KR20100008220A - Composition for preventing and treating colon cancer containing extract of mushroom and herb medicine - Google Patents
Composition for preventing and treating colon cancer containing extract of mushroom and herb medicine Download PDFInfo
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- KR20100008220A KR20100008220A KR1020080068676A KR20080068676A KR20100008220A KR 20100008220 A KR20100008220 A KR 20100008220A KR 1020080068676 A KR1020080068676 A KR 1020080068676A KR 20080068676 A KR20080068676 A KR 20080068676A KR 20100008220 A KR20100008220 A KR 20100008220A
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- red ginseng
- chaga
- preventing
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Abstract
Description
본 발명은 버섯 및 생약 추출물을 함유하는 대장암 예방 또는 치료용 조성물에 관한 것이다. 특히, 본 발명은 차가버섯 추출물을 함유하는 대장암 예방 또는 치료용 조성물에 관한 것이다. 더욱 상세하게는 본 발명은 차가버섯 추출물, 감초 추출물 및 홍삼 추출물의 혼합물을 유효성분으로 포함하는 대장암 예방 또는 치료용 조성물에 관한 것이다. The present invention relates to a composition for preventing or treating colorectal cancer containing mushroom and herbal extract. In particular, the present invention relates to a composition for preventing or treating colon cancer containing chaga extract. More specifically, the present invention relates to a composition for preventing or treating colon cancer, comprising a mixture of chaga extract, licorice extract, and red ginseng extract as an active ingredient.
차가버섯은 소나무 비닐버섯과(Hymenochaetaceae)에 속하는 다년생의 담자균버섯으로 북위 45도 이상의 춥고 습한 북반구에 분포하며 자연 상태에서 성장하면 검은색의 균핵 덩어리가 되어 자작나무에 기생하는 극내한성 버섯이다. 바이러스에 의해 착생하여 수액을 먹고 자라는데, 대개 15~20년 동안 성장한다. 오리나무, 버드나무 및 단풍나무 등에서도 발견되지만 이들은 효능이 낮은 것으로 알려져 있다. 수령 15년 이상 가운데 두께 10cm 이상, 수분 함량 14% 이하, 60℃ 이하에서 건조 된 1등급만 약용으로 사용하고 나머지는 폐기하거나 차를 끓이는 용도로 쓴다. 차가버섯의 성분으로는 천연색소인 멜라닌과 플라보노이드, 트리터펜, 오브리쿠올 (obliquol), 란노스테롤, 이노시톨, 아가산 (agaric acid), 폴리페놀, β-헤테로 글루칸, 리그닌 및 알칼로이드 등이 있으며, 무기질로는 Ca, Mg, Fe 및 Mn 등이 함유되어 있으며, 민간에서 혈압조절, 신체 저항력 증강 등에 사용되고 있을 뿐만 아니라 당뇨, 신경통, 신경쇠약 등 많은 질병의 치료를 위하여 이용되고 있다.Chaga is a perennial basidiomycete belonging to the genus Hyenochaetaceae, distributed in the cold and humid northern hemisphere above 45 degrees north latitude, and grows in black to form a black nucleus nucleus that is parasitic on birch. It is engrossed by the virus, eats sap, and grows, usually for 15 to 20 years. It is also found in alder, willow and maple trees, but these are known to have low efficacy. Among 15 years or more, only Grade 1 dried at a thickness of 10cm or more, moisture content of 14% or less and 60 ℃ or less is used for medicinal purposes, and the rest is used for brewing or making tea. Chaga's ingredients include melanin, flavonoids, triterpenes, obliquol, lannosterol, inositol, agaric acid, polyphenols, β-heteroglucans, lignin and alkaloids. The furnace contains Ca, Mg, Fe and Mn, and is used in the civilian to control blood pressure, enhance physical resistance, and to treat many diseases such as diabetes, neuralgia, and nervous breakdown.
차가버섯의 생리활성에 대한 연구로는 항돌연변이 (Saitoh et al., 道衛硏究報第46集 (1996)), 항바이러스 (Kahlos K et al., Fitoterapia 57:4 (1996); 및 Ichmura T et al., Biosci. Biotechnol. Biochem. 62:575 (1998)), 및 항산화 (Cui Y et al., J. Ethnopharmacol. 96(1-2):79 (2005); 및 Babitskai, VG et al., Prikladmaya Bioxhimiya Mikrobiologiya, 36:439 (2000)), 항당뇨(Mizuno T et al., Int. J. Med. Mushroom 1:301 (1999)) 등이 보고되었다.Studies on the physiological activity of chaga mushrooms include antimutagenicity (Saitoh et al., Dosa 46 46 (1996)), antiviral (Kahlos K et al., Fitoterapia 57: 4 (1996); and Ichmura T et al., Biosci. Biotechnol. Biochem. 62: 575 (1998), and antioxidant (Cui Y et al., J. Ethnopharmacol. 96 (1-2): 79 (2005); and Babitskai, VG et al. , Prikladmaya Bioxhimiya Mikrobiologiya, 36: 439 (2000)) and antidiabetic (Mizuno T et al., Int. J. Med. Mushroom 1: 301 (1999)).
감초는 장미목 콩과의 여러해살이 풀로 뿌리의 경우 단맛을 나타내는 감미료로 사용되며, 한의약에서 전통적으로 사용해온 약초로서 티벳이나 인도에서는 폐질환 및 염증질환에 대한 약재로 사용되어 왔다(Demizu S et al., Chem Pharm Bull 36: 3474-3479, 1988). 그러나 감초가 염증작용을 감소시키는 명확한 기작에 대하여는 아직 밝혀지지 않았다. 또한, 감초 추출물은 이러한 효과를 증강시키거나 약재의 쓴맛을 적게 느끼게 하기 위하여 첨가되어 왔다(Vaya J et al., Free Radic Biol Med 23: 302-313, 1997). Licorice is a perennial herb of the Rosacea legumes, used as a sweetener for sweet roots, and has been used traditionally in Chinese medicine as a medicine for lung and inflammatory diseases in Tibet and India (Demizu S et al. Chem Pharm Bull 36: 3474-3479, 1988). However, no clear mechanism of licorice's inflammatory effects has been identified. In addition, licorice extract has been added to enhance this effect or to make the medicinal herbs less bitter (Vaya J et al., Free Radic Biol Med 23: 302-313, 1997).
동양약물학에서 감초 (甘草, Glycyrrhizae radix)는 많은 복합 처방에 빈번 히 응용되는 일반적으로 안전한 한약제이다(Kamei, J., et al., Eur. J. Pharmacol., 469, pp159-163, 2003). 근경(根莖)은 원주상(圓柱狀)인데 주근(主根)은 매우 길고 거칠고 크며, 외피(外皮)는 적갈색에서 암갈색이다. 뿌리는 단맛이 나서 감미료, 한약재로 사용하여, 중국 동북부와 시베리아, 몽골 등지에 분포한다. 감초의 근(根)과 근경(根莖)에는 트리테르펜 (triterpene) 계(系) 사포닌(saponin), 글리시르히진 (glycyrrhizin)이 함유되어 있는데, 이것은 글리시르히진산의 2-글루쿠론 (glucuron)산 배당체로 감초의 감미성분이다. 이 배당체에는 혈액작용은 없으나 글리시르헤틴 (glycyrrhetin)산에는 있다. 감초(根)의 가수분해 성분 중에는 우랄렌 (uralen)산이 추출되어 이것이 18α-글리시르헤틴 산이라는 것이 증명되었다(정보섭 외 1인, 향약대사전, 영림사, pp684-687, 1988).Licorice (Glycyrrhizae radix) in oriental pharmacology is a generally safe herbal medicine frequently applied in many combination prescriptions (Kamei, J., et al., Eur. J. Pharmacol., 469, pp 159-163, 2003). Root stock is columnar, main root is very long, coarse and large, and the outer shell is reddish brown to dark brown. Root is sweet and is used as sweetener and herbal medicine. It is distributed in northeastern China, Siberia and Mongolia. The roots and roots of licorice contain triterpene system saponins and glycyrrhizin, which are 2-glucuron of glycyrrhizin acid. Acid glycoside, a sweet component of licorice. This glycoside has no blood but glycyrrhetin acid. Among the hydrolyzed components of licorice, uralene acid was extracted and it was proved that it was 18α-glycirrhetin acid (Information et al., Ph.D.
홍삼 (Ginseng radix)은 오갈피과 (Araliaceae)에 속한 인삼 (Panax ginseng C. A. MEYER)의 건조근이다. 홍삼은 인삼을 쪄서 말린 것으로 성미는 달고 조금 쓰며 성질은 평 (平)하며 비 (脾)와 폐 (肺)로 들어가 작용하며 한의학에서 대표적인 보기약으로 주치효능은 대보원기, 납기평천, 생진지갈하며 중추신경에 대한 진정작용과 흥분작용이 있고 순환계에 작용하여 고혈압이나 동맥경화 예방 효과가 있어 강심작용, 항산화작용, 항피로작용, 항방사능작용과 혈당강하작용 등이 있다. Red ginseng (Ginseng radix) is a dry root of Panax ginseng C. A. MEYER belonging to the Araliaceae. Red ginseng is steamed and dried ginseng, taste is sweet and slightly bitter, flat nature, and enters the nasal and lung (대표적인) and acts as a typical medicine in the main medicine is Daebowon period, delivery date Pyeongcheon, Saengjinji There is a sedation and excitement effect on the central nervous system, and the circulatory system prevents hypertension or atherosclerosis.
주요성분으로는 사포닌 (saponin: ginsenosides), 파낙시놀(panaxynol), 베타-엘레멘 (β-elemene), 말톨 (maltol) 등이 있다. 홍삼의 액상 추출액 (aqueous extract)은 빈혈 (anemia), 당뇨병, 불면증 (insomnia), 위염 (gastritis), 혈압이상, 소화불량 (dyspepsia), 과로 (overstrain), 그리고 피로 (fatigue)를 치료하는 데 사용되어 왔으며, 사포닌 (saponin:ginsenosides)이라고 하는 여러 가지 트립테르펜 배당체 (triterpene glycoside)를 함유하고 있다고 연구되었다(Baranov A.I., J.Ethnopharmacol., 6, 339-53, 1982; Chong S.K., et al., Postgrad Med. J., 64, 841-6, 1988). The main ingredients are saponin (ginsenosides), panaxynol, beta-elemene and maltol. Aqueous extract of red ginseng is used to treat anemia, diabetes, insomnia, gastritis, blood pressure abnormalities, dyspepsia, overstrain, and fatigue It has been studied to contain a variety of tryterpene glycosides called saponin (ginsenosides) (Baranov AI, J. Ethnopharmacol., 6, 339-53, 1982; Chong SK, et al., Postgrad Med. J., 64, 841-6, 1988).
또한, 홍삼은 항고혈압작용, 강심작용 (cardiotonic), 진정작용 (sedative), 최음작용 (aphrodisiac), 노화방지 및 항산화 작용을 포함한 다양한 약리 효과를 가지고 있는 것으로 보고 되고 있다 (Gillis C.N., Biochem. Pharmacol., 54, 1-8, 1997). In addition, red ginseng has been reported to have various pharmacological effects including antihypertensive, cardiotonic, sedative, aphrodisiac, anti-aging and antioxidant activities (Gillis CN, Biochem. Pharmacol). , 54, 1-8, 1997).
대장암을 치료하는 방법으로서, 수술법이 널리 사용되고 있다. 특히, 국소적으로 진행된 질병 또는 전이성 질병의 대장암 환자 사이에서, 예후는 높은 발병률과 사망률로 매우 불리하다. As a method of treating colorectal cancer, surgical methods are widely used. In particular, among colon cancer patients of locally advanced or metastatic disease, the prognosis is very disadvantageous due to high incidence and mortality.
한편, 대장암을 치료하는 방법으로서, 수술 보다는 덜 유리한 결과를 나타내는 약물 요법이 시도되고 있다. 항종양 화합물인 5-플루오로우라실 (5-FU)은 대장암의 치료에서 주요 선택 약물이고, 그의 사용은 단지 한계적으로 효과적인 것으로 증명되었다. 5-FU는 대장암 크기를 일시적으로 감소시킬 수 있지만, 환자의 생존 기간이 실질적으로 연장되었거나 "치유"된 (5년의 경감기를 기준으로) 것을 나타내는 증거는 거의 없다. 5-FU를 사용한 화학 요법이 질병이 간으로 전이된 환자에서 사용되고 있지만, 그러한 케이스의 단지 25% 또는 그 미만에서만 일시적인 개선이 관찰되며, 전체적으로 생존율은 유의한 영향을 받지 않는다 [라몽트, 제이.티.(LaMont, J.T.) 및 이젤배처, 케이.(Isselbacher, K.), Harrison's Principles of Internal Medicine (10판), McGraw-Hill, New York, p.1764 (1983)]. 5-FU의 한계적인 효과에도 불구하고, 확실하게 더 효과적인 것으로 나타나는 다른 약물이나 복합 치료는 없었다 [수가베이커, 피.에이치. 등, 상동; 울리, 피.브이.(Wolley, P.V.) 등, New Eng. J. Med., 312: 1465 (1985)].On the other hand, as a method for treating colorectal cancer, drug therapies that have less favorable results than surgery have been tried. The anti-tumor compound 5-fluorouracil (5-FU) is the main drug of choice in the treatment of colorectal cancer, and its use has only proven to be marginally effective. 5-FU may temporarily reduce colorectal cancer size, but little evidence indicates that the patient's survival is substantially extended or "healed" (based on a 5-year reduction). Although chemotherapy with 5-FU is used in patients with disease metastasis to the liver, only a temporary improvement is observed in only 25% or less of such cases, and overall survival is not significantly affected [Lamont, J. LaMont, JT and Easelbacher, K., Harrison's Principles of Internal Medicine (10th edition), McGraw-Hill, New York, p. 1764 (1983). Despite the marginal effects of 5-FU, there were no other drugs or combination treatments that apparently appeared to be more effective [Su Baker, P.H. Back, homology; Woolley, P. V., et al., New Eng. J. Med., 312: 1465 (1985).
대장암에 대한 종래의 치료, 예를 들면, 외과적 절제술 또는 5-FU를 사용하는 화학 요법을 받고 있는 환자에 있어서의 매우 빈약한 5년 생존율 (약 50% 또는 그 미만)을 고려하면, 수술 이후, 진단을 확정하거나 암의 체적을 제거하는 것을 보조하는 것과 같이, 약물 또는 화합물을 사용하여 사람의 악성 대장암을 효과적으로 치료하는 새로운 방법을 발견하는 것은 매우 유용할 것이다. 수술법이 암 조직 모두를 제거할 수는 없으므로, 약물 치료는 또한 각종 기관으로 전이되거나 퍼진, 진행된 질병의 환자를 위해 매우 유용할 것이다. Given the very poor 5-year survival rate (about 50% or less) in patients undergoing conventional treatment for colorectal cancer, such as surgical resection or chemotherapy using 5-FU, It would then be very useful to find new ways to effectively treat malignant colorectal cancer in humans using drugs or compounds, such as to help confirm the diagnosis or to remove the volume of cancer. Since surgery cannot remove all of the cancerous tissues, drug treatment will also be very useful for patients with advanced disease that have spread or spread to various organs.
본 발명의 일실시예는 대장암을 효과적으로 예방하고 치료하는 조성물을 제공하는 것을 목적으로 한다.One embodiment of the present invention is to provide a composition for effectively preventing and treating colorectal cancer.
본 발명의 일실시예는 여러 천연 추출물을 조합함으로써 대장암의 예방 및 치료 효과를 극대화시키는 것을 목적으로 한다. One embodiment of the present invention aims to maximize the prevention and treatment effect of colorectal cancer by combining several natural extracts.
본 발명의 일실시예는 천연 추출물을 사용함으로써 인체에 부작용이 현저히 낮은 대장암 예방 및 치료제를 제공하는 것을 목적으로 한다.One embodiment of the present invention is to provide a preventive and therapeutic agent for colorectal cancer with a significantly low side effects to the human body by using a natural extract.
본 발명의 일실시예는 유효성분으로서 차가버섯 추출물을 포함하는 것을 특징으로 한다. One embodiment of the present invention is characterized in that it comprises chaga extract as an active ingredient.
본 발명의 일실시예는 유효성분으로서 차가버섯 추출물, 감초 추출물 및 홍삼 추출물을 포함하는 것을 특징으로 한다. One embodiment of the present invention is characterized in that it comprises chaga mushroom extract, licorice extract and red ginseng extract as an active ingredient.
본 발명을 이용하면, 인체에 미치는 부작용이나 독성 없이 대장암을 효과적으로 예방 또는 치료할 수 있는 효과를 얻을 수 있다. Using the present invention, it is possible to obtain an effect that can effectively prevent or treat colorectal cancer without side effects or toxicity to the human body.
이하, 본 발명에 대하여 더욱 상세히 설명한다. Hereinafter, the present invention will be described in more detail.
차가버섯의 학명은 이노노투스 오블리쿠아 ( Inonotus obliqua) 또는 퍼스코포리아 오블리쿠아(Fuscoporia obliqua)(persoon ex Fires) 이다. 러시아에서는 차가(Chaga)로 불리우며, 일본에서는 가바노아나타케로 불리운다. 균핵 형태는 표면이 검고, 종횡으로 균열이 많으며, 내부는 황갈색으로 목질진흙버섯( Phellinus linteus )과 비슷하다. 균사가 조밀하게 모여 만드는 딱딱한 덩어리인 균핵이 주로 약용으로 사용하는 부분이다. 균핵의 직경은 10 내지 20cm 정도로 대형이다. 자실체의 두께는 2 내지 8mm 정도이고 전면에 관공이 있으며 강모체는 여러개이다.The scientific name of chaga is Inonotus obliqua or Fuscoporia obliqua (persoon ex Fires). In Russia it is called Chaga, and in Japan it is called Kabanoanatake. Mycobacterium forms a black surface, with many cracks on both sides, and yellowish brown inside, similar to Phellinus linteus. Mycelium, a hard mass made by densely packed mycelia, is mainly used for medicinal purposes. The diameter of the bacterium is large, about 10-20 cm. The fruiting body has a thickness of about 2 to 8mm, a hole on the front, and several bristle bodies.
차가버섯은 자작나무류( Betula sp. ), 특히 자작나무( Betula platyphylla var. japonica)에서 발생한다. 자작나무류에 검은 암 덩어리처럼 붙어 있다가 그 덩어리가 점차 커지면서 자작나무류가 점차 죽어가는 반활물 반사물 기생버섯이다.Chaga occurs in birch (Betula sp.), Especially birch (Betula platyphylla var. Japonica). It is a semi-reflective parasitic mushroom that is attached to a birch tree like a black rock mass, and the birch tree gradually dies as the mass grows larger.
차가버섯은 원래 자연산 채취로 이용되어 왔지만, 수량도 적고 또 채취에 많은 노력을 요하므로 인공배양 하는 것이 바람직하다. 배양방법으로는 여러가지 방법이 있지만, 그 중에서도 톱밥 배양 및 액체 배양에 의한 것이 바람직하다. 그 외에도 인공적으로 자작나무류의 생나무에 차가버섯 균사를 식균하여 증식시킨 균사 또는 그 균사를 생육시켜 얻은 균핵을 이용할 수도 있다. 톱밥 배양은 먼저 자작나무류의 수목의 톱밥을 준비하고 여기에 석회, 쌀을 넣고 혼합하며 수분을 조정한 후 혼합물을 내열성의 용기 또는 봉투에 넣고 이를 가열 멸균하여 톱밥 배양기를 얻는다. 이 톱밥 배양기를 차가버섯 균사의 생육온도, 바람직하게는 20℃이하로 냉 각한 후 균사체를 생육시킨다. 수개월동안 균사가 배양기에서 새하얗게 생육하면 이를 채취한 후 필요한 처리를 하여 유효성분을 추출하고, 이를 유효성분으로서 이용한다.Chaga was originally used for natural harvesting, but it is preferable to artificially cultivate because the quantity is small and requires a lot of effort to collect. There are various methods of culturing, but among them, sawdust culturing and liquid culturing are preferred. In addition, it is also possible to use a mycelium obtained by growing the mycelium or artificially grown mycelia of chaga mycelia on artificial green trees of birch. Sawdust cultivation is prepared by first preparing the sawdust of birch trees, lime, rice, mixed with water, and then adjusting the moisture, and heat sterilization of the mixture into a heat-resistant container or bag to obtain a sawdust incubator. The sawdust incubator is cooled to a growth temperature of chaga mycelium, preferably 20 ° C. or lower, and then the mycelium is grown. When mycelia grow white in the incubator for several months, it is collected and processed as needed to extract the active ingredient, which is used as an active ingredient.
차가버섯의 유효성분을 추출하는 방법에는 여러가지가 있다. 그 중에서도 천연 차가버섯 또는 배양 차가버섯의 균사를 PBS 용액, 부탄올, 에틸알콜, 초산에틸 또는 아세톤으로 처리하고 그 각각의 불용물로부터 활성성분을 취출할 수 있다. 또는, 천연 차가버섯 또는 배양 차가버섯의 균사성분 또는 균사 추출물을 카본 또는 숯으로 흡착처리하고, 그 각각의 비흡착물로부터 활성성분을 취출할 수도 있다. 또한, 천연 차가버섯 또는 배양 차가버섯을 다양한 pH의 물로 펄펄 끓이는(예컨대 60분간 펄펄 끓임) 열수 추출에 의해서도 유효 성분을 얻을 수 있다. 이들 추출 활성 성분은 수용성으로 내열성, 내산성 있는 안정한 물질인 것으로 인정된다. 이 추출 성분을, 그대로 경구 섭취하거나 의약품 또는 식품류에 혼합하고 그 혼합물을 섭취할 수 있다.There are several ways to extract the active ingredient of chaga. Especially, the mycelia of natural chaga or cultured chaga can be treated with PBS solution, butanol, ethyl alcohol, ethyl acetate or acetone, and the active ingredient can be taken out from each insoluble matter. Alternatively, the mycelium component or mycelium extract of natural chaga or cultured chaga may be adsorbed with carbon or charcoal, and the active ingredient may be taken out from each of the nonadsorbed substances. The active ingredient can also be obtained by hot water extraction in which natural chaga or cultured chaga are boiled with water at various pHs (eg, boiled for 60 minutes). These extract active ingredients are recognized to be water-soluble, heat-resistant and acid-resistant stable substances. This extract component may be taken orally as it is, or may be mixed with medicines or foodstuffs and consumed thereof.
본 발명의 일실시예에 있어서, 감초 조추출물은 물, 탄소수 1~4의 함수 또는 무수 저급 알코올, 상기 저급 알코올과 물과의 혼합 용매, 또는 아세톤, 에틸 아세테이트, 클로로포름, 1,3-부틸렌글리콜, 부틸 아세테이트 등의 추출 용매를 이용하여 수득될 수 있다. 바람직하게는, 감초 추출물은 함수 저급 알코올, 가장 바람직하게는 에탄올을 이용하여 얻어진 것이다. In one embodiment of the present invention, the crude licorice extract is water, water of 1 to 4 carbon atoms or anhydrous lower alcohol, mixed solvent of the lower alcohol and water, or acetone, ethyl acetate, chloroform, 1,3-butylene It can be obtained by using an extraction solvent such as glycol, butyl acetate and the like. Preferably, the licorice extract is obtained using a hydrous lower alcohol, most preferably ethanol.
예컨대, 먼저 감초를 건조 후 마쇄하여 분말화한 후, 건조 중량의 약 1 내지 10배, 바람직하게는 약 2 내지 6배의 물 또는 저급 알콜을 가하고 약 20 내지 60 ℃, 바람직하게는 약 30 내지 70 ℃로 가열하면서 약 1 내지 5시간 동안, 바람직하 게는 약 1.5 내지 3시간 동안 초음파 추출하고 냉각 및 여과한 후 회전증발기를 이용하여 감압 농축함으로써 수득될 수 있다. 이 때 여과 후 남은 잔사에 대하여 여과 과정을 2회 이상 반복하여 실시할 수 있다.For example, licorice is first dried and then ground and powdered, and then about 1 to 10 times the dry weight, preferably about 2 to 6 times water or lower alcohol, and about 20 to 60 ° C., preferably about 30 to It can be obtained by ultrasonic extraction, cooling and filtration for about 1 to 5 hours, preferably about 1.5 to 3 hours while heating to 70 ℃, and concentrated under reduced pressure using a rotary evaporator. At this time, the filtration process may be repeated two or more times with respect to the residue remaining after filtration.
본 발명의 일실시예에 있어서, 홍삼 조추출물은 물, 탄소수 1~4의 함수 또는 무수 저급 알코올, 상기 저급 알코올과 물과의 혼합 용매, 또는 아세톤, 에틸 아세테이트, 클로로포름, 1,3-부틸렌글리콜, 부틸 아세테이트 등의 추출 용매를 이용하여 수득될 수 있다. 바람직하게는, 홍삼 추출물은 함수 저급 알코올, 가장 바람직하게는 에탄올을 이용하여 얻어진 것이다. In one embodiment of the present invention, the crude red ginseng extract is water, water of 1 to 4 carbon atoms or anhydrous lower alcohol, a mixed solvent of the lower alcohol and water, or acetone, ethyl acetate, chloroform, 1,3-butylene It can be obtained by using an extraction solvent such as glycol, butyl acetate and the like. Preferably, the red ginseng extract is obtained using a hydrous lower alcohol, most preferably ethanol.
예컨대, 본 발명의 일실시예에 따른 홍삼 추출물은 다음과 같이 제조될 수 있다: 인삼을 쪄서 말리는 통상의 홍삼 제조 방식으로 제조된 홍삼을 물로 세척하고 1 내지 48시간 동안 냉침, 바람직하게는 10시간 동안 냉침한 홍삼을 1 내지 15배의 물, 에탄올 또는 메탄올과 같은 극성용매, 바람직하게는 5 내지 10 배의 물에 넣고 40 내지 100℃, 바람직하게는 70~90℃에서 가열한 후, 가열된 추출물을 1 내지 10회 반복하여 재추출하여, 감압여과하고 여과한 추출물을 혼합하여 회전 진공 농축기로 20 내지 100℃, 바람직하게는 50 내지 70℃에서 감압 농축하여 용매를 제거함으로써 물, 탄소수 1 내지 4의 저급 알콜 또는 이들의 혼합용매에 따른 가용 추출물인 조추출물을 수득할 수 있다.For example, the red ginseng extract according to an embodiment of the present invention may be prepared as follows: Red ginseng prepared by the conventional red ginseng manufacturing method by steaming ginseng is washed with water and cooled for 1 to 48 hours, preferably 10 hours. The red ginseng chilled for a while is put in a polar solvent such as 1 to 15 times water, ethanol or methanol, preferably 5 to 10 times water, heated at 40 to 100 ° C., preferably 70 to 90 ° C., and then heated. The extract was repeatedly extracted 1 to 10 times, filtered under reduced pressure, and the filtered extract was mixed and concentrated under reduced pressure at 20 to 100 ° C., preferably at 50 to 70 ° C., using a rotary vacuum concentrator to remove water and carbon atoms. Crude extract which is a soluble extract according to the lower alcohol of 4 or a mixed solvent thereof can be obtained.
한편, 본 발명의 추출물은 상기한 추출 용매 뿐만 아니라, 다른 추출 용매를 이용하여도 실질적으로 동일한 효과를 나타내는 감초 추출물이 얻어질 수 있다는 것은 당업자에게 자명한 것이다. On the other hand, it will be apparent to those skilled in the art that the extract of the present invention can be obtained not only the above-described extraction solvent but also other licorice extracts having substantially the same effect.
또한, 본 발명의 추출물은 상술한 추출 용매에 의한 추출물 뿐만 아니라, 통상적인 정제 과정을 거친 추출물도 포함한다. 예컨대, 일정한 분자량 컷-오프 값을 갖는 한외여과막을 이용한 분리, 다양한 크로마토그래피 (크기, 전하, 소수성 또는 친화성에 따른 분리를 위해 제작된 것)에 의한 분리 등 추가적으로 실시된 다양한 정제 방법을 통해 얻어진 활성 분획도 본 발명의 감초 추출물에 포함되는 것이다.In addition, the extract of the present invention includes not only the extract by the above-mentioned extraction solvent, but also the extract that has undergone a conventional purification process. Activity obtained through various purification methods additionally performed, for example, separation using ultrafiltration membranes having a constant molecular weight cut-off value, separation by various chromatography (manufactured for separation according to size, charge, hydrophobicity or affinity). The fraction is also included in the licorice extract of the present invention.
본 발명의 추출물은 감압 증류 및 동결 건조 또는 분무 건조 등과 같은 추가적인 과정에 의해 분말 상태로 제조될 수 있다.Extracts of the present invention may be prepared in powder form by additional processes such as distillation under reduced pressure and freeze drying or spray drying.
본 발명의 일실시예에 있어서, 상기 홍삼 추출물은 발효 홍삼 추출물일 수 있다. 홍삼을 발효시킴으로써 홍삼의 약효성분이 인체 내로 용이하게 흡수되도록 하며, 홍삼에 극미량으로 존재하는 성분들을 강화시킬 수 있다. 홍삼의 발효를 위해서, 홍삼을 장내 미생물을 이용하여 발효하거나 효소를 처리하는 방법 등이 사용되고 있다. 예컨대, 대한민국특허 공개공보 제2003-61756호에는 인삼을 아스퍼질러스로 발효한 후 전분 분해효소 및 단백질 분해효소로 분해하는 것을 특징으로 하는 기능성 및 관능성이 우수한 인삼 발효액의 제조방법이 개시되어 있다. 본 발명의 일실시예에 있어서, 상기와 같은 제조방법에 의해 제조된 발효 홍삼을 사용할 수 있다. In one embodiment of the present invention, the red ginseng extract may be a fermented red ginseng extract. By fermenting red ginseng, the active ingredients of red ginseng are easily absorbed into the human body, and the ingredients present in red ginseng in trace amounts can be strengthened. For fermentation of red ginseng, a method of fermenting red ginseng using intestinal microorganisms or treating enzymes is used. For example, Korean Patent Laid-Open Publication No. 2003-61756 discloses a method for producing a ginseng fermentation broth having excellent functionality and functionality, which is characterized by fermenting ginseng into aspergillus and then starch and protease. In one embodiment of the present invention, fermented red ginseng prepared by the method as described above can be used.
본 발명의 일실시예에 따른 조성물이 차가버섯 추출물, 감초 추출물 및 홍삼 추출물의 조합을 유효성분으로서 포함하는 경우, 상기 각 추출물의 중량비는 1~5 : 1~10 : 0.5~3일 수 있다. 이 범위에 속할 때 각 추출물 간의 시너지 효과가 극대화될 수 있다. When the composition according to an embodiment of the present invention includes a combination of chaga mushroom extract, licorice extract and red ginseng extract as an active ingredient, the weight ratio of each extract may be 1 to 5: 1 to 10: 0.5 to 3. When belonging to this range can be maximized synergistic effect between each extract.
본 발명에 의한 상기 조성물은 상기 차가버섯 추출물, 또는 차가버섯 추출물, 감초 추출물 및 홍삼 추출물의 조합을 전체 조성물 총 중량에 대하여 0.0001~99.9중량%의 양으로 함유할 수 있다. 유효한 효과와 안정성, 및 제형 안정성을 고려한다면 0.1~60.0중량%가 더 바람직하다.The composition according to the present invention may contain the chaga mushroom extract, or a combination of chaga mushroom extract, licorice extract and red ginseng extract in an amount of 0.0001 to 99.9% by weight based on the total weight of the composition. 0.1-60.0% by weight is more preferable in view of effective effects and stability and formulation stability.
본 발명에 따른 조성물은 약학 조성물일 수 있다. 약학 조성물인 경우, 경구, 비경구, 직장, 국소, 경피, 정맥 내, 근육 내, 복강 내, 피하 등으로 투여될 수 있으며, 가장 바람직한 투여 경로는 경구 투여이다. The composition according to the invention may be a pharmaceutical composition. In the case of pharmaceutical compositions, it may be administered orally, parenterally, rectally, topically, transdermally, intravenously, intramuscularly, intraperitoneally, subcutaneously, etc., with the most preferred route of administration being oral administration.
또한, 상기 활성성분의 투여량은 치료 받을 대상의 연령, 성별, 체중과, 치료할 특정 질환 또는 병리 상태, 질환 또는 병리 상태의 심각도, 투여경로 및 처방자의 판단에 따라 달라질 것이다. 이러한 인자에 기초한 투여량 결정은 당업자의 수준 내에 있다. 일반적으로 투여량은 0.0001mg/kg/일 내지 대략 2000g/kg/일 범위이다. In addition, the dosage of the active ingredient will vary depending on the age, sex and weight of the subject to be treated, the specific disease or pathology to be treated, the severity of the disease or pathology, the route of administration and the judgment of the prescriber. Dosage determination based on these factors is within the level of skill in the art. Generally dosages range from 0.0001 mg / kg / day to approximately 2000 g / kg / day.
한편, 의도된 투여양식에 따라 약학 조성물은 고체, 반고체 또는 액체 투여 형태일 수 있다. 투여 형태의 예는 정제, 캡슐, 츄잉정, 작은 봉지, 과립, 분말, 액체 용액, 현탁액, 분산액, 에멀젼, 시럽, 좌약 등을 포함하지만 이에 한정되지 않는다. 활성성분은 리포솜, 미세입자 또는 마이크로 캡슐 등에 캡슐화 될 수 있다. On the other hand, depending on the intended dosage form, the pharmaceutical composition may be in solid, semisolid or liquid dosage form. Examples of dosage forms include, but are not limited to, tablets, capsules, chewing tablets, small bags, granules, powders, liquid solutions, suspensions, dispersions, emulsions, syrups, suppositories, and the like. The active ingredient may be encapsulated in liposomes, microparticles or microcapsules.
한편, 경구 투여의 목적으로 본 발명의 유효성분인 추출물을 정제, 캡슐, 츄 잉정, 작은 봉지, 과립, 분말, 액체 용액, 현탁액, 분산액, 에멀젼, 시럽 등의 제제로 제형화하는 경우에 있어서는, 아라비아 고무, 옥수수 전분, 미세 결정질 셀룰로오스 또는 젤라틴과 같은 결합제, 인산 이칼슘 또는 락토오즈와 같은 부형제, 알긴산, 옥수수 전분 또는 감자 전분과 같은 붕해제, 스테아르산 마그네슘과 같은 윤활제, 슈크로오즈 또는 사카린과 같은 감미제 및 페퍼민트, 메틸 살리실산염 또는 과일향과 같은 향미제가 포함될 수 있으며, 투여 단위 형이 캡슐제인 경우에는 상기 성분 외에도 폴리에틸렌 글리콜 또는 지방유와 같은 액상 담체가 포함될 수 있다.On the other hand, in the case of formulating the extract of the active ingredient of the present invention in the form of tablets, capsules, chewing tablets, small bags, granules, powders, liquid solutions, suspensions, dispersions, emulsions, syrups for the purpose of oral administration, Gum arabic, corn starch, binders such as microcrystalline cellulose or gelatin, excipients such as dicalcium phosphate or lactose, disintegrants such as alginic acid, corn starch or potato starch, lubricants such as magnesium stearate, sucrose or saccharin and Such sweeteners and flavoring agents such as peppermint, methyl salicylate or fruit flavors may be included, and when the dosage unit form is a capsule, liquid carriers such as polyethylene glycol or fatty oils may be included in addition to the above components.
또한, 본 발명의 일실시예에 따른 식품 조성물은 상기 추출물에 식품학적으로 허용 가능한 식품보조 첨가제를 첨가한 건강기능성식품 조성물을 제공한다. 예를 들어, 츄잉껌, 캐러멜 제품, 캔디류, 빙과류, 과자류 등의 각종 식품류, 청량 음료, 미네랄 워터, 알코올 음료 등의 음료 제품, 비타민이나 미네랄 등을 포함한 건강기능성 식품류 등이 있다.In addition, the food composition according to an embodiment of the present invention provides a health functional food composition to which the food supplement is added to the food acceptable food supplement. For example, there are various foods such as chewing gum, caramel products, candy, ice cream and confectionery, beverage products such as soft drinks, mineral water and alcoholic beverages, and health functional foods including vitamins and minerals.
이 때, 상기 식품 중의 추출물의 양은 전체 식품 중량의 0.001 내지 99.9 중량%로 가할 수 있으며, 음료 중에는 100 ㎖를 기준으로 0.001 내지 0.1 g, 더 바람직하게는 0.05 내지 0.1 g의 비율로 가할 수 있다. At this time, the amount of the extract in the food may be added to 0.001 to 99.9% by weight of the total food weight, in the beverage may be added in a ratio of 0.001 to 0.1 g, more preferably 0.05 to 0.1 g based on 100 ml.
본 발명의 추출물을 함유하는 음료는 지시된 비율로 필수 성분으로서 상기 추출물을 함유하는 외에는 다른 성분에는 특별한 제한이 없으며 통상의 음료와 같이 여러 가지 향미제 또는 천연 탄수화물 등을 추가 성분으로서 함유할 수 있다. The beverage containing the extract of the present invention is not particularly limited to other ingredients except for containing the extract as an essential ingredient in the indicated ratio, and may contain various flavors or natural carbohydrates as additional ingredients, such as ordinary drinks. .
상기 외에 본 발명의 건강기능성 식품 조성물은 여러 가지 영양제, 비타민, 광물(전해질), 합성 풍미제 및 천연 풍미제 등의 풍미제, 착색제 및 증진제(치즈, 초콜릿 등), 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, pH 조절제, 안정화제, 방부제, 글리세린, 알콜, 탄산 음료에 사용되는 탄산화제 등을 함유할 수 있다. 그 밖에 본 발명의 건강기능성 식품 조성물들은 천연 과일 쥬스 및 과일 쥬스 음료 및 야채 음료의 제조를 위한 과육을 함유할 수 있다. 이러한 성분은 독립적으로 또는 조합하여 사용할 수 있다. 이러한 첨가제의 비율은 그렇게 중요하진 않지만 본 발명의 조성물 100 중량부 당 0 내지 약 20 중량부의 범위에서 선택되는 것이 일반적이다. In addition to the above, the functional food composition of the present invention includes various nutrients, vitamins, minerals (electrolytes), synthetic flavors such as synthetic and natural flavors, colorants and enhancers (such as cheese and chocolate), pectic acid and salts thereof, alginic acid And salts thereof, organic acids, protective colloid thickeners, pH adjusters, stabilizers, preservatives, glycerin, alcohols, carbonation agents used in carbonated beverages, and the like. In addition, the health functional food compositions of the present invention may contain fruit flesh for the production of natural fruit juices and fruit juice drinks and vegetable drinks. These components can be used independently or in combination. The proportion of such additives is not so critical but is generally selected from the range of 0 to about 20 parts by weight per 100 parts by weight of the composition of the present invention.
본 발명의 일실시예에 있어서, 상기 대장암 예방 또는 치료용 조성물은 대장암 치료를 위한 수술법과 병행하여 투여될 수 있다. 상기 조성물은 수술 전 또는/및 후에 투여될 수 있다. 또한, 본 발명의 일실시예에 있어서, 상기 조성물은 다른 약물과 조합되어 병행 투여될 수 있다. In one embodiment of the present invention, the composition for preventing or treating colorectal cancer may be administered in parallel with a surgical method for treating colorectal cancer. The composition can be administered before or after surgery. In addition, in one embodiment of the present invention, the composition may be administered in combination with other drugs.
이하에서는 실시예를 들어 본 발명을 더욱 상세히 설명하고자 하나, 본 발명의 권리범위가 하기 실시예에 의해 제한되는 것이 아님은 자명하다. Hereinafter, the present invention will be described in more detail with reference to Examples, but it is obvious that the scope of the present invention is not limited by the following Examples.
실시예Example
<실시예 1: 추출물의 제조>Example 1 Preparation of Extract
1-1. 차가버섯 추출물의 제조1-1. Preparation of Chaga Extract
분쇄한 차가버섯 200g을 에탄올 1000m에 넣고 30분간 교반시켰다. 그 후 용매를 제거하여 차가버섯 추출액을 얻었다. 이렇게 얻어진 추출액을 동결건조하였다. 200 g of crushed chaga was put in 1000m of ethanol and stirred for 30 minutes. Thereafter, the solvent was removed to obtain a chaga extract. The extract thus obtained was lyophilized.
1-2. 감초 에탄올 추출물의 제조1-2. Preparation of Licorice Ethanol Extract
건조 후 분쇄한 감초 4 ㎏에 15 ℓ의 100 % 메탄올을 가한 후, 37 ℃로 가열하면서 2시간 동안 초음파 추출하고 냉각 및 여과한 후 회전증발기를 이용하여 감압농축하여 감초의 에탄올 추출물 750 g을 얻었다.After drying, 15 L of 100% methanol was added to 4 kg of crushed licorice, sonicated for 2 hours while heating to 37 ° C, cooled and filtered, and concentrated under reduced pressure using a rotary evaporator to obtain 750 g of ethanol extract of licorice. .
1-3. 홍삼 추출물의 제조1-3. Preparation of Red Ginseng Extract
발효홍삼 분말((주)김정문 알로에 제, 대한민국)을 구입하여 사용하였다. Fermented red ginseng powder (Kim Jung Moon Co., Ltd., Aloe, Korea) was purchased and used.
<실험예 1: MTT 분석>Experimental Example 1 MTT Analysis
상황버섯 추출물, 차가버섯 추출물(실시예 1), 감초 추출물(실시예 1), 발효홍삼분말(실시예 1), 영지버섯 추출물, 백화사설초 추출물을 각각 대조군과 함께, 100ug/ml, 50ug/ml, 25ug/ml, 12.5ug/ml, 6.25ug/ml의 농도로 48시간동안 HT-29 Colon cancer cell 에 처리한 후 cell viability를 확인하였다. 그 결과는 도 1에 나타내었다. Situation mushroom extract, chaga mushroom extract (Example 1), licorice extract (Example 1), fermented red ginseng powder (Example 1), Ganoderma lucidum extract, white sperm extract with the control, 100ug / ml, 50ug / ml , 25ug / ml, 12.5ug / ml, 6.25ug / ml concentrations were treated in HT-29 Colon cancer cells for 48 hours and then cell viability was confirmed. The results are shown in FIG.
<실험예 2: 감초 추출물이 대장암 세포 스피어 형성에 미치는 영향에 대한 실험>Experimental Example 2 Experiments on the Effect of Licorice Extract on the Formation of Colorectal Cancer Cell Spheres
실시예 1에서 제조된 차가버섯 추출물을 100ml의 증류수에 33.33mg/ml의 농도로 넣고 휘저었다. 이렇게 제조된 용액을 각 25ug/ml, 50ug/ml, 100ug/ml의 농도로 HT-29 Colon cancer cell 에 가하였다. 그 후 HT-29 세포가 바닥에 붙지 못할 조건에서 3주간 배한 후 스피어(sphere)의 수를 세었다. 그 결과는 도 2에 나타난 바와 같다.Chaga mushroom extract prepared in Example 1 was added to 100ml of distilled water at a concentration of 33.33mg / ml and stirred. The solution thus prepared was added to HT-29 Colon cancer cells at concentrations of 25 ug / ml, 50 ug / ml and 100 ug / ml. Thereafter, HT-29 cells were seeded for 3 weeks in a condition where they could not adhere to the bottom, and the spheres were counted. The result is as shown in FIG.
도 2에 나타난 바와 같이, 차가버섯 추출물의 농도와 비례하여 HT-29 세포당 스피어의 수가 감소하는 것을 알 수 있다. 즉, 차가버섯 추출물이 HT-29 세포의 스피어 형성을 효과적으로 억제하는 것을 확인하였다. As shown in Figure 2, it can be seen that the number of spheres per HT-29 cells decreases in proportion to the concentration of chaga extract. That is, chaga extract was confirmed to effectively inhibit the spear formation of HT-29 cells.
제형예Formulation example
하기에 상기 조성물의 제제예를 설명하나, 본 발명은 이를 한정하고자 함이 아니라 단지 구체적으로 설명하고자 함이다. Hereinafter, the formulation examples of the composition will be described, but the present invention is not intended to be limited thereto but merely to be described in detail.
제제예Formulation example 1. 정제의 제조 1. Preparation of Tablets
실시예 1의 차가버섯 추출물................100 mgChaga extract of Example 1 ...... 100 mg
옥수수 전분...............................68 mgCorn starch ............... 68 mg
락토오즈..................................90 mgLactose ......... 90 mg
미세결정질 셀룰로즈.......................40 mgMicrocrystalline Cellulose ............. 40 mg
마그네슘 스테아레이트.....................2 mgMagnesium Stearate ..... 2 mg
통상적인 정제의 제조 방법에 따라, 상기 성분들을 제시된 함량으로 첨가하여 균일하게 혼합하고, 교반한 후, 과립화하였다. 건조 후 타정기를 사용하여 1 정당 유효 성분인 차가버섯 추출물이 100 mg씩 포함되어 있는 목적하는 정제를 제조하였다.According to the conventional method of preparing tablets, the above ingredients were added to the indicated contents, mixed uniformly, stirred and granulated. After drying, using a tableting machine, a desired tablet containing 100 mg of chaga extract, which is one active ingredient, was prepared.
제제예Formulation example 2. 캅셀제의 제조 2. Preparation of capsule
실시예 1의 차가버섯 추출물..................60 mgChaga extract of Example 1 .. 60 mg
실시예 1의 홍삼 추출물......................40mgRed ginseng extract of Example 1 ............ 40mg
옥수수 전분................................68 mgCorn starch ..... 68 mg
락토오즈...................................90 mgLactose ......... 90 mg
미세결정질 셀룰로즈........................40 mgMicrocrystalline Cellulose .............. 40 mg
마그네슘 스테아레이트......................2 mgMagnesium Stearate ......... 2 mg
통상적인 캅셀제의 제조 방법에 따라, 상기 성분들을 제시된 함량으로 첨가하여 균일하게 혼합한 후, 1 캅셀 당 100 mg의 추출물이 포함되도록 적절한 크기의 젤라틴 캅셀에 충진하여 목적하는 캅셀제를 제조하였다.According to the conventional method for preparing the capsules, the above-mentioned ingredients were added and mixed uniformly, and then the desired capsules were prepared by filling into gelatin capsules of an appropriate size to include 100 mg of extract per capsule.
제제예Formulation example 3. 3. 츄잉정의Chewing Definition 제조 Produce
실시예 1의 차가버섯 추출물..................30 mgChaga Extract of Example 1 ....... 30 mg
실시예 1의 감초 추출물......................60mgLicorice extract of Example 1 ... 60 mg
실시예 1의 홍삼 추출물......................10mgRed Ginseng Extract of Example 1 ...................................... 10mg
과립당 시럽.................................240 mgSyrup to granule ......... 240 mg
향료.........................................2 mgFragrance ......................................... 2 mg
옥수수 전분.................................60 mgCorn starch ..... 60 mg
만니톨......................................100 mgMannitol ......................................... 100 mg
마그네슘 스테아레이트........................20 mgMagnesium Stearate ............... 20 mg
정제수......................................적당량Purified water ............................
통상적인 츄잉정의 제조 방법에 따라, 상기 성분들을 적당량의 물에 혼합하고, 가열하면서 용해시킨 후, 냉각시키고 성형기에 넣어 목적하는 형상의 츄잉정을, 1개 당 100 mg의 추출물이 포함되도록 제조하였다.According to the conventional method of preparing chewing tablets, the above ingredients were mixed in an appropriate amount of water, dissolved while heating, cooled and placed in a molding machine to prepare chewing tablets of a desired shape, containing 100 mg of extract per one. .
제제예Formulation example 4. 캔디의 제조 4. Manufacture of Candy
실시예 1의 차가버섯 추출물..................100 mgChaga extract of Example 1 ....... 100 mg
과립당 시럽..................................640 mgSyrup to granule ......... 640 mg
향료..........................................2 mgFragrance ......................................... 2 mg
물엿.........................................230 mgStarch syrup ............... 230 mg
50% 타르타르산................................20 mg50% tartaric acid ................................. 20 mg
정제수.......................................적당량Purified water ...............
과립당 시럽을 소량의 물에 완전히 용해하면서 110 ℃까지 가열한 후, 참고 추출물을 용해한 나머지의 물과 물엿을 첨가하여, 145 ℃까지 온도를 올렸다. 불을 끄고, 향료와 타르타르산을 첨가하여 혼합하고, 75~80 ℃로 냉각시킨 후, 성형 롤러로 성형하여 추출물을 함유한 캔디를 제조하였다.The granulated sugar syrup was heated to 110 ° C. while completely dissolving in a small amount of water, and then the remaining water and starch syrup dissolved in the reference extract were added to raise the temperature to 145 ° C. The fire was turned off, the fragrance and tartaric acid were added, mixed, cooled to 75-80 ° C., and then molded with a forming roller to prepare a candy containing extract.
제제예Formulation example 5. 음료의 제조 5. Manufacture of drinks
실시예 1의 차가버섯 추출물......................100 mgChaga extract of Example 1 ............ 100 mg
농축 과즙........................................2 gConcentrated Juice ........... 2 g
슈크로즈.........................................12 gSucrose ......................................... 12 g
시트르산 나트륨..................................100 mgSodium Citrate ... 100 mg
향료.............................................70 mgFragrance ............... 70 mg
물...............................................적당량Water ............................................
통상적인 음료의 제조 방법에 따라, 상기 성분들을 제시된 함량으로 적당량의 물에 혼합하고, 가열하여 용해시킨 후, 냉각시키고 용기에 충전하여 200 ml 용량의 음료 1병당 100 mg의 차가버섯 추출물을 포함하는 음료를 제조하였다. According to a conventional method for preparing a beverage, the above ingredients are mixed in an appropriate amount of water to a given content, heated to dissolve, cooled, and filled into a container, which contains 100 mg of chaga extract per bottle of 200 ml of beverage. A beverage was prepared.
도 1은 차가버섯 추출물, 감초 추출물 및 홍삼 추출물을 HT-29 세포에 처리한 후 MTT ASSAY로 분석한 결과를 나타낸 것이다. Figure 1 shows the results of analysis by MTT ASSAY after processing chaga extract, licorice extract and red ginseng extract to HT-29 cells.
도 2는 차가버섯 추출물, 감초 추출물 및 홍삼 추출물을 HT-29 세포에 처리한 후 세포의 스피어 형성에 미치는 영향을 나타낸 그래프이다. Figure 2 is a graph showing the effect on the spear formation of cells after chaga extract, licorice extract and red ginseng extract to HT-29 cells.
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US20160082139A1 (en) * | 2014-09-18 | 2016-03-24 | Krista Koons WOODS | Deodorizing glove holder for athletic gloves and other equipment |
KR101699659B1 (en) | 2016-01-26 | 2017-01-24 | 부산대학교 산학협력단 | Composition preventing or treating cancer comprising (Z)-5-(4-hydroxy-3,5-dimethoxybenzylidene)-2-thioxoimidazolidin-4-one) |
KR101724425B1 (en) | 2016-01-26 | 2017-04-07 | 부산대학교 산학협력단 | Composition preventing or treating cancer comprising (Z)-2-acetamido-3-(4-hydroxy-3-methoxyphenyl)acrylic acid |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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US20160082139A1 (en) * | 2014-09-18 | 2016-03-24 | Krista Koons WOODS | Deodorizing glove holder for athletic gloves and other equipment |
KR101699659B1 (en) | 2016-01-26 | 2017-01-24 | 부산대학교 산학협력단 | Composition preventing or treating cancer comprising (Z)-5-(4-hydroxy-3,5-dimethoxybenzylidene)-2-thioxoimidazolidin-4-one) |
KR101724425B1 (en) | 2016-01-26 | 2017-04-07 | 부산대학교 산학협력단 | Composition preventing or treating cancer comprising (Z)-2-acetamido-3-(4-hydroxy-3-methoxyphenyl)acrylic acid |
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