KR20020080657A - Cosmetics comprising Albizzia bark extracts for antioxidation - Google Patents

Cosmetics comprising Albizzia bark extracts for antioxidation Download PDF

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KR20020080657A
KR20020080657A KR1020010020354A KR20010020354A KR20020080657A KR 20020080657 A KR20020080657 A KR 20020080657A KR 1020010020354 A KR1020010020354 A KR 1020010020354A KR 20010020354 A KR20010020354 A KR 20010020354A KR 20020080657 A KR20020080657 A KR 20020080657A
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extract
hwanhwanpi
antioxidant
cosmetics
antioxidant cosmetic
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김종헌
엄상용
정의수
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주식회사 참 존
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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
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/08Anti-ageing preparations
    • 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
    • A61K2800/52Stabilizers
    • A61K2800/522Antioxidants; Radical scavengers

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  • Public Health (AREA)
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  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dermatology (AREA)
  • Gerontology & Geriatric Medicine (AREA)
  • Biotechnology (AREA)
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  • Cosmetics (AREA)

Abstract

PURPOSE: An antioxidant cosmetic containing an Albizzia julibrissin Duraz. extract as a main component is provided. Because the extract is low in skin irritation and stability during mixing and shows an excellent free radical scavenging effect, it can provide an antioxidant cosmetic having an excellent prevention effect on wrinkles and skin aging. CONSTITUTION: The extract is prepared by extracting Albizzia julibrissin Duraz. in C1-3 anhydrous or hydrous alcohol, or ethyl acetate at 4 to 30deg.C for 3 to 20 days and then concentrating, wherein before or after execution of the extraction process, a diethylether soluble component is removed from the extract. The antioxidant cosmetic contains 0.0001 to 5% by weight of an Albizzia julibrissin Duraz. extract, based on the total dried weight of the antioxidant cosmetic.

Description

합환피 추출물을 함유하는 항산화 화장료{Cosmetics comprising Albizzia bark extracts for antioxidation}Cosmetics comprising Albizzia bark extracts for antioxidation

본 발명은 합환피 추출물을 함유하는 항산화 화장료에 관한 것이다.The present invention relates to an antioxidant cosmetic containing the haphwanpi extract.

자유라디칼 이론은 1950년대 중반 디 하만(D. Harman)에 의해서 제시되었으며, 최근들어 학회와 관련업계에서 주목을 받고 있다. 자유라디칼은 그 가장 바깥쪽의 궤도를 도는 전자가 쌍을 이루지 못하고 1개의 전자(부대전자) 상태로 있는 부대전자를 가진 분자, 원자를 의미한다. 이 부대전자를 가진 분자, 원자가 팀을 이루어 안정 상태에 들어가고자 다른 원자, 분자로 부터 전자 1개를 빼앗으려는 작용을 산화라고 한다. 라디칼이 인체에 존재하는 원인은 여러 가지 원인이 있으며, 이 라디칼은 세포를 파괴하거나 피부 진피층의 결합조직을 절단하거나 교차 결합을 일으키므로 주름형성, 피부암, 세포살상, 류마티스성 관절염, 아토피성 피부염, 여드름 등 여러 가지 문제를 발생시킨다. 이러한 자유라디칼을 없애거나 중화 시켜서 세포가 산화하는 것을 막는 역할을 하는 것이 항산화라고 하며 이 항산화 물질로는 베타 카로틴, 비타민 C, 비타민 E, 카테킨, 프로안소시아니징 등이 있다. 라디칼이생성되는 원인은 백혈구의 식작용, 미토콘드리아에서의 ATP 생산과정 중 전자 전달계, 미엘로퍼 옥사이드(Myeloper Oxide(MPO)) 의 작용, 자외선, 담배, 정상적인 대사 과정, 스트레스, 공해 물질, 세균 등이다.Free radical theory was proposed by D. Harman in the mid-1950s and has recently attracted attention in the academic and related industries. Free radicals mean molecules and atoms that have secondary electrons in their outermost orbital electrons that are not paired and in a single electron (sub electron). Oxidation is the act of taking away one electron from another atom or molecule in order to enter a stable state by forming a molecule and valence team with this secondary electron. Radicals exist in the human body for a number of reasons. These radicals destroy cells, cut connective tissue in the dermal layer of the skin, or cause cross-linking, resulting in wrinkles, skin cancer, cell killing, rheumatoid arthritis, atopic dermatitis, It can cause various problems such as acne. Antioxidants play a role in preventing or oxidizing cells by eliminating or neutralizing these free radicals. Antioxidants include beta carotene, vitamin C, vitamin E, catechin, and proanthocyanination. Radicals are produced by the phagocytosis of leukocytes, the electron transport system during the production of ATP in mitochondria, the action of Myeloper Oxide (MPO), ultraviolet light, tobacco, normal metabolic processes, stress, pollutants, bacteria, and the like.

물론 인체에도 항산화물질(라디칼 소거제)인 슈퍼옥사이드 디스뮤타제 (SuperOxide Dismatase:SOD), 카탈라아제, 비타민 E, 비타민 C, 유비퀴놀(Uviquinol) 등이 있다. 그러나 점차적으로 항산화 체계는 나이, 공해, 자외선, 스트레스 등에 의해 깨지기 시작한다. 그러므로 항 산화 체계가 무력화되고, 라디칼이 점차로 증가하게 된다.Of course, the human body also contains an antioxidant (radical scavenger), SuperOxide Dismatase (SOD), catalase, vitamin E, vitamin C, and ubiquinol. Increasingly, however, antioxidant systems begin to break down due to age, pollution, ultraviolet light, and stress. Thus the antioxidant system is neutralized and the radicals increase gradually.

이 증가된 라디칼은 진피의 결합조직인 콜라겐(Collagen), 엘라스틴(Elastin), 히아루론산(Hyaluronic aicd) 등을 파괴하여 피부의 일정 부위 침하 현상을 (주름) 일으키며 또한 세포막의 지질 부분을 산화시켜 세포의 파괴 현상을 일으켜 피부염, 여드름, 피부암 등의 질병을 유발하게 되는 것이다. 또한 이 라디칼은 멜라닌 형성과정 중 자발적인 산화반응 (도파퀴논 →멜라닌)에 관여하여 기미, 주근깨 등의 원인 및 주름생성의 원인이 되기도 한다. (참조 : 대한 화장품학회지 23권 1호 75~132) 따라서 종래에는 아스코르브산, α-토코페롤, SOD 등이 자유 라디칼 소거 효과를 가지는 물질로 화장료나 의약품에 배합함으로써 주름 및 기타 피부 질환을 방지하는 방법으로 이용되어 왔는데, 가격이 고가일 뿐만 아니라 배합시 안정성이 좋지 못하여 실질적인 효과를 얻기가 어려운 문제점이 있었다.The increased radicals destroy the dermal connective tissues, Collagen, Elastin and Hyaluronic acid, causing subsidence of certain areas of the skin (wrinkling), and also oxidizing the lipid part of the cell membrane to destroy cells. It causes symptoms such as dermatitis, acne, and skin cancer. In addition, this radical is involved in the spontaneous oxidation reaction (dopaquinone → melanin) during melanin formation, causing spots, freckles, and wrinkles. Therefore, conventionally, ascorbic acid, α-tocopherol, SOD, and the like have a free radical scavenging effect and are formulated into cosmetics or medicines to prevent wrinkles and other skin diseases. It has been used as, but not only the price is expensive but there is a problem that it is difficult to obtain a practical effect because the stability is not good at the time of formulation.

이에 본 발명자들은 상기 문제점을 해결하고, 보다 우수한 원료를 찾고자 하는연구의 일환으로 여러 천연물을 검색한 결과 합환피의 추출물이 라디칼 소거제로 효과가 우수하다는 것을 발견하여 본 발명을 완성하였다.Accordingly, the present inventors have completed the present invention by searching for several natural products as a part of the research to solve the above problems and to find a better raw material, and found that the extract of Haphwanpi is excellent as a radical scavenger.

따라서, 본 발명은 합환피 추출물을 함유하는 항산화 화장료를 제공하는 것을 목적으로 한다.Therefore, an object of the present invention is to provide an antioxidant cosmetic containing a synthetic ring extract.

본 발명은 합환피 추출물을 함유하는 항산화 화장료에 관한 것으로, 합환피 추출물이 항산와 화장료의 총 건조중량에 대하여 0.0001∼5중량%, 바람직하게는 0.001∼3중량%로 함유되는 것을 특징으로 한다. 합환피 추출물이 항산와 화장료의 총 건조중량에 대하여 0.0001중량% 이하의 농도인 경우에 라디칼소거의 실질적인 효과를 얻기 어려우며, 5중량% 이상의 농도인 경우에는 제품 안정성에 좋지 않은 영향을 미친다.The present invention relates to an antioxidant cosmetic containing haphwanpi extract, characterized in that the hwanhwanpi extract is contained in 0.0001 to 5% by weight, preferably 0.001 to 3% by weight relative to the total dry weight of the antioxidant and cosmetics. It is difficult to obtain the practical effect of radical elimination when the haphwanpi extract is less than 0.0001% by weight relative to the total dry weight of the acid and cosmetics, and when the concentration is more than 5% by weight, the product stability is adversely affected.

합환피(地楡)는 콩과 (Leguminosae) 식물인 자귀나무(Albizzia julibrissinDura)의 목피를 말한다. 합환피 추출액은 민간요법과 한의학에서 진정약, 이뇨, 진통약, 골절, 종창, 울결된 것을 풀어주고 혈을 조화시키며 마음을 가라앉히고 부스럼을 제거하는 효능, 종양, 유선암 , 고약, 강장, 흥분, 이뇨에 사용한다. (참조 : 약초의 성분과 이용(일월서각. 1994. 과학백과사전 출판사편), 신 약품 식물학(학창사. 1991), 사전식 동의보감(한국사전연구사), 중약대사전번역위 완역중약대사전(도서출판정담. 1997)).Haphwanpi (地 楡) refers to the bark of Albizzia julibrissin Dura, a legume (Leguminosae) plant. Hwanhwanpi extract can be used in folk medicine and oriental medicine to soothe sedatives, diuretics, pain medications, fractures, swelling, swelling, to balance blood, to calm the mind and to remove swelling, tumors, mammary cancer, plasters, tonics, excitement, Used for diuresis. (Reference: Ingredients and Use of Herbs (Ilwol Seok. 1994. Encyclopedia of Science Encyclopedia), New Medicine Botany (Hakchangsa, 1991), Dictionary Agreement (Korean Dictionary Researcher), Chinese Dictionary of Translation of Chinese Medicine Dictionary Jeongdam, 1997).

또한 합환피의 성분으로는 알비찐(Albizzin), 알칼로이드(Alkaloid), 탄닌(Tannin), 사포닌(Saponin), 빅찐(Bixin), 퀘세틴(Quercetin),비타민(Vitamin), 아라키닉산(Arachinic acid)등이 있다(참조 : 약초의 성분과 이용(일월서각. 1994. 과학백과사전 출판사편) ).In addition, the components of the compound skin include Albizzin, Alkaloid, Tannin, Saponin, Bixin, Quecetin, Vitamin, Vitamin A, Arachinic acid, etc. (See: Herbal Ingredients and Their Uses (Janwol Seokji, 1994. Encyclopedia of Science Encyclopedia)).

상기 합환피 추출물은 건조된 합환피를 탄소수 1∼3의 무수 또는 함수 알코올, 또는 에틸 아세테이트로 4∼30℃에서 3∼20일간 추출한 다음, 농축하여 제조할 수 있다.The haphwanpi extract can be prepared by extracting dried hwanhwanpi with anhydrous or hydrous alcohol having 1 to 3 carbon atoms, or ethyl acetate at 4 to 30 ° C. for 3 to 20 days, and then concentrating.

또한, 상기 합환피 추출물은 합환피를 물, 탄소수 1∼3의 무수 또는 함수 알코올, 또는 에틸 아세테이트로 50∼100℃에서 3∼24시간 동안 추출한 다음, 농축하여 제조할 수도 있다.In addition, the hwanhwanpi extract may be prepared by extracting hwanhwanpi with water, anhydrous or hydrous alcohol having 1 to 3 carbon atoms, or ethyl acetate for 3 to 24 hours at 50 to 100 ℃, and then concentrated.

한편, 추출공정의 수행 전 또는 후에 디에틸에테르 가용성분을 제거한 다음, 농축함으로써 더욱 정제된 합환피 추출물로 제조할 수 있다.Meanwhile, the diethyl ether soluble component may be removed before or after performing the extraction process, and then concentrated to prepare a more purified Hwanhwanpi extract.

상기 추출공정에 있어서, 합환피를 잘게 세절하여 사용하고, 추출용매는 시료중량에 대하여 1∼15배 부피량으로 가하는 것이 바람직하며, 유효 성분의 증발을 방지하기 위하여 냉각 콘덴서를 장착하여 추출하는 것이 바람직하다.In the extraction process, it is preferable to use finely pulverized blood, and the extraction solvent is added at a volume of 1 to 15 times the weight of the sample, and the extraction is carried out by mounting a cooling condenser to prevent evaporation of the active ingredient. desirable.

상기와 같이 제조된 합환피 추출물은 통상적인 기초 화장료, 예를 들면, 유연화장수(스킨), 영양화장수(밀크로션), 영양크림, 맛사지크림, 엣센스, 팩 등에 첨가되어 항산화 화장료로 제조될 수 있다.Haphwanpi extract prepared as described above may be added to a conventional basic cosmetics, for example, soft cosmetics (skin), nutritious cosmetics (milk lotion), nutrition cream, massage cream, essence, pack, etc. can be prepared as an antioxidant cosmetic .

이하, 본 발명을 하기 실시예 및 실험예을 통하여 더욱 상세히 설명하나 본 발명이 이에 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to the following Examples and Experimental Examples, but the present invention is not limited thereto.

실시예 1.Example 1.

합환피 100g를 잘게 세절하여 70% 에틸알코올 1L에 넣고 실온에서 10일간 침적시켜 추출한 후 300메쉬 여과지로 여과하고 1주일간 방치하여 침전물을 에드벤텍 7번 여과지로 2번 여과하였다. 그리고 감압 농축기를 이용하여 50℃에서 완전히 농축하여 건조 중량 13.93g을 얻었다.Finely pulverized 100g of hwanhwanpi was put in 1L of 70% ethyl alcohol, immersed for 10 days at room temperature and extracted, filtered through 300 mesh filter paper and left for 1 week, and the precipitate was filtered twice with filter paper of Adventech No. 7. And it concentrated completely at 50 degreeC using the vacuum concentrator, and obtained the dry weight 13.93g.

실시예 2.Example 2.

합환피 100g를 잘게 세절하여 30% 에틸알코올 1L에 넣고 실온에서 10일간 침적시켜 추출한 후 300메쉬 여과지로 여과하고 1주일간 방치하여 침전물을 에드벤텍 7번 여과지로 2번 여과하였다. 그리고 감압 농축기를 이용하여 50℃로 완전히 농축하여 건조 중량 14.16g을 얻었다.Finely pulverized 100g of hwanhwanpi was put in 1L of 30% ethyl alcohol, immersed for 10 days at room temperature, extracted, filtered with 300 mesh filter paper, and left for 1 week, and the precipitate was filtered twice with filter sheet of Adventech 7. Then, the resultant was concentrated completely at 50 ° C. using a vacuum concentrator to obtain a dry weight of 14.16 g.

실시예 3.Example 3.

합환피 100g를 잘게 세절하여 70% 에틸알코올 1L에 넣고 냉각 콘덴서가 달린 추출기에서 100℃로 8시간 끓여서 추출한 후 300메쉬 여과지로 여과하고 1주일간 방치하여 침전물을 에드벤텍 7번 여과지로 2번 여과하였다. 그리고 감압 농축기를 이용하여 50℃에서 완전히 농축하여 건조 중량 11.76g를 얻었다.Finely chopped 100g of hwanhwanpi in 1% of 70% ethyl alcohol, boiled at 100 ℃ in an extractor equipped with a cooling condenser for 8 hours, extracted with 300 mesh filter paper and left for 1 week, the precipitate was filtered twice by filter with Adventech No. 7 filter paper. . Then, the resultant was concentrated completely at 50 ° C. using a vacuum concentrator to obtain a dry weight of 11.76 g.

실시예 4.Example 4.

합환피 100g를 잘게 세절하여 30% 에틸알코올 1L에 넣고 냉각 콘덴서가 달린추출기에서 100℃로 8시간 끓여서 추출한 후 300메쉬 여과지로 여과하고 1주일간 방치하여 침전물을 에드벤텍 7번 여과지로 2번 여과하였다. 그리고 감압 농축기를 이용하여 50℃로 완전히 농축하여 건조 중량 6.32g를 얻었다.Finely chopped 100g of hwanhwanpi in 1L of 30% ethyl alcohol and boiled at 100 ℃ in an extractor equipped with a cooling condenser for 8 hours, extracted with 300 mesh filter paper and left for 1 week, the precipitate was filtered twice with filter No. 7 of Edbentech. . And it concentrated completely at 50 degreeC using the vacuum concentrator, and obtained the dry weight 6.32g.

실시예 5.Example 5.

합환피 100g를 잘게 세절하여 70% 에틸알코올 1L에 넣고 냉각 콘덴서가 달린 추출기에서 100℃로 8시간 끓여서 추출한 후 300메쉬 여과지로 여과하고 1주일간 방치하여 침전물을 에드벤텍 7번 여과지로 2번 여과하였다. 이 추출물을 디에틸에테르 1L를 가하여 잘 섞어준 후 두 층으로 완전히 분리시켜 하층인 수층에 다시 1L의 에틸아세테이트를 가하여 잘 섞어준 후 두 층으로 완전히 분리시켜 에틸아세테이트 층을 감압 농축기를 이용하여 50℃로 완전히 농축하여 건조 중량 2.78g를 얻었다.Finely chopped 100g of hwanhwanpi in 1% of 70% ethyl alcohol, boiled at 100 ℃ in an extractor equipped with a cooling condenser for 8 hours, extracted with 300 mesh filter paper and left for 1 week, the precipitate was filtered twice by filter with Adventech No. 7 filter paper. . 1L of diethyl ether was added to the mixture, and the mixture was thoroughly separated. The mixture was separated into two layers. Then, 1L of ethyl acetate was added to the lower aqueous layer, mixed well. The mixture was separated into two layers, and the ethyl acetate layer was separated using a reduced pressure concentrator. Concentration completely to ° C. gave 2.78 g of dry weight.

실험예 1.Experimental Example 1.

합환피 추출물 대하여 자유라디칼(Free Radical) 소거 효과를 측정하였으며, 비교 물질로 비타민 C를 사용하였다.Free Radical scavenging effect was measured on the extract of Hailhwanpi, and vitamin C was used as a comparative substance.

1) 실험방법1) Experiment Method

DPPH(1,1-디페닐-2피크릴-히드라질)방법(참조:Blois.M.S.Nature 181,1190,1958)을 사용하여 실험을 수행하였으며, DPPH는 시그마(SIGMA)사의 것을 사용하였다. 0.2mM DPPH 메탄올 용액 1ml에 여러 농도(0.0006, 0.0012, 0.0024,0.0036, 0.0048, 0.0060% w/v)의 합환피 추출물 또는 비타민 C의 에탄올 또는 메탄올 용액 2ml을 첨가하고 잘 교반한 후 실온에서 10분간 반응을 시킨다. 그리고 517nm에서 흡광도를 측정하였으며, 이때 대조군으로 합환피 추출물 대신 정제수를 사용하였다.Experiments were performed using the DPPH (1,1-diphenyl-2picryl-hydrazyl) method (Blois.M.S. Nature 181,1190,1958), and DPPH was used by SIGMA. To 1 ml of 0.2 mM DPPH methanol solution, 2 ml of ethanol or methanol solution of various concentrations (0.0006, 0.0012, 0.0024,0.0036, 0.0048, 0.0060% w / v) or ethanol or methanol solution of vitamin C were added and stirred well for 10 minutes at room temperature. Let reaction. The absorbance was measured at 517 nm, and purified water was used instead of the Hwanhwan skin extract as a control.

하기 수학식 1을 이용하여 자유라디칼 소거효과를 구하고 그 결과를 아래의 표 1에 기재하였다.The free radical scavenging effect was obtained using Equation 1 below and the results are shown in Table 1 below.

2) 실험결과2) Experiment result

합환피 추출물의 자유라디칼 소거 효과Free radical scavenging effect of Haphwanpi extract 실험물질Experimental substance 최종 실험 농도(%)Final experiment concentration (%) 자유라디칼소거율(%)Free radical scavenging rate (%) SC50 SC 50 실시예 1Example 1 0.006%0.006% 90.53%90.53% 0.0033V0.0033V 실시예 2Example 2 0.006%0.006% 91.26%91.26% 0.0031%0.0031% 실시예 3Example 3 0.006%0.006% 90.45%90.45% 0.0025%0.0025% 실시예 4Example 4 0.006%0.006% 91.49%91.49% 0.0025%0.0025% 실시예 5Example 5 0.006%0.006% 91.46%91.46% 0.0010%0.0010% 비타민 CVitamin c 0.002%0.002% 91.28%91.28% 0.0009%0.0009%

SC50: 자유라디칼을 50% 소거하는 시료의 농도 (50% ScavengingSC 50 : concentration of the sample that eliminates 50% of free radicals (50% scavenging

Concentration)Concentration

표 1에서 확인할 수 있는 바와 같이 실시예 5 합환피 추출물의 자유라디칼 50% 소거 농도(SC50)가 0.001% 이고 비타민 C는 0.0009% 이었다. 그러나 비타민 C가 불안정한 점을 고려하면 합환피 추출물(실시예 5)의 자유라디칼 소거 효과가 더 우수함을 알 수 있다.As can be seen in Table 1, the free radical 50% scavenging concentration (SC 50 ) of Example 5 Hailpi skin extract was 0.001% and vitamin C was 0.0009%. However, considering that the vitamin C is unstable, it can be seen that the free radical scavenging effect of the haphwanpi extract (Example 5) is more excellent.

처방예 1.Prescription Example 1.

합환피 추출물을 함유한 화장료 중 유연화장수(스킨)의 처방 예는 다음과 같으며, 여기서 합환피 추출물은 실시예 1에서 얻은 것을 말한다.Prescription example of supple cosmetics (skin) in the cosmetics containing the haphwanpi extract is as follows, where the hwanhwanpi extract is obtained in Example 1.

성분ingredient 함량(중량%)Content (% by weight) 편축 추출물Schist extract 3.03.0 부틸렌글리콜Butylene glycol 4.04.0 글리세린glycerin 8.08.0 카르복시비닐폴리머Carboxy Vinyl Polymer 0.060.06 디소디움 에틸렌디아민테트라아세틱에시드Disodium ethylenediaminetetraacetic acid 0.010.01 에탄올ethanol 7.07.0 트리에탄올아민Triethanolamine 0.20.2 소르비탄모노스테아레이트Sorbitan monostearate 0.80.8 하이드로지네이티드 캐스터 오일Hydrogenated Castor Oil 0.40.4 페닐트리메티콘Phenyltrimethicone 3.53.5 방부제antiseptic 0.40.4 향료Spices 0.10.1 색소Pigment 0.010.01 정제수Purified water 잔량Remaining amount system 100.0100.0

처방예 2Prescription Example 2

합환피 추출물을 함유한 화장료 중 로션의 처방 예는 다음과 같으며, 여기서 합환피 추출물은 실시예 1에서 얻은 것을 말한다.Prescription example of a lotion in the cosmetic containing the extract of hwanhwanpi is as follows, where hwanhwanpi extract refers to that obtained in Example 1.

성분ingredient 함량(중량%)Content (% by weight) 편축 추출물Schist extract 3.03.0 스테아린산Stearic acid 1.01.0 세틸알코올Cetyl alcohol 1.01.0 글리세릴모노스테아레이트Glyceryl Monostearate 1.01.0 폴리옥시에틸렌소르비탄모노스테아레이트Polyoxyethylene sorbitan monostearate 1.01.0 솔비탄세스퀴올레이트Sorbitan sesquioleate 1.01.0 유동파라핀Liquid paraffin 4.04.0 스쿠알란Squalane 3.03.0 카르릴릭/카프릭트리글리세라이드Carlylic / Capric Triglycerides 4.04.0 카르복시비닐폴리머Carboxy Vinyl Polymer 0.10.1 부틸렌글리콜Butylene glycol 5.05.0 트리에탄올아민Triethanolamine 0.20.2 방부제antiseptic 0.40.4 향료Spices 0.10.1 색소Pigment 0.010.01 정제수Purified water 잔량Remaining amount system 100.0100.0

처방예 3Prescription Example 3

합환피 추출물을 함유한 화장료 중 영양크림의 처방 예는 다음과 같으며, 여기서 합환피 추출물은 실시예 1에서 얻은 것을 말한다.Prescription example of nutrition cream in the cosmetic containing the extract of hwanhwanpi is as follows, where hwanhwanpi extract refers to that obtained in Example 1.

성분ingredient 함량(중량%)Content (% by weight) 편축 추출물Schist extract 5.05.0 스테아린산Stearic acid 2.02.0 세틸알코올Cetyl alcohol 2.02.0 글리세릴모노스테아레이트Glyceryl Monostearate 2.02.0 폴리옥시에틸렌소르비탄모노스테아레이트Polyoxyethylene sorbitan monostearate 0.50.5 솔비탄세스퀴올레이트Sorbitan sesquioleate 0.50.5 글리세릴모노스테아레이트/글리세릴스테아레이트/폴리옥시에틸렌스테아레이트Glyceryl Monostearate / Glyceryl Stearate / Polyoxyethylene Stearate 1.01.0 왁스Wax 1.01.0 유동파라핀Liquid paraffin 4.04.0 스쿠알란Squalane 4.04.0 카르릴릭/카프릭트리글리세라이드Carlylic / Capric Triglycerides 4.04.0 카르복시비닐폴리머Carboxy Vinyl Polymer 0.30.3 부틸렌글리콜Butylene glycol 5.05.0 글리세린glycerin 3.03.0 트리에탄올아민Triethanolamine 0.50.5 방부제antiseptic 0.40.4 향료Spices 0.10.1 색소Pigment 0.010.01 정제수Purified water 잔량Remaining amount system 100.0100.0

본 발명에 따른 합환피 추출물은 기존의 자유 라디칼 소거 물질과는 달리 천연물에서 추출한 성분이기 때문에 피부자극이 적고 자유라디칼 소거 효과가 우수하며 배합시 안정성이 뛰어나 주름 및 피부 노화의 방지에 탁월한 항산화 화장료를 제공할 수 있다.Unlike the existing free radical scavenging substances, Hwanhwan Phi extract according to the present invention is an ingredient extracted from natural products, so it has less skin irritation, excellent free radical scavenging effect, and excellent stability when formulated to provide an excellent antioxidant cosmetic for preventing wrinkles and skin aging. Can provide.

Claims (6)

합환피 추출물을 포함하는 항산화 화장료.Antioxidant cosmetics, including Haphwanpi extract. 제1항에 있어서, 합환피 추출물이 항산화 화장료의 총 건조중량에 대하여 0.0001∼5중량%의 양으로 함유되는 것을 특징으로 하는 항산화 화장료.The antioxidant cosmetic composition according to claim 1, wherein the extract of hwanhwanpi is contained in an amount of 0.0001 to 5% by weight based on the total dry weight of the antioxidant cosmetic. 제1항에 있어서, 합환피 추출물이 합환피를 탄소 수 1∼3의 무수 또는 함수 알코올, 또는 에틸 아세테이트로 4∼30℃에서 3∼20일간 추출한 다음, 농축하여 제조된 것임을 특징으로 하는 항산화 화장료.The anti-oxidant cosmetic according to claim 1, wherein the extract of hwanhwanpi is prepared by extracting hwanhwanpi with anhydrous or hydrous alcohol having 1 to 3 carbon atoms or ethyl acetate at 4-30 ° C for 3 to 20 days, and then concentrating. . 제1항에 있어서, 합환피 추출물이 합환피를 물, 탄소 수 1∼3의 무수 또는 함수 알코올, 또는 에틸 아세테이트로 50∼100℃에서 3∼24시간 동안 추출한 다음, 농축하여 제조된 것임을 특징으로 하는 항산화 화장료.The method of claim 1, wherein the extract of hwanhwanpi is prepared by extracting hwanhwanpi with water, anhydrous or hydrous alcohol having 1 to 3 carbon atoms, or ethyl acetate at 50-100 ° C for 3 to 24 hours, and then concentrating. Antioxidant cosmetics. 제3항 또는 제4항에 있어서, 합환피 추출물이 추출공정의 수행 전 또는 후에 디에틸에테르 가용성분을 제거한 다음, 농축하여 제조된 것임을 특징으로 하는 항산화 화장료.The antioxidant cosmetic composition according to claim 3 or 4, wherein the extract of Hwanhwan Phi is prepared by removing the diethyl ether soluble component before or after performing the extraction process and then concentrating. 제1항에 있어서, 합환피 추출물이 유연 화장수, 영양 화장수, 영양크림, 맛사지 크림, 엣센스 또는 팩 중에서 선택된 제형에 첨가된 것임을 특징으로 하는 항산화 화장료.The antioxidant cosmetic composition according to claim 1, wherein the extract of Hwanhwan Phi is added to the formulation selected from flexible lotion, nutrition lotion, nutrition cream, massage cream, essence or pack.
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KR100443588B1 (en) * 2002-01-25 2004-08-09 나드리화장품주식회사 Cosmetic composition containing paeonia suffruticosa andrews extract and albizzia julibrissin dura extract having anti-ageing effect
FR2871691A1 (en) * 2004-06-22 2005-12-23 Biolog Vegetale Yves Rocher Sa Cosmetic composition, useful to e.g. prevent/treat skin inflammations and cellulite, comprises an extract of leaves of Albizia adanthifolia
KR100733764B1 (en) * 2006-04-20 2007-07-02 주식회사 베터앤베터 Composition comprising the cortex extract of albizzia julibrissin or kuraridinol isolated therefrom for preventing or treating hyperlipidemia
WO2012108748A2 (en) * 2011-02-11 2012-08-16 주식회사 한국전통의학연구소 Composition and cosmetic composition for treating brain cancer comprising albizzia julibrissin extract
WO2013046137A2 (en) 2011-09-27 2013-04-04 Sederma New cosmetic use of an albizia julibrissin extract and corresponding topical composition
FR3007289A1 (en) * 2013-06-24 2014-12-26 Caster COSMETIC COMPOSITIONS COMPRISING PLANT EXTRACTS TO COMBAT SKIN AGING
KR20180112192A (en) 2017-03-31 2018-10-12 제주대학교 산학협력단 Composition for skin-lightening or antioxidant containing extract of Jeju camellia mistletoe
CN110638821A (en) * 2019-09-30 2020-01-03 江南大学 Albizzia julibrissin new lignan compound with antioxidant activity and application thereof
US10682381B2 (en) 2009-04-27 2020-06-16 Mary Kay Inc. Botanical formulations
US10780041B2 (en) 2011-12-19 2020-09-22 Mary Kay Inc. Combination of plant extracts to improve skin tone
CN112353722A (en) * 2020-11-19 2021-02-12 广州上悦生物科技有限公司 Moisturizing anti-aging repairing composition and preparation method and application thereof

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JPH04342519A (en) * 1990-10-11 1992-11-30 Kose Corp Skin cosmetic
JP2000143488A (en) * 1998-11-16 2000-05-23 Ichimaru Pharcos Co Ltd Cosmetic composition containing humectant plant extract

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100443588B1 (en) * 2002-01-25 2004-08-09 나드리화장품주식회사 Cosmetic composition containing paeonia suffruticosa andrews extract and albizzia julibrissin dura extract having anti-ageing effect
FR2871691A1 (en) * 2004-06-22 2005-12-23 Biolog Vegetale Yves Rocher Sa Cosmetic composition, useful to e.g. prevent/treat skin inflammations and cellulite, comprises an extract of leaves of Albizia adanthifolia
KR100733764B1 (en) * 2006-04-20 2007-07-02 주식회사 베터앤베터 Composition comprising the cortex extract of albizzia julibrissin or kuraridinol isolated therefrom for preventing or treating hyperlipidemia
US11638735B2 (en) 2009-04-27 2023-05-02 Mary Kay Inc. Botanical formulations
US10953058B2 (en) 2009-04-27 2021-03-23 Mary Kay Inc. Botanical formulations
US10682381B2 (en) 2009-04-27 2020-06-16 Mary Kay Inc. Botanical formulations
WO2012108748A2 (en) * 2011-02-11 2012-08-16 주식회사 한국전통의학연구소 Composition and cosmetic composition for treating brain cancer comprising albizzia julibrissin extract
WO2012108748A3 (en) * 2011-02-11 2012-12-27 주식회사 한국전통의학연구소 Composition and cosmetic composition for treating brain cancer comprising albizzia julibrissin extract
US9737476B2 (en) 2011-09-27 2017-08-22 Sederma Cosmetic use of an albizia julibrissin extract and corresponding topical composition
WO2013046137A2 (en) 2011-09-27 2013-04-04 Sederma New cosmetic use of an albizia julibrissin extract and corresponding topical composition
US10780041B2 (en) 2011-12-19 2020-09-22 Mary Kay Inc. Combination of plant extracts to improve skin tone
US11865202B2 (en) 2011-12-19 2024-01-09 Mary Kay Inc. Combination of plant extracts to improve skin tone
EP2818158A1 (en) 2013-06-24 2014-12-31 Caster Cosmetic compositions including plant extracts for controlling skin ageing
FR3007289A1 (en) * 2013-06-24 2014-12-26 Caster COSMETIC COMPOSITIONS COMPRISING PLANT EXTRACTS TO COMBAT SKIN AGING
KR20180112192A (en) 2017-03-31 2018-10-12 제주대학교 산학협력단 Composition for skin-lightening or antioxidant containing extract of Jeju camellia mistletoe
CN110638821A (en) * 2019-09-30 2020-01-03 江南大学 Albizzia julibrissin new lignan compound with antioxidant activity and application thereof
CN112353722A (en) * 2020-11-19 2021-02-12 广州上悦生物科技有限公司 Moisturizing anti-aging repairing composition and preparation method and application thereof

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