• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    PURPOSE: Provided are novel cosmetic or dermatological compositions for topical use, in particular for the photoprotection of the skin and/or hair, characterized in that they comprise, in a cosmetically acceptable vehicle, at least. CONSTITUTION: A topically applicable cosmetic/dermatological sunscreen composition suited for the UV-photoprotection of human skin and/or hair, characteristically comprises synergistically UV-APPD-enhancing amounts of (a) particulates of at least one insoluble organic UV-screening agent having a particle size ranging from 10 nanometer to 5 micrometer, and (b) at least one UV-screening amino-substituted 2-hydroxybenzophenone compound having the following structural formula(14) in which R1 and R2, which may be identical or different, are each a hydrogen atom, a C1-C20 alkyl radical, a C2-C10 alkenyl radical, a C3-C10 cycloalkyl radical or a C3-C10 cycloalkenyl radical, with the proviso that R1 and R2 can together form, with the nitrogen atom to which they are bonded, a 5- or 6-membered heterocyclic ring member; R3 and R4, which may be identical or different, are each a C1-C20 alkyl radical, a C2-C10 alkenyl radical, a C3-C10 cycloalkyl radical, a C3-C10 cycloalkenyl radical, a C1-C12 alkoxy radical, a (C1-C20) alkoxycarbonyl radical, a C1-C12 alkylamino radical, a di(C1-C12) alkylamino radical, an aryl radical or a heteroaryl radical which is optionally substituted, or a water-solubilizing substituent selected from among a carboxylate group, a sulfonate group or an ammonium residue; X is a hydrogen atom or a -COOR5 or -CONR6R7 radical; R5, R6 and R7, which may be identical or different, are each a hydrogen atom, a C1-C20 alkyl radical, a C2-C10 alkenyl radical, a C3-C10 cycloalkyl radical, a C3-C10 cycloalkenyl radical, a -(YO)o-Z radical or an aryl radical; Y is -(CH2)2-, -(CH2)3-, -(CH2)4- or -CH-CH3-CH2-; Z is -CH2-CH3, -CH2CH2CH3, -CH2-CH2-CH3 or -CH(CH3)-CH3; m is an integer ranging from 0 to 3; n is an integer ranging from 0 to 3; and o is an integer ranging from 1 to 2.
    公开号:KR20030047811A
    申请号:KR1020020077382
    申请日:2002-12-06
    公开日:2003-06-18
    发明作者:깡도디디에
    申请人:로레알；
    IPC主号:
    专利说明:

    Sunscreen cosmetic compositions based on synergistic mixtures of blockers, and use thereof {ANTISUN COSMETIC COMPOSITIONS BASED ON A SYNERGISTIC MIXTURE OF SCREENING AGENTS, AND USES}
    [1] The present invention relates to a new cosmetic or dermatological composition for topical use, in particular for photoprotection of skin and / or hair, characterized in that it contains the following in a cosmetically acceptable vehicle:
    [2] (a) a first screening agent, at least one insoluble organic UV blocker having a particle size of 10 nm to 5 μm, and
    [3] (b) at least one specific amino substituted 2-hydroxybenzophenone derivative as second blocking agent.
    [4] The combination of these two blockers allows a synergistic effect to be obtained for a given sunscreen factor UV-A PPD .
    [5] The invention also relates to their application in protecting skin and hair against the effects of ultraviolet radiation.
    [6] Light radiation of wavelength 280 nm to 400 nm can brown the human epidermis, and light rays of wavelength 280 nm to 320 nm known under the name UV-B can be detrimental to the development of natural tanning. It is known that this UV-B radiation should be blocked, as it causes erythema and skin burns.
    [7] It is also known that UV-A rays of wavelength 320 nm to 400 nm, which cause browning of the skin, can lead to harmful changes in the skin, in particular in the case of sensitive skin or in the case of continuous exposure to the sun. have. UV-A light causes, in particular, loss of elasticity and wrinkled appearance of the skin resulting in premature ejaculation. They promote the triggering of the lupus erythematosus reaction, or in some subjects, make the reaction prominent and even cause phototoxic or photoallergic reactions. Therefore, it is also desirable to block UV-A radiation.
    [8] Numerous cosmetic compositions intended to photoprotect skin (UV-A and / or UV-B) have been provided so far.
    [9] The efficacy of a sunscreen composition is commonly expressed as a sunscreen factor (SPF), which is mathematically needed to reach the erythema threshold with a UV blocker against the UV radiation dose required to reach the erythema threshold without a UV blocker. Expressed as the ratio of UV radiation dose. The factor thus relates to the protective effect on erythema whose spectrum of biological action is centered in the UV-B region, and consequently indicates protection against the UV-B radiation.
    [10] In view of the effects of UV-A radiation on the skin and the development of numerous compositions containing combinations of blocking agents capable of absorbing UV-B and / or UV-A radiation, protection against UV-A radiation is provided. Specific methods for evaluating have been developed
    [11] For identification of protection against UV-A radiation, the Persistent Pigment Darkening (PPD) method, which measures skin color observed 2-4 hours after skin exposure to UV-A radiation, is particularly recommended and used. do. This method was adopted in 1996 by the Japanese Cosmetic Industry Association (JCIA) as the official test procedure for UV-A labeling of products and is often used in laboratories in Europe and the United States (Japan Cosmetic Industry Association Technical Bulletin, Measurement Standards for UVA). protection efficacy.issued on November 21, 1995, implemented on January 1, 1996).
    [12] The sunscreen factor UV-A PPD (UV-A PPD PF) mathematically reaches the pigmentation threshold with a UV blocker against the UV-A radiation dose (MPPD np ) required to reach the pigmentation threshold without UV blocker. Expressed as the ratio of UV-A radiation dose (MPPD p ) needed to
    [13]
    [14] The sunscreen composition is often present in an oil-in-water emulsion form (ie, a cosmetically acceptable vehicle consisting of a continuous aqueous dispersion phase and a discontinuous oily dispersion phase), which are in various concentrations, one or more conventional lipophilic and / or It contains an organic blocker capable of selectively absorbing hydrophilic, harmful UV radiation, which blocker (and amount thereof) is selected according to the desired sunscreen factor.
    [15] Sunscreen compositions based on amino substituted 2-hydroxybenzophenone derivatives are known from patent applications EP-A-1 046 391 and DE 100 12 408.
    [16] In fact, following many of the studies conducted in the field of photoprotection described above, the Applicant is surprisingly and surprisingly, combining two specific sunscreens already known per se in the art at a rate within sufficiently defined limits, Due to the synergistic effect, it is possible in any case to obtain a sunscreen composition which exhibits a much higher, significantly improved sunscreen factor UV-A PPD than can be obtained by using one of the blockers alone. Found.
    [17] The above findings form the basis of the present invention.
    [18] Thus, according to one of the subject matter of the present invention, there is now provided a novel cosmetic composition for topical use, in particular for photoprotection of skin and / or hair, characterized in that it contains the following in a cosmetically acceptable vehicle: :
    [19] (a) at least one insoluble organic UV blocker having a particle size of 10 nm to 5 μm, as a first blocker, and
    [20] (b) at least one amino substituted 2-hydroxybenzophenone derivative of formula (14) as defined below as second blocking agent.
    [21] Another subject of the invention is the use of said composition in the preparation of the desired cosmetic composition for the protection of the skin and / or hair against ultraviolet radiation, in particular solar radiation.
    [22] Another subject of the invention is the purpose of providing a synergistic effect for a given sunscreen factor UV-A PPD and containing at least one insoluble organic UV blocker with a particle size of 10 nm to 5 μm, in particular against skin against ultraviolet radiation. And / or the use of an amino substituted 2-hydroxybenzophenone derivative of formula (14) as defined later in the preparation of the desired cosmetic or dermatological composition for protecting the hair.
    [23] The term "insoluble UV blocker" within the meaning of the present invention has a solubility of less than 0.1% by weight in water and includes liquid paraffins, fatty alcohol benzoates and fatty acid triglycerides such as Miglyol Of the majority of organic solvents such as 812 (available from Dynamit Nobel) is understood to mean any organic or inorganic UV blocker having a solubility of less than 1% by weight. At 70 ° C., the solubility, defined as the amount of product in solution in a solvent that is in equilibrium with the excess solids in suspension, can be readily assessed in the laboratory.
    [24] Other features, aspects, and advantages of the invention will become apparent upon reading the following detailed description.
    [25] Typically, insoluble UV blockers and amino substituted 2-hydroxybenzophenone derivatives are present in the composition at a rate that provides synergistic activity against a given sunscreen factor UV-A PPD .
    [26] Insoluble organic UV blockers according to the invention have an average particle size of 10 nm to 5 μm, more preferably 10 nm to 2 μm, more particularly 20 nm to 2 μm.
    [27] Insoluble organic blockers according to the invention are prepared by any means, such as, in particular, by dry milling or milling, sieving, atomizing, micronization, or spraying in a solvent medium. It can be made into a particulate form.
    [28] Insoluble organic blockers according to the invention in micronized form, in particular, the process of milling insoluble organic UV blockers in the form of coarse particles in the presence of a suitable surfactant which may allow for improved dispersion of the particles obtained in the cosmetic formulation. It can be obtained by.
    [29] Examples of processes for micronization of insoluble organic blockers are disclosed in applications GB-A-2 303 549 and EP-A-893 119, which form an integral part of the description. Milling devices used according to these documents are air jet mills, bead mills, vibratory mills or hammer mills, preferably high speed stirred mills or impact mills, more particularly rotary beads. Mill, vibratory mill, tube mill or rod mill.
    [30] According to the specific process, as a surfactant for milling of the blocking agent, the structural formula C n H 2n + 1 O (C 6 H 10 O 5 ) x H (wherein n is an integer of 8 to 16, x is ( C 6 H 10 O 5 ) alkylpolyglucosides having an average degree of polymerization of the monomers (between 1.4 and 1.6). These include at least one free OH functional group on the C 1 -C 12 ester of a compound having the structure C n H 2n + 1 O (C 6 H 10 O 5 ) x H, more particularly on the glucoside unit (C 6 H 10 O 5 ) And may be selected from esters obtained by the reaction of C 1 -C 12 carboxylic acids such as formic acid, acetic acid, propionic acid, butyric acid, sulfosuccinic acid, citric acid or tartaric acid. The surfactant is usually used in concentrations ranging from 1 to 50% by weight, more preferably from 5 to 40% by weight, relative to the insoluble blocker in micronized form.
    [31] Insoluble organic UV blocking agents according to the present invention are oxalanilide type, triazine type, benzotriazole type; Vinyl amide type; Cinnamic amide; Or indole forms comprising one or more benzazoles and / or benzofuran or benzothiophene groups; Aryl vinylene ketone type; Phenylenebis (benzoxazinone) derivative type; Or organic UV blockers of the acrylonitrile amide, sulfonamide or carbamate derivative type.
    [32] In the sense used in the present invention, the term benzazole includes benzothiazole, benzoxazole and benzimidazole simultaneously.
    [33] Among the oxalanilide type UV blocking agents according to the present invention, those corresponding to the following general formula (1) may be mentioned:
    [34]
    [35] (Wherein T 1 , T ′ 1 , T 2 and T ′ 2 are the same or different and represent a hydrogen atom, a C 1 -C 8 alkyl radical or a C 1 -C 8 alkoxy radical). These compounds are disclosed in patent application WO 95/22959.
    [36] For example, mention may be made of commercially available Tinuvin 315 and Tinuvin 312 (available from Ciba-Geigy), each having the following structure:
    [37]
    [38]
    [39] In addition, among the triazine type insoluble UV blockers according to the present invention, those corresponding to the following general formula (2) may be mentioned:
    [40]
    [41] Wherein T 3 , T 4 and T 5 are independently phenyl, phenoxy or pyrrolo, wherein the phenyl, phenoxy or pyrrolo group is OH, C 1 -C 18 alkyl or C 1 -C 18 alkoxy , C 1 -C 18 carboxyalkyl, C 5 -C 8 cycloalkyl, methylbenzylidenecamphor group,-(CH = CH) n (CO) -OT 6 group wherein T 6 is C 1 -C 18 alkyl or Cinnamic, n is a value of 0 or 1) or is substituted with 1, 2 or 3 substituents selected from).
    [42] These compounds are disclosed in WO 97/03642, GB 2 286 774, EP-743 309, WO 98/22447 and GB 2 319 523, which form an integral part of the description.
    [43] Among the triazine type UV blockers according to the invention, insoluble s-triazine derivatives carrying benzalmalonate and / or phenylcyanoacrylate groups, such as application EP-A-0 790 243 (which is an integral part of the description) May also be mentioned.
    [44] Among the triazine type insoluble UV blockers, more particularly the following compounds will be mentioned:
    [45] 2,4,6-tris (diethyl 4'-aminobenzalmalonate) -s-triazine,
    [46] 2,4,6-tris (diisopropyl 4'-aminobenzalmalonate) -s-triazine,
    [47] 2,4,6-tris (dimethyl 4'-aminobenzalmalonate) -s-triazine,
    [48] 2,4,6-tris (ethyl α-cyano-4-aminocinnamate) -s-triazine.
    [49] Among the triazine-type UV blockers according to the invention, insoluble s-triazine derivatives carrying benzotriazole and / or benzothiazole groups, such as application WO 98/25922, which form an integral part of the description. Mention may also be made of the disclosed.
    [50] Among these compounds, more particularly the following may be mentioned:
    [51] 2,4,6-tris [(3 '-(benzotriazol-2-yl) -2'-hydroxy-5'-methyl) phenylamino] -s-triazine,
    [52] 2,4,6-tris [(3 '-(benzotriazol-2-yl) -2'-hydroxy-5'-tert-octyl) phenylamino] -s-triazine.
    [53] Among the benzotriazole type insoluble organic UV blockers according to the invention, mention may be made of the following formula (3), as disclosed in the application WO 95/22959, which forms an integral part of the description.
    [54]
    [55] (Wherein T 7 represents a hydrogen atom or a C 1 -C 18 alkyl radical; T 8 and T 9 are the same or different and represent a C 1 -C 18 alkyl radical optionally substituted with phenyl).
    [56] As examples of the compound of the formula (3), mention may be made of commercially available Tinuvin 328, 320, 234 and 350 (manufactured by Ciba-Geigy) having the structure:
    [57]
    [58]
    [59]
    [60]
    [61] Among the insoluble organic UV blockers of the benzotriazole type according to the invention, the compounds as disclosed in patents US 5 687 521, US 5 373 037 and US 5 362 881, in particular, have the following structure, under the trade name Mixxim PB30 in Fairmount Chemical Commercially available [2,4'-dihydroxy-3- (2H-benzotriazol-2-yl) -5- (1,1,3,3-tetramethylbutyl) -2 '-(n-jade Methoxy) -5'-benzoyl] diphenylmethane may be mentioned:
    [62]
    [63] Among the benzotriazole type insoluble organic UV blockers according to the present invention, mention may be made of methylenebis (hydroxyphenylbenzotriazole) derivatives having the structure of formula (4):
    [64]
    [65] Wherein the T 10 and T 11 radicals are the same or different and are C 1 -C which may be substituted with one or more radicals selected from C 1 -C 4 alkyl radicals, C 5 -C 12 cycloalkyl radicals or aryl moieties 18 alkyl radicals). These compounds are known per se and have the applications US 5 237 071, US 5 166 355, GB-A-2 303 549, DE 197 26 184 and EP-A-893 119 (they form an integral part of the description). Is disclosed.
    [66] In Formula 4 as defined above: C 1 -C 18 alkyl groups can be linear or branched, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, tert-octyl, n-amyl, n-hexyl, n-heptyl, n-octyl, isooctyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, tetradecyl, hexadecyl or octadecyl; C 5 -C 12 cycloalkyl groups are, for example, cyclopentyl, cyclohexyl or cyclooctyl; Aryl groups are, for example, phenyl or benzyl.
    [67] Among the compounds of formula 4, those having the following structure are more particularly preferred:
    [68] Compound (a)
    [69] Compound (b)
    [70] Compound (c)
    [71] Compound (a), being the name 2,2'-methylenebis [6- (2H-benzotriazol-2-yl) -4- (1,1,3,3-tetramethylbutyl) phenol], is a Ciba Specialty Chemicals Commercially available in micronized form under the tradename Tinosorb M.
    [72] Compound (c), entitled 2,2'-methylenebis [6- (2H-benzotriazol-2-yl) -4-methylphenol], is commercially available from Fairmount Chemical under the trade name Mixxim BB / 200 in solid form.
    [73] Among the insoluble organic blockers of the vinyl amide type, mention may be made, for example, of compounds having the following formula as disclosed in the application WO 95/22959, which forms an integral part of the description.
    [74] T 12- (Y) r -C (= O) -C (T 13 ) = C (T 14 ) -N (T 15 ) (T 16 )
    [75] Wherein T 12 is an OH, a C 1 -C 18 alkyl radical, a C 1 -C 8 alkoxy radical, or a group -C (═O) -OT 17 , where T 17 is C 1 -C 18 alkyl Phenyl group optionally substituted with 1, 2 or 3 radicals selected from C 1 -C 18 , preferably C 1 -C 5 alkyl radicals; T 13 , T 14 , T 15 and T 16 are the same or different and represent a C 1 -C 18 , preferably C 1 -C 5 alkyl radical or a hydrogen atom; Y is N or O and r has a value of 0 or 1}.
    [76] Among these compounds, more particularly the following will be mentioned:
    [77] 4-octylamino-3-penten-2-one;
    [78] Ethyl 3-octylamino-3-butenoate;
    [79] 3-octylamino-1-phenyl-2-buten-1-one;
    [80] 3-dodecylamino-1-phenyl-2-buten-1-one.
    [81] Among the cinnamic insoluble organic blockers according to the invention, mention may also be made of compounds corresponding to the structure of the following formula (6), as disclosed in the application WO 95/22959, which forms an integral part of the description. :
    [82]
    [83] [Wherein OT 18 is a hydroxyl or C 1 -C 4 alkoxy radical, preferably a methoxy or ethoxy radical; T 19 is hydrogen or C 1 -C 4 alkyl, preferably methyl or ethyl; T 20 is — (CONH) s-phenyl group where s has a value of 0 or 1, and the phenyl group is OH, C 1 -C 18 alkyl, C 1 -C 8 alkoxy or -C (= O) -OT 21 May be substituted with 1, 2, or 3 groups selected from the group wherein T 21 is C 1 -C 18 alkyl and more preferably T 21 is a phenyl, 4-methoxyphenyl or phenylaminocarbonyl group }to be].
    [84] Mention may also be made of cinnamic dimers, such as those disclosed in patent US 5 888 481, for example compounds having the structure:
    [85]
    [86] Among the insoluble organic blockers of the benzazole type, mention may be made of one of the following formulas:
    [87]
    [88]
    [89]
    [90] {Wherein each X symbol independently represents an oxygen or sulfur atom, or an NR 2 group,
    [91] Each Z symbol independently represents a nitrogen atom or a CH group,
    [92] Each R 1 symbol independently represents a linear or branched C 1-8 alkyl group optionally containing an OH group, a halogen atom, a silicon atom, or a linear or branched C 1-8 alkoxy group,
    [93] Each number m is independently 0, 1 or 2,
    [94] n represents an integer of 1 to 4,
    [95] p is 0 or 1,
    [96] Each number q is independently 0 or 1,
    [97] Each R 2 symbol independently represents a benzyl or linear or branched C 1-8 alkyl group optionally containing a hydrogen atom or a silicon atom,
    [98] A represents a radical having valence n, selected from one of the formulas:
    [99]
    [100] (Wherein W represents N or CH; each R 3 symbol independently represents a halogen atom or a linear or branched C 1-4 alkyl or alkoxy group or a hydroxyl group, R 4 is a hydrogen atom, or Linear or branched C 1-4 alkyl group, c = 0 to 4, d = 0 to 3, e = 0 or 1, and f = 0 to 2)}.
    [101] These compounds are described in particular in patent DE 676 103 and CH 350 763, patent US 5 501 850, patent US 5 961 960, patent application EP 0 669 323, patent US 5 518 713, patent US 2 463 264, [J. Am. Chem. Soc., 79, 5706-5708, 1957, [J. Am. Chem. Soc., 82, 609-611, 1960, patent application EP 0 921 126 and patent application EP 712 855.
    [102] Examples of preferred compounds of formula (7) that are 2-arylbenzazoles include 2- (benzoxazol-2-yl) -4-methylphenol, 2- (1H-benzimidazol-2-yl) -4-methoxyphenol Or 2- (benzothiazol-2-yl) phenol, and these compounds may be prepared, for example, according to the process disclosed in patent CH 350 763.
    [103] Examples of preferred compounds of formula (7) which are benzimidazolylbenzazoles include 2,2'-bisbenzimidazole, 5,5 ', 6,6'-tetramethyl-2,2'-bisbenzimidazole, 5 , 5'-dimethyl-2,2'-bisbenzimidazole, 6-methoxy-2,2'-bisbenzimidazole, 2- (1H-benzimidazol-2-yl) benzothiazole, 2- (1H-benzimidazol-2-yl) benzoxazole and N, N'-dimethyl-2,2'-bisbenzimidazole will be mentioned and these compounds are disclosed in patents US 5 961 960 and US 2 463 264. Can be prepared according to the procedure.
    [104] Examples of preferred compounds of formula (7) which are phenylenebenzazoles include 1,4-phenylene bis (2-benzoxazolyl), 1,4-phenylenebis (2-benzimidazolyl), 1,3-phenyl Lenbis (2-benzoxazolyl), 1,2-phenylenebis (2-benzoxazolyl), 1,2-phenylenebis (benzimidazolyl), 1,4-phenylenebis (N- ( 2-ethylhexyl) -2-benzimidazolyl) and 1,4-phenylenebis (N-trimethylsilylmethyl-2-benzimidazolyl) will be mentioned and these compounds are described in US Pat. No. 2,463,264, and Publications [J. Am. Chem. Soc., 82, 609 (1960)] and [J. Am. Chem. Soc., 79, 5706-5708 (1957).
    [105] Examples of preferred compounds of formula (7) which are benzofuranyl benzoxazoles include 2- (2-benzofuranyl) benzoxazole, 2- (benzofuranyl) -5-methylbenzoxazole and 2- (3-methyl-2- Benzofuranyl) benzoxazoles will be mentioned and these compounds can be prepared according to the procedures disclosed in patent US Pat. No. 5,518,713.
    [106] Preferred compounds of formula (8) include, for example, 2,6-diphenyl-1,7-dihydrobenzo [1,2-d; 4,5-d '] diimidazole, corresponding to the formula:
    [107]
    [108] Or 2,6-distyryl-1,7-dihydrobenzo [1,2-d; 4,5-d '] diimidazole or 2,6-di (p-tert-butylstyryl) -1, Mention may be made of 7-dihydrobenzo [1,2-d; 4,5-d '] diimidazole and these compounds may be prepared according to application EP 0 669 323.
    [109] As preferred compounds of the formula (9), mention may be made of 5,5'-bis (2-phenylbenzimidazole) of the formula: Chim. Phys., 64, 1602 (1967).
    [110]
    [111] Among the above insoluble organic compounds that block UV radiation, very preferred are 2- (1H-benzimidazol-2-yl) benzoxazole, 6-methoxy-2,2'-bisbenzimidazole, 2- (1H-benzimidazol-2-yl) benzothiazole, 1,4-phenylenebis (2-benzoxazolyl), 1,4-phenylenebis (2-benzimidazolyl), 1, 3-phenylenebis (2-benzoxazolyl), 1,2-phenylenebis (2-benzoxazolyl), 1,2-phenylenebis (2-benzimidazolyl) and 1,4-phenylene Bis (N-trimethylsilylmethyl-2-benzimidazolyl) is given.
    [112] Among the insoluble organic blockers of the aryl vinylene ketone type, those corresponding to any one of the following Formulas 10 and 11 may be mentioned:
    [113]
    [114]
    [115] {Of the formulas,
    [116] n '= 1 or 2,
    [117] In formula (10) when n '= 1, or in formula (11), B is an aryl radical selected from formulas (a') to (d '), or in formula 10 when n' = 2, and a radical selected from (e ') to (h'):
    [118]
    [119] (In the meal,
    [120] Each R 8 symbol is independently an OH group, a halogen atom, a linear or branched C 1-6 alkyl group optionally containing a silicon atom, a linear or branched C 1-6 alkoxy group optionally containing a silicon atom, a linear or branched A topographic C 1-5 alkoxycarbonyl group or a linear or branched C 1-6 alkylsulfonamide group optionally containing a silicon atom or an amino acid functional group,
    [121] p 'represents an integer of 0 to 4,
    [122] q 'represents 0 or 1),
    [123] R 5 represents hydrogen or an OH group,
    [124] R 6 represents a linear or branched C 1-6 alkyl group, cyano group, C 1-6 alkylsulfonyl group or phenylsulfonyl group optionally containing hydrogen, a silicon atom,
    [125] R 7 represents a linear or branched C 1-6 alkyl group optionally comprising a phenyl group or a silicon atom capable of forming a bicyclic ring, optionally substituted by one or two R 4 radicals,
    [126] Or R 6 and R 7 together are optionally interrupted by one or more nitrogen, sulfur and oxygen atoms, may comprise another carbonyl, optionally substituted by a linear or branched C 1 -C 8 alkylsulfonamide group, Forms monocyclic, bicyclic or tricyclic C 2-10 hydrocarbonaceous residues, optionally comprising silicon atoms or amino acid functional groups; Provided that when n '= 1, R 6 and R 7 do not form a camphor nucleus.
    [127] As examples of compounds of formula 10, wherein n '= 1 and insoluble, block UV radiation and have an average particle size of 10 nm to 5 μm, the following classes may be mentioned:
    [128] Compounds of the styryl ketone type as disclosed in the application JP 04 134 042, for example 1- (3,4-dimethoxyphenyl) -4,4-dimethylpent-1-en-3-one:
    [129]
    [130] Compounds of the benzylidenecineol type, such as those described in the paper by E. Mariani et al. At the 16th IFSCC Society (New York (1990)), for example 1,3,3-trimethyl-5- (4-methoxy Benzylidene) -2-oxabicyclo [2.2.2] octan-6-one:
    [131]
    [132] Compounds of the benzylidenechromanone type, such as those disclosed in application JP 04 134 043, for example 3- (4-methoxybenzylidene) -2,3,4a, 8a-tetrahydrochromen-4-one:
    [133]
    [134] Compounds of the benzylidenethiochromemanone type, such as those disclosed in the application JP 04 134 043, for example 3- (4-methoxybenzylidene) -2,3,4a, 8a-tetrahydrochromen-4-thione:
    [135]
    [136] Compounds of the benzylidenequinuclidinone type, such as those disclosed in application EP 0 576 974, for example 4-methoxybenzylidene-1-azabicyclo [2.2.2] octan-3-one:
    [137]
    [138] Compounds of the benzylidenecycloalkanone type, such as those disclosed in the application FR 2 395 023, for example 2- (4-methoxybenzylidene) cyclopentanone and 2- (4-methoxybenzylidene) cyclohexanone :
    [139]
    [140] Compounds of the benzylidene hydantoin type, such as those disclosed in the application JP 01 158 090, for example 5- (3,4-dimethoxybenzylidene) imidazolidine-2,4-dione:
    [141]
    [142] Compounds of the benzylidene indanone type, such as those disclosed in the application JP 04 134 043, for example 2- (4-methoxybenzylidene) indan-1-one:
    [143]
    [144] Compounds of the benzylidene tetraralone type, such as those disclosed in the application JP 04 134 043, for example 2- (4-methoxybenzylidene) -3,4-dihydro-2H-naphthalen-1-one:
    [145]
    [146] Compounds of the benzylidenefuranone type, such as those disclosed in application EP 0 390 683, for example 4- (4-methoxybenzylidene) -2,2,5,5-tetramethyldihydrofuran-3-one:
    [147]
    [148] Compounds of the benzylidenebenzofuranone type, such as those disclosed in the application JP 04 134 041, for example 2-benzylidenebenzofuran-3-one:
    [149]
    [150] Compounds of the benzylidene indandione type, such as 2- (3,5-di (tert-butyl) -4-hydroxybenzylidene) indane-1,3-dione:
    [151]
    [152] Compounds of the benzylidenebenzothiofuranone type, such as those disclosed in the application JP 04 134 043, for example 2-benzylidenebenzo [b] thiophen-3-one:
    [153]
    [154] Compounds of the benzylidenebarbituric acid type, such as 5- (4-methoxybenzylidene) -1,3-dimethylpyrimidine-2,4,6-trione:
    [155]
    [156] Compounds of the benzylidenepyrazolone type, such as 4- (4-methoxybenzylidene) -5-methyl-2-phenyl-2,4-dihydropyrazol-3-one:
    [157]
    [158] Compounds of the benzylideneimidazolone type, such as 5- (4-methoxybenzylidene) -2-phenyl-3,5-dihydroimidazol-4-one:
    [159]
    [160] Chalcone type compounds, such as 1- (2-hydroxy-4-methoxyphenyl) -3-phenylpropenone:
    [161]
    [162] Benzylidene-one compounds as disclosed in document FR 2 506 156, for example 3-hydroxy-1- (2-hydroxy-4-methoxyphenyl) -3-phenylpropenone:
    [163]
    [164] As examples of compounds of the formula (10), in which n '= 2, insoluble, blocking UV radiation and having an average particle size of 10 nm to 5 μm, the following classes may be mentioned:
    [165] Compounds of the phenylenebis (methylidenenorcamphor) type as disclosed in document EP 0 693 471, for example 1,4-phenylenebis {3-methylidenebicyclo [2.2.1] heptan-2- On}:
    [166]
    [167] Compounds of the phenylenebis (methylidenecamphor) type as disclosed in document FR 2 528 420, for example 1,4-phenylenebis {3-methylidene-1,7,7-trimethyl bicyclo [2.2 .1] heptan-2-one}:
    [168]
    [169] Or 1,3-phenylenebis {3-methylidene-1,7,7-trimethylbicyclo [2.2.1] heptan-2-one}:
    [170]
    [171] Compounds of the phenylenebis (methylidenecamphorsulfonamide) type, such as those disclosed in document FR 2 529 887, for example 1,4-phenylenebis {3,3'-methylidenecamphor-10,10 '-Ethylsulfonamide or-(2-ethylhexyl) sulfonamide}:
    [172]
    [173] or
    [174]
    [175] Compounds of the phenylenebis (methylidenecineol) type as described in the paper of E. Mariani et al. In the 16th IFSCC Society (New York (1990)), for example 1,4-phenylenebis {5- Methylidene-3,3-dimethyl-2-oxabicyclo [2.2.2] octane-6-one}:
    [176]
    [177] Compounds of the phenylenebis (methylideneketotricyclodecane) type as disclosed in the application EP 0 694 521, such as 1,4-phenylenebis (octahydro-4,7-methano-6-indene-5- On):
    [178]
    [179] Compounds of the phenylenebis (alkylene ketone) type, such as those disclosed in the application JP 04 134 041, for example 1,4-phenylenebis (4,4-dimethylpent-1-en-3-one):
    [180]
    [181] Compounds of the phenylenebis (methylidenefuranone) type as disclosed in the application FR 2 638 354, for example 1,4-phenylenebis (4-methylidene-2,2,5,5-tetramethyldi Hydrofuran-3-one):
    [182]
    [183] Compounds of the phenylenebis (methylidenequinuclidinone) type, such as those disclosed in application EP 0 714 880, for example 1,4-phenylenebis {2-methylidene-1-aza bicyclo [2.2.2 ] Octan-3-one}:
    [184]
    [185] As the compound of formula 11, the following classes may be mentioned:
    [186] Compounds of the bis (benzylidene) cycloalkanone type, such as 2,5-di (benzylidene) cyclopentanone:
    [187]
    [188] Compounds of the γ-pyron type as disclosed in document JP 04 290 882, for example 2,6-bis (3,4-dimethoxyphenyl) pyran-4-one:
    [189]
    [190] Of the above insoluble organic compounds which block UV radiation, which are of the aryl vinylene ketone type, preference is given to compounds of the formula (10) in which very particularly n '= 2.
    [191] Among the insoluble organic blockers of the phenylenebis (benzoxazinone) type, those corresponding to the following formula (12) may be mentioned:
    [192]
    [193] Wherein R represents a divalent aromatic moiety selected from the following formulas (e ") to (h"):
    [194]
    [195] (Of the formulas,
    [196] Each R 9 symbol is independently a linear or branched C 1-6 alkyl group optionally containing an OH group, a halogen atom, a silicon atom, a linear or branched C 1-6 alkoxy group optionally comprising a silicon atom, a linear or A branched C 1-5 alkoxycarbonyl group or a linear or branched C 1-6 alkylsulfonamide group optionally containing a silicon atom or an amino acid functional group,
    [197] p "represents an integer of 0-4,
    [198] q "represents 0 or 1)}.
    [199] As examples of compounds of formula 12, which are insoluble, block UV radiation and have an average particle size of 10 nm to 5 μm, mention may be made of the following derivatives:
    [200] 2,2'-p-phenylenebis (3,1-benzoxazine-4-one), commercially available Cyasorb UV-3638 (manufactured by Cytec),
    [201] 2,2 '-(4,4'-biphenylene) bis (3,1-benzoxazin-4-one),
    [202] 2,2 '-(2,6-naphthylene) bis (3,1-benzoxazin-4-one).
    [203] Among the insoluble organic blockers of the acrylonitrile amide, sulfonamide or carbamate derivative type, those corresponding to the following formula (13) may be mentioned:
    [204]
    [205] (In the meal,
    [206] R 10 represents a linear or branched C 1-8 alkyl group,
    [207] n '' 'has a value of 0, 1 or 2,
    [208] X 2 is of the formula — (C═O) —R 11 — (C═O) —, —SO 2 —R 11 —SO 2 — or — (C═O) —OR 11 —O— (C═O) — Represents a divalent radical,
    [209] Y represents a-(C = 0) -R 12 or -SO 2 R 13 radical,
    [210] R 11 represents a single bond or may carry one or more hydroxyl substituents and may contain one or more heteroatoms selected from oxygen, nitrogen and silicon atoms in the carbonaceous chain, linear or branched divalent C 1- A C 30 alkylene or C 3 -C 30 alkenylene radical,
    [211] R 12 represents a -OR 14 or -NHR 14 radical,
    [212] R 13 represents a phenyl ring or a linear or branched C 1 -C 30 alkyl radical, optionally substituted with a C 1 -C 4 alkyl or alkoxy radical,
    [213] R 14 may carry one or more hydroxyl substituents and may comprise one or more heteroatoms selected from oxygen, nitrogen and silicon atoms in the carbonaceous chain, linear or branched C 1 -C 30 alkyl or C 3 -C 30 Alkenyl radicals).
    [214] Although only those isomers in which the cyano substituent is at the cis position relative to the para-aminophenyl substituent are represented in Formula 13, the above formula also includes the corresponding trans isomers; It is to be understood that for each of the two double bonds, and independently, the cyano and para-aminophenyl substituents may be cis or trans spaced relative to each other.
    [215] By way of example, mention may be made of dimers of 2-ethylhexyl 2-cyano-3- [4- (acetylamino) phenyl] acrylate of the formula:
    [216]
    [217] Another specific class of insoluble organic blockers according to the invention is the polyvalent metal salts of sulfone or carboxyl organic blockers (e.g., Ca 2+ , Zn 2+ , Mg 2+ , Ba 2+ , Al 3+). Or Zr 4+ ), for example polyvalent metal salts of sulfonated derivatives of benzylidene camphor, such as those disclosed in application FR-A 2 639 347; Polyvalent metal salts of sulfonated derivatives of benzimidazoles, such as those disclosed in application EP-A-893 119; Or polyvalent metal salts of cinnamic acid derivatives, such as those disclosed in application JP-87 166 517.
    [218] Mention may also be made of metals or ammonium or substituted ammonium complexes of UV-A and / or UV-B organic blockers as disclosed in the patent applications WO 93/10753, WO 93/11095 and WO 95/05150.
    [219] The insoluble UV blockers or blockers of the present invention are present at a total concentration of preferably about 1 to 10% by weight, more particularly 2 to 8% by weight relative to the total weight of the composition.
    [220] The amino substituted 2-hydroxybenzophenone derivatives according to the invention correspond to formula (14):
    [221]
    [222] (In the meal,
    [223] R 1 and R 2 are the same or different and represent a hydrogen atom, a C 1 -C 20 alkyl radical, a C 2 -C 10 alkenyl radical, a C 3 -C 10 cycloalkyl radical or a C 3 -C 10 cycloalkenyl radical Represent;
    [224] R 1 and R 2 may also form a 5 or 6 membered ring with the nitrogen atom bonded thereto;
    [225] R 3 and R 4 are the same or different and are C 1 -C 20 alkyl radicals, C 2 -C 10 alkenyl radicals, C 3 -C 10 cycloalkyl radicals, C 3 -C 10 cycloalkenyl radicals, C 1- C 12 alkoxy radical, (C 1 -C 20 ) alkoxycarbonyl radical, C 1 -C 12 alkylamino radical, di (C 1 -C 12 ) alkylamino radical, optionally substituted aryl radical or heteroaryl, or carboxyl A water-soluble substituent selected from a late group, a sulfonate group or an ammonium residue;
    [226] X represents a hydrogen atom or a COOR 5 or CONR 6 R 7 group;
    [227] R 5 , R 6 and R 7 are the same or different and represent a hydrogen atom, a C 1 -C 20 alkyl radical, a C 2 -C 10 alkenyl radical, a C 3 -C 10 cycloalkyl radical, a C 3 -C 10 cycloal A kenyl radical, a-(YO) o -Z group or an aryl group;
    [228] Y represents — (CH 2 ) 2 —, — (CH 2 ) 3 —, — (CH 2 ) 4 — or —CH— (CH 3 ) —CH 2 —;
    [229] Z represents -CH 2 -CH 3 , -CH 2 CH 2 CH 3 , -CH 2 CH 2 CH 2 CH 3 , or -CH (CH 3 ) -CH 3 ;
    [230] m is an integer from 0 to 3;
    [231] n is an integer from 0 to 3;
    [232] o is an integer from 1 to 2).
    [233] As C 1 -C 20 alkyl radicals, for example, mention may be made of: methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1- Dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1,1-dimethylpropyl, 1,2-dimethyl Propyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl, 1-ethyl-2-methylpropyl , n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-hepta Decyl, n-octadecyl, n-nonadecyl or n-icosyl.
    [234] As the C 2 -C 10 alkenyl group, for example, mention may be made of: vinyl, n-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 1-pentenyl, 2-pentenyl, 2-methyl-1-butenyl, 2-methyl-2-butenyl, 3-methyl-1-butenyl, 1-hexenyl, 2-hexenyl, 1-heptenyl, 2-heptenyl, 1-jade Tenyl or 2-octenyl.
    [235] As the C 1 -C 12 alkoxy radical, mention may be made of: methoxy, ethoxy, n-propoxy, n-butoxy, n-pentoxy, 1-methylpropoxy, 3-methylbutoxy, 2 , 2-dimethylpropoxy, 1-methyl-1-ethylpropoxy, octoxy, 2-methylpropoxy, 1,1-dimethylpropoxy, hexoxy, heptoxy or 2-ethylhexoxy.
    [236] As the C 3 -C 10 cycloalkyl radical, for example, the following may be mentioned: cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, 1-methylcyclopropyl, 2-ethylcyclopropyl, 1-propyl Cyclopropyl, 1-butylcyclopropyl, 1-pentylcyclopropyl, 1-methyl-1-butylcyclopropyl, 1,2-dimethylcyclopropyl, 1-methyl-2-ethylcyclopropyl, cyclooctyl, cyclononyl or cyclo Decyl.
    [237] As C 3 -C 10 cycloalkenyl radicals having one or more double bonds, the following may be mentioned: cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclopentadienyl, cyclohexenyl, 1,3-cyclo Hexadienyl, 1,4-cyclohexadienyl, cycloheptenyl, cycloheptatrienyl, cyclooctenyl, 1,5-cyclooctadienyl, cyclooctatetraenyl, cyclononenyl or cyclodecenyl.
    [238] Cycloalkyl or cycloalkenyl radicals may include, for example, one or more substituents (preferably 1 to 3) selected from: halogen, such as chlorine, fluorine or bromine; Cyano; Nitro; Amino; C 1 -C 4 alkylamino; Di (C 1 -C 4 ) alkylamino; C 1 -C 4 alkyl; C 1 -C 4 alkoxy; Or hydroxyl. They may also include one to three heteroatoms, such as sulfur, oxygen or nitrogen, whose free valences may be filled by hydrogen or C 1 -C 4 alkyl radicals.
    [239] The aryl group is preferably selected from phenyl or naphthyl rings, which may contain, for example, one or more substituents (preferably 1 to 3) selected from: halogens such as chlorine, fluorine or bromine; Cyano; Nitro; Amino; C 1 -C 4 alkylamino; Di (C 1 -C 4 ) alkylamino; C 1 -C 4 alkyl; C 1 -C 4 alkoxy; Or hydroxyl. More particularly, phenyl, methoxyphenyl and naphthyl are preferred.
    [240] Heteroaryl groups typically include one or more hetero atoms selected from sulfur, oxygen or nitrogen.
    [241] Water-soluble groups are, for example, carboxylate or sulfonate groups, more particularly physiologically acceptable cations and salts thereof, such as alkali metal salts or trialkylammonium salts such as tri (hydroxyalkyl) ammonium or 2 -Methylpropan-1-ol-2-ammonium salt. Mention may also be made of ammonium groups such as alkylammonium, and physiologically acceptable anions and their chlorinated forms.
    [242] As examples of 5- or 6-membered rings formed by R 1 and R 2 radicals and nitrogen atoms, mention may in particular be made of pyrrolidine or piperidine.
    [243] The amino group may be attached to the benzene ring in the ortho, meta or para position, more preferably in the para position relative to the carbonyl radical.
    [244] Preferred classes of compounds of formula 14 include those selected from those of formula 14a:
    [245]
    [246] (In the meal,
    [247] R 1 and R 2 are the same or different and represent a hydrogen atom or a C 1 -C 12 alkyl radical or form a 5 or 6 membered ring with the nitrogen atom bonded thereto;
    [248] X represents COOR 5 or CONR 6 R 7 ;
    [249] R 5 represents a hydrogen atom, a C 1 -C 12 alkyl radical or a C 3 -C 6 cycloalkyl radical;
    [250] R 6 and R 7 are the same or different and represent a hydrogen atom, a C 1 -C 12 alkyl radical or a C 5 -C 6 cycloalkyl radical).
    [251] More particularly preferred compounds of formula 14a are those wherein R 1 and R 2 are the same or different and represent a C 1 -C 4 alkyl radical, more particularly ethyl; R 5 represents a C 3 -C 8 alkyl radical; R 6 and R 7 are the same or different and represent C 1 -C 8 alkyl radicals.
    [252] Other preferred compounds of formula 14 include those selected from those of formula 14b:
    [253]
    [254] (In the meal,
    [255] R 1 and R 2 are the same or different and represent a C 1 -C 12 alkyl radical or form a 5 or 6 membered ring with the nitrogen atom bonded thereto).
    [256] Among the compounds of the formula (14b), more particularly the following may be mentioned:
    [257] 4-diethylamino-2-hydroxyphenyl phenyl ketone,
    [258] 4-pyrrolidino-2-hydroxyphenyl phenyl ketone.
    [259] More particularly preferred classes of compounds of formula 14 include those selected from those of formula 14c:
    [260]
    [261] (In the meal,
    [262] R 1 and R 2 are the same or different and represent a hydrogen atom or a C 1 -C 8 alkyl radical or form a 5 or 6 membered ring with the nitrogen atom bonded thereto;
    [263] R 5 represents a hydrogen atom, a C 1 -C 12 alkyl radical or a C 3 -C 6 cycloalkyl radical).
    [264] Among the compounds of formula 14c, mention may be made of:
    [265] 2- (4-pyrrolidino-2-hydroxybenzoyl) benzoate,
    [266] Methyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate,
    [267] 2-ethylhexyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate,
    [268] Cyclohexyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate,
    [269] n-hexyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate,
    [270] [lacuna] 2- (4-dibutylamino-2-hydroxybenzoyl) benzoate,
    [271] Methyl 2- (4-dibutylamino-2-hydroxybenzoyl) benzoate,
    [272] Isobutyl 2- (4-dibutylamino-2-hydroxybenzoyl) benzoate.
    [273] Very particularly preferred compound of formula 14 is n-hexyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate.
    [274] The compounds of formula 14 as defined above are known per se and their structures and their synthesis are described in patent applications EP-A-1 046 391 and DE 100 12 408 (which form an integral part of the description). Is disclosed.
    [275] The amino substituted 2-hydroxybenzophenone derivatives according to the invention are preferably 0.1 to 20% by weight, more preferably 0.1 to 15% by weight, more particularly 0.5 to 10, based on the total weight of the composition in the composition of the invention. It is present in ratios in the range by weight.
    [276] The composition according to the invention may also contain other additional water soluble or fat soluble organic UV blockers (absorbers) active in the UV-A and / or UV-B regions.
    [277] The additional organic UV blocker is in particular anthranilate; Cinnamic acid derivatives; Salicylic acid derivatives; Camphor derivatives other than the above formula; Triazine derivatives such as those disclosed in patent applications US 4 367 390, EP 863 145, EP 517 104, EP 570 838, EP 796 851, EP 775 698, EP 878 469 and EP 933 376; Benzophenone derivatives other than those of Formula 14; β, β-diphenylacrylate derivatives; Benzotriazole derivatives; Benzalmalonate derivatives; Benzimidazole derivatives; Imidazoline; Bisbenzoazolyl derivatives disclosed in patents EP 669 323 and US 2 463 264; p-aminobenzoic acid (PABA) derivatives; Methylenebis (hydroxyphenylbenzotriazole) derivatives disclosed in the applications US 5 237 071, US 5 166 355, GB 2 303 549, DE 197 26 184 and EP 893 119; Blocking polymers and blocking silicones such as those disclosed in particular in WO 93/04665; dimers derived from α-alkylstyrene, such as those disclosed in patent application DE 198 55 649; And 4,4-diarylbutadiene disclosed in applications EP 0 967 200, DE 197 46 654, DE 197 55 649, and EP-A-1 008 586.
    [278] As examples of additional organic blockers active in the UV-A and / or UV-B region, those indicated by the INCI name may be mentioned below:
    [279] Para-aminobenzoic acid derivatives:
    [280] -PABA,
    [281] Ethyl PABA,
    [282] Ethyl dihydroxypropyl PABA,
    [283] Ethylhexyl dimethyl PABA, especially those sold under the trade name "Escalol 507" by the ISP,
    [284] Glyceryl PABA,
    [285] PEG-25 PABA sold under the trade name "Uvinul P25" by BASF,
    [286] Salicylic Acid Derivatives:
    [287] Homosalates sold under the trade name "Eusolex HMS" by Rona / EM Industries,
    [288] Ethylhexyl salicylate sold by Haarmann and Reimer under the trade name "Neo Heliopan OS",
    [289] Dipropylene glycol salicylate sold by Scher under the trade name "Dipsal",
    [290] TEA salicylate sold by Haarmann and Reimer under the trade name "Neo Heliopan TS",
    [291] Dibenzoylmethane Derivatives:
    [292] Butyl methoxydibenzoylmethane, especially those sold under the trade name "Parsol 1789" by Hoffmann-LaRoche,
    [293] Isopropyl dibenzoylmethane,
    [294] Cinnamic acid derivatives:
    [295] Ethylhexyl methoxycinnamate, especially those sold under the trade name "Parsol MCX" by Hoffmann-LaRoche,
    [296] Isopropyl methoxy cinnamate,
    [297] Isoamyl methoxy cinnamate sold under the trade name "Neo Heliopan E 1000" by Haarmann and Reimer,
    [298] -Synoxate,
    [299] DEA methoxycinnamate,
    [300] Diisopropyl methylcinnamate,
    [301] Glyceryl ethylhexanoate dimethoxycinnamate,
    [302] β, β-diphenylacrylate derivatives:
    [303] Octocrylene, especially those sold under the trade name "Uvinul N539" by BASF,
    [304] Etocrylene, especially those sold under the trade name "Uvinul N35" by BASF,
    [305] Benzophenone Derivatives:
    [306] Benzophenone-1 sold under the trade name "Uvinul 400" by BASF,
    [307] Benzophenone-2 sold under the trade name "Uvinul D50" by BASF,
    [308] Benzophenone-3 or oxybenzone, sold under the trade name "Uvinul M40" by BASF,
    [309] Benzophenone-4 sold under the trade name "Uvinul MS4O" by BASF,
    [310] Benzophenone-5,
    [311] Benzophenone-6 sold under the trade name "Helisorb 11" by Norquay,
    [312] Benzophenone-8 sold under the trade name "Spectra-Sorb UV-24" by American Cyanamid,
    [313] Benzophenone-9 sold by BASF under the trade name "Uvinul DS-49",
    [314] Benzophenone-12,
    [315] Benzylidene Camphor Derivatives:
    [316] 3-benzylidene camphor made by Chimex under the trade name "Mexoryl SD",
    [317] 4-methylbenzylidene camphor sold under the trade name "Eusolex 6300" by Merck,
    [318] Benzylidene camphor sulfonic acid manufactured by Chimex under the trade name "Mexoryl SL",
    [319] Camphor benzalkonium methosulfate, manufactured under Chimex under the trade name "Mexoryl SO",
    [320] Polyacrylamidomethyl benzylidene camphor made by Chimex under the trade name "Mexoryl SW",
    [321] Phenylbenzimidazole Derivatives:
    [322] Phenylbenzimidazole sulfonic acid, especially those sold under the trade name "Eusolex 232" by Merck,
    [323] Disodium phenyl dibenzimidazole tetrasulfonate sold under the trade name "Neo Heliopan AP" by Haarmann and Reimer,
    [324] Triazine Derivatives:
    [325] -Anisotriazine sold under the trade name "Tinosorb S" by Ciba Specialty Chemicals,
    [326] Ethylhexyl triazone, especially those sold under the trade name "Uvinul T150" by BASF,
    [327] Diethylhexyl butamido triazone sold under the name "Uvasorb HEB" by Sigma 3V,
    [328] 2,4,6-tris (diisobutyl 4'-aminobenzalmalonate) -s-triazine,
    [329] Phenylbenzotriazole Derivatives:
    [330] -Drometrizol trisiloxane sold under the trade name "Silatrizole" by Rhodia Chimie,
    [331] Methylenebis (benzotriazolyltetramethylbutylphenol), commercially available under the trade name "Mixxim BB / 100" under Fairmount Chemical as a micronized form in an aqueous dispersion under the trade name "Tinosorb M" under Ciba Specialty Chemicals,
    [332] Anthranilic acid derivatives:
    [333] Menthyl anthranilate, sold under the trade name "Neo Heliopan MA" by Haarmann and Reimer,
    [334] Imidazoline Derivatives:
    [335] Ethylhexyl dimethoxybenzylidene dioxoimidazoline propionate,
    [336] Benzalmalonate Derivatives:
    [337] Polyorganosiloxanes comprising benzalmalonate functionality, marketed under the trade name "Parsol SLX" by Hoffmann-LaRoche,
    [338] 4,4-diarylbutadiene derivatives:
    [339] 1,1-dicarboxy (2,2'-dimethyl-propyl) -4,4-diphenylbutadiene,
    [340] And mixtures thereof.
    [341] More particularly preferred soluble organic UV blockers are selected from the following compounds:
    [342] Ethylhexyl salicylate,
    [343] -Octocrylene,
    [344] Ethylhexyl methoxycinnamate,
    [345] Butyl methoxydibenzoylmethane,
    [346] Phenylbenzimidazole sulfonic acid,
    [347] Benzophenone-3,
    [348] Benzophenone-4,
    [349] Benzophenone-5,
    [350] 4-methylbenzylidene camphor,
    [351] Disodium phenyl dibenzimidazole tetrasulfonate,
    [352] -Anisotriazine,
    [353] Ethylhexyl triazone,
    [354] Diethylhexyl butamido triazone,
    [355] 2,4,6-tris (diisobutyl 4'-aminobenzalmalonate) -s-triazine,
    [356] -Drometrizol trisiloxane,
    [357] Methylenebis (benzotriazolyltetramethylbutylphenol),
    [358] 1,1-dicarboxy (2,2'-dimethylpropyl) -4,4-diphenylbutadiene,
    [359] And mixtures thereof.
    [360] The cosmetic composition according to the invention also comprises a pigment, or alternatively a nanopigment formed from a coated or uncoated metal oxide (average size of primary particles: typically 5 nm to 100 nm, preferably 10 nm to 50 nm). For example, they may contain nanopigments formed from titanium oxide, iron oxide, zinc oxide, zirconium oxide or cerium oxide (which are amorphous or crystallized in rutile and / or anatase form), all of which are UV known per se. It is a photoprotectant. Common coatings are also alumina and / or aluminum stearate. Such coated and uncoated metal oxide nanopigments are described in particular in patent applications EP-A-0 518 772 and EP-A-0 518 773.
    [361] The composition according to the invention may also contain artificial tanning agents and / or browning agents (self-tanning agents) of the skin, for example dihydroxyacetone (DHA).
    [362] The compositions of the present invention may further contain customary cosmetic auxiliaries, in particular selected from: fatty substances, organic solvents, ionic or nonionic thickeners, softeners, antioxidants, free radical breakers, opacifiers, stabilizers , Emollients, silicones, α-hydroxy acids, antifoams, humectants, vitamins, insect repellents, fragrances, preservatives, surfactants, anti-inflammatory agents, P substance antagonists, fillers, polymers, propellants, basic or acidifying agents, colorants, Or any other component commonly used in the manufacture of cosmetics, in particular in sunscreen compositions in the form of emulsions.
    [363] Fatty substances may consist of oils or waxes, or mixtures thereof. The term "oil" is understood to mean a compound that is liquid at ambient temperature. The term "wax" is understood to mean a compound that is solid or substantially solid at ambient temperature and whose melting point is typically above 35 ° C. They also include derivatives of fatty acids, fatty alcohols and fatty acid esters, such as benzoic acid, trimellitic acid and hydroxybenzoic acid, linear or cyclic.
    [364] As oils, mention may be made of: mineral oils (liquid paraffin); Vegetable oils (sweet almonds, macadamia, currant or jojoba oil); Synthetic oils such as perhydrosqualene, fatty alcohols, acids or esters (e.g. C 12 -C 15 alkyl benzoates sold under the trade name "Finsolv TN" by Finetex, including those of capric acid / caprylic acid, Octyl palmitate, isopropyl ranolate or triglycerides), or oxyethylenated or oxypropyleneated fatty esters and ethers; Silicone oils (cyclomethicone, polydimethylsiloxane or PDMS); Fluorinated oils; Or polyalkylene.
    [365] As the waxy compound, mention may be made of paraffin wax, carnauba wax, beeswax or hydrogenated castor oil.
    [366] Among the organic solvents, lower alcohols and polyols may be mentioned.
    [367] Of course, those skilled in the art will appreciate that the advantageous properties added inherently to the composition according to the invention, in particular the synergistic effect thereof, are such that the additional compound and And / or choose their quantity carefully.
    [368] The compositions of the present invention can be prepared according to techniques known to those skilled in the art, in particular for the purpose of preparing oil-in-water or water-in-oil emulsions.
    [369] The compositions are provided in particular in the form of simple or complex emulsions (O / W, W / O, O / W / O or W / O / W), such as creams, milks, gels or cream gels, powders or solid tubes May be optionally packaged as an aerosol and provided in the form of a foam or spray.
    [370] If the emulsion is the issue, the latter aqueous phase may comprise a nonionic vesicular dispersion prepared according to known methods (Bangham, Standish and Watkins, J. Mol. Biol., 13, 238 (1965), FR 2 315 991 and FR 2 416 008).
    [371] The cosmetic composition of the present invention can be used as a composition, sunscreen composition or makeup product for protecting the human epidermis or hair against ultraviolet rays.
    [372] When the cosmetic composition according to the invention is used for the protection of the human epidermis against ultraviolet light or as a sunscreen composition, it is in the form of a suspension or dispersion in a solvent or fatty substance, in the form or emulsion of a nonionic vesicular dispersion, preferably in water It may be provided in the form of an emulsion, such as a cream or milk form, ointment, gel, cream gel, solid tube, powder, stick, aerosol foam or spray form.
    [373] When the cosmetic composition according to the invention is used for the protection of hair against ultraviolet rays, it may be provided in the form of a shampoo, lotion, gel, emulsion or nonionic vesicular dispersion, for example, before or after shampooing, dyeing or before or after bleaching. , Rinse-out compositions, styling or treatment lotions, or styling or treatment gels, blow-drying or hair setting lotions or gels applied before, during or after perm or hair straightening, Or it can comprise the composition for perming or straightening hair, hair dyeing, or discoloring.
    [374] Anhydrous or aqueous, paste or solid forms, when the composition is used as a cosmetic product for eyelashes, eyebrows or skin, such as epidermal treatment creams, foundations, lipstick tubes, eyeshadows, face powders, mascaras or eyeliners, Such as oil-in-water or water-in-oil emulsions, nonionic vesicular dispersions, or suspensions.
    [375] As an indication, for sunscreen formulations according to the invention which represent vehicles in oil-in-water emulsions, the aqueous phase (particularly including a hydrophilic blocker) is usually from 50 to 95% by weight, preferably relative to the total formulation. Represents 70 to 90% by weight, the oil phase (particularly comprising a lipophilic blocker) represents 5 to 50% by weight, preferably 10 to 30% by weight relative to the total formulation, and the (co) emulsifier (S) represents 0.5 to 20% by weight, preferably 2 to 10% by weight relative to the total formulation.
    [376] Specific but non-limiting examples illustrating the invention will now be provided.
    [377] Example
    [378] Example 1
    [379] 80/20 mixture of cetearyl alcohol and oxyethylenated (33 EO) cetearyl alcohol (Sinnowax AO, Henkel)7 g Glycerol Mono- and Distearate Mixtures (Cerasynt SD-V, ISP)2 g Cetyl alcohol1.5 g Polydimethylsiloxane (Dow Corning 200 Fluid, Dow Corning)1 g C 12 -C 15 alkyl benzoate (Witconol TN, Witco)10 g n-hexyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate2 g Glycerol10 g Methylenebis (benzotriazolyltetramethylbutylphenol) (Tinosorb M, Ciba)10 g PreservativeQuantity Demineralized waterSuitable quantity for 100 g
    [380] Example 2
    [381] Glycerol Mono / Distearate / Polyethylene Glycol (100 EO) Stearate Mixture (Arlacel 165 FL, ICI)2 g Stearyl Alcohol (Lanette 18, Henkel)1 g Palm oil stearic acid (Stearine TP, Stearinerie Dubois)2.5 g Polydimethylsiloxane (Dow Corning 200 Fluid, Dow Corning)0.5 g C 12 / C 15 alkyl benzoate (Witconol TN, Witco)15 g Triethanolamine0.5 g n-hexyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate2.5 g Glycerol5 g Hexadecyl phosphate, potassium salt (Amphisol K, Hoffmann-LaRoche)1 g Polyacrylic Acid (Synthalen K, 3V)0.3 g Hydroxypropyl methyl cellulose (Methocel F4M, Dow Chemical)0.1 g 2,2 '-(1,4-phenylene) bisbenzoxazole4 g TriethanolamineSuitable pH 7 PreservativeQuantity Demineralized waterSuitable quantity for 100 g
    [382] In the novel cosmetic compositions according to the invention, in particular for the photoprotection of skin and / or hair, the combination of the two blocking agents has a synergistic effect on a given sunscreen factor UV-A PPD .
    权利要求:
    Claims (69)
    [1" claim-type="Currently amended] A topical cosmetic or dermatological composition, such as skin, hair, or photoprotection of skin and hair, wherein the composition comprises the following in a cosmetically acceptable vehicle:
    (a) a first screening agent, at least one insoluble organic UV blocker having a particle size of 10 nm to 5 μm, and
    (b) at least one amino substituted 2-hydroxybenzophenone derivative of formula 14:
    [Formula 14]
    (In the meal,
    R 1 and R 2 are the same or different and represent a hydrogen atom, a C 1 -C 20 alkyl radical, a C 2 -C 10 alkenyl radical, a C 3 -C 10 cycloalkyl radical or a C 3 -C 10 cycloalkenyl radical Represent;
    R 1 and R 2 may also form a 5 or 6 membered ring with the nitrogen atom bonded thereto;
    R 3 and R 4 are the same or different and are C 1 -C 20 alkyl radicals, C 2 -C 10 alkenyl radicals, C 3 -C 10 cycloalkyl radicals, C 3 -C 10 cycloalkenyl radicals, C 1- C 12 alkoxy radical, (C 1 -C 20 ) alkoxycarbonyl radical, C 1 -C 12 alkylamino radical, di (C 1 -C 12 ) alkylamino radical, aryl radical which may be substituted or heteroaryl, or car A water soluble substituent selected from a carboxylate group, a sulfonate group or an ammonium moiety;
    X represents a hydrogen atom or a COOR 5 or CONR 6 R 7 group;
    R 5 , R 6 and R 7 are the same or different and represent a hydrogen atom, a C 1 -C 20 alkyl radical, a C 2 -C 10 alkenyl radical, a C 3 -C 10 cycloalkyl radical, a C 3 -C 10 cycloal A kenyl radical, a-(YO) o -Z group or an aryl group;
    Y represents — (CH 2 ) 2 —, — (CH 2 ) 3 —, — (CH 2 ) 4 — or —CH— (CH 3 ) —CH 2 —;
    Z represents -CH 2 -CH 3 , -CH 2 CH 2 CH 3 , -CH 2 CH 2 CH 2 CH 3 , or -CH (CH 3 ) -CH 3 ;
    m is an integer from 0 to 3;
    n is an integer from 0 to 3;
    o is an integer from 1 to 2).
    [2" claim-type="Currently amended] The composition of claim 1, wherein the first and second blockers are present in the composition at a rate that produces synergistic activity against a given sunscreen factor UV-A PPD .
    [3" claim-type="Currently amended] The composition according to claim 1 or 2, wherein the insoluble organic UV blocker or blockers are selected from organic UV blockers of the following types: oxalanilide type, triazine type, benzotriazole type; Vinyl amide type; Cinnamic amide; One or more benzazole, benzofuran or benzothiophene, or forms comprising benzazole and benzofuran or benzothiophene groups, or indole forms; Aryl vinylene ketone type; Phenylenebis (benzoxazinone) derivative type; Or acrylonitrile amide, sulfonamide or carbamate derivatives.
    [4" claim-type="Currently amended] The composition according to claim 3, wherein the oxalanilide type UV blocking agent is of the following general formula (1):
    [Formula 1]
    (Wherein T 1 , T ′ 1 , T 2 and T ′ 2 are the same or different and represent a hydrogen atom, a C 1 -C 8 alkyl radical or a C 1 -C 8 alkoxy radical).
    [5" claim-type="Currently amended] The composition according to claim 4, wherein the oxalanilide type UV blocking agent is selected from the following compounds:


    [6" claim-type="Currently amended] The composition according to claim 3, wherein the triazine type insoluble UV blocker is selected from the following Chemical Formula 2:
    [Formula 2]
    Wherein T 3 , T 4 and T 5 are independently phenyl, phenoxy or pyrrolo, wherein the phenyl, phenoxy and pyrrolo groups are OH, C 1 -C 18 alkyl or C 1 -C 18 alkoxy , C 1 -C 18 carboxyalkyl, C 5 -C 8 cycloalkyl, methylbenzylidenecamphor group,-(CH = CH) n (CO) -OT 6 group wherein T 6 is C 1 -C 18 alkyl or Cinnamic, n is a value of 0 or 1), and may be substituted with 1, 2 or 3 substituents selected from).
    [7" claim-type="Currently amended] The triazine type UV blocking agent is selected from benzalmalonate, phenylcyanoacrylate, or insoluble s-triazine derivatives carrying benzalmalonate and phenylcyanoacrylate groups. Composition.
    [8" claim-type="Currently amended] 8. Composition according to claim 7, wherein the triazine type UV blocker is selected from the following compounds:
    2,4,6-tris (diethyl 4'-aminobenzalmalonate) -s-triazine,
    2,4,6-tris (diisopropyl 4'-aminobenzalmalonate) -s-triazine,
    2,4,6-tris (dimethyl 4'-aminobenzalmalonate) -s-triazine,
    2,4,6-tris (ethyl α-cyano-4-aminocinnamate) -s-triazine.
    [9" claim-type="Currently amended] The composition according to claim 3, wherein the triazine type UV blocking agent is selected from benzotriazole, benzothiazole, or insoluble s-triazine derivatives carrying benzotriazole and benzothiazole groups.
    [10" claim-type="Currently amended] 10. The composition of claim 9, wherein the triazine type UV blocker is selected from:
    2,4,6-tris [(3 '-(benzotriazol-2-yl) -2'-hydroxy-5'-methyl) phenylamino] -s-triazine,
    2,4,6-tris [(3 '-(benzotriazol-2-yl) -2'-hydroxy-5'-tert-octyl) phenylamino] -s-triazine.
    [11" claim-type="Currently amended] The composition according to claim 3, wherein the benzotriazole type organic UV blocker corresponds to the formula
    [Formula 3]
    (Wherein T 7 represents a hydrogen atom or a C 1 -C 18 alkyl radical; T 8 and T 9 are the same or different and represent a C 1 -C 18 alkyl radical which may be substituted with phenyl).
    [12" claim-type="Currently amended] The composition of claim 11, wherein the compound of formula 3 is selected from the following compounds:




    [13" claim-type="Currently amended] 4. The insoluble UV blocker according to claim 3, wherein the insoluble UV blocker has the structure: [2,4'-dihydroxy-3- (2H-benzotriazol-2-yl) -5- (1,1,3,3- Tetramethylbutyl) -2 '-(n-octoxy) -5'-benzoyl] diphenylmethane

    [14" claim-type="Currently amended] The composition according to claim 3, wherein the benzotriazole type organic UV blocker is selected from methylenebis (hydroxyphenylbenzotriazole) derivatives having the structure
    [Formula 4]
    Wherein the T 10 and T 11 radicals are the same or different and are C 1 -C which may be substituted with one or more radicals selected from C 1 -C 4 alkyl radicals, C 5 -C 12 cycloalkyl radicals or aryl moieties 18 alkyl radicals).
    [15" claim-type="Currently amended] The composition of claim 14, wherein the compound of formula 4 is selected from the group consisting of compounds having the structure:
    Compound (a)
    Compound (b)
    Compound (c)
    [16" claim-type="Currently amended] The composition according to claim 3, wherein the vinyl amide type organic blocker corresponds to the formula (5):
    [Formula 5] T 12- (Y) r -C (= O) -C (T 13 ) = C (T 14 ) -N (T 15 ) (T 16 )
    Wherein T 12 is an OH, a C 1 -C 18 alkyl radical, a C 1 -C 8 alkoxy radical, or a group -C (═O) -OT 17 , where T 17 is C 1 -C 18 alkyl Phenyl group or C 1 -C 18 alkyl radical which may be substituted with 1, 2 or 3 radicals selected from; T 13 , T 14 , T 15 and T 16 are the same or different and represent a C 1 -C 18 alkyl radical or a hydrogen atom; Y is N or O and r has a value of 0 or 1}.
    [17" claim-type="Currently amended] The composition of claim 16, wherein the compound of formula 5 is selected from:
    4-octylamino-3-penten-2-one;
    Ethyl 3-octylamino-3-butenoate;
    3-octylamino-1-phenyl-2-buten-1-one;
    3-dodecylamino-1-phenyl-2-buten-1-one.
    [18" claim-type="Currently amended] The composition according to claim 3, wherein the cinnamic amide type organic blocker corresponds to the following formula (6):
    [Formula 6]
    [Wherein OT 18 is a hydroxyl or C 1 -C 4 alkoxy radical; T 19 is hydrogen or C 1 -C 4 alkyl; T 20 is — (CONH) s-phenyl group where s has a value of 0 or 1, and the phenyl group is OH, C 1 -C 18 alkyl, C 1 -C 8 alkoxy or -C (= O) -OT 21 Can be substituted with 1, 2, or 3 groups selected from the group wherein T 21 is C 1 -C 18 alkyl.
    [19" claim-type="Currently amended] 3. The composition of claim 2 wherein the insoluble UV blocker is cinnamic dimer.
    [20" claim-type="Currently amended] The composition of claim 19 wherein the insoluble UV blocker is a compound having the structure:

    [21" claim-type="Currently amended] The composition according to claim 3, wherein the benzazole type insoluble UV blocker is selected from those corresponding to one of the following Chemical Formulas 7, 8 and 9.
    [Formula 7]
    [Formula 8]
    [Formula 9]
    {Wherein each X symbol independently represents an oxygen or sulfur atom or an NR 2 group,
    Each Z symbol independently represents a nitrogen atom or a CH group,
    Each R 1 symbol independently represents a linear or branched C 1-8 alkyl group, or a linear or branched C 1-8 alkoxy group, which may include an OH group, a halogen atom, a silicon atom,
    Each number m is independently 0, 1 or 2,
    n represents an integer of 1 to 4,
    p is 0 or 1,
    Each number q is independently 0 or 1,
    Each R 2 symbol independently represents a benzyl or linear or branched C 1-8 alkyl group which may comprise a hydrogen atom or a silicon atom,
    A represents a radical having the valence n, selected from one of the formulas:

    Wherein W represents N or CH;
    Each R 3 symbol independently represents a halogen atom or a linear or branched C 1-4 alkyl or alkoxy group or a hydroxyl group,
    R 4 represents a hydrogen atom or a linear or branched C 1-4 alkyl group, c = 0 to 4, d = 0 to 3, e = 0 or 1, and f = 0 to 2)}.
    [22" claim-type="Currently amended] 22. The composition of claim 21, wherein the benzazole compound of formula 7 is selected from: 2- (benzoxazol-2-yl) -4-methylphenol, 2- (1H-benzimidazole-2- Yl) -4-methoxyphenol or 2- (benzothiazol-2-yl) phenol, 2,2'-bisbenzimidazole, 5,5 ', 6,6'-tetramethyl-2,2'- Bisbenzimidazole, 5,5'-dimethyl-2,2'-bisbenzimidazole, 6-methoxy-2,2'-bisbenzimidazole, 2- (1H-benzimidazol-2-yl) Benzothiazole, 2- (1H-benzimidazol-2-yl) benzoxazole and N, N'-dimethyl-2,2'-bisbenzimidazole, 1,4-phenylene bis (2-benzoxazolyl ), 1,4-phenylenebis (2-benzimidazolyl), 1,3-phenylenebis (2-benzoxazolyl), 1,2-phenylenebis (2-benzoxazolyl), 1, 2-phenylenebis (benzimidazolyl), 1,4-phenylenebis (N- (2-ethylhexyl) -2-benzimidazolyl) and 1,4-phenylenebis (N-trimethylsilylmethyl 2-benzimidazolyl), 2- (2-benzofuranyl) benzoxazole, 2- (benzofuranyl) -5-methylbenzone Azoles and 2- (3-methyl-2-benzofuranyl) benzoxazole.
    [23" claim-type="Currently amended] 22. The composition of claim 21, wherein the benzazole compound of formula 8 is selected from: 2,6-diphenyl-1,7-dihydrobenzo [1,2-d; 4,5-d ' ] Diimidazole, 2,6-distyryl-1,7-dihydrobenzo [1,2-d; 4,5-d '] diimidazole or 2,6-di (p-tert-butylstyryl ) -1,7-dihydrobenzo [1,2-d; 4,5-d '] diimidazole.
    [24" claim-type="Currently amended] 22. The composition of claim 21, wherein the benzazole compound of formula 9 is 5,5'-bis (2-phenylbenzimidazole).
    [25" claim-type="Currently amended] 22. A composition according to claim 21, wherein a benzazole type insoluble UV blocker is selected from: 2- (1H-benzimidazol-2-yl) benzoxazole, 6-methoxy-2,2'- Bisbenzimidazole, 2- (1H-benzimidazol-2-yl) benzothiazole, 1,4-phenylenebis (2-benzoxazolyl), 1,4-phenylenebis (2-benzimida) Zolyl), 1,3-phenylenebis (2-benzoxazolyl), 1,2-phenylenebis (2-benzoxazolyl), 1,2-phenylenebis (2-benzimidazolyl) and 1 , 4-phenylenebis (N-trimethylsilylmethyl-2-benzimidazolyl).
    [26" claim-type="Currently amended] The composition according to claim 3, wherein the insoluble organic blocker of the aryl vinylene ketone type corresponds to any one of the following Chemical Formulas 10 and 11.
    [Formula 10]
    [Formula 11]
    {Of the formulas,
    n '= 1 or 2,
    In formula (10) when n '= 1, or in formula (11), B is an aryl radical selected from formulas (a') to (d '), or in formula 10 when n' = 2, and a radical selected from (e ') to (h'):

    (In the meal,
    Each R 8 symbol is independently an OH group, a halogen atom, a linear or branched C 1-6 alkyl group which may include silicon atoms, a linear or branched C 1-6 alkoxy group that may contain silicon atoms, linear Or a branched C 1-5 alkoxycarbonyl group, or a linear or branched C 1-6 alkylsulfonamide group which may comprise a silicon atom or an amino acid functional group,
    p 'represents an integer of 0 to 4,
    q 'represents 0 or 1),
    R 5 represents hydrogen or an OH group,
    R 6 represents hydrogen, a linear or branched C 1-6 alkyl group, cyano group, C 1-6 alkylsulfonyl group or phenylsulfonyl group which may contain silicon atoms,
    R 7 represents a linear or branched C 1-6 alkyl group which may be substituted by one or two R 4 radicals and may comprise a phenyl group or silicon atom which may form a bicyclic ring, or
    Or R 6 and R 7 together may be interrupted by one or more nitrogen, sulfur and oxygen atoms and may comprise another carbonyl and be substituted with a linear or branched C 1 -C 8 alkylsulfonamide group and silicon To form monocyclic, bicyclic or tricyclic C 2-10 hydrocarbonaceous moieties, which may comprise atomic or amino acid functional groups; Provided that when n '= 1, R 6 and R 7 do not form a camphor nucleus.
    [27" claim-type="Currently amended] 27. The composition of claim 26, wherein the aryl vinylene ketone compound is selected from those corresponding to Formula 10 wherein n '= 1.
    [28" claim-type="Currently amended] The composition of claim 27 wherein the aryl vinylene ketone compound is selected from:
    Styryl ketone type compounds,
    -Benzylidenecineol type compounds,
    Compounds of the benzylidene chromanone type,
    Compounds of the benzylidene thiochromenone type,
    Benzylidenequinuclidinone type compounds,
    Compounds of the benzylidenecycloalkanone type,
    Compounds of the benzylidene hydantoin type,
    Compounds of the benzylidene indone type,
    -Benzylidene tetraral type compounds,
    Compounds of the benzylidenefuranone type,
    Compounds of the benzylidene benzofuranone type,
    Compounds of the benzylidene indandione type,
    Compounds of the benzylidene benzothiofuranone type,
    Compounds of the benzylidenebarbituric acid type,
    Compounds of the benzylidenepyrazolone type,
    Compounds of the benzylidene imidazolone type,
    -A chalcone type compound,
    A compound of benzylidene type.
    [29" claim-type="Currently amended] 29. The composition of claim 28, wherein the aryl vinylene ketone compound is selected from:
    1- (3,4-dimethoxyphenyl) -4,4-dimethylpent-1-en-3-one,
    1,3,3-trimethyl-5- (4-methoxybenzylidene) -2-oxabicyclo [2.2.2] octan-6-one,
    3- (4-methoxybenzylidene) -2,3,4a, 8a-tetrahydrochromen-4-one,
    3- (4-methoxybenzylidene) -2,3,4a, 8a-tetrahydrochromen-4-thione,
    4-methoxybenzylidene-1-azabicyclo [2.2.2] octan-3-one,
    2- (4-methoxybenzylidene) cyclopentanone and 2- (4-methoxybenzylidene) cyclohexanone,
    5- (3,4-dimethoxybenzylidene) imidazolidine-2,4-dione,
    2- (4-methoxybenzylidene) indan-1-one,
    2- (4-methoxybenzylidene) -3,4-dihydro-2H-naphthalen-1-one,
    4- (4-methoxybenzylidene) -2,2,5,5-tetramethyldihydrofuran-3-one,
    2-benzylidenebenzofuran-3-one,
    2- (3,5-di (tert-butyl) -4-hydroxybenzylidene) indane-1,3-dione,
    2-benzylidenebenzo [b] thiophen-3-one,
    5- (4-methoxybenzylidene) -1,3-dimethylpyrimidine-2,4,6-trione,
    4- (4-methoxybenzylidene) -5-methyl-2-phenyl-2,4-dihydropyrazol-3-one,
    5- (4-methoxybenzylidene) -2-phenyl-3,5-dihydroimidazol-4-one,
    1- (2-hydroxy-4-methoxyphenyl) -3-phenylpropenone,
    3-hydroxy-1- (2-hydroxy-4-methoxyphenyl) -3-phenylpropenone.
    [30" claim-type="Currently amended] 27. The composition of claim 26, wherein the aryl vinylene ketone compound is selected from those corresponding to Formula 10 wherein n '= 2.
    [31" claim-type="Currently amended] 31. The composition of claim 30, wherein the aryl vinylene ketone compound is selected from:
    Compounds of the phenylenebis (methylidenenorcamphor) type,
    Compounds of the phenylenebis (methylidenecamphor) type,
    Compounds of the phenylenebis (methylidenecamphorsulfonamide) type,
    Compounds of the phenylenebis (methylidenecineol) type,
    Compounds of the phenylene bis (methylideneketotricyclodecane) type,
    Compounds of the phenylenebis (alkylene ketone) type,
    Compounds of the phenylenebis (methylidenefuranone) type,
    A compound of the phenylenebis (methylidenequinuclidinone) type.
    [32" claim-type="Currently amended] 32. The composition of claim 31 wherein the aryl vinylene ketone compound is selected from:
    1,4-phenylenebis {3-methylidenebicyclo [2.2.1] heptan-2-one},
    1,4-phenylenebis {3-methylidene-1,7,7-trimethylbicyclo [2.2.1] heptan-2-one} or 1,3-phenylenebis {3-methylidene-1, 7,7-trimethylbicyclo [2.2.1] heptan-2-one},
    1,4-phenylenebis {3,3'-methylidenecamphor-10,10'-ethylsulfonamide or-(2-ethylhexyl) sulfonamide},
    1,4-phenylenebis {5-methylidene-3,3-dimethyl-2-oxabicyclo [2.2.2] octane-6-one},
    1,4-phenylenebis (octahydro-4,7-methano-6-inden-5-one),
    1,4-phenylenebis (4,4-dimethylpent-1-en-3-one),
    1,4-phenylenebis (4-methylidene-2,2,5,5-tetramethyldihydrofuran-3-one),
    1,4-phenylenebis {2-methylidene-1-azabicyclo [2.2.2] octan-3-one}.
    [33" claim-type="Currently amended] 27. The composition of claim 26, wherein the aryl vinylene ketone compound corresponds to formula 11 and is selected from:
    Compounds of the bis (benzylidene) cycloalkanone type;
    compounds of the γ-pyron type.
    [34" claim-type="Currently amended] 34. The composition of claim 33, wherein the aryl vinylene ketone compound corresponds to formula 11 and is selected from:
    2,5-di (benzylidene) cyclopentanone,
    2,6-bis (3,4-dimethoxyphenyl) pyran-4-one.
    [35" claim-type="Currently amended] The composition according to claim 3, wherein the insoluble organic blocker of the phenylenebis (benzoxazinone) type corresponds to the following formula (12):
    [Formula 12]
    Wherein R represents a divalent aromatic moiety selected from the following formulas (e ") to (h"):

    (Of the formulas,
    Each R 9 symbol is independently an OH group, a halogen atom, a linear or branched C 1-6 alkyl group which may include silicon atoms, a linear or branched C 1-6 alkoxy group which may include silicon atoms, Linear or branched C 1-5 alkoxycarbonyl group, or a linear or branched C 1-6 alkylsulfonamide group which may include silicon atoms or amino acid functional groups,
    p "represents an integer of 0-4,
    q "represents 0 or 1)}.
    [36" claim-type="Currently amended] The composition of claim 35 wherein the insoluble compound of formula 12 is selected from:
    2,2'-p-phenylenebis (3,1-benzoxazin-4-one),
    2,2 '-(4,4'-biphenylene) bis (3,1-benzoxazin-4-one),
    2,2 '-(2,6-naphthylene) bis (3,1-benzoxazin-4-one).
    [37" claim-type="Currently amended] The composition according to claim 3, wherein the insoluble organic blocker of the acrylonitrile amide, sulfonamide or carbamate derivative type is selected from those corresponding to the following formula (13) and isomers thereof:
    [Formula 13]
    (In the meal,
    R 10 represents a linear or branched C 1-8 alkyl group,
    n '' 'has a value of 0, 1 or 2,
    X 2 is of the formula — (C═O) —R 11 — (C═O) —, —SO 2 —R 11 —SO 2 — or — (C═O) —OR 11 —O— (C═O) — Represents a divalent radical,
    Y represents a-(C = 0) -R 12 or -SO 2 R 13 radical,
    R 11 represents a single bond or may carry one or more hydroxyl substituents and may comprise one or more heteroatoms selected from oxygen, nitrogen and silicon atoms in the carbonaceous chain, linear or branched divalent C 1 -C 30 alkylene or C 3 -C 30 alkenylene radical,
    R 12 represents a -OR 14 or -NHR 14 radical,
    R 13 represents a phenyl ring or a linear or branched C 1 -C 30 alkyl radical, optionally substituted with a C 1 -C 4 alkyl or alkoxy radical,
    R 14 may carry one or more hydroxyl substituents and may comprise one or more heteroatoms selected from oxygen, nitrogen and silicon atoms in the carbonaceous chain, linear or branched C 1 -C 30 alkyl or C 3 -C 30 Alkenyl radicals).
    [38" claim-type="Currently amended] 38. The composition of claim 37, wherein the insoluble blocker is a dimer of 2-ethylhexyl 2-cyano-3- [4- (acetylamino) phenyl] acrylate of the formula:

    [39" claim-type="Currently amended] The composition according to claim 1 or 2, wherein the insoluble UV blocker is a polyvalent metal salt of a sulfone or carboxyl organic UV blocker.
    [40" claim-type="Currently amended] 40. The method of claim 39, wherein the insoluble UV blocker is selected from the group consisting of polyvalent metal salts of sulfonated derivatives of benzylidene camphor; Polyvalent metal salts of sulfonated derivatives of benzimidazole; Or a polyvalent metal salt of cinnamic acid derivatives.
    [41" claim-type="Currently amended] The composition of claim 1 or 2, wherein the insoluble UV blocker is a UV-A, UV-B, or a polyvalent metal or an ammonium or substituted ammonium complex of UV-A and UV-B organic blockers.
    [42" claim-type="Currently amended] The composition of claim 1 or 2, wherein the insoluble UV blocker or blockers are present at a concentration ranging from approximately 1 to 10% by weight relative to the total weight of the composition.
    [43" claim-type="Currently amended] 43. The composition of claim 42, wherein the insoluble UV blocker or blockers are present at a concentration ranging from approximately 2 to 8% by weight relative to the total weight of the composition.
    [44" claim-type="Currently amended] The composition of claim 1 or 2, wherein the compound or compounds of formula 14 are selected from those of formula 14a:
    [Formula 14a]
    (In the meal,
    R 1 and R 2 are the same or different and represent a hydrogen atom or a C 1 -C 12 alkyl radical or form a 5 or 6 membered ring with the nitrogen atom bonded thereto;
    X represents COOR 5 or CONR 6 R 7 ;
    R 5 represents a hydrogen atom, a C 1 -C 12 alkyl radical or a C 3 -C 6 cycloalkyl radical;
    R 6 and R 7 are the same or different and represent a hydrogen atom, a C 1 -C 12 alkyl radical or a C 5 -C 6 cycloalkyl radical).
    [45" claim-type="Currently amended] 45. The compound of claim 44, wherein the compound of formula
    R 1 and R 2 are the same or different and represent a C 1 -C 4 alkyl radical such as ethyl;
    R 5 represents a C 3 -C 8 alkyl radical;
    R 6 and R 7 are the same or different and represent a C 1 -C 8 alkyl radical.
    [46" claim-type="Currently amended] The composition of claim 1 or 2, wherein the compound or compounds of formula 14 are selected from those of formula 14b:
    [Formula 14b]
    (In the meal,
    R 1 and R 2 are the same or different and represent a C 1 -C 12 alkyl radical or form a 5 or 6 membered ring with the nitrogen atom bonded thereto).
    [47" claim-type="Currently amended] 47. The composition of claim 46, wherein the compound of formula 14b is selected from:
    4-diethylamino-2-hydroxyphenyl phenyl ketone,
    4-pyrrolidino-2-hydroxyphenyl phenyl ketone.
    [48" claim-type="Currently amended] The composition of claim 1 or 2, wherein the compound or compounds of formula 14 are selected from those of formula 14c:
    [Formula 14c]
    (In the meal,
    R 1 and R 2 are the same or different and represent a hydrogen atom or a C 1 -C 8 alkyl radical or form a 5 or 6 membered ring with the nitrogen atom bonded thereto;
    R 5 represents a hydrogen atom, a C 1 -C 12 alkyl radical or a C 3 -C 6 cycloalkyl radical).
    [49" claim-type="Currently amended] 49. The composition of claim 48, wherein the compound of formula 14c is selected from:
    [lacuna] 2- (4-pyrrolidino-2-hydroxybenzoyl) benzoate,
    Methyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate,
    2-ethylhexyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate,
    Cyclohexyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate,
    n-hexyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate,
    [lacuna] 2- (4-dibutylamino-2-hydroxybenzoyl) benzoate,
    Methyl 2- (4-dibutylamino-2-hydroxybenzoyl) benzoate,
    Isobutyl 2- (4-dibutylamino-2-hydroxybenzoyl) benzoate.
    [50" claim-type="Currently amended] 50. The composition of claim 49, wherein the compound of formula 14c is n-hexyl 2- (4-diethylamino-2-hydroxybenzoyl) benzoate.
    [51" claim-type="Currently amended] A composition according to claim 1 or 2, wherein the amino substituted 2-hydroxybenzophenone derivatives or derivatives are present in the composition in a ratio ranging from 0.1 to 20% by weight, based on the total weight of the composition.
    [52" claim-type="Currently amended] 52. The composition of claim 51, wherein the amino substituted 2-hydroxybenzophenone derivatives or derivatives are present in the composition in a ratio ranging from 0.1 to 15% by weight relative to the total weight of the composition.
    [53" claim-type="Currently amended] 53. The composition of claim 52, wherein the amino substituted 2-hydroxybenzophenone derivatives or derivatives are present in the composition in a ratio ranging from 0.5 to 10% by weight relative to the total weight of the composition.
    [54" claim-type="Currently amended] The composition of claim 1 or 2, further comprising one or more agents for artificial tanning, browning, or tanning and browning of the skin.
    [55" claim-type="Currently amended] The composition of claim 1 or 2, further comprising at least one soluble organic UV blocker active in the UV-A, UV-B, or UV-A and UV-B regions.
    [56" claim-type="Currently amended] 56. The composition of claim 55, wherein the soluble organic UV blocker is selected from: anthranilate; Cinnamic acid derivatives; Dibenzoylmethane derivatives; Salicylic acid derivatives; Camphor derivatives; Triazine derivatives; Benzophenone derivatives other than those of the formula (14); β, β-diphenylacrylate derivatives; Benzotriazole derivatives; Benzalmalonate derivatives; Benzimidazole derivatives; Imidazoline; Bisbenzoazolyl derivatives; p-aminobenzoic acid (PABA) derivatives; Blocking polymers and blocking silicones; dimers derived from α-alkylstyrene; 4,4-diarylbutadiene; And mixtures thereof.
    [57" claim-type="Currently amended] The composition of claim 56, wherein the soluble organic UV blocker is selected from:
    Ethylhexyl salicylate,
    -Octocrylene,
    Ethylhexyl methoxycinnamate,
    Butyl methoxydibenzoylmethane,
    Phenylbenzimidazole sulfonic acid,
    Benzophenone-3,
    Benzophenone-4,
    Benzophenone-5,
    4-methylbenzylidene camphor,
    Disodium phenyl dibenzimidazole tetrasulfonate,
    -Anisotriazine,
    Ethylhexyl triazone,
    Diethylhexyl butamido triazone,
    2,4,6-tris (diisobutyl 4'-aminobenzalmalonate) -s-triazine,
    -Drometrizol trisiloxane,
    Methylenebis (benzotriazolyltetramethylbutylphenol),
    1,1-dicarboxy (2,2'-dimethylpropyl) -4,4-diphenylbutadiene,
    And mixtures thereof.
    [58" claim-type="Currently amended] The composition of claim 1 or 2, further comprising a coated or uncoated metal oxide pigment or nanopigment.
    [59" claim-type="Currently amended] 59. The composition of claim 58, wherein the pigment or nanopigment is selected from titanium oxide, zinc oxide, iron oxide, zirconium oxide or cerium oxide, and mixtures thereof, coated and uncoated.
    [60" claim-type="Currently amended] The composition according to claim 1 or 2, further comprising at least one cosmetic aid selected from: fatty substances, organic solvents, ionic or nonionic thickeners, softeners, antioxidants, free radical destruction Agents, opacifiers, stabilizers, emollients, silicones, α-hydroxy acids, antifoams, humectants, vitamins, insect repellents, flavorings, preservatives, surfactants, anti-inflammatory agents, P substance antagonists, fillers, polymers, propellants, basic Topical or acidifying agents, or colorants.
    [61" claim-type="Currently amended] The protective composition or sunscreen composition for human epidermis according to claim 1 or 2, which is a nonionic vesicular dispersion, emulsions such as oil-in-water emulsions, creams, milks, gels, cream gels, suspensions, dispersions, powders, solids. Composition provided in the form of a tube, foam or spray.
    [62" claim-type="Currently amended] The composition according to claim 1 or 2, which is a composition for makeup of eyelashes, eyebrows or skin and is provided in anhydrous or aqueous, paste or solid form, in emulsion, suspension or dispersion form.
    [63" claim-type="Currently amended] The composition according to claim 1 or 2, which is a composition intended for protecting hair against ultraviolet rays and is provided in the form of a shampoo, lotion, gel, emulsion or nonionic vesicular dispersion.
    [64" claim-type="Currently amended] The composition according to claim 1 or 2, which is used for the preparation of the intended cosmetic or dermatological composition for the protection of skin, hair, or skin and hair against ultraviolet rays such as insolation.
    [65" claim-type="Currently amended] For the purpose of providing a synergistic effect against a given sunscreen factor UV-A PPD , skin, hair, or skin against ultraviolet radiation, such as insolation, containing one or more insoluble organic blockers in the particle size range of 10 nm to 5 μm; A method of using an amino substituted 2-hydroxybenzophenone derivative of formula (14) as defined in claim 1 in the preparation of a cosmetic or dermatological composition intended for the protection of hair.
    [66" claim-type="Currently amended] The composition of claim 16 wherein T 12 in formula 5 is a C 1 -C 5 alkyl radical.
    [67" claim-type="Currently amended] 17. The composition of claim 16, wherein the same or different T 13 , T 14 , T 15 and T 16 in Formula 5 are C 1 -C 5 alkyl radicals.
    [68" claim-type="Currently amended] The composition of claim 18 wherein OT 18 in formula 6 is a methoxy or ethoxy radical.
    [69" claim-type="Currently amended] 19. The composition of claim 18 wherein T 19 in formula (6) is methyl or ethyl.
    类似技术:
    公开号 | 公开日 | 专利标题
    KR102052772B1|2019-12-05|Cosmetic and/or dermatological composition containing a merocyanine derivative comprising specific polar groups consisting of hydroxyl- and ether-functionalities
    US9162976B2|2015-10-20|Composition containing a dibenzoylmethane screening agent and a hydrophilic or water-soluble merocyanin uv-screening agent; process for photostabilizing the dibenzoylmethane screening agent
    US8003082B2|2011-08-23|Photostable organic sunscreen composition
    US5489431A|1996-02-06|Photoprotective/cosmetic compositions comprising 2,4,6-tris[p-|oxycarbonyl)anilino]-1,3,5-triazine and dioctyl malate
    JP3753224B2|2006-03-08|Photoprotective composition comprising a bisresorcinyltriazine derivative and a compound having a benzoazolyl or benzodiazolyl group
    US8747816B2|2014-06-10|UV-photoprotective compositions comprising diebenzoylmethane screening agents and silicon-containing s-triazine compounds substituted with two aminobenzoate or aminobenzamide groups
    US6607713B1|2003-08-19|Method for improving UV radiation stability of photosensitive sunscreen filters
    AU738645B2|2001-09-20|Photoprotectant cosmetic composition containing an anionic surfactant, compounds for screening out ultraviolet radiation and a cationic or zwitterionic amphiphilic compound, and use thereof
    EP1888009B1|2014-04-09|Method for photostabilizing a dibenzoylmethane derivative using a merocyanine sulphone derivative; photoprotective cosmetic compositions containing said combination
    US5882633A|1999-03-16|Compositions comprising a dibenzoylmethane derivative, a 1,3,5-triazine derivative and an amide compound, and methods of use therefor
    JP5001154B2|2012-08-15|Silane merocyanine sulfone derivatives; photoprotective compositions containing silane merocyanine sulfone derivatives; their use as UV filters
    AU765369B2|2003-09-18|Solubilization of 1,3,5-triazine derivatives with N-acyl amino acid esters
    US6495122B2|2002-12-17|Use of mixtures of micropigments for preventing tanning and for lightening skin and hair
    AU778175B2|2004-11-18|Micropigment mixture
    JP3848308B2|2006-11-22|Composition containing 4-tert-butyl-4'-methoxydibenzoylmethane, 1,3,5-triazine derivative and alkyl | -β, β'-diphenylacrylate and use thereof
    US6416748B1|2002-07-09|Emulsifier-free UV-photoprotecting emulsions comprising micronized insoluble screening agents
    US6616918B2|2003-09-09|Self-tanning composition containing an N-acyl amino acid ester and a self-tanning agent
    EP1441692B1|2008-01-02|Composition containing an amino acid n-acylated ester and a polyamide-structured uv filter
    AU2002300974B2|2004-11-25|Use of amphiphilic copolymers to stabilize dispersions of insoluble organic compounds for screening out UV radiation, dispersions stabilized with these copolymers and cosmetic compositions containing them
    JP2010535779A|2010-11-25|Method for quenching electronic excitation of chromophore-containing organic molecules in photoactive compositions
    US7250156B2|2007-07-31|Solid photoprotective compositions comprising octenylsuccinic anhydride-esterified starch salts
    JP4753550B2|2011-08-24|Use of blue light shielding agents to prevent the breakdown of endogenous carotenoids in the skin; novel aminoarylvinyl-S-triazine compounds and uses thereof
    US7153494B2|2006-12-26|Dibenzoylmethane sunscreen compositions photostabilized with amphiphilic block copolymers
    EP1353642B1|2008-05-07|Photoprotective compositions comprising an amphiphilic copoylmer comprising 2-acrylamido-2-propanesulfonic and |acrylates
    EP0823418B1|2002-10-09|Indanylidene derivatives and their use as UV-absorbers
    同族专利:
    公开号 | 公开日
    JP2003192557A|2003-07-09|
    BR0205462A|2004-07-27|
    ES2732182T3|2019-11-21|
    AU2002302148B2|2004-05-06|
    EP1317918B1|2019-05-01|
    EP1317918A1|2003-06-11|
    EP2196189A1|2010-06-16|
    FR2833164A1|2003-06-13|
    FR2833164B1|2004-07-16|
    AU2002302148A1|2003-06-19|
    CN1425368A|2003-06-25|
    ES2725152T3|2019-09-19|
    US6627180B2|2003-09-30|
    US20030152532A1|2003-08-14|
    CA2412807A1|2003-06-07|
    EP2196189B1|2019-03-06|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2001-12-07|Priority to FR0115860A
    2001-12-07|Priority to FR0115860
    2002-12-06|Application filed by 로레알
    2003-06-18|Publication of KR20030047811A
    2019-12-04|First worldwide family litigation filed
    优先权:
    申请号 | 申请日 | 专利标题
    FR0115860A|FR2833164B1|2001-12-07|2001-12-07|Antisolar cosmetic compositions based on a synergistic mixture of filters and uses|
    FR0115860|2001-12-07|
    [返回顶部]