KR101907179B1 - Method for production of sulforaphene-enriched raphanus sativus seeds extracts and Food composition, pharmaceutical composition, animal medicines for weight and blood glucose control, fatty liver prevention with the raphanus sativus seeds extracts therefrom - Google Patents

Method for production of sulforaphene-enriched raphanus sativus seeds extracts and Food composition, pharmaceutical composition, animal medicines for weight and blood glucose control, fatty liver prevention with the raphanus sativus seeds extracts therefrom Download PDF

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KR101907179B1
KR101907179B1 KR1020170055747A KR20170055747A KR101907179B1 KR 101907179 B1 KR101907179 B1 KR 101907179B1 KR 1020170055747 A KR1020170055747 A KR 1020170055747A KR 20170055747 A KR20170055747 A KR 20170055747A KR 101907179 B1 KR101907179 B1 KR 101907179B1
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extract
weight
ethanol
pharmaceutical composition
sulfolapin
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KR1020170055747A
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Korean (ko)
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장우정
석수진
서상권
윤정한
최명숙
최상호
이기원
양희
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서울대학교 산학협력단
경북대학교 산학협력단
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/105Plant extracts, their artificial duplicates or their derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/265Esters, e.g. nitroglycerine, selenocyanates of carbonic, thiocarbonic, or thiocarboxylic acids, e.g. thioacetic acid, xanthogenic acid, trithiocarbonic acid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/31Brassicaceae or Cruciferae (Mustard family), e.g. broccoli, cabbage or kohlrabi
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2200/00Function of food ingredients
    • A23V2200/30Foods, ingredients or supplements having a functional effect on health
    • A23V2200/328Foods, ingredients or supplements having a functional effect on health having effect on glycaemic control and diabetes
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2200/00Function of food ingredients
    • A23V2200/30Foods, ingredients or supplements having a functional effect on health
    • A23V2200/332Promoters of weight control and weight loss
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2300/00Processes
    • A23V2300/14Extraction
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2236/00Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
    • A61K2236/30Extraction of the material
    • A61K2236/33Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones
    • A61K2236/333Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones using mixed solvents, e.g. 70% EtOH
    • Y10S514/866
    • Y10S514/893

Abstract

The present invention relates to a method for manufacturing a radish seed extract containing a large amount of sulforaphene, a radish seed extract obtained therefrom and a composition for preventing or treating obesity, diabetes, and fatty liver containing the radish seed extract. The addition of 5-40% (v/v) ethanol as an extraction solvent to the pulverized product of radish seed can be used to extract sulforaphene from the radish seed by high yield, and the manufacturing process is simple and stable to be applied in the food industry. In addition, a food composition, a pharmaceutical composition and an animal medicine for ameliorating, preventing, and treating obesity, diabetes, and fatty liver containing the ethanol extract of radish seed of 5-40% (v/v) of the present invention exhibit more excellent effects of ameliorating, preventing, and treating obesity, diabetes, and fatty liver by extracting various active ingredients from the radish seed and the compound synergy effect.

Description

설포라핀을 다량 함유하는 무씨 추출물의 제조방법 및 이로부터 추출된 무씨 추출물을 함유하는 체중, 혈당조절용 및 지방간 예방용 식품 조성물, 약품 조성물, 동물용 의약품 {Method for production of sulforaphene-enriched raphanus sativus seeds extracts and Food composition, pharmaceutical composition, animal medicines for weight and blood glucose control, fatty liver prevention with the raphanus sativus seeds extracts therefrom}FIELD OF THE INVENTION [0001] The present invention relates to a method for producing a radish extract containing a large amount of sulforaphin and a method for producing a sulforaphane-enriched raphanus sativus seeds extracts and food composition, pharmaceutical composition, animal medicines for weight and blood glucose control, fatty liver prevention with the raphanus sativus seeds extracts therefrom}

본 발명은 설포라핀을 다량 함유하는 무씨 추출물의 제조방법 및 이로부터 추출된 무씨 추출물을 함유하는 비만, 당뇨, 지방간 개선, 예방, 치료용 조성물에 관한 것으로, 더욱 구체적으로는 무씨에 추출 용매로 5~40%(v/v) 에탄올을 첨가하여 설포라핀을 다량 함유하는 무씨 추출물을 제조하는 방법 및 이로부터 수득된 무씨 5~40%(v/v) 에탄올 추출물을 함유하는 비만, 당뇨, 지방간 개선, 예방, 치료용 식품 조성물, 약품 조성물, 동물용 의약품에 관한 것이다.The present invention relates to a method for preparing a radish extract containing a large amount of sulfo-fins and a composition for improving, preventing and treating obesity, diabetes and fatty liver, which contains the radish extract extracted therefrom. More specifically, The present invention relates to a method for producing a radish extract containing 5 to 40% (v / v) ethanol and a large amount of sulfolapin, and a method for producing obesity, diabetes mellitus, A food composition for improving, preventing, and treating fatty liver, a pharmaceutical composition, and an animal medicine.

서구화된 식습관과 운동량 감소로 인해 현재 비만 인구 비율은 전 세계적으로 급증하고 있는 추세이다. 비만과 과체중은 세계적으로 만연하고 있어서 조사 대상으로 한 국가(미국, 영국, 프랑스, 독일, 이탈리아, 스페인, 일본)의 인구 중 적어도 20%가, 또 많은 곳에서는 최대 45%가 과체중으로 알려져 있다. 비만은 그 자체의 문제뿐만 아니라 고지혈증, 당뇨, 지방간 등의 대사성 질환을 유발하는 주된 원인이 되기 때문에 체중을 조절하는 것이 건강유지에 매우 중요하다. 현재까지 개발된 비만 치료제들은 소화계 또는 신경계에 작용을 하는 기전을 가지고 있어 여러 부작용들이 보고되고 있으며, 대부분 시판이 금지되어 있다. 치료제의 안전성에 대한 우려 때문에 천연물에서 유래된 활성 성분으로 비만을 예방하거나 치료하기 위한 연구가 활발히 진행되고 있다.Due to westernized eating habits and a decrease in exercise, the proportion of obese people is rapidly increasing worldwide. Obesity and overweight are widespread worldwide and are known to be overweight in at least 20% of the population (US, UK, France, Germany, Italy, Spain and Japan) and up to 45% in many. Since obesity is a major cause of metabolic diseases such as hyperlipidemia, diabetes and fatty liver as well as its own problems, controlling body weight is very important for maintaining health. Many obesity drugs developed to date have a mechanism of acting on the digestive system or the nervous system, and many side effects have been reported, and most of them are forbidden on the market. Because of concerns about the safety of therapeutic agents, studies have been actively conducted to prevent or treat obesity as an active ingredient derived from natural products.

한편, 비만은 특히 제2형 당뇨를 유발시키는 중요한 위험요소이며 비만의 정도나 비만의 기간, 혹은 체지방의 분포에 따라 당뇨의 발병률이 달라진다. 체질량지수가 증가할수록 당뇨의 발생이 증가하는데, 체질량지수가 23 ㎏/㎡인 사람과 비교하였을 때 체질량지수가 35 ㎏/㎡이 넘은 사람은 당뇨 발병률이 40배 높게 나타난다는 보고가 있다. 하지만, 기존 당뇨 치료제는 위장장애, 저혈당유발, 부종 등을 유발하는 부작용이 있으며, 약물 투여 방법이 주사제이고 약한 약효를 가진다는 단점이 있어 새로운 개념의 치료제 개발이 매우 필요한 시점이다.Obesity, on the other hand, is an important risk factor for type 2 diabetes, and the incidence of diabetes varies according to the degree of obesity, duration of obesity, and distribution of body fat. It is reported that the incidence of diabetes increases with the increase of the body mass index, and the incidence of diabetes is 40 times higher in people with a BMI of 35 ㎏ / ㎡ than those with a body mass index of 23 ㎏ / ㎡. However, existing diabetes drugs have side effects that cause gastrointestinal disorders, hypoglycemia, edema, etc., and it is necessary to develop a new concept of therapeutic drugs because of the disadvantage that the drug administration method is injectable and has weak drug effect.

한편, 비만과 제2형 당뇨병은 간질환의 발생과 직접적으로 관련이 있는 대표적인 질환이다. 지방간이란 간 조직에 중성 지방이 과다하게 축적된 경우를 말하는데, 비만 또는 당뇨와 같은 대사 이상에 의해 발병된 경우를 비알콜성 지방간 질환이라고 한다. 현재까지는 이를 효과적으로 치료하기 위한 방법으로 체중 감량을 우선시하고 있고, 약물로는 메트포르민(metformin), 치아졸리딘디온(thiazolidinedione) 등의 당뇨병 약제나 스타틴(statin) 계열의 항고지혈제를 통해 호전 증세를 보인다는 보고가 있으나, 아직까지 효과적이면서 안전하게 장기간 사용 가능한 약물은 없는 실정이다. On the other hand, obesity and type 2 diabetes are major diseases directly related to the development of liver disease. Fatty liver is a case of excessive accumulation of triglyceride in liver tissue. It is called nonalcoholic fatty liver disease when it is caused by metabolic abnormality such as obesity or diabetes. To date, weight loss has been a priority for effective treatment of diabetes mellitus. Metformin, thiazolidinedione, and statin-based anticoagulants have been shown to improve symptoms However, there is no drug that can be used effectively and safely for a long period of time.

한편, 무씨(내복자)는 복부 창만, 트림, 위산 과다, 설사, 해수, 천식, 변비, 식욕부진, 오래된 담, 오래된 기침을 멈추게 하는 효과가 있다고 알려져 있고, 약리작용으로는 포도상구균 등의 억제작용, 피부진균 억제작용, 혈압강하작용, 항염증작용 등이 있음이 보고되어 있으며, 체중조절용 한약인 태음조위탕의 주성분으로 오랫동안 사용되어 왔다. 이러한 무씨의 지표성분으로 설포라핀, 에루익산, 리놀레익산, 글리세린시내픽산 에스테르, 시니그린 등이 알려져 있다.On the other hand, it is known that Mucus (abdomen) has the effect of stopping the abdominal cavity, trimming, gastric hyperplasia, diarrhea, seawater, asthma, constipation, anorexia, old skin and old cough. Pharmacological actions include inhibition of staphylococci Action, inhibition of skin fungi, hypotensive effect, anti-inflammatory action, etc. have been reported, and have been used for a long time as a main ingredient of Taeum Jowe-tang, a Chinese medicine for controlling body weight. As the indicator components of this kind of Si, sulfolapine, eruic acid, linoleic acid, glycerin locustic ester and cinchin are known.

한편, Pengqun Kuang(2013), Kuang P1(2013)의 논문에서는 무씨로부터 설포라핀을 분리하는 내용을 기재하고 있는데, 모두 컬럼을 사용하여 무씨로부터 설포라핀을 분리하고 있어 생산 단가가 높아 식품 산업에 적용이 어렵고, 안정성 문제가 대두된다 (Separation and purification of sulforaphene from radish seeds using macroporous resin and preparative high-performance liquid chromatography, Pengqun Kuang, Food Chemistry 136 (2013) 342-347, Preparative separation and purification of sulforaphene from radish seeds by high-speed countercurrent chromatography, Kuang P1, Food Chem, 2013 Jan 15;136(2):309-15.).On the other hand, Pengqun Kuang (2013) and Kuang P1 (2013) describe the separation of sulfo-fins from mushrooms. Since all of the columns are used to separate sulforaphane from mushrooms, (Pengqun Kuang, Food Chemistry 136 (2013) 342-347, Preparative Separation and Purification of Sulforaphene from Sulforaphene from Preparative Separation and Purification of Sulforaphane from Radish Seeds using Macroporous Resin and Preparative High-Performance Liquid Chromatography, radish seeds by high-speed countercurrent chromatography, Kuang P1, Food Chem, 2013 Jan 15; 136 (2): 309-15.).

또한, 대한민국 등록특허 제10-1028865호, 제10-1028864호에는 무의 가수분해물 또는 배무채의 가수분해물을 원심분리하여 수득한 상등액을 액체-액체식 추출법, 고체상 추출법을 이용하여 무 또는 배무채로부터 설포라핀을 분리하는 방법이 기재되어 있다. 하지만, 이 또한 공정이 복잡하며, 무씨가 아닌 무 또는 배무채로부터 설포라핀을 추출하는 방법이다.In addition, Korean Patent Nos. 10-1028865 and 10-1028864 disclose that the supernatant obtained by centrifuging the hydrolyzate of radish hydrolyzate or radish hydrolyzate is subjected to liquid-liquid extraction or solid-phase extraction, A method for separating sulforaphane from a sulforaphane is disclosed. However, this is also a complicated process, and is a method of extracting sulfolane from non-mucilage or non-mucilage.

본 발명은 무씨로부터 설포라핀을 효율적으로 추출할 수 있으며, 안전하고 간편한 공정으로 식품산업에 적용할 수 있는 무씨 추출물의 제조방법 및 이로부터 수득된 무씨 추출물을 제공하는 것을 목적으로 한다. It is an object of the present invention to provide a method for preparing a radish extract which can be efficiently extracted from mucus and can be applied to the food industry by a safe and simple process and a radish extract obtained therefrom.

또한, 본 발명은 무씨 5~40%(v/v) 에탄올 추출물 함유하는 비만, 당뇨, 지방간 개선, 예방, 치료용 식품 조성물, 약학 조성물, 동물용 의약품을 제공하는 것을 목적으로 한다.It is still another object of the present invention to provide a food composition, a pharmaceutical composition, and an animal medicine for obesity, diabetes, fatty liver improvement, prevention and treatment, containing 5 to 40% (v / v) ethanol extract of Cordyria.

상기 목적을 달성하기 위하여, 본 발명은 제1형태로 무씨에 추출 용매로 5~40%(v/v) 에탄올을 첨가하여 추출하는 것을 특징으로 하는 무씨 추출물의 제조방법을 제공한다.In order to achieve the above object, the present invention provides a method for preparing a radish extract, which comprises extracting 5 to 40% (v / v) ethanol as an extraction solvent in a first form of the present invention.

본 발명에 있어서, 상기 추출은 바람직하게 침지 추출일 수 있다.In the present invention, the extraction may be preferably an immersion extraction.

본 발명에 있어서, 상기 추출 용매는 바람직하게 5~10%(v/v) 에탄올일 수 있다.In the present invention, the extraction solvent may preferably be 5-10% (v / v) ethanol.

본 발명에 있어서, 상기 추출은 바람직하게 35~45℃의 온도로 10~15시간 동안 수행되는 것일 수 있다.In the present invention, the extraction may preferably be performed at a temperature of 35 to 45 DEG C for 10 to 15 hours.

한편, 본 발명은 제2형태로 무씨에 추출 용매로 5~40%(v/v) 에탄올을 첨가하여 추출된 것으로, 설포라핀 함량이 증가된 무씨 추출물을 제공한다.Meanwhile, the second aspect of the present invention provides a radish extract having an increased sulfolane content, which is extracted by adding 5 to 40% (v / v) ethanol as an extraction solvent to the radish.

상기 설포라핀 함량이 증가된 무씨 추출물의 설포라핀 함량은 바람직하게 추출물 중, 추출물 전체 고형분 1 g 대비 최소 18.36 mg일 수 있다.The sulfolane content of the radish extract with increased sulfolane content may preferably be at least 18.36 mg as compared to 1 g of the total solids in the extract.

한편, 본 발명은 제3형태로 무씨에 추출 용매로 5~40%(v/v) 에탄올을 첨가하여 추출한 추출물을 함유하는 비만 개선용 식품 조성물, 비만 예방 또는 치료용 약학 조성물 또는 비만 예방 또는 치료용 동물용 의약품 조성물을 제공한다.Meanwhile, the third aspect of the present invention is a food composition for improving obesity containing an extract obtained by adding 5 to 40% (v / v) ethanol as an extraction solvent to an alcoholic beverage, a pharmaceutical composition for preventing or treating obesity, An animal pharmaceutical composition is provided.

또한, 본 발명은 제4형태로 무씨에 추출 용매로 5~40%(v/v) 에탄올을 첨가하여 추출한 추출물을 함유하는 당뇨 개선용 식품 조성물, 당뇨 예방 또는 치료용 약학 조성물, 당뇨 예방 또는 치료용 동물용 의약품 조성물을 제공한다.The present invention also provides a food composition for improving diabetes, comprising a extract obtained by adding 5 to 40% (v / v) ethanol as an extraction solvent to an alcoholic beverage, a pharmaceutical composition for preventing or treating diabetes, An animal pharmaceutical composition is provided.

또한, 본 발명은 제5형태로 무씨에 추출 용매로 5~40%(v/v) 에탄올을 첨가하여 추출한 추출물을 함유하는 지방간 개선용 식품 조성물, 지방간 예방 또는 치료용 약학 조성물, 지방간 예방 또는 치료용 동물용 의약품 조성물을 제공한다.The fifth aspect of the present invention is a food composition for improving fatty liver comprising an extract obtained by adding 5 to 40% (v / v) ethanol as an extraction solvent to an alcoholic beverage, a pharmaceutical composition for prevention or treatment of fatty liver, An animal pharmaceutical composition is provided.

본 발명은 5~40%(v/v) 에탄올을 추출 용매로 사용하여 무씨로부터 설포라핀을 고수율로 추출할 수 있으며, 무씨 추출물의 제조공정이 간단하고 안정성이 우수하여 식품산업에 적용이 가능하다.The present invention can extract sulforaphin in high yield from mucilage using 5 ~ 40% (v / v) ethanol as an extraction solvent, and is easy to manufacture and has excellent stability in the food industry. It is possible.

또한, 본 발명은 무씨에 추출 용매로 5~40%(v/v) 에탄올을 첨가하여 추출된 추출물을 함유하여 우수한 비만, 당뇨, 지방간 개선, 예방, 치료 효과를 발휘하는 조성물을 제공할 수 있다. 본 발명의 무씨 5~40%(v/v) 에탄올 추출물은 무씨로부터 다양한 활성성분이 추출되어 이의 복합적 상승효과로 더욱 우수한 비만, 당뇨, 지방간 개선, 예방, 치료 효과를 발휘한다. In addition, the present invention can provide a composition exhibiting excellent obesity, diabetes, fatty liver improvement, prevention, and therapeutic effect by containing extract extracted from 5 to 40% (v / v) ethanol as an extraction solvent . The 5 to 40% (v / v) ethanol extract of the present invention extracts various active ingredients from mucilaginus, and exhibits a more excellent effect of obesity, diabetes, fatty liver improvement, prevention and treatment by its complex synergistic effect.

도 1은 설포라핀 표준품 및 표준곡선이다. 'SFEN'은 설포라핀을 의미한다.
도 2는 용매 조건에 따른 추출물의 추출물 중량, 추출물 내 설포라핀 농도, 총 설포라핀의 중량을 측정한 결과이다.
도 3은 10% 발효주정 무씨 추출물의 급여에 따른 체중 증가량 변화를 확인한 결과이다.
도 4는 10% 발효주정 무씨 추출물의 급여에 따른 사료 섭취량을 확인한 결과이다.
도 5는 10% 발효주정 무씨 추출물의 급여에 따른 공복 혈당 변화를 확인한 결과이다.
도 6은 10% 발효주정 무씨 추출물의 급여에 따른 공복 인슐린의 변화를 확인한 결과이다.
도 7은 10% 발효주정 무씨 추출물의 인슐린 민감도 개선 효과를 확인한 결과이다.
도 8은 10% 발효주정 무씨 추출물의 급여에 따른 혈당 조절 효과를 확인한 결과이다.
도 9는 쥐에게 10% 발효주정 무씨 추출물을 급여 후, 시간에 따른 혈당 곡선하면적을 계산한 결과이다.
도 10은 10% 발효주정 무씨 추출물 급여에 따른 간 무게 변화를 확인 결과이다.
도 11은 10% 발효주정 무씨 추출물 급여에 따른 간 내 지방구 감소 효과를 확인한 결과이다.
도 12는 10% 발효주정 무씨 추출물 급여에 따른 간 내 AST 수준을 확인한 결과이다.
도 13은 10% 발효주정 무씨 추출물 급여에 따른 간 내 ALT 수준을 확인한 결과이다.
도 14는 10% 발효주정 무씨 추출물의 급여에 따른 간 지질의 양을 측정한 결과이다.
도 15는 10% 발효주정 무씨 추출물의 급여에 따른 간 내 총 중성지방 양을 측정한 결과이다.
도 16은 10% 발효주정 무씨 추출물의 급여에 따른 간 내 총 콜레스테롤 양을 측정한 결과이다.
Figure 1 is a sulforapin standard and a standard curve. 'SFEN' means sulfolapin.
FIG. 2 shows the results of measuring the weight of the extract, the concentration of the sulfolane in the extract, and the weight of the total sulfolane according to the solvent conditions.
FIG. 3 shows the results of confirming the change in body weight gain due to the addition of 10% fermented alcoholic extract of Rumex.
FIG. 4 shows the results of the feed intake according to the feeding of 10% fermented mugwort extract.
FIG. 5 shows the results of confirming fasting blood glucose changes according to the feeding of 10% fermented alcoholic beverage extract.
FIG. 6 shows the results of confirming changes in fasting insulin according to the feeding of 10% fermented mugwort extract.
FIG. 7 shows the results of confirming the insulin sensitivity improving effect of the 10% fermented mugwort seed extract.
FIG. 8 shows the results of confirming the effect of controlling the blood glucose level by feeding 10% fermented mugwort extract.
FIG. 9 shows the result of calculating the blood glucose curve backward time after feeding 10% fermented mugwort extract to rats.
FIG. 10 shows the result of liver weight change according to the addition of 10% fermented mugwort extract.
FIG. 11 shows the results of confirming the effect of the 10% fermented mugwort extract on liver lipid reduction.
FIG. 12 shows the results of confirming the intra-liver AST level according to the 10% fermented alcoholic beverage extract.
FIG. 13 shows the results of confirming the level of ALT in liver according to the feeding of 10% fermented alcoholic beverages.
FIG. 14 shows the result of measurement of the amount of liver lipid according to the feeding of the 10% fermented alcoholic extract.
FIG. 15 shows the results of measurement of the total amount of triglyceride in liver according to the feeding of 10% fermented alcoholic extract of fermented rice.
FIG. 16 shows the results of measurement of the total cholesterol content in the liver according to the feeding of 10% fermented alcoholic extract of fermented rice.

본 발명의 발명자들은 이전 연구를 통해 무씨(내복자), 배무채 등의 십자화가 식물에는 글루코시놀레이트 성분들이 존재하며, 이 중 다량 함유되어 있는 파이토케미칼(phytochemical)인 4-메틸설포닐-3-부테닐 이소티오시아네이트(4-methylsulfinyl-3-butenyl isothiocyantate) 또는 4-메틸설포닐-3-부테닐 이소티오시아네이트 전구체 또는 유도체가 비만 예방 효과가 있음을 확인하였다 (대한민국 등록특허 제10-1213065).The inventors of the present invention have found that glucosinolate components are present in cruciferous plants such as mucilage (oboe) and rhizome, and phytochemicals such as 4-methylsulfonyl- It was confirmed that 4-methylsulfinyl-3-butenyl isothiocyanate or 4-methylsulfonyl-3-butenyl isothiocyanate precursor or derivative was effective for preventing obesity 10-1213065).

이로부터, 본 발명의 발명자들은 글루코시놀레이트의 일종인 설포라핀(sulforaphene, SFEN)에 주목하게 되었고, 본 발명에서는 무씨(내복자)로부터 설포라핀을 효율적으로 추출할 수 있는 무씨 추출물 제조 공정을 개발하였다.Accordingly, the inventors of the present invention have paid attention to sulforaphene (SFEN), which is a kind of glucosinolate. In the present invention, it is possible to efficiently produce sulforaphane from a rice bran Process.

종래에는 무씨로부터 설포라핀을 단순 분리하는 기술만이 있을 뿐, 무씨로부터 설포라핀을 고수율로 추출할 수 있으며, 공정이 간편하고 안전하여 식품산업에 적용이 가능한 기술은 개시된 바 없다.Conventionally, there is only a technology for simply separating sulforaphin from mucus, a technique for extracting sulforaphin from a mucilage at a high yield, and a simple and safe process that can be applied to the food industry have not been disclosed.

본 발명에 의할 경우, 무씨에 추출 용매로 5~40%(v/v) 에탄올을 첨가하여 추출함으로써 설포라핀이 다량 함유된 무씨 추출물을 수득할 수 있다. 특히, 5~10%(v/v) 에탄올을 추출 용매로 사용하는 경우 추출되는 설포라핀의 양이 현저히 높다. 아래 실시예에 의하면, 상기 범위를 벗어나는 에탄올 수용액, 물 또는 초산 에틸을 추출 용매로 사용하는 경우 설포라핀이 거의 추출되지 않거나, 추출량이 매우 낮다. In accordance with the present invention, a radish extract containing a large amount of sulfolapin can be obtained by adding 5 to 40% (v / v) ethanol to an extractor as an extraction solvent. Especially, when 5 ~ 10% (v / v) ethanol is used as the extraction solvent, the amount of sulfolapin to be extracted is remarkably high. According to the following examples, when an aqueous solution of ethanol, water or ethyl acetate deviating from the above range is used as an extraction solvent, sulfolapin is hardly extracted or the extraction amount is very low.

이때, 상기 에탄올은, 무수에탄올, 발효주정을 포함할 수 있으며, 식용 추출물을 제조하는 경우 에탄올은 발효주정인 것이 바람직하다.At this time, the ethanol may include anhydrous ethanol and fermented alcohol, and in the case of producing the edible alcohol, ethanol is preferably a fermentation alcohol.

한편, 상기 추출은, 바람직하게 침지 추출인 것이 좋다. 열수 추출시 무씨 내에 있는 미로시나아제의 활성을 제한할 수 있기 때문에 온도의 상승이 없는 추출 방법을 이용하는 것이다.On the other hand, the above extraction is preferably an immersion extraction. Since the activity of myosinase in Mo is limited during the extraction of hot water, the extraction method without elevation of temperature is used.

통상적으로 식용 추출물을 제조 시, 환류(refluxing) 추출법을 주로 사용하지만, 환류 추출법은 추출시 용매의 온도가 상승할 수 있으며, 침지 추출에 비해 공정이 복잡하다.The reflux extraction method is generally used for preparing edible extracts, but the reflux extraction method can increase the temperature of the solvent during extraction and complicate the process compared to the immersion extraction.

또한, 상기 추출은, 바람직하게 35~45℃의 온도에서 10~15시간 동안 수행되는 것이 좋다. 35℃ 미만이면 설포라핀이 충분히 추출되지 못하며, 45℃ 초과에서는 무씨 내에 있는 효소인 미로시나아제(myrosinase)(활성온도: 37~42℃)의 작용에 제한이 있기 때문이다. 즉, 상기 추출 온도를 벗어나면 설포라핀이 다량 함유된 내복자 추출물을 제조할 수 없는 것이다.The extraction is preferably carried out at a temperature of 35 to 45 DEG C for 10 to 15 hours. If the temperature is lower than 35 ° C, the sulfo-fins can not be extracted sufficiently. If the temperature exceeds 45 ° C, the action of myrosinase (activity temperature: 37-42 ° C) That is, when the temperature is above the extraction temperature, it is not possible to produce an extract of Alnus japonica containing a large amount of sulfolapin.

한편, 본 발명은 무씨 분쇄물에 추출 용매로 5~40%(v/v) 에탄올을 첨가하여 추출 통해 얻어진 설포라핀 함량이 증가된 무씨 추출물을 제공한다. 본 발명의 무씨 추출물은 추출물 전체 고형분 1 g 대비 최소 18.36 mg의 설포라핀을 함유한다. 본 발명의 무씨 추출물은 추출 용매로 에탄올을 사용하였기 때문에 바로 식품 소재로서 활용이 가능하며, 상기와 같이 얻어진 무씨 추출물은 설포라핀을 다량 함유하고 있어 다양한 약리효과를 기대할 수 있다. Meanwhile, the present invention provides a radish extract having increased sulforaphin content obtained by adding 5 to 40% (v / v) ethanol as an extraction solvent to pulverized muffins. The radish extract of the present invention contains at least 18.36 mg of sulforaphin per gram of the total solids of the extract. Since the radish extract of the present invention uses ethanol as an extraction solvent, it can be used directly as a food material. The thus obtained radish extract contains a large amount of sulfolapine, and thus various pharmacological effects can be expected.

한편, 본 발명은 무씨 5~40%(v/v) 에탄올 추출물 함유하는 비만, 당뇨, 지방간 개선, 예방, 치료용 식품 조성물, 약학 조성물 또는 동물용 의약품을 제공한다.Meanwhile, the present invention provides a food composition, a pharmaceutical composition, or an animal medicine for obesity, diabetes, fatty liver improvement, prevention and treatment, containing 5 to 40% (v / v) ethanol extract of SiC.

종래에 무씨(내복자)는 태음조위탕이라는 한약의 한 성분으로 주로 사용되어 왔으며, 무씨 열수 추출물 형태로 복용되어 왔다. 그런데, 본 발명의 발명자들은 무씨 열수 추출물보다 '5~40%(v/v) 에탄올 수용액을 추출 용매로 한 추출물'이 무씨로부터 다양한 활성 성분이 더욱 추출되어, 그 복합적 상승효과에 의해 더욱 우수한 비만, 당뇨, 지방간 개선, 예방, 치료 효과를 발휘함을 밝혀내었다.In the past, Moo (underwear) has been mainly used as a component of Chinese herb medicine called Taeum Joywantang, and has been taken in the form of hot water extract of Mujung. However, the inventors of the present invention have found that an extract of 5 to 40% (v / v) ethanol aqueous solution as an extraction solvent, rather than a hot-water extract of Succulent extract, further extracts various active ingredients from the sucrose, , Diabetes, fatty liver improvement, prevention and treatment effects were revealed.

이때, 상기 무씨 5~40%(v/v) 에탄올 추출물은 본 발명이 속하는 기술분야에서 통상적으로 사용하는 방법에 의해 추출될 수 있으나, 바람직하게는 무씨에 5~40%(v/v) 에탄올을 첨가한 후, 35~45℃의 온도에서 10~15시간 동안 추출된 것이 좋다.At this time, the 5 to 40% (v / v) ethanol extract of the present invention can be extracted by a method commonly used in the technical field of the present invention, but preferably 5 to 40% (v / v) ethanol And then extracted at a temperature of 35 to 45 ° C for 10 to 15 hours.

또한, 상기 에탄올은, 무수에탄올, 발효주정을 포함할 수 있다. In addition, the ethanol may include anhydrous ethanol, a fermented alcohol.

또한, 상기 지방간은, 고지방식이 섭취에 의해 유발되는 비알코올성 지방간일 수 있다. In addition, the fatty liver may be a non-alcoholic fatty liver caused by ingestion of a high fat diet.

한편, 본 발명의 식품 조성물은 무씨 5~40%(v/v) 에탄올 추출물을 함유하는 것을 특징으로 하는데, 상기 무씨 추출물은 바람직하게 식품 조성물 중 0.000001~50중량% 포함되는 것이 좋다. 0.000001중량% 미만일 경우에는 그 효과가 미비하고, 50중량%를 초과하는 경우에는 사용량 대비 효과 증가가 미미하여 비경제적이다.Meanwhile, the food composition of the present invention is characterized in that it contains 5 ~ 40% (v / v) ethanol extract of Si-Cu, and the extract is preferably 0.000001 ~ 50 wt% of the food composition. When the amount is less than 0.000001% by weight, the effect is insufficient. When the amount is more than 50% by weight, the increase in the effect on the usage amount is insignificant, which is uneconomical.

한편, 본 발명의 식품 조성물은 바람직하게 육류, 곡류, 카페인 음료, 일반음료, 초콜렛, 빵류, 스넥류, 과자류, 피자, 젤리, 면류, 껌류, 아이스크림류, 알코올성 음료, 술, 비타민 복합제 및 그 밖의 건강보조식품류 중 선택되는 어느 하나인 것인 것이 좋으나, 반드시 이에 한정되는 것은 아니다.On the other hand, the food composition of the present invention is preferably used in foods, cereals, caffeinated beverages, general drinks, chocolate, breads, And supplementary foods. However, the present invention is not limited thereto.

한편, 본 발명의 약학 조성물 또는 동물 의약품 조성물은 무씨 5~40%(v/v) 에탄올 추출물을 함유하는 것을 특징으로 하는데, 상기 무씨 추출물은 예방 및 치료제의 사용방법, 복용자(동물)의 상태, 질환의 종류 및 질환의 중증 정도에 따라 바람직하게 조절하는 것이 좋다. 본 발명의 약학 조성물 또는 동물 의약품 조성물에서 무씨 추출물의 함량은 약학 조성물 또는 동물 의약품 조성물 중 0.000001~50중량% 일 수 있으나, 반드시 이에 한정되는 것은 아니다. 그러나 그 함량이 0.000001중량% 미만인 경우 효과가 미비할 수 있으며, 50중량% 초과하는 경우에는 사용량 대비 효과 상승률이 낮아 비경제적일 수 있다.Meanwhile, the pharmaceutical composition or the veterinary pharmaceutical composition of the present invention is characterized in that it contains 5 ~ 40% (v / v) ethanol extract of Si-Ca, It is preferable to control it according to the type of disease and the severity of the disease. In the pharmaceutical composition or the veterinary pharmaceutical composition of the present invention, the content of the radish extract may be 0.000001 to 50% by weight in the pharmaceutical composition or the veterinary pharmaceutical composition, but is not limited thereto. However, when the content is less than 0.000001% by weight, the effect may be insufficient. When the content is more than 50% by weight, the rate of increase of the effect relative to the amount of use may be low.

한편, 본 발명의 약학 조성물 또는 동물 의약품 조성물은 유효성분 이외에 약제학적으로 허용 가능한 담체, 희석제 또는 부형제를 더욱 포함할 수 있다. 사용가능한 담체, 부형제 또는 희석제로는, 락토즈, 덱스트로즈, 수크로즈, 솔비톨, 만니톨, 자이리톨, 에리스리톨, 말티톨, 전분, 아카시아 고무, 알지네이트, 젤라틴, 칼슘 포스페이트, 칼슘 실리케이트, 셀룰로즈, 메틸 셀룰로즈, 미정질 셀룰로즈, 폴리비닐피롤리돈, 물, 메틸하이드록시벤조에이트, 프로필하이드록시벤조에이트, 탈크, 마그네슘 스테아레이트 및 광물유가 있으며, 이들은 1종 이상 사용될 수 있다. 또한, 예방 및 치료제가 약제인 경우 충진제, 항응집제, 윤활제, 습윤제, 향료, 유화제 또는 방부제 등이 추가적으로 포함될 수 있다.Meanwhile, the pharmaceutical composition or the animal pharmaceutical composition of the present invention may further comprise a pharmaceutically acceptable carrier, diluent or excipient in addition to the active ingredient. Examples of usable carriers, excipients or diluents include lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, acacia rubber, alginate, gelatin, calcium phosphate, calcium silicate, cellulose, methylcellulose, Microcrystalline cellulose, polyvinylpyrrolidone, water, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate and mineral oil. These may be used singly or in combination. When the preventive and therapeutic agent is a pharmaceutical agent, a filler, an anticoagulant, a lubricant, a wetting agent, a flavoring agent, an emulsifying agent or an antiseptic agent may be additionally included.

한편, 본 발명의 약학 조성물 또는 동물 의약품의 제형은 사용방법에 따라 바람직한 형태일 수 있으며, 특히 포유동물에 투여된 후 활성 성분의 신속, 지속 또는 지연된 방출을 제공할 수 있도록 당업계에 공지된 방법을 채택하여 제형화 하는 것이 좋다. 구체적인 제형의 예로는 경고제(PLASTERS), 과립제(GRANULES), 로션제(LPTIONS), 리니멘트제(LINIMENTS), 리모나데제(LEMONADES), 방향수제(AROMATIC WATERS), 산제(POWDERS), 시럽제(SYRUPS), 안연고제(OPHTALMIC OINTMENTS), 액제(LIQUIDS AND SOLUTIONS), 에어로솔제(AEROSOLS), 엑스제(EXTRACTS), 엘릭실제(ELIXIRS), 연고제(OINTMENTS), 유동엑스제(FLUIDEXTRACTS), 유제(EMULSIONS), 현탁제(SUSPESIONS), 전제(DECOCTIONS), 침제(INFUSIONS), 점안제(OPHTHALMIC SOLUTIONS), 정제(TABLETS), 좌제(SUPPOSITIORIES), 주사제(INJECTIONS), 주정제(SPIRITS), 카타플라스마제(CATAPLSMA), 캅셀제(CAPSULES), 크림제(CREAMS), 트로키제(TROCHES), 틴크제(TINCTURES), 파스타제(PASTES), 환제(PILLS), 연질 또는 경질 젤라틴 캅셀 중 선택되는 어느 하나일 수 있다.On the other hand, the formulation of the pharmaceutical composition or the veterinary medicament of the present invention may be in a desirable form depending on the method of use, and may be a method known in the art so as to provide rapid, sustained or delayed release of the active ingredient after administration to a mammal To be formulated. Examples of specific formulations include PLASTERS, GRANULES, LPTIONS, LINIMENTS, LEMONADES, AROMATIC WATERS, POWDERS, Syrups SYRUPS, OPHTALMIC OINTMENTS, LIQUIDS AND SOLUTIONS, AEROSOLS, EXTRACTS, ELIXIRS, OINTMENTS, FLUIDEXTRACTS, EMULSIONS, ), Suspensions, DECOCTIONS, INFUSIONS, OPHTHALMIC SOLUTIONS, TABLETS, SUPPOSITIORIES, INJECTIONS, SPIRITS, CATAPLSMA, ), Capsules, CREAMS, TROCHES, TINCTURES, PASTES, PILLS, soft or hard gelatin capsules.

한편, 본 발명의 약학 조성물 또는 동물 의약품 조성물의 투여량은 투여방법, 복용자(동물)의 연령, 성별 및 체중, 및 질환의 중증도 등을 고려하여 결정하는 것이 좋다. 일 예로, 본 발명의 비만 예방 또는 치료용 약학 조성물은 유효성분을 기준으로 하였을 때 1일 0.1 내지 100 ㎎/㎏(체중)으로 1회 이상 투여 가능하다. 그러나 상기의 투여량은 예시하기 위한 일 예에 불과하며, 복용자(동물)의 상태에 따라 의사의 처방에 의해 변화될 수 있다.On the other hand, the dosage of the pharmaceutical composition or the animal pharmaceutical composition of the present invention is preferably determined in consideration of the administration method, the age, sex and weight of the recipient (animal), severity of the disease, and the like. For example, the pharmaceutical composition for preventing or treating obesity of the present invention can be administered at least once at a dose of 0.1 to 100 mg / kg (body weight) per day based on the active ingredient. However, the above dosage is merely an example and can be changed by a physician's prescription depending on the condition of the recipient (animal).

이하, 본 발명의 내용에 대해 하기 실시예에서 더욱 상세히 설명하지만, 본 발명의 권리범위가 하기 실시예에만 한정되는 것은 아니고, 이와 등가의 기술적 사상의 변형까지를 포함한다.Hereinafter, the contents of the present invention will be described in more detail in the following examples, but the scope of the present invention is not limited to the following examples, but includes modifications of equivalent technical ideas.

[[ 실시예Example 1:  One: 설포라핀이Sulfolafine 다량 함유된 무씨 추출물 제조] Manufacture of a large amount of radish extract]

무씨로부터 설포라핀을 최적의 수율로 추출하고자, 물, 에탄올(발효주정), 초산에틸(ethyl acetate)을 이용하여 11가지 종류의 용매를 제조하였다 (0% 발효주정, 2% 발효주정, 5% 발효주정, 10% 발효주정, 30% 발효주정, 40% 발효주정, 50% 발효주정, 70% 발효주정, '30% 발효주정+10% 초산 에틸', '30% 발효주정+50% 초산 에틸', 100% 초산 에틸). 11 kinds of solvents were prepared by using water, ethanol (fermented alcohol) and ethyl acetate (0% fermented alcohol, 2% fermented alcohol, 5% fermented alcohol, 30% Fermented Spirits, 40% Fermented Spirits, 50% Fermented Spirits, 70% Fermented Spirits, 30% Fermented Spirits, 10% Ethyl Acetate, 30% Fermented Spirits, 50% Acetic Acid Ethyl ', 100% ethyl acetate).

믹서기를 이용하여 곱게 분쇄한 무씨(내복자) 100 g에 각 용매 800 ㎖를 넣고, 40℃의 온도에서 12시간 동안 침지 추출하여 무씨 추출물을 수득하였다. 이후, 각 무씨 추출물을 농축하고, 동결건조하여 분말 형태로 만들었다.800 ml of each solvent was added to 100 g of finely ground Mucilage (innerwear) using a blender, and the mixture was immersed and extracted at a temperature of 40 캜 for 12 hours to obtain a radish extract. After that, each of the Ricinus extracts was concentrated and lyophilized to a powder form.

[[ 실험예Experimental Example 1: 무씨 추출물 추출 수율 및 무씨 추출물 내  1: Extraction yield of radish extract and extracts of radish extract 설포라핀Sulfolapin 함량 측정]  Content measurement]

상기 실시예 1에 의해 용매별로 추출된 각 무씨 추출물의 추출 수율 및 무씨 추출물 내 설포라핀의 함량을 측정하였다.The extraction yield of each of the radish extracts extracted by solvent and the content of sulforaphane in the radish extract were measured by the above Example 1.

각 무씨 추출물의 중량을 측정하여 원물에 대비하여 추출 수율을 계산하였다.The weight of each extract was measured and the extraction yield was calculated against the raw material.

각 무씨 추출물 10 mg을 취하여 60% 에탄올 용액 1 ㎖에 녹인 후 0.45 ㎛ 시린지 필터(syringe filter)로 여과하여 시험용액을 준비하였다. 설포라핀 표준품을 여러 농도(25 ppm, 50 ppm, 125 ppm, 250 ppm, 500 ppm)로 준비하여 표준용액을 준비하였다. 상기에서 준비한 시험용액과 표준용액 속의 설포라핀 함량을 HPLC 기계를 통해 정량하였으며, XDB-C18 컬럼을 사용하였다. 유동상은 물, 인산용액, 아세토니트릴의 혼합용액을 사용하였으며, 215 nm에서 신호를 검출하였다. 그 후, 표준용액의 설포라핀 농도와 피크 면적 사이에 관계식을 구하고, 시험용액을 분석하여 나온 피크 면적을 관계식에 대입하여 시험용액의 설포라핀 농도를 계산하였다(도 1 참조). 도 1은 설포라핀 표준품 및 표준곡선이다. 'SFEN'은 설포라핀을 의미한다. 10 mg of each of the radish extracts was dissolved in 1 ml of a 60% ethanol solution, and the solution was filtered through a 0.45 μm syringe filter to prepare a test solution. Sulfolapin standards were prepared at various concentrations (25 ppm, 50 ppm, 125 ppm, 250 ppm, 500 ppm) to prepare standard solutions. The content of sulfolane in the test solution and the standard solution prepared above was quantitatively determined using an HPLC machine, and an XDB-C18 column was used. The liquid phase was a mixed solution of water, phosphoric acid solution and acetonitrile, and signals were detected at 215 nm. Thereafter, the relation between the sulfolane concentration and peak area of the standard solution was determined, and the peak area obtained by analyzing the test solution was substituted into the relational expression to calculate the sulfolane concentration of the test solution (see FIG. 1). Figure 1 is a sulforapin standard and a standard curve. 'SFEN' means sulfolapin.

또한, 추출 수율과 추출물 내 설포라핀의 농도를 곱하여 같은 양의 무씨(내복자)에서 추출된 설포라핀의 총 중량을 계산하였다.Also, the total yield of sulfolapin extracted from the same amount of Sucralose (underwear) was calculated by multiplying the extraction yield by the concentration of sulfolapin in the extract.

측정결과는 도 2와 같았다. 도 2는 용매 조건에 따른 추출물의 추출물 중량, 추출물 내 설포라핀 농도, 총 설포라핀의 중량을 측정한 결과이다.The measurement results are shown in Fig. FIG. 2 shows the results of measuring the weight of the extract, the concentration of the sulfolane in the extract, and the weight of the total sulfolane according to the solvent conditions.

도 2에서 확인되는 바와 같이, 5~40% 발효주정 무씨 추출물에 함유된 총 설포라핀 중량이 190 mg 이상으로 다른 조건보다 총 설포라핀 중량이 현저하게 높음을 확인할 수 있었다. 특히, 5~10% 발효주정 용매에서 추출물 중량, 추출물 내 설포라핀 농도, 총 설포라핀 중량이 높게 나타남을 확인할 수 있었다.As can be seen in FIG. 2, the total sulfolane weight of the 5 to 40% fermented mugwort seed extract was 190 mg or more, indicating that the total sulforaphane weight was significantly higher than other conditions. Especially, it was confirmed that the weight of extract, the concentration of sulfapyrin in the extract, and the weight of total sulforaphane were high in the 5 to 10% fermentation alcohol solution.

[[ 실험예Experimental Example 2: 무씨 에탄올 추출물의 체중 조절 효능 확인] 2: Checking the efficacy of ethanol extract of mucilage on weight control]

본 실험예에서는 무씨 에탄올 추출물의 체중 조절 효능을 확인하였다.In this experimental example, the effect of controlling the weight of the ethanol extract of sucrose was confirmed.

본 발명에서는 무씨 에탄올 추출물의 체중조절 효능을 비교하기 위한 실험을 진행하였다. 쥐에 16주간 일반식이(Control Diet, CD), 고지방식이(High Fat Diet, HFD), '고지방식이+10% 발효주정 무씨 추출물 0.3% (HFD+RSEL)', '고지방식이+10% 발효주정 무씨 추출물 1.5% (HFD+RSEH)'를 급여하면서 사료를 갈아줄 때 처음 제공하는 사료의 양을 측정하고, 다음에 사료를 갈아줄 때 섭취 후 남은 사료 양을 측정하여 사료섭취량을 계산하였고, 매주 체중 변화를 관찰하였다.In the present invention, an experiment was conducted to compare the effect of ethanol extract of sucrose on body weight. Control diet (CD), high fat diet (HFD), high fat diet + 10% fermented mushroom extract 0.3% (HFD + RSEL) and high fat diet +10 % Of fermented fermented mushroom extract (HFD + RSEH) ', and when the feed is changed, the amount of feed remaining after ingestion is measured to calculate the feed intake And weekly weight changes were observed.

측정 결과, 일반식이를 급여한 쥐는 16주간 약 8 g, 고지방식이를 단독으로 급여한 쥐는 일반식이를 급여한 쥐의 체중 증가량의 약 2.5배인 20 g의 체중이 증가하였고, 고지방식이와 함께 10% 발효주정 무씨 추출물을 급여한 쥐는 고지방식이를 단독으로 급여한 쥐의 체중증가량보다 유의적으로 낮음을 확인할 수 있었다 (도 3). 도 3은 10% 발효주정 무씨 추출물의 급여에 따른 체중 증가량 변화를 확인한 결과이다.As a result, the rats fed with the general diet showed a weight increase of about 8 g for 16 weeks and the rats fed the high fat diet alone increased the weight of 20 g, which is about 2.5 times the weight gain of the rats fed the normal diet, The mice fed the 10% fermented mugwort extract showed significantly lower weight gain than rats fed the high fat diet alone (Fig. 3). FIG. 3 shows the results of confirming the change in body weight gain due to the addition of 10% fermented mugwort extract.

한편, 10% 발효주정 무씨 추출물 급여에도 사료의 섭취량에는 큰 차이가 없었다(도 4). 도 4는 10% 발효주정 무씨 추출물의 급여에 따른 사료 섭취량을 확인한 결과이다.On the other hand, there was no significant difference in the amount of feed intake between the 10% fermented fermented milk extract (Fig. 4). FIG. 4 shows the results of the feed intake according to the feeding of 10% fermented mugwort extract.

이로부터, 10% 발효주정 무씨 추출물은 식욕을 억제하는 기존의 비만 치료제와는 다른 기전을 통해 고지방식이에 의한 체중 증가 현상을 완화함을 알 수 있었다. From the results, it was found that the 10% fermented mugwort extract significantly alleviated the weight gain due to the high fat diet through a mechanism different from that of the existing obesity treatment inhibiting the appetite.

[[ 실험예Experimental Example 3: 무씨 에탄올 추출물의 공복 혈당, 공복 인슐린, 인슐린 민감도에 미치는 영향 확인] 3: Effect of ethanol extract of sucrose on fasting plasma glucose, fasting insulin and insulin sensitivity]

본 실험예에서는 무씨 에탄올 추출물의 공복 혈당, 공복 인슐린, 인슐린 민감도에 미치는 영향을 확인하였다.In this experiment, the effects of ethanol extract of sucrose on fasting plasma glucose, fasting insulin and insulin sensitivity were examined.

쥐에 12주간 일반식이(Control Diet, CD), 고지방식이(High Fat Diet, HFD), '고지방식이+10% 발효주정 무씨 추출물 0.3% (HFD+RSEL)', '고지방식이+10% 발효주정 무씨 추출물 1.5% (HFD+RSEH)'를 급여한 후 굶긴 상태에서 공복 혈당과 공복 인슐린을 측정하였다. 그 후, HOMA IR(homeostatic model assessment)을 측정하였고 HOMA-IR 계산은 아래 수학식 1과 같이 진행되었다.Control diet (CD), high fat diet (HFD), high fat diet + 10% fermented mushroom extract 0.3% (HFD + RSEL) and high fat diet +10 % Fasting glucose and 1.5% (HFD + RSEH) 'in fasting state. Fasting blood glucose and fasting insulin were measured in fasted state. Thereafter, the HOMA IR (homeostatic model assessment) was measured, and the HOMA-IR calculation was performed as shown in the following equation (1).

[수학식 1][Equation 1]

HOMA IR= fasting insulin (μU/㎖) × fasting glucose (mg/dL)/405 HOMA IR = fasting insulin (μU / ml) × fasting glucose (mg / dL) / 405

측정결과, 일반식이를 급여한 쥐에 비해 고지방식이를 단독으로 급여한 쥐는 공복 혈당이 1.5배 정도 증가하였고, 고지방식이와 함께 10% 발효주정 무씨 추출물을 급여한 쥐의 공복 혈당은 고지방식이를 단독으로 급여한 쥐에 비해 감소하는 경향을 나타내었다 (도 5). 도 5는 10% 발효주정 무씨 추출물의 급여에 따른 공복 혈당 변화를 확인한 결과이다.As a result, fasting blood glucose level was 1.5 times higher in rats fed high fat diets than high fat diet fed rats, and fasting blood glucose levels in rats fed with 10% (Fig. 5). As shown in Fig. FIG. 5 shows the results of confirming fasting blood glucose changes according to the feeding of 10% fermented alcoholic beverage extract.

또한, 고지방식이와 함께 10% 발효주정 무씨 추출물을 급여한 쥐의 공복 인슐린 역시 고지방식이를 단독으로 급여한 쥐에 비해 감소하는 경향을 나타내었다(도 6). 도 6은 10% 발효주정 무씨 추출물의 급여에 따른 공복 인슐린의 변화를 확인한 결과이다.In addition, the fasting insulin of the rats fed the 10% fermented mugwort extract also showed a tendency to decrease compared with the rats fed the high fat diet alone (Fig. 6). FIG. 6 shows the results of confirming changes in fasting insulin according to the feeding of 10% fermented mugwort extract.

또한, HOMA IR 측정결과, 고지방식이에 10% 발효주정 무씨 추출물 고농도 투여군에서 유의적으로 인슐린 민감도를 개선시키는 것을 확인할 수 있었다 (도 7). 도 7은 10% 발효주정 무씨 추출물의 인슐린 민감도 개선 효과를 확인한 결과이다.In addition, as a result of the HOMA IR measurement, it was confirmed that the high-fat diet improves the insulin sensitivity significantly in the high-dose group of 10% fermented rumen extract (FIG. 7). FIG. 7 shows the results of confirming the insulin sensitivity improving effect of the 10% fermented mugwort seed extract.

[[ 실험예Experimental Example 4: 무씨 에탄올 추출물의 혈당 개선 효능 확인] 4: Confirmation of blood sugar-improving effect of ethanol extract of mucilage]

본 실험예에서는 무씨 에탄올 추출물의 혈당 개선 효능을 확인하였다.In this experimental example, the effect of improving the blood glucose level of the ethanol extract of sucrose was confirmed.

쥐에 14주간 일반식이(Control Diet, CD), 고지방식이(High Fat Diet, HFD), '고지방식이+10% 발효주정 무씨 추출물 0.3% (HFD+RSEL)', '고지방식이+10% 발효주정 무씨 추출물 1.5% (HFD+RSEH)'를 급여한 후, 16시간 동안 굶긴 상태에서 당부하 시험을 수행하였다. The control diet (CD), high fat diet (HFD), high fat diet + 10% fermented mushroom extract 0.3% (HFD + RSEL) and high fat diet +10 % Fermented mugwort extract (HFD + RSEH) ', and then starved for 16 hours.

쥐의 복강에 일정량의 포도당을 2 g/kg b.w.으로 주입한 후 시간에 따른 혈당의 변화를 관찰하였다. 또한, 0~120분 동안 혈당 변화에 따른 면적(Area under curve)를 계산하였다.A dose of 2 g / kg b.w. of glucose was injected into the abdominal cavity of the rats. The area under curve was calculated from 0 to 120 minutes.

확인결과, 일반식이를 급여한 쥐는 혈당이 조금 올라갔다가 금방 떨어졌지만, 고지방식이를 급여한 쥐는 혈당의 증가폭이 일반식이를 급여한 쥐보다 유의적으로 크며 잘 떨어지지 않음을 확인할 수 있었고, 고지방식이와 함께 10% 발효주정 무씨 추출물을 급여한 쥐는 고지방식이만 급여한 쥐에 비해 혈당의 증가폭도 작았으며, 혈당이 떨어지는 속도도 빠름을 확인할 수 있었다 (도 8, 도 9). 도 8은 10% 발효주정 무씨 추출물의 급여에 따른 혈당 조절 효과를 확인한 결과이고, 도 9는 쥐에게 10% 발효주정 무씨 추출물을 급여 후, 시간에 따른 혈당 곡선하면적을 계산한 결과이다.As a result, the rats fed with the normal diet showed a slight increase in blood glucose level but fell off immediately. However, the rats fed the high fat diet had significantly higher blood glucose levels than the rats fed the normal diet, In addition, the rats fed the 10% fermented mugwort extract showed a smaller increase in blood glucose and a lower rate of blood glucose lowering than rats fed the high fat diet (FIGS. 8 and 9). FIG. 8 is a graph showing the effect of the 10% fermented fermented mugwort extract on the blood glucose control effect, and FIG. 9 is a graph showing the blood glucose curves obtained after feeding 10% fermented mugwort extract to rats.

[[ 실험예Experimental Example 5: 무씨 에탄올 추출물의  5: Ethanol extract of mucilage 비알콜성Non-alcoholic 지방간 개선 효능 확인] Checking the efficacy of fatty liver improvement]

본 실험예에서는 무씨 에탄올 추출물이 고지방식이 섭취로 야기되는 비알콜성 지방간 개선 효능을 확인하였다.In this experimental example, the non-alcoholic fatty liver improvement effect caused by the ingestion of the high-fat type ethanol-ethanol extract was confirmed.

쥐에 16주간 일반식이(Control Diet, CD), 고지방식이(High Fat Diet, HFD), '고지방식이+10% 발효주정 무씨 추출물 0.3% (HFD+RSEL)', '고지방식이+10% 발효주정 무씨 추출물 1.5% (HFD+RSEH)'를 급여한 후, 각 쥐의 간을 적출하여 실험을 수행하였다.Control diet (CD), high fat diet (HFD), high fat diet + 10% fermented mushroom extract 0.3% (HFD + RSEL) and high fat diet +10 % HFD + RSEH ', and then liver was extracted from each rat.

(1) 간 무게 측정(1) Liver weighing

간 무게 측정결과, 고지방식이를 단독으로 급여한 쥐는 일반식이를 급여한 쥐보다 간 무게가 유의적으로 증가하였고, 고지방식이와 함께 10% 발효주정 무씨 추출물을 급여한 쥐의 간 무게는 고지방식이를 단독으로 급여한 쥐의 간 무게보다 유의적으로 낮음을 확인할 수 있었다 (도 10). 도 10은 10% 발효주정 무씨 추출물 급여에 따른 간 무게 변화를 확인 결과이다.As a result of liver weighing, the liver weight of the rats fed the high fat diet alone was significantly higher than that of the rats fed the normal diet, and the liver weight of the rats fed the 10% And the liver weight of the mice fed alone was significantly lower than the liver weight of the fed mice (Fig. 10). FIG. 10 shows the result of liver weight change according to the addition of 10% fermented mugwort extract.

(2) 간 내 지방구 감소 효과 확인(2) Confirming the effect of reducing the fat in the liver

병리조직학적 관찰을 위해 적출된 간은 즉시 4% 포르말린(formalin) 용액에 충분히 고정한 후 수세, 탈수, 투명, 침투, 포매 과정을 거쳐 파라핀(paraffin) 블록을 제작하였다. 제작한 블록은 절편으로 만들어 'H&E(hematoxylin-eosin) staining'을 시행한 후 광학현미경으로 관찰하였다.For histologic examination, the liver was immediately fixed in 4% formalin solution, and then paraffin block was prepared by washing, dehydrating, transparency, infiltration and embedding process. The prepared block was sectioned and stained with H & E (hematoxylin-eosin) and observed with an optical microscope.

간 조직을 'H&E staining' 처리한 결과, 고지방식이 군에서 지방 축적을 관찰할 수 있었으나, 10% 발효주정 무씨 추출물을 급여했을 때 간에 축적되어 있던 지방구들이 눈에 띄게 감소했음을 확인할 수 있었다 (도 11). 도 11은 10% 발효주정 무씨 추출물 급여에 따른 간 내 지방구 감소 효과를 확인한 결과이다.As a result of H & E staining of liver tissues, fat accumulation was observed in the high fat diet group, but fat fat accumulation in the liver was remarkably decreased when 10% fermented milk fat extract was fed ( 11). FIG. 11 shows the results of confirming the effect of the 10% fermented mugwort extract on liver lipid reduction.

(3) 혈청 생화학적 지표성분 분석(3) Analysis of serum biochemical indicators

AST(aspartate aminotransferase)와 ALT(alanine aminotransferase) 수준을 측정한 결과, 고지방식이군에 비해 10% 발효주정 무씨 추출물을 급여했을 때 AST와 ALT 수준이 모두 유의적으로 감소하며 간 손상을 개선하는 효과를 발휘함을 확인할 수 있었다 (도 12, 도 13). 도 12는 10% 발효주정 무씨 추출물 처리에 따른 간 내 AST 수준을 확인한 결과이고, 도 13은 10% 발효주정 무씨 추출물 처리에 따른 간 내 ALT 수준을 확인한 결과이다.The AST and alanine aminotransferase (ALT) levels were significantly lower in the AST and ALT levels compared to the high - fat diet group. (Fig. 12, Fig. 13). FIG. 12 shows the results of confirming the AST levels in the liver according to the treatment with 10% fermented alcoholic beverages and FIG. 13 shows the levels of ALT in the liver according to the treatment with 10% fermented alcoholic beverages.

(4) 간 조직의 지질분석(4) lipid analysis of liver tissue

간 조직의 지질분석을 위해 간 조직 250 mg에 3 M CaCl2 용액을 1 ㎖ 첨가하여 호모게나이저(homogenizer)로 마쇄한 후, Folch 용액(chloroform: methanol 혼합액(2:1, v/v))을 10 ㎖로 정용한 다음 정치시켜 지질을 추출하였고, 후드에서 유기 용매를 충분히 날리고 남은 순수 지질을 트리톤:에탄올 혼합액(triton: ethanol=1:3, v/v) 1 ㎖에 처리하여 충분히 녹여준 샘플을 사용하였다. 간 조직의 총 중성지방(Triglyceride, TG) 과 총 콜레스테롤은(Total Cholesterol, TC) 각각 TG 및 TC 측정용 상업 키트(kit)를 사용하여 분석하였다. For lipid analysis of hepatic tissues, 1 ml of 3 M CaCl 2 solution was added to 250 mg of liver tissue, and homogenized with a homogenizer. Folch solution (chloroform: methanol mixture (2: 1, v / v) The lipids were extracted from the hood by thoroughly draining the organic solvent, and the remaining pure lipid was treated with 1 ml of a mixture of triton: ethanol (1: 3, v / v) Were used. The total triglyceride (TG) and total cholesterol (TC) of liver tissues were analyzed by using a commercial kit for TG and TC measurement, respectively.

간의 지질, 총 중성지방, 총 콜레스테롤 양을 측정한 결과, 고지방식이만을 급여한 쥐에 비해 고지방식이와 함께 10% 발효주정 무씨 추출물을 급여한 쥐에서 간 지질, 중성지방, 총콜레스테롤이 모두 유의적으로 감소함을 확인할 수 있었다 (도 14 내지 16).Liver lipid, total triglyceride, total cholesterol, liver lipid, triglyceride, and total cholesterol were significantly higher in the rats fed the 10% (Figs. 14 to 16).

도 14는 10% 발효주정 무씨 추출물의 급여에 따른 간 지질의 양을 측정한 결과이고, 도 15는 10% 발효주정 무씨 추출물의 급여에 따른 간 내 총 중성지방 양을 측정한 결과이며, 도 16은 10% 발효주정 무씨 추출물의 급여에 따른 간 내 총 콜레스테롤 양을 측정한 결과이다.FIG. 14 shows the result of measuring the amount of liver lipid according to the feeding of the 10% fermented fermented mugwort extract, FIG. 15 shows the result of measuring the total amount of triglyceride in the liver according to the feeding of 10% fermented fermented mugwort extract, Is the result of measuring the total cholesterol content of liver according to the feeding of 10% fermented mugwort extract.

[제형예 1: 비만 개선용 식품 조성물 제조] [Formulation Example 1: Preparation of food composition for obesity improvement]

본 제형예에서는 하기와 같이 실시예 1에서 제조한 10%(v/v) 발효주정 무씨 추출물을 함유하는 비만 개선용 식품 조성물을 제조하였다.In the present formulation example, an obesity-improving food composition containing the 10% (v / v) fermented mugwort seed extract prepared in Example 1 was prepared as follows.

(1) 비스켓 제조(1) biscuit manufacture

박력 1급 25.59중량%, 중력 1급 22.22중량%, 정백당 4.80중량%, 식염 0.73중량%, 포도당 0.78중량%, 팜쇼트닝 11.78중량%, 암모니움 1.54중량%, 중조 0.17중량%, 중아황산나트륨 0.16중량%, 쌀가루 1.45중량%, 비타민 B1 0.0001중량%, 비타민 B2 0.0001중량%, 밀크향 0.04중량%, 물 20.6998중량%, 전지분유 1.16중량%, 대용분유 0.29중량%, 제일인산칼슘 0.03중량%, 살포염 0.29중량% 및 분무유 7.27중량%와 무씨 추출물 1중량%를 배합하여 통상의 방법으로 비스킷을 제조하였다.By weight of starch, 0.77% by weight of glucose, 0.78% by weight of glucose, 11.78% by weight of palm shortening, 1.54% by weight of ammonia, 0.17% by weight of sodium bicarbonate, 0.16% by weight of sodium bisulfite 1.45% by weight of rice flour, 0.0001% by weight of vitamin B1, 0.0001% by weight of vitamin B2, 0.04% by weight of milk fractions, 20.6998% by weight of water, 1.16% by weight of whole milk powder, 0.29% by weight of substitute milk powder, 0.29% by weight of salt and 7.27% by weight of spray oil and 1% by weight of the extract of Radix seed were mixed to prepare a biscuit by a conventional method.

(2) 건강음료 제조(2) Health drinks manufacturing

꿀 0.26중량%, 치옥토산아미드 0.0002중량%, 니코틴산아미드 0.0004중량%, 염산리보플라빈나트륨 0.0001중량%, 염산피리독신 0.0001중량%, 이노시톨 0.001중량%, 오르트산 0.002중량%, 물 98.7362중량% 및 무씨 추출물 1중량%를 배합하여 통상의 방법으로 건강 음료를 제조하였다.0.2% by weight of honey, 0.0002% by weight of chitosanic acid amide, 0.0004% by weight of nicotinic acid amide, 0.0001% by weight of riboflavin sodium chloride, 0.0001% by weight of pyridoxine hydrochloride, 0.001% by weight of inositol, 0.002% by weight of orthoacetic acid, 98.7362% 1% by weight was added to prepare a health drink.

(3) 건강보조식품 제조(3) health supplement manufacturing

스피루리나 55중량%, 구아검효소 분해물 10중량%, 비타민 B1 염산염 0.01중량%, 비타민 B6 염산염 0.01중량%, DL-메티오닌 0.23중량%, 스테아린산 마그네슘 0.7중량%, 유당 22.2중량% 및 옥수수전분 1.85중량%와 무씨 추출물 10중량%를 배합하여 통상의 방법으로 정제형 건강보조식품을 제조하였다.A mixture of 55% by weight of spirulina, 10% by weight of guar gum enzyme hydrolyzate, 0.01% by weight of vitamin B1 hydrochloride, 0.01% by weight of vitamin B6 hydrochloride, 0.23% by weight of DL-methionine, 0.7% by weight of magnesium stearate, And 10% by weight of the radish extract were blended to prepare a refillable health supplement food according to a conventional method.

[제형예 2: 비만 예방 또는 치료용 약학 조성물 제조][Formulation Example 2: Preparation of a pharmaceutical composition for preventing or treating obesity]

본 제형예에서는 하기와 같이 실시예 1에서 제조한 10%(v/v) 발효주정 무씨 추출물을 함유하는 비만 예방 또는 치료용 약학 조성물을 제조하였다.In this Formulation Example, a pharmaceutical composition for preventing or treating obesity containing the 10% (v / v) fermented mugwort seed extract prepared in Example 1 was prepared as follows.

(1) 산제 제조(1) Manufacture of powders

무씨 추출물 2 g에 유당 1 g을 혼합하고, 기밀포에 충진하여 산제를 제조하였다.2 g of the radish extract was mixed with 1 g of lactose and filled in an airtight container to prepare a powder.

(2) 정제 제조(2) Preparation of tablets

무씨 추출물 100 ㎎, 옥수수전분 100 ㎎, 유당 100 ㎎ 및 스테아린산 마그네슘 2 ㎎을 혼합한 후 통상의 정제 제조방법에 따라 타정하여 정제를 제조하였다.100 mg of the radish extract, 100 mg of the corn starch, 100 mg of the lactose and 2 mg of the magnesium stearate were mixed and tableted according to a conventional tablet preparation method.

(3) 캡슐제 제조(3) Manufacture of capsules

무씨 추출물 100 ㎎, 옥수수전분 100 ㎎, 유당 100 ㎎ 및 스테아린산 마그네슘 2 ㎎을 혼합한 후 젤라틴 캡슐에 충전하여 캡슐제를 제조하였다.100 mg of radish extract, 100 mg of corn starch, 100 mg of lactose and 2 mg of magnesium stearate were mixed and filled in gelatin capsules to prepare capsules.

(4) 주사제 제조(4) Injection preparation

무씨 추출물 100 ㎎에 주사용 증류수 적량을 가하여 용해시키고, pH를 약 7.5로 조절한 다음 2 ㎖ 용량의 앰플에 충진 및 멸균시하여 주사제를 제조하였다.100 mg of the radish extract was dissolved in an appropriate amount of distilled water for injection and the pH was adjusted to about 7.5. Then, the solution was filled and sterilized in a 2 ml capacity ampoule to prepare an injection.

[제형예 3: 비만 예방 또는 치료용 동물용 의약품 제조][Formulation Example 3: Preparation of animal drugs for prevention or treatment of obesity]

본 제형예에서는 하기와 같이 실시예 1에서 제조한 10%(v/v) 발효주정 무씨 추출물을 함유하는 비만 예방 또는 치료용 동물 의약품을 제조하였다.In the present formulation example, an animal drug for the prevention or treatment of obesity containing the 10% (v / v) fermented mugwort seed extract prepared in Example 1 was prepared as follows.

(1) 정제 제조(1) Preparation of tablets

무씨 추출물 100 ㎎에 단백질 혼합물 100 ㎎, 말분 100 ㎎을 혼합한 후 통상의 정제 제조방법에 따라 타정하여 정제를 제조하였다.100 mg of the radish extract was mixed with 100 mg of the protein mixture and 100 mg of the endosperm, and the tablets were prepared by tableting according to a conventional preparation method.

(2) 주사제 제조(2) Injection preparation

무씨 추출물 100 ㎎에 주사용 증류수 적량을 가하여 용해시키고, pH를 약 7.5로 조절한 다음 2 ㎖ 용량의 앰플에 충진 및 멸균시 하여 주사제를 제조하였다.100 mg of the radish extract was dissolved in an appropriate amount of distilled water for injection and the pH was adjusted to about 7.5. Then, the solution was filled and sterilized in a 2 ml capacity ampoule to prepare an injection.

[제형예 4: 당뇨 개선용 식품 조성물 제조] [Formulation Example 4: Preparation of food composition for diabetic improvement]

본 제형예에서는 하기와 같이 실시예 1에서 제조한 10%(v/v) 발효주정 무씨 추출물을 함유하는 당뇨 개선용 식품 조성물을 제조하였다.In this Formulation Example, a diabetic food composition containing the 10% (v / v) fermented mugwort extract prepared in Example 1 was prepared as follows.

(1) 비스켓 제조(1) biscuit manufacture

박력 1급 25.59중량%, 중력 1급 22.22중량%, 정백당 4.80중량%, 식염 0.73중량%, 포도당 0.78중량%, 팜쇼트닝 11.78중량%, 암모니움 1.54중량%, 중조 0.17중량%, 중아황산나트륨 0.16중량%, 쌀가루 1.45중량%, 비타민 B1 0.0001중량%, 비타민 B2 0.0001중량%, 밀크향 0.04중량%, 물 20.6998중량%, 전지분유 1.16중량%, 대용분유 0.29중량%, 제일인산칼슘 0.03중량%, 살포염 0.29중량% 및 분무유 7.27중량%와 무씨 추출물 1중량%를 배합하여 통상의 방법으로 비스킷을 제조하였다.By weight of starch, 0.77% by weight of glucose, 0.78% by weight of glucose, 11.78% by weight of palm shortening, 1.54% by weight of ammonia, 0.17% by weight of sodium bicarbonate, 0.16% by weight of sodium bisulfite 1.45% by weight of rice flour, 0.0001% by weight of vitamin B1, 0.0001% by weight of vitamin B2, 0.04% by weight of milk fractions, 20.6998% by weight of water, 1.16% by weight of whole milk powder, 0.29% by weight of substitute milk powder, 0.29% by weight of salt and 7.27% by weight of spray oil and 1% by weight of the extract of Radix seed were mixed to prepare a biscuit by a conventional method.

(2) 건강음료 제조(2) Health drinks manufacturing

꿀 0.26중량%, 치옥토산아미드 0.0002중량%, 니코틴산아미드 0.0004중량%, 염산리보플라빈나트륨 0.0001중량%, 염산피리독신 0.0001중량%, 이노시톨 0.001중량%, 오르트산 0.002중량%, 물 98.7362중량% 및 무씨 추출물 1중량%를 배합하여 통상의 방법으로 건강 음료를 제조하였다.0.2% by weight of honey, 0.0002% by weight of chitosanic acid amide, 0.0004% by weight of nicotinic acid amide, 0.0001% by weight of riboflavin sodium chloride, 0.0001% by weight of pyridoxine hydrochloride, 0.001% by weight of inositol, 0.002% by weight of orthoacetic acid, 98.7362% 1% by weight was added to prepare a health drink.

(3) 건강보조식품 제조(3) health supplement manufacturing

스피루리나 55중량%, 구아검효소 분해물 10중량%, 비타민 B1 염산염 0.01중량%, 비타민 B6 염산염 0.01중량%, DL-메티오닌 0.23중량%, 스테아린산 마그네슘 0.7중량%, 유당 22.2중량% 및 옥수수전분 1.85중량%와 무씨 추출물 10중량%를 배합하여 통상의 방법으로 정제형 건강보조식품을 제조하였다.A mixture of 55% by weight of spirulina, 10% by weight of guar gum enzyme hydrolyzate, 0.01% by weight of vitamin B1 hydrochloride, 0.01% by weight of vitamin B6 hydrochloride, 0.23% by weight of DL-methionine, 0.7% by weight of magnesium stearate, And 10% by weight of the radish extract were blended to prepare a refillable health supplement food according to a conventional method.

[제형예 5: 당뇨 예방 또는 치료용 약학 조성물 제조][Formulation Example 5: Preparation of pharmaceutical composition for prevention or treatment of diabetes]

본 제형예에서는 하기와 같이 실시예 1에서 제조한 10%(v/v) 발효주정 무씨 추출물을 함유하는 당뇨 예방 또는 치료용 약학 조성물을 제조하였다.In this Formulation Example, a pharmaceutical composition for preventing or treating diabetes containing 10% (v / v) fermented mugwort extract prepared in Example 1 was prepared as follows.

(1) 산제 제조(1) Manufacture of powders

무씨 추출물 2 g에 유당 1 g을 혼합하고, 기밀포에 충진하여 산제를 제조하였다.2 g of the radish extract was mixed with 1 g of lactose and filled in an airtight container to prepare a powder.

(2) 정제 제조(2) Preparation of tablets

무씨 추출물 100 ㎎, 옥수수전분 100 ㎎, 유당 100 ㎎ 및 스테아린산 마그네슘 2 ㎎을 혼합한 후 통상의 정제 제조방법에 따라 타정하여 정제를 제조하였다.100 mg of the radish extract, 100 mg of the corn starch, 100 mg of the lactose and 2 mg of the magnesium stearate were mixed and tableted according to a conventional tablet preparation method.

(3) 캡슐제 제조(3) Manufacture of capsules

무씨 추출물 100 ㎎, 옥수수전분 100 ㎎, 유당 100 ㎎ 및 스테아린산 마그네슘 2 ㎎을 혼합한 후 젤라틴 캡슐에 충전하여 캡슐제를 제조하였다.100 mg of radish extract, 100 mg of corn starch, 100 mg of lactose and 2 mg of magnesium stearate were mixed and filled in gelatin capsules to prepare capsules.

(4) 주사제 제조(4) Injection preparation

무씨 추출물 100 ㎎에 주사용 증류수 적량을 가하여 용해시키고, pH를 약 7.5로 조절한 다음 2 ㎖ 용량의 앰플에 충진 및 멸균시하여 주사제를 제조하였다.100 mg of the radish extract was dissolved in an appropriate amount of distilled water for injection and the pH was adjusted to about 7.5. Then, the solution was filled and sterilized in a 2 ml capacity ampoule to prepare an injection.

[제형예 6: 당뇨 예방 또는 치료용 동물용 의약품 제조][Formulation Example 6: Production of animal medicines for prevention or treatment of diabetes]

본 제형예에서는 하기와 같이 실시예 1에서 제조한 10%(v/v) 발효주정 무씨 추출물을 함유하는 당뇨 예방 또는 치료용 동물 의약품을 제조하였다.In this formulation example, an animal medicine for the prevention or treatment of diabetes containing the 10% (v / v) fermented mugwort extract prepared in Example 1 was prepared as follows.

(1) 정제 제조(1) Preparation of tablets

무씨 추출물 100 ㎎에 단백질 혼합물 100 ㎎, 말분 100 ㎎을 혼합한 후 통상의 정제 제조방법에 따라 타정하여 정제를 제조하였다.100 mg of the radish extract was mixed with 100 mg of the protein mixture and 100 mg of the endosperm, and the tablets were prepared by tableting according to a conventional preparation method.

(2) 주사제 제조(2) Injection preparation

무씨 추출물 100 ㎎에 주사용 증류수 적량을 가하여 용해시키고, pH를 약 7.5로 조절한 다음 2 ㎖ 용량의 앰플에 충진 및 멸균시 하여 주사제를 제조하였다.100 mg of the radish extract was dissolved in an appropriate amount of distilled water for injection and the pH was adjusted to about 7.5. Then, the solution was filled and sterilized in a 2 ml capacity ampoule to prepare an injection.

[[ 제형예Formulation Example 7: 지방간 개선용 식품 조성물 제조]  7: Preparation of food composition for fatty liver improvement]

본 제형예에서는 하기와 같이 실시예 1에서 제조한 10%(v/v) 발효주정 무씨 추출물을 함유하는 지방간 개선용 식품 조성물을 제조하였다.In the present formulation example, a food composition for improving fatty liver containing the 10% (v / v) fermented fermented mugwort extract prepared in Example 1 was prepared as follows.

(1) 비스켓 제조(1) biscuit manufacture

박력 1급 25.59중량%, 중력 1급 22.22중량%, 정백당 4.80중량%, 식염 0.73중량%, 포도당 0.78중량%, 팜쇼트닝 11.78중량%, 암모니움 1.54중량%, 중조 0.17중량%, 중아황산나트륨 0.16중량%, 쌀가루 1.45중량%, 비타민 B1 0.0001중량%, 비타민 B2 0.0001중량%, 밀크향 0.04중량%, 물 20.6998중량%, 전지분유 1.16중량%, 대용분유 0.29중량%, 제일인산칼슘 0.03중량%, 살포염 0.29중량% 및 분무유 7.27중량%와 무씨 추출물 1중량%를 배합하여 통상의 방법으로 비스킷을 제조하였다.By weight of starch, 0.77% by weight of glucose, 0.78% by weight of glucose, 11.78% by weight of palm shortening, 1.54% by weight of ammonia, 0.17% by weight of sodium bicarbonate, 0.16% by weight of sodium bisulfite 1.45% by weight of rice flour, 0.0001% by weight of vitamin B1, 0.0001% by weight of vitamin B2, 0.04% by weight of milk fractions, 20.6998% by weight of water, 1.16% by weight of whole milk powder, 0.29% by weight of substitute milk powder, 0.29% by weight of salt and 7.27% by weight of spray oil and 1% by weight of the extract of Radix seed were mixed to prepare a biscuit by a conventional method.

(2) 건강음료 제조(2) Health drinks manufacturing

꿀 0.26중량%, 치옥토산아미드 0.0002중량%, 니코틴산아미드 0.0004중량%, 염산리보플라빈나트륨 0.0001중량%, 염산피리독신 0.0001중량%, 이노시톨 0.001중량%, 오르트산 0.002중량%, 물 98.7362중량% 및 무씨 추출물 1중량%를 배합하여 통상의 방법으로 건강 음료를 제조하였다.0.2% by weight of honey, 0.0002% by weight of chitosanic acid amide, 0.0004% by weight of nicotinic acid amide, 0.0001% by weight of riboflavin sodium chloride, 0.0001% by weight of pyridoxine hydrochloride, 0.001% by weight of inositol, 0.002% by weight of orthoacetic acid, 98.7362% 1% by weight was added to prepare a health drink.

(3) 건강보조식품 제조(3) health supplement manufacturing

스피루리나 55중량%, 구아검효소 분해물 10중량%, 비타민 B1 염산염 0.01중량%, 비타민 B6 염산염 0.01중량%, DL-메티오닌 0.23중량%, 스테아린산 마그네슘 0.7중량%, 유당 22.2중량% 및 옥수수전분 1.85중량%와 무씨 추출물 10중량%를 배합하여 통상의 방법으로 정제형 건강보조식품을 제조하였다.A mixture of 55% by weight of spirulina, 10% by weight of guar gum enzyme hydrolyzate, 0.01% by weight of vitamin B1 hydrochloride, 0.01% by weight of vitamin B6 hydrochloride, 0.23% by weight of DL-methionine, 0.7% by weight of magnesium stearate, And 10% by weight of the radish extract were blended to prepare a refillable health supplement food according to a conventional method.

[제형예 8: 지방간 예방 또는 치료용 약학 조성물 제조][Formulation Example 8: Preparation of a pharmaceutical composition for prevention or treatment of fatty liver]

본 제형예에서는 하기와 같이 실시예 1에서 제조한 무씨 추출물을 함유하는 지방간 예방 또는 치료용 약학 조성물을 제조하였다.In this Formulation Example, a pharmaceutical composition for prevention or treatment of fatty liver containing the radish extract prepared in Example 1 was prepared as follows.

(1) 산제 제조(1) Manufacture of powders

무씨 추출물 2 g에 유당 1 g을 혼합하고, 기밀포에 충진하여 산제를 제조하였다.2 g of the radish extract was mixed with 1 g of lactose and filled in an airtight container to prepare a powder.

(2) 정제 제조(2) Preparation of tablets

무씨 추출물 100 ㎎, 옥수수전분 100 ㎎, 유당 100 ㎎ 및 스테아린산 마그네슘 2 ㎎을 혼합한 후 통상의 정제 제조방법에 따라 타정하여 정제를 제조하였다.100 mg of the radish extract, 100 mg of the corn starch, 100 mg of the lactose and 2 mg of the magnesium stearate were mixed and tableted according to a conventional tablet preparation method.

(3) 캡슐제 제조(3) Manufacture of capsules

무씨 추출물 100 ㎎, 옥수수전분 100 ㎎, 유당 100 ㎎ 및 스테아린산 마그네슘 2 ㎎을 혼합한 후 젤라틴 캡슐에 충전하여 캡슐제를 제조하였다.100 mg of radish extract, 100 mg of corn starch, 100 mg of lactose and 2 mg of magnesium stearate were mixed and filled in gelatin capsules to prepare capsules.

(4) 주사제 제조(4) Injection preparation

무씨 추출물 100 ㎎에 주사용 증류수 적량을 가하여 용해시키고, pH를 약 7.5로 조절한 다음 2 ㎖ 용량의 앰플에 충진 및 멸균시하여 주사제를 제조하였다.100 mg of the radish extract was dissolved in an appropriate amount of distilled water for injection and the pH was adjusted to about 7.5. Then, the solution was filled and sterilized in a 2 ml capacity ampoule to prepare an injection.

[제형예 9: 지방간 예방 또는 치료용 동물용 의약품 제조][Formulation Example 9: Preparation of animal medicines for prevention or treatment of fatty liver]

본 제형예에서는 하기와 같이 실시예 1에서 제조한 10%(v/v) 발효주정 무씨 추출물을 함유하는 지방간 예방 또는 치료용 동물 의약품을 제조하였다.In this formulation example, an animal medicine for prevention or treatment of fatty liver containing the 10% (v / v) fermented fermented mugwort extract prepared in Example 1 was prepared as follows.

(1) 정제 제조(1) Preparation of tablets

무씨 추출물 100 ㎎에 단백질 혼합물 100 ㎎, 말분 100 ㎎을 혼합한 후 통상의 정제 제조방법에 따라 타정하여 정제를 제조하였다.100 mg of the radish extract was mixed with 100 mg of the protein mixture and 100 mg of the endosperm, and the tablets were prepared by tableting according to a conventional preparation method.

(2) 주사제 제조(2) Injection preparation

무씨 추출물 100 ㎎에 주사용 증류수 적량을 가하여 용해시키고, pH를 약 7.5로 조절한 다음 2 ㎖ 용량의 앰플에 충진 및 멸균시 하여 주사제를 제조하였다.100 mg of the radish extract was dissolved in an appropriate amount of distilled water for injection and the pH was adjusted to about 7.5. Then, the solution was filled and sterilized in a 2 ml capacity ampoule to prepare an injection.

Claims (15)

무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출하되, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증대되는 것을 특징으로 하는 무씨 추출물의 제조방법.
Wherein the content of sulfolapin is increased such that the content of sulfolapin in the extract is in the range of 20.90 to 27.27 mg / g by adding 5 to 10% (v / v) ethanol as an extraction solvent to the sucrose. Way.
제1항에 있어서,
상기 추출은,
침지 추출인 것을 특징으로 하는 것을 무씨 추출물의 제조방법.
The method according to claim 1,
Preferably,
Wherein the extract is an immersion extract.
삭제delete 제1항에 있어서,
상기 추출은,
35~45℃의 온도로 10~15시간 동안 수행되는 것을 특징으로 하는 무씨 추출물의 제조방법.
The method according to claim 1,
Preferably,
Wherein the reaction is carried out at a temperature of 35 to 45 캜 for 10 to 15 hours.
무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출한 것으로, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증가된 무씨 추출물.
Extract of Sucroflavin, which is obtained by adding 5 ~ 10% (v / v) ethanol as an extraction solvent to sucrose and containing sulfolapin in the extract at 20.90 ~ 27.27 mg / g.
삭제delete 무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출한 것으로, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증가된 무씨 추출물을 함유하는 비만 개선용 식품 조성물.
The extracts were prepared by adding 5 ~ 10% (v / v) ethanol as an extraction solvent to sucrose. The extracts containing 20 ~ 27.27 mg / g sulfolapin in the extract Food composition.
무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출한 것으로, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증가된 무씨 추출물을 함유하는 비만 예방 또는 치료용 약학 조성물.
(Ii) an anti-obesity drug which contains an extract of Ricinus with an increased sulfolane content so that sulfolapin is contained in the extract at a concentration of from 20.90 to 27.27 mg / g, obtained by adding 5-10% (v / v) A pharmaceutical composition for therapeutic use.
무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출한 것으로, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증가된 무씨 추출물을 함유하는 비만 예방 또는 치료용 동물용 의약품 조성물.
(Ii) an anti-obesity drug which contains an extract of Ricinus with an increased sulfolane content so that sulfolapin is contained in the extract at a concentration of from 20.90 to 27.27 mg / g, obtained by adding 5-10% (v / v) A therapeutic veterinary pharmaceutical composition.
무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출한 것으로, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증가된 무씨 추출물을 함유하는 당뇨 개선용 식품 조성물.
It was extracted by adding 5 ~ 10% (v / v) ethanol as an extraction solvent to mucilage. It was used for the improvement of diabetes mellitus, which contained an extract of mucilaginous sulforaphin, which contained sulfolapin in the extract at 20.90 ~ 27.27 mg / Food composition.
무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출한 것으로, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증가된 무씨 추출물을 함유하는 당뇨 예방 또는 치료용 약학 조성물.
(V / v) ethanol as an extractive solvent to prevent the diabetes mellitus containing scorpion extract-rich radish extract so that sulfolapin is contained in the extract at 20.90 to 27.27 mg / g. A pharmaceutical composition for therapeutic use.
무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출한 것으로, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증가된 무씨 추출물을 함유하는 당뇨 예방 또는 치료용 동물용 의약품 조성물.
(V / v) ethanol as an extractive solvent to prevent the diabetes mellitus containing scorpion extract-rich radish extract so that sulfolapin is contained in the extract at 20.90 to 27.27 mg / g. A therapeutic veterinary pharmaceutical composition.
무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출한 것으로, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증가된 무씨 추출물을 함유하는 지방간 개선용 식품 조성물.
It was extracted by adding 5 ~ 10% (v / v) ethanol as an extraction solvent to sucrose, and it was found that the sulfolafin contained in the extract was contained at 20.90 ~ 27.27 mg / g. Food composition.
무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출한 것으로, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증가된 무씨 추출물을 함유하는 지방간 예방 또는 치료용 약학 조성물.
(V / v) ethanol as an extractive solvent, and it has been found that the prevention and / or prevention of fatty liver disease, which comprises the extract of the radish with increased sulfolane content so that sulfolapin is contained in the extract at 20.90 to 27.27 mg / A pharmaceutical composition for therapeutic use.
무씨에 추출 용매로 5~10%(v/v) 에탄올을 첨가하여 추출한 것으로, 설포라핀이 추출물 내 20.90~27.27 mg/g 함유되도록 설포라핀 함량이 증가된 무씨 추출물을 함유하는 지방간 예방 또는 치료용 동물용 의약품 조성물.(V / v) ethanol as an extractive solvent, and it has been found that the prevention and / or prevention of fatty liver disease, which comprises the extract of the radish with increased sulfolane content so that sulfolapin is contained in the extract at 20.90 to 27.27 mg / A therapeutic veterinary pharmaceutical composition.
KR1020170055747A 2017-04-28 2017-04-28 Method for production of sulforaphene-enriched raphanus sativus seeds extracts and Food composition, pharmaceutical composition, animal medicines for weight and blood glucose control, fatty liver prevention with the raphanus sativus seeds extracts therefrom KR101907179B1 (en)

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Publication number Priority date Publication date Assignee Title
KR102467837B1 (en) * 2022-02-07 2022-11-21 주식회사 밥스누 Composition comprising radish sprouts extract including increased isothiocyanate and method for preparing the same

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Sooyeon Lim 외 3인, 'Sulforaphene identified from radish (Raphanus sativus L.) seeds possesses antimicrobial properties against multidrug-resistant bacteria and methicillin-resistant Staphylococcus aure*
박경무 외 9인, ‘태음조위탕 관련 연구 분석’, 한방비만학회지 제9권 제1호 (2009) 23-36..*

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102467837B1 (en) * 2022-02-07 2022-11-21 주식회사 밥스누 Composition comprising radish sprouts extract including increased isothiocyanate and method for preparing the same

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