulfonic Acid, Benzophenone-3, Benzophenone-4 , Benzophenone-5, n-Hexyl 2- ( 4-diethylamino-2- hydroxybenzoyl ) benzoate, 4-Methylbenzylidene Camphor,
  • the inorganic UV filters may be selected from pigments (mean size of the primary particles: generally from 5 nm and 100 nm,
  • metal oxides which may or may not be coated, such as, for example, pigments formed of titanium oxide (amorphous or crystalline in the rutile and/or anatase form) , iron oxide, zinc oxide, zirconium oxide or cerium oxide, which are all well-known UV photoprotective agents.
  • the pigments may or may not be coated.
  • the coated pigments are pigments which have been subjected to one or more surface
  • anionic surfactants lecithins, sodium, potassium, zinc, iron or aluminum salts of fatty acids, metal alkoxides (titanium or aluminum alkoxides), polyethylene, silicones, proteins (collagen, elastin) , alkanolamines, silicon oxides, metal oxides or sodium hexametaphosphate .
  • the silicones are organosilicon polymers or oligomers comprising a linear or cyclic and branched or
  • crosslinked structure of variable molecular weight, obtained by polymerization and/or polycondensation of suitable functional silanes and essentially composed of a repetition of main units in which the silicon atoms are connected to one another via oxygen atoms (siloxane bond), optionally substituted hydrocarbon
  • radicals being connected directly to the said silicon atoms via a carbon atom.
  • silanes also encompasses the silanes necessary for their preparation, in particular alkylsilanes .
  • the silicones used for the coating of the pigments suitable for the present invention are preferably selected from the group consisting of alkylsilanes, polydialkylsiloxanes and
  • the silicones are selected from the group consisting of octyltrimethylsilane, polydimethylsiloxanes and polymethylhydrosiloxanes .
  • the pigments formed of metal oxides may, before their treatment with silicones, have been treated with other surfacing agents, in particular with cerium oxide, alumina, silica, aluminum compounds, silicon compounds or their mixtures.
  • coated pigments are more particularly titanium oxides coated: with silica, such as the product "Sunveil" from Ikeda;
  • silica and with alumina such as the products "Microtitanium Dioxide MT 500 SA” and “Microtitanium Dioxide MT 100 SA” from Tayca, “Tioveil” from Tioxide and “Mirasun TiW 60" from Rhodia; with alumina, such as the products “Tipaque TTO-55 (B) " and
  • TTO-55 (A) from Ishihara and "UVT 14/4" from Kemira; with alumina and with aluminum stearate, such as the product "Microtitanium Dioxide MT 100 T, MT 100 TX, MT 100 Z or MT-01" from Tayca, the products “Solaveil CT-10 W” and “Solaveil CT 100” from Uniqema and the product “Eusolex T-AVO" from Merck;
  • silica with silica, with alumina and with alginic acid, such as the product "MT-100 AQ" from Tayca;
  • silica with silica, with alumina and with aluminum stearate and treated with a silicone, such as the product "STT-30-DS" from Titan Kogyo;
  • sodium hexametaphosphate such as the product "Microtitanium Dioxide MT 150 W” from Tayca.
  • titanium oxide pigments treated with a silicone are preferably Ti0 2 treated with octyltrimethylsilane for which the mean size of the individual particles is from 25 and 40 nm, such as that marketed under the trademark "T 805" by Degussa Silices; Ti0 2 treated with a polydimethylsiloxane for which the mean size of the individual particles is 21 nm, such as that marketed under the trademark "70250 Cardre UF Ti02Sl3" by Cardre; and
  • the uncoated titanium oxide pigments are, for example, marketed by Tayca under the trademarks "Microtitanium Dioxide MT 500 B” or “Microtitanium Dioxide MT600 B", by Degussa under the trademark “P 25”, by Wacker under the trademark "Oxyde de titane
  • the uncoated zinc oxide pigments are, for example:
  • coated zinc oxide pigments are, for example:
  • Nanophase Technologies those marketed under the trademark “Nanogard Zinc Oxide FN” by Nanophase Technologies (as a 40% dispersion in Finsolv TN, Ci 2 -ci5 alkyl benzoate) ;
  • Daitopersion Zn-50 by Daito (dispersions in oxyethylenated polydimethylsiloxane/cyclopolymethylsiloxane comprising 30% or 50% of zinc nanooxides coated with silica and
  • Pigment ZnO coated with silica and polymethylsilsesquioxane
  • the uncoated cerium oxide pigments are marketed, for example, under the trademark "Colloidal Cerium Oxide” by Rhone-Poulenc .
  • the uncoated iron oxide pigments are, for example, marketed by Arnaud under the trademarks "Nanogard WCD 2002 (FE 45B)",
  • coated iron oxide pigments are, for example, marketed by
  • the UV filter can generally be present in the compositions according to the present invention in proportions ranging from 0.01% to 40% by weight, with respect to the total weight of the composition, and preferably ranging from 0.1% to 10% by weight, with respect to the total weight of the composition.
  • composition used for the present invention contains neither a reducing agent nor a source of carbonate ions of the formula:
  • X is a group selected from the group consisting of 0 “ , OH, NH 2 , 0- OH, and O-COO " .
  • the pH of the composition may range from 6 to 11, preferably between 6.0 and 9.0, and more preferably between 6.0 to 8.0.
  • the pH of the composition is not relatively high or low, damage to the keratin fibers by the composition can be reduced.
  • an acidic or alkali agent (s) other than sources of ions of the invention may be used alone or in combination.
  • the amount of the acidic or alkali agent (s) is not limited, but may be from 0.1 to 5% by weight relative to the total weight of the composition.
  • the acidic agents mention may be made of any inorganic or organic acids which are commonly used in cosmetic products such as citric acid, lactic acid, phosphoric acid or hydrochloric acid (HC1) . HC1 is preferable.
  • alkali agents mention may be made of any inorganic or organic basic agents which are commonly used in cosmetic products such as ammonia; alcanolamines such as mono-, di- and tri- ethanolamine, isopropanolamine; sodium and potassium hydroxides; urea, guanidine and their derivatives; basic amino acids such as lysine or arginine; and diamines such as those described in the structure below:
  • R denotes an alkylene such as propylene optionally
  • Ri, R 2 , R3 and R 4 independently denote a hydrogen atom, an alkyl radical or a C1-C4 hydroxyalkyl radical, which may be exemplified by 1,3- propanediamine and derivatives thereof.
  • monoethanolamine are preferred.
  • the composition used for the present invention may also comprise one or more additional cosmetic agent (s).
  • the amount of the additional cosmetic agent (s) is not limited, but may be from 0.1 to 10% by weight relative to the total weight of the composition.
  • the cosmetic agent (s) may be selected from the group consisting of volatile or non volatile, linear or cyclic, amine-type or not, silicones, cationic, anionic, non ionic or amphoteric polymers, peptides and derivatives thereof, protein hydrolyzates, synthetic or natural waxes, and especially fatty alcohols, swelling agents and penetrating agents, as well as other active compounds, such as anionic, cationic, non ionic, amphoteric or zwitterionic surfactants, agents for combating hair loss, anti-dandruff agents, associative-type or not, natural or synthetic thickeners,
  • suspending agents such as, but not limited to, benzyl alcohol, benzyl ether, benzyl ether, benzyl ether, benzyl ether, benzyl ether sulfate, benzyl ether sulfate, benzyl ether sulfate, benzyl ether sulfate, benzyl ether sulfate, benzyl ether sulfate, sorbitol, sorbitol, sulfate, benzyl sulfate, benzyl sulfate, benzyl sulfate, benzyl sulfate, benzyl sulfate, benzyl sulfate, sulfate, sulfate, sulfate, sulfate, sulfate, sulfate, sulfate, sulfate, sulfate, sulf
  • the vehicle for the composition used for the present invention is preferably an aqueous medium consisting of water and may
  • cosmetically acceptable organic solvents which particularly include alcohols, such as ethyl alcohol, isopropyl alcohol, benzyl alcohol and phenylethyl alcohol, or polyols or polyol ethers, such as ethylene glycol monomethyl, monoethyl and monobutyl ethers, propylene glycol or ethers thereof, such as propylene glycol monomethylether,
  • alcohols such as ethyl alcohol, isopropyl alcohol, benzyl alcohol and phenylethyl alcohol
  • polyols or polyol ethers such as ethylene glycol monomethyl, monoethyl and monobutyl ethers, propylene glycol or ethers thereof, such as propylene glycol monomethylether
  • butylene glycol dipropylene glycol as well as diethylene glycol alkyl ethers, such as diethylene glycol monoethylether or
  • the water may be present in a concentration of from 10 to 90% by weight relative to the total weight of the composition.
  • the organic solvent (s) may then be present in a concentration of from 0.1 to 20% by weight, and preferably from 1 to 10% by weight relative to the total weight of the composition.
  • composition used in the present invention may exist in any form such as a lotion, a gel, thickened or not, or a cream.
  • the process for treating keratin fibers according to the present invention can be performed by
  • composition comprising at least one UV filter, as described above;
  • keratin fibers such as hair are subjected to a specific heating process which is performed in an occlusive space.
  • the heating process can be performed by any heating means which can be freely controlled to realize the temperature desired for the process.
  • the heating process may preferably be performed by using a special heating device or devices that can form an occlusive space to restrict the evaporation of evaporable components such as water in the above-described composition from keratin fibers and keep a predetermined temperature in the heating device throughout the process.
  • a special heating device or devices that can form an occlusive space to restrict the evaporation of evaporable components such as water in the above-described composition from keratin fibers and keep a predetermined temperature in the heating device throughout the process.
  • the evaporable components such as water in the above-described composition evaporate from the keratin fibers, most of the heat energy applied to the keratin fibers will be consumed by the evaporation, and therefore the temperature of the keratin fibers cannot increase up to the predetermined temperature until all evaporable components in the composition evaporate.
  • the above heating device may comprise a heat energy source being either in contact with keratin fibers or apart from keratin fibers, and at least one means to form an occlusive space
  • the heat energy source is used to heat keratin fibers.
  • the heat energy source may be at least one heater providing at least one selected from the group consisting of hot air, hot steam, high frequency induction heating, microwave heating, infrared ray irradiation, laser, and flash lamp irradiation.
  • the occlusive space may be formed by at least one coating means.
  • a plurality of coating means may be used.
  • the coating means may be rigid or flexible.
  • the coating means may comprise at least one member selected from the group consisting of a film and a sheet.
  • the material of the film or the sheet is not limited.
  • the film or the sheet may comprise a thermoplastic or thermosetting resin, a paper, a textile, a bonnet, a metal foil such as aluminum foil, and the like.
  • the film or sheet may be set on a heating rod, a heating bar or a heating plate which is covered by keratin fibers.
  • the coating means may
  • the film or sheet which includes a heater may be set on a rod, a bar, or a plate which is covered by keratin fibers.
  • the occlusive conditions can restrict the evaporation of
  • evaporable components such as water in the above-described
  • composition applied to keratin fibers and therefore the
  • the temperature of the keratin fibers can be increased higher than that obtainable by a conventional heating process or device for the keratin fibers in open conditions. Furthermore, the keratin fibers can be heated effectively, and the keratin fibers can be heated evenly.
  • the occlusive space may comprise apertures, the surface area of which is less than 5%, preferably less than 3% and more particularly less than 0.5% of the total surface area of the coating means.
  • the total surface area of the coating means comprises the surface area of, when it is present, an opening means for the coating means.
  • the apertures may be passages, holes or orifices, which may allow an exchange of air between the occlusive space and the exterior thereof, especially when the reaction such as forming vapor inside the occlusive space is too great.
  • a person skilled in the art could form the apertures such that the diffusion of heat in the occlusive space is not impaired.
  • the keratin fibers can be heated at 45°C to 250°C, preferably 60°C to 200°C, more preferably 60°C to 150°C, more preferably 60°C to 90°C, during the step of heating the keratin fibers.
  • the heating process may be performed for an appropriate time which is required to treat keratin fibers.
  • the time length for the heating process is not limited, but it may be from 1 minute to 2 hours, preferably 1 minute to 1 hour, and more preferably 1 minute to 30 minutes.
  • the time for heating may be from 5 to 20 minutes, preferably 10 to 15 minutes.
  • the keratin fibers may be rinsed after the step of applying the composition onto the keratin fibers and/or after the step of heating the keratin fibers.
  • the keratin fiber may be subjected to mechanical tension which is typically used for permanent
  • mechanical tension is applied to keratin fibers may be performed as follows.
  • keratin fibers are subjected to mechanical tension for deformation.
  • the mechanical tension can be applied to the keratin fibers by any means to deform the keratin fibers to an intended shape.
  • the mechanical tension may be provided by at least one reshaping means selected from the group consisting of a curler, a roller, a clip, a plate and an iron.
  • the reshaping means may comprise at least one heater as described above. If the keratin fibers are rolled around a curler, this rolling-up may be performed on the entire length of the keratin fibers or, for example, on half the length of the keratin fibers. Depending on, for example, the desired hairstyle shape and amount of curls, the rolling-up may be performed with more or less thick locks .
  • the above-described composition is applied to the keratin fibers.
  • the application of the composition may be performed by any means, such as a brush and a comb.
  • the keratin fibers to which the mechanical tension has been applied should be treated with the composition. It may be possible that the keratin fibers are left as they are for a certain amount of time, if necessary.
  • the heat energy is applied to the keratin fibers under occlusive conditions as described above.
  • This process for permanent deformation of keratin fibers may be performed without any step of oxidizing the keratin fibers.
  • the time required for the process according to the present invention can be shorter than that for a conventional process which needs an oxidizing step. Furthermore, damage to the keratin fibers by the oxidizing step can be avoided.
  • the keratin fibers may be rinsed after the step of applying the composition onto the keratin fibers and/or after the step of heating the keratin fibers.
  • One embodiment of the hair treatment process according to the present invention may be a process for reshaping or permanent deforming keratin fibers, in particular hair, comprising:
  • the temperature can be set, adjusted and
  • thermo-measurement probe such as Digital Surface Sensor Module, reference MT-144, sold by Sakaguchi E.H VOC Corp (Japan), set on the keratin fibers.
  • the probe is set on a single keratin fiber.
  • the probe is set on the part of the keratin fibers which directly contacts with the occlusive space, and more preferably, the probe is set on the part of the keratin fibers which directly contacts with the occlusive space and forms the curl end of the keratin fibers, if a curler is used.
  • the temperature is measured at atmospheric pressure of 101325 Pa.
  • the temperature of the keratin fibers may be constant with a fluctuation of ⁇ 2 or 3°C over the head, if the keratin fibers are hair, of an individual, and the probe may be set on any type of keratin fibers .
  • keratin fibers are hair, according to the present
  • the constant temperature with a fluctuation of ⁇ 2 or 3°C can be obtained for any type of hair, and the temperature of the hair can be controlled to be constant + 2 or 3°C during the heating of the hair at a certain temperature.
  • the hair style becomes uniform and homogeneous for the entirety of the hair, and a more excellent hair style can be finally obtained.
  • the coating means may comprise one or more thermal insulating materials, and more advantageously, the coating means may consist of the material (s).
  • thermal insulating material means any material which has an electric conductivity of 0 to 1 W/m°C (PVC: 0.17 W/m°C) .
  • the heating means may be adjusted such that the temperature measured on the keratin fibers is 50 °C or more, more preferably 55°C to less than 150°C, and further more preferably less than 100°C. It is preferable that the heating is performed by heating via electrical resistance.
  • the coating means is impermeable with regard to the composition used in the step b) .
  • At least one of the reshaping or mechanical tensioning means and at least one of the covering means may include a heater.
  • occlusive space means that when the coating means is placed on the reshaping or mechanical tensioning means, or vice versa, they together form a closed structure in which heat can diffuse, but heat cannot diffuse out of or is difficult to diffuse out of the closed structure.
  • the coating means and the reshaping or mechanical tensioning means can form the occlusive space when they are set on the head, if the keratin fibers are hair.
  • the occlusive space may form a condensation cage in which water and a component or components in the composition used in the step b) may evaporate from the keratin fibers, adhere to the wall of the coating means, and drop onto the keratin fibers. This cycle may be repeated during the heating of the keratin fibers.
  • the keratin fibers can be always kept wet, and drying and deteriorating of the keratin fibers will be prevented.
  • occlusive space is an important characteristic of the present invention, because the keratin fibers in the occlusive space can be kept wet and the temperature of the keratin fibers can be constant.
  • the process of the present invention may comprise an additional step of tightening the coating means on the head of an individual, if the keratin fibers are hair, by an elastic cord, an extensible band, or a stretch.
  • the amount of a cosmetic component or components in the composition is advantageously reduced as compared to the processes in the prior art.
  • the amount of the cosmetic component (s) may be 0.3 to 3wt% of the composition .
  • a coating means may be placed on each hair curler as the reshaping or mechanically tensioning means, if the keratin fibers are hair.
  • each of the hair curlers if two or more hair curlers are- used, may be covered individually by a coating means. It is advantageous to cover each hair curler because leaking to the scalp of the composition which has been applied onto keratin fibers in the step b) can be prevented.
  • a coating means may cover all hair curlers, if two or more hair curlers are used.
  • the coating means may cover the entirety of the head if the keratin fibers are hair.
  • the occlusive space formed in the step d) may be maintained during the step e) .
  • the coating means may be removed only after the step e) or after the stop of the heating in the step e) .
  • the composition may be applied to keratin fibers before applying mechanical tension to the keratin fibers. It may be possible that the keratin fibers are left as they are for a certain amount of time, if necessary, before and/or after
  • the keratin fibers may be fixed by oxidation after being taken out from the coating means.
  • the present invention also relates to a composition for treating keratin fibers to be heated in an occlusive space, comprising at least one UV filter,
  • composition contains neither a reducing agent nor a source of carbonate ions of the formula:
  • X is a group selected from the group consisting of 0 “ , OH, NH 2 , 0- OH, and O-COO " .
  • This composition may not need to be used in combination with an oxidizing agent which is used in a conventional permanent
  • the composition may be used in one step, whereas two steps (reducing step and oxidizing step) are necessary in the conventional permanent deformation of keratin fibers.
  • This composition may have the same technical features as those of the composition described above.
  • the present invention also relates to a kit for treating keratin fibers, comprising: a device comprising
  • At least one reshaping means to provide the keratin fibers with mechanical tension
  • At least one coating means to form an occlusive space, and at least one heater to heat the keratin fibers in the
  • composition comprising at least one UV filter wherein the
  • composition contains neither a reducing agent nor a source of carbonate ions of the formula:
  • X is a group selected from the group consisting of 0 " , OH, NH 2 , O-OH, and 0-COO " .
  • the coating means and the heater, as well as the composition in the kit, may be the same as those described above.
  • composition 1 A hair treatment composition (referred to as "Composition 1") having the following composition shown in Table 1 was prepared (active ingredients in wt %) .
  • Composition 1 was applied to a lg natural Japanese hair swatch previously wrapped on a 1.7 cm heating perm-roller. Then, the perm-roller was covered by a plastic film and plugged into a Digital Perm Machine (Oohiro, model ODIS-2) . After the heating process at 90°C for 15 minutes, the hair was rinsed, removed from the perm-roller and dried.
  • ODIS-2 Digital Perm Machine
  • composition 2 The hair was resistant against various external aggressions.
  • composition 2 A hair treatment composition having the following composition shown in Table 2 was prepared (active ingredients in wt %).
  • Composition 2 was applied to a lg Japanese hair swatch. Then, the hair was wrapped by a plastic film and covered by a flexible heating film (FTH-050 from Tokyo Technological Labo) . The hair was heated in occlusive conditions for 10 minutes at 90°C. After the heating step, the hair was rinsed and dried.
  • FTH-050 from Tokyo Technological Labo

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Cosmetics (AREA)

Abstract

La présente invention concerne un procédé de traitement de fibres de kératine qui comprend les étapes consistant à: appliquer sur les fibres de kératine, une composition contenant au moins un filtre UV; placer ensuite les fibres de kératine dans un espace occlusif; puis chauffer les fibres de kératine. La composition ne contient pas d'agent réducteur ni de source d'ions carbonate de formule... Dans la formule, X représente un groupe sélectionné dans le groupe formé par: 0-, OH, NH2, 0- OH et 0-COO-. La présente invention concerne également la composition elle-même et une trousse à utiliser dans le procédé présenté ci-avant.
PCT/JP2009/071732 2009-12-18 2009-12-18 Procédé de traitement de fibres de kératine WO2011074141A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2012528136A JP2013514262A (ja) 2009-12-18 2009-12-18 ケラチン繊維を処理する方法
PCT/JP2009/071732 WO2011074141A1 (fr) 2009-12-18 2009-12-18 Procédé de traitement de fibres de kératine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2009/071732 WO2011074141A1 (fr) 2009-12-18 2009-12-18 Procédé de traitement de fibres de kératine

Publications (1)

Publication Number Publication Date
WO2011074141A1 true WO2011074141A1 (fr) 2011-06-23

Family

ID=42711717

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2009/071732 WO2011074141A1 (fr) 2009-12-18 2009-12-18 Procédé de traitement de fibres de kératine

Country Status (2)

Country Link
JP (1) JP2013514262A (fr)
WO (1) WO2011074141A1 (fr)

Citations (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2463264A (en) 1942-12-23 1949-03-01 Ciba Ltd Derivatives of cyclic amidines and process of making same
EP0133981A2 (fr) 1983-08-05 1985-03-13 Siemens Aktiengesellschaft Protection mécanique contre les surcharges
US5166355A (en) 1991-02-04 1992-11-24 Fairmount Chemical Co., Inc. Process for preparing substituted 2,2'-methylene-bis-[6-(2H-benzotriazol-2-yl)-4-hydrocarbyl-phenols]
WO1993004665A1 (fr) 1991-08-29 1993-03-18 L'oreal Composition cosmetique filtrante contenant un polymere filtre liposoluble a structure hydrocarbonee et une silicone filtre
US5237071A (en) 1991-01-22 1993-08-17 Fairmount Chemical Company, Inc. Process for preparing 2,2'-methylene-bis(6-(2H-benzotriazol-2-yl)-4-hydrocarbyl phenols)
EP0669323A1 (fr) 1994-02-24 1995-08-30 Haarmann & Reimer Gmbh Utilisation de benzazolen comme absorbeurs d'UV nouveaux benzazoles et procédé pour les préparation
GB2303549A (en) 1995-07-22 1997-02-26 Ciba Geigy Ag Micronising organic UV absorbers with alkyl polyglucosides
US5624663A (en) 1987-08-28 1997-04-29 L'oreal Photostable cosmetic filter composition cotaining a UV-A filter and a substituted dialkylbenzalmalonate, the use of substituted dialkylbenzalmalonates in cosmetics as broad-band solar filters and novel substituted dialkyl malonates
EP0832642A2 (fr) 1996-09-13 1998-04-01 3V SIGMA S.p.A Dérivés de benzoxazole et utilisation comme filtres ultraviolet
DE19726184A1 (de) 1997-06-20 1998-12-24 Beiersdorf Ag Kosmetische und dermatologische Lichtschutzformulierungen in Form von Emulsionen, insbesondere O/W-Makroemulsionen, O/W-Mikroemulsionen oder O/W/O-Emulsionen, mit einem Gehalt an lichtschutzwirksamen Benzotriazolderivaten
EP0893119A1 (fr) 1997-07-26 1999-01-27 Ciba SC Holding AG Formulation protectrice contre UV
DE19746654A1 (de) 1997-08-13 1999-02-18 Basf Ag Photostabile UV-Filter enthaltende kosmetische und pharmazeutische Zubereitungen
DE19755649A1 (de) 1997-12-15 1999-06-17 Basf Ag Photostabile UV-Filter enthaltende kosmetische und pharmazeutische Zubereitungen
EP0967200A1 (fr) 1998-06-26 1999-12-29 Basf Aktiengesellschaft 4,4-Diarylbutadiènes comme filtres UV hydrosolubles et photostables pour préparations cosmétiques et pharmaceutiques
DE19855649A1 (de) 1998-12-03 2000-06-08 Basf Ag Dimere alpha-Alkyl-Styrolderivate als photostabile UV-Filter in kosmetischen und pharmazeutischen Zubereitungen
EP1008586A1 (fr) 1998-12-11 2000-06-14 Basf Aktiengesellschaft Diarylbutadiènes oligomères
EP1027883A2 (fr) 1999-01-11 2000-08-16 3V SIGMA S.p.A Combinaison des agents antisolaires contre les rayonnements UV-A et UV-B
US6225467B1 (en) 2000-01-21 2001-05-01 Xerox Corporation Electroluminescent (EL) devices
EP1133980A2 (fr) 2000-03-15 2001-09-19 Basf Aktiengesellschaft Utilisation d'une combinaison d'agents photoprotecteurs comprenant en tant que composé essentiel des hydroxybenzophénones aminosubstituées comme filtres UV photostables dans des préparations cosmétiques et pharmaceutiques
EP1300137A2 (fr) 2001-10-02 2003-04-09 3V SIGMA S.p.A Combinations d'agents anti-solaires
DE10162844A1 (de) 2001-12-20 2003-07-03 Beiersdorf Ag Kosmetische und dermatologische Lichtschutzformulierungen mit einem Gehalt an Bis-Resorcinyltriazinderivaten und Benzoxazol-Derivaten
WO2004085412A2 (fr) 2003-03-24 2004-10-07 Ciba Specialty Chemicals Holding Inc. Derives de triazine symetriques
US20050166336A1 (en) 2004-01-29 2005-08-04 L'oreal Composition for protecting keratin material, process of making, uses thereof
WO2006035000A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Emulsion photoprotectrice a teneur elevee en pigments filtrants, photoprotecteurs
WO2006034991A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Emulsion eau dans l'huile contenant des pigments filtrants de protection solaire anti-uv
WO2006035007A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Preparation cosmetique de protection solaire a base de micropigments
WO2006034985A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Emulsion huile dans l'eau contenant des pigments filtrants de protection solaire anti-uv inorganiques et du sulfate d'alkyle
WO2006034992A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Emulsion cosmetique de protection solaire contenant des micropigments organiques
WO2006034982A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Concentre photoprotecteur a micropigments organiques
EP2022472A1 (fr) * 2007-08-07 2009-02-11 KPSS-Kao Professional Salon Services GmbH Composition de conditionnement pour cheveux
EP2111852A2 (fr) * 2008-04-21 2009-10-28 Henkel AG & Co. KGaA Procédé de traitement pour le soin des cheveux

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8921074D0 (en) * 1989-09-18 1989-11-01 Unilever Plc Hair conditioning composition
JPH06219931A (ja) * 1993-01-07 1994-08-09 Pola Chem Ind Inc 紫外線防護化粧料
JPH0824033A (ja) * 1994-07-11 1996-01-30 Michio Izawa 加温シート
DE19538094C1 (de) * 1995-10-13 1997-02-20 Kao Corp Gmbh Verwendung einer wäßrigen Emulsion oder Dispersion als Haarpflegemittel
JP4236365B2 (ja) * 2000-04-19 2009-03-11 花王株式会社 頭髪処理方法
JP2002017427A (ja) * 2000-07-06 2002-01-22 Kao Corp 頭髪処理方法
JP2002104935A (ja) * 2000-09-28 2002-04-10 Mitsubishi Chemicals Corp 毛髪化粧料
JP2002128645A (ja) * 2000-10-26 2002-05-09 Naiad:Kk 白髪用染毛剤及び白髪の染毛方法
JP4076355B2 (ja) * 2001-02-28 2008-04-16 花王株式会社 頭髪処理方法
JP2002338440A (ja) * 2001-05-17 2002-11-27 Kao Corp 毛髪処理方法
FR2865646B1 (fr) * 2004-01-29 2009-02-13 Oreal Procede de preparation d'une composition pour le traitement cosmetique des matieres keratiniques a partir de fluide sous pression et d'agents protecteurs
JP2006149698A (ja) * 2004-11-30 2006-06-15 Manabu Tanaka 毛髪形状の処理方法
FR2880801B1 (fr) * 2005-01-18 2008-12-19 Oreal Composition de traitement des fibres keratiniques comprenant un alcool aromatique, un acide carboxylique aromatique et un agent protecteur
JP4686295B2 (ja) * 2005-08-05 2011-05-25 株式会社大廣製作所 毛髪トリートメントの施術方法

Patent Citations (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2463264A (en) 1942-12-23 1949-03-01 Ciba Ltd Derivatives of cyclic amidines and process of making same
EP0133981A2 (fr) 1983-08-05 1985-03-13 Siemens Aktiengesellschaft Protection mécanique contre les surcharges
US5624663A (en) 1987-08-28 1997-04-29 L'oreal Photostable cosmetic filter composition cotaining a UV-A filter and a substituted dialkylbenzalmalonate, the use of substituted dialkylbenzalmalonates in cosmetics as broad-band solar filters and novel substituted dialkyl malonates
US5237071A (en) 1991-01-22 1993-08-17 Fairmount Chemical Company, Inc. Process for preparing 2,2'-methylene-bis(6-(2H-benzotriazol-2-yl)-4-hydrocarbyl phenols)
US5166355A (en) 1991-02-04 1992-11-24 Fairmount Chemical Co., Inc. Process for preparing substituted 2,2'-methylene-bis-[6-(2H-benzotriazol-2-yl)-4-hydrocarbyl-phenols]
WO1993004665A1 (fr) 1991-08-29 1993-03-18 L'oreal Composition cosmetique filtrante contenant un polymere filtre liposoluble a structure hydrocarbonee et une silicone filtre
EP0669323A1 (fr) 1994-02-24 1995-08-30 Haarmann & Reimer Gmbh Utilisation de benzazolen comme absorbeurs d'UV nouveaux benzazoles et procédé pour les préparation
GB2303549A (en) 1995-07-22 1997-02-26 Ciba Geigy Ag Micronising organic UV absorbers with alkyl polyglucosides
EP0832642A2 (fr) 1996-09-13 1998-04-01 3V SIGMA S.p.A Dérivés de benzoxazole et utilisation comme filtres ultraviolet
DE19726184A1 (de) 1997-06-20 1998-12-24 Beiersdorf Ag Kosmetische und dermatologische Lichtschutzformulierungen in Form von Emulsionen, insbesondere O/W-Makroemulsionen, O/W-Mikroemulsionen oder O/W/O-Emulsionen, mit einem Gehalt an lichtschutzwirksamen Benzotriazolderivaten
EP0893119A1 (fr) 1997-07-26 1999-01-27 Ciba SC Holding AG Formulation protectrice contre UV
DE19746654A1 (de) 1997-08-13 1999-02-18 Basf Ag Photostabile UV-Filter enthaltende kosmetische und pharmazeutische Zubereitungen
DE19755649A1 (de) 1997-12-15 1999-06-17 Basf Ag Photostabile UV-Filter enthaltende kosmetische und pharmazeutische Zubereitungen
EP0967200A1 (fr) 1998-06-26 1999-12-29 Basf Aktiengesellschaft 4,4-Diarylbutadiènes comme filtres UV hydrosolubles et photostables pour préparations cosmétiques et pharmaceutiques
DE19855649A1 (de) 1998-12-03 2000-06-08 Basf Ag Dimere alpha-Alkyl-Styrolderivate als photostabile UV-Filter in kosmetischen und pharmazeutischen Zubereitungen
EP1008586A1 (fr) 1998-12-11 2000-06-14 Basf Aktiengesellschaft Diarylbutadiènes oligomères
EP1027883A2 (fr) 1999-01-11 2000-08-16 3V SIGMA S.p.A Combinaison des agents antisolaires contre les rayonnements UV-A et UV-B
US6225467B1 (en) 2000-01-21 2001-05-01 Xerox Corporation Electroluminescent (EL) devices
EP1133980A2 (fr) 2000-03-15 2001-09-19 Basf Aktiengesellschaft Utilisation d'une combinaison d'agents photoprotecteurs comprenant en tant que composé essentiel des hydroxybenzophénones aminosubstituées comme filtres UV photostables dans des préparations cosmétiques et pharmaceutiques
EP1300137A2 (fr) 2001-10-02 2003-04-09 3V SIGMA S.p.A Combinations d'agents anti-solaires
DE10162844A1 (de) 2001-12-20 2003-07-03 Beiersdorf Ag Kosmetische und dermatologische Lichtschutzformulierungen mit einem Gehalt an Bis-Resorcinyltriazinderivaten und Benzoxazol-Derivaten
WO2004085412A2 (fr) 2003-03-24 2004-10-07 Ciba Specialty Chemicals Holding Inc. Derives de triazine symetriques
US20050166336A1 (en) 2004-01-29 2005-08-04 L'oreal Composition for protecting keratin material, process of making, uses thereof
WO2006035000A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Emulsion photoprotectrice a teneur elevee en pigments filtrants, photoprotecteurs
WO2006034991A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Emulsion eau dans l'huile contenant des pigments filtrants de protection solaire anti-uv
WO2006035007A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Preparation cosmetique de protection solaire a base de micropigments
WO2006034985A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Emulsion huile dans l'eau contenant des pigments filtrants de protection solaire anti-uv inorganiques et du sulfate d'alkyle
WO2006034992A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Emulsion cosmetique de protection solaire contenant des micropigments organiques
WO2006034982A1 (fr) 2004-09-27 2006-04-06 Beiersdorf Ag Concentre photoprotecteur a micropigments organiques
EP2022472A1 (fr) * 2007-08-07 2009-02-11 KPSS-Kao Professional Salon Services GmbH Composition de conditionnement pour cheveux
EP2111852A2 (fr) * 2008-04-21 2009-10-28 Henkel AG & Co. KGaA Procédé de traitement pour le soin des cheveux

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"IP.COM Journal", 20 September 2004, IP.COM INC, article "Symmetrical Triazine Derivatives"
COSMETICS & TOILETRIES, vol. 105, February 1990 (1990-02-01), pages 53 - 64

Also Published As

Publication number Publication date
JP2013514262A (ja) 2013-04-25

Similar Documents

Publication Publication Date Title
US20080019930A1 (en) Dibenzoylmethane sunscreens photostabilized with arylalkyl amide or ester compounds
CN108472515B (zh) 光保护性化妆品组合物及获得该组合物的方法
EP3193816B1 (fr) Composition à base de particules composites sphériques multicouches et d'agent anti-uv
JP2013507333A (ja) ２−アルコキシ−４−アルキルケトンフェノール化合物に基づく光保護組成物；太陽光線保護指数を増加させるための前記化合物の使用
JP2008001705A (ja) 日焼け防止指数を高めることが可能な薬剤としてのシリコーン材料の凹形または環状粒子の化粧品としての使用；それらを含む水性光防護組成物
US20200261748A1 (en) Photoprotective compositions comprising an aqueous phase and a low melting point apolar wax
US20080317685A1 (en) Photoprotective cosmetic compositions comprising photostabilized dibenzoylmethane compounds and siloxane-containing arylalkyl benzoate amide compounds
US20100003207A1 (en) Photoprotective compositions comprising photosensitive 1,3,5-triazine compounds, dibenzoylmethane compounds and siliceous s-triazines substituted with two aminobenzoate or aminobenzamide groups
WO2007080053A2 (fr) Composition cosmétique contenant un dérivé de dibenzoylméthane et un composé à base de phénol ou de bisphénol et procédé de photostabilisation du dérivé de dibenzoylméthane
KR102206407B1 (ko) 피지를 구성하는 하나 이상의 화합물과 오존 간의 반응으로부터 생성되는 카르보닐 화합물을 포획하기 위한 하나 이상의 친핵성 작용기를 포함하는 화합물의 용도
JP4732814B2 (ja) トリアジン誘導体、少なくとも１つの追加の光防護剤および安息香酸アリールアルキル誘導体を含む光防護組成物、これらの化粧用使用
JP4732813B2 (ja) 安息香酸アリールアルキル誘導体およびアミド系オイルの混合物で可溶化されたトリアジンスクリーニング剤を含有する光防護組成物；その化粧品使用
WO2007080052A1 (fr) Composition cosmétique contenant un dérivé de dibenzoylméthane et un composé de phénol ou de bisphénol contenant du siloxane, et procédé de photostabilisation du dérivé de dibenzoylméthane
KR20030047812A (ko) 차단제의 상승작용성 혼합물에 기초한 일광차단 화장조성물, 및 이의 용도
EP3989914B1 (fr) Composition comprenant des ingrédients pour un gel dic et un polyol
US20150064224A1 (en) Use of Certain Water-Insoluble Porous Polymeric Particles in Spherical Form as SPF Boosters
WO2011074141A1 (fr) Procédé de traitement de fibres de kératine
US7364720B2 (en) Photostabilization of dibenzoylmethane UV-screening agents with arylalkyl benzoate compounds/amide-based oils and photoprotective compositions comprised thereof
US11135149B2 (en) Salt activatable water resistant cosmetic composition
US20080008669A1 (en) Photostable sunscreen compositions comprising cinnamate ester UV-B filters and s-triazine compounds
WO2016008119A1 (fr) Composition d'écran solaire sans huile
JP4713251B2 (ja) 安息香酸アリールアルキル誘導体およびビス−レソルシニルトリアジン化合物を用いたジベンゾイルメタン誘導体を光防護する方法、ならびに光防護組成物
JP2006176516A (ja) 少なくとも一の金属酸化物の無機顔料と少なくとも一のヒドロキシアルキル尿素を含有する抗日光組成物
JP2008001706A (ja) ジベンゾイルメタン誘導体およびアリールアルキルアミドまたはエステル化合物を含む化粧品組成物、ジベンゾイルメタン誘導体を光安定化する方法
US20070196294A1 (en) Photostable sunscreen compositions comprising dibenzoylmethane compound UV-A filters and s-triazine compounds

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 09801566

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2012528136

Country of ref document: JP

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 09801566

Country of ref document: EP

Kind code of ref document: A1