Abstract:
본 발명은 타이포돈트와 로드셀을 이용한 교정력 측정기에 관한 것으로, 보다 상세하게는 타이포돈트에 교정력 인가용 와이어를 연결하고 로드셀을 도입하여 교정력을 측정함으로써 영상 기반의 측정방식에서 발생할 수 있는 측정오차를 줄여 정밀한 교정력의 측정과 동시에 3차원적인 교정력 측정이 가능한 타이포돈트와 로드셀을 이용한 교정력 측정기를 제공한다.
Abstract:
본 발명은 인지 기능 개선 조성물에 관한 것이다. 본 발명의 인지 기능 개선 조성물은 인삼을 유효 성분으로 함유하는 것을 특징으로 하여 이루어진다. 본 발명의 인삼을 유효 성분으로 함유하는 인지 기능 개선 조성물은 인삼을 함유하는 것으로 인해 시각적 언어학습능력과 시각적 기억 회상 능력이 개선되어 전체적으로 인지 기능의 향상에 기여하는 효과가 있다.
Abstract:
PURPOSE: A method for determining administration of talniflumate by SNP analysis and a gene used for the same are provided to determine proper administration amount of talniflumate by analyzing the relation of pharmacodynamic parameter and SNP. CONSTITUTION: A method for determining Cmax(maximum plasma concentration) of talniflumate by SNP comprises: a step of collecting biological sample from an individual; a step of analyzing gene of biological sample using SNP chip and identifying genotype thereof; a step of determining Cmax in a value indicated in each line of M1 row in case that the genotype of SNP is indicated in G1 row of figure 1a-1j; and a step of determining Cmax in a value indicated in each line of figure 1a-1j in case that the genotype of SNP is indicated in each line of G3 row of figure 1a-1j.
Abstract:
본 발명은 단일 염기 다형성의 분석에 의한 탈니플루메이트의 맞춤형 투여량의 결정방법 및 그에 사용되는 유전자에 관한 것으로, 개체가 갖는 단일 염기 다형성의 분석에 의해 탈니플루메이트의 약동학적 파라미터에 영향을 미치는 유전적 요인들을 확인하고, 상기 단일 염기 다형성과 상기 약동학적 파라미터의 관계를 분석하여 탈니플루메이트의 투여 계획에 활용함으로써 개체의 유전적 차이에 따라 탈니플루메이트의 적절한 투여량을 결정하는 데 유용하게 사용될 수 있다. 단일 염기 다형성, 탈니플루메이트, 약동학적 파라미터
Abstract:
PURPOSE: A composition containing ginseng for improving a cognitive function is provided to improve visual linguistics learning and visual memory recalling abilities. CONSTITUTION: A composition for improving a cognitive function contains ginseng as an active ingredient. The ginseng is white and red ginseng. The white ginseng is prepared removing peel of 4-year old raw ginsengs and drying. The red ginseng is prepared by steaming the raw ginseng. The cognitive function is a visual cognitive function.
Abstract:
PURPOSE: A composition containing garlic extract for anti-aging is provided to highly suppressing aging in skin cells. CONSTITUTION: A composition for skin anti-aging contains garlic extract as an active ingredient. The garlic extract is isolated using water, low alcohol of C1-C4, or their mixture solvent. The extract is an extract, dilutant, concentrate, dried product, or purified product. The composition for skin anti-aging is a cosmetic composition or food composition. The cosmetic composition also contains carrier and adjuvant such as antioxidant, stabilizing agent, solubilizing agent, vitamin, pigment, and perfume. The food composition contains citric acid, liquid fructose, sugar, glucose, acetic acid, and fruit juice.
Abstract:
PURPOSE: A composition containing garlic extract for anti-aging is provided to highly suppressing aging in skin cells. CONSTITUTION: A composition for skin anti-aging contains garlic extract as an active ingredient. The garlic extract is isolated using water, low alcohol of C1-C4, or their mixture solvent. The extract is an extract, dilutant, concentrate, dried product, or purified product. The composition for skin anti-aging is a cosmetic composition or food composition. The cosmetic composition also contains carrier and adjuvant such as antioxidant, stabilizing agent, solubilizing agent, vitamin, pigment, and perfume. The food composition contains citric acid, liquid fructose, sugar, glucose, acetic acid, and fruit juice.
Abstract:
PURPOSE: A method for determining dosage of pioglitazone by SANP analysis by analyzing the relation of dynamic parameter and SNP. CONSTITUTION: A method for determining pioglitazone Cmax(maximum plasma concentration) by SNA comprises: a step of collecting a biological sample from an individual; a step of analyzing genes of the biological sample using SNP chip to identify SNP and genotype thereof; and a step of determining the value of indicated in M1 row of piroglitazone in case that genotypes of SNP are indicated in each row of G1.
Abstract:
PURPOSE: A cDNA(complementary DNA) microarray chip using a gene having expression in inflammatory diseases is provided to early diagnose inflammatory diseases and develop a therapeutic agent. CONSTITUTION: A cDNA microarray chip for diagnosing inflammatory diseases contains a nucleotide of a gene of which expression is specifically increased or decreased in inflammatory diseases. Screening for inflammatory diseases is performed using a cDNA microarray chip. A method for screening inflammatory diseases comprises a step of inducing inflammatory reaction by treating LPS to Raw 246.7 cell line and selecting factor. A therapeutic agent for treating inflammatory diseases is a regulator of gene expression by binding to antisense oligonucleotide, peptide, small molecular compound, antibody or target promoter.
Abstract:
A therapeutic agent HJ001 isolated from Citrus reticulata Blanco is provided to inhibit growth of cancer cells and reduce expressions of IL-3(interleukin-3), IL-6, IL-12p40p70, IL-12p70 and SCF(stem cell factor) and increase expressions of IL-10 and TNF(tumor necrosis factor), so that it is useful for treatment of cancer and inflammatory disease. A method for preparing the extract of Citrus reticulata Blanco HJ001 comprises the steps of: dipping Citrus reticulata Blanco powder in water and filtering the solution; passing the filtered solution through the column packed with fillers HP-20 and collecting passed solution; mixing the collected solution with water-saturated ethylacetate to transfer it into an ethylacetate layer; inducing layer separation of the mixture into the ethylacetate layer and water layer, and separating the water layer; mixing the water layer with water-saturated butanol and separating a butanol layer; absorbing the butanol layer to TLC(thin layer chromatography) silica; subjecting the TLC silica by using chloroform, methanol and water as development solvent and separating the developed portion; dissolving the developed portion in butanol, and filtering and concentrating the solution; freeze-drying the filtered solution to obtain materials Fr1 and Fr2; and separating the Fr2 from the Fr1 and Fr2.