Compositions containing a UV-absorbing system including a UV-attenuating physical material, at least two polyols and at least one anionic polysaccharide thickening agent

A UV-absorbing system with physical UV-attenuating materials, polyols, and anionic polysaccharide thickening agents addresses the challenge of achieving high UV protection, stability, and pleasant texture in sunscreen compositions, ensuring balanced UVA and UVB protection without greasiness or whitening.

FR3169332A3Pending Publication Date: 2026-06-12LOREAL SA

Patent Information

Authority / Receiving Office
FR · FR
Patent Type
Utility models
Current Assignee / Owner
LOREAL SA
Filing Date
2024-12-10
Publication Date
2026-06-12

AI Technical Summary

Technical Problem

Existing sunscreen compositions struggle to achieve high UV protection with balanced UVA and UVB protection, stability, non-greasiness, and non-whitening while maintaining a pleasant texture, especially when using humectants like polyols.

Method used

A UV-absorbing system comprising at least one physical UV-attenuating material, at least two polyols, and at least one anionic polysaccharide thickening agent, which are combined to create stable, non-greasy, and non-whitening compositions.

Benefits of technology

The compositions provide high UV protection with balanced UVA and UVB protection, maintaining a pleasant texture and avoiding white marks on the skin, while being stable and non-greasy.

✦ Generated by Eureka AI based on patent content.
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Abstract

Compositions Containing a UV Absorbing System Including a UV Attenuating Physical Material, At Least Two Polyols, and At Least One Anionic Polysaccharide Thickening Agent. This disclosure relates to compositions including a UV absorbing system comprising at least one ultraviolet (UV) attenuating physical material, at least two polyols, and at least one anionic polysaccharide thickening agent, as well as methods for manufacturing and using such compositions. Figure for abstract: none
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Description

Title of the invention: COMPOSITIONS CONTAINING A UV-ABSORBING SYSTEM INCLUDING A PHYSICAL UV-ATTENUATING MATERIAL, AT LEAST TWO POLYOLS AND AT LEAST ONE AGENT ANIONIC POLYSACCHARIDE THICKENER FIELD OF THE INVENTION

[0001] The present disclosure relates to compositions comprising a UV-absorbing system comprising at least one physical ultraviolet (UV)-attenuating material, at least two polyols and at least one anionic polysaccharide thickening agent, as well as methods of making and using such compositions. DISCUSSION OF THE BACKGROUND

[0002] Radiation with wavelengths between 290 nm and 400 nm allows the human epidermis to tan, while radiation with wavelengths between 290 and 320 nm, called UVB rays, hinders the development of a natural tan. Exposure is also likely to cause a detrimental change in the biomechanical properties of the epidermis, resulting in the appearance of wrinkles and leading to premature skin aging (i.e., photoaging).

[0003] UVA rays with wavelengths between 320 and 400 nm penetrate the skin more deeply than UVB rays. UVA rays cause immediate and persistent tanning of the skin. Daily exposure to UVA rays, even for a short period under normal conditions, can damage collagen and elastin fibers, resulting in changes in the skin's microrelief, the appearance of wrinkles, and uneven pigmentation (spots, uneven skin tone).

[0004] Numerous studies show the need for effective protection against UVA and UVB to prevent sunburn, photoaging, and the like.

[0005] In order to obtain a high protection product, it is generally necessary to combine a large number of sunscreens and / or a large quantity of UV filters to achieve high levels of filtration efficiency.

[0006] However, high levels of UV filters do not lend themselves to the easy preparation of stable compositions with a pleasant texture. It is possible to obtain high UV protection by using one or more organic UV filters; however, Organic UV filters are often very greasy and unpleasant when applied to the skin, especially when used at high levels in a sunscreen formulation required for high UV protection efficacy.

[0007] Mineral UV filters such as titanium dioxide or zinc oxide are alternative UV filters to organic UV filters that can provide more pleasant textures; however, when one or more mineral UV filters are used, the resulting sunscreen formulation is far too whitening (also known as "white cast") when applied to the skin. When mineral UV filters are used at lower levels, it may be possible to produce sunscreen formulations with little or no whitening when applied to the skin; however, such formulations, containing low levels of mineral UV filters, are unable to produce the desired high levels of UV protection.

[0008] Finally, it can be difficult to combine an organic UV filter and a mineral UV filter in a single stable composition, particularly in order to achieve a stable, non-greasy, pleasant, non-whitening and high UV protection sunscreen formulation, especially when considering the need to balance the effectiveness of UVA and UVB protection in the presence of a humectant such as polyols.

[0009] There remains a need in the art of improved sunscreen compositions containing a humectant which have high UV protection and balanced UVA and UVB protection, which are stable, non-greasy, pleasant to apply and which are not whitening when applied to the skin.

[0010] Accordingly, one aspect of the present disclosure is a composition containing a humectant that is stable, non-greasy, non-whitening when applied to the skin, and that exhibits high UV protection. Summary of the invention

[0011] This disclosure relates to compositions comprising a UV-absorbing system including at least one physical ultraviolet (UV) attenuating material, at least two polyols, and at least one anionic polysaccharide thickening agent. Preferably, the compositions are stable, non-greasy, and / or non-bleaching (i.e., the compositions do not leave white marks) upon application.

[0012] This disclosure also relates to processes for the treatment, care, protection, enhancement of appearance and / or makeup of keratinous material, including the application of compositions of this disclosure to keratinous material in sufficient quantity to treat the keratinous material, care for it, enhance its appearance and / or make it up.

[0013] This disclosure also relates to methods of producing stable compositions comprising at least one ultraviolet (UV) attenuating physical material by combining at least one ultraviolet (UV) attenuating physical material, at least two polyols and at least one anionic polysaccharide thickening agent during the formation of the compositions to produce stable compositions.

[0014] It should be understood that both the preceding general description and the detailed description that follows are merely illustrative and explanatory and do not limit disclosure. DETAILED DESCRIPTION OF THE INVENTION

[0015] In the following description and the claims annexed thereto, it should be understood that the terms used have their ordinary and usual meanings in the art, unless otherwise specified.

[0016] “Approximately”, as used herein, means to within 10% of the stated number (for example, “ "Approximately 10%" means from 9% to 11% and "approximately 2%" means from 1.8% to 2.2%.

[0017] “At least one” means one or more and thus includes components individual products as well as mixtures / combinations.

[0018] As used herein, all proposed ranges are intended to include each specific point and range within the given ranges, as well as each combination of intermediate sub-ranges. Thus, a range from 1 to 5 specifically includes the integers in the range 1, 2, 3, 4 and 5, as well as sub-ranges such as 2 to 5, 3 to 5, 2 to 3, 2 to 4, 1 to 4, etc., and all fractional numbers in the range such as 1,2, 2,3, 3,4, etc., and sub-ranges including these fractional numbers such as 1.5 to 3.8, 2 to 4.3, 4.2 to 4.9, etc.

[0019] “Film-forming”, “film-forming polymer” or “film-forming agent” as used herein means a polymer or resin that is capable of leaving a film on the substrate to which it is applied, for example, after a solvent accompanying the film-forming agent has evaporated, been absorbed into the substrate and / or dissipated on it.

[0020] “Substituted” as used herein means comprising at least one substitute. Non-limiting examples of substituents include atoms, such as oxygen and nitrogen atoms, as well as functional groups, such as hydroxyl groups, ether groups, alkoxy groups, acyloxyalkyl groups, oxyalkylene groups, polyoxyalkylene groups, carboxylic acid groups, amine groups, acylamino groups, amide groups, halogen-containing groups, ester groups, thiol groups, sulfonate groups, thiosulfate groups, siloxane groups, and polysiloxane groups. The substituent(s) may, in addition, be substituted.

[0021] “Volatile”, as used here, means having a flash point of less than about 115 °C.

[0022] “Non-volatile”, as used here, means having a flash point greater than approximately 115 °C.

[0023] “Polymer” as used herein means a compound that is made up of at least two monomers.

[0024] “Exempt” or “substantially exempt” or “devoid of”, as used herein This means that, although it is preferable for no quantity of the specific component to be present in the composition, it is possible for very small quantities of it to be present in the compositions of the disclosure, provided that these quantities do not materially affect at least one, preferably most, of the advantageous properties of the compositions of the disclosure. Thus, for example, "oil-free" means that an effective quantity (i.e., greater than trace amounts) of oil(s) is omitted from the composition (i.e., about 0% by weight), "substantially oil-free" means that one or more oils are present in quantities not exceeding 0.1% by weight, and "oil-free" means that one or more oils are present in quantities not exceeding 0.25% by weight, based on the total weight of the composition.The same nomenclature applies to all other ingredients identified throughout the application and in this paragraph, such as, for example, specific UV filters and / or surfactants (the compositions in the disclosure that are "free of oxybenzone and / or octinoxate," "substantially free of oxybenzone and / or octinoxate," and "devoid of oxybenzone and / or octinoxate," as well as "free of surfactants," "substantially free of surfactants," and "devoid of surfactants" have meanings consistent with the discussion in this paragraph), even if they are not specifically mentioned for each ingredient identified in the application. The examples mentioned of the use of such language as that in this paragraph are intended to be provided by way of example, and not as a limitation.

[0025] “UV Filters” as used herein means approved sunscreen active agents by a government regulatory agency such as the Food and Drug Administration (FDA) in the United States or the European Commission in Europe and includes organic UV filters such as avobenzone, octocrylene, benzophenones, benzotriazoles and merocyanines, as well as physical ultraviolet (UV) attenuation materials.

[0026] “Whitening” or “white marks”, as used herein, refers to the appearance The visual appearance of the keratinous substance after a composition has been applied to the keratinous material, compared to the appearance of the keratinous material before the application of the composition. A composition is "non-bleaching". if it offers a minimal or non-existent visually white appearance (preferably no visually white appearance) of the keratinous material upon application.

[0027] “Anhydrous” as used here means that the compositions of the disclosure contain less than 3% water, which means that compositions may also contain less than 2% water, and less than 1% water, as well as being "water-free", "substantially water-free" and "water-free" as defined above.

[0028] A “UV-absorbing system containing essentially at least one ultraviolet (UV) attenuating physical material” as used herein means that the disclosure compositions contain less than 3% of UV filters other than the ultraviolet (UV) attenuating physical material(s), in particular less than 3% of organic UV filters, which means that in this definition as subcategories, there are compositions containing less than 2% of UV filters other than the ultraviolet (UV) attenuating physical material(s), in particular less than 2% of organic UV filters, and less than 1% of UV filters other than the ultraviolet (UV) attenuating physical material(s), in particular less than 1% of organic UV filters, as well as those “free of UV filters other than the ultraviolet (UV) attenuating physical material”,"substantially free of UV filters other than the physical ultraviolet (UV) attenuation material" and "devoid of UV filters other than the physical ultraviolet (UV) attenuation material" as defined above.

[0029] “System” and “component” are used interchangeably in the present request.

[0030] “Primary particle” as used in relation to the description of the material Ultraviolet (UV) attenuation physics here refers to inorganic or organic particles (structures) that can be held together by molecular or atomic bonding to form an ultraviolet (UV) attenuation physics material.

[0031] “Primary particle size” means the size of a non-aggregated primary particle in a physical material for attenuating ultraviolet (UV).

[0032] “Passive” as used in relation to the description of a physical material Ultraviolet (UV) attenuation here refers to a material that has been treated in such a way that the potential for the release of ionic species when in contact with water is reduced compared to the same non-passivated material.

[0033] “Keratinous materials” or “keratinous substance” means nails (nails fingers and / or toes), skin such as that of the body, face and around the eyes, scalp, keratinous fibers such as eyelashes, eyebrows and hair, and mucous membranes such as lips.

[0034] “Physiologically acceptable” means compatible with keratinous materials and having a pleasant color, smell and feel, and which does not cause unacceptable discomfort (tingling or pulling) likely to discourage a consumer from using the composition.

[0035] “UV protection efficiency” or “filtration efficiency” in the context of This disclosure is evaluated based on one or more of the following: FPS, FPUVA, critical wavelength, and UVA-I / UV ratio.

[0036] The "SPF" (Sun Protection Factor) measures the level of protection against erythema provided by a composition. The SPF value corresponds to the ratio between the minimum erythematous dose (MED) measured on skin covered with the composition and the MED measured on bare skin. "SPF" is a term known in the art of sunscreens and is defined, for example, in "A new substrate to measure sunscreen protection factors throughout the ultraviolet spectrum," J. Soc. Cosmet. Chem., 40, 127-133 (May / June 1989).

[0037] The evaluation of the SPF (Sun Protection Factor) can be carried out, for example, in vitro with a spectrophotometer from Labsphere (North Sutton, NH, USA). In such an evaluation, the plate is the material onto which the composition under test is applied. For such an evaluation, polymethyl methacrylate (PMMA) plates can be used. An example of an acceptable protocol is currently undergoing ISO accreditation under the name ISO Committee Draft 23675.

[0038] The evaluation of the sun protection factor (SPF) can also be performed in vivo in accordance with ISO 24444:2019 “Cosmetics-Sun protection test methods-In-vivo determination of the sun protection factor (SPF).” It can also be determined in accordance with FDA protocols, as described in the document “Labeling and Effectiveness Testing; Sunscreen Drug Products for Over-the-Counter Human Use” published in the U.S. Federal Register on May 7, 2011 (https: / / www.federalregister.gov / d / 2011-14766); 21 CFR Part 352 Subpart D § 352.72, updated and revised by the 2011 publication in the Federal Register.

[0039] “UVA protection factor” refers to an index characterizing the UVA protection provided by a composition. For example, the UVA protection factor (UPPF) can be measured in vivo according to the "PPD" (Persistent Pigment Darkening) method of the ISO-24442:2022 protocol, measuring the skin color observed 2 to 4 hours after UVA exposure. It can also be determined according to FDA protocols, as described again in 21 CFR Part 352 Subpart D § 352.72 as mentioned above in relation to SPF.

[0040] The evaluation of UVA protection can also be measured in vitro with the Labsphere® spectrophotometer under conditions such as those mentioned above in relation to FPS. The ISO 24443:2021 protocol describes such an in vitro process.

[0041] FDA broad-spectrum test procedures, particularly "critical wavelength" test procedures, are also available in 21 CFR Part 352 Subpart D § 352.72. In addition, broad-spectrum test procedures include the determination of the UVA1 / UV ratio as described in "Sunscreen Drug Products for Over-the-Counter-Human-Use" published in the Federal Register https: / / www.federalregister.gov / documents / 2019 / 02 / 26 / 2019-03019 / sunscreen-drug-products-for-over-the-counter-human-use.

[0042] According to this disclosure, the compositions in this disclosure preferably have one or more of the following properties:

[0043] The compositions have a critical wavelength, as determined by FDA critical wavelength procedures, of at least 370 nm;

[0044] The compositions have an FPS value of at least 15, preferably at least 30, preferably at least 50 and preferably at least 70;

[0045] The compositions have an FPUVA / FPS ratio of at least 1 / 3, and preferably of at least 2 / 5; and / or

[0046] The compositions have a UVA1 / UV ratio of 0.7 or more, preferably 0.75 or more, and preferably 0.8 or more.

[0047] “Makeup result”, as used herein, refers to compositions where The color remains the same or substantially the same as at the time of application, as observed with the naked eye, after a prolonged period. The "makeup result" can be evaluated by assessing the long-lasting properties using any method known in the art for evaluating such properties. For example, long-lasting performance can be assessed by a test involving the application of a composition to a keratinous material such as skin and evaluating the color of the composition after a prolonged period. For example, the color of a composition can be evaluated immediately after application to a keratinous material such as skin, and these characteristics can then be re-evaluated and compared after a certain duration. Furthermore, these characteristics can be evaluated in relation to other compositions, such as commercially available compositions.

[0048] “Natural” as in the expression “natural compound” means any compound derived directly from a natural substance such as a plant without having undergone chemical modification.

[0049] “Compound of natural origin” means any compound derived from a natural compound which has undergone one or more chemical modifications, for example by organic synthesis reaction, without the properties of the natural compound having been modified.

[0050] “Synthetic compound” means any compound that is neither a natural compound nor a composed of natural origin.

[0051] “Room temperature” means approximately 20-25 °C.

[0052] “Atmospheric pressure” means about 760 mmHg, i.e. about 105 pascals.

[0053] “UV filter” and “sunscreen agent” are used interchangeably in the present request.

[0054] “Effectiveness against UV”, “UV effectiveness” and “Effectiveness of UV protection” are used interchangeably in this application.

[0055] The compositions and methods of the present invention may include, consist of, or consist essentially of the essential elements and limitations of the disclosure described herein, as well as any additional or optional ingredients, components, or limitations described herein or otherwise useful. For example, the UV (ultraviolet) absorbing system of the compositions in the disclosure may "consist essentially of" at least one physical ultraviolet (UV) attenuating material.

[0056] For the purposes of this disclosure, the "fundamental novel property" associated with compositions, components and processes that "consist essentially of" identified ingredients, components or actions is "stability".

[0057] “Stable” or “stability” refers to a composition that has an appearance A homogeneous and smooth appearance (as opposed to perceptible aggregates or lumps) at a specified time, for example, immediately after manufacture (t0), after 4 hours of rest (t4h), and / or after 3 or 23 days of rest (t3d or t23d). Furthermore, or alternatively, "stable" or "stability" refers to a composition that does not undergo phase separation after a specified time (for example, those indicated in the preceding sentence).

[0058] The compositions of this disclosure may be in any form suitable for use as a personal care composition, such as a stick, paste, cream, anhydrous composition, emulsion (oil-in-water, water-in-oil, multiple emulsion such as water-in-oil-in-water), nanoemulsion, gel, liquid, solid, etc. These compositions may be used for all personal care purposes in cosmetic and / or dermatological products such as, for example, sunscreen, foundation, lip balms, lipsticks, concealers, mascaras, leave-in hair products, eyeshadows, powders, etc.

[0059] Reference is made herein to trade names of materials including, but not limited to, materials such as polymers and optional components. The materials are not intended to be limited by the materials described and referenced by a particular trade name herein. Equivalent materials (for example, those obtained from a different source under a different name or catalogue (reference) number) to those referenced by a trade name may be substituted for and used in the processes described and claimed herein.

[0060] Unless otherwise stated, all percentages and ratios are calculated by weight. Unless otherwise stated, all percentages are calculated relative to the total weight of a composition. All component or composition rates refer to the active rate of that component or composition and are understood to be exclusive of impurities, for example, residual solvents or by-products, which may be present in commercially available sources. COMPOSITION UV attenuating physical material

[0061] According to this disclosure, compositions comprising at least one ultraviolet (UV) attenuating physical material are proposed. "UV attenuating physical material" as used herein refers to solid inorganic ingredients that absorb incoming ultraviolet (UV) light and may optionally scatter incoming ultraviolet (UV) light, when present in the compositions disclosed herein. The UV attenuating physical material preferably comprises one or more metal oxides such as, for example, oxides of titanium, chromium, zinc, tin, alumina, cerium, and / or iron. Specific examples of suitable metal oxide(s) include, but are not limited to, at least one metal oxide selected from the group consisting of titanium dioxide, zinc oxide, iron oxide, chromium oxide, tin oxide, alumina, cerium oxide, and mixtures thereof.

[0062] The UV-attenuating physical material may be subjected to a surface treatment agent to improve the sensoriality, performance, and / or compatibility of the compositions disclosed herein. Suitable surface treatment agents may include hydrophobic or hydrophilic surface treatment agents such as, for example, those described in Cosmetics & Toiletries, February 1990, Vol. 105, pp. 53–64, including, but not limited to, specific examples such as amino acids, beeswax, fatty acids, fatty acid salts, fatty alcohols, anionic surfactants, lecithin, lecithin derivatives, metal alkoxides, polyethylene, silicones, proteins, alkanolamines, silicon oxides, metal oxides other than T, at least one ultraviolet (UV) attenuating physical material, sodium hexametaphosphate, alumina, and / or glycerol. Preferably, the physical UV attenuation material is passivated.

[0063] Preferably, the UV attenuation physical material comprises one or more zinc oxides and / or titanium dioxides. Preferably, the physical material UV attenuation material comprising one or more zinc oxides or titanium dioxides is passivated.

[0064] According to preferred embodiments, the UV attenuating physical material comprises titanium dioxide. The titanium dioxide may be present in any form in the compositions disclosed herein. Furthermore, the TiO2 may be treated (coated) or untreated.

[0065] According to preferred embodiments, the UV attenuating physical material comprises zinc oxide. The zinc oxide may be present in any form (for example, as wurtzite or a zinc mixture) in the compositions disclosed herein. Furthermore, the zinc oxide may be treated (coated) or untreated.

[0066] Preferably, the UV attenuation physical material comprises zinc oxide. Preferably, the zinc oxide is passivated.

[0067] Preferably, the UV attenuation physical material comprises titanium dioxide. Preferably, the titanium dioxide is passivated.

[0068] Preferably, the average primary particle size of the ultraviolet (UV) attenuating physical material is from 1 nm to 500 nm, preferably from 5 nm to 250 nm, preferably from 10 nm to 100 nm, and preferably from 20 nm to 50 nm, including all intermediate ranges and sub-ranges such as, for example, 25 nm to 40 nm, 10 nm to 75 nm, 10 nm to 40 nm, and 15 nm to 150 nm.

[0069] In some embodiments, the at least one ultraviolet (UV) attenuating physical material comprises zinc oxide and / or titanium dioxide, preferably coated with a coating agent, the coating agent preferably comprising at least one of hydrated silica, triethoxysilylethylpolydimethylsiloxyethyl, hexyldimethicone, hydrogenodimethicone, triethoxycaprylysilane and mixtures thereof.

[0070] Suitable examples of coated pigments include, but are not limited to, titanium dioxides that have been coated such as titanium dioxides:

[0071] - of hydrated silica, such as Tayca's MT-100WP product,

[0072] - of silica and iron oxide, such as the Sunveil F® product from Ikeda,

[0073] - of silica and alumina, such as Tayca's MT-500SA® and MT-100SA® products and Croda's Tioveil™ AQ-N,

[0074] - of alumina, such as Ishihara's TTO-55 (A)® product,

[0075] - of alumina and aluminum stearate, such as the MT-100TV® and MT-100Z products ® and MT-01® from Tayca, the Solaveil™ CT 100® product from Croda and the Eusolex T-AVO® product from Merck,

[0076] - of silica, alumina and alginic acid, such as Tayca's MT-100AQ® product,

[0077] - of alumina and aluminum laurate,

[0078] - of iron oxide and iron stearate,

[0079] - of zinc oxide and zinc stearate,

[0080] - of silica and alumina and treated with a silicone, such as the MTY-500SAS products ® or Microtitanium Dioxide MT-100SAS® from Tayca,

[0081] - of silica, alumina and aluminum stearate and treated with a silicone,

[0082] - of silica and treated with a silicone,

[0083] - of silica and treated with a silicone, such as Ishihara's TTO-55(S)® product,

[0084] - of triethanolamine,

[0085] - stearic acid, such as Ishihara's TTO-55 (C)® product,

[0086] - of sodium hexametaphosphate,

[0087] - of octyltrimethylsilane,

[0088] - of polydimethylsiloxane, of TiO2 anatase / rutile treated with a polydimethylhydrogenosiloxane

[0089] - of triethylhexanoin, aluminium stearate and alumina sold under the name commercial Solaveil™ CT-200 by Croda,

[0090] - of aluminium stearate, alumina and silicone, sold under the trade name Solaveil™ CT-12W by Croda,

[0091] - of lauroyl lysine, and / or

[0092] - of C9-Ci5 fluoroalcohol phosphate and aluminium hydroxide.

[0093] Other examples include TiO2 pigments doped with at least one transition metal such as iron, zinc, or manganese, preferably manganese. Preferably, the doped pigments are in the form of an oily dispersion. The oil present in the oily dispersion is preferably selected from triglycerides such as, for example, capric / caprylic acids. The oily dispersion of titanium dioxide particles may also include one or more dispersants, for example, a sorbitan ester, such as sorbitan isostearate, or a polyoxyalkylated glycerol fatty acid ester, such as tri-PPG-3 myristylether citrate and polyglyceryl-3 polyricinoleate. Preferably, the oily dispersion of titanium dioxide particles includes at least one dispersant selected from polyoxyalkylated glycerol fatty acid esters.One example is the oily dispersion of manganese-doped TiO2 particles in capric / caprylic acid triglyceride in the presence of tri-PPG-3 myristyl ether citrate and polyglyceryl-3 polyricinoleate and sorbitan isostearate, having the INCI name: titanium dioxide (and) TRLPPG-3 myristyl ether citrate (and) polyglyceryl-3 ricinoleate (and) sorbitan isostearate, for example the product sold under the trade name Optisol™ OTP-1 by Croda.

[0094] Suitable uncoated titanium oxide includes, but is not limited to, those sold by Tayca under the trade names MT-500B or MT-600B®, or by Evonik under the name Degussa P 25.

[0095] Appropriate examples of uncoated zinc oxide include, but are not limited to, zinc oxide marketed under the name "Z-COTE"® by BASF, zinc oxide marketed under the name "NanoArc® Zinc Oxide" by Nanophase Technologies, zinc oxide marketed under the name "MZ-500", "MZ-300", "MZ-200" or "MZ-150" by TAYCA.

[0096] Treated (coated) zinc oxide compounds are compounds that have undergone one or more surface treatments of a chemical, electronic, mechanochemical and / or mechanical nature with compounds such as described, for example, in Cosmetics & Toiletries, February 1990, Vol. 105, pp. 53-64, such as amino acids, beeswax, fatty acids, fatty alcohols, anionic surfactants, lecithins, sodium, potassium, zinc, iron or aluminum salts of fatty acids, metal alkoxides (titanium or aluminum), polyethylene, silicones, hydrated silica, proteins (collagen, elastin), alkanolamines, silicon oxides, triethoxycaprylylsilane, metal oxides or sodium hexametaphosphate.

[0097] Examples of suitable coated zinc oxide include, but are not limited to, polymethylhydrogenosiloxane-coated zinc oxide; zinc oxide dispersed in Cl2-15 alkyl benzoate (INCI: Zinc Oxide (and) Cl2-15 Alkyl Benzoate (and) Polyhydroxystearic Acid (and) Isostearic Acid), marketed by Croda under the trade name Solaveil CZ-100; zinc oxide dispersions in C9-12 alkane with a dispersing agent, marketed under the trade name "DAITOPERSION Zn-60VA"® by Daito Kasei; silicone-grafted acrylic polymer-coated ZnO dispersed in cyclodimethylsiloxane, marketed under the name "SPD-Z5®" by Shin-Etsu; ZnO coated with hydrated silica, marketed by TAYCA under the name "MZ-500HP"; ZnO coated with hydrated silica, triethoxysilyethyl polydimethylsiloxyethyl hexyl dimethicone and hydrogenodimethicone (H-Me-Si), marketed by TAYCA under the name MZ-510 HPSX;stearic acid-coated or isostearic acid-coated ZnO, such as those marketed by TAYCA under the name "MZ-505T", "MZY-505EX" or "MZY-304EX"; silicone oil-coated ZnO, such as those marketed by TAYCA under the name "MZX-510HPS", "MZY-505S", "MZY-510M3S", "MZ-505M", "MZY-303S", "MZY-303M", "MZY-203S", "MZY-210M3S" or "MZY-153S"; triethoxycaprylylsilane coated ZnO, such as those marketed by BASF under the name Z-COTE HP1, or by TAYCA under the name "MZX-508OTS", "MZY-203OTS" or "MZX-304OTS" or by DSM; under the name PARSOL ZX; for example: ZnO marketed under the brand name "Zinc Oxide CS-5" by Toshiba (ZnO coated with polymethylhydrosiloxane); ZnO marketed under the brand name "Nanogard Zinc Oxide FN" by Nanophase Technologies (as a 40% dispersion in Finsolv TN, C12-C15 alkyl benzoate); ZnO marketed under the brand names "Daitopersion Zn-30" and "Daitopersion Zn-50" by Daito (dispersions in oxyethylenated polydimethylsiloxane / cyclopolymethylsiloxane comprising 30% or 50% of zinc nanooxides coated with silica and polymethylhydrosiloxane); ZnO marketed under the brand name "NFD Ultrafine ZnO" by Daikin (ZnO coated with perfluoroalkyl phosphate and a perfluoroalkylethyl copolymer dispersed in cyclopentasiloxane); ZnO marketed under the brand name "SPD-Z1" by Shin-Etsu (ZnO coated with a silicone-grafted acrylic polymer dispersed in cyclodimethylsiloxane);ZnO marketed under the brand name "Escalol Z100" by ISP (alumina-treated ZnO dispersed in a copolymer mixture of ethylhexyl methoxycinnamate / PVP-hexadecene / methicone); ZnO marketed under the brand name "Fuji ZnO-SMS-10" by Fuji Pigment (ZnO coated with silica and polymethylsilsesquioxane); and ZnO marketed under the brand name "Nanox Gel TN" by Elementis (ZnO dispersed at 55% in C12-C15 alkyl benzoate with hydroxystearic acid polycondensate); ZnO marketed under the brand name Finex by SAKAI such as FINEX-50LP, FINEX-50S-LP2 and FINEX-30S-LPT (ZnO coated with hydrogenodimethicone); FINEX-33W (ZnO coated with hydrated silica), FINEX-52W-LP2 and FINEX-33W-LP2 (ZnO coated with hydrogenodimethicone and hydrated silica), FINEX-50-OTS and FINEX-30-OTS (ZnO coated with triethoxycaprylysilane). ;

[0098] Preferred coatings for zinc oxide preferably include one or more of the following: hydrated silica, triethoxysilylethyl polydimethylsiloxyethyl, hexyl dimethicone, hydrogenodimethicone, and / or triethoxycaprylysilane.

[0099] According to preferred embodiments of this disclosure, zinc oxide may be in the form of wafers, and may be coated or uncoated. Suitable examples of such forms are marketed by Croda under the name Solaveil (MicNo), such as Solaveil MXP3, MZP7, MZP8, MZ3-100, MZ3-300, and MZ7-100. Preferably, the zinc oxide wafers useful according to this disclosure (1) have a median specific surface area of ​​more than 25 square meters per gram, preferably greater than 30 square meters per gram, and / or (2) are transparent (i.e., transmission >30% at 600 nm). Suitable examples of such wafer forms may also be found in US Patent 11,608,275.

[0100] Suitable examples of other coated oxides include, but are not limited to, coated oxides preferably having amphiphilic properties such as:

[0101] cetyl phosphate and silica coated titanium oxides, such as Merck's "Eusolex® T-EASY" product;

[0102] titanium oxides coated with polyglyceryl-10 oleate and stearic acid, such as Tayca's "MTY-200STW";

[0103] zinc oxides coated with polyglyceryl-10 oleate and isostearic acid, such as Tayca's "MZY-505EXW";

[0104] titanium oxides coated with polysorbate 80 and isostearic acid, such as Tayca's "MT-10EXW"; and

[0105] zinc oxides coated with polysorbate 80 and isostearic acid, such as Tayca's "MZY-304EXW".

[0106] Preferably, the at least one ultraviolet (UV) attenuating physical material is present in the compositions of this disclosure in an amount of at least 5% by weight, preferably at least about 10% by weight, preferably at least about 12% by weight, preferably at least about 14% by weight, and preferably at least about 15% by weight, the upper end of the range of the at least one ultraviolet (UV) attenuating physical material present being preferably about 40% by weight (e.g., about 5 to 40%, about 10 to 40%, about 12 to 40%, etc.), preferably about 30% by weight (e.g., about 5 to 30%, about 10 to 30%, about 12 to 30%, etc.), preferably about 25% by weight (e.g., about 5 to 25%, about 10 to 25%, about 12 to 25%, etc.), and preferably about 20% by weight (for example, about 5 to 20%, about 10 to 20%, about 12 to 20%, etc.), all weights being based on the total weight of the composition.

[0107] According to preferred embodiments, the compositions of this disclosure contain a UV-absorbing system containing essentially one or more ultraviolet (UV) attenuating physical material(s) as defined above. Polyols

[0108] According to this disclosure, compositions comprising at least two polyols are proposed. Preferably, the polyol(s) in the compositions of this disclosure impart(s) humectant properties to the compositions.

[0109] “Polyol(s)” means compound(s) having two or more hydroxyl groups. Preferred polyols have from 2 to 20 carbon atoms, preferably from 2 to 8 carbon atoms, such as for example glycerol (glycerin), diglycerol, propylene glycol, isoprene glycol, dipropylene glycol, butylene glycol, hexane glycol, 1,3-propanediol, pentylene glycol, heptane glycol, caprylyl glycol, simple sugars and water-soluble polyalkylene glycols.

[0110] Preferred polyols in the compositions of this disclosure include glycerin and / or compounds with two hydroxyl groups (diols). Preferably, the compositions of this disclosure contain both (1) glycerin and (2) at least one diol.

[0111] According to preferred embodiments, the at least two polyols are present in the compositions of this disclosure in an effective combined amount of humectant such as, for example, about 0.1% to about 15% by weight relative to the total weight of the composition, about 0.25% to about 10% by weight, about 0.5% to about 7.5% by weight, and about 1% to about 5% by weight, including all intermediate ranges and sub-ranges such as, for example, about 4.5% to about 10% by weight, and about 2.5% to about 7.5% by weight, about 3% to about 15% by weight, about 5% to about 10% by weight, about 3% to about 10% by weight, etc., all weights being calculated relative to the total weight of the composition.According to preferred embodiments, the at least two polyols are present in compositions of this disclosure in an amount of at least about 3% by weight relative to the total weight of the composition.

[0112] According to preferred embodiments, where glycerin is present in compositions of this disclosure as one of the polyols, (1) the glycerin and (2) the other polyol(s) present in the composition are present in a weight % ratio of glycerin to other polyol(s) of about 10:1 to about 1:10, preferably about 8:1 to about 1:8, preferably about 7.5:1 to about 1:7.5, and preferably about 5:1 to about 1:5, including all intermediate ranges and sub-ranges, such as, for example, 5:1 to 2:1, 1:2 to 5:1, 8:1 to 1.5:1, 1:1.5 to 1:8, etc., all weights being based on the weight % of polyols present in the composition. Preferably, a higher weight % of glycerin is present in the compositions than the combined amount of other polyol(s). Anionic polysaccharide thickening agent

[0113] According to this disclosure, compositions comprising at least one anionic polysaccharide thickening agent are proposed. Suitable anionic polysaccharide thickening agents include anionic polysaccharide gums.

[0114] Suitable examples of anionic polysaccharide gums include, but are not limited to, polysaccharide gums produced by microorganisms; polysaccharide gums isolated from algae; and polysaccharide gums from higher plants, such as homogeneous polysaccharide gums, modified or unmodified, in particular celluloses, carrageenans, gellans, agars, xanthans, hyaluronates and alginates. In general, compounds of this type which may be used in compositions of the present disclosure may be found in Kirk-Othmer's Encyclopedia of Chemical Technology, Third Edition, 1982, Volume 3, pp. 896-900, and Volume 15, pp. 439-458, in Polymers in Nature by E.A. MacGregor and C.T. Greenwood, published by John Wiley & Sons, Chapter 6, p. 240-328, 1980, in the publication by Robert L. Davidson entitled Handbook of Water-Soluble Gums and Resins published by McGraw-Hill Book Company (1980) and in Industrial Gums - Polysaccharides and their Derivatives, edited by Roy L. Whistler, Second Edition, published by Academie Press Inc. Preferred polysaccharide thickening agents include carboxymethylcellulose, lambda-carrageenan, xanthan gum, sodium hyaluronate and mixtures thereof.

[0115] Preferably, the anionic polysaccharide thickening agent(s) is / are present in the compositions of the present invention in amounts ranging from about 0.1 to about 10% by weight, preferably from 0.2 to 5% by weight, preferably from 0.3 to 3% and preferably from 0.5 to 1.5% by weight, all weights being based on the weight of the composition as a whole, including all intermediate ranges and sub-ranges such as, for example, 0.1 to 1.5%, 0.5 to 1%, etc.

[0116] According to preferred embodiments, (1) the at least two polyols and (2) the at least one anionic polysaccharide thickening agent are present in compositions of this disclosure in a weight % ratio preferably of about 40:1 to about 1:10, preferably of about 20:1 to about 1:7.5, preferably of about 10:1 to about 1:5, and preferably of about 6:1 to about 1:1, including all intermediate ranges and sub-ranges, such as, for example, 5:1 to 2:1, 1:2 to 5:1, 8:1 to 1.5:1, 1:1.5 to 1:8, etc., all weights being based on the weight % of polyols and the weight % of anionic polysaccharide thickening agent(s) present in the composition. Preferably, a higher percentage by weight of polyols than of anionic polysaccharide thickening agent(s) is present in the compositions. Additional sunscreen agents

[0117] According to preferred embodiments of this disclosure, compositions optionally further comprising at least one additional UV filter (in addition to at least one physical ultraviolet (UV) attenuating material) selected from the group consisting of organic UV filters are proposed. However, as noted above, preferred embodiments of this disclosure include compositions of this disclosure containing a UV-absorbing system containing little or no organic UV filter as defined above.

[0118] The additional organic UV filter(s) may be hydrophilic or lipophilic. “Hydrophilic organic UV filter” means a water-soluble organic UV filter or a water-dispersible organic UV filter (in colloidal form). “Lipophilic organic UV filter” means a UV filter that is dissolved or dispersed in colloidal form in a liquid oil phase.

[0119] Suitable organic UV filters may be selected from the following non-exhaustive list of compounds: cinnamic compounds; anthranilate compounds; para-aminobenzoic acid compounds; salicylic compounds; dibenzoylmethane compounds; camphor compounds; benzophenone compounds; [3,[3-diphenylacrylate] compounds; triazine compounds such as bis-ethylhexyloxyphenol methoxyphenyl triazine; benzotriazole compounds; benzalmalonate compounds, including those cited in US patent 5,624,663; benzimidazole derivatives; imidazoline compounds; bis-benzoazolyl compounds as described in patents EP669323 and US 2,463,264; the compounds methylene bis(hydroxyphenylbenzotriazole) as described in applications US 5 237 071, US 5 166 355, GB2303549, DE197 26 184 and EP893119; the compounds benzoxazole as described in patent applications EP0832642, EP1027883, EP1300137 and DE10162844;Polymer filters and silicone filters such as those described in particular in application WO 93 / 04665; alkylstyrene-derived dimers such as those described in patent application DE19855649; 4,4-diarylbutadiene compounds such as those described in applications EP0967200, DE19746654, DE19755649, EP-A-1008586, EPI 133980 and EP133981, and mixtures thereof. Preferably, lipophilic organic UV filters are selected from salicylic compounds, dibenzoylmethane compounds, benzylidene camphor compounds; benzophenone compounds; triazine compounds; benzotriazole compounds; as well as other categories of compounds identified herein; and mixtures thereof.

[0120] Specific reference may be made to suitable salicylate compounds including Homosalate (homomentyl salicylate), for example marketed under the brand name "Eusolex HMS" by Rona / EM Industries; and ethylhexyl salicylate, for example marketed under the brand name "Neo Heliopan OS" by Symrise; and glycol salicylate. Other examples of salicylate compounds include phenyl salicylate; dipropylene glycol salicylate, for example marketed under the brand name "Dipsal" by Scher; and TEA salicylate, for example marketed under the brand name "Neo Heliopan TS" by Symrise.

[0121] Examples of suitable [3,[3-diphenylacrylate compounds include Octocrylene, for example marketed under the brand name "Uvinul N539" by BASF; and Etocrylene, for example marketed under the brand name "Uvinul N35" by BASF.

[0122] Suitable anthranilic compounds may include menthyl anthranilates, for example marketed under the brand name "Neo Heliopan MA" by Symrise.

[0123] Examples of dibenzoylmethane compounds include butyl methoxydibenzoylmethane, for example marketed under the brand name "Parsol 1789" by DSM; and isopropyl dibenzoylmethane.

[0124] Suitable cinnamyl compounds include ethylhexyl methoxycinnamate, marketed for example under the brand name "Parsol MCX" by DSM; isopropyl methoxycinnamate; isopropoxyl methoxycinnamate; isoamyl methoxycinnamate, marketed for example under the brand name "Neo Heliopan E 1000" by Symrise; cinoxate (2-ethoxyethyl-4-methoxycinnamate); DEA methoxycinnamate; diisopropyl methylcinnamate; and glyceryl dimethoxycinnamate ethylhexanoate.

[0125] Examples of camphor compounds include benzylidenecamphor derivatives: 3-benzylidene camphor, for example marketed under the brand name "Mexoryl SD" by Chimex; 4-methylbenzylidene camphor, for example marketed under the brand name "Eusolex 6300" by Merck; benzylidene camphor sulfonic acid, for example marketed under the brand name "Mexoryl SL" by Noveal; benzalkonium camphor methosulfate, for example marketed under the brand name "Mexoryl SO" by Noveal; terephthalylidene diamphrun sulfonic acid, for example marketed under the brand name "Mexoryl SX" by Noveal; and polyacrylamidomethyl benzylidene camphor, for example marketed under the brand name "Mexoryl SW" by Noveal.

[0126] Suitable benzophenone compounds include benzophenone-1 (2,4-dihydroxybenzophenone), such as that marketed under the brand name "Uvinul 400" by BASF; benzophenone-2 (tetrahydroxybenzophenone), such as that marketed under the brand name "Uvinul D50" by BASF; benzophenone-3 (2-hydroxy-4-methoxybenzophenone) or oxybenzone, such as that marketed under the brand name "Uvinul M40" by BASF; benzophenone-4 (hydroxymethoxybenzophonene sulfonic acid), such as that marketed under the brand name "Uvinul MS40" by BASF; benzophenone-5 (sodium hydroxymethoxybenzophenone sulfonate); benzophenone-6 (dihydroxy dimethoxybenzophenone), such as that marketed under the brand name "Helisorb 11" by Norquay; benzophenone-8, such as that marketed under the brand name "Spectra-Sorb UV-24" by American Cyanamid;benzophenone-9 (disodium dihydroxy dimethoxy benzophenonedisulfonate), such as that marketed under the brand name "Uvinul DS-49" by BASF, benzophenone-12 and 2-(4-diethylamino-; n-hexyl 2-hydroxybenzoyl)benzoate (such as that marketed under the brand name UVINUL A+ by BASF).

[0127] Examples of triazine compounds include 4-bis-{[4-(2-ethylhexyloxy)-2-hydroxy]-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine (INCI name: Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine (BEMT)), diethylhexyl butamido triazone, such as that marketed under the brand name "Uvasorb HEB" by Sigma 3V; 2,4,6-tris(dineopentyl 4'-aminobenzalmalonate)-s-triazine, bis-ethylhexyloxyphenol methoxyphenyl triazine, such as that marketed under the brand name "TINOSORB S" by BASF and ethylhexyl triazone, such as that marketed under the brand name "UVINUL T150" by BASF.

[0128] Suitable benzotriazole compounds include phenylbenzotriazole derivatives: 2-(2H-benzotriazole-2-yl)-6-dodecyl-4-methylpheno, branched and linear, and those described in USP 5240975.

[0129] Suitable benzalmalonate compounds include dineopentyl 4'-methoxybenzalmalonate and polyorganosiloxane comprising benzalmalonate functional groups, such as polysilicone-15, such as that marketed under the brand name "Parsol SLX" by Hoffmann-LaRoche.

[0130] Examples of benzimidazole compounds include, in particular, phenylbenzimidazole derivatives such as phenylbenzimidazole sulfonic acid, such as that marketed in particular under the brand name "Eusolex 232" by Merck, and phenyl dibenzimidazole tetrasulfonate disodium, such as that marketed under the brand name "Neo Heliopan AP" by Symrise.

[0131] Suitable imidazoline compounds include ethylhexyl dimethoxybenzylidene propionate dioxoimidazoline.

[0132] Examples of bis-benzoazolyl compounds include the compounds described in EP-669 323 and US patent no. 2 463 264.

[0133] Suitable para-aminobenzoic acid compounds include PABA (p-aminobenzoic acid), ethyl PABA, ethyl dihydroxypropyl PABA, pentyl dimethyl PABA, ethylhexyl dimethyl PABA, such as that marketed under the brand name "Escalol 507" by ISP, glyceryl PABA, and PEG-25 PABA, such as that marketed under the brand name "Uvinul P25" by BASF.

[0134] Suitable methylene bis-(hydroxyphenylbenzotriazole) compounds include 2,2'-methylenebis[6-(2H-benzotriazol-2-yl)-4-methylphenol] such as that marketed under the brand name "Mixxim BB / 200" by Fairmount Chemical, 2,2'-methylenebis[6-(2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)phenol], such as that marketed in micronized aqueous dispersion form under the brand name "Tinosorb M" by BASF or under the brand name "Mixxim BB / 100" by Fairmount Chemical, and derivatives as described in US patents Nos. 5,237,071 and 5,166 355, GB-2 303 549, DE-197 26 184 and EP-893 119, and drometrizole trisiloxane, such as that marketed under the brand name "Silatrizole" by Rhodia Chimie or - "Mexoryl XL" by L'Oréal.

[0135] Examples of benzoxazole compounds include 2,4-bis[5-l(dimethylpropyl)benzoxazol-2-yl-(4-phenyl)imino]-6-(2-ethylhexyl)imino-l,3,5-triazine, such as that marketed under the brand name Uvasorb K2A by Sigma 3V.

[0136] Suitable examples of shielding polymers and shielding silicones include the silicones described in WO 93 / 04665.

[0137] Suitable α-alkylstyrene derived dimers include the dimers described in DE-19855649.

[0138] Examples of 4,4-diarylbutadiene compounds include l,l-dicarboxy(2,2'-dimethylpropyl)-4,4-diphenylbutadiene.

[0139] If present, at least one additional organic UV filter is preferably present in the compositions of this disclosure in an amount of at least about 1% by weight, preferably at least about 5% by weight, preferably at least about 10% by weight, preferably at least about 12.5% ​​by weight, and preferably at least about 15% by weight, the upper end of the range of additional UV filter present preferably being about 40% by weight (e.g., about 1 to 40%, about 10 to 40%, about 12.5 to 40%, etc.), preferably about 30% by weight (e.g., about 5 to 30%, about 10 to 30%, about 15 to 30%, etc.), preferably about 25% by weight (e.g., about 5 to 25%, about 10 to 25%, about 15 to 25%, etc.), and preferably about 20% by weight (e.g., about 1 to 20%, about 5 to 20%, about 10 to 20%, etc.), all weights being based on the total weight of the composition.

[0140] According to preferred embodiments, the compositions of this disclosure comprise 10% or less by weight relative to the total weight of the composition of these optional additional UV filters, preferably less than 7.5% by weight relative to the total weight of the composition, preferably less than 5% by weight relative to the total weight of the composition, preferably less than 3% by weight relative to the total weight of the composition, and preferably less than 1% by weight relative to the total weight of the composition.

[0141] According to preferred embodiments, the compositions of this disclosure further comprise at least one additional organic UV filter selected from the group consisting of 4-bis-{[4-(2-ethylhexyloxy)-2-hydroxy]-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine (INCI name: Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine), avobenzone (butyl methoxydibenzoylmethane), octisalate (ethylhexyl salicylate), ensulizole (Phenylbenzimidazole sulfonic acid), homosalate, octocrylene, and mixtures thereof. In such embodiments, the UV-absorbing system may "consist of" or "consist essentially of" (1) at least one physical ultraviolet (UV) attenuating material and (2) at least one organic UV filter selected from the group consisting of 4-bis-{[4-(2-ethylhexyloxy)-2-hydroxy]-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine (INCI name: Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine), avobenzone (butyl methoxydibenzoylmethane), octisalate (ethylhexyl salicylate), ensulizole (Phenylbenzimidazole sulfonic acid), homosalate, octocrylene, and mixtures thereof.

[0142] According to other preferred embodiments, however, the compositions of this disclosure are "free", "substantially free" or "devoid" as defined above of one or more additional organic UV filters selected from the group consisting of 4-bis-{[4-(2-ethylhexyloxy)-2-hydroxy]-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine (INCI name: Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine), avobenzone (butyl methoxydibenzoylmethane), octisalate (ethylhexyl salicylate), ensulizole (Phenylbenzimidazole sulfonic acid), homosalate, and octocrylene, preferably two or more, preferably three or more, preferably four or more, or preferably all five of these sunscreen agents.

[0143] According to preferred embodiments, the compositions of this disclosure are "free", "substantially free" or "devoid", as defined above, of one or more additional organic UV filters selected from the group consisting of OXYBENZONE (benzophenone-3), OCTINOXATE (ethylhexyl methoxycinnamate), ETHYLHEXYL TRIAZONE, DROMETRIZOLE TRISILOXANE, METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYL PHENOL, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, DIETHYLHEXYL BUTAMIDO TRIAZONE, DTSOAMYL P-METHOXYCINNAMATE, POLYSILICONE-15, 4-METHYLBENZYLIDENE CAMPHOR, PHENYL DIBENZIMIDAZOLE DISODIUM TETRASULFONATE, METHOXYPROPYLAMINO CYCLOHEXENYLIDENE METHOXYETHYLCYANOACETATE, 4-bis-{[4-(2-ethyl hexyloxy)-2-hydroxy]-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine (INCI name: Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine), preferably two or more, preferably three or more, preferably four or more, etc.and preferably "free", "significantly free" or "devoid" of all these sunscreen agents.

[0144] According to preferred embodiments, the compositions of this disclosure are "free", "substantially free" or "devoid" of OXYBENZONE (benzophenone-3) and / or OCTINOXATE (ethylhexyl methoxycinnamate) and / or 4-bis-{[4-(2-ethylhexyloxy)-2-hydroxy]-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine (INCI name: Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine).

[0145] According to preferred embodiments, the UV-absorbing system of the compositions of this disclosure may "consist of" or "consist essentially of" at least one physical ultraviolet (UV) attenuating material.

[0146] According to preferred embodiments, this disclosure envisages omitting one or more of the specific UV filters mentioned above from the UV-absorbing system of the compositions of this disclosure. By way of example, octocrylene and / or octinoxate may be omitted from the compositions. A similar omission of one or more of the specific UV filters mentioned is thus envisaged. Oil

[0147] According to preferred embodiments of this disclosure, compositions further comprising at least one oil are proposed. “Oil” means a substance that is hydrophobic and lipophilic, and is a liquid at approximately room temperature (20 to 25 °C) and approximately atmospheric pressure (760 mm Hg).

[0148] Suitable oils include volatile and / or non-volatile oils. These oils may be any acceptable oil, including, but not limited to, silicone oils and / or hydrocarbon oils.

[0149] According to certain embodiments, the compositions of this disclosure preferably comprise one or more volatile silicone oils. Examples of such volatile silicone oils include linear or cyclic silicone oils having from 2 to 7 silicon atoms, these silicones optionally being substituted with alkyl or alkoxy groups of 1 to 10 carbon atoms. Specific oils that may be used in the disclosure include octamethyltetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane, heptamethyloctyltrisiloxane, hexamethyldisiloxane, decamethyltetrasiloxane, dodecamethylpentasiloxane, and mixtures thereof. Other volatile oils that may be used include KF 96A with a viscosity of 6 cSt, a commercial product from Shin Etsu with a flash point of 94 °C. Preferably, volatile silicone oils have a flash point of at least 40°C.

[0150] Non-limiting examples of volatile silicone oils are listed in Table 1 below.

[0151] [Tables 1] Compound Flash Point (°C) Viscosity (cSt) Octyltrimethicone 93 1.2 Hexyltrimethicone 79 1.2 Decamethylcyclopentasiloxane 72 4.2 (cyclopentasiloxane or D5) Octamethylcyclotetrasiloxane 55 2.5 (cyclotetramethylsiloxane or D4) Dodecamethylcyclohexasiloxane (D6) 93 7 Decamethyltetrasiloxane (L4) 63 1.7 KF-96 A from Shin Etsu 94 6 PDMS (polydimethylsiloxane) DC 200 (1.5 cSt) 56 1.5 from Dow Corning PDMS DC 200 (2 cSt) from Dow Corning 87 2

[0152] In addition, a linear volatile silicone oil may be used in this disclosure. Suitable linear volatile silicone oils include those described in US Patent No. 6,338,839 and in WO03 / 042221. In one embodiment, the linear volatile silicone oil is decamethyltetrasiloxane. In another embodiment, decamethyltetrasiloxane is further combined with another solvent that is more volatile than decamethyltetrasiloxane.

[0153] According to certain embodiments of this disclosure, the composition preferably comprises one or more non-silicone volatile oils, which may be selected from volatile hydrocarbon oils, volatile esters, and volatile ethers. Examples of such non-silicone volatile oils include, but are not limited to, volatile hydrocarbon oils having 8 to 16 carbon atoms and mixtures thereof, and in particular, C8-Ci6 branched alkanes such as C8-Ci6 isoalkanes (also known as isoparaffins), isohexadecane, isododecane, isodecane, and, for example, oils sold under the trade names Isopar or Permethyl. Preferably, the non-silicone volatile oils have a flash point of at least 40°C.

[0154] Non-limiting examples of non-silicone volatile oils are given in Table 2 below.

[0155] [Tables2] Compound Flash Point (°C) Isododecane 43 Propylene glycol n-butyl ether 60 Ethyl 3-Ethoxypropionate 58 Propylene glycol acetate methyl ether 46 Isopar L (Cn-Ci3 isoparaffin) 62 Isopar H (Cn-Ci2 isoparaffin) 56

[0156] According to certain embodiments of this disclosure, the composition includes at least one non-volatile oil. Examples of non-volatile oils that oils that may be used in this disclosure include, but are not limited to, polar oils such as, for example:

[0157] - esters and ethers, in particular fatty acids, such as oils of formula R1COOR2, in which RI represents the remainder of a fatty acid having from 8 to 29 carbon atoms, and R2 represents a hydrocarbon chain, branched or unbranched, containing from 2 to 30 carbon atoms, such as, for example, Purcellin oil, ethyl oleate, ethyl stearate, isononyl isononanoate, isopropyl myristate, ethyl-2-hexyl palmitate, octyl-2-dodecyl stearate, octyl-2-dodecyl erucate, isostearyl isostearate; hydroxylated esters such as isostearyl lactate, octylhydroxy stearate, octyldodecyl hydroxystearate, diisostearyl malate, triisocetyl citrate, heptanoates, octanoates, fatty alcohol decanoates; polyol esters, such as propylene glycol dioctanoate, neopentyl glycol diheptanoate and diethylene glycol diisononanoate;glyceryl triesters such as glycerol and C12-C22 fatty acid triesters, preferably C16-C18 fatty acid triesters, preferably C18 fatty acid triesters, such as glycerin and isostearic acid triester (triisostearine), glycerin and stearic acid triester (tristearine), glycerin and oleic acid triester (triolein), glyceryl tripalmitate, glyceryl trilaurate, etc.; and pentaerythritol esters such as pentaerythrityl tetraisostearate or dipentaerythrityl pentaisononanoate;

[0158] - ethers containing 10 to 40 carbon atoms;

[0159] - liquid C8 to C26 fatty alcohols, for example oleyl alcohol, alcohol cetyl alcohol, stearyl alcohol, octyldodecanol and cetearyl alcohol;

[0160] - hydrocarbon oils of animal origin, such as perhydrosqualene;

[0161] - vegetable hydrocarbon oils, such as liquid triglycerides of fatty acids having 4 to 10 carbon atoms such as triglycerides of heptanoic or octanoic acid, for example, sunflower, corn, soybean, cucurbit, grapeseed, sesame, hazelnut, apricot, macadamia, ara, sunflower, castor oil, avocado oil, triglycerides of caprylic / capric acid, such as those sold by the Stéarineries Dubois company or those sold under the names Miglyol 810, 812, and 818, by the Dynamit Nobel Company, coco-caprylate / caprate (esterified coconut oil), jojoba oil, shea butter oil; and

[0162] - their mixtures.

[0163] In addition, examples of non-volatile oils that may be used in this disclosure include, but are not limited to, non-polar oils such as branched and unbranched hydrocarbons, in particular Vaseline (petrolatum), paraffin oil, squalane, squalene, hydrogenated polyisobutene, hydrogenated polydecene, polybutene, a mineral oil, pentahydrosqualene and mixtures thereof.

[0164] According to certain embodiments of this disclosure, the compositions of this disclosure may include at least one non-volatile silicone oil. Appropriate examples of such silicone oils include, but are not limited to, non-volatile silicone fluids such as, for example, polyalkyl (aryl) siloxanes. Appropriate polyalkyl siloxanes include, but are not limited to, polydimethyl siloxanes, which are designated CTFA dimethicone, polydiethyl siloxane, phenyl trimethicone, trimethyl pentaphenyl trisiloxane, phenyldimethicone, phenyltrimethylsiloxydiphenylsiloxane, diphenyldimethicone, and diphenylmethyldiphenyltrisiloxane, and the siloxanes disclosed in US Patent Application Publication No. 2004 / 0126350.Specific examples of suitable high viscosity silicone oils include, but are not limited to, PCR 15 M 30 (500 cSt) or Wacker Belsil PDM 1000 (1000 cSt) and Dow Corning 200 (350 cSt) (values ​​in parentheses represent viscosities at 25 °C).

[0165] Particularly preferred oils include, but are not limited to, one or more of the following: diisopropyl sebacate, C12-15 alkyl benzoate, phenethyl benzoate, isopropyl lauroyl sarcosinate, diisopropyl adipate, dibutyl adipate, dicaprylyl carbonate, dicaprylate / dicaprate, coco glycerides, caprylic / capric triglyceride, isopropyl myristate, isopropyl palmitate, coco caprylate / caprate, ethylhexyl palmitate, isononyl isononanoate, octyl dodecanol, isohexadecane, isododecane, dicaprylyl ether, C15-19 alkane, and mixtures thereof.

[0166] According to preferred embodiments, at least one oil is present in the compositions of this disclosure in an amount ranging from about 1% to about 50% by weight, more preferably from about 5% to about 40% by weight, and preferably from about 10% to about 35% by weight, based on the total weight of the composition, including all ranges and sub-ranges within those ranges, such as 15% to 40%, 20% to 45%, etc. Aqueous Phase

[0167] The compositions of this disclosure may also optionally contain water. When the compositions of this disclosure contain water, they are preferably in the form of an emulsion. Preferably, when the compositions of this disclosure contain water, they are in the form of an emulsion containing an external aqueous phase such as an oil-in-water (O / W) emulsion or a water-in-oil-in-water (W / O / W) emulsion, or an emulsion containing an external oil phase such as a water-in-oil (W / O) emulsion or an oil-in-water-in-oil (W / O / O) emulsion. Preferably, when in the form of an emulsion, the oily phase may contain silicone oils (e.g., Si / E or E / Si emulsion) or hydrocarbon oils. When present, water is preferably present in an amount of about 10% to about 80% by weight, preferably about 20% to about 70% by weight, preferably about 35% to about 65% by weight, including all intermediate ranges and sub-ranges, all weights being based on the total weight of the composition.

[0168] If present in compositions of this disclosure, the aqueous phase may include at least one water-soluble organic solvent that is liquid at room temperature and atmospheric pressure. For example, such at least one water-soluble organic solvent may include C1-C5 monoalcohols having a C1-C5 alkane chain and a single hydroxyl (OH) group. Suitable C1-C5 monoalcohols include methanol, ethanol, propanol, isopropanol, butanol, and mixtures thereof.

[0169] If present, the water-soluble organic solvent(s) is / are preferably present in the compositions of this disclosure in an amount ranging from about 0.5% to about 40% by weight, preferably from about 3% to about 30% by weight, and preferably from about 5% to about 20% by weight relative to the total weight of the composition, including all intermediate ranges and sub-ranges such as, for example, 2% to 15%, 2% to 25%, 7.5% to 30%, etc. Additional optional ingredients

[0170] The compositions of this disclosure may also optionally include at least one additional additive or auxiliary commonly used in cosmetic compositions and known to a person skilled in the art as being capable of being incorporated into such compositions. Such additives or auxiliaries may be selected from film-forming agents, coloring agents (e.g., dyes and pigments), waxes, thixotropic agents (e.g., clays), fillers, preservatives, perfumes, surfactants, antioxidants, free radical scavengers, spreading agents, dispersing agents, antifoaming agents, neutralizing agents, stabilizing agents, active ingredients selected from essential oils, moisturizing agents, vitamins, active ingredients, proteins, ceramides, plant extracts, fibers and the like, wetting agents and mixtures thereof.However, preferably, the compositions in this disclosure are "free", "substantially free" or "devoid" of such additives.

[0171] A person skilled in the art shall ensure that the optional additional additives are chosen and / or their quantity so that the advantageous properties of the composition as disclosed are not, or are not substantially, compromised by the envisaged addition.

[0172] It goes without saying that the composition of the disclosure must be cosmetically or dermatologically acceptable, that is, it must contain a physiologically acceptable, non-toxic carrier. The composition may be in any pharmaceutical form normally used in the cosmetic and dermatological fields that is suitable for topical administration as mentioned above.

[0173] These auxiliary additives may be present in the composition in a proportion of 0% to 99% (such as 0.01% to 90%) relative to the total weight of the composition and furthermore such as 0.1% to 50% by weight (where appropriate), including all intermediate ranges and sub-ranges.

[0174] In accordance with this disclosure, the compositions of this disclosure may be a standalone product (for use alone), or they may be a product for use in conjunction with another composition, for example, a base coat composition (makeup base), a color coat composition, or a top coat composition (overcoat). It should be understood that when compositions of this disclosure are applied to keratinous materials in the form of any such composition, such application may include one or more coats of the product.Thus, for example, the application of at least one color layer composition may include one or more color layers; the application of at least one topcoat composition may include one or more topcoats; the application of at least one basecoat composition may include one or more basecoats. Preferably, such basecoat, color layer, and topcoat compositions contain three or fewer layers of compositions, preferably two or fewer layers of compositions, and preferably only one layer of compositions.

[0175] During the application of the compositions of this disclosure, the base coat (if present) is typically applied directly to the keratinous material, the color coat is typically applied either directly to the keratinous material (if no base coat is present), or to a previously applied base coat, and the top coat (if present) is typically applied to a color coat.

[0176] According to preferred embodiments of this disclosure, methods for treating, protecting, improving the appearance, caring for and / or making up a keratinous material by applying compositions of this disclosure to the keratinous material in a quantity sufficient to treat the keratinous material, improve its appearance, care for it and / or make it up, are proposed.

[0177] Preferably, the "makeup" of the keratinous material includes the application of a composition comprising at least one coloring agent to the keratinous material in a sufficient quantity to provide color and / or an optical effect to the keratinous material.

[0178] Preferably, the "protection" of the keratinous material includes the application of a composition of this disclosure to protect the keratinous material from damage resulting from exposure to UV rays.

[0179] According to the preceding embodiments, the compositions of this disclosure are applied topically to the keratinous material in a sufficient quantity to treat, improve the appearance of, care for, and / or conceal the keratinous material. The compositions can be applied to the desired area as needed, preferably once or twice daily, more preferably once daily, and then preferably allowed to dry before being subjected to contact such as with clothing or other objects (e.g., clothing or a top coat). Preferably, the composition is allowed to dry for about 1 minute or less, more preferably for about 45 seconds or less.

[0180] According to preferred embodiments of this disclosure, methods are proposed for producing stable compositions comprising at least one ultraviolet (UV) attenuating physical material by combining at least one ultraviolet (UV) attenuating physical material with at least two polyols and at least one anionic polysaccharide thickening agent in the compositions during the formation of the compositions to produce stable compositions.

[0181] This disclosure also considers kits and / or pre-packaged materials suitable for use by a consumer containing one or more compositions as described herein, alone or in combination with makeup products such as primers, top coats, makeup removers, etc. The packaging and application device for any subject of this disclosure may be selected and manufactured by persons skilled in the art based on their general knowledge and adapted according to the nature of the composition to be packaged. Indeed, the type of device to be used may be particularly related to the consistency of the composition, especially its viscosity; it may also depend on the nature of the constituents present in the composition, for example, the presence of volatile compounds.

[0182] Unless otherwise stated, all numbers expressing quantities of ingredients, reaction conditions, etc., used in the patent memorandum and claims are to be understood as modified in all cases by the term "approximately." Accordingly, unless otherwise stated, the numerical parameters presented in the following patent memorandum and the attached claims are approximations that may vary depending on the desired properties that are sought to be obtained through this disclosure.

[0183] Although the numerical ranges and parameters defining the general scope of disclosure are approximations, the numerical values ​​shown in the specific examples are reported as accurately as possible. However, every numerical value inherently contains some error that necessarily results from the standard deviation found in its respective measurements. The following examples are intended to illustrate disclosure without, however, limiting its scope. Percentages are provided on a weighted basis. Example 1

[0184] The following compositions were prepared at room temperature (1 kg total quantity) using a Rayneri VMI rotor-stator tool. The aqueous thickening agent was slowly incorporated into the aqueous phase (water, glycerin, and pentylene glycol). After 10 minutes of shearing with the rotor-stator (high shear, 3000 rpm), the ZnO powder was gradually added at the same high shear rate for an additional 20 minutes.

[0185] The stability of the prepared compositions was determined by visual observation, and the viscosity of the prepared compositions was measured at room temperature with a LAMY RM180 rotary viscometer equipped with a movable Ms R 2 immediately after preparation (t0), after 4 hours of rest (t4h), and / or after 3 or 23 days of rest (t3d or t23d) (as shown). The viscosity value was measured after 10 minutes of rotation of the tool in the cup to reach a plateau value, expressed in mPa·s using a lookup curve between the raw data expressed in deviation units (DU) and mPa·s. A. Compositions containing xanthan gum

[0186] [Tables3] Composition (% w / w) Inventive Composition 1 Comparative Composition IA Comparative Composition IB Comparative Composition IC ZnO 5.16 5.16 5.58 5.58 Hydrated Silica 0.6 0.6 0 0 Hydrogenodimethicone 0.24 0.24 0 0 Triethoxycaprylylsilane 0 0 0.42 0.42 Glycerin 3 0 3 0 Pentylene glycol 2 0 2 0 Xanthan Gum 1 1 1 1 Stability at t0 (visual observation) Smooth, fine, and homogeneous appearance Smooth, fine, and homogeneous appearance Coarse agglomerates, lumpy appearance Coarse agglomerates, lumpy appearance Evolution of viscosity between t0 and t4h 295 to 280 mPa·s -5% change 665 to 333 mPa·s -50% change Not measured Not measured

[0187] The inventive composition 1 was a stable composition with a smooth, fine, and homogeneous appearance, and a stable viscosity after manufacturing. The comparative compositions 1A-1C were neither unstable (composition IA - 50% decrease immediately after manufacturing) nor heterogeneous with coarse agglomerates and a lumpy appearance (compositions IB and IC). B. Compositions containing lambda carrageenan

[0188] [Tables4] Inventive Composition 2 Comparative Composition 2A Comparative Composition 2B Comparative Composition 2C ZnO 5.16 5.16 5.58 5.58 Hydrated Silica 0.6 0.6 0 0 Hydrogenodimethicone 0.24 0.24 0 0 Triethoxycapryl ylsilane 0 0 0.42 0.42 Glycerin 3 0 3 0 Pentylene glycol 2 0 2 0 Lambda carrageenan 1 1 1 1 Stability at t3d (visual observation) Smooth, thin and homogeneous appearance Smooth, thin and homogeneous appearance Phase separation with a thick and opaque upper phase Phase separation with a thick and opaque upper phase Evolution of appearance between t0 and t3d No change, fluid lotion Evolution from fluid lotion to cream Not evaluated No evaluated

[0189] The inventive composition 1 was a stable composition with a smooth, thin, and homogeneous appearance, and a stable viscosity after 3 days. The comparative compositions 2A-2C were neither unstable (composition 2A - significant increase in the cream form after 3 days) nor had undergone phase separation with a thick and opaque upper phase (compositions 2B and 2C).

[0190] C. Compositions containing sodium hyaluronate

[0191] [Tables5] Inventive Composition 3 Comparative Composition 3A Comparative Composition 3B Comparative Composition 3C ZnO 5.16 5.16 5.58 5.58 Hydrated Silica 0.6 0.6 0 0 Hydrogenodimethicone 0.24 0.24 0 0 Triethoxycaprylylsilane 0 0 0.42 0.42 Glycerin 3 0 3 0 Pentylene glycol 2 0 2 0 Sodium Hyaluronate 1 1 1 1 Stability at t23 days (visual observation) Smooth, fine and homogeneous appearance Phase separation with a thick and opaque upper phase Phase separation with a thick and opaque upper phase Phase separation with a thick and opaque upper phase

[0192] The inventive composition 3 was a stable composition with a smooth, thin, and homogeneous appearance, and a stable viscosity after 23 days. The comparative compositions 3A-3C had not undergone phase separation with a thick and opaque upper phase after 23 days.

Claims

Demands

1. Composition comprising at least one ultraviolet (UV) attenuating physical material, preferably at least one metal oxide, preferably at least one metal oxide selected from titanium, chromium, zinc, tin, alumina, cerium, and / or iron oxides, and more preferably zinc oxide and / or titanium dioxide; at least two polyols; and at least one anionic polysaccharide thickening agent, the at least one anionic polysaccharide thickening agent preferably being at least one anionic polysaccharide gum, preferably selected from the group consisting of carboxymethylcellulose, carrageenan, xanthan gum, hyaluronate and mixtures thereof.

2. Composition according to claim 1, wherein the at least two polyols comprise glycerin and / or at least one diol, preferably both.

3. Composition according to any one of claims 1 and 2, wherein the at least two polyols are present in a combined amount of at least 3% by weight relative to the total weight of the composition.

4. Composition according to any one of claims 1 to 3, wherein glycerin is present in the composition as one of at least two polyols, and preferably more glycerin is present in the composition than in the combined amount of other polyol(s) present in the composition.

5. Composition according to any one of claims 1 to 4, wherein at least one ultraviolet (UV) attenuating physical material is present in the composition in an amount of at least 5% by weight relative to the total weight of the composition, preferably from about 5% to about 40% by weight relative to the total weight of the composition.

6. Composition according to any one of claims 1 to 5, in the form of an emulsion.

7. Composition according to any one of claims 1 to 6, wherein at least one ultraviolet (UV) attenuating physical material is surface-treated with a surface treatment agent, the surface treatment agent preferably comprising at least one of amino acids, beeswax, fatty acids, salts of fatty acids, fatty alcohols, anionic surfactants, lecithin compounds, metal alkoxides, polyethylene, silicones, proteins, alkanolamines, silicon oxides, metal oxides other than at least one physical ultraviolet (UV) attenuating material, sodium hexametaphosphate, alumina, glycerol, and mixtures thereof.

8. Composition according to any one of claims 1 to 7, wherein at least one ultraviolet (UV) attenuating physical material comprises zinc oxide and / or titanium dioxide, preferably coated with a coating agent, the coating agent preferably comprising at least one of hydrated silica, triethoxysilylethylpolydimethylsiloxyethyl, hexyldimethicone, hydrogenodimethicone, triethoxycaprylysilane and mixtures thereof.

9. Composition according to any one of claims 1 to 8, wherein at least one ultraviolet (UV) attenuating physical material comprises zinc oxide, preferably passivated or coated with hydrated silica and / or hydrogenodimethicone.

10. Composition according to any one of claims 1 to 9, wherein at least one ultraviolet (UV) attenuating physical material has a primary average particle size of 1 nm to 500 nm, preferably 5 nm to 250 nm, preferably 10 nm to 100 nm, preferably 10 nm to 50 nm, preferably 20 nm to 40 nm.