WO2013047982A2 - Hydrogel composition for moisturizing skin and enhancing skin elasticity using properties of water - Google Patents

Hydrogel composition for moisturizing skin and enhancing skin elasticity using properties of water Download PDF

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WO2013047982A2
WO2013047982A2 PCT/KR2012/005295 KR2012005295W WO2013047982A2 WO 2013047982 A2 WO2013047982 A2 WO 2013047982A2 KR 2012005295 W KR2012005295 W KR 2012005295W WO 2013047982 A2 WO2013047982 A2 WO 2013047982A2
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skin
weight
hydrogel
moisturizing
hydrogel composition
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PCT/KR2012/005295
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French (fr)
Korean (ko)
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WO2013047982A3 (en
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추봉세
정성호
추예원
박경애
정주희
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Chu Bong Se
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241Containing particulates characterized by their shape and/or structure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/042Gels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds
    • A61K8/553Phospholipids, e.g. lecithin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/65Collagen; Gelatin; Keratin; Derivatives or degradation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/68Sphingolipids, e.g. ceramides, cerebrosides, gangliosides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/731Cellulose; Quaternized cellulose derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/41Particular ingredients further characterized by their size
    • A61K2800/413Nanosized, i.e. having sizes below 100 nm

Definitions

  • the present invention relates to a hydrogel composition for skin moisturizing and skin elasticity enhancement according to the maturity characteristics, more specifically, the hydration phenomenon over time due to the nature of the prescription hydrogel can not only obtain the cosmetic effect of the skin, but also nanoparticles
  • the ceramide component hwahwa the effect can be maintained for a long time
  • it relates to a hydrogel composition exhibiting excellent skin moisturizing and elasticity effect by inducing skin moisturizing, elasticity, collagen and elastin synthesis, etc. in the long-term use.
  • Hydrogels are used as dressings for wounds or lesions, as biological response modifiers, whereby dried hydrogels of hydrophilic-hygroscopic polymers or, more specifically, lyophilized hydrogels of polymeric carbohydrates.
  • hydrogels have been used mainly for the purpose of biopharmaceutical delivery systems or wound healing of skin, but in recent years, hydrogels have been applied to cosmetics.
  • Hydrogels which are biopharmaceutical carriers, mainly use hydrophilic polymers to facilitate skin penetration.
  • a polyethylene called conventional Pluronic is obtained by using a copolymer of polyarakelene glycol and polylactide or polyglycolide, polycaprolactone, which is a biodegradable polyester polymer.
  • Glycol and polyethylene oxide-polypropylene oxide-polyethylene oxide block copolymer are also used. These polymers are used to develop drug carrier hydrogels in the body.
  • Hydrogels developed for wound healing and the like serve to protect the wound from further trauma, environmental factors that slow down the healing process, or both.
  • Mannan including polysaccharides such as glucomannan and galactomannan, is used, which is widely used as a binder for the regulation of food tissues. Some encounters also show significant therapeutic properties.
  • Hydrogels used in cosmetics have been applied to the fields of skin care, skin care, skin treatment and the like. Mainly develops branched gelling polymer and electrolytic polymer according to product type. This is to make the delivery of drugs to the skin easy and rapid as affinity hydrogel.
  • the branched gelling polymer include galactomannan, glucomannan, guar gum, locust bean gum, and pluronic.
  • electrolytic gelling polymers agar, algin, carrageenan, xanthan and gellan are used. They can further formulate ingredients such as blends and moisturizers at appropriate temperatures to enhance skin intimacy, adhesion, and cosmetic effects.
  • Such polymers used in the hydrogel of cosmetics are rubbery substances present in plants or microorganisms, rubbery substances and mucus substances secreted from plants or microorganisms, and have high apparent viscosity and polysaccharides having unique properties.
  • Blacks are structurally hydrophilic (polar) or hydrophobic (non-polar) polymers of high molecular weight and usually exhibit colloidal properties and can form gels or produce high viscosity dispersions or solutions at low concentrations with the use of suitable solvents.
  • gum usually refers to plant or microbial polysaccharides or derivatives thereof that are dispersed in cold or hot water to form a viscous solution. Types include plant exudate gums, seaweed gums exuded from seaweed, seed gums exuded from plant seeds, starch and cellulose dervaties, microorganisms Microbial gums, and the like.
  • Agar is a rubbery material derived from algae extracted from viscous complex polysaccharides, which are cell wall components of red algae, including Gelidium and Gracilaria .
  • Agarose forms ⁇ -1,3 bonds of ⁇ -D-galactose and 3,6 anhydro- ⁇ -L-galactose
  • agaropectin is a sulfated ester of galactose in the basic structure of agarose, or D-glucuronic acid and a small amount of pyrivic acid Is combined. That is, they belong to polyelectrolytes in structure.
  • Agar is insoluble in cold water and is dissolved above 90 ° C to form colloidal solution. The properties of the agar are strong gelling, firm and form gels of brittle tissue, and do not dissolve well, ie have a high melting point.
  • Carrageenan was first extracted from Irish moss by residents of IRELAND Beach, County Carragheen, 600 years ago, and the term carrageen or carrageenan was first used in the patent literature on the separation and purification of irish moss from 1837 to 1871.
  • carrageenan is used in hundreds of products, from food to toothpaste, air fresheners and industrial suspensions.
  • Carrageenan from red seaweed forms the basic structure of the galactan family of repeating units of ⁇ -D-galactose linked by ⁇ -1,3 bond and ⁇ -D-galactose linked by ⁇ -1,4 bond. have.
  • alkali treatment is required for commercial purposes, and there are differences in structural changes such as kappa-type, lota-type, and lambda-type depending on the alkali treatment. appear.
  • Kappa carrageenan forms hard gels
  • lambda carrageenan does not form gels
  • rotacarrageenan forms semi-gels similar to vanadium gelatin.
  • Locust bean gum is a polysaccharide derived from the seeds of perennial legumes (Ceratonia siliqua, carob tree, ever green tree), widely grown in Spain, Italy, Sydney, Turkey, and Portugal.
  • the LBG powder may be ground or dissolved by dissolving in water, and after filtration, the polysaccharide thereof may be obtained by precipitation of alcohols.
  • Its structure is galactosmannan ⁇ galactose 1 unit per 4 units of mannose ⁇ .
  • Molecular weight of about 310,000 white or slightly yellowish brown powder, granular. It does not melt well in cold water, but melts well at about 80 °C and becomes mucus.
  • the viscosity is well formed at Ph 3.5 ⁇ 9.0 and the viscosity is decreased by salt, magnesium, inorganic acid or oxidizing agent. When used in combination with carrageenan or xanthan gum, it forms an elastic gel.
  • the hydrogel composition used in cosmetics is used by mixing agar or carrageenan and logger beast gum, moisturizer, pH adjuster, metal ion sequestrant, etc. and gelating them with appropriate monovalent or divalent cations.
  • Such a hydrogel composition exhibits a characteristic of adsorbing (absorbing) and releasing a large amount of solvents (solvents of water-soluble substances including water), that is, water release.
  • solvents solvents of water-soluble substances including water
  • the hydration of the hydrogel composition used in cosmetics is known to appear depending on the temperature of the skin (10 ⁇ 50 °C) (Korea Patent Registration No. 10-506543)
  • the hydrogel does not change to a fluid state by the temperature, Under the temperature of the hydrogel exposed to the air, the hydration occurs naturally. If the skin is closed under the temperature (10 ⁇ 50 °C) (ie, about 2 ⁇ 10 times larger than the area of the hydrogel mask), the hydration phenomenon according to temperature does not continue.
  • An object of the present invention for solving the above-mentioned conventional problems is that a hydrogel composition containing potassium alginate and potassium chloride, which are monovalent ions, in a hydrogel gel composition using a carrageenan and a locust bean gum, which are gelling polymers, are added in an appropriate combination Many phases appear, and the resulting moisturizing ingredients improve the adhesion of the skin as well as to provide a hydrogel composition that is effective in improving skin moisturizing, elasticity.
  • this study intends to make a hydrogel that can control the elasticity, strength and completion of the hydrogel.
  • the elasticity and strength of the gel depends on the content and mixing ratio of the gums used. Especially, the hydrogels can be optimized for the degree of breakage, hardness, adhesion, and elasticity through mixed ionic bonds with monovalent cations.
  • the technology seeks to develop products with optimized compatibility with suitable drug delivery materials.
  • Hydrogel composition for skin moisturizing and skin elasticity enhancement according to the characteristics of the present invention for solving the above problems, 0.5 to 3.0% by weight gelling polymer, 0.5 to 10.0% by weight collagen material, 5.0 to 20.0% by weight moisturizer, 0.04 ⁇ 1.0% by weight of monovalent cationic substance to adjust gel strength, 0.01 ⁇ 0.1% by weight of citric acid as acidity regulator, 0.02 ⁇ 0.1% by weight of metal ion sequestrant, 0.1 ⁇ 1.0% by weight of solubilizer (surfactant), combination It comprises 0.02-0.5% by weight fragrance, 0.2-0.6% preservative, and the remaining purified water.
  • the hydrogel composition is moisturizing retention effect is made by adding 0.1 to 5% by weight of the nano-material containing any one of ceramide, hydrogenated lecithin, caprylic / capric triglyceride, T-Cocoyl glutamate or cholesterol It is preferable at the point of view.
  • the gelling polymer is selected from the group consisting of agar, carrageenan, locust bean gum, gellan gum
  • the collagen material is marine collagen material extracted from fish dome scales
  • a substance selected from the group consisting of squalane, the monovalent cation material to control the gel strength is a material selected from the group consisting of potassium alginate, potassium chloride
  • the metal ion sequestrant is a disodium dithiate material
  • the solubilizing agent Is polysorbate and the preservative may be composed of methylparaben and phenoxyethanol.
  • the hydrogel composition of the present invention exhibits the best hydrate phenomenon, and thus has an excellent skin moisturizing effect.
  • the hydrogel composition can be maintained for a long time by adding particles in which nano-incorporated kinkin insoluble ceramide component is applied.
  • the hydrogel did not have fluidity under temperature response at 35 ° C., which is due to the hydrolysis of the hydrogel.
  • Figure 1 is a graph showing the weight loss rate as a fraction of the completion phenomenon according to time and temperature using a hydrogel of Sample No. S1.
  • Figure 2 is a graph showing the weight loss rate as a fraction of the completion phenomenon according to time and temperature using a hydrogel of Sample No. S2.
  • FIG. 3 is a graph showing the weight loss rate as a fraction of the completion phenomenon according to time and temperature using a hydrogel of Sample No. S3.
  • Figure 4 is a graph showing the completion of the development according to time and temperature using the hydrogel of Sample No. S4 as the weight loss ratio as a fraction.
  • FIG. 5 is a graph showing the weight loss rate as a fraction of the completion phenomenon according to time and temperature using a hydrogel of Sample No. S5.
  • FIG. 6 is a graph showing the weight loss rate as a fraction of the completion phenomenon according to time and temperature using a hydrogel of Sample No. S6.
  • Figure 7 is a graph measuring the moisturizing rate according to the hydrogel composition with time changes in a constant temperature and humidity conditions at 25 °C.
  • Figure 8 is a graph measuring the moisturizing rate with time by adding 0.5%, 1%, 3%, 5% each of the cosmetic ingredients using nanotechnology to each hydrogel prescription.
  • hydrogel composition for enhancing skin moisturizing and skin elasticity and its effects according to the maturity characteristics according to the present invention.
  • the hydrogel composition according to the present invention can be used to prepare a mask pack containing a cosmetic ingredient incorporating nanotechnology in a cloth mesh.
  • Hydrogel composition according to the present invention, gelling polymer 0.5 ⁇ 3.0% by weight, collagen material 0.5 ⁇ 10.0% by weight, moisturizer 5.0 ⁇ 20.0% by weight, monovalent cationic substance to adjust the gel strength 0.04-1.0% by weight, acidity regulator 0.01 ⁇ 0.1%, 0.02 ⁇ 0.1% by weight of metal ion blocker, 0.1 ⁇ 1.0% by weight of solubilizer (surfactant), 0.02 ⁇ 0.5% by weight of combination fragrance, 0.2 ⁇ 0.6% of preservative, 58.7 ⁇ 93.51% by weight of purified water
  • One nanomaterial may comprise 0.1-5%.
  • the hydrogel composition according to the present invention is 0.5wt% to 3.0wt% of a substance selected from the group consisting of gelling polymers agar, carrageenan, locust bean gum and gellan gum, and marine collagen material extracted from fish dome scales 0.5 to 10.0.
  • the content of the gum agar, carrageenan, logger bean bean gum, gellan gum and the like is preferably 0.5wt to 3wt% based on the total weight of the composition.
  • the content is preferably 5wt% to 20wt% based on the total weight of the composition.
  • the gel mask may fall easily when attached to the face when the content is less than 5 wt% based on the total blending amount, that is, when the content is 20 wt% or more, it may cause stickiness to the face after using the gel mask. Therefore, 5% to 20% of the content is appropriate to give skin moisturization without adhesion and stickiness of the hydrogel.
  • glycerin and butylene glycol which are used moisturizers, can easily maintain the moisturizing power according to the change over time after using the hydrogel mask.
  • the hydrogel composition according to the present invention may be appropriately mixed and administered in an appropriate amount in consideration of the required action, that is, diarrhea and moisturizing effect.
  • composition according to the present invention may further include a drug delivery material using other nanotechnology generally known.
  • Typical drug delivery agents that may be used include ceramides, phytosphingosines, oil-soluble cosmetics, and the like, such as tocopherol acetate, retinol, and the like, as well as bases, excipients, lubricants, and preservatives.
  • Samples of the hydrogel composition were prepared according to the preparation method of combining the six samples shown in the following [Table 1] with the following components.
  • Hydrogel composition was made using a total of six prescriptions from Sample.No.S1 to Sample.No.S6 as shown in Table 1 of the Examples.
  • the A and B phases are sequentially added to the HOMO mixer kiln, stirred from room temperature, gradually stirred at about 80 ° C, the temperature is raised, and sufficiently stirred and dispersed.
  • phase C was stirred at room temperature, and then charged into a mixer kiln, followed by gradual stirring to disperse.
  • phase D is added to a mixer kiln and slowly stirred to dissolve.
  • the E and F phases are sequentially added and stirred. After stirring for about 5 to 10 minutes using a coating machine to make a hydrogel using a PET material or OPP material and a mesh type mesh cloth used as a support for the hydrogel to make a gelled mask by cooling to about 30 °C.
  • the gelled hydrogel mask of the six samples described above was reduced to make samples corresponding to 4 ° C, 25 ° C, 35 ° C and 50 ° C. At this time, each sample is classified into an A-type in which the hydrogel is sealed and a B-type in the open state.
  • Figures 1 to 6 are graphs showing the weight loss rate as a fraction of the completion of development according to time and temperature using the hydrogels of Sample No. S1 to Sample No. S6.
  • Sample.No.S1 / A to Sample.No.S6 / A are in a sealed state
  • Sample.No.S1 / B to Sample.No.S6 / B mean an open state.
  • Moisturizing power was analyzed using Corneometer (CM820PC, Courage Khazka, Germany) at 25 ° C. under room constant temperature and humidity conditions.
  • hydrogel masks were prepared according to the prescription of Sample. No. S1 to S6, and then applied to the face and removed after 1 hour, and the change in moisturizing power over time was measured.
  • Figure 8 is a graph measuring the moisturizing rate with time by adding 0.5%, 1%, 3%, 5% each of the cosmetic ingredients using nanotechnology to each hydrogel prescription.
  • Ceramide, hydrogenated lecithin, caprylic / capric triglyceride, tie-cocoyl glutamate, and cholesterol components used as nanoderivatives and cosmetic ingredients are appropriately mixed to make nanoparticles using high pressure, and then 0.5wt% to 5wt%
  • the hydrogel mask was prepared by adding to the prescription of Sample.No.S6, and then the moisturizing power of the hydrogel mask was measured at 25 ° C. under constant temperature and humidity conditions.
  • Sample.No.S6 (0.0wt%) has 0.0wt% of nanomaterial added to Sample.No.S6, Sample.No.S6 (0.5wt%) has 0.5wt% of nanomaterial added to Sample.No.S6, Sample.No.S6 (1.0wt%) has 1.0wt% of nanomaterial added to Sample.No.S6, Sample.No.S6 (3.0wt%) has 3.0wt% of nanomaterial added to Sample.No.S6, Sample No. S6 (5.0 wt%) means that the nanomaterial addition rate is 5.0 wt% in Sample No. S 6.
  • ceramide with skin barrier function penetrates the skin according to hydration and relatively strengthens skin barrier function.
  • Caprylic / capric triglycerides and cholesterol components which are oil components contained in nano components, It is effective in maintaining moisturizing.
  • the hardness value according to the temperature of the contents according to the formulation of each hydrogel composition was measured.
  • the hardness measuring device was a FUDOH RHEOMETER. (Japan JAPAN), the plunger area (PLUNGER AREA) is 1cm2, the lift up speed (lift up speed) was measured the hardness of the hydrogel under 6cm / min.
  • the hardness change according to the temperature of the sealed hydrogel and the unsealed hydrogel shows a different tendency as a result of measuring the change in hardness.

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Abstract

The present invention relates to a hydrogel composition for moisturizing skin and enhancing skin elasticity using properties of water. More particularly, the present invention relates to a hydrogel composition enhancing moisture and elasticity of the skin, in which the hydrogel composition utilizes water over time due to hydrogel properties to provide skin care effects, also contains ceramide components of nanoparticles to maintain skin care effects over a long period of time, and induces skin moisturizing, skin elasticity, collagen and elastin synthesis during long-term use of the composition, thereby exhibiting excellent skin care effects. The hydrogel composition for moisturizing skin and enhancing skin elasticity using properties of water according to the present invention, comprises 0.5-3.0 wt% of a gelation polymer, 0.5-10.0 wt% of collagen, 5.0-20.0 wt% of a moisturizer, 0.04-1.0 wt% of a monovalent cationic ingredient for adjusting gel strength, 0.01-0.1 wt% of citric acid which is an acidity regulator, 0.02-0.1 wt% of a sequestering agent, 0.1-1.0 wt% of a solubilizing agent (surfactant), 0.02-0.5 wt% of combined perfumes, 0.2-0.6 wt% of a preserving agent, and the remainder being refined water.

Description

이수 특성에 따른 피부 보습 및 피부 탄력 증진용 하이드로 겔 조성물Hydrogel composition for skin moisturizing and skin elasticity improvement
본 발명은 이수 특성에 따른 피부 보습 및 피부 탄력 증진용 하이드로 겔 조성물에 관한 것으로서, 보다 상세하게는 처방상의 하이드로 겔의 특성상 시간 경과에 따른 이수현상이 피부의 미용효과를 얻을 수 있을 뿐만 아니라, 나노 입자화 시킨 세라마이드 성분을 함유함으로서 그 효과를 장시간 동안 유지할 수 있으며, 장기간 사용시 피부 보습, 탄력, 콜라겐 및 엘라스틴 합성등을 유도하여 피부 개선 효과가 우수한 피부 보습 및 탄력 효과를 나타내는 하이드로겔 조성물에 관한 것이다.The present invention relates to a hydrogel composition for skin moisturizing and skin elasticity enhancement according to the maturity characteristics, more specifically, the hydration phenomenon over time due to the nature of the prescription hydrogel can not only obtain the cosmetic effect of the skin, but also nanoparticles By containing the ceramide component hwahwa the effect can be maintained for a long time, it relates to a hydrogel composition exhibiting excellent skin moisturizing and elasticity effect by inducing skin moisturizing, elasticity, collagen and elastin synthesis, etc. in the long-term use.
하이드로 겔을 이용한 약물 전달체 개발을 위하여 자극(온도, pH, 광, 전장, 자장 등) 감응형 블록 공중합체를 이용한 각종 연구개발이 활발히 이루어지고 있다. 하이드로 겔은 상처 또는 병변용 드레싱, 생물학적 반응 조절제로서 사용되어지는데 이때는 친수성-흡습성 중합체의 건조된 하이드로겔 또는 보다 구체적으로는 중합체성 탄수화물의 동결 건조된 하이드로 겔을 사용하기도 한다. 이 처럼 하이드로 겔은 그동안 주로 생체 약물 전달 체계 또는 피부의 상처 치유등의 목적으로 사용되어졌으나, 최근에는 이를 화장품에 응용한 하이드로 겔이 개발되는 추세이다. In order to develop drug carriers using hydrogels, various researches and developments using stimulus-sensitive block copolymers (temperature, pH, light, electric field, magnetic field, etc.) have been actively conducted. Hydrogels are used as dressings for wounds or lesions, as biological response modifiers, whereby dried hydrogels of hydrophilic-hygroscopic polymers or, more specifically, lyophilized hydrogels of polymeric carbohydrates. As such, hydrogels have been used mainly for the purpose of biopharmaceutical delivery systems or wound healing of skin, but in recent years, hydrogels have been applied to cosmetics.
생체 약물 전달체인 하이드로 겔은 피부 침투를 용이하게 하기 위해 주로 친수성 고분자 폴리머를 사용한다. 하이드로 겔 형성에 사용되는 원료로는 폴리아라켈렌글리콜과 생분해성 폴리에스테르 고분자인 폴리락타이드 또는 폴리글리콜라이드, 폴리카프로락톤과의 공중합체를 이용하여 기존의 플루로닉(Pluronic)이라고 불리어진 폴리에틸렌글리콜과 폴리에틸렌옥사이드-폴리프로필렌옥사이드-폴리에틸렌옥사이드 블록 공중합체를 사용하기도 한다. 이러한 폴리머들은 체내의 약물전달체 하이드로 겔 개발 시 사용한다.Hydrogels, which are biopharmaceutical carriers, mainly use hydrophilic polymers to facilitate skin penetration. As a raw material for forming a hydrogel, a polyethylene called conventional Pluronic is obtained by using a copolymer of polyarakelene glycol and polylactide or polyglycolide, polycaprolactone, which is a biodegradable polyester polymer. Glycol and polyethylene oxide-polypropylene oxide-polyethylene oxide block copolymer are also used. These polymers are used to develop drug carrier hydrogels in the body.
상처치유 등의 목적으로 개발되는 하이드로 겔은 추가의 외상, 치유 과정을 늦추는 환경적요인 또는 이들 모두로부터 상처를 보호하는 역할을 한다. 주로 다당류인 글루코만난 및 갈락토만난등을 포함하는 만난을 사용하는데, 이는 식물성 검 형태의 갈락토만난은 식품 조직의 조절을 위해 결합제로서 널리 사용되고 있다. 또한 몇 가지 만난은 상당한 치료학적 특성을 나타낸다.Hydrogels developed for wound healing and the like serve to protect the wound from further trauma, environmental factors that slow down the healing process, or both. Mannan, including polysaccharides such as glucomannan and galactomannan, is used, which is widely used as a binder for the regulation of food tissues. Some encounters also show significant therapeutic properties.
화장품 등에 사용되는 하이드로 겔은 스킨 케어, 피부미용, 피부 치료 등의 분야에 적용하고 있다. 주로 가지형 겔화 고분자, 전해형 고분자 등을 적절히 섞어 제품의 형태에 맞게 개발한다. 이는 친화성이 큰 하이드로 겔로서 피부로 약물의 전달이 용이하고 신속하게 일어날 수 있도록 하기 위함이다. 가지형 겔화 고분자로서 갈락토만난, 글루코만난, 구아껌, 로카스트 빈 껌 및 플루로닉등이며, 전해형 겔화 고분자로서는 아가, 알긴, 카라기난, 잔탄 및 겔란 등을 사용한다. 이들은 적절한 온도에서 배합과 보습제등의 성분을 추가로 배합하여 피부의 친밀도, 밀착력, 미용효과등을 높힐 수 있다.Hydrogels used in cosmetics have been applied to the fields of skin care, skin care, skin treatment and the like. Mainly develops branched gelling polymer and electrolytic polymer according to product type. This is to make the delivery of drugs to the skin easy and rapid as affinity hydrogel. Examples of the branched gelling polymer include galactomannan, glucomannan, guar gum, locust bean gum, and pluronic. As electrolytic gelling polymers, agar, algin, carrageenan, xanthan and gellan are used. They can further formulate ingredients such as blends and moisturizers at appropriate temperatures to enhance skin intimacy, adhesion, and cosmetic effects.
화장품의 하이드로 겔에 사용되는 이와 같은 고분자 즉, 검류 등은 식물이나 미생물에 존재하는 고무질 물질, 식물이나 미생물에서 분비되는 고무질 물질들과 점액 물질들로 외관상의 점도가 크며, 특유한 성질을 가진 다당류를 말한다. 검은 구조적으로 친수(극성) 또는 소수성(비극성)의 고분자 중량을 가지는 분자들이며 보통 콜로이드 특성을 나타내며 적당한 용매의 사용하에서 낮은 농도에서도 겔을 형성하거나 고점도 분산액 또는 용액을 생성할 수 있다. 그러나 보통 검이라고하면 냉수 또는 열수에서 분산하여 점성이 있는 용액을 만드는 식물 또는 미생물 다당류 또는 그 유도체를 말한다. 그 종류로는 식물 조직의 고무질 물질(Plant exudate gums), 해조에서 삼출된 고무질 물질(Seaweed gums), 식물 종자에서 삼출된 고무질 물질(Seed gums), 전분 및 셀룰로스 유도체(Starch and cellulose dervaties), 미생물 유래 고무질 물질(Microbial gums)등으로 나눌 수 있다.Such polymers used in the hydrogel of cosmetics, such as gum, are rubbery substances present in plants or microorganisms, rubbery substances and mucus substances secreted from plants or microorganisms, and have high apparent viscosity and polysaccharides having unique properties. Say. Blacks are structurally hydrophilic (polar) or hydrophobic (non-polar) polymers of high molecular weight and usually exhibit colloidal properties and can form gels or produce high viscosity dispersions or solutions at low concentrations with the use of suitable solvents. However, gum usually refers to plant or microbial polysaccharides or derivatives thereof that are dispersed in cold or hot water to form a viscous solution. Types include plant exudate gums, seaweed gums exuded from seaweed, seed gums exuded from plant seeds, starch and cellulose dervaties, microorganisms Microbial gums, and the like.
주로 사용되는 검으로는 한천(agar), 카라기난(carrageenan), 로커스트 빈 검(Locust bean gum)등이 사용된다. 한천은 우뭇가사리(Gelidium)와 꼬시래기(Gracilaria속)를 비롯한 홍조류의 세포벽 구성 성분인 점질성 복합 다당류를 추출한 해조류 유래의 고무질 물질로서, 겔 형성능이 뛰어난 agarose와 agaropectin의 2중 helix 구조로 형성되어 있으며, agarose는 β-D-galactose와 3,6 anhydro-α-L-galactose의 β-1,3 결합을 형성하고 agaropectin 는 agarose의 기본 구조에 galactose가 황산에스테르화 되거나 D-glucuronic acid와 소량의 pyrivic acid가 결합되어있다. 즉 구조상 다가 전해질(polyelectrolytes)에 속한다. 한천은 냉수에 녹지 않고, 90℃ 이상에서용해되어 콜로이드 용액을 형성한다. 한천의 특성은 겔화력이 강하며 단단하며(firm) 퍼석한(brittle) 조직의 겔을 형성한다는 것과 잘 용해되지 않는 즉 융점이 높다.Commonly used gums include agar, carrageenan, and locust bean gum. Agar is a rubbery material derived from algae extracted from viscous complex polysaccharides, which are cell wall components of red algae, including Gelidium and Gracilaria . Agarose forms β-1,3 bonds of β-D-galactose and 3,6 anhydro-α-L-galactose, and agaropectin is a sulfated ester of galactose in the basic structure of agarose, or D-glucuronic acid and a small amount of pyrivic acid Is combined. That is, they belong to polyelectrolytes in structure. Agar is insoluble in cold water and is dissolved above 90 ° C to form colloidal solution. The properties of the agar are strong gelling, firm and form gels of brittle tissue, and do not dissolve well, ie have a high melting point.
카라기난은 600년전 County Carragheen 남 IRELAND 해변의 주민들이 Irish moss 를 추출한 것을 시작으로 1837~1871년 당시의 irish moss 의 분리 정제에 관한 특허 문언에서 carrageen 또는 carrageenan 이라는 말이 처음으로 사용되기 시작하였다. 오늘날 카라기난은 식품에서 치약, 공기청향제, 공업서스펜션까지 수백가지 제품에 쓰인다. 홍조류(red seaweed)에서 만들어지는 카라기난은 β-1,3 결합으로 연결된 β-D-galactose와 α-1,4 결합으로 연결된 α-D-galactose를 반복 단위로 하는 galactan 류의 기본 구조를 형성하고 있다. 자연상태와는 달리 상업적 목적을 위하여 알칼리 처리가 필요하며, 알칼리 처리에 따라 카파(Kappa-type)타입, 로타타입(lota-type), 람다타입(Lambda-type)등으로 구조적인 변화의 차이가 나타난다. 카파 카라기난은 단단한 겔을 형성하고 람다 카라기난은 겔을 형성하지 못하며 로타카라기난은 바나고체의 젤라틴과 유사한 겔(semi-gel)을 형성한다.Carrageenan was first extracted from Irish moss by residents of IRELAND Beach, County Carragheen, 600 years ago, and the term carrageen or carrageenan was first used in the patent literature on the separation and purification of irish moss from 1837 to 1871. Today, carrageenan is used in hundreds of products, from food to toothpaste, air fresheners and industrial suspensions. Carrageenan from red seaweed forms the basic structure of the galactan family of repeating units of β-D-galactose linked by β-1,3 bond and α-D-galactose linked by α-1,4 bond. have. Unlike the natural state, alkali treatment is required for commercial purposes, and there are differences in structural changes such as kappa-type, lota-type, and lambda-type depending on the alkali treatment. appear. Kappa carrageenan forms hard gels, lambda carrageenan does not form gels, and rotacarrageenan forms semi-gels similar to vanadium gelatin.
로거스트 빈 검(Locust bean gum)은 스페인, 이태리, 모로코, 터키, 포르투갈에서 널리 재배되고 있는 다년생 콩과 식물(Ceratonia siliqua, carob tree, ever green tree)의 종자에서 얻어지는 다당류로서 열매의 배유 부분을 분쇄하거나 LBG 분말을 물에 녹여 용해하고, 여과 후 그의 다당류를 알코올 류의 침전에 의해 얻을 수 있다. 구조는 갈락토만난으로 {만노스 4 unit당 갈락토스 1unit}되어 있다. 분자량이 약 31만의 백색 또는 약간의 황갈색의 분말, 과립상으로 되어 있따. 냉수에는 잘 녹지 않고 약 80℃ 에서 잘 녹고 점액질 상태가 된다. Ph 3.5~9.0에서 점도가 잘 형성되며 염, 마그네슘, 무기산 또는 산화제에 의해 점도가 떨어진다. 카라기난 또는 산탄검과 혼용하여 사용하였을때에 탄력있는 겔을 형성한다.Locust bean gum is a polysaccharide derived from the seeds of perennial legumes (Ceratonia siliqua, carob tree, ever green tree), widely grown in Spain, Italy, Morocco, Turkey, and Portugal. The LBG powder may be ground or dissolved by dissolving in water, and after filtration, the polysaccharide thereof may be obtained by precipitation of alcohols. Its structure is galactosmannan {galactose 1 unit per 4 units of mannose}. Molecular weight of about 310,000 white or slightly yellowish brown powder, granular. It does not melt well in cold water, but melts well at about 80 ℃ and becomes mucus. The viscosity is well formed at Ph 3.5 ~ 9.0 and the viscosity is decreased by salt, magnesium, inorganic acid or oxidizing agent. When used in combination with carrageenan or xanthan gum, it forms an elastic gel.
화장품에 사용되는 하이드로겔 조성물은 한천이나 카라기난 그리고 로거비스트 검등과 보습제, pH조절제, 금속이온봉쇄제등을 혼합하고 적절한 1가 내지 2가 양이온을 이용하여 겔화 시켜 사용한다. 이와 같은 하이드로 겔 조성물은 많은 양의 용매(물을 포함한 수용성 물질의 용매들)를 흡착(흡수)했다가 배출하는 특성 즉, 이수현상(water release)이 제각기 나타난다. 이수현상을 통해서 용매에 들어있는 미용성분들이 피부의 미용 효과를 가져다 준다.The hydrogel composition used in cosmetics is used by mixing agar or carrageenan and logger beast gum, moisturizer, pH adjuster, metal ion sequestrant, etc. and gelating them with appropriate monovalent or divalent cations. Such a hydrogel composition exhibits a characteristic of adsorbing (absorbing) and releasing a large amount of solvents (solvents of water-soluble substances including water), that is, water release. Through Isu phenomenon, the beauty ingredients in the solvent bring the beauty effect of the skin.
그러나 이처럼 화장품에 사용하는 하이드로겔 조성물의 이수현상이 피부의 온도에 따라(10~50℃) 나타나는 것으로 알려져 있으나(대한민국 특허등록 제10-506543호) 온도에 의하여 하이드로겔이 유동상태로 변하는 것이 아니라, 하이드로겔이 공기중으로 노출된 상태의 온도하에 이수현상이 자연스럽게 이루어 지는 것이다. 만일 피부의 온도하에(10~50℃) 밀폐된 상태(즉, 하이드로겔 마스크 면적대비 약 2~10배) 에서는 온도에 따른 이수현상이 계속 나타나지는 않는다. 또한 이수현상에 따른 하이드로 겔 조성물이 피부의 보습, 탄력에 어떠한 효과를 나타내는지 아직 알려진 바가 없다.However, the hydration of the hydrogel composition used in cosmetics is known to appear depending on the temperature of the skin (10 ~ 50 ℃) (Korea Patent Registration No. 10-506543) The hydrogel does not change to a fluid state by the temperature, Under the temperature of the hydrogel exposed to the air, the hydration occurs naturally. If the skin is closed under the temperature (10 ~ 50 ℃) (ie, about 2 ~ 10 times larger than the area of the hydrogel mask), the hydration phenomenon according to temperature does not continue. In addition, it is not yet known how the hydrogel composition according to the hydration effect on the moisturizing, elasticity of the skin.
상술한 종래의 문제점을 해결하기 위한 본 발명의 과제는, 겔화 고분자인 카라기난과 로거스트 빈검을 사용한 하이드로겔 겔 조성물에 1가 이온인 포타슘 알지네이트, 포타슘 클로라이드를 함께 적절한 배합으로 많든 하이드로겔 조성물은 이수현상이 많이 나타나며, 이로 인한 보습 성분 등이 피부의 밀착력을 향상시켜 줄 뿐만 아니라 피부 보습, 탄력 증진에 효과가 있는 하이드로 겔 조성물을 제공하고자 한다.SUMMARY OF THE INVENTION An object of the present invention for solving the above-mentioned conventional problems is that a hydrogel composition containing potassium alginate and potassium chloride, which are monovalent ions, in a hydrogel gel composition using a carrageenan and a locust bean gum, which are gelling polymers, are added in an appropriate combination Many phases appear, and the resulting moisturizing ingredients improve the adhesion of the skin as well as to provide a hydrogel composition that is effective in improving skin moisturizing, elasticity.
따라서 본 연구는 이와 같은 하이드로겔이 탄력과 강도 및 이수현상을 조절할 수 있는 하이드로겔을 만들고자 한다. Therefore, this study intends to make a hydrogel that can control the elasticity, strength and completion of the hydrogel.
겔의 탄력과 강도는 사용되어지는 검류의 함량과 혼합배율에 따라 달라지며 특히 1가의 양이온들과의 혼합된 이온결합을 통해 부러짐 정도, 경도, 밀착력, 탄성력 등이 최적화할 수 있는 하이드로겔에 나노기술을 적합한 약물전달 물질과의 상용성이 최적화된 제품을 개발하고자 한다.The elasticity and strength of the gel depends on the content and mixing ratio of the gums used. Especially, the hydrogels can be optimized for the degree of breakage, hardness, adhesion, and elasticity through mixed ionic bonds with monovalent cations. The technology seeks to develop products with optimized compatibility with suitable drug delivery materials.
상술한 과제를 해결하기 위한 본 발명에 따른 이수 특성에 따른 피부 보습 및 피부 탄력 증진용 하이드로겔 조성물은, 겔화 고분자 0.5~3.0중량%, 콜라겐 물질 0.5~10.0중량%, 보습제 5.0~20.0중량%, 겔 강도를 조절하는 1가 양이온 물질 0.04~1.0중량%, 산도조절제인 씨트릭애씨드 0.01~0.1중량%, 금속이온봉쇄제 0.02~0.1중량%, 가용화제(계면활성제) 0.1~1.0중량%, 조합향료 0.02~0.5중량%, 보존제 0.2~0.6%, 나머지 정제수를 포함하여 이루어진다. Hydrogel composition for skin moisturizing and skin elasticity enhancement according to the characteristics of the present invention for solving the above problems, 0.5 to 3.0% by weight gelling polymer, 0.5 to 10.0% by weight collagen material, 5.0 to 20.0% by weight moisturizer, 0.04 ~ 1.0% by weight of monovalent cationic substance to adjust gel strength, 0.01 ~ 0.1% by weight of citric acid as acidity regulator, 0.02 ~ 0.1% by weight of metal ion sequestrant, 0.1 ~ 1.0% by weight of solubilizer (surfactant), combination It comprises 0.02-0.5% by weight fragrance, 0.2-0.6% preservative, and the remaining purified water.
여기서, 상기 하이드로겔 조성물은 세라마이드, 수첨레시틴, 카프릴릭/카프릭 트리글리세라이드, 티이에이-코코일 글루타메이트 또는 콜레스테롤 중 어느 하나를 함유한 나노물질 0.1~5중량%를 첨가되어 이루어지는 것이 보습 유지 효과면에서 바람직하다.Here, the hydrogel composition is moisturizing retention effect is made by adding 0.1 to 5% by weight of the nano-material containing any one of ceramide, hydrogenated lecithin, caprylic / capric triglyceride, T-Cocoyl glutamate or cholesterol It is preferable at the point of view.
여기서, 상기 겔화 고분자는 한천, 카라기난, 로거스트빈검, 겔란검으로 이루어진 군에서 선택되며, 상기 콜라겐 물질은 생선 돔 비늘에서 추출한 해양성 콜라겐 물질이고, 상기 보습제는 글리세린, 부틸렌글라이콜, 베타인, 스쿠알란으로 이루어진 군에서 선택된 물질이며, 상기 겔 강도를 조절하는 1가 양이온 물질은 포타슘 알지네이트, 포타슘 클로라이드으로 이루어진 군에서 선택된 물질이고, 상기 금속이온 봉쇄제는 디소듐이디티에이 물질이고, 상기 가용화제는 폴리소르베이트이며, 상기 보존제는 메칠파라벤 및 페녹시에탄올로 이루어질 수 있다.Here, the gelling polymer is selected from the group consisting of agar, carrageenan, locust bean gum, gellan gum, the collagen material is marine collagen material extracted from fish dome scales, the moisturizing agent glycerin, butylene glycol, betaine, A substance selected from the group consisting of squalane, the monovalent cation material to control the gel strength is a material selected from the group consisting of potassium alginate, potassium chloride, the metal ion sequestrant is a disodium dithiate material, the solubilizing agent Is polysorbate, and the preservative may be composed of methylparaben and phenoxyethanol.
상술한 본 발명의 구성에 따르면, 본 발명의 하이드로겔 조성물은 이수현상이 가장 잘 나타나며, 이에 따라 피부 보습효과가 우수하다. According to the above-described configuration of the present invention, the hydrogel composition of the present invention exhibits the best hydrate phenomenon, and thus has an excellent skin moisturizing effect.
또한 본 하이드로겔 조성물에 나노기술을 접목식킨 불용성 세라마이드 성분을 나노화 시킨 입자를 첨가하여 보습력이 오래 유지될 수 있다. In addition, the hydrogel composition can be maintained for a long time by adding particles in which nano-incorporated kinkin insoluble ceramide component is applied.
이는 화장용 마스크팩으로서 보습효과가 우수한 특징인 생체 친화적으로 인해 마스크 팩으로서 피부 미용에 효과적이다.It is effective for skin beauty as a mask pack due to the bio-friendly characteristics of the excellent moisturizing effect as a cosmetic mask pack.
본 발명의 실시예에 따라 신체 피부인 35℃ 하에서 하이드로겔이 온도감응에 따른 유동성을 갖는 것이 아님을 알 수 있었으며, 이는 하이드로겔의 이수현상에 의한 것임을 알 수 있다.According to an embodiment of the present invention, it was found that the hydrogel did not have fluidity under temperature response at 35 ° C., which is due to the hydrolysis of the hydrogel.
도 1은 Sample.No.S1의 하이드로겔을 이용하여 시간과 온도에 따른 이수현상을 무게감소율을 분율로 하여 표시한 그래프이다.Figure 1 is a graph showing the weight loss rate as a fraction of the completion phenomenon according to time and temperature using a hydrogel of Sample No. S1.
도 2는 Sample.No.S2의 하이드로겔을 이용하여 시간과 온도에 따른 이수현상을 무게감소율을 분율로 하여 표시한 그래프이다.Figure 2 is a graph showing the weight loss rate as a fraction of the completion phenomenon according to time and temperature using a hydrogel of Sample No. S2.
도 3은 Sample.No.S3의 하이드로겔을 이용하여 시간과 온도에 따른 이수현상을 무게감소율을 분율로 하여 표시한 그래프이다.FIG. 3 is a graph showing the weight loss rate as a fraction of the completion phenomenon according to time and temperature using a hydrogel of Sample No. S3.
도 4는 Sample.No.S4의 하이드로겔을 이용하여 시간과 온도에 따른 이수현상을 무게감소율을 분율로 하여 표시한 그래프이다. Figure 4 is a graph showing the completion of the development according to time and temperature using the hydrogel of Sample No. S4 as the weight loss ratio as a fraction.
도 5는 Sample.No.S5의 하이드로겔을 이용하여 시간과 온도에 따른 이수현상을 무게감소율을 분율로 하여 표시한 그래프이다. FIG. 5 is a graph showing the weight loss rate as a fraction of the completion phenomenon according to time and temperature using a hydrogel of Sample No. S5.
도 6은 Sample.No.S6의 하이드로겔을 이용하여 시간과 온도에 따른 이수현상을 무게감소율을 분율로 하여 표시한 그래프이다.6 is a graph showing the weight loss rate as a fraction of the completion phenomenon according to time and temperature using a hydrogel of Sample No. S6.
도 7은 25℃ 하에 항온항습조건에서 시간변화에 따른 하이드로겔 조성물에 따른 보습율을 측정한 그래프이다.Figure 7 is a graph measuring the moisturizing rate according to the hydrogel composition with time changes in a constant temperature and humidity conditions at 25 ℃.
도 8은 하이드로겔 각 처방에 나노기술을 이용한 미용성분을 각 0.5%, 1%, 3%, 5% 씩 첨가하여 시간에 따른 보습율을 측정한 그래프이다.Figure 8 is a graph measuring the moisturizing rate with time by adding 0.5%, 1%, 3%, 5% each of the cosmetic ingredients using nanotechnology to each hydrogel prescription.
도 9는 각각의 하이드로겔 시료의 온도에 따른 경도 변화를 나타낸 그래프이다.9 is a graph showing the change in hardness according to the temperature of each hydrogel sample.
이하, 첨부된 도면을 참조하여 본 발명에 따른 이수 특성에 따른 피부 보습 및 피부 탄력 증진용 하이드로 겔 조성물 및 그에 따른 작용효과를 설명한다.Hereinafter, with reference to the accompanying drawings will be described a hydrogel composition for enhancing skin moisturizing and skin elasticity and its effects according to the maturity characteristics according to the present invention.
본 발명에 의한 하이드로겔 조성물은 천 재질의 망사에 나노기술을 접목시킨 미용성분이 함유된 마스크 팩을 제조하는 데 이용될 수 있다.The hydrogel composition according to the present invention can be used to prepare a mask pack containing a cosmetic ingredient incorporating nanotechnology in a cloth mesh.
본 발명에 따른 하이드로겔 조성물은, 겔화 고분자 0.5~3.0중량%, 콜라겐 물질 0.5~10.0중량%, 보습제 5.0~20.0중량%, 겔 강도를 조절하는 1가 양이온 물질 0.04~1.0중량%, 산도조절제 0.01~0.1%, 금속이온봉쇄제 0.02~0.1중량%, 가용화제(계면활성제) 0.1~1.0중량%, 조합향료 0.02~0.5중량%, 보존제 0.2~0.6%, 정제수 58.7~93.51중량%에 세라마이드를 함유한 나노물질 0.1~5%를 포함하여 이루어질 수 있다.Hydrogel composition according to the present invention, gelling polymer 0.5 ~ 3.0% by weight, collagen material 0.5 ~ 10.0% by weight, moisturizer 5.0 ~ 20.0% by weight, monovalent cationic substance to adjust the gel strength 0.04-1.0% by weight, acidity regulator 0.01 ~ 0.1%, 0.02 ~ 0.1% by weight of metal ion blocker, 0.1 ~ 1.0% by weight of solubilizer (surfactant), 0.02 ~ 0.5% by weight of combination fragrance, 0.2 ~ 0.6% of preservative, 58.7 ~ 93.51% by weight of purified water One nanomaterial may comprise 0.1-5%.
더욱 구체적으로는 본 발명에 따른 하이드로겔 조성물은 겔화 고분자인 한천, 카라기난, 로거스트빈검, 겔란검으로 이루어진 군에서 선택된 물질 0.5wt% 내지 3.0wt%, 생선 돔 비늘에서 추출한 해양성 콜라겐 물질 0.5~10.0중량%, 보습제인 글리세린, 부틸렌글라이콜, 베타인,스쿠알란으로 이루어진 군에서 선택된 물질 5.0wt% 내지 20.0wt%, 겔 강도를 조절하는 1가 양이온 물질인 포타슘 알지네이트, 포타슘 클로라이드으로 이루어진 군에서 선택된 물질 0.04~1.0중량%, 산도조절제인 씨트릭애씨드 물질 0.01~0.1중량%, 금속이온 봉쇄제인 디소듐이디티에이 물질 0.02~0.1중량%, 가용화제인 폴리소르베이트 20 물질인 0.1~1.0중량%, 조합향료 물질 0.02~0.5중량%, 보존제인 메칠파라벤,페녹시에탄올 물질 0.2~0.6중량%, 나노물질로서 세라마이드, 수첨레시틴, 카프릴릭/카프릭 트리글리세라이드, 티이에이-코코일 글루타메이트, 콜레스테롤으로 이루어진 나노 물질 0.1~5.0중량%, 정제수 58.7~93.51중량%를 포함하여 이루어질 수 있다.More specifically, the hydrogel composition according to the present invention is 0.5wt% to 3.0wt% of a substance selected from the group consisting of gelling polymers agar, carrageenan, locust bean gum and gellan gum, and marine collagen material extracted from fish dome scales 0.5 to 10.0. Weight%, moisturizing agents selected from the group consisting of glycerin, butylene glycol, betaine, squalane 5.0wt% to 20.0wt%, a monovalent cationic substance for controlling the gel strength potassium alginate, potassium chloride selected from the group consisting of 0.04 ~ 1.0% by weight of material, 0.01 ~ 0.1% by weight of citrate acid as acidity regulator, 0.02 ~ 0.1% by weight of disodium IDT, which is a metal ion sequestering agent, 0.1 ~ 1.0% by weight, which is 20 solubilizing agent of polysorbate 20, Combination fragrance substance 0.02 ~ 0.5% by weight, preservatives methylparaben, phenoxyethanol substance 0.2 ~ 0.6% by weight, nanomaterials ceramide, hydrogenated lecithin, caprylic / capric tree Lee triglyceride, tea yieyi-cocoyl glutamate, nanomaterials consisting of cholesterol, 0.1 may be formed, including 5.0% by weight purified water 58.7 - 93.51% by weight.
검류인 한천, 카라기난, 로거스트 빈 검, 겔란검등은 그 함량은 조성물의 총 중량 기준에서 0.5wt 내지 3wt%가 바람직하다.The content of the gum agar, carrageenan, logger bean bean gum, gellan gum and the like is preferably 0.5wt to 3wt% based on the total weight of the composition.
이는 총 배합함량 기준에서 그 함량이 0.5wt% 미만일 경우 겔의 경도가 나타나지 않으며, 그 함량이 3wt% 이상의 경우 겔의 경도가 너무 높아 상품적 가치가 떨어지기 때문이다.This is because the hardness of the gel does not appear when the content is less than 0.5wt% on the basis of the total blending content, because the hardness of the gel is too high when the content is more than 3wt%, the commercial value is lowered.
보습제인 글리세린, 부틸렌 글라이콜, 베타인,스쿠알란의 경우 함량은 조성물의 총 중량 기준에서 그 함량이 5wt% 내지 20wt%인 것이 바람직하다. In the case of the moisturizing glycerin, butylene glycol, betaine, squalane, the content is preferably 5wt% to 20wt% based on the total weight of the composition.
이는 총 배합량 기준에서 그 함량이 5wt%미만일 경우 겔 마스크가 얼굴에 부착될때에 쉽게 떨어지는 즉, 밀착력이 떨어지고, 그 함량이 20wt% 이상일 경우 겔 마스크 사용후의 얼굴에 끈적임을 유발할 수 있다. 따라서 하이드로 겔의 밀착력 및 끈적임 없이 피부 보습을 부여해 주는데는 그 함량을 5% 내지 20%가 타당하다.This may cause the gel mask to fall easily when attached to the face when the content is less than 5 wt% based on the total blending amount, that is, when the content is 20 wt% or more, it may cause stickiness to the face after using the gel mask. Therefore, 5% to 20% of the content is appropriate to give skin moisturization without adhesion and stickiness of the hydrogel.
나노유도체 및 미용성분으로 사용된 세라마이드, 수첨레시틴, 카프릴릭/카프릭 트리글리세라이드, 티이에이-코코일 글루타메이트, 콜레스테롤 성분을 적절히 배합하여 고유압을 이용해 나노입자를 만들 수 있는 마이크로 플루다이저(Midroflurdizer) 기기를 이용하여 3회 회전을 시켜 에멀젼 입자를 70nm 내지 300nm 의 나노 입자를 만든다. 나노 에멀젼 입자는 통상적으로 150nm 내지 300nm 하에 사용된다.Ceramide, hydrogenated lecithin, caprylic / capric triglyceride, tie-cocoyl glutamate, and cholesterol components used as nanoderivatives and cosmetic ingredients, which can make nanoparticles using high pressure Three rotations were carried out using a Midroflurdizer) instrument to produce nanoparticles with emulsion particles of 70 nm to 300 nm. Nanoemulsion particles are typically used under 150 nm to 300 nm.
하이드로겔 조성물의 경우 사용된 보습제인 글리세린 및 부틸렌 글라이콜의 경우, 하이드로겔 마스크를 사용 후 경시 변화에 따른 보습력 유지가 쉽게 떨어진다. In the case of the hydrogel composition, glycerin and butylene glycol, which are used moisturizers, can easily maintain the moisturizing power according to the change over time after using the hydrogel mask.
따라서 피부 장벽 기능을 갖는 세라마이드를 나노화 입자화한 나노물질을 0.1wt% 내지 5wt% 로 사용하여 하이드로겔에 사용하였을 때에 경시변화를 관찰한 결과 일반 보습제를 사용한 경우에 비해 현저히 그 보습력이 유지됨을 알 수 있다.Therefore, when the hydrogel was used with 0.1% to 5wt% of nanomaterial granulated with ceramide having a skin barrier function, it was found that the moisture retention was significantly maintained as compared with the case of using a general moisturizer. Can be.
킬레이트제인 디소듐이디티에이 0.02wt% 내지 0.1wt%, 겔화 고분자인 셀룰로오스 검 0.1wt% 내지 0.5wt%, 1가 양이온 물질인 포타슘 알지네이트, 포타슘 클로라이드, 산도조절제인 구연산등으로 이루어진 군에서 선택된 물질 0.01wt% 내지 0.1wt%는 제품의 안정성과 제품 경도에 영향을 주며, 적절한 상호 배합에 따라 하이드로겔 조성물의 이수현상에 커다란 영향을 미침을 알 수 있다.A substance selected from the group consisting of 0.02 wt% to 0.1 wt% of chelating agent, 0.1 wt% to 0.5 wt% of cellulose gum which is a gelling polymer, potassium alginate as monovalent cationic material, potassium chloride, and citric acid as acidity regulator 0.01wt% to 0.1wt% affects the stability of the product and the hardness of the product, it can be seen that it has a great effect on the completion of hydrogel composition according to the appropriate cross-linking.
방부제인 메칠파라벤, 페녹시에탄올으로 이루어진 군에서 0.2wt% 내지 0.6wt%, 가용화제인 폴리소르베이트 20 으로 0.05wt%, 조합향료 0.02wt% 내지 0.1wt%는 하이드로겔 조성물의 미생물에 의한 외부 오염을로부터 막아주며 제품의 질을 향상시키는 역할을 한다.0.2wt% to 0.6wt% in the group consisting of methylparaben and phenoxyethanol as preservatives, 0.05wt% as polysorbate 20 as a solubilizer, and 0.02wt% to 0.1wt% as a combination fragrance for external contamination by microorganisms of the hydrogel composition It prevents from and improves product quality.
본 발명에 따른 하이드로겔 조성물은 필요로 하는 작용 즉, 이수현상 및 보습효과 등을 고려하여 적합하게 혼합 및 적합한 양으로 투여될 수 있다. The hydrogel composition according to the present invention may be appropriately mixed and administered in an appropriate amount in consideration of the required action, that is, diarrhea and moisturizing effect.
또한 본 발명에 따른 조성물은 일반적으로 알려진 다른 나노기술을 이용한 약물전달용 물질 등을 더욱 포함할 수 있다. In addition, the composition according to the present invention may further include a drug delivery material using other nanotechnology generally known.
사용될 수 있는 일반적인 약물전달용으로는 세라마이드, 파이토 스핑고신, 유용성 미용성분으로 토코페롤아세테이트, 레티놀등의 통상적인 것이며, 이 외에 기제, 부형제, 윤활제, 보존제 등이 있다.Typical drug delivery agents that may be used include ceramides, phytosphingosines, oil-soluble cosmetics, and the like, such as tocopherol acetate, retinol, and the like, as well as bases, excipients, lubricants, and preservatives.
[실시예]EXAMPLE
하기 [표 1]에서 나타낸 6가지 시료들을 아래의 성분으로 조합한 제조방법에 따라 하이드로겔 조성물의 샘플을 만들었다. Samples of the hydrogel composition were prepared according to the preparation method of combining the six samples shown in the following [Table 1] with the following components.
표 1
No. Phase Trade Name Sample.No
S1 S2 S3 S4 S5 S6
1 A 한천 1 0 0 0 0 0
2 카라기난 1.000 1.000 1.000 1.000 1.000 1.000
3 로커스트빈검 1.000 1.000 1.000 1.000 1.000 1.000
4 글리세린 12.00 12.00 12.00 12.00 12.00 12.00
                 
5 B 디소듐이디티에이 0.10 0.10 0.10 0.10 0.10 0.10
6 메칠파라벤 0.15 0.15 0.15 0.15 0.15 0.15
7 베타인 0.01 0.01 0.01 0.01 0.01 0.01
8 정제수 76.37 77.37 77.29 77.28 77.20 77.33
                 
9 C 부틸렌글라이콜 7.00 7.00 7.00 7.00 7.00 7.00
10 셀룰로오스검 0.20 0.20 0.20 0.20 0.20 0.20
                 
11 D 포타슘알지네이트 0.00 0.00 0.08   0.08 0.00
12 포타슘클로라이드 0.00 0.00   0.09 0.09 0.00
13 씨트릭애씨드           0.04
                 
14 E 페녹시에탄올 0.1 0.1 0.1 0.1 0.1 0.1
15 스쿠알란 0.01 0.01 0.01 0.01 0.01 0.01
16 마린 콜라겐 1 1 1 1 1 1
17 폴리소르베이트20 0.05 0.05 0.05 0.05 0.05 0.05
18  F 0.01 0.01 0.01 0.01 0.01 0.01
to 100 to 100 to 100 to 100 to 100 to 100
Table 1
No. Phase Trade Name Sample.No
S1 S2 S3 S4 S5 S6
One A Agar One 0 0 0 0 0
2 Carrageenan 1.000 1.000 1.000 1.000 1.000 1.000
3 Locust Bean Sword 1.000 1.000 1.000 1.000 1.000 1.000
4 glycerin 12.00 12.00 12.00 12.00 12.00 12.00
 
5 B Disodium ID 0.10 0.10 0.10 0.10 0.10 0.10
6 Methylparaben 0.15 0.15 0.15 0.15 0.15 0.15
7 Betaine 0.01 0.01 0.01 0.01 0.01 0.01
8 Purified water 76.37 77.37 77.29 77.28 77.20 77.33
 
9 C Butylene Glycol 7.00 7.00 7.00 7.00 7.00 7.00
10 Cellulose gum 0.20 0.20 0.20 0.20 0.20 0.20
 
11 D Potassium alginate 0.00 0.00 0.08 0.08 0.00
12 Potassium chloride 0.00 0.00 0.09 0.09 0.00
13 Citric Acid 0.04
 
14 E Phenoxyethanol 0.1 0.1 0.1 0.1 0.1 0.1
15 Squalane 0.01 0.01 0.01 0.01 0.01 0.01
16 Marine collagen One One One One One One
17 Polysorbate 20 0.05 0.05 0.05 0.05 0.05 0.05
18 F incense 0.01 0.01 0.01 0.01 0.01 0.01
to 100 to 100 to 100 to 100 to 100 to 100
실시예의 [표 1]에서와 같이 Sample.No.S1 ~ Sample.No.S6 까지 총 6가지 처방을 이용하여 하이드로겔 조성물을 만들었다.Hydrogel composition was made using a total of six prescriptions from Sample.No.S1 to Sample.No.S6 as shown in Table 1 of the Examples.
하이드로겔 조성물은 A,B상을 차례로 HOMO 믹서용 가마에 투입, 실온에서부터 교반하여 약 80℃ 가지 서서히 교반하여 온도를 올려 충분히 교반하여 분산시킨다. In the hydrogel composition, the A and B phases are sequentially added to the HOMO mixer kiln, stirred from room temperature, gradually stirred at about 80 ° C, the temperature is raised, and sufficiently stirred and dispersed.
충분히 분산 확인 후 실온하에 C상을 교반한 후에 믹서용 가마에 투입, 서서히 교반하여 분산시키다. After sufficiently confirming the dispersion, the phase C was stirred at room temperature, and then charged into a mixer kiln, followed by gradual stirring to disperse.
충분히 분산 확인 후 D상을 믹서용 가마에 투입, 서서히 교반하여 용해 시킨다. After sufficiently confirming the dispersion, phase D is added to a mixer kiln and slowly stirred to dissolve.
용해 확인 후 E,F상을 차례로 투입, 교반하여 준다. 약 5~10분 교반 한 후에 코팅기기를 이용하여 하이드로겔의 지지체로 사용되어 지는 PET 재질 또는 OPP재질과 망사타입의 매쉬천을 이용하여 하이드로겔을 만들어 약 30℃까지 냉각하여 겔화된 마스크 만들었다. After confirming the dissolution, the E and F phases are sequentially added and stirred. After stirring for about 5 to 10 minutes using a coating machine to make a hydrogel using a PET material or OPP material and a mesh type mesh cloth used as a support for the hydrogel to make a gelled mask by cooling to about 30 ℃.
[이수현상 특성 분석][Feature Characteristics Analysis]
상술한 6가지 시료의 겔화된 하이드로겔 마스크를 적당량을 덜어 4℃, 25℃, 35℃, 50℃에 해당하는 샘플을 만든다. 이때 각 시료마다 하이드로겔을 밀폐시킨 상태의 A타입과, 하이드로겔을 개방된 상태의 B타입으로 뷴류한다.The gelled hydrogel mask of the six samples described above was reduced to make samples corresponding to 4 ° C, 25 ° C, 35 ° C and 50 ° C. At this time, each sample is classified into an A-type in which the hydrogel is sealed and a B-type in the open state.
도 1 내지 도 6 각각은 Sample.No.S1 내지 Sample.No.S6의 하이드로겔을 이용하여 시간과 온도에 따른 이수현상을 무게감소율을 분율로 하여 표시한 그래프이다. 여기서, Sample.No.S1/A 내지 Sample.No.S6/A는 밀봉상태이고, Sample.No.S1/B 내지 Sample.No.S6/B는 개봉상태를 의미한다. Figures 1 to 6 are graphs showing the weight loss rate as a fraction of the completion of development according to time and temperature using the hydrogels of Sample No. S1 to Sample No. S6. Here, Sample.No.S1 / A to Sample.No.S6 / A are in a sealed state, and Sample.No.S1 / B to Sample.No.S6 / B mean an open state.
각 온도별로 시료를 만들어 시간에 따른 이수현상을 무게로 측정하였다. 측정값은 백분율로 환산하여 도 1 내지 도 6에 나타내었다.Samples were prepared for each temperature, and the completion phenomenon over time was measured by weight. The measured values are shown in FIGS. 1 to 6 in terms of percentages.
도 1 내지 도 6의 처방에 따른 하이드로겔의 이수현상을 분석하여 보면, 검류인 한천을 베이스로 한 Sample.No.S1의 경우 나머지 카라기난과 로커스트빈검을 사용한 Sample.No.S2~ Sample.No. S6의 이수현상에 따른 무게변화율이 더 높았다.Analysis of the hydrogel hydration according to the prescription of Figures 1 to 6, in the case of Sample.No.S1 based on agar, which is a gum, using the remaining carrageenan and locust bean gum. The weight change rate was higher due to the completion of S6.
도 1 내지 도 6의 처방에 따른 하이드로겔의 이수현상을 보면, 하이드로겔을 밀봉한 상태와 개봉된 상태 모두에 이수현상이 나타났으나, 밀봉상태에 비해 개봉상태의 경우 이수현상이 더 나타났으며, 온도가 상승함에 따라 이수현상은 상대적으로 더 크게 나타났다. Looking at the completion of hydrogel according to the prescription of Figures 1 to 6, the completion of the phenomenon in both the sealed state and the opened state of the hydrogel, but the completion of the phenomenon in the opened state compared to the sealed state, As the temperature rose, the process was relatively larger.
또한, 도 1 내지 도 5의 경우 모두에서 밀봉된 상태의 경우 4 ℃ ~ 35℃하에서는 밀봉된 상태의 하이드로겔의 이수현상은 평균 5% 내외로 나타났으며, 50℃하에서는 도 1 내지 도 4(Sample.No.S1~S4)에서는 5%~6% 내로 이수현상이 나타났으며, 도 6(Sample.No.S6)은 20wt% 까지 이수현상이 나타났음을 알 수 있다.In addition, in the case of the sealed state in all of Figures 1 to 5 in 4 ℃ ~ 35 ℃ the degree of completion of the hydrogel in the sealed state was found to be around 5% on average, Figure 1 to Figure 4 (Sample under 50 ℃) In No. S1 to S4, the completion phenomenon appeared within 5% to 6%, and in FIG. 6 (Sample.No.S6), the completion phenomenon appeared to 20 wt%.
이러한 그래프 상에 나타난 실험값을 분석하여 보면, 35℃ 하에 Sample.No.S1~S5(도 1 내지 도 5)의 경우 밀봉된 상태와 개봉된 상태에서의 이수현상이 시간에 따라 차이가 있음을 알 수 있는데, 이에 비해 Sample.No. S6(도 6)처방의 경우 35℃ 하에서 밀봉된 상태와 개봉된 상태의 하이드로겔 마스크의 이수현상이 동일하게 낮아짐을 알 수 있다.Analyzing the experimental values shown on these graphs, it can be seen that in the case of Sample.No.S1 to S5 (FIGS. 1 to 5) at 35 ° C., the completion phenomenon in the sealed state and the unsealed state varies with time. Compared to this, Sample.No. In the case of S6 (FIG. 6), it can be seen that the hydrolysis of the hydrogel mask in the sealed state and the unsealed state under 35 ° C. is lowered equally.
즉, 도 1 내지 도 6의 6가지 하이드로겔 조성물의 처방에 따른 이수현상을 분석하여 본 결과 한천을 이용한 Sample.No.S1 보다 카라기난을 이용한 Sample.No.S2~S6 의 이수현상이 더 나타남을 알 수 있고, 또한 1가 양이온이 함유된 Sample.No.S3~S5의 경우보다 씨트릭애씨드가 함유된 Sample.No.S6의 처방의 이수현상이 더 크게 나타났음을 알 수 있다.In other words, the analysis of the completion of the six hydrogel composition according to the formulation of Figures 1 to 6 as a result of the analysis showed that the completion of the carbo nan sample.No.S2 ~ S6 using agar than the sample.No.S1 using agar. In addition, it can be seen that the completion of the prescription of Sample.No.S6 containing citric acid was larger than that of Sample.No.S3 to S5 containing monovalent cations.
[하이드로겔의 보습력 분석][Moisture Analysis of Hydrogels]
실내 항온항습 조건에서 25℃하에 Corneometer(CM820PC, Courage Khazka, Germany)를 사용하여 보습력을 분석하였다. Moisturizing power was analyzed using Corneometer (CM820PC, Courage Khazka, Germany) at 25 ° C. under room constant temperature and humidity conditions.
도 7에서와 같이 Sample.No.S1~S6 처방에 따라 하이드로겔 마스크를 만든 다음 얼굴에 도포하고 1시간 후에 떼어내고 시간에 따른 보습력 변화를 측정하였다.As shown in FIG. 7, hydrogel masks were prepared according to the prescription of Sample. No. S1 to S6, and then applied to the face and removed after 1 hour, and the change in moisturizing power over time was measured.
도 7에서와 같이 하이드로겔 조성물의 경우 하이드로겔 사용 직후 보습력 측정값은 올라가나 30분 경과후부터는 보습력이 떨어짐을 알 수 있었다. In the case of the hydrogel composition as shown in Figure 7, it was found that the measured value of the moisturizing force immediately after use of the hydrogel was lowered after 30 minutes.
상대적으로 Sample.No.S6 처방의 하이드로겔의 경우 상대적으로 높은 보습력을 유지함을 알 수 있다. 이는 보습제로 사용한 글리세린, 부틸렌글라이콜, 베타인등의 성분이 충분히 얼굴에 도포되면 어느 정도의 보습력을 유지함을 알 수 있었으며, 이는 앞서 나타난 이수현상에 따라 이수현상이 가장 두드러진 Sample.No.S6 처방의 하이드로겔의 경우와 상호 연관성이 있음을 나타내 준다.It can be seen that the relatively high moisturizing power of the hydrogel of the sample No. S6 prescription is relatively high. It was found that when the ingredients such as glycerin, butylene glycol, and betaine used as moisturizers were sufficiently applied to the face, it retained a certain amount of moisturizing power. Correlated with the case of hydrogels.
이러한 실험을 통해 하이드로겔의 이수현상이 피부의 보습력과 상호 연관성이 있음을 알 수 있다. These experiments show that the hydrogel is well correlated with the moisturizing properties of the skin.
그러나 하이드로겔에 사용한 보습제의 보습유지 효과는 30분을 지나서는 현저히 떨어짐을 알 수 있다.However, it can be seen that the moisturizing effect of the moisturizer used in the hydrogel is significantly reduced after 30 minutes.
[나노기술을 이용한 하이드로겔의 보습력 분석][Moisture Analysis of Hydrogel Using Nano Technology]
도 8은 하이드로겔 각 처방에 나노기술을 이용한 미용성분을 각 0.5%, 1%, 3%, 5% 씩 첨가하여 시간에 따른 보습율을 측정한 그래프이다.Figure 8 is a graph measuring the moisturizing rate with time by adding 0.5%, 1%, 3%, 5% each of the cosmetic ingredients using nanotechnology to each hydrogel prescription.
나노유도체 및 미용성분으로 사용된 세라마이드, 수첨레시틴, 카프릴릭/카프릭 트리글리세라이드, 티이에이-코코일 글루타메이트, 콜레스테롤 성분을 적절히 배합하여 고유압을 이용해 나노입자를 만든 다음 0.5wt% 내지 5wt% 까지 Sample.No.S6 처방에 첨가하여 하이드로겔 마스크를 만든 다음 항온항습 조건하에 25℃ 상태에서 시간에 따른 하이드로겔 마스크의 보습력을 측정하였다. Ceramide, hydrogenated lecithin, caprylic / capric triglyceride, tie-cocoyl glutamate, and cholesterol components used as nanoderivatives and cosmetic ingredients are appropriately mixed to make nanoparticles using high pressure, and then 0.5wt% to 5wt% The hydrogel mask was prepared by adding to the prescription of Sample.No.S6, and then the moisturizing power of the hydrogel mask was measured at 25 ° C. under constant temperature and humidity conditions.
Sample.No.S6(0.0wt%)는 Sample.No.S6에 나노물질 첨가율이 0.0wt%, Sample.No.S6(0.5wt%)는 Sample.No.S6에 나노물질 첨가율이 0.5wt%, Sample.No.S6(1.0wt%)는 Sample.No.S6에 나노물질 첨가율이 1.0wt%, Sample.No.S6(3.0wt%)는 Sample.No.S6에 나노물질 첨가율이 3.0wt%, Sample.No.S6(5.0wt%)는 Sample.No.S6에 나노물질 첨가율이 5.0wt%임을 의미한다.Sample.No.S6 (0.0wt%) has 0.0wt% of nanomaterial added to Sample.No.S6, Sample.No.S6 (0.5wt%) has 0.5wt% of nanomaterial added to Sample.No.S6, Sample.No.S6 (1.0wt%) has 1.0wt% of nanomaterial added to Sample.No.S6, Sample.No.S6 (3.0wt%) has 3.0wt% of nanomaterial added to Sample.No.S6, Sample No. S6 (5.0 wt%) means that the nanomaterial addition rate is 5.0 wt% in Sample No. S 6.
나노화 시킨 세라마이드 성분을 조성비에 따라 각각 함유한 후 보습력 측정을 한 결과 나노 세라마이드를 함유하지 않은 Sample.No.S6(0.0wt%) 보다 나노 세라마이드를 함유한 나머지 샘플에서 보습력이 더 지속성이 있음을 나타내 준다.Moisturizing power was measured after each of the nano-ceramic components were contained according to the composition ratio, and the results showed that the moisturizing power was more sustained in the remaining samples containing nano ceramide than Sample.No.S6 (0.0 wt%) without the nano ceramide. give.
하지만 상태적으로 나노 물질의 함유율인 0.5wt%, 1wt%, 3wt%, 5wt%에 따른 보습 유지 효과는 큰 차이가 없음을 알 수 있다. However, it can be seen that the moisturizing retention effect according to the content of the nanomaterials 0.5wt%, 1wt%, 3wt%, 5wt% is not significantly different.
이는 피부장벽기능을 갖는 세라마이드가 이수현상에 따라 피부에 스며들어 상대적으로 피부장벽기능을 강화한 것으로 생각하며 같이 나노 성분에 함유된 오일성분인 카프릴릭/카프릭 트리글리세라이드, 콜레스테롤 성분등이 피부의 보습을 지속적으로 유지하는데 효과가 있음을 나타내 준다.It is thought that ceramide with skin barrier function penetrates the skin according to hydration and relatively strengthens skin barrier function. Caprylic / capric triglycerides and cholesterol components, which are oil components contained in nano components, It is effective in maintaining moisturizing.
[하이드로겔 경도 분석]Hydrogel Hardness Analysis
도 9는 각각의 하이드로겔 시료의 온도에 따른 경도 변화를 나타낸 그래프이다.9 is a graph showing the change in hardness according to the temperature of each hydrogel sample.
각각의 하이드로겔 조성물의 처방에 따른 내용물의 온도에 따른 경도값을 측정하였다. The hardness value according to the temperature of the contents according to the formulation of each hydrogel composition was measured.
경도값 측정기기는 후도레오미터(FUDOH RHEOMETER. 제조국 JAPAN)로 플런저 면적(PLUNGER AREA)은 1cm2 이며, 리프트업 속도(lift up speed)는 6cm/min 하에 하이드로겔의 경도를 측정하였다. The hardness measuring device was a FUDOH RHEOMETER. (Japan JAPAN), the plunger area (PLUNGER AREA) is 1cm2, the lift up speed (lift up speed) was measured the hardness of the hydrogel under 6cm / min.
실험조건은 처방에 따른 하이드로겔을 만든 후 실험예 1와 동일한 조건에서 밀폐상태와 개봉상태에 따른 하이드로겔 내용물을 각 온도별로 incubater에 넣고 30분 후에 측정하였다. 표.10.의 경우 온도에 따른 하이드로겔 조성물의 경도 변화를 나타내 준다.Experimental conditions were made after the preparation of the hydrogel according to the prescription and the hydrogel contents according to the sealed state and the unsealed state in the same conditions as in Experimental Example 1 into the incubater for each temperature and measured after 30 minutes. Table 10 shows the change in hardness of the hydrogel composition with temperature.
도 9의 경우 경도의 변화값을 측정한 결과 밀폐된 하이드로겔과 개봉상태인 하이드로겔의 온도에 따른 경도변화는 서로 다른 경향을 나타낸다. In the case of FIG. 9, the hardness change according to the temperature of the sealed hydrogel and the unsealed hydrogel shows a different tendency as a result of measuring the change in hardness.
밀폐된 하이드로겔의 경우 온도에 따라 경도값의 변화는 조금씩 덜어지는 경향을 나타내나 그 변화값의 차이는 크지 않았으며, 개봉된 하이드로겔의 경우 4℃~ 35℃ 의 경우 일정하게 조금씩 떨어지는 경향을 보였으나 50℃ 온도에 따라 경도값의 변화는 크게 상승하는 것을 알 수 있다.In the case of closed hydrogels, the change in hardness value tends to decrease little by little depending on the temperature, but the difference in change is not large. It can be seen that the change in hardness value significantly increases with the temperature of 50 ℃.
이러한 실험결과를 통하여 하이드로겔의 이수현상과 경도값의 상호 관련은 통계적 유의성을 찾지 못하였으나, 오히려 개방된 하이드로겔의 경우 전체적으로 경도값이 증가함을 알 수 있다. 이는 이수현상에 따라 하이드로겔 표면이 건조되어 나타나는 현상임을 알 수 있다. The experimental results did not find statistical significance in the correlation between the hydrogel completion and hardness values, but in the case of open hydrogels, the hardness value increased. It can be seen that this phenomenon is caused by the surface of the hydrogel is dried according to the phenomenon.
이상 첨부된 도면을 참조하여 본 발명의 바람직한 실시예를 설명하였지만, 상술한 본 발명의 기술적 구성은 본 발명이 속하는 기술 분야의 당업자가 본 발명의 그 기술적 사상이나 필수적 특징을 변경하지 않고서 다른 구체적인 형태로 실시될 수 있다는 것을 이해할 수 있을 것이다. 그러므로 이상에서 기술한 실시예들은 모든 면에서 예시적인 것이며 한정적인 것이 아닌 것으로서 이해되어야 하고, 본 발명의 범위는 상기 상세한 설명보다는 후술하는 특허청구범위에 의하여 나타내어지며, 특허청구범위의 의미 및 범위 그리고 그 등가 개념으로부터 도출되는 모든 변경 또는 변형된 형태가 본 발명의 범위에 포함되는 것으로 해석되어야 한다.Although the preferred embodiments of the present invention have been described above with reference to the accompanying drawings, the above-described technical configuration of the present invention may be embodied by those skilled in the art to which the present invention pertains without changing its technical spirit or essential features of the present invention. It will be appreciated that the present invention may be practiced as. Therefore, the above-described embodiments are to be understood as illustrative and not restrictive in all respects, and the scope of the present invention is indicated by the appended claims rather than the detailed description, and the meaning and scope of the claims and All changes or modifications derived from the equivalent concept should be interpreted as being included in the scope of the present invention.

Claims (3)

  1. 겔화 고분자 0.5~3.0중량%, 콜라겐 물질 0.5~10.0중량%, 보습제 5.0~20.0중량%, 겔 강도를 조절하는 1가 양이온 물질 0.04~1.0중량%, 산도조절제인 씨트릭애씨드 0.01~0.1중량%, 금속이온봉쇄제 0.02~0.1중량%, 가용화제(계면활성제) 0.1~1.0중량%, 조합향료 0.02~0.5중량%, 보존제 0.2~0.6%, 나머지 정제수를 포함하여 이루어지는, 이수 특성에 따른 피부 보습 및 피부 탄력 증진용 하이드로겔 조성물.0.5 to 3.0% by weight of gelling polymer, 0.5 to 10.0% by weight of collagen material, 5.0 to 20.0% by weight of moisturizer, 0.04 to 1.0% by weight of monovalent cationic substance to adjust gel strength, 0.01 to 0.1% by weight of citric acid, an acidity regulator, Skin moisturizing according to the mucous characteristics, including 0.02 to 0.1% by weight of metal ion blocker, 0.1 to 1.0% by weight of solubilizer (surfactant), 0.02 to 0.5% by weight of combination fragrance, 0.2 to 0.6% of preservative, and the remaining purified water Hydrogel composition for enhancing skin elasticity.
  2. 제1항에 있어서,The method of claim 1,
    상기 하이드로겔 조성물은 세라마이드, 수첨레시틴, 카프릴릭/카프릭 트리글리세라이드, 티이에이-코코일 글루타메이트 또는 콜레스테롤 중 어느 하나를 함유한 나노물질 0.1~5중량%를 첨가되어 이루어지는, 이수 특성에 따른 피부 보습 및 피부 탄력 증진용 하이드로겔 조성물.The hydrogel composition comprises 0.1-5% by weight of nanomaterials containing any one of ceramide, hydrogenated lecithin, caprylic / capric triglyceride, TY-cocoil glutamate, or cholesterol, according to the skin characteristics. Hydrogel composition for moisturizing and enhancing skin elasticity.
  3. 제1항에 있어서,The method of claim 1,
    상기 겔화 고분자는 한천, 카라기난, 로거스트빈검, 겔란검으로 이루어진 군에서 선택되며, The gelling polymer is selected from the group consisting of agar, carrageenan, rogast bean gum, gellan gum,
    상기 콜라겐 물질은 생선 돔 비늘에서 추출한 해양성 콜라겐 물질이고, The collagen material is marine collagen material extracted from fish dome scales,
    상기 보습제는 글리세린, 부틸렌글라이콜, 베타인, 스쿠알란으로 이루어진 군에서 선택된 물질이며, The moisturizing agent is a material selected from the group consisting of glycerin, butylene glycol, betaine, squalane,
    상기 겔 강도를 조절하는 1가 양이온 물질은 포타슘 알지네이트, 포타슘 클로라이드으로 이루어진 군에서 선택된 물질이고,The monovalent cation material for controlling the gel strength is a material selected from the group consisting of potassium alginate, potassium chloride,
    상기 금속이온 봉쇄제는 디소듐이디티에이 물질이고,The metal ion sequestrant is a disodium id material,
    상기 가용화제는 폴리소르베이트이며, The solubilizer is polysorbate,
    상기 보존제는 메칠파라벤 및 페녹시에탄올로 이루어진, 이수 특성에 따른 피부 보습 및 피부 탄력 증진용 하이드로겔 조성물.The preservative is made of methyl paraben and phenoxy ethanol, hydrogel composition for enhancing skin moisturizing and skin elasticity according to diuretic properties.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113164333A (en) * 2018-11-30 2021-07-23 株式会社爱茉莉太平洋 Hydrogel mask composition, hydrogel mask prepared from same and preparation method of hydrogel mask
CN114533588A (en) * 2020-11-19 2022-05-27 (株)振科丝特 Hydrogel patch comprising dehydration shrinkage mode-regulated filling liquid and preparation method thereof
EP4023205A4 (en) * 2020-11-19 2022-09-14 Jincostech Co., Ltd. Hydrogel patch comprising syneresis pattern control filling solution, and method for manufacturing same

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102130482B1 (en) * 2017-10-26 2020-07-17 손동우 Water Soluble Gel Sheets and Manufacturing method thereof
WO2020091416A1 (en) * 2018-10-31 2020-05-07 ㈜아모레퍼시픽 Oil-in-water type cosmetic composition comprising nanoliposome
JP7470111B2 (en) * 2018-11-30 2024-04-17 アモーレパシフィック コーポレーション Hydrogel mask composition, hydrogel mask produced using the same, and method for producing the same

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3555937B2 (en) * 2000-08-14 2004-08-18 花王株式会社 Method for producing hydrogel particles
WO2007088038A1 (en) * 2006-02-02 2007-08-09 Euro-Celtique S.A. Hydrogel
JP2011098961A (en) * 2009-10-08 2011-05-19 Rohto Pharmaceutical Co Ltd Ophthalmic composition for nonionic silicone hydrogel contact lens
JP2011116690A (en) * 2009-12-02 2011-06-16 Rohto Pharmaceutical Co Ltd Ophthalmologic composition for nonionic silicone hydrogel contact lens

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3555937B2 (en) * 2000-08-14 2004-08-18 花王株式会社 Method for producing hydrogel particles
WO2007088038A1 (en) * 2006-02-02 2007-08-09 Euro-Celtique S.A. Hydrogel
JP2011098961A (en) * 2009-10-08 2011-05-19 Rohto Pharmaceutical Co Ltd Ophthalmic composition for nonionic silicone hydrogel contact lens
JP2011116690A (en) * 2009-12-02 2011-06-16 Rohto Pharmaceutical Co Ltd Ophthalmologic composition for nonionic silicone hydrogel contact lens

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113164333A (en) * 2018-11-30 2021-07-23 株式会社爱茉莉太平洋 Hydrogel mask composition, hydrogel mask prepared from same and preparation method of hydrogel mask
CN114533588A (en) * 2020-11-19 2022-05-27 (株)振科丝特 Hydrogel patch comprising dehydration shrinkage mode-regulated filling liquid and preparation method thereof
JP2022081439A (en) * 2020-11-19 2022-05-31 ジンコステック カンパニー,リミテッド Hydrogel patch including syneresis pattern adjustment filling fluid and production method thereof
EP4023205A4 (en) * 2020-11-19 2022-09-14 Jincostech Co., Ltd. Hydrogel patch comprising syneresis pattern control filling solution, and method for manufacturing same
JP7338891B2 (en) 2020-11-19 2023-09-05 ジンコステック カンパニー,リミテッド Hydrogel patch containing syneresis pattern control filling liquid and method for producing the same

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