KR20110085371A - Cosmetic composition for improving the scalp state containing natural plant extracts - Google Patents
Cosmetic composition for improving the scalp state containing natural plant extracts Download PDFInfo
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Abstract
본 발명은 천연식물 추출물을 함유하여 두피 상태를 개선시키는 화장료 조성물에 관한 것으로서, 보다 상세하게는 수련추출물, 생강추출물 및 대나무추출물을 포함하는 천연식물복합성분을 함유하여 두피 염증 반응을 억제시키고, 활성산소의 생성 및 작용을 억제하여 두피에 대한 정화 및 진정 효과가 우수한 화장료 조성물에 관한 것이다.The present invention relates to a cosmetic composition for improving the scalp state by containing a natural plant extract, more specifically, to inhibit the scalp inflammatory response by containing a natural plant complex components, including water extract, ginger extract and bamboo extract, It relates to a cosmetic composition excellent in the purification and soothing effect on the scalp by inhibiting the production and action of oxygen.
Description
본 발명은 천연식물 추출물을 함유하여 두피 상태를 개선시키는 화장료 조성물에 관한 것으로서, 보다 상세하게는 수련추출물, 생강추출물 및 대나무추출물을 포함하는 천연식물복합성분을 함유하여 두피 염증 반응을 억제시키고, 활성산소의 생성 및 작용을 억제하여 두피에 대한 정화 및 진정 효과가 우수한 화장료 조성물에 관한 것이다.
The present invention relates to a cosmetic composition for improving the scalp state by containing a natural plant extract, more specifically, to inhibit the scalp inflammatory response by containing a natural plant complex components, including water extract, ginger extract and bamboo extract, It relates to a cosmetic composition excellent in the purification and soothing effect on the scalp by inhibiting the production and action of oxygen.
두피는 표피(epidermis), 진피(dermis), 피하조직(subcutaneous tissue)으로 구성되어 있으며, 가장 바깥조직이 표피이다. 표피는 신체의 민감한 조직을 손상받지 않도록 보호해주는 기능을 한다. 그러나 외부의 온도, 습도의 변화, 공해물질 등의 여러 가지 물리적, 화학적 외부의 자극과 스트레스, 영향 결핍 등으로 인해 두피의 기능을 상실할 수 있으며, 나아가서는 탈모에도 영향을 미칠 수 있다. The scalp is composed of epidermis, dermis and subcutaneous tissue, with the outermost tissue being the epidermis. The epidermis functions to protect the sensitive tissues of the body from damage. However, various physical and chemical external stimuli such as external temperature, humidity, pollutants, stress, and lack of influence can cause the scalp to lose function, and can also affect hair loss.
한편 비듬이란 인체의 활발한 신진대사에 의해 생긴 두피의 죽거나 벗겨진 세포들이 두피 피지선의 분비물과 함께 말라붙어서 생긴 각질형태의 덩어리를 말한다. 비듬은 점차 정상 피부와 뚜렷한 경계를 가지며, 붉게 되어 두피에 인설이 증가하여 통상 가려움과 염증을 수반하는 지루피부염으로까지 진행된다.Dandruff, on the other hand, is a stratum corneum-like mass formed by the dead or peeled cells of the scalp caused by the active metabolism of the human body with the secretion of the scalp sebaceous glands. Dandruff gradually has a clear border with normal skin, becomes red, and increases the scale of the scalp, which usually leads to seborrheic dermatitis with itching and inflammation.
이러한 비듬의 발생과 관련하여 두피의 비듬균인 말라세지아균(Malassezia globosa)이 관련이 있으며 이 비듬균을 제거하기 위하여 많은 두피 케어 제품에서 효능성분으로 아연피리치온, 클림바졸, 이미다졸 등의 화학물질을 주로 사용하였다. Malassezia globosa, a dandruff bacterium of the scalp, is related to the occurrence of dandruff. In order to remove the dandruff, many chemicals such as zinc pyrithione, klimbazole, and imidazole are effective ingredients in many scalp care products. The material was mainly used.
그러나 상기 아연피리치온 등의 화학물질은 비듬균에 대한 항균력은 우수하나, 비듬증과 함께 수반되는 가려움증의 완화에 대해서는 효과가 약한 편이며, 피부 부작용 등에 안전하지 못하다는 점과 화학물질이라는 점에서 소비자들에게 부정적인 생각을 갖게 할 수 있다.However, the chemicals such as zinc pyrithione have excellent antibacterial activity against dandruff, but are less effective in relieving itching accompanying dandruff, and are not safe for skin side effects and chemicals. It can make consumers think negatively.
따라서, 두피의 상태를 개선시킬 수 있으면서 안정적인 천연식물성분을 함유한 조성물이 요구되고 있다.
Therefore, there is a need for a composition containing a stable natural plant component while improving the condition of the scalp.
이에 본 출원인들은 수련추출물, 생강추출물 및 대나무추출물을 포함하는 천연식물복합성분을 사용할 경우 이들 성분을 단독으로 사용할 때보다 항염 효능 및 항산화 효능이 우수하여 두피 정화 및 진정 효과가 뛰어남을 발견하고 본 발명을 완성하게 되었다.In this regard, the present applicants found that when using natural plant complex components including water lily extract, ginger extract, and bamboo extract, the anti-inflammatory and anti-oxidant effects were superior to those of using these components alone, so that the scalp purification and soothing effects were excellent. To complete.
따라서 본 발명은 두피 상태를 개선시키는 효과가 우수한 화장료 조성물을 제공하는 것을 목적으로 한다.
Therefore, an object of the present invention is to provide a cosmetic composition excellent in improving the scalp condition.
상기한 목적을 달성하기 위하여, 본 발명은 수련추출물, 생강추출물 및 대나무추출물을 포함하는 천연식물복합성분을 함유하는 두피 상태 개선용 화장료 조성물을 제공한다.
In order to achieve the above object, the present invention provides a cosmetic composition for improving the scalp state containing a natural plant complex components, including water lily extract, ginger extract and bamboo extract.
본 발명에 의한 화장료 조성물은 모발과 두피에 축적된 독소를 효과적으로 배출하여 두피를 정화하고, 비듬균의 증식과 성장을 억제하여 두피염증반응을 예방할 수 있으며, 또한 활성산소의 생성 및 작용을 억제하는 항산화 효능이 뛰어나 두피를 강화시키는 효과를 제공할 수 있다.
The cosmetic composition according to the present invention effectively cleans the scalp by releasing toxins accumulated in the hair and scalp, and prevents scalp inflammation by inhibiting the growth and growth of dandruff, and also inhibits the production and action of free radicals. Excellent efficacy can provide an effect to strengthen the scalp.
도 1은 천연식물복합성분의 비듬균에 의한 두피염증반응 억제 효과를 IL-8의 발현 정도로 나타낸 것이다.
도 2는 천연식물복합성분의 지방산에 의한 두피염증반응 억제 효과를 IL-8의 발현 정도로 나타낸 것이다.
도 3은 천연식물복합성분의 항산화 효능을 DPPH 분석법으로 측정한 결과를 나타낸 것이다.
도 4는 천연식물복합성분의 항산화 효능을 DCF-DA 분석법으로 측정한 지방산에 의해 생성되는 ROS에 대한 천연식물복합성분의 항산화 효과를 나타낸 것이다.
도 5는 천연식물복합성분의 항산화 효능을 DCF-DA 분석법으로 측정한 지방산 및 자외선에 의해 생성되는 ROS에 대한 천연식물복합성분의 항산화 효과를 나타낸 것이다.Figure 1 shows the inhibitory effect of the scalp inflammatory response by the dandruff bacteria of the natural plant complex components the degree of expression of IL-8.
Figure 2 shows the inhibitory effect of the scalp inflammatory reaction by the fatty acid of the natural plant complex components the degree of expression of IL-8.
Figure 3 shows the results of measuring the antioxidant efficacy of the natural plant complex components by DPPH assay.
Figure 4 shows the antioxidant effect of the natural plant compound against ROS produced by fatty acids measured the antioxidant efficacy of the natural plant compound by the DCF-DA assay.
Figure 5 shows the antioxidant effect of the natural plant complexes for ROS produced by fatty acids and ultraviolet rays measured the antioxidant efficacy of the natural plant complexes by DCF-DA analysis.
본 발명의 화장료 조성물은 수련추출물, 생강추출물 및 대나무추출물을 포함하는 천연식물복합성분을 유효성분으로 함유한다.The cosmetic composition of the present invention contains a natural plant complex component including water lily extract, ginger extract and bamboo extract as an active ingredient.
본 발명에서 사용되는 수련은 여러해살이 수중식물로서 굵고 짧은 땅속줄기에서 많은 잎자루가 자라서 물 위에서 잎을 편다. 잎몸은 질이 두꺼운 달걀 모양이고 밑부분은 화살밑처럼 깊게 갈라진다. 앞면은 녹색이고 윤기가 있으며, 뒷면은 자줏빛이고 질이 두껍다. 수련속의 식물은 꽃이 아름다우므로 연못이나 온실에서 관상용으로 재배된다. 또한 종자와 뿌리줄기는 녹말을 많이 함유하고 있어 세계 각지에서 식용되고 있다. 또한 뿌리줄기는 누파리딘을 함유하고 있어 위장약으로 사용된다.The water lily used in the present invention is a perennial aquatic plant, and many petioles grow in the thick and short undergrowth and fold the leaves on water. The leaf body is thick, egg-shaped, and the bottom part is deeply divided like an arrow. The front is green and glossy, and the back is purplish and thick. Water lily plants are beautiful because of their beautiful flowers, which are grown for ornamental purposes in ponds and greenhouses. Seeds and rhizomes also contain a lot of starch, which is edible all over the world. Root stems also contain nufariin, which is used as a gastrointestinal drug.
본 발명에서 사용되는 생강은 새앙, 새양이라고도 한다. 동남아시아가 원산지이고 채소로 재배한다. 뿌리줄기는 옆으로 자라고 다육질이며 덩어리 모양이고 황색이며 매운 맛과 향긋한 냄새가 있다. 뿌리줄기는 말려 갈아서 빵·과자·카레·소스·피클 등에 향신료로 사용하고, 껍질을 벗기고 끓인 후 시럽에 넣어 절이기도 하며 생강차와 생강주 등을 만들기도 한다. 한방에서는 뿌리줄기 말린 것을 건강(乾薑)이라는 약재로 쓰는데, 소화불량·구토·설사에 효과가 있고, 혈액 순환을 촉진하며, 항염증과 진통 효과가 있다. Ginger used in the present invention is also called a saeyang, a new sheep. It is native to Southeast Asia and is grown as a vegetable. Root stock grow sideways, fleshy, lumpy, yellow, with a spicy taste and aromatic odor. Root stems are dried and used as spices for breads, cookies, curry, sauces, and pickles. Peel and boil, add to syrup, and make ginger tea and ginger. In oriental medicine, dried root stem is used as a health medicine, which is effective for indigestion, vomiting and diarrhea, promotes blood circulation, and has anti-inflammatory and analgesic effects.
본 발명에서 사용되는 대나무는 외떡잎식물 벼목 화본과(벼과, Poaceae) 대나무아과(Bambusoideae)에 속하는 여러해살이 식물의 총칭으로 키가 큰 왕대속만을 대나무라고 일컫는 경우도 있다. 대나무는 건축재·가구재·낚싯대·식물 지지대를 비롯하여 바구니 등 죽세공품에 이르기까지 그 용도가 매우 다양하며 관상용으로 심기도 한다. 어린 순은 나물로 요리하여 먹는다.Bamboo used in the present invention is a generic term for perennial plants belonging to the monocotyledonous rice plant (Paceae, Poaceae) and the bamboo subfamily (Bambusoideae). Bamboo has a wide variety of uses, ranging from building materials, furniture, fishing rods, plant supports, to basketwork such as baskets, and is also planted for ornamental purposes. Young sprouts are cooked and eaten with herbs.
본 발명에서 상기 수련, 생강 및 대나무의 추출물은 각각의 건조된 원료를 수세 후 이온수에 투입하여 70~75℃에서 열수로 추출한다. 상온으로 냉각 후 탈취 및 여과하여 각각의 추출물을 얻는다. 상세한 제조방법은 하기의 참고예에 명기한다.In the present invention, the extracts of water lilies, ginger and bamboo are added to ionized water after washing each dried raw material and extracted with hot water at 70 ~ 75 ℃. After cooling to room temperature, each extract is obtained by deodorization and filtration. The detailed manufacturing method is specified in the following reference example.
본 발명에서 사용되는 천연식물복합성분에 포함되는 수련추출물, 생강추출물 및 대나무추출물은 1~10:1~10:1~10의 중량비율로 혼합되며, 바람직하게는 각 식물추출물들의 혼합으로 인한 시너지 효과를 얻기 위해 1:1:1의 비율로 혼합하는 것이 좋다. 또한 상기 천연식물복합성분은 수련추출물, 생강추출물 및 대나무추출물의 혼합물을 천연식물복합성분의 중량에 대하여 50.0~80.0중량%의 양으로 함유한다. 또한 천연식물복합성분은 원료의 보존성을 높이기 위해 제균목적으로 광범위하게 사용되는 방부제를 더 포함할 수 있으며, 바람직하게는 부틸렌글리콜과 페녹시에탄올을 사용할 수 있다.Water lily extract, ginger extract and bamboo extract included in the natural plant complexes used in the present invention are mixed in a weight ratio of 1 to 10: 1 to 10: 1 to 10, preferably synergistic due to the mixing of each plant extract It is recommended to mix at 1: 1: 1 to obtain the effect. In addition, the natural plant complex component contains a mixture of water lily extract, ginger extract and bamboo extract in an amount of 50.0 to 80.0% by weight based on the weight of the natural plant complex component. In addition, the natural plant complex component may further include a preservative widely used for bacteriostatic purposes in order to increase the preservation of the raw material, preferably butylene glycol and phenoxyethanol may be used.
또한, 본 발명의 조성물은 상기 천연식물복합성분을 조성물 총 중량에 대하여 0.01~10중량%의 양으로 함유한다. 이는 0.01중량% 미만에서는 그 효과가 매우 미약하고, 10중량% 초과에서는 제형의 안정도에 문제가 있기 때문이다.In addition, the composition of the present invention contains the natural plant complex component in an amount of 0.01 to 10% by weight based on the total weight of the composition. This is because the effect is very weak at less than 0.01% by weight, there is a problem in the stability of the formulation above 10% by weight.
본 발명의 조성물은 제형화하는데 있어서 특별히 한정되는 바가 없으나, 헤어토닉, 모발 영양화장수, 스칼프트리트먼트, 헤어트리트먼즈, 헤어샴푸, 헤어린스, 헤어로션 또는 두피 모발 겸용 트리트먼트 등으로 제형화될 수 있다.The composition of the present invention is not particularly limited in formulating, but may be formulated as a hair tonic, hair nourishing longevity, scalp treatment, hair treatments, hair shampoo, hair rinse, hair lotion, or scalp hair treatment. have.
또한, 각각의 제형에 있어서 상기한 필수성분 이외에 다른 성분들은 기타 외용제의 종류 또는 사용목적 등에 따라 당업자가 어려움 없이 적합하게 선정하여 배합할 수 있다. In addition, in each formulation, other ingredients in addition to the above-mentioned essential ingredients may be appropriately selected and blended by those skilled in the art without difficulty according to the kind or purpose of use of other external preparations.
본 발명에 의한 조성물은 모발과 두피에 축적된 독소를 효과적으로 배출하여 두피를 정화하고, 비듬균의 증식과 성장을 억제하여 두피염증반응을 예방할 수 있으며, 또한 활성산소의 생성 및 작용을 억제하는 항산화 효능이 뛰어나 두피를 진정시키고 강화시키며 본연의 방어력을 강화시키는 효과를 제공할 수 있다.
The composition according to the present invention effectively cleans the scalp by effectively discharging toxins accumulated in hair and scalp, and inhibits the growth and growth of dandruff bacteria to prevent scalp inflammatory reactions, and also inhibits the production and action of free radicals. This excellent soothing and strengthening of the scalp can provide the effect of strengthening the natural defenses.
이하, 실시예 및 시험예를 들어 본 발명의 보다 구체적으로 설명하지만, 본 발명이 이들 예로만 한정되는 것은 아니다.
Hereinafter, although an Example and a test example are given and demonstrated more concretely of this invention, this invention is not limited only to these examples.
[참고예 1] 수련추출물의 제조Reference Example 1 Preparation of Water Lily Extract
수련 1kg을 수세 후 25L의 이온수에 투입하여 70~75℃에서 3시간 동안 열수로 추출하였다. 상온으로 냉각 후 규조토를 이용하여 여과한 다음, 탈취를 위하여 제올라이트 0.5kg으로 처리하고 여과하여 추출액 21L를 획득하였다.
After washing with water 1kg was added to 25L of ionized water and extracted with hot water for 3 hours at 70 ~ 75 ℃. After cooling to room temperature, the mixture was filtered using diatomaceous earth, treated with 0.5 kg of zeolite for deodorization, and filtered to obtain 21 L of an extract.
[참고예 2] 생강추출물의 제조Reference Example 2 Preparation of Ginger Extract
건생강 2kg을 수세 후 25L의 이온수에 투입하여 70~75℃에서 3시간 동안 열수로 추출하였다. 상온으로 냉각 후 규조토를 이용하여 여과한 다음, 탈취를 위하여 제올라이트 0.5kg으로 처리하고 여과하여 추출액 21L를 획득하였다.
2 kg of dried ginger was washed with water in 25 L of ionized water and extracted with hot water at 70-75 ° C. for 3 hours. After cooling to room temperature, the mixture was filtered using diatomaceous earth, treated with 0.5 kg of zeolite for deodorization, and filtered to obtain 21 L of an extract.
[참고예 3] 대나무추출물의 제조Reference Example 3 Preparation of Bamboo Extract
건조된 대나무 5kg을 20cm 간격으로 자른 다음 수세 후 25L의 이온수에 투입하여 70~75℃에서 3시간 동안 열수로 추출하였다. 상온으로 냉각 후 규조토를 이용하여 여과하여 추출액 20L를 획득하였다.
5 kg of dried bamboo was cut at intervals of 20 cm, washed with water, and poured into 25 L of ionized water and extracted with hot water at 70 to 75 ° C. for 3 hours. After cooling to room temperature, 20L of extract was obtained by filtration using diatomaceous earth.
[참고예 4] 천연식물복합성분의 제조Reference Example 4 Preparation of Natural Plant Complex Ingredients
상기 참고예 1~3에서 획득한 추출액을 대나무 추출액 23.2중량%, 건생강 추출액 23.2중량%, 수련 추출액 23.1중량%를 비율에 맞추어 혼합한 후 방부액(1,3-부틸렌글라이콜 30중량%, 페녹시에탄올 0.5중량%)을 혼합하였다. 이를 1.0㎛ 필터를 이용하여 선여과(Pre-filteration) 처리하고, 0.45㎛ 필터를 이용하여 미세여과(Micro-filteration) 후 포장을 하였다.
Preservatives (1,3-
[시험예 1] 천연식물복합성분에 의한 항염효능Test Example 1 Anti-inflammatory Effect by Natural Plant Compounds
두피의 비듬균(Malassezia globosa)은 자신의 지방분해효소(Lipase)를 이용해서 두피 표면의 지방산을 분해한다. 이렇게 분해된 지방산들 중에서 불포화지방산은 두피 내부로 침투하여 염증반응 등의 병리적인 현상을 일으키고, 포화지방산들은 비듬균이 증식과 성장을 위한 에너지원으로 사용한다. 또한 두피의 비듬균과 비듬균이 생성하는 지방산은 두피 각질형성세포에서 IL-8의 발현을 증가시켜 두피 염증반응을 유발할 수 있다. 따라서 본 시험예에서는 본 발명의 천연식물복합성분이 비듬균과 지방산에 의한 피부 염증반응을 억제하는 효과를 측정하고자 하였다.Malassezia globosa decomposes fatty acids on the surface of the scalp using its Lipase. Among these decomposed fatty acids, unsaturated fatty acids penetrate into the scalp to cause pathological phenomena such as inflammatory reactions, and saturated fatty acids are used as energy sources for growth and growth of dandruff. In addition, fatty acids produced by dandruff and dandruff in the scalp may increase the expression of IL-8 in the scalp keratinocytes and induce scalp inflammation. Therefore, in this test example, the natural plant compound of the present invention was to determine the effect of inhibiting the skin inflammatory response caused by dandruff and fatty acids.
비듬균(Malassezia globosa)과 피부의 대표적인 지방산(리놀레산(Linoleic acid))을 인간각질형성세포에 처리하고 염증매개인자 분석을 통하여 염증반응을 관찰하고 항염효능을 확인하였다. 구체적인 실험방법은 하기와 같다.Malassezia globosa and typical fatty acids (linoleic acid) of the skin were treated to human keratinocytes and inflammatory responses were analyzed and anti-inflammatory effects were confirmed through analysis of inflammatory mediators. The specific experimental method is as follows.
1) 세포 배양 1) Cell Culture
인간의 불멸화된 각질형성세포인 HaCaT 세포를 10% FBS(Fetal Bovine Serum)와 100unit/ml 페니실린-스트렙토마이신이 들어 있는 DMEM(Dulbecco Modified Eagle's Medium)에 넣고 37℃, 5% CO2에서 배양하였다.HaCaT cells, human immortalized keratinocytes, were placed in DMEM (Dulbecco Modified Eagle's Medium) containing 10% FBS (Fetal Bovine Serum) and 100unit / ml penicillin-streptomycin and cultured at 37 ° C. and 5% CO 2 .
2) 비듬균 배양 및 비듬균 시료 준비 2) Dandruff culture and dandruff sample preparation
비듬균(Malassezia globosa)는 ATCC에서 구입(ATCC strain #96807)하였으며, Leeming & Notman 브로스(broth)에 접종하여 35℃에서 3일간 증식 후 실험에 사용하였다. 증식한 비듬균은 원심분리해서 비듬균과 배양배지로 분리하였다. 배양배지는 추가적인 정제 과정을 거치지 않고 냉동보관 하였다가 필요시 녹여서 사용하였으며, 비듬균은 PBS(Phosphate Buffered Saline)로 3회 세척한 후에 4℃에서 냉장보관 하였다가 시험에 사용하였다. Dandruff (Malassezia globosa) was purchased from ATCC (ATCC strain # 96807), inoculated in Leeming & Notman broth (broth) and used in the experiment after proliferation for 3 days at 35 ℃. The grown dandruff was centrifuged and separated into dandruff and culture medium. The culture medium was stored frozen without further purification, and then dissolved and used when necessary. Dandruff was washed three times with PBS (Phosphate Buffered Saline), and then refrigerated at 4 ° C and used for the test.
3) IL-8 분석3) IL-8 analysis
HaCaT 세포를 1x105 농도로 24웰 플레이트에 파종하였다. 파종 다음날 FBS 농도를 2%로 낮추고 페놀 레드(Phenol red)를 제거한 IL-8 분석용 배지로 교환하고 비듬균과 지방산류를 처리하였다. 물질 처리 24시간 후에 세포의 배양 배지를 수거하고 남아 있는 세포는 PBS로 두 번 세척 후 WST-1(Roche) 시약을 이용해서 세포 독성을 평가하였다. 수거한 배지는 원심분리로 잔여물을 제거하고 IL-8 ELISA 세트(BD Bioscience)를 이용해서 배지내의 IL-8 농도를 측정하였다. WST-1와 IL-8 ELISA는 제조사가 제공한 프로토콜을 따랐다.HaCaT cells were seeded in 24-well plates at 1 × 10 5 concentrations. The day after seeding, the FBS concentration was lowered to 2%, exchanged with IL-8 assay medium without phenol red, and treated with dandruff and fatty acids. After 24 hours of material treatment, the culture medium of the cells was collected, and the remaining cells were washed twice with PBS and then evaluated for cytotoxicity using the WST-1 (Roche) reagent. The collected medium was centrifuged to remove the residue and the IL-8 concentration in the medium was measured using an IL-8 ELISA set (BD Bioscience). WST-1 and IL-8 ELISA followed the protocol provided by the manufacturer.
4) 통계처리 4) Statistical Processing
배지에서 측정한 IL-8의 농도를 WST-1 값으로 나눠서 세포 독성에 의한 값 차이를 보정하였다. 이 보정값을 미니탭(Minitab 14 Korean) 통계 프로그램을 이용해서 각 군간의 유의성을 평가하였다. The concentration of IL-8 measured in the medium was divided by the value of WST-1 to correct for the difference in values due to cytotoxicity. The significance of each group was evaluated by using the Minitab statistical program.
측정결과는 도 1 및 도 2에 나타내었다.The measurement results are shown in FIGS. 1 and 2.
도 1 및 2를 보면, 생강추출물을 단독으로 처리한 경우에는 비듬균 및 지방산에 의한 두피 염증반응의 억제 효능이 거의 없음을 알 수 있다. 그러나 수련추출물, 생강추출물 및 대나무추출물을 포함한 천연식물복합성분은 비듬균과 지방산에 의한 IL-8의 증가를 농도 의존적으로 억제할 수 있으며, 특히 천연식물복합성분을 10ppm의 농도로 처리한 경우, 비듬균에 의한 두피 염증반응을 63% 정도, 지방산에 의한 두피염증반응을 65% 정도 억제할 수 있음을 확인할 수 있다.1 and 2, when the ginger extract is treated alone, it can be seen that the inhibitory effect of the scalp inflammatory reaction by dandruff and fatty acids. However, natural plant complexes, including water lily extract, ginger extract and bamboo extract, can suppress the increase of IL-8 by dandruff and fatty acids in a concentration-dependent manner, especially when the natural plant complex is treated at a concentration of 10 ppm It can be seen that the scalp inflammatory response by about 63%, it can suppress the scalp inflammation response by fatty acids about 65%.
이를 통해, 비듬균은 두피 각질형성세포에서 염증매개인자 IL-8의 발현을 증가시켜 두피염증반응을 유도할 수 있으나, 수련추출물, 생강추출물 및 대나무추출물로 구성된 천연식물복합성분은 이런 비듬균에 의한 두피 염증반응을 억제하여 항염효능을 제공할 수 있음을 알 수 있다.
Through this, dandruff bacteria can induce scalp inflammation by increasing the expression of IL-8 mediators in scalp keratinocytes, but the natural plant complex consisting of water extract, ginger extract and bamboo extract is the scalp It can be seen that it can provide an anti-inflammatory effect by inhibiting the inflammatory response.
[시험예 2] 천연식물복합성분에 의한 항산화 효능Test Example 2 Antioxidant Effect by Natural Plant Compounds
ROS(활성산소, Reactive oxygen stress)는 산소 원자를 포함한 자유 라디칼(free radical)을 지칭하는 것으로서, 평상시에는 대사과정 중 생성되는 부산물이나, 자외선과 같은 다양한 외부자극에 의해 세포가 지속적으로 영향을 받으면, 세포 내 ROS 생성 양이 급속하게 증가하게 된다. 이렇게 증가한 ROS는 세포의 DNA, RNA, 단백질 등에 영향을 주어 세포 괴사 혹은 염증 반응 등 세포에 손상을 입히는 다양한 현상들을 일으킨다. 따라서 본 시험예에서는 본 발명의 천연식물복합성분에 대하여 지방산에 의해 생성되는 ROS의 생성 및 작용을 막는 항산화 효과를 측정하고자 하였으며, DPPH 분석법과 DCF-DA 분석법을 이용하였다.
ROS (reactive oxygen stress) refers to free radicals containing oxygen atoms. When a cell is continuously affected by various external stimuli such as by-products generated during metabolism or ultraviolet rays, As a result, the amount of ROS produced in cells increases rapidly. This increased ROS affects the cell's DNA, RNA, and proteins, causing various phenomena that damage the cell, such as cell necrosis or inflammatory responses. Therefore, in this test example, the antioxidant effect to prevent the production and action of ROS produced by fatty acids to the natural plant complex of the present invention was measured, DPPH analysis and DCF-DA analysis was used.
1. DPPH 분석법1. DPPH Method
DPPH는 붉은색을 띄는 안정한 자유 라디칼인데, 이때 항산화 효능 물질에 의해 자유 라디칼의 수가 감소하면 점차 노란색으로 변하게 되므로, 이를 통해 세포 내 이미 생성된 ROS에 대한 물질의 항산화 효능을 판별할 수 있다.DPPH is a stable free radical with a reddish red color, and when the number of free radicals decreases due to antioxidant potency, it gradually turns yellow, thereby determining the antioxidant potency of the substance against ROS generated in the cell.
1) DPPH(2,2-Diphenyl-1-picrylhydrazyl) 준비1) Preparation of DPPH (2,2-Diphenyl-1-picrylhydrazyl)
실험을 시작하기 전에 에탄올에 녹여 100μM로 만들었다.Before starting the experiment, it was dissolved in ethanol to 100 μM.
2) 처리 물질 준비2) preparation of treated materials
DPPH 용액과 반응시킬 물질을 최종 처리 농도 x20로 에탄올에 녹였다.The material to react with the DPPH solution was dissolved in ethanol at the final treatment concentration x20.
3) 물질처리3) Material treatment
처리할 물질을 농도별로 10㎕씩 96-웰 플레이트에 넣었다. 이때 물질 처리 농도 구간마다 같은 농도의 처리 횟수를 3회로 하였다. 대조군에는 에탄올을 10 ㎕ 넣었다.Substances to be treated were placed in 96-well plates at 10 μl per concentration. At this time, the number of treatments having the same concentration was repeated three times for each substance treatment concentration section. 10 μl of ethanol was added to the control group.
4) DPPH 처리 및 반응4) DPPH Treatment and Reaction
100μM DPPH를 190㎕씩 멀티채널 피펫을 이용하여 넣었다. 그 후 37℃ 인큐베이터에서 30분간 보관하였다.100 μM DPPH was added in 190 μl each using a multichannel pipette. Then stored for 30 minutes in a 37 ℃ incubator.
5) 흡광도 측정 및 통계 처리5) absorbance measurement and statistical processing
Spectra Max 190을 이용하여 517nm에서의 흡광도를 측정하였다. 대조군을 기준으로 물질 처리군의 변화율을 계산하였다. 각 군간의 유의성은 미니탭(Minitab 14 Korean) 통계 프로그램을 이용하여 평가하였다. Absorbance at 517 nm was measured using Spectra Max 190. The rate of change of the material treatment group was calculated based on the control group. The significance of each group was assessed using the Minitab statistical program.
결과는 도 3에 나타내었다.The results are shown in FIG.
도 3을 보면 생강추출물 50μM 단독처리 시험군에서도 유의적인 자유 라디칼 소거능이 관찰되지만, 사용한 천연식물복합성분 보다 고농도이며 효능이 많이 떨어짐을 볼 수 있다. 반면, 수련추출물, 생강추출물 및 대나무추출물로 구성된 천연식물복합성분은 10μM의 농도로 처리시, 대조군 대비 60% 정도의 수준으로 자유 라디칼의 양이 감소하게 되며, 또한 95% 신뢰수준으로 검정 시, 10, 5μM 농도 모두에서 항산화능이 관찰되고, 이를 통해 본 발명의 천연식물복합성분은 농도의존적 항산화능을 보임을 알 수 있다.
In Figure 3, the ginger extract 50μM single treatment test group, but significant free radical scavenging ability is observed, it can be seen that the concentration is higher than the natural plant compound used, and the efficacy is much lower. On the other hand, natural plant complexes consisting of water lily extract, ginger extract and bamboo extract reduced the amount of free radicals to about 60% of the control group when treated at a concentration of 10 μM, and also when tested at 95% confidence level, Antioxidant activity is observed at both 10 and 5 μM concentrations, and it can be seen that the natural plant composites of the present invention show a concentration-dependent antioxidant activity.
2. DCF-DA 분석법2. DCF-DA Method
상기 방법은 세포내 ROS의 생성양을 측정할 수 있는 방법이다. 구체적으로 DCFH-DA가 세포 속으로 들어가면 DCFH 상태로 존재하는데, 이때 세포 내에 생성된 과산화수소(H2O2)를 만나면 형광도가 높은 DCF로 전환된다. 이때 DCF의 형광도 측정 및 관찰을 통해 녹색빛이 강해지거나 형광도 값이 높으면 ROS 생성이 높은 것으로 판단할 수 있으므로, 상기 방법으로 ROS의 생성 정도를 파악할 수 있다.
This method is a method capable of measuring the amount of intracellular ROS produced. Specifically, when DCFH-DA enters the cell, it is present in the DCFH state, where hydrogen peroxide (H 2 O 2 ) generated in the cell is converted into a highly fluorescent DCF. At this time, if the green light becomes strong or the fluorescence value is high through fluorescence measurement and observation of the DCF, the ROS generation may be determined to be high.
(1) 지방산에 의해 생성되는 ROS에 대한 천연식물복합성분의 항산화 효과 (1) Antioxidative Effect of Natural Plant Compounds on ROS Produced by Fatty Acids
1) 세포 배양1) Cell Culture
인간의 불멸화된 각질형성세포인 HaCaT 세포 1.0 X 105개/웰을 Ibidi 8웰 플레이트에 깔아, 10% FBS(Fetal Bovine Serum)와 100unit/ml 페니실린-스트렙토마이신이 들어 있는 DMEM(Dulbecco Modified Eagle's Medium)에 넣고 37℃, 5% CO2에서 24시간 배양하였다. Dulbecco Modified Eagle's Medium containing 10% FBS (Fetal Bovine Serum) and 100 unit / ml penicillin-streptomycin was laid down on an Ibidi 8-well plate with 1.0 × 10 5 / well HaCaT cells, human immortalized keratinocytes. ) Was incubated for 24 hours at 37 ℃, 5% CO 2 .
2) 물질 처리2) material processing
물질 처리군은 평가할 물질을 무혈청 배지에 넣고 24시간 전처리 하였다. 이때 세포독성이 나타나지 않는 물질 농도로 실험을 진행하였다. 그 외 평가군도 무혈청 배지로 갈아주었다. The substance treatment group was placed in a serum-free medium to be evaluated and pretreated for 24 hours. At this time, the experiment was carried out with a concentration of the substance does not appear cytotoxic. The other groups also changed to serum-free medium.
3) DCF da 처리 3) DCF da treatment
배지를 제거하고 HBSS로 한 번 세척하였다. DCF da 50 μM을 처리해 인큐베이터에서 20분간 반응시켰다. 반응이 끝난 후, HBSS로 2번 세척하였다.The medium was removed and washed once with HBSS. DCF da 50 μM was treated and reacted in an incubator for 20 minutes. After the reaction, the mixture was washed twice with HBSS.
4) 자극원 처리 및 공초점 현미경 관찰4) Stimulation source treatment and confocal microscopy
지방산(OA: 올레산) 100μM 처리 한 뒤, 1시간 뒤 공초점 현미경으로 488nm 파장으로 관찰하였다. 물질 처리군은 지방산 처리시 평가 물질을 함께 처리하였다.After treatment with 100 μM of fatty acid (OA: oleic acid), 1 hour later was observed at 488nm wavelength with a confocal microscope. The substance treatment group treated the evaluation substance together in the fatty acid treatment.
결과는 도 4에 나타내었다.The results are shown in FIG.
도 4를 보면, 지방산(OA)으로 처리하면 세포 내 ROS 생성양이 증가하게 되나, 본 발명에 의한 천연식물복합성분을 처리할 경우 지방산에 의한 ROS 생성의 증가가 억제됨을 확인할 수 있다.
Referring to Figure 4, the treatment with fatty acids (OA) increases the amount of intracellular ROS production, it can be seen that the increase in ROS production by fatty acids is suppressed when the natural plant complex component according to the present invention.
(2) 지방산과 자외선에 의해 생성되는 ROS에 대한 천연식물복합성분의 항산화 효과 (2) Antioxidant Effect of Natural Plant Compounds on ROS Produced by Fatty Acids and Ultraviolet Rays
1) 세포 배양1) Cell Culture
인간의 불멸화된 각질형성세포인 HaCaT 세포 1.0 X 105개/웰을 Ibidi 8웰 플레이트에 깔아, 10% FBS(Fetal Bovine Serum)와 100unit/ml 페니실린-스트렙토마이신이 들어 있는 DMEM(Dulbecco Modified Eagle's Medium)에 넣고 37℃, 5% CO2에서 24시간 배양하였다. Dulbecco Modified Eagle's Medium containing 10% FBS (Fetal Bovine Serum) and 100 unit / ml penicillin-streptomycin was laid down on an Ibidi 8-well plate with 1.0 × 10 5 / well HaCaT cells, human immortalized keratinocytes. ) Was incubated for 24 hours at 37 ℃, 5% CO2.
2) 물질 처리2) material processing
물질 처리군은 평가할 물질을 무혈청 배지에 넣고 24시간 전처리 하였다. 이때 세포독성이 나타나지 않는 물질 농도로 실험을 진행하였다. 그 외 평가군도 무혈청 배지로 갈아주었다. The substance treatment group was placed in a serum-free medium to be evaluated and pretreated for 24 hours. At this time, the experiment was carried out with a concentration of the substance does not appear cytotoxic. The other groups also changed to serum-free medium.
3) DCF da 처리 3) DCF da treatment
배지를 제거하고 HBSS로 한 번 세척하였다. DCF da 50 μM을 처리해 인큐베이터에서 20분간 반응시켰다. 반응이 끝난 후, HBSS로 2번 세척하였다.The medium was removed and washed once with HBSS. DCF da 50 μM was treated and reacted in an incubator for 20 minutes. After the reaction, the mixture was washed twice with HBSS.
4) 자극원 처리 및 공초점 현미경 관찰4) Stimulation source treatment and confocal microscopy
UVB를 처리하지 않는 대조군은 흡수막으로 가리고 UVB 30mJ을 처리하였다. UVB 처리가 끝나면, 지방산(OA: 올레산) 100μM 처리 한 뒤, 1시간 뒤 공초점 현미경으로 488nm 파장으로 관찰하였다. 물질 처리군은 지방산 처리시 평가 물질을 함께 처리하였다. The control group not treated with UVB was covered with an absorbent film and treated with UVB 30mJ. After the UVB treatment, the fatty acid (OA: oleic acid) 100μM treatment, after 1 hour was observed with a confocal microscope at 488nm wavelength. The substance treatment group treated the evaluation substance together in the fatty acid treatment.
결과는 도 5에 나타내었다.The results are shown in FIG.
도 5를 보면, 지방산(OA)과 자외선으로 처리하면 세포 내 ROS 생성양이 증가하게 되나, 본 발명에 의한 천연식물복합성분을 처리할 경우 지방산과 자외선에 의한 ROS 생성의 증가가 억제됨을 확인할 수 있다.
Referring to Figure 5, the treatment with fatty acids (OA) and ultraviolet light increases the amount of ROS production in the cell, the treatment of the natural plant compound according to the present invention can be confirmed that the increase in the production of ROS by fatty acids and ultraviolet light is suppressed. have.
[시험예 3] 사용 효능 및 품질 시험Test Example 3 Efficacy and Quality Test
20~30세 성인 남성, 여성 30명으로 구성되는 품평단(panel)을 대상으로 표 1의 실시예 1~2 및 비교예 1의 샴푸를 2주일 동안 매일 사용하도록 한 후, 하기 설문항목에 7점 척도(점수가 높을수록 우수함)로 답하게 하는 방식으로 사용 품질을 평가하였다. 그 결과는 하기 표 2에 나타내었다.After the shampoos of Examples 1 to 2 and Comparative Example 1 of Table 1 were used daily for two weeks for a panel consisting of 30 male and 20 adult males and females, 7 points were included in the following questionnaire. The quality of use was assessed by answering the scale (higher scores are better). The results are shown in Table 2 below.
(단위: 중량%)Comparative Example 1
(Unit: weight%)
(단위: 중량%)Example 1
(Unit: weight%)
(단위: 중량%)Example 2
(Unit: weight%)
(두피에 뾰루지나 홍반이 없는 정도)5. After 2 weeks, the scalp was clean.
(No rash or erythema on the scalp)
상기 표 2를 보면 본 발명에 따른 실시예 1~2를 사용할 경우 비교예 1을 사용할 경우보다 두피의 가려움이 많이 개선되고 두피의 상태가 깨끗해지게 되었음을 확인할 수 있다.
Looking at Table 2, when using Examples 1 to 2 according to the present invention it can be confirmed that the itching of the scalp is much improved and the state of the scalp is clean than when using Comparative Example 1.
Claims (7)
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020041955A (en) * | 2018-09-12 | 2020-03-19 | 株式会社マンダム | Inflammation risk evaluation method in scalp and anti-inflammatory substance screening method |
| JP2020115143A (en) * | 2016-03-29 | 2020-07-30 | ポーラ化成工業株式会社 | Peroxiredoxin expression enhancer |
| CN114569503A (en) * | 2020-12-02 | 2022-06-03 | 蔻诗曼嘉韩国股份公司 | Cosmetic composition for improving scalp state comprising natural complex extract |
| KR102529107B1 (en) * | 2022-06-24 | 2023-05-03 | 조선대학교산학협력단 | Cosmetic composition for scalp dandruff suppression and hair strengthening, containing Aurea Helianthus leaves as an active ingredient |
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| CN109866295A (en) * | 2019-03-22 | 2019-06-11 | 章健 | A kind of production method of phase-changing and temperature-regulating bamboo mat |
| US11786451B2 (en) | 2019-06-28 | 2023-10-17 | The Procter & Gamble Company | Skin care composition |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001122731A (en) * | 1999-10-26 | 2001-05-08 | Ichimaru Pharcos Co Ltd | Cosmetic composition containing moisturizing plant extract |
| KR20030070686A (en) * | 2002-02-26 | 2003-09-02 | 정성인 | External use medicine for promotion of wearing hair and prevention of fallen hair |
| KR20060016163A (en) * | 2004-08-17 | 2006-02-22 | 주식회사 알파인프로덕트 | Hair Loss Prevention & Hair Growth & Hair Growth Promoter |
| KR100715485B1 (en) * | 2006-05-03 | 2007-05-07 | 주식회사 바이오랜드 | Cosmetic composition containing water lily root extract having skin whitening and anti-aging effect |
-
2010
- 2010-01-20 KR KR1020100005125A patent/KR101691495B1/en not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001122731A (en) * | 1999-10-26 | 2001-05-08 | Ichimaru Pharcos Co Ltd | Cosmetic composition containing moisturizing plant extract |
| KR20030070686A (en) * | 2002-02-26 | 2003-09-02 | 정성인 | External use medicine for promotion of wearing hair and prevention of fallen hair |
| KR20060016163A (en) * | 2004-08-17 | 2006-02-22 | 주식회사 알파인프로덕트 | Hair Loss Prevention & Hair Growth & Hair Growth Promoter |
| KR100715485B1 (en) * | 2006-05-03 | 2007-05-07 | 주식회사 바이오랜드 | Cosmetic composition containing water lily root extract having skin whitening and anti-aging effect |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020115143A (en) * | 2016-03-29 | 2020-07-30 | ポーラ化成工業株式会社 | Peroxiredoxin expression enhancer |
| JP2020041955A (en) * | 2018-09-12 | 2020-03-19 | 株式会社マンダム | Inflammation risk evaluation method in scalp and anti-inflammatory substance screening method |
| CN114569503A (en) * | 2020-12-02 | 2022-06-03 | 蔻诗曼嘉韩国股份公司 | Cosmetic composition for improving scalp state comprising natural complex extract |
| CN114569503B (en) * | 2020-12-02 | 2024-01-02 | 蔻诗曼嘉韩国股份公司 | Cosmetic composition for improving scalp condition comprising natural complex extract |
| KR102529107B1 (en) * | 2022-06-24 | 2023-05-03 | 조선대학교산학협력단 | Cosmetic composition for scalp dandruff suppression and hair strengthening, containing Aurea Helianthus leaves as an active ingredient |
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