Abstract:
본 고안은 피지제거용 빗에 관한 것으로서, 복수의 빗살들로 마련된 빗살부가 구비된 빗 몸체; 및, 상기 빗살들이 각각 끼워질 수 있도록 상기 빗살부의 형상에 대응되게 마련되어 상기 빗살부에 착탈가능하게 결합되고, 두피의 피지를 흡착시키는 흡착제를 포함하는 피지흡착커버;를 포함하는 것을 특징으로 한다. 이에 의하여, 두피의 피지를 효과적으로 제거할 수 있다.
Abstract:
본 고안은 피지제거용 빗에 관한 것으로서, 길이방향을 따라 내부에 중공부가 형성된 복수의 빗살; 상기 빗살들로 마련된 빗살부가 구비된 빗 몸체; 및, 상기 빗살들의 단부에서 외부로 단부가 노출되도록 상기 빗살들 각각의 중공부에 수용된 흡착제 심;을 포함하는 것을 특징으로 한다. 이에 의하여, 두피의 피지를 효과적으로 제거할 수 있다.
Abstract:
본 고안은 피지제거용 빗에 관한 것으로서, 복수의 빗살들로 마련된 빗살부가 구비되고, 모발 영양제가 수용되는 컨디셔너 수용부가 내부에 구비된 빗 몸체; 및, 상기 빗살들의 단부에 두피의 피지를 흡착시키는 흡착제가 마련된 피지흡착부;를 포함하되, 상기 피지흡착부의 빗살들은, 다공성 재질로 마련되어 표면에 다수의 컨디셔너 배출공이 형성되고, 상기 컨디셔너 배출공과 상기 컨디셔너 수용부를 상호 연통시키는 컨디셔너 통로가 내부에 형성된 것을 특징으로 한다. 이에 의하여, 두피의 피지를 효과적으로 제거할 수 있다.
Abstract:
PURPOSE: A method for visibly measuring skin cell regeneration is provided to observe seed weight and bud length without special equipment. CONSTITUTION: A method visible measuring skin cell regeneration ability comprises: a step of preparing herb material extract; a step of measuring the weight of seeds; a step of the seeds using the extract for germination; a step of measuring the weight of the seeds and the length of the buds; and a step of determining skin regeneration.
Abstract:
PURPOSE: A method for preparing a green tea saponin 21-O-angeloyltheasapogenol E3 is provided to massively produce 21-O-angeloyltheasapogenol E3 through hydrolysis using microorganism. CONSTITUTION: A method for preparing 21-O-angeloyltheasapogenol E3 comprises: a step of collecting extract containing saponin from plant seeds using eater or organic solvent; and a step of hydrolyzing the extract using acid, base, enzyme, or microorganism producing the enzyme to isolate the 21-O-angeloyltheasapogenol E3 of chemical formula 1. The plant seed is green tea seed. The acid is hydrochloric acid, sulfuric acid, nitric acid, or ethanol, methanol, or butanol thereof. The base is sodium hydroxide, or potassium hydroxide, or base, ethanol, methanol, or butanol thereof. The enzyme is glucosidase, arabinosidase, rhamnosidase, xylosidase, cellulose, hesperidinase, naringinase, [glucuronidase, pectinase, galactosidase, or amyloglucosidase.
Abstract:
PURPOSE: A method and composition for promoting skin regeneration using icariside II is provided to promote proliferation of transient amplifying cells of epidermis base and promote skin regeneration. CONSTITUTION: An icariside II of chemical formula 1 promotes proliferation of skin cells in skin cells. The skin cell is transient amplifying cells(TA cells). A composition for promoting skin regeneration contains the icariside II as an active ingredient. The content of the active ingredient is 0.001-10 weight% based on total weight. The composition regenerates epidermis by promoting proliferation of the TA cells. The composition increases the number of TA cells which express CD71 protein (Cluster of Differentiation 71 Protein) and α6 integrin. The composition increases the expression of CD200(Cluster of Differentiation 200).
Abstract:
A composition for skin external application is provided to improve the skin wrinkle. A kaempferol-3-O-rutinoside suppresses a collagenase expression and accelerates a production of procollagen. A composition for skin external application for improving skin wrinkle contains the kaempferol-3-O-rutinoside expressed by a chemical formula 1. The composition is used as astringent cosmetic water, lotion, moisturizing cream, massage cream, essence, eye cream, eye essence, cleansing cream, cleansing foam, cleansing water, pack, powder, body lotion, body cream, body oil, body essence, makeup base, foundation, hair-dye, shampoo, rinse or the body cleansing agent. The kaempferol-3-O-rutinoside is separated from the green tea.
Abstract:
A method for preparing ortho-dihydroxyisoflavones having high antioxidative and skin-whitening effects through the biotransformation system is provided to improve the preparation yield of ortho-dihydroxyisoflavones by using microorganisms. The ortho-dihydroxyisoflavones including 7,8,4݆-trihydroxyisoflavone, 7,6,4݆-trihydroxyisoflavone, 7,3݆,4݆-trihydroxyisoflavone and 7,5,3݆,4݆-tetrahydroxyisoflavone are prepared by biotransforming daidzein and genistein with a microorganism derived from Actinomyces selected from Streptomyces evermitilis, Nocardia farcinica and Streptomyces lincolnesis through site specific hydroxylation at 3݆ site in a batch reactor to which oxygen is supplied.