Abstract:
The present invention provides a tooth whitening composition designed to relieve discoloration and stress caused by tooth discoloration, wherein a substrate or an oxidizing enzyme discharging hydrogen peroxide by decomposing a substrate is dipped in a macrocapsule. More specifically, the present invention relates to a tooth whitening composition and a tooth whitening food having the same as an active ingredient, wherein a substrate or an oxidizing enzyme discharging hydrogen peroxide by decomposing a substrate is firstly coated with a component that is decomposed by a chewing activity or a salivary enzyme; a macrocapsule of which thickness is adjusted to be dipped; and the rate of which the capsule and coating are disintegrated by the chewing activity or salivary enzyme is adjusted, thus enabling continuous generation of hydrogen peroxide so that whitening can be performed.
Abstract:
The present invention relates to a composition comprising at least one selected from the group consisting of Curcuma xanthorrhizae extract, curcumin, demethoxycurcumin, and xanthorrhizol for improving memory and learning ability. The composition of the present invention particularly has an effect of suppressing damage of nerve cells in cerebrum fundus by inhibiting activity of acetylcholinesterase. In addition, the composition of the present invention not only can improve memory and learning ability via effects of nerve cell protection and damage prevention, but also can prevent and treat cognitive disorders.
Abstract:
본 발명은 유효성분으로 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 세로토닌(serotonin), 멜라토닌(melatonin), α-토코페롤(α-Tocopherol), 진세노사이드-Rb1(ginsenoside-Rb1), 진세노사이드-Rg1(ginsenoside-Rg1) 및 나린제닌(naringenin)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 함유하는 식욕억제 호르몬인 렙틴(leptin) 분비 촉진용 조성물 및 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 세로토닌(serotonin), 멜라토닌(melatonin), α-토코페롤(α-Tocopherol), 진세노사이드-Rb1(ginsenoside-Rb1), 진세노사이드-Rg1(ginsenoside-Rg1) 및 나린제닌(naringenin)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 유효성분으로 함유하는 식욕억제 호르몬인 렙틴(leptin) 분비 촉진용 기능성 식품에 관한 것이다.
Abstract:
PURPOSE: A composition for memory ability and study ability enhancement with one or more selected from a group of Curcuma xanthorrhizae extract, curcumin, dimethoxy curcumin, and xanthorrihizol is provided to curb damage in a nerve cell, especially in a nerve cell of cerebrum base, through suppressing vitality of Acetylcholinesterase. CONSTITUTION: Composition for memory ability and study ability enhancement contains one or more selected from a group of Curcuma xanthorrhizae extract, curcumin, dimethoxy curcumin, and xanthorrihizol. The composition suppresses vitality of Acetylcholinesterase. A cognitive impairment is dementia, learning disability, agnosia, or delirium. A food composition for memory ability and study ability enhancement contains one or more selected from a group of Curcuma xanthorrhizae extract, curcumin, dimethoxy curcumin, and xanthorrihizol. A medicinal composition for prevention or treatment of cognitive impairment contains (a) a therapeutic effective dose of the component; and (b) a carrier allowed in pharmacology.
Abstract:
PURPOSE: A composition and a functional food for promoting leptin secretion are provided to effectively suppress appetite and to enable long-term administration without side effects. CONSTITUTION: A composition for promoting leptin secretion contains ascorbic acid, beta-D-glucan, hesperetin, serotonin, melatonin, alpha-tocopherol, ginsenoside-Rb1, ginsenoside-Rg1, or naringenin. The concentration of each ascorbic acid, hesperetin, serotonin, ginsenoside-Rg1, and naringenin is 0.1-10 ug/mg. The concentration of melatonin is 5-15 ug/ml. The concentration of each beta-D-glucan and alpha-tocopherol is 1-10 ug/ml. A health functional food for promoting leptin secretion contains ascorbic acid, beta-D-glucan, hesperetin, serotonin, melatonin, alpha-tocopherol, ginsenoside-Rg1, ginsenoside-Rg1, or naringenin as an active ingredient.
Abstract:
PURPOSE: A composition and a functional food for promoting leptin are provided to effectively suppress appetite and to ensure safety without side effects. CONSTITUTION: A composition for promoting leptin secretion contains 3-hydroxyflavone, hesperidin, quercetin, catechin, or caffeine ingredients. The concentration of each 3-hydroflavone, hesperidin, and catechin is 0.1-10 ug/ml. The composition is manufactured in the form of a powder, granules, a tablet, a capsule, a suspension, an emulsion, a syrup, an oral formulation of aerosol, an external use formulation, a suppository, or sterilization injection solution. A functional food for promoting leptin secretion contains the 3-hydroxyflavone, hesperidin, quercetin, catechin, or caffeine ingredients as active ingredients.
Abstract:
본 발명은 알코올발효 사과 사이다의 제조 방법에 관한 것으로, 더욱 상세하게는 껍질을 제거하지 않은 친환경사과를 세척하고 칼로 2-4 등분한 후, 잘게 조각을 내는 단계; 조각낸 사과에 천연 갈변 방지제인 루바브 주스 3~7 중량%를 혼합한 후 콜로이드 밀을 이용하여 분쇄하는 단계; 상기 분쇄된 사과 분쇄액에 유산균을 첨가하여 잡균을 제거한 후, 효모균을 첨가하여 알코올 발효하는 단계; 상기 알코올 발효된 사과 발효액을 착즙한 후 디켄트(decanter) 처리를 하는 단계; 및 상기 사과 발효액을 고전압 펄스(pulse)를 이용하여 살균하고 용기에 충진하거나 또는 사과 발효액을 용기에 충진하고 초고압 살균하는 단계를 포함하는 갈변이 방지되고, 첨가물이 첨가되지 않은 알코올발효 사과 사이다의 제조 방법 및 상기 방법에 의해 제조된 알코올발효 사과 사이다에 관한 것이다.
Abstract:
PURPOSE: A sandwich immunoassay biochip and an immunoassay using the same are provided to accurately and quickly detect pathogens. CONSTITUTION: A sandwich immunoassay biochip contains: a first protein which binds to Fc domain conjugated to a functional group of a surface-modified solid-support; a capture antibody conjugated to the first protein; a second protein which binds to Fc site of an antibody conjugated to a functional group of surface-modified polystyrene beads; and a detection antibody conjugated to the second protein. The functional groups of the solid-support and polystyrene beads are an amine group and a carboxyl group, respectively. The solid-support is a glass, polysterene, or metal. A sandwich immunoassay using the biochip comprises: a step of contacting a sample containing an antigen to the biochip; a step of specifically binding the antibody to the capture antibody; a step of binding the detection antibody to an epitope which is not conjugated with the capture antibody; and a step of detecting specific antigen-antibody binding.