KR101177888B1 - Composition for Relieving and Preventing Hangover - Google Patents

Composition for Relieving and Preventing Hangover Download PDF

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KR101177888B1
KR101177888B1 KR1020090011474A KR20090011474A KR101177888B1 KR 101177888 B1 KR101177888 B1 KR 101177888B1 KR 1020090011474 A KR1020090011474 A KR 1020090011474A KR 20090011474 A KR20090011474 A KR 20090011474A KR 101177888 B1 KR101177888 B1 KR 101177888B1
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vitamin
weight
acid
hangover
composition
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최병규
오한도
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주식회사 기영약품
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Abstract

본 발명은 식품 및 의약 조성물에 관한 것으로, 더욱 구체적으로는 호박산, 푸마르산, L-글루타민산 또는 L-글루타민산나트륨, 비타민 B군, L-주석산, 타우린, L-아르기닌, L-카르니틴, 글리신 및 오미자 추출물을 포함하는 것을 특징으로 하는 음주로 인한 숙취 증상의 예방, 해소용 조성물에 관한 것이다. 본 발명의 조성물은 임상실험 결과 혈중 알코올 농도와 아세트알데히드 농도를 격감시키는 것으로 나타나 우수한 숙취 증상 예방 및 숙취해소 효능을 발휘할 뿐만 아니라, 음주로 인해 유발되는 간수치 증대를 억제하므로 간을 해독, 보호하는 효과도 갖는다. 또한, 상기 숙취해소의 효과와 더불어 젖산의 분비를 감소시키므로 피로 회복의 효과도 갖는다.The present invention relates to food and pharmaceutical compositions, more specifically succinic acid, fumaric acid, L- glutamic acid or sodium L- glutamate, vitamin B group, L-tartrate, taurine, L-arginine, L-carnitine, glycine and Schizandra extract It relates to the prevention, remedy composition for the hangover symptoms due to drinking, characterized in that it comprises a. The composition of the present invention has been shown to reduce the blood alcohol and acetaldehyde concentration in clinical trials, not only to exhibit excellent hangover prevention and hangover efficacy, but also to detoxify and protect the liver by inhibiting the increase in liver values caused by drinking. Also have. In addition, since the secretion of lactic acid is reduced along with the effect of the hangover, it also has the effect of fatigue recovery.

숙취해소, 호박산, 푸마르산, L-글루타민산 또는 L-글루타민산나트륨, 비타민 B군, L-주석산 Hangover Relief, Succinic Acid, Fumaric Acid, L-Glutamic Acid or L-Glutamate, Vitamin B Group, L-Tartrate

Description

숙취 예방 및 해소용 조성물{Composition for Relieving and Preventing Hangover}Composition for Relieving and Preventing Hangover

본 발명은 식품 및 의약 조성물에 관한 것으로, 더욱 구체적으로는 호박산, 푸마르산, L-글루타민산 또는 L-글루타민산나트륨, 비타민 B군, L-주석산, 타우린, L-아르기닌, L-카르니틴, 글리신 및 오미자 추출물을 포함하는 것을 특징으로 하는 음주로 인한 숙취 증상의 예방, 해소용 조성물에 관한 것이다.The present invention relates to food and pharmaceutical compositions, more specifically succinic acid, fumaric acid, L- glutamic acid or sodium L- glutamate, vitamin B group, L-tartrate, taurine, L-arginine, L-carnitine, glycine and Schizandra extract It relates to the prevention, remedy composition for the hangover symptoms due to drinking, characterized in that it comprises a.

한국의 알코올 소비는 세계 최고의 수준이며, 간암이나 간경변으로 인한 사망이 한국인의 주요 사망원인이 되는 등 음주로 인한 사회경제적 및 보건학적 폐해는 엄청나며 이는 증가 추세에 있다. Korea's alcohol consumption is among the highest in the world, and the socioeconomic and health consequences of drinking alcohol are enormous and increasing, with deaths from liver cancer and cirrhosis becoming the leading cause of death for Koreans.

과다한 알코올 섭취는 갈증, 피로감/졸음, 두통/어지러움, 오심/구토, 무력감, 복부팽만감/위장관 불쾌감 등의 숙취현상(hangover)을 유발하며, 만성적으로는 간질환, 위염, 췌장염, 고혈압, 중풍, 식도염, 당뇨병 그리고 심장병 등 많은 질환을 일으키는 것으로 보고되고 있다. Excessive alcohol consumption can cause hangovers such as thirst, fatigue / drowsiness, headache / dizziness, nausea / vomiting, helplessness, bloating / gastrointestinal discomfort. Chronic liver disease, gastritis, pancreatitis, high blood pressure, stroke, It is reported to cause many diseases such as esophagitis, diabetes and heart disease.

정상적인 상태에서 알코올을 섭취할 경우 위장 또는 소장에서 흡수되어 혈관으로 들어가 간으로 옮겨지게 된다. 알코올은 알코올탈수소효소(Alcohol dehydrogenase, ADH)에 의해 아세트알데하이드(Acetaldehyde)로 전환되고, 이는 알데하이드 탈수소효소(Aldehyde dehydrogenase, ALDH)의 작용에 의해 아세테이트(Acetate)로 전환되어 순환계를 통해 간세포 밖으로 배설되어진다. If you consume alcohol in the normal state, it is absorbed by the stomach or small intestine, enters the blood vessels, and moves to the liver. Alcohol is converted to acetaldehyde by alcohol dehydrogenase (ADH), which is converted to acetate by the action of aldehyde dehydrogenase (ALDH) and excreted out of the liver cells through the circulation. Lose.

숙취 현상은 체내에 축적된 알코올(Alcohol) 및 에탄올의 최초 대사산물인 아세트알데하이드의 작용에 의해 발생하는 것으로 알려져 있다(Swift R et al., Alcohol Health Res World. 1998;22(1):54-60).Hangover is known to be caused by the action of acetaldehyde, the first metabolite of alcohol and alcohol (Scoft R et al ., Alcohol Health Res World. 1998; 22 (1): 54-). 60).

종래 이와 같은 숙취를 해소하기 위해서 콩나물, 북어 등을 이용한 음식물이 이용되어 왔으며 최근에는 숙취해소를 위한 많은 기능성 음료 또는 조성물들이 시판되고 있다.Conventionally, foods using bean sprouts, northern fish, etc. have been used to relieve such hangovers. Recently, many functional drinks or compositions for hangover relief have been marketed.

이들 종래 기술에 관련하여, 대한민국 공개특허 공보 제2005-0013073호에는 비타민과 허브추출물 분말을 포함하는 발포정의 제조방법이 개시되어 있고, 동 공개특허 공보 제2006-0117645호에는 천년초 추출액 및 엑스의 제조방법이 개시된 바 있으며, 대한민국 등록 특허 공보 제10-0372561호에는 천연 생약제 추출물을 포함하는 숙취해소용 조성물 및 이를 유효 성분으로 함유하는 건강보조식품이 개시되어 있는 등 다양한 천연소재 추출물에 의한 숙취해소제 특허들이 제안되어 있다.In relation to these prior arts, Korean Unexamined Patent Publication No. 2005-0013073 discloses a method for producing effervescent tablets containing vitamins and herbal extract powders, and Korean Patent Publication No. 2006-0117645 discloses preparation of extracts and extracts of cheonnyeoncho. The method has been disclosed, and the Republic of Korea Patent Publication No. 10-0372561 discloses hangover relief composition comprising a natural herbal extracts and health supplements containing the same as an active ingredient is disclosed hangover by various natural material extracts Patents have been proposed.

그러나, 위와 같은 숙취해소를 위한 다양한 노력에도 불구하고, 혈중 알코올 농도와 아세트알데히드 농도를 격감시켜, 간에서의 알코올 분해 효율이 더욱 증진된 기능성 조성물에 대한 요구가 여전히 있다.However, despite various efforts to relieve hangovers above, there is still a need for functional compositions in which blood alcohol and acetaldehyde levels are reduced, thereby further enhancing alcohol degradation efficiency in the liver.

본 발명자들은 인체에 우수한 숙취해소 및 예방 기능을 가지는 숙취해소용 조성물을 개발하기 위하여 연구를 거듭하던 중, 후술하는 바의 호박산, 푸마르산, L-글루타민산 또는 L-글루타민산나트륨, 비타민 B군, L-주석산, 타우린, L-아르기닌, L-카르니틴, 글리신 및 오미자 추출물을 함유한 조성물이 뛰어난 숙취 해소 효과를 나타내어 이것이 기능성 식품 및 의약으로 효율적으로 이용될 수 있음을 확인하고 본 발명을 완성하기에 이르렀다.The inventors of the present invention during the development of a hangover relief composition having excellent hangover relief and prevention function to the human body, succinic acid, fumaric acid, L- glutamic acid or L- glutamate, sodium vitamin B group, L- The composition containing tartaric acid, taurine, L-arginine, L-carnitine, glycine, and Schisandra chinensis extract exhibited excellent hangover-relieving effect, confirming that it can be efficiently used as a functional food and medicine, and completed the present invention.

따라서, 본 발명의 목적은 상술한 바와 같은 종래의 문제점을 해결하고, 음주로 인한 숙취증상을 효과적으로 예방하거나 숙취증상을 신속히 해소할 수 있는 의약 및 기능성 식품 조성물을 제공하는데 있다.Accordingly, an object of the present invention is to solve the conventional problems as described above, and to provide a medicinal and functional food composition that can effectively prevent the hangover symptoms due to drinking or to quickly resolve the hangover symptoms.

본 발명의 다른 목적은 간수치 증대를 억제하여 해독 작용 및 간을 보호하는 효과와 피로회복 효과를 갖는 조성물을 제공하는 데 있다.Another object of the present invention is to provide a composition having an effect of preventing detoxification, protecting the liver, and a fatigue recovery effect by inhibiting increase in liver values.

본 발명의 추가의 목적은 일반 소비자가 기호 또는 기능성 식품으로 이용할 수 있는 식품 조성물을 제공하는 데 있다.A further object of the present invention is to provide a food composition which can be used by consumers as a favorite or functional food.

본 발명의 조성물은 혈중 알코올 및 아세트알데히드 농도를 격감시키는 것으로 나타나 우수한 숙취 증상의 예방 및 숙취 해소의 효능을 발휘할 뿐만 아니라, 음주로 인해 유발되는 간수치 증대를 억제하므로 간을 해독, 보호하는 효과도 갖는다. 또한, 상기 숙취해소의 효과와 더불어 젖산의 분비를 감소시키므로 피로 회복의 효과도 갖는다. The composition of the present invention has been shown to significantly reduce the concentration of alcohol and acetaldehyde in the blood, thereby exerting the effect of preventing the hangover and preventing hangover, as well as inhibiting the increase in liver values caused by drinking, and thus detoxifying and protecting the liver. . In addition, since the release of lactic acid is reduced in addition to the effect of the hangover, it also has the effect of fatigue recovery.

본 발명은, 일면에 있어서, 호박산, 푸마르산, L-글루타민산 또는 L-글루타민산나트륨, 비타민 B군, L-주석산, 타우린, L-아르기닌, L-카르니틴, 글리신 및 오미자 추출물을 포함하는 것을 특징으로 하는 음주로 인한 숙취 증상의 예방 및 숙취해소용 조성물을 제공한다.The present invention, in one aspect, succinic acid, fumaric acid, L- glutamic acid or L- glutamate, sodium vitamin B group, L-tin acid, taurine, L- arginine, L- carnitine, glycine and Schizandra extract, characterized in that it comprises an extract Provided is a composition for preventing and preventing hangover symptoms caused by drinking.

본 발명은, 추가의 일면에 있어서, 상기 조성물에 더하여 액상 과당, 벌꿀, 황금 추출액, 유카 추출액, 배 추출액, 대추 추출액, 갈근 추출액, 감초 추출액, 매실 추출액, 홍삼향, 쌍화차향, 허브향, 및 과일향으로 이루어진 군 중에서 선택된 하나 이상의 성분을 포함하는 숙취 예방 및 숙취해소용 기능성 조성물을 제공한다.In still another aspect, the present invention provides liquid fructose, honey, golden extract, yucca extract, pear extract, jujube extract, brown root extract, licorice extract, plum extract, red ginseng flavor, biscented tea, herbal flavor, It provides a hangover prevention and hangover functional composition comprising at least one component selected from the group consisting of fruit flavor.

본 명세서에서 용어 "숙취(Hangover)"는 알코올 섭취 후에 나타나는 부작용, 즉 갈증, 전신권태, 피로감, 기억상실, 복부팽만감, 소화 불량, 구토, 설사, 비타민 결핍 등과 같이 섭취한 알코올 및 이의 대사물 알데하이드에 의해 유도되는 여러 가지 부작용을 의미한다. As used herein, the term "hang" refers to side effects that occur after alcohol consumption, such as thirst, systemic boredom, fatigue, memory loss, bloating, indigestion, vomiting, diarrhea, vitamin deficiency, and the like and their metabolite aldehydes. Means a number of side effects induced by.

이하, 본 발명을 더욱 상세하게 설명하기로 한다.Hereinafter, the present invention will be described in more detail.

본 발명의 조성물에 사용된 성분 중, 호박산은 숙신산(succinic acid)으로도 불리우며, 천연으로는 호박 속에 그 유도체가 함유되어 있으며, 이 밖에 테레빈유, 지의류, 균류 등에도 분포하고 알코올 발효시에도 소량 생성되며 청주 속에도 함유되어 있다. 무색무취이며 특이한 신맛을 지닌다. 열수(熱水), 알코올, 아세톤에 녹으나 에테르, 냉수에는 녹지 않는다. 끓는점까지 가열하면 한 분자의 물을 잃고 호박산무수물이 된다. 생체 내에서는 시트르산회로 등 여러 가지 대사과정의 중간물질로서 중요한 역할을 하고 있다. 호박산은 NADN-디하이드로게나이즈와는 독립적으로 아세트알데히드에 작용하여 아세트알데히드가 저산소증(Hypoxia)을 일으키지 못하도록 한다.Among the components used in the composition of the present invention, succinic acid is also referred to as succinic acid, and its derivative is naturally contained in amber, and is also distributed in terebin oil, lichens, fungi, etc. Produced and contained in sake. It is colorless and odorless and has an unusual sour taste. Soluble in hot water, alcohol, acetone, but insoluble in ether and cold water. Heating to the boiling point loses one molecule of water and turns into succinic anhydride. In vivo, it plays an important role as an intermediate of various metabolic processes such as the citric acid cycle. Succinic acid acts on acetaldehyde independently of NADN-dehydrogenase, preventing acetaldehyde from causing hypoxia.

상기 푸마르산(Fumaric Acid)은 불포화 디카르복시산의 일종으로 화학식은 C4H4O4이며, 녹는점 300~302℃(밀폐된 용기)의 특이한 신맛이 나는 바늘모양 결정으로, 약 200℃에서 승화한다. 에틸알코올에 녹으며, 물, 에테르, 아세톤에 잘 녹지 않는다. 생화학적으로 TCA 회로 중간생성물의 하나로 숙신산의 산화에 의해 만들어진다. 아미노산 대사에 있어서는 티로신과 페닐알라닌의 일부가 푸마르산을 거쳐 TCA회로에 들어간다. 또한 TCA회로의 다른 중간생성물과 함께 포스포에글피루브산을 거쳐 당을 생성하는 데도 이용된다.The fumaric acid (Fumaric Acid) is a kind of unsaturated dicarboxylic acid, the formula is C 4 H 4 O 4 , a unique sour needle crystal of melting point 300 ~ 302 ℃ (closed container), sublimation at about 200 ℃ . Soluble in ethyl alcohol, insoluble in water, ether and acetone. Biochemically produced by oxidation of succinic acid as one of the TCA cycle intermediates. In amino acid metabolism, some of tyrosine and phenylalanine enter the TCA cycle via fumaric acid. It is also used to produce sugars via phosphoeglypyruvic acid along with other intermediates of the TCA cycle.

상기 L-글루타민산(L-Glutamate), 또는 L-글루타민산나트륨(Monosodium L-Glutamate)은 아미노산의 주성분으로서 상기 분해반응식에 첨가되어 아세트알데히드의 무독성화에 핵심적 역할을 하는 미토콘드리아의 Cytosolic Malate-Aspartate의 속도를 높이며, 상기 호박산의 산화과정 속도도 촉진하게 된다. 또한 상기 L-글루타민은 크랩스 회로에서 빠른 산화과정을 거치는 동안 α-Ketoglutarate로 변형되며 최종적으로 뇌에 있어서 GAMC 시냅스와 글루타메이트(Glutamate)에 긍정적인 영향을 미쳐 알콜의 무독화를 촉진시킴으로써 알코올이 뇌에 미치는 악영향을 차단하는 기능을 한다.L-Glutamate, or L-Glutamate, is the main component of amino acids, and is added to the decomposition scheme to play a key role in the detoxification of acetaldehyde. To increase the speed of oxidation of the succinic acid. In addition, L-glutamine is transformed into α-Ketoglutarate during the rapid oxidation process in the Crab's circuit and finally has a positive effect on GAMC synapses and glutamate in the brain, promoting alcohol detoxification, It is a function to block adverse effects on the product.

상기 비타민 B는 일명 면역비타민으로 불리며, 비타민 B가 부족하면 흉선이 점점 축소되고 T-임파구의 생산도 감소되는 것으로 알려져 있다. 비타민 B에는 B1, B2, B3, B6, 판토텐산, 엽산, 비오틴, 콜린, 이노시톨 등 10여 종이 있으며, 본 발명에서는 특정의 것에 제한되지 않고 사용될 수 있으나, 특히 비타민 B1, 비타민 B2, 비타민 B6 또는 이들의 혼합물이 바람직하다.The vitamin B is known as immunovitamin, and it is known that the deficiency of vitamin B gradually reduces the thymus and reduces the production of T-lymphocytes. Vitamin B has about 10 species such as B 1 , B 2 , B 3 , B 6 , pantothenic acid, folic acid, biotin, choline, inositol, etc., but may be used without particular limitation in the present invention, in particular, vitamin B 1 , vitamin B 2 , vitamin B 6 or mixtures thereof are preferred.

L-주석산(타르타르산)은 흰색 결정을 지닌 유기산의 일종이다. 주석산은 포도, 바나나, 타마린드와 같은 많은 식물에서 존재하며, 와인에서 발견되는 주요한 산의 일종이다. 신맛을 가하기 위해 식품에 첨가되기도 하며, 산화방지제로서 사용되기도 한다.L-Tartaric acid (tartaric acid) is a type of organic acid with white crystals. Tartaric acid is present in many plants, such as grapes, bananas, and tamarinds, and is a major acid found in wine. It can be added to foods to add sourness, or used as an antioxidant.

상기 본 발명의 숙취해소용 조성물은 타우린, L-아르기닌, L-카르니틴, 글리신, 오미자 추출물, 액상과당, 벌꿀, 황금 추출액, 유카 추출액, 배 추출액, 대추 추출액, 갈근 추출액, 감초 추출액, 매실 추출액, 홍삼향, 쌍화차향, 허브향, 및 과일향으로 이루어진 군 중에서 선택된 하나 이상의 성분을 포함할 수 있다.The hangover composition of the present invention is taurine, L-arginine, L-carnitine, glycine, Schisandra extract, liquid fructose, honey, golden extract, yucca extract, pear extract, jujube extract, root extract, licorice extract, plum extract, It may include one or more components selected from the group consisting of red ginseng flavor, scented tea flavor, herbal flavor, and fruit flavor.

본 발명의 조성물에 있어서 타우린은 타우로콜산(taurocholic acid)과 같은 담즙산을 만들어 지방의 소화 흡수에 관여하며, 체내에서 간질발작을 억제하는 기능이 있고, 세포막의 보호기능이 있으며, 혈구와 폐조직의 산화를 방지하는 기능이 있다. 또한 중추신경계에 작용하고, 혈소판의 응집과 심장수축에 작용하며, 해독작용과 인슐린 유사기능도 보이고 있다. In the composition of the present invention, taurine is involved in the digestion and absorption of fat by making bile acids such as taurocholic acid, has the function of inhibiting epileptic seizures in the body, has a protective function of cell membranes, blood cells and lung tissue Has the function of preventing oxidation. It also acts on the central nervous system, on platelet aggregation and heart contraction, and also has detoxification and insulin-like functions.

또한, 오미자는 혈압강하 및 진해 거담작용을 갖고 있어서 한약재로 널리 이용되고 있을 뿐 아니라 위액 분비의 조절 및 담즙분비 촉진작용을 갖고 있어서 건 강 식품의 성분으로 널리 이용되고 있다. 특히 오미자는 단맛, 쓴맛, 신맛, 매운맛, 짠맛 등이 복합된 특이한 맛을 갖고 있으며 고유의 특이한 향을 나타내므로 다류와 주정 음료의 원료로도 이용되고 있다. In addition, Schisandra chinensis has a blood pressure lowering and antitussive expectorant action, which is not only widely used as a herbal medicine but also has a regulation of gastric juice secretion and biliary secretion, and thus is widely used as a component of healthy foods. In particular, Schisandra chinensis has a unique taste that combines sweetness, bitterness, sourness, spicy taste, salty taste, etc., and it is also used as a raw material for teas and spirit drinks.

상기 오미자, 황금, 유카, 배, 대추, 갈근, 감초, 매실 등의 추출물은 물과 각각의 재료를 용기에 넣고 물의 중량을 기준으로 1~5중량부로 혼합하여 고압멸균솥에 넣고 2~5 시간 동안 추출하여 여과하여 농축한 액을 재료로 사용하거나 분말 건조화 하여 분말상태로 사용한다. 별법으로, 상기 추출물들은 각 재료를 분쇄한 후에 물 또는 알코올로 추출할 수 있다. 또한 수증기 증류하여 추출하는 것도 바람직한 결과를 초래할 수 있다.The extract of Schisandra chinensis, golden, yucca, pear, jujube, brown root, licorice, plum, etc., put water and each material in a container and mix in 1 to 5 parts by weight based on the weight of water and put into a autoclave for 2 to 5 hours Extracted, filtered and concentrated to use the concentrated solution as a material, or powder dried to use as a powder. Alternatively, the extracts can be extracted with water or alcohol after grinding each material. Extraction by steam distillation can also produce desirable results.

본 발명의 숙취해소용 조성물은 후술하는 시험예로부터 확인할 수 있는 바와 같이 건강 기능성 식품 및 숙취의 해소, 예방 및 개선을 위한 약제학적 제제로 이용될 수 있다. 상기 건강기능성 식품은 일반 건강식품 또는 다이어트나 피로회복, 숙취해소용 등의 다목적 기능을 갖는 기능성 건강 식품으로도 이용될 수 있다.Hangover composition of the present invention can be used as a pharmaceutical preparation for the elimination, prevention and improvement of health functional food and hangover as can be seen from the test examples described below. The health functional food may also be used as a general health food or a functional health food having a multipurpose function such as diet or fatigue, hangover relief.

본 발명에 따른 의약 및 기능성 식품 조성물은 당해 분야에서의 통상적인 방법에 따라, 예를 들면 분말, 과립, 환, 정제, 캡슐, 액상 또는 음료 형태를 포함하는 제형으로 제공할 수 있다.The pharmaceutical and functional food compositions according to the invention may be provided in formulations comprising, for example, powders, granules, pills, tablets, capsules, liquids or beverages according to conventional methods in the art.

본 발명의 제약 또는 식품 조성물의 섭취량은 그 제제 형태, 투여 방법, 사용 목적 및 이것에 적용되는 개체의 연령, 체중, 증상에 따라서 적절히 설정되고, 일정하지 않지만 일반적으로는 제제 중에 함유되는 유효성분의 양은 성인 1일당, 예컨대 25 mg~5,000 ㎎/㎏이다. 물론 복용량은, 각종 조건에 의해서 변동하기 때 문에, 상기 섭취량보다 적은 양으로 충분한 경우도 있고, 또는 범위를 초과하여 필요한 경우도 있다.The intake amount of the pharmaceutical or food composition of the present invention is appropriately set according to the form of the preparation, the method of administration, the purpose of use, and the age, weight, and symptoms of the individual to which it is applied. The amount is, for example, 25 mg to 5,000 mg / kg per adult. Of course, since the dose varies depending on various conditions, an amount smaller than the intake amount may be sufficient, or it may be necessary beyond the range.

본 발명의 조성물이 약제학적 조성물로 제조되는 경우에는 약제학적으로 허용되는 담체를 추가적으로 포함한다. 약제학적으로 허용되는 담체는 제제시에 통상적으로 이용되는 것으로서, 탄수화물류 화합물(예: 락토오스, 아밀로스, 덱스트로스, 수크로오스, 솔비톨, 만니톨, 전분, 셀룰로오스 등), 아카시아 고무, 인산 칼슘, 알기네이트, 젤라틴, 규산 칼슘, 미세결정성 셀룰로오스, 폴리비닐피롤리돈, 셀룰로오스, 물, 시럽, 염 용액, 알코올, 아라비아 고무, 식물성 기름(예: 옥수수 기름, 목화 종자유, 두유, 올리브유, 코코넛유), 폴리에틸렌 글리콜, 메틸 셀룰로오스, 메틸히드록시 벤조에이트, 프로필히드록시 벤조에이트, 활석, 스테아르산 마그네슘 및 미네랄 오일 등을 포함하나, 이에 한정되는 것은 아니다. 본 발명의 약제학적 조성물은 상기 성분들 이외에 윤활제, 습윤제, 감미제, 향미제, 유화제, 현탁제, 보존제 등을 추가로 포함하나, 이에 한정되는 것은 아니다.When the composition of the present invention is prepared as a pharmaceutical composition, it further includes a pharmaceutically acceptable carrier. Pharmaceutically acceptable carriers are those commonly used in the preparation of carbohydrates (e.g., lactose, amylose, dextrose, sucrose, sorbitol, mannitol, starch, cellulose, etc.), acacia rubber, calcium phosphate, alginate, Gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water, syrup, salt solution, alcohol, gum arabic, vegetable oils (e.g. corn oil, cotton seed oil, soy milk, olive oil, coconut oil), polyethylene Glycol, methyl cellulose, methylhydroxy benzoate, propylhydroxy benzoate, talc, magnesium stearate and mineral oil, and the like. The pharmaceutical composition of the present invention further includes, but is not limited to, lubricants, wetting agents, sweeteners, flavoring agents, emulsifiers, suspending agents, preservatives, and the like, in addition to the above components.

또한, 본 발명의 조성물이 기능성 식품(건강기능식품 및 일반 식품) 조성물로 제조되는 경우에는 식품에 통상적으로 첨가되는 성분을 포함할 수 있으며, 예를 들어, 단백질, 탄수화물, 지방, 감미료를 포함한 식품첨가물을 포함한다. In addition, when the composition of the present invention is prepared as a functional food (health functional food and general food) composition may include ingredients that are commonly added to food, for example, food, including protein, carbohydrates, fat, sweeteners Contains additives.

본 발명에 따른 숙취해소용 의약 및 식품 조성물은 더욱 바람직한 실시형태에 있어서, 호박산 10~48 중량%, 푸마르산 5~27 중량%, L-글루타민산 또는 L-글루타민산나트륨 1~19 중량%, 비타민 B1, 비타민 B2, 비타민 B6 또는 이들의 혼합물 중에서 선택된 비타민 B 0.05~6 중량%, L-주석산 0.5~4 중량%, 타우린 4~20 중량%, L-아르기닌 0.5~4 중량%, L-카르니틴 0.5~4 중량%, 글리신 1~6 중량%, 및 오미자 추출분말(고형분) 0.5~4 중량%을 포함한다.
상기 조성물은 추가로 본 발명의 조성물의 전체 중량을 기준으로 액상과당 0.01~20 중량%, 벌꿀 0.01~2 중량%, 황금 추출액 0.01~2 중량%, 유카 추출액 0.01~2 중량%, 배 추출액 0.01~2 중량%, 대추 추출액 0.01~2 중량%, 갈근 추출액 0.01~2 중량%, 감초 추출액 0.01~2 중량%, 및 매실 추출액 0.01~2 중량%로 이루어진 군 중에서 선택된 하나 이상의 성분을 포함할 수도 있다.
Hangover medicament and food composition according to the present invention in a more preferred embodiment, 10 to 48% by weight of succinic acid, 5 to 27% by weight of fumaric acid, 1 to 19% by weight of L- glutamic acid or L- glutamate, vitamin B 1 Selected from vitamin B 2 , vitamin B 6, or a mixture thereof, 0.05 to 6% by weight of vitamin B, 0.5 to 4% by weight of L-tartrate, 4 to 20% by weight of taurine, 0.5 to 4% by weight of L-arginine, L-carnitine 0.5-4% by weight, glycine 1-6% by weight, and Schizandra chinensis extract powder (solid content).
The composition is further based on the total weight of the composition of the present invention 0.01 to 20% by weight of liquid fructose, 0.01 to 2% by weight of honey, 0.01 to 2% by weight of golden extract, 0.01 to 2% by weight of yucca extract, 0.01 to 0.01% of pear extract It may include one or more components selected from the group consisting of 2% by weight, jujube extract 0.01 ~ 2% by weight, root extract extract 0.01 ~ 2% by weight, licorice extract 0.01 ~ 2% by weight, and plum extract 0.01 ~ 2% by weight.

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추가로 상기 조성물에 향을 부여하기 위하여 향미료를 첨가할 수 있으며, 예를 들면 쌍화차향, 허브향, 홍삼향 및 과일향 등을 사용할 수 있다.In addition, flavoring may be added to impart flavor to the composition, and for example, ssanghwa tea, herbal flavor, red ginseng flavor and fruit flavor may be used.

음료의 경우, 본 발명에 따른 숙취해소용 조성물을 정제수로 5~200배 희석하여 제조할 수 있다. 따라서, 본 발명은 구체적인 실시형태에 있어서, 호박산 10~48 중량%, 푸마르산 5~27 중량%, L-글루타민산 또는 L-글루타민산나트륨 1~19 중량%, 비타민 B 0.05~6 중량%, L-주석산 0.5~4 중량%, 타우린 4~20 중량%, L-아르기닌 0.5~4 중량%, L-카르니틴 0.5~4 중량%, 글리신 1~6 중량%, 및 오미자 추출분말(고형분) 0.5~4 중량%을 포함하는 조성물을 5~200배 희석하여 제조된 것인 음주로 인한 숙취 예방 및 숙취해소용 음료를 제공한다.In the case of beverages, the composition for releasing hangovers according to the present invention may be prepared by diluting 5-200 times with purified water. Thus, in a specific embodiment of the present invention, 10 to 48% by weight of succinic acid, 5 to 27% by weight of fumaric acid, 1 to 19% by weight of L-glutamic acid or L-glutamic acid, 0.05 to 6% by weight of vitamin B, L-tartrate 0.5-4% by weight, 4-20% by weight of taurine, 0.5-4% by weight of L-arginine, 0.5-4% by weight of L-carnitine, 1-6% by weight of glycine, and 0.5-4% by weight of Schizandra chinensis powder (solid) It provides a drink for preventing hangover and hangover caused by drinking that is prepared by diluting a composition containing 5 to 200 times.

<실시예><Examples>

이하, 본 발명에 따른 숙취해소용 조성물을 바람직한 실시예를 통해 설명하고자 한다. 이 실시예는 오로지 본 발명을 보다 구체적으로 설명하기 위한 것으로서, 본 발명의 요지에 따라 본 발명의 범위가 이 실시예에 의해 제한되지 않는다는 것은 본 발명이 속하는 기술 분야에서 통상의 지식을 가진 자에게 있어서 자명할 것이다. Hereinafter, the hangover composition according to the present invention will be described through preferred embodiments. This embodiment is only for illustrating the present invention in more detail, and the scope of the present invention is not limited by this embodiment according to the gist of the present invention to those skilled in the art. Will be self-evident.

실시예 1: 식물 추출물의 제조Example 1: Preparation of Plant Extract

각각의 오미자, 황금, 유카, 배, 대추, 갈근, 감초, 매실 500g을 잘 세척한 후, 정제수 2 리터를 가하여 고압멸균솥에서 3 시간 동안 추출하였다. 이어서 여과하여 농축한 액을 분말화하여 각각의 분말 50g을 얻어 이를 후속 실시예에 사용하였다.500 g of each Schizandra chinensis, golden, yucca, pear, jujube, brown root, licorice and plums were washed well, and then, 2 liters of purified water was added and extracted in a autoclave for 3 hours. The filtrate was then concentrated to powder to give 50 g of each powder which was used in the subsequent examples.

실시예 2: 기능성 식품 조성물의 제조Example 2: Preparation of Functional Food Composition

다음의 표 1에 나타낸 성분을 혼합하여 기능성 정제 형태의 식품 조성물을 제조하였다.The ingredients shown in Table 1 were mixed to prepare a food composition in the form of a functional tablet.

성 분       ingredient 함량(단위: g)Content in g 비타민 B1Vitamin B1 0.480.48 비타민 B2Vitamin B2 0.480.48 비타민 B6Vitamin B6 0.720.72 호박산Succinic acid 240240 푸마르산Fumaric acid 160160 타우린Taurine 120120 L-글루타민산나트륨Sodium L-Glutamate 117.28117.28 글리신Glycine 3636 L-주석산L-Tartrate 2020 L-아르기닌L-arginine 2020 L-카르니틴L-carnitine 2020 오미자추출분말Schisandra chinensis powder 5.605.60

상기 각 실시예의 성분과 히드록시 프로필메틸 셀룰로오스 8g, 결정셀룰로오스 43.44g, 스테아린산 마그네슘 8g을 혼합하여 정제로 타정하였다. 본 실시예에서는 식물 추출물로서 오미자 추출분말을 사용하였으나, 본 발명은 이에 제한되지 않고, 상기한 각각의 추출물을 필요에 따라서 첨가할 수 있음은 자명하다.8 g of hydroxypropylmethyl cellulose, 43.44 g of crystalline cellulose, and 8 g of magnesium stearate were mixed and compressed into tablets. In the present embodiment, the Schizandra chinensis extract powder was used as the plant extract, but the present invention is not limited thereto, and it is apparent that each of the extracts may be added as necessary.

실시예 3~7: 정제의 제조Examples 3-7: Preparation of Tablets

다음의 표 2에 나타낸 성분을 혼합하여 기능성 정제 형태의 식품 조성물을 제조하였다.Food ingredients in the form of functional tablets were prepared by mixing the ingredients shown in Table 2 below.

성 분    ingredient 함량(g)                    Content (g) 실시예 3Example 3 실시예 4Example 4 실시예 5Example 5 실시예 6Example 6 실시예 7Example 7 호박산 Succinic acid 240 240 240 240 108 108 100 100 300 300 푸마르산 Fumaric acid 160 160 160 160 60  60 50  50 200 200 L-글루타민산 L-glutamic acid 23.4 23.4 117.36 117.36 42  42 10  10 100 100 비타민 B1 Vitamin B1 0.48 0.48 0.16 0.16 6   6 0.15 0.15 5   5 비타민 B2 Vitamin B2 0.48 0.48 0.24 0.24 3   3 0.15 0.15 5   5 비타민 B6 Vitamin B6 0.72 0.72 0.24 0.24 3   3 0.25 0.25 8   8 L-주석산 L-Tartrate 20  20 20  20 7.5 7.5 5  5 25  25 타우린 Taurine 120 120 120 120 45  45 45 45 150 150 L-아르기닌 L-arginine 20  20 20  20 7.5 7.5 5  5 25  25 L-카르니틴 L-carnitine 20  20 20  20 7.5 7.5 5  5 25  25 글리신 Glycine 36  36 36  36 13.5 13.5 12 12 45  45 오미자추출물 Schisandra chinensis extract 5.6 5.6 5.6 5.6 6   6 5  5 25  25

상기 각 실시예의 성분과 히드록시프로필메틸 셀룰로오스 8g, 결정셀룰로오스 43.44g, 스테아린산 마그네슘 8g을 혼합하여 정제로 타정하였다.8 g of hydroxypropylmethyl cellulose, 43.44 g of crystalline cellulose, and 8 g of magnesium stearate were mixed and compressed into tablets.

실시예 8: 캡슐의 제조Example 8: Preparation of Capsules

1,000 캡슐을 기준으로 호박산 108 g, 푸마르산 60 g, L-글루타민산나트륨 42 g, L-주석산 7.5 g, 비타민 B1 6 g, 비타민 B2 3 g 및 비타민 B6 3 g을 균질하게 혼합하고 이를 통상의 방식에 의하여 캡슐(1,000 캡슐 기준)을 제조하였다.On a 1,000 capsule basis, homogeneously mix 108 g of succinic acid, 60 g of fumaric acid, 42 g of sodium L-glutamate, 7.5 g of L-tartrate, 6 g of Vitamin B1, 3 g of Vitamin B2 and 3 g of Vitamin B6 and mix it in a conventional manner. Capsules (based on 1,000 capsules) were prepared.

실시예 9: 캡슐의 제조Example 9 Preparation of Capsules

1,000 캡슐을 기준으로 호박산 108g, 푸마르산 60g, L-글루타민산나트륨 42g, L-주석산 7.5g, 비타민 B1 6g, 비타민 B2 3g 및 비타민 B6 3g, 글리신 13.5g, 황납 13.5g, 대두레시틴 9g, L-아르기닌 7.5g, L-카르니틴 1.25g, 오미자추출분말 6g을 혼합하고 이를 통상의 방식에 의하여 캡슐을 제조하였다.Based on 1,000 capsules, 108 g of succinic acid, 60 g of fumaric acid, 42 g of sodium L-glutamate, 7.5 g of L-tartrate, 6 g of vitamin B1, 3 g of vitamin B2 and 3 g of vitamin B6, 13.5 g of glycine, 13.5 g of soy lecithin, 9 g of soy lecithin, L-arginine 7.5g, L-carnitine 1.25g, 6g of Schisandra chinensis powder was mixed and it was prepared capsules in a conventional manner.

실시예 10 : 음료의 제조Example 10 Preparation of Beverages

상기 실시예 3에서 제조한 조성물 6.4668g을 혼합한 후, 나머지는 정제수로 첨가한 후 음료수 1ℓ를 제조한 다음, 미량의 액상과당, 벌꿀과 향료를 첨가하여 저온살균하여 본 발명의 조성물로 제조하였다. 결과적으로 본 발명 음료수는 종래의 음료수 제품과 입안 감촉, 맛 그리고 종합평가 면에서 양호한 반응을 얻었다.After mixing 6.4668 g of the composition prepared in Example 3, the rest was added to purified water, and then 1 liter of beverage was prepared, followed by pasteurization by adding a small amount of liquid fructose, honey and flavoring to prepare a composition of the present invention. . As a result, the beverage of the present invention obtained a favorable response from the conventional beverage product in terms of mouth feel, taste and comprehensive evaluation.

실험예 1 : 혈중 알코올 농도 감소 효과 측정Experimental Example 1: Measurement of the effect of reducing blood alcohol concentration

본 발명에 따른 조성물의 숙취 예방 및 개선 효능을 확인하기 위해 20에서 50대의 남녀 20명을 무작위로 선발하여 각각 실험군과 대조군으로 나누고 이들을 대상으로 임상실험을 실시하였다. 실험을 시작하기 전 일주일간은 금주하도록 하였다. 알코올 음료를 섭취하기 30분 전 실험군은 상기 표 1의 조성물 800mg을 섭취하도록 하고, 대조군에는 동일한 부피의 위약을 섭취하도록 하였다. 실험대상자들은 각각 30분 후 20%의 알코올 음료 200㎖를 15분간 마시게 하였다. 섭취가 끝난 후 0, 30분, 1, 2, 3시간 경과한 시점에서 혈액을 채취하여 Enzymatic bioanalysis UV-method(F-Kit Roche, Cat. No.0176290)로 사용한 Kit의 조작법에 의해 혈중 알코올 농도를 측정하여, 그 결과를 표 3에 나타내었다.In order to confirm the effect of preventing and improving hangover of the composition according to the present invention, 20 men and women in their 50s were randomly selected and divided into experimental groups and control groups, respectively, and clinical trials were performed on them. This week was a week before the experiment. Thirty minutes before ingesting the alcoholic beverage, the experimental group was to take 800 mg of the composition of Table 1, and the control group to take the same volume of placebo. Subjects were allowed to drink 200 ml of 20% alcoholic beverages for 15 minutes after 30 minutes each. Blood alcohol concentration was measured by kit operation using Enzymatic bioanalysis UV-method (F-Kit Roche, Cat.No.0176290) at 0, 30 minutes, 1, 2, 3 hours after ingestion. Was measured, and the results are shown in Table 3.

본 발명에 따른 조성물의 혈중 알코올 농도 시험 결과Blood alcohol concentration test result of the composition according to the present invention 구분division 혈중 알코올 농도 (mg %)Blood Alcohol Concentration (mg%) 경과시간 (시간)Elapsed time (hours) 00 0.50.5 1One 22 33 대조군Control group 136.2136.2 127.3127.3 118.24118.24 95.6295.62 71.5871.58 실험군Experimental group 132.4132.4 111.1111.1 71.4971.49 59.8159.81 55.0355.03 혈중 알코올 농도 감소율(%)% Decrease in blood alcohol level 2.792.79 12.7312.73 39.5439.54 37.4537.45 23.1223.12

실험예 2 : 혈중 아세트알데히드 농도 감소 효과 측정Experimental Example 2: Determination of the Effect of Acetaldehyde Concentration in Blood

상기 실험예 1의 실험대상자에 대하여 혈중 아세트알데히드 농도를 Enzymatic bioanalysis UV-method(F-Kit Roche, Cat. No.0668613)로 사용한 Kit의 조작법에 의해 혈중 아세트알데히드 농도를 측정하였다. 측정한 결과를 평균화하였으며, 그 결과를 표 4에 나타내었다.Blood acetaldehyde concentration was measured by the kit operation using Enzymatic bioanalysis UV-method (F-Kit Roche, Cat. No.0668613). The measured results were averaged and the results are shown in Table 4.

본 발명에 따른 조성물의 혈중 아세트알데히드 농도 시험 결과Blood acetaldehyde concentration test result of the composition according to the present invention 구분division 혈중 아세트알데히드 농도 (mg %)Acetaldehyde concentration in blood (mg%) 경과시간 (시간)Elapsed time (hours) 00 0.50.5 1One 22 33 대조군Control group 1010 66 2.32.3 3.63.6 3.13.1 실험군Experimental group 7.27.2 5.85.8 1.11.1 1.81.8 1.41.4 혈중 아세트알데히드 농도 감소율(%)% Decrease in acetaldehyde concentration in blood 28.0028.00 3.333.33 52.1752.17 50.0050.00 54.8454.84

표 3 및 4에 나타낸 바와 같이, 본 발명의 조성물은 임상실험 결과 섭취가 끝난 후 0, 30분, 1, 2, 3 시간에 혈중 알코올 농도 감소율(%)이 2.79, 12.73, 39.54, 37.45, 23.12로 감소하였고, 혈중 아세트알데히드 농도가 28.00, 3.33, 52.17, 50.00, 54.84로 감소하는 것을 확인하였으며, 이는 도 1에서 나타내었다. As shown in Tables 3 and 4, the composition of the present invention showed that the percentage of decrease in blood alcohol concentration (%) was 2.79, 12.73, 39.54, 37.45, 23.12 at 0, 30 minutes, 1, 2, and 3 hours after the end of the clinical trial. It was confirmed that the concentration of acetaldehyde in blood decreased to 28.00, 3.33, 52.17, 50.00, 54.84, which is shown in FIG.

따라서, 기능성 식품 조성물이 뚜렷한 숙취해소 효과를 나타냄을 확인하였다.Therefore, it was confirmed that the functional food composition exhibits a clear hangover effect.

실험예 3 : 간 기능 검사 (SGPT(ALT), SGOT(AST)Experimental Example 3 Liver Function Test (SGPT (ALT), SGOT (AST)

상기 실험예 1의 실험군의 대상자에 한하여 알코올 음료 복용 전 최초 채혈시와 마지막 채혈시 혈액의 SGPT(ALT), SGOT(AST) 를 측정하였다. SGPT (ALT), SGOT (AST) of blood at the time of the first blood collection and the last blood collection before the alcoholic beverage was measured only for the subjects of the experimental group of Experimental Example 1.

측정한 결과를 표 5에 나타내었으며, SGPT(ALT), SGOT(AST)가 유의적으로 감소하는 것을 확인하였다. The measurement results are shown in Table 5, and it was confirmed that SGPT (ALT) and SGOT (AST) were significantly decreased.

본 발명의 간 기능 검사 결과Liver function test result of this invention 변인 Variable 알코올 음료 복용전
최초 채혈시
Before taking alcoholic drinks
At first blood collection
알코올 음료 복용후
마지막 채혈시
After taking alcoholic beverages
At the last blood collection
SGPT (ALT) SGPT (ALT) 28.56±23.40 28.56 ± 23.40 26.10±9.22 26.10 ± 9.22 SGOT (AST) SGOT (AST) 45.81±15.60 45.81 ± 15.60 34.16±6.74 34.16 ± 6.74

실험예 4 : 피로 회복 능력 평가Experimental Example 4: Evaluation of fatigue recovery ability

피로 회복 능력을 평가하기 위해 20에서 50대의 남녀 20명을 무작위로 선별하여 각각 실험군과 대조군으로 나누고, 운동검사 시작 1시간 전에 표 1에 나타낸 조성물을 각각 투여하였다. 이들을 대상으로 혈액 변인인 혈중 젖산 농도를 안정시, 운동 직 후, 회복기 3분, 10분, 20분에 측정하여 그 결과를 표 6에 나타내었다.To evaluate fatigue recovery ability, 20 men and women in their 20s and 50s were randomly selected and divided into experimental and control groups, respectively, and the compositions shown in Table 1 were administered 1 hour before the start of the exercise test. The blood lactate concentration, a blood variable, was measured at rest, 3 minutes, 10 minutes and 20 minutes immediately after exercise, and the results are shown in Table 6.

본 발명 조성물의 혈중 젖산 농도 시험 결과Blood lactic acid concentration test result of the composition of the present invention 변인
Variable
그룹
group
시기
Time
안정시
At rest
운동직후
Right after exercise
회복기           Recovery period
3분   3 minutes 10분   10 minutes 20분  20 minutes
Lactate(mmol/L)

Lactate (mmol / L)
실험군Experimental group 처치 전Before kill 1.3±0.461.3 ± 0.46 7.2±1.347.2 ± 1.34 6.8±1.406.8 ± 1.40 5.7±1.185.7 ± 1.18 3.8±1.033.8 ± 1.03
처치 후After treatment 0.7±0.220.7 ± 0.22 6.2±0.956.2 ± 0.95 5.7±1.035.7 ± 1.03 4.4±0.864.4 ± 0.86 3.0±0.703.0 ± 0.70 대조군
Control group
처치 전Before kill 1.0±0.331.0 ± 0.33 5.1±0.855.1 ± 0.85 4.6±0.774.6 ± 0.77 3.6±0.913.6 ± 0.91 2.6±0.682.6 ± 0.68
처치 후After treatment 1.2±0.271.2 ± 0.27 5.8±1.485.8 ± 1.48 5.5±1.355.5 ± 1.35 4.0±1.044.0 ± 1.04 3.1±1.313.1 ± 1.31

상기 표 6의 결과에서 알 수 있는 바와 같이, 본 발명의 조성물은 임상실험 결과 혈중 젖산 농도를 유의적으로 감소시켜, 피로회복에 영향을 미침을 확인하였다. As can be seen from the results of Table 6, the composition of the present invention was confirmed to significantly reduce blood lactate concentration in clinical trials, affecting fatigue recovery.

본 발명의 숙취해소 조성물은 임상실험 결과 혈중 알코올 농도 및 아세트알데히드 농도를 격감시키는 것으로 나타나 우수한 숙취 증상의 예방 및 숙취해소의 효능을 발휘할 뿐만 아니라, 음주로 인해 유발되는 간수치 증대를 억제하므로 간을 해독, 보호하는 효과도 갖는다. 또한, 상기 숙취해소의 효과와 더불어 젖산의 분비를 감소시키므로 피로 회복의 효과도 가지므로, 이를 기능성 식품 및 의약 제형으로 제공될 수 있다.The hangover relief composition of the present invention has been shown to reduce blood alcohol and acetaldehyde concentration in clinical trials, and not only exerts the effect of preventing hangover symptoms and relieving hangover, but also inhibits the increase in liver values caused by drinking, thus detoxifying the liver. It also has a protective effect. In addition, since the effect of relieving hangover and reducing the secretion of lactic acid also has the effect of fatigue recovery, it can be provided as a functional food and pharmaceutical formulation.

도 1은 본 발명에 따른 조성물의 혈중 알코올 농도와 혈중 아세트알데히드 농도 시험 결과를 나타내는 그라프도.1 is a graph showing blood alcohol concentration and blood acetaldehyde concentration test results of the composition according to the present invention.

Claims (8)

호박산 10~48 중량%, 푸마르산 5~27 중량%, L-글루타민산 또는 L-글루타민산나트륨 1~19 중량%, 비타민 B1, 비타민 B2, 비타민 B6 또는 이들의 혼합물 중에서 선택된 비타민 B 0.05~6 중량%, L-주석산 0.5~4 중량%, 타우린 4~20 중량%, L-아르기닌 0.5~4 중량%, L-카르니틴 0.5~4 중량%, 글리신 1~6 중량% 및 오미자 추출분말 0.5~4 중량%를 포함하는 것을 특징으로 하는 음주로 인한 숙취 예방 및 숙취해소용 식품 조성물.Vitamin B 0.05 to 6 selected from 10 to 48% by weight of succinic acid, 5 to 27% by weight of fumaric acid, 1 to 19% by weight of L-glutamic acid or sodium L-glutamate, vitamin B 1 , vitamin B 2 , vitamin B 6 or mixtures thereof Weight%, L-Tartic acid 0.5-4%, Taurine 4-20%, L-Arginine 0.5-4%, L-Carnitine 0.5-4%, Glycine 1-6%, and Schizandra chinensis extract 0.5-4 Hangover prevention and hangover food composition for drinking characterized in that it comprises a weight%. 삭제delete 제1항에 있어서, 상기 조성물이 알코올 탈수소효소와 아세트알데하이드 탈수소효소의 활성을 증가시키는 것을 특징으로 하는 것인 식품 조성물.The food composition of claim 1, wherein the composition increases the activity of alcohol dehydrogenase and acetaldehyde dehydrogenase. 제1항에 있어서, 상기 조성물이 분말, 과립, 환, 정제, 캡슐, 액상 또는 음료 형태인 것을 특징으로 하는 식품 조성물.2. A food composition according to claim 1, wherein said composition is in powder, granule, pill, tablet, capsule, liquid or beverage form. 삭제delete 삭제delete 삭제delete 호박산 10~48 중량%, 푸마르산 5~27 중량%, L-글루타민산 또는 L-글루타민산나트륨 1~19 중량%, 비타민 B1, 비타민 B2, 비타민 B6 또는 이들의 혼합물 중에서 선택된 비타민 B 0.05~6 중량%, L-주석산 0.5~4 중량%, 타우린 4~20 중량%, L-아르기닌 0.5~4 중량%, L-카르니틴 0.5~4 중량%, 글리신 1~6 중량% 및 오미자 추출분말 0.5~4 중량%를 포함하는 것을 특징으로 하는 간수치 증대를 억제하여 해독 작용 및 간을 보호하는 효과와 피로회복 효과를 갖는 것인 제약 조성물. Vitamin B 0.05 to 6 selected from 10 to 48% by weight of succinic acid, 5 to 27% by weight of fumaric acid, 1 to 19% by weight of L-glutamic acid or sodium L-glutamate, vitamin B 1 , vitamin B 2 , vitamin B 6 or mixtures thereof Weight%, L-Tartic acid 0.5-4%, Taurine 4-20%, L-Arginine 0.5-4%, L-Carnitine 0.5-4%, Glycine 1-6%, and Schizandra chinensis extract 0.5-4 Pharmaceutical composition that has a detoxification effect and the effect of protecting the liver and the fatigue recovery effect by inhibiting the increase in liver values, characterized in that it comprises a weight%.
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JP2000128784A (en) * 1998-10-20 2000-05-09 Kuressendo Corporation:Kk Hangover symptom
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