KR0143385B1 - Collegen capsule for cosmetics - Google Patents

Collegen capsule for cosmetics

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Publication number
KR0143385B1
KR0143385B1 KR1019940020674A KR19940020674A KR0143385B1 KR 0143385 B1 KR0143385 B1 KR 0143385B1 KR 1019940020674 A KR1019940020674 A KR 1019940020674A KR 19940020674 A KR19940020674 A KR 19940020674A KR 0143385 B1 KR0143385 B1 KR 0143385B1
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KR
South Korea
Prior art keywords
collagen
capsule
atelocollagen
cosmetic
cosmetics
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KR1019940020674A
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Korean (ko)
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KR960006909A (en
Inventor
고종성
김광희
이승화
Original Assignee
한동근
주식회사태평양
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Priority to KR1019940020674A priority Critical patent/KR0143385B1/en
Publication of KR960006909A publication Critical patent/KR960006909A/en
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Publication of KR0143385B1 publication Critical patent/KR0143385B1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics 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
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/11Encapsulated compositions
    • 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
    • A61K2800/412Microsized, i.e. having sizes between 0.1 and 100 microns

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

본 발명은 가압붕괴성이 우수하고, 분산성이 우수한 화장료용 콜라겐 캡슐을 제공하며, 이 화장료용 콜라겐 캡슐은 콜라겐 및 그의 유도체를 피막재로 하며, 그리시딜기를 2~4개 갖고 있는 화합물을 가교제로 사용하여 제조된 것임을 특징으로 한다.The present invention provides a cosmetic collagen capsule having excellent pressure disintegration properties and excellent dispersibility, the cosmetic collagen capsule comprising a collagen and its derivative as a coating material, and having a compound having 2 to 4 glycidyl groups as a crosslinking agent. It is characterized in that it is manufactured using.

Description

[발명의 명칭][Name of invention]

화장료용 콜라겐 캡슐Cosmetic Collagen Capsule

[발병의 상세한 설명][Detailed Description of Onset]

본 발명은 화장료용 캡슐에 관한 것으로, 더욱 상세하게는 피막재로 콜라겐 및 그의 유도체를, 가교제로 글리시딜기를 2~4개 갖고 있는 화합물을 함유함을 특징으로 하는 화장료용 콜라겐 캡슐에 관한 것이다.The present invention relates to a cosmetic capsule, and more particularly to a collagen capsule for cosmetics, characterized in that it contains collagen and derivatives thereof as a coating material, and a compound having 2 to 4 glycidyl groups as a crosslinking agent. .

현재, 일반적으로 시판되고 있는 화장료용 캡슐로는 경질캡슐, 연질캡슐 및 이음새 없는 캡슐이 있다. 이들 캡슐에 주로 사용되어 온 피막재로는 젤라틴, 알긴산 또는 한천 등을 들 수 있는데, 젤라틴을 피막재로 사용하여 캡슐을 제조하는 경우 막후가 두꺼워서 파열이 어려워 기구를 이용하여 깨뜨려 써야 하고, 사용 후에는 피막재가 피부에 남아 사용성이 나쁘고 피부에 자극을 주는 문제점이 있다. 또한 젤라틴은 수용성이어서 이를 피막재로 한 캡슐을 화장료에 배합할 때 수상의 화장료에는 분산시킬 수가 없어 그 사용범위가 제한되고 있다. 즉, 수용성 젤라틴으로 캡슐을 제조하여 수상의 화장료에 분산시킬 경우, 피막재인 젤라틴은 약 1시간 경과후 팽윤되기 시작하며, 장시간 후에는 수상의 화장료에 용해되어 캡슐 내용물이 용출되기 때문에 캡슐로의 기능을 상실하며, 또 젤라틴은 그의 용해온도가 37℃이기 때문에 수상의 화장료에 배합시 온도가 40℃이상인 경우 쉽게 용해되어 버리는 문제점이 있어 수상의 화장료에는 배합하기 어려운 문제가 있다. 이음새 없는 캡슐은 그 피막재로 알긴산 나트륨이나 젤라틴, 한천 등을 사용하고 있는데, 다가 금속 이온으로 경화시킨 알긴산 나트륨을 피막재로 사용하는 경우, 사용시 가압 붕괴성이 좋지 않아서 마찬가지로 기구를 사용하여 파열시켜야 하며, 하용후 껍질이 남아 피부에 자극을 주는 문제점이 있다. 이러한 문제점을 해소하기 위해 제안된 것이 한천을 피막재로 한 이음새 없는 캡슐로서, 이는 실제 유통 조건의 온도 범위에서 수상의 분산매체에 안정하여 주목받고 있으나, 한천 자체는 피부 도포시 피부에 보습효과를 부여 할 수 없는 문제점이 있다.Currently, commercially available cosmetic capsules include hard capsules, soft capsules, and seamless capsules. The encapsulating materials mainly used in these capsules include gelatin, alginic acid, or agar, and when the capsule is manufactured using gelatin as the encapsulating material, it is difficult to rupture due to the thick film and must be broken using a device. The encapsulant remains on the skin, which causes poor usability and irritates the skin. In addition, since gelatin is water-soluble, it is impossible to disperse it in the cosmetics of the water phase when formulating a capsule made of the coating material in the cosmetics, and thus its use range is limited. In other words, when the capsule is made of water-soluble gelatin and dispersed in the cosmetic of the aqueous phase, the coating material gelatin begins to swell after about 1 hour, and after a long time it dissolves in the cosmetic of the aqueous phase and the contents of the capsule are eluted, which functions as a capsule. Also, since gelatin has a melting temperature of 37 ° C., the gelatin has a problem in that it dissolves easily when the temperature is 40 ° C. or higher when it is added to the cosmetic of the aqueous phase. The seamless capsule uses sodium alginate, gelatin, or agar as the coating material.If sodium alginate cured with polyvalent metal ions is used as the coating material, it must be ruptured using an instrument because of its poor pressure collapse. And, there is a problem that remains after peeling irritate the skin. In order to solve these problems, the proposed capsule is a seamless capsule made of agar, which is stable and attracting attention to the dispersion medium of the water phase in the temperature range of the actual distribution conditions, but the agar itself has a moisturizing effect on the skin when the skin is applied. There is a problem that cannot be granted.

이에, 본 발명자들은 상기와 같은 종래 기술의 문제점을 해결하고, 가압붕괴성이 우수하며 수상의 분산매체에서도 그 분산성이 안정한 화장료용 캡슐을 제공하고자 예의연구한 결과, 콜라겐 또는 그의 유도체를 피막재로 하고, 그리시딜기를 2~4개 갖고 있는 화합물을 가교제로 사용하여 얻어진 가교 콜라겐 캡슐을 화장료에 배합하면 상기 목적을 달성할 수 있음을 발견하고 본 발명을 완성하게 되었다.Accordingly, the present inventors have solved the problems of the prior art as described above, and as a result of earnestly research to provide a cosmetic capsule having excellent pressure disintegration property and stable dispersibility even in the dispersion medium of the aqueous phase, collagen or derivatives thereof as a coating material When the compound obtained by using a compound having 2 to 4 glycidyl groups as a crosslinking agent was added to the cosmetic, it was found that the above object can be achieved and the present invention has been completed.

따라서, 본 발명의 목적은 가압붕괴성이 우수하고, 분산성이 우수한 화장료용 콜라겐 캡슐을 제공하는 것이다. 즉, 본 발명의 화장료용 콜라겐 캡슐은 콜라겐 및 그의 유도체를 피막재로 하며, 글리시딜기를 2~4개 갖고 있는 화합물을 가교제로 사용하여 제조된 것임을 특징으로 한다.Accordingly, it is an object of the present invention to provide a cosmetic collagen capsule excellent in pressure disintegration and excellent in dispersibility. That is, the cosmetic collagen capsule of the present invention is characterized in that the collagen and its derivatives are prepared as a coating material, and the compound having 2 to 4 glycidyl groups is used as a crosslinking agent.

이하, 구체적으로 본 발명의 화장료용 콜라겐 캡슐을 설명한다.Hereinafter, the collagen capsule for cosmetics of the present invention will be described in detail.

본 발명에 따른 캡슐에 있어서, 피막재로 사용되는 콜라겐은 인체를 구성하는 단백질의 일종으로 생체에 섬유상으로 존재하며 주로 식품, 화장품원료, 수술용 봉합사, 인공 피부 등에 실용화되어 있으며, 저항 원성 및 생물학적 분해성을 지니고 있어 화장품에 사용시 피부의 노화 방지 역할이 예측되는 물질이다.In the capsule according to the present invention, collagen used as a coating material is a kind of protein constituting the human body and is present in the form of fibers in the living body, and is mainly used for food, cosmetic raw materials, surgical sutures, artificial skin, and the like. As it has degradability, it is expected to play a role in anti-aging of skin when used in cosmetics.

본 발명에서는 콜라겐으로서 아텔로콜라겐, 미리스틸화 아텔로콜라겐, 석시닐화 아텔로콜라겐, 밀스틸화석시닐화 아텔로콜라겐 및 프탈화 아텔로콜라겐으로 이루어진 군에서 선택된 1종 또는 2종 이상의 것을 사용할 수 있다. 콜라겐은 수용액 형태로 이용되며, 그 농도는 0.5~4%(w/v)가 적당하고, 바람직하게는 1%(w/v)가 좋다.In the present invention, one or two or more selected from the group consisting of atelocollagen, myristylated atelocollagen, succinylated atelocollagen, millyl succinylated atelocollagen, and phthalated atelocollagen may be used as collagen. have. Collagen is used in the form of an aqueous solution, the concentration of 0.5 ~ 4% (w / v) is suitable, preferably 1% (w / v).

캡슐의 제조는 콜라겐 수용액에 친수성 유효성분 수용액을 혼합, 또는 소수성 유효성분을 분산시킨 후, 이를 유기분산매에 가하여 교반하에 분산시킨 후, 여기에 가교제의 유기용매 용액을 가하여 가교시킴으로써 행할 수 있다. 이렇게 제조된 캡슐은 용매 및 미반응물을 제거하기 위하여 수회 수세한다.The preparation of the capsule can be carried out by mixing a hydrophilic active ingredient solution in a collagen aqueous solution or dispersing a hydrophobic active ingredient, adding it to an organic dispersion medium and dispersing it under stirring, and then adding and crosslinking it with an organic solvent solution of a crosslinking agent. The capsules thus prepared are washed several times to remove the solvent and unreacted materials.

캡슐의 제조에 사용될 수 있는 가교제로는 그리시딜기를 2~4개 갖고있는 화합물이다. 구체적인 예로는 트리메칠올프로판폴리글리시딜에테르, 네오펜틸글리콜디글리시딜에테르, 글리세롤폴리글리시딜에테르, 폴리프로필렌글리콜디글리시딜에테르, 에틸렌글리콜디글리시딜에테르, 폴리에틸렌글리콜디글리시딜에테르, 솔비톨폴리글리시딜에테르 등을 들 수 있으며, 가교제는 분산매와 동일한 용매 또는 분산매와 상용성 있는 용매에 용해하여 용액의 형태로 사용한다. 그 농도는 3~15%(w/v)가 바람직한데, 15%(w/v) 이상인 경우에는 제조된 캡슐을 화장료에 배합하여 사용하는 경우 캡슐의 가압붕괴성이 불량하며, 3%(w/v) 미만인 경우에는 캡슐의 제조시 수세 등의 작업에 의해 또는 화장료에 배합하는 도중에 캡슐이 붕괴되어 버리는 문제점이 있다.A crosslinking agent that can be used in the manufacture of capsules is a compound having 2 to 4 glycidyl groups. Specific examples include trimethylolpropane polyglycidyl ether, neopentyl glycol diglycidyl ether, glycerol polyglycidyl ether, polypropylene glycol diglycidyl ether, ethylene glycol diglycidyl ether, polyethylene glycol digly Cylyl ether, sorbitol polyglycidyl ether, etc. are mentioned, A crosslinking agent is melt | dissolved in the same solvent as a dispersion medium, or a solvent compatible with a dispersion medium, and is used in the form of a solution. The concentration is preferably 3 to 15% (w / v). If the concentration is 15% (w / v) or more, the capsules used in combination with the cosmetics are poor in pressure decay and 3% (w). / v), there is a problem that the capsule is collapsed by the operation of washing with water or the like during the preparation of the capsule during the preparation of the capsule.

이때, 캡슐의 제조에 있어 콜라겐의 충분한 가교가 이루어지도록 하기 위해서는 콜라겐 대 가교제의 함량을 중량비로 1:1.5~2.5의 범위로 하는 것이 바람직하다.At this time, in order to ensure sufficient crosslinking of collagen in the preparation of the capsule, it is preferable to make the content of collagen to the crosslinking agent in the range of 1: 1.5 to 2.5 by weight ratio.

본 발명에서 콜라켄 캡슐안에 함유되는 유효성분으로는 통상 사용되는 친유성 화장료나 친수성 화장료 모두 좋고, 또한 색상을 부여하기 위한 유기 또는 무기 안료 및 무기염료도 콜라켄 캡슐중에 함유시킬 수 있다.As the active ingredient contained in the collagen capsule in the present invention, both lipophilic cosmetics and hydrophilic cosmetics commonly used may be used, and organic or inorganic pigments and inorganic dyes for imparting color may also be contained in the collagen capsules.

본 발명에 따르면 캡슐의 바람직한 직경으로는 1~5,000㎛이다.According to the present invention, the preferred diameter of the capsule is 1 to 5,000 μm.

본 발명의 유효성분 함유 콜라겐 캡슐을 포함하는 화장료 조성물은 캡슐의 내용물이 자외선등에 의해 변질되는 것을 방지할 수 있으며, 또한 피부에 도포시 콜라겐의 역할에 인해 부드럽고 매끄럽게 그리고 고르게 도포되어 사요감도 우수하다.The cosmetic composition including the active ingredient-containing collagen capsule of the present invention can prevent the contents of the capsule from being deteriorated by ultraviolet light, and is also soft and smooth and evenly applied due to the role of collagen when applied to the skin.

이하 실시예를 들어 본 발명을 보다 상세히 설명하지만, 볼 발명이 이들 실시예에 한정되는 것은 아니다.Although an Example is given to the following and this invention is demonstrated in more detail, a ball invention is not limited to these Examples.

[실시예 1]Example 1

미리스틸화석시닐화 아텔로콜라겐[일본 고껜 아테로콜라겐 MS] 1% 수용액 500g에 아스코르빈산인산마그네슘 1g을 용해하였다. 유동파라핀 LP#70 2,000g을 혼합기를 이용하여 6,000rpm 으로 교반하면서 여기에 상기 용액을 적가시킨 후 교반을 계속하였다. 여기에 가교제인 폴리에틸렌글리콜디글리시딜에테르 5%의 이소프로필미리스테이트 용액 200g을 가한 후, 6,000rpm으로 교반하면서 2시간동안 가교반응시켰다. 반응이 끝난 후 용매를 제거하기 위해 수회에 걸쳐 수세한 후 여과하였다. 평균 직경 30㎛의 캡슐을 얻었다.1 g of magnesium ascorbic acid phosphate was dissolved in 500 g of myristylate fossilylated atelocollagen (Japanese Kobe Aterocollagen MS) 1% aqueous solution. The solution was added dropwise thereto while stirring 2,000 g of liquid paraffin LP # 70 at 6,000 rpm using a mixer, and then stirring was continued. 200 g of isopropyl myristate solution of polyethylene glycol diglycidyl ether as a crosslinking agent was added thereto, followed by crosslinking reaction for 2 hours while stirring at 6,000 rpm. After the reaction was completed, washed several times to remove the solvent and filtered. A capsule having an average diameter of 30 µm was obtained.

[실시예 2]Example 2

석시닐화 아텔로콜라겐[일본 고껜 아테로콜라겐 SS] 2% 수용액 500g에 세라미이드 50g을 용해하였다. 사이클로 헥산 2,000g을 혼합기를 이용하여 500rpm으로 교반하면서 여기에 상기 용액을 적가시킨 후 교반을 계속하엿다. 여기에 가교제인 글리세롤디글리시딜에테르 5%의 이소프로필미리스테이트 용액 300g을 가한 후, 500rpm으로 교반하면서 2시간동안 가교반응시켰다. 반응이 끝난 후 용매를 제거하기 위해 수회에 걸쳐 수세한 후 여과하였다. 평균 직경 150㎛의 캡슐을 얻었다.50 g of ceramide was dissolved in 500 g of a succinylated atelocollagen (Japan Goya Aterocollagen SS) 2% aqueous solution. 2,000 g of cyclohexane was added dropwise thereto while stirring at 500 rpm using a mixer, followed by continued stirring. To this was added 300 g of a 5% isopropyl myristate solution of glycerol diglycidyl ether as a crosslinking agent, and then crosslinked for 2 hours with stirring at 500 rpm. After the reaction was rinsed several times to remove the solvent and filtered. A capsule having an average diameter of 150 µm was obtained.

[실시예 3]Example 3

실시예 2에서 얻은 캡슐 20g을 하기 조성을 갖는 외상액 100g에 혼합하여 캡슐 화장료를 제조하였다.20 g of the capsule obtained in Example 2 was mixed with 100 g of the supernatant having the following composition to prepare a capsule cosmetic.

[비교예 1]Comparative Example 1

피막재로 젤라틴을 사용한 것을 제외하고는 상기 실시예 2와 동일하게 실시하여 평균 직경 150㎛의 캡슐을 얻었다.A capsule having an average diameter of 150 µm was obtained in the same manner as in Example 2, except that gelatin was used as the coating material.

이렇게 하여 얻은 젤라틴 캡슐 20g을 상기 실시예 3과 동일 조성을 갖는 외상액 100g에 혼합하여 캡슐화장료를 얻었다.20 g of the obtained gelatin capsules were mixed with 100 g of the supernatant having the same composition as in Example 3 to obtain a capsule cosmetic.

[시험예 1][Test Example 1]

가압붕괴성 시험Pressure Collapse Test

캡슐의 가압붕괴성의 정도를 비교하기 위해 실시예 1과 2에서 얻은 캡슐과 비교예 1에서 얻은 캡슐을 레오미터(SUN SCIENTIFIC社, 모델 CR-200)로 상승속도 45㎜/min, 직경 2.5㎝의 로드로 10회 측정하여 평균값을 측정하였다. 결과는 표 1과 같았다.In order to compare the degree of pressure collapse of the capsules, the capsules obtained in Examples 1 and 2 and the capsules obtained in Comparative Example 1 were used with a rheometer (SUN SCIENTIFIC, Model CR-200) to increase the speed of 45 mm / min and the diameter of 2.5 cm. The average value was measured 10 times with a rod. The results were shown in Table 1.

[시험예 2][Test Example 2]

사요감 비교Comparison of feelings

본 발명의 실시예 3에서 얻은 화장료와 비교예 1에서 얻은 화장료와의 가압붕괴후 사용성을 비교하기 위해 19~40세의 전문검사요원 남녀 50명에 의한 3점 평가법으로 비교하여 얻은 점수의 평균치를 얻었다. 그 결과는 표 2와 같았다.Average value of scores obtained by comparing the cosmetics obtained in Example 3 of the present invention with the cosmetics obtained in Comparative Example 1 by the three-point evaluation method by 50 men and women of professional inspection personnel aged 19-40 years Got it. The results were shown in Table 2.

1:껍질 잔존, 피부에 거친 느낌이 있음.1: Peel remaining, rough skin.

2:껍질 미량 잔존, 피부에 약간의 물리적 자극을 느낌.2: A small amount of skin remaining, feeling a slight physical irritation to the skin.

3:잔존 껍질 없음, 피부에 매끄럽게 도포됨.3: No remaining crust, applied to skin smoothly.

Claims (4)

화장료용 콜라겐 캡슐에 있어서, 피막제로서 콜라겐 또는 그의 유도체를, 가교제로서 글리시딜기를 2~4개 갖고 있는 화합물을 사용하고, 가교제의 함량을 콜라겐에 대한 중량비로 1:1.5~2.5의 범위 내로, 가교제의 농도를 3~15%(w/v)의 범위로 조정하여 얻은 것임을 특징으로 하는 화장료용 콜라겐 캡슐.In the collagen capsule for cosmetics, a compound having 2 to 4 glycidyl groups as a crosslinking agent and collagen or a derivative thereof is used, and the content of the crosslinking agent is in the range of 1: 1.5 to 2.5 in a weight ratio to collagen, Collagen capsules for cosmetics, characterized in that obtained by adjusting the concentration of the crosslinking agent in the range of 3 to 15% (w / v). 제1항에 있어서, 콜라겐 또는 그의 유도체는 아텔로콜라겐, 미리스틸화 아텔로콜라겐, 석시닐화 아텔로콜라겐, 미리스틸석시닐화 아텔로콜라겐 및 프탈화아텔로콜라겐으로 이루어진 군에서 선택된 1종 또는 2종 이상임을 특징으로 하는 화장료용 콜라겐 캡슐.The collagen or derivative thereof is one or more selected from the group consisting of atelocollagen, myristylated atelocollagen, succinylation atelocollagen, myristylosynylated atelocollagen, and phthalated atelocollagen. Cosmetic collagen capsules, characterized in that two or more. 제1항에 있어서, 글리시딜기를 2~4개 갖고 있는 화합물은 트리메칠올프로판폴리글리시딜에테르, 네오펜틸글리콜디글리시딜에테르, 그리세롤폴리글리시딜에테르, 폴리프로필렌글리콜디글리시딜에테르, 에틸렌글리콜디글리시딜에테르, 폴리에틸렌글리콜디글리시딜에테르 및 솔비톨폴리글리시딜에테르로 이루어진 군에서 선택된 것임을 특징으로 하는 화장료용 콜라겐 캡슐.The compound having 2 to 4 glycidyl groups according to claim 1, wherein the compound having 2 to 4 glycidyl groups is trimethylolpropanepolyglycidyl ether, neopentyl glycol diglycidyl ether, gglycerol polyglycidyl ether, polypropylene glycol digly Cosmetic collagen capsules, characterized in that selected from the group consisting of cydyl ether, ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether and sorbitol polyglycidyl ether. 제1항에 있어서, 캡슐은 평균 직경이 1~5,000㎛임을 특징으로 하느 화장료요 콜라겐 캡슐.The cosmetic collagen capsule of claim 1, wherein the capsule has an average diameter of 1 to 5,000 μm.
KR1019940020674A 1994-08-22 1994-08-22 Collegen capsule for cosmetics KR0143385B1 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11612172B2 (en) 2018-10-25 2023-03-28 Amorepacific Corporation Processed products of tea with quick dispersibility in water and method for manufacturing processed products of tea
US11653665B2 (en) 2019-08-21 2023-05-23 Amorepacific Corporation Processed products of tea and method for manufacturing the same

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Publication number Priority date Publication date Assignee Title
KR100308769B1 (en) * 1999-02-19 2001-09-24 장호균 Freeze dried retinol microsphere and a lip-care cosmetic composition containing the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11612172B2 (en) 2018-10-25 2023-03-28 Amorepacific Corporation Processed products of tea with quick dispersibility in water and method for manufacturing processed products of tea
US11653665B2 (en) 2019-08-21 2023-05-23 Amorepacific Corporation Processed products of tea and method for manufacturing the same

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