KR20050025454A - Cosmetic compositions with adsorber stabilized with concentrated red ginseng extract - Google Patents

Cosmetic compositions with adsorber stabilized with concentrated red ginseng extract Download PDF

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KR20050025454A
KR20050025454A KR1020030062679A KR20030062679A KR20050025454A KR 20050025454 A KR20050025454 A KR 20050025454A KR 1020030062679 A KR1020030062679 A KR 1020030062679A KR 20030062679 A KR20030062679 A KR 20030062679A KR 20050025454 A KR20050025454 A KR 20050025454A
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red ginseng
cosmetic composition
adsorber
ginseng concentrate
concentrated red
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KR100525506B1 (en
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박명기
이홍선
서정민
이천일
표형배
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한불화장품주식회사
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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
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9789Magnoliopsida [dicotyledons]
    • 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
    • A61K8/0279Porous; Hollow
    • 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
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • 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
    • A61K2800/60Particulates further characterized by their structure or composition
    • A61K2800/61Surface treated
    • A61K2800/62Coated

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  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
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  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Botany (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Cosmetics (AREA)

Abstract

A cosmetic composition comprising an adsorber stabilized with concentrated red ginseng extract is provided, which cosmetic composition has no distinct smell of red ginseng, improved stability against temperature change and light, and improved skin protection and enhancement. The cosmetic composition comprises (a) a concentrated red ginseng solution containing concentrated red ginseng extract and purified water in a volume ratio of 2:8 to 7:3; (b) one or two compounds selected from lauryl metacrylate/glycol dimetacrylate crosspolymer and allyl metacrylate crosspolymer as an adsorber; and (c) one or two or more polyhydric alcohols selected from butyleneglycol, propyleneglycol or glycerin, wherein the cosmetic composition is prepared by adsorbing the component (a) into the adsorber of component (b), and coating the adsorber with the component (c); and the cosmetic composition comprises 1.5 to 25.0 wt.% of the adsorber stabilized with concentrated red ginseng extract.

Description

홍삼 농축액 포집체를 함유한 화장료 조성물{Cosmetic compositions with adsorber stabilized with concentrated red ginseng extract}Cosmetic compositions containing red ginseng concentrate collectors {Cosmetic compositions with adsorber stabilized with concentrated red ginseng extract}

본 발명은 홍삼농축액을 라우릴메타크릴레이트/글리콜디메타크릴레이트 크로스폴리머 또는 알릴메타크릴레이트 크로스폴리머에 포집한 후 보습제로 코팅한 포집체 및 이 포집체를 함유한 화장료 조성물에 관한 것이며, 보다 상세하게는 끈적임이 적고 온도변화에 따른 색상이나 취변화가 없는 안정성과 사용감이 우수한 화장료를 만들기 위하여 홍삼농축액을 라우릴메타크릴레이트/글리콜디메타크릴레이트 크로스 폴리머 또는 알릴메타크릴레이트크로스폴리머에 흡착시킨 후 코팅한 포집체 및 이 포집체를 함유하는 화장료 조성물에 관한 것이다.The present invention relates to a collector coated with a moisturizer after collecting red ginseng concentrate in a lauryl methacrylate / glycol dimethacrylate crosspolymer or an allyl methacrylate crosspolymer, and a cosmetic composition containing the collector. In detail, red ginseng concentrate is adsorbed on lauryl methacrylate / glycol dimethacrylate cross polymer or allyl methacrylate cross polymer to make cosmetics with less stickiness and excellent stability and usability without color or brittleness due to temperature change. The present invention relates to a coated collector and a cosmetic composition containing the collected after the coating.

홍삼의 원료인 수삼은 보통 75%내외의 수분을 함유하고 있어 1주일 이상 보관이 어려워 단순 건조한 백삼으로 널리 유통되어오다 좀더 장기간 보관이 가능한 증숙한 홍삼이 약 1,000년전부터 중국에서 활용되었으나 한국의 풍토나 기후가 인삼재배에 가장 이상적이며 품질및 약효 또한 중국산과 비교할 수 없이 월등한 것으로 알려져 있다.Red ginseng, which is the raw material of red ginseng, contains about 75% of moisture, so it is difficult to store for more than a week, so it is widely distributed as a simple dry white ginseng. The climate is the most ideal for ginseng cultivation, and the quality and efficacy are known to be superior to those of China.

홍삼의 주요 성분인 사포닌은 식물의 뿌리, 줄기, 잎, 껍질, 씨 등에 흔히 함유되어 있는 물질로 의약품 및 건강식품 등에 널리 활용되고 있다. 홍삼의 주성분인 사포닌은 화학적으로 배당체라 부르는 화합물의 일종으로서 사포닌이란 흔들면 비누처럼 거품을 낸다고 하여 붙여진 이름이며 사포닌 함유 식물은 예로부터 세정, 거담, 진해를 목적으로 의약품에 활용되었으며 최근에는 소염, 해열, 건위, 배농, 항종양, 이뇨, 강장, 강정 등에 널리 활용되고 있다.Saponin, the main ingredient of red ginseng, is a substance commonly contained in roots, stems, leaves, bark, and seeds of plants, and is widely used in medicine and health foods. Saponin, the main ingredient of red ginseng, is a chemical compound called glycoside. Saponin is a name given to foam like soap when shaken. Saponin-containing plants have been used in medicine for the purpose of washing, expectoration and antitussive. It is widely used in health, stomach, drainage, anti-tumor, diuresis, tonic and gangjeong.

사포닌은 당부분(sugar 또는 glycone), 비당부분(non-sugar 또는 aglycone)으로 구성되어있는 배당체로서 홍삼 사포닌은 트리테르페노이드(triterpenoid)계의 담마란(dammarane)계의 사포닌으로 인삼속 식물에만 존재한다. 홍삼은 증숙등 제조과정중 비효소적 갈색화 반응이 촉진되어 많은 갈색화 반응 생성물이 형성되고 그 중 말톨(maltol)등과 같은 항산화 성분도 다량 생성되어 암세포 증식을 억제하는 진세노사이드(ginsenoside)와 파낙시트리올(panaxytrol)등과 같은 성분이 생성된다. 사포닌은 도라지나 콩, 은행에도 들어있는 성분으로 특히 인삼, 홍삼, 산삼에 함유된 사포닌 성분을 진세노사이드라고 부른다. 이중 진세노사이드 Rh2와 Rg3는 인삼에는 전혀 없고 산삼과 홍삼에만 극미량 포함되어 있다.Saponins are glycosides consisting of sugar (sugar or glycone) and non-sugar (a-glycone). Red ginseng saponins are triterpenoid dammarane saponins. exist. Red ginseng promotes the non-enzymatic browning reaction during the steaming process, and many browning reaction products are formed. Among them, a large amount of antioxidants such as maltol are generated, which inhibits cancer cell proliferation. Ingredients such as panaxytrol are produced. Saponins are also found in bellflower, soybeans, and ginkgo. Especially, saponins contained in ginseng, red ginseng, and wild ginseng are called ginsenosides. Ginsenosides Rh2 and Rg3 are not present in ginseng at all and are contained only in wild ginseng and red ginseng.

이러한 홍삼 성분의 피부 작용으로는 피부기능을 개선시키고, 피부탄력 및 노화방지, 피부세포 부활, 보습작용, 피부트러블 해결, 지친 피부개선, 유해한 환경으로부터 건강한 피부를 유지할 수 있게 도와 주는 역할을 한다. 최근에 한방화장품이 유행하여 홍삼추출물, 인삼추출물, 산삼 및 장뇌삼 등이 화장료에 많이 이용되고 있다.The skin action of these red ginseng components improves skin function, and helps to maintain skin elasticity and anti-aging, rejuvenation of skin cells, moisturizing, resolving skin problems, tired skin improvement, and maintaining healthy skin from harmful environment. In recent years, herbal cosmetics have become popular, and red ginseng extract, ginseng extract, wild ginseng and camphor ginseng are widely used in cosmetics.

본 발명에서 '홍삼농축액'이라는 용어는 식품공전(한국식품공업협회 발간)에서의 정의대로 홍삼으로부터 가용성 홍삼성분을 추출하여 농축한 것을 말한다. 즉 이 홍삼농축액 안에는 홍삼성분 사포닌이 70mg/g 이상이 함유된 것을 말한다. 이 홍삼농축액은 매우 끈적이고 특이한 취와 색상을 가지고 있어 홍삼 농축액을 그대로 사용하여 화장료에 적용할 경우 홍삼농축액이 가지고 있는 고유의 색깔, 취 및 계면활성제 역할을 할 수 있는 사포닌에 의한 제형의 교란 등으로 제품의 안정도가 영향을 받을 수 있으며, 홍삼 농축액 특유의 진한 취와 색깔로 인해 거부감이 생겨 제품화가 쉽지 않은 것으로 알려져 있다. 향취면에서는 홍삼농축액을 0.25% 정도이상으로 화장료에 배합해도 홍삼농축액 특유의 취의 강함 때문에 일반소비자들은 거부감을 가지게 되고, 함량이 높아지는 경우에는 섭씨 40℃ 이상에서 수주간 방치시 탈색이 일어나 화장료에 응용하기가 어렵다. 홍삼농축액에 함유되어 있는 사포닌은 계면활성작용이 있어서 화장품에 있어서 제형의 안정화에 역할을 하는 계면활성제와 상호간섭을 일으켜 화장품의 안정도에 영향을 끼치기 때문에 안정도를 유지하기 위해서는 계면활성제나 안정화제를 추가로 배합할 필요가 있다. 그러나 이러한 추가로 인해서 사용에 거부감을 주는 끈적임이나 색조화장품 사용시 밀림현상이 발생해서 색조화장이 잘 되지 않을 수도 있다. 이에 본 연구자들은 홍삼농축액이 안정하게 함유된 제제 개발을 연구하게 되었다. In the present invention, the term 'red ginseng concentrate' refers to a concentrated and extracted soluble red ginseng component from red ginseng as defined by the Food Code (published by the Korea Food Industry Association). That is, the red ginseng concentrate contains more than 70mg / g of red ginseng component saponin. This red ginseng concentrate has a very sticky and unusual odor and color. When applied to cosmetics using the red ginseng concentrate as it is, the red ginseng concentrate has its own color, odor, and disturbance of the formulation by saponin that can act as a surfactant. The stability of the product may be affected, and it is known that it is not easy to commercialize due to the strong smell and color of red ginseng concentrate. On the fragrance side, even if the red ginseng concentrate is blended to the cosmetics at about 0.25% or more, the general consumer has a sense of rejection due to the strong odor of the red ginseng concentrate. Difficult to apply Saponin contained in red ginseng concentrate has surfactant activity, so it interferes with the surfactant which plays a role in stabilization of the formulation in cosmetics and affects the stability of cosmetics. Therefore, surfactant or stabilizer is added to maintain stability. It is necessary to mix | blend with. However, this addition may cause stickiness that causes a disapproval of use, or the use of color cosmetics may cause a jungle phenomenon, which may result in poor color cosmetics. We therefore studied the development of a formulation containing red ginseng concentrates stably.

본 발명자들은 상기 홍삼농축액의 문제점을 갖지 않으면서 온도변화에도 안정하며 또 사용성이 좋은, 화장료에 유용한 홍삼농축액을 사용할 수 있도록 안정화 연구를 행하였고, 그 결과 라우릴메타크릴레이트/글리콜디메타크릴레이트 크로스 폴리머 또는 알릴메타크릴레이트크로스폴리머에 홍삼농축액을 흡착시킨 뒤 보습제로서 코팅한 포집체를 만들어 화장료에 투입하므로서 상기 목적들을 달성할 수 있음을 발견하고 본 발명을 완성하기에 이르렀다.The present inventors conducted a stabilization study to be able to use the red ginseng concentrate useful in cosmetics, which is stable and easy to change in temperature without having the problem of the red ginseng concentrate, and as a result, lauryl methacrylate / glycol dimethacrylate. After adsorbing the red ginseng concentrate on the cross polymer or allyl methacrylate cross polymer, it was found that the above-mentioned objects can be achieved by making a collector coated with a moisturizing agent and applying it to a cosmetic.

따라서, 본 발명의 목적은 홍삼농축액이 안정하게 흡착된 화장료용 포집체를 제공하는 것이다. Accordingly, it is an object of the present invention to provide a cosmetic collector in which red ginseng concentrate is stably adsorbed.

본 발명의 또다른 목적은 상기 코팅 포집체를 함유하는 홍삼농축액의 특이취를 감소시키고, 안정하고 사용성이 좋은 화장료 조성물을 제공하는 것이다. Still another object of the present invention is to reduce the specific odor of the red ginseng concentrate containing the coating collector, and to provide a stable and usable cosmetic composition.

본 명세서에서 '홍삼농축액'이라는 용어는 식품공전(한국식품공업협회 간)에서의 정의대로 홍삼으로부터 가용성 홍삼성분을 추출하여 농축한 것을 말한다. 즉 이 홍삼농축액 안에는 홍삼성분 사포닌이 70mg/g 이상이 함유된 것을 말한다.As used herein, the term 'red ginseng concentrate' refers to a concentrated and extracted soluble red ginseng component from red ginseng as defined by the Food Code (Korea Food Industry Association). That is, the red ginseng concentrate contains more than 70mg / g of red ginseng component saponin.

본 발명에 사용되는 흡착제, 라우릴메타크릴레이트/글리콜디메타크릴레이트 크로스폴리머는 입자의 크기가 200 ∼ 1,200㎛ 크기의 백색의 다공성 파우더이며 피부의 유분을 흡착하는 성질이 강하면서 사용성이 좋은 원료이다.The adsorbent used in the present invention, lauryl methacrylate / glycol dimethacrylate crosspolymer, is a white porous powder having a particle size of 200 to 1,200 μm, and has a strong property of adsorbing skin oil and good usability. to be.

그리고, 알릴메타크릴레이트 크로스폴리머는 크기는 20㎛ 정도의 크기로서 표면적이 150 m2/g 이상이 되는 다공성 물질이다.The allyl methacrylate crosspolymer is a porous material having a size of about 20 μm and a surface area of 150 m 2 / g or more.

그리고, 코팅제로서 사용되는 다가알콜(폴리올)로서는 부틸렌글리콜, 프로필렌글리콜 및 글리세린 등을 예시할 수 있으며 1종 단독 혹은 2종이상의 혼합물을 사용할 수 있다. 상기 다가알콜이 코팅제로서 사용될 수 있는 이유는 부틸렌글리콜 또는 프로필렌글리콜은 홍삼농축액 자체와 혼합하면 용해성을 보이지 않고 엉겨서 침전 현상을 나타내지만 홍삼농축액이 포집된 라우릴메타크릴레이트/글리콜디메타크릴레이트 크로스폴리머 또는 알릴메타크릴레이트크로스폴리머에는 응집 및 침전 현상을 보이지 않고 이 두 종류의 다공성 파우더 표면에 포집된 홍삼농축액의 방출을 방해하여 변취나 변색에 대하여 안정성을 유지시키고 끈적임을 유발하는 홍삼농축액이 피부에 빨리 흡수되는 것을 방해하여 사용성을 좋게 할 수 있고 홍삼농축액 특유의 취를 감소시켜 홍삼농축액의 화장료에의 사용량을 증가시킬 수 있기 때문이다.As the polyhydric alcohol (polyol) used as the coating agent, butylene glycol, propylene glycol, glycerin, and the like can be exemplified, and one kind or a mixture of two or more kinds can be used. The reason why the polyhydric alcohol can be used as a coating agent is that butylene glycol or propylene glycol does not show solubility when mixed with the red ginseng concentrate itself and becomes tangled, causing precipitation, but the lauryl methacrylate / glycol dimethacryl collected with the red ginseng concentrate. Red ginseng concentrate which does not show aggregation or precipitation phenomenon in late crosspolymer or allyl methacrylate crosspolymer and prevents the release of red ginseng concentrate collected on the surface of these two porous powders to maintain stability against discoloration or discoloration and cause stickiness This is because the use of red ginseng concentrate in cosmetics can be increased by preventing the absorption into the skin quickly and improving usability.

이들 성분들은 (가)홍삼농축액 : 정제수의 비율이 2:8 ∼7:3인 홍삼농축액 수용액 (나)흡착제인 라우릴메타크릴레이트/글리콜디메타크릴레이트 크로스폴리머 또는 알릴메타크릴레이트크로스폴리머에서 선택된 1종 또는 2종의 혼합물 (다) 부틸렌글리콜, 프로필렌글리콜 또는 글리세린등의 다가알콜 1종 혹은 2종이상의 혼합물로 구성되는데 (가):(나) 의 비율이 0.5:1 ∼ 7:1 로 되게 흡착시킨 뒤 이 흡착된 (가+나) :(다) 의 비율이 0.1:4 ∼ 4:4로 혼합 코팅하여 제조된 포집체를 제공하는 것이다.These components are (a) red ginseng concentrate: red ginseng concentrate aqueous solution with ratio of purified water 2: 8-7: 3 (b) in lauryl methacrylate / glycol dimethacrylate crosspolymer or allyl methacrylate crosspolymer One or two selected mixtures (C) Polyhydric alcohols such as butylene glycol, propylene glycol or glycerin, or one or more mixtures of two or more thereof. The ratio of (A) :( B) is 0.5: 1 to 7: 1. After adsorbing, the adsorbed (ga + na) :( c) ratio is 0.1: 4 to 4: 4 to provide a collector prepared by mixing coating.

본 발명의 포집체를 각종 화장료에 배합하는 경우 화장료 총 중량에 대하여 약 1.50 ∼ 25.0중량%의 양으로 사용될 수 있다. 1.50중량% 미만인 경우 홍삼농축액의 피부미용효과가 미미하며, 25.0중량%를 넘는 경우에는 냄새 및 끈적임에 있어서 바람직하지 않다.When the collector of the present invention is blended into various cosmetics, it may be used in an amount of about 1.50 to 25.0% by weight based on the total weight of the cosmetic. If less than 1.50% by weight of the red ginseng concentrate skin care effect is insignificant, if it exceeds 25.0% by weight is not preferable in the smell and stickiness.

이하 실시예에서 본 발명을 상세히 설명하지만 본 발명이 이들 실시예에만 국한되는 것은 아니다. 각 실시예에서 모든 성분의 함량은 특별한 언급이 없는 한 중량부이다.The present invention is described in detail in the following Examples, but the present invention is not limited to these Examples. The content of all components in each example is parts by weight unless otherwise specified.

<실시예 1∼6 : 코팅 포집체 제조><Examples 1-6: Preparation of Coating Collector>

하기 표1에 나타낸 성분들을 이용하여 다음 방법에 따라 포집체를 제조하였다.Using the components shown in Table 1 below to prepare a collector according to the following method.

가) 원료1을 원료 2에 투입, 상온에서 용해한다.A) Raw material 1 is added to raw material 2 and dissolved at room temperature.

나) 용해된 가) 성분을 원료 3이나 4에 서서히 투입하면서 혼합(포집)시킨다.B) The dissolved a) ingredients are mixed (collected) while gradually being added to raw materials 3 and 4.

다) 혼합된 나)에 원료 5 또는 6 또는 7을 투입 혼합 코팅시켜 포집체를 완성한다.C) Mixed material b) Input mixed coating 5 or 6 or 7 to complete the collector.

항목Item 원료명Raw material name 실시예Example 비교예Comparative example 1One 22 33 44 55 66 1One 22 A상A phase 1.홍삼농축액Red ginseng concentrate 15.62515.625 15.62515.625 15.62515.625 15.89815.898 15.89815.898 15.89815.898 15.62515.625 15.89815.898 2.정제수2.purified water 15.62515.625 15.62515.625 15.62515.625 15.89815.898 15.89815.898 15.89815.898 잔량Remaining amount 잔량Remaining amount B상B phase 3.라우릴메타크릴레이트/글리콜디메타크릴레이트 크로스 폴리머3.lauryl methacrylate / glycol dimethacrylate cross polymer 6.2506.250 6.2506.250 6.2506.250 -- -- -- 6.2506.250 -- 4. 알릴메타크릴레이트 크로스 폴리머4. Allyl methacrylate cross polymer -- -- -- 4.6114.611 4.6114.611 4.6114.611 -- 4.6114.611 C상C phase 5.부틸렌글리콜5.butylene glycol 62.50062.500 -- -- 63.59363.593 -- -- -- -- 6.프로필렌글리콜6.propylene glycol -- 62.50062.500 -- -- 63.59363.593 -- -- -- 7.글리세린7.glycerine -- -- 62.50062.500 -- -- 63.59363.593 -- --

<비교예 1,2 비코팅 포집체 제조><Comparative Examples 1 and 2 Uncoated Collector Preparation>

가) 원료 1을 원료 2에 투입하여 용해한다.A) Raw material 1 is added to raw material 2 and dissolved.

나) 용해된 가) 성분을 원료 3이나 4에 서서히 투입하면서 혼합시킨다.B) The dissolved a) ingredients are mixed with raw materials 3 or 4 gradually.

상기 제조 공정에 따라 제조된 포집체를 이용하여 본 발명의 실시예 및 비교예를 들어 본 발명을 좀더 상세하게 설명한다. The present invention will be described in more detail by way of examples and comparative examples of the present invention using a collector prepared according to the above manufacturing process.

<실시예 7~10 및 비교예 3~5> 크림상 화장료 조성물의 제조<Examples 7-10 and Comparative Examples 3-5> Preparation of creamy cosmetic composition

항목Item 원료명Raw material name 실시예Example 비교예Comparative example 77 88 99 1010 33 44 55 A상A phase 1.디소듐 이디티에이1.Disodium ID 0.010.01 0.010.01 0.010.01 0.010.01 0.010.01 0.010.01 0.010.01 2.메칠파라벤2.Methylparaben 0.200.20 0.200.20 0.200.20 0.200.20 0.200.20 0.200.20 0.200.20 3.카보머 2% 수용액3.Carbomer 2% aqueous solution 6.006.00 6.006.00 6.006.00 6.006.00 6.006.00 6.006.00 6.006.00 4. 정제수4. Purified water 잔량Remaining amount 잔량Remaining amount 잔량Remaining amount 잔량Remaining amount 잔량Remaining amount 잔량Remaining amount 잔량Remaining amount B상B phase 5.부틸파라벤5.butylparaben 0.100.10 0.100.10 0.100.10 0.100.10 0.100.10 0.100.10 0.100.10 6.토코페릴아세테이트6.Tocopheryl Acetate 0.100.10 0.100.10 0.100.10 0.100.10 0.100.10 0.100.10 0.100.10 7.세테아릴알코올7.cetearyl alcohol 1.601.60 1.601.60 1.601.60 1.601.60 1.601.60 1.601.60 1.601.60 8.메칠글루코스디올레이트8.Methylglucose dioleate 0.300.30 0.300.30 0.300.30 0.300.30 0.300.30 0.300.30 0.300.30 9.피이지-20 메칠글루코스세스퀴스테아레이트9.Pig-20 Methylglucosesesquistearate 1.001.00 1.001.00 1.001.00 1.001.00 1.001.00 1.001.00 1.001.00 10.폴리글리세릴-3 메칠글루코스디스테아레이트10.Polyglyceryl-3 Methylglucose distearate 1.201.20 1.201.20 1.201.20 1.201.20 1.201.20 1.201.20 1.201.20 11.글리세릴스테아레이트/피이지-100스테아레이트11.Glyceryl Stearate / Pig-100stearate 1.501.50 1.501.50 1.501.50 1.501.50 1.501.50 1.501.50 1.501.50 12.스테아린산12.Stearic acid 1.001.00 1.001.00 1.001.00 1.001.00 1.001.00 1.001.00 1.001.00 13.스쿠알란13.Squalane 4.004.00 4.004.00 4.004.00 4.004.00 4.004.00 4.004.00 4.004.00 14.호호바오일14.Jojoba oil 5.005.00 5.005.00 5.005.00 5.005.00 5.005.00 5.005.00 5.005.00 C상C phase 15.트리에탄올아민15.Triethanolamine 0.140.14 0.140.14 0.140.14 0.140.14 0.140.14 0.140.14 0.140.14 16.정제수16.Purified water 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 D상D phase 17.홍삼농축액17.Red ginseng concentrate -- -- -- -- 1.001.00 -- 3.003.00 18.실시예 118.Example 1 6.406.40 19.2019.20 -- -- -- -- -- 19.실시예 219.Example 2 -- -- 6.406.40 -- -- -- -- 20.실시예 420.Example 4 -- -- -- 6.406.40 -- -- -- 21.비교예 121.Comparative Example 1 -- -- -- -- -- 6.46.4 --

상기 표 2.의 원료 1∼4의 원료를 80℃까지 가열하여 균일하게 한 다음 80℃로 원료 5∼14의 유상을 균일하게 하여 원료 5∼14의 유상을 원료 1∼4의 수상에 서서히 투입하면서 3,000rpm으로 7분동안 유화시킨다. 그리고 유화물에 정제수 즉 원료 16에 용해된 중화제, 원료 15를 투입하여 3,500rpm으로 7분동안 중화시킨다. 그리고 내용물을 40∼44℃로 냉각시킨 후 나머지 원료들을 투입 교반하여 30℃까지 냉각한 후 최종 크림상 화장료 조성물을 얻는다.The raw materials 1-4 of Table 2 were heated to 80 ° C. to be uniform, and then the oil phases of raw materials 5-14 were uniformized at 80 ° C., and the oil phases of raw materials 5-14 were gradually added to the aqueous phase of raw materials 1-4. While emulsifying at 3,000 rpm for 7 minutes. In the emulsion, purified water, that is, neutralizer dissolved in raw material 16 and raw material 15 were added and neutralized at 3,500 rpm for 7 minutes. After the contents are cooled to 40 to 44 ° C., the remaining raw materials are added and stirred, cooled to 30 ° C., and a final creamy cosmetic composition is obtained.

<실시예 11∼14 및 비교예 6∼8> 로션류 화장료 조성물의 제조<Examples 11-14 and Comparative Examples 6-8> Preparation of lotion cosmetic composition

항목Item 원료명Raw material name 실시예Example 비교예Comparative example 1111 1212 1313 1414 66 77 88 A상A phase 1.디소듐이디티에이1.Disodium IDT 0.010.01 0.010.01 0.010.01 0.010.01 0.010.01 0.010.01 0.010.01 2.아크릴레이트/씨10-30 알킬아크릴레이트 크로스폴리머 2% 수용액2. 2% aqueous solution of acrylate / C10-30 alkyl acrylate crosspolymer 5.005.00 5.005.00 5.005.00 5.005.00 5.005.00 5.005.00 5.005.00 3.카보머 2% 수용액3.Carbomer 2% aqueous solution 9.009.00 9.009.00 9.009.00 9.009.00 9.009.00 9.009.00 9.009.00 4.정제수4.purified water 잔량Remaining amount 잔량Remaining amount 잔량Remaining amount 잔량Remaining amount 잔량Remaining amount 잔량Remaining amount 잔량Remaining amount B상B phase 5.메칠클루코스디올레이트5.Methyl Clocosdiolate 0.400.40 0.400.40 0.400.40 0.400.40 0.400.40 0.400.40 0.400.40 6.피이지-20 메칠글루코스세스퀴스테아레이트6.Pig-20 Methylglucosesesquistearate 1.401.40 1.401.40 1.401.40 1.401.40 1.401.40 1.401.40 1.401.40 7.친유형 글리세릴 스테아레이트7.lipophilic glyceryl stearate 0.600.60 0.600.60 0.600.60 0.600.60 0.600.60 0.600.60 0.600.60 8.세테아릴아코올8.cetearyl alcohol 0.800.80 0.800.80 0.800.80 0.800.80 0.800.80 0.800.80 0.800.80 9. 스테아린산9. Stearic Acid 0.300.30 0.300.30 0.300.30 0.300.30 0.300.30 0.300.30 0.300.30 10.스쿠알란10.Squalane 8.008.00 8.008.00 8.008.00 8.008.00 8.008.00 8.008.00 8.008.00 11.호호바오일11.Jojoba oil 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 12.사이클로펜타실록산12.cyclopentasiloxane 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 13.디메치콘13.Dimethicone 0.300.30 0.300.30 0.300.30 0.300.30 0.300.30 0.300.30 0.300.30 14.프로필파라벤14.Profile paraben 0.100.10 0.100.10 0.100.10 0.100.10 0.100.10 0.100.10 0.100.10 15.부틸레이티드하이드록시톨루엔15.butylated hydroxytoluene 0.020.02 0.020.02 0.020.02 0.020.02 0.020.02 0.020.02 0.020.02 C상C phase 16.트리에탄올아민16.Triethanolamine 0.290.29 0.290.29 0.290.29 0.290.29 0.290.29 0.290.29 0.290.29 17.정제수17.Purified water 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 D상D phase 18.홍삼농축액18.Red ginseng concentrate -- -- -- -- 1.001.00 -- 3.003.00 19.실시예 119.Example 1 6.406.40 19.2019.20 -- -- -- -- -- 20.실시예 220.Example 2 -- -- 6.406.40 -- -- -- -- 21.실시예 421.Example 4 -- -- -- 6.406.40 -- -- -- 24.비교예 124. Comparative Example 1 -- -- -- -- -- 6.406.40 --

상기 표 3.의 원료 1∼4의 원료를 80℃까지 가열하여 균일하게 한 다음, 80℃로 원료 5∼15의 유상을 균일하게 하여 원료 5∼15의 오일상을 원료 1∼4의 수상에 서서히 투입하면서 3,000rpm으로 7분동안 유화시킨다. 그리고 유화물에 정제수 즉 원료 17에 용해된 중화제, 원료 16을 투입하여 3,500rpm으로 7분동안 중화시킨다. 그리고 내용물을 40∼44℃로 냉각시킨 후 나머지 원료들을 투입 교반하여 30℃까지 냉각한 후 최종 로션상 화장료 조성물을 얻는다The raw materials 1-4 of Table 3 above were heated to 80 ° C. to be uniform, and then the oil phases of raw materials 5-15 were uniformed at 80 ° C., and the oil phases of raw materials 5-15 were transferred to the aqueous phase of raw materials 1-4. Emulsify for 7 minutes at 3,000 rpm while slowly adding. In the emulsion, purified water, that is, neutralizer dissolved in raw material 17 and raw material 16 were added and neutralized at 3,500 rpm for 7 minutes. After the contents are cooled to 40 to 44 ° C., the remaining raw materials are added and stirred, cooled to 30 ° C., and a final lotion-like cosmetic composition is obtained.

<실험예 1>Experimental Example 1

상기 실시예 7,10,11 및 비교예 3,4,6에서 화장료의 향취의 강도를 비교하기 위하여 상온(25℃)과 고온(42℃)에서 45일동안 보관한 후 향료 전문가 10명이 관능평가하였다. 그 결과를 표 4에 나타내었다. Sensory evaluation of 10 flavor experts after storing for 45 days at room temperature (25 ℃) and high temperature (42 ℃) in order to compare the strength of the perfume of the cosmetics in Examples 7,10,11 and Comparative Examples 3,4,6 It was. The results are shown in Table 4.

실시예 7Example 7 실시예 10Example 10 실시예 11Example 11 비교예 3Comparative Example 3 비교예 4Comparative Example 4 비교예 6Comparative Example 6 향의 강도(25℃ 평균값, 비교예 3을 100으로 잡음)Fragrance intensity (25 ℃ average value, comparable example 3 to 100) 2525 3030 2525 100100 9595 9595 향의 강도(42℃ 평균값, 비교예 3을 100으로 잡음)Fragrance intensity (42 ℃ average value, comparable example 3 to 100) 2525 3030 2525 100100 9595 9595

<실험예 2: 취 선호도 비교>Experimental Example 2: Comparison of Odor Preference

상기 실시예 7, 10, 11 및 비교예 3, 6에서 화장료의 향취의 선호도를 조사비교하기 위하여 상온(25℃)과 고온(42℃)에서 45일동안 보관한 후 일반남녀 40 명이 관능평가하였다. 그 결과를 표 5에 나타내었다. In order to investigate and compare the taste preference of the cosmetics in Examples 7, 10, 11 and Comparative Examples 3, 6, 40 general men and women after sensory evaluation at room temperature (25 ℃) and high temperature (42 ℃) sensory evaluation . The results are shown in Table 5.

항목Item 실시예 7(인원수)Example 7 (number of people) 실시예 10(인원수)Example 10 (number of people) 실시예 11(인원수)Example 11 (number of people) 비교예 3(인원수)Comparative Example 3 (Number of People) 비교예 6(인원수)Comparative Example 6 (Number of People) 상당히 좋다Pretty good -- -- -- -- -- 좋다good 3030 2525 2727 -- -- 그저그렇다so so 1010 1515 1313 -- -- 별로 좋지 않다Not so good -- -- -- 55 66 전혀 좋지 않다Not good at all -- -- -- 3535 3434

<실험예 3: 색상변화 평가>Experimental Example 3: Evaluation of Color Change

상기 실시예 6,7,11,12 및 비교예 3,5,8에서 화장료의 색상의 변화를 비교하고자 상온(25℃), 형광등, 자외선, 순환, 저온(4℃) 및 고온(42℃)에서 60일동안 보관한 후 평가하였다. 그 결과를 표 6에 나타내었다.Examples 6, 7, 11, 12 and Comparative Examples 3, 5, 8 to compare the color change of the cosmetics at room temperature (25 ℃), fluorescent lamps, UV, circulation, low temperature (4 ℃) and high temperature (42 ℃) Evaluation after storage for 60 days at. The results are shown in Table 6.

실시예 7Example 7 실시예 8Example 8 실시예 11Example 11 실시예 12Example 12 비교예 3Comparative Example 3 비교예 5Comparative Example 5 비교예 8Comparative Example 8 25℃25 ℃ 42℃42 ℃ ×× ×× ×× 자외선UV-rays ×× 형광Neon 순환cycle 4℃(저온)4 ° C (low temperature)

평가기준: ○: 변화 없음Evaluation criteria: ○: No change

▲: 약간의 변화 있음               ▲: slight change

×: 변화가 심한 편임               ×: change is severe

<실험예 4. 사용성 평가>Experimental Example 4. Usability Evaluation

상기 실시예 7,10,11 및 비교예 3,6에서 얻은 화장료의 사용성을 비교하기 위하여 피부 도포 후의 끈적임 정도를 23세∼40세의 일반인 40명에 의한 3점 평가법으로 비교하여 얻은 점수의 평균치를 얻었다. 그 결과는 표 7에 나타내었다.In order to compare the usability of the cosmetics obtained in Examples 7,10,11 and Comparative Examples 3,6, the average value of the scores obtained by comparing the degree of sticking after applying the skin by a three-point evaluation method by 40 people aged 23 to 40 years Got. The results are shown in Table 7.

실시예 7Example 7 실시예 10Example 10 실시예 11Example 11 비교예 3Comparative Example 3 비교예 6Comparative Example 6 평균값medium 2.72.7 2.82.8 2.82.8 1.21.2 1.31.3

1: 끈적임이 심함1: severe stickiness

2: 약간 끈적임2: slightly sticky

3: 끈적임이 없음3: no stickiness

상기 결과에서 알 수 있듯이 본 발명의 홍삼농축액이 포집된 포집체를 함유하는 화장료 조성물은 취 선호도 , 온도변화 및 빛에 의한 안정성, 사용성 등의 측면에서 홍삼농축액을 직접 화장료에 투입한 것 및 코팅시키지 않고 다공성 고분자에만 홍삼농축액을 흡착시켜 화장료에 투입한 통상의 화장료에 비하여 품질적인 면에서 월등하다.As can be seen from the above results, the cosmetic composition containing the red ginseng concentrate collected in the present invention is not directly coated and coated with red ginseng concentrate in cosmetics in terms of odor preference, temperature change, light stability, and usability. Red ginseng concentrate is adsorbed only on the porous polymer, and is superior in quality in comparison with the conventional cosmetics put into cosmetics.

Claims (2)

(가) 홍삼농축액:정제수의 비율이 2:8 ∼ 7:3인 홍삼농축액 수용액; (A) Red ginseng concentrate: Aqueous solution of red ginseng concentrate with ratio of purified water 2: 8-7: 3; (나) 흡착제로서 라우릴메타크릴레이트/글리콜디메타크릴레이트크로스폴리머 또는 알릴메타크릴레이트크로스폴리머에서 선택된 1종 또는 2종의 혼합물;(B) one or two mixtures selected from lauryl methacrylate / glycol dimethacrylate crosspolymer or allyl methacrylate crosspolymer as adsorbents; (다) 부틸렌글리콜, 프로필렌글리콜 또는 글리세린등의 다가 알코올 1종 혹은 2종 이상의 혼합물로 구성되며,(C) polyhydric alcohols such as butylene glycol, propylene glycol or glycerin, or a mixture of two or more thereof; (가):(나) 의 비율이 0.5:1 ∼ 7:1이 되도록 흡착시킨 후, (가+나):(다)의 비율이 0.1:4 ∼ 4:4 의 비율이 되도록 코팅하여 제조되는 홍삼농축액 포집체를 함유한 화장료조성물.Adsorbed so that the ratio of (A) :( B) is 0.5: 1 to 7: 1, and then coated so that the ratio of (A + B) :( C) is 0.1: 4 to 4: 4. Cosmetic composition containing red ginseng concentrate collector. 제1항에 있어서, 상기 홍삼농축액 포집체는 전체 화장료 조성물 중량대비 1.5 ∼ 25.0 중량% 함유함을 특징으로 하는, 홍삼농축액 포집체를 함유한 화장료 조성물.According to claim 1, wherein the red ginseng concentrate is characterized in that containing 1.5 to 25.0% by weight relative to the total weight of the cosmetic composition, cosmetic composition containing a red ginseng concentrate.
KR10-2003-0062679A 2003-09-08 2003-09-08 Cosmetic compositions with adsorber stabilized with concentrated red ginseng extract KR100525506B1 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100840508B1 (en) * 2007-02-08 2008-06-23 박상도 A manufacturing method of bodycleaner using red ginseng maltol and a bodycleaner thereof
KR100847662B1 (en) * 2007-03-09 2008-07-21 박상도 A manufacturing method of shampoo using red ginseng maltol and a shampoo thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100840508B1 (en) * 2007-02-08 2008-06-23 박상도 A manufacturing method of bodycleaner using red ginseng maltol and a bodycleaner thereof
KR100847662B1 (en) * 2007-03-09 2008-07-21 박상도 A manufacturing method of shampoo using red ginseng maltol and a shampoo thereof

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