KR101902932B1 - A composition for preventing, improving or treating alcoholic gastritis of the extracts from the aerial parts except flower and root of Cirsium japonicum and Taraxacum coreanum - Google Patents
A composition for preventing, improving or treating alcoholic gastritis of the extracts from the aerial parts except flower and root of Cirsium japonicum and Taraxacum coreanum Download PDFInfo
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- KR101902932B1 KR101902932B1 KR1020160179611A KR20160179611A KR101902932B1 KR 101902932 B1 KR101902932 B1 KR 101902932B1 KR 1020160179611 A KR1020160179611 A KR 1020160179611A KR 20160179611 A KR20160179611 A KR 20160179611A KR 101902932 B1 KR101902932 B1 KR 101902932B1
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- extract
- thistle
- mixture
- white dandelion
- preventing
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Abstract
본 발명은 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 간 손상 또는 알코올성 위염의 예방, 개선 또는 치료용 조성물에 관한 것으로, 더욱 상세하게는 GOT 및 GPT의 활성을 저해하거나 또는 증가된 간 조직의 무게를 감소시키는 효과 및/또는 위 조직에서 활성산소종을 감소시키거나 위 조직의 염증을 완화시키는 효과를 나타내는 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 이용하여 알코올성 간 손상 및/또는 알코올성 위염의 예방, 개선 또는 치료용 약학적 조성물 및 건강기능식품을 제공한다.The present invention relates to a composition for preventing, ameliorating or treating alcoholic liver damage or alcoholic gastritis containing, as an active ingredient, a mixture of thistle and white dandelion outpost extract, and more particularly to a composition for preventing, improving or treating GOT and GPT activity, A mixture of thistle and white dandelion outpost extract, which has the effect of reducing the weight of the liver tissue and / or reducing the active oxygen species in the stomach tissue or alleviating the inflammation of the stomach tissue, is used to treat alcoholic liver damage and / or alcoholic gastritis A pharmaceutical composition for preventing, ameliorating or treating the aforementioned diseases, and a health functional food.
Description
본 발명은 엉겅퀴 및 흰민들레 전초 추출물을 유효성분으로 함유하는 알코올성 간 손상 또는 알코올성 위염의 예방, 개선 또는 치료용 조성물에 관한 것으로, 더욱 상세하게는 GOT 및 GPT의 활성을 저해하거나 또는 증가된 간 조직의 무게를 감소시키는 효과 및/또는 위 조직에서 활성산소종을 감소시키거나 위 조직의 염증을 완화시키는 효과를 나타내는 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 이용하여 알코올성 간 손상 및/또는 알코올성 위염의 예방, 개선 또는 치료용 약학적 조성물 및 건강기능식품을 제공한다.The present invention relates to a composition for preventing, ameliorating or treating alcoholic liver damage or alcoholic gastritis containing thistle and white dandelion outbreak extract as an active ingredient, and more particularly to a composition for preventing, improving or treating GOT and GPT, And / or prevention of alcoholic liver damage and / or alcoholic gastritis by using a mixture of thistle and white dandelion outpost extract which has the effect of reducing the weight of the stomach and / or reducing the active oxygen species in the stomach tissue or alleviating the inflammation of the stomach tissue , A pharmaceutical composition for improvement or treatment, and a health functional food.
우리나라의 경우 20세 이상 성인 남자의 음주율은 83.3%로 매우 높고 여성의 음주율 또한 54.9%로 급격히 증가하는 추세에 있으며, 잘못된 음주문화로 인하여 과음에 심각하게 노출되어 있다. 알코올의 과다 섭취로 인한 폐해는 간질환을 비롯하여 각종 질환의 병인이 됨은 물론 개인, 가정, 사회의 정서와 생활에 부정적인 영향을 미침으로써 국가적으로 막대한 경제, 사회적 손실을 야기하고 있다.In Korea, the drinking rate of men over 20 years old is very high (83.3%), and the rate of women drinking is also rapidly increasing to 54.9%, which is seriously exposed to excessive drinking due to wrong drinking culture. The harmful effects caused by excessive consumption of alcohol are not only a pathogen of various diseases such as liver disease but also have a negative effect on the emotion and life of the individual, family and society, resulting in enormous national and economic losses.
급성 알코올 섭취는 사람들에게 있어 직접적으로 또는 간접적으로 독성작용을 일으키는 것으로 알려져 있으며, 아세트알데하이드와 아세테이트와 같은 생성물은 간세포에 손상을 야기한다. 섭취한 에탄올의 80-90% 이상이 간에서 대사되며 에탄올은 아세트알데하이드로 산화된다. 간에서의 에탄올 독성은 에탄올 대사에 의해 야기되는 산화적 스트레스로 설명된다. 에탄올 또는 이의 대사산물은 간세포에서 자동산화를 일으키며 산화촉진성(pro-oxidative) 인자로서의 작용 또는 항산화 수준을 감소시킴으로써 간염을 일으킨다. 또한 지질산화와 막 손상과의 관련은 에탄올성 간 손상에서 중요한 특징이다.Acute alcohol consumption is known to cause direct or indirect toxic effects in people, and products such as acetaldehyde and acetate cause damage to the hepatocytes. More than 80-90% of the ethanol ingested is metabolized in the liver and ethanol is oxidized to acetaldehyde. Ethanol toxicity in the liver is explained by oxidative stress caused by ethanol metabolism. Ethanol or its metabolites cause autoxidation in hepatocytes and produce hepatitis by acting as a pro-oxidative factor or reducing antioxidant levels. The association of lipid oxidation with membrane damage is also an important feature of ethanolic liver damage.
따라서, 이들의 초기반응을 저해할 수 있는 간 보호활성물질이나 간염 치료제의 개발이 요구되고 있다. 최근 개발된 디메닐 디메톡시 비페닐레이트(dimethyl dimethoxybiphenylate)는 오미자의 성분인 쉬잔드린(schizandrin)과 유사한 합성물질로 간독성 치료 효과가 보고된 바 있으나, 이들 질환의 심각성과 빈도수를 고려해 효과적으로 작용하기 위한 천연물에서의 간질환 예방 또는 치료제의 개발이 절실히 필요한 실정이다. Accordingly, development of a hepatoprotective agent and a hepatitis therapeutic agent capable of inhibiting the initial reaction thereof is required. Recently, dimethyl dimethoxybiphenylate has been reported to be a synthetic substance similar to schizandrin, a component of Schizandrin, and has been reported to be effective against hepatotoxicity in consideration of the severity and frequency of these diseases The development of a preventive or therapeutic agent for liver diseases in natural products is urgently needed.
또한, 알코올성 위염은 알코올로 인한 만성적인 자극에 의해 위 점막이 손상된 상태를 일컫는다. 알코올성 위염에 걸리면 소화가 잘 되지 않고 쓰린 느낌을 호소하는 경우도 있지만 대부분 특별한 증상이 없다가 내시경 검사와 초음파 검사를 통해 심각한 증상이 발견된다. 만성적으로 술을 마시는 경우 위염뿐만 아니라 췌장이나 간 등도 손상시켜 관련질환을 유발하며, 또한 식도암, 위암, 대장암의 위험도 높아진다.In addition, alcoholic gastritis refers to a condition in which the gastric mucosa is damaged by chronic stimuli due to alcohol. Alcoholic gastritis is not easy to digest and sometimes feel sore, but most of the symptoms are not specific symptoms through endoscopy and ultrasonography is found. Chronic drinking does not only lead to gastritis, but also damage the pancreas and liver, leading to related diseases, and also increases the risk of esophageal cancer, stomach cancer and colon cancer.
특히, 알코올로 인한 위염 및 위궤양은 가장 주의를 요하는데, 알코올은 위벽의 세포를 자극해 산 분비를 증가시키며, 과도한 알코올 섭취는 위점막의 부종을 발생시켜 출혈을 일으키고 염증세포들의 생성을 유도한다. 또한, 산화적 스트레스로 인한 괴사 혹은 세포사멸을 유도하여 위점막을 손상시키고, 위출혈이 나타나게 된다.In particular, gastritis and gastric ulceration due to alcohol require the most attention. Alcohol stimulates the cells of the gastric wall to increase acid secretion. Excessive alcohol consumption causes edema of the gastric mucosa, leading to bleeding and induction of inflammatory cells . In addition, it induces necrosis or cell death due to oxidative stress, damaging the gastric mucosa and causing gastrointestinal bleeding.
종래의 위염 및 위궤양의 치료제로는 과다 분비된 위산을 중화시키는 제산제(antacid), 산 분비 억제 목적의 히스타민 길항제(histamine antagonist), 프로톤 펌프 저해제(proton pump inhibitor), 콜린 억제제, 위내막의 내성을 증가시키고 회복을 돕는 위점막보호제 등이 있다. 다만, 이와 같은 치료제들은 합성 의약품으로 식욕감퇴, 무력감, 알레르기 등의 부작용이 발생하는 문제점이 있었다.Conventional treatments for gastritis and gastric ulcers include antacids that neutralize excess secreted acid, histamine antagonists to inhibit acid secretion, proton pump inhibitors, cholinergic inhibitors, and resistance to gastric lining And gastric mucosal protective agents that help increase recovery. However, such therapeutic agents are synthetic drugs and have side effects such as loss of appetite, weakness, and allergy.
이에, 대한민국 공개특허 제10-2009-0046425호(천마 추출물을 함유하는 위염 또는 위궤양의 예방 또는 치료용 조성물), 대한민국 등록특허 제10-1091025호(복분자 추출물을 함유하는 비스테로이드성 항염증제에 의해 유발된 위염 및 위궤양 예방 및 치료용 조성물), 대한민국 공개특허 제10-2012-0051904호(옻나무 추출물을 포함하는 위염 및 위궤양 치료제 조성물), 대한민국 등록특허 제10-1204981호(고로쇠 수액을 함유하는 위염 및 위궤양의 예방 및 치료용 조성물) 등 위염 및 위궤양의 예방 및 치료 효과가 있는 천연 추출물에 대한 관심이 높아지고 있다. Accordingly, Korean Patent Publication No. 10-2009-0046425 (composition for preventing or treating gastritis or gastric ulcer containing Ganoderma extract), Korean Patent No. 10-1091025 (induced by non-steroidal anti-inflammatory drug containing bokbunja extract Korean Patent Laid-Open Publication No. 10-2012-0051904 (composition for treating gastritis and gastric ulcer including Rhus verniciflua extract), Korean Patent No. 10-1204981 (composition for prevention and treatment of gastritis and gastric ulcer comprising Gonorrhea sap) There is a growing interest in natural extracts having preventive and therapeutic effects of gastritis and gastric ulcer.
이러한 배경 하에, 본 발명자들은 엉겅퀴와 흰민들레 전초 추출물의 혼합물이 알코올성 간 손상과 알코올성 위염을 개선시키는 효과가 있음을 확인하고 본 발명을 완성하였다.Under these circumstances, the present inventors have confirmed that a mixture of thistle and white dandelion outpost extract has the effect of improving alcoholic liver damage and alcoholic gastritis, and completed the present invention.
본 발명은 상기와 같은 문제점을 해결하기 위해 안출된 것으로, 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 간 손상의 예방, 개선 또는 치료용 조성물을 제공하는데 목적이 있다.SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned problems, and it is an object of the present invention to provide a composition for preventing, improving or treating alcoholic liver damage containing a mixture of thistle and white dandelion seedling extract as an active ingredient.
본 발명의 다른 목적은 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 위염의 예방, 개선 또는 치료용 조성물을 제공하는데 목적이 있다.It is another object of the present invention to provide a composition for preventing, improving or treating alcoholic gastritis containing a mixture of thistle and white dandelion seed extract as an active ingredient.
상술한 과제를 해결하기 위해, 본 발명은 엉겅퀴(Cirsium japonicum) 및 흰민들레(Taraxacum coreanum) 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 간 손상의 예방 또는 치료용 약학적 조성물을 제공한다.In order to solve the above problems, the present invention thistle (Cirsium The present invention also provides a pharmaceutical composition for preventing or treating alcoholic liver damage containing a mixture of an extract of Taraxacum coreanum and an extract of Taraxacum coreanum as an active ingredient.
본 발명은 또한, 엉겅퀴 추출물(Cirsium japonicum)와 흰민들레(Taraxacum coreanum) 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 간 손상의 예방 또는 개선용 건강기능식품 조성물을 제공한다.The present invention also provides a health functional food composition for preventing or ameliorating alcoholic liver damage containing a mixture of Cirsium japonicum and Taraxacum coreanum outpost extract as an active ingredient.
본 발명의 바람직한 일실시예에 따르면, 상기 엉겅퀴와 흰민들레 엉겅퀴와 흰민들레 전초 추출물은 물, C1 ~ C4의 알코올 또는 이들의 혼합용매로 추출할 수 있다.According to a preferred embodiment of the present invention, the thistle, the white dandelion thistle and the white dandelion outpost extract can be extracted with water, a C 1 to C 4 alcohol, or a mixed solvent thereof.
본 발명의 바람직한 다른 일실시예에 따르면, 상기 엉겅퀴와 흰민들레 전초 추출물은 1:0.25 내지 1:1의 중량비로 함유될 수 있다.According to another preferred embodiment of the present invention, the thistle and the white dandelion outpost extract may be contained in a weight ratio of 1: 0.25 to 1: 1.
본 발명의 바람직한 또 다른 일실시예에 따르면, 상기 조성물은 GOT 및 GPT의 활성을 저해하거나 또는 증가된 간 조직의 무게를 감소시킬 수 있다.According to another preferred embodiment of the present invention, the composition may inhibit the activity of GOT and GPT or may reduce the weight of the increased liver tissue.
나아가, 본 발명은 엉겅퀴(Cirsium japonicum) 및 흰민들레(Taraxacum coreanum) 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 위염의 예방 또는 치료용 약학적 조성물을 제공한다.Furthermore, the present invention thistle (Cirsium japonicum ) and white dandelion ( Taraxacum The present invention provides a pharmaceutical composition for preventing or treating alcoholic gastritis containing as an active ingredient a mixture of a coreanum extract.
본 발명은 또한, 엉겅퀴(Cirsium japonicum) 및 흰민들레(Taraxacum coreanum) 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 위염의 예방 또는 개선용 건강기능식품 조성물을 제공한다.The present invention also relates to a method for the treatment of cirsium The present invention provides a health functional food composition for preventing or alleviating an alcoholic gastritis containing, as an active ingredient, a mixture of an extract of Taraxacum coreanum and an extract of a white dandelion ( Taraxacum coreanum ).
본 발명의 바람직한 일실시예에 따르면, 상기 엉겅퀴와 흰민들레 전초 추출물은 물, C1 ~ C4의 알코올 또는 이들의 혼합용매로 추출할 수 있다.According to a preferred embodiment of the present invention, the thistle and the white dandelion seedling extract can be extracted with water, a C 1 to C 4 alcohol, or a mixed solvent thereof.
본 발명의 바람직한 다른 일실시예에 따르면, 상기 엉겅퀴와 흰민들레 전초 추출물은 1:0.25 내지 1:4의 중량비로 함유될 수 있다.According to another preferred embodiment of the present invention, the thistle and the white dandelion outpost extract may be contained in a weight ratio of 1: 0.25 to 1: 4.
본 발명의 바람직한 또 다른 일실시예에 따르면, 상기 조성물은 위 조직에서 활성산소종(reactive oxygen species)을 감소시키거나 위 조직의 염증을 완화시킬 수 있다.According to another preferred embodiment of the present invention, the composition may reduce reactive oxygen species in the stomach tissue or alleviate inflammation of the stomach tissue.
본 발명에 따른 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 유효성분으로 함유하는 조성물은 알코올에 의해 손상된 간 조직에서 GOT 및 GPT의 활성을 저해하는 효과가 매우 우수하고, 증가된 간 무게의 감소 및 간세포의 괴사와 변성을 감소시켜 알코올성 간 손상을 예방, 개선 또는 치료하는데 유용하다. 또한, 본 발명의 조성물은 알코올로 유발된 위 조직의 산화 스트레스 감소 및 염증 완화 효과가 뛰어나 알코올성 위염을 예방, 개선 또는 치료하는데 유용하다.The composition containing the mixture of thistle and white dandelion seed extract according to the present invention as an active ingredient has excellent effect of inhibiting the activity of GOT and GPT in liver damaged by alcohol, It is useful for preventing, ameliorating or treating alcoholic liver damage by reducing necrosis and degeneration. In addition, the composition of the present invention is useful for preventing, ameliorating or treating alcoholic gastritis by excelling in the reduction of oxidative stress and inflammation of the stomach tissue induced by alcohol.
나아가, 본 발명의 조성물은 천연물 소재의 추출물을 유효성분으로 하여 인체에 안전하고, 부작용이 적어 의약품, 의약외품 및 건강기능식품등의 개발에 소재로 적합하다.Furthermore, the composition of the present invention is safe as a human body and has few side effects, and is suitable as a material for the development of medicines, quasi-drugs and health functional foods.
도 1은 알코올 투여로 간 손상을 일으킨 쥐에서 엉겅퀴와 흰민들레 전초 추출물의 다양한 중량비로 혼합된 혼합물 처리에 따른 GOP 수치(A) 및 GPT 수치(B) 저해 효과를 나타낸 그래프이다.
도 2는 알코올로 투여로 간 무게가 증가된 쥐에서 엉겅퀴와 흰민들레 전초 추출물의 다양한 중량비로 혼합된 혼합물 처리에 따른 간 무게 감소 효과를 나타낸 그래프이다.
도 3은 알코올 투여로 간 손상을 일으킨 쥐에서 엉겅퀴와 흰민들레 전초 추출물의 다양한 중량비로 혼합된 혼합물 처리에 따른 간 조직의 미세구조 변화를 보여주는 사진이다.
도 4는 알코올 투여로 산화적 스트레스가 증가된 쥐의 위 조직에서 엉겅퀴와 흰민들레 전초 추출물의 다양한 중량비로 혼합된 혼합물 처리에 따른 활성산소종(ROS)의 감소 효과를 나타낸 그래프이다.
도 5는 알코올 투여로 위염이 유발된 쥐의 위 조직에서 엉겅퀴와 흰민들레 전초 추출물의 다양한 중량비로 혼합된 혼합물 처리에 따른 염증 완화 정도를 보여주는 사진이다.FIG. 1 is a graph showing the inhibitory effects of GOP values (A) and GPT values (B) upon treatment of mixed mixtures at various weight ratios of thistle and white dandelion outpost extract in liver damaged by alcohol administration.
FIG. 2 is a graph showing the effect of liver weight reduction according to various mixture treatments at various weight ratios of thistle and white dandelion outpost extract in rats in which liver weight was increased by alcohol administration.
FIG. 3 is a photograph showing changes in the microstructure of liver tissues according to various mixture treatments at various weight ratios of thistle and white dandelion outpost extract in rats caused by alcohol administration by alcohol administration.
FIG. 4 is a graph showing a reduction effect of reactive oxygen species (ROS) according to various mixture treatments at various weight ratios of thistle and white dandelion outpost extract in rat stomach tissues in which oxidative stress was increased by alcohol administration.
FIG. 5 is a photograph showing the degree of inflammation relief according to the treatment of the mixture mixed at various weight ratios of thistle and white dandelion outpost extract in the stomach tissue of gastritis induced by alcohol administration.
이하, 본 발명을 더욱 상세히 설명한다.Hereinafter, the present invention will be described in more detail.
상술한 바와 같이, 알코올로 인한 간 손상으로 유발되는 간 질환은 그 심각성과 빈도수를 고려해 효과적으로 작용하는 천연물 소재의 치료제 개발이 요구되고 있다. 또한, 종래의 위염 또는 위궤양 치료제의 부작용은 천연물 소재의 알코올성 위염 치료제 개발 및 치료방법에 대한 요구를 증가시키고 있다.As described above, it is required to develop a therapeutic agent for a natural material which effectively acts on liver disease caused by liver damage due to alcohol, taking into consideration the severity and the frequency. In addition, the conventional side effects of the gastritis or gastric ulcer therapeutic agent are increasingly demanded for the development and treatment of alcoholic gastritis treatment of natural materials.
이에, 본 발명은 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 유효성분으로 함유하는 조성물을 제공함으로써 상술한 문제의 해결방안을 모색하였다. 본 발명에 따른 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 유효성분으로 함유하는 약학적 조성물 및 건강기능식품 조성물은 GOT 및 GPT의 활성을 저해하는 효과가 매우 우수하고, 증가된 간 무게의 감소 및 간세포의 괴사와 변성을 감소시켜 알코올성 간 손상을 예방, 개선 또는 치료하는데 유용하고, 또한, 알코올로 유발된 위 조직의 산화 스트레스 감소 및 염증 완화 효과가 뛰어나 알코올성 위염을 예방, 개선 또는 치료하는데 유용하다.Accordingly, the present invention has solved the above-mentioned problem by providing a composition containing a mixture of thistle and white dandelion seedling extract as an active ingredient. The pharmaceutical composition and the health functional food composition containing the mixture of the thistle and the white dandelion seed extract according to the present invention as an active ingredient are excellent in the effect of inhibiting the activity of GOT and GPT, It is useful for prevention, improvement or treatment of alcoholic liver damage by reducing necrosis and degeneration. It is also useful for preventing, ameliorating or treating alcoholic gastritis by excelling in reduction of oxidative stress and inflammation of alcohol induced gastric tissue.
본 발명에서 사용되는 용어는 다음과 같이 정의된다.The terms used in the present invention are defined as follows.
용어 “약학적 조성물(pharmaceutical composition)”은 본 발명의 엉겅퀴와 흰민들레 전초 추출물의 혼합물에 희석제 또는 담체와 같은 다른 화학 성분들을 혼합한 혼합물을 의미한다.The term " pharmaceutical composition " means a mixture of a mixture of thistle and white dandelion outpost extract of the present invention with other chemical components such as diluent or carrier.
용어 “담체(carrier)”는 세포 또는 조직 내로의 화합물의 부가를 용이하게 하는 화합물로 정의된다. 예를 들어, 디메틸술폭사이드(DMSO)는 생물체의 세포 또는 조직 내로의 많은 유기 화합물들의 투입을 용이하게 하는 통상 사용되는 담체이다.The term " carrier " is defined as a compound that facilitates the addition of a compound into a cell or tissue. For example, dimethylsulfoxide (DMSO) is a commonly used carrier that facilitates the introduction of many organic compounds into cells or tissues of an organism.
용어 “희석제(diluent)”는 대상 화합물의 생물학적 활성 형태를 안정화시킬 뿐만 아니라, 화합물을 용해시키게 되는 물에서 희석되는 화합물로 정의된다. 버퍼 용액에 용해되어 있는 염은 당해 분야에서 희석제로 사용된다. 통상 사용되는 버퍼 용액은 포스페이트 버퍼 식염수이며, 이는 인간 용액의 염 상태를 모방하고 있기 때문이다. 버퍼 염은 낮은 농도에서 용액의 pH를 제어할 수 있기 때문에, 버퍼 희석제가 화합물의 생물학적 활성을 변형하는 일은 드물다.The term " diluent " is defined as a compound that not only stabilizes the biologically active form of the compound of interest, but also dilutes in water to which the compound is dissolved. Salts dissolved in buffer solutions are used as diluents in the art. A commonly used buffer solution is phosphate buffered saline, since it mimics the salt state of the human solution. Since buffer salts can control the pH of the solution at low concentrations, buffer diluents rarely modify the biological activity of the compounds.
용어 “치료”는 이롭거나 바람직한 임상적 결과를 수득하기 위한 접근을 의미한다. 본 발명의 목적을 위해서, 이롭거나 바람직한 임상적 결과는 비제한적으로, 증상의 완화, 질병 범위의 감소, 질병 상태의 안정화(즉, 악화되지 않음), 질병 진행의 지연 또는 속도의 감소, 질병 상태의 개선 또는 일시적 완화 및 경감 (부분적이거나 전체적으로), 검출가능하거나 또는 검출되지 않거나의 여부를 포함한다. 또한, “치료”는 치료를 받지 않았을 때 예상되는 생존율과 비교하여 생존율을 늘이는 것을 의미할 수도 있다. “치료”는 치료학적 치료 및 예방적 또는 예방조치 방법 모두를 가리킨다. 상기 치료들은 예방되는 장애뿐만 아니라 이미 발생한 장애에 있어서 요구되는 치료를 포함한다. 질병을 “완화(alleviating)”하는 것은 치료를 하지 않은 경우와 비교하여, 질병상태의 범위 및/또는 바람직하지 않은 임상적 징후가 감소되거나 및/또는 진행의 시간적 추이(time course)가 늦춰지거나 길어지는 것을 의미한다.The term " treatment " means an approach to obtaining beneficial or desired clinical results. For purposes of the present invention, beneficial or desired clinical results include, but are not limited to, alleviation of symptoms, reduction in the extent of disease, stabilization (i.e., not worsening) of the disease state, (Either partially or totally), detectable or undetected, whether or not an improvement or temporary relief or reduction Also, " treatment " may mean increasing the survival rate compared to the expected survival rate when not receiving treatment. &Quot; Treatment " refers to both therapeutic treatment and prophylactic or preventative measures. Such treatments include treatments required for disorders that have already occurred as well as disorders to be prevented. "Alleviating" a disease may result in a reduction in the extent of the disease state and / or undesirable clinical symptoms and / or a slower or longer time course of the progression, It means to lose.
본 발명에서 사용되는 모든 기술용어는, 달리 정의되지 않는 이상, 본 발명의 관련 분야에서 통상의 당업자가 일반적으로 이해하는 바와 같은 의미로 사용된다. 또한 본 명세서에는 바람직한 방법이나 시료가 기재되나, 이와 유사하거나 동등한 것들도 본 발명의 범주에 포함된다.All technical terms used in the present invention are used in the sense that they are generally understood by those of ordinary skill in the relevant field of the present invention unless otherwise defined. Also, preferred methods or samples are described in this specification, but similar or equivalent ones are also included in the scope of the present invention.
본 발명은 엉겅퀴(Cirsium japonicum) 및 흰민들레(Taraxacum coreanum) 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 간 손상의 예방 또는 치료용 약학적 조성물을 제공한다.The present invention relates to a method for the treatment of cirsium japonicum ) and white dandelion ( Taraxacum The present invention also provides a pharmaceutical composition for prevention or treatment of alcoholic liver damage containing a mixture of coreanum extract.
또한, 본 발명은 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 간 손상의 예방 또는 개선용 건강기능식품을 제공한다.The present invention also provides a health functional food for preventing or ameliorating an alcoholic liver injury containing a mixture of thistle and white dandelion seed extract as an active ingredient.
본 발명에서 사용된 엉겅퀴(Cirsium japonicum)는 국화과의 여러해살이풀로 연한 식물체와 어린순은 나물로 먹고 성숙한 뿌리는 약으로 쓴다. 약효는 지혈작용이 현저하여 소변출혈, 대변출혈, 코피, 자궁출혈, 외상출혈에 활용된다. 본 발명에서는 엉겅퀴의 전초를 원료로 하여 추출물을 제조하였다.The thistle used in the present invention (Cirsium japonicum ) is a perennial plant of the Asteraceae family. The plant is eaten as a herb and the mature root is a medicine. The drug efficacy is remarkable in hemostatic effect, and it is used for urine hemorrhage, fecal hemorrhage, nosebleed, uterine hemorrhage, trauma hemorrhage. In the present invention, an extract was prepared from thistle seeds as a raw material.
본 발명에서 사용된 흰민들레(Taraxacum coreanum)는 국화과(compositae)에 속한 다년초로 한방에서는 전초를 건조한 것을 봄과 여름에 꽃이 피기 전이나 후에 채취하여 청열해독, 소염, 이뇨의 목적으로 하는 약물로 이용되어 왔다. 본 발명에서는 흰민들레의 전초를 원료로 하여 추출물을 제조하였다.The taraxacum coreanum used in the present invention is a perennial plant belonging to the genus Chrysanthemum (Compositae). It is a drug for the purpose of detoxification, anti-inflammation and diuretic, Have been used. In the present invention, an extract was prepared from the outpast of white dandelion as a raw material.
본 발명의 엉겅퀴와 흰민들레는 상업적으로 판매되는 것을 구입하여 사용하거나, 자연에서 직접 채취 또는 재배한 것을 사용할 수 있다.The thistle and the white dandelion of the present invention may be commercially purchased or used, or may be directly harvested or cultivated.
본 발명의 바람직한 일실시예에서는 엉겅퀴와 흰민들레 전초 추출물을 혼합하여 사용하였다. 상기 엉겅퀴와 흰민들레 전초 추출물을 제조하는 방법은 정치 추출법, 초음파 추출법, 여과법 및 환류 추출법 등 당업계의 통상적인 추출방법을 사용할 수 있다. 바람직하게는 세척 및 건조로 이물질이 제거된 엉겅퀴와 흰민들레 전초를 동결건조한 후 분쇄하여 추출용매로 3회 반복하여 정치 추출하였다. 상기 추출용매는 당업계의 통상적인 추출용매라면 제한없이 사용할 수 있고, 바람직하게는 물, C1~C4의 알코올 또는 이들의 혼합용매일 수 있으며, 보다 바람직하게는 메탄올 또는 에탄올일 수 있고, 가장 바람직하게는 99% 에탄올일 수 있다. 필요한 경우에는 당업계에 공지된 방법에 따라 여과, 농축 및 동결건조 등의 단계를 추가적으로 거쳐 분말로 제조될 수 있다.In a preferred embodiment of the present invention, thistle and white dandelion outpost extract were mixed and used. The method for preparing the thistle and the white dandelion seedling extract may be a conventional extraction method such as a stationary extraction method, an ultrasonic extraction method, a filtration method and a reflux extraction method. Preferably, the thistle and the white dandelion outpost, which have been freed from foreign matter by washing and drying, are lyophilized, pulverized, and extracted three times with an extraction solvent. The extraction solvent may be any conventional extraction solvent in the art, and may be water, C 1 -C 4 alcohol or a mixture thereof, more preferably methanol or ethanol, Most preferably 99% ethanol. If necessary, the powder may be further subjected to steps such as filtration, concentration and freeze-drying according to methods known in the art.
간과 관련된 여러 질환들을 감별하기 위해서는 몇 가지 화학적 검사들을 종합적으로 해석하는 것이 필요한데, 이를 위하여 몇 가지 검사항목들을 묶어 간 기능 검사로 통칭한다. 주요 검사로는 GOT, GPT 등이 있고, 이외에도 총 단백질, 알부민, 암모니아 등의 항목을 더하여 검사하는 경우도 많다.In order to distinguish the various diseases related to the liver, it is necessary to comprehensively analyze several chemical tests. For this purpose, some test items are collectively referred to as liver function tests. Major tests include GOT and GPT. In addition, there are many cases in which total protein, albumin, and ammonia are added to the test.
GOT(glutamic oxaloacetic transaminase, 아스파르트산 아미노기전달효소)는 L-아스파르트산의 아미노기를 α-케토글루타르산으로 전달하여 옥살로아세트산과 L-글루탐산을 생성하는 가역반응을 촉매하는 효소이다. 간염, 심근경색 등의 진단 시 혈중에서의 이 효소 활성에 대한 측정이 자주 이용된다.GOT (glutamic oxaloacetic transaminase) is an enzyme that catalyzes the reversible reaction of producing oxaloacetic acid and L-glutamic acid by transferring the amino group of L-aspartic acid to? -Ketoglutaric acid. In the diagnosis of hepatitis and myocardial infarction, measurement of this enzyme activity in the blood is frequently used.
GPT(glutamic-pyruvic transaminase, 알라닌 아미노기전달효소)는 알라닌의 아미노기를 α-케토글루타르산에 전달하여 피루브산과 글루탐산 생성반응을 촉매하는 효소이다. 간·담도계 질환의 진단을 위해 혈액 중의 이 효소의 활성 측정이 자주 이루어진다.GPT (glutamic-pyruvic transaminase) is an enzyme that catalyzes pyruvic acid and glutamic acid production by transferring the amino group of alanine to α-keto glutaric acid. In order to diagnose liver and biliary system diseases, the activity of this enzyme in blood is frequently measured.
따라서, 본 발명에서는 알코올성 간 손상 개선 효과를 GOT 및 GPT 수치 측정을 통해 확인하였다. 본 발명의 엉겅퀴와 흰민들레 전초 추출물을 함유하는 조성물은 알코올, 바람직하게는 에탄올 투여로 증가된 GOT 및 GPT 수치를 현저하게 저해할 수 있고(도 1), 증가된 간 조직의 무게를 감소시킬 수 있다(도 2). 또한 에탄올로 손상된 간 조직의 간세포 괴사(hepatocyte necrosis)와 변성(degeneration), 지방변성(fatty change), 염증 세포 침윤(inflammatory cell infiltration) 및 간세포의 세포질 공포화(cytoplasmic vacuolation of hepatocyte)를 완화시켜 알코올성 간 손상을 효과적으로 개선시킬 수 있음을 확인하였다(도 3).Therefore, in the present invention, the improvement effect of alcoholic liver damage was confirmed by measuring the GOT and GPT values. The compositions containing the thistle and white dandelion outpost extract of the present invention can significantly inhibit increased GOT and GPT levels from alcohol, preferably ethanol administration (Fig. 1), and can reduce the weight of the increased liver tissue (Fig. 2). In addition, hepatocyte necrosis, degeneration, fatty change, inflammatory cell infiltration, and cytoplasmic vacuolation of hepatocyte of hepatocyte necrosis damaged by ethanol are alleviated, Liver damage can be effectively improved (Fig. 3).
본 발명의 조성물에 있어서, 엉겅퀴와 흰민들레 전초 추출물은 알코올성 간 손상을 치료하기 위한 최적의 효과를 나타내기 위해 특정 중량비로 혼합될 수 있다. 바람직한 혼합 중량비는 1:0.25 내지 1:1이며, 가장 바람직한 혼합 중량비는 1:0.25일 수 있다. 엉겅퀴와 흰민들레 전초 추출물을 상기 범위를 벗어난 중량비로 혼합할 경우, 두 가지 추출물의 복합 상승효과가 감소하여 최적의 활성을 나타낼 수 없으므로(도 1 내지 3), 상기 중량비 범위 내에서 두 가지 추출물을 혼합하는 것이 바람직하다.In the composition of the present invention, thistle and white dandelion outpost extract may be mixed in a specific weight ratio to exhibit optimal effects for treating alcoholic liver damage. The preferred mixing weight ratio is 1: 0.25 to 1: 1, and the most preferred mixing weight ratio can be 1: 0.25. When the thistle and white dandelion seedling extracts were mixed at a weight ratio out of the above range, the complex synergistic effect of the two extracts was reduced and the optimum activity could not be exhibited (Figs. 1 to 3) Mixing is preferred.
나아가, 본 발명은 엉겅퀴(Cirsium japonicum) 및 흰민들레(Taraxacum coreanum) 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 위염의 예방 또는 치료용 약학적 조성물을 제공한다.Furthermore, the present invention thistle (Cirsium japonicum ) and white dandelion ( Taraxacum The present invention provides a pharmaceutical composition for preventing or treating alcoholic gastritis containing as an active ingredient a mixture of a coreanum extract.
본 발명은 또한, 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 유효성분으로 함유하는 알코올성 위염의 예방 또는 개선용 건강기능식품 조성물을 제공한다.The present invention also provides a health functional food composition for preventing or alleviating an alcoholic gastritis containing a mixture of thistle and white dandelion seed extract as an active ingredient.
상기 조성물에서 엉겅퀴와 흰민들레 전초 추출물에 대한 설명은 전술한 바와 동일하므로, 중복 기재에 따른 본 명세서의 과도한 복잡성을 피하기 위하여 그 기재를 생략한다.The description of thistle and white dandelion outpost extract in the composition is the same as that described above, so that the description thereof is omitted in order to avoid the excessive complexity of the present specification according to the overlapping description.
본 발명의 바람직한 일실시예에서는, 본 발명의 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 함유하는 조성물의 알코올성 위염 개선 효과를 확인하기 위해 알코올, 바람직하게는 에탄올 투여로 증가된 산화적 스트레스의 개선 효과를 활성산소종을 측정함으로써 확인하였다. 본 발명의 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 함유하는 조성물은 증가된 활성산소종의 수준을 정상군과 유사한 정도로 감소시켜 알코올에 의해 위 조직에서 증가된 산화스트레스를 매우 효과적으로 감소시켰다(도 4). 또한, 알코올로 유발된 위 조직의 염증을 현저하게 완화시켜 알코올성 위염 완화에 탁월한 효능이 있음을 확인하였다(도 5).In a preferred embodiment of the present invention, in order to confirm the effect of improving the alcoholic gastritis of the composition containing the mixture of thistle and white dandelion seed extract of the present invention, the effect of improving the oxidative stress increased by the administration of alcohol, preferably ethanol, And was confirmed by measuring the active oxygen species. The composition containing the mixture of thistle and white dandelion outpost extract of the present invention reduced the level of the increased active oxygen species to a similar level to that of the normal group, thereby effectively reducing the increased oxidative stress in the stomach tissue by alcohol (Fig. 4) . In addition, it was confirmed that the inflammation of the stomach tissue induced by alcohol was remarkably alleviated to exert an excellent effect in alleviating alcoholic gastritis (FIG. 5).
본 발명의 조성물에 있어서, 엉겅퀴와 흰민들레 전초 추출물은 알코올성 위염을 치료하기 위한 최적의 효과를 나타내기 위해 특정 중량비로 혼합될 수 있다. 바람직한 혼합 중량비는 1:0.25 내지 1:4이며, 더욱 바람직하게는 1:1 내지 1:4이며, 가장 바람직한 혼합 중량비는 1:4일 수 있다. 엉겅퀴와 흰민들레 전초 추출물을 상기 범위를 벗어난 중량비로 혼합할 경우, 두 가지 추출물의 복합 상승효과가 감소하여 최적의 활성을 나타낼 수 없으므로(도 4 및 5), 상기 중량비 범위 내에서 두 가지 추출물을 혼합하는 것이 바람직하다.In the composition of the present invention, thistle and white dandelion outpost extract may be mixed at specific weight ratios to exhibit optimal effects for treating alcoholic gastritis. The preferred mixing weight ratio is 1: 0.25 to 1: 4, more preferably 1: 1 to 1: 4, and most preferably 1: 4. When the thistle and white dandelion seedling extracts were mixed at a weight ratio out of the above range, the complex synergistic effect of the two extracts was reduced and the optimum activity could not be exhibited (FIGS. 4 and 5) Mixing is preferred.
본 발명의 약학적 조성물은 약학적 조성물의 제조에 통상적으로 사용하는 적절한 담체, 부형제 및 희석제를 더 포함할 수 있다.The pharmaceutical compositions of the present invention may further comprise suitable carriers, excipients and diluents conventionally used in the manufacture of pharmaceutical compositions.
본 발명에 따른 약학적 조성물은, 각각 통상의 방법에 따라 산제, 과립제, 정제, 캡슐제, 현탁액, 에멀젼, 시럽, 에어로졸 등의 경구형 제형, 외용제, 좌제 및 멸균 주사용액의 형태로 제형화하여 사용될 수 있다.The pharmaceutical composition according to the present invention can be formulated in the form of oral, granule, tablet, capsule, suspension, emulsion, syrup, aerosol or the like oral preparation, external preparation, suppository and sterilized injection solution according to a conventional method Can be used.
본 발명의 조성물에 함유될 수 있는 담체, 부형제 및 희석제로는 락토오즈(lactose), 덱스트로즈, 수크로스(sucrose), 솔비톨, 만니톨, 자일리톨, 에리스리톨, 말티톨, 전분, 아카시아 고무, 알지네이트, 젤라틴, 칼슘 포스페이트, 칼슘 실리케이트, 셀룰로즈, 메틸 셀룰로즈, 미정질 셀룰로스, 폴리비닐 피롤리돈, 물, 메틸히드록시벤조에이트, 프로필히드록시벤조에이트, 탈크, 마그네슘 스테아레이트 및 광물유를 들 수 있다.Examples of carriers, excipients and diluents that may be contained in the composition of the present invention 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.
제제화할 경우에는 보통 사용하는 충진제, 증량제, 결합제, 습윤제, 붕해제, 계면활성제 등의 희석제 또는 부형제를 사용하여 조제된다.In the case of formulation, a diluent or excipient such as a filler, an extender, a binder, a wetting agent, a disintegrant, or a surfactant is usually used.
경구투여를 위한 고형제제에는 정제, 환제, 산제, 과립제, 캡슐제 등이 포함되며, 이러한 고형제제는 상기 화합물에 적어도 하나 이상의 부형제 예를 들면, 전분, 칼슘카보네이트(calcium carbonate), 수크로스 또는 락토오스, 젤라틴 등을 섞어 조제된다. 또한 단순한 부형제 이외에 마그네슘 스테아레이트, 탈크 같은 윤활제들도 사용된다. 경구를 위한 액상 제제로는 현탁제, 내용액제, 유제, 시럽제 등이 해당되는데 흔히 사용되는 단순 희석제인 물, 리퀴드 파라핀 이외에 여러 가지 부형제, 예를 들면 습윤제, 감미제, 방향제, 보존제 등이 포함될 수 있다.Solid formulations for oral administration include tablets, pills, powders, granules, capsules and the like, which may contain at least one excipient such as starch, calcium carbonate, sucrose or lactose , Gelatin, and the like. In addition to simple excipients, lubricants such as magnesium stearate and talc are also used. Examples of the liquid preparation for oral use include suspensions, solutions, emulsions, and syrups. In addition to water and liquid paraffin, simple diluents commonly used, various excipients such as wetting agents, sweeteners, fragrances, preservatives and the like may be included .
비경구 투여를 위한 제제에는 멸균된 수용액, 비수성용제, 현탁제, 유제, 동결건조 제제, 좌제가 포함된다. 비수성용제, 현탁제로는 프로필렌글리콜(propylene glycol), 폴리에틸렌 글리콜, 올리브 오일과 같은 식물성 기름, 에틸올레이트와 같은 주사 가능한 에스테르 등이 사용될 수 있다. 좌제의 기제로는 위텝솔(witepsol), 마크로골, 트윈(tween) 61, 카카오지, 라우린지, 글리세로제라틴 등이 사용될 수 있다.Formulations for parenteral administration include sterilized aqueous solutions, non-aqueous solutions, suspensions, emulsions, freeze-dried preparations, and suppositories. Examples of the suspending agent include propylene glycol, polyethylene glycol, vegetable oil such as olive oil, injectable ester such as ethyl oleate, and the like. As a base for suppositories, witepsol, macrogol, tween 61, cacao paper, laurin, glycerogelatin and the like can be used.
상기 본 발명의 약학적 조성물은 약제학적으로 유효한 양으로 투여한다.The pharmaceutical composition of the present invention is administered in a pharmaceutically effective amount.
본 발명에서 용어 "약제학적으로 유효한 양"은 의학적 치료에 적용 가능한 합리적인 수혜/위험 비율로 질환을 치료하기에 충분한 양을 의미하며, 유효 용량 수준은 개체 종류 및 중증도, 연령, 성별, 감염된 바이러스 종류, 약물의 활성, 약물에 대한 민감도, 투여 시간, 투여 경로 및 배출 비율, 치료기간, 동시 사용되는 약물을 포함한 요소 및 기타 의학 분야에 잘 알려진 요소에 따라 결정될 수 있다. 본 발명의 조성물은 개별 치료제로 투여하거나 다른 치료제와 병용하여 투여될 수 있고 종래의 치료제와는 순차적 또는 동시에 투여될 수 있다. 그리고 단일 또는 다중 투여될 수 있다. 상기 요소를 모두 고려하여 부작용없이 최소한의 양으로 최대 효과를 얻을 수 있는 양을 투여하는 것이 중요하며, 당업자에 의해 용이하게 결정될 수 있다.The term "pharmaceutically effective amount " as used herein means an amount sufficient to treat a disease at a reasonable benefit / risk ratio applicable to medical treatment, and the effective dose level will vary depending on the species and severity, age, sex, , The activity of the drug, the sensitivity to the drug, the time of administration, the route of administration and rate of release, the duration of the treatment, factors including co-administered drugs, and other factors well known in the medical arts. The composition of the present invention may be administered as an individual therapeutic agent or in combination with other therapeutic agents, and may be administered sequentially or simultaneously with conventional therapeutic agents. And can be administered singly or multiply. It is important to take into account all of the above factors and to administer the amount in which the maximum effect can be obtained in a minimal amount without adverse effect, and can be easily determined by those skilled in the art.
본 발명의 약학적 조성물은 단순포진바이러스 감염의 예방 또는 치료를 위하여 단독으로, 또는 수술, 호르몬 치료, 약물 치료 및 생물학적 반응 조절제를 사용하는 방법들과 병용하여 사용할 수 있다.The pharmaceutical composition of the present invention can be used alone or in combination with methods for the prevention or treatment of herpes simplex virus infection or using surgery, hormone therapy, drug therapy and biological response modifiers.
상기 조성물은 쥐, 생쥐, 가축, 인간 등의 포유동물에 다양한 경로로 투여될 수 있다. 투여의 모든 방식은 예상될 수 있는데, 예를 들면, 경구, 직장 또는 정맥, 근육, 피하, 자궁 내 경막 또는 뇌혈관 내 주사에 의해 투여될 수 있다.The composition can be administered to mammals such as rats, mice, livestock, humans, and the like in a variety of routes. All modes of administration may be expected, for example, by oral, rectal or intravenous, intramuscular, subcutaneous, intra-uterine dural or intracerebral injection.
본 발명의 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 식품 첨가물로 사용할 경우, 상기 혼합물을 그대로 첨가하거나 다른 식품 또는 식품 성분과 함께 사용될 수 있고, 통상적인 방법에 따라 적절하게 사용될 수 있다. 유효성분의 혼합량은 사용 목적 (예방, 건강 또는 치료적 처치)에 따라 적합하게 결정될 수 있다. 일반적으로, 식품 또는 음료의 제조 시에는 본 발명의 조성물은 원료에 대하여 0.01 ~ 10 중량%, 바람직하게는 0.05 ~ 1 중량%의 양으로 첨가된다. 그러나 건강 및 위생을 목적으로 하거나 또는 건강 조절을 목적으로 하는 장기간의 섭취의 경우에는 상기 양은 상기 범위 이하로도 사용될 수 있다.When the mixture of thistle and white dandelion outpost extract of the present invention is used as a food additive, the mixture can be used as it is, or can be used together with other food or food ingredients, and can be suitably used according to a conventional method. The amount of the active ingredient to be mixed can be suitably determined according to the intended use (prevention, health or therapeutic treatment). Generally, in the production of food or beverage, the composition of the present invention is added in an amount of 0.01 to 10% by weight, preferably 0.05 to 1% by weight based on the raw material. However, in the case of long-term ingestion intended for health and hygiene purposes or for the purpose of controlling health, the amount can also be used in the above-mentioned range.
상기 건강기능식품은 여러 가지 영양제, 비타민, 광물(전해질), 합성 풍미제 및 천연 풍미제 등의 풍미제, 착색제 및 중진제(치즈, 초콜릿 등), 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, pH 조절제, 안정화제, 방부제, 글리세린, 알코올, 탄산음료에 사용되는 탄산화제 등을 함유할 수 있다. 그 밖에 천연 과일 주스 및 과일 주스 및 야채 음료의 제조를 위한 과육을 함유할 수 있다. 이러한 성분은 독립적으로 또는 조합하여 사용할 수 있다. 또한, 건강기능식품은 육류, 소세지, 빵, 초콜릿, 캔디류, 스넥류, 과자류, 피자, 라면, 껌류, 아이스크림류, 스프, 음료수, 차, 기능수, 드링크제, 알코올 및 비타민 복합제 중 어느 하나의 형태일 수 있다.The health functional food may contain flavoring agents such as various nutrients, vitamins, minerals (electrolytes), synthetic flavors and natural flavors, coloring agents and thickening agents (cheese, chocolate etc.), pectic acid and its salts, alginic acid and its salts, Organic acids, protective colloid thickeners, pH adjusting agents, stabilizers, preservatives, glycerin, alcohols, carbonating agents used in carbonated drinks, and the like. It can also contain natural fruit juices and pulp for the production of fruit juices and vegetable drinks. These components may be used independently or in combination. The health functional food may be any one of meat, sausage, bread, chocolate, candy, snack, confectionery, pizza, ramen, gum, ice cream, soup, beverage, tea, functional water, drink, alcohol and vitamin .
본 발명의 건강 음료 조성물은 엉겅퀴와 흰민들레 전초 추출물의 혼합물을 함유하는 것 외에는 액체성분에는 특별한 제한은 없으며 통상의 음료와 같이 여러 가지 향미제 또는 천연 탄수화물 등을 추가 성분으로서 함유할 수 있다.The health beverage composition of the present invention is not particularly limited to a liquid ingredient except that it contains a mixture of thistle and white dandelion outpost extract, and may contain various flavors or natural carbohydrates as an additional ingredient such as ordinary beverages.
또한, 상기 건강기능식품은 식품첨가물을 추가로 포함할 수 있으며, “식품첨가물”로서의 적합여부는 다른 규정이 없는 한 식품의약품안정청에 승인된 식품첨가물공전의 총칙 및 일반시험법 등에 따라 해당 품목에 관한 규격 및 기준에 의하여 판정한다.In addition, the health functional food may further include food additives, and the suitability of the food functional food as a " food additive " is not limited to the corresponding items in general rules and general test methods approved by the Food and Drug Administration Shall be determined according to the relevant standards and standards.
상기 “식품첨가물공전”에 수재된 품목으로 예를 들어, 케톤류, 글리신, 구연산 칼륨, 니코틴산, 계피산 등의 화학적 합성품, 감색소, 감초추출물, 결정셀룰로오스, 고랭색소, 구아검 등의 천연첨가물, L-글루타민산나트륨제제, 면류첨가알칼리제, 보존료제제, 타르색소제제 등의 혼합 제제류 등을 들 수 있다.Examples of the products that have been used in the above-mentioned "food additives" include natural products such as ketones, chemical products such as glycine, potassium citrate, nicotinic acid and cinnamic acid, sensory coloring matter, licorice extract, crystalline cellulose, high- - Mixed preparations such as a sodium glutamate preparation, a noodle-added alkaline agent, a preservative preparation, a tar coloring agent and the like.
하기의 실시예를 통하여 본 발명을 더욱 구체적으로 설명하기로 하지만, 하기의 실시예가 본 발명의 범위를 제한하는 것은 아니며, 이는 본 발명의 이해를 돕기 위한 것으로 해석되어야 할 것이다.The present invention will now be described more specifically with reference to the following examples. However, the following examples should not be construed as limiting the scope of the present invention, but should be construed to facilitate understanding of the present invention.
1-1. 엉겅퀴와 1-1. Thistle 흰민들레White dandelion 전초outpost 추출물의 제조 Preparation of extract
수확한 엉겅퀴(Cirsium japonicum)와 흰민들레(Taraxacum coreanum)의 꽃과 뿌리를 제거한 전초를 물로 세척하고 동결건조기(Martin Christ, Osterode, Germany)로 동결건조하였다. 동결건조된 시료를 분쇄 후 99% 에탄올(EtOH)로 실온에서 24시간 3회 반복하여 정치추출하였다. 추출물은 여과지(Filter paper, No.4)를 이용하여 여과하고, 여과된 추출물은 회전감압농축기(Heidolph, Germanay)로 45℃에서 감압농축하였다. 농축물은 동결건조 후 분말형태로 수득하였다. Cirsium with harvested thistle japonicum ) and taraxacum coreanum were washed with water and lyophilized with a freeze dryer (Martin Christ, Osterode, Germany). The lyophilized sample was pulverized and then subjected to repeated extraction with 99% ethanol (EtOH) at room temperature for 24 hours three times. The extract was filtered using a filter paper (No. 4), and the filtered extract was concentrated under reduced pressure at 45 ° C with a rotary evaporator (Heidolph, Germanay). The concentrate was obtained as a powder after lyophilization.
1-2. 1-2. 실험 동물Experimental animal
6 주령 된 C57BL/6 수컷 마우스를 (주)중앙실험동물로부터 구입하였다. 22℃에서 명/암 주기를 12시간 간격으로 설정하고, 식이와 물을 자유롭게 공급하여 1 주일간 기본식이로 적응시켰다.Six-week-old C57BL / 6 male mice were purchased from the Central laboratory animals. The light / dark cycle was set at 12 hours at 22 ° C, and the diet and water were freely fed and adapted to the basic diet for one week.
알코올성 간 손상 개선 효과의 확인Identification of Alcoholic Liver Damage Improvement Effect
2-1. 2-1. 실험군Experimental group 설정 및 시료 투여 Setting and sample administration
상기 실시예 1-2의 실험동물을 각 군당 5마리씩, 아무것도 처리하지 않은 정상군, 5.0g/kg의 에탄올만을 투여한 대조군, 및 5.0g/kg의 에탄올에 용해된 각각의 실험시료를 투여한 5개의 실험군으로 나누어 실험을 진행하였다. 각 실험군에 투여된 실험시료는 하기 표 1에 기재된 바와 같다. 에탄올에 용해된 실험시료는 12시간마다 200mg/kg씩 3회 경구투여 하였고, 대조군에는 에탄올만을 12시간마다 3회 경구투여 하였다. 실험기간 동안 물과 식이는 자유롭게 공급하였고, 실험시료(엉겅퀴 추출물과 흰민들레 추출물)는 매일 동일한 시간에 경구 투여하였다. 마지막 경구투여 24시간 후 에테르 마취하여 개복 후 심장채혈 및 간 조직과 위조직을 적출하였다.The experimental animals of Example 1-2 were injected with 5 mice per group, a normal group without any treatment, a control group with 5.0 g / kg of ethanol alone, and each experimental sample dissolved in 5.0 g / kg of ethanol The experiment was divided into five experimental groups. The experimental samples administered to each experimental group are as shown in Table 1 below. Experimental samples dissolved in ethanol were orally administered three times at 200 mg / kg every 12 hours, and the control group was orally administered only three times every 12 hours. Water and diet were freely supplied during the experiment, and experimental samples (thistle extract and white dandelion extract) were orally administered at the same time every day. Twenty-four hours after the last oral administration, ether anesthesia was performed, and then the heart was harvested and liver tissues and stomach tissues were extracted.
실험군
Experimental group
추출물Thistle outpost
extract
추출물White dandelion outpost
extract
2-2. 혈청 2-2. serum 중 간middle 기능 지표효소 활성 측정 Functional indicator Enzyme activity measurement
제조사의 지시에 따라 진단 키트(Procedure No. 505, Sigma Chemical Co., St Louis, MO)를 사용하여 비색법으로(colorimetrically) GOT (glutamic oxaloacetic transaminase) 및 GPT (glutamic-pyruvic transaminase) 활성을 측정하였다.Glutamic oxaloacetic transaminase (GOT) and glutamic-pyruvic transaminase (GPT) activity were measured colorimetrically using a diagnostic kit (Procedure No. 505, Sigma Chemical Co., St Louis, MO) according to the manufacturer's instructions.
그 결과, 도 1(A) 및 (B)에 나타난 바와 같이 에탄올 투여로 GOT 및 GPT 수치(대조군)가 증가하였고, 엉겅퀴와 흰민들레 전초 추출물을 각각 단독으로 투여한 군에서는 GOT 및 GPT 수치가 감소되었으나 정상군 수준에는 미치지 못했다. 이에 반해, 엉겅퀴와 흰민들레 전초 추출물이 1:0.25 및 1:1 중량비로 혼합된 혼합물 A군 및 혼합물 B군은 대조군에 비해 GOT 및 GPT 수치가 현저하게 감소하였으며, 특히 혼합물 A군은 엉겅퀴와 흰민들레 전초 추출물을 각각 단독으로 투여한 군 보다 GOT 및 GPT 수치를 효과적으로 감소시켜 정상군 수준과 유사한 수준으로 간수치가 회복됨을 확인하였다. 이러한 혼합물 상승효과는 엉겅퀴와 흰민들레 전초추출물을 1:0.25의 중량비로 혼합하였을 때 가장 극대화됨을 알 수 있다.As a result, as shown in Figs. 1 (A) and (B), the GOT and GPT values (control group) were increased by ethanol administration and the GOT and GPT values were decreased in the group administered with thistle and white dandelion seed extract But it did not reach the normal level. Compared with the control group, the concentrations of GOT and GPT in the mixtures A and B, in which 1: 0.25 and 1: 1 weight ratio of thistle and white dandelion seeds extracts were mixed, The results showed that GOT and GPT levels were reduced more effectively than those treated with dandelion seedlings alone. The synergistic effect of this mixture is maximized when thistle and white dandelion outpost extract are mixed at a weight ratio of 1: 0.25.
2-3. 간 무게 측정2-3. Liver weighing
적출된 간 무게를 측정한 결과, 도 2에 나타난 바와 같이 체중(100g) 당 간 무게는 에탄올 투여에 의해 통계적으로 유의하게 증가하였다(대조군). 엉겅퀴 전초 추출물 투여군, 혼합물 A 투여군 및 혼합물 B 투여군은 에탄올에 의해 증가된 간 무게를 유의적으로 감소시켰고, 이들 중 혼합물 A 투여군의 간 무게 감소 효과가 가장 우수하였다. 특히, 혼합물 A군의 경우, 에탄올에 의해 증가된 간 무게를 정상군 수준으로 감소시켰다. 이러한 효과는 엉겅퀴와 흰민들레 전초 추출물을 각각 단독으로 투여한 군 보다 개선된 것으로, 엉겅퀴 전초 추출물과 흰민들레 전초 추출물을 1:0.25의 중량비로 혼합하였을 때 혼합물 상승효과가 가장 극대화됨을 알 수 있다.As shown in FIG. 2, liver weight per body weight (100 g) was statistically significantly increased by ethanol administration (control group). The effects of thistle outpost extract, mixture A, and mixture B on ethanol - induced liver weight were significantly decreased. Especially, in the case of mixture A group, the liver weight increased by ethanol was reduced to the normal group level. These effects were more improved than those of the thistle and white dandelion outpost extracts alone, and the synergistic effect of the mixture was maximized when the thistle outpost extract and white dandelion outpost extract were mixed at a weight ratio of 1: 0.25.
2-4. 간 조직 검사2-4. Liver biopsy
간 조직을 ~3mm 두께의 얇은 조각(slice)으로 자르고 10% 중화 포르말린으로 고정하고, 조직 조각을 파라플라스트(paraplast)에 포매하였다. 5μm의 조직 조각을 H&E(hematoxylin and eosin)으로 염색하고 Nikon Eclipse E400 광학 현미경으로 관찰하였다.Liver tissue was cut into ~ 3 mm thick slices, fixed with 10% neutralized formalin, and tissue pieces embedded in paraplast. Tissue pieces of 5 mu m were stained with H & E (hematoxylin and eosin) and observed with a Nikon Eclipse E400 optical microscope.
그 결과, 도 3에 나타난 바와 같이 에탄올만 투여한 군의 마우스 간 조직은 괴사와 함께 미세소포성 지방증(microvesicular steatosis)이 두드러지게 나타나 간 조직이 손상되었음을 확인하였다. 이러한 알코올성 간 손상은 엉겅퀴 전초 추출물 투여군, 혼합물 A, B 및 C 투여군에서 개선되었고, 특히, 엉겅퀴와 흰민들레 전초 추출물을 1:0.25의 중량비로 혼합한 혼합물 A군에서 가장 현저하게 개선되었다. 간 조직 검사에서도 마찬가지로 엉겅퀴와 흰민들레 전초 추출물을 1:0.25의 중량비로 혼합하였을 때 혼합물 상승효과가 가장 두드러지게 나타남을 확인하였다.As a result, as shown in FIG. 3, it was confirmed that mouse liver tissue of ethanol-only group showed prominent microvesicular steatosis together with necrosis, and liver tissue was damaged. These alcoholic liver injuries were improved in thistle outpost extract group, mixture A, B and C administration group, and most remarkably improved in mixture A group in which thistle and white dandelion outpost extract were mixed at a weight ratio of 1: 0.25. The liver biopsy showed that the synergistic effect was most pronounced when the thistle and white dandelion outpost extracts were mixed at a weight ratio of 1: 0.25.
이상의 실험 결과를 통해, 엉겅퀴와 흰민들레 전초 추출물이 1:0.25 내지 1:1의 중량비로 혼합된 혼합물이 알코올성 간 손상을 치료하는데 매우 유용함을 확인하였다.From the above results, it was confirmed that a mixture of thistle and white dandelion seedling extract at a weight ratio of 1: 0.25 to 1: 1 is very useful for treating alcoholic liver damage.
알코올성 위염 개선 효과의 확인Identification of alcoholic gastritis improvement
3-1. 위 조직의 3-1. Above 산화적Oxidative 스트레스 개선 Stress Improvement
상기 실시예 2-1에서 적출한 위 조직 내 산화적 스트레스를 ROS(reactive oxidative species)를 이용하여 측정하였다. 위 조직은 1 mM EDTA-50 mM 소듐 포스페이트 버퍼(pH 7.4)를 이용하여 분쇄한 후 ROS를 측정하기 위하여 25 mM DCFH-DA를 혼합하였다. 그 다음 형광 광도계를 이용하여 0분부터 매 10분씩 530 nm의 방출 파장(emission wavelength)과 486nm의 여기 파장(excitation wavelength)에서 30분간 측정한 산출 값을 계산하였다.The oxidative stress in the stomach tissues extracted in Example 2-1 was measured using ROS (reactive oxidative species). The stomach tissue was pulverized with 1 mM EDTA-50 mM sodium phosphate buffer (pH 7.4) and 25 mM DCFH-DA was mixed to measure ROS. Then, using a fluorescence spectrophotometer, the emission value measured at 530 nm and the excitation wavelength at 486 nm for 30 minutes was calculated every 10 minutes from 0 minutes.
그 결과, 도 4에 나타난 바와 같이 에탄올만을 투여한 대조군은 정상군에 비해 ROS 수치가 증가하였고 엉겅퀴 전초 추출물 또는 흰민들레 전초 추출물을 단독으로 투여한 군에서는 ROS 수치가 유의적으로 감소하였다. 특히 혼합물 A, B 및 C 투여군은 각각 상기 단독 투여군보다 ROS 수치가 더욱 감소하여 정상군 수준에 도달하였고, 혼합물 A와 혼합물 C 투여군의 경우 혼합물 상승 효과로 인해 산화적 스트레스 감소가 두드러지게 나타났다.As a result, as shown in FIG. 4, the ROS level of the control group treated with ethanol alone was increased compared to that of the normal group, and the ROS level was significantly decreased in the group administered with thistle outpost extract or white dandelion outpost extract alone. In particular, the ROS levels of the mixtures A, B and C were lower than those of the single administration group, and the concentrations of the mixture reached to the normal level. In the case of mixture A and mixture C, oxidative stress decreased remarkably due to synergistic effect.
3-2. 위 조직의 염증 개선3-2. Improved inflammation of stomach tissue
각 군에서 적출한 위 조직을 고정하여 손상된 범위 및 손상 정도를 관찰하였다. 그 결과, 도 5에 나타난 바와 같이 에탄올만 투여한 대조군의 경우, 위 조직의 염증, 출혈, 발적 및 부종이 발생하였고 손상 부위 면적 또한 매우 넓었다. 이러한 위 조직 손상은 혼합물 B 및 C 투여군에서 눈에 띄게 회복되었으며, 특히 다른 실험군들에 비해 엉겅퀴 전초 추출물과 흰민들레 전초 추출물이 1:4의 중량비로 혼합된 혼합물 C군에서 상승 효과가 최대로 나타나 위 조직 손상이 극적으로 완화되어 정상군 수준으로 회복됨을 확인하였다.The stomach tissues extracted from each group were fixed and the degree of damage and degree of damage were observed. As a result, as shown in FIG. 5, in the control group in which only ethanol was administered, inflammation, hemorrhage, erythema and edema occurred in the stomach tissue and the area of the damaged area was also very wide. These stomach injuries were remarkably recovered in the mixtures B and C, and the synergistic effect was maximized in the mixture C, in which the thistle outpost extract and the white dandelion outpost extract were mixed at a weight ratio of 1: 4, It was confirmed that the stomach injuries were dramatically relieved and recovered to normal levels.
이상의 실험 결과를 통해, 엉겅퀴와 흰민들레 전초 추출물이 1:0.25 내지 1:4, 바람직하게는 1:1 내지 1:4의 중량비로 혼합된 혼합물이 알코올성 위염을 치료하는데 매우 유용함을 확인하였다.From the above experimental results, it was confirmed that the mixture of thistle and white dandelion seedling extract at a weight ratio of 1: 0.25 to 1: 4, preferably 1: 1 to 1: 4 is very useful for treating alcoholic gastritis.
제조예Manufacturing example 1: 약학적 제제의 제조 1: Preparation of pharmaceutical preparations
1-1. 1-1. 산제의Sanje 제조 Produce
엉겅퀴 전초 추출물 2g과 흰민들레 전초 추출물 0.5g의 혼합물 또는 엉겅퀴 전초 추출물 0.5g과 흰민들레 전초 추출물 2g의 혼합물을 유당 1g과 혼합한 후, 기밀포에 충진하여 산제를 제조하였다.A mixture of 2 g of the thistle outpost extract and 0.5 g of the white dandelion outpost extract or 0.5 g of the thistle outpost extract and 2 g of the white dandelion outpost extract was mixed with 1 g of lactose and filled in airtight bags to prepare a powder.
1-2. 정제의 제조1-2. Manufacture of tablets
엉겅퀴 전초 추출물 100mg과 흰민들레 전초 추출물 25mg의 혼합물 또는 엉겅퀴 전초 추출물 25mg과 흰민들레 전초 추출물 100mg의 혼합물을 옥수수 전분 100 ㎎, 유당 100 ㎎ 및 스테아린산 마그네슘 2 ㎎과 혼합한 후, 통상의 정제의 제조방법에 따라서 타정하여 정제를 제조하였다.The mixture of 100 mg of corn starch, 100 mg of lactose and 2 mg of magnesium stearate was mixed with a mixture of 100 mg of the thistle outpost extract and 25 mg of the white dandelion outpost extract or 25 mg of the thistle outpost extract and 100 mg of the white dandelion outpost extract, To prepare tablets.
1-3. 캡슐제의 제조1-3. Preparation of capsules
엉겅퀴 전초 추출물 2g과 흰민들레 전초 추출물 0.5g의 혼합물 또는 엉겅퀴 전초 추출물 0.5g과 흰민들레 전초 추출물 2g의 혼합물을 옥수수 전분 100 ㎎, 유당 100 ㎎ 및 스테아린산 마그네슘 2 ㎎과 혼합한 후, 통상의 캡슐제의 제조방법에 따라서 젤라틴 캡슐에 충전하여 캡슐제를 제조하였다.A mixture of 2 g of the thistle outpost extract and 0.5 g of the white dandelion seedling extract or 0.5 g of the thistle outpost extract and 2 g of the white dandelion seedling extract were mixed with 100 mg of corn starch, 100 mg of lactose and 2 mg of magnesium stearate, The capsule was packed in a gelatin capsule according to the manufacturing method of the capsule.
1-4. 주사액제의 제조1-4. Injection preparation
적당한 주사용 염화나트륨 BP에 엉겅퀴 전초 추출물 10 ㎍/㎖와 흰민들레 전초 추출물 2.5㎍/㎖의 혼합물 또는 엉겅퀴 전초 추출물 2.5 ㎍/㎖와 흰민들레 전초 추출물 10㎍/㎖의 혼합물을 용해시키고, 생성된 용액의 pH를 묽은염산 BP를 사용하여 pH 3.5로 조절하고, 주사용 염화나트륨 BP(최대 1 ㎖)를 사용하여 용적을 조절하여 충분히 혼합하였다. 용액을 투명 유리로 된 5 ㎖ 타입 I 앰플 중에 충전시키고, 유리를 용해시킴으로써 공기의 상부 격자하에 봉입시키고, 120 ℃에서 15분 이상 오토클래이브시켜 살균하여 주사액제를 제조하였다.A mixture of 10 占 퐂 / ml of thistle outpost extract and 2.5 占 퐂 / ml of a mixture of thistle outpost extract and 2.5 占 퐂 / ml of thistle outpost extract and 10 占 퐂 / ml of white dandelion outpost extract was dissolved in a suitable injectable sodium chloride BP and the resulting solution Was adjusted to pH 3.5 with diluted hydrochloric acid BP and mixed well by adjusting the volume using injectable sodium chloride BP (max. 1 ml). The solution was filled in a 5 ml type I ampoule made of transparent glass, sealed in an upper lattice of air by dissolving the glass, sterilized by autoclaving at 120 DEG C for 15 minutes or longer, and an injection solution was prepared.
제조예Manufacturing example 2: 건강식품의 제조 2: Manufacture of health food
2-1. 조리용 양념의 제조2-1. Manufacture of cooking seasonings
엉겅퀴 전초 추출물과 흰민들레 전초 추출물을 1:0.25 내지 1:4의 중량비로 혼합한 혼합물을 0.2 ~ 10 중량%로 첨가하여 건강 증진용 조리용 양념을 제조하였다.A mixture prepared by mixing the thistle outpost extract and the white dandelion outpour extract at a weight ratio of 1: 0.25 to 1: 4 was added in an amount of 0.2 to 10 wt% to prepare a cooking sauce for health promotion.
2-2. 토마토 2-2. tomato 케찹ketchup 및 소스의 제조 And source
엉겅퀴 전초 추출물과 흰민들레 전초 추출물을 1:0.25 내지 1:4의 중량비로 혼합한 혼합물 0.2 ~ 1.0 중량%를 토마토 케찹 또는 소스에 첨가하여 건강 증진용 토마토 케찹 또는 소스를 제조하였다.A tomato ketchup or sauce for health promotion was prepared by adding 0.2-1.0 wt% of a mixture prepared by mixing thistle outpost extract and white dandelion seed extract at a weight ratio of 1: 0.25 to 1: 4 to tomato ketchup or sauce.
2-3. 밀가루 식품의 제조2-3. Manufacture of flour food products
엉겅퀴 전초 추출물과 흰민들레 전초 추출물을 1:0.25 내지 1:4의 중량비로 혼합한 혼합물 0.1 ~ 5.0 중량%를 밀가루에 첨가하고, 이 혼합물을 이용하여 빵, 케이크, 쿠키, 크래커 및 면류를 제조하여 건강 증진용 식품을 제조하였다.Bread, cake, cookies, crackers and noodles were prepared by adding 0.1 to 5.0% by weight of a mixture obtained by mixing thistle outpost extract and white dandelion seedling extract at a weight ratio of 1: 0.25 to 1: 4 to wheat flour Health enhancing foods were prepared.
2-4. 2-4. 스프soup 및 육즙 (gravies)의 제조 And gravies
엉겅퀴 전초 추출물과 흰민들레 전초 추출물을 1:0.25 내지 1:4의 중량비로 혼합한 혼합물 0.1 ~ 1.0 중량%를 스프 및 육즙에 첨가하여 건강 증진용 육가공 제품, 면류의 수프 및 육즙을 제조하였다.0.1-1.0 wt% of a mixture of thistle outpost extract and white dandelion outpost extract at a weight ratio of 1: 0.25 to 1: 4 was added to the soup and juice to prepare health promotion meat product, noodle soup and juice.
2-5. 그라운드 2-5. ground 비프Beef (ground beef)의 제조 manufacture of ground beef
엉겅퀴 전초 추출물과 흰민들레 전초 추출물을 1:0.25 내지 1:4의 중량비로 혼합한 혼합물 10 중량%를 그라운드 비프에 첨가하여 건강 증진용 그라운드 비프를 제조하였다.A ground beef for health promotion was prepared by adding 10% by weight of a mixture obtained by mixing thistle outpost extract and white dandelion seedling extract at a weight ratio of 1: 0.25 to 1: 4 to ground beef.
2-6. 유제품 (dairy products)의 제조2-6. Manufacture of dairy products
엉겅퀴 전초 추출물과 흰민들레 전초 추출물을 1:0.25 내지 1:4의 중량비로 혼합한 혼합물 0.1 ~ 1.0 중량%를 우유에 첨가하고, 상기 우유를 이용하여 버터 및 아이스크림과 같은 다양한 유제품을 제조하였다.0.1 to 1.0 wt.% Of a mixture obtained by mixing the thistle outpost extract and the white dandelion seedling extract at a weight ratio of 1: 0.25 to 1: 4 was added to milk, and various dairy products such as butter and ice cream were prepared using the milk.
2-7. 2-7. 선식의Solar 제조 Produce
현미, 보리, 찹쌀, 율무를 공지된 방법으로 알파화시켜 건조시킨 것을 배전한 후 분쇄기로 입도 60 메쉬의 분말로 제조하였다.The brown rice, barley, glutinous rice, and yulmu were dried by a known method and dried, and the powder was prepared into a powder having a particle size of 60 mesh by a pulverizer.
검정콩, 검정깨, 들깨도 공지된 방법으로 쪄서 건조시킨 것을 배전한 후 분쇄기로 입도 60 메쉬의 분말로 제조하였다.Black beans, black sesame seeds, and perilla seeds were steamed and dried by a known method, and then they were prepared into powders having a particle size of 60 mesh by a pulverizer.
엉겅퀴 전초 추출물과 흰민들레 전초 추출물을 1:0.25 내지 1:4의 중량비로 혼합한 혼합물을 진공 농축기에서 감압농축하고, 분무, 열풍 건조기로 건조하여 얻은 건조물을 분쇄기로 입도 60 메쉬로 분쇄하여 건조분말을 얻었다.The mixture obtained by mixing the thistle outpost extract and the white dandelion seedling extract at a weight ratio of 1: 0.25 to 1: 4 was concentrated under reduced pressure in a vacuum concentrator, sprayed and dried with a hot air drier, and the resulting dried material was pulverized to a particle size of 60 mesh using a pulverizer, ≪ / RTI >
상기에서 제조한 곡물류, 종실류 및 감초 추출물의 건조분말을 다음의 비율로 배합하여 제조하였다.The above-prepared cereal grains, seeds and dried powder of the licorice extract were blended in the following proportions.
곡물류 (현미 30 중량%, 율무 15 중량%, 보리 20 중량%),Cereals (30% by weight of brown rice, 15% by weight of yulmu, 20% by weight of barley)
종실류 (들깨 7 중량%, 검정콩 8 중량%, 검정깨 7 중량%),Seeds (7% by weight of perilla, 8% by weight of black beans, 7% by weight of black sesame seeds)
엉겅퀴 전초 추출물과 흰민들레 전초 추출물이 1:0.25 내지 1:4의 중량비로 혼합된 혼합물의 건조분말 (1 중량%),Dried powder (1% by weight) of a mixture of thistle outpost extract and white dandelion outpour extract mixed at a weight ratio of 1: 0.25 to 1: 4,
영지 (0.5 중량%), 및Manure (0.5% by weight), and
지황 (0.5 중량%)(0.5% by weight)
2-8. 탄산음료의 제조2-8. Manufacture of carbonated drinks
설탕 5~10%, 구연산 0.05 ~ 0.3 %, 카라멜 0.005 ~ 0.02 %, 비타민 C 0.1 ~ 1 %의 첨가물을 혼합하고, 여기에 79 ~ 94 %의 정제수를 섞어서 시럽을 만들었다. 상기에서 제조한 시럽을 85 ~ 98 ℃에서 20 ~ 180초 동안 살균하여 냉각수와 1 : 4의 비율로 혼합시킨 다음, 탄산가스를 0.5 ~ 0.82 % 주입하여 엉겅퀴 전초 추출물과 흰민들레 전초 추출물이 1:0.25 내지 1:4의 중량비로 혼합된 혼합물을 함유하는 탄산음료를 제조하였다.Syrup was prepared by mixing additives of 5 to 10% of sugar, 0.05 to 0.3% of citric acid, 0.005 to 0.02% of caramel and 0.1 to 1% of vitamin C and 79 to 94% of purified water. The syrup prepared above was sterilized at 85 to 98 ° C for 20 to 180 seconds, mixed with cooling water at a ratio of 1: 4, then carbon dioxide gas was injected at 0.5 to 0.82%, and the thistle outpost extract and white dandelion outpour extract were mixed at a ratio of 1: 0.25 to 1: 4 in the weight ratio.
2-9. 건강음료의 제조2-9. Manufacture of health drinks
액상과당 (0.5 %), 올리고당 (2 %), 설탕 (2 %), 식염 (0.5 %), 물 (75 %)과 같은 부재료에 엉겅퀴 전초 추출물과 흰민들레 전초 추출물이 1:0.25 내지 1:4의 중량비로 혼합된 혼합물을 균질하게 배합하여 순간 살균을 한 후 이를 유리병, 패트병 등 소포장 용기에 포장하여 건강음료를 제조하였다.The thistle outpost extract and the white dandelion outpost extract were added to the raw materials such as liquid fructose (0.5%), oligosaccharide (2%), sugar (2%), salt (0.5%) and water (75% , The mixture was homogenized and sterilized instantaneously, and then packaged in a glass bottle, plastic bottle or other plastic container to prepare a health drink.
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---|
약학회지. 2011. 제55권제2호, pp.160-167..* |
인터넷 기사. "민들레와 엉겅퀴, 약대 효과로 UP!". 메디컬 한의. (2013.01.13.).* |
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