Method for producing a cosmetic composition comprising a sucrose ester and a solvent

By employing specific sucrose esters and solvents with defined parameters, the solubility and sensory feel of cosmetic compositions are enhanced, addressing the solubility challenges of sucrose esters in cosmetic formulations.

JP7620104B2Active Publication Date: 2025-01-22PROCTER & GAMBLE CO
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Patent Information

Application Number
JP2023534891
Authority / Receiving Office
JP · JP
Patent Type
Patents
Current Assignee / Owner
Priority Date
2020-12-14
Filing Date
2021-12-08
Publication Date
2025-01-22
Estimated Expiration
2041-12-08

AI Technical Summary

Technical Problem

Sucrose esters, when included at higher levels or in the aqueous phase of cosmetic compositions, face solubility challenges, and there is a need for a method to dissolve them while maintaining a fresh/light feel.

Method used

A method involving sucrose esters with specific fatty acid carbon ranges and solvents with defined solubility parameters is used to ensure sucrose esters dissolve in cosmetic compositions, even at higher concentrations, by incorporating an aqueous carrier through controlled mixing steps.

Benefits of technology

The method enables sucrose esters to dissolve in cosmetic compositions, providing their benefits with a light, non-greasy sensory feel.

✦ Generated by Eureka AI based on patent content.

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Abstract

The present invention provides a method for producing a sucrose ester comprising: (a) one or more esters of sucrose and fatty acids, wherein the fatty acids are selected from those having from about 12 to about 24 carbon atoms, and the sucrose esters are selected from the group consisting of monoesters, diesters, triesters, tetraesters, and mixtures thereof; and (b) one or more esters of sucrose having a viscosity of from about 23 to about 31.5 (J / cm 3 ) 1 / 2 and a Hildebrand solubility parameter of about 4.5 to about 10.5 (J / cm 3 ) 1 / 2 and one or more solvents selected from those having a polar component with a Hansen solubility parameter of 0.05 to 0.05, and a solvent having a polar component with a Hansen solubility parameter of 0.05 to 0.05, respectively. The method for producing a cosmetic composition of the present invention makes it possible to dissolve a sucrose ester in a cosmetic composition even when the sucrose ester is contained in a high concentration in the composition and / or when the sucrose ester is contained in the aqueous phase of the cosmetic composition.
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Description

[Technical field]

[0001] The present invention relates to a method for producing a sucrose ester comprising the steps of: (a) one or more esters of sucrose and fatty acids, the fatty acids being selected from those having from about 12 to about 24 carbon atoms, the sucrose esters being selected from the group consisting of monoesters, diesters, triesters, tetraesters, and mixtures thereof; and (b) one or more esters having a viscosity of from about 23 to about 31.5 (J / cm 3 ) 1 / 2 and a Hildebrand solubility parameter of about 4.5 to about 10.5 (J / cm 3 ) 1 / 2 and one or more solvents selected from those having a polar component with a Hansen solubility parameter of 0.05 to 0.05, and a mixture of 0.05 to 0.05% by weight of the sucrose ester. By the method for producing a cosmetic composition of the present invention, even when the sucrose ester is contained in a high concentration in the composition and / or when the sucrose ester is contained in the aqueous phase of the cosmetic composition, the sucrose ester can be dissolved in the cosmetic composition. [Background technology]

[0002] Mammalian keratinous tissue, particularly human skin, is exposed to various damages caused by both exogenous and intrinsic factors. Such exogenous factors include ultraviolet light, environmental pollution, wind, heat, infrared rays, low humidity, harsh surfactants, abrasives, etc. Meanwhile, intrinsic factors include chronological aging and other biochemical changes from within the skin. Whether exogenous or intrinsic, these factors result in visible signs of skin damage. Typical skin damage in aged or damaged skin includes fine lines, wrinkles, hyperpigmentation, yellowing, sagging, dark circles under the eyes, puffy eyes, enlarged pores, slow turnover rate, and abnormal desquamation or peeling. Further damage resulting from both exogenous and intrinsic factors includes visible dead skin, i.e. peeling, desquamation, dryness, and roughness.

[0003] Currently, many personal care products are available to consumers that are aimed at improving the health and physical appearance of keratinous tissues such as skin, hair, and nails. Most of these products are aimed at delaying, minimizing, or even eliminating wrinkles, age spots, and other histological changes of the skin that accompany skin aging or environmental damage to human skin. Consumers prefer topically applied products because they are not only effective, but also safe and comfortable to use.

[0004] In these products, various ingredients are used to provide the above-mentioned advantages.The inventors have found that one of these ingredients, namely sucrose ester, can be difficult to dissolve in product composition, especially when sucrose ester is contained in higher levels in the product composition, and / or especially when sucrose ester is contained in the water phase of the product composition.While providing the advantages of sucrose ester, it has also been found that in terms of providing fresh / light feeling from the composition, it may be preferable for sucrose ester to be dissolved in the water phase of the product composition rather than in the oil phase. Summary of the Invention [Problem to be solved by the invention]

[0005] Based on the above, there is a need for a method of making a cosmetic composition that dissolves sucrose esters in the cosmetic composition, especially when the sucrose esters are included in the composition at higher levels, and / or especially when the sucrose esters are included in the aqueous phase of the cosmetic composition. Additionally, there is a need for a method of making a cosmetic composition, where the produced cosmetic composition provides the benefits of the sucrose esters while providing a fresh / light feel from the composition. [Means for solving the problem]

[0006] The present invention provides a method for producing a cosmetic composition, comprising the steps of: (a) one or more esters of sucrose and fatty acids, the fatty acids being selected from those having from about 12 to about 24 carbon atoms, and the sucrose esters being selected from the group consisting of monoesters, diesters, triesters, tetraesters, and mixtures thereof; (b) Approx. 23~31.5 (J / cm) 3 ) 1 / 2 and a Hildebrand solubility parameter of about 4.5 to about 10.5 (J / cm 3 ) 1 / 2 and one or more solvents selected from those having a polar component of the Hansen Solubility Parameters of:

[0007] Surprisingly, it has now been found that the method of producing the cosmetic composition of the present invention allows for the dissolution of sucrose esters in the cosmetic composition, even when the sucrose esters are contained in the composition at higher levels and / or when the sucrose esters are contained in the aqueous phase of the cosmetic composition.

[0008] Without being limited to theory, it is believed that in this manner, when the composition contains an aqueous carrier, the majority of the sucrose ester is contained in the aqueous phase of the composition. Without being limited to theory, it is believed that such a composition provides the benefits of the sucrose ester while providing a sensory feel that is light, non-sticky, and / or fresh from the composition. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0009] References herein to an "embodiment" or the like mean that a particular material, feature, structure, and / or characteristic described in connection with that embodiment is included in at least one embodiment, and optionally multiple embodiments, but do not mean that all embodiments incorporate the described material, feature, structure, and / or characteristic. Moreover, materials, features, structures, and / or characteristics may be combined in any suitable manner across different embodiments, and materials, features, structures, and / or characteristics may be omitted or substituted from those described. Thus, the embodiments and aspects described herein may include or be combined with elements or components of other embodiments and / or aspects, even if not expressly illustrated in combination, unless otherwise stated or incompatibility is expressly stated.

[0010] In all embodiments, unless specifically stated otherwise, all percentages of ingredients are based on the weight of the cosmetic composition. Unless specifically stated otherwise, all ratios are by weight. The number of significant digits does not represent a limitation on the amounts indicated, nor does it represent a limitation on the precision of the measurements. Unless specifically stated otherwise, all quantities are understood to be modified by the word "about". Unless otherwise stated, all measurements are understood to be made at ambient conditions of approximately 25°C, where "ambient conditions" means conditions of approximately 1 atmosphere pressure and approximately 50% relative humidity. All numerical ranges are inclusive and can be combined to form narrower ranges not expressly disclosed. For example, the upper and lower range limits delimited are interchangeable to create further ranges.

[0011] The compositions of the present invention can comprise, consist essentially of, or consist of the essential and optional ingredients described herein. As used herein, "consist essentially of" means that the composition or component may contain only additional ingredients that do not materially alter the basic and novel characteristics of the claimed composition or method. As used in this specification and the appended claims, the singular forms "a," "an," and "the" are intended to include the plural forms unless the context clearly indicates otherwise.

[0012] definition "About" modifies a particular value by referring to a range equal to plus or minus twenty percent (±20%) or less of the stated value (e.g., less than 15%, 10%, or even 5%).

[0013] "Applying" or "application" as used in reference to a composition means applying or spreading a composition of the present invention onto a human skin surface, such as the epidermis.

[0014] As used herein, "derivative" refers to the amide, ether, ester, amino, carboxyl, acetyl, and / or alcohol derivatives of a given compound.

[0015] "Effective amount" refers to an amount of the compounds and compositions sufficient to significantly induce a positive effect on keratinous tissue over the course of a treatment period. The positive effect may be a health, appearance, and / or feel effect, including the effects disclosed herein, either individually or in combination.

[0016] "Cosmetic agent" means any substance and any components thereof intended to be rubbed, poured, sprinkled, sprayed, introduced, or otherwise applied to the mammalian body or any part thereof to provide a cosmetic effect. Cosmetic agents may include substances Generally Recognized as Safe (GRAS) by the U.S. Food and Drug Administration, food additives, and materials used in non-cosmetic consumer products such as over-the-counter drugs.

[0017] "Cosmetic composition" means a composition that includes a cosmetic agent. Examples of cosmetic compositions include color cosmetics (e.g., foundations, lipsticks, concealers, and mascaras), skin care compositions (e.g., moisturizers and sunscreens), personal care compositions (e.g., leave-on and leave-in body washes and soaps), and hair care compositions (e.g., shampoos and conditioners).

[0018] "Skin care" refers to regulating and / or improving the condition of the skin (e.g., the health, appearance, or texture / feel of the skin). Some non-limiting examples of improving the condition of the skin include improving the appearance and / or feel of the skin by providing a smoother and more uniform appearance and / or feel, increasing the thickness of one or more layers of the skin, improving the elasticity or resilience of the skin, improving the firmness of the skin, reducing the oily, shiny, and / or dull appearance of the skin, improving the hydration condition or moisturization of the skin, improving the appearance of fine lines and / or wrinkles, improving skin exfoliation or scaling, plumping the skin, improving skin barrier properties, improving skin tone, reducing the appearance of redness or skin blemishes, and / or improving the brightness, luster, or clarity of the skin.

[0019] "Skin care active" means a compound or combination of compounds that, when applied to the skin, provides an acute and / or chronic effect on the skin or a type of cell normally found in the skin. Skin care actives may regulate and / or improve the skin or cells associated therewith (e.g., improve skin elasticity, skin hydration, skin barrier function, and / or cell metabolism).

[0020] "Skin care composition" means a composition that contains skin care actives and that regulates and / or improves the condition of the skin.

[0021] "Synergism" and variations thereof mean that the effect provided by the combination of two or more substances is greater than the expected additive effect of those substances.

[0022] As used herein, "treatment period" refers to the length of time and / or frequency that a material or composition is applied to a targeted skin surface.

[0023] Manufacturing method The method for producing the cosmetic composition comprises the following steps: (a) one or more esters of sucrose and fatty acids, the fatty acids being selected from those having from about 12 to about 24 carbon atoms, and the sucrose esters being selected from the group consisting of monoesters, diesters, triesters, and tetraesters, and mixtures thereof; (b) Approx. 23~31.5 (J / cm) 3 ) 1 / 2 and a Hildebrand solubility parameter of about 4.5 to about 10.5 (J / cm 3 ) 1 / 2 and one or more solvents selected from those having a polar component of the Hansen Solubility Parameters of 0.1 to 0.5.

[0024] From the viewpoint of solubilizing the sucrose ester, the mixture preferably contains a total amount of sucrose ester and solvent of about 70% by weight to about 100% by weight, more preferably about 80% by weight to about 100% by weight, and even more preferably about 90% by weight to about 100% by weight of the mixture.

[0025] In the mixture, the weight ratio of the sucrose ester to the solvent is preferably about 1:1000 to about 1000:1, more preferably about 1:100 to about 100:1, even more preferably about 10:1 to about 1:10, even more preferably about 5:1 to 1:5, and even more preferably about 2.5:1 to 1:2.5, from the viewpoint of solubilizing the sucrose ester. In another embodiment, the weight ratio of the sucrose ester to the solvent is about 2.5:1 to about 1:10, preferably about 2.5:1 to about 1:5, from the viewpoint of solubilizing the sucrose ester.

[0026] The method preferably further comprises a step of mixing the mixture with an aqueous carrier. The weight ratio of the aqueous carrier to the mixture is preferably about 1000:1 to about 1:1000, more preferably about 1:100 to about 100:1, even more preferably about 1:10 to about 10:1, even more preferably about 5:1 to about 1:5, even more preferably about 2:1 to about 1:5. The addition of an aqueous carrier to the mixture may provide improved sucrose ester solubility. Too much aqueous carrier may cause a decrease in transparency / translucency and / or a decrease in solubility of the sucrose ester, and too little aqueous carrier may not result in such improved solubility of the sucrose ester.

[0027] The above step of mixing the mixture with an aqueous carrier may include two sub-steps, namely, a first dilution and a second dilution. The first dilution is dilution of the mixture with an aqueous carrier. The second dilution is dilution of the diluted mixture obtained from the first dilution to make the final product formulation of the cosmetic composition. In the second dilution, the diluent can be any diluent contained in the cosmetic composition, including but not limited to the aqueous carrier. In the first dilution, the weight ratio of the aqueous carrier to the mixture is preferably about 1:10 to about 10:1, more preferably about 5:1 to about 1:5, and even more preferably about 2:1 to about 1:5. In the second dilution to make the final cosmetic composition, the diluent and other optional ingredients are added in an appropriate amount up to 100% of the cosmetic composition. In the second dilution, other ingredients (if included), such as thickeners, moisturizers, surfactants, pigments, powders, oils, are added simultaneously and subsequently.

[0028] Sucrose Esters Sucrose esters useful herein are esters of sucrose and fatty acids, the fatty acids being selected from those having from about 12 to about 24 carbon atoms, preferably from about 12 to about 22 carbon atoms, more preferably from about 12 to about 18 carbon atoms, the sucrose esters being selected from the group consisting of monoesters, diesters, triesters, tetraesters, and mixtures thereof. Preferably, the fatty acids are selected from those having saturated alkyl groups having the above numbers of carbon atoms.

[0029] Preferably, the sucrose ester is included in the composition at a level of from about 0.01% to about 50% by weight, preferably from about 0.1% to about 35% by weight, more preferably from about 0.5% to about 25% by weight, and even more preferably from about 1% to about 20% by weight.

[0030] Preferably, the sucrose esters useful herein contain from about 10% to about 100%, preferably from about 20% to about 100%, and more preferably from about 50% to about 90% higher esters selected from the group consisting of diesters, triesters, tetraesters, and mixtures thereof.

[0031] In some cases, the sucrose ester may be a blend of two or more sucrose esters, where the two or more sucrose esters are present in a ratio of 1:10 to 1:1 (e.g., 1:7, 1:5, 1:3, or 1:2) of any one sucrose ester to another. In some cases, the sucrose ester may be a blend of sucrose laurate and sucrose dilaurate, where the sucrose laurate is present at 50% to 80% by weight of the sucrose ester and the sucrose dilaurate is present at 20% to 45% by weight of the sucrose ester. Alternatively, the sucrose ester may be a blend of sucrose laurate, sucrose dilaurate, and sucrose trilaurate, where the sucrose dilaurate is present at 35% or more by weight of the sucrose ester. An example of a sucrose ester particularly suitable for use herein is Sucrose Dilaurate BC10034 available from BASF.

[0032] solvent Solvents useful herein have a viscosity of about 23 to about 31.5, preferably about 23 to about 29 (J / cm) from the standpoint of solubilizing sucrose esters. 3 ) 1 / 2 and about 4.5 to about 10.5, preferably about 5 to about 9, more preferably about 5.5 to about 8 (J / cm 3 ) 1 / 2 The polar component of the Hansen solubility parameter is selected from those having a polar component of the Hansen solubility parameter of 0.1 to 0.5.

[0033] One or a mixture of several of the above solvents can be used as long as each solvent meets the above parameters. Such solvents include, for example, the following materials in the table below:

[0034] [Table 1]

[0035] Of these, pentylene glycol is highly preferred, considering the balance between the improved solubility of sucrose esters and minimal potential for skin irritation.

[0036] The solvent may be contained in the cosmetic composition at a concentration of about 0.01% to about 90%, preferably about 0.1% to about 50%, and more preferably about 0.5% to about 30%.

[0037] Below, for reference purposes only, are provided the polar components of the Hildebrand and Hansen solubility parameters for ingredients that are not solvents as defined herein but are frequently used in cosmetic compositions.

[0038] [Table 2]

[0039] Aqueous Carrier The aqueous carrier useful herein is excluding the solvent defined above.Preferably, the aqueous carrier is substantially water.Preferably, deionized water is used.Water from natural sources containing mineral cations can also be used, depending on the desired properties of the product.

[0040] In one embodiment, the aqueous carrier may be present at a level of from about 50% to about 99%, preferably from about 60% to about 98%, more preferably from about 70% to about 98%, and even more preferably from about 80% to about 95% of the composition.

[0041] Cosmetic Composition The cosmetic compositions herein are intended for topical application to human skin and contain a sucrose ester and a solvent, and preferably also contain an aqueous carrier. The skin care compositions may optionally contain one or more additional skin active ingredients or other ingredients of the type commonly included in topical skin care compositions.

[0042] The cosmetic composition herein may be a cosmetic composition, a pharmaceutical composition, or a cosmeceutical composition, and may be provided in various product forms, including, but not limited to, solutions, suspensions, lotions, creams, gels, toners, sticks, sprays, aerosols, ointments, cleansing liquid washes and solid bars, pastes, foams, mousses, shaving creams, wipes, strips, patches, powered patches, hydrogels, film-forming products, facial and skin masks (with and without insoluble sheets); make-up such as foundations, eyeliners and eyeshadows, and the like. In some cases, the form of the composition may be in accordance with the particular dermatologically acceptable carrier selected. For example, the composition (and carrier) may be provided in the form of an emulsion (e.g., water-in-oil, oil-in-water, or water-in-oil-in-water) or an aqueous dispersion. Preferably, the cosmetic composition of the present invention is in the form of an oil-in-water emulsion.

[0043] Dermatologically acceptable carrier The compositions disclosed herein may include a dermatologically acceptable carrier (which may be referred to as a "carrier"). The phrase "dermatologically acceptable carrier" means that the carrier is suitable for topical application to keratinous tissue, has good aesthetic properties, is compatible with the actives in the composition, and does not raise any undue safety or toxicity concerns. In one embodiment, the carrier is present at a level of about 50% to about 99% by weight, about 60% to about 98% by weight, about 70% to about 98% by weight, or alternatively about 80% to about 95% by weight.

[0044] The carrier may be in a wide variety of forms. In some cases, the solubility or dispersibility of the components (e.g., extracts, sunscreen actives, additional ingredients) may determine the form and characteristics of the carrier. Non-limiting examples include simple solutions (e.g., aqueous or anhydrous), dispersions, emulsions, and solid forms (e.g., gels, sticks, flowable solids, or amorphous materials). In some cases, the dermatologically acceptable carrier is in the form of an emulsion. An emulsion may have a continuous aqueous phase (e.g., oil-in-water or water-in-oil-in-water emulsions) or a continuous oil phase (e.g., water-in-oil or oil-in-water-in-oil emulsions). The oil phase of the present invention may include non-silicone oils such as silicone oils, hydrocarbon oils, esters, ethers, and mixtures thereof. The aqueous phase typically includes water and water-soluble components (e.g., water-soluble moisturizers, conditioning agents, antibacterial agents, humectants, and / or other skin care actives). In some cases, however, the aqueous phase may contain components other than water, including, but not limited to, water-soluble moisturizers, conditioning agents, antimicrobial agents, humectants, and / or other water-soluble skin care actives. In some cases, the non-aqueous components of the composition include humectants, such as glycerin and / or other polyols.

[0045] In some cases, the compositions herein are in the form of oil-in-water ("O / W") emulsions that provide a light, non-greasy sensory feel. Suitable O / W emulsions herein may comprise more than 50% by weight of the composition of a continuous water phase, with the remainder being a dispersed oil phase. The water phase may comprise 1% to 99% water, based on the weight of the water phase, along with any water-soluble and / or water-miscible ingredients. In these cases, the dispersed oil phase is typically present at less than 30% by weight of the composition (e.g., 1% to 20%, 2% to 15%, 3% to 12%, 4% to 10%, or even 5% to 8%) to help avoid some of the undesirable sensory effects of oil-based compositions. The oil phase may comprise one or more volatile and / or non-volatile oils (e.g., vegetable oils, silicone oils, and / or hydrocarbon oils).

[0046] Skin conditioning agents Optionally, the compositions of the present invention may further comprise a skin conditioning agent. These agents may be selected from moisturizers and emollients. The amount of the skin conditioning agent may range from about 1% to about 50% by weight of the composition, preferably from about 2% to about 40% by weight, more preferably from about 5% to about 30% by weight.

[0047] Moisturizing agents are polyhydric alcohols that are intended to moisturize, reduce scale, and stimulate the exfoliation of accumulated scale from the skin.Typical polyhydric alcohols include polyalkylene glycols, more preferably alkylene polyols and their derivatives.Examples include propylene glycol, dipropylene glycol, polypropylene glycol, polyethylene glycol, sorbitol, hydroxypropyl sorbitol, hexylene glycol, 1,3-butylene glycol, 1,2,6-hexanetriol, ethoxylated glycerin, propoxylated glycerin, and mixtures thereof.Most preferably, the moisturizing agent is glycerol.

[0048] When the conditioning agent is an emollient, it may be selected from hydrocarbons, fatty acids, fatty alcohols, and esters.

[0049] Fatty alcohol The compositions herein may include fatty alcohols, which refer to high molecular weight, straight-chain primary alcohols having the following general structure:

[0050] [ka] In the formula, n=8 to 32.

[0051] Fatty alcohols can be natural or synthetic, saturated or unsaturated, branched or straight chain. Some non-limiting examples of fatty alcohols commonly used in cosmetic compositions include caprylic, caprylic, lauryl, myristyl, cetyl, stearyl, and behenyl alcohol. Fatty alcohols herein can be generically referred to by the number of carbon atoms in the molecule. For example, "C12 alcohol" refers to an alcohol with 12 carbon atoms in its chain (i.e., dodecanol).

[0052] The sucrose ester may be included in the composition at 0.0001% to 15% (e.g., 0.0002% to 10%, 0.001% to 15%, 0.025% to 10%, 0.05% to 7%, 0.05% to 5%, or even 0.1% to 3%) by weight of the composition.

[0053] Skin whitening agents The composition may contain a whitening agent.Whitening agents useful herein refer to active ingredients that not only change the appearance of skin, but also improve hyperpigmentation compared to before treatment.Whitening agents useful herein include ascorbic acid compounds, vitamin B3 compounds, azelaic acid, butyl hydroxyanisole, gallic acid and its derivatives, hydroquinone, kojic acid, arbutin, mulberry extract, tetrahydrocurcumin and mixtures thereof.The use of a combination of whitening agents is also considered to be advantageous in that they may provide whitening effect through different mechanisms.

[0054] If used, the compositions preferably contain from about 0.1% to about 10%, more preferably from about 0.2% to about 5%, by weight of the composition, of a skin lightening agent.

[0055] Ascorbic acid compounds are useful skin lightening agents, and ascorbyl glucoside is a preferred derivative of ascorbic acid compounds.

[0056] Conditioning Agent The compositions herein may include 0.1% to 50% by weight of conditioning agents (e.g., 0.5% to 30%, 1% to 20%, or even 2% to 15%). The addition of conditioning agents may help provide the composition with desirable feel characteristics (e.g., silky smooth feel upon application). Some non-limiting examples of conditioning agents include hydrocarbon oils and waxes, silicones, fatty acid derivatives, cholesterol, cholesterol derivatives, diglycerides, triglycerides, vegetable oils, vegetable oil derivatives, acetoglyceride esters, alkyl esters, alkenyl esters, lanolin, wax esters, beeswax derivatives, sterols and phospholipids, salts, isomers, and derivatives thereof, and combinations thereof. Particularly suitable examples of conditioning agents include volatile or non-volatile silicone fluids such as dimethicone copolyol, dimethylpolysiloxane, diethylpolysiloxane, mixed C1-30 alkylpolysiloxane, phenyldimethicone, dimethiconol, dimethicone, dimethiconol, silicone crosspolymers, and combinations thereof.Dimethicone may be particularly suitable because some consumers associate the feel properties provided by certain dimethicone fluids with good moisturization.Other examples of silicone fluids that may be suitable for use as conditioning agents are described in U.S. Pat. No. 5,011,681.

[0057] Thickener The compositions of the present invention may further comprise one or more thickening agents.

[0058] Non-limiting classes of thickening agents include those selected from the following: carboxylic acid polymers, crosslinked polyacrylate polymers, polyacrylamide polymers, polysaccharides, and gums.

[0059] If present, the composition preferably comprises from about 0.01% to about 5%, more preferably from about 0.1% to about 4%, and even more preferably from about 0.1% to about 3%, by weight of the composition, of a thickening agent.

[0060] emulsifier When the composition is in the form of an emulsion, it may contain an emulsifier. The emulsifier may be nonionic, anionic, cationic, or zwitterionic. Some non-limiting examples of emulsifiers are disclosed in U.S. Pat. Nos. 3,755,560, 4,421,769, U.S. Patent Application Publication No. 2006 / 0275237, and McCutcheon's Detergents and Emulsifiers, North American Edition, pages 317-324 (1986). Suitable examples of emulsifiers include nonionic emulsifiers such as polysorbate 20, polysorbate 80, polyglyceryl-4 caprate, and glycereth-25 pyrrolidone carboxylic acid isostearate. A particularly suitable example of an emulsifier for use in the compositions described herein is polysorbate 20.

[0061] Other optional ingredients. The composition suitable for use in the method herein may contain one or more optional ingredients known for use in topical skin care compositions, provided that the optional ingredients do not unacceptably change the desired effect of the composition.In some cases, it may be desirable to select cosmetic active ingredients that function through different biological pathways so that the active ingredients do not interfere with each other.When the composition is in the form of an emulsion, the additional ingredient must not introduce instability (e.g., syneresis) to the emulsion.For example, it may be desirable to select optional ingredients that do not form complexes with other ingredients in the composition, especially pH-sensitive ingredients such as vitamin B3 compounds, salicylates, and peptides.

[0062] The additional components should be suitable for use in contact with human skin tissue without undue toxicity, incompatibility, instability, allergic response, etc. If present, the optional components may be included in an amount of about 0.001% to 50% by weight (e.g., 0.01% to 40%, 0.1% to 30%, 0.5% to 20%, or 1% to 10% by weight) of the composition. Some non-limiting examples of additional ingredients include vitamins, minerals, peptides and peptide derivatives, sugar amines, sunscreens, oil control agents, microparticles, flavonoid compounds, hair growth regulators, antioxidants and / or antioxidant precursors, preservatives, protease inhibitors, tyrosinase inhibitors, anti-inflammatory agents, moisturizers, exfoliants, skin lightening agents, sunscreens, sunless tanning agents, lubricants, anti-acne agents, anti-cellulite agents, chelating agents, anti-wrinkle actives, anti-atrophy actives, phytosterols and / or plant hormones, N-acyl amino acid compounds, antibacterial agents, and antifungal agents. Some particularly suitable examples of additional ingredients include one or more skin care actives selected from the group consisting of vitamin B3 compounds (e.g., niacinamide), n-acyl amino acids (e.g., undecylenoyl phenylalanine), vitamin E compounds (e.g., tocopheryl acetate), palmitoylated dipeptides (e.g., palmitoyl-lysine-threonine), palmitoylated pentapeptides (e.g., palmitoyl-lysine-threonine-threonine-lysine-serine), vitamin A compounds (e.g., retinol and retinyl propionate), and combinations thereof.Other non-limiting examples of optional ingredients and / or skin care actives that may be suitable for use herein are described in U.S. Patent Application Publication Nos. 2002 / 0022040, 2003 / 0049212, 2004 / 0175347, 2006 / 0275237, 2007 / 0196344, 2008 / 0181956, 2008 / 0206373, 2010 / 0092408, 2008 / 0206373, 2010 / 0239510, 2010 / 0189669, 2010 / 0189702, 2010 / 0189704, 2010 / 0189706, 2010 / 0189708, 2010 / 0189709 ... Nos. 2010 / 0272667, 2011 / 0262025, 2011 / 0097286, 2012 / 0197016, 2012 / 0128683, 2012 / 0148515, 2012 / 0156146, and 2013 / 0022557, as well as U.S. Patent Nos. 5,939,082, 5,872,112, 6,492,326, 6,696,049, 6,524,598, 5,972,359, and 6,174,533.

[0063] Method of using the cosmetic composition The method of use herein involves identifying a target area of ​​skin of a person in need of treatment and applying the composition to the target area of ​​skin for a treatment period. The target area of ​​skin may be on the skin surface of the face, such as the forehead, perioral, chin, periorbital, nose, and / or cheeks, or on another part of the body (e.g., hands, arms, legs, back, chest). A person in need of treatment is one whose skin exhibits signs of oxidative stress, such as fine lines, wrinkles, hyperpigmentation, uneven skin tone, and / or other visible skin features that are commonly associated with aging. In some cases, the target area of ​​skin may not exhibit visible signs of skin aging, but a user (e.g., a relatively young user) may still wish to target such areas of skin if they are areas that develop such problems with aging. In this way, the method of the present invention may be used as a preventative measure to delay the onset of visible signs of skin aging.

[0064] The composition may be applied daily to the target area of ​​skin and, if desired, to the surrounding skin at least once a day, twice a day, or more frequently during the treatment period. When applied twice a day, the first and second applications are separated by at least 1-12 hours. The composition is typically applied in the morning and / or at night before going to bed. The treatment period may last for at least one week (e.g., about 2, 4, 8, or even 12 weeks). In some cases, the treatment period will extend for several months (i.e., 3-12 months). In some cases, the composition may be applied at least once a day, or even twice a day, for the majority of days of the week (e.g., at least 4, 5, or 6 days a week) during a treatment period of at least 2, 4, 8, or 12 weeks.

[0065] The step of applying the composition can be accomplished by topical application. With respect to the application of the composition, the terms "topical", "topical" or "topically" mean that the composition is delivered to the target area (e.g., wrinkles or lines) while minimizing delivery to skin surfaces where treatment is not desired. The composition can be applied to a skin area and massaged gently. The form of the composition or dermatologically acceptable carrier should be selected to facilitate topical application. Although certain embodiments herein contemplate applying the composition topically to an area, it will be understood that the composition herein can be applied broadly to one or more skin surfaces. In certain embodiments, the composition herein can be used as part of a multi-step cosmetic regimen, in which the composition can be applied before and / or after one or more other compositions.

[0066] combination A. A method for producing a cosmetic composition comprising: (a) one or more esters of sucrose and fatty acids, wherein the fatty acids are selected from those having from about 12 to about 24 carbon atoms, preferably from about 12 to about 22 carbon atoms, more preferably from about 12 to about 18 carbon atoms, and the sucrose esters are selected from the group consisting of monoesters, diesters, triesters, tetraesters, and mixtures thereof; (b) about 23 to about 31.5, preferably about 23 to about 29 (J / cm 3 ) 1 / 2 and about 4.5 to about 10.5, preferably about 5 to about 9, more preferably about 5.5 to about 8 (J / cm 3 ) 1 / 2 and one or more solvents selected from those having a polar component of a Hansen Solubility Parameter of 0.01 to 0.01. B. The method of any preceding feature, wherein the mixture comprises a combined amount of sucrose ester and solvent of about 70% to about 100%, preferably about 80% to about 100%, and more preferably about 90% to about 100%. C. The method of any of the preceding features, wherein the fatty acid is selected from those having a saturated alkyl group having from about 12 to about 24 carbon atoms. D. The method of any of the preceding features, wherein the weight ratio of sucrose ester to solvent is from about 1:1000 to about 1000:1, preferably from about 1:100 to about 100:1, more preferably from about 10:1 to about 1:10, even more preferably from about 5:1 to 1:5, and even more preferably from about 2.5:1 to 1:2.5. E. The method of any of the preceding features, further comprising the step of combining the mixture with an aqueous carrier. F. The method of any of the preceding features, wherein the weight ratio of the aqueous carrier to the mixture is from about 1000:1 to about 1:1000, preferably from about 1:100 to about 100:1, more preferably from about 1:10 to about 10:1, even more preferably from about 5:1 to about 1:5, and even more preferably from about 2:1 to about 1:5. G. The method of any of the preceding features, wherein the step of mixing the mixture with the aqueous carrier includes a first dilution step and a second dilution step, and in the first dilution step, the weight ratio of the aqueous carrier to the mixture is from about 1:10 to about 10:1, preferably from about 5:1 to about 1:5, and more preferably from about 2:1 to about 1:5. H. The method of any of the preceding features, wherein the sucrose esters contain from about 10% to about 100%, preferably from about 20% to about 100%, and more preferably from about 50% to about 90% of higher esters selected from the group consisting of diesters, triesters, tetraesters, and mixtures thereof. I. The method of any of the preceding features, wherein the cosmetic composition comprises from about 0.01% to about 50%, preferably from about 0.1% to about 35%, more preferably from about 0.5% to about 25%, and even more preferably from about 1% to about 20% of a sucrose ester. EXAMPLES

[0067] [Table 3] ** i) Mix for 60 minutes at 80°C and then visually observe 24 hours later.

[0068] [Table 4] ** ii) Visual observation after mixing the mixture with deionized water at room temperature for 1 minute.

[0069] [Table 5] ** iii) Visual observation after mixing as follows: (a) The aqueous phase ingredients are mixed at room temperature until homogenous. (b) Mix such homogenized aqueous phase ingredients from (a) with the first dilution from Table 2 for 5 minutes. (c) Mix such blended ingredients from (b) with oil phase ingredients in a homomixer at 5000 rpm at room temperature for 5 minutes.

[0070] [Table 6]

[0071] Second Dilution Example 1 to Example 5 are skin care compositions made by the manufacturing method of the present invention. Second Dilution CEx.i is a skin care composition made by a manufacturing method different from the present invention and is provided as a comparative example. As shown in each table above, the method of the present invention can dissolve sucrose esters in the skin care composition, but the comparative example cannot dissolve sucrose esters.

[0072] Dimensions and values ​​disclosed herein should not be understood as being strictly limited to the exact numerical values ​​recited. Instead, unless otherwise indicated, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as "40 mm" is intended to mean "about 40 mm."

[0073] All documents cited herein, including any cross-referenced or related patents or patent applications, and any patent applications or patents to which this application claims priority or the benefit thereof, are incorporated herein by reference in their entirety, unless expressly excluded or otherwise limited. The citation of any document shall not be deemed to be prior art to any invention disclosed or claimed herein, or to teach, suggest or disclose such invention, either alone or in combination with any other reference(s). Furthermore, to the extent that any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall apply.

[0074] While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.

Claims

1. A method for producing a cosmetic composition comprising a sucrose ester, said sucrose ester being dissolved in a continuous aqueous phase of said composition, (a) one or more esters of sucrose and fatty acids, the fatty acids being selected from those having from 12 to 24 carbon atoms, the sucrose esters comprising from 10% to 100%, by weight of the sucrose ester, of higher esters selected from the group consisting of diesters, triesters, tetraesters, and mixtures thereof; (b) 23-31.5 (J / cm 3 ) 1 / 2 and a Hildebrand solubility parameter of 4.5 to 10.5 (J / cm 3 ) 1 / 2 one or more solvents selected from those having a polar component of the Hansen Solubility Parameters of wherein the one or more solvents comprise pentylene glycol.

2. 2. The method of claim 1, wherein the mixture comprises 70% to 100% of the combined amount of the sucrose ester and the solvent.

3. 2. The method of claim 1, wherein the fatty acid is selected from those having saturated alkyl groups with 12 to 24 carbon atoms.

4. 2. The method of claim 1, wherein the weight ratio of the sucrose ester to the solvent is from 1:1000 to 1000:

1.

5. The method of claim 1 further comprising the step of combining the mixture with an aqueous carrier.

6. The method of claim 5, wherein the weight ratio of the aqueous carrier to the mixture is from 1000:1 to 1:1000.

7. 6. The method of claim 5, wherein the step of mixing the mixture with an aqueous carrier comprises a first dilution step and a second dilution step, and in the first dilution step, the weight ratio of the aqueous carrier to the mixture is from 1:10 to 10:

1.

8. The method of claim 1 , wherein the cosmetic composition comprises from 0.01% to 50% of the sucrose ester.

Citation Information

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