Abstract:
본 발명은 알파-락트알부민과 덱스트란의 마이얄반응을 통해 생성된 당단백질을 유효성분으로 함유하는 면역 증강용 조성물에 관한 것으로, 더 상세하게는 알파-락트알부민(alpha-lactalbumin)과 덱스트란(dextran)의 마이얄반응(Maillard reaction)을 통해 생성된 당단백질을 유효성분으로 함유하는 면역 증강용 또는 암 개선용 식품용 조성물, 면역력 저하로 인한 질환 치료용 또는 암 치료용 약학적 조성물에 관한 것이다. 본 발명의 당단백질은 면역 증진에 필요한 사이토킨 및 백혈구의 수를 늘려주고, 종양을 억제하는 효능이 있어, 면역 증진용 조성물 및 암 치료용 조성물의 제조에 효과적이다.
Abstract:
The present invention relates to a composition for immune enhancement containing, as an active ingredient, glycoprotein produced through a Maillard reaction of alpha-lactalbumin and dextran, and more specifically, to a composition for immune enhancement or a food composition for cancer alleviation, containing, as an active ingredient, glycoprotein produced through a Maillard reaction of alpha-lactalbumin and dextran, and to a pharmaceutical composition for treating disease caused by decreased immunity or treating cancer. The glycoprotein of the present invention has an effect of increasing the number of cytokines and leukocytes, which are necessary for immunological enhancement, and suppressing tumor, and thus is effective in preparing a composition for immune enhancement and a composition for cancer treatment.
Abstract:
본 발명은, 루테올린에 하기 화학식 1로 표시되는 카테콜기를 작용기로 포함하는 화합물을 첨가함으로써 생체내에서의 항염증 효능이 증가된 루테올린 혼합 조성물을 제조하는 방법에 관한 것이다. 본 발명에 의하면, 생체내에서의 루테올린의 항염증 효능을 증가시키기 위하여 특정한 구조의 천연 화합물을 생체내 루테올린 간 대사의 competitor로서 혼합하는 혼합 조성물의 제조방법 및 그 제조방법에 의하여 제조된 생체내에서의 항염증 효능이 증가된 루테올린 혼합 조성물을 제공할 수 있다.
Abstract:
The present invention relates to a fraction of rice wine lees derived-glycoprotein, which is characterized in having a molecular weight of 15 to 110 kDa, and a method of producing the same and, more specifically, to a fraction of rice wine lees-derived glycoprotein and the uses thereof, which is prepared by a method comprising: (a) a step of removing fat in rice wine lees; (b) a step of mixing the rice wine lees in a buffer solution having a pH level of 7.0 to 8.0; (c) a step of obtaining a supernatant by centrifugation; (d) a step of dialyzing the supernatant with a dialysis semipermeable membrane (MWCO 6000-8000); (e) a step of adding a salt precipitating protein in the dialyzed supernatant to precipitate glycoprotein; (f) a step of dissolving the precipitate in a buffer solution having a pH level of 7.0 to 8.0 with a dialysis semipermeable membrane (MWCO 6000-8000); and (g) a step of obtaining a fraction of glycoprotein from the dialyzed and precipitated lysate. The fraction of glycoprotein of the present invention has a better effectiveness of promoting histiocyte vitality than Krestin (PSK), which is a medicine for enhancing immune vitality, and has no cytotoxicity, thereby being effective in producing a new functional food and a medicine for enhancing immune function.
Abstract:
PURPOSE: A separating method is provided to extract capsaicinoid and carotenoid from red pepper without using organic solvent, and to prevent the denaturation and destruction of effective component. CONSTITUTION: (a) One to four percent of yield fraction is collected from red pepper by supercritical carbon dioxide extraction on condition that the temperature is 30-50°C and the pressure is 1500-2500 psi. (b) One to four percent of yield fraction is collected from red pepper of (a) step by supercritical carbon dioxide extraction on condition that the temperature is 30-50°C and the pressure is 6000-7500 psi. (c) One to four percent of yield fraction is collected from the red pepper by supercritical carbon dioxide extraction on condition that the temperature is 30-50°C and the pressure is 6000-7500 psi. The pressure condition in (a) step is 1500-2000 psi. The temperature condition in (a) step is 35-45°C. The temperature condition in (b) step is 35-45°C.
Abstract:
PURPOSE: A manufacturing method is provided to manufacture spice and the taste component of red pepper without the denaturation and the destruction of effective component. CONSTITUTION: Red pepper extract and the extract remnant are manufactured by supercritical extraction. It is the supercritical extraction and the red pepper extract and extracted cake is manufactured. An enzymatic lysate is manufactured by reacting the produced extract remnant with at least one of cell wall enzyme or proteinase. The extract includes oleoresin The oleoresin is added to the enzymatic lysate and mixed together. The supercritical extraction condition is as in the following: 35-45°C of temperature; 4500-7500 psi; and 5-10 of CO2 / sample rate. The cell wall degrading enzyme is viscozyme, celluclast, pectinex, or ultraflo. The proteinase is alcalase or protamex. The Reaction occurs at 45-55°C. The spice composition includes the enzymatic lysate. The enzymatic lysate comprises at least one of amino nitrogen, reducing sugar or organic acid.