PASTE-TYPE COSMETIC CONTAINING NATURAL MOISTURIZING FACTOR

20230329999 · 2023-10-19

    Inventors

    Cpc classification

    International classification

    Abstract

    Provided is a cosmetic composition that is used for imparting corneum improving effect and exhibits reduced skin irritation. A microneedle type cosmetic composition containing: 30 to 100 mass % of a water-soluble or water-swellable polymer compound; and one or more types of natural moisturizing factors, wherein when the microneedle type cosmetic composition contains 100 mass % of the water-soluble or water-swellable polymer compound, the water-soluble or water-swellable polymer compound is the natural moisturizing factors; and a method for producing the microneedle type cosmetic composition, including: preparing an aqueous solution of a water-soluble or water-swellable polymer compound, and mixing the aqueous solution with one or more types of natural moisturizing factors to produce a cosmetic raw material liquid.

    Claims

    1. A microneedle type cosmetic composition comprising: 30 to 100 mass % of a water-soluble or water-swellable polymer compound; and one or more types of natural moisturizing factors, wherein when the composition contains 100 mass % of the water-soluble or water-swellable polymer compound, the water-soluble or water-swellable polymer compound is the natural moisturizing factors.

    2. The cosmetic composition according to claim 1, wherein the water-soluble or water-swellable polymer compound is one or more types of water-soluble polymer compounds selected from the group consisting of hyaluronic acid, PEG-grafted-hyaluronic acid and salts thereof, hydroxypropyl cellulose, carboxymethyl cellulose, sodium chondroitin sulfate, polyvinyl alcohol, and proteoglycan, or a water-swellable polymer compound that is a crosslinked product of the water-soluble polymer compound.

    3. The cosmetic composition according to claim 1, wherein the natural moisturizing factors are contained in an amount of 0.1 mass % or more based on a total mass of the composition.

    4. The cosmetic composition according to claim 1, wherein the natural moisturizing factors are contained in an amount of 8 mass % or more based on a total mass of the composition.

    5. The cosmetic composition according to claim 1, wherein a component having a molecular weight of 1,000 or less of the natural moisturizing factors is contained in an amount of 70 mass % or less based on a total mass of the composition.

    6. The cosmetic composition according to claim 1, wherein the natural moisturizing factors are present in a dissolved or dispersed state in the microneedle type cosmetic composition.

    7. The cosmetic composition according to claim 1, wherein the natural moisturizing factors are one or more types selected from substances including amino acids, metabolites of amino acids, pyrrolidone carboxylic acid and salts thereof, ureas, inorganic ions and inorganic salts, and organic acid salts.

    8. The cosmetic composition according to claim 7, wherein the ureas are a substance selected from the group consisting of urea, ammonia, uric acid, glucosamine, creatinine, and urocanic acid.

    9. The cosmetic composition according to claim 7, wherein the ureas are glucosamine, or a combination of glucosamine and one or more types of substances selected from the group consisting of urea, ammonia, uric acid, creatinine, and urocanic acid.

    10. A method for producing a microneedle type cosmetic composition, comprising: preparing an aqueous solution of a water-soluble or water-swellable polymer compound, and mixing one or more types of natural moisturizing factors in the aqueous solution to produce a cosmetic raw material liquid; casting the cosmetic raw material liquid into a mold for a microneedle; heating the mold to dry the cosmetic raw material liquid; and taking out a cosmetic composition molded into a microneedle from the mold.

    11. The method for producing a microneedle type cosmetic composition according to claim 10, wherein the cosmetic raw material liquid is produced by dissolving or suspending the natural moisturizing factors in a mixed liquid of water and alcohol, water and polyhydric alcohol, or water, alcohol and polyhydric alcohol.

    Description

    BRIEF DESCRIPTION OF THE DRAWINGS

    [0031] FIG. 1 is a cross-sectional view showing an example of a method for producing a microneedle array of the present invention.

    MODE FOR CARRYING OUT THE INVENTION

    [0032] The microneedle type cosmetic composition has the following constitution.

    Microneedle Array

    [0033] Conide-like, pyramidal, or needle-like microneedles having a height of 100 to 400 μm stand on a substrate having a thickness of 10 to 200 μm. In the constituent substance of the microneedle, valuable substances are dispersed in a state of being dissolved or suspended in a base.

    [0034] The valuable substance contains a natural moisturizing factor as a main component. In the present invention, the natural moisturizing factor plays a role of maintaining the physical properties of the stratum corneum in the skin.

    [0035] The natural moisturizing factor is composed of many substances, and these substances are classified into six types of components. Hereinafter, six components and substances belonging thereto are listed.

    [0036] Component 1. Amino acids (substances including betaine, aspartic acid, glutamic acid, leucine, isoleucine, methionine, tryptophan, histidine, phenylalanine, threonine, serine, valine, proline, glycine, alanine, lysine, arginine, ornithine, and the like, but not limited thereto)

    [0037] Component 2. Metabolites of amino acids (substances including pyruvic acid, 2-oxoglutaric acid, succinyl-CoA, fumaric acid, oxaloacetic acid, acetyl-CoA, acetoacetic acid, and the like, but not limited thereto)

    [0038] Component 3. Pyrrolidone carboxylic acids (pyrrolidone carboxylic acid and salts thereof)

    [0039] Component 4. Ureas (substances including urea, ammonia, uric acid, glucosamine, creatinine, urocanic acid, and the like, but not limited thereto)

    [0040] Component 5. Inorganic ions and inorganic salts (substances including sodium, potassium, calcium, magnesium, sodium phosphate, chloride, and the like, but not limited thereto)

    [0041] Component 6. Organic acid salts (substance including sodium lactate, sodium citrate, sodium hyaluronate, and the like, but not limited thereto)

    [0042] From the viewpoint of its effect, the ureas are preferably glucosamine, or a combination of glucosamine and one or more types of substances selected from the group consisting of urea, ammonia, uric acid, creatinine, and urocanic acid.

    [0043] The natural moisturizing factor may be contained in an amount of 0.1 to 100 mass %, preferably 1 to 95 mass %, more preferably 5 to 92 mass %, still more preferably 11 to 70 mass %, and most preferably 12 to 70 mass % based on the total mass of the microneedle. When the natural moisturizing factor is contained in an amount of less than 0.1 mass %, the effect of the natural moisturizing factor becomes too small. A compound such as sodium hyaluronate (organic acid salt), which itself has a structure forming strength and moisture retaining ability, may be contained in an amount of 100 mass %. When the base such as carboxymethyl cellulose (CMC) has low moisture retaining ability, the content of the natural moisturizing factor is desirably 8 mass % or more, more preferably 11 to 70 mass %, and still more preferably 12 to 70 mass %. Low molecular weight components such as inorganic ions, salts, and amino acids have no structure-forming ability by themselves, and thus it is necessary to provide the strength required as a microneedle by blending with a water-soluble or water-swellable polymer compound.

    [0044] The cosmetic composition of the present invention can further contain a moisturizer, for example, a polyol such as glycerin, dipropylene glycol, or butylene glycol, as other components.

    [0045] The cosmetic composition of the present invention can further contain all types of components usable in normal cosmetics as other components, for example, an ultraviolet shielding agent, a neutralizer, a thickener, a fragrance, an antiseptic, an antioxidant, and a dye.

    [0046] For formation of microneedles, a base for maintaining the needle shape while containing a natural moisturizing factor as a main component in a dissolved or dispersed state and also maintaining the stiffness to withstand application to the skin is essential. As the base, a water-soluble polymer compound and a crosslinked product thereof are suitable. For example, non-crosslinked products such as hyaluronic acid, hydroxypropyl cellulose, sodium chondroitin sulfate, polyvinyl alcohol, proteoglycan, and PEG-grafted hyaluronic acid (for example, compounds described in JP 2017-019791 A) are suitable. When these water-soluble polymer compounds are crosslinked at an appropriate crosslinking density using a crosslinking agent, they are not soluble in water but swellable. In the present invention, these compounds are referred to as water-swellable polymer compounds. Among them, a crosslinked product of hyaluronic acid has been reported in many cases, and can be suitably used in the present invention.

    [0047] The proportion of the base in the total mass of the microneedle is 30 to 100 mass %, and 30 to 90 mass % is appropriate. When the proportion is less than 30 mass %, the mechanical strength of the microneedle is weakened, and when the proportion is more than 90 mass %, there is a risk that the effectiveness is weakened.

    [0048] However, when the proportion of the water-soluble or water-swellable polymer compound as the base is 100 mass %, the water-soluble or water-swellable polymer compound is a natural moisturizing factor, specifically, sodium hyaluronate as an organic acid salt, proteoglycan, sodium chondroitin sulfate, crosslinked hyaluronic acid, and the like.

    [0049] In addition, when a large amount of a low molecular weight component of the natural moisturizing factor is contained, the mechanical strength of the microneedle is weakened. Thus, the proportion of a component having a molecular weight of 1,000 or less of the natural moisturizing factor in the total mass is preferably 70 mass % or less.

    Method for Producing Microneedle Type Cosmetic Composition

    [0050] The production method of the present invention includes the following steps (1) to (4): [0051] (1) preparing an aqueous solution of a water-soluble or water-swellable polymer compound, and mixing the aqueous solution with one or more types of natural moisturizing factors to produce a cosmetic raw material liquid; [0052] (2) casting the cosmetic raw material liquid into a mold for a microneedle; [0053] (3) heating the mold to dry the cosmetic raw material liquid; and [0054] (4) taking out the cosmetic composition molded into a microneedle from the mold.

    [0055] The steps (1) to (4) are not particularly limited, and any publicly known step can be used. Examples of the method include a method in which a cosmetic raw material liquid (aqueous solution or suspension) produced in the above step (1) with other components added thereto as necessary is cast into a mold having a microneedle shape, and dried, and a cosmetic composition molded into a microneedle is released and taken out. After releasing from the mold, the cosmetic composition is cut into an arbitrary shape (patch), and the cut product is lined with an adhesive support as necessary, and used.

    [0056] In the step (1), a cosmetic raw material liquid is preferably produced by dissolving or suspending the natural moisturizing factor in a mixed liquid of water and alcohol, water and polyhydric alcohol, or water, alcohol and polyhydric alcohol.

    [0057] Here, examples of the alcohol include ethanol and isopropanol, and examples of the polyhydric alcohol include glycerin and propylene glycol. As the combination of the alcohol and the polyhydric alcohol, a combination of ethanol and glycerin, and a combination of ethanol and propylene glycol are preferable. The alcohol and/or the polyhydric alcohol contained in the mixed liquid can be appropriately selected according to the type and content of the natural moisturizing factor. The ratio of water to alcohol and/or polyhydric alcohol can also be appropriately set according to the type and content of the natural moisturizing factor.

    [0058] The size of the patch (microneedle patch) including a microneedle array is 1 to 50 square cm. When the size of the patch is less than 1 square cm, the effect is limited and the effectiveness is not easily exhibited. When the size of the patch exceeds 50 square cm, a problem in adhesion is likely to occur in covering the body surface. In order to cover a wide body surface, a plurality of microneedle patches each having a size of 50 square cm or less may be used.

    [0059] In order to stably apply the microneedle patch to the skin and hold the microneedle patch on the skin, the microneedle patch more preferably, but not essentially, have an adhesive support on the back surface thereof. The adhesive support is a support film having an adhesive layer on one side thereof.

    [0060] The adhesive layer in the present invention is determined in consideration of adhesion to the skin and attachment to the support film. Specifically, a material of the adhesive layer is selected from an acrylic adhesive, a rubber-based adhesive, a silicone-based adhesive, a urethane-based adhesive, and the like. In order to improve the stickiness to the skin, a plasticizer such as isopropyl myristate or isopropyl palmitate, a tackifier, a liquid hydrocarbon, or the like may be added to these adhesives. The thickness of the adhesive layer is desirably 10 μm to 250 μm.

    [0061] As the support film, a film made of a synthetic polymer is preferable, and specifically, polyvinyl alcohol, polyolefin, polyurethane, polyethylene terephthalate (PET), or the like is used.

    EXAMPLES

    [0062] Hereinafter, the present invention will be described in more detail by the following Examples. These examples are merely examples for specifically describing the present invention, and the scope of the present invention is not limited to these examples.

    Example 1

    Preparation of Microneedle Array

    [0063] FIG. 1 is a cross-sectional view showing an example of a method for producing a microneedle array of the present invention. In the drawing, reference numeral 1 denotes a mold with a conide type microneedle forming concave portion 11 formed through a process of: forming a conide-type microneedle pattern by a lithography method of irradiating a photosensitive resin with light; and then performing electroforming to transfer the conide-type microneedle pattern. Reference numeral 2 denotes a cosmetic raw material liquid cast into the microneedle forming concave portion 11.

    [0064] The microneedle forming concave portions 11 are a conide type with a bottom diameter of 0.6 mm, a tip diameter of 0.02 mm, and a depth of 0.25 mm, and are arranged in a lattice pattern at intervals of 0.8 mm.

    [0065] An aqueous hyaluronic acid solution (cosmetic raw material liquid) prepared by dissolving 20 parts by mass of hyaluronic acid (manufactured by Kikkoman Biochemifa Company, trade name “FCH-SU”, molecular weight: 100,000) and 20 parts by mass of a composite wetting agent (manufactured by Ajinomoto Healthy Supply Co., Inc., trade name PRODEW, composed of a plurality of amino acids <component 1> and pyrrolidone carboxylic acid <component 2>) in 100 parts by mass of water at room temperature was cast into the mold 1, and heated to evaporate moisture in the aqueous hyaluronic acid solution layer. Then, a dried product was released from the mold 1 and punched into an elliptical shape with a size of 7 (minor axis)×50 mm (major axis).

    Preparation of Microarray with Protective Adhesive Tape

    [0066] An elliptical microneedle array with a size of 7 (minor axis)×50 mm (major axis) was set in the central portion of an adhesive tape (HiPAS (registered trademark) 10, adhesive manufactured by CosMED Pharmaceutical Co. Ltd., thickness: 30 μm) with a rectangular (9×56 mm) support (polyethylene film, thickness: 40 μm) having rounded corners to obtain a microneedle array (sheet A) with a protective adhesive tape of the present invention.

    Example 2

    Evaluation of Skin Texture

    [Outline of Test]

    [0067] The sheet A of Example 1 was applied to the facial part of five subjects and peeled off after five hours. On the next day, the application site on the face of the subject and the adjacent non-application site were observed with a microscope, and the state of the texture was compared with that before use to perform evaluation.

    [Evaluation Results]

    <Evaluation Results of Skin Texture Improving Effect>

    [0068] In Example 1, regarding the improvement of the skin texture after use of the sheet A, the skin texture was better and improved than before use in all five out of the five subjects. Therefore, it was determined that the sheet A was useful for improving the skin texture.

    Examples 3 to 12

    [0069] Preparation of Microneedle Array Containing Various Natural Moisturizing Factor Components

    [0070] Three types of microneedle arrays containing a natural moisturizing factor were prepared in accordance with Example 1. The numbers in the table below are parts by mass in the composition after drying. These compositions were dissolved or suspended in 70 parts of water and 10 parts of an ethanol solution so as to be 20 parts by mass, and dried to form a microneedle array. Note that, in Example 4, hyaluronic acid serves as both the base and the natural moisturizing factor.

    TABLE-US-00001 TABLE 1 Natural moisturizing factor component (part by mass) Base Component Component Component Component Component Examples (part by mass) 1 3 4 5 6 3 Sodium Alanine hyaluronate (0.05) (99.9) Arginine (0.05) 4 Sodium hyaluronate (100) 5 Sodium Alanine Pyrrolidone Urea (2) hyaluronate (20) carboxylic (73) acid (5) 6 Sodium Proline (1) Sodium Glucosamine NaCl (0.5) hyaluronate pyrrolidone (5) (92) carboxylate (1) 7 Sodium PEG- Arginine Sodium Urocanic KCI (0.5) Sodium grafted (0.1) pyrrolidone acid (0.5) citrate hyaluronate carboxylate (0.5) (97.4) (1) 8 Crosslinked Proline (3) Sodium Glucosamine product of pyrrolidone (67) sodium carboxylate hyaluronate (1) (30) 9 Sodium Alanine (3) Pyrrolidone Urea (5) hyaluronate carboxylic Glucosamine (72) acid (5) (15) 10 Hydroxypropyl Arginine Glucosamine cellulose (0.5) (67) (HPC-M) (31) Alanine (0.5) Proline (1.0) 11 Carboxymethyl Urea (5) cellulose (85) Glucosamine (10) 12 Sodium Arginine Sodium chondroitin (3) pyrrolidone sulfate (96) carboxylate (1)

    [0071] All of the natural moisturizing factor-containing microneedles produced in Examples 1 to 12 had sufficient mechanical strength for skin application.

    TABLE-US-00002 TABLE 2 Natural moisturizing factor component (part by mass) Comparative Base Component Component Component Component Component Example (part by mass) 1 2 3 4 5 1 Sodium Arginine Glucosamine hyaluronate (9) (1) (90) 2 Sodium Sodium chondroitin pyrrolidone sulfate (20) carboxylate (80)

    [0072] In Comparative Example 1 and Comparative Example 2, the microneedles are brittle and have poor film properties.

    DESCRIPTION OF REFERENCE SYMBOLS

    [0073] 1 Mold [0074] 2 Cosmetic raw material liquid [0075] 11 Microneedle forming concave portion