KR20200099326A - Method for extracting isoflavones from soybean - Google Patents
Method for extracting isoflavones from soybean Download PDFInfo
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- CJWQYWQDLBZGPD-UHFFFAOYSA-N isoflavone Natural products C1=C(OC)C(OC)=CC(OC)=C1C1=COC2=C(C=CC(C)(C)O3)C3=C(OC)C=C2C1=O CJWQYWQDLBZGPD-UHFFFAOYSA-N 0.000 title claims abstract description 50
- 235000008696 isoflavones Nutrition 0.000 title claims abstract description 50
- 235000010469 Glycine max Nutrition 0.000 title claims abstract description 28
- 244000068988 Glycine max Species 0.000 title claims abstract description 27
- 150000002515 isoflavone derivatives Chemical class 0.000 title abstract description 34
- 238000000034 method Methods 0.000 title abstract description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 37
- 238000010992 reflux Methods 0.000 claims abstract description 19
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- 239000002904 solvent Substances 0.000 claims abstract description 17
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- 238000000605 extraction Methods 0.000 claims description 58
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- 150000002338 glycosides Chemical class 0.000 description 14
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- ZQSIJRDFPHDXIC-UHFFFAOYSA-N daidzein Chemical compound C1=CC(O)=CC=C1C1=COC2=CC(O)=CC=C2C1=O ZQSIJRDFPHDXIC-UHFFFAOYSA-N 0.000 description 6
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- ZCOLJUOHXJRHDI-FZHKGVQDSA-N Genistein 7-O-glucoside Natural products O([C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1)c1cc(O)c2C(=O)C(c3ccc(O)cc3)=COc2c1 ZCOLJUOHXJRHDI-FZHKGVQDSA-N 0.000 description 1
- CJPNHKPXZYYCME-UHFFFAOYSA-N Genistin Natural products OCC1OC(Oc2ccc(O)c3OC(=CC(=O)c23)c4ccc(O)cc4)C(O)C(O)C1O CJPNHKPXZYYCME-UHFFFAOYSA-N 0.000 description 1
- 102000005741 Metalloproteases Human genes 0.000 description 1
- 108010006035 Metalloproteases Proteins 0.000 description 1
- YCUNGEJJOMKCGZ-UHFFFAOYSA-N Pallidiflorin Natural products C1=CC(OC)=CC=C1C1=COC2=CC=CC(O)=C2C1=O YCUNGEJJOMKCGZ-UHFFFAOYSA-N 0.000 description 1
- 239000004231 Riboflavin-5-Sodium Phosphate Substances 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L11/00—Pulses, i.e. fruits of leguminous plants, for production of food; Products from legumes; Preparation or treatment thereof
- A23L11/05—Mashed or comminuted pulses or legumes; Products made therefrom
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L11/00—Pulses, i.e. fruits of leguminous plants, for production of food; Products from legumes; Preparation or treatment thereof
- A23L11/05—Mashed or comminuted pulses or legumes; Products made therefrom
- A23L11/07—Soya beans, e.g. oil-extracted soya bean flakes
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/38—Other non-alcoholic beverages
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/318—Foods, ingredients or supplements having a functional effect on health having an effect on skin health and hair or coat
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2250/00—Food ingredients
- A23V2250/20—Natural extracts
- A23V2250/21—Plant extracts
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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- A23V2250/00—Food ingredients
- A23V2250/20—Natural extracts
- A23V2250/21—Plant extracts
- A23V2250/2116—Flavonoids, isoflavones
- A23V2250/21172—Soy Isoflavones, daidzein, genistein
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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Abstract
Description
본 발명은 콩에 함유된 이소플라본(isoflavone)을 추출하는 방법에 관한 것이다.The present invention relates to a method for extracting isoflavones contained in soybeans.
자극적으로 변해가는 외부 환경, 잘못된 생활 습관, 각종 스트레스 속에 놓인 현대인들에게 있어 피부 노화 방지는 남녀노소할 것 없이 꾸준하고 지속적인 관심의 대상이다.For modern people who are exposed to stimulating changing external environments, wrong lifestyles, and various stresses, skin aging prevention is a subject of constant and continuous interest, regardless of age or sex.
피부 노화가 외형적으로 나타나는 형태는 주름이다. 외인성 노화에 해당하는 자외선 노출 등에 진행되는 노화는 MMPs(Matrix Metallo Proteases), 특히 MMP-1의 발현이 주요인이다. MMP-1은 콜라겐을 분해 하는 효소로서 피부 주름의 개선을 위해 MMP-1의 발현 억제를 위한 생리활성 성분의 탐색이 요구된다.The appearance of skin aging is wrinkles. Aging that progresses through exposure to ultraviolet rays, which is an exogenous aging process, is mainly due to the expression of Matrix Metallo Proteases (MMPs), especially MMP-1. MMP-1 is an enzyme that decomposes collagen, and it is required to search for a physiologically active component to inhibit the expression of MMP-1 in order to improve skin wrinkles.
여성 호르몬인 에스트로겐(estrogen)이 감소하면 피부 속 수분과 콜라겐이 감소하고 피부 노화 및 피부의 주름으로 진행이 된다고 알려져 있다. 이소플라본은 에스트로겐과 유사한 분자 구조를 가지며 우리 몸에서의 효능도 유사하다고 알려져 있다. 콩에 천연적으로 존재하는 이소플라본 성분을 이용한 MMP-1 발현의 억제 등 피부 노화 방지 및 개선 효과가 기대된다.It is known that when the female hormone estrogen decreases, moisture and collagen in the skin decrease, leading to skin aging and wrinkles in the skin. Isoflavones have a molecular structure similar to estrogen and are known to have similar efficacy in our body. It is expected to prevent and improve skin aging, such as inhibition of MMP-1 expression using isoflavones that are naturally present in soybeans.
콩은 한국 사람의 식생활에서 가장 비중이 큰 단백질 공급원일 뿐만 아니라 수많은 화학제품의 원료로도 활용되고 있다. 콩의 수분 8.6%, 단백질 40%, 지방18%, 섬유질 3.5%, 회분 4.6%, 펜토산 4.4%, 당분 7% 등으로 이루어져 있다.Soybeans are not only the largest source of protein in Korean diet, but are also used as a raw material for numerous chemical products. It consists of 8.6% moisture, 40% protein, 18% fat, 3.5% fiber, 4.6% ash, 4.4% pentosan, and 7% sugar.
이소플라본은 콩에서 유래된 플라보노이드(flavonoid)계 물질로 비배당체인 제니스테인(genistein), 다이드제인(daidzein), 글리시테인(glycitein)과 이들의 배당체(glucoside) 등으로 구성되어 있다. 콩의 이소플라본 함유량은 약 0.1~0.4% 정도이고 그 대부분은 제니스틴(genistin) 및 다이드진(daizin)과 같은 배당체 형태인 것으로 알려져 있다.Isoflavones are flavonoid-based substances derived from soybeans, and are composed of non-glycosides such as genistein, daidzein, glycitein, and their glycosides. Soybean isoflavone content is about 0.1 to 0.4%, and most of it is known to be in the form of glycosides such as genistin and daizin.
이소플라본에 대한 연구는 국내·외에서 활발히 진행되고 있으며, 주요 효능은 항산화제, 암 유발 억제, 항염증 활성, 심근경색증 및 동맥경화증의 예방 등으로 보고되고 있는 것으로 보인다.Research on isoflavones is being actively conducted both at home and abroad, and its main effects appear to be antioxidants, suppression of cancer induction, anti-inflammatory activity, and prevention of myocardial infarction and arteriosclerosis.
국내 콩 유전자원의 이소플라본 함량 변이에 관한 논문[한국작물학회지, 51(S):146~151(2006)]에 의하면, 한국산 콩 주요 43품종의 평균 함량은 다이드제인은 484.4±223.9μg/g, 제니스테인은 448.4±156.2μg/g 그리고 글리시테인은 84.9±48.7μg/g으로 콩 100g당 평균 다이드제인은 48.44mg, 제니스테인은 44.84mg 그리고 글리시테인은 8.49mg 정도이다. According to the article on the variation of isoflavone content in domestic soybean genetic resources [Journal of the Korean Society of Crop Science, 51(S):146~151(2006)], the average content of 43 major varieties of Korean soybeans was 484.4±223.9μg/ g, genistein is 448.4±156.2 μg/g, and glycitane is 84.9±48.7 μg/g.The average daidzein per 100 g of soybeans is 48.44 mg, genistein is 44.84 mg, and glycitane is 8.49 mg.
콩에 함유된 비배당체 형태의 이소플라본 함량이 극히 적어 종래에는 염산(1N-HCL), 메탄올(methanol), 헥산(hexane) 등 식품용에는 적용할 수 없는 용매를 사용하여 콩에서 이소플라본을 추출하고 성분 분석을 한 것이 대부분이다. 콩에 천연적으로 존재하는 이소플라본 성분을 식품이나 음료용으로도 활용할 수 있는 개선된 이소플라본 추출방법이 요구된다.Because the content of isoflavones in the form of non-glycosylated soybeans is extremely low, isoflavones are extracted from soybeans using solvents that are not applicable for food, such as hydrochloric acid (1N-HCL), methanol, and hexane. Most of them were analyzed for ingredients. There is a need for an improved method for extracting isoflavones that can utilize isoflavones naturally present in soybeans for food or beverages.
본 발명은 위와 같은 종래기술에 대한 인식에 기초한 것으로, 콩에서 추출된 이소플라본 성분을 식품으로 사용할 수 있도록 보다 개선된 콩 함유 이소플라본 추출방법을 제공하고자 한다.The present invention is based on the recognition of the prior art as described above, to provide a more improved soybean-containing isoflavone extraction method so that the isoflavone component extracted from soy can be used as food.
본 발명에서 해결하고자 하는 과제는 반드시 위에 언급된 사항에 국한되지 않으며, 미처 언급되지 않은 또 다른 과제들은 이하 기재되는 사항에 의해서도 이해될 수 있을 수 있을 것이다.The problem to be solved in the present invention is not necessarily limited to the above-mentioned matters, and other problems that are not already mentioned may be understood by the matters described below.
위 목적을 달성하기 위한 본 발명에 따른 콩 함유 이소플라본 추출방법은 건조된 선유 콩을 분쇄한 후, 분쇄된 콩을 증류수 또는 증류수와 혼합된 에탄올을 용매로 하여 환류 추출하는 것을 특징으로 한다.The soybean-containing isoflavone extraction method according to the present invention for achieving the above object is characterized in that after pulverizing the dried seonyu soybeans, the pulverized soybeans are subjected to reflux extraction using distilled water or ethanol mixed with distilled water as a solvent.
상기 에탄올 혼합 용매로는 증류가가 혼합된 60~75%의 에탄올을 용매가 바람직하며, 추출시간은 2~5, 나아가 3~5시간이 바람직하다.The ethanol mixed solvent is preferably a solvent of 60 to 75% ethanol in which a distillation value is mixed, and the extraction time is preferably 2 to 5, furthermore, 3 to 5 hours.
상술한 바와 같은 본 발명에 따른 콩 함유 이소플라본 추출방법에 의하면, 콩에서 이소플라본 성분을 상대적으로 다량 추출할 수 있으며 헥산 등의 화학 용매를 사용하지 않으므로 추출된 이소플라본 성분을 식품으로 사용할 수 있다.According to the soybean-containing isoflavone extraction method according to the present invention as described above, a relatively large amount of the isoflavone component can be extracted from the soybean, and since a chemical solvent such as hexane is not used, the extracted isoflavone component can be used as food. .
환류 추출에 의해 생체 활성이 높은 비배당체 성분을 기존보다 상대적으로 다량 추출 가능하다.By reflux extraction, it is possible to extract a relatively large amount of non-glycoside components with high bioactivity than before.
도 1은 본 발명의 다양한 예에 따른 추출 방법과 그에 따른 이소플라본의 수득율을 보인 것이다.
도 2는 도 1의 결과에서 용매 조건별 이소플라본의 수득율을 보인 것이다.
도 3은 도 1의 결과에서 추출 시간별 소플라본의 수득율을 보인 것이다.1 shows an extraction method according to various examples of the present invention and a yield of isoflavones according thereto.
2 shows the yield of isoflavones by solvent conditions in the results of FIG. 1.
3 shows the yield of soflavones by extraction time from the results of FIG. 1.
이하 본 발명의 여러 특징적인 측면을 이해할 수 있도록 실시예를 들어 보다 상세히 살펴보기로 한다. 첨부된 도면들에서 동일 또는 동등한 구성요소들 또는 부품들은 설명의 편의를 위해 가능한 한 동일한 참조부호로 표시될 수 있고, 도면들은 본 발명의 특징에 대한 명확한 이해와 설명을 위해 과장되게 그리고 개략적으로 도시될 수 있다.Hereinafter, examples will be described in more detail in order to understand various characteristic aspects of the present invention. In the accompanying drawings, the same or equivalent components or parts may be indicated by the same reference numerals as possible for convenience of description, and the drawings are exaggerated and schematically illustrated for clear understanding and description of the features of the present invention. Can be.
식품이나 음료용으로도 사용할 수 있는 최적의 이소플라본 추출법 도출을 위해 다양한 방법을 이용하여 콩으로부터 이소플라본을 추출하는 연구를 수행하였다. 유의미한 추출법으로 최종적으로는 환류 추출, 냉침 추출 및 초음파(sonication) 추출을 선택하였고, 이 중에서도 환류 추출이 가장 적합하다는 결론을 얻게 되었다.In order to derive an optimal isoflavone extraction method that can be used for food or beverage, a study was conducted to extract isoflavones from soybeans using various methods. Finally, reflux extraction, cold needle extraction, and sonication extraction were selected as meaningful extraction methods, and among them, reflux extraction was concluded to be the most suitable.
이하 콩 함유 이소플라본 추출방법을 살펴본다.Hereinafter, a method for extracting isoflavones containing soybeans will be described.
2004, 2005년도 하계작물 신품종개발 공동연구 보고서에 따르면 선유콩은 표준 품종인 태광콩에 비해 이소플라본의 비배당체에 해당하는 다이드제인, 제니스테인, 글리시테인과 과 아미노산의 조성이 높고 개화기와 성숙기 또한 빠르며 수확량도 더 9% 높고 전국 어디서나 재배가 가능한 품종으로 알려져 있다.According to a joint research report on the development of new varieties of summer crops in 2004 and 2005, Seonyu beans have a higher composition of daidzein, genistein, glycitein and amino acids, which are non-glycosides of isoflavones, compared to the standard cultivar Taekwang. It is known as a variety that is fast and has a higher yield of 9% and can be grown anywhere in the country.
항노화 활성 효능이 있는 비배당체 이소플라본의 함량이 높은 선유콩이 총 이소플라본 함량의 최적 추출 조건의 탐색에 부합하며, 나아가 이소플라본이 함유된 추출물을 이용한 식품 개발 및 기능성 음료 개발에서도 이소플라본 함량에 대한 경쟁력을 가질 것으로 판단된다. 이하 실험 예에서 콩은 전남산 선유가 사용되었다.Seonyu soybeans with a high content of non-glycosylated isoflavones with anti-aging activity meet the search for the optimal extraction conditions for total isoflavone content, and furthermore, isoflavone content in food development and functional beverage development using extracts containing isoflavones It is expected to have competitiveness in In the experimental examples below, the soybeans were made from Jeonnam-san Seonyu.
환류 추출은 건조된 콩을 분쇄기로 분쇄한 후, 분쇄된 콩 100g을 이에 20배수에 해당하는 2L의 증류수(D.W.) 혹은 증류수와 혼합된 주정, 즉 에탄올(ethanol: EtoOH)을 넣고 환류장치(미성과학기기, MS-E106, 한국)를 이용하여 열수 추출하는 과정을 반복하는 방식으로 진행되었다. 증류수의 경우 100℃ 도달 후 여러 조건으로 나누어 추출하고, 에탄올 혼합 용매에 의한 추출은 70~80℃ 도달 후 여러 시간 추출하였다. 추출 후에는 종이필터(filter paper)를 이용하여 여과 후 성분 분석을 하였다.For reflux extraction, the dried beans are pulverized with a grinder, and then 100 g of the crushed beans are put in 2L of distilled water (DW) equivalent to 20 times the amount of distilled water or alcohol mixed with distilled water, that is, ethanol (EtoOH). Scientific equipment, MS-E106, Korea) was used to repeat the process of extracting hot water. Distilled water was extracted by dividing into various conditions after reaching 100°C, and extraction with an ethanol mixed solvent was extracted for several hours after reaching 70-80°C. After extraction, the components were analyzed after filtration using a filter paper.
초음파 추출은 앞서 환류 추출에서와 동일하게 건조된 콩을 분쇄기로 분쇄한 후, 초음파 세정기(성동초음파, SDd-350H, 한국)를 이용하여 40℃의 항온수조에서 여러 조건으로 나누어 열수 및 용매 추출을 반복적으로 수행하는 방식으로 진행되었다. 추출 후에는 종이필터를 이용하여 여과 후 성분 분석을 하였다.In the ultrasonic extraction, the dried beans are pulverized in the same manner as in the previous reflux extraction, and then hot water and solvent extraction are performed by dividing into various conditions in a constant temperature water bath at 40℃ using an ultrasonic cleaner (Sungdong Ultrasonic, SDd-350H, Korea). It proceeded in a way that was performed repeatedly. After extraction, the components were analyzed after filtration using a paper filter.
초음파 추출은 앞서 환류 추출에서와 동일하게 건조된 콩을 분쇄기로 분쇄한 후, 삼각 플라스크를 이용하여 4℃ 냉장 조건에서 3~5일에 걸쳐 여러 조건으로 반복 추출하는 방식으로 진행되었다. 추출 후에는 종이필터를 이용하여 여과 후 성분 분석을 하였다.The ultrasonic extraction was carried out by pulverizing the dried beans with a grinder in the same manner as in the previous reflux extraction, and then repeatedly extracting under various conditions over 3 to 5 days in a 4°C refrigerated condition using an Erlenmeyer flask. After extraction, the components were analyzed after filtration using a paper filter.
아래 표 1은 여러 실험예들 중에서 몇 가지의 대표적인 추출 조건을추출 방법, 용매별, 시간별로 세분화하여 나타낸 것이다.Table 1 below shows several representative extraction conditions among various experimental examples, divided by extraction method, solvent, and time.
아래 표 2에는 표 1의 추출 조건별 이소플라본의 수득율을 나타낸 것이다. 각 추출 조건별 수득률의 편차를 조정하기 위해 각각 3회 반복 추출을 한 후 평균값을 기재하였다.Table 2 below shows the yield of isoflavones according to the extraction conditions of Table 1. In order to adjust the deviation of the yield for each extraction condition, the average value was described after repeated extraction three times each.
도 1에는 추출방법별 이소플라본 수득률이 도시되어 있다. 도 1에서 보듯이 환류 추출이 가장 수득률이 높은 것으로 나타났으며, 초음파 추출과 냉침 추출 순으로 유의성 있게 수득률이 나타났으나 초음파 추출과 냉침 추출의 두 조건에서는 큰 수득률 차이가 없는 것을 확인할 수 있다.Figure 1 shows the yield of isoflavones by extraction method. As shown in FIG. 1, the reflux extraction was found to have the highest yield, and the yield was significantly in the order of ultrasonic extraction and cold needle extraction, but it can be seen that there is no significant difference in yield under the two conditions of ultrasonic extraction and cold needle extraction.
도 2에는 용매별 방법별 이소플라본 수득률이 도시되어 있다. 도 2에서 보듯이 100% 열수 추출이 가장 높은 수득률을 보이는 것으로 나타났으며, 에탄올 용매를 사용한 경우는 열수 추출에 비해 수득량은 낮게 나타났고, 에탄올 용매 60%와 70%의 두 조건에서는 큰 수득률 차이가 없는 것으로 나타났다.Figure 2 shows the yield of isoflavones by method for each solvent. As shown in FIG. 2, 100% hot water extraction showed the highest yield, and when ethanol solvent was used, the yield was lower compared to hot water extraction, and in the two conditions of
도 3에는 추출시간별 이소플라본 수득률이 도시되어 있다. 도 3에서 보듯이 에탄올 용매의 환류 추출법에 3시간과 5 시간은 큰 수득률 차이를 나타나지 않으나, 열수 추출에서는 추출 방법과 상관없이 상대적으로 큰 차이를 나타내는 것으로 나타났다.Figure 3 shows the isoflavone yield by extraction time. As shown in FIG. 3, there was no significant difference in yield between 3 hours and 5 hours in the reflux extraction method of the ethanol solvent, but the hot water extraction showed a relatively large difference regardless of the extraction method.
위와 같은 추출 방법, 용매별 방법 및 추출 시간에 결과를 종합해 보면, 추출방법으로는 환류 추출이 가장 좋은 것으로 나타났다. 초음파 추출은 이소플라본 추출 수득률이 높게 나타나기도 했으나 콩 추출 이소플라본을 식, 음료로 적용하고자 하는 경우 초음파 추출에 의한 대규모 양산은 어려울 것으로 판단된다. 한편 극성이 상대적으로 강한 100% 열수 추출에서 높은 수득률을 나타나 콩에서는 비교적 극성에 해당하는 성분이 많이 차지하고 있는 것으로 판단된다.When the results are summarized in the above extraction method, solvent-specific method and extraction time, reflux extraction is the best extraction method. Although ultrasonic extraction showed a high yield of isoflavone extraction, large-scale mass production by ultrasonic extraction is likely to be difficult if the isoflavone extracted from soybeans is to be applied as food or beverage. On the other hand, 100% hot water extraction, which has a relatively strong polarity, shows a high yield, so it is judged that soybeans occupy a lot of components corresponding to relatively polarity.
아래 표 3에는 환류 추출법에 의해 추출된 이소플라본 6종에 대한 성분 분석을 한 결과를 나타낸 것이다.Table 3 below shows the results of component analysis for six isoflavones extracted by the reflux extraction method.
표 3에서 보듯이 이소플라본 함량 결과를 보면 배당체 형태의 이소플라본 총 함량이 상대적으로 높은 샘플은 10-A, 10-B, 10-C, 10-D, 10-J, 10-Q, 10-R 등 으로 60% EtOH 환류 추출법과 60% EtOH 냉침 추출법 그리고 100% 증류수 초음파 추출법 에서는 추출 시간과 상관없이 상대적으로 많은 함량이 검출되는 것을 알 수 있다. 특히 샘플 10-C와 10-D에 해당하는 60% EtOH 냉침 추출법이 배당체 형태의 이소플라본을 추출 하는데 가장 최적화 된 추출법으로 판단된다.As shown in Table 3, when looking at the results of the isoflavone content, samples with a relatively high total content of isoflavones in the form of glycosides were 10-A, 10-B, 10-C, 10-D, 10-J, 10-Q, 10- It can be seen that in the 60% EtOH reflux extraction method, the 60% EtOH cold needle extraction method, and the 100% distilled water ultrasonic extraction method with R, etc., relatively large amounts are detected regardless of the extraction time. In particular, the 60% EtOH cold needle extraction method for samples 10-C and 10-D is judged to be the most optimized extraction method for extracting isoflavones in the form of glycosides.
활성 성분인 비배당체 형태의 이소플라본 총 함량이 상대적으로 높은 샘플은 10-E, 10-F, 10-G, 10-H로서, 상대적으로 두드러지게 높은 함량을 보이는 것으로 나타나는 것을 알 수 확인할 수 있다. 10-G, 10-H에 해당하는 70% EtOH 환류 추출법은 활성 성분인 비배당체 형태의 이소플라본 총 함량뿐만 아니라 배당체 형태의 이소플라본 총 함량도 비교적 높은 편이다. 이들 중 샘플 10-H인 70% EtOH 환류 5hr 추출법이 비배당체 형태의 이소플라본은 물론이고 배당체 형태의 이소플라본의 함량도 비교적 높게 나타나, 콩에 천연적으로 존재하는 이소플라본을 추출하는데 가장 최적화 된 추출법이라 판단된다.It can be seen that the samples with a relatively high total content of isoflavones in the form of non-glycosides, which are active ingredients, are 10-E, 10-F, 10-G, and 10-H, which appear to show a relatively high content. . The 70% EtOH reflux extraction method corresponding to 10-G and 10-H has a relatively high total content of isoflavones in the form of glycosides as well as the total content of isoflavones in the form of a glycoside as an active ingredient. Of these, the 70% EtOH reflux 5hr extraction method, sample 10-H, showed a relatively high content of isoflavones in the form of glycosides as well as in the non-glycoside form, and is the most optimized for extracting isoflavones naturally present in soybeans. It is considered an extraction method.
이소플라본 최적 추출조건으로 확립한 70% EtOH 환류 5시간 추출법을 토대로 더 명확한 추출조건을 확립하기 위해 추출 시간을 늘려 7시간의 조건을 추가하고, 용매의 양을 원물의 각 30배수와 40배수의 조건을 추가하여 연구해 보았으며 그 결과는 아래 표 4와 표 5에 나타냈다.Based on the 70% EtOH reflux 5-hour extraction method established as the optimum extraction condition for isoflavones, the extraction time was increased to add 7 hours to establish a clearer extraction condition, and the amount of solvent was increased by 30 times and 40 times the amount of the raw material. Research was conducted by adding conditions, and the results are shown in Tables 4 and 5 below.
표 4 및 도 5에서 보듯이 배당체 형태의 이소플라본은 추출시간과 용매의 양이 늘어남에 따라 비교적 더 많은 함량이 나타났고, 비배당체 형태의 이소플라본은 확립된 최적추출 조건보다 추출시간 7시간에서 비교적 더 많은 함량이 나타났으나 용매의 양과는 함량 변화의 차이가 크게 나타나지 않는 것을 알 수 있다.As shown in Table 4 and Figure 5, the content of isoflavones in the form of glycosides was relatively higher as the extraction time and the amount of solvent increased, and the isoflavones in the form of non-glycosides were extracted at 7 hours than the established optimal extraction conditions. It can be seen that a relatively higher content was shown, but the difference in content change did not appear significantly with the amount of the solvent.
종합해 보면 이소플라본 최적 추출조건으로 확립한 70% EtOH 환류 5시간에 비해 추출시간과 용매의 양을 늘리면 이소플라본의 함량은 비교적 높게 나타날 수 있으나, 제품화에 투자되는 시간과 비용을 대비해보면 70% EtOH 환류 5시간의 조건이 더 생산성에 적합한 추출 조건이라 판단할 수 있다.Overall, the content of isoflavones may appear relatively high when the extraction time and the amount of solvent are increased compared to the 70%
이상 본 발명의 특정 실시예에 관하여 도시하고 설명하였지만, 하기의 특허청구범위에 기재된 발명의 기술적 사상으로부터 벗어나지 않는 범위 내에서 본 발명은 다양하게 수정 또는 변형될 수 있다는 것이 이해될 필요가 있다.Although shown and described above with respect to specific embodiments of the present invention, it is necessary to understand that the present invention can be variously modified or modified within the scope not departing from the technical spirit of the invention described in the following claims.
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